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Volume 91, Number 4<br />

2004<br />

Croat<br />

Revision of Dieffenbachia<br />

more attractive to beetle pollinators, since only the apparently absent, with the fertile staminate and<br />

lowermost flowers are eaten (Fig. 1B).<br />

fertile pistillate portions essentially contiguous. The<br />

length of the sterile portion of the spadix is here<br />

ANDROECIUM<br />

defined as that portion which lies between the lowermost<br />

functional androecium and the uppermost<br />

Staminate flowers consist of 4 stamens united functional pistil regardless of the presence of pisinto<br />

a 4- or 5-sulcate truncate synandrium (Figs. tillodes and staminodes along its length. However,<br />

2E, 5G, 23G, 26E). The apex of the synandrium the sterile portion of the spadix is usually quite<br />

often has a minute slit or an equidistant series of obvious since a significant proportion of the sterile<br />

3 minute slits connected at the center. Upon drying section is devoid of flowers. The axis of the sterile<br />

the apex of the synandrium may become wrinkled portion is typically convex as if the terete axis of<br />

along the margin and may also have a concave sur- the spadix (now fused) was half sunken into the<br />

face. The anthers are contiguous or nearly so, af- leafy tissue of the spathe.<br />

fixed near the upper edge of the synandrium. The<br />

thecae are obovoid to cylindroid, opening by apical<br />

PISTII,I,ATE SPADIX<br />

slits just below the upper edge of the synandrium.<br />

The pollen is dispersed in slender, subterete filaments<br />

and typically projects up to 1 cm above the<br />

surface of the synandrium. When the stamens are<br />

at anthesis, the shedding pollen can completely fill<br />

the now closing spathe (Fig. 5F).<br />

The pistillate portion of the spadix is fused<br />

throughout its entire length to the spathe. What appears<br />

to be a stipe is readily apparent at the base.<br />

The pistillate flowers rarely extend very close to the<br />

base of the spathe (Fig. 4C). After the presence or<br />

absence of a sterile segment in the spadix, the<br />

POLI,EN<br />

number and disposition of the pistils is perhaps the<br />

Pollen of Dieffenbachia is released in monads most important taxonomi( character in the infloresthat<br />

are inaperturate, subisopolar to virtually polar, cence. Unlike many genera in the Philodendroi(leae<br />

boat-shaped-ellipti( to oblong, or nearly spherie al. that have the pistillate flowers closely aggregate(l<br />

They are bilaterally symmetrie al or radiosymmetrie on the spa(lix, the pistillate flowers of DiefJenbachia<br />

(Grayum, 1992).<br />

are moderately dispersed on the spadix. The degree<br />

Dieffenbachia pollen is moderately large for Ar- of (lispersal on the spadix is in itself different from<br />

aveae, ranging from 54 to 99 1lm (as in D. oerstedii) spee ies to spee ies. There are generally only 2 or 3<br />

and avelaging 79 11m. Exine sculpturing is psilate<br />

pistils aeross the width of the spadix axis (regardto<br />

obs(urely verrueulate (as in D. oer.steflii) an(l/or<br />

less of whether they are lined up or not). Rarely,<br />

sparingly punctate-foveate to densely foveate with as in the ease of D. killivii, there up to 6 pistils<br />

scattered compound foveolae (as in D. pittieri and visible across the width of the spadix. At the op-<br />

D. seguine). Grayum (1992) pointed out that the posite extreme, D. Iongispatha sometimes has a solcompound<br />

foveolae found on the pollen of D. pittieri itary row of pistils across the spadix axis. The arand<br />

D. seguine resemble those of Chlorospatha<br />

rangement of the pistils is generally quite irregular,<br />

croatiana Grayum.<br />

lacking any obvious equidistant spacing or alignment<br />

in rows, but sometimes a series of pistils<br />

STERILE SPADIX SECTION<br />

might be arranged in a loose row (as in D. killipii)<br />

or even in a broad arc across the width of the spa-<br />

Dieffienbachia typically has a nearly barren sec- dix.<br />

tion of the spadix lying between the fertile stami- Pistils are 2- or 3-carpellate, sometimes l-carnate<br />

portion at the apex and the pistillate portion pellate, sessile, depressed-globose to depressedat<br />

the base (Figs. 5D, 23F). This section occurs in ovoid, pale green, semiglossy, and smooth or 2- or<br />

the area where the spadix first becomes free from 3-lobate. The stigma is a 2- or 3-lobate cushionthe<br />

spathe. Only rarely is the transition between like layer that covers the entire apex of the pistil.<br />

the fertile staminate and the sterile }ortion of the The stigmatic papillae are orange or yellow. The<br />

spadix clearly defined with the fertile flowers papillae are close, dense, and moderately short,<br />

abruptly ending on a clear flowerless sterile portion. similar to those of Philodendron, but appear less<br />

Instead, there is usually an assortment of sterile interspersed with the gelatinous matrix that is so<br />

male flowers toward the apex of the sterile segment common on the stigmas of that genus. The stylar<br />

(Fig. 7E). Less frequently there are pistillodes in region is inconspicuous. With the stigma removed,<br />

the lower half of the sterile segment. In D. beachi- the surface is truncate or broadly sulcate with a<br />

ana and D. killipii (Fig. 15H) the sterile section is solitary medial or near-medial pore. Ovules are<br />

679

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