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A SPATIAL ANALYSIS OF GREATER BILBY (MACROTIS LAGOTIS) HABITAT IN SOUTH-WEST QUEENSLAND

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Greater Bilbies (Macrotis lagotis) once occupied 70% of Australia but are now an endangered species under the Environment Protection and Biodiversity Conservation Act (C'wlth) 1999. A dedicated 29 km 2 enclosure to protect reintroduced bilbies from predators was built in Currawinya National Park in southwest Queensland in 2003. Ten bilbies (three male and seven female) were released in the enclosure during the period of December 2005 to September 2006. The objective of this research was to develop a method to identify suitable Greater Bilby habitat from remote sensing imagery. A related objective was to spatially characterize how bilbies used their environment for feeding and resting. Aerial photographs (1:40,000) were used to classify the vegetation and land cover. Soil samples were used to construct a detailed soils map. Radio tracking (2005-06) and field tracking data (2008) were used to identify spatial associations between bilby activities and land cover and soils features in order to spatially characterize bilby micro-habitats. These results formed the basis of a Weighted Sum model that accurately identified potential bilby micro-habitats within the enclosure.
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E. Dunwoody, X. Liu and K. McDougall
A SPATIAL ANALYSIS OF GREATER BILBY (MACROTIS
LAGOTIS) HABITAT IN SOUTH-WEST QUEENSLAND
Ernest. Dunwoody1, Xiaoye. Liu1, and Kevin. McDougall1
1Faculty of Engineering and Surveying, University of Southern Queensland
Toowoomba, QLD, 4350, Australia
Email: edunwoody1@bigpond.com
KEYWORDS: Greater Bilby, marsupial habitat, spatial analysis, remote sensing
ABSTRACT
Greater Bilbies (Macrotis lagotis) once occupied 70% of Australia but are now an
endangered species under the Environment Protection and Biodiversity Conservation
Act (C’wlth) 1999. A dedicated 29 km2 enclosure to protect reintroduced bilbies from
predators was built in Currawinya National Park in south-west Queensland in 2003.
Ten bilbies (three male and seven female) were released in the enclosure during the
period of December 2005 to September 2006.
The objective of this research was to develop a method to identify suitable Greater
Bilby habitat from remote sensing imagery. A related objective was to spatially
characterize how bilbies used their environment for feeding and resting. Aerial
photographs (1:40,000) were used to classify the vegetation and land cover. Soil
samples were used to construct a detailed soils map. Radio tracking (2005-06) and
field tracking data (2008) were used to identify spatial associations between bilby
activities and land cover and soils features in order to spatially characterize bilby
micro-habitats. These results formed the basis of a Weighted Sum model that
accurately identified potential bilby micro-habitats within the enclosure.
The analysis showed that bilbies prefer to dig burrows in Acidic Rudosol soils with
Shrubland with Dead Wood landcover. Their feed sites occur fairly evenly on Acidic,
Basic and Salic Rudosol soils but they preferred Shrubland landcover in which to
feed.
The modelling results showed that; (i) bilby feeding and resting micro-habitat could be
accurately predicted within the confines of the enclosure, (ii) bilbies were active in
only a small part of the larger area available to them, (iii) bilbies exhibited distinct
preferences for specific soil and landcover types for constructing burrows and feeding
and (iv) micro-habitats suitable for bilbies represent only a small percentage of the
enclosure.
E. Dunwoody, X. Liu and K. McDougall
2
INTRODUCTION
The Greater Bilby (Macrotis lagotis) is a small, cryptic, nocturnal, fossorial marsupial
in the Peramelidae Family (Figure 1). It is one of Australia’s most endangered
marsupials
1
, its range having declined 99.7 % since 1836 (McRae 2004, p. 111). It
remains in the wild in
only small areas of arid
inland Australia
(McRae 2004, p. 106;
Southgate 1990a, pp.
295-298). Populations
are maintained in
protected areas in
South Australia
(Moseby & Donnell
2003), New South
Wales (Finlayson,
Vieira, Priddel et al.
2008, p. 320) and
Queensland (Mayhew
2006, p. 5).
Figure 1. Greater Bilby (Macrotis lagotis) (© QEPA)
The Greater Bilby is a generalist omnivore that can live in a wide range of habitats as
evidenced by its historically broad distribution. Vegetation types range from Acacia
rich woodlands through shrub steppe communities to tussock and forbs grasslands
(Southgate 1990b, p. 111). Lavery and Kirkpatrick (1997, p. 274) reported bilbys
burrowing in “stone free Cretaceous sediments of cracking clays” that occur in
grassland downs adjacent to the watercourses in Davenport Downs (SW QLD). McRae
(2004, pp. 10, 71-72) reported that the bilbies in Astrebla Downs National Park built
burrows in areas of suitable soil structure and stability that included “Compacted
sandstone outcrops in deep cracking clay soils of the ashy plains --- along drainage
depressions”. Bilbies in the Tanami Desert (NW of Alice Springs) were reported to
preferentially occupy palaeodrainage habitats (Paltridge & Southgate 2001, p. 255).
