A new Genus of Proctotrupidae from Japan (Hymenoptera: Proctotrupoidea).

Der Autor beschreibt eine neue Gattung, Watanabeia n. g. (Proctotrupidae), mit Disogmus afissae Watanabe (Japan) als Genotypus. Die phylogenetische Stellung der neuen Gattung wird kurz erörtert und abschließend ein Bestimmungsschlüssel der Proctotrupiden-Gattungen der Welt (einschließlich ihrer Synonymie) gegeben.Nomenklatorische HandlungenWatanabeia Masner, 1958 (Proctotrupoidea), gen. n.The author has established a new genus - Watanabeia n. g. (Proctotrupidae) - for Disogmus afissae Watanabe, originally described from Japan. A short discussion concerning phylogenetic evaluation of the new genus is added. Finally a key to genera of Proctotrupidae of the world with their synonymy is given. Nomenclatural ActsWatanabeia Masner, 1958 (Proctotrupoidea), gen. n

Systematics of Old World Odontacolus Kieffer s.l. (Hymenoptera, Platygastridae s.l.): Parasitoids of spider eggs

The genera Odontacolus Kieffer and Cyphacolus Priesner are among the most distinctive platygastroid wasps because of their laterally compressed metasomal horn; however, their generic status has remained unclear. We present a morphological phylogenetic analysis comprising all 38 Old World and four Neotropical Odontacolus species and 13 Cyphacolus species, which demonstrates that the latter is monophyletic but nested within a somewhat poorly resolved Odontacolus. Based on these results Cyphacolus syn. n. is placed as a junior synonym of Odontacolus which is here redefined. The taxonomy of Old World Odontacolus s.str. is revised; the previously known species Odontacolus longiceps Kieffer (Seychelles), Odontacolus markadicus Veenakumari (India), Odontacolus spinosus (Dodd) (Australia) and Odontacolus hackeri (Dodd) (Australia) are re-described, and 32 new species are described: Odontacolus africanus Valerio & Austin sp. n. (Congo, Guinea, Kenya, Madagascar, Mozambique, South Africa, Uganda, Zimbabwe), Odontacolus aldrovandii Valerio & Austin sp. n. (Nepal), Odontacolus anningae Valerio & Austin sp. n. (Cameroon), Odontacolus australiensis Valerio & Austin sp. n. (Australia), Odontacolus baeri Valerio & Austin sp. n. (Australia), Odontacolus berryae Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus bosei Valerio & Austin sp. n. (India, Malaysia, Sri Lanka), Odontacolus cardaleae Valerio & Austin sp. n. (Australia), Odontacolus darwini Valerio & Austin sp. n. (Thailand), Odontacolus dayi Valerio & Austin sp. n. (Indonesia), Odontacolus gallowayi Valerio & Austin sp. n. (Australia), Odontacolus gentingensis Valerio & Austin sp. n. (Malaysia), Odontacolus guineensis Valerio & Austin sp. n. (Guinea), Odontacolus harveyi Valerio & Austin sp. n. (Australia), Odontacolus heratyi Valerio & Austin sp. n. (Fiji), Odontacolus heydoni Valerio & Austin sp. n. (Malaysia, Thailand), Odontacolus irwini Valerio & Austin sp. n. (Fiji), Odontacolus jacksonae Valerio & Austin sp. n. (Cameroon, Guinea, Madagascar), Odontacolus kiau Valerio & Austin sp. n. (Papua New Guinea), Odontacolus lamarcki Valerio & Austin sp. n. (Thailand), Odontacolus madagascarensis Valerio & Austin sp. n. (Madagascar), Odontacolus mayri Valerio & Austin sp. n. (Indonesia, Thailand), Odontacolus mot Valerio & Austin sp. n. (India), Odontacolus noyesi Valerio & Austin sp. n. (India, Indonesia), Odontacolus pintoi Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus schlingeri Valerio & Austin sp. n. (Fiji), Odontacolus sharkeyi Valerio & Austin sp. n. (Thailand), Odontacolus veroae Valerio & Austin sp. n. (Fiji), Odontacolus wallacei Valerio & Austin sp. n. (Australia, Indonesia, Malawi, Papua New Guinea), Odontacolus whitfieldi Valerio & Austin sp. n. (China, India, Indonesia, Sulawesi, Malaysia, Thailand, Vietnam), Odontacolus zborowskii Valerio & Austin sp. n. (Australia), and Odontacolus zimi Valerio & Austin sp. n. (Madagascar). In addition, all species of Cyphacolus are here transferred to Odontacolus: Odontacolus asheri (Valerio, Masner & Austin) comb. n. (Sri Lanka), Odontacolus axfordi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus bhowaliensis (Mani & Mukerjee) comb. n. (India), Odontacolus bouceki (Austin & Iqbal) comb. n. (Australia), Odontacolus copelandi (Valerio, Masner & Austin) comb. n. (Kenya, Nigeria, Zimbabwe, Thailand), Odontacolus diazae (Valerio, Masner & Austin) comb. n. (Kenya), Odontacolus harteni (Valerio, Masner & Austin) comb. n. (Yemen, Ivory Coast, Paskistan), Odontacolus jenningsi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus leblanci (Valerio, Masner & Austin) comb. n. (Guinea), Odontacolus lucianae (Valerio, Masner & Austin) comb. n. (Ivory Coast, Madagascar, South Af rica, Swaziland, Zimbabwe), Odontacolus normani (Valerio, Masner & Austin) comb. n. (India, United Arab Emirates), Odontacolus sallyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tes...Alejandro A.Valerio , Andrew D. Austin , Lubomír Masner , Norman F. Johnso

