A New Combination and New Synonymy in Synsepalum (Sapotaceae) from Central Africa

Kew Bulletin ◽  
1999 ◽  
Vol 54 (1) ◽  
pp. 80
Author(s):  
D. J. Harris
1978 ◽  
Vol 9 (1) ◽  
pp. 75-76
Author(s):  
Leif Lyneborg

AbstractNeotherevella n.gen. is proposed as a replacement for Neothereva Kröber sensu Lyneborg (1976). Neothereva Kröber, 1912, is placed in new synonymy with Thereva Latreille, 1796, as the consequence of an overlooked designation of a type-species for Neothereva Kröber, 1912, by Kröber (1935). Neotherevella is fully described. Five specific names are placed in new combination with Neotherevella, which is known from Namibia, Mauritania, Algeria, Sudan, Egypt, Israel, Uzbechistan and Mongolia. It is demonstrated that two species described in combination with Neothereva by Zaitzev (1970) do not belong to Neotherevella.


Zootaxa ◽  
2007 ◽  
Vol 1504 (1) ◽  
pp. 1-51 ◽  
Author(s):  
DIRK AHRENS

This paper presents some results of the ongoing taxonomic investigations of the Asian Sericini (Scarabaeidae: Melolonthinae) beetle fauna with an updated catalogue to the Palaearctic members of this tribe. The following new synonymies and combinations are introduced: Archeohomaloplia Nikolajev, 1982 (= Melanomaladera Miyake & Yamaya, 2001, new synonymy); Trioserica Moser, 1922 (= Sinoserica Miyake & Yamaya, 2001, new synonymy); Nipponoserica koltzei (Reitter, 1897) (= Nipponoserica opacicarina Kim & Kim, 2003, new synonymy); Maladera lignicolor (Fairmaire, 1887) (= Autoserica laboriosa Brenske, 1897, Aserica fusiana Murayama, 1934, and Serica tenebrosa Frey, 1972, new synonymy); Neosericania nitida (Kobayashi, 1985) new combination; Eumaladera subrugata (Moser, 1926) new combination; Eumaladera opaciventris (Moser, 1915) new combination (= Maladera coreana Kim & Kim, 2003, new synonymy); Maladera verticalis (Fairmaire, 1888) (= Maladera castanea koreana Kim & Kim, 2003, new synonymy); Archeohomaloplia abbreviata (Fairmaire, 1897) new combination (= Areohomaloplia potanini Nikoleav, 1982, new synonymy); Archeohomaloplia yunnana (Miyake & Yamaya, 2001) new combination; Trioserica maculipennis (Miyake & Yamaya) new combination; Serica (Taiwanoserica) anmashana (Kobayashi, 1993) new combination; S. (T.) bihluhensis (Kobayashi & Yu, 2000) new combination; S. (T.) chunlinlii (Ahrens, 2002) new combination; S. (T.) elongata (Nomura, 1974) new combination; S. (T.) gracilipes (Nomura, 1974) new combination; S. (T.) kubotai (Kobayashi, 1983) new


Zootaxa ◽  
2019 ◽  
Vol 4683 (3) ◽  
pp. 301-335 ◽  
Author(s):  
FRANK E. ETZLER

