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Artykuły w czasopismach na temat "Chelodina longicollis Ecology"

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Chessman, BC. "Seasonal and Diel Activity of Fresh-Water Turtles in the Murray Valley, Victoria and New South-Wales". Wildlife Research 15, nr 3 (1988): 267. http://dx.doi.org/10.1071/wr9880267.

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Activity cycles of Chelodina expansa, C. longicollis and Emydura macquarii were inferred from captures in baited traps set in the Murray River and Lake Boga. C. expansa and E, macquarii were caught only from October to April, while C. longicollis was taken in all months but June and July. Minimum water temperatures at capture were highest for C. expansa and lowest for C. longicollis. Diel cycles of catch rate were often weak, but tended to be bimodal for all species, with peaks near dawn and in the afternoon or evening. Unlike the Chelodina species, E. macquarii was ofen caught near midnight. In the laboratory (at c.24�C with light:dark 12:12 h), the average diel pattern of locomotor activity was weakly bimodal in C. expansa, strongly bimodal in C. longicollis and unimodal in E. macquarii.
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Chessman, BC. "Habitat Preferences of Fresh-Water Turtles in the Murray Valley, Victoria and New-South-Wales". Wildlife Research 15, nr 5 (1988): 485. http://dx.doi.org/10.1071/wr9880485.

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Preferences of Chelodina expansa, Chelodina longicollis and Emydura macquarii (Testudines : Chelidae) for different types of aquatic habitat on the Murray River flood plain in south-eastern Australia were inferred from catch statistics. E. macquarii was the species most often caught in the river itself and river backwaters, whereas C. longicollis formed the majority of captures from oxbow lakes, anabranches, ponds, rain pools and a swamp. Relative abundance of E. macquarii was significantly positively correlated with water body depth, transparency, persistence during dry conditions and flow speed, and negatively correlated with remoteness from the river. C. longicollis demonstrated the opposite pattern, and the proportional catch of C. expansa was weakly correlated with environmental variables. The capacity of C. longicollis for colonising and surviving in small, remote and ephemeral ponds and pools relates to its ability to aestivate and resist desiccation and its propensity for overland migration.
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Georges, a., RH Norris i L. Wensing. "Diet of the Fresh-Water Turtle Chelodina-Longicollis (Testudines, Chelidae) From the Coastal Dune Lakes of the Jervis Bay Territory". Wildlife Research 13, nr 2 (1986): 301. http://dx.doi.org/10.1071/wr9860301.

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Chelodina longicollis is an opportunistic carnivore that obtains its food from a wide variety of sourcesplankton, nekton, benthic macro-organisms, carrion, and terrestrial organisms that fall upon the water. Although there are some quantitative differences between the littoral components of the diet and the composition of the littoral fauna, these can be attributed to differences in accessibility or 'noticeability' among prey species. There is no evidence to suggest that C, longicollis is selective in what it eats, within the confines of carnivory. Comparison of the diet of C. longicollis with those of other sympatric chelids reveals considerable overlap; the relevance of this to geographic variation in abundance of the species is discussed.
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Chessman, Bruce C. "Effects of temperature and exercise on metabolism of three species of Australian freshwater turtles: implications for responses to climate change". Australian Journal of Zoology 66, nr 6 (2018): 317. http://dx.doi.org/10.1071/zo18062.

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Oxygen consumption () of Chelodina expansa, C. longicollis and Emydura macquarii (Pleurodira: Chelidae) was measured at rest and during induced exercise at 8, 13, 18, 22, 26, 30 and 34°C. Resting varied significantly among species, being lowest in C. expansa, which is the most sedentary of the three species in nature, and highest in E. macquarii, which is the most energetic, but active did not differ significantly among the three species overall. For both Chelodina species, resting was appreciably lower than expected from regression of on body mass for non-marine turtles globally, a result that reinforces previous evidence of low resting metabolism in Australian chelid turtles. Active of all three species at higher temperatures was similar to reported for active freshwater cryptodires. Resting of all three species increased similarly with temperature, but active and aerobic scope did not. In C. expansa and E. macquarii, active and aerobic scope increased over the full temperature range assessed but in C. longicollis these variables reached a plateau above 22°C. Projected increases in freshwater temperatures in south-eastern Australia as a result of global warming are likely to enhance activity, feeding and growth of the three species (subject to food availability), especially in cooler seasons for C. longicollis and warmer seasons for C. expansa and E. macquarii. However, other aspects of predicted climate change, especially increased drought, are likely to be detrimental.
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Chessman, Bruce C. "Behavioural thermoregulation by Australian freshwater turtles: interspecific differences and implications for responses to climate change". Australian Journal of Zoology 67, nr 2 (2019): 94. http://dx.doi.org/10.1071/zo20004.

