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Contrary to what its name suggests, Nemesia arboricola is not strictly arboreal in habit. Here we compare female specimens of N. arboricola collected from arboreal and terrestrial nests. We furthermore describe the male of N. arboricola for the first time as well as two recently discovered species of Nemesia (N. maltensis sp. nov. and N. cominensis sp. nov.). Nemesia maltensis is described from both sexes, N. cominensis is described from the female and a juvenile male specimen. For N. cominensis we discuss the sexual dimorphism of juvenile male and female spiders. Field observations and laboratory observations show remarkable features of the Maltese Nemesia fauna that are unknown from Nemesia species found elsewhere. Particularly, the arboreal dwellings of N. arboricola and the absence of a trapdoor to close off the burrow entrance in N. maltensis appear to be exceptional. The composition of the Maltese Nemesia fauna, as located in the central Mediterranean, is finally discussed in relation to the different Nemesia species-complexes occurring in the eastern and western Mediterranean basin.
This paper offers an explanation of each of the 44 scientific names given by Leopold Krüger (1861-1942) to odonate taxa together with that for the names of all the genera into which they are sorted now. But prior to that there is some information about the life and work of this scientist, and in the final part his preferences in odonatological nomenclature are compared with those in the names created by F.M. Brauer and F. Ris and some impressions of his studies on Neuroptera are presented and considerations about his aspirations in his work are given.
Our expanded efforts in genomic sequencing to cover additional skipper butterfly (Lepidoptera: Hesperiidae) species and populations, including primary type specimens, call for taxonomic changes to restore monophyly and correct misidentifications by moving taxa between genera and proposing new names. Reconciliation between phenotypic characters and genomic trees suggests three new tribes, two new subtribes, 23 new genera, 17 new subgenera and 10 new species that are proposed here: Psolosini Grishin, new tribe (type genus Psolos Staudinger, 1889), Ismini Grishin, new tribe (type genus Isma Distant, 1886), Eetionini Grishin, new tribe (type genus Eetion de Nicéville, 1895), Orphina Grishin, new subtribe (type genus Orphe Godman, 1901), Carystoidina Grishin, new subtribe (type genus Carystoides Godman, 1901), Fulvatis Grishin, new genus (type species Telegonus fulvius Plötz, 1882), Adina Grishin, new genus (type species Nascus adrastor Mabille and Boullet, 1912), Ornilius Grishin, new genus (type species Ornilius rotundus Grishin, new species), Tolius Grishin, new genus (type species Antigonus tolimus Plötz, 1884), Lennia Grishin, new genus (type species Leona lena Evans, 1937), Trida Grishin, new genus (type species Cyclopides barberae Trimen, 1873), Noxys Grishin, new genus (type species Oxynthes viricuculla Hayward, 1951), Gracilata Grishin, new genus (type species Enosis quadrinotata Mabille, 1889), Hermio Grishin, new genus (type species Falga ? hermione Schaus, 1913), Eutus Grishin, new genus (type species Cobalus rastaca Schaus, 1902), Gufa Grishin, new genus (type species Phlebodes gulala Schaus, 1902), Godmia Grishin, new genus (type species Euroto chlorocephala Godman, 1900), Rhomba Grishin, new genus (type species Eutychide gertschi Bell, 1937), Rectava Grishin, new genus (type species Megistias ignarus Bell, 1932), Contrastia Grishin, new genus (type species Hesperia distigma Plötz, 1882), Mit Grishin, new genus (type species Mnasitheus badius Bell, 1930), Picova Grishin, new genus (type species Vorates steinbachi Bell, 1930), Lattus Grishin, new genus (type species Eutocus arabupuana Bell, 1932), Gubrus Grishin, new genus (type species Vehilius lugubris Lindsey, 1925), Koria Grishin, new genus (type species Hesperia kora Hewitson, 1877), Corta Grishin, new genus (type species Eutychide lycortas Godman, 1900), Calvetta Grishin, new genus (type species Hesperia calvina Hewitson, 1866), Oz Grishin, new genus (type species Astictopterus ozias Hewitson, 1878), Praxa Grishin, new subgenus (type species Nascus prax Evans, 1952), Bron Grishin, new subgenus (type species Papilio broteas Cramer, 1780), Turis Grishin, new subgenus (type species Pyrgus 1955, and Synale Mabille, 1904 of Carystus Hübner, [1819]. The following 20 genera are treated as junior subjective synonyms: Leucochitonea Wallengren, 1857 of Abantis Hopffer, 1855; Sapaea Plötz, 1879 and Netrobalane Mabille, 1903 of Caprona Wallengren, 1857; Parasovia Devyatkin, 1996 of Sebastonyma Watson, 1893; Pemara Eliot, 1978 of Oerane Elwes and Edwards, 1897; Ankola Evans, 1937 of Pardaleodes Butler, 1870; Arotis Mabille, 1904 of Mnaseas Godman, 1901; Chalcone Evans, 1955, Hansa Evans, 1955, and Propertius Evans, 1955 of Metrocles Godman, 1900; Jongiana O. Mielke and Casagrande, 2002 of Cobaloides Hayward, 1939; Pamba Evans, 1955 of Psoralis Mabille, 1904; Brownus Grishin, 2019 of Styriodes Schaus, 1913; Mnasilus Godman, 1900 of Papias Godman, 1900; Sucova Evans, 1955 of Mnasitheus Godman, 1900; Pyrrhocalles Mabille, 1904 and Asbolis Mabille, 1904 of Choranthus Scudder, 1872; Miltomiges Mabille, 1903 of Methionopsis Godman, 1901; Sacrator Evans, 1955 of Thracides Hübner, [1819]; and Lychnuchoides Godman, 1901 of Perichares Scudder, 1872. Arunena Swinhoe, 1919 is a junior subjective synonym of Stimula de Nicéville, 1898 (not of Koruthaialos Watson, 1893). The following 27 names are species-level taxa (some in new combinations) reinstated from synonymy: Salantoia gildo (Mabille, 1888) (not Salatis cebrenus (Cramer, 1777)), Bungalotis corentinus (Plötz, 1882) (not Bungalotis midas (Cramer, 1775)), Telegonus cretellus (Herrich-Schäffer, 1869) (not Telegonus cassander (Fabricius, 1793)), Santa palica (Mabille, 1888) (not Chiothion asychis (Stoll, 1780)), Camptopleura cincta Mabille and Boullet, 1917 (not Camptopleura auxo (Möschler, 1879)), Camptopleura orsus (Mabille, 1889) (not Nisoniades mimas (Cramer, 1775)), Metron voranus (Mabille, 1891) and Metron fasciata (Möschler, 1877) (not Metron zimra (Hewitson, 1877)), Limochores catahorma (Dyar, 1916) (not Limochores pupillus (Plötz, 1882)), Pares viridiceps (Mabille, 1889) (not Thoon modius (Mabille, 1889)), Tigasis wellingi (Freeman, 1969) (not Tigasis arita (Schaus, 1902)), Rectava sobrinus (Schaus, 1902) (not Papias phainis Godman, 1900), Nastra subsordida (Mabille, 1891) (not Adlerodea asema (Mabille, 1891), previously in Eutychide Godman, 1900), Lerema pattenii Scudder, 1872 (not Lerema accius (J. E. Smith, 1797)), Lerema (Morys) ancus (Möschler, 1879) (not Cymaenes tripunctus theogenis (Capronnier, 1874)), Cobalopsis zetus (Bell, 1942) (not Cobalopsis nero (Herrich-Schäffer, 1869)), Lerema (Geia) etelka (Schaus, 1902) (not Lerema (Geia) geisa (Möschler, 1879), previously in Morys Godman, 1900), Cymaenes isus (Godman, 1900) (not Cymaenes trebius (Mabille, 1891)), Vehilius labdacus (Godman, 1900) (not Vehilius inca (Scudder, 1872)), Papias amyrna (Mabille, 1891) (not Papias allubita (Butler, 1877), previously in Mnasilus Godman, 1900), Papias integra (Mabille, 1891) (not Papias subcostulata (Herrich-Schäffer, 1870)), Metiscus atheas Godman, 1900 (not Hesperia achelous Plötz, 1882), Dion agassus (Mabille, 1891) (not Dion uza (Hewitson, 1877), previously in Enosis Mabille, 1889), Picova incompta (Hayward, 1942) (not Lerema (Morys) micythus (Godman, 1900), previously in Morys Godman, 1900), Lucida melitaea (Draudt, 1923) (not Lucida lucia (Capronnier, 1874)), Methionopsis modestus Godman, 1901 (not Methionopsis ina (Plötz, 1882)), and Thargella (Volus) volasus (Godman, 1901) (not Eutocus facilis (Plötz, 1884)). The following 57 taxa are elevated from subspecies to species, new status (some in new combinations): Dyscophellus doriscus (Hewitson, 1867) (not Dyscophellus porcius (C. Felder and R. Felder, 1862), Phocides vida (A. Butler, 1872) (not Phocides urania (Westwood, 1852)), Tagiades (Daimio) ceylonica Evans, 1932 (not Tagiades litigiosa Möschler, 1878), Tagiades (Daimio) tubulus Fruhstorfer, 1910 (not Tagiades sambavana Elwes and Edwards, 1897), Tagiades (Daimio) kina Evans, 1934, Tagiades (Daimio) sheba