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Fig. 22 in Taxonomy of the Crematogaster degeeri-species-assemblage in the Malagasy region (Hymenoptera: Formicidae)
Fig. 22. Crematogaster tricolor Gerstäcker, 1859 stat. rev., worker and queen. A-C. Worker (CASENT0120944). A. Full-face. B. Profile. C. Dorsal. D-F. Queen (CASENT0120949). D. Full-face. E. Profile. F. Dorsal.
Figure 4 in Aquatic Diptera (Insecta) assemblages in four sympatric Eryngium (Apiaceae) phytotelmata in flowering and senescent times
Figure 4. Median number of Metriocnemus eryngiotelmatus larvae per plant in four Eryngium phytotelmata. The box indicates the 25th and 75th centiles, the line within the box indicates the median and the whiskers indicate the 90th and 10th centiles. Different letters indicate significant differences detected by Dunn's test (p <0.05).
Figure 3 in Aquatic Diptera (Insecta) assemblages in four sympatric Eryngium (Apiaceae) phytotelmata in flowering and senescent times
Figure 3. Median number of Polypedilum parthenogeneticum larvae per plant in four Eryngium phytotelmata. The box indicates the 25th and 75th centiles, the line within the box indicates the median and the whiskers indicate the 90th and 10th centiles. Different letters indicate significant differences detected by Dunn's test (p <0.05).
Figure 2 in Aquatic Diptera (Insecta) assemblages in four sympatric Eryngium (Apiaceae) phytotelmata in flowering and senescent times
Figure 2. Cumulative total of Diptera observed in successive plants (n = 40 plants for each species in autumn and in spring). (A) Eryngium horridum; (B) Eryngium stenophyllum; (C) Eryngium aff. serra; (D) Eryngium elegans. Logarithmic equations with R2 values; p <0.001 for all R2 except for E. stenophyllum in autumn (p = 0.09).
Data 1 for "Population- and age-specific patterns of haemosporidian assemblages and infection levels in European Bee-eaters (Merops apiaster)"
<p>Data related to the article "Population- and age-specific patterns of haemosporidian assemblages and infection levels in European Bee-eaters (<em>Merops apiaster</em>)" in the format .xlsx. The 1st sheet contains all variables for analyses done with the R script (see 10.5281/zenodo.3968360). The 2nd sheet contains explanations about the variables in sheet 1.</p>
Figure 1 in Assessing high compositional differences of beetle assemblages across vertical woodland strata in the New Forest, Hampshire, England
Figure 1. Correspondence analysis ordination of subfamily/family level showing separation between the sampling methods. Eigenvalue axis 1: 0.4953, variation 45.14; axis 2: 0.2668, variation 69.47. Key to subfamily/family abbreviations – Carabida: Carabidae, Hydrophl: Hydrophilidae, Leiodida: Leiodidae, Omaliina: Omaliinae, Pselaphn: Pselaphinae, Phloeocr: Phloeocharinae, Tachypor: Tachyporinae, Habrocer: Habrocerinae, Aleochar: Aleocharinae, Oxytelin: Oxytelinae, Scaphidi: Scaphidiinae, Scydmaen: Scydmaeninae, Paederin: Paederinae, Staphyln: Staphylininae, Geotrupd: Geotrupidae, Scirtida: Scirtidae, Throscid: Throscidae, Elaterid: Elateridae, Canthard: Cantharidae, Ptiliida: Ptiliidae, Anobiida: Anobiinae, Malachii: Malachiidae, Sphindid: Sphindidae, Nitiduld: Nitidulidae, Cryptoph: Cryptophagidae, Coccinel: Coccinellidae, Coryloph: Corylophidae, Latridii: Latridiidae, Melandry: Melandryidae, Tenebrio: Tenebrionidae, Salpingd: Salpingidae, Scraptii: Scraptiidae, Cerambyc: Cerambycidae, Crytocp: Cryptocephalinae, Chrysoml: Chrysomelinae, Galerucn: Galerucinae, Rhynchit: Rhynchitidae, Apionida: Apionidae, Curculio: Curculioninae, Cossonin: Cossninae, Entimina: Entiminae, Molytina: Molytinae, Scolytin: Scolytinae.
Figure 4 in Patterns of spatial variability of mobile macro-invertebrate assemblages within a Posidonia oceanica meadow
Figure 4. Non-metric multidimensional scaling (nMDS) ordination on macro-invertebrate assemblages of Pianosa Island. S = shallow, I = intermediate, D = deep; e = east, s = south, w = west.
