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61 results for “881”
Figure 6 from: Xu Y, Li Y, Zhan Z, Xu K (2019) Morphology and phylogenetic analysis of two new deep-sea species of Chrysogorgia (Cnidaria, Octocorallia, Chrysogorgiidae) from Kocebu Guyot (Magellan seamounts) in the Pacific Ocean. ZooKeys 881: 91-107. https://doi.org/10.3897/zookeys.881.34759
Figure 6 Sclerites of Chrysogorgia binata sp. nov. A Sclerites in the basal part of the polyp body B Sclerites in the point at the base of a naked tract below each tentacle. Scale bar: 300 μm (all at the same scale).
Figure 4 from: Xu Y, Li Y, Zhan Z, Xu K (2019) Morphology and phylogenetic analysis of two new deep-sea species of Chrysogorgia (Cnidaria, Octocorallia, Chrysogorgiidae) from Kocebu Guyot (Magellan seamounts) in the Pacific Ocean. ZooKeys 881: 91-107. https://doi.org/10.3897/zookeys.881.34759
Figure 4 External morphology of the holotype and polyps of Chrysogorgia binata sp. nov. A Two planar fans of the colony after fixation B The holotype (arrow) in situ. Laser dots spaced at 33 cm used for measuring dimensions C The colony after collection D A single polyp under SEME Single terminal polyp under light microscope F Short trunk with the first bifurcation of branches after fixation. Scale bars: 10 cm (A); 5 cm (C); 1 mm (D, E); 1 cm (F).
Figure 2 from: Xu Y, Li Y, Zhan Z, Xu K (2019) Morphology and phylogenetic analysis of two new deep-sea species of Chrysogorgia (Cnidaria, Octocorallia, Chrysogorgiidae) from Kocebu Guyot (Magellan seamounts) in the Pacific Ocean. ZooKeys 881: 91-107. https://doi.org/10.3897/zookeys.881.34759
Figure 2 External morphology and polyps of Chrysogorgia ramificans sp. nov.: A The holotype in situ B Close-up of branches and polyps in situ C The colony after collection D A single polyp under light microscope E Single polyp under SEM. Scale bars: 20 cm (C); 1 mm (D, E).
Figure 3 from: Xu Y, Li Y, Zhan Z, Xu K (2019) Morphology and phylogenetic analysis of two new deep-sea species of Chrysogorgia (Cnidaria, Octocorallia, Chrysogorgiidae) from Kocebu Guyot (Magellan seamounts) in the Pacific Ocean. ZooKeys 881: 91-107. https://doi.org/10.3897/zookeys.881.34759
Figure 3 Sclerites of Chrysogorgia ramificans sp. nov. A Sclerites of polyp neck extending to the rachis of tentacles B Sclerites in the pinnules C Sclerites at the body base D Sclerites of coenenchyme. Scale bars: 200 μm (A, C, D); 50 μm (B).
Figure 6 from: Chen Y-M, Gibson GAP, Peng L-F, Iqbal A, Zang L-S (2019) Anastatus Motschulsky (Hymenoptera, Eupelmidae): egg parasitoids of Caligula japonica Moore (Lepidoptera, Saturniidae) in China. ZooKeys 881: 109-134. https://doi.org/10.3897/zookeys.881.34646
Figure 6 Anastatus meilingensisA–E female (2): A dorsal habitus B lateral habitus C dorsal mesosoma D lateral mesosoma E fore wing, dorsal view. F–H male (19): F lateral habitus G antenna H clava and apical three funiculars (three lower bars indicate length of clava compared to combined length of apical funiculars). Abbreviations: cbr = remnant of hyaline cross band, clv = clava, flx = flagellomere number.
