Maternal legacy: Unraveling the crucial role of the parental population against larval nutrition and its profound impact on developmental trajectories and morphological outcomes in Pseudechinus huttoni (Echinoidea: Temnopleuridae) larvae
Downloads
This study examined the relative contribution of parental population and larval diet on development and larval characteristics in Pseudechinus huttoni. We further investigated the effects of parental population on egg traits. Two populations of sea urchins were selected—shallow and deep—with a known difference in nutritional history, where the deep population showed poor nutritional condition and lower egg size. However, eggs from both populations had the same nutritional content. However, larvae from the lower-nutrition population were more advanced in growth and development, and their body shape was more flexible. More rapid growth and development and flexibility in body shape were seen in the larvae reared with high-plankton food. More importantly, the parental population contributed more towards variations in larval growth and shape than to the diet received by larvae. Additionally, larvae from the low-nutrition parental population were nutritionally increased, which could indicate that this parental effect is more than just a simple change in egg composition.
Downloads
Bertram D.F., Strathmann R. (1998). Effects of maternal and larval nutrition on growth and form of planktotrophy larvae. Ecology, 79: 315-327.
Boidron-Metairon I. F. (1988). Morphological plasticity in laboratory-reared echinoplutei of Dendraster excentricus (Eschscholtz) and Lytechinus variegatus (Lamarck) in response to food conditions. Journal of Experimental Marine Biology and Ecology, 119: 31-41.
Bradford M.M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72: 248-254.
Bryan P.J. (2004). Energetic cost of development through metamorphosis for the seastar Mediaster aequalis (Stimpson). Marine Biology, 145: 293-302.
Byrne M., Sewell M.A., Prowse T.A.A. (2008). Nutritional ecology of sea urchin larvae: influence of endogenous and exogenous nutrition on echinopluteal growth and phenotypic plasticity in Tripneustes gratilla. Functional Ecology, 22: 643-648.
Chu F.-L.E., Casey B.B. (1986). A comparison of protein assays for oyster larval proteins using two different standards. Marine Chemistry, 19: 1-7.
Ebert T.A. (1980). Relative growth of sea urchin jaws: an example of plastic resources allocation. Bulletin of Marine Science, 30: 467-474.
Emlet R.B., Hoegh-Guldberg O. (1997). Effects of egg size on postlarval perrformance: Experimental evidence from a sea urchin. Evolution, 51: 141-152.
Emlet R.B., McEdward L.R., Strathmann R.R. (1987). Echinoderm larval ecology viewed from the egg. In: M. Jangoux and J.M. Lawrence (Ed.). Echinoderm studies, vol. 2. Rotterdam, A.A. Balkema. pp: 55-136
Everitt B.S., Dunn G. (1991). Applied multivariate data analysis. Edward Arnold. London. 304 p.
George S. B. (1996). Echinoderm egg and larval quality as a function of adult nutritional state. Oceanologica Acta, 19: 297-308.
George S.B. (1999). Egg quality, larval growth and phenotypic plasticity in a forcipulate seastar. Journal of Experimental Marine Biology and Ecology, 237: 203-224.
George S.B., Cellario C., Fenaux L. (1990). Population differences in egg quality of Arbacia lixula (Echinodermata: Echinoidea): proximate composition of eggs and larval development. Journal of Experimental Marine Biology and Ecology, 141: 107-118.
George S.B., Lawrence J.M., Fenaux L. (1991). The effect of food ration on the quality of eggs of Luidia clathrata (Say) (Echinodermata: Asteroidea). Invertebrate Reproduction and Development, 20: 237-242.
George S.B., Young C.M., Fenaux L. (1997). Proximate composition of eggs and larvae of the sand dollar Encope michelini (Agassiz): the advantage of higher investment in planktotrophic eggs. Invertebrate Reproduction and Development, 32: 11-19.
Gnaiger E. (1983). Calculation of energetic and biochemical equivalents of respiratory oxygen consumption. In: E. Gnaiger, H. Forstner (Eds.). Polarographic oxygen sensors: Aquatic and physiological applications. New York, Springer-Verlag. pp: 337-345.