Figure 3 in Patterns of spatial variability of mobile macro-invertebrate assemblages within a Posidonia oceanica meadow
Figure 3. (a) Mean species number and (b) number of individuals per sample of mobile macroinvertebrate assemblages of Posidonia oceanica meadow (mean ± standard error, SE; n = 24).
Figure 2 in Patterns of spatial variability of mobile macro-invertebrate assemblages within a Posidonia oceanica meadow
Figure 2. (a) Shoot density and (b) mean leaf length of Posidonia oceanica meadow of Pianosa Island (mean ± standard error, SE; n = 120).
Figure 2 in Influence of riparian quality on macroinvertebrate assemblages in subtropical mountain streams
Figure 2. Redundancy analysis (RDA) of macroinvertebrate density in sites of good (white dots), poor (grey dots) and bad (black dots) riparian quality according with the QBRy index. References: DO = dissolved oxygen; Bh = bank-full height; DW = dry channel width; Temp = water temperature; Cond = conductivity; FPOM = fine particulate organic matter.
Illuminating the planktonic stages of salmon lice: a unique fluorescence signal for rapid identification of a rare copepod in zooplankton assemblages.
<p>The Excitation Emission Matrix (EEM) measurements were taken with Shimadzu's proprietary software ‘LabSolutions RF’. All files are in the exported csv format with columns representing the excitation wavelengths and rows the emission wavelengths. Wavelengths range from 200-600 nm with a 2 nm increment. Fluorescence intensity was influenced by the fluctuating number of animals in the path of the excitation beam during the 5 minute measurement. We compensated for this artefact by repeating measurements of each sample five times, calculating the mean, and applying a smoothing function which found the median value within 10 nm. The fluorescence intensity was further normalized on a 0 to 1 scale by dividing intensity by the maximum fluorescence within each EEM measurement.</p> <p>Supplemental Table 1. The metadata of EEM measurements. The measurements were used for the spectrum section analysis and correspond to those depicted in Figures 2, 3, 4, & 5. See sections 3.1, 3.1.1, & 3.1.2. The Sample column indicates which lab culture cohort the sea lice came from (BGO*), which wild caught fish sample they came from (WC*), or the sampling date of non-target copepods (DDMMYY). The filename of each mean measurement is listed and indicates the first of 5 repeated measurements. Corresponding files can be found in the deposited.csv files at Zendo. In those files, data columns represent the excitation wavelengths, 200nm to 600nm increasing in 2 nm increments. Likewise, the rows represent the emission wavelengths. NaN’s are present where scattering layers were removed. All fluorescence intensity values are normalized to the maximum within each EEM.</p>
FIG. 8 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 8. — Photomicrographs of the radiolarians from the Orbuklukeli section; A-H, Acanthotetrapaurinella kennecottensis (Carter in Longridge, Carter, Smith & Tipper, 2007); A-E, G, Orbuk-26, F, H, Orbuk-27; I-O, Paurinella liassica Tekin, n. sp.; I, Holotype, Orbuk-27; J-O, Paratypes; J, N, Orbuk-27; K-M, Orbuk-32; O, Orbuk-26; P-V, Tetrapaurinella sphaerica Tekin, n. sp.; P, Holotype, Orbuk-32; Q-V, Paratypes; Q, Orbuk-32; R-T, Orbuk-27, U, Orbuk-26; V, Orbuk-31; W-Y, Orbiculiformella callosa (Yeh, 1987); W, X, Orbuk-36; Y, Orbuk-41. Scale bar: G-H, 100 µm; A-F, I-V, 150 µm; W-Y, 200 µm.
