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310 results for “Caribbean Islands”
FIGURE 4 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 4. Characterization of pattern elements in skinks of the Subfamily Mabuyinae (top, dorsal view; bottom, side view). For species with dark dorsolateral stripes, the pale middorsal stripe is defined as the zone between the dark dorsolateral stripes.
FIGURE 3 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 3. Head scalation in Neotropical skinks (Mabuyidae, Mabuyinae). Locations and names of head scales on side (A) and top (B) of head. Abbreviations are AL (anterior loreal), F (frontal), FN (frontonasal), FP (frontoparietal), IP (interparietal), LST (lower secondary temporal), M (mental), NU (nuchal), P (parietal), PF (prefrontal), PL (posterior loreal), PT (primary temporal), R (rostral), UST (upper secondary temporal), and UTT (upper tertiary temporal). Selected (non-standard) measurements on side (C) and top (D) of head. Length of eyelid window, supraciliary-2, narial opening, and supranasal scale defined by longest axis. Other scale length measurements (not shown) follow axis of body. Chin scale configuration: (E) no contact between chin shields and infralabials; (F) two
FIGURE 1 in A new skink fauna from Caribbean islands (Squamata, Mabuyidae, Mabuyinae) 3288
FIGURE 1. Map of Caribbean region. Neotropical skinks occur, or once occurred, on the islands indicated.
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms. in Leporidae
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms.
Distribution. Panama (W to Chiriqui, and including Isla del Rey and Isla Saboga in the Gulf of Panama), N & W Colombia, N Venezuela (N of the Orinoco River), and on several islands on the continental shelf of South America and the Caribbean (Margarita, Trinidad, Tobago, and Grenada). in Didelphidae
Distribution. Panama (W to Chiriqui, and including Isla del Rey and Isla Saboga in the Gulf of Panama), N & W Colombia, N Venezuela (N of the Orinoco River), and on several islands on the continental shelf of South America and the Caribbean (Margarita, Trinidad, Tobago, and Grenada).
Distribution. SE Ghana (E of Volta River), Togo, Benin, Nigeria, and NW Cameroon (to a little S of the Sanaga River). The species has been introduced to the Gulf of Guinea islands of Sao Tomé and Principe, and into the Caribbean islands of Grenada, Saint Kitts, and Nevis. in Cercopithecidae
Distribution. SE Ghana (E of Volta River), Togo, Benin, Nigeria, and NW Cameroon (to a little S of the Sanaga River). The species has been introduced to the Gulf of Guinea islands of Sao Tomé and Principe, and into the Caribbean islands of Grenada, Saint Kitts, and Nevis.
Subspecies and Distribution. E.p.patasSchreber,1774—sub-SaharanAfricafromSMauritaniaandSenegaltoChadandCentralAfricanRepublic;isolatedpopulationsinhabittherockyAirMassifofNNigerandtheEnnediMassif,Chad. E.p.baumstarkiMatschie,1905—NCTanzania(SerengetiandAthiPlainsandtheWsideofMt.Kilimanjaro),butthedistributionisnotwelldocumented. E. p. pyrrhonotus Hemprich & Erhenburg, 1829 — Sudan (N to Nubia), South Sudan, W Ethiopia, N DR Congo, N Uganda, and Kenya. Introduced into south-western Puerto Rico in the Caribbean Islands. in Cercopithecidae
Subspecies and Distribution. E.p.patasSchreber,1774—sub-SaharanAfricafromSMauritaniaandSenegaltoChadandCentralAfricanRepublic;isolatedpopulationsinhabittherockyAirMassifofNNigerandtheEnnediMassif,Chad. E.p.baumstarkiMatschie,1905—NCTanzania(SerengetiandAthiPlainsandtheWsideofMt.Kilimanjaro),butthedistributionisnotwelldocumented. E. p. pyrrhonotus Hemprich & Erhenburg, 1829 — Sudan (N to Nubia), South Sudan, W Ethiopia, N DR Congo, N Uganda, and Kenya. Introduced into south-western Puerto Rico in the Caribbean Islands.
