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1,478 results for “Sulawesi”
Figure 2 in A new molluscivore crab from Lake Poso confirms multiple colonization of ancient lakes in Sulawesi by freshwater crabs (Decapoda: Brachyura)
Figure 2. Sundathelphusa molluscivora sp. nov. Major chelae. A, male (23.5 by 19.0 mm) (ZRC 2000.1703); B, holotype male (24.6 by 20.4 mm) (MZB 1480); C, female (24.3 by 20.0 mm) (ZRC 2000.1703).
Figure 1 in A new species of Schismatogobius (Teleostei: Gobiidae) from Sulawesi (Indonesia)
Figure 1. – Most likely ML tree inferred using the TIM+I model (–lnL = 3711.2906, I = 0.6520, f(A) = 0.2382, f(C) = 0.3018, f(G) = 0.1692, f(T) = 0.2909, AC = GT = 1.0, AT = CG = 0.6842, AG = 12.0806, CT = 6.0413). BP are given above each branch. Schismatogobius limmoni branch is highlighted in bold.
Figure 4. – Schismatogobius limmoni n in A new species of Schismatogobius (Teleostei: Gobiidae) from Sulawesi (Indonesia)
Figure 4. – Schismatogobius limmoni n. sp., female, paratype in MNHN-IC 2020-0176 (SL 24.7 mm; BIF 10054) (Photo N. Hubert).
Figure 2 in SYNOPSIS OF BEGONIA (BEGONIACEAE) FROM THE NORTHERN ARM OF SULAWESI AND SANGIHE ISLAND, INDONESIA, INCLUDING THREE NEW SPECIES
Figure 2. Distribution maps of Begonia species occurring on the northern arm of Sulawesi. Distribution points are from georeferenced collections from major herbarium collections (B, BO, E, K, KRB, L, SING), the Begonia Resource Centre (Hughes et al., 2015–) and the Sulawesi Begonia Data Portal (Thomas et al., 2013, continuously updated).
Figure 12. Begonia rieckei. A in SYNOPSIS OF BEGONIA (BEGONIACEAE) FROM THE NORTHERN ARM OF SULAWESI AND SANGIHE ISLAND, INDONESIA, INCLUDING THREE NEW SPECIES
Figure 12. Begonia rieckei. A, Habit, reddish leaves with white dots along the margin and between the veins; B, inflorescence; C, male flowers; D, female flower; E and F, infructescence; G, ovary (crosssection of middle part). A from W.H. Ardi WI410; B, D and F from W.H. Ardi WI207; C, E and G from W.H. Ardi WI391. Photographs: W. H. Ardi.
Fig. 3 in Five new species and a new record of Manota (Diptera: Mycetophilidae) from Sulawesi
Fig. 3. Manota licina sp. nov. (holotype). A – antennal flagellomere 4, lateral view. B – hypopygium, ventral view. C – hypopygium, dorsal view. D – hypoproct and aedeagus, ventral view. E – posterior part of gonocoxa, dorsal view. Scales 0.10 mm.
Fig. 1 in Five new species and a new record of Manota (Diptera: Mycetophilidae) from Sulawesi
Fig. 1. Manota abscissa sp. nov. (holotype). A – antennal flagellomere 4, lateral view. B – hypopygium, dorsal view. C – hypopygium, ventral view. D – hypoproct and aedeagus, ventral view. Scales 0.10 mm. 1 = sternite 9, 2 = gonocoxa, 3 = ventral mesial margin of gonocoxa, 4 = parastylar lobe, 5 = paraapodemal lobe, 6 = gonostylus, 7 = apex of aedeagus, 8 = aedeagal apodeme, 9 = juxtagonostylar setae, 10 = dorsal mesial margin of gonocoxa, 11 = lobes at dorsal posterior margin of gonocoxa, 12 = gonocoxal apodemes, 13 = tergite 9, 14 = hypoproct, 15 = cercus.
Fig. 4 in Five new species and a new record of Manota (Diptera: Mycetophilidae) from Sulawesi
Fig. 4. Manota loricata sp. nov. (holotype). A – antennal flagellomere 4, lateral view. B – hypopygium, ventral view. C – hypopygium, dorsal view. D – hypoproct and aedeagus, ventral view. Scales 0.10 mm.