Figure 1 from: Chen Y-M, Gibson GAP, Peng L-F, Iqbal A, Zang L-S (2019) Anastatus Motschulsky (Hymenoptera, Eupelmidae): egg parasitoids of Caligula japonica Moore (Lepidoptera, Saturniidae) in China. ZooKeys 881: 109-134. https://doi.org/10.3897/zookeys.881.34646
Figure 1 Anastatus fulloiA–E female: A dorsal habitus (13) B lateral habitus (12) C dorsal mesosoma (13) D lateral mesosoma (12) E fore wing (14). F–H male: F lateral habitus (22) G antenna (32) H clava and apical three funiculars (32) (three lower bars indicate length of clava compared to combined length of apical funiculars). Abbreviations: clv = clava, flx = flagellomere number.
Figure 5 from: Chen Y-M, Gibson GAP, Peng L-F, Iqbal A, Zang L-S (2019) Anastatus Motschulsky (Hymenoptera, Eupelmidae): egg parasitoids of Caligula japonica Moore (Lepidoptera, Saturniidae) in China. ZooKeys 881: 109-134. https://doi.org/10.3897/zookeys.881.34646
Figure 5 Anastatus japonicusA–E female: A dorsal habitus (6) B lateral habitus (4) C mesosoma in dorsal view (6) D same in lateral view (4) E fore wing (5). F–H male: F lateral habitus (25) G antenna (25) H clava and apical three funiculars (25) (three lower bars indicate length of clava compared to combined length of apical funiculars). Abbreviations: clv = clava, flx = flagellomere number.
Figure 1 from: Beltrão H, Zuanon J, Ferreira E (2019) Checklist of the ichthyofauna of the Rio Negro basin in Brazilian Amazon. ZooKeys 881: 53-89. https://doi.org/10.3897/zookeys.881.32055
Figure 1 Map of the Rio Negro basin in the northwestern portion of Brazil and adjacent countries, depicting its main tributaries and sampling localities (red dots) obtained from the descriptions of new species 2003–2019, fish collection records, and published ichthyofaunal inventories.
Figure 4 from: Chen Y-M, Gibson GAP, Peng L-F, Iqbal A, Zang L-S (2019) Anastatus Motschulsky (Hymenoptera, Eupelmidae): egg parasitoids of Caligula japonica Moore (Lepidoptera, Saturniidae) in China. ZooKeys 881: 109-134. https://doi.org/10.3897/zookeys.881.34646
Figure 4 Anastatus gansuensis, male A dorsal habitus (17) B lateral habitus (16) C head in frontal view (19) D mesosoma in lateral view (16) E propodeum (17) F fore wing (17) G antenna (18) H pedicel and basal three funiculars (18) (three lower bars indicate length of clava compared to combined length of apical funiculars). Abbreviations: clv = clava, flx = flagellomere number.
Supplementary material 1 from: Beltrão H, Zuanon J, Ferreira E (2019) Checklist of the ichthyofauna of the Rio Negro basin in Brazilian Amazon. ZooKeys 881: 53-89. https://doi.org/10.3897/zookeys.881.32055
: Data type: species data
Figure 3 from: Chen Y-M, Gibson GAP, Peng L-F, Iqbal A, Zang L-S (2019) Anastatus Motschulsky (Hymenoptera, Eupelmidae): egg parasitoids of Caligula japonica Moore (Lepidoptera, Saturniidae) in China. ZooKeys 881: 109-134. https://doi.org/10.3897/zookeys.881.34646
Figure 3 Anastatus spp., female A–EA. gansuensis: A fore wing (8) B basal half of fore wing (29) C enlargement of medial part of wing disc (8) D gaster in dorsal view (9) E mesotarsus and apex of mesotibia, in anterior view (7). F, GA. fulloi, mesotarsus and apex of mesotibia (12): F in anterior view G in posterodorsal view. Abbreviations: Gtx = gastral tergite number, syn = syntergum.
Figure 3 from: Beltrão H, Zuanon J, Ferreira E (2019) Checklist of the ichthyofauna of the Rio Negro basin in Brazilian Amazon. ZooKeys 881: 53-89. https://doi.org/10.3897/zookeys.881.32055
Figure 3 Taxonomic characterization (proportions of species by order) of fish assemblages found in different aquatic habitats of Rio Negro, Amazon Basin, Brazil.
