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Progressive Crop Consultant May/June 2021

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<strong>May</strong> / <strong>June</strong> <strong>2021</strong><br />

The Potential of Ultraviolet Light to Suppress<br />

Grapevine Powdery Mildew<br />

Developing a Nitrogen Fertilizer Plan for Olive Orchards<br />

Soil Health on Every Farm<br />

Transitioning from Hand to Machine Harvesting<br />

of Blueberries<br />

<strong>May</strong>/<strong>June</strong> <strong>2021</strong><br />

VINEYARD REVIEW<br />

Pages 37-51<br />

Register at progressivecrop.com/conference<br />

<strong>2021</strong><br />

DAY<br />

REGISTER NOW AT<br />

wcngg.com/almond-day-<strong>2021</strong>/<br />

Volume 6: Issue 3<br />

Photo courtesy of David Gadoury, Cornell Agritech.


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4<br />

IN THIS ISSUE<br />

Transitioning from Hand<br />

to Machine Harvesting<br />

of Blueberries for Fresh<br />

Market<br />

PUBLISHER: Jason Scott<br />

Email: jason@jcsmarketinginc.com<br />

EDITOR: Marni Katz<br />

ASSOCIATE EDITOR: Cecilia Parsons<br />

Email: article@jcsmarketinginc.com<br />

PRODUCTION: design@jcsmarketinginc.com<br />

Phone: 559.352.4456<br />

Fax: 559.472.3113<br />

Web: www.progressivecrop.com<br />

CONTRIBUTING WRITERS & INDUSTRY SUPPORT<br />

12<br />

Developing a Nitrogen<br />

Fertilizer Plan for Olive<br />

Orchards<br />

Kris Beal<br />

Vineyard Team<br />

Robert Blundell<br />

Graduate Studen Researcher,<br />

UC Davis<br />

Akif Eskalen<br />

UCCE Specialist, Plant Pathologist,<br />

UC Davis<br />

Sonia Rios<br />

UCCE Subtropical Horticulture<br />

Farm Advisor, Riverside and San<br />

Diego Counties<br />

Steven Sargent<br />

University of Florida<br />

Fumiomi Takeda<br />

USDA-ARS<br />

16<br />

Pre-Plant Weed<br />

Management Followed<br />

by for Alfalfa Stand and<br />

Yield<br />

4<br />

Elizabeth J. Fichtner<br />

UCCE Farm Advisor, Kings and<br />

Tulare Counties<br />

David M. Gadoury<br />

Senior Research Associate, Plant<br />

Pathology and Plant-Microbe<br />

Biology Section, Cornell AgriTech,<br />

Geneva, NY<br />

Lisa Wasko DeVetter<br />

Washington State University<br />

Jeffrey Williamson<br />

University of Florida<br />

Eryn Wingate<br />

Agronomist, Tri-Tech Ag Products,<br />

Inc.<br />

22<br />

26<br />

Managing Soil and<br />

Structure Quality<br />

Avocado Invasive Insect<br />

Pests<br />

Mark S. Hoddle<br />

UCCE Specialist, Biological Control,<br />

UC Riverside<br />

Changying Li<br />

University of Georgia<br />

Sarah Light<br />

UCCE Agronomy Advisor, Sutter<br />

and Yuba Counties<br />

Craig Macmillan<br />

Niner Wine Estates<br />

Dr. Karl Wyant<br />

Vice President of Ag Science,<br />

Heliae Agriculture, Board of<br />

Directors, Western Region<br />

Certified <strong>Crop</strong> Adviser<br />

Wei Q. Yang<br />

Oregon State University<br />

32<br />

VINEYARD REVIEW<br />

38<br />

46<br />

Soil Health on Every Farm<br />

The Potential of Ultraviolet<br />

Light to Suppress<br />

Grapevine Powdery<br />

Mildew<br />

Irrigation Scheduling In<br />

Winegrape Vineyards<br />

16<br />

UC COOPERATIVE EXTENSION<br />

ADVISORY BOARD<br />

Surendra Dara<br />

UCCE Entomology and<br />

Biologicals Advisor, San Luis<br />

Obispo and Santa Barbara<br />

Counties<br />

Kevin Day<br />

UCCE Pomology Farm Advisor,<br />

Tulare and Kings Counties<br />

Elizabeth Fichtner<br />

UCCE Farm Advisor,<br />

Kings and Tulare Counties<br />

Katherine Jarvis-Shean<br />

UCCE Orchard Systems<br />

Advisor, Sacramento, Solano<br />

and Yolo Counties<br />

Steven Koike<br />

Tri-Cal Diagnostics<br />

Jhalendra Rijal<br />

UCCE Integrated Pest<br />

Management Advisor,<br />

Stanislaus County<br />

Kris Tollerup<br />

UCCE Integrated Pest Management<br />

Advisor, Fresno, CA<br />

Mohammad Yaghmour<br />

UCCE Area Orchard Systems<br />

Advisor, Kern County<br />

48<br />

Grapevine Trunk Diseases<br />

48<br />

The articles, research, industry updates, company profiles, and advertisements<br />

in this publication are the professional opinions of writers<br />

and advertisers. <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> does not assume any<br />

responsibility for the opinions given in the publication.<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 3


TRANSITIONING FROM HAND TO MACHINE<br />

HARVESTING OF BLUEBERRIES FOR<br />

FRESH MARKET<br />

A look at machine harvesting in blueberries research from around the country.<br />

By FUMIOMI TAKEDA | USDA-ARS<br />

CHANGYING LI | University of Georgia<br />

LISA WASKO DEVETTER | Washington State University<br />

JEFFREY WILLIAMSON | University of Florida<br />

STEVEN SARGENT | University of Florida<br />

WEI Q. YANG | Oregon State University<br />

Blueberry production acreage in<br />

the U.S. is expanding. Across the<br />

country, commercial blueberry<br />

growers are increasingly using over-therow<br />

(OTR) mechanical harvesters (MH)<br />

to pick their blueberries for fresh market<br />

(Figure 1). Growers everywhere are experiencing<br />

difficulties in finding sufficient<br />

labor for hand harvest operations and<br />

due to the rising costs of labor. Harvesting<br />

blueberries with OTR harvesters can<br />

significantly reduce the overall cost of<br />

harvesting to a fraction of that needed for<br />

hand harvesting (HH) and workers needed<br />

for harvest operations from about 500<br />

hours of labor per acre per year to as little<br />

as three hours of labor per acre per year.<br />

However, compared to hand harvesting,<br />

OTR harvesting causes more berry loss<br />

due to falling on the ground and green/<br />

red berries are harvested along with ripe,<br />

blue fruit.<br />

Detailed field testing of OTR harvesters<br />

for picking blueberries for the fresh market<br />

was conducted nearly 30 years ago in<br />

Michigan. That research in South Haven,<br />

Mich. evaluated the quality of blueberries<br />

harvested by hand and by four rotary<br />

and slapper harvesters that were used by<br />

growers at that time to harvest blueberries<br />

for processing. MH blueberries were<br />

sorted at the packinghouse (Figure 2).<br />

The most significant findings were a high<br />

percentage of detached blueberries had<br />

impact damage (Figure 3) and more<br />

than 20% of detached blueberries fell on<br />

the ground. The bruise damage was attributed<br />

to iImpact to the fruit created by<br />

the rapid actions of shaking rods and detached<br />

berries landing on the hard catching<br />

surface. Those studies revealed that<br />

blueberries harvested by the machines<br />

had a high percentage of blueberries with<br />

more than 20% of sliced surface area<br />

showing bruise damage (Figure 3 and 4,<br />

see page 5). Also, MH blueberries were<br />

much softer compared to hand harvested<br />

fruit. Their conclusion was that MH<br />

blueberries should not be cold-stored for<br />

more than two weeks while HH blueberries<br />

could go in controlled atmosphere<br />

storage for six weeks and air-shipped to<br />

Europe in excellent condition.<br />

Soon after, USDA engineers developed<br />

an experimental harvester called the V45<br />

harvester designed specifically to harvest<br />

fresh-market blueberries. It used a<br />

direct-drive shaker with an angled, double-spike-drum,<br />

a unique cane dividing<br />

and positioning system to push the canes<br />

out diagonally and cushioned catching<br />

Figure 1. A front view of Oxbo over-therow<br />

(OTR) blueberry harvester (all photos<br />

courtesy F. Takeda.)<br />

Figure 3. Bruise damage caused by mechanical<br />

harvesting makes the flesh dark and soft. Half of<br />

these berries have excessive bruising.<br />

Figure 2. Mechanical harvesting detaches<br />

unripe green fruit and clusters that<br />

must be sorted out on the grading line.<br />

4 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


Figure 4. Sliced examples of mechanically harvested blueberries. From left to right:<br />

Fruit with no internal bruise as indicated by no large discolored tissue; Fruit with<br />

impact damage at the stem end as indicated by discoloration inside the seed core;<br />

Fruit exhibiting damaged area from impact force to that triangular shaped, discolored<br />

section; and Discolored area has been highlighted in purple with SketchAndCalc<br />

program to calculate bruised area as 17% of the total cut surface area.<br />

surfaces to harvest fruit with minimum damage. With the V45<br />

harvester design, the detached blueberries dropped less than 15<br />

inches onto a soft neoprene sheet glued to a hard catch plate and<br />

soft sheet over the conveyor belt.<br />

These soft surfaces reduced impact force on the fruit detached<br />

by the V45 harvester. However, gluing a soft surface onto a hard<br />

surface has proven to show little reduction in bruise damage<br />

when harvesting is performed with conventional harvesters<br />

with two vertical drum shakers and berries falling more than 30<br />

inches. Only five V45 harvesters were sold by the now defunct<br />

B.E.I Inc. (South Haven, Mich.), although it was thought to have<br />

good fruit selectivity (low green fruit removal) compared to<br />

slapper models, little ground loss (fruiting cane pushed away<br />

from the crown) and superior quality over existing commercial<br />

harvesters at the time with two vertical drum shakers and either<br />

a metal or hard plastic catch surface.<br />

Sometimes, the fruit harvested by the V45 harvester had quality<br />

as good as commercially HH fruit. Its limitations were: 1) It<br />

needed to be driven much slower to avoid damaging bushes; 2) It<br />

could not harvest trellised rows or those with overhead sprinklers;<br />

and 3) It could not harvest all varieties, especially those<br />

with stiff, upright canes like ‘Jersey’ and many rabbiteye cultivars.<br />

The Fulcrum harvester made by A&B Packing Equipment<br />

(Lawrence, Mich.) has features like those of the V45 harvester.<br />

In the last ten years or so, U.S. blueberry farmers targeting the<br />

fresh market have been facing challenging economic situations<br />

(e.g., rising cost of hand picking, shrinking labor force, global<br />

competition, etc.) They and other specialty crop farmers have<br />

a greater interest in using automation and OTR machines to<br />

harvest their crop. The authors of this article have participated<br />

in different aspects of machine harvesting and sorting of<br />

blueberries to reduce the amount of internal bruise damage<br />

and in packing line sorting technology and damage detection<br />

systems to improve the quality of packed fruit. Several blueberry<br />

MH manufacturers (e.g., Oxbo International, Lynden, Wash.;<br />

A&B Packing Equipment, Lawrence, Mich.; BSK, Serbia; and<br />

FineFields, the Netherlands) have put more efforts devoted to<br />

developing MH systems that would impart low or no bruise<br />

damage so that fruits can be packed for fresh market. Following<br />

is a summary of recent developments in MH.<br />

Bruised Berries from Mechanical Harvesting<br />

Most OTR harvesters currently available are better suited for<br />

harvesting processed blueberries because they can cause<br />

excessive fruit damage. However, OTR machines have<br />

been used to pick blueberries for fresh market. In these<br />

instances, the fruit should be packed and transported to<br />

consumers as quickly as possible. When blueberries are<br />

HH, typically the picker gently picks ripe fruit selectively.<br />

In Chile and China, for example, ripe berries are picked<br />

individually to obtain high fresh quality.<br />

In the Pacific Northwest and elsewhere in North America,<br />

ripe fruit is often harvested by rubbing fruit cluster<br />

or sometimes by “tickling” them between the thumb<br />

and index finger and catching the detached berries in the palm<br />

and then placing them in a small harvesting bucket. In contrast,<br />

MH involves the shaking of the entire bush with rapid action of<br />

shaking rods to move canes back and forth. The cane movement<br />

causes ripe berries that need less fruit removal force than green/<br />

red berries to be displaced from the fruit stem (pedicel) and<br />

fall onto catching surfaces. Experienced MH operators make<br />

slight adjustments on machine settings to obtain good selectivity<br />

(minimize green/red berry removal and maximize ripe fruit<br />

removal).<br />

The blueberry bush can range from 3 to about 6 feet tall with<br />

fruit located from the tip of the canes to branches near the<br />

ground, which causes the berries located on the top part of bush<br />

to fall as much as 50 inches. When an OTR harvester picks blueberries<br />

and fruit falls from that height onto plastic catch plates<br />

and conveyor belts, one can hear berries hitting the hard catch<br />

surfaces.<br />

Based on this simplified description of the blueberry MH process,<br />

it was apparent that the interaction between the machine<br />

and fruit should be better understood. To do this, we used a<br />

custom-made miniature electronic sphere called the BIRD<br />

(blueberry impact recording device developed at the University<br />

of Georgia) to measure the fruit impacts during MH process in<br />

2010 and 2011. The BIRD sensor for this study weighed 14 g. The<br />

later version, BIRD II, was built to closely approximate the size<br />

and weight of a large blueberry (9/16-in diameter and weighed 6<br />

g) (Figure 5, see page 6).<br />

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<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 5


Peak acceleration(g)<br />

250<br />

200<br />

Day of bruise assessment<br />

Drop height (ft) Day of drop After 14 days<br />

150<br />

2 11.4 16.2<br />

3 100 14.4 19.7<br />

4 20.3 25.6<br />

2 50 3.1 4.9<br />

3 3.7 2.0<br />

0 0 6 12 18 24 30 36 42 48<br />

4 2.9 6.6<br />

0 0.6 2.0<br />

Drop height (inch)<br />

Continued from Page 5<br />

Along with documenting fruit impacts<br />

with a BIRD, a closeup video camera recorded<br />

the harvesting to pinpoint critical<br />

control points where most impacts were<br />

created. The results showed that the drop<br />

to the plastic catch plates on the harvester<br />

accounted for over 30% of all impacts<br />

on the BIRD, followed by the drop from<br />

the grading belt on the harvester into an<br />

empty lug (20%). When the lug is filled<br />

with blueberries, fruit-to-fruit impacts<br />

occur, which are much lower than when<br />

the fruit fall into an empty lug.<br />

Impacts created by the conveyor, including<br />

secondary bounce from the catch<br />

plates, and shaking rods combined for<br />

another 25% of recorded impacts. The<br />

remaining 25% of impacts that occurred<br />

before the sphere contacted the catch<br />

plate were classified as obscured impact<br />

events which could not be identified<br />

clearly from the video and were attributed<br />

to contact with the shaking rod,<br />

branches and the vertical tunnel panels.<br />

These measurements suggested that<br />

the most significant reduction in fruit<br />

impacts could be achieved by 1) Modifying<br />

the catch plates; 2) Reducing drop<br />

heights, either by restricting bush size,<br />

placing catching surfaces closer to the<br />

fruit or decreasing drop heights at other<br />

transition points; and 3) Placing softer<br />

surfaces at the transition points (e.g.,<br />

at transfer points in the fruit handing<br />

equipment on the top of platform.)<br />

The two parts of the impacts include<br />

the number of encounters between the<br />

sphere and different surfaces of the<br />

harvester and the magnitude of these<br />

impacts. In our study, the harvesting<br />

process was documented with video that<br />

recorded time-stamped impact events<br />

with the larger, heavier BIRD I sensor.<br />

Legend<br />

Stainless steel plate<br />

Glued foam pad on<br />

stainless steel plate<br />

Suspended foam pad<br />

Suspended fabric net<br />

Figure 6. The relationship between various contact surface materials and drop height. The<br />

impacts were collected with a BIRD II sphere dropped from different heights.<br />

Using these parameters, the OTR MH<br />

process was divided into four phases:<br />

Phase I (detachment and falling), Phase<br />

II (fruit hitting the catch plate/conveyor<br />

belt), Phase III (elevation from the<br />

conveyor/transfer belt to the top platform<br />

and conveyance through a trash blower)<br />

and Phase IV (dropping from the conveyor<br />

belt into the lug).<br />

Results showed that for the rotary drum<br />

shaker, the BIRD sensor recorded an<br />

average of 18 impacts in Phases I to IV.<br />

During Phase I, it is assumed blueberries<br />

detached by fast-moving harvesting rods<br />

that shake left and right, impact branches<br />

as they fall and/or are flung out to the<br />

side panel. There were about five impact<br />

events in Phase I, but magnitudes of<br />

these impacts proved to be less significant<br />

than initially assumed. In Phase<br />

II, the BIRD contacted the catch plate<br />

and usually only one or two events were<br />

recorded. The magnitude of the impacts<br />

in Phase II was extremely high compared<br />

to impacts recorded in Phases I, III and<br />

IV. Our results strongly suggested that<br />

the high impact that the falling blueberries<br />

receive at the point of contact with<br />

the catch plate injures the fruit, resulting<br />

in fruit softening and larger bruise while<br />

the fruit is in storage (Figures 3 and 4,<br />

see page 5).<br />

Further analysis was performed by<br />

dropping the large, heavier BIRD I sensor<br />

onto a hard-plastic catch plate from<br />

different heights (6, 12, 24, 36 and 48 in)<br />

(Figure 6). As expected, the impact values<br />

(peak acceleration at impact (g) increased<br />

sharply linearly with increasing<br />

drop height, ranging from 280 g at 6 in<br />

to about 800 g at 48 in (data not shown).<br />

In subsequent studies, impact measurements<br />

were made using the smaller and<br />

lighter-weight BIRD II sphere by dropping<br />

onto soft surfaces created by placing<br />

Figure 5 . BIRD II (red sphere) connected<br />

with a 4-pin connector to a laptop to<br />

charge its internal battery, initiate impact<br />

measurements or download collected data<br />

to a laptop or mobile device.<br />

cushioned padding on top of the hard<br />

plastic plates or by suspending the soft<br />

material (no hard surface underneath.)<br />

A wide range of impact values were obtained<br />

depending on the hardness of the<br />

catch plate (Figure 6). Impacts greater<br />

than 200 g were recorded on hard surfaces<br />

such as a stainless-steel sheet and a<br />

plastic catch plate even when the BIRD II<br />

was dropped from a height less than 30<br />

cm (12 in). Gluing a soft surface to a hard<br />

surface reduced impact; however, this<br />

type of surface still created high impact<br />

above a one-foot drop height such that<br />

blueberries falling 30 inches onto such a<br />

surface would still be bruised. For example,<br />

the suspended foam sheet we used<br />

in our harvest-assist blueberry picking<br />

machine in 2017 generated less than 200<br />

g even when the drop height was 42 in,<br />

but well above the 120 g at which ripe<br />

blueberries can be bruised by impact<br />

force. Only the netted fabric that acted<br />

like a hammock produced low enough<br />

impact force and kept the blueberries<br />

from getting bruised even when the fruit<br />

was dropped from a 48-in height. Thus,<br />

it was thought that replacing the hard,<br />

plastic fruit catching and collection surfaces<br />

with soft and durable catching surface<br />

materials and plate design features<br />

that prevent soft surface from contacting<br />

any hard surfaces underneath had the<br />

potential to improve the quality of MH<br />

blueberries and reduce bruise damage<br />

associated with high mechanical impact.<br />

In terms of mechanical impact to blueberry<br />

fruit, our research has shown that<br />

bruise damage and the loss of firmness<br />

in MH fruit can be decreased by reducing<br />

space between blueberries on<br />

the bush and the catching surface to 12<br />

Continued on Page 8<br />

6 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


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Continued from Page 6<br />

inches in the case of hard plastic fruit<br />

catching surfaces or by modifying the<br />

fruit catching surfaces to create a softer<br />

fruit landing surface. Ideally, the fruit<br />

catching surface should not exceed<br />

120 g impact even when the BIRD II is<br />

dropped from a height of 48 in (equivalent<br />

to the distance between the top of a<br />

large mature blueberry bush and catch<br />

plates on the harvester).<br />

The design of soft surfaces can be<br />

achieved by either incorporating netted<br />

material or a soft “rubber” sheet with no<br />

hard surfaces beneath for catching the<br />

fruit (Takeda and Wolford, U.S. Patent<br />

No. 9,750,188 and the Oxbo SoftSurface<br />

kit). For example, even with a soft<br />

surface insert in a hollowed-out plexiglass<br />

catch plate, the margins of the plate<br />

contributed to more than 20% of the<br />

exposed surface area. In addition, catch<br />

plates on the harvester overlapped with<br />

adjacent plates and rested on top of another<br />

plate. The outline of the plate below<br />

another created about 10% additional<br />

hard surfaces.<br />

When blueberries are HH, the packout<br />

is about 95% or better and fruit usually<br />

have little or no internal bruise damage<br />

(Table 1). The packout of MH blueberries<br />

is lower and typically ranges from 70% to<br />

slightly more than 80%. The remaining<br />

20% consists of soft, overripe and immature<br />

green- and red-colored berries.<br />

Commercial packing operations, for<br />

the most part, do not check for internal<br />

bruise damage in their MH blueberries.<br />

However, close inspections of MH<br />

blueberries packed into clamshells after<br />

sorting on commercial packing lines<br />

revealed berries were bruised (Figure 3,<br />

see page 4). Our studies evaluated different<br />

catch surface designs by inserting<br />

soft, flexible material to reduce internal<br />

bruise damage. We did record improvements<br />

in packout. However, neither<br />

the improvement in packout nor berry<br />

firmness approached that of HH fruit<br />

in the case of varieties Duke, Draper<br />

or southern highbush blueberry (SHB)<br />

Optimus even when they were harvested<br />

with OTR machines equipped with soft,<br />

flexible catch surfaces. The only exception<br />

to date has been the variety Last<br />

Day of bruise assessment<br />

Surface Drop height (ft) Day of drop After 14 days<br />

2 11 .4 1 6.2<br />

Hard<br />

3 14.4 1 9.7<br />

4 20.3 25.6<br />

2 3.1 4.9<br />

Soft<br />

3 3.7 2.0<br />

4 2.9 6.6<br />

Not dropped 0 0.6 2.0<br />

Table 1. Effect of catch surface (hard or soft) and drop height on internal bruise damage<br />

within one day of drop and after 14 days in cold storage (32 degrees F to 37 degrees F).<br />

