Skip to main content
Log in

Defining patch contribution in source-sink metapopulations: the importance of including dispersal and its relevance to marine systems

  • Original Article
  • Published:
Population Ecology

An Erratum to this article was published on 13 August 2009

Abstract

In metapopulations, individual patch contribution (source or sink) is typically calculated as a patch growth rate (the “intrinsic” lambda, λI) dependent only upon local demographics. We demonstrate that when dispersal is explicitly included in the model, the growth rates for all patches calculated in an analogous manner (the “observed” lambda, λO) equilibrate to the overall metapopulation growth rate and thus no longer serve as a useful reflection of the demographic and dispersive characteristics of a given patch. In these situations we suggest an alternative method of estimating patch contribution (the “contribution” lambda, λC) in which a patch is decremented for losses that occur within it and credited for gains that occur anywhere in the metapopulation because of it. We compare values of λI, λO, and λC for individual patches in discrete-time density-independent metapopulation models of two organisms with very different life histories, mayflies with adult dispersal, and reef fish with larval dispersal. Results confirm that when dispersal is included only λC clearly indicates the contribution of a particular patch. λIλC comparisons indicate that inclusion of dispersal in the mayfly model was only important if connectivity patterns were random or directional. In the reef fish model, however, results were very different when dispersal was included and there were many cases of patches being misidentified (e.g., as a source when it was really a sink) depending upon the metric used (λI or λC). Our results demonstrate the importance of including dispersal in metapopulation models when considering the contribution of individual patches.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Armsworth PR (2002) Recruitment limitation, population regulation, and larval connectivity in reef fish metapopulations. Ecology 83:1092–1104

    Google Scholar 

  • Blondel J, Perret P, Maistre M, Dias PC (1992) Do harlequin Mediterranean environments function as source sink for blue tits (Parus caeruleus L)? Landscape Ecol 6:213–219

    Article  Google Scholar 

  • Boehlert GW (1996) Larval dispersal and survival in tropical reef fishes. In: Polunin NVC, Roberts CM (eds) Reef fisheries. Chapman and Hall, New York, pp 61–84

    Google Scholar 

  • Botsford LW, Moloney CL, Hastings A, Largier JL, Powell TM, Higgins K, Quinn JF (1994) The influence of spatially and temporally varying oceanographic conditions on meroplanktonic metapopulations. Deep Sea Res 41:107–145

    Article  Google Scholar 

  • Caswell H (2001) Matrix population models: construction, analysis and interpretation, Sinauer, Sunderland

    Google Scholar 

  • Caudill CC (2005) Trout predators and demographic sources and sinks in a mayfly metapopulation. Ecology 86:935–946

    Google Scholar 

  • Cooper AB, Mangel M (1999) The dangers of ignoring metapopulation structure for the conservation of salmonids. Fish Bull 97:213–226

    Google Scholar 

  • Cowen RK, Lwiza KMM, Sponaugle S, Paris CB, Olson DB (2000) Connectivity of marine populations: open or closed? Science 287:857–859

    Article  PubMed  Google Scholar 

  • Cowen RK, Gawarkiewicz G, Pineda J, Thorrold SR, Werner F (2003) Population connectivity in marine systems. Report of a workshop to develop science recommendations for the National Science Foundation. EOS Trans 84:119–119

    Google Scholar 

  • Dias PC (1996) Sources and sinks in population biology. Trends Ecol Evol 11:326–330

    Article  Google Scholar 

  • Dight IJ (1995) Understanding larval dispersal and habitat connectivity in tropical marine systems. A tool for management. In: Agardy T (ed) The science of conservation in the coastal zone: new insights on how to design, implement, and monitor marine protected areas. IUCN, Gland (Switzerland), pp 41–46

  • Doak DF (1995) Source-sink models and the problem of habitat degradation: General models and applications to the Yellowstone grizzly. Conserv Biol 9:1370–1379

    Article  Google Scholar 

  • Dobey S, Masters DV, Scheick BK, Clark JD, Pelton MR, Sunquist ME (2005) Ecology of Florida black bears in the Okefenokee-Osceola ecosystem. Wildlife Monogr 158:1–41

