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Figure 6 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 6. Behavioural activities recorded for sub adult female vs. total time spent during different season(s).
Figure 3 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 3. Behavioural activities recorded for adult male vs. total time spent during different season(s).
Figure 4 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 4. Behavioural activities recorded for adult female vs. total time spent during different season(s).
Figure 8 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 8. Average % time spent annually versus activities by different age sex group (Error bars with standard error and treatment bars with different letters differ significantly at P ≤ 0.05 based on Duncan Multiple Range Test).
Figure 7 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 7. Major behavioural activities vs. total time spent on each activity by different age-sex animal.
Text-fig. 5. Distribution of age classes of deningeri bears from Middle Pleistocene deposits from Za Hájovnou Cave (Moravia, the Czech Republic) based on wear stage of M2 dext. and m2 dext. (I–III: juveniles, IV–VII: prime adults, VIII–IX: senile adults; according to Stiner 1998). Juveniles distinctly outnumber adults. in Basic Population And Taphonomic Analysis Of Bear Assemblages From Za Hájovnou Cave (Moravia, The Czech Republic): A Fossil Record From 1987-2007
Text-fig. 5. Distribution of age classes of deningeri bears from Middle Pleistocene deposits from Za Hájovnou Cave (Moravia, the Czech Republic) based on wear stage of M2 dext. and m2 dext. (I–III: juveniles, IV–VII: prime adults, VIII–IX: senile adults; according to Stiner 1998). Juveniles distinctly outnumber adults.
Text-fig. 1: Distribution of Cenozoic volcanites (gray shaded areas) along the Ohře/Eger rift and the position of localities with Protothymallus elongatus (KRAMBERGER, 1885) including their K-Ar ages (from Bellon et al. 1998). in Revision Of The Cyprinids From The Early Oligocene Of The České Středohoří Mountains, And The Phylogenetic Relationships Of Protothymallus Laube, 1901 (Teleostei, Cyprinidae, Gobioninae)
Text-fig. 1: Distribution of Cenozoic volcanites (gray shaded areas) along the Ohře/Eger rift and the position of localities with Protothymallus elongatus (KRAMBERGER, 1885) including their K-Ar ages (from Bellon et al. 1998).
Figure 1 in Age structure of Hemidactylus turcicus (L., 1758) (Sauria: Gekkonidae) from southwestern Anatolia (Muğla, Turkey)
Figure 1. Cross-sections of the femur diaphysis: a) 1-year-old juvenile; b) 4-year-old female; c) 5-year-old male; d) 6-year-old male; e) 7-year-old female; f) 9-year-old female. mc: medullar cavity, eb: endosteal bone, O: double LAG,: LAG.
Figure 1 in The first record of age structure and body size of the Suphan Racerunner, Eremias suphani Başoğlu & Hellmich, 1968
Figure 1. Cross-section (18 µm thick) at the diaphysis level of a phalanx of male E. suphani, 60.52 mm SVL, 7 years old. Six LAGs were observed in the periosteal bone. The first LAG was destroyed by endosteal resorption and endosteal bone was present. Periphery was not regarded as a LAG. Arrows indicate endosteal resorption and periphery, and arrowheads indicate LAGs. e.b. = endosteal bone, m.c. = marrow cavity, r.l. = reversal line, p = periphery.
Figure 2 in Body size and age in three populations of the northern banded newt Ommatotriton ophryticus (Berthold, 1846) from Turkey
Figure 2. Cross-sections through phalanges of O. ophryticus. A) An 8-year-old female from Bahçesultan. Each LAG corresponds to a year. B) An 8-year-old female from Tosya. The first LAG was destroyed by endosteal resorption. Periphery was not regarded as a LAG. Arrowheads show the LAGs and red arrow shows the false LAG (e.b. = endosteal bone, e.r. = endosteal resorption, k.l. = Kastschenko line, m.c. = marrow cavity, p. = periphery).
