Camera traps in the canopy: surveying wildlife at tree hollow entrances

2016 ◽  
Vol 22 (1) ◽  
pp. 48 ◽  
Author(s):  
Nigel Cotsell ◽  
Karl Vernes

This is the first comprehensive camera trap study to examine hollow usage by wildlife in the canopy of trees. Eighty cameras directed at tree hollows were deployed across eight sites in nine species of eucalypt in north-east New South Wales. In total, 38 species (including 21 birds, 9 mammals and 8 reptiles) were recorded at hollow entrances over a three-month period. There was a significant difference between wildlife hollow usage associated with site disturbance and tree growth stage (ANOSIM, P > 0.05); however, there was no significant difference associated with tree hollow diameter (ANOSIM, P > 0.05). The level of anthropogenic disturbance at each site, including vegetation modification of the understorey, was a significant predictor of species presence. Despite the limitations of using camera traps in the canopy of trees this study demonstrates the potential to garner useful insights into the ecology and behaviour of arboreal wildlife.

2014 ◽  
Vol 36 (1) ◽  
pp. 60 ◽  
Author(s):  
Brendan D. Taylor ◽  
Ross L. Goldingay ◽  
John M. Lindsay

Camera traps can detect rare and cryptic species, and may enable description of the stability of populations of threatened species. We investigated the relative performance of cameras oriented horizontally or vertically, and recording mode (still and video) to detect the vulnerable long-nosed potoroo (Potorous tridactylus) as a precursor to population monitoring. We established camera traps for periods of 13–21 days across 21 sites in Richmond Range National Park in north-east New South Wales. Each camera trap set consisted of three KeepGuard KG680V cameras directed at a bait container – one horizontal and one vertical camera in still mode and one horizontal camera in video mode. Potoroos and bandicoots (Perameles nasuta and Isoodon macrourus) were detected at 14 sites and pademelons (Thylogale stigmatica and T. thetis) were detected at 19 sites. We used program Presence to compare detection probabilities for each camera category. The detection probability for all three taxa groups was lowest for the vertical still and similar for the horizontal cameras. The detection probability (horizontal still) was highest for the potoroos (0.43) compared with the bandicoots (0.16) and pademelons (0.25). We estimate that the horizontal stills camera could achieve a 95% probability of detection of a potoroo within 6 days compared with 8 days using a vertical stills camera. This suggests that horizontal cameras in still mode have great potential for monitoring the dynamics of this potoroo population.


2017 ◽  
Vol 23 (3) ◽  
pp. 302 ◽  
Author(s):  
Paul D. Meek ◽  
Jason Wishart

Camera traps provide a novel and quasicovert method of gathering information on animal behaviour that may otherwise remain undetected without sophisticated and expensive filming equipment. In a rangelands pest management project at Mt Hope in the central west of New South Wales, Australia, we recorded foxes seemingly hunting kangaroos on three occasions. While we did not record direct instances of predation, our observations provide camera trap photographic evidence suggesting that foxes will attempt to tackle mammals above the critical weight range, including large macropod species such as western grey kangaroos.


2007 ◽  
Vol 34 (6) ◽  
pp. 484 ◽  
Author(s):  
Ross L. Goldingay ◽  
Matthew J. Grimson ◽  
Geoffrey C. Smith

Although nest boxes have considerable application in the research and management of hollow-using arboreal marsupials, few studies have assessed whether species show a preference for particular nest box designs. This study aimed to determine whether the feathertail glider (Acrobates pygmaeus) showed a preference when offered four different designs, each of which had been used in earlier studies. We established one of each design in 45 plots across five locations, spanning north-east New South Wales and south-east Queensland. Feathertail gliders used 34 nest boxes at four locations but avoided a medium-sized rear-entry box with a 45-mm-diameter entrance. No clear preference was shown for three designs with narrow (≤25 mm) entrances. Feathertail gliders used 15 small rear-entry boxes, 10 large slit-entrance boxes and 9 wedge-shaped bat boxes. A slight preference was shown by breeding groups to occur in the non-wedge boxes compared with the wedge boxes. Squirrel gliders (Petaurus norfolcensis) used 51% of medium rear-entry boxes at four locations. This may account for the avoidance of this box design by feathertail gliders at these locations. Breeding and prolonged use of nest boxes by resident feathertail gliders and squirrel gliders at two locations in eucalypt plantations suggest that nest boxes can support local populations of arboreal marsupials where tree hollows are absent or scarce.


