Relict (biology)

In biogeography and paleontology a relict is a population or taxon of organisms that was more widespread or more diverse in the past. A relictual population is a population that presently occurs in a restricted area, but whose original range was far wider during a previous geologic epoch. Similarly, a relictual taxon is a taxon (e.g. species or other lineage) that is the sole surviving representative of a formerly diverse group.[1]

Definition

A relict (or relic) plant or animal is a taxon that persists as a remnant of what was once a diverse and widespread population. Relictualism occurs when a widespread habitat or range changes and a small area becomes cut off from the whole. A subset of the population is then confined to the available hospitable area, and survives there while the broader population either shrinks or evolves divergently. This phenomenon differs from endemism in that the range of the population was not always restricted to the local region. In other words, the species or group did not necessarily arise in that small area, but rather was stranded, or insularized, by changes over time. The agent of change could be anything from competition from other organisms, continental drift, or climate change such as an ice age.

Examples

A notable example is the thylacine of Tasmania, a relict marsupial carnivore that survived into modern times on an island whereas the rest of its species on mainland Australia had long ago gone extinct.[2] When a relict is representative of taxa found in the fossil record, and yet is still living, such an organism is sometimes referred to as a living fossil. However, a relict need not be currently living. An evolutionary relict is any organism that was characteristic of the flora or fauna of one age and that persisted into a later age, with the later age being characterized by newly evolved flora or fauna significantly different from those that came before.

An example from the fossil record would be a specimen of Nimravidae, an extinct branch of carnivores in the mammalian evolutionary tree, if said specimen came from Europe in the Miocene epoch. If that was the case, the specimen would represent, not the main population, but a last surviving remnant of the nimravid lineage. These carnivores were common and widespread in the previous epoch, the Oligocene, and disappeared when the climate changed and woodlands were replaced by savanna. They persisted in Europe in the last remaining forests as a relict of the Oligocene: a relict species in a relict habitat.[3]

An example of divergent evolution creating relicts is found in the shrews of the islands off the coast of Alaska, namely the Pribilof Island shrew and the St. Lawrence Island shrew. These species are apparently relicts of a time when the islands were connected to the mainland, and these species were once conspecific with a more widespread species, now the cinereus shrew, the three populations having diverged through speciation.[4]

In botany, an example of an ice age relict plant population is the Snowdon lily, notable as being precariously rare in Wales. The Welsh population is confined to the north-facing slopes of Snowdonia, where climatic conditions are apparently similar to ice age Europe. Some have expressed concern that the warming climate will cause the lily to die out in Great Britain.[5] Other populations of the same plant can be found in the Arctic and in the mountains of Europe and North America, where it is known as the common alplily. One of the best-known botanical examples of a living fossil is Ginkgo biloba, because Ginkgoales other than G. biloba are not known from the fossil record after the Pliocene.[6][7]

Relevance

The concept of relictualism is useful in understanding the ecology and conservation status of populations that have become insularized, meaning confined to one small area or multiple small areas with no chance of movement between populations. Insularization makes a population vulnerable to forces that can lead to extinction, such as disease, inbreeding, habitat destruction, competition from introduced species, and global warming. Consider the case of the white-eyed river martin, a very localized species of bird found only in Southeast Asia, and extremely rare, if not already extinct. Its closest and only surviving living relative is the African river martin, also very localized in central Africa. These two species are the only known members of the subfamily Pseudochelidoninae, and their widely disjunct populations suggest they are relict populations of a more common and widespread ancestor. Known to science only since 1968, it seems to have disappeared.[8]

Studies have been done on relict populations in isolated mountain and valley habitats in western North America, where the basin and range topography creates areas that are insular in nature, such as forested mountains surrounded by inhospitable desert, called sky islands. Such situations can serve as refuges for certain Pleistocene relicts, such as Townsend's pocket gopher,[4] while at the same time creating barriers for biological dispersal. Studies have shown that such insular habitats have a tendency toward decreasing species richness. This observation has significant implications for conservation biology, because habitat fragmentation can also lead to the insularization of stranded populations.[2][9]

So-called "relics of cultivation"[10] are plant species that were grown in the past for various purposes (medicinal, food, dyes, etc.), but are no longer utilized. They are naturalized and can be found at archaeological sites.

See also

References

  1. Habel, Jan C.; Assmann, Thorsten; Schmitt, Thomas; Avise, John C. (2010). "Relict Species: From Past to Future". In Habel, Jan Christian; Assmann, Thorsten. Relict species: Phylogeography and Conservation Biology. Berlin: Springer-Verlag. pp. 1–5. ISBN 9783540921608.
  2. 1 2 Quammen, David (2004). The Song of the Dodo: Island Biogeography in An Age of Extinctions. New York: Scribner. pp. 287–288, 436–447, 631. ISBN 978-0-684-82712-4.
  3. Prothero, Donald R. (2006). After the Dinosaurs: The Age of Mammals. Bloomington, Indiana: Indiana University Press. pp. 9, 132–134, 160, 174, 176, 198, 222–233. ISBN 978-0-253-34733-6.
  4. 1 2 Wilson, Don; Ruff, Sue (1999). The Smithsonian Book of North American Mammals. Washington, DC: Smithsonian Institution Press. pp. 20, 27–30. ISBN 1-56098-845-2.
  5. Brown, Paul (27 March 2003). "Global warming threatens Snowdonian plant". Guardian. London: Guardian Unlimited. Retrieved 9 April 2011.
  6. Zhou, Zhiyan; Zheng, Shaolin (2003). "Palaeobiology: The missing link in Ginkgo evolution". Nature. 423 (6942): 821–2. PMID 12815417. doi:10.1038/423821a.
  7. Julie Jalalpour; Matt Malkin; Peter Poon; Liz Rehrmann; Jerry Yu (1997). "Ginkgoales: Fossil Record". University of California, Berkeley. Retrieved 3 June 2008.
  8. Turner, Angela K.; Rose, Chris (1989). Swallows & Martins. Boston: Houghton Mifflin. pp. 5, 34, 85–87. ISBN 0-395-51174-7.
  9. Harris, Larry D. (1984). The Fragmented Forest: Island Biogeography Theory and the Preservation of Biotic Diversity. Chicago: University of Chicago Press. pp. 71–92. ISBN 0-226-31763-3.
  10. Celka Z., Drapikowska M. 2008. Relics of cultivation in Central Europe: Malva alcea L. as an example. Vegetation History and Archaeobotany. Volume 17, Supplement 1, 251-255, ] doi:10.1007/s00334-008-0151-0
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