    Google Scholar 

  • Doebeli M (1995) Dispersal and dynamics. Theor Popul Biol 47:82–106

    Article  Google Scholar 

  • Donovan TM, Thompson FR III, Faaborg J, Probst JR (1995) Reproductive success of migratory birds in habitat sources and sinks. Conserv Biol 9:1380–1395

    Article  Google Scholar 

  • Eriksson O (1996) Regional dynamics of plants: a review of evidence for remnant, source-sink and metapopulations. Oikos 77:248–258

    Google Scholar 

  • Fahrig L, Merriam G (1994) Conservation of fragmented populations. Conserv Biol 8:50–59

    Article  Google Scholar 

  • Figueira WF (2002) Metapopulation dynamics of coral reef fish: Understanding habitat, demography, and connectivity in source-sink systems. PhD dissertation, Duke University

    Google Scholar 

  • Hanski IA (1999) Metapopulation ecology. Oxford University Press, Oxford

  • Harveson PM, Lopez RR, Silvy NJ, Frank PA (2004) Source-sink dynamics of Florida Key deer on Big Pine Key, Florida. J Wildlife Manage 68:909–915

    Article  Google Scholar 

  • Hellgren EC, Onorato DP, Skiles JR (2005) Dynamics of a black bear population within a desert metapopulation. Biol Conserv 122:131–140

    Article  Google Scholar 

  • James MK, Armsworth PR, Mason LB, Bode L (2002) The structure of reef fish metapopulations: modelling larval dispersal and retention patterns. Proc R Soc B Biol Sci 269:2079–2086

    Article  Google Scholar 

  • Johnson DM, Horvitz CC (2005) Estimating postnatal dispersal: tracking the unseen dispersers. Ecology 86:1185–1190

    Google Scholar 

  • Kauffman MJ, Pollock JF, Walton B (2004) Spatial structure, dispersal, and management of a recovering raptor population. Am Nat 164:582–597

    Article  PubMed  Google Scholar 

  • Kawecki TJ, Holt RD (2002) Evolutionary consequences of asymmetric dispersal rates. Am Nat 160:333–347

    Article  Google Scholar 

  • Keddy PA (1981) Experimental demography of the sand-dune annual, Kakile edentula, growing along an environmental gradient in Nova Scotia. J Ecol 69:615–630

    Google Scholar 

  • Levins R (1969) Some demographic and genetic consequences of environmental heterogeneity for biological control. Bull Entomol Soc Am 12:237 – 240

    Google Scholar 

  • Lipcius RN, Stockhausen WT, Eggleston DB, Marshall LS Jr, Hickey B (1997) Hydrodynamic decoupling of recruitment, habitat quality and adult abundance in the Caribbean spiny lobster: source-sink dynamics? Mar Freshwater Res 48:807–815

    Article  Google Scholar 

  • Lipcius RN, Stockhausen WT, Eggleston DB (2001) Marine reserves for Caribbean spiny lobster: empirical evaluation and theoretical metapopulation recruitment dynamics. Mar Freshwater Res 52:1589–1598

    Article  Google Scholar 

  • Lipcius RN, Crowder LB, Morgan LE (2005) Metapopulation structure and marine reserves. In: Norse EA, Crowder LB (eds) Marine conservation biology: the science of maintaining the sea’s biodiversity. Island, Washington, pp 328–349

    Google Scholar 

  • McGehee MA (1995) Juvenile settlement, survivorship and in situ growth rates of four species of Caribbean damselfishes in the genus Stegastes. Environ Biol Fish 44:393–401

    Article  Google Scholar 

  • Meijden E van der, van der Veen-van Wijk CAM (1997) Tritrophic metapopulation dynamics: a case study of ragwort, the cinnabar moth, and the parasitoid Cotesia popularis. In: Hanski IA, Gilpin ME (eds) Metapopulation biology: ecology, genetics, and evolution. Academic, San Diego, pp 387–405

    Google Scholar 

  • Mennechez G, Petit S, Schtickzelle N, Baguette M (2004) Modelling mortality and dispersal: consequences of parameter generalisation on metapopulation dynamics. Oikos 106:243–252

    Article  Google Scholar 

  • Nemeth RS (1997) Spatial patterns of bicolor damselfish in Jamaica and St Croix are determined by similar post-settlement processes. In: Proceedings of the 8th international coral reef symposium, vol. 1, pp 1017–1022

