Activity budgets and habitat use of the Green Pygmy-goose (Nettapus pulchellus) on dry-season refuges in Kakadu National Park, Northern Territory

2005 ◽  
Vol 105 (3) ◽  
pp. 217-222 ◽  
Author(s):  
Errol R. Nye ◽  
Chris R. Dickman
Keyword(s):  
Habitat Use ◽  
National Park ◽  
Northern Territory ◽  
Dry Season ◽  
Activity Budgets

Dry-season use of space, habitats and shelters by the short-eared rock-wallaby (Petrogale brachyotis) in the monsoon tropics

2006 ◽  
Vol 33 (3) ◽  
pp. 207 ◽  
Author(s):  
Wendy R. Telfer ◽  
Anthony D. Griffiths
Keyword(s):  
Home Range ◽  
National Park ◽  
Northern Territory ◽  
Dry Season ◽  
Strong Preference ◽  
Use Of Space ◽  
Resting Sites ◽  
Significant Difference ◽  
Simultaneous Use ◽  
Rocky Habitats

It is widely recognised that the use of fixed diurnal shelters by rock-wallabies greatly affects their ecology. However, the details of how shelters and surrounding habitats are used, and how similar these characteristics are across rock-wallaby species, remain scarcely understood. The dry season home range, and use of habitats and den sites, of the short-eared rock wallaby (Petrogale brachyotis) were examined at Litchfield National Park, Northern Territory, Australia. We radio-tracked 10 individuals on foot to locate diurnal shelters, and with fixed towers to determine their nocturnal positions. P. brachyotis used a range of rock piles and outcrops for dens, and showed a strong preference for rocky habitats and adjacent woodland. On average, animals used four dens within outcrops, as well as more exposed resting sites. Individual rock-wallabies sometimes shared dens, but there appeared to be male–male intolerance of simultaneous use of dens. Mean home range in the dry season was 18.3 ha, and there was no significant difference in home-range area between sexes. Use of space by P. brachyotis was very similar to that reported for another tropical rock-wallaby species, P. assimilis, and many behavioural traits were also similar to those found in other species of Petrogale.

New species of Drymopsalta Heath Cicadas (Cicadidae: Cicadettinae: Cicadettini) from Queensland and Northern Territory, Australia, with overview of genus

Zootaxa ◽  
2013 ◽  
Vol 3620 (1) ◽  
pp. 1-42
Author(s):  
A. EWART ◽  
L. W. POPPLE
Keyword(s):  
New Species ◽  
High Frequency ◽  
Similar Pattern ◽  
National Park ◽  
Northern Territory ◽  
Allopatric Species ◽  
Temporal Structures ◽  
Cape York ◽  
Three New Species ◽  
Tree Foliage

Three new species are described in the genus Drymopsalta Ewart, previously known only from D. crepitum Ewart and D. daemeli Distant. The three new species occur in Southern Queensland and Northern Territory. D. wallumi sp. nov. occurs along coastal S.E. Queensland, whereas D. hobsoni sp. nov. is restricted to the Bringalily State Forest, near Inglewood, southern inland Queensland. D. acrotela sp. nov. is found in the Litchfield National Park and other locations near Jabaluka, Cahills Crossing, E. Alligator River and Nourlangie, all across the northern Northern Territory. D. crepitum occurs on the Cape York Peninsular extending into the southern Gulf, while D. daemeli occurs in two localised regions in central coastal N.S.W. Each of the species inhabits heath vegetation, often spilling-over into adjacent tree foliage. The species of Drymopsalta are small and inconspicuous cicadas (<15 mm body length) with relatively high frequency songs (~15 to 22 kHz). The temporal structures of the normal calling songs follow a similar pattern in each species, consisting of the emission of short chirps (comprising 2–16 ticks). Between the chirps are emitted one (D. wallumi, D. hobsoni, D. acrotela), two (D. daemeli) or 1–9 (D. crepitum) intervening single ticks. The species can be distinguished by the timing and the number of these single ticks relative to the adjacent chirps with the notable exception of D. hobsoni and D. acrotela. The calling songs of these two allopatric species are indistinguishable, an unusual feature in Australian cicadas. Two additional song variants are described, a more unstructured chirping song without intervening single ticks observed in each of the species except D. crepitum, and periodic extended buzzing echemes emitted within the calling songs (excepting the D. wallumi song).

