Measuring environmental niche isolation between genetically management units of Goitered gazelle, Gazella subgutturosa (Guldenstadt, 1970) in Iran

Authors

  • Rasoul Khosravi Department of Natural Resources, Isfahan University of Technology, Isfahan, Iran
  • Roya Adavoudi Department of Environmental Sciences, Faculty of Natural Resources, University of Tehran, Karaj, Iran
  • Mansoureh Malekian Department of Natural Resources, Isfahan University of Technology, Isfahan, Iran
  • Mohmoud-Reza Hemami Department of Natural Resources, Isfahan University of Technology, Isfahan, Iran

DOI:

https://doi.org/10.22120/jwb.2017.28178

Keywords:

Goitered gazelle, Management unit, Niche equivalency, Niche overlap, Niche similarity

Abstract

The interactions between species and their environments can shape the distribution of spatial genetic variations. Evaluation of niche overlap and environmental dissimilarity provides valuable opportunities to investigate how niche differences contribute to genetic divergence between populations that differ in their geographical distributions and environmental conditions. Nowadays, the formerly large continuous populations of Goitered gazelle in Iran have been confined to fragmented habitats due to natural and anthropogenic factors. A statistical framework based on an ecological niche modeling at the genetical management units (MUs) level was used to compare environmental niches and evaluate the effect of niche differentiation on genetic patterns of two management units of Goitered gazelle in Central Iran. We found low values of niche overlap between the management units. The niche equivalency hypothesis revealed that the niche of MUs is more significantly distinct than expected by chance. Also, the niche similarity test for both comparisons falls within the 95% confidence limits of the null distribution. These findings demonstrate that the niche of two MUs is rarely identical, but they tend to be more similar than expected based on random predictions and environmental background, which they occur. We concluded that, besides landscape resistance and geographic distance, ecological niche isolation is another factor affecting the genetic structure of gazelle populations in Iran. Conservation planning of this vulnerable species should focus on isolated populations as separate management units and landscape linkages to maintain gene flow between the genetically similar populations.

References

Aguirre-Gutiérrez J., Serna-Chavez H.M., Villalobos-Arambula A.R., Pérez de la Rosa J.A., Raes N. 2015. Similar but not equivalent: ecological niche comparison across closely–related Mexican white pines. Diversity and distributions 21(3): 245-257.

Balkenhol N., Cushman S., Storfer A., Waits L. 2016. Landscape genetics: concepts, methods, applications. John Wiley and Sons, pp.272.

Broennimann O., Fitzpatrick M.C., Pearman P.B., Petitpierre B., Pellissier L., Yoccoz N.G., Thuiller W., Fortin M.J., Randin C., Zimmermann, N.E. 2012. Measuring ecological niche overlap from occurrence and spatial environmental data. Global Ecology and Biogeography 21: 481–497.

Elton C.S. 1927. Animal ecology. London: Sidgwick and Jackson. pp. 130

Fitzpatrick M.C., Weltzin J.F., Sanders N.J., Dunn R.R. 2007. The biogeography of prediction error: why does the introduced range of the fire ant over-predict its native range. Global Ecology and Biogeography 16(1): 24–33.

Flint L.E., Flint A.L. 2012. Downscaling future climate scenarios to fine scales for hydrologic and ecological modeling and analysis. Ecological Process 1(1):123–140.

Graham C.H., Ron S.R., Santos J.C., Schneider C.J., Moritz C. 2004. Integrating phylogenetics and environmental niche models to explore speciation mechanisms in dendrobatid frogs. Evolution 58(8): 1781-1793.

Grinnell J. 1917. The niche-relationships of the California thrasher. The Auk 34: 427–433.

Guisan A., Thuiller W. 2005. Predicting species distribution: offering more than simple habitat models. Ecology Letters 8(9): 993–1009.

Hijmans R.J., Cameron S.E., Parra J.L., Jones P.G., Jarvis A. 2005. Very high resolution interpolated climate surfaces for global land areas. International Journal of Climatology 25(15): 1965–1978.

¬¬

Hof C., Rahbek C., Araújo M.B. 2010. Phylogenetic signals in the climatic niches of the world’s amphibians. Ecography 33(2): 242–250.

Hutchinson G.E. 1957. Population studies – animal ecology and demography – concluding remarks. Cold Spring Harbor Symposia on Quantitative Biology 22: 415–427.

Khosravi R., Hemami M.R., Malekian M., Flint A., Flint L. 2016. Maxent modeling for predicting potential distribution of goitered gazelle in central Iran: the effect of extent and grain size on performance of the model. Turk. Journal Zoology 40(4): 574–585.

Khosravi R., Hemami M.R., Malekian M., Silva T.L., Rezaei H.R., Brito J.C. 2016. Effect of landscape features on genetic structure of the Goitered gazelle (Gazella subgutturosa) in Central Iran. Conservation Genetic (https://doi.org/10.1007/s10592-017-1002-2).