Bruise damage is expressed as the percentage of cut surface area indicated by dark color<br />

(see Figure 4, see page 5).<br />

Call, where MH produced the quality<br />

approaching that of HH berries. MH of<br />

SHB Optimus produced higher-quality<br />

packout than other SHB varieties, such<br />

as Jewel, Star and Farthing, but even<br />

Optimus should not be cold-stored for<br />

more than one week. Our studies have<br />

shown that fresh market pack-out can<br />

be increased by installing a soft catch<br />

surface on the harvester, but the quality<br />

of HH blueberries has been better.<br />

Cultivar Susceptibility<br />

In a study conducted in Oregon, the<br />

susceptibility of 11 blueberry cultivars<br />

to impact damage was determined by<br />

dropping the fruit from 2-, 3-, and 4-foot<br />

heights onto a hard, plastic catch plate.<br />

Bruises developed more rapidly in rabbiteye<br />

cultivars (Ochlocknee, Powderblue<br />

and Overtime) than in northern highbush<br />

(NHB) and SHB cultivars. NHB<br />

cultivars Aurora, Cargo, Draper and Last<br />

Call had the least amount of bruising<br />

after two weeks in cold storage. Blue Ribbon,<br />

Legacy and Liberty had a moderate<br />

amount of bruising.<br />

These studies showed that simulated<br />

drop tests are useful in determining the<br />

potential of varieties for long-term cold<br />

storage and, more importantly, their<br />

potential to MH for fresh market. In a<br />

study in 2020 in Oregon, Draper and<br />

Legacy were MH with two OTR Oxbo<br />

harvesters, one fitted with and the other<br />

without the SOFTSurface kit. To date,<br />

the challenge for Oxbo Corporation and<br />

other machine manufacturers has been<br />

to procure soft materials that meet food<br />

safety standards and are durable for<br />

harvesting blueberries.<br />

The preliminary findings of this study<br />

were: 1) Machine harvesting with the<br />

SOFTSurface kit reduced fruit internal<br />

bruise damage in both Draper and Legacy<br />

fruits compared to those harvested<br />

with the unmodified OTR harvester as<br />

shown with a laboratory test (Table 1); 2)<br />

Draper and Legacy fruit harvested with<br />

the machine fitted with the SOFTSurface<br />

kit and sampled before sorting in the<br />

packing house were firmer compared<br />

to fruit harvested by the unmodified<br />

harvester; and 3) After one and two<br />

weeks in cold storage, there was no difference<br />

in firmness of berries harvested<br />

by machines fitted with and without the<br />

SOFTSurface kit.<br />

We found that fruit firmness-based sorting<br />

by itself may not be a good predictor<br />

of berry quality when MH blueberries<br />

are cold-stored for two weeks or more,<br />

but both Draper and Legacy blueberries<br />

picked by the OTR machine fitted with<br />

the SOFTSurface kit maintained better<br />

fruit firmness (>160 g/mm) values and<br />

lower internal bruise ratings in cold<br />

storage (Table 1). The improvements in<br />

fruit quality may well have been from a<br />

70% reduction in hard catch surface area<br />

in the SOFTSurface kit compared to the<br />

hard polycarbonate fruit catching surfaces<br />

in the regular harvesters. A laboratory<br />

test determined the effects of dropping<br />

blueberries from different heights onto<br />

either a hard (e.g., polycarbonate catch<br />

plate on conventional harvesters) or soft<br />

catch surface (e.g., prototype SOFTSurface<br />

kit) on internal bruise development<br />

(Table 1). Blueberries were sliced to<br />

visually assess bruise damage on the day<br />

of the drop test and after cold storage for<br />

two weeks.<br />

Young (~3-ft-tall) and mature (6-ft-tall)<br />

trellised Last Call blueberry plants were<br />

either HH or picked with a modified<br />

OTR machine. Fruit samples from both<br />

methods were manually sorted and<br />

evaluated for internal bruise damage<br />

on the day of harvest and the remaining<br />

samples were placed in cold storage.<br />

Cold-stored samples were taken out after<br />

8 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


two and four weeks and evaluated for internal bruise damage<br />

(Table 2). On the day of harvest (zero days after harvest), about<br />

80% of blueberries showed no bruise damage, and the remainder<br />

showed damage ranging from 1% to more than 50%. There<br />

was little change in internal bruise for samples from matures<br />

bushes that were either HH or MH. However, there was a<br />

dramatic decline in the percentage of fruit with no internal<br />

damage among the samples from machine harvesting of young<br />

plants.<br />

Our field observations of the Last Call bushes used in this<br />

study indicated that the canes of young plants were upright<br />

during the harvest and detached fruit fell straight down. In<br />

contrast, on the taller, mature bushes, the canes had grown<br />

well above the height of the trellis and they were leaning<br />

outward at the time of harvest. This placed the fruit away from<br />

the crown and less than 30 inches above the catching surface<br />

and may have contributed to reducing mechanical impacts in<br />

terms of numbers and magnitude, thus reducing the amount of<br />

internal bruise damage.<br />

Sorting Out Bruised Berries<br />

Blueberry growers in the Pacific Northwest and in Chile have<br />

expressed an interest in machine harvesting blueberries for the<br />

export market. The consensus among them is that the varieties<br />

for the export market must be firm and arrive at the destination<br />

in excellent condition after more than three weeks of cold<br />

storage and a transoceanic travel period. Our machine harvesting<br />

research has consistently shown that the MH blueberries<br />

generally had more internal bruise damage and shorter shelf<br />

life than the HH blueberries.<br />

Commercial optical sorting equipment are now available<br />

for grading blueberries. In the last three years, HH and MH<br />

blueberries have been processed on commercial blueberry<br />

packing lines in Oregon and Washington equipped with an<br />

optical sorter (e.g., UNITEC, BBC and MAF). For each packing<br />

line, samples of Draper and Legacy were taken from lugs prior<br />

to unloading onto the conveyor system, and a second group<br />

of samples were collected after the fruit had gone through the<br />

optical sorting machine. Samples from both locations were assessed<br />

for bruise damage (% bruised area). The bruise data are<br />

presented in Table 3 in which the data are expressed in terms<br />

of how the samples were distributed (e.g., blueberries with no<br />

damage to those that were severely bruised.) The analysis indicated<br />

that sorting by optical sorters did not remove blueberries<br />

with moderate to severe internal bruise damage.<br />

Next, we compared the blueberry fruit firmness value with the<br />

area of internal bruise damage on the sliced surface. One would<br />

likely assume that softer fruit will have more bruise damage.<br />

Our results and those from a report by Chilean researchers<br />

showed that this was not the case as shown by the low correlation<br />

coefficient (r-value) for these two fruit quality parameters.<br />

Whether the fruit had been collected from the packing line<br />

before or after the optical sorting machine, the correlation<br />

coefficients for berry firmness and bruise damage were less<br />

than 0.4 in NHB cultivars. This suggested that optical sorters<br />

in commercial blueberry packing houses were not effective in<br />

removing blueberries with internal bruise damage.<br />

Once more in the laboratory, we conducted drop tests in which<br />

HH Duke blueberries were dropped from a height of 62 inches<br />

to ensure that the samples would be bruised. A hyperspectral<br />

imaging system was used to locate and quantify bruise damage<br />

in each whole fruit (25 berries at a time). We then measured<br />

fruit firmness with a FirmTech II at the site of the bruise impact<br />

as determined by the imaging system. Then, the same fruit was<br />

rotated and additional firmness measurements were taken at 90<br />

and 180 degrees from the bruised site.<br />

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0 1 2 3 4 5<br />

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OTR machine Old 89 0 3 3 4 2<br />

Hand Old 7 8 1 6 1 0 5 1<br />

After 1 4 days in cold storage<br />

OTR machine Young 47 3 9 9 1 3 21<br />

OTR machine Old 7 7 2 6 6 6 4<br />

Hand Old 80 2 1 0 3 5 2<br />

After 28 days in cold storage<br />

OTR machine Young 43 2 8 15 16 16<br />

OTR machine Old 86 1 3 6 2 3<br />

Hand Old 86 1 3 6 2<br />

*The IBD categories are on a scale of 0 to 5, with 0 representing 0% IBD, 1 representing 1 % to 5% IBD, 2<br />

representing 6% to 1 0%, 3 representing 1 1 % to 20%IBD, 4 representing 21 % to 50% IBD and 5<br />

representing more than 51 % IBD.<br />

**Fruit samples were randomly collected on the day of harvest.<br />

Table 2. Percent of blueberries in each internal bruise damage (IBD) category<br />

as affected by hand harvesting and harvesting with a modified OTR<br />

machine and the age of ‘Last Call’ northern highbush blueberry immediately<br />

after harvesting and after two and four weeks in cold storage.<br />

Continued on Page 10<br />

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Internal bruise damage (% of samples in each category)<br />

Cultivar Location 0 1 2 3 4 5<br />

Draper Before 33.5 1 .5 21 .5 30.0 1 1 .0 2.5<br />

After 22.5 7.5 26.5 30.0 1 1 .0 2.5<br />

Legacy Before 47.0 1 .0 21 .5 20.5 1 3.0 2.0<br />

After 23.5 1 .0 1 7.5 30.0 1 8.5 9.5<br />

Table 3. Determination of internal bruise damage in machine-harvested Draper and Legacy<br />

blueberry samples collected from packing line locations either before or after inspection<br />

with an optical sorter. Samples were sliced through their equator and the bruised area was<br />

assessed visually as the percentage of sliced area and converted to a value between 0 and 5<br />

using a 5rating scale: 0= no bruise, 1= 1% to 5% bruised, 2= 6% to 10%, 3= 11% to 20%, 4=21%<br />

to 50% and 5= greater than 50%.<br />

Continued from Page 9<br />

The analysis showed that at the site of<br />

the bruise damage, the average fruit<br />

firmness was 149 g/mm. However, at the<br />

sites that were 90 and 180 degrees from<br />

the impacted location, the firmness was<br />

greater than 162 g/mm. This meant that<br />

a lower firmness value was detected<br />

when the damaged area was purposely<br />

used to determine firmness, resulting<br />

in a much higher r-value between fruit<br />

firmness and internal bruise damage<br />

values. Fruit that were firm at the time<br />

of packing (e.g., >180 g/mm value using<br />

a FirmTech II instrument) were found to<br />

have internal bruise damage exceeding<br />

15%. In the near future, our research<br />

team will sort MH blueberries with<br />

this imaging system to separate whole<br />

unbruised and bruised blueberries and<br />

conduct postharvest quality evaluation<br />

for unbruised and bruised MH blueberries<br />

to determine the shelf life of each<br />

group with an eye toward exporting MH<br />

blueberries to distant Asian markets. Of<br />

course, taking this non-destructive imaging<br />

system from the laboratory bench<br />

to integrating it into commercial optical<br />

sorting machines for IBD detection and<br />

sorting is a challenge facing the machine<br />

manufacturers.<br />

Conclusions<br />

More blueberries for fresh market are<br />

being machine harvested.<br />

Machine harvested blueberries have<br />

more internal bruise damage.<br />

On-going research is developing a better<br />

understanding of what causes bruising<br />

and working with harvest machine manufacturer<br />

to reduce bruise damage.<br />

New sensor technologies for blueberry<br />

sorting could assist in reducing bruised<br />

berries in fresh packs.<br />

Our research has shown that to make<br />

MH more profitable for blueberry growers,<br />

the current OTR harvesters must<br />

be modified to reduce impact damage<br />

and ground loss. Cultivars with superior<br />

machine harvestability are being<br />

released by blueberry breeding programs,<br />

and research must continue to develop<br />

equipment capable of harvesting blueberries<br />

with less bruise damage. The sorting<br />

system on the packing line for MH<br />

fruit must be improved with a greater<br />

precision to eliminate fruit with severe<br />

internal bruise damage. This would ensure<br />

that the quality of MH blueberries<br />

going into clamshells would be as good<br />

as HH fruit. Blueberry growers in some<br />

regions can then contemplate having<br />

MH blueberries packed for export. Also,<br />

proper training and pruning of blueberry<br />

bushes to maintain a small crown can<br />

increase MH efficiency. These changes<br />

will help in making small, incremental<br />

improvements in increasing pack-outs<br />

and fresh quality of packed blueberries.<br />

Finally, in order for MH blueberries to<br />

have quality that is as good as HH fruit,<br />

the blueberry industry needs to be willing<br />

to make changes by growing superior<br />

varieties, modifying how blueberry bushes<br />

are grown and harvested, and improving<br />

how the fruit is sorted. This will take<br />

a concerted effort from growers, breeders,<br />

horticulturists, engineers and supply<br />

chain specialists. These changes could<br />

lead to blueberry fields that look different<br />

from what we see today, with radically<br />

different ways of harvesting blueberries<br />

and technological advancements for sorting<br />

blueberries with the goal of improving<br />

the quality of MH blueberries going<br />

into clamshells.<br />

In terms of harvesting and packing technology,<br />

it is envisioned that U.S. blueberry<br />

growers will be using robotic harvesting<br />

systems in the field or in warehouses<br />

with specialized automated or semi-automated<br />

harvesting machines that will<br />

avoid damaging berries, have better<br />

selectivity to reduce green berries picked<br />

and sort out over-ripe and diseased<br />

berries in the field. In packing houses,<br />

new non-destructive technologies are<br />

needed that will be capable of analyzing<br />

the blueberry fruit surface and below the<br />

skin and sort fruit for quality (large size,<br />

high sweetness, flavor, bloom, no bruise<br />

damage and color). These advances will<br />

facilitate market segmentation and high<br />

prices as one U.S. and several European<br />

blueberry distributors are doing already<br />

with HH blueberries.<br />

This research was supported in part by<br />

the U.S. Department of Agriculture<br />

agencies (Agricultural Research Service<br />

(Project No. 8080-21000-028, National<br />

Institute for Food and Agriculture<br />

(Agreement No. : 2008-51180-19579 and<br />

2014-51181-22471), Agricultural Marketing<br />

Service (FY 18 Oregon Department<br />

of Agriculture SCBG to WQY and<br />

FY18 Washington SCBG to LWD), U.S.<br />

Highbush Blueberry Council, Chilean<br />

Blueberry Committee and Naturipe<br />

Farms Blue Challenge.<br />

Our gratitude goes to blueberry growers<br />

and packers in Waldo, Fla.; Alma<br />

and Homerville, Ga.; South Haven and<br />

Grand Junction, Mich.; Kingsburg and<br />

Stockton, Calif.; Hillsboro, Independence<br />

and Roseburg, Ore.; and Burlington,<br />

Prosser, Lynden and Sumas, Wash.,<br />

and in Chile who provided much needed<br />

in-kind support to the harvest project. A<br />

special thanks goes to Oxbo International<br />

Corporation which has collaborated<br />

with the group since 2014.<br />

Authors are employees of USDA-ARS (FT,<br />

fumi.takeda@usda.gov) Oregon State<br />

University (WQY, wei.yang@oregonstate.<br />

edu), University of Georgia (CL, cyli@uga.<br />

edu), Washington State University (LWV,<br />

lisa.devetter@wsu.edu) and University of<br />

Florida (SS, sasa@ufl.edu and JW, jgrw@<br />

ufl.edu).<br />

Mention of trade names or commercial products<br />

in this publication is solely for the purpose<br />

of providing specific information and does not<br />

imply recommendation or endorsement by<br />

the U.S. Department of Agriculture. USDA is an<br />

equal opportunity provider and employer.<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

10 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


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Developing a Nitrogen<br />

Fertilizer Plan for Olive<br />

Orchards<br />

By ELIZABETH J. FICHTNER | UCCE Farm Advisor, Kings and Tulare Counties<br />

Plant tissues pruned from the trees are typically flail mowed for reincorporation into the orchard floor. Nitrogen<br />

incorporated in this biomass will be released by mineralization (courtesy E. Fichtner.)<br />

Nitrogen management plans<br />

(NMP) for California olive<br />

orchards are essential for the Irrigated<br />

Lands Regulatory Program and<br />

can increase net return. A good NMP<br />

has the potential to increase yield, improve<br />

oil quality and mitigate biotic and<br />

abiotic stresses while reducing nitrogen<br />

losses from the orchard.<br />

Olives differ from other orchard crops<br />

in California in that they are both evergreen<br />

and alternate bearing. Individual<br />

leaves may persist on the tree for two to<br />

three years. Leaf abscission is somewhat<br />

seasonal, with most leaf drop occurring<br />

in late spring.<br />

Rapid shoot expansion occurs on<br />

non-bearing branches during the hottest<br />

part of the summer (July/August)<br />

on ‘Manzanillo’ olives in California.<br />

The fruit on bearing branches limits<br />

current-season vegetative growth.<br />

Olives bear fruit on the prior year’s<br />

growth, and the alternate bearing cycle<br />

is characterized by extensive vegetative<br />

growth in one year followed by<br />

reproductive growth the following year<br />

(Figure 1). With bloom occurring in<br />

late April to mid-<strong>May</strong>, fruit set can be<br />

estimated in early July, allowing for<br />

consideration of crop load while interpreting<br />

foliar nutritional analysis in late<br />

July-early August.<br />

Critical Nitrogen Values<br />

Foliar nitrogen content in July/August<br />

should range from approximately 1.3%<br />

to 1.7% to maintain adequate plant<br />

health. The symptoms of nitrogen<br />

deficiency manifest when foliar nitrogen<br />

content drops to 1.1% N. As leaves<br />

become increasingly nitrogen deficient,<br />

foliar chlorosis progresses from yellow-green<br />

to yellow. Leaf abscission is<br />

common at nitrogen levels below 0.9%.<br />

Nitro-<br />

gen deficiency in olive is associated<br />

with a reduced number of flowers per<br />

inflorescence, low fruit set and reduced<br />

yield.<br />

Table 1. The quantity of nitrogen removed per ton of fruit at harvest<br />

varies by variety.<br />

Variety<br />

1 ton per acre<br />

crop<br />

(lbs. Nitrogen)<br />

Arbequina 6.81<br />

Arbosana<br />

Koroneiki<br />

Manzanillo<br />

6.39<br />

7.45<br />

8.04<br />

5 ton per acre<br />

crop<br />

(lbs. Nitrogen)<br />

34.07<br />

31.97<br />

37.26<br />

40.22<br />

Year 1: Spring ON bloom<br />

Year 1 - Summer ON crop<br />

Year 2 - Spring OFF bloom<br />

Year 2 - Summer OFF crop<br />

10 ton per acre<br />

crop<br />

(lbs. Nitrogen)<br />

68.14<br />

63.94<br />

74.51<br />

80.44<br />

Source: Total Fruit Nutrient Removal Calculator for Olive in California B. Krueger (UCCE Glenn County)<br />

and R. Rosecrance (California State University, Chico).<br />

Year 3 - Spring ON bloom<br />

Figure 1. Illustrative model of the alternate bearing cycle of olive (courtesy<br />

