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FIG. 2 in On the last occurrence of Marginella Lamarck, 1799 (Gastropoda, Marginellidae) in the Mediterranean: description of a new species from the Early Pleistocene and paleoceanographic implications
FIG. 2. — Sample of 36 shells used for morphometry and shape analysis, with identification number. Scale bar: 5 mm.
FIG. 1. — A in On the last occurrence of Marginella Lamarck, 1799 (Gastropoda, Marginellidae) in the Mediterranean: description of a new species from the Early Pleistocene and paleoceanographic implications
FIG. 1. — A, Map of the Messina Strait; B, location of the outcrop; C, schematic stratigraphy of the outcrop (asterisk indicates the sampled bed). Abbreviations:see text.
Evaluation of the shucking of certain species of scallops contaminated with domoic acid with a view to the production of edible parts meeting the safety requirements foreseen in the Union legislation - Summary statistics on occurrence and consumption data and exposure assessment results
<p>DomoicAcid_Raw_Occurrence_Data.CSV contains the raw occurrence dataset on Domoic Acid contaminant in scallops as extracted from EFSA DWH on the 9 June 2020, 16,369 samples presented in the opinion as described in its section 1.3.2. Occurrence data submitted to EFSA. The data is provided in .csv format. This dataset is compliant with EFSA SSD model and contains two additional columns documenting issues identified in the cleaning process (column: issue) and the action taken (column: outcome) to address the issue (e.g. delete record or update values in specific fields).</p> <p>The link to the catalogues of controlled terminologies can be found under "Related identifiers”.</p> <p><strong>Annex_</strong> DomoicAcid</p> <p>Table of contents</p> <p><br> Table A1</p> <p>Description of FoodEx2 codes used to describe scallop species and their anatomical parts</p> <p>Table A2</p> <p>Data cleaning steps applied to occurrence data on domoic acid in scallops</p> <p>Table A3</p> <p>Percentage of Left-Censored data and descriptive statistics for Limits of detection (LODs) and Limits of quantification (LOQs) for domoic acid in scallops (mg/kg)</p> <p>Table A4</p> <p>Descriptive statistics for domoic acid in scallops (mg/kg) as reported in the cleaned database (statistics weighted by number of units per sample)</p> <p>Table A5</p> <p>Descriptive statistics of body tissue weights (g) of scallops as submitted by data providers</p>
Figure 2 in The occurrence and phylogenetic implications of the ovipositor clip within the Figitidae (Insecta: Hymenoptera: Cynipoidea)
Figure 2. Electron micrographs of the ovipositor clip of Trybliographa (Eucoilinae). (A) Overview, ventral side; (B) enlargment of boxed area in (A). 2vlv, second valvulae; L, lobe; LL, lateral lip; Se, sensillae; T, teeth. Scale bar: 10 Mm.
Figure 5 in The occurrence and phylogenetic implications of the ovipositor clip within the Figitidae (Insecta: Hymenoptera: Cynipoidea)
Figure 5. Examples of the ovipositor clip within Eucoilinae. (A) Aganaspis daci (Weld); (B) Leptopilina; (C) Dieucoila; (D) Nordlandiella; (E) ''Eucoila'' impatiens Say; (F) Odontosema anastrephae Kieffer; (G) Ganaspis mundata Foerster; (H) Triplasta; (I) Glauraspidia; (J) Trybliographa; (K) Kleidotoma; (L) Aporeucoela. 2 vlv, fused ovipositor valve.
Figure 1 in The occurrence and phylogenetic implications of the ovipositor clip within the Figitidae (Insecta: Hymenoptera: Cynipoidea)
Figure 1. Electron micrographs of the ovipositor clip of Neralsia (Figitinae). (A) Overview of ovipositor tip, lateral side; (B) enlargement of boxed area in (A). 1vlv, first valvulae; 2vlv, second valvulae; L, lobe; S, slot, Ser, apical serration. Scale bar: 10 Mm.
Figure 4 in The occurrence and phylogenetic implications of the ovipositor clip within the Figitidae (Insecta: Hymenoptera: Cynipoidea)
Figure 4. Examples of the ovipositor clip present within Figitinae. (A) Neralsia; (B) Amphithectus; (C) Trischiza; (D) Xyalophora. The viewing angle in (B) is dorsal and not lateral; the asterisk and lines are meant to delineate the extent of the clip. 2 vlv, fused ovipositor valve.
