Anhoraeomorphus vadoni (Franz) Jałoszyński, 2024
publication ID |
https://doi.org/ 10.11646/zootaxa.5505.1.1 |
publication LSID |
lsid:zoobank.org:pub:93F5E9F6-9EDC-4ED2-8F2B-1E6D0C18F893 |
persistent identifier |
https://treatment.plazi.org/id/03E7FF50-FFC3-5034-FF23-FF5BFDE247F2 |
treatment provided by |
Plazi |
scientific name |
Anhoraeomorphus vadoni (Franz) |
status |
comb. nov. |
Anhoraeomorphus vadoni (Franz) , comb. n.
Horaeomorphus vadoni Franz, 1986b: 152 View in CoL .
Remarks. According to Franz (1986b), the type series of this species is composed of a holotype and one paratype, and the holotype male is deposited in Tervuren, while a paratype male in “der Sammlung des Bayerischen Staates in München”. The holotype was not found in Musée Royal de l’Afrique Centrale, Tervuren, Belgium (email from Stéphane Hanot dated 02.04.2024), and the paratype was not found in Zoologische Staatssammlung München, Germany (email from Ditta Balke dated 03.04.2024). They are also missing from Franz Coll. at NHMW (pers. obs.).
Franz (1986b) described this species as most similar to A. roussettensis , and judging from the illustrated aedeagus ( Franz 1986b: fig. 135) it is possible that these two names are synonyms. Because of the aedeagal structure almost identical with that in A. roussettensis , there is no doubt that Horaeomorphus vadoni is a member of Anhoraeomorphus .
Distribution. Northern Madagascar (Analanjirofo Region).
Genus Euconnus Thomson
Euconnus Thomson, 1859: 61 View in CoL . Type species: Pselaphus hirticollis Illiger, 1798 (des. orig.).
Remarks. The chaotic subgeneric system of Euconnus and Euconnus -like genera in recent years were the subject of extensive study ( Jałoszyński 2012b, 2013, 2015b, c, d, 2016a, b, c, d, 2017a, b, c, d, e, f, 2018a, b, 2019, 2020a, b, 2021b, c, 2022, Jałoszyński & Newton 2017). However, this megadiverse genus (one of the largest within Coleoptera ) is still inadequately studied and its subgeneric division needs further work.
The key features of Euconnus are: eyes (if present) situated closer to mandibular bases and antennal fossae than to occipital constriction (e.g., Fig. 196 View FIGURES 195–197 ); hypostomal sutures lacking (e.g., Fig. 196 View FIGURES 195–197 ); mesoventral intercoxal process present, carinate (e.g., Fig. 197 View FIGURES 195–197 ); notosternal sutures complete (e.g., Fig. 196 View FIGURES 195–197 ); hypomeral ridges at least partly developed (e.g., Fig. 196 View FIGURES 195–197 ) or at least inner regions of hypomera delimited from outer regions by abrupt change in microsculpture; each elytron with two asetose basal pits (reduced in some species) (e.g., Fig. 217 View FIGURES 217–219 ); metaventral intercoxal process widely or narrowly (but clearly) separating metacoxae (e.g., Fig. 197 View FIGURES 195–197 ); and aedeagus with free rod-like parameres (e.g., Figs 191–194 View FIGURES 187–194 ).
A number of western Indian Ocean species were originally placed in Euconnus by Franz (1986b), but nomenclatural issues described in the Introduction resulted in placing them in Horaeomorphus . They are revised below, and most of them were found to belong in Euconnus , subgenus Tetramelus Motschulsky, 1869 .
Subgenus Tetramelus Motschulsky
Tetramelus Motschulsky, 1869: 257 . Type species: Scydmaenus oblongus Sturm, 1838 (des. by Franz in Newton & Franz (1998): 147).
Drastophus Casey, 1897: 389 View in CoL . Type species: Drastophus laevicollis Casey, 1897 (monotypy). Synonymized with Euconnus View in CoL s. str. by Franz (1985b); resurrected as subgenus by O’Keefe (1998); synonymized with Tetramelus by Jałoszyński (2017a).
Euconnoides Croissandeau, 1898: 154 (as subgenus of Euconnus View in CoL ). Type species: Scydmaenus styriacus Grimmer, 1841 View in CoL (des. Franz in Newton & Franz (1998): 147). Synonymized with Tetramelus by Csiki (1919).
Vinsoniana Lhoste, 1956: 283 (as subgenus of Scydmaenus View in CoL ). Type species: Scydmaenus mauritiensis Lhoste, 1956 View in CoL (monotypy). Erroneously synonymized with Horaeomorphus View in CoL by Franz (1986b); herein placed as junior synonym of Tetramelus .