Carol Lovatt, UC Riverside.)<br />

12 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


Excess nitrogen (>1.7%) adversely affects oil quality. Oil with<br />

low polyphenol concentration is associated with orchards<br />

exhibiting excess nitrogen fertility. Since polyphenols are<br />

the main antioxidant in olive oil, reduced polyphenol levels<br />

are associated with reduced oxidative stability.<br />

Nitrogen content may impact orchard susceptibility to biotic<br />

and abiotic stresses. For example, while excess nitrogen<br />

content has been associated with increased tolerance to<br />

frost prior to dormancy, it is associated with sensitivity to<br />

low temperatures in spring (post-dormancy). High nitrogen<br />

content has also been associated with increased susceptibility<br />

to peacock spot, a foliar fungal disease on olive.<br />

Foliar Sampling for Nitrogen Analysis<br />

By convention, foliar nutrient analysis is conducted in late<br />

July to early August in California. Fully-expanded leaves<br />

are collected from the middle to basal region of the current<br />

year’s growth at a height of about five to eight feet from<br />

the ground. To capture a general estimate of the nitrogen<br />

status of the orchard, samples should be taken from 15 to 30<br />

trees, with approximately five to eight leaf samples collected<br />

per tree. Leaves for analysis should only be collected from<br />

non-bearing branches. Growers may find it beneficial to<br />

make note of the ‘ON’ and ‘OFF’ status in the historical<br />

records of each block. The orchard bearing status, combined<br />

with anticipated yield and foliar analysis, will guide decisions<br />

for nitrogen applications the following<br />

year.<br />

Figure 2. Approximate distribution of nitrogen in the aboveground<br />

portion of olive trees.<br />

33% 19%<br />

44%<br />

4%<br />

Leaves<br />

Twigs/Branches/Trunk<br />

Fruit (pulp)<br />

Fruit (pit)<br />

Adapted from: Rodrigues et al. 2012<br />

Figure 2. Approximate distribution of nitrogen in the aboveground portion of<br />

olive trees (source: Rodrigues et al. 2012.)<br />

Estimation of Nitrogen<br />

Removed from the Orchard<br />

The easiest component of orchard nitrogen<br />

loss to estimate is the N in the harvested<br />

fruit. A ton of harvested olives removes<br />

approximately 6-8 lbs N from the orchard.<br />

The quantity of nitrogen in the fruit varies<br />

slightly between olive varieties (Table 1,<br />

see page 12). Growers can use the Fruit<br />

Removal Nutrient Calculator for Olive on<br />

the CSU Chico website to gain estimates of<br />

N removal by the three oil varieties (Arbequina,<br />

Arbosana and Koroneiki) and the<br />

Manzanillo table olive. This tool was developed<br />

by Dr. Richard Rosecrance, a professor<br />

at CSU Chico, and Bill Krueger UCCE farm advisor. To<br />

access the Fruit Removal Nutrient Calculator for Olive, visit<br />

rrosecrance.yourweb.csuchico.edu/Model/OliveCalculator/<br />

OliveCalculator.html.<br />

Pruning may generate a second component of nitrogen loss<br />

Continued on Page 14<br />

Nitrogen Distribution in the Tree<br />

Over 75% of the aboveground nitrogen in<br />

the olive tree is incorporated in the vegetative<br />

biomass (Figure 2). The twigs, secondary<br />

branches, main branches and trunk<br />

account for approximately 33% of aboveground<br />

nitrogen. 23% of the aboveground<br />

nitrogen is harbored in the fruit, with the<br />

majority in the pulp (19%). Fruit is only an<br />

important nitrogen sink during the initial<br />

phase of growth. As fruit size increases, the<br />

N concentration decreases due to dilution.<br />

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Continued from Page 13<br />

from orchards. The best practice to mitigate<br />

nitrogen loss from pruning is to<br />

reincorporate the pruned material into<br />

the orchard floor by flail mowing. The<br />

nitrogen in this organic material will<br />

gradually become available to the trees<br />

through mineralization.<br />

In mature orchards, the wood removed<br />

by annually pruning is approximately<br />

equal to the annual vegetative growth.<br />

Consequently, the input and removal of<br />

nitrogen in vegetative growth is cyclic<br />

and almost equal in mature orchards.<br />

In young orchards, nitrogen inputs are<br />

utilized to support vegetative growth<br />

and little N is removed from the<br />

orchard in prunings or crop. During<br />

this time, nitrogen must be supplied to<br />

meet the demand to support vegetative<br />

growth. It is estimated that approximately<br />

2.5 lbs N is required to produce<br />

1000 lbs fresh weight of tree growth.<br />

Nitrogen Use Efficiency<br />

Not all the nitrogen supplied to the orchard<br />

from fertilizer and other inputs<br />

(i.e., organic matter, irrigation water) is<br />

utilized for tree growth and crop production.<br />

A fraction of nitrogen is lost<br />

from the orchard ecosystem through<br />

processes such as runoff, leaching and<br />

denitrification. Efficiency varies among<br />

orchards, with some orchard systems<br />

exhibiting higher nitrogen utilization<br />

rates than others. The efficiency generally<br />

varies from 60% to 90%. Higher<br />

values denote more efficient use of nitrogen<br />

inputs. To estimate the amount<br />

of nitrogen to supply an orchard, the<br />

demand is divided by the estimated<br />

efficiency. For example, if nitrogen demand<br />

is 50 lbs. per acre and efficiency<br />

is estimated at 0.8, then 62.5 lbs N per<br />

acre should be applied.<br />

Nitrogen management plans are<br />

site-specific and designed to meet orchard<br />

and crop demand while reducing<br />

environmental losses. Nitrogen utilization<br />

is never 100% efficient. Nitrogen<br />

use efficiency can be maximized by<br />

minimizing losses from irrigation and<br />

fertilization practices while utilizing foliar<br />

analysis and knowledge of alternate<br />

bearing status to fine-tune applications.<br />

References<br />

Fernández-Escobar, et al. 2011. Scientia Horticulturae<br />

127:452–454.<br />

Hartman, H.T. 1958. Cal Ag. Pgs 6-10.<br />

Rodrigues, M.A. et al. 2012. Scientia Horticulturae<br />

142:205-211.<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

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PRE-PLANT WEED MANAGEMENT FOLLOWED BY IN-SEASON<br />

CONTROL FOR IMPROVED ALFALFA STAND AND YIELD<br />

By SARAH LIGHT | UCCE Agronomy Advisor, Sutter and Yuba Counties<br />

Good stand establishment is<br />

critical for productivity of an<br />

alfalfa field both in year one<br />

and in subsequent years. Weed competition<br />

during stand establishment<br />

may be irreversible because it can<br />

reduce alfalfa root growth and lead<br />

to thinner alfalfa stands and lower<br />

forage quality. Thus, it is important to<br />

have good weed control during alfalfa<br />

stand establishment.<br />

This project evaluated the efficacy of<br />

weed control options for both conventional<br />

and organic growers. Pre-plant<br />

mechanical cultivation and glyphosate<br />

spray were evaluated with the<br />

goal of providing regionally relevant<br />

information about an integrated weed<br />

management tool for improved stand<br />

establishment.<br />

Methods<br />

Six treatments (Table 1) were replicated<br />

three times in the field. Main plots<br />

were a pre-plant treatment (either no<br />

pre-plant treatment, pre-plant tillage<br />

or pre-plant glyphosate). Additionally,<br />

half of the plots received later in-season<br />

treatment (Table 1): either no treatment<br />

or Raptor application in-season after<br />

the crop had emerged.<br />

This field was planted in the spring in<br />

the Sacramento Valley of California.<br />

Weeds were germinated with winter<br />

rains. On some plots (treatments 3 and<br />

6), pre-plant glyphosate was sprayed<br />

on plots on January 31, 2020 at a rate of<br />

three pints glyphosate/acre. On other<br />

plots (treatments 2 and 5), mechanical<br />

cultivation was implemented on<br />

February 11, 2020 once the soil was<br />

dry enough. This cultivation was very<br />

shallow (top few inches of the soil) to<br />

avoid bringing new weed seeds to the<br />

soil surface.<br />

Alfalfa seed was flown on the field on<br />

March 4, 2020, and the field was then<br />

EXPERIMENTAL TREATMENTS<br />

T RE A TMENT N UM BER PRE -PLA NT TREA TMEN T IN -S E A S O N TRE ATMEN T HERBICIDE R A TE (S )<br />

1 N o n e N o n e N / A<br />

2 T illa g e N o n e N / A<br />

3 G ly p h o s a te N o n e 3 p t / a c r e<br />

4 N o n e R a p to r 6 fl o z / a c r e<br />

5 T illa g e R a p to r 6 fl o z / a c r e<br />

6 G ly p h o s a te R a p to r 3 p t / a c r e + 6 fl o z / a c r e<br />

Table 1. Six treatments were replicated three times in the field.<br />

ring-rolled to cover seed and get good<br />

seed-to-soil contact. The field was then<br />

irrigated for germination a week later.<br />

In-season weeds were controlled on<br />

some of the plots (treatments 4, 5 and<br />

6) with a tank mix of Raptor (Imazamox<br />

Ammonium Salt) at 6 fl oz per<br />

acre and Buctril (Bromoxnil) on April<br />

25, 2020.<br />

Data Collected<br />

Baseline weed counts were taken on<br />

January 29, 2020 from all plots before<br />

treatment implementation but after<br />

weed germination. Individual broadleaf<br />

weeds and grasses + sedges were counted<br />

in three random 20x20 cm quadrats<br />

per plot. Plants were counted on this<br />

date because weeds and alfalfa plants<br />

were small and percent cover would not<br />

have captured potential differences.<br />

Weed counts were taken an additional<br />

three times between planting and first<br />

cutting from all plots. In-season weed<br />

counts were taken as percent cover<br />

in which the area of the quadrat was<br />

broken up in percent covered with<br />

broadleaves, grasses + sedges, bare soil<br />

and alfalfa. On April 9 and <strong>May</strong> 14,<br />

2020, weed counts were taken in three<br />

random 20x20 cm quadrats per plot,<br />

and on <strong>June</strong> 8, 2020, percent cover was<br />

observed in three random square-meter<br />

quadrats per plot. The larger quadrat<br />

was used for percent cover on <strong>June</strong> 8<br />

because alfalfa and weeds were tall<br />

at this time and the meter by meter<br />

square allowed for more accurate representation<br />

of each plot.<br />

Plots were hand harvested on <strong>June</strong> 8,<br />

2020 prior to first cutting by the grower,<br />

which occurred on <strong>June</strong> 10. Two<br />

square-meter areas of each plot, which<br />

were representative of the larger plot,<br />

were cut. Yield biomass was separated<br />

into weeds and alfalfa, dried, weighed<br />

separately and then converted to a<br />

pounds dry matter/acre basis.<br />

Finally, on <strong>June</strong> 23, 2020, following first<br />

cutting, alfalfa stand counts were taken<br />

in all plots by counting the number<br />

of alfalfa plants in three 20x20 cm<br />

quadrats.<br />

Baseline and Early Weed Counts<br />

The first weed counts (January 29, 2020)<br />

collected before treatment implementation<br />

showed the average count for<br />

grasses + sedges for all plots was zero at<br />

this count. For broadleaves, there were<br />

no significant differences by treatment,<br />

but there were significantly more weeds<br />

in the side of the field with no in-season<br />

control compared to the side where<br />

Raptor was applied in-season.<br />

April 9, 2020 Weed Counts<br />

Grasses + sedges: There were not many<br />

grasses or sedges in the field.<br />

Broadleaves: There were significantly<br />

less broadleaves in the plots that had<br />

pre-plant weed control (glyphosate or<br />

tillage).<br />

Alfalfa: Alfalfa plants were small at this<br />

counting date; however, there were<br />

significant treatment differences with<br />

Continued on Page 18<br />

16 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


THE BEST WAY TO MANAGE PATHOGENS<br />

BEFORE THEY BECOME AN ISSUE.<br />

TriClor is chloropicrin based and can be used as a standalone or as a complement to Telone® depending<br />

on your orchard redevelopment needs. When targeting soil borne disease and nematodes, TriClor<br />

and Telone® can be applied in a single pass. This reduces application costs, promotes early root development,<br />

and improves soil health. For more information about TriClor and Telone or to schedule an<br />

application contact TriCal, Inc.<br />

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*TriClor and Telone are federally Restricted Use Pesticides.<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 17


Percent Broadleaf Weeds<br />

Percent Alfalfa Plants<br />

Yield (lb/A in 100% dry weight<br />

100<br />

75<br />

50<br />

25<br />

0<br />

100<br />

75<br />

50<br />

25<br />

0<br />

4000<br />

3000<br />

2000<br />

1000<br />

0<br />

PERCENT COVER OF BROADLEAVES AT FIRST CUTTING (6/8/20)<br />

No pre-plant treatment Glyphosate pre-plant Tillage pre-plant<br />

Raptor In-season<br />

PERCENT COVER OF ALFALFA AT FIRST CUTTING (6/8/20)<br />

No pre-plant treatment<br />

Glyphosate pre-plant<br />

Raptor In-season<br />

No In-season control<br />

ALFALFA YIELDS AT FIRST CUTTING (6/8/20)<br />

Tillage pre-plant<br />

Figure 2. Effect of early weed management and follow-up in-season weed management on<br />

percent cover of alfalfa at first cutting.<br />

No pre-plant treatment Glyphosate pre-plant Tillage pre-plant<br />

Raptor In-season<br />

No In-season control<br />

Figure 1. Broadleaf weed cover at first harvest as affected by pre-plant and<br />

in-season weed control (<strong>June</strong> 8, 2020) (all figures courtesy S. Light.)<br />

No In-season control<br />

Figure 3. Yield of the first cutting of alfalfa as affected by affected by early season and<br />

in-season weed management.<br />

# Alfalfa plants per 20x20cm quadrant<br />

ALFALFA STAND COUNTS AFTER FIRST CUTTING<br />

No pre-plant treatment Glyphosate pre-plant Tillage pre-plant<br />

Raptor In-season<br />

No In-season control<br />

Figure 4. Alfalfa stand counts at first cutting showing significant effects of early<br />

pre-plant treatments as well as the effect of in-season herbicide treatment.<br />

Stand count data was collected after first cutting (see results in Figure 4.) (All<br />

photos by S. Light.)<br />

Continued from Page 16<br />

the pre-plant weed control treatments having more<br />

alfalfa than the control.<br />

<strong>May</strong> 14, 2020 Weed Counts*<br />

Grasses + sedges: There were not many grasses or<br />

sedges in the field.<br />

Broadleaves: There were significantly less broadleaves<br />

in the plots that had pre-plant weed control<br />

(glyphosate or tillage) and in the plots that had<br />

Raptor applied in-season.<br />

Alfalfa: There was significantly more alfalfa in the<br />

plots that had pre-plant weed control (glyphosate<br />

or tillage) and in the plots that had an in-season<br />

herbicide.<br />

*Data not shown<br />

Broadleaf Weeds Dominated at First Cutting<br />

There were significantly more broadleaf weeds in<br />

the plots that had no pre-plant weed control (glyphosate<br />

or tillage) (Figure 1). Additionally, the plots<br />

that had Raptor applied in-season reduced broadleaf<br />

weeds down to negligible levels compared with<br />

no in-season treatment (Figure 1). There were not<br />

many grasses or sedges in the field; however, there<br />

were more grasses in the side of the field with no<br />

in-season herbicide application.<br />

Alfalfa Stand<br />

There was significantly more alfalfa at first cutting<br />

in the plots that had pre-plant weed control<br />

(glyphosate or tillage) and in the plots that had an<br />

in-season herbicide (Figure 2). Weeds in the no<br />

pre-plant treatment essentially killed many of the<br />

young seedlings due to weed competition. This is a<br />

key issue since early growth and establishment of<br />

alfalfa seedlings sets the stage for vigorous growth<br />

over many years of production. This is demonstrated<br />

by the number of alfalfa plants in a 20x20<br />

cm quadrant after first cutting (Figure 4). There<br />

were significant differences in the alfalfa stand after<br />

first cutting. With regard to pre-plant treatments,<br />

both glyphosate spray and tillage pre-plant significantly<br />

increased alfalfa stand compared to the plots<br />

with no pre-plant treatment.<br />

Enhanced Yields<br />

Alfalfa yields were near zero for the plots where early<br />

control was not applied (Figure 4). Additionally,<br />

yields were improved over 90% when an in-season<br />

weed control was applied (Figure 4). This yield data<br />

is only for the first cutting of the stand, not for the<br />

full first year of production. There were significant<br />

differences in alfalfa yield between pre-plant treatments<br />

and plots that had no pre-plant weed control<br />

(Figure 3). Both the glyphosate and tillage pre-plant<br />

18 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


treatments increased yields. In addition,<br />

the Raptor spray significantly increased<br />

yields compared to plots without<br />

in-season control.<br />

A combination of early weed control<br />

combined with in-season weed control<br />

was the most successful at controlling<br />

weeds and enhancing alfalfa yields.<br />

Biomass was separated into alfalfa<br />

(Figure 3, see page 18) and weeds after<br />

plots were hand-harvested. Alfalfa and<br />

weeds were then weighed separately<br />

by plot. There were significantly more<br />

weeds by weight in the side of the field<br />

that did not get the herbicide spray in<br />

season compared to the side that did<br />

get an herbicide spray. However, within<br />

one side of the field (Raptor or not),<br />

there were no significant differences<br />

by pre-plant treatment. In other words,<br />

even though there was more alfalfa in<br />

the plots with pre-plant weed control,<br />

there were also more weeds. The photo<br />

taken at harvest show how heavy the<br />

weed pressure was even in plots with<br />

Glyphosate and tillage pre-plant that<br />

did not have in-season herbicide application.<br />

When comparing plots with the same<br />

pre-plant treatments with or without<br />

in-season herbicide spray, plots that<br />

were tilled pre-plant did not have<br />

significantly different stand counts<br />

regardless of in-season herbicide treatment.<br />

However, within the plots that<br />

were sprayed with glyphosate pre-plant,<br />

those that also were sprayed with Raptor<br />

in-season had significantly higher<br />

alfalfa stand counts than those without<br />

in-season control.<br />

Conclusions<br />

The data shows that controlling weeds<br />

prior to planting, either with shallow<br />

tillage or an herbicide spray (glyphosate),<br />

will reduce weed pressure,<br />

increase yields and lead to a stronger<br />

alfalfa stand after first cutting. There<br />

were also differences between plots<br />

that got an in-season herbicide and<br />

those that did not. Yields were highest<br />

in plots that had both pre-plant weed<br />

control and an in-season herbicide. The<br />

plots with the highest stand counts after<br />

first cutting were also the plots that had<br />

Continued on Page 20<br />

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<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 19


A combination of early weed control combined with in-season<br />

weed control was the most successful at controlling weeds and<br />

enhancing alfalfa yields.<br />

This photo taken at harvest shows how heavy the weed pressure was even<br />

in plots with glyphosate or tillage pre-plant that did not have in-season<br />

herbicide application.<br />

<strong>Crop</strong> Resilience<br />

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Beneficial fungi also help suppress<br />

disease and mitigate abiotic stresses<br />

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Biological fertility programs renew<br />

the soil with diverse fungi, which<br />

increases humus and water-holding<br />

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Continued from Page 19<br />

both pre-plant and in-season weed<br />

control. However, the stand in the preplant<br />

treatment plots that did not have<br />

an in-season herbicide application still<br />

had relatively high alfalfa stand counts<br />

after first cutting. This means that with<br />

early effective weed control, the alfalfa<br />

stand may be more robust for future<br />

cuttings, even if weed pressure was<br />

high initially. As shown in the provided<br />

photos, the alfalfa was robust in the<br />

understory of the canopy, even when<br />

broadleaf weeds were very large. By<br />

first cutting, many broad leaf weeds<br />

had gone to flower, so they likely would<br />

not return after first cutting. However,<br />

when included in the harvest, these<br />

weeds reduce quality and price of the<br />

hay and also contribute seed to the<br />

weed-seed population in the field.<br />

Ideally, both pre-plant and in-season<br />

weed control would be implemented to<br />

get highest yields, quality, a vigorous<br />

stand and ensure animal safety. However,<br />

growers (particularly organic) may<br />

be able to do a pre-plant tillage to control<br />

weeds and establish a good alfalfa<br />

stand, accept some yield reduction and<br />

additional weed pressure leading up<br />

to first cutting and then have a strong<br />

alfalfa stand for subsequent cuttings.<br />

The author would like to thank the California<br />

Alfalfa & Forage Association for<br />

funding this project and River Garden<br />

Farms for their collaboration on this<br />

project.<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

20 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


Managing Soil<br />

Structure and Quality<br />

Biological Management Practices to Maximize Soil Quality<br />

By DR. KARL WYANT | Vice President of Ag Science, Heliae Agriculture<br />

Board of Directors, Western Region Certified <strong>Crop</strong> Advisers<br />

