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1,186 results for “Scolytinae”
Figs 113–117. 113 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 113–117. 113 – Endeochetus canui Perrin, 2000, habitus of a male from Wadi Ayhaft. 114, 116 – Endeochetus crassirostris sp. nov.: 114 – habitus of the holotype; 116 – aedeagus of a paratype in dorsal view. 115, 117 – Endeochetus helenae sp. nov., holotype: 115 – habitus; 117 – aedeagus in dorsal view.
Figs 103–106 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 103–106. Molybdotus vermiculosus (Waterhouse, 1881). 103–104 – female lectotype (103 – habitus; 104 – labels borne by the same); 105–106 – male paralectotype (105 – aedeagus in dorsal view; 106 – the same in side view).
Figs 107–112. 107, 110 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 107–112. 107, 110 – Molybdotus minor sp. nov.: 107 – habitus of the holotype; 110 – aedeagus of a paratype in dorsal view. 108, 111 — Molybdotus viridiaureus sp. nov. 108 – habitus of the holotype; 111 – aedeagus of a paratype in dorsal view. 109, 112 – Molybdotus mixtus sp. nov., holotype. 109 – habitus; 112 – aedeagus in dorsal view.
Figs 98–102. 98–99 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 98–102. 98–99 – Systates spinipennis sp. nov., holotype: 98 – habitus; 99 – habitus in side view. 100–102 – Tuberates pustulatus sp. nov.: 100 – habitus of the holotype; 101 – habitus of the holotype in side view; 102 – aedeagus of a paratype in dorsal view.
Figs 79–84. 79–81, 83 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 79–84. 79–81, 83 – Socotracerus delumbis sp. nov. 79 – habitus of the holotype; 80 – head, antenna and right fore legs of the same; 81 – habitus of a female paratype; 83 – aedeagus of a paratype in dorsal view. 82, 84 – Socotracerus contortipes sp. nov., holotype. 82 – habitus; 84 – aedeagus in dorsal view.
Figs 85–91. 85–89 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 85–91. 85–89 – Socotractus angusticollis (Taschenberg): 85 – habitus of the male lectotype; 86 – locality label borne by the lectotype; 87 – collection label after which is placed the lectotype; 88 –aedeagus of a male from Wadi Madar in dorsal view; 89 – habitus of a female from Scant Mt. 90–91 – Socotractus peteri sp. nov., holotype: 90 – habitus; 91 – aedeagus in dorsal view.
Figs 73–78. 73–75 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 73–78. 73–75 – Nesotocerus labeculatus sp. nov.: 73 – habitus of the holotype; 74 – habitus of a female paratype; 75 – aedeagus of a paratype in dorsal view. 76–78 – Nesotocerus griseovestitus sp. nov.: 76 – habitus of the holotype; 77 – habitus of a female paratype; 78 – aedeagus of a paratype in dorsal view.
Figs 131–138. 131, 134 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 131–138. 131, 134 – Endeochetus parvus sp. nov., holotype: 131 – habitus; 134 – broken aedeagus in dorsal view. 132–133, 135 – Endeochetus minimus sp. nov.: 132 – habitus of the holotype; 133 – habitus of the holotype in side view; 135 – aedeagus of a paratype in dorsal view. 136–138 – Hagherius sculptus sp. nov.: 136 – habitus of a female paratype; 137 – aedeagus of the holotype in dorsal view; 138 – spermatheca of a paratype.
Figs 67–72. 67–69, 71 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 67–72. 67–69, 71 – Nesotocerus complanatus sp. nov.: 67 – habitus of the holotype; 68 – the same in side view; 69 – aedeagus of a paratype in dorsal view; 71 – spermatheca of a paratype. 70, 72 – Nesotocerus rectus sp. nov. 70 – aedeagus of a paratype in dorsal view; 72 – spermatheca of a paratype.
Figs 62–66. 62–64 in Apionidae, Nanophyidae, Brachyceridae and Curculionidae except Scolytinae (Coleoptera) from Socotra Island
Figs 62–66. 62–64 – Nematocerus spinifemur sp. nov.: 62 – habitus of the holotype; 63 – head, pronotum and front legs of the same to show the spine at the base of femora; 64 – aedeagus of a paratype in dorsal view. 65–66 – Nesotocerus rectus sp. nov. 65 – habitus of the holotype; 66– the same in side view
Scolytinae Xyleborini host plants dataset
<p>The present database includes all Xyleborini species known and described prior to October 30<sup>th</sup> 2022 and their relative host plants.</p>
Scolytinae former Cryphalini host plant dataset
<p>The present database includes all Coriacephilini, Corthylini, Ernoporini, Trypophloeini, Xyloctonini, and Xyloterini species known and described prior to February 28th 2023 and their relative host plants.</p>
Figure 7 in Revision of the Bark Beetle Genera Within the Former Cryphalini (Curculionidae: Scolytinae)
Figure 7. Phylogeny of Cryphalini, Coriacephilini, Xyloterini, andTrypophloeini, Part 2.