Bilbys released at the Arid Recovery Reserve north of Roxby Downs (SA) were found
to prefer clay swale habitat, dunes and sand plains (Moseby & Donnell 2003, p. 19).
The reduction in their population and range has been caused primarily by predation
from red foxes (Vulpes vulpes) and cats (Felis catus), habitat destruction by domestic
and feral herbivores, increased provision of watering points and by past government
bounty policies (Hrdina 1997). Recolonisation of bilbies into “wild like” protected
areas from which predators have been excluded has been successful at Thistle Island
and Yookamurra Sanctuary in South Australia (Moseby & Donnell 2003), Scotia
Sanctuary in New South Wales (Finlayson et al. 2008, p. 320) and in the Bilby
Enclosure (BE) in Currawinya National Park (CNP) in Queensland (Mayhew 2006, p.
5).
1
Vulnerable under Schedule 1 of the Environment Protection and Biodiversity Conservation Act (Cwlth) of 1999
(Pavey, C. 2006, National recovery plan for the Greater Bilby Macrotis lagotis., Darwin)
E. Dunwoody, X. Liu and K. McDougall
3
Small animals cannot be detected directly by aerial or satellite photography. Their
habitats can only be determined indirectly by detecting and mapping combinations of
vegetation, soil and landscape elements and developing associations between these
features and the target animal. Southgate et al (2005) assessed bilby abundance in the
Tanami Desert by looking for their footprints, scats and diggings. Their ability to
identify bilby tracks was not obscured by vegetation or rabbits. McRae (2004, p. 77)
reported that “bilby burrows were readily visible from the air” due to their excavation
of different coloured subsoil in the open treeless area between the Diamantina River
and the Simpson Desert. Such knowledge must be able to be summarised and
represented spatially before it can be used in habitat mapping.
GIS systems allow interaction between data at different spatial and temporal scales
(Store & Jokimäki 2003). Multi-Criteria Evaluation (MCE) in a GIS environment
allows cartographic combination of multiple habitat factors so as to detect their
influence on the suitability of the habitat for a species. Store and Kangas (2001, p. 79)
demonstrated this approach to predicting habitat suitability for the polypore fungal
species Skeletocutis odora and subsequently with three species simultaneously, the
Redstart (Phoenicurus phoenicurus), Pied Flycatcher (Ficedula hypoleuca ) and S.
odora (Store & Jokimäki 2003). Apan et al (2004, p. 812) used a knowledge based
MCE GIS method to identify areas of high priority for revegetation to ameliorate
dryland salinity in the Hodgson Creek watershed (Darling Downs, Qld).
The absence of a geographical knowledge base about bilby activity at CNP
necessitated the development of an empirical data set. This required obtaining detailed
evidence of bilby activity in a wooded environment containing a significant rabbit
population and the extraction of indicator relationships for bilby activity.
The objective of this research was to test the use of aerial photography for detecting
suitable landscape elements with which to predict the suitability of habitat for Greater
Bilbys in the BE at CNP. Imagery captured prior to release of bilbys was used to
develop a model of suitable burrowing and feeding sites based on activity records of
the bilbies that were subsequently released. The accuracy of the model for detecting
bilby activity elsewhere in the enclosure was tested on separate validation areas.
METHODS
Study Areas
The study area was the 29 km2 BE in CNP built in 2003-2004 (Figure 2). It is
designed to exclude all ground based predators of bilbys while retaining the released
bilbys and their offspring.
Field Data Collection
Detailed data about soil characteristics and bilby activity were collected at eight
investigation areas selected at random within the BE (Figure 2). Trimble GeoXT hand
held GPS units loaded with TerraSynch software were used to collect both base station
and field observations. All GPS data were differentially corrected.
E. Dunwoody, X. Liu and K. McDougall
4
Figure 2. Study Area
The key GPS settings were: observation interval, 5 sec.; observations per feature, 20
(min); and HDOP, 6 (max). These values resulted in data with the following precision.
Differentially corrected feature
Non-differentially corrected feature
Mean = 2.18 m
Mean = 10.32 m
SD (95%) = 0.12 m
SD (95%) = 0.11 m
Signs of bilbies were recorded in a GPS data dictionary by a trained observer walking
in a series of roughly concentric circles through each vegetation zone in each of the
eight investigation areas.
