Cite this paper:
LI Chen, NIU Cuijuan. Effects of sexual reproduction of the inferior competitor Brachionus calycifl orus on its fi tness against Brachionus angularis[J]. Journal of Oceanology and Limnology, 2015, 33(2): 356-363

Effects of sexual reproduction of the inferior competitor Brachionus calycifl orus on its fi tness against Brachionus angularis

LI Chen, NIU Cuijuan
Ministry of Education Key Laboratory for Biodiversity Science and Ecological Engineering, College of Life Sciences, Beijing Normal University, Beijing 100875, China
Abstract:
Sexual reproduction adversely affects the population growth of cyclic parthenogenetic animals. The density-dependent sexual reproduction of a superior competitor could mediate the coexistence. However, the cost of sex may make the inferior competitor more vulnerable. To investigate the effect of sexual reproduction on the inferior competitor, we experimentally paired the competition of one Brachionus angularis clone against three Brachionus calycifl orus clones. One of the B. calycifl orus clones showed a low propensity for sexual reproduction, while the other two showed high propensities. The results show that all B. calycifl orus clones were excluded in the competition for resources at low food level. The increased food level promoted the competition persistence, but the clones did not show a clear pattern. Both the cumulative population density and resting egg production increased with the food level. The cumulative population density decreased with the mixis investment, while the resting egg production increased with the mixis investment. A trade-off between the population growth and sexual reproduction was observed in this research. The results indicate that although higher mixis investment resulted in a lower population density, it would not determinately accelerate the exclusion process of the inferior competitor. On the contrary, higher mixis investment promoted resting egg production before being excluded and thus promised a longterm benefit. In conclusion, our results suggest that mixis investment, to some extent, favored the excluded inferior competitor under fierce competition or some other adverse conditions.
Key words:    sexual reproduction|competition|resting egg|Brachionus   
Received: 2014-03-20   Revised: 2014-06-09
Tools
PDF (408 KB) Free
Print this page
Add to favorites
Email this article to others
Authors
Articles by LI Chen
Articles by NIU Cuijuan
References:
Carmona M, Dimas-Flores N, García Roger E, Serra M. 2009. Selection of low investment in sex in a cyclically parthenogenetic rotifer. Journal of Evolutionary Biology, 22 (10): 1 975-1 983.
Chesson P. 2000. Mechanisms of maintenance of species diversity. Annual review of Ecology and Systematics, 31 : 343-366. http://dx.doi.org/10.1146/annurev.ecolsys.31.1. 343.
Ciros-Pérez J, Carmona M J, Lapesa S, Serra M. 2004. Predation as a factor mediating resource competition among rotifer sibling species. Limnology and Oceanography, 49 (1): 40-50.
Ciros-Pérez J, Carmona M J, Serra M. 2001. Resource competition between sympatric sibling rotifer species. Limnology and Oceanography, 46 (6): 1 511-1 523.
Ciros-Pérez J, Carmona M J, Serra M. 2002. Resource competition and patterns of sexual reproduction in sympatric sibling rotifer species. Oecologia, 131 (1): 35-42.
Dimas-Flores N, Serra M, Carmona M J. 2013. Does genetic diversity reduce intraspecific competition in rotifer populations? Hydrobiologia, 705 (1): 43-54.
Dumont H J, Sarma S S S, Ali A J. 1995. Laboratory studies on the population dynamics of Anuraeopsis fi ssa (Rotifera) in relation to food density. Freshwater Biology, 33 (1): 39- 46.
FACHB-Collection. 2014. SE (Brostol's solution) from Freshwater Algae Culture Collection of the Institute of Hydrobiology. http://algae.ihb.ac.cn/Products/ProductDetail. aspx?product=3. Accessed on 2014-03-11.
García-Roger E M, Dias N, Carmona M J, Serra M. 2009. Crossed induction of sex in sympatric congeneric rotifer populations. Limnology and Oceanography, 54 (6): 1 845- 1 854.
