Fragmentation and destruction of Great Ape habitat in Central Africa, from the GLOBIO and GRASP projects.

Habitat fragmentation describes the emergence of discontinuities (fragmentation) in an organism's preferred environment (habitat), causing population fragmentation and ecosystem decay. Habitat fragmentation can be caused by geological processes that slowly alter the layout of the physical environment[1] (suspected of being one of the major causes of speciation[1]), or by human activity such as land conversion, which can alter the environment much faster and causes extinctions of many species.

Deforestation and increased road-building in the Amazon Rainforest are a significant concern because of increased human encroachment upon wild areas, increased resource extraction and further threats to biodiversity.



The term habitat fragmentation includes five discrete phenomena:

  • Reduction in the total area of the habitat
  • Decrease of the interior: edge ratio
  • Isolation of one habitat fragment from other areas of habitat
  • Breaking up of one patch of habitat into several smaller patches
  • Decrease in the average size of each patch of habitat

"fragmentation ... not only causes loss of the amount of habitat, but by creating small, isolated patches it also changes the properties of the remaining habitat" (van den Berg et al. 2001). Habitat fragmentation is the landscape level of the phenomenon, and patch level process. Thus meaning, it covers; the patch areas, edge effects, and patch shape complexity.[2]

Natural causesEdit

Evidence of habitat destruction through natural processes such as volcanism, fire, and climate change is found in the fossil record.[1] For example, habitat fragmentation of tropical rainforests in Euramerica 300 million years ago led to a great loss of amphibian diversity, but simultaneously the drier climate spurred on a burst of diversity among reptiles.[1]

Human causesEdit

Habitat fragmentation is frequently caused by humans when native vegetation is cleared for human activities such as agriculture, rural development, urbanization and the creation of hydroelectric reservoirs. Habitats which were once continuous become divided into separate fragments. After intensive clearing, the separate fragments tend to be very small islands isolated from each other by cropland, pasture, pavement, or even barren land. The latter is often the result of slash and burn farming in tropical forests. In the wheat belt of central western New South Wales, Australia, 90% of the native vegetation has been cleared and over 99% of the tall grass prairie of North America has been cleared, resulting in extreme habitat fragmentation.


One of the major ways that habitat fragmentation affects biodiversity is by reducing the amount of suitable habitat available for organisms. Habitat fragmentation often involves both habitat destruction and the subdivision of previously continuous habitat.[3] Plants and other sessile organisms are disproportionately affected by some types of habitat fragmentation because they cannot respond quickly to the altered spatial configuration of the habitat.[4]

As the remaining habitat patches are smaller, they tend to support smaller populations of species.[5] Small populations are at an increased risk of a variety of genetic consequences that influence their long-term survival.[6] Remnant populations often contain only a subset of the genetic diversity found in the previously continuous habitat. Processes that act upon underlying genetic diversity such as adaptation have a smaller pool of fitness-maintaining alleles to survive in the face of environmental change.

Populations can maintain genetic diversity through migration. In continuous habitats, migrants have few barriers to establish themselves in suitable sites. In fragmented habitats however, the separation between suitable sites disrupts migration, and therefore gene flow, limiting a populations capacity to supplement the reduced genetic diversity of the remnant populations. With lower migration, inbreeding becomes a of increasing concern as the level of homozygosity increases, facilitating the expression of deleterious alleles that reduce the fitness of the population called inbreeding depression.

The percentage preservation of contiguous habitats is closely related to both genetic and species biodiversity preservation. Generally a 10% remnant contiguous habitat will result in a 50% biodiversity loss.[7]

Reduced viabilityEdit

Habitat fragmented by numerous roads near the Indiana Dunes National Lakeshore.