FIG. 13 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 13. — Photomicrographs of the radiolarians and conodonts from the Orbuklukeli section: A, Saitoum sp. aff. S. triumphense Whalen & Carter in Carter, Whalen & Guex, 1998, Orbuk-32; B, Saitoum sp. A, Orbuk-32; C-E, Katroma ninstintsi Carter in Carter, Cameron & Smith, 1988, Orbuk-46; F-G, Ares sutherlandi Whalen & Carter in Carter, Whalen & Guex, 1998, Orbuk-32; H-I, Bipedis douglasi Whalen & Carter in Carter, Whalen & Guex, 1998, Orbuk-32; J-L, Bipedis hannai Whalen & Carter in Carter, Whalen & Guex, 1998; J, Orbuk-27; K, L, Orbuk-32; M, Bipedis helenae Whalen & Carter in Carter, Whalen & Guex, 1998, Orbuk-27; N, Epigondolella sp. cf. E. postera Kozur & Mostler, 1971, Orbuk-2; O, Hindeodella sp., Orbuk-12; P, Misikella hernsteini (Mostler, 1967), Orbuk-9; Q-T, Misikella posthernsteini Kozur & Mock, 1974; Q-R, Orbuk-13, S, T, Orbuk-15; U, Misikella rhaetica Mostler, 1978, Orbuk-9; V-X, Misikella ultima Kozur & Mock, 1991, Orbuk-15. Scale bar: A-B, F-M, 100 µm; N-X, 150 µm; C-E, 180 µm.
FIG. 11 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 11. — Photomicrographs of the radiolarians from the Orbuklukeli section; A, B, Droltus sp. aff. D. eurasiaticus Kozur & Mostler, 1990, Orbuk-32; C, Droltus hecatensis Pessagno & Whalen, 1982, Orbuk-32; D-F, Droltus laseekensis Pessagno & Whalen, 1982, Orbuk-27; G-J, Trexus dodgensis Whalen & Carter in Carter, Whalen & Guex, 1998; G-H, Orbuk-27; I, J, Orbuk-32; K-O, Canoptum cephalobulbosum Tekin, n. sp.; K, Holotype, Orbuk-15; L-O, Paratypes, Orbuk-15; P, Canoptum columbiaense Whalen & Carter in Carter, Whalen & Guex, 1998, Orbuk-27; Q, Canoptum merum Pessagno & Whalen, 1982, Orbuk-15; R-U, Canoptum productum Tekin, n. sp.; R, Holotype, Orbuk-15; S-U, Paratypes, Orbuk-15; V-X, Canoptum rarum Tekin, n. sp.; V, Holotype, Orbuk-15; W-X, Paratypes, Orbuk-15. Scale bar: A, B, 200 µm; C, P, 120 µm; D-J, 100 µm; K-O, R-X, 80 µm.
FIG. 5 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 5. — Field photographs from the Lower Jurassic part of the section: A, Thin to medium-bedded, gray, red to purple-colored limestones with red-colored chert interlayers from where the sample Orbuk-39 was collected; B, Alternating thin-bedded, purple-colored limestone, and thin-bedded, red-colored chert corresponding to the level of sample Orbuk-42; C, Thin-bedded, red-colored cherts with thin-bedded, purple-colored limestone interlayers of the sample point Orbuk-45; D, General view of purple-colored, nodular limestones showing typical features of Ammonitico Rosso facies from the top of the section; E-J, Different ammonite taxa from the Ammonitico rosso facies in the section place and Kuzyurt region to the 850 m NE of section place (E, Pseudomercaticeras sp.; F, phylloceratid; G, H, J,? harpoceratid; I, lytoceratid); K, General view from southwest to northeast showing section location; L, General view from southeast to northwest showing the eastern side of Orbuklukeli hill. Abbreviation: A.R., Ammonitico rosso.
FIG. 2 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 2. — Detailed geological map of the Orbuklukeli hill surroundings, northwest of Mersin city (after Tekin et al. 2016a). Key: a, Mersin Mélange; 1, Middle Permian brecciated limestone; 2, Middle Triassic basic volcanic rocks; 3, Upper Triassic conglomerate, sandstone, and silt-claystone; 4, Upper Triassic massive platform limestone; 5, Upper Triassic alternating tuff, tuffite with limestone; 6, Upper Triassic cherty limestone; 7, Lower Jurassic alternating chert and limestone (including Ammonitico rosso facies); 8, Middle-Upper Jurassic radiolarite and mudstone; 9, Lower Cretaceous alternating chert and mudstone; 10, Undifferentiated mélange (mainly matrix); b, Stratigraphic contact; c, Fault; d, Strike-slip fault; e, Thrust; f, Toarcian ammonite fauna near the Kuzyurt region; g, Section location (revised after Tekin et al. 2016a).
