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> Goniobasis floridensis timidus Goodrich 1942
> Habitat & distribution
Populations of G. floridensis
are widespread throughout the northern half of Florida and the Gulf
drainages of Georgia (Clench & Turner 1956, Chambers 1980, Thompson
2004), in rivers, springs, and the nearshore regions of lakes
with low to moderate current. Hanley & Ultsch (1999)
reported individuals on all available substrates, to depths of 1.5
meters, in waters with temperatures of 14 - 26 C and a pH of 7.55 - 8.45.
The occurrence of G. floridensis
in Atlantic drainages of Georgia was not suspected until the population
genetic survey of Dillon & Robinson (in review). We have recently documented several populations of G. floridensis
bearing weakly-sculptured shells inhabiting springs and springfed
streams in the vicinty of Hawkinsville. These populations were
originally described as "Goniobasis mutabilis timidus" by Goodrich (1942). But since mutabilis is a synonym of catenaria, we suggested that the subspecific nomen be transferred to G. floridensis.
> Ecology & Life history
In peninsular
Florida, eggs are laid from February to October, and are embedded in
sand-grain matrices affixed to plants and hard objects (Chambers 1980). Although there have been no detailed studies of G. floridensis life
history, I imagine that two years are required for maturity, and that
several years of iteroparous reproduction can be expected thereafter,
as is the case for pleurocerids generally (Dazo 1965). This is
life cycle G of Dillon (2000:
156 - 162).
Hanley & Ultsch (1999) reported that G. floridensis
grazes on algae and other periphyton, as is typical of pleurocerids
generally. Grazing by high densities of pleurocerids can have a
significant impact on
energy flow in streams (Dillon 2000: 86 - 91).
> Taxonomy & Systematics
Genetic divergence at allozyme-encoding loci among populations of G. floridensis
from Florida and the Gulf drainages of Georgia has
been characterized by Chambers (1978, 1980, 1990). The survey of
Dillon & Robinson (in review) included one of the Chambers (1980)
populations as a control, as well as samples of G. floridensis timidus
from Mile Creek (on the southern edge of Hawkinsville) and a Flint
River tributary near Vienna. All three were quite similar
genetically.
Mihalcik & Thompson (2002) reported that the mitochondrial CO1 gene sequences of two timidus individuals sampled from the vicinity of Hawkinsville were very similar to individual G. floridensis sampled from tributaries of the Flint River ("induta") and Chatttahoochee River ("glarea"). They nonethless raised Goodrich's taxon to the specific level and recognized three subspecies beneath it, "Elimia" timida timida, E. timida exul, and E. timida nymphaea. These are all synonyms of G. floridensis timidus.
Cytogenetic data have been reported by Chambers (1982) and Dillon (1989, 1991). The diploid number is 2N = 36.
Burch resurrected the name "Elimia" to include catenaria and approximately 80 other pleurocerid species traditionally assigned to Goniobasis (Lea 1862). But Elimia (H. & A. Adams 1854) is a composite group, explicitly rejected by Tryon, Walker, Pilsbry and Goodrich (Dillon 1989). See essay below.
> Essay
See my 28Sept04 post to the FWGNA web site for a review of the Goniobasis/Elimia taxonomic
controversy.
>Map of Goniobasis distribution (PDF)
Robert T. Dillon, Jr.
Department of Biology, College of
Charleston
Charleston, SC 29424
P: 843.953.8087
F: 843.953.5453