Revision of Scelio pulchripennis - group species (Hymenoptera, Platygastroidea, Platygastridae)

The charismatic pulchripennis-group of Scelio Latreille is revised and 18 species are treated. The species group is described and diagnosed. Eight new species are described: S. clarkei Yoder, sp. n. (India, Sri Lanka); S. ememeye Yoder, sp. n. (Sri Lanka, Nepal); S. leipo Yoder, sp. n. (Madagascar); S. parapulchripennis Yoder, sp. n. (Madagascar); S. masneri Yoder, sp. n. (Botswana, South Africa); S. paranitens Yoder, sp. n. (Botswana, Kenya, South Africa, Zimbabwe); S. tria, Yoder & Masner, sp. n. (India); and S. turbidus Yoder, sp. n. (Botswana, South Africa, Tanzania). Scelio princeps Nixon is treated as a junior synonym of S. poecilopterus Priesner (syn. n.). Scelio variegatus Kozlov & Kononova is removed from synonymy with S. poecilopterus Priesner and treated as a valid species (stat. n.). Lectotypes are designated for Scelio baoli Risbec, S. corion Nixon, and S. pulchripennis Brues. Known hosts are eggs of grasshoppers in the family Acrididae (Orthoptera). The electronic version of this paper contains numerous hyperlinks that make use of biodiversity informatics standards to reference supporting data

Monitoring of Wild Animal Species in the Czech Republic

AbstractIn the paper, the method of data collection, processing and visualization of the occurrence of non-indigenous and endangered animal species in the Czech Republic is described. Our new software enables easy data entry about the observation of monitored species to the expert public. The data obtained is then used by expert and scientific institutions in order to search for optimal solutions of nature protection and population management and results are open to the public.This analytic and software solution was developed by the Department of Information Technologies, Czech University of Life Sciences; the data has been also used by the Forestry and Wood Faculty and the Faculty of Life Sciences

World Species of the Genus Chromoteleia Ashmead (Hymenoptera, Platygastridae, Scelioninae)