Management practices that<br />

improve soil health and soil<br />

quality have gained considerable<br />

attention over the past few years. If you<br />

are wondering how to get started and<br />

what to focus on, you have come to the<br />

right place! In Part 2 of this article series,<br />

I focus on how the living, biologic<br />

components of the soil, the microbes,<br />

directly impact your soil, including the<br />

structure (e.g., aggregation and pore<br />

space). My focus on bacteria and fungi<br />

in the soil is a perfect complement to<br />

Part 1 of this article series, where we<br />

explored the physical and chemical<br />

components behind soil structure. Part<br />

1 can be found in the January/February<br />

<strong>2021</strong> edition of <strong>Progressive</strong> <strong>Crop</strong><br />

<strong>Consultant</strong>.<br />

Let us kick things off with a quick<br />

reminder of some terminology and<br />

drive home the connection between<br />

soil quality (structure) and soil health<br />

(biology).<br />

Soil quality: This term has broad application<br />

on your farm. Soil quality refers<br />

to how well a soil functions physically,<br />

chemically and biologically and does<br />

its “job” (Figure 1). Many factors influence<br />

the soil quality on a farm and are<br />

summed up in Figure 2. In this article,<br />

we will focus on the biological management<br />

practices that maximize soil<br />

quality, expressed here as soil structure.<br />

Soil health: This term refers to the<br />

interaction between organisms and<br />

their environment in a soil ecosystem<br />

and the properties provided by such<br />

Figure 1. Holistic soil management can be used to help improve soil structure and soil quality.<br />

We explored the physical and chemical controls in Part 1 and explore the biological controls in<br />

Part 2 of this article series (all figures and tables courtesy K. Wyant.)<br />

interactions. When you think of soil<br />

health, think of the biological integrity<br />

of your field (e.g., microbial population<br />

and diversity) and how the soil biology<br />

supports plant growth.<br />

There is a direct link between soil<br />

health (the living component) and soil<br />

quality (the structural component).<br />

The linkage is fungi and bacteria in the<br />

soil and the byproducts they secrete.<br />

These byproducts help restore your<br />

soil structure (Figure 3, see page 23).<br />

Furthermore, well-structured soils are<br />

characterized by excellent soil health,<br />

which indicates a feedback loop between<br />

the soil biology and soil particles.<br />

But how exactly do the microbes<br />

put your soil back together?<br />

Figure 2. <strong>Crop</strong> productivity is influenced by<br />

several interrelated concepts, which have an<br />

impact on the soil quality of a field.<br />

22 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


Component<br />

Practice<br />

Feed Existing Biology<br />

Add Biology<br />

Mulches and Compost<br />

Cover <strong>Crop</strong>ping<br />

Reduce tillage<br />

Glue and Nets<br />

Abundant and diverse soil microbial<br />

communities produce lots of “free”-<br />

services for your farm soil. When<br />

your soil is healthy, microbes speed up<br />

nutrient release rates back to the crop,<br />

influence the water holding capacity of<br />

the soil, and help restore soil structure.<br />

How exactly do they go about sticking<br />

the soil together? The answer can be<br />

summed up in two terms: glues and<br />

nets.<br />

When you have a healthy and abundant<br />

soil bacteria population, they produce<br />

a sticky, glue-like gel called extracellular<br />

polymeric substances (EPS) that<br />

forms a protective slime layer around<br />

bacteria as they grow. EPS, since it is<br />

sticky, acts as a glue for soil particles,<br />

sticking them together and improving<br />

overall soil structure.<br />

Another important group of soil<br />

microbes, called fungi, is most known<br />

Provides the soil microbiome a food source<br />

Provide certain species of bacteria and fungi to soil<br />

Provides a bulk carbon and nutrient source to the soil<br />

Keeps living roots in the soil and protects soil from erosion<br />

Helps keep soil structure and microbial communities intact<br />

Table 1. Practices that can help improve soil biology and improve soil structure.<br />

by its aboveground structures like<br />

mushrooms. However, most soil fungi<br />

exist where you cannot see them below<br />

ground. In the soil, fungi produce millions<br />

of miles of microscopic threads<br />

called hyphae. These structures help<br />

fungi find resources and grow. The<br />

threads also help to capture and tie<br />

soil particles together like a net, which<br />

improves soil structure. Now that you<br />

know the connection between your soil<br />

biology and soil structure, let us turn<br />

our attention to management practices<br />

that can help optimize the contribution<br />

of microbes to improving your farm<br />

soil (Table 1).<br />

Soil Biology Management<br />

Guidelines<br />

Feed the Soil Biology<br />

This might seem like an obvious<br />

management choice, but this practice<br />

is often missed in the yearly crop plan.<br />

Continued on Page 24<br />

With a focus on abiotic<br />

stress, diKaP (0-31-50)<br />

improves nitrogen<br />

metabolism that can<br />

lead to reduced<br />

incidence of hull rot.<br />

Scan code<br />

to learn more.<br />

Scan the code with your<br />

camera app or Google Lens<br />

Figure 3. The soil on the left has poor soil structure while the soil on the right has excellent<br />

aggregation and structure. The samples also have vastly different living components in the<br />

soil, as shown in the agar plates. The soil with the best aggregation is characterized by having<br />

a healthy soil microbiome (right).<br />

redoxgrows.com<br />

@redoxgrows<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 23


Continued from Page 23<br />

Your soil is teeming with fungi and<br />

bacteria and they are ready to go to<br />

work for you. The problem? They are<br />

starving and will go dormant on you<br />

until conditions improve. Research<br />

shows that farm soils are generally low<br />

in the food stuffs that microbes like to<br />

eat, and that food scarcity will limit<br />

the activity of your soil biology. The<br />

answer? Provide them with a regular<br />

installment of something they like to<br />

eat to keep their populations up. You<br />

have many choices, including microalgae,<br />

molasses, fish emulsions, etc.<br />

Add Soil Biology<br />

Another option is to add biology to the<br />

soil. I do not have space to cover all<br />

the products out there, but the main<br />

concept is to provide selected species<br />

of bacteria or fungi to the soil and put<br />

them to work for you. Keep in mind<br />

that the inoculant must stay alive to get<br />

the benefit you are looking for. This can<br />

be quite a challenge considering how<br />

sensitive microbes are to changes in<br />

temperature and humidity from shipping<br />

to storage in the farm shop to field<br />

application. If you choose this option,<br />

make sure your product is viable and<br />

high quality when going out into the<br />

field.<br />

Mulches and Compost<br />

This practice is like the first management<br />

suggestion but provides more<br />

of a “slow release” food source for the<br />

microbes. Not all the carbon in plant<br />

mulch and compost is available as<br />

microbial food. Instead, it must be<br />

chemically and physically broken down<br />

before the microbes can take advantage<br />

of it. Another advantage is that mulches<br />

and compost provide a nutrient<br />

source to the soil. A potential disadvantage<br />

here is that mulches and compost<br />

can contain excess salts and weed seeds<br />

if not prepared correctly.<br />

Reduce Tillage and Improve Soil<br />

Biology<br />

Field activities like tillage can be hard<br />

on your soil biology, particularly the<br />

soil fungi. For example, when a disk<br />

moves through the field, it not only<br />

slices through the soil (what you want<br />

to happen) but it also slices and dices<br />

through all the fungi threads you<br />

are trying to grow (what you do not<br />

want to happen.) This unintentional<br />

result can have a severe impact on the<br />

biological contribution to soil structure.<br />

Moreover, excessive tillage can<br />

crush and compact your soil structure,<br />

which can set you back from a physical<br />

management perspective. Reducing<br />

tillage, therefore, can improve your soil<br />

structure on two fronts. Talk about a<br />

2-for-1 deal!<br />

Cover <strong>Crop</strong>s and Soil Biology<br />

The cover crop, usually grown in<br />

between the rows of permanent crops<br />

(e.g., trees and vines) or in the ‘off-season’<br />

for annual crops, can be used to<br />

help feed soil microbes. Cover crop<br />

roots secrete carbon substances, called<br />

exudates, which can help boost the soil<br />

fungi and bacteria when a crop is not<br />

in the ground. Keeping your soil alive<br />

year-round is key to optimizing the<br />

biological contribution to soil quality.<br />

Fine root hairs can also tie soil particles<br />

together, improving soil structure and<br />

quality. Another two-for-one deal!<br />

Testing for Soil Biology<br />

No doubt you are familiar with soil<br />

tests from your favorite agricultural<br />

laboratory. Traditional soil tests have<br />

mainly focused on measuring the<br />

chemical constituents of the soil (e.g.,<br />

nitrate, phosphate, etc.) or the physical<br />

aspects of the soil (e.g., soil texture,<br />

cation exchange capacity). However, as<br />

useful as these tests are, they fail to explain<br />

how “alive” the soils are. There is<br />

good news though! Many laboratories<br />

are starting to offer soil health testing<br />

services which can help you get a better<br />

understanding of the biological components<br />

of your soil. Certified <strong>Crop</strong> Advisors<br />

(CCA) help guide growers through<br />

which test to order and, more importantly,<br />

help them interpret it. Common<br />

tests include measurements of carbon<br />

dioxide respiration, extraction of DNA<br />

for microbial community analysis<br />

and even direct counting of fungi and<br />

bacteria populations. There are many<br />

choices and sound advice from an<br />

experienced crop advisor that can help<br />

direct you down the right path and<br />

reduce the learning curve.<br />

Conclusion<br />

Biological factors can have a profound<br />

impact on overall soil structure and,<br />

thus, the soil quality of the field. Generally,<br />

poorly structured soils have a difficult<br />

time supporting optimized crop<br />

growth due to the severe reduction<br />

in water storage capacity, low oxygen,<br />

surface crusting and seed bed issues,<br />

accumulation of salinity, etc. If the soil<br />

looks like the example on the left side<br />

of Figure 3, it may be well worth your<br />

time and money to start implementing<br />

soil biology improvement practices as<br />

outlined in this article and revisit some<br />

of the physical and chemical practices<br />

discussed in Part 1 of this series. I<br />

strongly recommend that you put your<br />

field detective hat on to diagnose why<br />

your field is not performing as expected.<br />

A bit of detective work beforehand can<br />

pay off in turning your field around<br />

and using your input dollars most<br />

effectively.<br />

Dr. Karl Wyant currently serves as the<br />

Vice President of Ag Science at Heliae ®<br />

Agriculture where he oversees the internal<br />

and external PhycoTerra ® trials, assists<br />

with building regenerative agriculture<br />

implementation and oversees agronomy<br />

training.<br />

Resources<br />

Soil Health Partnership Blog: https://<br />

www.soilhealthpartnership.org/shp-blog/<br />

Soil Health Institute Blog: https://soilhealthinstitute.org/resources/<br />

The Applied Side of Soil Health Measurements:<br />

https://phycoterra.com/<br />

the-applied-side-of-soil-health-measurements-2/<br />

The Connection Between Your Soil<br />

Structure and Soil Moisture: https://phycoterra.com/connection-between-soilstructure-soil-moisture-crop/<br />

Physical and Chemical Controls of<br />

Soil Structure: http://progressivecrop.<br />

com/<strong>2021</strong>/01/managing-soil-and-structure-quality/<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

24 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


Avocado Invasive Insect Pests<br />

Current, Potential and Recent Threats to<br />

Southern California’s Avocado Industry<br />

By SONIA RIOS | UCCE Subtropical Horticulture Farm Advisor, Riverside and San Diego Counties<br />

AKIF ESKALEN | UCCE Specialist, Grapevine, Fruit Trees and Small Fruits Pathology<br />

