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Abstracts of Papers - Harvard Forest - Harvard University

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Australian National <strong>University</strong>, Canberra, A.C.T.<br />

2601. - Differing ontogenetic origin <strong>of</strong> PCR<br />

("Kranz") sheaths in leaf blades <strong>of</strong> C, grasses<br />

(Poaceae)<br />

The origin and development <strong>of</strong> ground meristem and<br />

provascular tissue have been examined in leaf blades<br />

<strong>of</strong> eight C4 grasses, representing different taxonomic<br />

groups and the three recognized biochemical C4 types<br />

(NADP-ME, NAD-ME and PCK types). Comparisons were<br />

made with the C3 species, Festuca arundinacea (pooid).<br />

In NAD-ME (Panicum effusum, eupanicoid; Eleusine<br />

coracana, chloridoid) and PCK (Sporobolus elongatus,<br />

chloridoid) species, the provascular tissue <strong>of</strong><br />

primary veins gives rise to xylem, phloem and a<br />

mestome sheath; associated ground meristem differ-<br />

entiates as PCA ("C4 mesophyll") and the PCR ("Kranz")<br />

sheath. This parallels development in the C3 grass,<br />

except that associated ground meristem differentiates<br />

into mesophyll and a parenchymatous bundle sheath.<br />

By contrast, the provascular tissue <strong>of</strong> NADP-ME C4<br />

species (Panicum bulbosum and Digitaria brownii, eu-<br />

panicoid; Cymbopogon exaltatus, andropogonoid)<br />

differentiates into xylem, phloem and a PCR sheath;<br />

associated ground meristem giving rise only to PCA<br />

tissue. Findings support W.V. Brown's hypothesis<br />

that the PCR sheaths <strong>of</strong> NAD-ME and PCK-type C4 grasses<br />

are homologous with the parenchymatous bundle sheaths<br />

<strong>of</strong> C grasses, whereas in NAD-ME C4 grasses, they are<br />

homologous with mestome sheaths. Aristida<br />

biglandulosa and Arundinella nepalensis have unusual<br />

C4leaf anatomy <strong>of</strong> special interest to this hypo-<br />

thesis.<br />

DERSTINE, KITTIE S.* and SHIRLEY C. TUCKER.<br />

Department <strong>of</strong> Botany, Louisiana State <strong>University</strong>,<br />

Baton Rouge, LA 70803<br />

-Comparative floral ontogeny <strong>of</strong> Parkinsonia<br />

aculeata (Caesalpinioideae), Lupinus havardii<br />

(Papilionoideae) and Acacia baileyana (Mimos-<br />

oideae).<br />

The three subfamilies <strong>of</strong> Fabaceae are distinguished<br />

on the basis <strong>of</strong> floral symmetry, aestivation <strong>of</strong><br />

petals in bud (valvate or imbricate), degree <strong>of</strong><br />

fusion in calyx and corolla, and morphology <strong>of</strong> seeds<br />

and leaves. The first three characteristics will be<br />

addressed, using SEM primarily. Ontogenetic studies<br />

<strong>of</strong> a representative taxon in each subfamily are<br />

intended to determine when during development these<br />

diagnostic features first become evident. In each<br />

taxon, order <strong>of</strong> initiation <strong>of</strong> sepals and petals is<br />

used to establish first evidence <strong>of</strong> symmetry. Middle<br />

developmental stages elucidate first indications <strong>of</strong><br />

aestivation and/or apparent fusion among sepals,<br />

petals and filaments. Final flower form is seen in<br />

later developmental stages with petal expansion into<br />

divergent forms and cell differentiation as well as<br />

degree <strong>of</strong> filament fusion and further apparant petal<br />

fusion.<br />

DICKISON, WILLIAM C. Department <strong>of</strong> Biology,<br />

<strong>University</strong> <strong>of</strong> North Carolina, Chapel Hill, NC<br />

