131 Annotated Checklist of Anomuran Decapod

131 Annotated Checklist of Anomuran Decapod

THE RAFFLES BULLETIN OF ZOOLOGY 2010 Supplement No. 23: 131–137 Date of Publication: 31 Oct.2010 © National University of Singapore ANNOTATED CHECKLIST OF ANOMURAN DECAPOD CRUSTACEANS OF THE WORLD (EXCLUSIVE OF THE KIWAOIDEA AND FAMILIES CHIROSTYLIDAE AND GALATHEIDAE OF THE GALATHEOIDEA) PART III – AEGLOIDEA Patsy A. McLaughlin Shannon Point Marine Center, Western Washington University, 1900 Shannon Point Road, Anacortes, WA 98221-4042, USA Email: hermit@fi dalgo.net Rafael Lemaitre Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution, 4210 Silver Hill Road, Suitland, Maryland 20746, USA Email: [email protected] Keith A. Crandall Department of Biology and Monte L. Bean Life Science Museum 401 Widtsoe Building, Brigham Young University, Provo, UT 84602, USA Email: [email protected] INTRODUCTION distinctiveness. Ortmann’s (1902) insistence that Aegla was a monotypic genus prevailed, and for the next 40 years, most, The Recent Aegloidea Dana, 1852, represented by the single if not all, studies of Aegla were reported as dealing only with genus, Aegla Leach, 1820, is unique among anomurans, not A. laevis. Despite being exclusively freshwater in habitat, only because of its occurrence exclusively in freshwater, but aeglids closest relatives were thought to be found somewhere because of its endemicity to South America. The fi rst detailed among the galatheids (Schmitt, 1942b), and, until recently report on the genus was given by Schmitt (1942b) in which (McLaughlin et al., 2007) the family was classifi ed as a 15 new species and two new subspecies were added to the member of the superfamily Galatheoidea, despite mounting four species recognized in the genus at the time. Schmitt’s evidence to the contrary. treatise was superseded recently by the monograph of Bond- Buckup and Buckup (1994) who reviewed most of the 43 described taxa, placed four in synonymy and added 20 new INFRAORDER ANOMURA MACLEAY, 1838 species. There have been nine additional new species reported since their publication, with another three potentially new Extant Superfamily Aegloidea, family Aeglidae species identifi ed through molecular studies awaiting formal Superfamily Aegloidea Dana, 1852 descriptions. Thus, the current tally of aeglid species is 69 Aeglidae Dana, 1852 with another three suspected and currently under study. DESCRIPTIVE TERMS AND CURRENT STATUS HISTORY OF CLASSIFICATION General morphology. – The depressed and flattened The fi rst aeglid to be described was assigned to the genus carapace is separated into a narrow anterior region and Galathea Fabricius, 1793 by Latreille (1818). Schmitt broader posterior region by a distinct cervical groove. The (1942b), who provided a historical account of the Aeglidae, integumental surface may be smooth or granular and often is presumed that Latreille had not realized that his species, marked by setiferous punctuations. The prominent rostrum Galathea laevis Latreille, 1818, had been collected in is usually provided with a dorsal carina that extends to the freshwater. The generic distinctiveness of G. laevis was epigastric prominence, to the protogastric lobe, or rarely recognized by Leach (1820) who transferred the species the entire length of the carapace. The ocular orbits are to his newly proposed genus, Aegla. Although two or well developed and each may or may not be armed with three additional species were subsequently described, an acute orbital spine; each anterolateral carapace angle is specifi c differences were subtle, which cast doubt on their drawn out into an anterolateral spine. Each ocular peduncle 131 McLaughlin et al.: Checklist of world Aegloidea is provided with a basal ring of small sclerites. While CHECKLIST Martin & Abele (1986) scored the aeglids as lacking ocular acicles, McLaughlin et al. (2007) considered these sclerites Family Aeglidae Dana, 1852 homologous with paguroid ocular acicles. The corneas of the aeglid eyes are deeply pigmented. The antennules are Aegla Leach, 1820 {1} three-segmented; the antennae fi ve-segmented with segments = Aegla Leach, 1820 (type species Galathea laevis 2 and 3 fused. Each third maxilliped is provided with a crista Latreille, 1818, by monotypy; gender feminine) dentata, but no accessory tooth. Martin & Abele (1988) = Aeglea Desmarest, 1825 (incorrect spelling) reported that aeglid gills resembled trichobranchiate gills Aegla abtao Schmitt, 1942 distally and phyllobranchiate gills proximally. However, = Aeglea abato Schmitt, 1942 (misspelling of Boyko (2002) was convinced that the gill structure of aeglids Aegla) was truly trichobranchiate. These gills are 13 in number Aegla affi nis Schmitt, 1942 and consist of one arthrobranch on the arthroidal membrane = Aegla maulensis Bahamonde & López, 1963 of