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976 results for “Pacific Islands”
FIGURES 59–63 in A Revision of the Wasp Genus Pison Jurine, 1808 of Australia and New Zealand, New Guinea, and the Pacific Islands (Hymenoptera: Crabronidae)
FIGURES 59–63. Pison antennatum Pulawski, sp. nov. (59) Female clypeus and mandibles; (60) Male clypeus and mandibles; (61) Upper frons of female showing pair of setal patches; (62) Female metapleuron (arrow on each side of metapleuron shows foveolate sulcus); (63) Basal flagellomeres of male.
FIGURES 108–113 in A Revision of the Wasp Genus Pison Jurine, 1808 of Australia and New Zealand, New Guinea, and the Pacific Islands (Hymenoptera: Crabronidae)
FIGURES 108–113. Pison aridum Pulawski, sp. nov. (108) Female clypeus and mandibles; (109) Middle clypeal section of female; (110) Female head in dorsal view; (111) Male clypeus and mandibles; (112) Male head in dorsal view; (113) Female tergum VI.
FIGURES 51–54 in A Revision of the Wasp Genus Pison Jurine, 1808 of Australia and New Zealand, New Guinea, and the Pacific Islands (Hymenoptera: Crabronidae)
FIGURES 51–54. Pison angustivertex Pulawski, sp. nov. (51) Female clypeus and mandibles; (52) Male clypeus and mandibles; (53) Female frons; (54) Female head in dorsal view.
FIGURES 125–130 in A Revision of the Wasp Genus Pison Jurine, 1808 of Australia and New Zealand, New Guinea, and the Pacific Islands (Hymenoptera: Crabronidae)
FIGURES 125–130. Pison aterrimum Pulawski, sp. nov. (125) Female forewing; (126) Female gaster in dorsal view; male: (127) Sternum VIII (ventral surface); (128) Sternum VIII in lateral view; (129) Genitalia in dorsal view; (130) Genitalia in lateral view (damaged specimen).
FIGURES 119–124 in A Revision of the Wasp Genus Pison Jurine, 1808 of Australia and New Zealand, New Guinea, and the Pacific Islands (Hymenoptera: Crabronidae)
FIGURES 119–124. Pison aterrimum Pulawski, sp. nov. (119) Female clypeus and mandibles; (120) Male clypeus and mandibles; (121) Upper frons of female; (122) Female head in dorsal view; (123) Female tegula and adjacent scutum; (124) Propodeal dorsum of female.
FIGURES 47–49 in A Revision of the Wasp Genus Pison Jurine, 1808 of Australia and New Zealand, New Guinea, and the Pacific Islands (Hymenoptera: Crabronidae)
FIGURES 47–49. Pison angulare Pulawski, sp. nov., male. (47) Sternum VIII (ventral surface); (48) Genitalia in dorsal view; (49) Genitalia in lateral view. FIGURE 50. Collecting localities of Pison angulare Pulawski, sp. nov.
FIGURE 1 in Morphological and molecular diversity of rissoellids (Mollusca, Gastropoda, Heterobranchia) from the Northwest Pacific island of Hokkaido, Japan
FIGURE 1. Sampling sites in Hokkaido island, Japan.
FIGURE 14 in Indo-West Pacific species of Trachinotus with spots on their sides as adults, with description of a new species endemic to the Marquesas Islands (Teleostei: Carangidae)
FIGURE 14. Original drawing of Russell's (1803) "botla parah," plate 142
FIGURE 12. Trachinotus botla, ANSP 148732, 343 in Indo-West Pacific species of Trachinotus with spots on their sides as adults, with description of a new species endemic to the Marquesas Islands (Teleostei: Carangidae)
FIGURE 12. Trachinotus botla, ANSP 148732, 343 mm FL, Sri Lanka. Drawn by Tracy D. Pedersen.
FIGURE 1 in A new species of Proterhinus Sharp, 1878 (Coleoptera: Curculionoidea: Belidae) from Miti'aro, Cook Islands, South Pacific
FIGURE 1. Distribution of known Proterhinus species
Fig. 2 in First Records and Community Pattern of Arcellinida Inhabiting a Pristine and Remote Island from Southeastern Pacific, Chile
Fig. 2. Both images correspond to the northeastern side of the Guamblin Island ('closest' area to mainland). These images are useful to show the contrasting nature of the two types of sampled environments (treeless and forested environments). A – this photo corresponds to the sampled coastal swamp, which is located in sector Punta Piedra (see Fig. 1). This environment is dominated by Gunnera spp. and Juncus sp.; B – this photo corresponds to sector Punta Arena (see Fig. 1), and was taken from an elevation of 150 m a.s.l. In the foreground are some ferns (Lomatia ferruginea) and trees (Nothofagus spp., Amomyrtus luma and Maytenus boaria). In the background is the North Patagonian rain forest (which is mainly dominated by Nothofagus spp.) and towards the end the Southeastern Pacific. Photo credits by J. Pérez.
