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Abstracts of Papers - Harvard Forest - Harvard University

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in the concept <strong>of</strong> "serial homology", and the more<br />

concise notion <strong>of</strong> strict homology which (by defini-<br />

tion) is due to descent. A historical perspective is<br />

particularly illuminating, especially as the basic<br />

principles <strong>of</strong> comparative morphology are largely<br />

conceived in a pre-evolutionary environment. Em-<br />

phasis will be placed on developmental analysis in<br />

comparative morphology as a basic process in the<br />

generation <strong>of</strong> the modular organism. Knowledge <strong>of</strong><br />

development can frequently illuminate comparative<br />

analysis. Examples will be cited where the organiza-<br />

tional plasticity almost defeats the possibility <strong>of</strong><br />

evolutionary morphological analysis in modular organ-<br />

isms.<br />

W. H. WAGNER, JR., Department <strong>of</strong> Botany, <strong>University</strong><br />

<strong>of</strong> Michigan, Ann Arbor, Michigan 48109. -<br />

Homology and the early<br />

plants.<br />

diversification <strong>of</strong> vascular<br />

Primitive vascular plants are the ones that first appeared<br />

in the fossil record, that possess simple life<br />

cycles,and are most similar to the outside group, the<br />

bryophytes. Because <strong>of</strong> their diversity, homology <strong>of</strong><br />

even major organs has been controversial. Theories<br />

like the Stelar Theory or the Telome Theory try to<br />

fit the morphics <strong>of</strong> plants into preconceived molds<br />

Objectivity is best accomplished by using classical<br />

tests <strong>of</strong> position, ontogeny, mature structure, and<br />

absence <strong>of</strong> intermediates. Evidence <strong>of</strong> early diversification<br />

<strong>of</strong> vascular plants comes from cladistic analysis<br />

<strong>of</strong> living groups, psilotopsids, lycopsids,<br />

equisetopsids, and polypodiopsids, together with the<br />

fossil remains <strong>of</strong> trimerophytes, zosterophytes, and<br />

rhyniophytes, a motley assemblage. Our problem is<br />

to connect different organs in different groups, because<br />

there are such large gaps, and intermediate<br />

stages or trends are lacking. How teratology fits<br />

into this is a question. In addition to varlous tissue<br />

types, the major organs are discussed:stem, root,<br />

leaf, sporangium, spore, gametophyte, gametangia,<br />

gametes, embryo, and foot. Because <strong>of</strong> homoplasy,<br />

homology is, by itself, not necessarily a criterion<br />

<strong>of</strong> relationship. At the tissue level, the stele provides<br />

a challenge; at the organ level, the foliar<br />

appendages. Parsimony suggests that at least in the<br />

case <strong>of</strong> the leaf, all <strong>of</strong> the appendages were originally<br />

emergences. The position <strong>of</strong> sporangia, so fundamental,<br />

apparently, in the early differentiation<br />

<strong>of</strong> vascular plants, is a good example, <strong>of</strong> the absence<br />

