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Population‐specific life histories contribute to metapopulation viability
Author(s) -
Halsey Samniqueka J.,
Bell Timothy J.,
McEachern Kathryn,
Pavlovic Noel B.
Publication year - 2016
Publication title -
ecosphere
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.255
H-Index - 57
ISSN - 2150-8925
DOI - 10.1002/ecs2.1536
Subject(s) - metapopulation , population viability analysis , biology , threatened species , ecology , population , fecundity , population growth , ecological succession , extinction (optical mineralogy) , demography , habitat , endangered species , biological dispersal , paleontology , sociology
Restoration efforts can be improved by understanding how variations in life‐history traits occur within populations of the same species living in different environments. This can be done by first understanding the demographic responses of natural occurring populations. Population viability analysis continues to be useful to species management and conservation with sensitivity analysis aiding in the understanding of population dynamics. In this study, using life‐table response experiments and elasticity analyses, we investigated how population‐specific life‐history demographic responses contributed to the metapopulation viability of the Federally threatened Pitcher's thistle ( Cirsium pitcheri ). Specifically, we tested the following hypotheses: (1) Subpopulations occupying different environments within a metapopulation have independent demographic responses and (2) advancing succession results in a shift from a demographic response focused on growth and fecundity to one dominated by stasis. Our results showed that reintroductions had a positive contribution to the metapopulation growth rate as compared to native populations which had a negative contribution. We found no difference in succession on the contribution to metapopulation viability. In addition, we identified distinct population‐specific contributions to metapopulation viability and were able to associate specific life‐history demographic responses. For example, the positive impact of Miller High Dunes population on the metapopulation growth rate resulted from high growth contributions, whereas increased time of plant in stasis for the State Park Big Blowout population resulted in negative contributions. A greater understanding of how separate populations respond in their corresponding environment may ultimately lead to more effective management strategies aimed at reducing extinction risk. We propose the continued use of sensitivity analyses to evaluate population‐specific demographic influences on metapopulation viability. In understanding the underlying causes of the projected extinction probabilities of each population and identifying broad‐scale contributions of different populations to the metapopulation, the process of pinpointing target populations is simplified. More detailed analyses can then be applied to the target populations to increase population viability and consequently metapopulation viability. Based on our research, we suggest that the best approach to improve the overall metapopulation viability is to manage the contributions to population growth for each population separately.

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