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Fig. 3 in A new basal actinopterygian fish from the Anisian (Middle Triassic) of Luoping, Yunnan Province, Southwest China
Fig. 3. Skull of the basal actinopterygian fish Luoxiongichthys hyperdorsalis gen. et sp. nov., Guanling Formation, Anisian, Middle Triassic; Daaozi Quarry, Luoping, Yunnan Province, Southwest China. A. LPV−10625 in dorso−lateral view. B. LPV−10120 in dorsal view.
Fig. 2 in A new basal actinopterygian fish from the Anisian (Middle Triassic) of Luoping, Yunnan Province, Southwest China
Fig. 2. Holotype of the basal actinopterygian fish Luoxiongichthys hyperdorsalis gen. et sp. nov., LPV−10144, Guanling Formation, Anisian, Middle Triassic; Daaozi Quarry, Luoping, Yunnan Province, Southwest China; in lateral view (A), interpretive drawing (B).
Fig. 7 in A new basal actinopterygian fish from the Anisian (Middle Triassic) of Luoping, Yunnan Province, Southwest China
Fig. 7. Reconstruction of the basal actinopterygian fish Luoxiongichthys hyperdorsalis gen. et sp. nov., Guanling Formation, Anisian, Middle Triassic; Daaozi Quarry, Luoping, Yunnan Province, Southwest China; in lateral view.
Fig. 3 in Prevalence of fish-borne zoonotic trematode infection in Jilin Province, China
Fig. 3. The phylogenetic tree of FZTs obtained in this study with other trematodes based on ITS sequences. ITS sequences of C. sinensis, M. orientalis and E. japonicus from fish were obtained and compared. They had the same similarity and were deposited into NCBI (No. MW828640, MW828729 and MW828605). The phylogenetic relationship between the FZTs obtained in this study and other trematodes based on ITS sequences was analyzed via MP, NJ and ML using A. chongqingens as the outgroup. The scale bar indicates an evolutionary distance of 0.10 substitutions per site in the sequence. The ITS sequences of C. sinensis, M. orientalis and E. japonicus obtained in this study (marked with *) was 100% consistent with the sequences of C. sinensis (MF319654), M. orientalis (MK482055) and E. japonicus (KT873314) deposited in NCBI GenBank.
Fig. 5 in Prevalence of fish-borne zoonotic trematode infection in Jilin Province, China
Fig. 5. The prevalence of FZTs in different months in wild freshwater fish in Jilin Province, China. The prevalence of FZTs in freshwater fish gradually increased and then decreased, with the highest prevalence of C. sinensis and E. japonicus in August and the highest prevalence of M. orientalis in September. *p <0.05 was considered to be a significant difference, and the prevalence in November was used as a control. The significances of C. sinensis, M. orientalis and E. japonicus in different months are marked in red *, green * and blue *, respectively. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Prevalence of fish-borne zoonotic trematode infection in Jilin Province, China
Fig. 2. The metacercariae and eggs of C. sinensis, M. orientalis and E. japonicus.C. sinensis metacercariae encysted on the flesh of P. parva, scale bar = 50 μm (A). M. orientalis metacercariae encysted on the flesh of P. parva, scale bar = 50 μm (B). E. japonicus metacercariae encysted on the gills of R. sinensis, scale bar = 50 μm (C). C. sinensis metacercariae isolated from P. parva, scale bar = 50 μm (D). M. orientalis metacercariae isolated from P. parva, scale bar = 50 μm (E); E. japonicus metacercariae isolated from R. sinensis, scale bar = 50 μm (F). C. sinensis egg in feces of canine, scale bar = 10 μm (G). M. orientalis egg in feces of duck, scale bar = 10 μm (H). E. japonicus eggs in feces of canine and duck, scale bar = 10 μm (I, J). EC, excretion cyst; ET, excretion tube; EO, egg operculum; IW, inner cyst wall; OW, outer cyst wall; ME, metacercariae; MI, miracidium; SP, shoulder peaks; SE, small spine at the rear end; OS, oral sucker; VS, ventral sucker.
Figure 5 in Motivations and contributions of volunteer groups in the management of invasive alien plants in South Africa's Western Cape province
Figure 5. Challenges (n = 56) faced by individual volunteers in the management of invasive alien plant management in Western Cape, South Africa.
Figure 4 in Motivations and contributions of volunteer groups in the management of invasive alien plants in South Africa's Western Cape province
Figure 4. Reasons for initial engagement (n = 71) in volunteering and the current motivations (n = 86) for volunteers to be involved in the management of invasive alien plant species in Western Cape, South Africa.
Figure 2 in Motivations and contributions of volunteer groups in the management of invasive alien plants in South Africa's Western Cape province
Figure 2. Motivations (n = 35) for forming volunteer groups that remove alien invasive plants in Western Cape, South Africa.
Figure 1 in Motivations and contributions of volunteer groups in the management of invasive alien plants in South Africa's Western Cape province
Figure 1. Identified volunteer groups (52) in Western Cape of South Africa. Groups that participated in the survey (26) are indicated by circles that also show group sizes (individual members per group). Groups that did not participate in the survey are indicated by blue circles. The green area on the map represents the fynbos biome.
