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Fig. 6 in Tolerance to Anhydrobiotic Conditions Among Two Coexisting Tardigrade Species Differing in Life Strategies.
Fig. 6. Relation of the measured activity indices to time spent in the tun stage in Milnesium inceptum: (A) time to first movement of any first individual (FM); (B) time to first movement of all individuals (FAA); (C) time to full activity of any first individual (FA); (D) time to full activity of all individuals (FAA). Curves were ± SE fitted with Local Polynomial Regression Fitting (LOESS).
Fig. 5 in Tolerance to Anhydrobiotic Conditions Among Two Coexisting Tardigrade Species Differing in Life Strategies.
Fig. 5. Relationship between the measured activity indices and time spent during the tun stage for Ramazzottius subanomalus: (A) time to first movement of any first individuals (FM); (B) time to first movement of all individuals (FAA); (C) time to full activity of any first individual (FA); (D) time to full activity of all individuals (FAA). Curves ± SE were fitted with Local Polynomial Regression Fitting (LOESS).
Fig. 3. A in Tolerance to Anhydrobiotic Conditions Among Two Coexisting Tardigrade Species Differing in Life Strategies.
Fig. 3. A time from the start of rehydration to the first movement (FM) of any first individual and all individuals (FMA) in the experimental groups representing increasing duration of the tun stage for Milnesium inceptum (A, C) and Ramazzottius subanomalus (B, D). The number of replicate samples for each group n = 10.
Fig. 4. A in Tolerance to Anhydrobiotic Conditions Among Two Coexisting Tardigrade Species Differing in Life Strategies.
Fig. 4. A time from the start of rehydration to the full activity (FA) of any first individual and all individuals (FAA) in the experimental groups representing increasing duration of the tun stage for Milnesium inceptum (A, C) and Ramazzottius subanomalus (B, D). The number of replicate samples for each group n = 10.
Fig. 2 in Tolerance to Anhydrobiotic Conditions Among Two Coexisting Tardigrade Species Differing in Life Strategies.
Fig. 2. Differences in the number of non-moving (NM) and not fully active (NFA) individuals between experimental groups representing increasing duration of the tun stage for Milnesium inceptum (A, C) and Ramazzottius subanomalus (B, D). The number of replicate samples for each group n = 10.
Fig. 3 in Notes on the Genus Mamaev (Diptera: Cecidomyiidae) with Description of Two New Species from China.
Fig. 3. Brachyneurina rhombica sp. nov. Male holotype (NKUCecid. No. BBL001) (A-C): (A), Genitalia (dorsal view, cerci and hypoproct removed). (B), Genitalia (dorsal view). (C), cerci and hypoproct (dorsal view).
Fig. 1 in Notes on the Genus Mamaev (Diptera: Cecidomyiidae) with Description of Two New Species from China.
Fig. 1. Brachyneurina hemisphaerica sp. nov. Male holotype (NKUCecid. No. BBI001) (A-C): (A), 3rd flagellomere (dorsal view). (B), Wing (dorsal view). (C), Fore acropod (lateral view).
Fig. 2 in Notes on the Genus Mamaev (Diptera: Cecidomyiidae) with Description of Two New Species from China.
Fig. 2. Brachyneurina hemisphaerica sp. nov. Male holotype (NKUCecid. No. BBI001) (A-C): (A), Genitalia (dorsal view, cerci and hypoproct removed). (B), Genitalia (dorsal view). (C), cerci and hypoproct (dorsal view).
Fig. 4 in Fig. 17. Periclimenaeus djiboutensis Bruce, 1970, ovigerous female specimen pocl 3.7 in Two New Species and a Further Country Record of the Caridean Shrimp Genus Borradaile, 1915 from Korea (Decapoda: Palaemonidae).
Fig. 4. Distribution of the Olpiidae, Cheiridiidae, Atemnidae, Garypinidae, Geogarypidae, Cheliferidae, Chernetidae and Withiidae taxa in Albania. A, Amblyolpium dollfusi (purple colour), Apocheiridium ferum (grey colour), Atemnus syriacus (red colour), Calocheiridius libanoticus (blue colour), Geogarypus italicus (green colour), Geogarypus minor (orange colour), Withius piger (yellow colour). B, Beierochelifer peloponnesiacus (blue colour), Chelifer cancroides (red colour), Dactylochelifer latreillii (yellow colour), Hysterochelifer meridianus (green colour). C, Hysterochelifer cyprius (green colour), Rhacochelifer maculatus (yellow colour), Rhacochelifer peculiaris (red colour). D, Dendrochernes cyrneus (yellow colour), Dinocheirus panzeri (orange colour), Lamprochernes chyzeri (green colour), Lamprochernes nodosus (grey colour), Lasiochernes graecus (purple colour), Pselaphochernes lacertosus (red colour), Pselaphochernes scorpioides (blue colour). Circles indicate the published data, stars indicate the new data. For the locality codes, see table 1.
Fig. 2 in Fig. 17. Periclimenaeus djiboutensis Bruce, 1970, ovigerous female specimen pocl 3.7 in Two New Species and a Further Country Record of the Caridean Shrimp Genus Borradaile, 1915 from Korea (Decapoda: Palaemonidae).