<strong>of</strong> intermediates, suggesting abrupt, rapid changes.<br />

There is a spectrum <strong>of</strong> degrees<br />

organs <strong>of</strong> early vascular plants<br />

to very questionable.<br />

<strong>of</strong> homology <strong>of</strong> the<br />

-- from very obvious<br />

Poster Session<br />

BASILE, DOMINICK V. and MARGARET R. BASILE<br />

Department <strong>of</strong> Biological Sciences, H. H.<br />

Lehman College <strong>of</strong> CUNY, Bronx, N.Y. 10468.<br />

- Auxin antagonist-induced desuppression<br />

<strong>of</strong> leaf primordia <strong>of</strong> Plagiochila arctica<br />

(Hepaticae): Possible integration <strong>of</strong><br />

auxin, ethylene and hydroxyproline-alterable<br />

proteins in correlative control <strong>of</strong><br />

cellular suppression.<br />

Two inhibitors <strong>of</strong> auxin transport, triiodobenzoic<br />

acid (TIBA) and N-l-naphthylphthalamic<br />

acid<br />

auxin action, i -<br />

(NPA), and an inhibitor <strong>of</strong><br />

(p-chlorophenoxy) isobutyric<br />

acid (PCIB), induced the same kind <strong>of</strong> pheno-<br />

Developmental and Structural Section 13<br />

variation in Plagiochila arctica Bryhn &<br />

Kaal. (Hepaticae) as do antagonists <strong>of</strong> ethy-<br />

lene synthesis/action and antagonists <strong>of</strong><br />

hydroxyproline-protein (hyp-protein) syn-<br />

thesis. This indicates that the two phyto-<br />

hormones and a cell surface protein sensi-<br />

tive to antagonists <strong>of</strong> hyp-protein synthesis<br />

play an integrated role in the correlative<br />

control <strong>of</strong> cellular suppression - primordium<br />

development. Auxin-induced ethylene syn-<br />

thesis and ethylene-induced cell surface<br />

hydroxyproline protein deposition correlated<br />

with suppressed development have been re-<br />

ported byothers, previously. This, however,<br />

is the first experimental evidence to impli-<br />

cate all three molecules, two phytohormones<br />

and a cell surface glycoprotein, in the same<br />

morphoregulatory system. This correlative<br />

control system conceivably plays an impor-<br />

tany role in other, if not all, groups <strong>of</strong><br />

land plants (Embryophyta).<br />

CAESAR, J. C. AND A. D. MACDONALD*. Department<br />

<strong>of</strong> Biology, Lakehead <strong>University</strong>, Thunder Bay,<br />

Ontario. P7B 5EI.<br />

- Comparison <strong>of</strong> early growth <strong>of</strong> vegetative and<br />

reproductive short shoots <strong>of</strong> Betula papyrifera.<br />

This study shows the cost to short shoot growth <strong>of</strong><br />

female inflorescence development. Expanding and<br />

flushing short shoot buds were collected from mature<br />

trees from April-June 1982. Quantitative analyses<br />

were made on fresh and FAA-fixed material for<br />

relative growth rates (RGR) <strong>of</strong> leaves and buds,<br />

specific leaf area (SLA), leaf area ratio (LAR), leaf<br />

area (LA) and number <strong>of</strong> leaf side nerve pairs (SNP).<br />

Material was partially dissected to determine whether<br />

the bud was reproductive or vegetative. Short shoot<br />

buds may be vegetative or may bear a female<br />

inflorescence; these buds may be proximal on a long<br />

shoot or terminal on a short shoot. Axillary short<br />

shoot buds flush later than 2-4 year old short shoot<br />

terminal buds, which flush later than 5-10 year old<br />

shoots. Mean RGR <strong>of</strong> 5-10 year old short shoot buds<br />

is greater than that <strong>of</strong> younger short-shoot buds. It<br />

is suggested that older short shoot buds are<br />

relatively autonomous and that the flushing long<br />

shoot exhibits an inhibitory influence on the<br />

proximal axillary buds and possibly on young short<br />

shoot terminal buds. Reproductive short shoots diffr<br />

from vegetative short shoots in that they have lower<br />

LAR's and leaf RGR's, higher SLA's, smaller LA's,<br />

fewer SNP's and they seem to grow more in length<br />

than in width. These findings are related to<br />

reproductive cost. The developing inflorescences<br />

act as preferred 'sinks' for resource allocation.<br />

CECICH, ROBERT A. <strong>Forest</strong>ry Sciences Laboratory,<br />

P.O. Box 898, Rhinelander, WI 54501 -<br />

Histochemical and ultrastructural changes in<br />

microsporangia <strong>of</strong> jack pine during the winter.<br />

The development <strong>of</strong> jack pine (Pinus banksiana Lamb.)<br />

microsporangia from October to April was investigated.<br />

DNA, RNA, and protein content <strong>of</strong> sporogenous<br />

cells was measured with a microdensitometer at<br />

monthly intervals. DNA was unreplicated (2c) until<br />

March when DNA synthesis was first noted, coinciding<br />

with a loss <strong>of</strong> condensed chromatin. Protein staini<br />

ng i ncreased i n Apri . RNA stai-n i ng i ncreased i n<br />

December, followed by a loss <strong>of</strong> staining in January.

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