The genus Chromoteleia was originally described by William H. Ashmead (1893), based on the colorful type species Chromoteleia semicyanea from the Caribbean island of Saint Vincent. Currently, six species have been recorded from the New World and a single species from Africa. One fossil species, C. theobaldi Maneval, was reported from Baltic amber (from 40~60 mya), but the status of this species is not clear. These creatures are parasites of insect eggs, but which host they attack is still unclear. Since its original description Chromoteleia has never been comprehensively reviewed. In this study, a total of 27 species are recognized worldwide, of which 21 are new to science. All species are described and illustrated. Several important morphological characters are provided for the identification of the species of Chromoteleia and the geographical distribution records of the genus are expanded to 29 countries in Central and South America, the Caribbean, and Africa. The documentation of the species diversity is crucial to the understanding of the evolution and interrelationships in this genus, as well as informing conservation policies

Linoleic and oleic acids enhance cell migration by altering the dynamics of microtubules and the remodeling of the actin cytoskeleton at the leading edge

Fatty acids (FA) have a multitude of biological actions on living cells. A target of their action is cell motility, a process of critical importance during cancer cell dissemination. Here, we studied the effect of unsaturated FA on ovarian cancer cell migration in vitro and its role in regulating cytoskeleton structures that are essential for cell motility. Scratch wound assays on human ovary cancer SKOV-3 cell monolayers revealed that low doses (16 μM) of linoleic acid (LA, 18:2 ω6) and oleic acid (OA; 18:1 ω9) promoted migration, while α-linolenic acid (ALA, 18:3 ω3), showed a migration rate similar to that of the control group. Single cell tracking demonstrated that LA and OA-treated cells migrated faster and were more orientated towards the wound closure than control. In vitro addition of those FA resulted in an increased number, length and protrusion speed of filopodia and also in a prominent and dynamic lamellipodia at the cell leading edge. Using time-lapse video-microscopy and FRAP we observed an increase in both the speed and frequency of actin waves associated with more mobile actin and augmented Rac1 activity. We also observed that FA induced microtubule-organizing center (MTOC)-orientation towards the cell front and affected the dynamics of microtubules (MT) in the direction of cell migration. We propose that environmental cues such as OA and LA present in ascitic fluid, should be taken into account as key factors for the regulation of cell migration.Fil: Masner Moratorio, Martin. Instituto Universitario de Ciencias Biomédicas de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa | Universidad Nacional de Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa | Instituto de Investigación Médica Mercedes y Martín Ferreyra. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa; ArgentinaFil: Lujea, Noelia Carolina. Instituto Universitario de Ciencias Biomédicas de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa | Universidad Nacional de Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa | Instituto de Investigación Médica Mercedes y Martín Ferreyra. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa; ArgentinaFil: Bisbal, Mariano. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Universidad Nacional de Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra; ArgentinaFil: Acosta, Cristian Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; ArgentinaFil: Kunda, Patricia Elena. Instituto Universitario de Ciencias Biomédicas de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa | Universidad Nacional de Córdoba. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa | Instituto de Investigación Médica Mercedes y Martín Ferreyra. Instituto de Investigación Médica Mercedes y Martín Ferreyra. Grupo Vinculado Centro de Investigación en Medicina Traslacional Severo R. Amuchástegui - Cimetsa; Argentin

Calixomeria, a new genus of Sceliotrachelinae (Hymenoptera, Platygastridae) from Australia

Calixomeria lasallei gen. n. et sp. n. is described as a new genus and species of Sceliotrachelinae. Calixomeria most closely resembles genera of the Aphanomerus-cluster but possesses several characters that readily separate it from other sceliotracheline genera. The key of Masner and Huggert (1989) is modified to accommodate Calixomeria, and the relationship of the genus to other members of the subfamily is discussed

New World Diapriinae.