FIGURES 42–51. Dasyhelea rhopaloparamera n in The Biting Midges of the Caribbean island Curaçao (Diptera: Ceratopogonidae) I. Species in the genus Dasyhelea Kieffer
FIGURES 42–51. Dasyhelea rhopaloparamera n. sp. Holotype male, 42–45, allotype female, 46–51. 42, 46 head. 43, 48 palpus. 44, 50 wing. 45 genitalia. 47 clypeus. 49 thorax. 51 apex of abdomen and spermatheca. Scale bars = 0.05 mm.
FIGURES 31–41. Dasyhelea curacaoensis n in The Biting Midges of the Caribbean island Curaçao (Diptera: Ceratopogonidae) I. Species in the genus Dasyhelea Kieffer
FIGURES 31–41. Dasyhelea curacaoensis n. sp. Holotype male, 31–34, allotype female, 35-41. 31, 35 head. 32, 38 palpus. 33, 40 wing. 34 genitalia. 36 frontal sclerite. 37 clypeus. 39 thorax and abdomen. 41 apex of abdomen and spermatheca. Scale bars = 0.05 mm.
FIGURES 1–5. Dasyhelea aliciae n in The Biting Midges of the Caribbean island Curaçao (Diptera: Ceratopogonidae) I. Species in the genus Dasyhelea Kieffer
FIGURES 1–5. Dasyhelea aliciae n. sp. Holotype male. 6-10. Dasyhelea recurva n. sp. Holotype male. 1, 6 head. 2, 7. palpus. 3, 8 thorax and abdomen. 4, 9 wing. 5, 10 genitalia. Scale bars = 0.05 mm.
FIGURES 22–30. Dasyhelea cyrtostyla n in The Biting Midges of the Caribbean island Curaçao (Diptera: Ceratopogonidae) I. Species in the genus Dasyhelea Kieffer
FIGURES 22–30. Dasyhelea cyrtostyla n. sp. Holotype male, 22–25, allotype female, 26–30. 22, 26 head. 23, 28 palpus. 24, 29 wing. 25 genitalia. 27 clypeus. 30 apex of abdomen and spermatheca. Scale bars = 0.05 mm.
FIGURES 11–21. Dasyhelea latiala n in The Biting Midges of the Caribbean island Curaçao (Diptera: Ceratopogonidae) I. Species in the genus Dasyhelea Kieffer
FIGURES 11–21. Dasyhelea latiala n. sp. Holotype male, 11–15, allotype female, 16–21. 11, 16 head. 12, 17 clypeus. 13, 18 palpus. 14, 20 wing. 15 genitalia. 19 thorax. 21 apex of abdomen and spermatheca. Scale bars = 0.05 mm.
FIGURES 52–69 in The Biting Midges of the Caribbean island Curaçao (Diptera: Ceratopogonidae) I. Species in the genus Dasyhelea Kieffer
FIGURES 52–69. Male Dasyhelea genitalia structures: sternites 9 (left column), gonocoxal apodemes and parameres (middle column), and aedeagi (right column). 52–54 D. aliciae n. sp., 55–57 D. recurva n. sp., 58–60 D. latiala n. sp., 61–63 D. cyrtostyla n. sp., 64–66 D. curacaoensis n. sp., 67–69 D. rhopaloparamera n. sp. Scale bars = 0.05 mm.
FIGURE 1 in An annotated checklist of the Branchiopoda (Crustacea) of the Dutch Caribbean islands
FIGURE 1. Sample locations on St. Maarten. 1—Fresh Pond North, 2—Fresh Pond South, 3—Little Bay Pond, 4—Great Salt Pond West and 5 –Great Salt Pond East.
FIG. 6 in Deciphering Geographical Affinity and Reconstructing Invasion Scenarios of Boa imperator on the Caribbean Island of Cozumel
FIG. 6. Bayesian clustering for two main continental clades of Boa imperator (Gulf of Mexico and Yucatán Peninsula) and the Cozumel population using STRUCTURE (Pritchard et al., 2000), based on the resulting K ¼ 3 for (A) microsatellite loci and (B) cytochrome b haplotypes. Maps show spatial interpolations of individual assignment into the three genetic clusters obtained with (C) microsatellites and (D) cyt b. Circles indicate individuals from the Gulf of Mexico clade (n ¼ 30), triangles from the Yucatán Peninsula clade (n ¼ 54), and diamonds from Cozumel (n ¼ 16).
