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FIGURES 22‑29 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 22‑29: Pectiniunguis gaigei (Chamberlin, 1921), (female paratype MCZ TC-161; GUYANA: Dunoon), (Reference Adenoschendyla gaigei): (22) Sternum II; (23) Sternum VII; (24) Pore field on sternum VIII; (25) Pore field on sternum XXIV; (26) Pore field on sternum XXVI; (27) Pore field on sternum XXXII; (28) Pore field on sternum XLVIII; (29) Pore field on sternum LIII. Scale bars: 0.4 mm (22, 23); 0.1 mm (24-29).
FIGURES 44‑50 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 44‑50: (44-49): Pectiniunguis gaigei (Chamberlin, 1921), (male paratype MCZ TC-162 (A), GUYANA: Dunoon, Sand-hill forest), (Reference Adenoschendyla gaigei): (44) Last leg-bearing segment and terminal segments, dorsal; (45) Last leg-bearing segment and terminal segments, ventral; (46) Detail of distal end of last podomere of left last leg, ventral; (47) Detail of distal end of last podomere of right last leg, ventral; (48) Left gonopod, ventral; (49) Penis, dorsal. (50): Pectiniunguis gaigei (Chamberlin, 1921), (male paratype MCZ TC-162 (C), GUYANA: Dunoon: Sand-hill forest), (specimen collected during an incomplete moulting cycle), (Reference Adenoschendyla gaigei): Right anterior coxal organ and anterior half of right posterior coxal organ, ventral (a: exuvial remnants). Scale bars: 0.3 mm (44, 45); 0.1 mm (49, 50); 0.05 mm (46, 47, 48).
FIGURES 37‑43 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 37‑43: (37-39): Pectiniunguis gaigei (Chamberlin, 1921), (female paratype MCZ TC-162 (B), GUYANA: Dunoon: Sandhill forest), (Reference Adenoschendyla gaigei): (37) Detail of anterior margin of forcipular coxosternum and basal internal edge of trochanteropraefemur; (38) Apical article of left last leg with abnormal (claw-like) praetarsus, ventral; (39) Detail of abnormal praetarsus of left last leg, ventral. (40-43): Pectiniunguis gaigei (Chamberlin, 1921), (male paratype MCZ TC-162 (A), GUYANA: Dunoon, Sand-hill forest), (Reference Adenoschendyla gaigei): (40) Right a.a. I-VI, dorsal; (41) Right a.a. VII-XIV, dorsal; (42) Detail of right a.a. XIV, ventral (a: claviform sensilla, b: apical specialized sensilla, c: internal chitinous thickening); (43) Detail of anterior margin of forcipular coxosternum and basal internal edge of trochanteropraefemur. Scale bars: 0.2 mm (37, 38, 43); 0.04 mm (39); 0.5 mm (40, 41); 0.1 mm (42).
FIGURES 60‑62 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 60‑62: (60-61): Pectiniunguis geayi (Brölemann & Ribaut, 1911), (male (specimen A); BRAZIL: Amazonas: Lago Janauarí): (60) Last leg-bearing segment and terminal segments, ventral; (61) Penis and gonopods, ventral. (62): Pectiniunguis geayi (Brölemann & Ribaut, 1911), (female (specimen B); BRAZIL: Amazonas: Lago Janauarí): Last leg-bearing segment and terminal segments, dorsal. (After Pereira et al., 2000). Scale bars: 0.3 mm (60, 62); 0.05 mm (61).
FIGURES 13‑21 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 13‑21: Pectiniunguis gaigei (Chamberlin, 1921), (female paratype MCZ TC-161; GUYANA: Dunoon), (Reference Adenoschendyla gaigei): (13) Left first maxilla, dorsal; (14) Detail of coxosternum and pleurites of right second maxilla, ventral; (15) Detail of coxosternum and pleurites of left second maxilla, dorsal; (16) Telopodite of left second maxilla, dorsal; (17) Claw of telopodite of right second maxilla, ventral; (18) Forcipular segment, ventral; (19) Detail of conduct and calyx of poison gland, in left forcipular telopodite, dorsal; (20) Right leg I, ventral; (21) Claw of right leg I, ventral. Scale bars: 0.2 mm (13); 0.3 mm (14, 15, 19, 20); 0.15 mm (16); 0.1 mm (17); 0.4 mm (18); 0.03 mm (21).