The genus Limonius Eschscholtz, 1829 was last treated as a whole by Candèze (1860). Since then, members have been placed in eight other genera: Cidnopus Thomson, 1859; Gambrinus LeConte, 1853; Elathous Reitter, 1890; Kibunea Kishii, 1966; Limoniscus Reitter, 1905; Nothodes LeConte, 1861; Pheletes Kiesenwetter, 1858; and Solskyana Dolin, 1978. Based on the examination of adult and larval characters, five genera are recognized: Elathous Reitter, 1890; Gambrinus LeConte, 1853; Limonius Eschscholtz, 1829; Pheletes Kiesenwetter, 1858; and Tetralimonius new genus. Limoniscus Reitter, 1905 and Sichuanelater Platia and Gudenzi, 2006 are new synonymies of Gambrinus LeConte, 1853; Micrathous Lane, 1971, Neoathousius Schimmel and Platia, 1991 and Solskyana Dolin, 1978 are all new synonymies of Limonius. A total of 84 new combinations are proposed: Nearctic: Elathous huguenini (Van Dyke, 1932) new combination; Gambrinus angulatus (Motschulsky, 1859) new combination; Gambrinus bicolor (Van Dyke, 1932) new combination; Gambrinus clypeatus (Motschulsky, 1859) new combination; Gambrinus confusus (LeConte, 1853) new combination; Gambrinus cribriceps (Van Dyke, 1943) new combination; Gambrinus crotchii (Horn, 1872) new combination; Gambrinus flavomarginatus (Knull, 1938) new combination; Gambrinus fulvipilis (Candèze, 1860) new combination; Gambrinus griseus (Beauvois, 1805) new combination; Gambrinus humidus (Lane, 1941) new combination; Gambrinus interstitialis (Melsheimer, 1846) new combination; Gambrinus lanchesteri (Lane, 1941) new combination; Gambrinus meridianus (Knull, 1947) new combination; Gambrinus mirus (LeConte, 1853) new combination; Gambrinus norahae (Al Dhafer, 2009) new combination; Gambrinus olentangyi (Knull, 1947) new combination; Gambrinus plebejus (Say, 1825) new combination; Gambrinus propexus (Candèze, 1860) new combination; Gambrinus rudis (Brown, 1933) new combination; Gambrinus rufihumeralis (Lane, 1941) new combination; Gambrinus seminudus (Van Dyke, 1932) new combination; Gambrinus shircki (Lane, 1965) new combination; Gambrinus sinuifrons (Fall, 1907) new combination; Gambrinus snakensis (Lane, 1965) new combination; Gambrinus stigma (Herbst, 1806) new combination; Gambrinus pictus (Van Dyke, 1932) new combination; Gambrinus ulkei (Horn, 1871) new combination; Gambrinus ursinus (Van Dyke, 1932) new combination; Gambrinus venablesi (Wickham, 1913) new combination; Limonius brevis (Van Dyke, 1932) new combination; Limonius sordidus (Van Dyke, 1932) new combination; Pheletes lecontei (Lane, 1971) new combination; Tetralimonius definitus (Ziegler, 1845) new combination; Tetralimonius humeralis (Candèze, 1860) new combination; Tetralimonius maculicollis (Motschulsky, 1860) new combination; Tetralimonius nimbatus (Say, 1825) new combination; Tetralimonius ornatulus (LeConte, 1857) new combination. Palearctic: Gambrinus elegans (Buysson, 1891) new combination; Gambrinus gibbosus (Platia and Gudenzi, 2006) new combination. Gambrinus henanensis (Schimmel, 2006) new combination; Gambrinus hinakurai (Kishii, 1998) new combination; Gambrinus katoi (Kishii, 2002) new combination; Gambrinus kawaharai (Kishii, 2002) new combination; Gambrinus kucerai (Schimmel, 2006) new combination; Gambrinus nanshanensis (Arimoto and Hiramatsu, 2013) new combination; Gambrinus naomii (Kishii, 1997) new combination; Gambrinus shaanxiensis (Schimmel, 2006) new combination; Gambrinus