FIG. 2 in Deciphering Geographical Affinity and Reconstructing Invasion Scenarios of Boa imperator on the Caribbean Island of Cozumel
FIG. 2. Graphical representation of the demographical reconstruction based on ABC analyses implemented in DIYABC (Cournet et al., 2014) considering different molecular datasets and priors schemes (see text for a detailed explanation).
FIG. 3 in Deciphering Geographical Affinity and Reconstructing Invasion Scenarios of Boa imperator on the Caribbean Island of Cozumel
FIG. 3. (A) Bayesian maximum clade credibility tree based on 220 unique cytochrome b haplotypes for the genus Boa inferred with BEAST (Drummond et al., 2012). Black dots represent the main clades obtained. Posterior probabilities and bootstrap support values are shown above and below the diagonal, respectively. (B) Rooted network based on the same 220 unique cyt b haplotypes, inferred with SPLITSTREE (Huson and Bryant, 2006). Arrows indicate the position of the Cozumel unique haplotypes within Boa imperator. See Data Accessibility for tree file.
FIG. 5 in Deciphering Geographical Affinity and Reconstructing Invasion Scenarios of Boa imperator on the Caribbean Island of Cozumel
FIG. 5. (A–C) Main demographic scenarios modeled with DIYABC (Cournet et al., 2014) based on two molecular datasets and the Constrained Optimization scheme of Boa imperator from Cozumel, the Yucatán Peninsula, and the Gulf of Mexico. Note that time is not to scale. (D–E) Prior distribution of parameters corresponding to the three invasion scenarios tested, where the first two axes are shown. (F–G) Posterior predictive test of model fit corresponding to Scenario 1. (H–I) Direct and (J–K) logistic approaches of the three scenario model comparisons. In all cases, left panels (D, F, H, J) and right panels (E, G, I, K) show results from the Original Reduced Datasets (ORD) and the Polymorphic Microsatellite-based Dataset (PMD), respectively.
Figs. 1–4. Sueus niisimai female, 1.6 in The First Report of Sueus niisimai (Eggers, 1923) (Coleoptera: Curculionidae: Scolytinae: Hyorrhynchini) from the Western Hemisphere, from the Caribbean Island of Martinique
Figs. 1–4. Sueus niisimai female, 1.6 mm. 1) Dorsal habitus; 2) Lateral habitus; 3) Head anterior; 4) Elytral declivity.
FIGURES 1–6 in Gato hyalinus gen. et sp. nov., an unusual araphid tube-dwelling diatom from Western Pacific and Caribbean islands
FIGURES 1–6: Gato hyalinus light microscopy. Figs 1–4: Live colonies and cells showing mucilage tubes and plastids. Fig. 1. Colony showing branching. A Striatella unipunctata cell (S.u.) has attached to the end of one tube and there appear to be naviculoid cells inside the tubes (some indicated by arrows). Top part of colony partially overlain by a ribbon of Hyalosira interrupta (H.i.) (GU44O-F). Fig. 2: Dividing cell in near-girdle view at apex of colony, at two focal planes. A Licmophora sp. cell (L.) is attached to the outside of the tube (GU44O-F). Fig. 3. Cell in valve view (GU44O-F). Fig. 4: Cells in valve and girdle view with some evidence of a septum (arrow) within the mucilage tube (GU44W-10). Figs 5–6: Acid cleaned valves in LM, oriented with basal pole to left. Fig. 5: Valve at two focal planes showing rimoportulae at both poles (arrows) and faint sternum (GU44Z-15). Fig. 6: Valve with two rimoportulae (arrows), sternum not visible (GU44Z-15). Scale bars: Figs 1–4 = 20 µm; Figs 5, 6 = 10 µm.
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