FIGURES 54‑59 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 54‑59: Pectiniunguis geayi (Brölemann & Ribaut, 1911), (male (specimen A); BRAZIL: Amazonas: Lago Janauarí): (54) Right antenna, ventral; (55) Labrum; (56) First and second maxillae, ventral; (57) Forcipular segment, ventral; (58) Detail of calyx and conduct of poison gland in left forcipular telopodite, ventral; (59) Last leg-bearing segment and terminal segments, dorsal. (After Pereira et al., 2000). Scale bars: 0.3 mm (54, 57, 59); 0.1 mm (55); 0.2 mm (56, 58).
FIGURES 34‑36 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 34‑36: Pectiniunguis gaigei (Chamberlin, 1921), (female paratype MCZ TC-161; GUYANA: Dunoon), (Reference Adenoschendyla gaigei): (34) Detail of internal cuticular structure of two lobes on right anterior coxal organ, ventral (a: common channels; b: individualized areas of mucous layer; (external contour of lobes not delineated)); (35) Detail of internal cuticular structure of a lobe on right anterior coxal organ, ventral (a: common channel; b: individualized areas of mucous layer; c: contour of lobe); (36) Last leg-bearing segment and terminal segments, dorsal. Scale bars: 0.05 mm (34, 35); 0.4 mm (36).
FIGURES 30‑33 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 30‑33: Pectiniunguis gaigei (Chamberlin, 1921), (female paratype MCZ TC-161; GUYANA: Dunoon), (Reference Adenoschendyla gaigei): (30) Last leg-bearing segment and terminal segments, ventral; (31) Detail of distal end of last podomere of right last leg, ventral; (32) Right coxal organs, ventral; (33) Right anterior coxal organ, ventral. Scale bars: 0.3 mm (30, 32); 0.1 mm (33); 0.01 mm (31).
FIGURES 6‑12 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 6‑12: Pectiniunguis gaigei (Chamberlin, 1921), (female paratype MCZ TC-161; GUYANA: Dunoon), (Reference Adenoschendyla gaigei): (6) Cephalic shield and basis of antennae; (7) head capsule and basis of antennae, ventral; (8) clypeal area; (9) labrum; (10) dentate lamella of left mandible; (11) dentate lamella of right mandible; (12) first and second maxillae, ventral. Scale bars: 0.5 mm (6, 7); 0.1 mm (8); 0.3 mm (9, 12); 0.05 mm (10, 11).
FIGURES 1‑5 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 1‑5: Pectiniunguis gaigei (Chamberlin, 1921), (female paratype MCZ TC-161; GUYANA: Dunoon), (Reference Adenoschendyla gaigei): (1) Right a.a. I-VI, ventral; (2) Right a.a. VII-XIV, ventral; (3) Distal portion of right a.a. XIV, ventral (a: claviform sensilla, b: apical specialized sensilla); (4) Right a.a. XIII, ventral (a, b: a, b type sensilla); (5) Right a.a. XIII, dorsal (a, b, c: a, b, c type sensilla). Scale bars: 0.4 mm (1, 2); 0.05 mm (3); 0.1 mm (4, 5).
FIGURES 51‑53 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 51‑53: Pectiniunguis geayi (Brölemann & Ribaut, 1911), (male juvenile; BRAZIL: Amazonas: Manaus): (51) Last leg-bearing segment and terminal segments, ventral; (52) Detail of right coxal organs, ventral; (53) Detail of left coxal organs, ventral. Scale bars: 0.2 mm (51); 0.1 mm (52, 53).
FIGURES 67‑68 in Redescription Of Pectiniunguis Gaigei (Chamberlin, 1921) From Guyana, With New Distributional Data And Complementary Descriptive Notes On Similar Neotropical Species (Chilopoda: Geophilomorpha: Schendylidae)
FIGURES 67‑68: Pectiniunguis ducalis Pereira, Minelli & Barbieri, 1995, (female juvenile (A); BRAZIL: Amazonas: Reserva Florestal A. Ducke): (67) Last leg-bearing segment and terminal segments showing coxal organs, ventral; (68) Detail of coxal organs, ventral. (After Pereira et al., 1995). Scale bars: 0.3 mm (67); 0.1 mm (68).