Hart M.W., Scheibling R. E. (1988). Comparing shapes of echinoplutei using principal components analysis, with an application to larvae of Strongylocentrotus droebachiensis. In: R.D. Burke, P.V. Mladenov, P. Lambert, R.L. Parsley (Ed.). Echinoderm biology. A.A. Balkema, Rotterdam. pp: 277-284.
Hart M.W., Strathmann R.R. (1994). Functional consequences of phenotypic plasticity in echinoid larvae. Biological Bulletin, 186: 291-299.
Havenhand J.N. (1995). Evolutionary ecology of larval types. In: L.M. McEdward (Ed.). Ecology of marine invertebrate larvae. CRC Press, Inc. pp: 79-122.
Heyland A., Reitzel A.M., Hodin J. (2004). Thyroid hormones determine developmental mode in sand dollars (Echinodermata: Echinoidea). Evolution and Development, 6: 382-392.
Jaeckle W.B. (1995). Variation in egg size, energy content, and biochemical composition of invertebrate eggs: correlates to the mode of larval development. In: L.M. McEdward (Ed.). Ecology of marine invertebrate larvae. CRC Press, Inc. pp: 49-78.
Jong-Westman M.D., Qian P.-Y., March B.E., Carefoot T.H. (1995). Artificial diets in sea urchin culture: effects of dietary protein level and other additives on egg quality, larval morphometrics, and larval survival in the green sea urchin, Strongylocentrotus droebachiensis. Canadian Journal of Zoology, 73: 2080-2090.
Kirby S., Lamare M.D., Barker M.F. (2006). Growth and morphometrics in the New Zealand sea urchin Pseudechinus huttoni (Echinoidea: Temnopleuridae). New Zealand Journal of Marine and Freshwater Research, 40: 413-428.
Lamare M.D., Barker M.F. (1999). In situ estimates of larval development and mortality in the New Zealand sea urchin Evechinus chloroticus (Echinodermata: Echinoidea). Marine Ecology Progress Series, 180: 197-211.
Levitan D.R. (1993). The importance of sperm limitation to the evolution of egg size in marine invertebrates. American Naturalist, 141: 517-536.
Mann R., Gallager S.M. (1985). Physiological and biochemical energetics of larvae of Teredo navalis L. and Bankia gouldi (Bartsch). Journal of Experimental Marine Biology and Ecology, 85: 211-228.
Maxwell S.E., Delaney H.D. (2004). Designing experiments and analyzing data: a model comparison perspective (2nd edition). Lawrence Erlbaum Associates, Inc. Mahwah, New Jersey, 1104 p.
McAlister J.S. (2007). Egg size and the evolution of phenotypic plasticity in larvae of the echinoid genus Strongylocentrotus. Journal of Experimental Marine Biology and Ecology, 352: 306-316.
McAlister J.S. (2008). Evolutionary responses to environmental heterogeneity in central American echinoid larvae: plastic versus constant phenotypes. Evolution, 62-6: 1358-1372.
McClary D., Barker M. (1998). Reproductive isolation? interannual variability in the timing of reproduction in sympatric sea urchins, genus Pseudechinus. Invertebrate Biology, 117: 75-93.
McEdward L.R. (1986a). Comparative morphometrics of echinoderm larvae. I. some relationships between egg size and initial larval form in echinoids. Journal of Experimental Marine Biology and Ecology, 96: 251-265.
McEdward L.R. (1986b). Comparative morphometrics of echinoderm larvae. II. larval size, shape, growth, and the scaling of feeding and metabolism in echinoplutei. Journal of Experimental Marine Biology and Ecology, 96: 267-286.
McEdward L.R., Carson S.F. (1987). Variation in egg organic content and its relationship with egg size in the starfish Solaster stimpsoni. Marine Ecology Progress Series, 37: 159-169.
McEdward L.R., Chia F.-S. (1991). Size and energy content of eggs from echinoderms with pelagic lecithotrophic development. Journal of Experimental Marine Biology and Ecology, 147: 95-102.
McEdward L.R., Janies D.A. (1997). Relationship among development, ecology, and morphology in the evolution of Echinoderm larvae and life cycles. Biological Journal of the Linnean Society, 60: 381-400.