E. Dunwoody, X. Liu and K. McDougall
5
Data Pre-processing
Six aerial photographs acquired in June 2003 by a private contractor (Jacobs 2003)
were used based on their availability, clarity and resolution. The images were captured
during the period 18-23 May 2003 at a flying height of 3,229 m with a calibrated 80
mm focal length Hasselblad lens resulting in imagery with a scale of 1:38,800. The
pixel size was 0.6682 m. Each image was georeferenced and the images were
mosaiced with ERDAS Imagine software (Ver.9.3). The mosaiced image was linearly
stretched and dehazed prior to Supervised Classification using the maximum
likelihood classifier. The resulting raster was reclassified into 5 Landcover Classes and
a final Accuracy Assessment performed using 50 randomly stratified sites. A soils
map was created by heads-up digitising based on an observed association between the
soil types and broad vegetation zones.
DATA ANALYSIS
The spatial association of burrows and feed sites with soil and landcover types was
determined by spatially joining the data sets and extracting the positive joins. The area
of soil types and landcover classes that were inspected was obtained by buffering each
track path (5m either side) and extracting the area of each soil and landcover type.
The frequencies of burrows and feed sites were used as class weights in multiple
Weighted Sum Overlay (WSO) calculations to determine the combination of layer
weights and classification break points that maximised the number of bilby signs in
high priority areas. The predictive accuracy of these values was determined by
vectorising the WSO rasters, spatially joining them with field records and analysing
the distribution of the joins between priority areas.
RESULTS
When averaged, normalised, and expressed on a common basis (0-10) the burrow and
feed site weights had the following values (Tables 1 and 2).
Table 1. Burrow Site Weights
Soil Class
Weight
L’cover Class
Weight
Hydrosol
0
Claypan
0
Salic Rudosol
3.58
Red Soil
1.54
Basic Rudosol
0
Shrubland
0
Acidic Rudosol
6.42
S’land with dead wood
6.83
Thick Vegetation
1.63
Total
10.00
Total
10.00
Table 2. Feed Site Weights
Soil Class
Weight
L’cover Class
Weight
Hydrosol
0
Claypan
0
Salic Rudosol
3.24
Red Soil
1.65
Basic Rudosol
3.09
Shrubland
3.73
Acidic Rudosol
3.66
S’land with dead wood
2.22
Thick Vegetation
2.39
Total
10.00
Total
10.00
E. Dunwoody, X. Liu and K. McDougall
6
The most accurate prediction of burrow sites and feed sites was obtained by weighting
the landcover layer as twice as important as the soil layer. Manual classification break
values that yielded the highest accuracy are shown in Table 3.
Table 3. Classification Break Values
Priority
Burrow Site Break
Value
Feed Site Break
Value
Low
0 4
0 6
Medium
4 14
6 7
High
14 21
7 - 10
These values were used to produce maps of Burrow and Feed Site Priority areas for the
whole of the BE. Figure 3 shows an illustration of such mapping for Study Area 4.
The model predicted high priority locations for burrow sites and feed sites with a 67%
and 84% accuracy respectively in the areas in which it was developed (Areas 2, 4 and
7) (Table 4).
Table 4. Study Area Accuracy
Parameter
Feature
Predicted priority of sites
High
SD
Medium
SD
Low
SD
Total
Totals
Burrows
4
1.53
2
0.58
0
0
6
Scrapes
64
5.77
7
2.31
5
1.53
76
Percent
Burrows
67%
33%
0%
100%
Scrapes
84%
9%
7%
100%
When validated in independent areas (Areas 1, 3, 5, 6, and 8) the model predicted high
priority locations for burrow sites and feed sites with 84% and 80.5% accuracy
respectively (Table 5).
Table 5. Validation Area Accuracy
Parameter
Feature
Predicted priority of sites
High
SD
Medium
SD
Low
SD
Total
Totals
Burrows
16
4.60
1
0.45
2
0.65
19
Scrapes
70
9.08
10
2.35
7
1.52
87
Percent
Burrows
84%
5%
11%
100%
Scrapes
80.5%
11.5%
8
5
100%
Combining the burrow and feed site priorities into an overall Habitat Suitability Map
identified areas in which both or either criteria was a high priority. This is illustrated in
Figure 4.
DISCUSSION
The model is based on a Weighted Sum Overlay approach to predicting suitable
burrow and feeding locations for bilbys in the BE at CNP. It uses data derived from
aerial photography, soil sampling and ground presence tracking. The model was
validated by using a subset of the ground truth records. It predicted high priority
burrow and feed sites with 84% and 80.5% accuracy respectively. No reports of other
E. Dunwoody, X. Liu and K. McDougall
7
studies on predicting specific habitats for small marsupials were found. These results
need to be considered in the light of the limitations inherent in the procedures.
Figure 3. Burrow and Feed Site Priority Locations for Area 4
Figure 4. Combined Habitat Suitability detail for Test Area 4
E. Dunwoody, X. Liu and K. McDougall
8
Burrow and Feed Sites
Previous studies have established the importance of soil type in habitat selection by
bilbies. This study found that bilbies dug burrows in Acidic Rudosol soils twice as
frequently (6.42) as in Salic Rudosol soils (3.58). There was no evidence of bilby
burrows in Basic Rudosol soils or in Hydrosols. They chose Shrubland with Dead
Wood landcover twice as frequently (6.83) in which to burrow compared to exposed
Red Soil (1.54) and Thick Vegetation landcover (1.63). These findings are consistent
with Mayhew’s (2006, p. 79) more generalised findings for the BE.