Figure 7 in The occurrence and phylogenetic implications of the ovipositor clip within the Figitidae (Insecta: Hymenoptera: Cynipoidea)
Figure 7. Presence of the ovipositor clip mapped on to two possible cladograms for relationships of Figitidae (from Buffington et al. forthcoming). (A) Parsimony analysis; (B) Bayesian analysis. Numbers next to terminal names indicate the number of taxa sampled. Letters in boxes at tree tips refer to niche type in which the host is attacked: C, concealed; S, semi-concealed; E, exposed; G, gall inducer/inquilline;?, unknown. Black bars indicate clades for which all members possess the ovipositor clip. ''+ACC'' indicates presence of character based on ACCTRAN optimization; ''+ DEL'' indicates presence of character based on DELTRAN optimization (Swofford and Maddison 1987).
Figure 3 in The occurrence and phylogenetic implications of the ovipositor clip within the Figitidae (Insecta: Hymenoptera: Cynipoidea)
Figure 3. Examples of Figitidae that lack the ovipositor clip. (A–C) Anacharitinae: (A) Aegilips, (B) Xyalaspis, (C) Anacharis; (D, E) Aspicerinae: (D) Melanips; (E) Callaspidea; (F) Charipinae (Alloxysta); (G) Emargininae (Thoreauella); (H) Thrasorinae (Euceroptres). 2 vlv, fused ovipositor valve.
Fig. 19 in Confirmed occurrence of Hydroscapha granulum in Iran, with notes on its biology (Coleoptera: Myxophaga: Hydroscaphidae)
Fig. 19. Known distribution of West-Palaearctic Hydroscapha derived from the published data (see the text for details). Asian records are mapped by full circles, Spanish record of H. granulum (Motschulsky, 1855) by JÄCH et al. (1999) by an empty circle. Species whose synonymy with H. granulum requires revision are mapped in dotted line.
Figs. 1–9 in Confirmed occurrence of Hydroscapha granulum in Iran, with notes on its biology (Coleoptera: Myxophaga: Hydroscaphidae)
Figs. 1–9. Iranian specimens of Hydroscapha granulum (Motschulsky, 1855) and their typical habitat. 1 – egg size in comparison to female beetle (locality no. 6); 2 – air bubble under elytra; 3 – typical habitat of the species (rocks covered by algae, locality no. 12); 4–6 – mites (possibly parasitic) infecting Hydroscapha adults at localities 6 and 12 (4, 5 – mites on abdominal tergites; 6 – microscopic slide of the mite, scale bar 0.1 mm); 7–9 – habitus of different larval instars.
Fig. 1. Occurrence points for 12 in Projected Climate Change Effects On Nuthatch Distribution And Diversity Across Asia
Fig. 1. Occurrence points for 12 Sitta species and one Tichodroma species used in this study. Sitta solangiae and S. victoriae each had fewer than 5 occurrence points and were excluded from the analysis.
Fig. 1 in Co-occurrence of two sympatric galliform species on a landscape-scale
Fig. 1. Map of Cat Tien NP with five survey transects each in bamboo, mixed deciduous, and mosaic forests, and seven transects in evergreen forest.
Fig. 1 in Pattern of co-occurrence between ant-mimicking jumping spiders and sympatric ants in a Bornean tropical rainforest
Fig. 1. Dorsal views of the model ants and their ant-mimicking spiders, showing the body parts removed legs and antennae. A, Camponotus saundersi; B, Myrmarachne alticephalon; C, Polyrhachis olybia; D, Myrmarachne maxillosa; E, Polyrhachis boltoni; F, Polyrhachis phalerata; G. Myrmarachne malayana.
Figure 1-4. Megacopta cribraria. 1 in Occurrence of the Old World bug Megacopta cribraria (Fabricius) (Heteroptera: Plataspidae) in Georgia: a serious home invader and potential legume pest
Figure 1-4. Megacopta cribraria. 1) Male, dorsal view. 2) Female, ventral view. 3) Male, ventral view. 4) Fifth instar nymph, dorsal view. Dimensional line equals 1.0 mm.