Fig. 2. Distribution of the Chthoniidae and Neobisiidae taxa in Albania. A, Chthonius gjirokastri (red colour), Chthonius jonicus (orange colour), Chthonius rhodochelatus (green colour), Chthonius tenuis (blue colour), Globochthonius argirocastronis (yellow colour). B, Ephippiochthonius rogoi (red colour), Ephippiochthonius serbicus (green colour), Ephippiochthonius tuberculatus (yellow colour). C, Neobisium albanicum (purple colour), Neobisium doderoi (orange colour), Neobisium georgecastriotae (yellow colour), Neobisium latellai (red colour), Neobisium sylvaticum (blue colour), Neobisium valsuanii (green colour), Neobisium cf. vjetrenicae (brown colour), Neobisium sp. 1 (grey colour). D, Neobisium cephalonicum (red colour), Neobisium fuscimanum (blue colour), Neobisium hellenum (grey colour), Neobisium sublaeve (orange colour), Neobisium sp. 2 (green colour), Roncus lonai (purple colour), Roncus lubricus (brown colour), Roncus spp. (yellow colour). Circles indicate the published data, stars indicate the new data. For the locality codes, see table 1.
Fig. 3. First pseudoscorpion records for Albania from the families Chthoniidae and Garypinidae. A in Fig. 17. Periclimenaeus djiboutensis Bruce, 1970, ovigerous female specimen pocl 3.7 in Two New Species and a Further Country Record of the Caridean Shrimp Genus Borradaile, 1915 from Korea (Decapoda: Palaemonidae).
Fig. 3. First pseudoscorpion records for Albania from the families Chthoniidae and Garypinidae. A, Chthonius jonicus (female). B, Chthonius rhodochelatus (female). C, Chthonius tenuis (male). D, Ephippiochthonius serbicus (female). E, Ephippiochthonius tuberculatus (female). F, Amblyolpium dollfusi (male). Scale bars = 1 mm.
Fig. 1 in Fig. 17. Periclimenaeus djiboutensis Bruce, 1970, ovigerous female specimen pocl 3.7 in Two New Species and a Further Country Record of the Caridean Shrimp Genus Borradaile, 1915 from Korea (Decapoda: Palaemonidae).
Fig. 1. Map of all studied localities in Albania. Red circles indicate the published data, yellow stars indicate the new data. For the locality codes, see table 1.
Fig. 5 in Fig. 17. Periclimenaeus djiboutensis Bruce, 1970, ovigerous female specimen pocl 3.7 in Two New Species and a Further Country Record of the Caridean Shrimp Genus Borradaile, 1915 from Korea (Decapoda: Palaemonidae).
Fig. 5. First pseudoscorpion records for Albania from the families Geogarypidae, Cheiridiidae, Atemnidae and Cheliferidae. A, Geogarypus italicus (female). B, Apocheiridium ferum (female). C, Atemnus syriacus (male). D, Beierochelifer peloponnesiacus (female). E, Hysterochelifer cyprius (female). F, Hysterochelifer meridianus (male). Scale bars = 1 mm.
Fig. 6 in Fig. 17. Periclimenaeus djiboutensis Bruce, 1970, ovigerous female specimen pocl 3.7 in Two New Species and a Further Country Record of the Caridean Shrimp Genus Borradaile, 1915 from Korea (Decapoda: Palaemonidae).
Fig. 6. First pseudoscorpion records for Albania from the families Cheliferidae, Chernetidae and Withiidae. A, Rhacochelifer peculiaris (male). B, Dinocheirus panzeri (male). C, Lamprochernes chyzeri (male). D, Withius piger (female). Scale bars = 1 mm.
Fig. 3 in Morphological Differentiation of the Skull in Two Closely-related Mustelid Species (Carnivora: Mustelidae)
Fig. 3. Projections specific (M. putorius and M. eversmanii) morphospace models on first two coordinates E1-E2 and K1-K2.
Fig. 2 in Morphological Differentiation of the Skull in Two Closely-related Mustelid Species (Carnivora: Mustelidae)
Fig. 2. NJ trees of skull measurements in M. putorius and M. eversmanii based on the absolute values of Spearman Rank Order Correlation coefficients from Tables 3-4.
Fig. 1 in Morphological Differentiation of the Skull in Two Closely-related Mustelid Species (Carnivora: Mustelidae)
Fig. 1. Two-species (M. putorius, M. eversmanii) morphospace models: (A) skull size morphospace based on NMDS axes E1, E2, and skull shape morphospace based on NMDS axes K1, K2; (B) three-dimensional joint 'size/shape' diversity morphospace based on principal components PC1-PC3.
Fig. 5 in Morphological Differentiation of the Skull in Two Closely-related Mustelid Species (Carnivora: Mustelidae)
Fig. 5. (A) Allometry of (CbL), the neurocranium length (NcL), the viscerocranium length (VcL) in M. putorius. (B-D) allometry of the postorbital width (PoW), width of auditory bulla (AbW) and the minimal palatal width (MpW) in M. putorius and M. eversmanii. First coordinate of the morphospaces (E1) is a general size factor of the skull.
Fig. 4 in Morphological Differentiation of the Skull in Two Closely-related Mustelid Species (Carnivora: Mustelidae)
Fig. 4. Scatterplots of PC1 vs. PC2 (A) and PC1 vs. PC3 (B) showing the relative positions of the European and steppe polecats and other mustelines species. (C) UPGMA dendrogram of morphological diversity macroparameters based on factor loadings from Table 6: ds, df - dimensionality of the morphospace models, Hs, Hf - entropy, Hds, Hdf - the average entropy, MOs, MOf - the measures of morphosystem organization; abbreviations s and f mark the macroparameters of 'size' diversity and 'shape' diversity of the skull correspondently.
Fig. 5 in Helminth community structure in two species of arctic-breeding waterfowl
Fig. 5. Predicted helminth infection intensity for combined cestodes identified in Pacific black brant (BLBR) and greater white-fronted geese (GWFG) collected in two locations (i.e., Arctic and Subarctic) in Alaska (2014). Circles represent predicted means and error bars denote 85% confidence intervals. Predictions are based off the most supported model from AICc selection and all interactions include lower-order effects (see title).
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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.