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The abilities of freshwater turtles to control their body temperatures by behavioural means have implications for activity, food ingestion and digestion, growth, reproduction and potential responses to climate change. I compared various forms of basking in nature, and responses to aquatic and aerial photothermal gradients in the laboratory, among three species of Australian chelid turtles: Chelodina expansa, C. longicollis and Emydura macquarii. Proclivity for behavioural thermoregulation varied substantially among these species, being highest in C. longicollis and lowest in C. expansa. However, C. expansa had a thermophilic response to feeding. For C. longicollis and E. macquarii, behavioural thermoregulation may enhance colonisation of more southerly latitudes or higher elevations as climatic warming proceeds. However, increasing air temperatures may pose a hazard to turtles dispersing or sheltering terrestrially (for example, when water bodies dry during drought). C. longicollis appears the best placed of the three species to avoid this hazard through its abilities to thermoregulate behaviourally and to aestivate in terrestrial microenvironments that are buffered against temperature extremes.
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Palmer-Allen, M., F. Beynon i a. Georges. "Hatchling Sex Ratios are Independent of Temperature in Field Nests of the Long-necked Turtle, Chelodina longicollis (Testudinata : Chelidae)". Wildlife Research 18, nr 2 (1991): 225. http://dx.doi.org/10.1071/wr9910225.

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Eastern long-necked turtles, Chelodina longicollis, are known to lack heteromorphic sex chromosomes and to lack temperature-dependent sex determination when incubated under constant conditions. This study determined whether sex ratios of hatchlings emerging from natural nests of C. longicollis were different from that expected from constant temperature experiments. Temperatures in the eight nests monitored varied considerably each day (by 1.7-12.6�C), with eggs at the top of the nest experiencing the greatest variation (mean range 9.0�C) and eggs at the bottom experiencing least variation (mean range 5.3�C). Temperatures experienced by the top and bottom eggs differed by as much as 5.7�C at any one time. No monotonic seasonal trend was evident, but rainfall caused a sharp drop in nest temperatures. Sex ratios in hatchlings from 14 field nests of C. longicollis did not differ significantly from 1:1, a result in agreement with previous studies conducted at constant incubation temperatures in the laboratory.
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Graham, Terry, Arthur Georges i Neil McElhinney. "Terrestrial Orientation by the Eastern Long-Necked Turtle, Chelodina longicollis, from Australia". Journal of Herpetology 30, nr 4 (grudzień 1996): 467. http://dx.doi.org/10.2307/1565689.

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Stokeld, Danielle, Andrew J. Hamer, Rodney van der Ree, Vincent Pettigrove i Graeme Gillespie. "Factors influencing occurrence of a freshwater turtle in an urban landscape: a resilient species?" Wildlife Research 41, nr 2 (2014): 163. http://dx.doi.org/10.1071/wr13205.

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Context Species vary broadly in their ability to adapt to urbanisation. Freshwater turtles are vulnerable to the loss and degradation of terrestrial and aquatic habitat in urban environments. There have been few publications investigating impacts of urbanisation on freshwater turtles in Australia. Aims We investigated the effects of urbanisation on the distribution and abundance of the eastern long-necked turtle (Chelodina longicollis) in greater Melbourne. Methods We examined occurrence and relative abundance of C. longicollis at 55 wetlands across an urban–rural gradient in relation to site- and landscape-level factors. Occupancy was modelled using the program PRESENCE, and incorporated landscape and habitat covariates. A negative binomial regression model was used to examine the influence of landscape and habitat factors on relative abundance by using WinBUGS. Key results C. longicollis occupied 85% of the 55 wetlands we surveyed, and we found no evidence that wetland occupancy was influenced by the variables we measured. However, relative abundance was highest at wetlands with low water conductivity and heavy metal pollution, and in wetlands furthest from rivers. Conclusions C. longicollis appears to be resilient to urbanisation and is likely to persist in urban landscapes, possibly because of the creation of new wetlands in Australian cities. However, long-term studies focussed on demographic parameters, or survivorship, may elucidate as yet undetected effects of urbanisation. Although no specific management recommendations may be necessary for C. longicollis in urban areas at this time, this species may be in decline in non-urban areas as a result of climatic changes and wetland drying. Implications Our findings suggest that caution is required before drawing generalised conclusions on the impacts of urbanisation on turtles, as the effects are likely to be species-specific, dependent on specific ecology and life-history requirements. Further studies are required to ascertain these relationships for a wider array of species and over longer time spans.
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Doody, J. Sean, John Roe, Phillip Mayes i Lesley Ishiyama. "Telemetry tagging methods for some freshwater reptiles". Marine and Freshwater Research 60, nr 4 (2009): 293. http://dx.doi.org/10.1071/mf08158.

