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799 results for “island endemism”
Figure 8 in Dissecting an island radiation: systematic revision of endemic land snails on Lord Howe Island (Gastropoda: Stylommatophora: Microcystidae)
Figure 8. Reproductive system of Innesoconcha catletti. A–C, AM C.532590, Erskine Valley. A, reproductive system. B, penis with tunica opened. C, penis interior. D, AM C.446502, Goat House. Scale bar: 1 mm.
Figure 1 in Dissecting an island radiation: systematic revision of endemic land snails on Lord Howe Island (Gastropoda: Stylommatophora: Microcystidae)
Figure 1. Map showing location and major morphological features of Lord Howe Island and surrounding islands. From
Fig. 2 in Role of microhabitat and temporal activity in facilitating coexistence of endemic carnivores on the California Channel Islands
Fig. 2.— Kernel density estimates of fine-scale circadian activity of island spotted skunks (Spilogale gracilis amphiala; solid line) and island foxes (Urocyon littoralis; dotted line) from camera data collected on Santa Cruz Island, California, USA, in 2016 and 2017 (A) and on Santa Rosa Island, California, USA, in 2017 (B). The coefficient of overlap in activity between skunks and foxes, represented by the shaded area, was Δ = 0.66 (95% CI 0.60 – 0.72) on Santa Cruz Island and Δ = 0.55 (95% CI 0.49 – 0.62) on Santa Rosa Island.
Fig. 1.—Coefficient estimates with 95 in Role of microhabitat and temporal activity in facilitating coexistence of endemic carnivores on the California Channel Islands
Fig. 1.—Coefficient estimates with 95% confidence intervals for important predictors (i.e., top models ≤ 2 ΔAIC) of microhabitat associations of island spotted skunks (Spilogale gracilis amphiala) and island foxes (Urocyon littoralis) from zero-inflated Poisson generalized linear mixed models (GLMMs; skunks) and Poisson GLMMs (foxes) using trap data collected on Santa Cruz and Santa Rosa islands, California, United States, in 2015–2017 (A and B, respectively), and from negative binomial GLMMs using camera data collected on Santa Cruz Island in 2016 and 2017 (C) and camera data collected on Santa Rosa Island in 2017 (D). Figure includes coefficient estimates for each species responding to the important predictors for the other. Gray triangles represent skunks, black circles represent foxes, solid lines for confidence intervals indicate the estimate is an important predictor for the species, and dotted lines for confidence intervals indicate the estimate is not an important predictor for the species. See Table 1 for descriptions of microhabitat variables.
FIGURE 6 in Molecular phylogeny and taxonomy of the genus Nanocnide (Urticaceae) with particular attention to the Ryukyu Islands endemic N. lobata
FIGURE 6. The phylogenetic tree of Nanocnide compared to the key. The labels A, B and C on the tree branches correspond to the distinguishing morphologies in the key. The up and down of the labels also correspond to the order of the key. For example, the upper branch with the label A corresponds to the first key of A.
FIGURE 4. A in Molecular phylogeny and taxonomy of the genus Nanocnide (Urticaceae) with particular attention to the Ryukyu Islands endemic N. lobata
FIGURE 4. A photography of a staminate flower of N. japonica (left) and its hollow (right). The hollow is arrowed and edged by a broken line. (Japan, Chiba Pref., Katori, 28 March 2018.)
FIGURE 3. Genetic structure between N. lobata and N in Molecular phylogeny and taxonomy of the genus Nanocnide (Urticaceae) with particular attention to the Ryukyu Islands endemic N. lobata
FIGURE 3. Genetic structure between N. lobata and N. pilosa based on averaged MIG-seq data inferred using structure. The sample 1–4 and 5–9 correspond to N. lobata and N. pilosa. More precisely, the numbers correspond to the samples as follows: 1: R2. 2: R9. 3: R10. 4: R19. 5: R23. 6: KY18. 7: 33028. 8: H30528. 9: H30337.
FIGURE 2 in Molecular phylogeny and taxonomy of the genus Nanocnide (Urticaceae) with particular attention to the Ryukyu Islands endemic N. lobata
FIGURE 2. Genetic structure in Nanocnide based on averaged MIG-seq data inferred using structure. The samples 1–4, 5–9 and 10–34 correspond to N. lobata, N. pilosa and N. japonica, respectively. More precisely, the numbers correspond to the samples as follows: 1: R2. 2: R9. 3: R10. 4: R19. 5: R23. 6: KY18. 7: 33028. 8: H30528. 9: H30337. 10: Tai. 11: 602. 12: A1. 13: B2. 14: C1. 15: S2. 16: KY2. 17: KY25. 18: KY29. 19: TC2. 20: KO2. 21: KO7. 22: CH4. 23: CH10. 24: CH25. 25: CH29. 26: CH33. 27: NG2. 28: HK2. 29:HK9. 30: TH2. 31: TH16. 32: 827. 33: H30608. 34: L150039.
