FWGNA > Species Accounts > Pleuroceridae > Lithasia armigera duttoniana
Lithasia armigera duttoniana (Lea 1841)
  • click to view larger

> Habitat & Distribution

Goodrich (1940) considered Lithasia duttoniana endemic to the Duck River of Middle Tennessee.  Our extensive observations on clinal variation in both allozyme frequency and shell morphology in Duck River Lithasia populations (see below) have led us to suggest lowering duttoniana to subspecific level underneath L. armigera and broadening its range to include the Harpeth and Caney/Smith tributaries of the Cumberland, as well as Cypress Creek of the Tennessee.

As is true for the genus generally, populations of L. armigera duttoniana reach maximum abundance grazing on solid substrates, including interstitial gravel and cobble.  They are characteristic of large, rich, free-flowing rivers with broad riffles and good water quality
. FWGNA incidence rank I-4.

> Ecology & Life History

Pleurocerids are heavily-shelled, conspicuous freshwater gastropods, typically inhabiting firm substrates in shallow waters.  Males are aphallic; females can be distinguished by an egg laying groove on the right side of their foot.  Most populations are perennial and iteroparous, typically requiring more than a year to mature and living several years (Life cycle Hi of Dillon 2000: 156-162).  Eggs are affixed to hard substrates singly or in small clusters from spring to midsummer.  Pleurocerids are generalized grazers, and where present in high density can have significant effects on energy flow in streams (Dillon 2000: 86-91).

> Taxonomy & Systematics

Tryon (1873) catalogued 25 species in the genus Lithasia/Angitrema, primarily inhabiting the Tennessee/Cumberland but ranging throughout the interior drainages of seven states.  Goodrich (1940) boiled these down to 10 species and 14 subspecies.  Burch (1989) left Goodrich's system almost untouched, trimming out one species and 8 subspecies, but adding one species more recently described, to bring the total back to 10.

Minton & Lydeard (2003) obtained mtDNA CO1 sequence data from 5 populations they identified as L. armigera:  Ohio R (2 individuals), Wabash R (2), Tennessee R (1), Stones R (6), and Harpeth R (3).  All 14 of these individuals were genetically indistinguishable.  Minton & Lydeard did, however, document 4% divergence between their 14 Lithasia armigera CO1 sequences sequences and a set of 19 sequences sampled from the Duck River of Middle Tennessee.  The snails from which these 19 sequences were obtained were identified by five separate names on the basis of shell morphology: L. geniculata pinguis (6), L. geniculata fuliginosa (7), L. geniculata geniculata (1), L. jayana (1), and L. duttoniana (4).

The allozyme surveys of Dillon (2020) returned evidence, however, of reproductive isolation between Duck River populations identified as L. geniculata (all subspecies) and those identified as L. duttoniana.  No evidence of reproductive isolation was apparent between populations identified as L. duttoniana and L. jayana.  See my DATE series of essays from the links below.

Populations conventionally identified as Lithasia duttoniana are more lightly-shelled and inhabit smaller rivers but are otherwise indistinguishable from typical L. armigera.  Indeed, Lithasia bearing shells of the duttoniana form in upper regions of the Duck River intergrade smoothly with heavily-shelled populations in the lower Duck identified as L. jayana.  And L. jayana is entirely indistinguishable from L. armigera in all respects.

We have therefore suggested that jayana (Lea 1841) is a junior synonym of armigera (Say 1821) and that duttoniana (Lea 1841) is best lowered to subspecific rank under armigera, the shell morphological distinction between duttoniana and armigera being a case of cryptic phenotypic plasticity.  See my 2013-14 essays on CPP from the links below to learn more about this important phenomenon
.

> Supplementary Resources

> Essays

  • Goodrich's (1934) paper on the Duck River Lithasia geniculata population was the primary inspiration behind my essay of 20Feb07, Goodrichian Taxon Shift.  See that essay for a detail from Goodrich's Figure 1.
  • I generalized the concept of Goodrichian taxon shift to "cryptic phenotypic plasticity" in two subsequent essays on pleurocerid systematics, Pleurocera acuta is Pleurocera canaliculata (3June13) and Elimia livescens and Lithasia obovata are Pleurocera semicarinata (11July14).   That latter essay featured a scan of Goodrich's (1934) figure 1 in its entirety.
  • I reviewed the phenomenon of mitochondrial superheterogeneity in the North American Pleuroceridae in a series of essays published from March to May, 2016: What We Know, What It Means, and Speciation.
  • I returned to the subject of the Duck River Lithasia in a series of posts published from X to Y, titles.  In those essays I reported a series of population genetic surveys designed to sort out all six of the specific nomina recently applied to Duck River populations: pinguis, fuliginosa, geniculata, duttoniana, jayana, and armigera.