Evans, 1934, Tagiades (Daimio) martinus Plötz, 1884, Tagiades (Daimio) sem Mabille, 1883, and Tagiades (Daimio) neira Plötz, 1885 (not Tagiades trebellius (Hopffer, 1874)), Tagiades (Daimio) korela Mabille, 1891 and Tagiades (Daimio) presbyter Butler, 1882 (not Tagiades nestus (C. Felder, 1860)), Tagiades obscurus Mabille, 1876, Tagiades ravi (Moore, [1866]), Tagiades atticus (Fabricius, 1793), Tagiades titus Plötz, 1884, Tagiades janetta Butler, 1870, Tagiades inconspicua Rothschild, 1915, and Tagiades hovia Swinhoe, 1904 (not Tagiades japetus (Stoll, [1781])), Tagiades silvia Evans, 1934 and Tagiades elegans Mabille, 1877 (not Tagiades gana (Moore, [1866])), Tapena bornea Evans, 1941 and Tapena minuscula Elwes and Edwards, 1897 (not Tapena thwaitesi Moore, [1881]), Darpa dealbata (Distant, 1886) (not Darpa pteria (Hewitson, 1868)), Perus manx (Evans, 1953) (not Perus minor (Schaus, 1902)), Canesia pallida (Röber, 1925) (not Carrhenes canescens (R. Felder, 1869)), Carrhenes conia Evans, 1953 (not Carrhenes fuscescens (Mabille, 1891)), Anisochoria extincta Hayward, 1933 and Anisochoria polysticta Mabille, 1876 (not Anisochoria pedaliodina (Butler, 1870)), Anisochoria verda Evans, 1953 (not Anisochoria minorella Mabille, 1898), Bralus alco (Evans, 1953) (not Bralus albida (Mabille, 1888)), Ephyriades jamaicensis (Möschler, 1879) (not Ephyriades brunnea (Herrich-Schäffer, 1865)), Koruthaialos (Stimula) frena Evans, 1949 (not Koruthaialos focula (Plötz, 1882)), Euphyes kiowah (Reakirt, 1866) (not Euphyes vestris (Boisduval, 1852)), Mnaseas inca Bell, 1930 (not Mnaseas bicolor (Mabille, 1889)), Metron hypochlora (Draudt, 1923) (not Metrocles schrottkyi (Giacomelli, 1911), previously in Metron Godman, 1900), Decinea huasteca (H. Freeman, 1969), Decinea denta Evans, 1955, and Decinea antus (Mabille, 1895) (not Decinea decinea (Hewitson, 1876)), Xeniades pteras Godman, 1900 (not Xeniades chalestra (Hewitson, 1866)), Xeniades difficilis Draudt, 1923 (not Xeniades orchamus (Cramer, 1777)), Xeniades hermoda (Hewitson, 1870) (not Tisias quadrata (HerrichSchäffer, 1869)), Hermio vina (Evans, 1955) (not Hermio hermione (Schaus, 1913), previously in Lento Evans, 1955), Cymaenes loxa Evans, 1955, (not Cymaenes laureolus (Schaus, 1913)), Niconiades peri (Evans, 1955) (not Rhinthon bajula (Schaus, 1902), previously in Neoxeniades Hayward, 1938), Gallio danius (Bell, 1941) (not Vehilius seriatus (Mabille, 1891)), Gallio massarus (E. Bell, 1940) (not Gallio garima (Schaus, 1902) previously in Tigasis Godman, 1900), Cymaenes edata (Plötz, 1882), Cymaenes miqua (Dyar, 1913) and Cymaenes aequatoria (Hayward, 1940) (not Cymaenes odilia (Burmeister, 1878)), Lychnuchus (Enosis) demon (Evans, 1955) (not Lychnuchus (Enosis) immaculata (Hewitson, 1868), previously in Enosis Mabille, 1889), Naevolus naevus Evans, 1955 (not Naevolus orius (Mabille, 1883)), Lucida scopas (Mabille, 1891), Lucida oebasus (Godman, 1900), and Lucida leopardus (Weeks, 1901) (not Lucida lucia (Capronnier, 1874)), Corticea schwarzi (E. Bell, 1941) and Corticea sylva (Hayward, 1942) (not Corticea mendica (Mabille, 1898)), and Choranthus orientis (Skinner, 1920) (not Choranthus antiqua (Herrich-Schäffer, 1863), previously in Pyrrhocalles Mabille, 1904). Borbo impar bipunctata (Elwes and J. Edwards, 1897) is a valid subspecies, not a synonym of Borbo impar tetragraphus (Mabille, 1891), here placed in synonymy with Lotongus calathus (Hewitson, 1876), new synonym. We confirm the species status of Telegonus cassius (Evans, 1952) and Lerema (Morys) valda Evans, 1955. Euphyes chamuli Freeman, 1969 is placed as a subspecies of Euphyes kiowah (Reakirt, 1866), new status. The following 41 taxa are junior subjective synonyms, either newly proposed or transferred from synonymy with other species or subspecies: Telegonus mutius Plötz, 1882 of Euriphellus phraxanor (Hewitson, 1876), Telegonus erythras Mabille, 1888 of Dyscophellus damias (Plötz, 1882), Aethilla jaira Butler, 1870 of Telegonus cretellus (Herrich-Schäffer, 1869), Paches era Evans, 1953 of Santa palica (Mabille, 1888), Antigonus alburnea Plötz, 1884 of Tolius tolimus robigus (Plötz, 1884) (not of Echelatus sempiternus simplicior (Möschler, 1877)), Echelatus depenicillus Strand, 1921 of E. sempiternus simplicior (not of T. tolimus robigus), Antigonus aura Plötz, 1884 of Theagenes dichrous (Mabille, 1878) (not of Helias phalaenoides palpalis (Latreille, [1824])), Achlyodes impressus Mabille, 1889 of Camptopleura orsus (Mabille, 1889), Augiades tania Schaus, 1902 of Metron voranus (Mabille, 1891), Pamphila verdanta Weeks, 1906 of Metron fasciata (Möschler, 1877), Niconiades viridis vista Evans, 1955 of Niconiades derisor (Mabille, 1891), Pamphila binaria Mabille, 1891 of Conga chydaea (A. Butler, 1877) (not of Cynea cynea (Hewitson, 1876)), Psoralis concolor Nicolay, 1980 of Ralis immaculatus (Hayward, 1940), Hesperia dido Plötz, 1882 of Cynea (Quinta) cannae (Herrich-Schäffer, 1869) (not of Lerema lochius (Plötz, 1882)), Proteides osembo Möschler, 1883 of Cynea (Cynea) diluta (Herrich-Schäffer, 1869) (not of Cynea (Quinta) cannae (Herrich-Schäffer, 1869)), Cobalopsis brema E. Bell, 1959 of Eutus rastaca (Schaus, 1902), Psoralis panamensis Anderson and Nakamura, 2019 of Rhomba gertschi (Bell, 1937), Cobalus asella Herrich-Schäffer, 1869 of Amblyscirtes alternata (Grote and Robinson, 1867) (not of Amblyscirtes vialis (W. H. Edwards, 1862)), Papias trimacula Nicolay, 1973 of Nastra subsordida (Mabille, 1891), Pamphila bipunctata Mabille, 1889 and Sarega staurus Mabille, 1904 of Lerema pattenii Scudder, 1872 (not of Cymaenes lumina (Herrich-Schäffer, 1869), previously in Lerema Scudder, 1872), Hesperia aethra Plötz, 1886 of Lerema lineosa (Herrich-Schäffer, 1865) (not of Lerema (Morys) compta Butler, 1877), Megistias miaba Schaus, 1902 of Cobalopsis valerius (Möschler, 1879), Phanis sylvia Kaye, 1914 of Lerema etelka (Schaus, 1902) (not of Lerema (Geia) geisa (Möschler, 1879), previously in Morys Godman, 1900), Carystus odilia Burmeister, 1878, Pamphila trebius Mabille, 1891 and Megistias corescene Schaus, 1902 of Cymaenes lumina (Herrich-Schäffer, 1869), Hesperia phocylides Plötz, 1882 of Cymaenes edata (Plötz, 1882) (not of Lerema accius (J. E. Smith, 1797)), Pamphila xenos Mabille, 1898 of Vehilius inca (Scudder, 1872), Mnasilus guianae Lindsey, 1925 of Papias amyrna (Mabille, 1891), Pamphila nubila Mabille, 1891 of Papias integra (Mabille, 1891) (not of Cynea corisana (Plötz, 1882)), Enosis matheri H. Freeman, 1969 of Metiscus atheas Godman, 1900 (previously in Enosis Mabille, 1889), Hesperia infuscata Plötz, 1882 of Mnaseas derasa derasa (Herrich-Schäffer, 1870) (previously Arotis Mabille, 1904), (not of Papias subcostulata (Herrich-Schäffer, 1870)), Pamphila astur Mabille, 1891 of Metiscus angularis (Möschler, 1877) (not of Cymaenes tripunctus theogenis (Capronnier, 1874)), Anthoptus macalpinei H. Freeman, 1969 of Anthoptus inculta (Dyar, 1918), Methionopsis typhon Godman, 1901 of Methionopsis ina (Plötz, 1882), Methionopsis dolor Evans, 1955 of Thargella volasus (Godman, 1901), Hesperia cinica Plötz, 1882 of Dubiella dubius (Stoll, 1781), Cobalus disjuncta Herrich-Schäffer, 1869 of Dubiella dubius (Stoll, 1781) (not of Vettius lafrenaye (Latreille, [1824])), and Saliana vixen Evans, 1955 of Neoxeniades parna (Evans, 1955). The following are new and revised genusspecies combinations: Euriphellus cebrenus (Cramer, 1777) (not Salatis Evans, 1952), Gorgopas extensa (Mabille, 1891) (not Polyctor Evans, 1953), Clytius shola (Evans, 1953) (not Staphylus Godman and Salvin, 1896), Perus narycus (Mabille, 1889) (not Ouleus Lindsey, 1925), Perus parvus (Steinhauser and Austin, 1993) (not Staphylus Godman and Salvin, 1896), Pholisora litus (Dyar, 1912) (not Bolla Mabille, 1903), Carrhenes decens (A. Butler, 1874) (not Antigonus Hübner, [1819]), Santa palica (Mabille, 1888) (not Chiothion Grishin, 2019), Bralus nadia (Nicolay, 1980) (not Anisochoria Mabille, 1876), Acerbas sarala (de Nicéville, 1889) (not Lotongus Distant, 1886), Caenides sophia (Evans, 1937) (not Hypoleucis Mabille, 1891), Hypoleucis dacena (Hewitson, 1876) (not Caenides Holland, 1896), Dotta tura (Evans, 1951) (not Astictopterus C. Felder and R. Felder, 1860), Nervia wallengrenii (Trimen, 1883) (not Kedestes Watson, 1893), Testia mammaea (Hewitson, 1876) (not Decinea Evans, 1955), Oxynthes trinka (Evans, 1955) (not Orthos Evans, 1955), Metrocles argentea (Weeks, 1901) (not Paratrytone Godman, 1900), Metrocles scitula (Hayward, 1951) (not Mucia Godman, 1900), Metrocles schrottkyi (Giacomelli, 1911) (not Metron Godman, 1900), Niconiades derisor (Mabille, 1891) (not Decinea Evans, 1955), Paratrytone samenta (Dyar, 1914) (not Ochlodes Scudder, 1872), Oligoria (Cobaloides) locutia (Hewitson, 1876) (not Quinta Evans, 1955), Psoralis (Saniba) laska (Evans, 1955) (not Vidius Evans, 1955), Psoralis (Saniba) arva (Evans, 1955) and Psoralis (Saniba) umbrata (Erschoff, 1876) (not Vettius Godman, 1901), Psoralis (Saniba) calcarea (Schaus, 1902) and Psoralis (Saniba) visendus (E. Bell, 1942) (not Molo Godman, 1900), Alychna gota (Evans, 1955) (not Psoralis Mabille, 1904), Adlerodea asema (Mabille, 1891) and Adlerodea subpunctata (Hayward, 1940) (not Eutychide Godman, 1900), Ralis immaculatus (Hayward, 1940) (not Mucia Godman, 1900), Rhinthon braesia (Hewitson, 1867) and Rhinthon bajula (Schaus, 1902) (not Neoxeniades Hayward, 1938), Cymaenes lochius Plötz, 1882 (not Lerema Scudder, 1872), Paracarystus ranka (Evans, 1955) (not Thoon Godman, 1900), Tricrista aethus (Hayward, 1951), Tricrista canta (Evans, 1955), Tricrista slopa (Evans, 1955), Tricrista circellata (Plötz, 1882), and Tricrista taxes (Godman, 1900) (not Thoon Godman, 1900), Gallio madius (E. Bell, 1941) and Gallio seriatus (Mabille, 1891) (not Vehilius Godman, 1900), Gallio garima (Schaus, 1902) (not Tigasis Godman, 1900), Tigasis corope (HerrichSchäffer, 1869) (not Cynea Evans, 1955), Tigasis perloides (Plötz, 1882) (not Cymaenes Scudder, 1872), Amblyscirtes (Flor) florus (Godman, 1900) (not Repens Evans, 1955), Vidius fraus (Godman, 1900) (not Cymaenes Scudder, 1872), Nastra celeus (Mabille, 1891) (not Vehilius Godman, 1900), Nastra nappa (Evans, 1955) (not Vidius Evans, 1955), Vehilius warreni (Weeks, 1901) and Vehilius limae (Lindsey, 1925) (not Cymaenes Scudder, 1872), Cymaenes lumina (Herrich-Schäffer, 1869) (not Lerema Scudder, 1872), Cobalopsis valerius (Möschler, 1879) (not Cobalopsis Godman, 1900), Cobalopsis dictys (Godman, 1900) (not Papias Godman, 1900), Lerema (Morys) venias (Bell, 1942) (not Cobalopsis Godman, 1900), Papias latonia (Schaus, 1913) (not Cobalopsis Godman, 1900), Dion iccius (Evans, 1955) and Dion uza (Hewitson, 1877) (not Enosis Mabille, 1889), Vistigma (Vistigma) opus (Steinhauser, 2008) (not Thoon Godman, 1900), Saturnus fartuga (Schaus, 1902) (not Parphorus Godman, 1900), Phlebodes fuldai (E. Bell, 1930) (not Vettius Godman, 1901), Mnasitheus padus (Evans, 1955) (not Moeris Godman, 1900), Naevolus brunnescens (Hayward, 1939) (not Psoralis Mabille, 1904), Lamponia ploetzii (Capronnier, 1874) (not Vettius Godman, 1901), Mnestheus silvaticus Hayward, 1940 (not Ludens Evans, 1955), Rigga spangla (Evans, 1955) (not Sodalia Evans, 1955), Corticea vicinus (Plötz, 1884) (not Lento Evans, 1955), Mnasalcas thymoetes (Hayward, 1942) (not Mnasicles Godman, 1901), Mnasalcas boyaca (Nicolay, 1973) (not Pamba Evans, 1955), Vertica brasta (Evans, 1955) (not Lychnuchus Hübner, [1831]), Carystina discors Plötz, 1882 (not Cobalus Hübner, [1819]), Zetka irena (Evans, 1955) (not Neoxeniades Hayward, 1938), and Neoxeniades parna (Evans, 1955) (not Niconiades Hübner, [1821]). The following are new or revised species-subspecies combinations: Tagiades neira moti Evans, 1934, Tagiades neira canonicus Fruhstorfer, 1910, Tagiades sheba vella Evans, 1934, Tagiades sheba lola Evans, 1945, Tagiades korela biakana Evans, 1934, Tagiades korela mefora Evans, 1934, Tagiades korela suffusus Rothschild, 1915, Tagiades korela brunta Evans, 1949, Tagiades ravi ravina Fruhstorfer, 1910, Tagiades atticus carnica Evans, 1934, Tagiades atticus nankowra Evans, 1934, Tagiades atticus helferi C. Felder, 1862, Tagiades atticus balana Fruhstorfer, 1910, Tagiades inconspicua mathias Evans, 1934, Tagiades hovia kazana Evans, 1934, Tagiades elegans fuscata de Jong and Treadaway, 2007, Tagiades elegans semperi Fruhstorfer, 1910, Metron hypochlora tomba Evans, 1955, Decinea denta pruda Evans, 1955, and Choranthus orientis eleutherae (Bates, 1934) (previously in Pyrrhocalles Mabille, 1904). In addition to the abovementioned changes, the following new combinations involve newly proposed genus group names: Fulvatis fulvius (Plötz, 1882) and Fulvatis scyrus (E. Bell, 1934) (not Salatis Evans, 1952); Adina adrastor (Mabille and Boullet, 1912) (not Bungalotis Watson, 1893); Nascus (Praxa) prax Evans, 1952, Nascus (Bron) broteas (Cramer, 1780), and Nascus (Bron) solon (Plötz, 1882) (not Pseudonascus Austin, 2008); Chirgus (Turis) veturius (Plötz, 1884); Paches (Tiges) liborius (Plötz, 1884), and Paches (Tiges) mutilatus (Hopffer, 1874) (not Antigonus Hübner, [1819]); Paches (Tiges) exosa (A. Butler, 1877); Tolius tolimus (Plötz, 1884) and Tolius luctuosus (Godman & Salvin, 1894) (not Echelatus Godman and Salvin, 1894); Ancistroides (Ocrypta) caerulea (Evans, 1928), Ancistroides (Ocrypta) renardi (Oberthür, 1878), Ancistroides (Ocrypta) waigensis (Plötz, 1882), Ancistroides (Ocrypta) aluensis (Swinhoe, 1907), Ancistroides (Ocrypta) flavipes (Janson, 1886), and Ancistroides (Ocrypta) maria (Evans, 1949) (not Notocrypta de Nicéville, 1889); Lennia lena (Evans, 1937), Lennia binoevatus (Mabille, 1891), Lennia maracanda (Hewitson, 1876), and Lennia lota (Evans, 1937) (not Leona Evans, 1937); Trida barberae (Trimen, 1873) and Trida sarahae (Henning and Henning, 1998) (not Kedestes Watson, 1893); Noxys viricuculla (Hayward, 1951) (not Oxynthes Godman, 1900); Xeniades (Tixe) quadrata (Herrich-Schäffer, 1869), Xeniades (Tixe) rinda (Evans, 1955), Xeniades (Tixe) putumayo (Constantino and Salazar, 2013) (not Tisias Godman, 1901); Gracilata quadrinotata (Mabille, 1889) (not Styriodes Schaus, 1913); Hermio hermione (Schaus, 1913) (not Lento Evans, 1955); Cynea (Nycea) hycsos (Mabille, 1891), Cynea (Nycea) corisana (Plötz, 1882), Cynea (Nycea) popla Evans, 1955, Cynea (Nycea) iquita (E. Bell, 1941), Cynea (Nycea) robba Evans, 1955, Cynea (Nycea) melius (Geyer, 1832), and Cynea (Nycea) irma (Möschler, 1879); Eutus rastaca (Schaus, 1902) (not Eutychide Godman, 1900); Eutus yesta (Evans, 1955) (not Thoon Godman, 1900); Eutus mubevensis (E. Bell, 1932) (not Tigasis Godman, 1900); Gufa gulala (Schaus, 1902) (not Mucia Godman, 1900); Gufa fusca (Hayward, 1940) (not Tigasis Godman, 1900); Godmia chlorocephala (Godman, 1900) (not Onophas Godman, 1900); Rhomba gertschi (E. Bell, 1937) (not Justinia Evans, 1955); Mnasicles (Nausia) nausiphanes (Schaus, 1913) (not Tigasis Godman, 1900); Amblyscirtes (Flor) florus (Godman, 1900) (not Repens Evans, 1955); Rectava ignarus (E. Bell, 1932) (not Papias Godman, 1900); Rectava vorgia (Schaus, 1902) (not Cobalopsis Godman, 1900); Rectava nostra (Evans, 1955) (not not Vidius Evans, 1955); Lerema (Geia) geisa (Möschler, 1879) and Lerema (Geia) lyde (Godman, 1900) (not Morys Godman, 1900); Contrastia distigma (Plötz, 1882) (not Cymaenes Scudder, 1872); Mit (Mit) badius (E. Bell, 1930) (not Styriodes Schaus, 1913); Mit (Mit) gemignanii (Hayward, 1940), (not Mnasitheus Godman, 1900); Mit (Rotundia) schausi (Mielke and Casagrande, 2002), (not Enosis Mabille, 1889); Picova steinbachi (E. Bell, 1930) (not Saturnus Evans, 1955); Lattus arabupuana (E. Bell, 1932) (not Eutocus Godman, 1901); Gubrus lugubris (Lindsey, 1925) (not Vehilius Godman, 1900); Thargella (Pseudopapias) tristissimus (Schaus, 1902) (not Papias Godman, 1900); Koria kora (Hewitson, 1877) (not Justinia Evans, 1955); Justinia (Septia) septa Evans, 1955; Corta lycortas (Godman, 1900) (not Orthos Evans, 1955); Vertica (Brasta) brasta (Evans, 1955) (not Lychnuchus Hübner, [1831]); Calvetta calvina (Hewitson, 1866) (not Cobalus Hübner, [1819]); Neoxeniades (Bina) gabina (Godman, 1900) (not Orthos Evans, 1955); Oz ozias (Hewitson, 1878) and Oz sebastiani Salazar and Constantino, 2013 (not Lychnuchoides Godman, 1901); and Carystoides (Balma) balza Evans, 1955 and Carystoides (Balma) maroma (Möschler, 1877). Finally, unless stated otherwise, all subgenera, species, subspecies and synonyms of mentioned genera and species are transferred together with their parent taxa, and taxa not mentioned in this work remain as previously classified.
