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SI Figure 3: Compositional difference among eukaryotic microinvertebrate external and internal microbiomes, using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars centroid location of each microbiome type. Communities do not cluster by animal, microbiome type, mat type, or stream. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 3: Compositional difference among eukaryotic microinvertebrate external and internal microbiomes, using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars centroid location of each microbiome type. Communities do not cluster by animal, microbiome type, mat type, or stream.
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats.
SI Figure 1: Dispersion values (a boxplot using distance to centroids based on Bray Curtis distance matrix) of external and internal bacterial microbiome composition for different hosts. In a mixed linear model, microinvertebrates did not significantly impact dispersion (P=0.44), but microbiome type did (P=0.03). Pairwise contrasts show that while external microbiomes of P. murrayi and Tardigrada are more variable than their internal microbiomes, E. antarcticus external and internal microbiomes are equally variable. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 1: Dispersion values (a boxplot using distance to centroids based on Bray Curtis distance matrix) of external and internal bacterial microbiome composition for different hosts. In a mixed linear model, microinvertebrates did not significantly impact dispersion (P=0.44), but microbiome type did (P=0.03). Pairwise contrasts show that while external microbiomes of P. murrayi and Tardigrada are more variable than their internal microbiomes, E. antarcticus external and internal microbiomes are equally variable.
Fig. 5 in Species Accumulation Curves And Similarity Traits Of A Species-Rich Fly (Diptera) Community
Fig. 5. Jackknifed NESS indices relating to the kth and (k + 1)th group of 50, k = 1,2,…, 19. In case of k = 8 and k = 14 samples from different years are compared
Fig. 2. Sample-based curve for 2003–2005 in Species Accumulation Curves And Similarity Traits Of A Species-Rich Fly (Diptera) Community
Fig. 2. Sample-based curve for 2003–2005. Two points, corresponding to species numbers after adding the first group of ten to the sample in 2004 and 2005 are denoted by empty symbol
Рис. 1. ÀенΔрограмма схоΔства (коэффициент Жаккара) состава насеΛения герпетобионтных жесткокрыΛых поймы разных Λет (2008–2011 гг.) Fig. 1. The dendrogram of faunistic similarity (Jacquard coefficient) for the population composition of herpetobiont beetles in different years (2008–2011) in Population Dynamics For Herpetobiont Beetles (Coleoptera) In The Floodplain Of A Small Tributary In The Lower Reaches Of The Irtysh
Рис. 1. ÀенΔрограмма схоΔства (коэффициент Жаккара) состава насеΛения герпетобионтных жесткокрыΛых поймы разных Λет (2008–2011 гг.) Fig. 1. The dendrogram of faunistic similarity (Jacquard coefficient) for the population composition of herpetobiont beetles in different years (2008–2011)
FIGURE 12 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 12. Time span of the species of Pygocephalomorpha during the Carboniferous of North America, the UK and continental Europe. Abbreviation: Ks, Kasimovian.
FIGURE 11 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 11. Frequency plot of the distribution of ingroups of Eumalacostraca and of its sister-group Phyllocarida, during the Carboniferous (A) of North America, the UK and continental Europe, the Mississippian (B) and the Pennsylvanian (C).
FIGURE 10 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 10. Restoration drawings of the pygocephalmorphan Anthracaris gracilis (Meek and Worthen, 1865) and Pygocephalus cooperi Huxley, 1857. (A–C) A. gracilis. (A) Dorsal aspect. (B) Ventral aspect of putative female, note the pouch on the last thorax segment. (C) Ventral aspect of putative male. (D–F) P. cooperi. (D) Dorsal aspect. (E) Ventral aspect of female with thorax sternites hidden by oostegites. (F) Putative male in ventral aspect.
FIGURE 8 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 8. Restoration drawings of shields of pygocephalmorphans. (A) Specimen 1.587, (B) 1.228 and (C) Pal.590-2 of Anthracaris gracilis (Meek and Worthen, 1865) from the Carboniferous of Germany. (D) Anthracaris gracilis, based on Brooks (1962, pl. 32, fig. 2). (E) Pygocephalus cooperi Huxley, 1857, based on Schram (1979, fig. 39a). (F) Pygocephalus dubius (Prestwich, 1840), based on Schram (1979, fig. 39c).