MARK S. HODDLE | UCCE Specialist, Biological Control, UC Riverside<br />

Globally, invasive insect pests<br />

cause substantial damage to agricultural<br />

crops and natural environments.<br />

In the U.S. alone, crop and forest<br />

production losses from invasive insects<br />

and pathogens have been estimated at<br />

almost $40 billion per year (Pimentel et<br />

al. 2005). On average, a new non-native<br />

invertebrate is introduced into California<br />

every 40 days. With respect to insects and<br />

mites, about one-third of these become<br />

pests (Dowell et al. 2016), and economic<br />

losses in California are estimated at more<br />

than $3 billion per year (Metcalf 1995).<br />

Rapid growth of U.S. demand for fresh<br />

avocados has increased the fruit’s prominence<br />

in retail sales and diets. California<br />

is the largest producer of avocados grown<br />

in the U.S. The value of U.S. avocado<br />

production measured at approximately<br />

$392 million in 2017, (NASS, 2018). There<br />

are more than 3,000 avocado growers<br />

in the state farming on approximately<br />

50,000 acres of land, with Ventura County<br />

leading the state in most acres planted<br />

and harvested in recent years (California<br />

Avocado Commission [CAC], 2020).<br />

California avocados are particularly<br />

special because less than 1% of the state<br />

is suitable for growing them. A healthy,<br />

single ‘Hass’ avocado tree can produce<br />

up to 200 pounds of fresh fruit each<br />

year, which is ~500 pieces. In 2018 alone,<br />

California produced around 350 million<br />

pounds. Avocados are considered a<br />

specialty crop and are not cheap to grow<br />

because of water and land costs, and<br />

fruit therefore usually demands a high<br />

premium price.<br />

Traditionally, insecticide use in California<br />

avocado orchards has been minimal<br />

due to relatively few pest species, which,<br />

for the most part, have been under adequate<br />

levels of biological control (Hoddle<br />

2005). However, due to the increase of<br />

international trade, illegal importation<br />

and the smuggling of foliage, branches<br />

with leaves, whole plants and budwood,<br />

invasive insect and mite pests have begun<br />

to threaten the economic viability of<br />

avocado production in California.<br />

Polyphagous and Kuroshio<br />

Shot Hole Borers<br />

Polyphagous Shot Hole Bore (PSHB)<br />

is an invasive ambrosia beetle from<br />

Southeast Asia that was first detected in<br />

Los Angeles County in 2003 (Gomez et al.<br />

2018, Rabaglia et al. 2006). PSHB is a pest<br />

of great concern in Southern California<br />

as it can attack over 300 tree species and<br />

reproduce on a subset of these that are<br />

capable of supporting beetle reproduction<br />

and growing the fungi that cause<br />

fusarium dieback.<br />

PSHB has a strong symbiotic relationship<br />

with several fungi, including Fusarium<br />

euwallaceae and Fusarium kuroshium,<br />

the causal agent of Fusarium Dieback<br />

(FD) disease (Eskalen et al. 2013). The<br />

list of reproductive hosts includes several<br />

native oaks, maples, sycamores, willows<br />

and avocado. The fungus disrupts the<br />

vascular transport of water and nutrients<br />

on their host tree that eventually causes<br />

branch dieback. The most common<br />

symptoms of the disease include sugar<br />

or gum exudates, dieback, wilt and<br />

ultimately host tree mortality. Reports<br />

of dieback symptoms in El Cajon, San<br />

Diego County led to the discovery of<br />

another species, the Kuroshio shot hole<br />

borer (KSHB) in 2013.<br />

KSHB is also present in commercial<br />

avocado orchards in San Diego County.<br />

KSHB was originally limited to the San<br />

Diego region but has since spread to<br />

Orange, Los Angeles, Ventura and Santa<br />

Barbara counties. Presumably, PSHB and<br />

KSHB were introduced accidentally into<br />

Southern California via wooden products<br />

and/or shipping material (e.g., pallets and<br />

dunnage) from Southeast Asia. KSHB is<br />

morphologically indistinguishable from<br />

PSHB, but species can be separated using<br />

molecular techniques.<br />

The fungus gets into the woody tissue of<br />

the tree when a female PSHB excavates a<br />

gallery and inoculates the gallery walls<br />

with fungal spores that it carries in special<br />

structures called mycangia (Beaver,<br />

1989). The female PSHB and her offspring<br />

feed exclusively on the fungal spores.<br />

PSHB adults engage in sibling mating<br />

within the natal gallery. Offspring sex<br />

ratios are female biased to maximize reproductive<br />

output such that one male can<br />

inseminate many of his female siblings.<br />

Once fully developed and mated, female<br />

PSHB exit their natal gallery to start a<br />

gallery of their own and repeat the cycle.<br />

Unlike their sisters, male PSHB do not<br />

disperse since they are not capable of flying<br />

and do not possess mycangia, which<br />

are specialized structures for fungus<br />

storage.<br />

Pesticide efficacy may be limited, and<br />

this is attributed to the fact that PSHB<br />

feeds on fungi and not directly on wood<br />

tissue. This reduces exposure to active<br />

ingredients when feeding (Eatough<br />

Jones et al. 2017). Cultural management<br />

practices include: 1) removal of infected<br />

branches to reduce local beetle numbers<br />

and fungal spread in the infested area;<br />

2) chipping (< 1 inch) and solarizing infested<br />

wood; and 3) avoiding movement<br />

of infested materials to new areas (if<br />

26 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


A female PSHB boring (photo by A. Eskalen.)<br />

Beetle gallery formation in an avocado branch (photo by<br />

A. Eskalen.)<br />

transportation of materials is necessary,<br />

it must be covered(UC IPM 2017).<br />

These management strategies can perhaps<br />

abate the severity of local infestations.<br />

Also, limiting the spread of infected/infested<br />

trees include minimizing firewood<br />

transportation. Sterilizing pruning<br />

tools with household bleach or another<br />

cleaning solution can reduce the spread<br />

of the FD pathogen. The PSHB was found<br />

in Israel in 2009 in commercial avocado<br />

orchards where it damages trees. To date,<br />

there has been no avocado tree fatality<br />

due to the PSHB or FD in California. For<br />

more information regarding PSHB, visit<br />

ucanr.edu/sites/pshb/.<br />

Redbay Ambrosia Beetle<br />

and Laurel Wilt Complex<br />

An invasive ambrosia beetle, the redbay<br />

ambrosia beetle (RAB; Xyleborus glabratus)<br />

is a serious pest currently spreading<br />

through the Florida avocado industry<br />

and has been responsible for significant<br />

yield reductions since its discovery in<br />

2005. The beetle was first detected in the<br />

U.S. in Port Wentworth, Ga. in 2002 and<br />

was probably introduced via infested<br />

wooden packaging material (Crane 2011).<br />

This beetle has been slowly spreading<br />

across the southeastern U.S. and is<br />

currently found as far west as east Texas.<br />

Therefore, California growers need to<br />

be aware that this pest-disease complex<br />

may spread to California avocados. What<br />

makes this complex dangerous is that the<br />

vector, RAB, has a symbiotic relationship<br />

with the fungal pathogen Raffaelea<br />

lauricola that causes Laurel Wilt Disease<br />

(LWD). Native to Southeast Asia, RAB<br />

has similarities to our current ambrosia<br />

pest, PSHB. However, the fungus as-<br />

Continued on Page 28<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 27


Continued from Page 27<br />

sociated with LWD is unlike the disease<br />

here in California. Trees become infected<br />

when female beetles attack host trees and<br />

introduce the pathogen into the xylem<br />

while boring their galleries. The infection<br />

restricts the flow of water in the tree,<br />

induces a black discoloration in the outer<br />

sapwood and causes the leaves to wilt.<br />

Tree mortality is so rapid that leaves do<br />

not fall from dying branches.<br />

Symptoms of RAB beetle and LWD infestations<br />

include (Carrillo et al. 2017):<br />

• Wilting of leaves and young stems.<br />

You can usually see dead leaves<br />

hanging on branches.<br />

• Color change in leaves from light<br />

green to dark purplish green or<br />

greenish brown.<br />

• Stem and limb dieback.<br />

• Trunk and major limbs that<br />

show dried sap which has a white<br />

appearance and is a crystalline,<br />

powder-like material.<br />

• Dark streaks in the sapwood.<br />

Normally sapwood should be white<br />

to yellowish white in coloration<br />

with no dark staining or streaking.<br />

To check for this symptom simply<br />

remove a section of the bark to<br />

check for discoloration, which,<br />

if present, may indicate fungal<br />

infection.<br />

• Small, dark holes in the sapwood<br />

and what looks like loose wood<br />

dust and frass indicate wood boring<br />

beetles are present.<br />

LWD affects redbay (Persea borbonia)<br />

and other tree species of the Laurel<br />

family (Lauraceae), including avocado.<br />

R. lauricola is introduced into host trees<br />

when adult RAB colonizes a tree. Adult<br />

RAB are very small (~1/16-inch-long),<br />

dark brown to black in color and spend<br />

most of their life within the tree. Larvae<br />

are white, legless grubs with an amber<br />

colored head capsule and are found within<br />

galleries throughout infected trees. Female<br />

beetles can produce flightless male<br />

offspring without mating, but females<br />

may mate with their male offspring or<br />

brothers to produce males and females.<br />

Females greatly outnumber males in<br />

populations. In the Southeast U.S.,<br />

RAB’s lifecycle from egg to adult appears<br />

to take 50 to 60 days, and there appear to<br />

be multiple overlapping generations per<br />

year (Hanula et al. 2008). Female beetles<br />

emerging from galleries may reinfest the<br />

same tree or disperse in search of new<br />

hosts. Host trees can remain standing<br />

for years and may continue to serve<br />

as host material for beetles for several<br />

months after initial colonization. Flight<br />

activity peaks in the late afternoon and<br />

early evening.<br />

It is known that ambrosia beetles are<br />

notoriously difficult to control with<br />

insecticides because they are protected<br />

from residues by living inside the tree<br />

most of their life versus being outside<br />

the tree. RAB can fly short distances,<br />

but LW fungus spreads more quickly<br />

through the movement of insect-infested<br />

plant material, such as firewood.<br />

Additionally, the pathogen also spreads<br />

to other ambrosia beetle vectors. This<br />

happens when beetles feed on diseased<br />

trees and become contaminated with<br />

spores of R. lauricola. Spread can also<br />

occur through root grafting between<br />

trees. Sanitation is the most effective way<br />

to manage this problem. Scouting for<br />

wilted branches and quickly removing<br />

them has been key to successful early<br />

intervention and eradication.<br />

It has been suggested to remove symptomatic<br />

trees immediately upon their<br />

identification. However, once the<br />

appearance of frass and streaks start to<br />

show in the wood, this is a sign that the<br />

tree has already been infected and has<br />

been for some time. As soon as a grower<br />

sees the wilt in the branches, it’s time<br />

to move quickly. Verticillium wilt and<br />

Phytophthora root rot can be mistaken<br />

for LW, so avocado growers should check<br />

for these diseases before removing trees.<br />

The Florida avocado industry has<br />

implemented a universal detection and<br />

suppression program with the goal of<br />

preventing or limiting the incidence of<br />

Continued on Page 30<br />

Severe Laurel wilt vascular staining on avocado<br />

(photo by A. Eskalen.)<br />

Laurel wilt branch die back on avocado (photo by<br />

S. Rios.)<br />

RAB entry holes in avocado (photo by S. Rios.)<br />

The presence of frass indicates the presence of<br />

RAB (photo by A. Eskalen.)<br />

28 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


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Continued from Page 28<br />

LW in commercial groves and depressing<br />

ambrosia beetle populations (Carrillo et.<br />

al 2017). Surveying for the symptoms of<br />

LW is a key component to limiting the<br />

spread of the disease. Growers and their<br />

workers should survey groves weekly or<br />

more often if an infestation is detected<br />

in an adjacent grove. Early detection,<br />

removal and destruction of LW affected<br />

trees is the most important practice for<br />

controlling LW.<br />

Contact insecticides are ineffective<br />

because the pathogen vectors (i.e., the<br />

ambrosia beetles) are primarily inside the<br />

tree. The first goal is to avoid infestation<br />

with the beetles by maintaining a healthy<br />

tree as stressed trees are more attractive<br />

to colonizing beetles. Beetles prefer trees<br />

in orchards that have dense canopies<br />

with overlapping leaves and branches.<br />

Chipping infected trees is effective in reducing<br />

the spread of the disease. However,<br />

chips must be as small as possible (one<br />

square inch or smaller) and dried quickly<br />

so that the wood is not conducive to fungal<br />

growth. A potential drawback to this<br />

method is that the aroma of the chipped<br />

wood can attract other wood boring<br />

insects. Research in Florida is currently<br />

being conducted to determine if different<br />

Avocado lace bug adult and eggs (photo by M. Hoddle.)<br />

commercial formulations of insecticides<br />

can be effective in controlling the beetle.<br />

For more information regarding LW and<br />

RAB, please visit sfyl.ifas.ufl.edu/miami-dade/agriculture/laurel-wilt---a-disease-impacting-avocados/.<br />

Avocado Lacebug<br />

The avocado lacebug (ALB), Pseudacysta<br />

perseae (Hemiptera: Tingidae), was first<br />

detected in California on backyard avocado<br />

trees in Chula Vista and National<br />

City, San Diego County in 2004. This<br />

pest was first described in Florida in 1908<br />

and has since been reported from Mexico,<br />

Guatemala, Puerto Rico, Jamaica, the<br />

Dominican Republic and parts of northeastern<br />

South America. The native range<br />

of ALB is uncertain. Molecular studies<br />

suggest that the western areas of Mexico<br />

may be the evolutionary center of origin<br />

for this pest and it was spread unintentionally<br />

from this area, probably on avocado<br />

trees into eastern Mexico, Florida<br />

and the Caribbean (Rugman-Jones et al.<br />

2012).<br />

After a lull of approximately 13 years,<br />

reports started coming of ALB damage<br />

to avocados outside of San Diego. In October<br />

2017, well established, reproducing<br />

populations of lace bugs were confirmed<br />

in commercial Hass avocado groves in<br />

Oceanside and De Luz in San<br />

Diego County and in Temecula<br />

in Riverside County (CAC, 2017).<br />

Around this time, infestations<br />

were reported from backyard<br />

avocados in Culver City in Los<br />

Angeles County. Genetic analysis<br />

suggested that these new, more<br />

damaging populations of ALB<br />

were different to those originally<br />

detected in San Diego in 2004, and<br />

it’s likely that a second introduction<br />

of ALB into California has<br />

occurred, possibly from Florida<br />

(Rugman-Jones and Stouthamer<br />

unpublished molecular data).<br />

ALB has been recorded feeding<br />

on avocado, red bay and camphor,<br />

which are all in the Lauraceae<br />

family.<br />

Avocado lace bug is a true bug<br />

with sucking mouth parts. Lace<br />

bugs use these needle-like mouthparts<br />

to feed on the undersides of<br />

leaves. Through feeding, leaf cells and<br />

pierced cell contents are extracted and<br />

ingested, preventing photosynthesis.<br />

Adult avocado lace bugs are small,<br />

winged insects, about 2 mm in length<br />

(slightly longer than 1/16 in), with black<br />

bodies, yellow legs and antennae, and are<br />

visible to the naked eye (UC IPM <strong>2021</strong>).<br />

ALB live in colonies on the lower surfaces<br />

of mature leaves, often adults, eggs and<br />

nymphs are found together. Eggs are<br />

laid in an irregular pattern, sometimes<br />

in loose rows, attached to the lower leaf<br />

surface and are covered with irregular<br />

globules of a black, sticky, tar-like substance<br />

excreted by adults. To the naked<br />

eye, eggs will appear like grains of black<br />

pepper or dirt.<br />

Eggs hatch into wingless nymphs that are<br />

capable of walking. Nymphs go through<br />

a gradual metamorphosis, shedding their<br />

exoskeleton several times as they grow in<br />

size, finally developing wings and becoming<br />

flying adults. Nymphs are dark redbrown<br />

to black and covered with spines.<br />

They feed for approximately two to three<br />

weeks before maturing into adult males<br />

and females which mate, and females<br />

then lay eggs, starting the cycle over. In<br />

California, ALB populations tend to peak<br />

over early summer, around <strong>June</strong>, then<br />

decline in fall, sometime around September<br />

(Humeres et al. 2009).<br />

ALB restrict their feeding to the undersides<br />

of leaves. Feeding initially causes<br />

small white or yellow spots on the<br />

surface of the leaves as individual cells<br />

dry out. These necrotic areas look like<br />

tip-burn caused by excessive salts, but in<br />

this case, the necrotic areas are islands<br />

of dead tissue in the interior of the leaf<br />

surrounded by living tissue. It is suspected<br />

that feeding damage can provide<br />

entrance for pathogenic fungi, in particular<br />

Colletotrichum spp., which are leaf<br />

anthracnose fungi. As lace bug colonies<br />

grow, brown necrotic areas develop<br />

where there has been heavy feeding damage.<br />

Heavy feeding can cause striking leaf<br />

discoloration and early leaf drop (Hoddle<br />

2004; Hoddle et al. 2005). Avocado lace<br />

bug nymphs and adults do not feed on<br />

fruit. However, heavy feeding damage to<br />

leaves will likely have a detrimental effect<br />

on yield, which may result from the loss<br />

30 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


of photosynthetic capacity in damaged<br />

leaves.<br />

Relatively little is known about biology<br />

and ecology of ALB in California. In<br />

Florida, the most important biological<br />

control agents are two egg parasitoids<br />

including Oligosita sp. (a Trichogrammatid<br />

wasp) and an unidentified mymarid<br />

wasp. Green lace wing larvae and other<br />

generalist predators are also thought to<br />

be important natural enemies. A predatory<br />

thrips, Franklinothrips vespiformis,<br />

is reported to be the most important<br />

natural enemy of the avocado lace bug in<br />

the Dominican Republic and is similarly<br />

abundant on ALB-infested avocados in<br />

Escuintla Guatemala.<br />

Insecticide treatments for other sucking<br />

pests currently registered for use on<br />

avocado in California will likely provide<br />

control of avocado lace bugs (Hoddle et<br />

al. 2005). In a trial reported in 1998, J. E.<br />

Peña, University of Florida (UF), showed<br />

that citrus oil, M-Pede (insecticidal<br />

soap) and Mycotrol (a Beauveria fungal<br />

species) all controlled lace bug, but it was<br />

not indicated how long the effect lasted.<br />

Researchers at UF have shown that citrus<br />

oil and M-Pede provided short-term lace<br />

bug control. Results of small tree trials<br />

or weathered residue tests have indicated<br />

that carbaryl, imidicloprid, cyfluthrin,<br />

carbaryl, fenpropathrin and malathion<br />

provide excellent control of avocado lace<br />

bug nymphs. Spinosad, abamectin and<br />

mineral oil are much less effective at<br />

providing control (Humeres et al. 2009b;<br />

Byrne et al. 2010). For more information<br />

on lace bugs, please visit biocontrol.ucr.<br />

edu/avocado-lace-bug.<br />

Severe feeding damage to avocado leaves caused by avocado lace bug (photo by M.<br />

Hoddle.)<br />

Ideally, finding a new pest species in the<br />

early stages of the invasion and quickly<br />

containing and treating the new infestation<br />

may reduce costly long-term<br />

management, especially if eradication is<br />

possible. Rapid and decisive containment<br />

actions are an important consideration as<br />

controlling invasive pests, especially fruit<br />

feeders, in California avocado orchards<br />

will always be a challenge and expensive<br />

should they establish widely.<br />

References<br />

Byrne, F. J., Almanzor, J., Tellez, I., Eskalen, A., Grosman, D. M., & Morse, J. G. 2020.<br />

Evaluation of trunk-injected emamectin benzoate as a potential management<br />

strategy for Kuroshio shot hole borer in avocado trees. <strong>Crop</strong> Protection, 132, 105136.<br />

Byrne, F. J., Humeres, E. C., Urena, A. A., Hoddle, M. S., and Morse, J. G. 2010. Field<br />

evaluation of systemic imidacloprid for the management of avocado thrips and<br />

avocado lace bug in California avocado groves. Pest management science, 66(10),<br />

1129-1136.<br />

Carrillo, D., J. Crane, R. Ploetz, E. Evans, and J. Wasielewski. 2017. Brief Update to<br />

Laurel Wilt Recommendations – Ambrosia Beetles. Univ. of Florida, IFAS Extension<br />

Notice.<br />

Crane, J. (2011) Laurel Wilt and the Redbay Ambrosia Beetle threaten Florida’s<br />

avocado and native trees in the Laurel Family. Univ. of Florida, IFAS Extension<br />

Homeowner informational brochure.<br />

Coleman, T. W., Poloni, A. L., Chen, Y., Thu, P. Q., Li, Q., Sun, J., and Seybold, S. J. 2019.<br />

Hardwood injury and mortality associated with two shot hole borers, Euwallacea<br />

spp., in the invaded region of southern California, USA, and the native region of<br />

Southeast Asia. Annals of Forest Science, 76(3), 1-18.<br />

Hughes, M.A., Smith, J.A., Ploetz, R.C., Kendra, P.E., <strong>May</strong>field, A.B., Hanula, J., Hulcr,<br />

J., Stelinski, L.L., Cameron, S., Riggins, J.J. and Carrillo, D. 2015. Recovery plan for laurel<br />

wilt on redbay and other forest species caused by Raffaelea lauricola and<br />

disseminated by Xyleborus glabratus. Plant Health Progress, 16(4), pp.174-210.<br />

Humeres, E. C., Morse, J. G., Stouthamer, R., Roltsch, W., & Hoddle, M. S. 2009a.<br />

Detection surveys and population monitoring for Pseudacysta perseae on<br />

avocados in southern California. Florida Entomologist 92(2): 382-385.<br />

Humeres, E. C., Morse, J. G., Stouthamer, R., Roltsch, W., & Hoddle, M. S. 2009b.<br />

Evaluation of natural enemies and insecticides for control of Pseudacysta<br />

perseae (Hemiptera: Tingidae) on avocados in Southern California. Florida<br />

Entomologist, 92(1), 35-42.<br />

Lu, M., Hulcr, J., and Sun, J. 2016. The role of symbiotic microbes in insect invasions.<br />

Annual Review of Ecology, Evolution, and Systematics, 47, 487-505.<br />

<strong>May</strong>field, A.E. III, Barnard, E.L., Smith, J.A., Bernick, S.C. , Eickwort, J.M., and T.J.<br />

Dreaden. 2008. Effect of propiconazole on laurel wilt disease development in redbay<br />

trees and on the pathogen in vitro. Arboriculture & Urban Forestry 35: 317-324<br />

<strong>May</strong>orquin, J. S., Carrillo, J. D., Twizeyimana, M., Peacock, B. B., Sugino, K. Y., Na,<br />

F., and Eskalen, A. 2018. Chemical management of invasive shot hole borer and<br />

Fusarium dieback in California sycamore (Platanus racemosa) in southern<br />

California. Plant disease, 102(7), 1307-1315.<br />

Mead, F. W., and Peña, J. E. 2016. Avocado lace bug, Pseudacysta perseae<br />

(Heidemann)(Insecta: Hemiptera: Tingidae). Entomol. Circ, (346).<br />

Metcalf, R. L. 1995. Invasion of California by exotic insects. California Agriculture<br />

49(1): 2.<br />

Pimentel D, Zuniga R, and Morrison D. 2005.Update on the environmental and<br />

economic costs associated with alien-invasive species in the United States. Ecol<br />

Econ 52(3):273–288.<br />

Ploetz, R. C., Pérez‐Martínez, J. M., Smith, J. A., Hughes, M., Dreaden, T. J., Inch, S. A.,<br />

and Fu, Y. 2012. Responses of avocado to laurel wilt, caused by Raffaelea lauricola.<br />

Plant Pathology, 61(4), 801-808.<br />

Rios, S., B. Faber, P. Mauk, A. Eskalen, and M.L. Arpaia. 2018. Redbay Ambrosia Beetle<br />

Poses Potential Threat to California’s Avocado Industry. California Association of<br />

Pest Control Advisors. February 2018. 22(1):36-38, Pp 36-38.<br />

Proactive Management<br />

and Early Detection<br />

The concept of early detection and rapid<br />

response is fundamental to effective invasive<br />

species management. Developing<br />

collaborative relationships with avocado<br />

research colleagues in different countries<br />

can provide insight into new potential<br />

pest problems that could eventually find<br />

their way to California (Hoddle et al.<br />

2009). Developing this idea further can<br />

result in the development of proactive<br />

biological control and IPM programs in<br />

advance of the anticipated arrival of new<br />

pest species (Hoddle et al. 2018).<br />

Dowell, R. V., R. J. Gill, D. R. Jeske, and M. S. Hoddle. 2016. Exotic macro-invertebrate<br />

invaders in California from 1700 to 2015: An analysis of records. Proceedings<br />

of the California Academy of Sciences Series 4 63(3): 63-157.<br />

Hanula, J.L, <strong>May</strong>field, A.E. III, Fraedrich, S.W., and Rabaglia, R.J. 2008. Biology and<br />

host associations of the redbay ambrosia beetle, (Coleoptera: Curculionidae:<br />

Scolytinae), exotic vector of laurel wilt killing redbay trees in the southeastern<br />

United States. Journal of Economic Entomology 101: pp. 1276-1286.<br />

Hoddle, M. S. 2004. Invasions of leaf feeding arthropods: why are so many<br />

new pests attacking California-grown avocados? California Avocado Society<br />

Yearbook, 87, 65-81.<br />

Hoddle, Mark S., J. G. Morse, Richard Stouthamer, Eduardo Humeres, Gilsang Jeong,<br />

William Roltsch, Gary S. Bender. 2005. “Avocado lace bug in California.” California<br />

Avocado Society Yearbook 88: 67-79.<br />

Hoddle, M. S., Arpaia, M. L., and Hofshi, R. 2009. Mitigating invasion threats to the<br />

California avocado industry through collaboration. Calif. Avo. Soc. Yrbk., 92, 43-64.<br />

Hoddle, M. S., K. Mace, and J. Steggall. 2018. Proactive biocontrol: A cost effective<br />

management option for invasive pests. California Agriculture 72(3): 1-3.<br />

Rivera, M. J., Martini, X., Conover, D., Mafra-Neto, A., Carrillo, D., & Stelinski, L.<br />

L. 2020. Evaluation of semiochemical based push-pull strategy for population<br />

suppression of ambrosia beetle vectors of laurel wilt disease in avocado. Scientific<br />

reports, 10(1), 1-12.<br />

Rugman-Jones, P. F., M. S. Hoddle, P. A. Phillips, G. Jeong, & R. Stouthamer. 2012.<br />

Strong genetic structure among populations of the invasive avocado pest<br />

Pseudacysta perseae (Heidemann) (Hemiptera: Tingidae) reveals the source<br />

of introduced populations. Biological Invasions 14: 1079-1100.<br />

University of California Integrated Pest Management Guidelines for Avocado<br />

Accessed 20 March <strong>2021</strong>.<br />

Umeda, C., Eskalen, A., and Paine, T. D. 2016. Polyphagous shot hole borer and<br />

Fusarium dieback in California. In Insects and diseases of Mediterranean forest<br />

systems (pp. 757-767). Springer, Cham.<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 31


Soil Health on Every Farm<br />

A Guide to Soil Health Testing and<br />

Interpretation<br />

By ERYN WINGATE | Agronomist, Tri-Tech Ag Products, Inc.<br />

Commercial farms throughout<br />

the U.S. consistently turn out<br />

impressive yields, supplying the<br />

nation and the world with quality fruits,<br />

vegetables and staple grains. However,<br />

every year we lose organic matter and<br />

watch topsoil erode with wind and<br />

runoff. Heavy tillage, powerful biocides<br />

and mineral fertilizers support high<br />

production even on suboptimal ground.<br />

Safer crop protection products and efficient<br />

fertigation practices significantly<br />

contribute to extending the longevity of<br />

America’s agricultural lands, yet growers<br />

still struggle to maintain yields on tired,<br />

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32 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