McEdward L.R., Miner B.G. (2003). Fecundity-time models of reproductive strategies in marine benthic invertebrates: fitness differences under fluctuating environmental conditions. Marine Ecology Progress Series, 256: 111-121.
Meidel S.K., Scheibling R.E., Metaxas A. (1999). Relative importance of parental and larval nutrition on larval development and metamorphosis of the sea urchin Strongylocentrotus droebachiensis. Journal of Experimental Marine Biology and Ecology, 240: 161-178.
Miner B.G. (2005). Evolution of feeding structure plasticity in marine invertebrate larvae: a possible trade-off between arm length and stomach size. Journal of Experimental Marine Biology and Ecology, 315: 117-125.
Moran A.L. (2004). Egg size evolution in Tropical American arcid bivalves: the comparative method and the fossil record. Evolution, 58: 2718–2733.
Moran A.L., Manahan D.T. (2004). Physiological recovery from prolonged 'starvation' in larvae of the Pacific oyster Crossostrea gigas. Journal of Experimental Marine Biology and Ecology, 306: 17-36.
Moran A.L., McAlister J.S. (2009). Egg size as a life history character of marine invertebrates: is it all it's cracked up to be? Biological Bulletin, 216: 226-242.
Podolsky R.D., Strathmann R.R. (1996). Evolution of egg size in free-spawners: consequences of the fertilization-fecundity trade-off. American Naturalist, 148: 160-173.
Poorbagher H., Lamare M.D., Barker M.F., Rayment W. (2010). Relative importance of parental diet versus larval nutrition on development and phenotypic plasticity of Pseudechinus huttoni larvae (Echinodermata: Echinoidea). Marine Biology Research, 6: 302-314.
Quinn G.P. and M. J. Keough (2002). Experimental design and data analysis for biologists. Cambridge University Press. New York, 537 p.
Reitzel A.M., Heyland A. (2007). Reduction in morphological plasticity in echinoid larvae: relationship of plasticity with maternal investment and food availability. Evolutionary Ecology Research, 9: 109–121.
Reitzel A.M., Miles C.M., Heyland A., Cowart J.D., McEdward L.R. (2005). The contribution of the facultative feeding period to echinoid larval development and size at metamorphosis: a comparative approach. Journal of Experimental Marine Biology and Ecology, 317: 189-201.
Saito M., Seki M., Amemiya S., Yamasu K., Suyemitsu T., Ishihara K. (1998). Induction of metamorphosis in the sand dollar Peronella japonica by thyroid hormones. Development, Growth and Differentiation, 40: 307-312.
Sewell M.A., Cameron M.J., McArdle B.H. (2004). Developmental plasticity in larval development in the echinometrid sea urchin Evechinus chloroticus with varying food ration. Journal of Experimental Marine Biology and Ecology, 309: 219-237.
Soars N.A., Prowse T.A.A., Byrne M. (2009). Overview of phenotypic plasticity in echinoid larvae, ‘Echinopluteus transversus’ type vs. typical echinoplutei. Marine Ecology Progress Series, 383: 113-125.
Strathmann M.F. (1987). Reproduction and development of marine invertebrates of the northern Pacific coast. University of Washington Press. 670 p.
Strathmann R.R., Fenaux L., Strathmann M.F. (1992). Heterochronic developmental plasticity in larval sea urchins and its implications for evolution of nonfeeding larvae. Evolution, 46: 972-986.
Strathmann R.R., Vedder K. (1977). Size and organic content of eggs of echinoderms and other invertebrates as related to developmental strategies and egg eating. Marine Biology, 39: 305-309.
Strathmann R.S. (1985). Feeding and nonfeeding larval development and life-history evolution in marine invertebrates. Annual Review of Ecology and Systematics, 16: 339-61.
Tsushima M., Byrne M., Amemiya S., Matsuno T. (1995). Comparative biochemical studies of carotenoids in sea urchins--III. Relationship between developmental mode and carotenoids in the Australian echinoids Heliocidaris erythrogramma and H. tuberculata and a comparison with Japanese species. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 110: 719-723.
Copyright (c) 2024 International Journal of Aquatic Biology
This work is licensed under a Creative Commons Attribution 4.0 International License.