Sharp, T., & Saunders, G. mustering of feral horses.
Abstract: Background
Feral horses (Equus caballus) can cause significant environmental damage and losses to
rural industries. Although considered pests, feral horses are also a resource, providing
products such as pet meat for the domestic market and meat for human consumption
for the export market. Control methods include trapping, mustering exclusion fencing,
ground shooting and shooting from helicopters.
Feral horses are mustered by helicopter, motorbike or on horseback, sometimes with the
assistance of coacher horses. Once mustered into yards, net traps or fenced paddocks, the
horses are usually sold to abattoirs for slaughter which can offset the costs of capture and
handling. Less commonly, they are sold as riding horses or relocated to reserves or horse
sanctuaries. Where there is no market for them or where removal may be too costly or
impractical e.g. in conservation areas or remote areas without access to transportation,
horses are sometimes destroyed by shooting in the yards.
This standard operating procedure (SOP) is a guide only; it does not replace or
override the legislation that applies in the relevant State or Territory jurisdiction.
The SOP should only be used subject to the applicable legal requirements (including
OH&S) operating in the relevant jurisdiction.
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In Zentall T.R, G. B. G. (Ed.). Social Learning: Psychological and Biological Perspectives. Lawrence Erlbaum Associates.
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Mednikov Bm, G. J. Zur systematischen Stellung des Kulans.
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Heyes, C., & Galef, B. G. (Eds.). (1996). Social learning in animals: the roots of culture. San Diego, CA: Academic Press, Inc.
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Castley, J. G., & Knight, M. H. (1997). Population status of plains zebra, Equus burchelli, in South African National Parks. Scientific Services, National Parks Board, .
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Saucier, D. M., Shultz, S. R., Keller, A. J., Cook, C. M., & Binsted, G. (2007). Sex differences in object location memory and spatial navigation in Long-Evans rats. Anim. Cogn., .
Abstract: In both humans and rodents, males typically excel on a number of tasks requiring spatial ability. However, human females exhibit advantages in memory for the spatial location of objects. This study investigated whether rats would exhibit similar sex differences on a task of object location memory (OLM) and on the watermaze (WM). We predicted that females should outperform males on the OLM task and that males should outperform females on the WM. To control for possible effects of housing environment, rats were housed in either complex environments or in standard shoebox housing. Eighty Long-Evans rats (40 males and 40 females) were housed in either complex (Complex rats) or standard shoebox housing (Control rats). Results indicated that males had superior performance on the WM, whereas females outperformed males on the OLM task, regardless of housing environment. As these sex differences cannot be easily attributed to differences in cognitive style related to linguistic processing of environmental features or to selection pressures related to the hunting gathering evolutionary prehistory of humans, these data suggest that sex differences in spatial ability may be related to traits selected for by polygynous mating strategies.
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Mohr, E., Speed, J. G.(D.), & Goodall D.M..(Translator) (Eds.). The Asiatic Wild Horse.
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Hvorecny, L. M., Grudowski, J. L., Blakeslee, C. J., Simmons, T. L., Roy, P. R., Brooks, J. A., et al. (2007). Octopuses (Octopus bimaculoides) and cuttlefishes (Sepia pharaonis, S. officinalis) can conditionally discriminate. Anim. Cogn., .
Abstract: In complex navigation using landmarks, an animal must discriminate between potential cues and show context (condition) sensitivity. Such conditional discrimination is considered a form of complex learning and has been associated primarily with vertebrates. We tested the hypothesis that octopuses and cuttlefish are capable of conditional discrimination. Subjects were trained in two maze configurations (the conditions) in which they were required to select one of two particular escape routes within each maze (the discrimination). Conditional discrimination could be demonstrated by selecting the correct escape route in each maze. Six of ten mud-flat octopuses (Octopus bimaculoides), 6 of 13 pharaoh cuttlefish (Sepia pharaonis), and one of four common cuttlefish (S. officinalis) demonstrated conditional discrimination by successfully solving both mazes. These experiments demonstrate that cephalopods are capable of conditional discrimination and extend the limits of invertebrate complex learning.
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Mauck, B., & Dehnhardt, G. (2007). Spatial multiple-choice matching in a harbour seal (Phoca vitulina): differential encoding of landscape versus local feature information? Anim. Cogn., .
Abstract: The nature of spatial information used for memorizing and recalling places is largely unclear. Earlier studies tested integration of geometric and feature information mostly during reorientation in artificial environments without including time as a memory-critical component. Here, we tested a harbour seal in a delayed matching-to-sample task (DMTS) in a familiar environment under two spatial multiple-choice conditions. The feature condition consisted of a DMTS task with four comparison stimuli presented on fixed positions in a classic matching apparatus and was designed to make stimulus features the most prominent information. The landscape condition consisted of a DMTS task in a familiar environment with four places marked by comparison stimuli and allowed the use of all available spatial information including geometrical and feature information. The seal's performance was impaired by delays of 3, 6, 9 or 12 s only in the feature condition; a delay of 12 s resulted in chance level performance. Replacing the comparison stimuli at the apparatus with identical spheres resulted in impaired performance. Performance in the landscape condition was impaired neither by delays nor by replacing comparison stimuli with spheres. Landscape information obviously was encoded redundantly and could be recalled more reliably and longer than feature information, which reveals feature information to be a less valuable type of spatial information for memorizing and recalling places.
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