Lee C.R., Mitchell-Olds T. 2011. Quantifying effects of environmental and geographical factors on patterns of genetic differentiation. Molecular Ecology 20(22): 4631–4642.

Marvier M., Kareiva P. 2015. Conservation Science: Balancing the Needs of People and Nature. Second Edition. Roberts and Company Publishers, Greenwood Village, pp. 543.

McCormack J.E., Zellmer A.J., Knowles L.L. 2010. Does niche divergence accompany allopatric divergence in Aphelocoma jays as predicted under ecological speciation? insights from tests with niche models. Evolution 64(5): 1231– 1244.

McRae B.H., Beier P. 2007. Circuit theory predicts gene flow in plant and animal populations. Proceedings of the National Academy of Sciences 104(50): 19885–19890.

Medley K.A. 2010. Niche shifts during the global invasion of the Asian tiger mosquito, Aedes albopictus Skuse (Culicidae), revealed by reciprocal distribution models. Global Ecology and Biogeography 19(1): 122–133.

Moqanaki E.M., Cushman S.A. 2016. All roads lead to Iran: Predicting landscape connectivity of the last stronghold for the critically endangered Asiatic cheetah. Animal Conservation 20(1): 29-41.

Moritz C. 1994. Defining evolutionary significant unit for conservation. Trends in Ecology and Evolution 9(10): 373-211.

Mosca E., Eckert A.J., Di Pierro E.A., Rocchini D., La Porta N., Belletti P., Neale D.B. 2012. The geographical and environmental determinants of genetic diversity for four alpine conifers of the European Alps. Molecular Ecology 21(22): 5530–5545.

Raasanen K., Hendry A.P. 2008. Disentangling interactions between adaptive divergence and gene flow when ecolo gy drives diversification. Ecology Letters 11(6): 624–636.

Raxworthy C.J., Ingram C.M., Rabibisoa N., Pearson R.G. 2007. Applications of ecological niche modeling for species delimitation: a review and empirical evaluation using day geckos (Phelsuma) from Madagascar. Systematic Biology 56(6): 907–923.

Schoener T.W. 1968. Anolis lizards of Bimini: resource partitioning in a complex fauna. Ecology 49(4): 704-726.

Steiner F.M., Schlick-Steiner B.C., VanDerWal J., Reuther K.D., Christian E., Stauffer C., Suarez A.V., Williams S.E., Crozier R.H. 2008. Combined modelling of distribution and niche in invasion biology: a case study of two invasive Tetramorium ant species. Diversity and Distributions 14(3): 538– 545.

Storfer A., Murphy M.A., Spear S. F., Holderegger R., Waits L.P. 2010. Landscape genetics: Where are we now? Molecular Ecology 19(17): 3496–514.

Svendsen G. M., Romero M. A., Williams G. N., Gagliardini D. A., Crespo E. A., Dans S. L., González R. A. 2015. Environmental Niche Overlap between Common and Dusky Dolphins in North Patagonia, Argentina. PloS one 10(6): e0126182.

Team R.C. 2016. A language and environment for statistical computing. R Foundation for statistical computing. 2015. Vienna, Austria, pp.3-36.

Thuiller W., Lavorel S., Araújo M.B. 2005. Niche properties and geographical extent as predictors of species sensitivity to climate change. Global Ecology and Biogeography 14(4): 347– 357.

Wang I.J., Summers K. 2010. Genetic structure is correlated with phenotypic divergence rather than geographic isolation in the highly polymorphic strawberry poison-dart frog. Molecular Ecology 19(3): 447–458.

Warren D.L., Glor R.E., Turelli M. 2008. Environmental niche equivalency versus conservatism: quantitative approaches to niche evolution. Evolution 62(11): 2868–2883.

Wielstra B., Beukema W., Arntzen J.W., Skidmore A.K., Toxopeus A.G., Raes N. 2012. Corresponding Mitochondrial DNA and Niche Divergence for Crested Newt Candidate Species. PLoS One 7(9): e46671

Wiens J.J., Graham C.H. 2005. Niche conservatism: integrating evolution, ecology and conservation biology. Annual Review of Ecology, Evolution, and Systematics 36: 519–539.

Wright S. 1943. Isolation by distance. Genetics 28(2): 114–138.

Zachos F.E., Karami M., Ibenouazi Z., Hartl G.B., Eckert I., Kirschning J. 2010. First genetic analysis of a free-living population of the threatened goitered gazelle (Gazella subgutturosa). Mammalian Biology 75(3): 277–282.

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Published

2017-10-30

How to Cite

Khosravi, R. ., Adavoudi, R. ., Malekian, M. ., & Hemami, M.-R. . (2017). Measuring environmental niche isolation between genetically management units of Goitered gazelle, Gazella subgutturosa (Guldenstadt, 1970) in Iran . Journal of Wildlife and Biodiversity, 1(2), 60–68. https://doi.org/10.22120/jwb.2017.28178