The West Indian genus Onychotillus Chapin (Coleoptera: Cleridae: Tillinae) is revised and includes O. androwi Opitz, new species, O. apiculus Opitz, new species, O. cinctipennis (Chevrolat,1874), O. cubana de Zayas,1988, O. dimidiatus de Zayas,1988, O. lineatus Opitz, new species, O. minutus de Zayas,1988, O. trinitatis de Zayas,1988, O. woodruffi Opitz, new species, and O. vittatus Chapin,1945.
Lissomus quisqueya new species and L. woodruffi new species are described. Both species are reported from the Dominican Republic on the island of Hispaniola. These are the first species of Lissomus Dalman reported from the Greater Antilles. Lissomus quisqueya is recorded from montane mesic forests in the Cordillera Central from Dajadon and La Vega provinces. Lissomus woodruffi is recorded from Barahona, Independencia and Pedernales provinces from montane mesic forest in the Sierra de Bahoruco. Morphologically, these species are most similar to members of the L. discedens Bonvouloir species group from Mesoamerica and South America. Known sites of occurrence of L. quisqueya and L. woodruffi are remnants of formerly more extensive mesic forests. Some of the specimens were found in secondary forests and ecotonal areas at sites near to primary forest or remnants, and all these forests are threatened by anthropogenic activities and stochastic climate changes.
The tornoceratid ammonoids from the Roteisenstein Formation of Dillenburg (Cephalopoda, Ammonoidea)
(2022)
The ammonoids of the suborder Tornoceratina from the Middle to Late Devonian Red Ironstone Formation of the area around Dillenburg (eastern Rhenish Mountains) are revised, mainly based on historical collections stored in the Museum für Naturkunde, Berlin. The species Tornoceras typus (Sandberger & Sandberger, 1851), Tornoceras frechi Wedekind, 1918 and Epitornoceras mithracoides (Frech, 1888) are re-described based on the original material from the Red Ironstone. The new genus Lentitornoceras gen. nov. is proposed for the new species L. materni gen. et sp. nov.; the new genus Paucitornoceras gen. nov. is proposed with the type species Goniatites paucistriatus. Epitornoceras transmediterraneum sp. nov. is described from the Anti-Atlas of Morocco and compared with E. mithracoides.
Two new species of shrubs in the genus Lasianthus Jack (Rubiaceae), L. naikii V.S.Dang & Vuong sp. nov. and L. sonlangensis V.S.Dang, Vuong & Quan sp. nov. from Kon Chu Rang Nature Reserve of Gia Lai Province in southern Vietnam, are described and illustrated. The similarities and differences of two new species with the morphologically closest allies are presented. Descriptions, illustrations, colour plates and vernacular names are provided.
Labahitha spiders (Arachnida: Araneae: Filistatidae) from islands in the Indian and Pacific Ocean
(2022)
The genus Labahitha has hitherto comprised two species from peninsular Malaysia and Christmas Island (Australia). We here demonstrate that the genus is widespread in islands and territories across the Indian and Pacific Oceans, including the following species that have been previously assigned to other filistatid genera: Labahitha marginata (Kishida, 1936) comb. nov. (= Filistata bakeri Berland, 1938 syn. nov.), Labahitha garciai (Simon, 1892) comb. nov. (= Pritha heikkii Saaristo, 1978 syn. nov., = Pritha sechellana Benoit, 1978 syn. nov.), Labahitha nicobarensis (Tikader, 1977) comb. nov., Labahitha littoralis (Roewer, 1938) comb. nov., Labahitha insularis (Thorell, 1891) comb. nov., Labahitha sundaica (Kulczyński, 1908) comb. nov. (all transferred from Pritha, the latter three provisionally, pending re-examination of the type material); Labahitha fuscata (Nakatsudi, 1943) comb. nov. and Labahitha ryukyuensis (Ono, 2013) comb. nov. (both transferred from Tricalamus). Many of these species have been collected in synanthropic settings and from disparate islands thousands of kilometers apart. This suggests either high dispersal capabilities or, more likely, human-mediated introductions. At least L. marginata has been introduced to continental America. Two new species of Labahitha are described: Labahitha platnicki sp. nov. from New Caledonia and the Bismarck Islands and Labahitha incerta sp. nov. from Queensland, Australia. The male of Labahitha gibsonhilli (Savory, 1943) is reported for the first time. Wandella loloata sp. nov. is described from Papua New Guinea, representing the first record of this genus outside Australia. Pritha hasselti (Simon, 1906) from Indonesia is shown to be a Filistatinae, and thus the species is provisionally transferred back to Filistata.
The western Indian Ocean genus Paracephaelis is revised. Sixteen species are endemic to Madagascar, 12 of which are new for science: P. aristata sp. nov., P. bardotiae sp. nov., P. capitulifera sp. nov., P. gautieri sp. nov., P. grandifructa sp. nov., P. longipedicellata sp. nov., P. orientalis sp. nov., P. pauciflora sp. nov., P. ranirisonii sp. nov., P. russata sp. nov., P. sambavensis sp. nov., and P. seyrigii sp. nov. Paracephaelis trichantha occurs on the east coast of continental Africa and on the islands of the Aldabra Group. One other species is newly described from the Comoros, P. comorensis sp. nov. Paracephaelis is characterized by sessile inflorescences, pubescent inflorescence and flower parts, ovules arranged at the periphery of the placenta, laterally flattened seeds with entire endosperm and a shallow elongate hilum, and pollen with supratectal elements. Of the Malagasy endemics, five species are assessed as Critically Endangered with P. sambavensis sp. nov. possibly Extinct in the Wild, three are Endangered, four are Vulnerable, one is Near Threatened, and three are Least Concern. Outside Madagascar, P. trichantha and P. comorensis sp. nov. are assessed as Vulnerable.
Four new species of limnoterrestrial rhabdocoels (‘Typhloplanidae’ Graff, 1905) are described. One of these – Faunulus nielsi Houben, Proesmans & Artois gen. et sp. nov. – could not be unambiguously placed within an existing genus. Faunulus nielsi most closely resembles species of the genus Adenocerca Reisinger, 1924 but can be clearly distinguished by the position of the testes. The three other new species described are Bryoplana belgica Houben, Proesmans & Artois sp. nov., Hoplopera isis Houben, Proesmans & Artois sp. nov., and Protoplanella leiae Houben, Proesmans & Artois sp. nov. All three belong to the subfamily ‘Protoplanellinae’ Reisinger, 1924 and are distinguished based on a detailed description of the reproductive system. Finally, new data are provided for nine other, known typhloplanids: Adenocerca minima Kolasa, 1981; Chorizogynopora italica Kolasa, 1981; Hoplopera opaca Reisinger, 1924; K. subterranea Reisinger, 1933; Krumbachia virginiana (Kepner & Carter, 1931) Ruebush, 1938; Olisthanellinella rotundula Reisinger, 1924; Prorhynchella minuta Ruebush, 1939; Protoplanella simplex Reisinger, 1924; and Ventrociliella romanae Kolasa, 1977. A detailed comparison of our material of V. romanae to what is described for Bockia deses Reisinger, 1924, leads us to consider the latter a nomen dubium.
