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Abstracts of Papers - Harvard Forest - Harvard University

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Tsuga canadensis, which may be a reflection <strong>of</strong> .the<br />

stronger apical dominance in the former species. The<br />

pipe model would have to be modified to account for<br />

the above data, such that each unit pipe system had<br />

many more but smaller tracheids near the top than the<br />

bottom <strong>of</strong> the tree, and such that the trunk component<br />

<strong>of</strong> a unit pipe had more and wider tracheids than the<br />

lateral branch component. A more useful morphogenetic<br />

model involves hormonal gradients that control tracheid<br />

size and number in the plant. Hydraulically the ar-<br />

chitecture <strong>of</strong> these species favors the trunk over<br />

lateral branches and may thus help the upper leaves on<br />

the tree to compete with lower leaves for water and<br />

minerals.<br />

FAGERBERG, WAYNE, R. Dept. <strong>of</strong> Biology,<br />

Southern Methodist <strong>University</strong>, Dallas, TX<br />

75275.- A morphometric analysis <strong>of</strong> the<br />

homogeneity <strong>of</strong> palisade cell structure in<br />

leaves <strong>of</strong> Helianthus annuus. L.<br />

Leaves were divided into four quadrants and<br />

random samples taken from each quadrant.<br />

The ratio descriptors, Vv and Sv were cal-<br />

culated to describe the relationship between<br />

organelle compartment and cell size for the<br />

chloroplast, mitochondria, vacuole, micro-<br />

body, oil, starch, and mitochondrial -<br />

chloroplast membrane compartments. Since<br />

ratio values do not <strong>of</strong>ten reflect changes<br />

in mean cell volume, cell volumes and actual<br />

compartment sizes were also determined. In<br />

mature fully expanded leaves statistically<br />

significant variations were found between<br />

quadrants in Vv ratio <strong>of</strong> the chloroplast,<br />

vacuolar and starch compartments and in the<br />

Sv ratios <strong>of</strong> the granal membranes. The<br />

granal membrane compartment was the most<br />

variable, between sampled quadrants. The<br />

starch compartment was significantly smaller<br />

in the bottom 1/2 <strong>of</strong> the leaf suggesting<br />

that starch may be more rapidly mobilized<br />

from the lower half <strong>of</strong> the leaf. This study<br />

suggests that palisade cells are not homo-<br />

genous throughout the whole leaf due to<br />

variation in organelle compartments involved<br />

with photosynthesis. These results will be<br />

compared to similar data derived from<br />

developing leaves.<br />

FIORES, EUGENIA M. Escuela de Biologia, Univer-<br />

sidad de Costa Rica, San Josg, Costa Rica, Amgrica<br />

Central. - Cauline glands <strong>of</strong> Gunnera insignis.<br />

Cauline glands <strong>of</strong> Gunnera insignis were studied with<br />

light and scanning electron microscopy. Two types<br />

are recognized: (1) stellate glandular trichomes<br />

secreting mucous material and (2) whitish lobulated<br />

bodies covered by stomata which release water. The<br />

glandular trichomes develop around the leaf<br />

primordia and between the numerous squamules. These<br />

organs, as well as the shoot apex, are immersed in<br />

the mucous secretion. Many filaments <strong>of</strong> Nostoc and<br />

other organisms (algae, fungi, nematodes, insect<br />

larvae) are observed living in the mucilage. Nostoc<br />

is also recognized inside the trichomes and cauline<br />

tissues. Eventually, these trichormes degenerate and<br />

form brownish spots associated with Nostoc. The<br />

structures wich release water develop later and<br />

occupy the spaces left by the glandular trichomes.<br />

They cease functioning, turn green and extend<br />

longitudinally when the leaf~ which they surround<br />

Developmental and Structural Section 21<br />

reaches maturity. The interaction Gunnera - Nostoc<br />

represents the only known symbiosis between an<br />

angiosperm and a nitrogen-fixing bluegreen alga.<br />

This relationship is still not well known.<br />

Apparently in Gunnera the alga Nostoc penetrates<br />

through the glandular trichomes. It seems pertinent<br />

to study the role <strong>of</strong> these glands in relation with<br />

Nostoc penetration and the nitrogen fixing mechanism.<br />

FOLSOM, MICHAEL W. Dept <strong>of</strong> Botany, Univ. <strong>of</strong> Alberta,<br />

