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Compendium of Potato Diseases - (PDF, 101 mb) - USAID

Compendium of Potato Diseases - (PDF, 101 mb) - USAID

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Fig. 1.A, Lower portion <strong>of</strong> young potato plant showing: a, stem; b, stolons; c, roots; and d, seed tuber. B, Bud on stolon tip (bar represents<br />

100 ,m). C, Starch grains within cells <strong>of</strong> a potato tuber (bar represents 10pm), showing characteristic refraction patterns within the grain.<br />

Tubers<br />

The tuber (Fig. 2) is formed at the tip <strong>of</strong> the stolon (rhizome)<br />

as a lateral proliferation <strong>of</strong> storage tissue resulting from rapid<br />

cell division and enlargement. Enlargement approximates a<br />

64-fold cell volme increase.<br />

'Re stolon usually breaks <strong>of</strong>fclose to the tuber during harvest<br />

or dies with the plant on maturity and is evident either as a short<br />

stub o r sm all scar .,E<br />

In stens, stolons, and tubers, vascular tissue initiallv forms as<br />

bikollateral bundles with groups <strong>of</strong> thin-walled phloem cells<br />

outside <strong>of</strong>'the xylem (outer phloem) and toward the center and<br />

inside the xyleml(inner phloem). As th' stolon enlarges to form<br />

the tuber. parenchyna developing within the bundles tends to<br />

split the separa it iroups. and the vascular ring becomes spread<br />

olt. New groups <strong>of</strong> phloem including sieve tubes, companion<br />

cells, and conducting parenchyma elements are formed as the<br />

tuber enlarges. Carbohydrates are stored within storage parenchyima<br />

ce',s <strong>of</strong> pith and cortex in the form <strong>of</strong> starch granules<br />

with characteristic markings.<br />

Tuber constitucnts vary with cultivar and growing conditions.<br />

E:stimated amounts <strong>of</strong> constituents may also reflect differences<br />

in methods <strong>of</strong>chemical analysis. Ranges in the whole fresh tuber<br />

are: water, 63-87i: carbohydrates, 13-30("i (including a fiber<br />

content <strong>of</strong>N. 17-3.48Ci ): protein, 0.7-4.61"; fat, 0.02-0.96(' ; and<br />

ash, 0.44-1.91". Additional constituents include sugars, notnstarchy<br />

polysaccharides, enzymes, ascorbic acid and other<br />

vitamins, phenolic substances, and nucleic acids,<br />

The tuber surface permits or excludes entrance <strong>of</strong> pathogens,<br />

regulates rate <strong>of</strong>gas exchange or water loss, and protects against<br />

mechanical damage. The surface is not fixed and static but will<br />

maintain and regenerate itself through wound healing reactions<br />

which influence disease incidence and severity, preservation in<br />

storage, and seed germinability and performance,<br />

Tle epidermis exists for only a short time on tile youngest<br />

tubers <strong>of</strong> approximately I cm or less in diameter. Stomata are<br />

scattered ir the epidermis and permit gas exchange. A shortlived<br />

penuerm is derived from tile epidermis and is soon<br />

replaced by a more permanent periderm or cork layer arising<br />

from meristenatic ca<strong>mb</strong>ium cells below the epidermis. This<br />

periderm in mature tubers is composed <strong>of</strong> 6-10 layers <strong>of</strong> bricklike,<br />

thin-wvalled cells, one on top <strong>of</strong> tie otiher, without<br />

intercellular spaces and with suberized cell walls. Periderm<br />

STEM ED J<br />

0<br />

\,\<br />

. ".<br />

" APEX<br />

BUDEND<br />

NEEL E, ROSE END<br />

STOLO<br />

,<br />

R ID, ' A C A L U D<br />

ORSK-N ' OR'eye<br />

CORTEX' LATERAL UD<br />

VASCULAR RING LAOR EYE<br />

VASCULAR ITORASE BO OFEY<br />

ARENCHYA !<br />

its Trts<br />

Fig. 2. The potato tuber and its parts.<br />

characteristics vary considerably with cultivar (Fig. 3).<br />

Wound healing (Fig. 3) develops under cut, bruised, or torn<br />

surfaces. Suberin forms within 3-5 days in walls <strong>of</strong> living cells<br />

under the wound. A cork ca<strong>mb</strong>ium layer developing under the<br />

suberized cells gives rise to a wound periderm. The promptness<br />

with which wound healing develops is Jependent upon environment<br />

(temperature, humidity, and aeration) and the physiology<br />

<strong>of</strong> the tuber.<br />

Cut tuber surfaces exposed to dr. ing air may seem to have a<br />

tough, resistant covering. Drying kills living surface cells and<br />

interferes with normal wound-healing activity. Dried surfaces<br />

do not exclude pathogens nor prevent dehydration and should<br />

not be confused with wound healing.<br />

Rates <strong>of</strong>' wound healing, including both suberization and<br />

periderm development, increase approximately threefold<br />

between 5 and 10' C and again threefold between 10 and 200 C.<br />

Oxygen supply less than that <strong>of</strong> the atmosphere and carbon<br />

dioxide greater than that <strong>of</strong> tile atomosphere progressively<br />

inhibit wound healing. Wound healing is most rapid between 80<br />

and 100%rh: however, the presence <strong>of</strong> free water on the surface<br />

that excludes oxygen is detrimental. Wound healing is more<br />

rapid in stored, recently harvested tubers, and as the tubers age,<br />

ability to heal wounds gradually diminishes. Also, periderm<br />

development in the cortical areas is more rapid than in the<br />

medullary region. Irradiation by sunlight or by ionizinggamma<br />

3

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