期刊论文详细信息
Movement Ecology
Identifying the time scale of synchronous movement: a study on tropical snakes
Richard Shine2  Gregory P Brown2  Benjamin L Phillips3  Tom Lindström1 
[1] Department of Physics, Biology and Chemistry, Linköping University, Linköping, 58183, Sweden;School of Biological Sciences, University of Sydney, Sydney 2006, NSW, Australia;School of Biosciences, University of Melbourne, Melbourne 3010, VIC, Australia
关键词: Ectotherms;    Elapidae;    Relocation data;    Hierarchical Bayes;    Periodogram;   
Others  :  1182904
DOI  :  10.1186/s40462-015-0038-5
 received in 2015-02-02, accepted in 2015-03-09,  发布年份 2015
PDF
【 摘 要 】

Background

Individual movement is critical to organismal fitness and also influences broader population processes such as demographic stochasticity and gene flow. Climatic change and habitat fragmentation render the drivers of individual movement especially critical to understand. Rates of movement of free-ranging animals through the landscape are influenced both by intrinsic attributes of an organism (e.g., size, body condition, age), and by external forces (e.g., weather, predation risk). Statistical modelling can clarify the relative importance of those processes, because externally-imposed pressures should generate synchronous displacements among individuals within a population, whereas intrinsic factors should generate consistency through time within each individual. External and intrinsic factors may vary in importance at different time scales.

Results

In this study we focused on daily displacement of an ambush-foraging snake from tropical Australia (the Northern Death Adder Acanthophis praelongus), based on a radiotelemetric study. We used a mixture of spectral representation and Bayesian inference to study synchrony in snake displacement by phase shift analysis. We further studied autocorrelation in fluctuations of displacement distances as “one over f noise”. Displacement distances were positively autocorrelated with all considered noise colour parameters estimated as >0. We show how the methodology can reveal time scales of particular interest for synchrony and found that for the analysed data, synchrony was only present at time scales above approximately three weeks.

Conclusion

We conclude that the spectral representation combined with Bayesian inference is a promising approach for analysis of movement data. Applying the framework to telemetry data of A. praelongus, we were able to identify a cut-off time scale above which we found support for synchrony, thus revealing a time scale where global external drivers have a larger impact on the movement behaviour. Our results suggest that for the considered study period, movement at shorter time scales was primarily driven by factors at the individual level; daily fluctuations in weather conditions had little effect on snake movement.