A new species of the gecarcinucid freshwater crab genus, Spiralothelphusa Bott, 1968, is described from the Andhra Pradesh State of South India, with supporting data from mitochondrial cytochrome c oxidase subunit I. This brings the number of known species of Spiralothelphusa to seven, five from India and two from Sri Lanka. The identity of S. wuellerstorfi (Heller, 1862) has remained uncertain because the former lectotype designation was not clear. Bott (1968), while designating a male lectotype of S. wuellerstorfi from the Naturhistorisches Museum Wien, Vienna, Austria, had neither stated the catalogue number nor the size of the specimen. It is now difficult to trace the particular lectotype among several paralectotypes of the depository. A new lectotype is, therefore, designated herein for S. wuellerstorfi, and the species is redescribed. The new species, S. andhra sp. nov., has morphological affinities with S. wuellerstorfi, but can be distinguished from the latter species by the shape of the male telson and outer margin of the non-twisted portion of the male first gonopod. Phylogenetic analyses of the molecular data also corroborate their separation. An illustrated identification key is provided for the species of Spiralothelphusa.
Descriptions of the following 23 species of Macrotomoderus Pic, 1901 new to science, from continental China, are provided as an addition to the recently published review of the genus from China and Taiwan (Telnov 2018): M. angelinii, M. belousovi, M. bicrispus, M. boops, M. bordonii, M. dali, M. daxiangling, M. femoridens, M. hajeki, M. hartmanni, M. hengduan, M. imitator, M. kabaki, M. korolevi, M. lapidarius, M. muli, M. palaung, M. similis, M. tenuis, M. transitans, M. truncatulus, M. usitatus, and M. wudu spp. nov. Additional records are provided for some poorly known species. The identification key to the species of Macrotomoderus from China, the Japanese Archipelago, and Taiwan is herewith significantly supplemented and updated. Biogeographical peculiarities and altitudinal gradient of Macrotomoderus distribution in continental China are briefly discussed.
We describe a new species of Theloderma from northeastern Vietnam based on morphological differences and molecular divergence. Theloderma khoii sp. nov. is distinguishable from its congeners on the basis of a combination of the following characters: large size, SVL 52.1 mm in male, 59.4 mm in female; head length and width equal; vomerine teeth present; snout pointed and truncated, eye large, ED 4.7 mm in male, 5.6 mm in female, spinules on upper eyelid; tibiotarsal articulation reaches to the posterior border of the eye or the tip of the snout; dorsal skin very rough with large irregular gland ridges and warts, ventral surface of body granular; tips of all digits dilated but all considerably smaller than tympanum; dorsal surface mossy green or olive mottled with dark magenta. The distribution of the new species is unknown but probably extends into adjacent high elevation forested areas in Ha Giang Province, Vietnam and in Yunnan Province, China with an extent of occurrence of only < 1000 km2 and continuing decline in the quality of its habitat due to deforestation. Thus, we suggest the species should be considered Endangered following IUCN’s Red List categories.
Revisions of Holocnemus and Crossopriza: the spotted-leg clade of Smeringopinae (Araneae, Pholcidae)
(2022)
The genera Holocnemus Simon, 1873 and Crossopriza Simon, 1893 are revised. Together with Stygopholcus Kratochvíl, 1932 (revised recently) and the newly described genus Maghreba gen. nov., they constitute the spotted-leg clade within the northern clade of Smeringopinae. Males and females in this group are characterized by dark marks on the leg femora and tibiae. The native area of the spotted-leg clade ranges from northern Africa and the Mediterranean to Central Asia and NW India. A morphological cladistic analysis suggests that Holocnemus is paraphyletic while Crossopriza is monophyletic, but morphology seems only partly adequate to resolve phylogenetic relationships convincingly. The genus Holocnemus includes four species, all of which are redescribed: H. pluchei (Scopoli, 1763); H. reini (C. Koch, 1873) comb. nov. (transferred from Pholcus); H. caudatus (Dufour, 1820); and H. hispanicus Wiehle, 1933. The genus Maghreba gen. nov. includes eight species from NW Africa: M. aurouxi (Barrientos, 2019) gen. et comb. nov. (transferred from Holocnemus; redescribed, female newly described) and seven newly described species. The genus Crossopriza includes six previously described species (of which five are redescribed), and 18 newly described species. The Madagascan C. nigrescens Millot, 1946 is synonymized with C. lyoni (Blackwall, 1867). All new species are described on the basis of both sexes.
La distribución geográfica y las características morfológicas de Ectinogonia chalyboeiventris chalyboeiventris Germain y Kerremans, 1906 y E. chalyboeiventris wagenknechti Cobos, 1954 (Coleoptera: Buprestidae) fueron identificadas a partir del estudio de parte de sus ejemplares tipo. Como resultado de la comparación de estos taxones con ejemplares de Ectinogonia Spinola recolectados en las provincias de Elqui y Choapa (Región de Coquimbo), se reconocen y describen dos nuevas especies del norte de Chile: E. gemmula Pineda y Mondaca, nueva especie y E. interruptissima Pineda y Mondaca, nueva especie. Se presentan caracteres diagnósticos, fotografías de los adultos y de los órganos genitales del macho y de la hembra, junto a observaciones sobre el hábitat, historia natural, y distribución de los nuevos taxa. Adicionalmente, se presenta una lista actualizada que incluye a la totalidad de las especies del subgénero Ectinogonia descritas hasta el momento.
ZooBank registration. urn:lsid:zoobank.org:pub:7DC20EF3-1568-484B-B1C9-3D1A9F12460E
The original description of Rivudiva trichobasis Lugo-Ortiz & McCafferty, 1998 is short, with few illustrations. The lack of information resulted in a broad specific diagnosis, with emphasis on the spine-like setae on the antenna. Our hypothesis is that the lack of information resulted in many species being hidden behind R. trichobasis name. We evaluated the species R. coveloae (Traver, 1971) and R. venezuelensis (Traver, 1943) considering the new evidence. After analyzing the paratype of R. trichobasis and records of the species in Brazil, the hidden-species hypothesis was corroborated. Five new species were identified among the published records of R. trichobasis of which four are described here: R. amazona sp. nov. (Roraima State), R. oxum sp. nov. (Rondônia State), R. uiara sp. nov. (Amazonas State), R. naia sp. nov. (Roraima State). The fifth species, Rivudiva sp. X from Maranhão State, could not be described due to the poor conservation of the specimen and is therefore left in open nomenclature. Records from Espírito Santo State (Brazil) and from Paraguay are treated as putative and must be evaluated considering the new evidence. Rivudiva venezuelensis and Rivudiva coveloae are diagnosed and illustrated based on type material. After analyzing these two species, we hypothesize that only R. coveloae likely belongs to the genus Rivudiva. However, information on the nymphal stage is needed to corroborate this hypothesis.
Early Carboniferous coiled nautiloids from North Africa are virtually unknown. An assemblage of nine species, all from the family Trigonoceratidae, from the Dalle à Merocanites (Tournaisian-Viséan boundary interval) of Timimoun in western Algeria is described, being the most diverse Carboniferous nautiloid assemblage known from North Africa but much less diverse than the time-equivalent assemblages from Belgium and Ireland. The assemblage consists of the species Maccoyoceras pentagonum sp. nov., Lispoceras orbis sp. nov., Thrincoceras devolvere sp. nov., Rineceras multituberculatum sp. nov., Rineceras rectangulatum sp. nov., Vestinautilus padus sp. nov., Vestinautilus concinnus sp. nov., Planetoceras destrictum sp. nov. and Planetoceras transforme sp. nov. A morphometric analysis of Maccoyoceras pentagonum sp. nov. and Lispoceras orbis sp. nov. shows that the intraspecific variation in these species is within rather narrow limits.
Perinereis anderssoni Kinberg, 1865 originally described from Brazil has been attributed with a wide distribution on the American Atlantic coasts, ranging from Brazil to Bermuda, due to the synonymy of Nereis bairdii Webster, 1884 and Nereis (Perinereis) melanocephala McIntosh, 1885. In this paper, the synonymy of Nereis bairdii with Perinereis anderssoni is rejected based on a re-examination of the syntypes of N. bairdii which are found to contain two species requiring designation of a lectotype and paralectotypes here redescribed as Perinereis bairdii (Webster, 1884) and the remaining specimens are here described as Perinereis websteri sp. nov. The synonymy of Nereis (Perinereis) melanocephala with P. anderssoni is rejected and the synonymy with P. bairdii proposed by previous authors is accepted here. A description of P. anderssoni, a redescription of P. floridana, and a description of the males of P. cariboea with additional material are provided for comparison. A key to identifying all Atlantic Perinereis species is also included.
A new genus, Thaicypris gen. nov., in the tribe Herpetocypridini Kaufmann, 1900 of the subfamily Herpetocypridinae Kaufmann, 1900 is established to accommodate a new species from Thailand. The present contribution deals with the description of a new genus and species, Thaicypris panhai gen. et sp. nov., which is mainly characterized by the distinctive and raised, inwardly displaced selvage at the postero-ventral part of the right valve (RV) that is not parallel to the valve margin, the absence of an anterior inner list on the RV, the prominent and elevated double inner list on the posterior part of the left valve, the small and three-segmented Rome organ on the first antenna (A1), the spatulated terminal segment of the maxillular (Mx1) palp, the slender caudal ramus (CR) with long and thin Sp seta, the presence of basal triangle on the CR attachment, and the pointed projection at the terminal segment base of the prehensile palps. The hemipenis of the new genus and species is outstanding, especially the medial lateral shield which has a long, beak-shaped protrusion on the distal part. The discovery of this Thai taxon is the first record of the tribe Herpetocypridini in Thailand and the second species of the tribe in Southeast Asia.
