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Home > Academics > Department Pages > Biology > Faculty > Chmielewski, Jerry G. > Research Interests
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SYSTEMATICS OF ANTENNARIA

The genus Antennaria is a dioecious member of the tribe Inuleae and is distributed throughout the cold temperate and arctic regions of the northern hemisphere. In North America the taxonomy of the genus is difficult and therefore no unanimity of opinion exists with respect to the most suitable taxonomic treatment. Apomixis in the genus led to the formation of many distinct polyploid races or clones, many of which were named as species by turn of, to mid century taxonomists. Unfortunately, many of these species were based on single collections from local populations that have never been recollected. Most recent workers on the genus have adopted a more conservative classification for this group.

 

Antennaria probably comprises 25-30 sexual diploid species and several large polyploid agamic complexes derived from them. Taxonomic differences are presumably due to the occurrence of polyploidy, apomixis, and hybridization. In North America it has been suggested that Antennaria is comprised of six large polyploid complexes, namely A. howellii and A. parlinii, mostly from eastern North America, and A. alpina, A. media, A. parvifolia, and A. rosea, mainly from western or arctic North America. In attempting to delimit patterns of variation and thereby resolve taxonomic confusion in the genus, the classification of taxa should be derived not only from morphology and chromosome number determinations (knowledge of cytogeographic distributions of taxa is useful in determining the limits of distribution of infraspecific variants, in constructing biogeographic histories of species, and in testing hypotheses on the evolution of infraspecific polyploidy), but also from experimental studies.

 

Although most recent studies have focused on the use of classical morphological analyses to ascertain phenetic relationships within the genus, molecular techniques, specifically random amplified polymorphic DNA (RAPD), is being used to examine the phylogeny of the genus.

SEED ECOLOGY

One of the more stable morphological characteristics of many plant species is seed weight. Despite this cited stability, variability in seed weight has been documented among species, populations, cytotypes, individuals, and even within an inflorescence.

 

When variability in seed weight is recognized, it is generally greater among those species in which flowering is determinate as opposed to indeterminate. Presumably those species with an indeterminate flowering pattern will more likely exhibit variation which is attributable to environmental change as seed maturation occurs over an extended portion of the growing season. Variation in seed weight within an inflorescence indicates that those factors responsible are likely nongenetic in origin, and that environmental change during maturation is a probable cause. Others have argued that seed weight is genetically controlled and thus subject to evolutionary change.

 

Many examples of seed polymorphism, that is, the production of seeds with differing morphologies and or behaviors occur within the Asteraceae, Brassicaceae, Chenopodiaceae, and Poaceae. The production of dimorphic achenes has facilitated the evolution of alternative strategies relative to dispersal, germination, and dormancy.

 

Some previous studies on members of the Asteraceae have differentiated between germination in dimorphic ray and disc achenes. Reduced dispersability and delayed germination are characteristic of the outer (typically associated with the ligulate ray floret) achenes, conversely, distance dispersal and quick germination are characteristic of the central (typically associated with the tubular disc floret) achenes.

 

The inflorescence in Aster is actually a capitulescence consisting of one, to possibly a thousand, capitula. These capitula are typically differentiated into the centripetally maturing peripheral, ligulate, imperfect pistillate ray florets and the central, tubular, perfect disc florets. The achenes of Aster pose yet a different question, that is, whether these apparently monomorphic products of dimorphic florets exhibit comparable tendencies to those of dimorphic achenes.

 

Previous life history studies on Aster in which values were reported for both achene (actually a cypsela) weight and germination concurrently did not differentiate between achenes produced from either ray or disc florets. Additionally, a distinction was not made for germination per se, irrespective of achene weight, for achenes produced by these two types of florets.

 

Although the florets per se of Aster are typically morphologically different, ray and disc achenes are morphologically indistinguishable. The senescence of floret parts (both ray floret ligule and disc floret tube) in species of Aster prior to complete achene maturation negate the possibility of reliable separation of achenes based strictly on the position of a floret in the capitulum. Inasmuch as these studies did recognize that our inability to separate ray and disc achenes was a potential source of variation, we concurrently did not know whether character associations which were noted for the respective species were real or incidental. Were character associations being obscured because of our inability to separate ray achenes from disc achenes? Dissatisfied with this possibility, a protocol was devised which resolved this dilemma.

 

The primary focus of this research is to determine whether ray and disc achenes of Aster spp. differ relative to the relationship of achene weight and its components of pericarp weight and embryo weight to each other, to germination, and to the time required to germinate (germination time). These results will be used to compare evolutionary trends among those species which perennate through herbaceous rhizomes, corms, or caudex.

 


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