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Two new species of ants (Hymenoptera: Formicidae) collected from New Caledonia are described and figured based on worker specimens: Leptogenys loarelae Ramage sp. nov. (Ponerinae, Ponerini) and Lioponera neocaledonica Jouault, Ramage & Perrichot sp. nov. (Dorylinae, Cerapachyini). All specimens were collected from the South Province of Grande Terre. These two new species are primarily distinguished from the other New Caledonian relatives by the size and shape of petiole for L. loarelae Ramage sp. nov. and by the presence of dorsolateral margins on the mesosoma for L. neocaledonica Jouault, Ramage & Perrichot sp. nov. Keys to New Caledonian Leptogenys and Lioponera are provided.
Thirty four species of Zethus are enumerated from Venezuela, providing known and new locality records. Six new species are described: Z. rubioi and Z. vincenti in the subgenus Zethusculus, Z. carpenteri and Z. milleri in the subgenus Zethoides, and Z. bolivarensis and Z. yepezi in the nominate subgenus. A key to the species of Venezuela is provided. The distribution patterns of Zethus are discussed.
The first Cenozoic roproniid wasp from the Paleocene of Menat, France (Hymenoptera: Proctotrupoidea)
(2016)
Paleoropronia salamonei gen. et sp. nov., the first Cenozoic Roproniidae, is described from the Paleocene of Menat (Massif Central, France) on the basis of its fore wing venation. The Roproniidae range between the Mesozoic and the present time. P. salamonei gen. et sp. nov. was perhaps a parasitoid on tenthredinid sawfly larvae, as these insects were present in the wasp fauna from Menat outcrop.
The first key is completed for the Palaearctic Pristiphora Latereille, 1810 species. Pristiphora araratensis sp. n. is descdbed. Pristiphora kamtchatica Malaise, 1931, Pristiphora mesatlantica Lacourt, 1976 and Pristiphora amelanchieris (Takeuchi, 1922) are new synonyms of Pristiphora insularis Rohwer, 1910.
We revised the species of the genus Pristomerus Curtis, 1836 in the Afrotropical Region. Fortynine species are recognized, of which 31 are newly described. The following new species are described: P. afrikaner, P. aka, P. babinga, P. bemba, P. dikidiki, P. herero, P. hutu, P. kagga, P. khoikhoi, P. kuku, P. masai, P. mbaka, P. mbama, P. mboum, P. nzakara, P. protea, P. restio, P. san, P. sara, P. sotho, P. swahili, P. teke, P. tutsi, P. venda, P. wolof, P. xhosa, P. yakoma, P. yangere, P. yoccolo, P. zande and P. zulu spp. nov. New synonyms: P. africator, P. cunctator and P. luteolus are new junior synonyms of P. pallidus. New records: new host records are reported for the widespread P. pallidus; new country-level distribution records are added for P. bullis, P. keyka, P. kelikely and P. pallidus; and reports of Trathala concolor and P. veloma in South Africa are shown to have been erroneous. An illustrated dichotomous key to females is provided; an online Lucid interactive matrix key is also available at www.waspweb.org. Finally, the ecological and geographical correlates of colour patterns exhibited by Pristomerus in the Afrotropical region are discussed.