each third maxilliped and paired arthrobranchs on these = Aegla montana Ringuelet, 1960 membranes of pereopods 1–4; one pleurobranch is present = Aegla neuquensis affi nis Ringuelet, 1948 on the body wall above each of pereopods 2–5. Aegla alacalufi Jara & López, 1981 Aegla araucaniensis Jara, 1980 The first pereopods are large, usually largest in males, Aegla bahamondei Jara, 1982 chelate and asymmetrical. Pereopods 2–4 are developed as Aegla camargoi Buckup & Rossi, 1977 ambulatory legs; pereopod 5 is reduced, modifi ed and usually Aegla castro Schmitt, 1942 carried under the carapace. Coxae of the fi fth pereopods in Aegla cavernicola Türkay, 1972 adult males each has the vas deferens extruded into a short Aegla cholchol Jara & Palacios, 1999 sexual tube. The pleon is well developed, calcified and Aegla concepcionensis Schmitt, 1942 carried folded under the cephalothorax. It is composed of = Aeglea concepcionensis Schmitt, 1942 (misspelling six pleomeres and a telson. of Aegla) Aegla denticulata denticulata Nicolet, 1849 Adult male pleopods on pleomere 2–5 are reduced to small = Aeglea denticulata Nicolet, 1849 (misspelling of “knobs” or are absent. Females have two-segmented, Aegla) uniramous pleopods on pleomeres 2–5. Uropods are Aegla denticulata lacustris Jara, 1989 biramous, fl attened and together with the telson form a Aegla expansa Jara, 1992 tail-fan. The telson usually, but not always, is divided by Aegla franca Schmitt, 1942 a longitudinal suture. Aegla franciscana Buckup & Rossi, 1977 Aegla grisella Bond-Buckup & Buckup, 1994 Development. – Development in aegloids is direct; there Aegla hueicollensis Jara & Palacios, 1999 are no zoeal stages. Females brood their eggs for 50 days Aegla humahuaca Schmitt, 1942 to upward of six months (Greco et al., 2004; Rodrigues & Aegla inconspicua Bond-Buckup & Buckup, 1994 Hebling, 1978), and the newly hatched juveniles remain Aegla inermis Bond-Buckup & Buckup, 1994 beneath or in close proximity to the female’s pleon for 3–12 Aegla intercalata Bond-Buckup & Buckup, 1994 days, initially attached to the pleopods and other structures Aegla intermedia Girard, 1855 and subsequently exploratory in their movements, but always = Aeglea intermedia Girard, 1855 (misspelling of returning to the safety of the maternal pleon. Aegla) Aegla itacolomiensis Bond-Buckup & Buckup, 1994 Current status. – The fi rst real concern directed to the Aegla jarai Bond-Buckup & Buckup, 1994 traditional inclusion of the Aeglidae in the superfamily Aegla jujuyana Schmitt, 1942 Galatheoidea was that of Martin & Abele (1986), who, Aegla laevis (Latreille, 1818) [Galathea] while not excluding the family, suggested a “more remote = Aegla laevigata H. Milne Edwards & Lucas, origin for aeglids than modern galatheoids.” Additional 1843 {2} morphological evidence for major differences of the aeglids = Aeglea levis Dana, 1855 (misspelling of Aegla from the other galatheoids was provided by Martin & Abele and laevis) (1988). Based on spermatological data, Tudge & Scheltinga Aegla lata Bond-Buckup & Buckup, 1994 (2002) suggested an independent and basal lineage for the Aegla leptochela Bond-Buckup & Buckup, 1994 Aeglidae. Even more convincing evidence for separation Aegla leptodactyla Buckup & Rossi, 1977 of the aeglids from the other galatheoids was provided by Aegla ligulata Bond-Buckup & Buckup, 1994 the molecular studies of Pérez-Losada et al. (2002a, 2002b, Aegla longirostri Bond-Buckup & Buckup, 1994 {3} 2004) and the combined molecular and morphological studies Aegla manni Jara, 1980 of Ahyong & O’Meally (2004). However, it was only after Aegla marginata Bond-Buckup & Buckup, 1994 another morphological review that the aeglids were formally Aegla manunifl ata Bond-Buckup & Santos, in Santos et removed from the Galatheoidea and transferred to their own al., 2009 {4} major taxon, the Aegloidea (McLaughlin et al., 2007). Aegla microphthalma Bond-Buckup & Buckup, 1994 132 THE RAFFLES BULLETIN OF ZOOLOGY 2010 Aegla muelleri Bond-Buckup & Buckup, in Bond-Buckup 1820 [1821] without explanation. Some subsequent et al, 2010 {4} references to Leach’s publication have listed the Aegla neuquensis Schmitt, 1942 date as 1821 (e.g., Martin & Abele, 1988; Jara et al., Aegla obstipa Bond-Buckup & Buckup, 1994 2003) while others (e.g., Tudge & Scheltinga, 2002; Aegla occidentalis Jara, Pérez-Losada & Crandall, Pérez-Losada et al., 2004; De Grave et al., 2008) have 2003 cited it as 1820. The correct date of publication is Aegla odebrechtii Müller, 1876 ambiguous because the cover page for the volume = Aeglea odebrechtii Müller, 1876 (misspelling of gives the publication date as 1821, whereas the title Aegla) page gives it as 1820. The Nomenclator Zoologicus = Aeglea intermedia Moreira, 1901 (misspelling of (Neaves, 1939)

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