Figure 2 in A brief on the current occurrence of Gorsachius spp. in mainland China
Figure 2. Sketch map of occurrence of the Japanese Night Heron in mainland China. Localities on the map presented in black letters are to follow Threatened Birds of Asia (BirdLife, 2001) but remaining the ones at the county and/or city level; whilst, those localities presented in red letters are the newly reported ones since 2006. Abbreviation. AM/XM, Amoy/Xiamen; BBB, Beibu Bay [Tonkin Gulf]; BJ, Beijing; BH, Beihai; DD, Dandong; FCh, Fangcheng; FZh, Fuzhou; GL, Guilin; HK/HK, Hong Kong; HP, Hepu; HT, Haitan Is.; HX, Hengxian; HY, Haiyan; HZh, Hangzhou; LSh, Lishui; NB, Ningbo; NP, Nanping; NT, Nantong; QZh, Qinzhou; RD, Rudong; ShH, Shanghai; SWS, Shaweishan; WY, Wuyuan; WZh, Wenzhou.
Figure 3 in A brief on the current occurrence of Gorsachius spp. in mainland China
Figure 3. Sketch map of occurrence of the Malay Night Heron in mainland China. Localities on the map presented in black letters are to follow Yang et al. (1995) and Zhou et al. (2011), whilst, those localities presented in red letters are either the newly reported site or the sites surely with recent records since 2008. Abbreviation. ChZ, Chongzuo; DaX, Daxing; DX, Dongxing; FCh, Fangcheng; FS, Fusui; HP, Hepu; JX, Jinxiu; L'An, Long'an; LZh, Longzhou; ML, Mengla; NN, Nanning; NM, Ningming; QZh, Qinzhou; ShS, Shangsi; ShZ, Shenzhen.
Figure 1 in A brief on the current occurrence of Gorsachius spp. in mainland China
Figure 1. Sketch map of occurrence of the White-eared Night Heron. Localities on the map presented in numerals are to follow Threatened Birds of Asia (BirdLife, 2001) but for those localities in Guangxi only the ones at the county level remained; whilst, those localities presented in letters are either the newly found ones or the historical ones but newly annotated (He et al, 2007a, b, 2011, 2014a); and those letters in red color are to illustrate the localities reported since 2008. Abbreviation. BH, Beihai; BHL, Baihualing; BK, Baokang; BS, Baise; B&X, Ban Thi & Xuan Lac (Vietnam); Ch'An, Chun'an; DCh, Duchang; DJK, Danjiangkou; DX, Dongxing; GT, Gutian; GY, Guangyuan; GZ, Guangze; HH, Huaihua; HSh, Huangshan; HX, Hengxian; HZh, Hezhou; J'An, Jing'an; JD, Jingde; JGSh, Jinggangshan; LL, Lung`(Vietnam); LM, Longmen; LN, Longnan; LS, Leishan; LSh, Lushan; LuZ, Luzhai; LY, Liuyang; LZh, Liuzhou; MShH, Manshuihe; NJ, Nanjian; PJ, Pingjiang; PT, Putian; R'An, Rong'An; RY, Ruyuan; SCh, Suichuan; TD, Tongdao; TN, Taining; WCh, Wuchuan; WF, Wufeng; WN, Wuning; WX, Wuxuan; WeiY, Weiyuan; WY, Wuyuan; XCh, Xuancheng; XH, Xinhua; XP, Xinpin; XSh, Xiushui; XY, Xinyu; YN, Yongning; Ysh, Yushan; ZhF, Zhongfang.
Text-fig. 6. Distribution of Oligocene continental sediments of Africa, revealing the patchy and incomplete coverage of the occurrences. The Tunisian sedimentary outcrops represent an important resource for the north-western part of the continent. in Arsinoitherium (Embrithopoda) And Other Large Mammals And Plants From The Oligocene Of Tunisia
Text-fig. 6. Distribution of Oligocene continental sediments of Africa, revealing the patchy and incomplete coverage of the occurrences. The Tunisian sedimentary outcrops represent an important resource for the north-western part of the continent.
FIG. 1 in The first Old World occurrence of the North American mustelid (Mammalia, Carnivora)
FIG. 1. — Locality map of Sthenictis neimengguensis n. sp. (IVPP V15873) and known occurrences of the genus Sthenictis Peterson, 1910 in North America: ☆, locations of holotype specimens of species of Sthenictis; ◯, localities of specimens referred to the genus; Ð, locality of occurrence in Inner Mongolia; 1, Mandelin Chabu; 2, Aoershun Chaba; 3, Zhunwuguer; 4, Moergen loc; 5, Platybelodon Quarry; 6, Wolf Camp; 7, 346 locality; 8, Aletexire loc; 9, Huerguolajin loc; 10, PM-08 loc; 11, South Camp.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.