138 p. : ill. ; 26 cm.Includes bibliographical references (p. 122-125) and index.The subfamily Diapriinae (Diapriidae: Proctotrupoidea) in the New World is reviewed at the supra specific level. Three tribes and 52 genera are recognized. Sixteen new genera are proposed: Apopria (Diapriini), Avoca (Diapriini), Chilomicrus (Spilomicrini), Cruzium (Diapriini), Doddius (Spilomicrini), Eladio (Diapriini), Epomium (Spilomicrini), Ferrugenus (Spilomicrini), Hansona (Diapriini), Leucopria (Diapriini), Mimopriella (Diapriini), Omopria (Diapriini), Ortona (Psilini), Peckidium (incertae sedis) Psychopria (Diapriini), and Turripria (Diapriini). The following new species are described: Apopria coveri [female] (USA), Asolenopsia gibba [female] (Costa Rica), Avoca collaris [female] (USA), Chilomicrus pecki [male] (Chile), Cruzium amphorale [female] (Costa Rica), Eladio cruzi [female] (Costa Rica), Epomium cicatrix [female] (Chile), Ferrugenus chilensis [female] (Chile), Hansona pauli [female] (Costa Rica), Leucopria cylindricornis [female] (Ecuador, Costa Rica), Omopria brevipalpis [female] (Brazil), Ortona hansoni [female] (Costa Rica), Peckidium enigmaticum [female] (Antilles, Central and South America, West Africa, Philippines), Psychopria hoguei [male] (Costa Rica), Turripria woldai [female] (Panama). New generic synonymies are proposed: Acanthopria Ashmead (= Adelioneiva Fischer), Asolenopria Kieffer (= Euplacopria Ferrière), Bruchopria Kieffer (= Aulatopria Brèthes), Doliopria Kieffer (= Martinica Risbec), Megaplastopria Ashmead (= Xyalopria Kieffer), Notoxoides Ashmead (= Psilogasteroides Brèthes), Pentapria Kieffer (= Antipapria Fabritius, Bakeria Kieffer, Plutopria Kieffer, Spilomicrinus Ogloblin), Spilomicrus Westwood (= Hoplopria Ashmead, Linkiola Kieffer), Szelenyiopria Fabritius (= Gymnopria Loiácono). New combinations are proposed: Aulatopria tucumana Brèthes to Bruchopria, Bakeria rugosa Dodd to Doddius, Gymnopria lucens Loiácono to Szelenyiopria, Mimopria pentatoma Borgmeier and Mimopria splendens Borgmeier to Mimopriella, and Xanthopria nitida Brues to Acanthopria. The 52 genera are keyed (keys in both English and Spanish); for each genus the synonymies, diagnoses, descriptions, recognition and relationships, distribution, and biology are given. Twelve plates with 107 figures are included

A semantically enriched taxonomic revision of Gryonoides Dodd, 1920 (Hymenoptera, Scelionidae), with a review of the hosts of Teleasinae

Teleasinae are commonly collected scelionids that are the only known egg parasitoids of carabid beetles and therefore play a crucial role in shaping carabid populations in natural and agricultural ecosystems. We review the available host information of Teleasinae, report a new host record, and revise Gryonoides Dodd, 1920, a morphologically distinct teleasine genus. We review the generic concept of Gryonoides and provide diagnoses and descriptions of thirteen Gryonoides species and two varieties: G. glabriceps Dodd, 1920, G. pulchellus Dodd, 1920 (= G. doddi Ogloblin, 1967, syn. nov. and G. pulchricornis Ogloblin, 1967, syn. nov.), G. brasiliensis Masner & Miko, sp. nov., G. flaviclavus Masner & Miko, sp. nov., G. fuscoclavatus Masner & Miko, sp. nov., G. garciai Masner & Miko, sp. nov., G. mexicali Masner & Miko, sp. nov., G. mirabilicornis Masner & Miko, sp. nov., G. obtusus Masner & Miko, sp. nov., G. paraguayensis Masner & Miko, sp. nov., G. rugosus Masner & Miko, sp. nov., G. uruguayensis Masner & Miko, sp. nov. We treat Gryonoides scutellaris Dodd, 1920, as status uncertain. Gryonoides mirabilicornis Masner & Miko, sp. nov. is the only known teleasine with tyloids on two consecutive flagellomeres, a well-known trait of Sparasionidae. An illustrated identification key to species of Gryonoides, a queryable semantic representation of species descriptions using PhenoScript, and a simple approach for making Darwin Core Archive files in taxonomic revisions accessible are provided.Peer reviewe