Figure 1. A in Preliminary data on the age structure of Asaccus barani (Baran's leaf-toed gecko) from southeastern Anatolia, Turkey
Figure 1. A cross-section (17 µm thick) of the femur bone of a 5-year-old Asaccus barani individual (m.c. = marrow cavity, p. = periosteal bone). The 5 LAGs are indicated by black arrows. A double LAG is highlighted by red arrow.
Figure 3 in Impact of dike age on biodiversity and functional composition of soil macrofaunal communities in poplar forests in a reclaimed coastal area
Figure 3. PCoA ordinal configuration of soil macrofaunal communities from different habitats by Euclidean distance similarity index. In the code of the samples, the prefix means the code of the habitat, and the suffix means the number of the sample.
Figure 2 in Impact of dike age on biodiversity and functional composition of soil macrofaunal communities in poplar forests in a reclaimed coastal area
Figure 2. One-way ANOVA of taxonomic richness and abundance (A) and Margalef 's richness index R and Shannon– Weaver diversity index H' (B) across different habitats (mean ± SE). Means with different scripts are significantly different by Dunnett's T3 test (A) and LSD test (B), α = 0.05.
Figure. Age-specific survival rate (lx) and natality (m x) of Axinoscymnus apioides at different temperatures (20 °C, 23 °C, 26 °C, 29 °C, and 32 °C). in Temperature influences the development, survival, and life history of Axinoscymnus apioides Kuznetsov & Ren (Coleoptera: Coccinellidae), a predator of whitefly
Figure. Age-specific survival rate (lx) and natality (m x) of Axinoscymnus apioides at different temperatures (20 °C, 23 °C, 26 °C, 29 °C, and 32 °C).
Fig. 3 in The trade-off between the transmission of chemical cues and parasites: behavioral interactions between leaf-cutting ant workers of different age classes
Fig. 3. Mean ± s.e. frequencies that young and old ants were observed giving or receiving allogrooming during a 15 s observation period.
Fig. 2 in The trade-off between the transmission of chemical cues and parasites: behavioral interactions between leaf-cutting ant workers of different age classes
Fig. 2. Mean ± s.e. frequencies that young and old ants were: (a) observed selfgrooming and (b) observed engaged in mandible scraping with another ant, during a 15 s observation period.
Fig. 1 in The trade-off between the transmission of chemical cues and parasites: behavioral interactions between leaf-cutting ant workers of different age classes
Fig. 1. Overall activity levels. Mean ± s.e. frequencies that young and old ants were: (a) observed engaging in one of the focal behaviors and (b) observed engaged in antennation with another ant, during a 15 s observation period.
Figure 3 in Spalax denizliensis sp. nov. (Spalacidae, Rodentia) from an Early Pleistocene-aged locality in the Denizli Basin (southwestern Turkey)
Figure 3. Occlusal views of Spalax denizliensis sp. nov. from Gökpınar (GOP): A) left M1 (GOP-7001); B) left M2 (GOP- 6002); C) right m1 (GOP-7003); D) left m1 (GOP-7004); E) right m2 (GOP-7005); F) right m3 (GOP-7007).
Figure 4 in Spalax denizliensis sp. nov. (Spalacidae, Rodentia) from an Early Pleistocene-aged locality in the Denizli Basin (southwestern Turkey)
Figure 4. Comparison of the upper and lower molars of Spalax denizliensis sp. nov. with Spalax odessanus. The length of teeth has been made the same in order to facilitate morphological comparison and to draw attention to differences in shape. Illustrations used in the chart are from: A) Spalax denizliensis sp. nov. (M1, M2), B) Spalax odessanus (M1, M2) (Topachevski, 1969, fig. 2), C) Spalax denizliensis sp. nov. (m1–m3), Spalax odessanus (m1–m3) (Topachevski, 1969, fig. 2).
Figure 1. A in Spalax denizliensis sp. nov. (Spalacidae, Rodentia) from an Early Pleistocene-aged locality in the Denizli Basin (southwestern Turkey)
Figure 1. A) Gökpınar location of the Denizli Basin in western Turkey (modified from Bozkurt, 2003); B) geological map of the Denizli Basin modified from Erten (2017) with the position of Gökpınar locality.
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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.