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22 results for “Macropus”
Figs. 38–44 Macroponema comani Mawson, 1978 from Macropus giganteus. 38 in Revision of MaCroponema Mawson, 1978 (Nematoda: Strongylida) from macropodid marsupials with the description of two new species
Figs. 38–44 Macroponema comani Mawson, 1978 from Macropus giganteus. 38 Posterior end of male, ventral view, showing lateral (L) and central cordate (C) thickenings of spicule sheaths. 39 Posterior end of male, left lateral view, showing thickenings of spicule sheaths. 40 Bursa, apical view. 41 Genital cone, dorsal view. 42 Female tail, right lateral view. 43 Vagina and ovejector, left, lateral view. 44 Female genital system, showing uteri and seminal receptacles. Scale-bars: 0.1 mm
Figs. 29–37 Macroponema comani Mawson, 1978 from Macropus giganteus. 29 Anterior region, left lateral view. 30 Buccal capsule, lateral view. 31 Buccal capsule, ventral view. 32 Anterior extremity, apical view. 33 in Revision of MaCroponema Mawson, 1978 (Nematoda: Strongylida) from macropodid marsupials with the description of two new species
Figs. 29–37 Macroponema comani Mawson, 1978 from Macropus giganteus. 29 Anterior region, left lateral view. 30 Buccal capsule, lateral view. 31 Buccal capsule, ventral view. 32 Anterior extremity, apical view. 33 Mouth opening, apical view, showing detail of cephalic papillae and amphids. 34 Transverse optical section through oesophagus at level of oesophageal bulb, showing anterior extension of intestine. 35 Oesophageal corpus, showing bead-like sclerotisations of lining. 36 Transverse section of oesophageal corpus, showing bead-like sclerotisations of lining. 37 Spicule tip, left lateral view. Scale-bars: 29–32, 34–37, 0.1 mm; 33, 0.01 mm
Fig. 5 in A retrospective study of Babesia macropus associated with morbidity and mortality in eastern grey kangaroos (Macropus giganteus) and agile wallabies (Macropus agilis)
Fig. 5. Phylogenetic tree of heat shock protein 70 (hsp70) gene sequences of eastern grey kangaroo and agile wallaby Babesia and other piroplasm hsp70 sequences in the GenBank nucleotide database. For each sequence, the GenBank GI number is followed by the species name. The representative Babesia isolates from eastern grey kangaroos and an agile wallaby in this study are shown with a - and a ♦ respectively. The evolutionary history was inferred using the Maximum Likelihood method based on the TamuraNei model (Tamura and Nei, 1993). The tree with the highest log likelihood (−6290.3774) is shown. Initial tree for the heuristic search was obtained automatically as follows. When the number of common sites was <100 or less than one fourth of the total number of sites, the maximum parsimony method was used; otherwise, BIONJ method with MCL distance matrix was used. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The scale bar represents the number of substitutions per nucleotide. All positions containing gaps and missing data were eliminated. There are limited data available on this locus within the public data repositories and as such there is some lack of consistency with the 18S ribosomal RNA tree.
Fig. 4 in A retrospective study of Babesia macropus associated with morbidity and mortality in eastern grey kangaroos (Macropus giganteus) and agile wallabies (Macropus agilis)
Fig. 4. Phylogenetic tree of 18S ribosomal RNA (18S rRNA) gene sequences of eastern grey kangaroo and agile wallaby Babesia and other piroplasms that are in the GenBank nucleotide database. For each sequence, the GenBank GI number is followed by the species name. The representative Babesia isolates from eastern grey kangaroos and an agile wallaby in this study are shown with a - and a ♦ respectively. Evolutionary history was inferred using the Maximum Likelihood method based on the Tamura 3-parameter model. The tree with the highest log likelihood (−1820.5242) is shown. Initial tree for the heuristic search was obtained automatically as follows. When the number of common sites was <100 or less than one fourth of the total number of sites, the maximum parsimony method was used; otherwise, BIONJ method with MCL distance matrix was used. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The scale bar represents the number of substitutions per nucleotide. All positions containing gaps and missing data were eliminated. Evolutionary analyses were conducted in MEGA6 (Tamura et al., 2011).
Fig. 1 in A retrospective study of Babesia macropus associated with morbidity and mortality in eastern grey kangaroos (Macropus giganteus) and agile wallabies (Macropus agilis)
Fig. 1. Map showing the distribution of the 38 cases of Babesia infection in eastern grey kangaroos in coastal New South Wales and southeastern Queensland over the period 1995–2013. Insert also shows the two locations of the three cases identified in agile wallabies in northern Queensland in 2009 and 2013. The locations of cases were converted to GPS coordinates and mapped using GPS Visualizer on 21/05/2014 (www.gpsvisualizer.com).