2008 ◽  
Vol 56 (1) ◽  
pp. 13 ◽  
Author(s):  
Georgia L. Beyer ◽  
Ross L. Goldingay ◽  
David J. Sharpe

Effective management of tree-hollow-dependent wildlife requires a sound knowledge of the characteristics of the trees used for shelter or breeding. We used radio-tracking to identify the den trees of squirrel gliders (Petaurus norfolcensis) in south-east Queensland (Qld) and north-east New South Wales (NSW). Squirrel gliders used dead trees as well as 13 species of living tree for dens across the two locations. Dead trees accounted for a large percentage of dens (54% of 48 dens in Qld, and 50% of 18 dens in NSW) despite comprising only 3–10% of the forest (trees >20 cm diameter at breast height (dbh)) at each location. This preference is largely due to dead trees being more likely to contain hollows, accounting for 26–44% of available hollow-bearing trees. Mean den tree size (dbh) was 48.9 ± 2.4 cm in Qld and 62.8 ± 5.6 cm in NSW. Den entrance height averaged 6.8 ± 1.2 m in Qld and 11.9 ± 1.3 m in NSW. Fissures in the trunk and holes in branches were the most common of six hollow types used. At one location branch end hollows were ignored relative to their availability. Den entrances varied in size (2.5–12 cm wide) but most were ≤5 cm in diameter. Entrance size of hollows appears to be the hollow attribute of most importance to squirrel gliders. Monitoring of these den trees over several years revealed the collapse of three dead den trees at each location, which is equivalent to an annual loss of 3% of den trees. Further research is needed to determine whether this will lead to a future shortage of den trees.


2007 ◽  
Vol 55 (2) ◽  
pp. 117 ◽  
Author(s):  
C. A. Belcher ◽  
J. L. Nelson ◽  
J. P. Darrant

Analysis of 338 tiger quoll scats from tableland moist forest in south-eastern New South Wales found that the greater glider was the major prey species occurring in 54.1% of scats and contributing an estimated 51.01% of the biomass consumed by tiger quolls. Medium-sized (0.5–5 kg) mammals were the most important prey group by occurrence (53.9%), frequency (66.0%) and estimated biomass contribution to diet (62.93%). Other medium-sized prey taken by tiger quolls included: long-nosed bandicoot, rabbit, brushtail possum and ringtail possum. Macropods and wombats were also present in the scats and had been presumably taken as carrion. There was no significant difference in the diets of male and female tiger quolls. Tiger quolls were recorded hunting greater gliders in their tree hollows during the day, hunting rabbits in their burrows both during the day and at night and were observed eating road-killed macropods and wombats around dawn and dusk.


2019 ◽  
Vol 41 (2) ◽  
pp. 283 ◽  
Author(s):  
Stephanie K. Courtney Jones ◽  
Katarina M. Mikac

Activity levels of spotted-tailed quolls were investigated using camera traps over 12 months. There were 33 independent camera trap photos with 17 individual quolls identified. Latency to initial detection was 40 days. Quolls were nocturnal/crepuscular, spending 35% of the day they were detected active. Highest activity levels were recorded in summer.