The bilby burrow data used in this study were an amalgamation of burrow location
data collected by previous investigators by radio-tracking in 2005-2006 (McRae 2008
pers. comms.) and visual tracking data collected for this study. Prediction of burrow
habitats was based on 6 burrows in the three study areas and the results were validated
using a further 19 independent burrow locations. The small sample size of the
predictor burrow habitat is recognised as being less than optimal, however the
validation on a further 19 burrow locations supports the model outcomes.
Feed sites selected by bilbies were relatively evenly distributed between all three
Rudosol soil types but there were none in Hydrosols. Shrubland landcover was
preferred for feed sites (3.73) over Shrubland with Dead Wood (2.22) and Thick
Vegetation landcover (2.39). These findings were based on 76 clusters of scrapes in
the study areas and a further 87 clusters in the areas used for validation.
Analysis of the whole enclosure found that there were more areas of high priority for
feeding than for burrowing (Figure 3). This finding was anticipated. Combining the
burrow and feed site priority areas defines the areas suitable for both resting and
feeding. The combined map of burrow and feed sites (Figure 4) shows the areas in
which both are a high priority, or either one of the two is a high priority. McRae (2004,
p. sec. 2.3.2) documented the capacity of bilbies to forage at distances of hundreds of
meters from their refugia. It is therefore not surprising to find some record of feed sites
outside the high and medium priority habitat areas.
Precision and Accuracy
The Overall Classification Accuracy of 80% and Kappa Index of Agreement of 0.76
were considered satisfactory for classification of aerial imagery without an NIR band
into 5 landcover classes. The model accuracy results (Tables 4 and 5) are comparable
to or better than accuracies obtained by other models. Pasher, King and Lindsay
(2007), using Landsat 5 and Ikonos imagery, reported model accuracy of 70% for nest
sites for the Hooded Warbler (Wilsonia citrinia) in the validation area. Allowing for a
10 m error zone increased their accuracy to 87%. The bilby model’s use of a 95%
probability level resulted in a more stringent accuracy test than if a 99% probability
level had been used. The accuracy was scored according to the highest priority
polygon that lay partially or wholly within the 95% horizontal precision zone (Figure
4, subset).
E. Dunwoody, X. Liu and K. McDougall
9
CONCLUSION
This study demonstrated a procedure by which aerial photography can be used to
identify areas suitable for Greater Bilby burrow and feed sites with a high level of
accuracy. Physical tracking and GPS recording of bilby signs was shown to be a
practical and effective method of collecting geographically referenced information
about bilby habitat. Bilbys exhibited strong preference for specific types of soil and
landcover in which to burrow. Application of the model to the 29 km2 enclosure
established that there are extensive feeding sites within foraging range of all potential
burrow sites in the Enclosure. The applicability of these results is limited by their
dependence on aerial photography. Use of more widely available imagery with greater
spectral and less spatial resolution would allow (i) application to a wider area, (ii)
more accurate soil type classification, and (iii) integration with other land management
issues.
ACKNOWLEDGEMENTS
Special appreciation is acknowledged to Mr Peter McRae, Senior Zoologist,
Threatened Species Unit, QEPA for his assistance with bilby burrow data, aerial
photography and tracking and for the use of the Save The Bilby Facilities, Mr Brett
Ford, USQ student in land studies and photogrammetry, Maclean, NSW, for his very
capable research assistance in GPS recording of bilby tracks, maintaining the GPS
base station and photography and to Dr. Manda Page, Australian Wildlife
Conservancy, Perth, for suggesting the topic. Financially assistance from the Save the
Bilby Fund is gratefully acknowledged.
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of revegetation sites for dryland salinity management: an analytical framework
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Finlayson, G. R., Vieira, E. M., Priddel, D., Wheeler, R., Bentley, J. & Dickman, C. R.
2008, 'Multi-scale patterns of habitat use by re-introduced mammals: A case
study using medium-sized marsupials', Biological Conservation, vol. 141, no.
1, pp. 320-331.
Hrdina, F. 1997, 'Marsupial Destruction in Queensland 1877-1930', Australian
Zoologist, vol. 30, pp. 272-286.
Jacobs, I. O. 2003, Aerial Photographs of the Bilby Enclosure at Currawinya National
Park, I Melbourne.
Lavery, H. J. & Kirkpatrick, T. H. 1997, 'Field management of the bilby Macrotis
lagotis in an area of south-western Queensland', Biological Conservation, vol.
79, no. 2-3, pp. 271-281.
