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35 results for “wombats”

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dryad36/100

Abundance and population growth estimates for bare-nosed wombats

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publicAug 2023View details →
dryad36/100

Data from: Cranial remains of Ramsayia magna from the Late Pleistocene of Australia and the evolution of gigantism in wombats (Vombatidae; Marsupialia)

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publicDec 2022View details →
zenodo32/100

Neutron powder diffraction from NIST 660c LaB6 standard for calibration of Wombat high-intensity neutron powder diffractometer

<p>Calibration data for the Wombat high intensity powder diffractometer, ANSTO, collected at a nominal wavelength of 1.64A from NIST 660c LaB<sub>6</sub> standard using the [224] reflection from a single crystal Ge monochromator, [335] cut. Note that B in this standard is enriched to 99% with isotope <sup>11</sup>B. The sample was loaded in a 6mm diameter vanadium cylindrical sample can.</p>

opencc-by-4.0Feb 2020View details →
zenodo32/100

Figure 8 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 8. Architectural parameters of muscle groups crossing the shoulder, elbow, and wrist in the koala (K) and the common wombat (W). The less y axis relates to stacked bars and shows (A) summed PCSA and (B) mean fascicle length (normalized by body mass). The right y axis relates to circle (koala) and square (wombat) points, and shows the ratio between these PCSA and FL values for each antagonistic muscle group, as a measure of relative emphasis placed by these species on opposing actions at each of the forelimb joints. Muscles assigned to each functional group are detailed in Table 5.

opennotspecifiedJun 2023View details →
zenodo32/100

Figure 4 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 4. Muscle aưachment sites on the right humerus of the koala (A) and common wombat (B) in lateral, cranial, medial, and caudal views. For abbreviations see Table 2. Articulated versions of these muscle maps are available in the Supporting Information, Model S2.

opennotspecifiedJun 2023View details →
zenodo32/100

Figure 7 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 7. Functional morphospace showing PCSA and fascicle length values for muscles of the forelimb in the (A) koala and the (B) common wombat. Values have been normalized by individual body mass. For abbreviations see Table 2.

opennotspecifiedJun 2023View details →
zenodo32/100

Figure 1 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 1. Muscle topology of the right forelimb of the (A) koala and the (B) common wombat in lateral view at sequential depths of dissection from superficial (top) to deep (boưom). For abbreviations see Table 2. An interactive version of this figure is available in the Supporting Information, Model S1.

opennotspecifiedJun 2023View details →
zenodo32/100

Figure 3 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 3. Muscle aưachment sites on the right scapula of the koala (A) and common wombat (B) in lateral, medial, distal, and inferior views. For abbreviations see Table 2. Articulated versions of these muscle maps are available in the Supporting Information, Model S2.

opennotspecifiedJun 2023View details →
zenodo32/100

Figure 2 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 2. Muscle topology of the right forelimb of the (A) koala and the (B) common wombat in medial view at sequential depths of dissection from superficial (top) to deep (boưom). For abbreviations see Table 2. An interactive version of this figure is available in the Supporting Information, Model S1.

opennotspecifiedJun 2023View details →
zenodo32/100

Figure 6 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 6. Muscle aưachment sites on the right manus of the koala (A) and common wombat (B) in ulnar, dorsal, radial, and palmar views. For abbreviations see Table 2. Articulated versions of these muscle maps are available in the Supporting Information, Model S2.

opennotspecifiedJun 2023View details →
zenodo32/100

Figure 5 in Hanging on and digging deep: comparative forelimb myology of the koala (Phascolarctos cinereus) and common wombat (Vombatus ursinus)

Figure 5. Muscle aưachment sites on the right radius and ulna of the koala (A) and the common wombat (B) in lateral, cranial, medial, and caudal views. For abbreviations see Table 2. Articulated versions of these muscle maps are available in the Supporting Information, Model S2.

opennotspecifiedJun 2023View details →
dryad32/100

Data from: Isolation, marine transgression, and translocation of the bare-nosed wombat (Vombatus ursinus)

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publicFeb 2019View details →
dryad28/100

Data from: Invasive pathogen drives host population collapse: effects of a travelling wave of sarcoptic mange on bare-nosed wombats

1.Emerging and invasive pathogens can have long-lasting impacts on susceptible wildlife populations, including localised collapse and extirpation. Management of threatening disease is of widespread interest and requires knowledge of spatiotemporal patterns of pathogen spread. 2.Theory suggests disease spread often occurs via two patterns: homogenous mixing and travelling waves. However, high resolution empirical data demonstrating localised (within population) disease spread patterns are rare. 3.This study examined the spread of sarcoptic mange (aetiological agent Sarcoptes scabiei) in a population of bare-nosed wombats (Vombatus ursinus), and investigated whether pathogen spread occurred by homogenous mixing or a travelling wave. 4.Using seven years of population surveys and four years of disease severity surveys, we show that mange was first detected in the east of a wombat population in northern Tasmania, and progressed westward as a travelling wave. Wombat mortality rates reached 100% behind the wave, with a 94% decline in overall wombat abundance within the park. 5.Synthesis and applications. Globally distributed pathogens may have severe impacts on susceptible host species. This is the first study to quantify population level impacts of sarcoptic mange upon bare-nosed wombats, showing a wave of mange disease which resulted in a dramatic population decline. Successful management of the spread of this and similar pathogens may hinge on the capacity to establish transmission barriers at local or between-population scales.

opencc-zeroDec 2016View details →
zenodo28/100

On following page: 3. Northern Hairy-nosed Wombat (Lasiorhinus krefftii). in Vombatidae

On following page: 3. Northern Hairy-nosed Wombat (Lasiorhinus krefftii).

opennotspecifiedJun 2015View details →
dryad28/100

Data from: Invasive pathogen drives host population collapse: effects of a travelling wave of sarcoptic mange on bare-nosed wombats

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publicJun 2018View details →

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