Fig. 3 in A retrospective study of Babesia macropus associated with morbidity and mortality in eastern grey kangaroos (Macropus giganteus) and agile wallabies (Macropus agilis)
Fig. 3. Transmission electron micrographs showing the intravascular location and structure of Babesia organisms in the kidney and brain of eastern grey kangaroos. (A) Kidney, the cytoplasm of two adjacent erythrocytes contains Babesia merozoites (arrows) with a membrane-bound nucleus (N) and cytoplasm containing polymorphic vacuoles and some electron dense particles (C) (scale bar = 1.0 μm). (B) Brain, adjacent to an intact erythrocyte and the nucleus of an endothelial cell is a cluster of extraerythrocytic Babesia organisms containing electron dense micronemes and developing pellicles (arrows) (scale bar = 2.0 μm). (C) Brain, within the capillary lumen is a cluster of eight or nine extraerythrocytic organisms (thick arrow) and a distorted erythrocyte (thin arrow) containing four intracytoplasmic parasites (scale bar = 5.0 μm).
Fig. 2 in A retrospective study of Babesia macropus associated with morbidity and mortality in eastern grey kangaroos (Macropus giganteus) and agile wallabies (Macropus agilis)
Fig. 2. Photomicrographs showing the forms of Babesia seen in cytological preparations and tissue sections in macropods. (A) Agile wallaby. Giemsa stained peripheral blood smear showing extraerythrocytic zoites (thin arrow) and merozoites (thick arrow) within an intact erythrocyte. (B) Eastern grey kangaroo. Diff-Quik-stained renal impression smear demonstrating 2 or 4 merozoites within intact erythrocytes (thick arrows) and clusters of extraerythrocytic zoites (thin arrows). (C) Eastern grey kangaroo. DiffQuik-stained brain squash preparation showing large clusters of intravascular zoites (arrows). (D) Eastern grey kangaroo. H&E stained section of kidney glomerulus showing merozoites within intact erythrocytes (thick arrows) and as large extraerythrocytic clusters of zoites (thin arrows). All scale bars = 20 μm.
Fig. 1 in Observation of a novel Babesia spp. in Eastern Grey Kangaroos (Macropus giganteus) in Australia
Fig. 1. Photomicrograph of a blood smear from an Eastern Grey kangaroo stained with Giemsa and showing the presence of Babesia species merozoites. Bar = 10 µm.
Fig. 3 in Observation of a novel Babesia spp. in Eastern Grey Kangaroos (Macropus giganteus) in Australia
Fig. 3. Electron micrographs of Babesia spp. (Case 2) within an erythrocyte. Nucleus (N); host cytoplasm (HC); endoplasmic reticulum (ER); ribosome (RI); mitochondria (MC), and invagination (I). Bar = 0.5 µm.
Fig. 2 in Observation of a novel Babesia spp. in Eastern Grey Kangaroos (Macropus giganteus) in Australia
Fig. 2. Photomicrograph of blood smears stained with Diff-Quik (A) and Giemsa (B–F) from eastern grey kangaroos (Cases 2 and 3) showing diverse forms of Babesia including paired merozoites (2A), multiple ring-shaped trophozoites with a chromatin dot (2B), a large ring-shaped trophozoite with three chromatin dots (2C), ring-shaped trophozoite with a pair of buds in early dividing stage (2D), two dividing trophozoites with a cytoplasmic bridge (2E), and a clump of diverse forms of extraerythrocytic Babesia (3F). Bar = 10 µm.
Fig. 4 in Observation of a novel Babesia spp. in Eastern Grey Kangaroos (Macropus giganteus) in Australia
Fig. 4. Minimum evolution phylogenetic tree based on a 1560 bp 18S rRNA alignment for representatives of the genus Babesia including the new kangaroo-infecting species (in bold and underlined) originating from Cases 1 and 2. Also underlined and in bold are other species sequenced as part of this study. Branch support is shown with a ‡ where all tree building methods (parsimony, distance and likelihood) had at least 70% bootstrap and Bayesian support.
Fig. 1 in Toxoplasma gondii in four captive kangaroos (Macropus spp.) in China: Isolation of a strain of a new genotype from an eastern grey kangaroo (Macropus giganteus)
Fig. 1. Toxoplasma gondii cysts in kangaroos or mice. A. Toxoplasma gondii cysts in the diaphragm of case 2 kangaroo, H&E. B. Toxoplasma gondii cysts in the tongue of case 2 kangaroo, H&E. C. Toxoplasma gondii cysts in the diaphragm of case 2 kangaroo, IHC. D. Toxoplasma gondii cysts in the tongue of case 2 kangaroo, IHC. E. Toxoplasma gondii-like cysts in the myocardium of case 4 kangaroo, squashed section, unstained. F. Many TgRooCHn1 Toxoplasma gondii cysts were observed in the mouse brain, 27 DPI, squashed section, unstained. Bar = 50 μm.
Magnetic Resonance Imaging Scan of the Brain of a Red kangaroo (Macropus rufus)
<p>Magnetic Resonance Imaging Scan of the Brain of a Red kangaroo (<i>Macropus rufus</i>) from http://braincatalogue.org/Red_kangaroo</p>
Assessing physiological, behavioral and movement responses to Suprelorin® implant delivery methods in free-ranging eastern grey kangaroos (Macropus giganteus)
Open the record for dataset details and reuse information.