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Mayhew, M. A. 2006, 'Habitat Preference and Burrow Use of Reintroduced Bilbies
(Macrotis lagotis) in Semi-Arid Mulga Lands', University of Queensland,
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McRae, P. 2004, 'Aspects of the ecology of the Greater Bilby, Macrotis lagotis, in
Queensland', Masters thesis, University of Sydney.
Moseby, K. E. & Donnell, E. 2003, 'Reintroduction of the greater bilby, (Macrotis
lagotis) (Reid) (Marsupialia: Thylacomyidae), to northern South Australia:
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lagotis Reid (Marsupialia: Peramelidae)', in J. H. Seebeck, P. R. Brown, R. I.
Wallis & C. M. Kemper (eds), Bandicoots and Bilbies, Surrey beatty and Sons,
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Peramelidae)', in J. H. Seebeck, Brown, P.R., Wallis, R.L. and C.M. Kemper
(ed.), Bandicoots and Bilbies, Surrey Beatty and Sons, Sydney, pp. 303-309.
Southgate, R. I., Paltridge, R., Masters, P. & Nano, T. 2005, 'An evaluation of transect,
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BIOGRAPHY OF PRESENTER
Ernest Dunwoody is a post-graduate student at the University of Southern Queensland
studying for a Masters Degree in Spatial Science Technology. He holds a Bachelor’s
Degree in Agricultural Science (Entomology) from the University of Queensland, and
a Graduate Diploma in Geomatic Studies from the University of Southern Queensland.
... The greater bilby ( Fig. 1) is one of Australia's most endangered native fauna with an estimated 600 individuals remaining in the wild (Dunwoody et al. 2009). The species is listed as Vulnerable [C1 ver 3.1] to extinction by the Red Species list of the International Union for Conservation of Nature (Friend et al. 2008). ...
... The species is listed as Vulnerable [C1 ver 3.1] to extinction by the Red Species list of the International Union for Conservation of Nature (Friend et al. 2008). The greater bilby is a medium-sized, semi-fossorial, strictly nocturnal marsupial with large ears and a long pointed snout (Dunwoody et al. 2009). The diet of the bilby ranges from insectivory to herbivory depending on habitat and food availability (Southgate and Carthew 2006). ...
Article
Natural weathering conditions can influence faecal cortisol metabolite (FCM) measurements in wildlife if fresh faeces cannot be collected immediately following defaecation. In this study, we evaluated this issue in a threatened Australian marsupial, the greater bilby (Macrotis lagotis). Fresh (<12h since defaecation) faecal samples (n=19 pellets per bilby) were collected one morning from seven adult bilbies kept in captivity. One control faecal sample (Day 1) from each bilby was immediately frozen. The remaining faecal pellets were randomly positioned outdoors. Subsequently, we froze one faecal pellet every 24h for 19 days. FCM levels in bilby faeces were quantified using an enzyme-immunoassay. Mean FCM levels showed variation (daily mean coefficients of variation [CV %]) of 56.83-171.65% over 19 days. Overall, FCM levels were affected by exposure time; however, multiple comparisons showed that no significant change in FCM occurred after environmental exposure (no significant difference in mean FCM between control (Day 1) with any of the exposure days (Days 2-19). Individuals and sex also affected FCM levels. We found no correlation between mean daily CVs with daily minimum-maximum temperatures or rainfall. Our results indicate that FCM in bilby faeces is fairly stable to long-term environmental exposure (19 days). In future, freshly excreted bilby faeces (where the sample maintains a distinct odour for 9-13 days) should be used to study FCM levels in wild bilbies.
... Study sites: semi-free ranging Currawinya National Park (semi-wild population 1; SW-1), located in south-western Queensland (28.6817 S, 144.6978 E) contains a 25-km 2 predator-proof enclosure that was built in the National Park in 2003 to protect the reintroduced population of the greater bilby from ground dwelling predators (Dunwoody et al. 2009;DEHP 2012). Unfortunately, during the time of sampling the predator-proof exclusion fence had been compromised by recurrent rains that caused corrosion and enabled the infiltration of feral cats (F. ...
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Rapid and reliable physiological evaluation of stress is necessary for understanding the potential impacts of environmental changes on managed populations of threatened mammals. In situ populations of Australia’s iconic marsupial, the greater bilby (Macrotis lagotis), are nearing extinction due to the impacts of competition and predation by feral animals and unpredictable climatic events (summer heat waves). In this study, we focussed our aim to identify a non-invasive method to measure adrenal activity in the species and also to identify potential factors that should be considered when comparing physiological stress in semi-free ranging populations of the species. We validated an enzyme immunoassay (EIA) for detecting fecal cortisol metabolites (FCM) from fresh fecal pellets taken from bilbies within four captive sites and two semi-free ranging populations around Queensland and New South Wales, Australia. Our FCM EIA successfully detected the ‘raise and fall’ pattern of FCM levels within 3 days of exogenous adrenocorticotropic hormone (ACTH) challenge. Mean FCM levels differed significantly between the captive sites and between sexes. All male bilbies grouped outdoor in captivity expressed the highest mean FCM level in comparison to all captive males that were housed individually or as groups indoors. Also, semi-free ranging bilbies expressed higher mean FCM levels than the captive bilbies. Overall, our study successfully validated a non-invasive tool for monitoring physiological stress in the greater bilby. In the future, it will be worthwhile to consider factors such as housing conditions, sex and location when comparing the adrenal sensitivity to environmental changes, to help evaluate the success of management interventions (such as predator free enclosures) and support the survival of the species.