Two new species of Ageniella Banks, 1912 (Hymenoptera: Pompilidae) from Brazil and updated keys
(2022)
Ageniella Banks, 1912 is a paraphyletic group exclusive to the Nearctic and Neotropical regions. The genus has a remarkable morphological diversity among species and strong sexual dimorphism, hampering taxonomic studies of it. Herein, we add two new species to the Neotropical fauna of Ageniella: A. caerulea sp. nov. belonging to the subgenus Ameragenia and A. ruschi sp. nov. belonging to the subgenus Priophanes; both species are described and illustrated. A brief discussion of subgeneric characters and an updated taxonomic key to the species of Ageniella known from Brazil are provided.
Three new species of Mesacanthion Filipjev, 1927 were found along Patagonian coasts (Argentina). Mesacanthion bifidum sp. nov. is characterized by short labial and cephalic setae, onchia of equal size, spicule arcuate, and gubernaculum with caudal apophysis, ending in two teeth. The species is related to M. virile (Ditlevsen, 1930) De Coninck & Schuurmans Stekhoven, 1933. However, the spicules and gubernaculum of both species are different in shape. Mesacanthion longigubernaculum sp. nov. is characterized by its long and slender body, striated cuticle, relatively long cephalic and cervical setae, onchia of different sizes, amphidial fovea lentil-shaped, spicule arcuate, gubernaculum surrounding the spicule, and tail conical-cylindrical with terminal setae. Mesacanthion sanantoniensis sp. nov. is characterized by its long and stout body, striated cuticle, long cephalic setae, onchia of different sizes, amphidial fovea pouch-shaped, spicule arcuate, gubernaculum with dorsal apophysis, and tail conical without terminal setae. Following the key of Jeong et al. (2019), the last two species are related to M. pali Wieser, 1959 and M. longissimesetosum Wieser, 1953, so we provide a key to differentiate the four species.
Pseudocetherinae (Hemiptera: Reduviidae) revisited: phylogeny and taxonomy of the lobe-headed bugs
(2022)
The concept of the previously monogeneric subfamily Pseudocetherinae (Hemiptera: Heteroptera: Reduviidae) is revised and expanded. We here transfer Gerbelius Distant, 1903, Kayanocoris Miller, 1954, Microvarus Jeannel, 1917, Paragerbelius Miller, 1958, and Voconia Stål, 1866 from Reduviinae to Pseudocetherinae and treat Kayanocoris, Microvarus, Paragerbelius, and Pseudocethera Villiers, 1963 as junior synonyms of Voconia, resulting in new combinations for Voconia conradti (Jeannel, 1917) comb. nov., V. ifana (Villiers, 1963) comb. nov., V. monodi (Villiers, 1963) comb. nov., V. motoensis (Schouteden, 1929) comb. nov., V. ornata (Distant, 1903) comb. nov., V. schoutedeni (Villiers, 1964) comb. nov., V. typica (Miller, 1958) comb. nov., and V. wegneri (Miller, 1954) comb. nov. We also describe 23 new species of Voconia: V. bakeri sp. nov., V. bracata sp. nov., V. brachycephala sp. nov., V. chrysoptera sp. nov., V. coronata sp. nov., V. decorata sp. nov., V. dolichocephala sp. nov., V. fasciata sp. nov., V. grandioculata sp. nov., V. hemera sp. nov., V. isosceles sp. nov., V. laosensis sp. nov., V. lasiosoma sp. nov., V. lirophleps sp. nov., V. loki sp. nov., V. mexicana sp. nov., V. minima sp. nov., V. nyx sp. nov., V. smithae sp. nov., V. tridens sp. nov., V. trinidadensis sp. nov., V. tuberculata sp. nov., and V. vittata sp. nov. Lectotypes are designated for Gerbelius confluens Distant, 1903, G. typicus Distant, 1903, V. conradti comb. nov., V. ornata comb. nov., and V. pallidipes Stål, 1866. A revised diagnosis and description of Pseudocetherinae are provided along with photographs of the species and of the male genitalia of 13 pseudocetherine and five closely related reduviine species. An identification key to the two genera of Pseudocetherinae as well as a key to species of Voconia are presented. A phylogenetic hypothesis is proposed for the relationships of Pseudocetherinae using parsimony analyses of 77 morphological characters.
We provide keys, descriptions and illustrations for 16 species of Scoliidae Latreille, 1802 found in Hong Kong, of which nine are new records for the territory, one is new to China and one is new to science: Scolia pakshaoensis sp. nov. The status of one species (Megacampsomeris sp. 1) remains uncertain; it may represent an additional new species.
An illustrated checklist of the Mollusca of Galicia Bank, a large and deep seamount off the NW Iberian Peninsula, is provided. The studied material was collected in 8 samples of Seamount 1 cruise (1987), 7 samples of ECOMARG 0709 (2009) and 36 samples of BANGAL 0711 (2011), between 615 and 1768 m. A total of 212 species are known to occur at the Galicia Bank (1 Monoplacophora, 7 Solenogastres, 3 Polyplacophora, 132 Gastropoda, 54 Bivalvia, 6 Scaphopoda, and 9 Cephalopoda), 21 of which from previous studies only. Four species are described as new, 34 species are first record in Spanish waters and another 20 species first record for the Northern Spanish waters. Over 7500 specimens, representing 104 species, were collected alive, and 87 species were represented by empty shells only. Only 53 species were detected in both Seamount 1 and BANGAL 0711; most of the species are rare and more species can be expected if exploration is continued. There is a marked difference in species composition between the summit platform (615‒1000 m) and the deeper part below 1500 m, with some genera (e.g., Colus and Limopsis) represented by alternative species. Endemism, if any, is very low and most of the species are widespread.
The diversity of Palpigradi is not evenly distributed among its different branches. The widespread genus Eukoenenia includes 80% of the species, while the other genera are poorly known. Allokoenenia certainly is the most understudied genus because it is represented only by the African species Allokoenenia afra Silvestri, 1913. Its description is short and does not include many features depicted in modern taxonomy of Palpigradi. In this paper, we describe two troglobitic species of Allokoenenia, report the occurrence of a third species represented by an immature specimen from Brazilian caves, and provide brief notes on the morphology of A. afra. Allokoenenia canhembora sp. nov., A. stygia sp. nov., and Allokoenenia sp. differ from A. afra by several morphological features, including more elongated appendages and a greater number of blades on lateral organs. Thus, they are considered troglomorphic. These new species are vulnerable to extinction because they are endemic to a single or few caves directly impacted by mining activities and groundwater exploitation. This study represents the first step for the conservation of these species and their habitats, since Brazilian caves with rare troglobites cannot be irreversibly impacted. Also, it brings important contributions on the distribution and morphology of this enigmatic genus.
Oxyethira Eaton, 1873 is one of the most diverse genera of Hydroptilidae, comprising over 240 species distributed in all biogeographical regions. Here three new species of Oxyethira (Trichoglene) Neboiss, 1977 are described and illustrated from male specimens collected in New Caledonia: O. (Trichoglene) hamus sp. nov., recognized by the hook-shaped apex of the long inferior appendages in lateral view and by the posterior margin of segment IX with a trilobed appearance in ventral view; O. (Trichoglene) rectangulata sp. nov., recognized by the rectangular shape of the inferior appendages, which are totally fused and with two pairs of small setae on the inner face; and O. (Trichoglene) spiralis sp. nov., recognized by the strongly curvilinear shape of the subgenital process in dorsal and lateral views and by the long process spiralling around the ejaculatory duct at the phallus apex.
New synonymies and notes in Criodion Audinet-Serville (Coleoptera: Cerambycidae: Cerambycinae)
(2021)
Criodion angustatum Buquet, 1852 a nd C. pilosum Lucas, 1857 (Coleoptera: Cerambycidae: Cerambycinae) are synonymized with C. tomentosum Audinet-Serville, 1834. The holotypes of C. angustatum and C. hirsutum, and syntypes of C. pilosum and of C. tuberculatum Gahan, 1892 are illustrated for the first time. One of the type localities of C. tuberculatum is corrected.
This paper is the conclusion of the “Spaghetti Project” aiming to revise French species of Terebellidae sensu lato (s.l.) belonging to the five families: Polycirridae, Telothelepodidae, Terebellidae sensu stricto (s.s.), Thelepodidae and Trichobranchidae. During this project, 41 species were observed, 31 of them new for science: eight species of Polycirridae, eleven species of Terebellidae s.s., three species of Thelepodidae and nine species of Trichobranchidae. We provide a comprehensive key for all European species of terebellids with a focus on the important diagnostic characters for each family. Finally, we discuss issues on taxonomy, biodiversity and cryptic and pseudo-cryptic species of polychaetes in European waters, based on results obtained during this project.
We describe and illustrate a new Neotropical predaceous midge, Parabezzia carlae Huerta, Spinelli and Grogan, new species (Diptera: Ceratopogonidae) from males collected by Malaise trap in La Union, Ayutla de los Libres, state of Guerrero, Mexico. We also report a second record of P. alexanderi Wirth from Veracruz, Mexico. A key to the known species in Mexico is included.
