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December 2012 Number 1 - Utah Native Plant Society

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Calochortiana <strong>December</strong> <strong>2012</strong> <strong>Number</strong> 1<br />

vetch), a species of ponderosa pine forests in northcentral<br />

New Mexico and south-central Colorado, reproduces<br />

by seed, but plants tend to allocate resources toward<br />

survival of individual plants, and it is believed to<br />

build up root stock reserves when aboveground parts are<br />

consumed (Ladyman 2003). Direct evidence supports an<br />

ability to lie dormant for two years, but monitoring has<br />

not yet been used to establish if it can remain dormant<br />

for a longer period.<br />

Although a number of Astragalus species contain<br />

toxins (such as miserotoxin or swainsonine) or accumulate<br />

selenium, thus making them poisonous to livestock,<br />

there are also many species that are highly desirable to<br />

herbivores. Lesica (1995) found fecundity losses in A.<br />

scaphoides due to livestock and insect herbivory ranging<br />

from 14-90% at two sites. Observations have confirmed<br />

that inflorescences are consumed by ants and<br />

moth larvae. Loss of seeds to weevil predation ranged<br />

from 0-33%. Sugars such as those found in flower nectar<br />

may increase palatability. Lesica also found very low<br />

recruitment, accounting for less than 17% of population<br />

growth. However, despite heavy losses in reproductive<br />

output and low recruitment, populations can continue to<br />

persist and increase in size. He suspects that persistence<br />

of many populations of long-lived plants may be more<br />

reliant on growth and survival of established plants than<br />

on recruitment from seed. Herbivory by cattle and game<br />

has also been observed in A. terminalis (railhead milkvetch),<br />

and seed predation in A. ripleyi may be the cause<br />

of significant seed loss (Heidel and Vanderhorst 1996,<br />

Ladyman 2003). Apparently, like A. scaphoides, this<br />

species has low recruitment rates and allocates a significant<br />

amount of resources toward maintenance of the<br />

root system. A. ripleyi is also consumed by a number of<br />

arthropods (aphids, treehoppers, carpenter ants), rodents<br />

and large mammals, including cattle, elk, deer, sheep<br />

and goats. A ninety percent reduction in fruit production<br />

due to herbivory was observed in A. ampullarioides<br />

(Shivwits milkvetch), which the authors suggest could<br />

have a significant impact on reproductive output (Miller<br />

et al. 2007). The toxicity of A. rusbyi is unknown.<br />

The effects of disturbances, such as tree thinning or<br />

burning, on Astragalus species vary widely. A. ripleyi is<br />

thought to be a “fire evader” rather than a stress tolerator<br />

(Ladyman 2003). Following fire, plants have been<br />

observed in areas where they have not been detected<br />

before, presumably emerging from dormant root systems<br />

underground. However, the stress-tolerator category<br />

may be appropriate, for a pattern of rapid colonization<br />

following fire and drought has also been observed<br />

in this species (Ladyman 2003).<br />

Thinning activities in pinyon-juniper woodlands at<br />

Mesa Verde National Park appeared to cause an increase<br />

in Poa fendleriana (muttongrass) that could result in<br />

undesirable competition impacts on A. schmolliae<br />

(Anderson 2004). Grass seeding post-fire also has the<br />

potential to cause negative impacts on this species.<br />

Drought is deleterious, but it is likely tolerant of fire<br />

because of a deep taproot. However, monitoring indicates<br />

that while fire may confer short-term benefits, it<br />

may also have long-term detrimental impacts (Anderson<br />

2004).<br />

OBSERVATIONS FROM FIELD STUDIES<br />

A. rusbyi has a very small range in northern Arizona,<br />

with the bulk of its population limited to a band approximately<br />

18 x 7 km (11 x 4.5 mi) in size to the west<br />

and north of the San Francisco Peaks and a few scattered<br />

populations to the west (Figure 1). Some of its<br />

habitat has been subjected to large wildfires over the last<br />

few decades; other areas have undergone ecological restoration<br />

treatments (tree thinning and prescribed burning);<br />

and much of its range in ponderosa pine forest is<br />

slated to undergo such treatments in the near future. Increasing<br />

tree densities of ponderosa pine, and a cessation<br />

of frequent fires in ponderosa pine forests since<br />

Euro-American settlement of this area of the Southwest<br />

have been well documented (Covington and Moore<br />

1994, Fulé et al. 1997).<br />

We currently do not have a thorough understanding<br />

of the basic ecology of this species. Additionally, we<br />

have insufficient knowledge of the effects of increased<br />

tree densities, tree thinning, or fire on the population<br />

dynamics. However, some limited information is available<br />

from large landscape scale studies within its range.<br />

Fisher and Fulé (2004) installed 121 20x50 m permanent<br />

monitoring plots on the south side of the San Francisco<br />

Peaks (specifically Agassiz Peak). Plots were established<br />

in five forest types: ponderosa pine, mixed<br />

conifer, aspen, spruce/fir and bristlecone pine. Overstory<br />

measurements and plant community data were<br />

collected between 2000 and 2003. A. rusbyi was found<br />

to be an indicator species for ponderosa pine forest, with<br />

an indicator value of 36.5 (p

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