Environments ◽  
2021 ◽  
Vol 8 (1) ◽  
pp. 2
Author(s):  
Peter Brimblecombe ◽  
Yonghang Lai

The COVID-19 pandemic made it critical to limit the spread of the disease by enforcing human isolation, restricting travel and reducing social activities. Dramatic improvements to air quality, especially NO2, have often characterised places under COVID-19 restrictions. Air pollution measurements in Sydney in April 2019 and during the lockdown period in April 2020 show reduced daily averaged NO2 concentrations: 8.52 ± 1.92 and 7.85 ± 2.92 ppb, though not significantly so (p1~0.15) and PM2.5 8.91 ± 4.94 and 7.95 ± 2.64 µg m−3, again a non-significant difference (p1~0.18). Satellite imagery suggests changes that parallel those at ground level, but the column densities averaged over space and time, in false-colour, are more dramatic. Changed human mobility could be traced in increasing times spent at home, assessed from Google Mobility Reports and mirrored in decreased traffic flow on a major road, suggesting compliance with the restrictions. Electricity demand for the State of New South Wales was low under lockdown in early April 2020, but it recovered rapidly. Analysis of the uses of search terms: bushfires, air quality, haze and air pollution using Google Trends showed strong links between bushfires and pollution-related terms. The smoke from bushfires in late 2019 may well have added to the general impression of improved air quality during lockdown, despite only modest changes in the ground level measurements. This gives hints that successful regulation of air quality requires maintaining a delicate balance between our social perceptions and the physical reality.


1994 ◽  
Vol 17 (1) ◽  
pp. 19
Author(s):  
J. Barker ◽  
D. Lunney ◽  
T. Bubela

Mammal surveys were carried out on the Carrai Plateau and Richmond Range in north-east New South Wales between March 1988 and November 1989. The emphasis was placed on rainforest mammals, following the recognition by Adam ( 1987) that the species lists of mammals in the state's rainforests were incomplete and that more research was needed. The mammals were surveyed primarily by analysis of prey remains in Dog and Fox scats, collected from roads throughout the forests, and from bat trapping. The bat fauna at both the Carrai Plateau and Richmond Range is rich (1 0 species and nine species respectively, including the rare Golden-tipped Bat, Kerivoula papuensis, in the Richmond Range). Scat analysis revealed the presence of 24 native species on the Carrai Plateau, and on the Richmond Range there were 17 species, including high numbers of two pademelon species. Feral prey species are almost completely absent, although the Fox is an established predator in both areas. A sharp division was identified between the mammal faunas of closed and open forests. Differences were found also between the mammal fauna composition of the two rainforest sites, and with those of nearby eucalypt forests. The mammal fauna of New South Wales rainforests is distinct from open forests and future mammal surveys are needed to ensure an adequate level of knowledge to identify and conserve these areas.


2000 ◽  
Vol 6 (3) ◽  
pp. 218 ◽  
Author(s):  
P Gibbons ◽  
D. B. Lindenmayer ◽  
S. C. Barry ◽  
M. T. Tanton

We examined factors associated with the occurrence of tree hollows in four eucalypt species from temperate forest in southeastern New South Wales and East Gippsland. A total of 1 256 standing trees and 328 felled trees was examined. The proportion of trees containing hollows with small entrances (2-5 cm) was significantly negatively associated with dbh, while the proportion of trees containing hollows with medium (5-10 cm) and large (>10 cm) entrances was positively associated with dbh. There was a significant, but weak, relationship between hollow depth and minimum entrance width that was improved with the addition to the model of the variables branch diameter and branch health. Trees of all sizes and ages contained hollows, although larger and older trees had a higher probability of doing so. For two tree species (Brown Barrel or Cuttail Eucalyptus fastigata and Messmate E. obliqua), the probability of live trees containing hollows remained below 0.5 for stems less than 180 years of age. Un logged forest supported, on average, 22.0 hollowbearing trees per ha ? 18.5% of which were dead trees. For all values of dbh, trees were more likely to contain hollows if either dead or in poor physiological condition, indicating the potential for hollow development to be accelerated in eucalypts by killing or injuring suitably-sized trees.


Sign in / Sign up

Export Citation Format

Share Document