FIGURE 5. A in Molecular phylogeny and taxonomy of the genus Nanocnide (Urticaceae) with particular attention to the Ryukyu Islands endemic N. lobata
FIGURE 5. A seed and its mucilage of N. japonica on a tip of tweezers (Cultivated, originally collected from Japan, Tochigi Pref. Mt. Futamata on 14 April 2018.)
FIGURE 1 in Molecular phylogeny and taxonomy of the genus Nanocnide (Urticaceae) with particular attention to the Ryukyu Islands endemic N. lobata
FIGURE 1. The obtained phylogenetic trees. Left: The ML tree of ITS sequence for Nanocnide. The identical genotypes are collapsed at the right side of a triangular. Numbers near a branch stand for ML bootstrap value, MP bootstrap value, and BI posterior probability of the branch. The support in MP tree is based on the most frequent values of all the multiple MP trees. Hyphens mean the branch did not appear in the corresponding analysis. Samples with identical sequences are collapsed and listed in the same line, but a triangle on a tip of the tree shows a single sequence corresponding to the samples on listed in two lines. The sample name abbreviations for the samples from GenBank are listed in Table 3. Right: The ML tree of Nanocnide based on MIG-seq. Numbers below a branch stand for bootstrap values (1000 times) for min_samples_locus = 1 / min_samples_locus = 4. Bootstrap values less than 50 in both parameters were omitted. Abbreviation after the sample locality shows the country of the locality. (C): Mainland China, (J): Japan and (T): Taiwan.
FIGURE 5. Tillandsia alcatrazensis phenotypical variation. A–C in Tillandsia alcatrazensis (Bromeliaceae), a new endemic species from Alcatrazes Island in southeastern Brazil
FIGURE 5. Tillandsia alcatrazensis phenotypical variation. A–C. Front view of the inflorescences. D–F. Lateral view of the inflorescences. G–I. Habit. Bars: A–F = 1 cm; G–I = 2 cm. Photos by G.P. Sabino based on G.P. Sabino et al. 772 (A,D,G), GPS et al. 773 (B,E,H) and GPS et al. 774 (C,F,I).
FIGURE 4. A–J in Tillandsia alcatrazensis (Bromeliaceae), a new endemic species from Alcatrazes Island in southeastern Brazil
FIGURE 4. A–J Tillandsia alcatrazensis (G.P. Sabino 551). A. Habit. B. Inflorescence branch. C. Floral bract and flower. D. Detail of the lepidote sepal. E. Floral bracts. F. Sepals. G. Petals. H. Stigma. I. Gynoecium. J. Stamen. (Illustration by Danilo Ulbrich Tavares).
FIGURE 3. Tillandsia alcatrazensis. A. Habit. B in Tillandsia alcatrazensis (Bromeliaceae), a new endemic species from Alcatrazes Island in southeastern Brazil
FIGURE 3. Tillandsia alcatrazensis. A. Habit. B. Primary branch (left) and primary branch with a secondary branch (right). C. flower with a floral bract. D. Floral bracts. E. Sepals. F. Petals. G. Stamens. H. Gynoecium. Bars: A = 2 cm; B–C= 1 cm; D= 1 cm; E= 1 cm; F= 1 cm; G, H = 0.5 cm. (Photos by G.P. Sabino based on G.P. Sabino 551, 772).
FIGURE 2 in Tillandsia alcatrazensis (Bromeliaceae), a new endemic species from Alcatrazes Island in southeastern Brazil
FIGURE 2. Tillandsia alcatrazensis in habitat. A. Growing as a rupicole on rocky substrate of the granitic outcrops, photo by Gabriel Pavan Sabino. B. Close up of the flowers, photo by Vitor de Andrade Kamimura.
FIGURE 1 in Tillandsia alcatrazensis (Bromeliaceae), a new endemic species from Alcatrazes Island in southeastern Brazil
FIGURE 1. Geographical location and habitat of Tillandsia alcatrazensis in Alcatrazes Island, state of São Paulo, southeastern Brazil. A. South America and Alcatrazes Island location, São Paulo state, southeastern Brazil. B. Red dots indicating the collection points of T. alcatrazensis on the island (adapted from Google Earth Pro). C. Overview of Alcatrazes Island, photo by Luciano Candisani. D. Overview of a granitic outcrop where Tillandsia alcatrazensis grows together with Tillandsia cf. araujei and Coleocephalocereus fluminensis, photo by Gabriel Pavan Sabino.
Data from: The relevance of gene flow in metapopulation dynamics of an oceanic island endemic, Olea europaea subsp guanchica
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Data from: Genetic characterization of the endangered and endemic anchialine squat lobster Munidopsis polymorpha from Lanzarote (Canary Islands): management implications
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Data from: Speciation processes in putative island endemic sister bat species: false impressions from mitochondrial DNA and microsatellite data
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Data from: Partial support for the central–marginal hypothesis within a population: reduced genetic diversity but not increased differentiation at the range edge of an island endemic bird
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Data from: Microhabitat heterogeneity and a non-native avian frugivore drive the population dynamics of an island endemic shrub, Cyrtandra dentata
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Allen Brain Atlas
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International Brain Laboratory public data
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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.