NAVEL ORANGEWORM MANAGEMENT<br />

disease ridden and salt affected soils.<br />

Tillage, poor water quality, drought<br />

and soil borne disease slowly degrade<br />

soil health. Growers must invest in<br />

more water, fertilizer and pesticides to<br />

maintain their yields and crop quality<br />

on declining ground.<br />

Organic Matter and<br />

Regenerative Practices<br />

Healthy soils are well aerated, have<br />

good water and nutrient holding capacity,<br />

have little to no disease pressure<br />

and house beneficial microbial ecosystems.<br />

Each positive attribute relies<br />

on soil organic matter. Annual net<br />

carbon loss drives soil degradation and<br />

threatens our country’s food security.<br />

Tillage is one of the main practices<br />

contributing to organic matter loss.<br />

Turning the soil introduces an influx<br />

of oxygen, temporarily accelerating<br />

microbial activity. Bacteria and fungi,<br />

no longer limited by O 2<br />

availability,<br />

rapidly feed on organic matter, releasing<br />

carbon dioxide to the atmosphere<br />

as they respire. Tillage increases soil<br />

carbon loss beyond annual carbon gain.<br />

Reducing tillage, or converting to a notill<br />

system, can reverse carbon loss and<br />

begin rebuilding soil organic matter.<br />

Other practices, such as cover cropping,<br />

intercropping and composting, also<br />

contribute to carbon sequestration.<br />

Specialized agronomists can assist<br />

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© <strong>2021</strong>, Trécé Inc., Adair, OK USA • TRECE, PHEROCON and CIDETRAK are registered trademarks of Trece, Inc., Adair, OK USA • TRE-1855, 12/20<br />

Continued on Page 34<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 33


Physical<br />

Chemical<br />

Biological<br />

Indicator<br />

Available Water Capacity<br />

Surface Hardness<br />

Subsurface Hardness<br />

Aggregate Stability<br />

Bulk Density<br />

Water Infiltration<br />

Indicator<br />

Electrical Conductivity (EC)<br />

Sodium Absorption Ratio (SAR)<br />

pH<br />

Essential Nutrients (N, P, K, Ca,<br />

Mg, S, etc.)<br />

Heavy Metals<br />

Cation Exchange Capacity<br />

Indicator<br />

Organic Matter<br />

(combustion)<br />

Soil Protein Index<br />

Soil Respiration<br />

Water Extractable Organic Carbon<br />

Microbially Active Carbon (%MAC)<br />

Water Extractable Organic Nitrogen<br />

Soil Health Metrics<br />

Active Carbon (potassium permanganate<br />

oxidation)<br />

Phospholipid Fatty Acid Analysis (PLFA)<br />

Microscopy<br />

Genomics<br />

Enzymes - B-Glucosidase, N-Acetyl-B-D<br />

Glucosaminidase, Phosphomonoesterase,<br />

arylsulfatase<br />

Description<br />

Measures the amount of water soils can hold and<br />

release to plant roots. Soils with higher OM have<br />

higher AWC.<br />

Measures compaction at the soil surface implicating<br />

susceptibility to runoff.<br />

Measures soil compaction between 6 to 18 inches.<br />

Measures how well soil aggregates stick together<br />

when struck by simulated rain drops. Soils with better<br />

aggregate stability resist erosion and generally have<br />

good water infiltration and aeration.<br />

Indicates soil structure, compaction, and organic<br />

matter content. Soils with high bulk density may have<br />

poor structure, compaction, and low organic matter.<br />

Measures the soil's ability to absorb water.<br />

Description<br />

Measures overall soil salinity<br />

Calculation comparing sodium to calcium and<br />

magnesium content to determine soil sodicity.<br />

Soil acidity and alkalinity influence nutrient availability<br />

Macro and micronutrient concentrations are<br />

measured to determine fertilization requirements and<br />

address potential deficiencies or toxicities.<br />

Measured to determine presence of metals that may<br />

harm plant, animal, or human health.<br />

Measures the soil's ability to retain essential nutrients.<br />

Description<br />

Measures the quantity of all carbon containing<br />

materials in the soil.<br />

Measures the fraction of organic matter containing<br />

amino acids, peptides, and proteins. Organic<br />

nitrogen availability influences the soil's nitrogen<br />

mineralization potential.<br />

Measures microbial activity upon rewetting oven<br />

dried soil.<br />

Small fraction of Soil Organic Matter that is readily<br />

available for microbial consumption.<br />

Percentage of WEOC used by microbes during the<br />

soil respiration test. High values above 80% indicate<br />

that microbial activity may become limited by carbon<br />

availability and the soil would benefit from increasing<br />

carbon inputs.<br />

Includes proteins and amino acids available for<br />

microbial use. Higher WEON levels indicate better<br />

nitrogen mineralization potential and decreases<br />

mineral N fertilizer requirement.<br />

Carbon readily available for microbial decomposition.<br />

Estimates the quantity and type of bacteria, fungi, and<br />

other microbes in the soil.<br />

Microorganism identification<br />

DNA sequencing to determine microbial genera and<br />

species present in the soil.<br />

Enzymes indicate microbial community composition<br />

and the soil's capacity to cycle nutrients.<br />

Note: This is not an exhaustive list. Contact your local soil health test lab to inquire about the soil health metrics they offer.<br />

Continued from Page 33<br />

growers in transitioning to a suite of<br />

practices to begin rebuilding soil.<br />

No-till cover cropped systems represent<br />

the gold standard for carbon sequestration<br />

and soil health, yet logistical and<br />

economic factors prevent many growers<br />

from adopting regenerative practices.<br />

When cover cropping and no till are<br />

unfeasible, growers can support healthy<br />

microbial communities by applying<br />

carbon rich liquid amendments and<br />

biostimulants. Many organic fertilizers<br />

and amendments contain high levels of<br />

carbon, amino acids and metabolites<br />

to support beneficial microbial activity<br />

during crop growth. Carbon-rich<br />

fertilizers made from food scraps feed<br />

the soil microbiome while providing a<br />

societal benefit by diverting waste from<br />

landfills. Liquid organic fertilizers,<br />

compost and other amendments can<br />

improve soil fertility, mitigate salinity<br />

and enhance the crop’s stress tolerance.<br />

No matter where your farm lies on the<br />

sustainability spectrum, you can monitor<br />

and manage the land to improve its<br />

long-term production capacity.<br />

Soil Health Metrics<br />

Soil health testing can guide management<br />

decisions and gauge progress after<br />

implementing new practices. Many<br />

commercial and university labs provide<br />

soil quality panels to assess a wide<br />

array of metrics influencing the soil’s<br />

production capacity and environmental<br />

impact. Some labs offer soil health<br />

assessment frameworks that rate soil<br />

health based on results for several key<br />

indicators. Lab test results for each<br />

indicator are mathematically transformed<br />

into unitless scores reflecting<br />

the level of functionality. Scores for<br />

each indicator are combined to give an<br />

overall soil health rating. Widely respected<br />

soil health frameworks include<br />

the Cornell Soil Health Assessment, the<br />

Soil Management Assessment Framework<br />

(Andrews et al., 2004) and the<br />

Haney Test provided by Ward Laboratories.<br />

Metrics included in the assessments<br />

vary between labs, but they all aim to<br />

34 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


include physical, chemical and biological<br />

components. Familiar measurements<br />

including pH, electrical conductivity<br />

(EC) and essential nutrients<br />

appear on soil health panels as do<br />

traditional field evaluations like water<br />

infiltration and wet aggregate stability.<br />

Biological indicators include combustible<br />

soil organic matter, water soluble<br />

organic carbon and soil respiration.<br />

Several biological indicators must be<br />

viewed together to accurately interpret<br />

field conditions. For instance, increased<br />

microbial respiration does not always<br />

indicate improved soil health. High<br />

respiration rates combined with high<br />

organic matter likely indicate good soil<br />

health, but when the soil shows high<br />

respiration and low organic matter, the<br />

microbes may be burning soil carbon<br />

faster than it can be captured. Respiration<br />

that outpaces carbon sequestration<br />

leads to organic matter loss and soil<br />

degradation.<br />

Advances in Biological Testing<br />

Other biological metrics provide<br />

insight into nutrient cycling, disease<br />

pressure and crop stress tolerance. Enzyme<br />

analysis indicates the microbial<br />

community’s capacity to mineralize N,<br />

P, K and micronutrients. Pathologists<br />

can diagnose fungal, bacterial, nematode<br />

and viral pathogens so that growers<br />

can choose the right fumigants and<br />

crop rotations to keep disease pressure<br />

in check.<br />

Phospholipid Fatty Acid Analysis<br />

(PLFA) helps determine the abundance<br />

and types of microbes in the soil. Identifying<br />

some of the beneficial microbes<br />

helps us predict the soil’s ability to inhibit<br />

disease, enhance crop growth and<br />

increase nutrient availability. Recent<br />

advances in genomics offer exciting<br />

opportunities to sequence all the DNA<br />

found in a soil sample and map microbial<br />

community composition and<br />

functioning. Genomics offer a more<br />

comprehensive analysis of microbial<br />

community than PLFA can provide.<br />

Tracking shifts in the microbiome may<br />

help determine how land management<br />

influences the soil’s trajectory towards<br />

improved sustainability.<br />

Choosing Soil Health Indicators<br />

Healthy soils share many common<br />

characteristics, but growers may<br />

prioritize some attributes over others<br />

depending on their needs. Growers can<br />

select soil health indicators relevant to<br />

their unique goals, production system,<br />

climate and soil type. Farmers converting<br />

to no-till can monitor progress<br />

by measuring organic matter. Those<br />

who continue tilling but begin cover<br />

cropping may not observe significant<br />

OM increases, but they might find<br />

decreased compaction and improved<br />

soil aggregate stability. Biostimulant<br />

and organic amendment efficacy may<br />

be measured by analyzing enzymatic<br />

activity and changes in the soil microbiome.<br />

Soil health tests are accessible, affordable<br />

and offer practical insights into<br />

Continued on Page 36<br />

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Office: 559-686-3833 Fax: 559-686-1453<br />

2904 E. Oakdale Ave. | Tulare, CA 93274<br />

newerafarmservice.com<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 35


Continued from Page 35<br />

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progress by annually measuring soil<br />

health indicators most likely to change<br />

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implemented. Every farm can<br />

contribute to agricultural sustainability<br />

by adopting simple practices like<br />

applying carbon-based amendments<br />

or launching advanced regenerative<br />

programs such as no-till and intercropping.<br />

Soil health can also improve by<br />

knocking out disease pressure with soil<br />

fumigation and allowing beneficials to<br />

repopulate. Soil health tests can guide<br />

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Eryn Wingate is an agronomist with<br />

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County, California. Eryn provides soil<br />

health and nutrient management consulting<br />

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production while meeting sustainability<br />

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Citations & Resources<br />

Andrews, S.S., Karlen, D.L., and Cambardella, C.A.<br />

2004. The soil management assessment framework:<br />

a quantitative soil quality evaluation method. Soil<br />

Science Society of America Journal 68: 1945-1962.<br />

Moebius-Clune, B.N. et al. 2016. Comprehensive<br />

Assessment of Soil Health – The Cornell Framework<br />

Manual, Edition 3.1, Cornell University,<br />

Geneva, NY.<br />

Soil Health Institute – North American Project<br />

to Evaluate Soil Health Indicators: soilhealth-<br />

Natural Resources Conservation District Soil<br />

Health Assessment Resources: nrcs.usda.gov/<br />

institute.org/north-american-project-to-evalu-<br />

ate-soil-health-measurements/<br />

wps/portal/nrcs/detail/soils/health/assessment/?cid=stelprdb1237387<br />

Ward Laboratories Haney Test Information: wardlab.com/haney-test/<br />

EPA Reg. No. 264-616-87865<br />

Belchim <strong>Crop</strong> Protection USA, LLC<br />

2751 Centerville Road | Suite 100<br />

Wilmington, DE 19808<br />

Phone: 855-445-7990<br />

Email: info.usa@belchim.com<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

36 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


<strong>May</strong>/<strong>June</strong> <strong>2021</strong><br />

VINEYARD REVIEW<br />

FEATURED ARTICLES:<br />

The Potential of Ultraviolet Light to Suppress<br />

Grapevine Powdery Mildew<br />

Pg.38<br />

Irrigation Scheduling In Winegrape Vineyards<br />

Pg.46<br />

Grapevine Trunk Diseases<br />

Pg.48<br />

An All New Daily Radio Show<br />

Available now on the MyAgLife App, Download Today


VINEYARD REVIEW<br />

The Potential of<br />

Ultraviolet Light to<br />

Suppress Grapevine<br />

Powdery Mildew<br />

By DAVID M. GADOURY | Senior Research Associate,<br />

Plant Pathology and Plant-Microbe Biology Section, Cornell<br />

AgriTech, Geneva, NY<br />

Figure 1. Grape powdery mildew occupies a niche bathed in<br />

sunlight, and it senses and uses light to direct its development.<br />

Researchers are learning new ways to use that evolved process<br />

against the pathogen to suppress disease (all photos courtesy<br />

D. Gadoury.)<br />

Global winegrape production is<br />

largely based upon the production<br />

of the European winegrape Vitis<br />

vinifera, a host species comprised of cultivars<br />

that are all highly susceptible to<br />

infection by the grape powdery mildew<br />

pathogen Erisyphe necator as well as several<br />

other fungal and oomycete pathogens.<br />

Irrespective of the center of origin<br />

of Vitis vinifera or the major pathogen<br />

groups, the global ubiquity of both the<br />

host and various pathogens is now a<br />

fact faced by grape and wine producers<br />

everywhere.<br />

In particular, fungicidal suppression of<br />

grapevine powdery mildew is problematic.<br />

Resistance to many FRAC<br />

classes, including sterol demethylation<br />

inhibitors (DMI), strobilurins, benzimidazoles<br />

and succinate dehydrogenase<br />

inhibitor (SDHI) fungicides is sufficiently<br />

widespread that the forgoing<br />

classes are no longer effective in some<br />

viticultural regions. Organic production<br />

systems are also threatened. There are<br />

very few practical organic options for<br />

controlling powdery mildews. Many<br />

organic options entail undesirable<br />

non-target effects or are marginally<br />

effective. Additionally, many viticultural<br />

regions are located in Mediterranean<br />

climates with little rainfall during the<br />

crop production season. All of the<br />

foregoing creates the present situation:<br />

grapevine powdery mildew predominates<br />

as the principal threat to healthy<br />

fruit and foliage worldwide.<br />

UV Light to Suppress Pathogens<br />

Nearly all of the biomass of powdery<br />

mildews is wholly external to the host<br />

(Figure 1). They live in a world bathed<br />

in sunlight throughout the disease<br />

process. With the exception of the<br />

walls of their overwintering structures<br />

(chasmothecia), they possess none<br />

of the pigmentation that would offer<br />

protection from biocidal wavelengths<br />

of the solar spectrum (wavelengths<br />

of UVB between 280 and 290 nm.)<br />

Powdery mildews are favored by shade<br />

and repressed to some degree by direct<br />

sunlight exposure. They persist in the<br />

above niche due in part to their ability<br />

to repair UV-inflicted damage to their<br />

DNA through a robust photolyase<br />

mechanism driven by blue light and<br />

UVA.<br />

In 1990, we began work that led to<br />

the use of germicidal UVC lamps to<br />

suppress E. necator. The treatments<br />

were effective, but UVC also damaged<br />

38 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


VINEYARD REVIEW<br />

Figure 2. Researchers at Cornell used UVC applications to suppress grape powdery mildew as early<br />

as 1991. While effective, the treatments also caused damage to both the leaves and fruit. A breakthrough<br />

discovery several years later by a PhD student in Norway unlocked the key to effective<br />

treatments without plant injury.<br />

the vines, and the technology was never<br />

widely adopted (Figure 2). It took 20<br />

years before a critical breakthrough by<br />

a Ph.D. student in Norway (Aruppillai<br />

Suthparan) fundamentally changed<br />

how we could use UV light against<br />

plant pathogens. He found that if UV<br />

light was applied during night hours,<br />

we could use much lower doses than<br />

were required during daylight. That<br />

breakthrough largely resolved the issue<br />

of plant damage at the high UV doses<br />

required for daytime applications.<br />

Today, UV technology for plant disease<br />

suppression is being investigated by several<br />

working groups. Most exploit the<br />

link between darkness and the inability<br />

to withstand exposure to UV. When<br />

damage to pathogen DNA during darkness<br />

is not repaired within four hours, it<br />

is usually lethal.<br />

The UV spectrum used in such studies<br />

has ranged from a UVB waveband<br />

between 280 to 290 nm into the UVC<br />

range produced by low pressure discharge<br />

lamps yielding a peak output<br />

near 254 nm. Reduction of the severity<br />

of several powdery mildews has been<br />

attributed to direct damage to the<br />

pathogen by UV exposure. UVC has<br />

been reported to be directly inhibi-<br />

Continued on Page 40<br />

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<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 39