Article
Rapid and reliable physiological evaluation of stress is necessary for understanding the potential impacts of environmental changes on managed populations of threatened mammals. In-situ populations of Australia’s iconic marsupial, the greater bilby (Macrotis lagotis) are nearing extinction due to the impacts of competition and predation by feral animals and unpredictable climatic events (summer heat waves). In this study, we focussed our aim to identify a non-invasive method to measure adrenal activity in the species and also to identify potential factors that should be considered when comparing physiological stress in semi-free ranging populations of the species. We validated an enzyme-immunoassay (EIA) for detecting fecal cortisol metabolites (FCM) from fresh fecal pellets taken from bilbies within four captive sites and two semi-free ranging populations around Queensland and New South Wales, Australia. Our FCM EIA successfully detected the “raise and fall” pattern of FCMs levels within 3 days of exogenous adrenocorticotropic hormone (ACTH) challenge. Mean FCMs levels differed significantly between the captive sites and between sexes. All male bilbies grouped outdoor in captivity expressed the highest mean FCM level in comparison to all captive males that were housed individually or as groups indoors. Also, semi-free ranging bilbies expressed higher mean FCMs levels than the captive bilbies. Overall, our study successfully validated a non-invasive tool for monitoring physiological stress in the greater bilby. In future, it will be worthwhile to consider factors such as housing conditions, sex and location when comparing the adrenal sensitivity to environmental changes, to help evaluate the success of management interventions (such as predator free enclosures) and support the survival of the species.
Article
Natural weathering conditions can influence faecal cortisol metabolite (FCM) measurements in wildlife if fresh faeces cannot be collected immediately following defaecation. In this study, we evaluated this issue in a threatened Australian marsupial, the greater bilby (Macrotis lagotis). Fresh (<12 h since defaecation) faecal samples (n = 19 pellets per bilby) were collected one morning from seven adult bilbies kept in captivity. One control faecal sample (Day 1) from each bilby was immediately frozen. The remaining faecal pellets were randomly positioned outdoors. Subsequently, we froze one faecal pellet every 24 h for 19 days. FCM levels in bilby faeces were quantified using an enzyme-immunoassay. Mean FCM levels showed variation (daily mean coefficients of variation [CV %]) of 56.83–171.65% over 19 days. Overall, FCM levels were affected by exposure time; however, multiple comparisons showed that no significant change in FCM occurred after environmental exposure (no significant difference in meanFCMbetween control (Day 1) with any of the exposure days (Days 2–19). Individuals and sex also affected FCM levels. We found no correlation between mean daily CVs with daily minimum–maximum temperatures or rainfall. Our results indicate that FCM in bilby faeces is fairly stable to long-term environmental exposure (19 days). In future, freshly excreted bilby faeces (where the sample maintains a distinct odour for 9–13 days) should be used to study FCM levels in wild bilbies.
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The Greater Bilby (Macrotis lagotis) in as IUCN listed Vulnerable (C1 ver 3.1) marsupial species in Australia. Proper monitoring of physiological stress hormone responses in the individuals involved in captive breeding programs is important. In this study, we used a fecal cortisol enzyme-immunoassay (EIA) and validated it to measure stress hormone (cortisol) metabolites in adult male and female bilbies (n = 7) in captivity at the Dreamworld Theme park, Queensland. The fecal cortisol EIA was validated via parallelism and recovery of exogenous cortisol added to pooled fecal extracts (greater than 99 % recovery). Female bilbies had higher mean baseline cortisol concentrations than male bilbies however there was no relationship with bilby age. There was high day-to-day variation in fecal cortisol metabolites, larger in females than males. Cortisol levels for most individuals varied widely through time with numerous peaks and troughs following long-term stressors (illnesses, injury and reproductive issues) and known short-term stressors such as use in shows at Dreamworld or public displays in local schools, manual restraint and short-term veterinary procedures (e.g. general anaesthesia). Overall, the higher mean baseline cortisol metabolite levels of long-term stressed individuals appear to be, at least partially, related to their higher response to short-term stressors. This suggests an interaction between responses to short and long-term stressors, which have been explained in relation to habituation and/or facilitation of long-term stressors. In future, non-invasive fecal monitoring of stress hormones could be applied within wild populations to quantify the impact of survey programs on wild populations.