Fig. 1 in First Records and Community Pattern of Arcellinida Inhabiting a Pristine and Remote Island from Southeastern Pacific, Chile
Fig. 1. Map of the Guamblin Island National Park. Samples were taken at equidistant distances, ranging from sector Punta Piedra (sampling site number 1) to sector Punta Arena (sampling site number 15).
Fig. 4 in First Records and Community Pattern of Arcellinida Inhabiting a Pristine and Remote Island from Southeastern Pacific, Chile
Fig. 4. Species-accumulation curve for testate amoebae collected in the Guamblin Island. Our observed number of species was 33 (black horizontal line). This value was consistent with the estimate species richness curve based on Chao1 (black irregular line). Upper and lower confidence intervals are shown as gray dotted lines (calculated using 1,000 permutations without replacement).
Figure 2 A–C in Host Plant Records for Fruit Flies (Diptera: Tephritidae: Dacini) in the Pacific Islands: 2. Infestation Statistics on Economic Hosts
Figure 2 A–C. Mean number of flies emerged per kg fruit and percent samples infested for the most infested hosts for mango fly (Bactrocera frauenfeldi) (A), B. kirki (B), and B. passiflorae (C).
Figure 1 A–C in Host Plant Records for Fruit Flies (Diptera: Tephritidae: Dacini) in the Pacific Islands: 2. Infestation Statistics on Economic Hosts
Figure 1 A–C. Mean number of flies emerged per kg fruit and percent samples infested for the most infested hosts for oriental fruit fly (Bactrocera dorsalis) (A), Queensland fruit fly (B. tryoni) (B), and melon fly (B. cucurbitae) (C).
Pacific Atoll Island Change Dataset
Open the record for dataset details and reuse information.
FIGURE 1 in New and rare bivalve species for the fauna of the Kuril Islands (northwestern Pacific Ocean): A study of materials collected over 70 years of expeditions (from 1949 to 2019)
FIGURE 1. Map of the study area.
Phylogeography of Meimuna cicadas on continental and oceanic islands of Japan in the north-western Pacific region
<p><span><span><span><span><span><span><span><span><span><span><span>Islands are a challenging habitat for organisms with weak dispersal power. We aimed to elucidate how geological history, geography, accidental dispersal events and species ecology affected different colonisation and genetic divergence patterns on continental and oceanic islands among species of a cicada group, which are poor dispersers.</span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span><b>Location: </b>Japanese Archipelago, Ogasawara Islands, Ryukyu Archipelago.</span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span><b>Taxon:</b> Cicadas of the genus <i>Meimuna </i>(Hemiptera: Cicadidae).</span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span>We performed phylogenetic analysis, divergence time estimation, and ancestral area reconstruction using two mitochondrial and four nuclear gene sequences and population genetics analyses, including Bayesian skyline plotting using a mitochondrial gene sequence. </span></span></span></span></span></span></span></span></span></span></span><span><span><span><span><span><span><span><span><span><span><span><i>Meimuna opalifera</i> in the Japanese Archipelago, which was connected to the continent during the glacial periods, diverged from the continental populations 0.4 million years ago (Ma). In the Ryukyu Archipelago, which became disconnected from the continent earlier, two endemic species <i>M. kuroiwae</i> and <i>M. oshimensis</i> diverged 2.5 Ma; these species showed differences in intraspecific genetic differentiation and range expansion. Furthermore, <i>M. iwasakii</i>colonised the South Ryukyus from Taiwan Island later than 1.4 Ma, whereas<i> M. boninensis</i>, which is endemic to the oceanic Ogasawara Islands, diverged from <i>M. kuroiwae</i> in the Middle Ryukyus 1.4 Ma. </span></span></span></span></span></span></span></span></span></span></span><span><span><span><span><span><span><span><span><span><span><span>Genetic divergence among <i>Meimuna</i> species was larger on the continental islands that disconnected earlier, as was expected from the geological history of the islands. However, the pattern of intraspecific genetic differentiation differed between species within the same island region, possibly due to their ecological characteristics. In addition, colonisation of oceanic islands was achieved by long-distance (possibly wind-borne) dispersal from the continental islands. Thus, the formation of island cicada fauna was affected by islands' geological history and species' ecological characteristics, as well as accidental long-distance dispersal events. </span></span></span></span></span></span></span></span></span></span></span></p>
Fig. 3 in A New Species of Bush-Warbler from Bougainville Island and a Monophyletic Origin for Southwest Pacific Cettia
Fig. 3. Scatterplot of Cettia species and subspecies on the first two principal components derived from analysis of species means for six external measurements (tables 1, 2, and 3).
Figure 10 in Morphological and molecular description of new species of squat lobster (Crustacea: Decapoda: Galatheidae) from the Solomon and Fiji Islands (South-West Pacific)
Figure 10. Neighbour-joining (NJ) tree based on the combined data set (16S rRNA and COI genes), showing phylogenetic relationships between Paramunida and Plesionida. Numbers above branches indicate bootstrap values for the NJ and maximum parsimony (MP) analyses. Numbers below branches indicate bootstrap values for the maximum likelihood (ML) analyses and Bayesian posterior probabilities (BPPs).
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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
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.