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Figure 2 in Reproductive phenology and pre-dispersal seed-feeding in Protium tovarense (Burseraceae), with a description of the first known phytophagous ''Bracon'' species (Hymenoptera: Braconidae: Braconinae)
Figure 2. Short-term flowering and fruiting phenology of Protium tovarense including phenophase occurrence (a) and intensity (b). See text for explanation.
Figure 7 in Reproductive phenology and pre-dispersal seed-feeding in Protium tovarense (Burseraceae), with a description of the first known phytophagous ''Bracon'' species (Hymenoptera: Braconidae: Braconinae)
Figure 7. Features of final instar larva of Bracon phytophagus sp. n. taken from chill-killed specimens. (a) Frontal view of head capsule showing large, multi-toothed, heavily sclerotized mandibles; (b) oblique view of head showing (arrowed) the small papilliform antenna; (c) lateral view of mature larva showing large humps on abdominal segments 2–7.
Figure 6 in Reproductive phenology and pre-dispersal seed-feeding in Protium tovarense (Burseraceae), with a description of the first known phytophagous ''Bracon'' species (Hymenoptera: Braconidae: Braconinae)
Figure 6. Habitus and features of the metasoma of males of Bracon phytophagus sp. n. illustrated using Automontageẹ. (a, c) Dark morph; (b, d) yellow form.
Figure 1 in Reproductive phenology and pre-dispersal seed-feeding in Protium tovarense (Burseraceae), with a description of the first known phytophagous ''Bracon'' species (Hymenoptera: Braconidae: Braconinae)
Figure 1. Long-term flowering and fruiting phenology of Protium tovarense in northern Venezuela, including periodicity of El Niño and La Niña events.
Figure 8 in Reproductive phenology and pre-dispersal seed-feeding in Protium tovarense (Burseraceae), with a description of the first known phytophagous ''Bracon'' species (Hymenoptera: Braconidae: Braconinae)
Figure 8. Prepupa, pupa, and traces of silk in pupation chamber of Bracon phytophagus sp. n. (a, b) Prepupa, in lateral and ventral views, showing ''S''-shaped curvature and beginning of development of ovipositor structures posteriorly (lower left); (c) posterior of pupa in situ showing ovipositor with remains of larval skin (head capsule: arrowed) adhering to ovipositor; (d) frass from inside pupation hole with traces of thin silk-like material.
Figure 5 in Reproductive phenology and pre-dispersal seed-feeding in Protium tovarense (Burseraceae), with a description of the first known phytophagous ''Bracon'' species (Hymenoptera: Braconidae: Braconinae)
Figure 5. Habitus and details of claw and ovipositor of Bracon phytophagus sp. n., holotype female. (a) Habitus; (b) oblique ventral view of mid-telotarsus showing large basal lobe; (c) apex of ovipositor and ovipositor sheaths; (d) detail of apex of ovipositor showing extra serrations.
Figure 4 in Reproductive phenology and pre-dispersal seed-feeding in Protium tovarense (Burseraceae), with a description of the first known phytophagous ''Bracon'' species (Hymenoptera: Braconidae: Braconinae)
Figure 4. Fruit (volume), seed embryo (volume), and larval growth (length) in Protium tovarense from 1-monthold fruits until fruit ripening (a) and percentage of fruits infested during the same interval of time (b).
Figure 1 in The first substantiated case of trans-oceanic tortoise dispersal
Figure 1. The Aldabra tortoise at Kimbiji, shortly after its discovery in December 2004. Photograph: C. Muir.
Fig.1. Bipartite graph depicting a plant-animal mutualistic network involving 10 in The Role Of Macaca Spp. (Primates: Cercopithecidae) In Seed Dispersal Networks
Fig.1. Bipartite graph depicting a plant-animal mutualistic network involving 10 frugivores (left) and 170 of the plant species (right) they disperse at Khao Yai National Park, Thailand. The list of plant species is based on Kitamura et al. (2002), then the list of frugivores dispersing each species has been completed thanks to data from bin Kassim (1987), Kitamura et al. (2005), Datta & Rawat (2008), Brockelman (2009), McConkey & Brockelman (2011), Albert et al. (2013), Ngoprasert (2012), Khamcha (pers. comm.), Latinne (pers. comm.), Martmoon (pers. comm.).
Fig. 1 in Fig Wasp Dispersal In Urban Singapore
Fig. 1. Distribution of dioecious and monoecious pollinators between 25 m, 10 m, and 2 m trap heights.
Fig. 1 in Secondary removal of seeds dispersed by gibbons (Hylobates lar) in a tropical dry forest in Thailand
Fig. 1. Distribution of experimental sites where seeds were dispersed by 4 groups of white-handed gibbons (Hylobates lar). Home range maps of the gibbons are based on Light (2016) and Phiphatsuwannachai et al. (2018), plus newly-discovered areas (extended home ranges) by the author. Fruiting trees and gibbon defecation locations were recorded in a GPS. Each site when active contained a camera trap and a paired control/treatment.
Fig 2 in Secondary removal of seeds dispersed by gibbons (Hylobates lar) in a tropical dry forest in Thailand
Fig 2. Estimates of beta-coefficients from binomial regressions with parameter estimates derived from model averaging with 95% confidence intervals. A variable is considered significant if the confidence interval does not overlap zero.