Figure 3. Tractor-drawn UVC array used in<br />

the first large-scale field trials on strawberries.<br />

Side-by-side arrays allowed two rows<br />

to be treated in each pass.<br />

Continued from Page 39<br />

tory to Botrytis cinerea on strawberry<br />

(Janisiewicz et al. 2016). In contrast,<br />

pathogens other than powdery<br />

mildews have been suppressed by<br />

exposure of their hosts to UV prior to<br />

inoculation, possibly due to enhancement<br />

of host resistance.<br />

The adaptation of nighttime UV treatments<br />

to commercial field plantings<br />

has necessitated the development of<br />

UV arrays powerful enough to apply<br />

effective doses at speeds that allow<br />

the equipment to complete treatments<br />

during the available night interval,<br />

often in late spring and early summer<br />

during some of the shortest nights of<br />

the year. Remember: we need about<br />

four hours of darkness after UV exposure<br />

in order to achieve the maximum<br />

suppression. A tractor-drawn UVC<br />

apparatus described in a report by<br />

Onofre et al (2019) was developed to<br />

suppress strawberry powdery mildew.<br />

This apparatus contained two hemicylindrical<br />

arrays of UVC lamps and was<br />

the basis of a later array design fitted<br />

to an autonomous robotic carriage<br />

produced by Saga Robotics, LLC. UVC<br />

treatments applied once or twice weekly<br />

at doses ranging from 70 to 200 J/m 2<br />

effectively suppressed strawberry powdery<br />

mildew (Podosphaera aphanis) to a<br />

degree that equaled or exceeded that of<br />

some of the best available fungicides.<br />

The potential for nighttime UV treatments<br />

to eliminate the threat posed by<br />

E. necator could greatly reduce the need<br />

for fungicide applications. In regions<br />

with higher rainfall and multiple fungal<br />

pathogens, the potential for nighttime<br />

UV treatments to remove the threat<br />

of powdery mildew would improve<br />

options for the remaining members of<br />

the pathogen and pest complex, such<br />

as downy mildew (Plasmopara viticola),<br />

bunch rot (Botrytis cinerea) and various<br />

arthropod pests.<br />

For all of the foregoing reasons, our<br />

objectives in the present study were to<br />

1) Determine the potential of nighttime<br />

UV applications to suppress grapevine<br />

powdery mildew; 2) Determine if UVC<br />

at disease-suppressive doses and frequency<br />

of application has any deleteri-<br />

40 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


Figure 4. Thorvald, an autonomous robotic<br />

device developed in collaboration with<br />

SAGA Robotics in Norway, can carry and<br />

power the same UV array used in tractor<br />

drawn devices.<br />

ous effects on vine growth, yield or crop<br />

quality; and 3) Determine if nighttime<br />

UV applications targeting powdery mildew<br />

have effects on other selected pests<br />

or diseases of grapevine.<br />

In summary, the mechanism underlying<br />

the success of nighttime UV applications<br />

is related to how pathogens deal<br />

with naturally-occurring ultraviolet<br />

light from the sun. Shorter-wave UVB<br />

and UVB both damage DNA in all living<br />

organisms. Exposure to UV causes<br />

thymine base pairs in the DNA to bind<br />

together, changing the genetic code<br />

to genetic gobbledygook. Pathogens<br />

sense visible light, but they also possess<br />

evolved systems that can repair the<br />

foregoing damage to their DNA caused<br />

Figure 5. Efficacy of UVC treatments for suppression<br />

of powdery mildew on Chardonnay grapes, 2019.<br />

by incoming UV. We now know that<br />

those biochemical and genetic repair<br />

systems are recharged by blue light and<br />

UV-A, and are reduced by red light and<br />

darkness. This photolyase-based repair<br />

mechanism effectively “unglues” the<br />

thymine base pairs as fast as they are<br />

created by UV, but the repair mechanism<br />

does not operate at night.<br />

Lamps producing UV light have been<br />

commonly available for over 75 years.<br />

Those that produce an effective wavelength<br />

and are powerful enough to<br />

be practically used against powdery<br />

mildews produce either UVC (100 to<br />

280 nm) or UVB (280 to 315 nm). Both<br />

UVC and UVB affect DNA in the same<br />

way by the aforementioned creation<br />

of thymine dimmers. UVB poses less<br />

potential to harm plants, and may<br />

therefore be preferred for static and<br />

permanent installations in greenhouses.<br />

However, with precise dosing, UVC<br />

can be used safely on even UV-sensitive<br />

crops.<br />

Low-pressure discharge lamps are the<br />

most common available technology.<br />

Low-pressure discharge UVC lamps<br />

are generally clear quartz-glass tubes<br />

containing a small amount of mercury<br />

vapor. Passing an electric arc through<br />

this vapor results in the efficient production<br />

of a narrow waveband centered<br />

on 254 nm, which is excellent for<br />

germicidal applications. UVB low-pressure<br />

discharge lamps are similar, but<br />

incorporate a fluorophore powder<br />

coating on the inside of the tube. When<br />

this is struck by the internally produced<br />

UVC, the fluorophore absorbs the<br />

UVC and emits the longer wavelength<br />

UVB. This process is also relatively<br />

inefficient, and nearly 95% of the<br />

usable germicidal energy is lost in<br />

the conversion from UVC to UVB.<br />

So, low-pressure discharge UVC<br />

lamps can produce much more<br />

usable power than comparably sized<br />

UVB lamps. While UV LEDs are<br />

available, they are presently far too<br />

expensive and underpowered to be<br />

useful for treating crops.<br />

Results Adapted to Grapevine<br />

Field trials for suppression of<br />

strawberry powdery mildew were<br />

initiated in Florida in 2017. Weekly<br />

applications of UVC provided suppression<br />

of foliar powdery mildew across<br />

the duration of the experiment that was<br />

substantially better than that provided<br />

by the best fungicide treatment in the<br />

trial, which was a combination of two<br />

materials sold under the trade names<br />

Quintec and Torino. We also confirmed<br />

in parallel measurements that the UV<br />

treatments did not reduce plant size or<br />

the yield of harvested berries. Continued<br />

trials on field plantings of strawberries<br />

duplicated the efficacy of the 2017<br />

trials.<br />

In our initial trials, we used a tractor-drawn<br />

array (Figure 3, see page<br />

40). Additional trials adapted modified<br />

designs of the original tractor-drawn<br />

array to an autonomous robotic<br />

device (Figure 4) manufactured by<br />

SAGA Robotics, a Norwegian company<br />

collaborating with our research<br />

group in developing this technology<br />

for multiple crops. The use of a robotic<br />

carriage provides additional flexibility<br />

in nighttime applications. At temperate<br />

latitudes, the duration of night near the<br />

summer solstice can be less than eight<br />

hours, leaving only about four hours<br />

during which the UV treatments could<br />

be applied with optimal effect. In situations<br />

where employing nighttime labor<br />

to make applications split over several<br />

relatively short night intervals would<br />

be problematic, an autonomous robotic<br />

device offers a practical alternative.<br />

In 2019, we came full circle and were<br />

ready to resume UV treatments on<br />

grapevine. As in our work on strawberry,<br />

we began by using a UV array and<br />

tractor-drawn carriage. UV Treatments<br />

were applied once per week at 100 or<br />

200 J/m 2 to Chardonnay vines that<br />

received no other fungicide treatments.<br />

Laboratory experiments had indicated<br />

that the UV doses used would stop 80%<br />

to nearly 100% of the conidia of E. necator<br />

from germinating. The incidence<br />

and severity of powdery mildew was<br />

assessed on leaves and fruit of UV treated<br />

vines, vines treated with an effective<br />

conventional fungicide and completely<br />

untreated vines. 2019 was a moderately<br />

severe year for powdery mildew.<br />

Continued on Page 42<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 41


VINEYARD REVIEW<br />

Disease Severity (%)<br />

50<br />

40<br />

30<br />

20<br />

Disease Severity (%)<br />

12<br />

10<br />

8<br />

6<br />

4<br />

2<br />

A<br />

B<br />

C<br />

10<br />

0<br />

Untreated<br />

Oxidate<br />

UVC<br />

0<br />

Fungicide Untreated 100 J/m 2 200 J/m 2<br />

Figure 6. Foliar severity of grapevine downy mildew on Chardonnay<br />

vines treated weekly with UVC at 100 or 200 J/m2 compared to a standard<br />

fungicide treatment and untreated control.<br />

Figure 7. Suppression of sour rot on Vignoles grapes treated<br />

with UVC at 200 J/m2 compared to a standard fungicide<br />

treatment and untreated control.<br />

40<br />

12<br />

A<br />

Figure 8. The egg and 10 immature stages of<br />

mites are susceptible to UV treatments, and<br />

this technology is now widely 8 used, particularly<br />

in the Netherlands for suppression<br />

of mites in greenhouses and high tunnel<br />

6<br />

production systems.<br />

Disease Severity (%)<br />

Continued from Page 2 41<br />

Both the 100 J/m 2 and 0 200 J/m 2 UVC<br />

treatments significantly but Untreated equivalently<br />

reduced the severity of powdery mildew<br />

on berries compared to the untreated<br />

vines, albeit not to the degree provided<br />

by the standard fungicide treatments<br />

(Figure 5, see page 41). What surprised<br />

us was that both the 100 J/m 2 and 200 J/<br />

m 2 UV treatments also suppressed foliar<br />

downy mildew (Plasmopara viticola),<br />

and did so better than the fungicide<br />

standard (Figure 6). Laboratory studies<br />

indicated that the suppression of the<br />

4<br />

10<br />

Figure B 9. A tractor-drawn UVC lamp array used to treat grapevines at Cornell Agritech, and<br />

the same array carried by the autonomous robot Thorvald, manufactured by Saga Robotics.<br />

0<br />

Untreated<br />

C<br />

downy mildew pathogen was due to<br />

a pre-inoculation increase in host<br />

resistance. This was distinct from the<br />

Oxidate impact of UV on UVC powdery mildew,<br />

which was primarily a direct effect of<br />

UV on the pathogen itself. However, in<br />

our 2020 trials, weather conditions were<br />

especially conducive to downy mildew,<br />

and the level of suppression of downy<br />

mildew from UV was only around 50%.<br />

That’s helpful, but it is nowhere near<br />

acceptable commerical control. So, we<br />

obviously have more work to do in this<br />

area.<br />

Disease Severity (%)<br />

30<br />

20<br />

The 2019 trials produced another<br />

surprise: the UV treatments effectively<br />

suppressed sour rot (Figure 7). This<br />

disease is a complex mess involving<br />

bacteria, fungi and fruit-feeding insects.<br />

We still don’t understand how UV is<br />

accomplishing this reduction, but given<br />

that there are very few effective means<br />

to suppress sour rot, any efficacy due to<br />

UV treatments is worth further investigation.<br />

In addition to suppressing plant pathogenic<br />

fungi, UV treatments can also<br />

suppress populations of phytophagous<br />

U<br />

42 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


VINEYARD REVIEW<br />

40<br />

NAVEL ORANGEWORM MONITORING SYSTEMS<br />

Disease Severity (%)<br />

30<br />

20<br />

10<br />

0<br />

Untreated UVC<br />

Fungicide<br />

Figure 10. Efficacy of UVC treatments for<br />

suppression of powdery mildew on Chardonnay<br />

grapes, 2020.<br />

mites (Figure 8). A number of studies<br />

have noted that UVB and UVC treatments<br />

can kill eggs of spider mites and<br />

European Red Mites. In addition to<br />

these effects, our preliminary trials indicate<br />

that the UV treatments can also<br />

alter behavior of adult mites, reduce egg<br />

laying, and reduce fecundity of the generation<br />

of surviving mites that emerge<br />

from UV treated eggs.<br />

As in our strawberry work, we eventually<br />

wanted to adapt the tractor-drawn<br />

grape UV array to a robotic carriage,<br />

and our partnership with SAGA robotics<br />

made this possible (Figure 9, see<br />

page 42). The navigation autonomy of<br />

the SAGA robot (Thorvald) is capable<br />

of tracking within a few centimeters of<br />

the trellis center at operational speeds<br />

between 1.25 to 2.5 mph. We evaluated<br />

UV doses between 100 J/m 2 and 200 J/<br />

m 2 at frequencies of either once weekly<br />

or twice weekly. All of the evaluated<br />

doses significantly suppressed powdery<br />

mildew on both fruit and foliage, and<br />

the twice-weekly 200 J/m2 treatment<br />

provided control that was superior to<br />

the fungicide standard (Figure 10).<br />

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What’s Next?<br />

We are collaborating with growers and<br />

scientists at multiple locations in the<br />

U.S. and Europe, including Bully Hill<br />

Vineyards in Hammondsport, N.Y.;<br />

Washington State University’s research<br />

and extension center in Prosser, and<br />

the USDA Horticultural <strong>Crop</strong>s Research<br />

Center in Corvallis, Ore. as<br />

well as multiple locations in California,<br />

Continued on Page 44<br />

— Brad Higbee,<br />

Field R&D Mgr, Trécé, Inc<br />

INCORPORAT ED<br />

INSECT PHEROMONE & KAIROMONE SYSTEMS<br />

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<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 43


VINEYARD REVIEW<br />

Continued from Page 43<br />

with designs and materials for UVC<br />

lamp arrays adapted for their vineyard<br />

pruning and training systems. These<br />

trials will be conducted over the course<br />

of the <strong>2021</strong> growing season. More<br />

about the autonomous robot Thorvald<br />

can be found at sagarobotics.com/.<br />

Our international working group<br />

is described on our project website:<br />

LightAndPlantHealth.org. It is a large,<br />

multidisciplinary, multi-institutional<br />

and international group representing<br />

several U.S. and overseas universities<br />

and government agencies, with industrial<br />

partnerships (Figure 11).<br />

The design of a lamp array to match a<br />

particular crop canopy and target pest<br />

biology is a critical aspect determining<br />

of the success of the treatments. Our<br />

cooperative projects with growers<br />

across the US have always involved our<br />

array designs and electronics. Some<br />

growers have designed and fabricated<br />

the various carriages for the arrays.<br />

But the UV array itself is NOT a DIY<br />

project, nor is calibration and the<br />

photobiological and epidemiological<br />

calculations that enter into calculations<br />

of a proper UV dose for specific applications.<br />

In addition to the engineering<br />

and biological considerations, both<br />

UVB and UVC can be injurious to you<br />

unless devices are properly designed<br />

and the lamps are properly shielded<br />

from direct view. No person should ever<br />

have an unshielded view of germicidal<br />

UV lamps, as there is a significant risk<br />

of eye and skin damage from exposure<br />

UVB and UVC. The protective gear that<br />

is required for safe applications is not<br />

expensive, and consists of UV-opaque<br />

clothing that covers all exposed skin,<br />

disposable gloves and a face-shield and<br />

eye protection rated for protection from<br />

UV. The arrays shown in this article<br />

also incorporate clear PVC curtains at<br />

each end of the array to limit escape<br />

of UV from the array. As would be the<br />

case with any IPM technology, UV does<br />

not pose undue risks to operators or the<br />

environment if used properly. Proper<br />

training and use protocols are the key<br />

to safe and effective applications.<br />

Figure 11. Group photo: Members of the research/extension team and advisory committee<br />

for our USDA-OREI project. Left to right: Laura Pedersen, Pedersen Farms, Geneva, NY; Eric<br />

Sideman, NOFA; Arupplillai Suthaparan, NMBU, Norway; Arne Stensvand, NIBIO Norway;<br />

Mariana Figueiro, Mount Sinai Light and Health Research Center (LHRC); Mark Rea, Mount<br />

Sinai LHRC; David Gadoury, Cornell University; Ole Myhrene, Myhrene AS, Norway; Rebecca<br />

Sideman, University of New Hampshire; and Robert Seem, Cornell University. Below (left to<br />

right), other members of the research and extension project team: Dr. Natalia Peres and PhD<br />

student Rodrigo Onofre, UFL Gulf Coast Research and Education Center; Dr. Lance Cadle-Davidson,<br />

USDA Grape Genetics Research Unit; Dr. Jan Nyrop, Department of Entomology,<br />

Cornell University and Director at Cornell AgriTech; Dr. Walt Mahaffee, USDA-ARS, Corvallis,<br />

OR; and Dr. Michelle Moyer, University of Washington, Irrigated Agriculture Research and<br />

Extension Center, Prosser.<br />

Our work has been funded by competitive<br />

grants from the USDA Organic Research<br />

and Extension Initiative, and the<br />

USDA Specialty <strong>Crop</strong>s Research Initiative.<br />

Additional support has been provided<br />

by the National Research Council<br />

of Norway, the New York Farm Viability<br />

Institute, the USDA Sustainable<br />

Agriculture Research and Extension<br />

Program and Bully Hill Vineyards. We<br />

work as a diverse international group<br />

to promote this research area and its<br />

applications, and to act as a resource to<br />

train others. The work spans disciplines<br />

from plant growth and photobiology to<br />

physics and lighting technology.<br />

David M. Gadoury is a senior research<br />

associate in Cornell’s Plant Pathology<br />

and Plant-Microbe Biology Section at<br />

Cornell AgriTech, where his program<br />

focuses on pathogen ecology, pathogen<br />

biology and disease management. He<br />

leads the Light and Plant Health Group.<br />

References<br />

Gadoury, D.M., Pearson, R.C., Seem, R.C., Henick-Kling,<br />

T., Creasy, L.L., and Michaloski, A. 1992. Control of<br />

diseases of grapevine by short-wave ultraviolet<br />

light. Phytopathology 82:243.<br />

Janisiewicz, W. J., Takeda, F., Glenn, D. M., Camp, M.<br />

J., & Jurick, W. M. (2016a). Dark Period Following<br />

UV-C Treatment Enhances Killing of Botrytis cinerea<br />

3.Conidia and Controls Gray Mold of Strawberries.<br />

Phytopathology, 106(4), 386–394. https://doi.<br />

org/10.1094/PHYTO-09-15-0240-R<br />

Michaloski, A.J. 1991. Method and apparatus for<br />

ultraviolet treatment of plants. U.S. Patent no.<br />

5,040,329.<br />

Onofre, R. B., Gadoury, D. M., Stensvand, A., Bierman,<br />

A., Rea, M., and Peres, N. A. 2019. Use of ultraviolet<br />

light to suppress powdery mildew in strawberry<br />

fruit production fields. Plant Dis. 105:0000-0000<br />

(in press).<br />

Suthaparan, A., Stensvand, A., Solhaug, K. A., Torre,<br />

S., Mortensen, L. M., Gadoury, D. M., Seem, R. C., and<br />

Gislerød, H. R. 2012. Suppression of powdery mildew<br />

(Podosphaera pannosa) in greenhouse roses by brief<br />

exposure to supplemental UV-B radiation. Plant Dis.<br />

96:1653-1660.<br />

Suthaparan, A., Stensvand, A., Solhaug, K. A., Torre, S.,<br />

Telfer, K. H., Ruud, A. K., Mortensen, L. M., Gadoury, D.<br />

M., Seem, R. C., and Gislerød, H. R. 2014. Suppression<br />

of cucumber powdery mildew by supplemental<br />

UV-B radiation in greenhouses can be augmented or<br />

reduced by background radiation quality. Plant Dis.<br />

98:1349-1357.<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

44 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


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our website at www.Bayer<strong>Crop</strong>Science.us. Bayer <strong>Crop</strong>Science LP, 800 North Lindbergh Boulevard, St. Louis, MO 63167. ©<strong>2021</strong> Bayer Group. All rights reserved.


VINEYARD REVIEW<br />

Irrigation Scheduling In<br />

Winegrape Vineyards<br />

Combine technology tools to confirm grapevine water needs.<br />

BY CRAIG MACMILLAN | Niner Wine Estates<br />

and KRIS BEAL | Vineyard Team<br />

The vine’s response to irrigation depends on soil physics, changes in weather patterns year to year, vine age, crop load, canopy size and<br />

disease status (photo courtesy C. Macmillan.)<br />

Irrigation is probably the most powerful<br />

tool a winegrape grower has in<br />

their tool box. Intelligent use of irrigation<br />

can control canopy size, manage vine<br />

stress, manipulate berry size, improve<br />

wine quality and conserve water. The key<br />

to achieving a grower’s viticultural goals<br />

through irrigation is data-driven scheduling<br />

to determine when and how much to<br />

irrigate.<br />

The tools growers have available for<br />

irrigation scheduling generally fall into<br />

five categories: soil-based, plant-based,<br />

weather-based, remote sensing and visual<br />

assessment of the vine’s water status.<br />

Soil-Based Methods and Technologies<br />

Soil moisture sensors are an effective way<br />

of measuring how much water is in the<br />

soil, where it is in the profile and how<br />

and when the vine is taking up that water.<br />

Another benefit of soil moisture sensors is<br />

the ability to measure the effect of winter<br />

rain on the soil profile<br />

For the best resolution, multiple sensors<br />

are needed per block reflecting soil types<br />

and topography. The key is placing sensors<br />

in locations which are representative<br />

of larger areas. Soil maps can help identify<br />

the best locations. Ideally, a soil map<br />

was made prior to vineyard installation.<br />

Mapping can still be done after installation<br />

with the help of a professional agricultural<br />

soils expert. Identifying representative<br />

areas within a vineyard can also<br />

be done using Normalized Difference<br />

Vegetative Index (NDVI) mapping. These<br />

maps identify areas of weak or excessive<br />

vigor. Those areas should be avoided as<br />

locations for sensors.<br />

The best depths for sensor placement can<br />

be determined by taking soil cores with<br />

a hand auger. Look for changes between<br />

soil horizons which might impact water<br />

holding capacity. Depths should represent<br />

rooting depths and just below<br />

to monitor deep percolation. Place the<br />

sensor in the vine row approximately 18<br />

inches from the vine trunk and four to<br />

six inches from the emitter.<br />

Types of soil moisture sensors include<br />

quantitative technologies such as time<br />

domain transmissometry, capacitance<br />

measurements, time domain reflectometry<br />

and qualitative methods such as<br />

matric potential. Each has its advantages<br />

and disadvantages in terms of cost, soil<br />

volume measured and ease of installation.<br />

No one type of sensor is ideal for all<br />

situations, so some research and ground<br />

truthing against other methods like visual<br />

assessment is required to find the best<br />

fit for your particular vineyard.<br />

Plant-Based Methods<br />

and Technologies<br />

Probably the most common method for<br />

evaluating vine water status is leaf or<br />

stem water potential using a device such<br />

as a pressure bomb. This method measures<br />

the tension (or “potential”) between<br />

the pull of water through the plant from<br />

evapotranspiration and how tightly water<br />

is held to the soil. A leaf is cut from the<br />

vine. The blade is placed under pressure<br />

forcing water back through the xylem of<br />

the petiole. The more pressure required to<br />

force the water out, the drier the vine is.<br />

A porometer is another tool which directly<br />

measures an indicator of vine water<br />

status. Porometers provide a reading of<br />

how relatively open or closed the stomata<br />

are on the leaf. Stomata are open when<br />

there is water available for evapotranspiration.<br />

When stomata start to close,<br />

the vine is protecting itself from drying<br />

out—a sign of stress. A sensor is clipped<br />

to a leaf blade and a measurement is taken<br />

automatically.<br />

An indirect measurement of stomatal<br />

46 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


VINEYARD REVIEW<br />

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Register at progressivecrop.com/conference<br />