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Reptiles are often ignored or under-studied in freshwater systems. An understanding of their biology and thus their role in aquatic communities can be greatly advanced by studies using radio telemetry. In turn, the value of radio telemetry for research depends on the availability of suitable and reliable methods of attaching or implanting radio transmitters. The present study describes transmitter attachment and implantation techniques for selected freshwater reptiles, including the eastern and northern long-necked turtles (Chelodina longicollis and Chelodina rugosa, respectively), the pig-nosed turtle (Carettochelys insculpta), Mertens’ water monitor (Varanus mertensi) and the water dragon (Physignathus lesueurii). The effectiveness of the methods for each species is described and the potential pitfalls and challenges of each method are discussed. The literature abounds with techniques for attachment and implantation techniques, and the methods used in the present study are not wholly novel. The aim, however, is to provide detailed summaries, in one paper, of effective methods for attachment and implantation of radio-tags for freshwater reptiles with a diversity of sizes, shapes and attachment surfaces. Despite the focus on Australian freshwater reptiles, these methods are applicable to aquatic reptiles worldwide.
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Georges, Arthur. "Sex Determination Is Independent of Incubation Temperature in Another Chelid Turtle, Chelodina longicollis". Copeia 1988, nr 1 (5.02.1988): 248. http://dx.doi.org/10.2307/1445946.

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Rozprawy doktorskie na temat "Chelodina longicollis Ecology"

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Stott, Philip. "Terrestrial movements of the freshwater tortoise Chelodina longicollis". Title page, contents and summary only, 1988. http://web4.library.adelaide.edu.au/theses/09SM/09sms888.pdf.

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Roe, John H., i n/a. "THE TERRESTRIAL ECOLOGY OF A FRESHWATER TURTLE, CHELODINA LONGICOLLIS, IN BOODEREE NATIONAL PARK, AUSTRALIA". University of Canberra. Institute for Applied Ecology, 2007. http://erl.canberra.edu.au./public/adt-AUC20081009.143208.