Figure 3 in Motivations and contributions of volunteer groups in the management of invasive alien plants in South Africa's Western Cape province
Figure 3. Challenges (n = 26) faced by volunteering by groups in the management of invasive alien plants in Western Cape, South Africa.
Fig. 4 in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 4. Haplotype network of G1/G3 haplotypes identified on the basis of partial nad5 gene (628 bp). The G1 isolates obtained in this study (Hap01-Hap04), G3 isolates (Hap05, Hap06). Hatch marks represent the number of mutations between the haplotypes and the size of circle corresponds to the frequency of each haplotype in the population. Haplotypes formed by the isolates obtained in this study are marked with an asterisk.
Fig. 3. Haplotype network for E in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 3. Haplotype network for E. canadensis (G6/G7) using cox1 gene (616 bp) sequences of different countries. The E. canadensis (G6/G7) isolate obtained in this investigation (Hap_01) and the sequences identified as G7 in the Genbank database were utilized. Circle size relative to haplotype data set frequency. Each hatch mark is representative of one nucleotide change. Haplotypes formed by the isolates obtained in this study are marked with an asterisk.
Fig. 1 in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 1. Hydatid cyst image obtained from the lung (A) and liver (B) and C. tenuicollis (C,D) image obtained from its mesentery of wild boar.
Fig. 2. Haplotype network constructed using cox1 in Prevalence, molecular characterisation and phylogenetic analyses of hydatid cysts and cysticercus tenuicollis isolates and first report of E. canadensis (G6/G7) in wild boars in Bingol province, Türkiye
Fig. 2. Haplotype network constructed using cox1 (744 bp) gene sequences of T. hydatigena. Seven haplotypes formed by the T. hydatigena isolates obtained in this study: (Hap 1-Hap 7). Circle size relative to haplotype data set frequency. Each hatch mark is representative of one nucleotide change. Haplotypes formed by the isolates obtained in this study are marked with an asterisk.
FIGURE 9 in Identification of fossilized eggshells from the Taung hominin locality, Taung, Northwest Province, South Afric
FIGURE 9. Cross-plot of oxygen and carbon isotope values from fossil eggshells and sediment, base of the Dart Pinnacle, Taung. There is a high degree of consistency between replicate samples, and each eggshell fragment shows a distinct isotopic signature, indicating that the eggshells are derived from different individuals (with the possible exception of TDES 2 & TDES 3). The δ13C values indicate that all eggshells have a predominantly C4 (savannah grass) dietary signal, with the exception of T93-17 which has a pure (or almost pure) C3 diet.
FIGURE 4 in Identification of fossilized eggshells from the Taung hominin locality, Taung, Northwest Province, South Afric
FIGURE 4. All specimens, both extant eggs and fossil eggshells, showing surface morphology at 57X magnification.
FIGURE 5 in Identification of fossilized eggshells from the Taung hominin locality, Taung, Northwest Province, South Afric
FIGURE 5. Renderings of fossil eggshell fragments embedded in matrix (1-2) and indication of the internal boundary between eggshell and matrix (3-4). Images 1 and 3 are fossil eggshell fragment T92-88, and images 2 and 4 are fossil eggshell fragment T93-17. Note the relatively consistent thickness at the edges and how this maintained surface curvatures indicated by the external surfaces.
FIGURE 6. Fossil eggshell fragments T92-88 in Identification of fossilized eggshells from the Taung hominin locality, Taung, Northwest Province, South Afric
FIGURE 6. Fossil eggshell fragments T92-88 (blue) and T93-17 (yellow) fit to eggs from five extant birds. Fits depicted visually in the figure (rigidly constrained size) correspond to root mean square (RMS) values reported in Table 2. Note that visual correspondence supports quantification of RMS values in that fossil eggshell fragment T92-88 fits best with the blunt pole of the extant guinea fowl egg. Extant black eagle (blunt pole) and giant eagle owl (apical pole) eggs provide the next closest, but still worse fits. Fossil eggshell fragment T93-17 fits best with the equatorial region of the black eagle egg. The extant guinea fowl egg provides the next closest fit for fossil eggshell fragment T93-17.
FIGURE 8 in Identification of fossilized eggshells from the Taung hominin locality, Taung, Northwest Province, South Afric
FIGURE 8. (1) Fossilized eggshell fragments T92-88 (blue) and T93-17 (yellow) indicating best fit to the same black eagle egg as illustrated in Figure 6, plus six additional black eagle eggs. Note despite intraspecific variability in egg shape, the fits are quite similar (also see Table 3). This suggests even accounting for intraspecific variability in egg shape Results in Table 2 should be robust. (2) Fossil eggshell fragments T92-88 (blue) and T93-17 (yellow) indicating best fit to the same guinea fowl egg as illustrated in Figure 6 (far left), plus four additional guinea fowl eggs. Note that despite intraspecific variability in egg shape, the fits are quite consistent (also see Table 3). This suggests that even accounting for intraspecific variability in egg shape results of the surface curvature analyses are robust.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.