Area is the primary determinant of the number of species in a fragment [8] and the relative contributions of demographic and genetic processes to the risk of global population extinction depend on habitat configuration, stochastic environmental variation and species features.[9] Minor fluctuations in climate, resources, or other factors that would be unremarkable and quickly corrected in large populations can be catastrophic in small, isolated populations. Thus fragmentation of habitat is an important cause of species extinction.[8] Population dynamics of subdivided populations tend to vary asynchronously. In an unfragmented landscape a declining population can be "rescued" by immigration from a nearby expanding population. In fragmented landscapes, the distance between fragments may prevent this from happening. Additionally, unoccupied fragments of habitat that are separated from a source of immigrants by some barrier are less likely to be repopulated than adjoining fragments. Even small species such as the Columbia spotted frog are reliant on the rescue effect. Studies showed 25% of juveniles travel a distance over 200m compared to 4% of adults. Of these, 95% remain in their new locale, demonstrating that this journey is necessary for survival.[10]

Additionally, habitat fragmentation leads to edge effects. Microclimatic changes in light, temperature and wind can alter the ecology around the fragment, and in the interior and exterior portions of the fragment. Fires become more likely in the area as humidity drops and temperature and wind levels rise. Exotic and pest species may establish themselves easily in such disturbed environments, and the proximity of domestic animals often upsets the natural ecology. Also, habitat along the edge of a fragment has a different climate and favours different species from the interior habitat. Small fragments are therefore unfavourable for species which require interior habitat.

Conservation implicationsEdit

Habitat fragmentation is often a cause of species becoming threatened or endangered. The existence of viable habitat is critical to the survival of any species, and in many cases the fragmentation of any remaining habitat can lead to difficult decisions for conservation biologists. Given a limited amount of resources available for conservation is it preferable to protect the existing isolated patches of habitat or to buy back land to get the largest possible continuous piece of land? This ongoing debate is often referred to as SLOSS (Single Large or Several Small).

One solution to the problem of habitat fragmentation is to link the fragments by preserving or planting corridors of native vegetation. This has the potential to mitigate the problem of isolation but not the loss of interior habitat. In rare cases a conservation reliant species may gain some measure of disease protection by being distributed in isolated habitats.

Another mitigation measure is the enlargement of small remnants in order to increase the amount of interior habitat. This may be impractical since developed land is often more expensive and could require significant time and effort to restore.

The best solution is generally dependent on the particular species or ecosystem that is being considered. More mobile species, like most birds, do not need connected habitat while some smaller animals, like rodents, may be more exposed to predation in open land. These questions generally fall under the headings of metapopulations island biogeography.

Forest fragmentationEdit

Forest fragmentation is a form of habitat fragmentation where forests are reduced (either naturally or man-made) to relatively small, isolated patches of forest known as forest fragments or forest remnants.[1] The intervening matrix that separates the remaining woodland patches can be natural open areas, farmland, or developed areas. Following the principles of island biogeography, remnant woodlands act like islands of forest in a sea of pastures, fields, subdivisions, shopping malls, etc. These fragments will then begin to undergo the process of ecosystem decay.

Forest fragmentation also includes less subtle forms of discontinuities such as utility right-of-ways (ROWs). Utility ROWs are of ecological interest because they have become pervasive in many forest communities, spanning areas as large as 5 million acres in the United States.[11] Utility ROWs include electricity transmission ROWs, gas pipeline and telecommunication ROWs. Electricity transmission ROWs are created to prevent vegetation interference with transmission lines. Some studies have shown that electricity transmission ROWs harbor more plant species than adjoining forest areas,[12] due to alterations in the microclimate in and around the corridor. Discontinuities in forest areas associated with utility right-of-ways can serve as biodiversity havens for native bees [11] and grassland species,[13] as the right-of-ways are preserved in an early successional stage.


Forest fragmentation is one of the greatest threats to biodiversity in forests, especially in the tropics.[14] The problem of habitat destruction that caused the fragmentation in the first place is compounded by:

  • the inability of individual forest fragments to support viable populations, especially of large vertebrates
  • the local extinction of species that do not have at least one fragment capable of supporting a viable population
  • edge effects that alter the conditions of the outer areas of the fragment, greatly reducing the amount of true forest interior habitat.[15]

The effect of fragmentation on the flora and fauna of a forest patch depends on a) the size of the patch, and b) its degree of isolation. Isolation depends on the distance to the nearest similar patch, and the contrast with the surrounding areas. For example, if a cleared area is reforested or allowed to regenerate, the increasing structural diversity of the vegetation will lessen the isolation of the forest fragments. However, when formerly forested lands are converted permanently to pastures, agricultural fields, or human-inhabited developed areas, the remaining forest fragments, and the biota within them, are often highly isolated.