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Most studies of wetlands tend to focus on the biotic and abiotic interactions within the aquatic habitat. Though wetlands and associated biota may appear to be somewhat isolated from the influence of the wider landscape, wetland habitats are critically linked with adjacent terrestrial habitats and other wetlands through the two-way flows of energy and nutrients and provision of structure. While an understanding of these inter-habitat linkages is breaking down the perceived boundaries between "aquatic" and "terrestrial" ecosystems, there is more limited knowledge on the ecology of wetland animals that must meet critical needs in both aquatic and terrestrial habitats at some time during their life or seasonal cycles. Here, I examine the terrestrial ecology of a freshwater turtle, the eastern long-necked turtle (Chelodina longicollis) in the temporally dynamic and heterogeneous landscape of Booderee national park in south-east Australia by 1) providing a description of terrestrial behaviours, 2) identifying the factors driving terrestrial behaviour and its functional significance, 3) examining factors that may limit or constrain terrestrial behaviour and 4) demonstrating how various terrestrial behaviours can factor prominently in the overall biology of a nominally aquatic animal. Chelodina longicollis used terrestrial habitats for reasons other than nesting, including aestivation and movements between wetlands. Radio-telemetry of 60 turtles revealed that nearly 25 % of all locations were in terrestrial habitats up to 505 m from the wetland, where turtles remained for extended periods (up to 480 consecutive days) buried under sand and leaf litter in the forest. Individuals also maintained an association with a permanent lake and at least one temporary wetland within 1470 m, though some inter-wetland dispersal movements were much longer (5248 m). As a result of their associations with several wetlands and terrestrial aestivation sites, C. longicollis traversed large areas and long distances (13.8 +/- 2.8 ha home range, 2608 +/- 305 m moved), indicating that this species is highly vagile. In fact, a three-year capture-mark-recapture study conducted in 25 wetlands revealed that 33% of the population moved overland between wetlands. After scaling this rate to the number of generations elapsed during the study, C. longicollis moved between discrete water bodies at a rate of 88-132% per generation. This rate is not only high for freshwater turtles, but is among the highest rates of inter-patch movement for any vertebrate or invertebrate. Chelodina longicollis demonstrated an impressive capacity for individual variation in nearly every aspect of its behaviour examined. Most of the variation in space use, movements, terrestrial aestivation and activity could be attributed to extrinsic local and landscape factors, seasonal influences and rainfall, whereas intrinsic attributes of the individual such as sex, body size, body condition and maturity status were less important. Turtles increased movement distance and home range size in regions where inter-wetland distances were farther and with increasing wetland size. Individuals spent more time in terrestrial habitats with decreasing wetland hydroperiod and increasing distance to the nearest permanent lake. Overland movements between wetlands were correlated with rainfall, but the directionality of these movements and the frequency with which they occurred varied according to the prevalent rainfall patterns; movements were to permanent lakes during drought, but turtles returned to temporary wetlands en masse upon the return of heavy rainfall. However, deteriorating conditions in drying wetlands forced turtles to move even in the absence of rainfall. Captures at a terrestrial drift fence revealed that immature turtles as small as 72.3 mm plastron length may move overland between wetlands with similar frequency as larger adults. Taken together, these results suggest that C. longicollis behaviour is in part conditional or state-dependent (i.e., plastic) and shaped by the spatiotemporal variation and heterogeneity of the landscape. Perhaps the most surprising aspect of individual variation was the alternate responses to wetland drying. Turtles either aestivated in terrestrial habitats (for variable lengths of time), or moved to other wetlands. Movement to other wetlands was the near universal strategy when only a short distance from permanent lakes, but the proportion of individuals that aestivated terrestrially increased with distance to the nearest permanent lake. When long distances must be travelled, both behaviours were employed by turtles in the same wetland, suggesting that individuals differentially weigh the costs and benefits of residing terrestrially versus those of long-distance movement. I propose that diversity in response to wetland drying in the population is maintained by stochastic fluctuations in resource quality. The quality of temporary wetlands relative to permanent wetlands at our study site varies considerably and unpredictably with annual rainfall and with it the cost-benefit ratio of each strategy or tactic. Residency in or near temporary wetlands is more successful during wet periods due to production benefits (high growth, reproduction and increased body condition), but movement to permanent wetlands is more successful, or least costly, during dry periods due to the fitness benefits of increased survival and body condition. I used the doubly-labelled water (DLW) method to provide the first estimates of water and energy costs of aestivation and overland movement for any freshwater turtle behaving naturally in the field. Chelodina longicollis remained hydrated while terrestrial with water flux rates (14.3-19.3 ml kg-1 d-1) on par with those of strictly terrestrial turtles, but field metabolic rate during aestivation (20.0-24.6 kJ kg-1 d-1) did not indicate substantial physiological specializations in metabolism during aestivation. Energy reserves, but not water, are predicted to limit survival in aestivation to an estimated 49-261 days, which is in close agreement with the durations of natural aestivation. The energy costs of overland movement were 46-99 kJ (kg d)-1, or 1.6-1.7 times more expensive than aestivation. When a wetland dries, a turtle that foregoes movement to other wetlands can free sufficient energy to fuel up to 134 days in aestivation. The increasing value of this energy "trade-off" with travel distance fits our behavioural observations of variance in response to wetland drying. Taken together, this evidence indicates that terrestrial habitats provide more than just organic and structural inputs and filtering services and that nearby wetlands are important for reasons other than potential sources of occasional colonists to a population. Terrestrial habitats are used for aestivation in response to wetland drying and different wetlands are diverse in their functions of meeting the annual or life-cycle requirements of C. longicollis in temporally dynamic wetland systems. As overland movements between these various habitat types are in response to spatiotemporal variation in habitat quality and associated shifts in the fitness gradient between them, I suggest that terrestrial and different aquatic habitats in Booderee offer complementary resources contributing to regional carrying capacity and population persistence of the turtle population. Thus, important ecological processes regulating C. longicollis in a focal wetland should not be viewed as operating independently of other nearby wetlands and their adjacent terrestrial habitats. Collectively, these findings highlight the complex and dynamic associations between a population of freshwater turtles and the wider terrestrial and aquatic landscape, demonstrating that turtle populations and the factors that impact them can extend well beyond the boundaries of a focal wetland.
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