In this study, the thallus-forming Laboulbeniomycetes (Herpomycetales and Laboulbeniales) from Denmark are presented as an illustrated monograph. Sixteen species and one genus are newly described based on morphology and ecology (host association). The new genus is named Tanmaurkiella Santam. gen. nov. and includes two species: T. pselaphi Santam. gen. et sp. nov. (type species) and T. huggertii Santam. gen. et sp. nov., both on Pselaphus heisei Herbst, 1792 (Col. Staphylinidae Pselaphinae). The other 14 new species are Amorphomyces ventricosus Santam. sp. nov. on Myrmecocephalus concinnus (Erichson, 1839) (Col. Staphylinidae Aleocharinae), Cantharomyces papillatus Santam. sp. nov. on Bledius terebrans (Schiødte, 1866) (Col. Staphylinidae Oxytelinae), Cryptandromyces cryptophagi Santam. sp. nov. on Cryptophagus distinguendus Sturm, 1845 (Col. Cryptophagidae), Cryptandromyces danicus Santam. sp. nov. on Euconnus wetterhallii (Gyllenhal, 1813) (Col. Staphylinidae Scydmaeninae), Dimeromyces oculatus Santam. sp. nov. on Longitarsus luridus (Scopoli, 1763) (Col. Chrysomelidae), Euphoriomyces enghoffii Santam. sp. nov. on Leiodes rugosa Stephens, 1829 (Col. Leiodidae), Euphoriomyces smicri Santam. sp. nov. on Smicrus filicornis (Fairmaire & Laboulbène, 1855) (Col. Ptiliidae), Laboulbenia inexpectata Santam. sp. nov. on Acupalpus exiguus Dejean, 1829 (Col. Carabidae), Laboulbenia pygidicola Santam. sp. nov. on Syntomus truncatellus (Linnaeus, 1761) (Col. Carabidae), Monoicomyces brachiatus Santam. sp. nov. on Atheta sodalis (Erichson, 1837) and Ocyusa picina (Aubé, 1850) (Col. Staphylinidae Aleocharinae), Monoicomyces crassicaulis Santam. sp. nov. on Oxypoda elongatula Aubé, 1850 (Col. Staphylinidae Aleocharinae), Monoicomyces reboleirae Santam. sp. nov. on Gnypeta carbonaria (Mannerheim, 1830) (Col. Staphylinidae Aleocharinae), Monoicomyces validus Santam. sp. nov. on Atheta vestita (Gravenhorst, 1806), Aleochara grisea Kraatz, 1856, and Geostiba circellaris (Gravenhorst, 1806) (Col. Staphylinidae Aleocharinae), and Stigmatomyces thoracochaetae Santam. sp. nov. on Thoracochaeta brachystoma (Stenhammer, 1855) (Diptera Sphaeroceridae). The total number of laboulbeniaceous species from Denmark rises from 29 to 195, which means that 166 are here reported as new country records. Among these, Kainomyces isomali Thaxt. deserves special mention as it is a new European record. The same applies to nine species which are reported here for the first time after their original description. For this study, an intensive sampling programme has been realized, with 429 Danish localities screened including around 1900 collections with fungi. Two new synonymies are established: Laboulbenia acupalpi Speg. (Spegazzini 1915a) syn. nov. for Laboulbenia stenolophi Speg. (Spegazzini 1914), and Monoicomyces oxytelis Huldén (Huldén 1983) syn. nov. for Monoicomyces invisibilis Thaxt. (Thaxter 1900). The new combination Peyritschiella oxyteli (Cépède & F.Picard) Santam. comb. nov. is proposed for Rheophila oxyteli Cépède & F.Picard including neotypification, and delimitation of Peyritschiella protea Thaxt. is incorporated. Lectotypes for Laboulbenia polyphaga Thaxt. and Symplectromyces vulgaris (Thaxt.) Thaxt. are designated. Nineteen species are illustrated here with photographs for the first time. Three species: Eumonoicomyces papuanus Thaxt., Peyritschiella protea, and Stigmatomyces euconni F.Picard, which were reported from Denmark in the literature should be removed from the Danish Funga. We have examined the following types of Thaxter from FH (Farlow Herbarium, Harvard University Herbaria): Asaphomyces cholevae Thaxt., Dimorphomyces myrmedoniae Thaxt., Eumonoicomyces papuanus, Laboulbenia polyphaga, Peyritschiella protea, Rhadinomyces pallidus Thaxt., and Symplectromyces vulgaris. Ceratomyces pyrenaeus Santam. is newly recorded from USA, and this is also a new record from the American continent. Description of the genus Cryptandromyces Thaxt. has been emended to incorporate the new species here described. Morphology of the antheridium in Eumonoicomyces papuanus is studied, and the status of the genus Eumonoicomyces Thaxt. vis-à-vis Monoicomyces Thaxt. is discussed. Identification keys are provided for genera and species. In support of the additional aim of this work to serve as a reference for the study of Laboulbeniomycetes fungi in Europe, we include maps and the Appendix 1 for comparison of the known species in the ten most diverse, better studied, European countries.
A new species of the genus Bomansius Lacroix (Coleoptera: Lucanidae), which had been illustrated in the literature but never formally named, is described from Aneityum Island, Vanuatu (former New Hebrides) under the name of Bomansius cheesmanae Kakinuma, new species. The generic redescription of Bomansius and the redescription of B. gabrieli Lacroix, 1978 are also given based on additional specimens. Bomansius is transferred to tribe Aegini Huang and Chen, 2013.
Genomic sequencing and analysis of worldwide skipper butterfly (Lepidoptera: Hesperiidae) fauna points to imperfections in their current classification. Some tribes, subtribes and genera as they are circumscribed today are not monophyletic. Rationalizing genomic results from the perspective of phenotypic characters suggests two new tribes, two new subtribes and 50 new genera that are named here: Ceratrichiini Grishin, trib. n., Gretnini Grishin, trib. n., Falgina Grishin, subtr. n., Apaustina Grishin, subtr. n., Flattoides Grishin, gen. n., Aurivittia Grishin, gen. n., Viuria Grishin, gen. n., Clytius Grishin, gen. n., Incisus Grishin, gen. n., Perus Grishin, gen. n., Livida Grishin, gen. n., Festivia Grishin, gen. n., Hoodus Grishin, gen. n., Anaxas Grishin, gen. n., Chiothion Grishin, gen. n., Crenda Grishin, gen. n., Santa Grishin, gen. n., Canesia Grishin, gen. n., Bralus Grishin, gen. n., Ladda Grishin, gen. n., Willema Grishin, gen. n., Argemma Grishin, gen. n., Nervia Grishin, gen. n., Dotta Grishin, gen. n., Lissia Grishin, gen. n., Xanthonymus Grishin, gen. n., Cerba Grishin, gen. n., Avestia Grishin, gen. n., Zetka Grishin, gen. n., Turmosa Grishin, gen. n., Mielkeus Grishin, gen. n., Coolus Grishin, gen. n., Daron Grishin, gen. n., Barrolla Grishin, gen. n., Brownus Grishin, gen. n., Tava Grishin, gen. n., Rigga Grishin, gen. n., Haza Grishin, gen. n., Dubia Grishin, gen. n., Pares Grishin, gen. n., Chitta Grishin, gen. n., Artonia Grishin, gen. n., Lurida Grishin, gen. n., Corra Grishin, gen. n., Fidius Grishin, gen. n., Veadda Grishin, gen. n., Tricrista Grishin, gen. n., Viridina Grishin, gen. n., Alychna Grishin, gen. n., Ralis Grishin, gen. n., Testia Grishin, gen. n., Buzella Grishin, gen. n., Vernia Grishin, gen. n., and Lon Grishin, gen. n. In addition, the following taxonomic changes are suggested. Prada Evans is transferred from Hesperiinae to Trapezitinae. Echelatus Godman and Salvin, Systaspes Weeks, and Oenides Mabille are removed from synonymy and are treated as valid genera. The following genera are new junior subjective synonyms: Tosta Evans of Eantis Boisduval; Turmada Evans of Neoxeniades Hayward, Arita Evans of Tigasis Godman, and Alera Mabille of Perichares Scudder. Eantis pallida (R. Felder) (not Achlyodes Hübner), Gindanes kelso (Evans) (not Onenses Godman and Salvin), Isoteinon abjecta (Snellen) (not Astictopterus C. and R. Felder), Neoxeniades ethoda (Hewitson) (not Xeniades Godman), Moeris anna (Mabille) (not Vidius Evans), and Molo pelta Evans (not Lychnuchus Hübner) are new genus-species combinations. The following are species-level taxa: Livida assecla (Mabille) (not a subspecies of Livida grandis (Mabille), formerly Pythonides Hübner) and Alychna zenus (E. Bell) (not a junior subjective synonym of Alychna exclamationis (Mabille), formerly Psoralis Mabille); and Barrolla molla E. Bell (formerly Vacerra Godman) is a junior subjective synonym of Barrolla barroni Evans (formerly Paratrytone Godman). All these changes to taxonomic status of names are propagated to all names currently treated as subspecies (for species), subgenera (for genera) and synonyms of these taxa. Finally, taxa not mentioned in this work are considered to remain at the ranks and in taxonomic groups they have been previously assigned to.
Systematic, faunistic and ecological aspects of the six families and 34 species and subspecies in the order Ephemeroptera currently recorded from Cuba are reviewed based primarily on a reference collection located at the Universidad de Oriente (Santiago de Cuba), collections at the Institute of Ecology and Systematics (Havana) and historic literature. A key to nymphs is included with photographs of significant features of many species. An annotated list of species is presented with comments on type localities, species ecology and distribution. The morpho- ecological types of the nymphs are updated according to current taxonomic changes, and indicator species of organic contamination are analyzed according to the BMWP-Cub index. Based on present data, mayflies are best collected between January and June although many species are present throughout the year, and almost half of the species are widely distributed. Possible routes of penetration from the continents toward Cuba are from South America through the arc of islands formed by the Lesser Antilles, from Central and South America through the peninsula of Yucatan, and via an ancient landspan or island chain from northern South America (GAARlandia). With one exception, there is no evidence for dispersal of species from North America (through Florida) to Cuba (and then to the Antilles) or vice versa. The pattern of geographical distribution of Ephemeroptera inside Cuba is very similar to that of the orders Trichoptera and Odonata. The greatest number of species is found in the Eastern region and the fewest in the Central and Central-East regions. The high endemism (76.5%) is probably due to geographical isolation and processes that bring about this phenomenon together with the low vagility that characterizes the order.