Forest patches that are smaller or more isolated will lose species faster than those that are larger or less isolated. A large number of small forest "islands" typically cannot support the same biodiversity that a single contiguous forest would hold, even if their combined area is much greater than the single forest. However, forest islands in rural landscapes greatly increase their biodiversity.[16]

See alsoEdit


  1. ^ a b c d e Sahney, S., Benton, M.J. & Falcon-Lang, H.J. (2010). "Rainforest collapse triggered Pennsylvanian tetrapod diversification in Euramerica" (PDF). Geology. 38 (12): 1079–1082. doi:10.1130/G31182.1. 
  2. ^ van den Berg LJL, Bullock JM, Clarke RT, Langsten RHW, Rose RJ. 2001. Territory selection by the Dartford warbler (Sylvia undata) in Dorset, England: the role of vegetation type, habitat fragmentation and population size. Biol. Conserv. 101:217-28
  3. ^ Fahrig, Lenore (November 2003). "Effects of Habitat Fragmentation on Biodiversity". Annual Review of Ecology, Evolution, and Systematics. 34 (1): 487–515. doi:10.1146/annurev.ecolsys.34.011802.132419. 
  4. ^ Lienert, Judit (July 2004). "Habitat fragmentation effects on fitness of plant populations – a review". Journal for Nature Conservation. 12 (1): 53–72. doi:10.1016/j.jnc.2003.07.002. 
  5. ^ Simberloff, Daniel (1 January 1998). "Small and Declining Populations". Conservation Science and Action. Blackwell Publishing Ltd.: 116–134. doi:10.1002/9781444313499.ch6/summary. 
  6. ^ Frankham, Richard; Ballou, Jonathan D.; Briscoe, David A. (2009). Introduction to conservation genetics (2nd ed.). Cambridge: Cambridge University Press. ISBN 9780521702713. 
  7. ^ Quammen, David (1997), "The Song of the Dodo: Island Biogeography in an Age of Extinction" (Scribner)
  8. ^ a b Rosenzweig, Michael L. (1995). Species diversity in space and time. Cambridge: Cambridge University Press. 
  9. ^ Robert, A. (2011) Find the weakest link. A comparison between demographic, genetic and demo-genetic metapopulation extinction times. BMC Evolutionary Biology 11: 260. doi= 10.1186/1471-2148-11-260
  10. ^ Funk W.C.; Greene A.E.; Corn P.S.; Allendorf F.W. (2005). "High dispersal in a frog species suggests that it is vulnerable to habitat fragmentation". Biol. Lett. 1 (1): 13–6. doi:10.1098/rsbl.2004.0270. 
  11. ^ a b Russell, K. N.; Ikerd, H.; Droege, S. (2005-07-01). "The potential conservation value of unmowed powerline strips for native bees". Biological Conservation. 124 (1): 133–148. doi:10.1016/j.biocon.2005.01.022. 
  12. ^ Wagner, David L.; Metzler, Kenneth J.; Leicht-Young, Stacey A.; Motzkin, Glenn (2014-09-01). "Vegetation composition along a New England transmission line corridor and its implications for other trophic levels". Forest Ecology and Management. 327: 231–239. doi:10.1016/j.foreco.2014.04.026. 
  13. ^ Lampinen, Jussi; Ruokolainen, Kalle; Huhta, Ari-Pekka (2015-11-13). "Urban Power Line Corridors as Novel Habitats for Grassland and Alien Plant Species in South-Western Finland". PLOS ONE. 10 (11): e0142236. doi:10.1371/journal.pone.0142236. ISSN 1932-6203. PMC 4643934 . PMID 26565700. 
  14. ^ Bierregaard, Richard (2001). Claude Gascon; Thomas E. Lovejoy; Rita Mesquita, eds. Lessons from Amazonia: The Ecology and Conservation of a Fragmented Forest. ISBN 0-300-08483-8. 
  15. ^ Harris, Larry D. (1984). The Fragmented Forest: Island Biogeography Theory and the Preservation of Biotic Diversity. The University of Chicago Press. ISBN 0-226-31763-3. 
  16. ^ Banaszak J. (ed.) 2000. Ecology of Forest Islands. Bydgoszcz University Press, Bydgoszcz, Poland, 313 pp.

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