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2,247 results for “Western Australia”
Figure 2 in A New Bat Species from Southwestern Western Australia, Previously Assigned to Gould's Long-eared Bat Nyctophilus gouldi Tomes, 1858
Figure 2. Specimen scores on the first two axes of a PCA based on a correlation matrix of nine cranial characters of adult male N. holtorum sp. nov. (squares, n = 6) and N. gouldi sensu stricto (circles, n = 79): (a) PCA scores grouped by species, and (b) same plot with N. gouldi coded by four geographic localities: montane and subcoastal NSW and far southeastern Qld (closed circles); southern and eastern Victorian montane regions (closed diamonds); inland and northern Qld (open circles) and inland NSW and northern Victoria (triangles).
Figure 3 in A New Bat Species from Southwestern Western Australia, Previously Assigned to Gould's Long-eared Bat Nyctophilus gouldi Tomes, 1858
Figure 3. Bivariate plots (mm) showing overlap in measurements of adult N. holtorum sp. nov. (squares, polygons) and adult N. gouldi sensu stricto (circles). Solid symbols are females, open symbols male: (a), condylo-basal skull length (CON) vs. least inter-temporal breadth (INT); (b) CON vs. mastoid breadth (MASB); (c), CON vs. braincase height (BRH); (d) forearm length (FA) vs. greatest skull length (GSL), and (e) FA vs. length from canine to upper rear molar (CM3).
Figure 6 in A New Bat Species from Southwestern Western Australia, Previously Assigned to Gould's Long-eared Bat Nyctophilus gouldi Tomes, 1858
Figure 6. Distributional records of N. holtorum sp. nov. based on AM and WAM voucher specimens examined (n = 26 localities) and bioregional boundaries of the Interim Biological Regionalization Scheme (IBRS version 7; DSEWPAC, 2012). Regions are: AVW, Avon Wheatbelt; JAF, Jarrah Forests; SWA, Swan Coastal Plain and WAR, Warren.
Figure 1 in A New Bat Species from Southwestern Western Australia, Previously Assigned to Gould's Long-eared Bat Nyctophilus gouldi Tomes, 1858
Figure 1. Highest maximum likelihood tree of relationships amongst Nyctophilus using: (a) 28 COI haplotypes, and (b) 21 CytB haplotypes. Bootstrap support (%) is shown at branch nodes. All M numbers refer to AM specimens except where indicated.
Figure 10 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 10. Inferred relative phylogenetic position of Macroderma handae sp. nov. based on observable synapomorphic features (modified after Hand, 1996; numbers indicate the development of potential apomorphic character states, as detailed in that reference).
Figure 5 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 5. Scanning electron micrographs of paratype material of Macroderma handae sp. nov. (A) fragment of the right maxilla with alveoli of the C1 and P4, paratype WAM 2020.4.5; (B) palatal fragment of left maxilla with lingual alveoli of P4 and M1, paratype WAM 2020.4.4; (C) detail of the blood vessel fenestrations in paratype WAM 2020.4.4; (D) probable wear striations on the M3, paratype WAM 2020.4.11; (E) wear striations from M. gigas ANWC CM568. Scale bars 1 mm, except where indicated otherwise.
Figure 8 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 8. Scanning electron micrographs of paratype material of Macroderma handae sp. nov. (A, B, D) lingual, labial and occlusal views of a left P2, paratype WAM 2020.4.8; (C) labial view of the left P2 of M. gigas ANWC CM568; (E, G, H) occlusal, lingual-oblique, and posterior views of a damaged left P4, paratype WAM 2020.4.12; (F) occlusal view of a left P4 of M. gigas ANWC CM568. Scale bars 1 mm.
Figure 4 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 4. Scanning electron micrographs of holotype and paratype material of Macroderma handae sp. nov. (A, C, E, G) occlusal, lingual, labial, and labial-oblique views of the left M2 from the holotype WAM 2020.4.1; (B, D, F, H) corresponding views of the left M2 of M. gigas ANWC CM568; (I) occlusal view of left M3, paratype WAM 2020.4.11; (J) left M3 of M. gigas ANWC CM568. Scale bars 1 mm.