Seven new species of Cacostola Fairmaire and Germain, 1859 (Coleoptera: Cerambycidae: Lamiinae: Onciderini) are described: C. plotkini Wappes and Santos-Silva from Costa Rica; C. galenae Wappes and Santos- Silva from Panama; C. opitzi Wappes and Santos-Silva from Bolivia; C. howdenae Wappes and Santos-Silva from Guatemala; C. thomasorum Wappes and Santos-Silva from Brazil; C. nearnsi Wappes and Santos-Silva from Bolivia and Panama; and C. rothschildi Wappes and Santos-Silva from Argentina and Brazil. Notes on C. simplex (Pascoe, 1859), and C. mexicana (Breuning, 1943) are also included.
The following new species of Eupogonius LeConte, 1852 (Coleoptera: Cerambycidae: Lamiinae) are described: E. tlanchinolensis Wappes and Santos-Silva (Mexico, Hidalgo); E. albofasciatus Wappes and Santos- Silva (Mexico, Puebla); E. sonorensis Wappes and Santos-Silva (Mexico, Sonora); E. guerrerensis Wappes and Santos-Silva (Mexico, Guerrero); E. boteroi Wappes and Santos-Silva (Mexico, Guerrero); E. nascimentoi Wappes and Santo-Silva (Mexico, Jalisco and Colima); and E. monzoni Wappes and Santos-Silva (Guatemala, Alta Verapaz). Additionally, a detailed description of the female of Eupogonius fulvovestitus Schaeffer, 1905 is provided for the first time, along with notes on the likely host of the species. New state records in Mexico are provided for Eupogonius comus Bates, 1885, and E. stellatus Chemsak and Noguera, 1995. Other taxonomic or nomenclatural actions included herein are: Eupogonius knabi Fisher, 1925 is transferred to Atelodesmis Chevrolat, 1841, new combination; the gender of the species-group name in Eupogonius azteca Martins, Santos-Silva and Galileo, 2015 is commented on; notes on the geographical distribution of Eupogonius affinis Breuning, 1942, and the problematic morphology of E. infimus (Thomson, 1868) are presented; Eupogonius subaeneus Bates, 1872, and E. marmoratus Fisher, 1925 are revalidated, and E. columbianus Breuning, 1942 is a new synonym of E. subaeneus”.
In the course of working on new species of North American Phyllophaga Harris, 1827 (Coleoptera: Scarabaeidae: Melolonthinae) some synonyms have been found and are proposed here. New synonymies: Phyllophaga knausii (Schaeffer, 1907) is synonymized with Phyllophaga sociata (Horn, 1878); Phyllophaga chippewa Saylor, 1939 is synonymized with Phyllophaga rugosa (Melsheimer, 1845); and Phyllophaga falta Sanderson, 1950 is synonymized with Phyllophaga bipartita (Horn, 1887). Lectotypes are here designated for the following species: Listrochelus knausii Schaeffer, Listrochelus sociatus Horn, and Lachnosterna bipartita Horn. A neotype for Ancylonycha rugosa Melsheimer is here designated from the Horn Collection.
Revision of the species confused with "Nereis falsa" de Quatrefages, 1866 (Annelida, Nereididae)
(2021)
Nereis falsa de Quatrefages, 1866 has been regarded as a cosmopolitan species, and several species described from different localities have been regarded as junior synonyms of N. falsa. The present study is an attempt to resolve the taxonomic confusion in N. falsa, which seems to contain several distinct species due to previous inappropriate synonymy, widely distributed in the Atlantic and eastern Pacific Oceans. For this purpose, the authors first propose the resurrection of the synonymy of N. falsa with Hediste diversicolor that was concluded during the 19th century but disregarded later. After the fixation of the identity of N. falsa sensu stricto, the authors re-evaluate the proper taxonomic status of species which have previously been confused with N. falsa. Type, topotype and non-type specimens were examined; most species are redescribed, and others are reinstated. Nereis splendida Grube, 1840 is a valid Mediterranean species, and a neotype is proposed; it includes the Mediterranean populations of what is currently regarded as N. falsa. Consequently, N. falsa is transferred to Hediste Malmgren, 1867, and some taxonomic comments are added for the latter genus and a key to species is also included. Nereis callaona Grube & Kröyer in Grube, 1857, N. marginata Grube & Örsted in Grube, 1857 and N. riisei Grube & Örsted in Grube, 1857 are restricted to tropical American shores and are all redescribed. Nereis pelagica lunulata Ehlers, 1901, formerly regarded as a junior synonym of N. falsa by Fauvel (1941), is redescribed and elevated in rank to species level. Nereis lucipeta Ehlers, 1908, formerly regarded as a junior synonym of N. splendida by Ehlers (1913) and of N. falsa by Fauvel (1919), is reinstated. Nereis occidentalis Hartman, 1945 is also redescribed. Furthermore, N. ambigua Treadwell, 1937, formerly regarded as a junior synonym of N. riisei by Monro (1933), deserves to be reinstated. Western Africa specimens recorded as N. falsa are newly described as N. mezianei sp. nov.
Three species of Corethrella Coquillett, 1902 from the state of Amazonas, Brazil are described as new to science based on female adult specimens. Corethrella cabocla Feijó, Belchior, Marialva & Pessoa sp. nov. possesses four large setae on the frons between the ventromedial area of ommatidia, a wide clypeus with 1–4 setae, a wing with the apex of R2 basal to the apex of M2 and with a midlength band, and with the abdomen entirely dark brown. Corethrella ielemdei Feijó, Ramires, Lima & Pessoa sp. nov. possesses an elongated coronal suture, four large setae on the frons between the ventromedial area of ommatidia, a clypeus squarish with 42–43 setae, a wing with the apex of R2 basal to the apex of M1 and with a midlength band and dark scales on the basal and subbasal areas of the anterior margin, legs with dark scales, and with the abdomen entirely dark brown. Corethrella menini Feijó, Picelli, Ríos-Velásquez & Pessoa sp. nov. possesses wings with the apex of R2 basal to the apex of M2 and a midlength band, with darker basal scales along all veins, basal band dark scales on C, Sc, R, M, and Cu and the abdomen entirely dark brown. With the addition of the new species, the numbers of frog-biting midges described in the Amazon basin, Brazil and in Neotropical region are now 31, 49 and 80 species, respectively.
Two new genera of Acanthocinini (Coleoptera: Cerambycidae), Luctithonus Lingafelter and Duocristala Lingafelter, are described from Hispaniola. Two new species of Luctithonus are described: Luctithonus aski Lingafelter and L. duartensis Lingafelter. A third species, L. pantherinus (Zayas), is newly recorded from Hispaniola and the Dominican Republic (new country record), and transferred from Sternidius Haldeman as a new combination. Additional new species of Lamiinae are described from Hispaniola: Eugamandus albipumilus Lingafelter; Leptostylopsis opuntiae Lingafelter; and Lethes turnbowi Lingafelter. Keys to tribes of Lamiinae, genera of Acanthocinini, and species of Luctithonus in Hispaniola are included.
Crioprosopus baldwini Eya (Coleoptera: Cerambycidae: Cerambycinae: Trachyderini), sp. nov., from Costa Rica and Panama, is described. An amendment to the key to species of Crioprosopus Audinet-Serville, 1834, as presented in Eya (2015), is provided along with illustrations of the key characteristics to differentiate C. baldwini from other species.
The tribal allocation of Xalitla Lane, 1959 (Cerambycidae: Cerambycinae) is discussed. Xalitla limoni Santos-Silva and Skillman, new species,is described from Mexico (Jalisco). Xalitla lezamai Galileo and Martins,2008 is determined to be synonymous with X. genuina Martins,1970 and formally placed in synonymy. A key to the species of Xalitla, which includes the new species and synonymy, is provided.
The number of specimens in the type series of Hemilophus leuconotus Laporte, 1840 (= Cirrhicera leuconota) is corrected. Cirrhicera leucronota Thomson, 1857 (Coleoptera: Cerambycidae: Lamiinae: Hemilophini), currently considered lapsus calami or an error to C. leuconotus, and the number of specimens in the type series is also corrected. Cirrhicera leuconota is recorded from Guatemala for the first time. The sex of the holotype of Lamacoscylus albatus Martins, Santos-Silva and Galileo, 2015, is corrected, and a new state record in Mexico is provided. The description of the antennae in females of Lamacoscylus Martins and Galileo,1991 is discussed; Malacoscylus humilis Bates,1881 (currently Lamacoscylus humilis) sensu Gahan (1892) is discussed and the two varieties described by him, M. humilis var. fulvescens and M. humilis var. grisescens (only part of the speci-mens), as well as M. usingeri Linsley,1935 are transferred to Schmidarius Santos-Silva, Heffern, Botero and Nascimento, new genus. Additionally, a new species from Mexico (Mexico) is described in Schmidarius as S. kondratieffi Santos-Silva, Heffern, Botero and Nascimento. The correct type-species of Phoebe Audinet-Serville,1835 is determined as Saperda bicornis Olivier,1800 and Phoebe phoebe Lepeletier and Audinet-Serville,1825 and Phoebe tinga Martins and Galileo,1998 are transferred to Phoebella Lane,1966, which is redescribed. Leucophoebe Lane,1976 is synonymized with Phoebe. A key to species of Hemilophini with 12-segmented antennae is provided. The differences between Callanga Lane,1973 and Lapazina Lane,1973 are discussed, and a new species of Callanga from Peru is described as C. ashaninka Santos-Silva, Heffern, Botero and Nascimento. A new species of Fredlanea Martins and Galileo,1996 from Colombia is described as F. lazulina Santos-Silva, Heffern, Botero and Nascimento; a new department record in Colombia is provided for Fredlanea consobrina (Lane,1970) and a chromatic variation in this species is discussed.