original description
Dall, W. H. (1890-1903). Contributions to the Tertiary fauna of Florida with especial reference to the Miocene silex-beds of Tampa and the Pliocene beds of the Caloosahatchie River. <em>Transactions of the Wagner Free Institute of Science.</em> 3(1): 1-200 [1890]; 3(2): 201-474 [1892]; 3(3): 475-570, and plates for part 1: pp. 179-190, pl. 1-12; plates for part 2: pp. 449-458, pl. 13-22 [1895]; 3(4): [i]-viii, 571-948, pl. 23-35; [1898]; 3(5): 949-1218, pl. 36-47 [1900]; 3(6): [i]-xiv, 1219-1654, pl. 48-60 [27 October1903]., available online at http://www.biodiversitylibrary.org/item/98240
page(s): 3(3): 517 [details]
additional source
Bieler, R.; Carter, J. G.; Coan, E. V. (2010). Classification of Bivalve families. Pp. 113-133, in: Bouchet P. & Rocroi J.-P. (2010), Nomenclator of Bivalve Families. <em>Malacologia.</em> 52(2): 1-184. [details]
additional source
Janssen, R. (2015). A review of the Oligocene Limopsidae of the North Sea Basin (Mollusca: Bivalvia). <em>Geologica Saxonica.</em> 61 (1): 7-33., available online at https://www.senckenberg.de/wp-content/uploads/2019/08/02_geologica-saxonica61-1_2015_janssen.pdf [details] Available for editors [request]
additional source
Valentich-Scott, P.; Coan, E. V.; Zelaya, D. (2020). <i>Bivalve seashells of western South America. Marine bivalve mollusks from Punta Aguja, Peru to Isla Chiloé, Chile</i>. Santa Barbara: Santa Barbara Museum of Natural History. vii + 593 pp.
page(s): 136-137 [details]
additional source
Oliver, P. G. (1981). The functional morphology and evolution of Recent Limopsidae. <em>Malacologia.</em> 21/1-2): 61-93., available online at https://www.biodiversitylibrary.org/page/13111004 [details]
redescription
Coan, E. V.; Valentich-Scott, P. (2012). Bivalve seashells of tropical West America. Marine bivalve mollusks from Baja California to northern Peru. 2 vols, 1258 pp. [details]
Present Inaccurate Introduced: alien Containing type locality
From editor or global species database
Taxonomy There is no general agreement over the definition of genera in this family. Whereas Tevesz (1977) accepted two genera, Limopsis and Empleconia Dall 1908, Oliver (1981) recognised only Limopsis despite arranging the various Recent species into 13 morphological groups. Coan et al. (2000) accepted Limopsis, Empleconia and Nipponolimopsis Habe 1951, thus assigning generic status to former subgenera. Beu (2006) again accepted the only genus Limopsis. Huber (2010) acknowledged the morphological groups distinguished by Oliver, but treated them as subgenera and added two further new subgenera.
This was challenged by Janssen (2015) who argued that "As long as no molecular studies are available which could demonstrate natural relationships among species groups, conchologically separable groups should be treated as distinct on generic level". This is here followed for the genus-group taxa which have been formally raised to genus level by recent authors, whereas others so far used only at subgeneric level are left in Limopsis until forthcoming authors address their placement. [details]