27514. - Fruits and seeds <strong>of</strong> the Cunoniaceae.<br />

Cunoniaceae fruit morphology varies from ventrally<br />

dehiscent follicles, and dry, septicidally dehiscent<br />

capsules, to dry, indehiscent capsules, fleshy<br />

drupes, berries, and winged fruit types. The fol-<br />

licular fruit is the primitive condition in the<br />

family from which dehiscent capsules and indehiscent<br />

forms evolved. The majority <strong>of</strong> species produce<br />

fruit in which the pericarp is differentiated into<br />

exocarp, mesocarp, and lignified, fibrous endocarp.<br />

Developmental and Structural Section 19<br />

Major shifts ih dispersal strategy resulted in more<br />

advanced taxa in which the entire fruit is modified<br />

for seed dispersal and protection. Most dehiscent-<br />

fruited genera produce seeds with dispersal append-<br />

ages in the form <strong>of</strong> wings or hairs. Hairs are<br />

generally apically comate, less commonly distributed<br />

in other patterns. Genera with indehiscent fruits<br />

possess a variety <strong>of</strong> seed morphologies but all are<br />

devoid <strong>of</strong> wings or hairs. Seed coats are exotegmic<br />

in construction, that is, the outer epidermis <strong>of</strong><br />

the inner integument differentiates into the<br />

mechanical layer. Two distinct trends are recog-<br />

nized in seed coat structure: (1) reduction in seed<br />

coat thickness, including loss <strong>of</strong> a mechanical layer,<br />

and (2) amplification <strong>of</strong> the seed coat by secondary<br />

divisions <strong>of</strong> integumentary cells in the post-<br />

fertilization ovule. The diversity <strong>of</strong> seed surface<br />

patterns will be described and illustrated.<br />

DIGGLE, PAMELA K.* and DARLEEN A. DEMASON. Botany<br />

and Plant Sciences, <strong>University</strong><br />

Riverside, 92521. - Developmental<br />

<strong>of</strong> California,<br />

relationship<br />

between the PTM and the STM in Yucca whipplei.<br />

Histological and anatomical observations were made<br />

on plants ranging from embryos to three-year-old<br />

plants <strong>of</strong> Yucca whipplei Torr. var. percursa Haines.<br />

Our objective was to determine the time and position<br />

<strong>of</strong> origin, ontogenetic relationship, and function<br />

<strong>of</strong> the primary thickening meristem (PTM) and the<br />

secondary thickening meristem (STM) during development<br />

<strong>of</strong> the vegetative axis. The PTM arises in<br />

the stem periphery during germination. It is longitudinally<br />

continuous from beneath the youngest<br />

leaf primordia to the primary root, and functions<br />

in the production <strong>of</strong> primary vascular bundles and<br />

ground tissue. The STM arises ontogenetically from<br />

the PTM in the base <strong>of</strong> two- to three-month seedlings<br />

and produces secondary vascular bundles and ground<br />

tissue. Parenchyma in the ground tissue is arranged<br />

in anticlinal cell files continuous from beneath the<br />

leaf bases, through the cortex and central cylinder<br />

to the pith. Individual vascular bundles in the<br />

primary body are collateral. The parenchyma cells<br />

<strong>of</strong> the ground tissue <strong>of</strong> the secondary body are also<br />

arranged in files continuous with those <strong>of</strong> the primary<br />

parenchyma. Secondary vascular bundles are<br />

amphivasal and have an undulating path with frequent<br />

anastomoses. The PTM and STM, primary and secondary<br />

vascular bundles, and files <strong>of</strong> primary and secondary<br />

ground tissue are continuous at all developmental<br />

stages studied. Development <strong>of</strong> the primary body is<br />

histologically and quantitatively similar to development<br />

in monocotyledons which possess only a PTI;<br />

and secondary growth is interpreted as a developmental<br />

continuation <strong>of</strong> the process <strong>of</strong> primary thickening.<br />

DUTE, ROLAND<br />

R. Department <strong>of</strong> Botany, Plant<br />

Pathology, and Microbiology, Auburn <strong>University</strong>,<br />

Auburn, AL 36849.<br />

- Features <strong>of</strong> sieve-element ontogeny in Ginkgo<br />

biloba.<br />

In an effort to enhance our knowledge <strong>of</strong> the phloem<br />

<strong>of</strong> gymnosperms, an ultrastructural investigation was<br />

conducted into the development <strong>of</strong> petiolar sieve<br />

elements <strong>of</strong> Ginkgo biloba. As in the sieve elements<br />

<strong>of</strong> other species, there is a stage <strong>of</strong> ER stacking<br />

which precedes cytoplasmic lysis. In some cases the<br />

ER forms concentric layers enclosing portions <strong>of</strong><br />

ribosome-rich cytoplasm. These concentric layers are<br />

held together by bridges <strong>of</strong> 7 nm in length which

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