  • Nemeth RS (1998) The effect of natural variation in substrate architecture on the survival of juvenile bicolor damselfish. Environ Biol Fish 53:129–141

    Article  Google Scholar 

  • Ovaskainen O, Hanski I (2001) Spatially structured metapopulation models: global and local assessment of metapopulation capacity. Theor Popul Biol 60:281–302

    Article  PubMed  Google Scholar 

  • Pulliam HR (1988) Sources, sinks, and population regulation. Am Nat 132:652–661

    Article  Google Scholar 

  • Pulliam HR, Danielson BJ (1991) Sources, sinks and habitat selection: a landscape perspective on population dynamics. Am Nat 137:S50–S66

    Article  Google Scholar 

  • Roberts CM (1997) Connectivity and management of Caribbean coral reefs. Science 278:1454–1457

    Article  PubMed  Google Scholar 

  • Roberts CM (1998) Sources, sinks, and the design of marine reserve networks. Fisheries 23:16–19

    Article  Google Scholar 

  • Roberts CM, Polunin NVC (1991) Are marine reserves effective in management of reef fisheries? Rev Fish Biol Fisher 1:65–91

    Article  Google Scholar 

  • Roberts CM, Polunin NVC (1993) Marine reserves: simple solutions to managing complex fisheries? Ambio 22:363–368

    Google Scholar 

  • Roughgarden J, Iwasa Y (1986) Dynamics of a metapopulation with space-limited subpopulations. Theor Popul Biol 29:235–261

    Article  Google Scholar 

  • Rousset F (1999) Reproductive value vs sources and sinks. Oikos 86:591–596

    Google Scholar 

  • Roy M, Holt RD, Barfield M (2005) Temporal autocorrelation can enhance the persistence and abundance of metapopulations comprised of coupled sinks. Am Nat 166:246–261

    Article  PubMed  Google Scholar 

  • Saether BE, Ringsby TH, Bakke O, Solberg EJ (1999) Spatial and temporal variation in demography of a house sparrow metapopulation. J Anim Ecol 68:628–637

    Article  Google Scholar 

  • Sale PF, Hanski I, Kritzer JP (2006) The merging of metapopulation theory and marine ecology: establishing the historical context. In: Kritzer JP, Sale PF (eds) Marine metapopulations. Academic, New York, pp 3–28

    Google Scholar 

  • Schlosser IJ, Angermeier PL (1995) Spatial variation in demographic processes of lotic fishes: conceptual models, empirical evidence, and implications for conservation. Am Fish Soc Symp 17:392–401

    Google Scholar 

  • Sladek Nowlis JS (2000) Short- and long-term effects of three fishery-management tools on depleted fisheries. Bull Mar Sci 66:651–662

    Google Scholar 

  • Smedbol RK, McPherson A, Hansen MM, Kenchington E (2002) Myths and moderation in marine ‘metapopulations’? Fish Fisheries 3:20–35

    Article  Google Scholar 

  • Stobutzki IC, Bellwood DR (1997) Sustained swimming abilities of the late pelagic stages of coral reef fishes. Mar Ecol Prog Ser 149:35–41

    Google Scholar 

  • Valverde T, Silvertown J (1997) A metapopulation model for Primula vulgaris, a temperate forest understorey herb. J Ecol 85:193–210

    Google Scholar 

  • Wolanski E, Doherty P, Carleton J (1997) Directional swimming of fish larvae determines connectivity of fish populations on the Great Barrier Reef. Naturwissenschaften 84:262–268

    Article  Google Scholar 

Download references

Acknowledgments

We wish to thank S. Lyman, L. Botsford, and three anonymous reviewers for their valuable input to this manuscript. Funding was provided to W.F.F. by the Duke University Marine Lab Fellowship and McCurdy Endowment Funds. We also thank Environmental Defense, the Pew Charitable Trusts, the Sloan Census of Marine Life, and the Gordon and Betty Moore Foundation for support.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Will F. Figueira.

Additional information

An erratum to this article is available at http://dx.doi.org/10.1007/s10144-009-0173-1.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Figueira, W.F., Crowder, L.B. Defining patch contribution in source-sink metapopulations: the importance of including dispersal and its relevance to marine systems. Popul Ecol 48, 215–224 (2006). https://doi.org/10.1007/s10144-006-0265-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10144-006-0265-0

Keywords

Navigation