Environmental integration: patterns of correlation between environmental factors, early life decisions, and their long-term consequences

被引:0
作者
Lee, Who-Seung [1 ,2 ]
Mangel, Marc [2 ,3 ]
Peres-Neto, Pedro [1 ]
机构
[1] Univ Quebec, Dept Biol Sci, Montreal, PQ H3C 3P8, Canada
[2] Univ Calif Santa Cruz, Ctr Stock Assessment Res, Santa Cruz, CA 95064 USA
[3] Univ Bergen, Dept Biol, Bergen, Norway
基金
加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
climate change; developmental phenotype; dynamic state model; growth; life history; reproduction; PHENOTYPIC PLASTICITY; EVOLUTION; GROWTH; PRECIPITATION; TRAJECTORIES; FITNESS; TRAITS; STRESS; MODELS; DAMAGE;
D O I
暂无
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Questions: How does the temporal correlation of key environmental variables (here temperature and precipitation) affect life-history decisions in early life, and what are the long-term consequences (accumulated damage, survival, and expected reproductive success)? Hypothesis: Strong environmental correlation (environmental integration) is an important signal for the development of life-history traits, such as growth rate, phenotype, and reproduction, leading to higher fitness; plastic and fixed developmental strategies have different fitness depending upon the level of environmental integration. Mathematical methods: A dynamic state-dependent model in which the state of the organism is characterized by mass, reproductive investment, and accumulated damage, all of which are affected by feeding activity and developmental costs mediated by the environment. Fitness is measured as expected lifetime reproduction. Key assumptions: We assume that at each time step the resources gained by an individual through foraging activity are determined by developmental phenotype, which itself is the result of a decision process, and are then allocated to somatic growth, repair of cellular damage (e.g. oxidative stress) or gonadal tissue. Results/Conclusions: (1) The differences in growth rate and reproductive investment between the plastic and fixed phenotypic strategies are greater at low levels (both positive and negative directions) of environmental integration. (2) Optimal resource allocation changes as a function of environmental gradient only for the plastic phenotypic strategy, and the difference in the onset of resource allocation between the plastic and fixed strategies is greater at low levels of environmental integration (i.e. the correlation between environmental factors and their fluctuation affects the reproductive timing decision though modification of resource allocation). (3) There is a marked difference in fitness when there is a low correlation and high fluctuation - conversely, the correlation has little effect when environmental fluctuation is low. (4) Even with costs, the investment in phenotype-environment matching has greater payoffs for individuals who are better able to track changes in their environment. Our results highlight that to understand the interactions between developmental decisions, we need to take into account not only the average environmental conditions but also their dynamics through time (variance and covariance).
引用
收藏
页码:1 / 19
页数:19
相关论文
共 55 条
  • [1] Reopening the climate envelope reveals macroscale associations with climate in European birds
    Araujo, Miguel B.
    Thuiller, Wilfried
    Yoccoz, Nigel G.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (16) : E45 - E46
  • [2] Re-evaluating the costs and limits of adaptive phenotypic plasticity
    Auld, Josh R.
    Agrawal, Anurag A.
    Relyea, Rick A.
    [J]. PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2010, 277 (1681) : 503 - 511
  • [3] How wild is the ocean? Assessing the intensity of anthropogenic marine activities in British Columbia, Canada
    Ban, Natalie
    Alder, Jackie
    [J]. AQUATIC CONSERVATION-MARINE AND FRESHWATER ECOSYSTEMS, 2008, 18 (01) : 55 - 85
  • [4] The importance of the variance around the mean effect size of ecological processes
    Benedetti-Cecchi, L
    [J]. ECOLOGY, 2003, 84 (09) : 2335 - 2346
  • [5] Breitburg DL, 1998, SUCCESSES, LIMITATIONS, AND FRONTIERS IN ECOSYSTEM SCIENCE, P416
  • [6] Brett J.R., 1979, FISH PHYSL VOL 8, VVIII, P162
  • [7] Phenotypic Plasticity, Costs of Phenotypes, and Costs of Plasticity Toward an Integrative View
    Callahan, Hilary S.
    Maughan, Heather
    Steiner, Ulrich K.
    [J]. YEAR IN EVOLUTIONARY BIOLOGY 2008, 2008, 1133 : 44 - 66
  • [8] CLARK CW, 2000, OX ECOL EV, P3
  • [9] Interactive and cumulative effects of multiple human stressors in marine systems
    Crain, Caitlin Mullan
    Kroeker, Kristy
    Halpern, Benjamin S.
    [J]. ECOLOGY LETTERS, 2008, 11 (12) : 1304 - 1315
  • [10] Temporal stability of an endemic Mexican treefrog
    Cruz-Ruiz, Griselda
    Venegas-Barrera, Crystian S.
    Sanchez-Sanchez, Hermilo
    Manjarrez, Javier
    [J]. PEERJ, 2015, 3