suturalis (Gebler, 1844) new combination; Gambrinus takabai (Kishii, 1997) new combination; Gambrinus violaceus (Müller, 1821) new combination; Gambrinus wittmeri (Chassain, 1998) new combination; Gambrinus yamato (Kishii, 1998) new combination; Gambrinus yujii (Arimoto, 2013) new combination; Gambrinus zhejiangensis (Schimmel, 2015) new combination; Limonius brancuccii (Schimmel and Platia, 1991) new combination; Limonius decorus (Gurjeva, 1975) new combination; Limonius exiguus (Schimmel and Platia, 1991) new combination; Limonius hartmanni (Schimmel, 1998) new combination; Limonius hiermeieri (Schimmel and Platia, 1991) new combination; Limonius hirtus (Dolin, 1978) new combination; Limonius hubeiensis (Kishii and Jiang, 1996) new combination; Limonius kubani (Schimmel, 1996) new combination; Limonius loebli (Schimmel and Platia, 1991) new combination; Limonius longicornis (Schimmel and Platia, 1991) new combination; Limonius macedonicus (Cate and Platia, 1989) new combination; Limonius marginellus brusteli (Leseigneur, 2004) new combination; Limonius manaliensis (Schimmel and Platia, 1991) new combination; Limonius miandamensis (Schimmel and Platia, 1991) new combination; Limonius minusculus (Schimmel and Platia, 1991) new combination; Limonius nigronitidus (Han and Lee, 2012) new combination; Limonius platiai (Mertlik, 1996) new combination; Limonius pseudopilosus (Platia and Gudenzi 1985) new combination; Limonius recticornis (Schimmel and Platia, 1991) new combination; Limonius riesei (Platia, 1988) new combination; Limonius rusticus (Schimmel and Platia, 1991) new combination; Limonius schurmanni (Platia and Gudenzi, 1998) new combination; Limonius sinensis (Schimmel and Platia, 1994) new combination; Limonius singularis (Schimmeland Platia, 1991) new combination; Limonius stapfi (Schimmel, 2007) new combination; Limonius turcicus (Platia, 2004) new combination; Limonius wittmeri (Schimmel and Platia, 1991) new combination; Tetralimonius quercus (Olivier, 1790) new combination; Tetralimonius reitteri (Gurjeva, 1976) new combination. The following 12 North American species are removed from synonymy and recognized as valid species: Gambrinus interstitialis (Melsheimer, 1846) status resurrected; Gambrinus propexus (Candèze, 1860) status resurrected; Gambrinus shircki (Lane, 1965) status resurrected; Gambrinus snakensis (Lane, 1965) status resurrected; Gambrinus ulkei (Horn, 1871) status resurrected; Limonius anceps LeConte, 1853 status resurrected; Limonius dubitans LeConte, 1853 status resurrected; Limonius infuscatus Motschulsky, 1859 status resurrected; Limonius pilosulus Candèze, 1891 status resurrected; Limonis semianeus LeConte, 1853 status resurrected. Tetralimonius humeralis (Candèze, 1860) status resurrected; Tetralimonius maculicollis (Motschulsky, 1860) status resurrected. New replacement names are proposed for three homynyms: Limonius schimmeli Etzler new name for Neoathousius ferrugineus Schimmel and Platia, 1991; Elathous malatyanus Etzler new name for Elathous bicolor Platia, 2010, not Elathous bicolor (LeConte, 1853); and Microdesmes carteri Etzler new name for Limonius angulatus Carter, 1939 (= Microdesmes angulatus). Limonius kondratieffi Al Dhafer, 2009 is a new synonymy of Elathous bicolor (LeConte, 1853). A key to genera, generic descriptions, notes on species, and definitions of important characters are provided. 