FIGURE 7 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 7. Plot of the eumalacostracan shields of Anthracaris gracilis (Meek and Worthen, 1865) from the Carboniferous of Germany (1.587A, Pal.590-2, 1.228A) and of A. gracilis from Mazon Creek, USA. Values for A. gracilis from Brooks (1962).
FIGURE 5 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 5. Anthracaris gracilis (Meek and Worthen, 1865) from the Carboniferous of Germany. (A) Virtually overlaid part and counterpart of specimen 1.529. (B) Same as A, but structures colour marked. Abbreviations: ab = antenna basipod; ant = antenna; atl = antennula; ec = eye cornea; es = eye stalk; lb = labrum; md = mandible; ml = maxillula; mx = maxilla; pl = pleon; sc = scaphocerite; tp1–8 = thoracopod 1–8; ts1–8 = thoracic segment 1–8.
FIGURE 4 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 4. Anthracaris gracilis (Meek and Worthen, 1865) from the Carboniferous of Germany. Digital microscopy images of shields. (A–G) Specimen 1.587 in dorsal view. (A–C) Part. (D, E) Counterpart. (A, D) Non-polarized co-axial light. (B, E) Polarized co-axial light. (C) Ring light. (F) Detail of B, antero-lateral shield corner. (G) Detail of B, rostrum. (H) Detail of Pal590-2, antero-lateral shield corner, mirrored. Images of the counterpart are mirrored. Abbreviations: als = antero-lateral spine; g = groove; ls = lateral spine; p = punctuations; r = rostrum.
FIGURE 2 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 2. Anthracaris gracilis (Meek and Worthen, 1865) from the Carboniferous of Germany. Digital microscopy image of part (A–C) and counterpart (D–F) (specimen 1.529), in ventral view. (A, D) Ring light. (B, D) non-polarized coaxial light. (C, F) polarized co-axial light.
FIGURE 3 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 3. Anthracaris gracilis (Meek and Worthen, 1865) from the Carboniferous of Germany. Digital microscopy images of shields. (A–D) Dorsal view of specimen 1.228. (A, B) Part. (C, D) Counterpart. (E, F) Dorsal view of specimen Pal590-2. (A, C, E) Non-polarized co-axial light. (B, D, F) Polarized co-axial light. Images of the counterparts are mirrored. Abbreviations: als = antero-lateral spine; ls = lateral spine; r = rostrum.
FIGURE 1 in Pygocephalomorphan crustaceans further emphasise the similarities between the Carboniferous Piesberg quarry in Germany and the Mazon Creek Lagerstätte in North America
FIGURE 1. Schematic drawing of a pygocephalomorphan shield in dorsal aspect, showing the measurements taken for the morphometric analysis. 1: Length of rostrum, 2: Length of shield, 3: Width of anterior (outer) margin, 4: Medial width, 5: Width of posterior margin, 6: Length of antero-lateral spine.
Figure 1 in Reproductive and ecological similarity between Caretta caretta (Linnaeus, 1758) and Eretmochelys imbricata (Linnaeus, 1766) in southern Bahia (Brazil)
Figure 1. Location of the study area on the Brazilian coast. The river mouth corresponds to the Tijuípe River (Bahia, Brazil).
Figure 3 in Reproductive and ecological similarity between Caretta caretta (Linnaeus, 1758) and Eretmochelys imbricata (Linnaeus, 1766) in southern Bahia (Brazil)
Figure 3. Similarity of hatchlings between species. a = Caretta caretta and x = Eretmochelys imbricata. The numbers and red circles highlight the three groups of ecological similarity among hatchlings.
Figure 6 in Reproductive and ecological similarity between Caretta caretta (Linnaeus, 1758) and Eretmochelys imbricata (Linnaeus, 1766) in southern Bahia (Brazil)
Figure 6. Correlation between the hatch response of (A) Eretmochelys imbricata and (B) Caretta caretta and temperature.
Figure 2 in Reproductive and ecological similarity between Caretta caretta (Linnaeus, 1758) and Eretmochelys imbricata (Linnaeus, 1766) in southern Bahia (Brazil)
Figure 2. Correlation between the number of nests observed for the Caretta caretta and Eretmochelys imbricata. The descending line shows the correlation pattern. The number of nests ranged from 0 to 3 for each sample (n=102).
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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.