Tigriopus californicus

From Wikipedia, the free encyclopedia

Tigriopus californicus
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Copepoda
Order: Harpacticoida
Family: Harpacticidae
Genus: Tigriopus
Species:
T. californicus
Binomial name
Tigriopus californicus
(Baker, 1912)[1][2]
Synonyms [3]
  • Tigriopus triangulus Campbell, 1930
  • Tisbe californica Baker, 1912

Tigriopus californicus is an intertidal copepod species that occurs on the Pacific coast of North America. This species has been the subject of numerous scientific studies on subjects ranging from ecology and evolution to neurobiology.

Ecology and environment[edit]

Found from central Baja California, Mexico to Alaska, USA along the Pacific coast of North America, T. californicus inhabits splash pools in rocky intertidal habitat. T. californicus is limited to pools in the upper end of the intertidal apparently by predation,[4] but it can reach quite high population densities in this habitat. One study found that population densities on Vancouver Island averaged about 800 copepods per liter with some dense pools having as many as 20,000 copepods per liter.[5]

These splash pools are often isolated from the moderating influence of the ocean and therefore the pools can vary dramatically in environmental factors such as salinity and temperature over the course of hours or days. T. californicus has the ability to thrive under these variable environmental conditions (factors that limit predators such as fish to lower pools in the intertidal zone).[4] Temperature in the pools that this copepod inhabits tend to track air temperatures more closely than ocean temperatures and salinities in pools can change as pools evaporate, receive freshwater inputs from rain, or saltwater from wave actions.

The ability of T. californicus to handle extreme high temperatures varies among populations with southern California populations able to handle higher temperatures than those further north.[6] This pattern of higher thermal tolerance in southern populations mirrors the temperature variation seen in copepod pools with southern populations experiencing more extreme high temperatures (over 40 °C or 104 °F on occasion).[7] The genetic basis of this potential thermal adaptation has been studied by looking at genome-wide studies of gene expression and this study showed that differential expression of Hsp70 genes and a number of other genes could contribute to differences in thermal tolerance between these populations.[8]

They have been known to have survived up to six months in laboratory conditions, however their longevity in natural conditions has yet to be determined.[9]

Genetics and evolution[edit]

Populations of T. californicus along the Pacific coast of North America show a striking pattern of genetic differentiation among populations. Mitochondrial DNA shows particularly large divergences among populations often exceeding twenty percent total sequence divergence.[10][11] Genetic divergence of a smaller magnitude extends down to a more local scale and this divergence can be stable for longer than two decades for outcrops that are as little as 500 m (0.31 mi) apart, suggesting that dispersal between outcrops must be relatively rare for this copepod.[12] Surprisingly, genetic divergence is much lower among copepod populations from Washington north to Alaska suggesting that copepods may have recolonized these areas since the end of the last ice age.[13] Crosses of copepods from different populations of T. californicus have been used to study how reproductive isolation accumulates between diverging population to gain insights into the process of speciation. For crosses between many populations a pattern that has been called hybrid breakdown is observed; this means that first generation hybrids have high survival and reproduction (fitness), while the second generation hybrids have lower and more variable fitness.[14] Deleterious interactions between the mitochondrial genome and nuclear genome may play a large role in the reduction in hybrid fitness observed in many of these crosses.[15] Sex determination in T. californicus does not appear to be caused by sex chromosomes and is likely to be polygenic, potentially influenced by environmental conditions. The ratios of males to females produced by females differs among families and in some families seems to be genetically determined largely by the father in a pair.[16] Another interesting feature of the mating system of this species is that the males use their large clasping antennules to clutch females until they are ready to mate.[17] Females will mate only once during their lives but produce multiple clutches of offspring.

Physiology[edit]

This copepod species has also been used as a model system in which to look at some questions in animal physiology including both neurobiology and osmoregulation. In response to increasing or decreasing environmental salinities T. californicus changes the amount of amino acids within its cells to maintain water balance.[18] The amino acid proline is subject to strict regulation in response to changes in salinity and this may be a common mechanism of osmoregulation across crustaceans.[19] For neurobiology, one study looked at the central nervous system of this copepod to get an idea of the organization of the central nervous system of the ancestors to the crustaceans and insects to complement the neurobiological work that has been done in a group of distantly related copepods (the calanoid copepods).[20]

Commercial sources[edit]

https://www.carolina.com/crustaceans/marine-copepod-tigriopus-californicus-living/142366.pr?question=Tigriopus https://www.podyourreef.com/products/tigriopus-californicus-reef-copepods

