Interactions between dingoes and introduced wild ungulates: concepts, evidence and knowledge gaps

2019 ◽  
Vol 41 (1) ◽  
pp. 12 ◽  
Author(s):  
David M. Forsyth ◽  
A. David M. Latham ◽  
Naomi E. Davis ◽  
Peter Caley ◽  
Mike Letnic ◽  
...  

The dingo (Canis dingo or C. familiaris, including hybrids with feral dogs) is the apex carnivore on mainland Australia. Fifteen non-native ungulate species have established wild populations in Australia. Dingoes are managed to reduce impacts on domestic ungulates, and introduced wild ungulates are managed to reduce impacts on natural ecosystems and to minimise competition with domestic ungulates. There is speculation about the extent to which (1) dingoes limit the abundances of introduced wild ungulates, and (2) introduced wild ungulates sustain dingo populations. We reviewed the literature to identify potential ecological interactions between dingoes and introduced wild ungulates, and to synthesise evidence for interactions between dingoes and each ungulate species (including the percentage frequency occurrence (%FO) of ungulates in dingo diets). Eleven of the 15 ungulate species were recorded in the diet of dingoes, with the highest %FO occurrences reported for feral goats (73%) and cattle (60%). Two studies concluded that dingoes reduced ungulate abundances (feral goat (Capra hircus) and feral donkey (Equus asinus)), and two studies concluded that dingoes did not regulate feral pig (Sus scrofa) abundances. A fifth study concluded that dingoes exhibited a Type III functional response to increasing sambar deer (Cervus unicolor) abundances. A sixth study concluded that dingoes made relatively little use of hunter-shot sambar deer carcasses. We propose that interactions between dingoes and introduced wild ungulates depend on the sex–age classes vulnerable to dingo predation, dingo pack sizes, the availability of escape terrain for ungulates and the availability of alternative foods for dingoes. The interplay between environmental conditions and the population growth rate of ungulates, and hence their ability to sustain losses from predation, could also be important. We predict that dingoes will have most impact on the abundance of smaller ungulate species and neonates.

2013 ◽  
Vol 9 (3) ◽  
Author(s):  
Juan Herrero ◽  
Olatz Fernández ◽  
Carlos Prada ◽  
Alicia García-Serrano

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Ting-Yeu Dai ◽  
Chih-Hua Wang ◽  
Kun-Nan Chen ◽  
I-Nung Huang ◽  
Wei-Sheng Hong ◽  
...  

We assayed the effects of velvet antler (VA) of Formosan sambar deer (Cervus unicolor swinhoei) and its extracts on the anti-infective activity against pathogenicStaphylococcus aureus in vitroandin vivoin this study.In vitrodata indicated that the VA extracts stimulated the proliferation of resting splenocytes and macrophages in a dose-dependent manner up to the highest concentration used (150 μg mL−1). The production of proinflammatory cytokines (TNF-α, IL-6, IL-12) by lipoteichoic acid was significantly suppressed after being cocultured with the VA extracts in a dose-dependent manner. Animal test inS. aureus-infected mice demonstrated that the numbers of bacteria determined in the kidneys and peritoneal lavage fluid ofS. aureus-infected mice were significantly higher than those found in the same organs of mice pretreated with the VA samples. Moreover, the highly enhanced phagocytic activity of macrophages was further verified afterin vitrotreatment with the VA samples. The protective mechanisms of the VA samples might include an immune enhancer and an inflammatory cytokine suppressor.


1986 ◽  
Vol 22 (1) ◽  
pp. 136-136 ◽  
Author(s):  
K. K. Bhattacharjee ◽  
A. W. Franzmann

2014 ◽  
Vol 13 (2) ◽  
pp. 3967-3971 ◽  
Author(s):  
D.Y. Lin ◽  
T.Y. Chiang ◽  
C.C. Huang ◽  
H.D. Lin ◽  
S.J. Tzeng ◽  
...  

2008 ◽  
Vol 30 (2) ◽  
pp. 83 ◽  
Author(s):  
A. Bennett ◽  
G. Coulson

To study the effects of grazing and browsing by Sambar deer (Cervus unicolor), swamp wallaby (Wallabia bicolor) and wombats (Vombatus ursinus) exclosure plots measuring 10 m x 10 m were erected in the Upper Yarra and O'Shannassy water catchments near Melbourne, Victoria. Total exclusion fences and partial exclusion fences were erected. Design details and costs are provided. Operational problems are discussed.


1997 ◽  
Vol 9 (6) ◽  
pp. 587 ◽  
Author(s):  
G. W. Asher ◽  
P. D. Muir ◽  
G. Semiadi ◽  
K. T. O'Neill ◽  
I. C. Scott ◽  
...  

Seasonal onset of pubertal ovulation and incidence of luteal cyclicity was assessed from plasma progesterone proles over 15 months for tame red deer (n = 7) and sambar deer (n = 7) hinds. Seasonal responses to photoperiod were determined from plasma prolactin proles. All red deer attained puberty at 17-18 months of age in May-June and expressed 3-6 luteal cycles of length 20·0 ± 10·4 days (mean ± s.e.m.) over 52-102 days. Six sambar deer attained puberty at 7-19 months of age, between August and December. Duration of luteal cyclicity was variable. While one animal remained continuously cyclic for 13 months, most entered anoestrus between November and February. The mean length of the luteal cycle was 17·2 ± 0·3 days. While red deer exhibited strongly seasonal patterns of prolactin secretion, sambar deer showed no such seasonal trends. The data collectively indicate that young sambar hinds at temperate latitudes exhibit loosely dened patterns of reproductive seasonality that are 4-6 months out of phase with those of red deer, although some individuals may be non-seasonal. Failure to express seasonal patterns of prolactin secretion indicates that sambar deer may not perceive photoperiodic cues to the same extent as do red deer.


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