Edmonton, Alberta, CANADA T6G 2E9. -Structural aspects <strong>of</strong> the<br />

central cell gf Soybean. Glycine max (L) Merr. with respect to<br />

fixation technique.<br />

Ultrastructure <strong>of</strong> the eight nucleate embryo sac <strong>of</strong> soybean Glycine<br />

max (L.) Merr. demonstrates an unusual sequence <strong>of</strong> events in the<br />

central cell. Metabolites enter the embryo sac, are polymerized into<br />

starch grains, and are degraded mostly disdppearing from the<br />

central cell before fertilization. These starch grains are organized<br />

into groups that have been referred to as "packets" by previous<br />

workers. Unlike starch grains reported in most plant cells these<br />

packets do not appear to be membrane bound. The absence <strong>of</strong> a<br />

membrane is most likely not caused by fixation problems since<br />

other membrane bound organelles <strong>of</strong> the central cell exhibit normal<br />

membranes. The addition <strong>of</strong> Alcian Blue 8GX (AB) to the fixation<br />

process shows that rather than being naked or bound by a plastid<br />

membrane, these paskets are at least partially enclosed in a layer <strong>of</strong><br />

amorphous material, a mucopolysaccharide, deposited some time<br />

after the starch grains begin to form. Coomassie Brilliant Blue has<br />

shown that the material surrounding the starch packets has a protein<br />

component. The role <strong>of</strong> Alcian Blue acting as stabilizing agent for<br />

this glycoprotein and the preservation <strong>of</strong> cellular components by<br />

various fixation techniques (e.g. GA/Os04, GA + AB/Os04,<br />

GA/OsOi/TA/OsO4, and freeze substitution) will be discussed with<br />

respect to the starch packets and associated glycoprotein in the<br />

central cell.<br />

FREEMAN, THOMAS P., MURRAY E. DUYSEN AND<br />

THOMAS J. GULYA. Departments <strong>of</strong> Botany and<br />

Plant Pathology, North Dakota State<br />

<strong>University</strong> and U.S.D.A. Agricultural<br />

Research Service, Fargo, N.D. 58105.<br />

chloroplasts caused by Pseudomonas<br />

syringae pv. ta etis.<br />

Severe chlorosis and ultrastructural modifi-<br />

cations <strong>of</strong> chloroplasts occur in sunflowers<br />

in response to infections <strong>of</strong> Pseudomonas<br />

syringae pv. tagetis. Chlorosis became<br />

apparent within two days after the cotyledons<br />

<strong>of</strong> ten day old sunflower seedlings were<br />

inoculated with the bacteria. The first<br />

symptoms gererally appeared in the center <strong>of</strong><br />

leaves at the second node above the cotyle-<br />

dons. During the rext few days the chlorosis<br />

progressed to include leaves at several<br />

nodes. Despite the fact that some <strong>of</strong> these<br />

leaves lost essentially alL <strong>of</strong> their pigmen-<br />

tation they remained turgid and continued to<br />

expand. The loss <strong>of</strong> pigmentation is<br />

directly related to ultrastructural changes<br />

within the chloroplast. Grana thylakoids<br />

became dilated and separated from the granal<br />

stacks. These thylakoid membranes were not<br />

altered as in the cases <strong>of</strong> chromoplast<br />

formation or normal senescence. Both grana<br />

and stroms thylakoid membranes coalesced to<br />

form a large membrane sheet in the center <strong>of</strong><br />

the plastid. Starch and plastid ribosomes<br />

were lost early in the chlorotic cycle.<br />

Other cellular organelles do not appear to be<br />

altered by the bacterial i nf ection .

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