References[edit]

  1. ^ Baker, C. F. 1912. [1] Notes on the Crustacea of Laguna Beach. Ann. Rep. Laguna Marine Lab. 1: 100-117
  2. ^ Cecil R. Monk. 1941.[2] Marine Harpacticoid Copepods from California. Transactions of the American Microscopical Society , Vol. 60 pp. 75-99
  3. ^ T. Chad Walter (2013). Walter TC, Boxshall G (eds.). "Tigriopus californicus (Baker, 1912)". World of Copepods database. World Register of Marine Species. Retrieved December 17, 2013.
  4. ^ a b Dethier, M. F. 1980 [3] Tidepools as refuges: Predation and the limits of the harpacticoid copepod Tigriopus californicus (Baker) Journal of Experimental Marine Biology and Ecology, Volume 42, Issue 2, 22 January 1980, Pages 99-111.
  5. ^ Powlik. J. F. 1998 [4] Seasonal Abundance and Population Flux of Tigriopus californicus (Copepoda: Harpacticoida) in Barkley Sound, British Columbia. J. Mar. Biol. Ass. UK. 78, 467-481.
  6. ^ Willett 2010 [5] Potential fitness tradeoffs for thermal tolerance in the intertidal copepod Tigriopus californicus. Evolution 64: 2521-2534.
  7. ^ Kelly, M. W., E. Sanford, and R. K. Grosberg [6] Limited potential for adaptation to climate change in a broadly distributed marine crustacean. Proc. R. Soc. B. 2012 279 1727 349-356doi:10.1098/rspb.2011.0542
  8. ^ Schoville, S. D., Barreto, F. S., Moy, G. W., Wolff, A. & Burton, R. S. (2012). [7] Investigating the molecular basis of local adaptation to thermal stress: population differences in gene expression across the transcriptome of the copepod Tigriopus californicus, BMC Evolutionary Biology, 12:170.
  9. ^ "Hawkins, B. The Biology of the marine copepod Tigriopus Californicus (Baker) (Doctoral dissertation) 13-14". 1962.
  10. ^ Burton, R. S., R. J. Byrne & P. D. Rawson. 2007 [8] Three divergent mitochondrial genomes from California populations of the copepod Tigriopus californicus. Gene 403:53-59.
  11. ^ Willett, C. S. and J. T. Ladner. 2009. [9] Investigations of fine-scale phylogeography in Tigriopus californicus reveal historical patterns of population divergence. BMC Evolution. 9:139.
  12. ^ Burton, R. S. 1997. [10] Genetic evidence for long term persistence of marine invertebrate populations in an ephemeral environment. Evolution 51:993-998.
  13. ^ Edmands, S. 2001. [11] Phylogeography of the intertidal copepod Tigriopus californicus reveals substantially reduced population differentiation at northern latitudes. Molecular Ecology 10:1743-1750.
  14. ^ Edmands, S. 1999. [12] Heterosis and outbreeding depression in interpopulation crosses spanning a wide range of divergence. Evolution 53:1757-1768.
  15. ^ Ellison, C. K. & R. S. Burton. 2008. [13] Interpopulation hybrid breakdown maps to the mitochondrial genome. Evolution 62: 631-638.
  16. ^ Voordouw, M. J., Robinson H. E. & Anholt, B. R. (2005) [14], Paternal inheritance of the primary sex ratio in a copepod. Journal of Evolutionary Biology, 18: 1304–1314.
  17. ^ Burton, R. S. (1985). [15] Mating system of the intertidal copepod Tigriopus californicus, Marine Biology, 86:247-252.
  18. ^ Burton, R. S. & Feldman, M. W. (1982) [16] Changes in free amino acid concentrations during osmotic response in the intertidal copepod Tigriopus californicus. Comp. Biochem. Physiol. 73A, 441-445.
  19. ^ Burton, R. S. (1992) [17] Proline synthesis during osmotic stress in megalopa stage larval of the blue crab, Callinectes sapidus. Biol. Bull. 182, 409-415.
  20. ^ Andrew, D. R., Brown, S. M. and Strausfeld, N. J. (2012), [18] The minute brain of the copepod Tigriopus californicus supports a complex ancestral ground pattern of the tetraconate cerebral nervous systems. J. Comp. Neurol., 520: 3446–3470.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Tigriopus_californicus&oldid=1135029096"