Zootaxa ◽  
2010 ◽  
Vol 2565 (1) ◽  
pp. 55 ◽  
Author(s):  
CATHERINE A. TAUBER ◽  
OLIVER S. FLINT, JR.

With the purpose of promoting nomenclatural stability, this paper addresses a number of errors, omissions, and controversial conclusions in a recent revision of the green lacewing genus Ceraeochrysa by Freitas et al. (2009). 1. Valid species, new combinations and synonymies: (a) We identified Ceraeochrysa chiricahuae Freitas and Penny (in Freitas et al. 2009), Chrysopa forreri Navás, and Chrysopa intacta Navás as subjective synonyms. Thus, Ceraeochrysa intacta, a species that was previously synonymized under Ceraeochrysa placita (Banks), becomes the valid name of the species [New status, new combination]. Chrysopa forreri is now synonymized under Cer. intacta, not Cer. placita [New synonymy]. And, Cer. chiricahuae becomes a junior synonym of Cer. intacta, not a valid species of Ceraeochrysa [New synonymy]. (b) We enumerate specific internal and external features of the Chrysopa cornuta Navás type that identify it as conspecific with Ceraeochrysa caligata (Banks), not Ceraeochrysa cincta (Schneider) as proposed by Freitas et al. (2009). Thus, Ceraeochrysa cornuta (Navás), which has priority, is reinstated as the valid name [Reinstated status, reinstated combination], and Ceraeochrysa caligata (Banks) is reinstated as a junior subjective synonym of Cer. cornuta, not a valid species [Reinstated synonymy]. (c) We provide documented evidence for reinstating three synonymies that Freitas et al. had reversed [Reinstated synonymies]: (i) Allochrysa parvula Banks is a junior subjective synonym of Ceraeochrysa lineaticornis (Fitch); (ii) Chrysopa columbiana Banks is a junior subjective synonym of Ceraeochrysa lineaticornis (Fitch); (iii) Chrysopa rochina (Navás) is a junior subjective synonym of Ceraeochrysa cincta (Schneider). 2. Generic assignments: (a) Visual evidence is provided for the placement of Ceraeochrysa laufferi (Navás) in Ungla. Therefore, Ungla laufferi (Navás) is reinstated as the valid name [Reinstated combination]. (b) We question Freitas et al.’s rationale for including Cer. placita (Banks) and Cer. intacta (Navás) (as Cer. chiricahuae Freitas and Penny) in the genus Ceraeochrysa; female and larval features of the two species differ markedly from those used to characterize Ceraeochrysa species. As an alternative that recognizes the uncertainty surrounding the generic placement of these species and that avoids additional, unnecessary name changes, we propose including the caveat “genus incertae sedis” with the names, as follows: Ceraeochrysa placita (Banks), genus incertae sedis, and Ceraeochrysa intacta (Navás), genus incertae sedis. 3. Type designations: (a) Errors concerning the Chrysopa furculata Navás type in the Muséum national d’Histoire naturelle, Paris (MNHN), are corrected, and doubts raised by Freitas et al. (2009) concerning the identification of this specimen as the holotype are removed. (b) The earlier designation of the Chrysopa rochina (Navás) type in the MNHN as the lectotype (not holotype) is verified.


Zootaxa ◽  
2009 ◽  
Vol 2237 (1) ◽  
pp. 59-66 ◽  
Author(s):  
LUBOMÍR MASNER ◽  
NORMAN F. JOHNSON ◽  
LUCIANA MUSETTI

The monobasic genus Caenoteleia Kieffer (Hymenoptera: Platygastridae) is considered to be a junior synonym of the widespread and common genus Calliscelio Ashmead, new synonymy. Calliscelio elegans (Perkins) is redescribed, transferred to Calliscelio, new combination, and its geographic distribution documented. Originally described from Hawai‘i, this species is widespread through the tropics. The species likely is distributed by human commerce, possibly in association with cricket pests (Orthoptera: Gryllidae) of sugar cane.


Zootaxa ◽  
2006 ◽  
Vol 1226 (1) ◽  
pp. 1 ◽  
Author(s):  
ARKADY S. LELEJ ◽  
ANTONIUS VAN HARTEN