On following pages: 452. Long-toed Myotis (Myotis secundus); 453. Bornean Whiskered Myotis (Myotis borneoensis); 454. Malaysian Whiskered Myotis (Myotis federatus): 455. Indochinese Myotis (Myotis indochinensis); 456. Peyton's Myotis (Myotis peyton); 457. Burmese Whiskered Myotis (Myotis montivagus); 458. Long-fingered Myotis (Myotis capaccinii); 459. Chinese Water Myotis (Myotis laniger); 460. Csorba's Myotis (Myotis csorbal); 461. Kashmir Cave Myotis (Myotis longipes); 462. Annamit Myotis (Myotis annamiticus); 463. Phan Luong's Myotis (Myotis phanluongi); 464. Himalayan Whiskered Myotis (Myotis siligorensis); 465. Chestnut Myotis (Myotis badius); 466. Ridley's Myotis (Myotis ridley); 467. Thick-thumbed Myotis (Myotis rosseti); 468. Horsfield's Myotis (Myotis horsfieldi); 469. Pallid Large-footed Myotis (Myotis macrotarsus); 470. Stalker's Myotis (Myotis stalkeri); 471. Gray Large-footed Myotis (Myotis adversus); 472. Maluku Myotis (Myotis moluccarum); 473. Southern Myotis (Myotis macropus); 474. Lesser Large-footed Myotis (Myotis hasselti). in Vespertilionidae
On following pages: 452. Long-toed Myotis (Myotis secundus); 453. Bornean Whiskered Myotis (Myotis borneoensis); 454. Malaysian Whiskered Myotis (Myotis federatus): 455. Indochinese Myotis (Myotis indochinensis); 456. Peyton's Myotis (Myotis peyton); 457. Burmese Whiskered Myotis (Myotis montivagus); 458. Long-fingered Myotis (Myotis capaccinii); 459. Chinese Water Myotis (Myotis laniger); 460. Csorba's Myotis (Myotis csorbal); 461. Kashmir Cave Myotis (Myotis longipes); 462. Annamit Myotis (Myotis annamiticus); 463. Phan Luong's Myotis (Myotis phanluongi); 464. Himalayan Whiskered Myotis (Myotis siligorensis); 465. Chestnut Myotis (Myotis badius); 466. Ridley's Myotis (Myotis ridley); 467. Thick-thumbed Myotis (Myotis rosseti); 468. Horsfield's Myotis (Myotis horsfieldi); 469. Pallid Large-footed Myotis (Myotis macrotarsus); 470. Stalker's Myotis (Myotis stalkeri); 471. Gray Large-footed Myotis (Myotis adversus); 472. Maluku Myotis (Myotis moluccarum); 473. Southern Myotis (Myotis macropus); 474. Lesser Large-footed Myotis (Myotis hasselti).
FIGURE 1 in A new species of Helvella (Helvellaceae, Pezizomycetes) within the H. macropus group from China
FIGURE 1. Maximum likelihood (ML) tree of Helvella and its allies within Helvellaceae inferred from a combined LSU, TEF and HSP90 dataset. Bootstrap support values for ML ≥ 80 of SH-aLRT or 95 of UFB and posterior probability for BIPP ≥ 0.95 are indicated above the nodes and separated by '-/-/-' (SH-aLRT/UFB/BIPP). Specimens of the current study are given in red. Type specimens are in bold. The letter ET after the sample stands for epitype, HT for holotype, and IET for isoepitype.
FIGURE 2. Helvella guttata. a–e in A new species of Helvella (Helvellaceae, Pezizomycetes) within the H. macropus group from China
FIGURE 2. Helvella guttata. a–e Typical mature specimens (a HKAS 67836; b HKAS 87759; c HKAS 69046; d, e HKAS 69733); f–g Receptacle surface of pileus; h Stipitipellis; i,j Asci and paraphyses; k–n Asci; o,p Ascospores. Scale bars: a–e = 1 cm; f–h = 50 μm; i–p = 20 μm.
FIGURE 1. Maximum likelihood phylogenetic tree generated from combined 5.8S in A new addition to the Helvella macropus group (Helvellaceae) from Southwestern China
FIGURE 1. Maximum likelihood phylogenetic tree generated from combined 5.8S+ITS2, LSU, tef-1α, and hsp90 sequenced dataset. Maximum likelihood bootstrap (ML-BP) ≥ 70% and Bayesian posterior probabilities (BI-PP) ≥ 0.95 are indicated above the nodes. Specimen vouchers are noted after the species names. New samples collected in this study are indicated in red. Type specimens are in bold.
FIGURE 2. Helvella submacropus. a–d in A new addition to the Helvella macropus group (Helvellaceae) from Southwestern China
FIGURE 2. Helvella submacropus. a–d Typical mature specimens (a HKAS 70217, holotype; b HKAS 78930; c HKAS 90592; d HKAS 90593); e Receptacle surface; f Stipal ecto-excipulum; g Asci and paraphyses; h–j Asci; k Ascospores. Scale bars: a–d = 1 cm; e, f = 50 μm; g–k = 20 μm. (e–j treated with Melzer reagent solution).
Analysis of the Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development.
GEO Series GSE30372. Notamacropus eugenii. 10 samples. Type: Non-coding RNA profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
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