Figure 2 from: Chen Y-M, Gibson GAP, Peng L-F, Iqbal A, Zang L-S (2019) Anastatus Motschulsky (Hymenoptera, Eupelmidae): egg parasitoids of Caligula japonica Moore (Lepidoptera, Saturniidae) in China. ZooKeys 881: 109-134. https://doi.org/10.3897/zookeys.881.34646
Figure 2 Anastatus gansuensis, female A dorsal habitus (9) B lateral habitus (7) C head in frontal view (10) D, same in dorsal view (9) E mesosoma in dorsal view (9) F same in lateral view (7) G antenna (10) H pedicel and basal three funiculars (10) I clava and apical three funiculars (10). Abbreviations: clv = clava, flx = flagellomere number; pdl = pedicel
Figure 2 from: Beltrão H, Zuanon J, Ferreira E (2019) Checklist of the ichthyofauna of the Rio Negro basin in Brazilian Amazon. ZooKeys 881: 53-89. https://doi.org/10.3897/zookeys.881.32055
Figure 2 Cumulative curve of valid fish species numbers described from type localities in the Rio Negro basin between 1821 and 2019, based on the catalogs of Reis et al. (2003) and Buckup et al. (2007), and species descriptions published after those compilations.
Data from: Distinctive architecture of the chloroplast genome in the chlorodendrophycean green algae Scherffelia dub and Tetraselmis sp. CCMP 881
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Figure 6 from: Kohlmann B, Solís Á, Alvarado G (2019) Description of Onthophagus humboldti and Uroxys bonplandi, two new scarab beetles (Coleoptera, Scarabaeidae, Scarabaeinae) from Costa Rica, with notes on tropical mountain brachyptery and endemicity. ZooKeys 881: 23-51. https://doi.org/10.3897/zookeys.881.38026
Figure 6 Known distribution of brachypterous Scarabaeinae in Costa Rica.
Figure 1 from: Mvogo Ndongo PA, von Rintelen T, Cumberlidge N (2019) Taxonomic revision of the endemic Cameroonian freshwater crab genus Louisea Cumberlidge, 1994 (Crustacea, Decapoda, Brachyura, Potamonautidae), with descriptions of two new species from Nkongsamba and Yabassi. ZooKeys 881: 135-164. https://doi.org/10.3897/zookeys.881.36744
Figure 1 Collection localities of the four species of Louisea in Cameroon.
Figure 1A from: Lu Y-Y, Zorn C, Král D, Bai M (2019) Description of Callistethus hamus sp. nov. (Coleoptera, Scarabaeidae, Rutelinae) from continental Southeast Asia using synchrotron to illustrate the aedeagus. ZooKeys 881: 1-11. https://doi.org/10.3897/zookeys.881.34821
Figure 1A 3D model for aedeagus of Callistethus hamus Lu & Zorn, sp. nov. in pdf format.
Figure 4 from: Kohlmann B, Solís Á, Alvarado G (2019) Description of Onthophagus humboldti and Uroxys bonplandi, two new scarab beetles (Coleoptera, Scarabaeidae, Scarabaeinae) from Costa Rica, with notes on tropical mountain brachyptery and endemicity. ZooKeys 881: 23-51. https://doi.org/10.3897/zookeys.881.38026
Figure 4 Dorsal drawing of a male Uroxys bonplandi sp. nov.
Figure 1 from: Kohlmann B, Solís Á, Alvarado G (2019) Description of Onthophagus humboldti and Uroxys bonplandi, two new scarab beetles (Coleoptera, Scarabaeidae, Scarabaeinae) from Costa Rica, with notes on tropical mountain brachyptery and endemicity. ZooKeys 881: 23-51. https://doi.org/10.3897/zookeys.881.38026
Figure 1 Dorsal drawing of a male Onthophagus humboldti sp. nov.
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