Figure 7 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 7. Scanning electron micrographs of paratype material of Macroderma handae sp. nov. (A) anterior half of a right C1, paratype WAM 2020.4.7; (B) lingual view of a right C1 of M. gigas ANWC CM568; (C, D) labial and lingual views of a right C1 with a damaged paracone, paratype WAM 2020.4.9. Scale bars 1 mm.
Figure 6 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 6. Scanning electron micrographs of paratype material of Macroderma handae sp. nov. (A, C) occlusal-oblique views of a right M1, paratype WAM 2020.4.6; (B, D) corresponding views of the right M1 of M. gigas ANWC CM568; (E) occlusal view of a fragment of a right M2, paratype WAM 2020.4.10; (F) corresponding view of the right M2 of M. gigas ANWC CM568. Scale bars 1 mm.
Figure 9 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 9. Scanning electron micrographs of other unidentified and undescribed bat material recovered from the same deposit at Dingo Gap. (A–D) WAM 2020.4.13; (E–G) right C1 of an emballonurid, WAM 2020.4.14; (H) right C1 of an emballonurid, WAM 2020.4.15; (I, J) left C1 of an emballonurid, WAM 2020.4.16; (K, L) left C1 of an emballonurid, WAM 2020.4.17; (M, N) lingual and occlusal views of a fragment of dentary of a vespertilionid containing M1–M3 (M1 is on the right in both views), WAM 2020.4.18. Scale bars 1 mm.
Figure 3 in A New Species of Extinct False Vampire Bat (Megadermatidae: Macroderma) from the Kimberley Region of Western Australia
Figure 3. Scanning electron micrographs of holotype and paratype material of Macroderma handae sp. nov. (A) lateral view of the left dentary of holotype WAM 2020.4.1 with mostly intact M2, broken P4, M1 and M3, and alveoli of single-rooted P2 and C1; (B) occlusal view of the holotype WAM 2020.4.1 anterior to the M2; (C) occlusal view of a fragment of left dentary, paratype WAM 2020.4.3; (D, E) lateral and occlusal view of a fragment of left dentary, paratype WAM 2020.4.2; (F) digital photograph of the left dentary of M. gigas WAM M18284. Scale bars 1 mm.
Datasets for: Climate change and conservation of Caladenia orchids in Western Australia
<p>Occurence data for 26 <em>Caladenia </em>species for the paper: "<strong>Climate change and conservation of Caladenia orchids in Western Australia" </strong></p> <p><strong>Abstract</strong></p> <p>Understanding how species distributions are being shaped by current rises in atmospheric temperature is of immediate conservation importance. Orchids are a globally threatened plant family, with many species having narrow ranges and low abundances that heighten extinction risk due to rising atmospheric temperature. Using 26 rare and common <em>Caladenia </em>orchid species in Western Australia, we first performed a conservation assessment by calculating the proportion of populations that currently occur in conservation areas. We then compared current range extents with past and future climate scenarios. We performed a niche overlap test with a future climate scenario to test how the current population level climatic niche of these species will change. As some of these orchids frequently hybridize, we then quantified how ecogeographical isolation will change under future climates. Only 27% of all <em>Caladenia </em>populations are currently found in protected areas. Most species had reduced range extents in historically warmer climates. However, only three species will experience range extent contractions under future climate scenarios. The current population climatic niche has a 36% overlap with future climates, indicating that current population level conditions may change. Ecogeographical isolation will potentially increase in hybridizing species, thereby acting as a stronger barrier against hybridization. As <em>Caladenia </em>species evolved in seasonally dry conditions, this suggests that there is potential preadaptation to survive under elevated temperatures. Despite their physiological tolerances to elevated temperature, conservation of <em>Caladenia </em>species will depend on the availability of habitat to allow migration within future range limits, and the presence of their key mutualists. </p>
FIGURE 13 in The role of allopatric speciation and ancient origins of Bathynellidae (Crustacea) in the Pilbara (Western Australia): two new genera from the De Grey River catchment
FIGURE 13 Male and female thoracopods VIII of the four genera described for WA. (A, B) male ThVIII of Pilbaranella ethelensis; (C, D) male ThVIII of Fortescuenella serenitatis; (E, F) male ThVIII of Anguillanella callawaensis; (G, H) male ThVIII of Muccanella cundalinensis; (I) female ThVIII of Pilbaranella ethelensis; (J) female ThVIII of Fortescuenella serenitatis; (K) female ThVIII of Anguillanella callawaensis; (L) female ThVIII of Muccanella cundalinensis. Scale bar in mm
FIGURE 10 in The role of allopatric speciation and ancient origins of Bathynellidae (Crustacea) in the Pilbara (Western Australia): two new genera from the De Grey River catchment
FIGURE 10 Muccanella cundalinensis gen. et sp. nov., male holotype (A, B, D, F, H, I); female allotype (E, G); male paratype (C). (A) Antennula (dorsal view); (B) antenna (dorsal view); (C) Paragnath male WAMC57343; (D) labrum; (E) labrum female WAMC57341; (F) palp and mandible male holotype; (G) palp and mandible female allotype; (H) maxillule; (I) maxilla. Scale bar in mm.