Forty species in 19 genera are recorded from Yemen. Three new genera are described: Paglianotilla gen. nov. (type species P. hogenesi sp. nov.), Rasnitsynitilla gen. nov. (type species R. brachyptera sp. nov.), and Vanhartenidia gen. nov. (type species V. felix sp. nov.). Ten new species are described: Arnoldtilla achterbergi sp. nov. (Yemen), Dentilla ehrenbergi sp. nov. (Yemen, Saudi Arabia), P. hogenesi sp. nov. (Yemen), R. brachyptera sp. nov. (Yemen), R. invreai sp. nov. (Yemen), R. schmideggeri sp. nov. (Yemen), V. arabica sp. nov. (Yemen), V. felix sp. nov. (Yemen), V. tihama sp. nov. (Yemen), and Spinulomutilla yemenita sp. nov. (Yemen). Hitherto unknown females are recognized for Arnoldtilla Nonveiller, Omotilla Invrea, and Tropidotilla milmili (Magretti). New synonymy is proposed for Omotilla Invrea 1943 = Conjunctotilla Nonveiller 1996, syn. nov.; Pseudophotopsis aurea (Klug 1829) = Mutilla kassalina Magretti 1898, syn. nov., P. continua arabica Hammer 1962, syn. nov. New status is proposed for Arnoldtilla Nonveiller, Myrmilla rubida Magretti, M. parvula Magretti, Glossotilla djiboutiensis Bischoff, V. kassalana (Bischoff), V. pyrrhospilota (Bischoff). New combination is proposed for: A. bischoffi (Arnold), A. silvestris (Arnold), O. conjuncta (Klug), O. conjunctoides (Magretti), O. grazianii (Invrea), Dentilla arabica (Hammer), V. dives (Smith), V. kassalana (Bischoff), V. pyrrhospilota (Bischoff), V. tricolor (Klug), and V. unguiculata (Magretti). Eleven genera are recorded for the first time from Yemen: Arnoldtilla Nonveiller, Omotilla Invrea, Macromyrme Lelej, Ronisia Costa, Strangulotilla Nonveiller, Tropidotilla Bischoff, Dentilla Lelej, Glossotilla Bischoff, Dentotilla Nonveiller, Spinulomutilla Nonveiller, and Dasylabris Radoszkowski. Seventeen species are recorded for the first time from Yemen: Pseudophotopsis maura Bischoff, P. mascatiana Invrea, Myrmilla parvula Magretti, M. rubida Magretti, T. bellii (Magretti), T. carinulifera Bischoff, T. frontalis (Klug), T. milmili (Magretti), Strangulotilla samharica (Magretti), Ronisia idonea (André), Dentilla testacea (Klug), Glossotilla djiboutiensis Bischoff, Dentotilla auricoma (Bischoff), Dasylabris biblica Invrea, Tricholabiodes niloticus Suárez, T. pedunculatoides Bischoff, and T. sudanensis Suárez. Dentilla testacea (Klug) and Tricholabiodes chloroticus (Gribodo) are recorded for the first time from Saudi Arabia. Tricholabiodes sudanensis Suárez is recorded for the first time from Oman. Glossotilla djiboutiensis Bischoff is recorded for the first time from Eritrea. Keys to eight species of Vanhartenidia and three species of Rasnitsynitilla are given.


Zootaxa ◽  
2011 ◽  
Vol 2866 (1) ◽  
pp. 1 ◽  
Author(s):  
JONGOK LIM ◽  
JONGWOOK LEE ◽  
SANGHYUN KOH ◽  
BONGWOO LEE ◽  
CELSO O. Azevedo ◽  
...  

Nineteen Epyris species are recorded from Korea. Ten new species: E. aequalis Lim et S. Lee, sp. nov., E. breviclypeatus Lim et S. Lee, sp. nov., E. dulicus Lim et S. Lee, sp. nov., E. finitus Lim et S. Lee, sp. nov., E. jeonbukensis Lim et S. Lee, sp. nov., E. limatulus Lim et S. Lee, sp. nov., E. longiantennatus Lim et S. Lee, sp. nov., E. mureungensis Lim et S. Lee, sp. nov., E. yetus Lim et S. Lee, sp. nov., and E. sudosanensis Lim et S. Lee, sp. nov. are described from Korea. Hitherto unknown females are described for E. fuscipes (Kieffer 1906) and E. yamatonis Terayama 1999. New synonymy is proposed for E. sauteri (Enderlein 1920) = E. formosus Terayama 2006, syn. nov. New combination is proposed for E. fuscipes (Kieffer 1906), comb. nov. (from Rhabdepyris). Seven species: E. asura Terayama 2006, E. darani Terayama 2006, E. fuscipes (Kieffer 1906), E. idaten Terayama 2006, E. niwoh Terayama 2006, E. sauteri (Enderlein 1920), and E. yamatonis Terayama 1999 are recorded for the first time from Korea. Descriptions, illustrations of diagnostic characteristics for each species are presented with a key to the Korean Epyris species.