【 授权许可】

   
2015 Lindström et al.; licensee BioMed Central.

【 预 览 】
附件列表
Files Size Format View
20150518080331130.pdf 761KB PDF download
Figure 2. 11KB Image download
Figure 1. 51KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]Brown GP, Shine R. Influence of weather conditions on activity of tropical snakes. Austral Ecol. 2002; 27:596-605.
  • [2]Latimer AM, Wu S, Gelfand AE, Silander JA. Building statistical models to analyze species distributions. Ecol Appl. 2006; 16:33-50.
  • [3]Ives AR, Abbott KC, Ziebarth NL. Analysis of ecological time series with ARMA(p, q) models. Ecology. 2010; 91:858-71.
  • [4]Brown GP, Phillips BL, Shine R. The ecological impact of invasive cane toads on tropical snakes: field data do not support laboratory-based predictions. Ecology. 2011; 92:422-31.
  • [5]King MB, Duvall D. Prairie rattlesnake seasonal migrations: episodes of movement, vernal foraging and sex differences. Anim Behav. 1990; 39:924-35.
  • [6]Madsen T, Shine R. Seasonal migration of predators and prey–a study of pythons and rats in tropical Australia. Ecology. 1996; 77:149-56.
  • [7]Froy O, Gotter AL, Casselman AL, Reppert SM. Illuminating the circadian clock in monarch butterfly migration. Science. 2003; 300:1303-5.
  • [8]Boone RB, Thirgood SJ, Hopcraft JGC. Serengeti wildebeest migratory patterns modeled from rainfall and new vegetation growth. Ecology. 2006; 87:1987-94.
  • [9]Hailey A, Davies PMC. Activity and thermoregulation of the snake Natrix maura. 2. A synoptic model of thermal biology and the physiological ecology of performance. J Zool. 1988; 214:325-42.
  • [10]Lelièvre H, Hénanff M, Blouin-Demers G, Naulleau G, Lourdais O. Thermal strategies and energetics in two sympatric colubrid snakes with contrasted exposure. J Comp Physiol B. 2010; 180:415-25.
  • [11]Kearney M, Shine R, Porter WP. The potential for behavioral thermoregulation to buffer “cold-blooded” animals against climate warming. Proc Natl Acad Sci. 2009; 106:3835.
  • [12]Shine R, Madsen T. Is thermoregulation unimportant for most reptiles? An example using water pythons (Liasis fuscus) in tropical Australia. Physiol Zool. 1996; 69:252-69.
  • [13]Daltry JC, Ross T, Thorpe RS, Wüster W. Evidence that humidity influences snake activity patterns: a field study of the Malayan pit viper Calloselasma rhodostoma. Ecography (Cop). 1998; 21:25-34.
  • [14]Moore JA, Gillingham JC. Spatial ecology and multi-scale habitat selection by a threatened rattlesnake: the Eastern Massasauga (Sistrurus Catenatus Catenatus). Copeia. 2006; 2006:742-51.
  • [15]Subach A, Scharf I, Ovadia O. Foraging behavior and predation success of the sand viper (Cerastes vipera). Can J Zool. 2009; 87:520-8.
  • [16]Clark DR, Fleet RR. The rough earth snake (Virginia striatula): ecology of a Texas population. Southwest Nat. 1976; 20:467-78.
  • [17]Bonnet X, Naulleau G, Shine R. The dangers of leaving home: dispersal and mortality in snakes. Biol Conserv. 1999; 89:39-50.
  • [18]Whitaker PB, Shine R. Thermal biology and activity patterns of the eastern brownsnake (Pseudonaja textilis): a radiotelemetric study. Herpetologica. 2002; 58:436-52.
  • [19]Hastings A. Timescales, dynamics, and ecological understanding. Ecology. 2010; 91:3471-80.
  • [20]Spiegelhalter DJ, Best NG, Carlin BP. Bayesian measures of model complexity and fit. J R Stat Soc B. 2002; 64:583-639.
  • [21]Halley JM. Ecology, evolution and 1/f-noise. Trends Ecol Evol. 1996; 11:33-7.
  • [22]Phillips BL, Greenlees MJ, Brown GP, Shine R. Predator behaviour and morphology mediates the impact of an invasive species: cane toads and death adders in Australia. Anim Conserv. 2010; 13:53-9.
  • [23]Webb JK, Shine R, Christian KA. Does intraspecific niche partitioning in a native predator influence its response to an invasion by a toxic prey species? Austral Ecol. 2005; 30:201-9.
  • [24]Fowler MS, Ruokolainen L. Confounding environmental colour and distribution shape leads to underestimation of population extinction risk. PLoS One. 2013; 8:e55855.
  • [25]Lindström T, Sisson SA, Håkansson N, Bergman K-O, Wennergren U. A spectral and Bayesian approach for analysis of fluctuations and synchrony in ecological datasets. Methods Ecol Evol. 2012; 3:1019-27.
  • [26]Gelman A, Carlin JB, Stern HS, Rubin DB. Bayesian data analysis. 2nd ed. Chapman & Hall/CRC, New York; 2004.
  • [27]Kerr GD, Bottema MJ, Bull CM. Lizards with rhythm? Multi-day patterns in total daily movement. J Zool. 2008; 275:79-88.
  • [28]Polansky L, Wittemyer G, Cross PC, Tambling CJ, Getz WM. From moonlight to movement and synchronized randomness: fourier and wavelet analyses of animal location time series data. Ecology. 2010; 91:1506-18.
  • [29]Vasseur DA, Yodzis P. The color of environmental noise. Ecology. 2004; 85:1146-52.
  • [30]Lindström T, Håkansson N, Wennergren U. The shape of the spatial kernel and its implications for biological invasions in patchy environments. Proc R Soc B Biol Sci. 2011; 278:1564-71.
  • [31]Whittle P. Curve and periodogram smoothing. J R Stat Soc Ser B Methodol. 1957; 19:38-63.
  • [32]Christian K, Webb JK, Schultz T, Green B. Effects of seasonal variation in prey abundance on field metabolism, water flux, and activity of a tropical ambush foraging snake. Physiol Biochem Zool. 2007; 80:522-3.
  • [33]Pimm SL, Redfearn A. The variability of population densities. Nature. 1988; 334:613-4.
  • [34]Buonaccorsi JP, Elkingston JP, Evans SR, Liebhold AM. Measuring and testing for spatial synchrony. Ecology. 2001; 82:1668-79.
  • [35]Brown GP, Shine R, Madsen T. Spatial ecology of slatey-grey snakes (Stegonotus cucullatus, Colubridae) on a tropical Australian floodplain. J Trop Ecol. 2005; 21:605.
  • [36]Lindström T, Brown GP, Sisson SA, Phillips BL, Shine R. Rapid shifts in dispersal behavior on an expanding range edge. Proc Natl Acad Sci. 2013; 110:13452-6.
  • [37]Price-Rees SJ, Lindström T, Brown GP, Shine R. The effects of weather conditions on dispersal behaviour of free-ranging lizards (Tiliqua, Scincidae) in tropical Australia. Funct Ecol. 2014; 28:440-9.
  • [38]Bjørnstad ON, Ims RA, Lambin X. Spatial population dynamics: analyzing patterns and processes of population synchrony. Trends Ecol Evol. 1999; 14:427-32.
  文献评价指标  
  下载次数:26次 浏览次数:17次