A world revision of the four entedonine (Hymenoptera: Eulophidae: Entedoninae) genera of larval parasitoids of thrips (Thysanoptera) is presented: Ceranisus Walker, 1841, Entedonomphale Girault, 1915 stat. rev. (reinstated as a valid taxon from previous synonymy under Ceranisus, with type species E. margiscutum Girault, 1915 stat. rev.), Goetheana Girault, 1920, and Thripobius Ferrière, 1938. The following new generic synonymies are proposed: Cryptomphale Girault, 1917, Entedonastichus Girault, 1920, Pirenoidea Girault, 1922, and Thripoctenoides Erdös, 1954 under Entedonomphale. The proposed new combinations are as follows: Entedonomphale bicolorata (Ishii, 1933), E. nubilipennis (Williams, 1916), and Thripobius javae (Girault, 1917) from Ceranisus; Entedonomphale carbonaria (Erdös, 1954), E. dei (Girault, 1922), E. kaulbarsi (Yoshimoto, 1981), and E. mira (Girault, 1920) from Entedonastichus. New synonymies are proposed for the following species: Ceranisus vinctus (Gahan, 1932) under Ceranisus menes (Walker, 1839), Diglyphus aculeo Walker, 1848 under Ceranisus pacuvius (Walker, 1838); Ceranisus maculatus (Waterston, 1930) and Thripobius semiluteus Boucek, 1976 under Thripobius javae (Girault, 1917); Entedonastichus albicoxis (Szelényi, 1982) under Entedonomphale carbonaria (Erdös, 1954), and Entedonastichus gaussi (Ferrière, 1958) under Entedonomphale bicolorata (Ishii, 1933). Eleven new species are described: Ceranisus barsoomensis and C. votetoda (Australia), C. udnamtak (Nepal); Entedonomphale boccaccioi (USA), E. esenini (Madagascar), E. lermontovi (South Africa), E. quasimodo and E. zakavyka (Australia); Goetheana pushkini (Japan and Republic of Korea) and G. rabelaisi (Australia); and Thripobius melikai (China). Three species are excluded from Ceranisus: C. ancylae (Girault, 1917) (mistakenly listed in Ceranisus) as well as C. nigricornis Motschulsky, 1863 and C. semitestaceus Motschulsky, 1863, both taxa incertae sedis. New data are provided on the distribution and host associations of many of the species included in this review.
Yemen is provided for the first time. The following genera are recorded in the southern Arabian Peninsula for the first time: tribe Doryctini – Hemispathius Belokobylskij & Quicke, 2000 and Doryctes Haliday, 1836; tribe Spathiini – Parana Nixon, 1941 and Spathius Nees, 1819; tribe Hecabolini – Hemidoryctes Belokobylskij, 1992 and Parallorhogas Marsh, 1993; tribe Heterospilini – Heterospilus Haliday 1936; tribe Rhaconotini – Platyspathius Viereck, 1911 and Rhaconotinus Hedqvist, 1965. Sixteen species and one subspecies are described as new for science: Dendrosotinus (Gildoria) maculipennis Belokobylskij sp. nov., D. (G.) subelongatus Belokobylskij sp. nov., Doryctes (Neodoryctes) arrujumi Belokobylskij sp. nov., Parana arabica Belokobylskij sp. nov., Spathius alkadanus Belokobylskij sp. nov., S. austroarabicus Belokobylskij sp. nov., S. lahji Belokobylskij sp. nov., S. subafricanus Belokobylskij sp. nov., Hecabalodes maculatus Belokobylskij sp. nov., Platyspathius (Platyspathius) longicaudis Belokobylskij sp. nov., P. (P.) brevis Belokobylskij sp. nov., Rhaconotinus albosetosus Belokobylskij sp. nov., Rhaconotus brevicellularis Belokobylskij sp. nov., Rh. magniareolus Belokobylskij sp. nov., Rh. microexcavatus Belokobylskij sp. nov., Rh. vanharteni Belokobylskij sp. nov. and Hemidoryctes carbonarius postfurcalis Belokobylskij subsp. nov. Two new generic combinations are proposed: Hemispathius pilosus (Granger, 1949) comb. nov. (transferred from Doryctes) and Parallorhogas testaceus (Szépligeti, 1914) comb. nov. (transferred from Opius). Rhaconotus decaryi Granger, 1949 is here synonymised with Rh. menippus Nixon, 1939 (syn. nov.). A lectotype for Doryctes pilosus Granger, 1949 is designated. The following species are recorded for the UAE and/or Yemen for the first time: Dendrosotinus ferrugineus (Marshall, 1888), Hemispathius pilosus (Granger, 1949), Mimodoryctes proprius Belokobylskij, 2001, M. arabicus Edmardash, Gadallah & Soliman, 2020, Spathius nixoni Belokobylskij & Maetô, 2009, Hecabalodes anthaxiae Wilkinson, 1929, H. radialis Tobias, 1962, H. xylophagi Fischer, 1962, Parallorhogas testaceus (Szépligeti, 1914), Heterospilus (Eoheterospilus) rubrocinctus (Ashmead, 1905), Rhaconotinus menippus (Nixon, 1939), Rhaconotus arabicus Belokobylskij, 2001, Rh. manolus Nixon, 1941, Rh. scirpophagae Wilkinson, 1927 and Rh. sudanensis Wilkinson, 1927.