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Nine bilbies were reintroduced to a 14-km2 reserve free of rabbits, cats and foxes in South Australia in April 2000. The survival, growth and ecology of the population were studied for 17 months after release by means of radio-tracking and trapping. Reproduction was continuous over the study period, with juveniles successfully recruited into the population. Home-range size of female bilbies averaged 0.18 km2 and was significantly smaller than home ranges of males, which averaged 3.16 km2. Wild-born subadults had smaller home ranges than adults. While male home ranges, and male and female home ranges overlapped considerably, females appeared to maintain areas discrete from other adult females. Bilbies showed a significant preference for dune habitat. As swale habitat appears too hard for burrow construction and males moved greater distances from diurnal burrows than females, males are likely to access food reserves that are under-used by females. Both males and females reused at least 30% of their burrows, and females displayed long-term site fidelity. The release was considered successful and suggests that despite historical damage from rabbits and stock, bilbies are able to successfully recolonise parts of their former range in arid South Australia once rabbits, cats and foxes are removed.
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To address the limited application of analytical and modelling techniques in prioritizing revegetation sites for dryland salinity (saline land) management, a case study of the Hodgson Creek catchment in Queensland, Australia, was conducted. An analytical framework was developed, incorporating the use of spatial datasets (Landsat 7 image, DEM, soil map, and salinity map), which were processed using digital image processing techniques and a geographic information system (GIS). Revegetation sites were mapped and their priority determined based on recharge area, land use/cover and sub-catchment salinity. The analytical framework presented here enhances the systematic use of land information, widens the scope for scenario testing, and improves the testing of alternative revegetation options. The spatial patterns of revegetation sites could provide an additional set of information relevant in the design of revegetation strategies.
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The aim of this study is to develop a method by means of which it is possible to produce georeferenced ecological information about the habitat requirements of different species. The integrated habitat suitability index approach includes the steps of constructing habitat suitability models, producing data needed in models, evaluating of target areas based on habitat factors, and combining various suitability indices. The method relies on the combined use of empirical evaluation models and models based on expertise in geographical information system (GIS) environment. GIS was used to produce the data needed in the models, and as a platform to execute the models and to present the results of the analysis. Furthermore, multi-criteria evaluation methods (MCEs) provide the technical tools for modeling the expertise and for connecting (standardizing, weighting, and combining) the habitat needs of different species. The main advantages of the method were connected to possibilities to consider the habitat factors on different scales, to combine habitat suitability evaluations for several species and to weight different species in different ways, and to integrate empirical models and expert knowledge. The method is illustrated by a case study in which an integrated habitat suitability map is produced for a group of old-forest species.
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Greater bilby was once widely distributed throughout arid and semiarid Australia. It has suffered a rapid decline since European settlement and is now restricted to parts of the Tanami, Great Sandy and Gibson Deserts with outlying populations in SW Queensland and N of Alice Springs, Northern Territory. Its distribution is examined in relation to historic and scientific records, climatic and soil features, land use and the distribution of rabbits Oryctolagus cuniculus and foxes Vulpes vulpes. -from Author
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So-called Marsupial Destruction Acts were in force in Queensland from 1877 to 1930. The Acts were administered by District Boards which paid bonuses (bounties on presentation of scalps) and kept annual records of their activities. During that period over 27 million macropods and bandicoots, as well as dingoes and foxes (which were included under the Acts) were destroyed. The cost to Queensland was over £1,187,000 in bonuses paid by the boards which included £349,000 in government subsidies. The annual reports on these Acts, which do not always provide information on individual boards, provide essentially reliable data reflecting the number of animals in existence. It is seen that despite the large number of "pests" destroyed, the original purpose of Acts was not achieved in that the larger marsupials and the dingo successfully proliferated; no effect on fox numbers was discernible, the numbers of some medium-sized species remained static, and the smaller species declined.
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Australian deserts are characterised by highly patterned plant productivity and an extremely unpredictable climate. The Tanami Desert in central Australia is dominated by vast sandplains interspersed with more productive habitats such as palaeodrainage lines. During 1996 and 1997 fauna surveys were conducted in two areas of the Tanami Desert to investigate the relative importance of palaeodrainage habitat for fauna under different seasonal conditions. The two areas were at latitudes separated by approximately 400 km, and during the study period the northern study area (Tennant) received considerably more rainfall than the southern study area (Kintore). The species richness and abundance of a range of taxonomic groups were compared between the two study areas and between palaeodrainage habitat and adjacent sandplain habitat. The only significant difference between habitats was that small reptiles were more abundant in sandplain than palaeodrainage habitat. Overall, bilbies, bustards and macropods were significantly more abundant at Tennant than Kintore, but significantly more small mammals were captured at Kintore. In both habitats and areas, capture rates, track counts and species richness of reptiles varied significantly with season. The biomass of invertebrates captured also showed significant temporal fluctuations. Burrowing frogs were active only after rain, and birds showed significant fluctuations in abundance and species richness associated with rainfall. The abundance of small mammals did not vary significantly during this study. Overall, local seasonal conditions were generally more important determinants of the abundance of fauna in the spinifex grasslands of central Australia than was habitat type.