2001 ◽  
Vol 32 (1) ◽  
pp. 45-89 ◽  
Author(s):  
Kelly B. Miller

AbstractCharacters from adult morphology are analyzed cladistically to infer the phylogeny of the family Dytiscidae. The analysis is based on examination of 233 species of Dytiscidae and several outgroup taxa including members of Noteridae, Amphizoidae, Hygrobiidae and Carabidae. Members of all currently recognized tribes of Dytiscidae are represented except Anisomeriini Brinck, Hydronebriini Guignot and Carabhydrini Watts. Emphasis is placed on identifying informative characters from the female genital system that comprise 34 of the resulting 101 total characters. The consensus of the most parsimonious trees is well resolved and supports recognition of ten subfamilies of Dytiscidae including; Matinae van den Branden, Laccophilinae Gistel, Coptotominae van den Branden, Copelatinae Erichson, Hydroporinae Aubé, Agabinae Thomson, Colymbetinae Erichson, Lancetinae van den Branden and Dytiscinae Leach. Also, Hydrodytes Miller, NEW GENUS, is erected and placed in its own subfamily, Hydrodytinae, NEW SUBFAMILY, to include two species previously placed in Agaporomorphus Zimmermann (Copelatinae), H. opalinus (Zimmermann) (NEW COMBINATION) and H. dodgei (Young) (NEW COMBINATION). Hydrodytinae is sister group to Hydroporinae and is diagnosed by the presence of anterior apodemes on the gonocoxae, several characters of the metendosternite (each synapomorphic with Hydroporinae), lack of pseudotetramerous pro- and mesotarsi, lack of a declivitous prosternum and prosternal process, the scutellum visible with the elytra closed (all plesiomorphic), the rami of the female genitalia sinuate and dorsally with an opalescent sheen (each autapomorphic for Hydrodytinae). Matinae is resolved as the sister group to the remaining Dytiscidae. Hyphydrini Sharp is found to be paraphyletic with respect to Pachydrini Biström, Nilsson and Wewalka, and the latter is relegated to a junior subjective synonym of the former (NEW SYNONYMY). Hydroporini Aubé and Hygrotini Portevin are found to be para- or polyphyletic. No changes are made to the classification of these taxa since character evidence is relatively weak, and taxon sampling within Hydroporinae is inadequate to justify changes. Carabdytes Balke, Hendrich and Wewalka is found to be the sister taxon to the remaining Colymbetinae, and because of its unique combination of characters and phylogenetic placement it is included in its own tribe, Carabdytini Pederzani (RESURRECTED). All other examined tribes of Dytiscidae are monophyletic. The female genitalia are described and figured for numerous taxa across the family, and numerous other characters are described and figured. The evolution of various features of the female genitalia within Dytiscidae is discussed. The resulting phylogenetic hypothesis is compared and contrasted with other phylogenetic proposals.