Die Grabwespen (Sphecidae sensu Bohart & Menke 1976; Sphecidae sensu lato in neueren, phylogenetischen Arbeiten), zu denen nach Day (1984) und späteren Autoren auch die Heterogynaidae zählen, umfassen derzeit 266 Gattungen mit 9559 beschriebene Arten (Pulawski 2006). Zusammen mit den Bienen (= Apiformes nach Michener 2000, bzw. Anthophila nach Engel 2005) bilden die Grabwespen ein gut begründetes Monophylum, das nach Michener (1986) den Namen Apoidea trägt und eine der drei Hauptlinien innerhalb der aculeaten Hymenoptera ist. Die Monophylie der aculeaten Hymenoptera, der Apoidea sowie die der Bienen ist jeweils gut begründet (z.B. Brothers 1975, Königsmann 1978, Lomholdt 1982, Alexander 1992, Brothers & Carpenter 1993). Anders verhält es sich mit den Grabwespen. Neben der phylogenetischen Untersuchung von Brothers & (1993), die die Monophylie der Grabwespen unterstützt, haben andere morphologische als auch molekularsystematische Analysen starken Zweifel an dieser Hypothese aufkommen lassen (z.B. Königsmann 1978, Lomholdt 1982, Alexander 1992, Prentice 1998, Melo 1999, Ohl & Bleidorn 2006).
Pholetesor acrocercophagus sp. nov., P. camerariae sp. nov. and P. indicus sp. nov.(Hymenoptera: Braconidae: Microgastrinae) are described as new to science. These three species were reared from Acrocercops sp., Acrocercops phaeospora Meyrick, 1916 and Cameraria virgulata Meyrick, 1914 (Lepidoptera: Gracillariidae), respectively. Characteristics of these new species and their affinities with related taxa are discussed. Data on habitat, host records and host plant species for all the parasitoid species is provided. A key to the Indian species of the genus Pholetesor Mason, 1981 reared from lepidopteran leafminers is also given.
The origins of the Cuban bee fauna are reviewed. This fauna began to form 40 million years ago during the Proto Antilles period, through ancestors that arrived in successive invasions from adjacent continental areas. The composition of the Antillean fauna has evolved continuously over millions of years until the present time. The native bee fauna of Cuba is represented by 89 species, contained in 29 genera and 4 families. The number of genera represented per family is as follows: Colletidae (3), Halictidae (8), Megachilidae (4), and Apidae (14). The Cuban apifauna contains four principal groups with distinct biogeographic histories: endemic species of Cuba (43.8%); endemic species of the Antilles shared among multiple islands (33.1%); continental species whose distribution includes the Antilles (16.8%); and species introduced through human activity (6.3%). An analysis of the distributions of Cuban bee species reveals that areas of highest species endemism coincide with the main mountainous nuclei of the East, Center and West. These were: the Sierra Maestra mountain range (with 25 species), Nipe-Sagua-Baracoa (15), the Mountain range of Guaniguanico (14) and the Massif of Guamuaya (14). The distribution of the bees in the Cuban Archipelago was not uniform, possibly due to the ecological conditions of the respective habitats, the diversity and presence of specific food plants, and interspecific competition. The endemism of bees in Greater Antilles is considered high keeping in mind the mobility of the group, as observed not only in Cuba (43.8%) but also Jamaica (50%), Hispaniola (45.6%), and in Puerto Rico and adjacent islands (26.5 %).