scholarly journals The Kruger National Park: Provision of Water for Wild Life

Oryx ◽  
1951 ◽  
Vol 1 (4) ◽  
pp. 187-189
Keyword(s):  
National Park ◽  
Dry Season ◽  
Kruger National Park ◽  
Rain Water ◽  
General Fund ◽  
Run Off ◽  
Wild Life

Two years have passed since Colonel J. A. B. Sandenbergh, the Warden of the Kruger National Park, launched a public appeal to provide water for the wild life of the park. Subscriptions were invited for two purposes: the first to provide boreholes so that in the dry season animals could find water within reach of their grazing, the second to form a general fund to build dams to retard the run-off of rain water.

Dry season diets and habitat use of sympatric Asian elephants (Elephas maximus) and greater one-horned rhinoceros (Rhinocerus unicornis) in Nepal

2005 ◽  
Vol 265 (4) ◽  
pp. 377-385 ◽  
Author(s):  
Geir Steinheim ◽  
Per Wegge ◽  
Jo I. Fjellstad ◽  
Shant R. Jnawali ◽  
Robert B. Weladji
Keyword(s):  
Habitat Use ◽  
Dry Season ◽  
Elephas Maximus ◽  
Asian Elephants

scholarly journals Changes in number and distribution of hippoptamus (Hippopotamus amphibius) in the Sabie River, Kruger National Park, during the 1992 drought

Koedoe ◽  
1995 ◽  
Vol 38 (2) ◽  
Author(s):  
P.C. Viljoen
Keyword(s):  
Southern Africa ◽  
National Park ◽  
Dry Season ◽  
Kruger National Park ◽  
Population Densities ◽  
Drought Period ◽  
Aerial Surveys ◽  
Hippopotamus Amphibius ◽  
Reduced Flow

The 1991/92 drought in Southern Africa and the effect of the resultant reduced flow of the Sabie River on hippopotami was investigated. Hippopotami are counted annually in the Kruger National Park's (KNP) major rivers as part of the park's monitoring pro- gramme. Two additional aerial surveys were conducted to document changes in hippopotamus population densities in the Sabie River during the drought period. The hippopotamus population decreased during the drought by 12.6 to 672 animals between July 1991 and October 1992. The highest and lowest hippopotamus densities recorded were 11.6 and 2.2 animals/km river length respectively in different river sections. Only 12 hippopotamus mortalities were recorded at the end of the 1992 dry season (October).

Thinking honeyeater: nectar maps for the Northern Territory, Australia

2000 ◽  
Vol 6 (1) ◽  
pp. 61 ◽  
Author(s):  
John C. Z. Woinarski ◽  
Greg Connors ◽  
Don C. Franklin
Keyword(s):  
Northern Territory ◽  
Dry Season ◽  
Spatial And Temporal Variation ◽  
Wet Season ◽  
Nectar Production ◽  
The World ◽  
Eucalypt Forests ◽  
The Times ◽  
Species Specific ◽  
Nectar Availability

We create monthly maps of nectar availability for the 1.4 x 106 km2 jurisdiction of the Northern Territory, Australia. These are based on a combination of vegetation mapping and a series of indices of plant species specific nectar scoring. The maps reveal complex spatial and temporal variation in nectar availability, but most notably a greater nectar resource in the monsoon-influenced north than in the arid south, and a peak in nectar availability in the dry season. The latter is associated with the extensive tropical eucalypt forests (especially those co-dominated by Eucalyptus miniata and E. tetrodonta). In contrast, wet season nectar availability in these forests is limited, but riparian and swampland forests, typically dominated by Melaleuca species, provide rich but spatially restricted nectar resources. The extensive and rich nectar resources available in eucalypt forests in the dry season supplement the diets of many species which are not primarily nectarivorous. This resource helps shape the singularity of northern Australian eucalypt forests relative to other extensive forests elsewhere in the world. Nectarivores remain in the system through a combination of movements across a number of scales, habitat shifting, and diet shifting. The latter is aided by the peaking of invertebrate and fruit resources at the times of minimum nectar production; a shuffling in resource availability brought about by the extreme climatic seasonality.

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