FIGURE 11 in The role of allopatric speciation and ancient origins of Bathynellidae (Crustacea) in the Pilbara (Western Australia): two new genera from the De Grey River catchment
FIGURE 11 Muccanella cundalinensis gen. et sp. nov., male holotype. (A) Thoracopod I; (B) thoracopod II; (C) thoracopod III; (D) thoracopod IV; (E) thoracopod V; (F) Thoracopod VI; (G) thoracopod VII. Scale bar in mm.
FIGURE 7 in The role of allopatric speciation and ancient origins of Bathynellidae (Crustacea) in the Pilbara (Western Australia): two new genera from the De Grey River catchment
FIGURE 7 Anguillanella callawaensis gen. et sp. nov., male holotype. (A) Thoracopod I; (B) thoracopod II; (C) thoracopod III; (D) thoracopod IV; (E) thoracopod V; (F) Thoracopod VI; (G) thoracopod VII. Scale bar in mm.
FIGURE 6 in The role of allopatric speciation and ancient origins of Bathynellidae (Crustacea) in the Pilbara (Western Australia): two new genera from the De Grey River catchment
FIGURE 6 Anguillanella callawaensis gen. et sp. nov., male holotype (A–E, G); female allotype (F, H, K, L); male paratype (I, J). (A) Antennula (dorsal view); (B) antenna (dorsal view); (C) max Maxilla; (D) maxillula; (E) mandibular palp male holotype; (F) palp female allotype; (G) mandible male holotype; (H) mandi- ble female allotype; (I) paragnath male WAMC57657 (J) labrum male WAMC57423 (ventral view); (K) Paragnath female allotype; (L) labrum female allotype (dorsal view Downloaded). Scalefrom bar in Brill. mm com. 08/31/2023 03:13:03AM via free access
FIGURE 8 in The role of allopatric speciation and ancient origins of Bathynellidae (Crustacea) in the Pilbara (Western Australia): two new genera from the De Grey River catchment
FIGURE 8 Anguillanella callawaensis gen. et sp. nov., (A–D, F, G, H) male holotype. (A, B) thoracopod VIII (posterior view); (C, D) thoracopod VIII (frontal view); (E) thoracopod VIII female allotype (frontal view); (F) first pleopod; (G) furcal rami and dorsal seta (dorsal view); (H) uropod (latero-internal view). Scale bar in mm. Abbreviations: O. lb, outer lobe; Bsp, basipod; Endp, endopod; Exp, exopod; P.pr, posterior projection; Fr.pr, frontal projection.
FIGURE 4 Maximum Clade Credibility Tree inferred using a concatenate COI, 16S, 28S and 18S alignment using BEAST. Node bars are 95 in The role of allopatric speciation and ancient origins of Bathynellidae (Crustacea) in the Pilbara (Western Australia): two new genera from the De Grey River catchment
FIGURE 4 Maximum Clade Credibility Tree inferred using a concatenate COI, 16S, 28S and 18S alignment using BEAST. Node bars are 95% Higher Posterior Density, scale bar is in million years ago (Ma), starting from present 0. Numbers above bars = node age; numbers below bars (bold) = posterior probability of the node.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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
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