FIG. 1 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 1. — Geological base map showing the distribution of the Mersin Ophiolitic Complex and surrounding tectonic units in the northwest of Mersin city, southern Turkey (revised after Senel 2002 and Alan et al. 2007). For a detailed geological sketch of the Orbuklukeli section, see Fig. 2. Inset: Distribution of ophiolites and mélanges in Turkey with the location of Fig. 1.
FIG. 3 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 3. — Columnar section of the Orbuklukeli section and sampling points. Key: a, Limestone; b, Limestone with chert nodules; c, Alternating chert and limestone with chert nodules; d, Brecciated limestone; e, Nodular limestone with ammonites; f, Tuffite; g, Radiolarian occurrence; h, Conodont occurrence; i, Tuffite sample. Abbreviations: Sinemur., Sinemurian; Toar., Toarcian.
FIG. 4 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 4. — Field photographs of the Orbuklukeli section: A-G, Upper Triassic part of the section; A, General view of the Orbuklukeli section around Orbuklukeli hill, view from southwest to northeast; B, Basal part of the section represented by medium to thick-bedded, gray-colored limestones with chert nodules; C, Medium-bedded, gray to yellow-colored limestones with chert nodules where sample Orbuk-3 was collected, overlain by meter-thick mass-flow bed; D, Thin to medium-bedded, gray to beige-colored limestones of sample Orbuk-10 with thin-bedded, gray-colored chert interlayers; E, Medium-bedded, gray to beige-colored, brecciated limestones with rare gray-colored chert nodules and beds where sample Orbuk-12 was obtained; F, Brecciated limestones with pyritized chert and limestone pebbles from where sample Orbuk-13 was collected; G, The upper part of the Upper Triassic sequence of the section representing by thin to medium-bedded, gray to beige-colored, locally brecciated limestones with chert nodules; H, The upper part of the limestones with chert nodules of Late Triassic age followed by Early Jurassic chert-rich platy limestone; I, The boundary between Upper Triassic limestones with chert nodules, tuffite layer and thin-bedded, chert-rich limestone of Early Jurassic age; J, Basal part of the Lower Jurassic sequence characterized by alternating thin-bedded, gray-colored limestone and thin-bedded, gray-colored chert from where samples from Orbuk-16 to Orbuk-20 have been collected; K, Alternating thin-bedded, gray-colored limestone, and thin-bedded, gray-colored chert corresponding to the level of sample Orbuk-30. Abbreviation: T., Tuffite.
FIG. 9 in Late Triassic to Early Jurassic radiolarian, conodont and ammonite assemblages from the Tavuscayiri block, Mersin Mélange, southern Turkey: Time constraints for the T/J boundary and sedimentary evolution of the southern margin of the northern Neotethys
FIG. 9. — Photomicrographs of the radiolarians from the Orbuklukeli section: A-E, Orbiculiformella pulchra Tekin, n. sp.; A, Holotype, Orbuk-32; B-E, Paratypes; B, Orbuk-31; C-E, Orbuk-32; F-G, Orbiculiformella? trispina trispina (Yeh, 1987), Orbuk-32; H, Orbiculiformella sp. A, Orbuk-27; I, Danubea sp. A, Orbuk-27; J-L, Charlottea elegantissima Tekin, n. sp.; J, Orbuk-32, Holotype; K-L, Paratypes; K, Orbuk-27; L, Orbuk-32; M, N, Charlottea johnsoni Whalen & Carter in Carter, Whalen & Guex, 1998, Orbuk-32; O, Charlottea sp. A sensu Whalen & Carter (2002), Orbuk-41; P-R, Tozerium orbuklukeliense Tekin, n. sp.; P, Holotype, Orbuk-32; Q-R. Paratypes; Q, Orbuk-32; R, Orbuk-31; S-T, Tozerium sp. A; S, Orbuk-41; T, Orbuk-44; U, Ferresium sp. cf. F. teekwoonense Carter, 1993, Orbuk-15; V, Palaeosaturnalis blomei Kozur & Mostler, 1990, Orbuk-32; W, Palaeosaturnalis liassicus Kozur & Mostler, 1990, Orbuk-38; X, Palaeosaturnalis schaafi Kozur & Mostler, 1990, Orbuk-38; Y, Palaeosaturnalis subovalis Kozur & Mostler, 1990, Orbuk-38. Scale bar: A-E, 200 µm; F-H, 170 µm; I, 80 µm; J-L, P-R, 120 µm; M-O, S-U, 150 µm; W, X, 220 µm.
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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.