Fig. 2 in Five new species and a new record of Manota (Diptera: Mycetophilidae) from Sulawesi
Fig. 2. Manota aciculata sp. nov. (A – paratype; B, C, D – holotype). A – antennal flagellomere 4, lateral view. B – hypopygium, ventral view. C – hypopygium, dorsal view. D – hypoproct and aedeagus, ventral view. Scales 0.10 mm.
FIG. 39 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 39. Map of Sulawesi showing localities sampled for shrews. Colored areas enclose localities with known records of members of the Ordinary Group. To maintain clarity of presentation, the widespread Crocidura nigripes is not included.
FIG. 32 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 32. Bivariate plots showing the results of principal components analyses of the two Thick-Tailed Group species using A, five external and B, 12 cranial measurements. Loadings and variance explained are given in tables 10 and 11, respectively.
FIG. 20 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 20. Map of Sulawesi showing localities sampled for shrews. Colored areas enclose localities with known records of members of the Rhoditis Group of Sulawesi Crocidura.
FIG. 10 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 10. Box plots of relative skull measures showing braincase breadth (BB), interorbital width (IOW), and rostral length (RL) divided by condyloincisive length (CIL) and BB divided by IOW for all species of Sulawesi shrew. Plots show the median, 1st and 3rd quartiles, the maximum value within 1.5 × interquartile range (distance between 1st and 3rd quartiles; IQR), the minimum value within 1.5 × IQR, and outliers (black circles). Sample sizes are shown along the x-axis. Species are ordered according to the species groups used in the text (Thick = Thick-Tailed Group).
FIG. 25 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 25. Map of Sulawesi showing localities sampled for shrews. Colored areas enclose localities with known records of members of the Small-Bodied Group of Sulawesi Crocidura.
FIG. 16 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 16. Map of Sulawesi showing localities sampled for shrews. Colored areas enclose localities with known records of members of the Elongata Subgroup. Although we excluded Pinedapa from the estimated geographic ranges, we suspect the two USNM specimens referred to Crocidura elongata by Miller and Hollister (1921) from this site represent C. microelongata.
FIG. 8. Estimated phylogenetic relationships from a in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 8. Estimated phylogenetic relationships from a maximum likelihood analysis of 983 concatenated ultraconserved elements. Samples from Sulawesi are labeled with the species name, locality, and catalog number. Asterisks indicate type specimens from Miller and Hollister (1921). Ultrafast bootstrap values <95 are shown.
FIG. 7 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 7. Estimated species tree from analysis of 3940 ultraconserved element loci in ASTRAL. Samples from Sulawesi are labeled with the species name, locality, and catalog number. Asterisks indicate type specimens from Miller and Hollister (1921). Local posterior probabilities <0.95 are shown. Tip branch lengths are arbitrary.
FIG. 4 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 4. Maximum-likelihood estimate of the gene tree of Sulawesi Crocidura derived from an alignment of 851 individuals and 1111 characters from the mitochondrial gene cytochrome b. Bootstrap support is shown along branches. Clades corresponding to species are collapsed for ease of presentation. Tips are labeled with the species name, the number of tips (T), and number of localities (L), as labeled in figure 1, and the maximum intraspecific (MI) Jukes-Cantor distance calculated from a reduced alignment. Two species are paraphyletic and their respective, within-clade MI values are shown separately. For species described by Miller and Hollister (1921), the holotype or paratypes are included for C. elongata, C. lea, and C. rhoditis. Branch lengths between C. nigripes and other taxa are shortened for presentation. See supplementary data S2 for the full tree.
FIG. 43 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 43. Bivariate plots showing the first two axes from principal components analyses of A, five external and B, 12 cranial measurements from Crocidura solita and C. ordinaria, two members of the Ordinary Group. Loadings and variance explained are given in tables 17 and 18, respectively.
FIG. 42 in Fourteen New, Endemic Species Of Shrew (Genus Crocidura) From Sulawesi Reveal A Spectacular Island Radiation
FIG. 42. Box plots showing subtle differences in cranial measurements between Crocidura solita and C. ordinaria, two members of the Ordinary Group. Plots show the median, 1st and 3rd quartiles, the maximum value within 1.5 × interquartile range (distance between 1st and 3rd quartiles; IQR), the minimum value within 1.5 × IQR, and outliers (black circles). Sample sizes are shown along the x-axis. All measurements in mm.
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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.