Gilbert J J, Dieguez M C. 2010. Low crowding threshold for induction of sexual reproduction and diapause in a Patagonian rotifer. Freshwater Biology, 55 (8): 1 705- 1 718.
Gilbert J J, Schröder T. 2007. Intraclonal variation in propensity for mixis in several rotifers: variation among females and with maternal age. Hydrobiologia, 593 (1): 121-128.
Gilbert J J. 1963. Mictic female production in the rotifer Brachionus calycifl orus. Journal of Experimental Zoology, 153 :113-123.
Gilbert J J. 1974. Dormancy in rotifers. Transactions of the American Microscopical Society, 93 (4): 490-513.
Gilbert J J. 2004. Population density, sexual reproduction and diapause in monogonont rotifers: new data for Brachionus and a review. Journal of Limnology, 63 (1s): 32-36.
Gilbert J J. 2010. Effect of food concentration on the production and viability of resting eggs of the rotifer Brachionus : implications for the timing of sexual reproduction. Freshwater Biology, 55 (12): 2 437-2 446.
Grover J P. 1997. Resource Competition. Chapman & Hall, London. 342p.
Montero-Pau J, Serra M. 2011. Life-cycle switching and coexistence of species with no niche differentiation. PloS One, 6 (5): e20314. http://dx.doi.org/10.1371/journal. pone. 0020314.
Pourriot R, Snell T W. 1983. Resting eggs in rotifers. Hydrobiologia, 104 (1): 213-224.
Sarma S, Fernández Araiza M A, Nandini S. 1999. Competition between Brachionus calycifl orus Pallas and Brachionus patulus (M黮ler) (Rotifera) in relation to algal food concentration and initial population density. Aquatic E cology, 33 (4): 339-345.
Schröder T, Gilbert J. 2004. Transgenerational plasticity for sexual reproduction and diapause in the life cycle of monogonont rotifers: intraclonal, intraspecific and interspecific variation in the response to crowding. Functional Ecology, 18 (3): 458-466.
Schröder T, Howard S, Arroyo M, Walsh E. 2007. Sexual reproduction and diapause of Hexarthra sp. (Rotifera) in short-lived ponds in the Chihuahuan Desert. Freshwater B iology, 52 (6): 1 033-1 042.
Serra M, King C. 1999. Optimal rates of bisexual reproduction in cyclical parthenogens with density-dependent growth. Journal of Evolutionary Biology, 12 (2): 263-271.
Serra M, Snell T W, Gilbert J J. 2005. Delayed mixis in rotifers: an adaptive response to the effects of density-dependent sex on population growth. Journal of P lankton R esearch, 27 (1): 37-45.
Simon J C, Rispe C, Sunnucks P. 2002. Ecology and evolution of sex in aphids. Trends in Ecology & Evolution, 17 (1): 34-39.
Stelzer C P. 2012. Population regulation in sexual and asexual rotifers: an eco-evolutionary feedback to population size? Functional Ecology, 26 (1): 180-188.
Stemberger R S, Gilbert J J. 1985. Body size, food concentration, and population growth in planktonic rotifers. Ecology, 66 (4): 1 151-1 159.
Stemberger R S, Gilbert J J. 1987. Rotifer threshold food concentrations and the size-effi ciency hypothesis. Ecology, 68 (1): 181-187.
Stemberger R S. 1981. A general approach to the culture of planktonic rotifers. Canadian Journal of Fisheries and Aquatic Sciences, 38 (6): 721-724.
Tilman D. 1982. Resource Competition and Community Structure. Princeton University Press, Princeton. 296p. Yin X W, Niu C J. 2008. Predatory rotifer Asplanchna brightwellii mediated competition outcome between Brachionus calycifl orus and Brachionus patulus (Rotifera). Hydrobiologia, 610 (1): 131-138.
Zhang D Y, Hanski I. 1998. Sexual reproduction and stable coexistence of identical competitors. Journal of T heoretical B iology, 193 (3): 465-473.
Copyright © Haiyang Xuebao