> References


Burch, J. B. (1989)
 North American Freshwater Snails.  Malacological Publications, Hamburg, MI.
Dillon, R. T., Jr. (1989)
  Karyotypic evolution in pleurocerid snails: I. Genomic DNA estimated by flow cytometry. Malacologia, 31: 197-203. 
Dillon, R. T., Jr. (2000)  The Ecology of Freshwater Molluscs. Cambridge, Cambridge University Press.  509 pp.

Dillon, R. T., Jr. (2011)  Robust shell phenotype is a local response to stream size in the genus Pleurocera.  Malacologia 53: 265-277.  [pdf]
Dillon, R. T., Jr.  (2014) Cryptic phenotypic plasticity in populations of the North American freshwater gastropod, Pleurocera semicarinata.  Zoological Studies 53:31. [html] [pdf]
Dillon, R. T., Jr. (2020) Reproductive isolation between Lithasia populations of the geniculata and duttoniana forms in the Duck River, Tennessee.  Ellipsaria 22(3): 6 - 8.  [PDF]
Dillon, R. T., Jr., S. J. Jacquemin & M. Pyron (2013) Cryptic phenotypic plasticity in populations of the freshwater prosobranch snail, Pleurocera canaliculata.  Hydrobiologia 709: 117-127. [html] [pdf]
Goodrich, C. (1934) Studies of the gastropod family Pleuroceridae - I.  Occas. Pprs. Mus. Zool. Univ. Mich. 286: 1 - 17.
Goodrich, C. (1940) The Pleuroceridae of the Ohio River drainage system.  Occas. Pprs. Mus. Zool. Univ. Mich., 417: 1-21.
Goodrich, C. (1941) Studies of the gastropod family Pleuroceridae VIII.  Occas. Pprs. Mus. Zool. Univ. Mich. 447: 1 - 13.
Holznagel, W. E. & C. Lydeard (2000)  A molecular phylogeny of North American Pleuroceridae (Gastropoda: Cerithioidea) based on mitochondrial 16S rDNA sequences.  Journal of Molluscan Studies 66: 233 - 257.
Minton, R. L. (2002)  A cladistic analysis of Lithasia (Gastropoda: Pleuroceridae) using morphological characters.  The Nautilus 116: 39-49.
Minton, R. L. (2013) A new species of Lithasia (Gastropoda: Pleuroceridae) from the Buffalo River, Tennessee, USA.  The Nautilus 127: 119 - 124.
Minton, R. L., K. C. Hart, R. Fiorillo, & C. Brown (2018)  Correlates of snail shell variation along a unidirectional freshwater gradient in Lithasia geniculata (Haldeman, 1840) (Caenogastropoda: Pleuroceridae) from the Duck River, Tennessee, USA.  Folia Malacologica 26: 95 - 102.
Minton, R. L. & C. Lydeard (2003) Phylogeny, taxonomy, genetics, and global heritage ranks of an imperiled, freshwater snail genus Lithasia (Pleuroceridae)  Molecular Ecology 12: 75-87.
Minton, R. L., A. P. Norwood & D. M. Hayes (2008) Quantifying phenotypic gradients in freshwater snails: a case study in Lithasia (Gastropoda: Pleuroceridae)  Hydrobiologia 605: 173-182
.
Minton, R. L., S. P. Savarese & D. C. Campbell (2005) A new species of "Lithasia" (Mollusca: Caenogastropoda: Pleuroceridae) from the Harpeth River, Tennessee, USA.  Zootaxa 1054: 31 - 42.
Tiemann, J. S., W. R. Posey, K. S. Cummings, K. J. Irwin, and B. Turner (2013)  First occurrences of Lithasia armigera and Lithasia verrucosa (Gastropoda: Pleuroceridae) in the Mississippi River.  Southeastern Naturalist 12: N35 - N39.
Tryon, G. W. (1873) Land and Fresh-water shells of North America.  Part IV, Strepomatidae.  Smithsonial Miscellaneous Collections 253: 1- 434.