Fig. 3 in Do we similarly assess diversity with microscopy and high-throughput sequencing? Case of microalgae in lakes
Fig. 3 Correlation between the samples positions obtained on the first axes of the PCA based on microscopy and HTS diatom composition of the samples. There is a highly significant correlation (p <0.001, R 2 = 31%) between both axes
Fig. 4 in Do we similarly assess diversity with microscopy and high-throughput sequencing? Case of microalgae in lakes
Fig. 4 Comparison of the diatom assemblages heterogeneity inside each lake, obtained with HTS and microscopy. Inside lake assemblage heterogeneity is the sum of the Bray-Curtis distances between the three samples of a lake. Correlation is significant (Pearson correlation p <0.001) and follows a linear model (p <0.001, R 2 = 50.8%) (see black line)
Fig. 6 in Do we similarly assess diversity with microscopy and high-throughput sequencing? Case of microalgae in lakes
Fig. 6 Correlations of diversity indices obtained with microscopy and HTS. All correlations are significant and follow linear models (see Table 1)
Fig. 2 in Do we similarly assess diversity with microscopy and high-throughput sequencing? Case of microalgae in lakes
Fig. 2 Correlation between both distance matrices (Bray-Curtis distances) calculated between diatom compositions of samples obtained with microscopy and HTS
Fig. 5 in Do we similarly assess diversity with microscopy and high-throughput sequencing? Case of microalgae in lakes
Fig. 5 Comparison of diversity indices obtained with microscopy and HTS. Classes boundaries for α diversity: c1 <0.675 ≤ c2 <1.100 ≤ c3 <1.525 ≤ c4 <1.950 ≤ c5 <2.375 ≤ c6 <2.800 ≤ c7 <3.225 ≤ c8 <3.650 ≤ c9 <4.075 ≤ c10. For β diversity: c1 <0.7 ≤ c2 <0.8 ≤ c3 <0.9 ≤ c4 <1.0 ≤ c5 <1.1 ≤ c6 <1.2 ≤ c7 <1.3 ≤ c8 <1.4 ≤ c9 <1.5 ≤ c10. For ϒ diversity: c1 <1.04 ≤ c2 <1.48 ≤ c3 <1.92 ≤ c4 <2.36 ≤ c5 <2.80 ≤ c6 <3.24 ≤ c7 <3.68 ≤ c8 <4.12 ≤ c9 <4.56 ≤ c10
Fig. 7 in Analysis of major sperm proteins in two nematode species from two classes, Enoplus brevis (Enoplea, Enoplida) and Panagrellus redivivus (Chromadorea, Rhabditida), reveals similar localization, but less homology of protein sequences than expected for Nematoda phylum
Fig. 7 Immunolocalization of MSP in E. brevis sperm. a Immature spermatozoon from male. MSP is diffusely distributed in cytoplasm and concentrated in large granules (scale bar 10 µm). b Spermatozoon recovered from male and partially activated by 10-min incubation in sea water. MSP undergoes transformation resulting in appearance of
Fig. 5 in Analysis of major sperm proteins in two nematode species from two classes, Enoplus brevis (Enoplea, Enoplida) and Panagrellus redivivus (Chromadorea, Rhabditida), reveals similar localization, but less homology of protein sequences than expected for Nematoda phylum
Fig. 5 Western blot analysis of MSP in E. brevis. a MSP has unusual mobility in gel and is found as protein with weight 36–38 kDa. Both male and female samples reveal MSP signal, because the latter include inseminated females. α-Tubulin was used as a loading control (approximate weight 55 kDa). b Peptide competition assay confirms reactivity of anti-MSP antibodies with protein band of 36–38 kDa
Fig. 2 in Analysis of major sperm proteins in two nematode species from two classes, Enoplus brevis (Enoplea, Enoplida) and Panagrellus redivivus (Chromadorea, Rhabditida), reveals similar localization, but less homology of protein sequences than expected for Nematoda phylum
Fig. 2 Western blot analysis of MSP in P. redivivus. In adult animals, MSP is detected as double band with approximate weight 15 and 16 kDa. a Both male and female samples reveal MSP signal, because the latter include mated females. α-Tubulin was used as a loading control (approximate weight 55 kDa). b Analysis of young males and females. MSP is not detected in females, because most of them are unmated. Abbreviations: m, males; f, females
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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)
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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.