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We evaluated three monitoring techniques to determine the spatial pattern and relative abundance of the bilby (Macrotis lagotis) in the Tanami Desert, Northern Territory. All the methods examined relied on the identification of animal sign (foot imprints or diggings) to indicate the presence of a species. With fixed transects, a 10-km prepared tracking surface was monitored regularly using an all-terrain vehicle. With random plots, an unprepared tracking surface within a 200 x 300 m area was searched on foot for sign of the species. A helicopter was used in an aerial survey to identify bilby diggings from an altitude of 15-20 m while travelling at a speed of 30-40 knots along a predefined transect. The results for each method were stratified in relation to latitude and substrate to facilitate comparison of the efficacy of each technique. The fixed transects returned the least number of bilby records for most effort. The aerial transect technique resulted in few (<4%) false negative records but a sizeable (42%) number of false positive records. It is suggested that the aerial survey technique combined with ground-truth survey plots would provide reliable information on the extent of occurrence and status of the bilby in the remote spinifex deserts of central Australia.
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A study is reported of a population of bilbies Macrotis lagotis Reid at Davenport Downs, a 15 100 km2 cattle property in the Channel Country of Queensland. Systematic traverses first established that bilby burrows were located throughout the tussock grasslands on downs near major watercourses on the property. A 10-month survey of burrows subsequently revealed that fewer than one-half of those studied were in permanent use. Moreover, daily burrow use in a typical burrow aggregation ranged from one-third to two-thirds of the total over a 45-day observation period. From regular observations made of 27 burrow aggregations consisting (at the end of the period) of 169 burrows, the data suggested that these may have accommodated 40 bilbies, that each added an extra burrow over 10 months, and that each used one, two or three burrows each night. Further research needs are identified from these introductory observations. These include monitoring the distribution and relationships between burrow and bilby numbers. Property management guidelines to minimize disturbance to areas of bilby activity, including by overgrazing by stock, have been recommended to, and adopted by, the landholders involved.
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Knowledge of the habitat requirements of threatened species at both local and landscape scales is crucial for maintaining viable populations and for making conservation and management decisions. Here, we use live trapping and radio-tracking to investigate habitat use by four species of threatened marsupials - burrowing bettongs (Bettongia lesueur), brush-tailed bettongs (B. penicillata), greater bilbies (Macrotis lagotis), and bridled nailtail wallabies (Onychogalea fraenata). The study populations had been re-introduced to Scotia Sanctuary in western New South Wales, Australia, within a predator-proof area. All showed preferences for particular macrohabitats while resting by day, with M. lagotis and B. penicillata selecting Eucalyptus woodland with Triodia understorey and B. lesueur and O. fraenato selecting Eucalyptus woodland with shrubs. However, they showed no such partiality at night. Bettongia penicillata used areas with Triodia and litter but few herbs for shelter, while burrows of M. lagotis avoided shrubs. Habitat components that influenced trap captures were: crust cover and herb layer cover (negative) for B. penicillata, trees <5 in in height and number of shrubs (both negative) for B. lesueur, crust cover for M. lagotis, and crust cover and trees <5 in high for O. fraenata (both negative). There was also a negative association at this scale between B. penicillata and both B. lesueur and M. lagotis, suggesting the possibility of competition. our results support the idea that studies at multiple spatial scales are crucial to understand the habitat use and requirements of threatened fauna, and should therefore be incorporated into future re-introduction programs. (C) 2007 Elsevier Ltd. All rights reserved.
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GIS data processing and spatial analysis, together with modern decision analysis techniques, were used in this study to improve habitat suitability evaluation over large areas. Both empirical evaluation models and models based on expert knowledge can be applied in this approach. The habitat requirements of species were described as map layers within GIS so that each map layer represented one criterion. GIS was used as the platform in managing, combining and displaying the criterion data and also as a tool for producing new data, especially by utilising spatial analysis functions.Criterion standardisation, weighting and combining were accomplished by means of multi-criteria evaluation (MCE) methods, the theoretical background being based on the multi-attribute utility theory (MAUT). By using continuous priority and sub-priority functions in the evaluation, no classification of continuous attributes was needed and also non-linear relationships between habitat suitability and the attributes could be considered. Sensitivity analysis was applied to consider the temporal factor in the analysis and to find out the effect of different criteria weights on the spatial pattern of the suitability index. Changing the weights of permanent and time-changeable habitat factors shifted the location of optimal habitats for the species. In the long run, permanent factors such as soil properties define the habitat potential, which is important to take into consideration; e.g. in forest management planning and species conservation. The method is illustrated by a case study in which habitat suitability maps were produced for an old-forest polypore, Skeletocutis odora.