New non-native pseudocryptic Cyclorhipidion species (Coleoptera: Curculionidae: Scolytinae: Xyleborini) found in the United States as revealed in a multigene phylogeny
<p>Pseudocryptic species, those that are difficult to diagnose using traditional taxonomic methods, are serious impediments for recognizing the introduction of non-native species. Rapid identification of species facilitates a rapid response to newly introduced species which can lessen their damaging effects. This situation is acute for known pest species such as xyleborine ambrosia beetles which are difficult to identify given minute morphological, often variable, diagnostic characters. These beetles have been introduced into non-native temperate regions and have caused economic and ecological havoc. In this study, we produced DNA-based phylogenies using four genes for individuals of <em>Cyclorhipidion bodoanum</em> (Reitter, 1913)<em>, C. distinguendum </em>(Eggers, 1930), and <em>C. pelliculosum </em>(Eichhoff, 1878) sampled from their introduced and native Asian ranges and as well as other <em>Cyclorhipidion </em>species. In addition, we review subtle morphological characters for diagnostic potential for these similar species. Bayesian phylogenetic analysis produced well-resolved and supported phylogeny that provided evidence for multiple introductions of <em>C. bodoanum and C. distinguendum</em> into the US and the occurrence of pseudocryptic species. The ambrosia beetles <em>Cyclorhipidion tenuigraphum </em>(Schedl, 1953)<em> </em>and<em> C. nemesis </em>Smith & Cognato, sp. nov. are reported in North America for the first time. We find that the pattern of elytral interstrial setae is an unrealized source for the identification of <em>Cyclorhipidion</em> species. This study resulted in the recognition of six species adventive to the US with the revised status of <em>C. californicum</em> (Wood, 1975). All species known from North American are diagnosed, illustrated and a key is provided.</p>
New xyleborine (Coleoptera: Curculionidae: Scolytinae) genus with an Afrotropical-Neotropical distribution
<p>Plant-associated arthropods have been shown to cross large oceanic distances on floating plant material and to establish themselves on distant landmasses. Xyleborini (Coleoptera: Curculionidae: Scolytinae) ambrosia beetles occur in forests worldwide and are likely capable of long range dispersal. In less than 20 million years, this group dispersed from Asia to tropical regions of Africa and South America. The phylogeny, taxonomy, and biogeography of one <em>Xyleborus </em>species group which occurs on both continents are reviewed for this study. Based on a well-resolved molecular phylogeny resulting from parsimony, likelihood, and Bayesian analyses of four gene loci, we describe a new monophyletic genus, <em>Xenoxylebora </em>Osborn, Smith & Cognato, gen. nov., for this bicontinental <em>Xyleborus </em>species group with seven Afrotropical and six Neotropical species. Six new species are described: <em>Xenoxylebora pilosa </em>Osborn, Smith & Cognato, sp. nov. from Africa, and <em>Xenoxylebora addenda </em>Osborn, Smith & Cognato, sp. nov., <em>Xenoxylebora calculosa </em>Osborn, Smith & Cognato, sp. nov., <em>Xenoxylebora hystricosa</em> Osborn, Smith & Cognato, sp. nov., <em>Xenoxylebora serrata </em>Osborn, Smith & Cognato, sp. nov., and <em>Xenoxylebora sulcata </em>Osborn, Smith & Cognato, sp. nov., from South America. Seven new combinations from <em>Xyleborus </em>are proposed: <em>Xenoxylebora caudata</em> (Schedl, 1957) comb. nov., <em>Xenoxylebora collarti</em> (Eggers, 1932) comb. nov., <em>Xenoxylebora perdiligens</em> (Schedl, 1937) comb. nov., <em>Xenoxylebora sphenos</em> (Sampson, 1912) comb. nov., <em>Xenoxylebora subcrenulata</em> (Eggers, 1932) comb. nov., and <em>Xenoxylebora syzygii</em> (Nunberg, 1959) comb. nov. from Africa, and<em> Xenoxylebora neosphenos</em> (Schedl, 1976) comb. nov. from South America. One new synonym is proposed: <em>Xenoxylebora sphenos </em>(Sampson, 1912) =<em>Xyleborus tenellus </em>Schedl, 1957 syn. nov. Descriptions, diagnoses, images, and a key to the identification of all 13 species are provided. The sequence of colonization between Africa and South America is uncertain for <em>Xenoxylebora</em>. Prevailing ocean currents and predominant locality patterns observed for other organisms suggests an African <em>Xenoxylebora</em> origin. However, the phylogeny, biogeographical analyses, and a calibrated divergence time suggests a possible South American origin for African <em>Xenoxylebora</em> (2.3 Ma, 95% HDP 4.5 – 0.6 Ma) which is supported by the occurrence of ocean counter currents between the continents and evidence of dispersal from South America to Africa among some plant and arthropod taxa. </p>
Fig. 9 in Microsculpture and chaetotaxy of abdominal tergites of bark and ambrosia beetles (Coleoptera: Curculionidae, Scolytinae): morphology and nomenclature
Fig. 9. Elements of chaetom and microsculpture of abdominal tergites of Scolytinae. a –
Fig. 8 in Microsculpture and chaetotaxy of abdominal tergites of bark and ambrosia beetles (Coleoptera: Curculionidae, Scolytinae): morphology and nomenclature
Fig. 8. Elements of chaetom and microsculpture of abdominal tergites of Scolytinae. a –
Fig. 11 in Microsculpture and chaetotaxy of abdominal tergites of bark and ambrosia beetles (Coleoptera: Curculionidae, Scolytinae): morphology and nomenclature
Fig. 11. Microscuptural fields and chaetom of Scolytinae (glass slides). a – Camptocerus
Figs 1–7 in Microsculpture and chaetotaxy of abdominal tergites of bark and ambrosia beetles (Coleoptera: Curculionidae, Scolytinae): morphology and nomenclature
Figs 1–7. Microscuptural fields and chaetom elements of Scolytinae. 1, 6 – Hylurgus
Fig. 10 in Microsculpture and chaetotaxy of abdominal tergites of bark and ambrosia beetles (Coleoptera: Curculionidae, Scolytinae): morphology and nomenclature
Fig. 10. Different setae of tergite 7 of Scolytinae. n – feathery furcate; d – feathery; a –
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
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OpenNeuro
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