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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.
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.
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.
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).
The worldwide transport of species beyond their native range is an increasing problem, e.g. for global biodiversity. Many introduced species are able to establish in new environments and some even become invasive. However, we do not know which traits enable them to survive and reproduce in new environments. This study aims to identify the characteristics of exotic ants, and to quantitatively test previously postulated but insufficiently tested assumptions. We collected data on nine traits of 93 exotic ant species (42 of them being invasive) and 323 native ant species in North America. The dataset includes 2536 entries from over 300 different sources; data on worker head width were mostly measured ourselves. We analyzed the data with three complementary analyses: univariate and multivariate analyses of the raw data, and multivariate analyses of phylogenetically independent contrasts. These analyses revealed significant differences between the traits of native and exotic ant species. In the multivariate analyses, only one trait was consistently included in the best models, estimated with AICc values: colony size. Thus, of the nine investigated traits, the most important characteristic of exotic ants as compared to native ants appears to be their large colony size. Other traits are also important, however, indicating that native and exotic ants differ by a suite of traits.
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.
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.
Four new species of the braconid wasp genus Hecabolus Curtis, 1834 (Doryctinae Foerster, 1863) are described for the Neotropical region in south and southwestern Brazil: H. acutus sp. nov., H. chrisaxeli sp. nov., H. gavinbroadi sp. nov., and H. transversalis sp. nov. We also report the morphological variation of females and males of H. mexicanus Zaldívar-Riverón & Belokobylskij, 2009, originally described based on a single female, and provide its first precise geographical distribution records. An updated key to the 13 described species of Hecabolus is provided.