Zootaxa ◽  
2017 ◽  
Vol 4269 (3) ◽  
pp. 346 ◽  
Author(s):  
M.J. PAULSEN

The endemic North American stag beetle tribe Platyceroidini Paulsen & Hawks (Coleoptera: Lucanidae: Lucaninae) is reviewed. All primary types were studied and the existing generic and species concepts are subsequently corrected. Based on study of the male genitalia and external morphology, the previously monotypic genus Platyceropsis Benesh is reduced to subgeneric status under Platyceroides Benesh, new status, and the species Platyceroides laticollis (Casey) and Platyceroides keeni (Casey) new combination are transferred to this subgenus. Praocerus, new subgenus, is created to contain the species Platyceroides latus (Fall), and P. viriditinctus (Benesh). In the nominal subgenus, confusion has resulted from the historic misapplication of the oldest available name, Platyceroides agassii (LeConte), resulting in significant underestimation of the number of extant taxa. Lectotypes are designated for four species-group names (listed in their original combinations): Platycerus latus Fall, Platycerus opacus Fall, Platycerus pacificus Casey, and Platycerus parvicollis Casey. Four new species (Platyceroides barrae, P. infernus, P. pampinatus, and P. umpquus) are described from California and Oregon, United States of America. The following species are valid and are removed from synonymy with P. agassii: P. pacificus (Casey), revised status, and P. californicus (Casey), revised status. The synonym Platycerus parvicollis Casey is transferred from Platyceroides agassii to P. californicus, new synonymy. With the addition of four new species and the correction of the mistaken synonymies the total number of species in the tribe Platyceroidini is now 16.


2013 ◽  
Vol 58 ◽  
pp. 107-338
Author(s):  
Barbara Baehr ◽  
◽  
Mark Harvey ◽  
H.M. Smith ◽  
R. Ott ◽  
...  

The widespread and highly diverse goblin spider genus Opopaea Simon is a pantropical genus with biodiversity hotspots in Africa, Asia and Australia. We revise the Australian and Pacific species of the genus, provide redescriptions of the Australian species O. banksi (Hickman) and the Micronesian species O. foveolata Roewer, and new records of the pantropical O. deserticola Simon and O. concolor (Blackwall), as well as O. apicalis (Simon) which is newly transferred from Epectris, after the new synonymy of Epectris with Opopaea. The following species are provisionally transferred from Epectris to Opopaea, pending investigations into their generic affinities: O. conujaingensis (Xu), new combination from China; and O. mollis (Simon), new combination from Sri Lanka. Most Pacific Islands are inhabited by the four above-mentioned species but the following 15 newly described species are most likely native to the islands: from Fiji (O. fiji), Hawaii (O. hawaii), Palau (O. palau), New Caledonia (O. amieu, O. bicolor, O. burwelli, O. calcaris, O. goloboffi, O. monteithi, O. ndoua, O. platnicki, O. raveni, O. striata, O. touho, O. tuberculata). We treat the Australian Opopaea fauna and recognise 84 species including 71 new and 13 previously described species. The new Australian species include 21 species from New South Wales (O. acuminata, O. addsae, O. bushblitz, O. gerstmeieri, O. lebretoni, O. linea (also occurs in Queensland), O. magna, O. margaretehoffmannae, O. martini, O. michaeli, O. milledgei, O. nitens, O. ottoi, O. plana, O. simplex, O. sturt, O. suelewisae, O. sylvestrella, O. tenuis, O. ursulae, O. yorki); six from Northern Territory (O. ephemera, O. fishriver, O. gilliesi, O. johardingae, O. preecei, O. wongalara); 13 from Queensland (O. ameyi, O. brisbanensis, O. broadwater, O. carnarvon, O. carteri, O. chrisconwayi, O. douglasi, O. lambkinae, O. leichhardti, O. mcleani, O. proserpine, O. stanisici, O. ulrichi); three from South Australia (O. millbrook, O. mundy, O. stevensi); and 28 from Western Australia (O. aculeata, O. aurantiaca, O. billroth, O. callani, O. cowra, O. durranti, O. exoculata, O. flava, O. fragilis, O. framenaui, O. gracilis, O. gracillima, O. harmsi, O. johannae, O. julianneae, O. marangaroo, O. millstream, O. nadineae, O. pallida, O. pannawonica, O. pilbara, O. rixi, O. robusta, O. rugosa, O. subtilis, O. triangularis, O. wheelarra, O. whim). New records are provided for O. sown Baehr. Seven area-based keys to species are provided.


Sign in / Sign up

Export Citation Format

Share Document