Propeamussium, DE GREGORIO, 1884

Hickman, Carole S., 2023, Paleogene marine bivalves of the deep-water Keasey Formation in Oregon, Part II: The pteriomorphs, PaleoBios 40 (5), pp. 1-51 : 31-32

publication ID

https://doi.org/ 10.5070/P940561331

publication LSID

lsid:zoobank.org:pub:1756B24A-813B-423F-896F-91B21FF58A79

DOI

https://doi.org/10.5281/zenodo.10913553

persistent identifier

https://treatment.plazi.org/id/C23987DD-FFD8-291D-FC23-FBEDEB69BC99

treatment provided by

Felipe

scientific name

Propeamussium
status

 

PROPEAMUSSIUM DE GREGORIO, 1884 View in CoL

Type species —by monotypy, Pecten (Propeamussium) ceciliae de Gregorio (1884) . Miocene , Sicily .

There are many available genus-group names for the fossil glass scallops. Although Propeamussium View in CoL itself is based on a Miocene fossil, shell morphology is distinctive. The free-living P.jeffreysii (E.A. Smith, 1885) View in CoL ( Fig. 20A, B View Figure 20 ) illustrates the difference between the functionally dorsal right valve (A) with its uncalcified flexible prismatic apron, which is adpressed against the rigid interior margin of the fully calcified (functionally ventral) left valve (B) when the valves are closed. Although swimming has never been observed in live specimens, Morton and Thurston (1989) inferred rapid valve adduction and strong swimming capability by combining shell morphology with detailed study of adductor muscle components and insertions on the shell. Their reconstruction is presented in an elegant series of illustrations (Morton and Thurston 1989 figs. 3; 4a, b; and 5a, b) of the airfoil shape, opening and closure of the shell, and flexure of the apron during valve adduction.

An early functional reconstruction of the Keasey propeamussiid ( Hickman 1984, Fig. 8A, B View Figure 8 ), recognized the design of jet propulsion system, swimming in an edge upward orientation but without evidence of the lateral gape that is more evident in Propeamussium View in CoL s.s. Potential multiple functions of the gape during valve opening and adduction in swimming and carnivorous feeding (swimming jets, intake of meiobenthonic prey, and cleansing of the mantle cavity) have not been explored, and theory requires additional anatomical data and testing in live animals. There is strong evidence of sex-selective predation on meiobenthonic copepods ( Hicks and Marshall 1985), although hypothesized mechanisms are yet to be tested.

Propeamussiids are the only pectinoideans in which the right valve is functionally dorsal or uppermost. If they do not comprise a monophyletic group, it is even more remarkable that an uppermost right valve and discrepant shell size and surface sculpture have evolved multiple times.

The well-developed slat-like ribs of lathic calcite, which act as buttresses in both valves, are partially imbedded in the shell interior layer of crossed lamellar aragonite. Interior ribs are often visible externally through the thin translucent shells ( Fig. 20A, B View Figure 20 ). All species are apparently capable of swimming even if normally attached by a weak byssus (Waller 2006), and all available evidence suggests that propeamussiids are living “relicts of the past” (Waller 1971), surviving extinctions at the close of the Paleozoic and Mesozoic to persist and radiate at bathyal and abyssal depths during the Cenozoic.

Stratigraphic range —Jurassic–Holocene.

Kingdom

Animalia

Phylum

Mollusca

Class

Bivalvia

Order

Pectinida

Family

Propeamussiidae

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