FIG. 1. — Stiphodon mele n in Stiphodon mele n. sp., a new species of freshwater goby from Vanuatu and New Caledonia (Teleostei, Gobiidae, Sicydiinae), and comments about amphidromy and regional dispersion
FIG. 1. — Stiphodon mele n. sp., holotype ♂ 27.2 mm SL (MNHN 2008-1920), Efate, Mele waterfall, 22.VII.2002, Vanuatu, Keith and Keith coll. Photo: É. Vigneux.
Text-fig. 4. Known geographic distribution of Microtscoptini on a modern-day biome map (Arc-GIS feature TNC terrestrial ecoregions). 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole. 1–20, 30–32 – Steppe biomes, 21–29, 33 – xeric shrubland biomes. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 4. Known geographic distribution of Microtscoptini on a modern-day biome map (Arc-GIS feature TNC terrestrial ecoregions). 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole. 1–20, 30–32 – Steppe biomes, 21–29, 33 – xeric shrubland biomes.
Text-fig. 3 Comparison of various stratigraphic subdivisions: European (ELMA), North American (NALMA) (Hilgen et al. 2012) and Chinese (CLMA) (Qiu Zhanxiang et al. 2013, Qiu Zhuding et al. 2013) Land Mammal Ages and Eastern Paratethys stages. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 3 Comparison of various stratigraphic subdivisions: European (ELMA), North American (NALMA) (Hilgen et al. 2012) and Chinese (CLMA) (Qiu Zhanxiang et al. 2013, Qiu Zhuding et al. 2013) Land Mammal Ages and Eastern Paratethys stages.
Text-fig. 2. Stratigraphic ranges of Microtoscoptini-bearing sites. Correlation of ELMA and NALMA with earth years is according to Hilgen et al. (2012). Localities of very broad stratigraphic range (e.g., the entire Turolian or Hemphillian, as for Vasilivka 1, Lobkove, Little Valley, Cambridge), do not contribute to detail the range, and are omitted in this figure. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 2. Stratigraphic ranges of Microtoscoptini-bearing sites. Correlation of ELMA and NALMA with earth years is according to Hilgen et al. (2012). Localities of very broad stratigraphic range (e.g., the entire Turolian or Hemphillian, as for Vasilivka 1, Lobkove, Little Valley, Cambridge), do not contribute to detail the range, and are omitted in this figure.
Text-fig. 1. Known geographic distribution of Microtoscoptini. 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 1. Known geographic distribution of Microtoscoptini. 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole.
Text-fig. 6. a. Vertical section showing part of body-chamber of a Cenoceras in the top of the Main Cenoceras Bed associated with attached oysters below and stringers of crinoid debris below and stretching laterally. Coin 23 mm in diameter. b. Complete lateral half of conch showing intact and elastically deformed septa on which rests crinoid debris that spreads across the exposed septa and onto the adjacent substrate. Conch approximately 180 mm in diameter. c. Individual showing dispersed crinoid and molluscan debris within body-chamber and septa in the crushed inner whorls that have taken a sparite cement prior to, and after having undergone brittle deformation. 160 mm in diameter. d. Vertically embedded specimen showing the loss of septa in the inner whorls that are infilled with matrix mottled by bioturbation. Tape measure provides scale. in 'Cenoceras Islands' In The Blue Lias Formation (Lower Jurassic) Of West Somerset, Uk: Nautilid Dominance And Influence On Benthic Faunas
Text-fig. 6. a. Vertical section showing part of body-chamber of a Cenoceras in the top of the Main Cenoceras Bed associated with attached oysters below and stringers of crinoid debris below and stretching laterally. Coin 23 mm in diameter. b. Complete lateral half of conch showing intact and elastically deformed septa on which rests crinoid debris that spreads across the exposed septa and onto the adjacent substrate. Conch approximately 180 mm in diameter. c. Individual showing dispersed crinoid and molluscan debris within body-chamber and septa in the crushed inner whorls that have taken a sparite cement prior to, and after having undergone brittle deformation. 160 mm in diameter. d. Vertically embedded specimen showing the loss of septa in the inner whorls that are infilled with matrix mottled by bioturbation. Tape measure provides scale.
Figure 8 in First European evidence for transcontinental dispersal of Crocodylus (late Neogene of southern Italy)
Figure 8. Osteoderms in dorsal (A, B, D) and lateral (C) views. A, RGM 454946; B, RGM 453781; C, RGM 454947; D, RGM 454948. Scale bar equals 10 mm.
Figure 9 in First European evidence for transcontinental dispersal of Crocodylus (late Neogene of southern Italy)
Figure 9. Late Miocene crocodylian localities in the Mediterranean area. Black dots, early Tortonian localities with tomistomine fossils; open circles, Tortonian and Messinian localities with crocodylians of unresolved phylogenetic relationships; black square, Gargano fossil locality with Crocodylus sp. (Miocene–Pliocene transition); open square, Sahabi fossil locality with Crocodylus checchiai (Late Neogene – Miocene–Pliocene transition?). Data from Böhme & Ilg (2003).
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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)
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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.