Vinsonia Franz, 1986b: 174 View in CoL . Misspelling of Vinsoniana .
Heteroconnus Franz, 1963: 40 (as subgenus of Euconnus View in CoL ). Type species: Euconnus impressicollis Franz, 1963 View in CoL (des. orig.). Synonymized with Tetramelus by Jałoszyński (2021b).
Paratetramelus Franz, 1963: 25 (as subgenus of Euconnus View in CoL ). Type species: Euconnus kenyae Franz, 1963 View in CoL (des.orig.). Synonymized with Tetramelus by Jałoszyński (2021b).
Dimorphoconnus Franz, 1975: 177 (as subgenus of Euconnus View in CoL ). Type species: Scydmaenus insigniventris Lea, 1912 (des. orig.). Synonymized with Tetramelus by Jałoszyński (2021b).
Drasterophus Franz, 1985b: 171 (subsequent misspelling of Drastophus View in CoL ).
Remarks. Morphological structures illustrated and emended diagnosis given in Jałoszyński (2015d); further notes on character variability in Jałoszyński (2017a, 2021b).
Tetramelus , as currently defined, can be identified using the following set of co-occurring characters: hypostomal ridges running posteromesally (e.g., Figs 196 View FIGURES 195–197 , 207 View FIGURES 206–208 , 218 View FIGURES 217–219 ); head ventrally lacking deep narrow longitudinal groove connecting gular plate and submentum (e.g., Figs 196 View FIGURES 195–197 , 207 View FIGURES 206–208 , 218 View FIGURES 217–219 ); prothorax lacking longitudinal hypomeral grooves; pronotum broadest in front of middle (e.g., Figs 195 View FIGURES 195–197 , 206 View FIGURES 206–208 , 217 View FIGURES 217–219 ); antenna in male unmodified, gradually thickened or with variously distinct tetramerous club (e.g., Figs 190 View FIGURES 187–194 , 212 View FIGURES 209–216 , 223 View FIGURES 220–227 ); and tarsomere 4 in all legs lacking long distoventral lobe (for key to subgenera of Euconnus see Jałoszyński (2022)).
Distribution. Africa: Algeria, Cameroon, Comoros, Kenya, Lesotho, Madagascar, RSA, Swaziland, Tanzania; Asia: Asian Turkey, Nagorno-Karabakh, Nepal, “Syria”; Australia: Australia (incl. Franklin Is., Lord Howe Is., Reevesby Is., Tasmania); Caribbean: Jamaica; Europe: Albania, Andorra, Armenia, Austria, Belgium, Bosnia & Herzegovina, Bulgaria, Croatia, Czech Rep., France, Georgia, Germany, Greece, Hungary, Italy, Kosovo, Lithuania, Macedonia, Montenegro, Netherlands, Poland, Portugal, Romania, European Russia, Slovakia, Slovenia, Spain, Switzerland, European Turkey, Ukraine; North America: Canada, USA; Pacific: New Caledonia, New Zealand; South America: Bolivia, Brazil, Peru.
Composition. 251 species and 2 subspecies. During the present study, 18 species of Tetramelus were recognized to occur in Madagascar, and one in Grande Comore (one originally placed in Euconnus subgenus Paratetramelus (currently a junior synonym of Tetramelus ), 17 herein transferred from Horaeomorphus ). However, judging from descriptions and illustrations in Franz (1986b), it seems that some species placed by him in Euconnus (s. str.) in fact belong in Tetramelus (this problem is beyond the scope of the present paper). Only species previously placed in Horaeomorphus are treated here.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
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Phylum |
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Class |
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Order |
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Family |
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Genus |
Anhoraeomorphus vadoni (Franz)
Jałoszyński, Paweł 2024 |
Horaeomorphus vadoni
Franz, H. 1986: 152 |
Vinsonia
Franz, H. 1986: 174 |
Drasterophus
Franz, H. 1985: 171 |
Dimorphoconnus
Franz, H. 1975: 177 |
Heteroconnus
Franz, H. 1963: 40 |
Paratetramelus
Franz, H. 1963: 25 |
Vinsoniana
Lhoste, J. 1956: 283 |
Euconnoides
Newton, A. F. & Franz, H. 1998: 147 |
Croissandeau, J. 1898: 154 |
Drastophus
Casey, T. L. 1897: 389 |
Tetramelus
Newton, A. F. & Franz, H. 1998: 147 |
Motschulsky, V. 1869: 257 |
Euconnus
Thomson, C. G. 1859: 61 |