closure can be done with an Infrared<br />

thermometer. Transpiration cools the<br />

surface of the leaf, making it cooler<br />

than the ambient air temperature. As<br />

stomata close, the temperature of the<br />

leaf blade increases. Readings are taken<br />

by simply pointing an infrared thermometer<br />

at the canopy. This method is<br />

simple, quick and generates good quality<br />

data that is easy to interpret when<br />

analyzed over time.<br />

Weather-Based Methods<br />

and Technologies<br />

While not a direct measure of vine<br />

water status, weather-based methods<br />

allow for data-informed scheduling<br />

decisions for the vineyard as a whole.<br />

By estimating how much water vines<br />

have transpired, a grower can decide<br />

how much water to put back into the<br />

soil, or not, in the case of deficit irrigation.<br />

This is done by estimating the<br />

daily water loss of the vine using evapotranspiration<br />

(ET) rates. The baseline<br />

for comparison is the reference ET, also<br />

called ET O<br />

or “full ET”. The California<br />

Irrigation Management Information<br />

System (CIMIS) maintains remote stations<br />

throughout California to provide<br />

reliable estimates of ET. Many weather<br />

stations available today also estimate<br />

ET O<br />

.<br />

Grapevines do not transpire at the full<br />

ET rate, so a crop coefficient (K C<br />

) is<br />

required to better reflect how the vine<br />

is behaving under these conditions.<br />

Essentially, the more canopy, the more<br />

water is transpired by the vine. As<br />

canopy size varies during the course of<br />

the growing season, the ratio of water<br />

transpired by the vine to reference ET<br />

changes. Therefore, the crop coefficient<br />

needs to be calculated at multiple times<br />

during the season. Calculating the crop<br />

ET (ET C<br />

) uses the equation ET O<br />

× K C<br />

=<br />

ET C<br />

.<br />

K C<br />

is determined by measuring the<br />

percent of the vineyard floor shaded<br />

at solar noon. This can be done with a<br />

gridded board to estimate the width of<br />

the shade and the percent of gaps in the<br />

shaded area. The percentage of shaded<br />

floor area is then used in the following<br />

equation to calculate the crop coefficient:<br />

K C<br />

= Percent shaded area × 0.017<br />

Using ET C<br />

is especially helpful for<br />

successful deficit irrigation. A crop<br />

coefficient for deficit irrigations, called<br />

K RDI<br />

, can be calculated by multiplying<br />

K C<br />

by the percent deficit desired using<br />

the equation K C<br />

× %RDI target = K RDI<br />

.<br />

This gives the grower confidence that<br />

they are hitting their specific target for<br />

deficit irrigation taking current weather<br />

conditions into account.<br />

An example:<br />

The percent of vineyard floor shaded is<br />

25%.<br />

This gives a K C<br />

of 0.425.<br />

If the RDI target is 75% the K RDI<br />

is 0.319.<br />

If the ET O<br />

rate for the week is two inches,<br />

0.638 acre-inches should be applied<br />

to maintain vines at their current water<br />

status.<br />

Remote Sensing<br />

Remote sensing using the Normalized<br />

Difference Vegetative Index (NDVI) is<br />

a powerful tool as it provides a literal<br />

picture of vine vigor across a large area<br />

to a high degree of resolution. Maps are<br />

created by flying over the vineyard with<br />

a drone or fixed wing aircraft. Cameras<br />

on the aircraft record the amounts<br />

of near infrared and red wave lengths<br />

reflected by the vineyard canopy.<br />

NDVI is calculated using an equation<br />

that compares these wavelengths. The<br />

resulting numbers correlate to the<br />

relative photosynthetic activity of the<br />

canopy which is directly tied to vine<br />

water status.<br />

Visual Assessment<br />

Purely qualitative practices for assessing<br />

vine water status are commonly<br />

used by growers. One can simply look<br />

at the appearance of vines searching for<br />

tell-tale signs of stress without the need<br />

for any devices. This is an excellent way<br />

of ground truthing other methods.<br />

Vine response to stress can readily be<br />

seen in the growth pattern of shoots<br />

and angle of leaf blades. When tendrils<br />

extend far beyond the shoot tip, the<br />

vine is growing rapidly and is under no<br />

stress. As the soil and vine begin to dry<br />

out, tendrils become shorter.<br />

Shoot tips are another good indicator.<br />

The state of a shoot tip can be determined<br />

by folding the last fully opened<br />

leaf up toward the tip. If the shoot tip<br />

extends past the leaves, it is active. If<br />

the folded leaves cover the shoot tip, it<br />

has stopped growing. Eventually, the<br />

tip will die altogether.<br />

Leaves provide another clue to vine<br />

stress. Under stress, leaves begin to<br />

droop. Leaves on an unstressed vine<br />

will form an obtuse angle to the petiole.<br />

As stress progresses, this angle becomes<br />

less and less until it is acute.<br />

Using visual inspection of the vine<br />

successfully requires many years of<br />

experience to perfect. Combining experience<br />

with quantifying technology<br />

may give the grower more confidence<br />

that their “read” of the vines is correct.<br />

One serious drawback of relying solely<br />

on looking at vines for indicators of<br />

stress is that there is a delay between<br />

the onset of stress and the symptoms<br />

becoming apparent in the state of the<br />

canopy. Overshooting a stress goal under<br />

RDI can be difficult to recover from,<br />

especially during late season.<br />

Consider using a combination of at<br />

least two different types of irrigation<br />

scheduling methods as each measures<br />

different variables and provides a different<br />

viewpoint of what is happening<br />

in the field. The vine’s response to irrigation<br />

depends on soil physics, changes<br />

in weather patterns year to year, vine<br />

age, crop load, canopy size and disease<br />

status. Taking all those variables into<br />

account is challenging even with the<br />

best tools. The more tools in the tool<br />

box, the better equipped the grower is<br />

to harness the power of well scheduled<br />

irrigation.<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us at<br />

article@jcsmarketinginc.com<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 47


VINEYARD REVIEW<br />

Grapevine Trunk<br />

Diseases<br />

Research Updates for<br />

Pruning Wound Protection<br />

Strategies<br />

A<br />

By ROBERT BLUNDELL | Robert Blundell, Graduate Student Researcher,<br />

UC Davis<br />

AKIF ESKALEN | Plant Pathologist, UCCE Specialist, UC Davis<br />

Grapevine trunk diseases (GTDs)<br />

are currently considered one of<br />

the most important challenges for<br />

viticulture worldwide. These widespread<br />

damaging diseases are caused by a<br />

broad range of permanent, wood-colonizing<br />

fungal pathogens, which<br />

primarily gain entry into grapevines<br />

via pruning wounds. GTDs can also<br />

reside latently within tissue as part of<br />

the normal grapevine microbiota, and<br />

environmental factors may trigger their<br />

switch to pathogenic.<br />

The economic impact of GTDs can be<br />

significant in both young and mature<br />

vines, with Black foot disease and Petri<br />

disease being predominant in young<br />

vines. In mature vines, Esca (Figure 1),<br />

Botryosphaeria dieback (Figure 2a and<br />

2b, see page 49), Eutypa dieback (Fig.<br />

2c and 2d, see page 49) and Phomopsis<br />

dieback are damaging and referred to<br />

as canker diseases due to characteristic<br />

cankers they cause in vines. Other<br />

major symptoms of their presence<br />

include poor vigor, leaf chlorosis (Fig.<br />

1a), berry specks and shoot and tendril<br />

dieback. Perennial cankers cause spur,<br />

cordon and trunk dieback and ultimately<br />

result in death of the entire vine.<br />

The majority of the fungal pathogens<br />

responsible for GTDs produce overwintering<br />

fruiting structures containing<br />

the infectious spores of the pathogen.<br />

These overwintering structures<br />

can be found on the bark surface of<br />

infected vines as well as on pruning<br />

and harvesting debris on vineyard<br />

floors. Another source of GTD fungal<br />

inoculum (spores) is from other woody<br />

perennial crops such as nut trees which<br />

are known to be infected by GTDs.<br />

Under conducive environmental<br />

conditions, largely precipitation events,<br />

the fruiting bodies release fungal<br />

spores which land on exposed pruning<br />

wounds, causing infection and thus<br />

completing their life cycle. Research<br />

has identified that the majority of spore<br />

release in California occurs during<br />

winter following precipitation (December<br />

to February), which also overlaps<br />

with pruning timing, thus creating<br />

a window for GTDs to infect vines.<br />

With this knowledge, pruning wound<br />

protection strategies alongside cultural<br />

practices are the best strategies to<br />

mitigate GTDs. Cultural practices are<br />

focused around sanitation, including<br />

using clean material when establishing<br />

a new vineyard, removal of pruned<br />

and infected material and pruning<br />

dead shoots, spurs and cordons below<br />

symptomatic tissue. Delayed pruning<br />

after the high disease pressure period<br />

has passed is another good option in<br />

California to mitigate GTD infection.<br />

The most effective way to protect<br />

pruning wounds from airborne fungal<br />

spores of GTDs is to apply registered<br />

chemical and/or biological pruning<br />

wound protectants. Ideally, these protectants<br />

should be applied shortly after<br />

pruning and in a dry weather window<br />

to avoid rain washing the solution away.<br />

B<br />

C<br />

Figure 1. Symptoms of esca vine decline:<br />

a) classic leaf stripe symptoms of esca;<br />

b) cross-section showing central white<br />

rot and canker on esca infected vine; and<br />

c) black spot and sectorial necrosis of<br />

esca-infected vine.<br />

48 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


A<br />

C<br />

B<br />

D<br />

VINEYARD REVIEW<br />

Methodology<br />

This comprehensive study was performed<br />

to evaluate a variety of registered<br />

and experimental chemical and<br />

biological agents to protect pruning<br />

wounds (Table 1) from the fungal<br />

pathogens Neofusicoccum parvum and<br />

Eutypa lata, which are aggressive causal<br />

agents of the GTDs Botryosphaeria<br />

dieback and Eutypa dieback, respectively.<br />

This study was set up in both a<br />

wine grape and table grape commercial<br />

vineyard in Sacramento County (cv<br />

Cabernet Sauvignon) and Kern County<br />

(cv Allison), respectively.<br />

Figure 2. Symptoms of grapevine trunk diseases on mature vines: a) classic dead arm<br />

symptoms of Botryosphaeria dieback disease; b) wedge-shaped canker characteristic of<br />

Botryosphaeria dieback; c) Eutypa dieback include stunted shoots with necrotic leaves; and d)<br />

canker and internal necrotic wedge-shaped staining in cross section of cordon characteristic of<br />

Eutypa dieback.<br />

The damaging effects of GTDs on vineyard<br />

longevity are likely to be reduced<br />

significantly if protectants are adopted<br />

when vines are young and subsequently<br />

applied annually.<br />

Commercial chemical protectants such<br />

as a combination of Rally and Topsin M<br />

have been shown to be effective in controlling<br />

GTDs. With a need for sustainable<br />

alternatives, there is huge interest<br />

in the research, development and use of<br />

biological pruning wound protectants.<br />

Biological pruning wound protectants<br />

exploit beneficial micro-organisms<br />

that possess either natural antagonistic<br />

activity or compete with the pathogen<br />

by colonizing the pruning wound faster<br />

to provide protection from GTD pathogens.<br />

Several commercially available<br />

beneficial microorganisms, including<br />

Trichoderma spp. and Bacillus spp.,<br />

have been shown to provide protection<br />

against GTDs (Brown et al. 2020; Kotze<br />

et al. 2011; Halleen et al. 2010; John<br />

et al. 2008). As well as being an alternative<br />

to fungicides, it is thought that<br />

biologicals could provide prolonged<br />

protection once they have colonized the<br />

pruning wound.<br />

All study vines were pruned (one foot<br />

long) in February (Figure 3a, see page<br />

50), and within 24 hours of pruning,<br />

the liquid protectants were sprayed<br />

with a one-liter hand-held spray<br />

bottle on the pruning wound until<br />

runoff (Figure 3b, see page 50). All<br />

protectants were prepared according<br />

to their label recommendations. The<br />

following day, canes treated with a<br />

chemical protectant were inoculated<br />

with roughly 2000 spores of either N.<br />

parvum or E. lata. Canes treated with<br />

a biological protectant were inoculated<br />

with the same amount of spores of<br />

either N. parvum or E. lata seven days<br />

after treatment application (Figure<br />

3c, see page 50). The positive control<br />

treatment had sterile distilled water<br />

applied to wounds and was inoculated<br />

with the same amount of spores<br />

of each pathogen. Eight months after<br />

Continued on Page 50<br />

Treatment or Trade Name Active Ingredient Manufacturer<br />

Application rate<br />

per acre (100gal)<br />

Table 1. List of all treatments used in the study, including their active ingredient, manufacturer and application rate.<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 49


VINEYARD REVIEW<br />

pathogen that was inoculated (Figure<br />

3e). After incubation for 5 to 14 days at<br />

room temperature, recovery of fungal<br />

pathogens was recorded by their morphological<br />

characteristics. The efficacy<br />

of the treatments controlling the GTDs<br />

was calculated as the Mean Percent of<br />

Infection (MPI) using the following<br />

formula: Number of GTD-infected<br />

samples (canes from which the pathogen<br />

could be re-isolated)/total number<br />

of canes inoculated x 100.<br />

Figure 3. a) Spur pruning of vines in February 2020: b) application of protectants; c) inoculation<br />

of pruned canes with GTDs; d) treated canes split longitudinally; and e) isolated segments<br />

cultured on growth media.<br />

Continued from Page 49<br />

inoculation, treated canes were collected<br />

and brought to the lab for further<br />

evaluation. Each cane was split with a<br />

knife longitudinally (Figure 3d) and<br />

segments were excised and plated<br />

on a growth medium to confirm the<br />

Results<br />

Our results from both field studies show<br />

that Biotam, a Trichoderma-based biological<br />

product, was the superior protectant<br />

overall, providing a consistently<br />

high level of pruning wound protection<br />

compared to the water-treated, inoculated<br />

positive control. In the Sacramento<br />

County trial, Biotam application<br />

resulted in an MPI of 5% and 0% for E.<br />

lata and N. parvum, respectively, compared<br />

to the water-treated, inoculated<br />

positive control with an MPI of 40%<br />

and 70% for E. lata and N. parvum, respectively<br />

(Figure. 4a and 4b). In Kern<br />

County, Biotam application resulted in<br />

an MPI of 0% and 10% for E. lata and<br />

N. parvum, respectively, compared to<br />

Mean Percent Infection of<br />

E. Lata (MPI)%<br />

Mean Percent Infection of<br />

N. parvum (MPI)%<br />

50<br />

40<br />

30<br />

20<br />

10<br />

0<br />

80<br />

60<br />

40<br />

20<br />

0<br />

Biotam<br />

Botector<br />

Topsin M + Rally<br />

Water treated - Non<br />

inoculated negative control<br />

Biotam<br />

Vintec<br />

BioTam + Crab Life-Powder<br />

GCM<br />

Sacramento County<br />

UCD 8745<br />

Vintec<br />

UCD 8189<br />

Topsin M + Rally<br />

Water treated - Non<br />

inoculated negative control<br />

UCD 8189<br />

Luna Sensation<br />

Serenade<br />

UCD 8717<br />

Botector<br />

Serenade<br />

GCM<br />

Terramera (Exp B)<br />

BioTam + Crab Life-Powder<br />

Crab Powder<br />

UCD 8717<br />

Water treated - Inoculated<br />

positive control<br />

UCD 8745<br />

UCD 8189<br />

Crab Life Powder<br />

Luna Sensation<br />

Terramera (Exp B)<br />

Water treated - Inoculated<br />

positive control<br />

Mean Percent Infection of<br />

E. Lata (MPI)%<br />

Mean Percent Infection of<br />

N. parvum (MPI)%<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

Biotam<br />

Topsin M + Rally<br />

50<br />

40<br />

30<br />

20<br />

10<br />

0<br />

Serenade<br />

Vintec<br />

Biotam<br />

Topsin M + Rally<br />

Water treated - Non<br />

inoculated negative control<br />

Kern County<br />

Vintec<br />

UCD 8717<br />

GCM<br />

Luna Sensation<br />

BioTam + Crab Life-Powder<br />

Serenade<br />

UCD 8189<br />

UCD 8745<br />

Luna Sensation<br />

Bacillus veleze fermented product<br />

Botector<br />

Water treated - Non<br />

inoculated negative control<br />

Terramera (Exp B)<br />

Crab Life Powder<br />

Botector<br />

Water treated - Inoculated<br />

positive control<br />

Terramera (Exp B)<br />

UCD 8745<br />

BioTam + Crab Life-Powder<br />

UCD 8717<br />

Crab Life Powder<br />

UCD 8189<br />

Water treated - Inoculated<br />

positive control<br />

Figure 4. Evaluation of treatments for pruning wound protection<br />

of E. lata (a) and N. parvum (b) in Sacramento County.<br />

Figure 5. Evaluation of treatments for pruning wound protection of<br />

E. lata (a) and N. parvum (b) in Kern County.<br />

50 <strong>Progressive</strong> <strong>Crop</strong> <strong>Consultant</strong> <strong>May</strong> / <strong>June</strong> <strong>2021</strong>


VINEYARD REVIEW<br />

the water-treated, inoculated positive<br />

control with an MPI of 25% and 45%<br />

for E. lata and N. parvum, respectively<br />

(Figure 5a and 5b, see page 50). This<br />

shows that Biotam is capable of providing<br />

simultaneous pruning wound<br />

protection against multiple fungal<br />

pathogens of GTDs, which is often<br />

challenging for protectants to achieve.<br />

Another Trichoderma-based biological<br />

product, Vintec, was also effective<br />

at protecting wounds. Application of<br />

Vintec (2.8 oz/A) resulted in an MPI of<br />

15% and 5% for E. lata and N. parvum,<br />

respectively, in Sacramento County<br />

(Figure 4a and 4b, see page 50) and an<br />

MPI of 5% and 10% for E. lata and N.<br />

parvum, respectively, in Kern County<br />

(Figure 5a and 5b, see page 50).<br />

Our results also showed that the chemical<br />

protectants Topsin M + Rally and<br />

Luna Sensation were effective at providing<br />

simultaneous pruning wound<br />

protection of E. lata and N. parvum<br />

in both Sacramento and Kern County<br />

trials. Application of Topsin M + Rally<br />

resulted in an MPI of 10% for both<br />

E. lata and N. parvum in Sacramento<br />

County (Fig. 4a and 4b, see page 50)<br />

and an MPI of 5% and 10% for E. lata<br />

and N. parvum, respectively, in Kern<br />

County (Figure 5a and 5b, see page<br />

50). Several naturally occurring biocontrol<br />

agents, including Trichoderma<br />

hamatum (UCD 8717), Aureobasidium<br />

pullulans (UCD 8189) and Bacillus<br />

sp. (UCD 8745), that were identified<br />

in California vineyards were also<br />

performing very well compared with<br />

other commercially available products<br />

(Figure 4 and 5, see page 50).<br />

Baumgartner, K. <strong>2021</strong>. Pruning-wound<br />

protectants for trunk-disease management<br />

in California table grapes. <strong>Crop</strong><br />

Protection, 141.<br />

Halleen, F., Fourie, P.H., and Lombard,<br />

P.J. 2010. Protection of grapevine<br />

pruning wounds against Eutypa lata<br />

by biological and chemical methods. A.<br />

Afr. J. Enol. Vitic. 31: 125–132.<br />

Kotze, C., Van Niekerk, J., Mostert,<br />

L., Halleen, F., and Fourie, P. 2011.<br />

Evaluation of biocontrol agents for<br />

®<br />

grapevine pruning wound protection<br />

against trunk pathogen infection. Phytopathol.<br />

Mediterr. 50: 247–263.<br />

John, S., Wicks, T.J., Hunt, J.S., and<br />

Scott, E.S. 2008. Colonisation of<br />

grapevine wood by Trichoderma harzianum<br />

and Eutypa lata. Aust. J. Grape<br />

Wine Res. 14:18-24.<br />

Comments about this article? We want<br />

to hear from you. Feel free to email us<br />

at article@jcsmarketinginc.com<br />

The Grower’s Advantage<br />

Since 1982<br />

Effective Plant Nutrients and Biopesticides<br />

to Improve <strong>Crop</strong> Quality & Yield<br />

©<br />

In conclusion, our 2020 field trials<br />

have shown that several biological and<br />

chemical treatments can provide efficient<br />

protection of pruning wounds of<br />

grapevine against one or more fungal<br />

pathogens responsible for the major<br />

grapevine trunk diseases (Esca, Botryosphaeria<br />

dieback and Eutypa dieback).<br />

Moreover, improving accurate<br />

diagnosis of GTDs will be essential in<br />

determining an effective product.<br />

ORGANIC<br />

Contains Auxiliary Soil & Plant Substances<br />

Botector ®<br />

Biofungicide<br />

®<br />

ORGANIC<br />

Plant Nutrients & Adjuvants<br />

®<br />

GARGOIL<br />

INSECT, MITE & DISEASE CONTROL<br />

Blossom Protect <br />

Biopesticide<br />

®<br />

Herbicide EC<br />

®<br />

References<br />

Brown, A.A., Travadon, R., Lawrence<br />

D.P., Torres, G., Zhuang., and<br />

For more information, call (800) 876-2767 or visit www.westbridge.com<br />

<strong>May</strong> / <strong>June</strong> <strong>2021</strong> www.progressivecrop.com 51


®<br />

IMAGINATION<br />

INNOVATION<br />

SCIENCE IN ACTION

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