scholarly journals From Individual Behavior to Metapopulation Dynamics: Unifying the Patchy Population and Classic Metapopulation Models

2004 ◽  
Vol 164 (3) ◽  
pp. 364-377 ◽  
Author(s):  
Otso Ovaskainen ◽  
Ilkka Hanski
2007 ◽  
Vol 85 (10) ◽  
pp. 1031-1048 ◽  
Author(s):  
D.A. Driscoll

Where habitat loss and fragmentation is severe, many native species are likely to have reduced levels of dispersal between remnant populations. For those species to avoid regional extinction in fragmented landscapes, they must undergo some kind of metapopulation dynamics so that local extinctions are countered by recolonisation. The importance of spatial dynamics for regional survival means that research into metapopulation dynamics is essential. In this review I explore the approaches taken to examine metapopulation dynamics, highlight the analytical methods used to get the most information out of field data, and discover some of the major research gaps. Statistical models, including Hanski’s incidence function model (IFM) are frequently applied to presence–absence data, an approach that is often strengthened using long-term data sets that document extinctions and colonisations. Recent developments are making the IFM more biologically realistic and expanding the range of situations for which the model is relevant. Although accurate predictions using the IFM seem unlikely, it may be useful for ranking management decisions. A key weakness of presence–absence modelling is that the mechanisms underlying spatial dynamics remain inferential, so combining modelling approaches with detailed demographic research is warranted. For species where very large data sets cannot be obtained to facilitate statistical modelling, a demographic approach alone or with stochastic modelling may be the only viable research angle to take. Dispersal is a central process in metapopulation dynamics. Research combining mark–recapture or telemetry methods with model-selection procedures demonstrate that dispersal is frequently oversimplified in conceptual and statistical metapopulation models. Dispersal models like the island model that underlies classic metapopulation theory do not approximate the behaviour of real species in fragmented landscapes. Nevertheless, it remains uncertain if additional biological realism will improve predictions of statistical metapopulation models. Genetic methods can give better estimates of dispersal than direct methods and take less effort, so they should be routinely explored alongside direct ecological methods. Recent development of metacommunity theory (communities connected by dispersal) emphasises a range of mechanisms that complement metapopulation theory. Taking both theories into account will enhance interpretation of field data. The extent of metapopulation dynamics in human modified landscapes remains uncertain, but we have a powerful array of field and analytical approaches for reducing this knowledge gap. The most informative way forward requires that many species are studied in the same fragmented landscape by applying a selection of approaches that reveal complementary aspects of spatial dynamics.


Oikos ◽  
2002 ◽  
Vol 97 (3) ◽  
pp. 349-360 ◽  
Author(s):  
Nicolas Schtickzelle ◽  
Eric Le Boulenge ◽  
Michel Baguette

1998 ◽  
Vol 152 (2) ◽  
pp. 298
Author(s):  
Amarasekare

Insects ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 392
Author(s):  
Antonio Pulido-Pastor ◽  
Ana Luz Márquez ◽  
José Carlos Guerrero ◽  
Enrique García-Barros ◽  
Raimundo Real

Metapopulation theory considers that the populations of many species are fragmented into patches connected by the migration of individuals through an interterritorial matrix. We applied fuzzy set theory and environmental favorability (F) functions to reveal the metapopulational structure of the 222 butterfly species in the Iberian Peninsula. We used the sets of contiguous grid cells with high favorability (F ≥ 0.8), to identify the favorable patches for each species. We superimposed the known occurrence data to reveal the occupied and empty favorable patches, as unoccupied patches are functional in a metapopulation dynamics analysis. We analyzed the connectivity between patches of each metapopulation by focusing on the territory of intermediate and low favorability for the species (F < 0.8). The friction that each cell opposes to the passage of individuals was computed as 1-F. We used the r.cost function of QGIS to calculate the cost of reaching each cell from a favorable patch. The inverse of the cost was computed as connectivity. Only 126 species can be considered to have a metapopulation structure. These metapopulation structures are part of the dark biodiversity of butterflies because their identification is not evident from the observation of the occurrence data but was revealed using favorability functions.


Author(s):  
Apolline Louvet ◽  
Nathalie Machon ◽  
Jean‐Baptiste Mihoub ◽  
Alexandre Robert

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