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Ontogenetic shifts in swimming capacity of echinoderm propagules: a comparison of species with planktotrophic and lecithotrophic larvae

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Abstract

While developmental strategies can modulate the dispersal and recruitment of marine benthic species, the significance and drivers of propagule motility throughout ontogeny remain incompletely understood. Species with lecithotrophic (non-feeding) development are rarely studied, despite their predominance in some taxa, including echinoderms. Quantification of the swimming capacity (i.e. speed and trajectory) of early life history stages and its variability with environmental factors is required to improve the ability to predict population connectivity and assess trade-offs associated with complex life histories. In general, lecithotrophic larvae of echinoderms are ascribed weak swimming abilities relative to planktotrophic larvae, although explicit measures are scarce. Here, we explored selected metrics of swimming capacity in four co-occurring species of North Atlantic echinoderms displaying different types of pelagic development: planktotrophs represented by the sea star Asterias rubens and the sea urchin Strongylocentrotus droebachiensis, and lecithotrophs represented by the sea star Crossaster papposus and the sea cucumber Cucumaria frondosa. Swimming was characterized in still water based on the horizontal speed and path straightness of early life-history stages, from late blastula (hatched embryo) to late-stage larva. We tested the hypotheses that swimming capacity of propagules increases with progression through developmental stages and with increasing seawater temperature. Swimming speed increased with ontogeny in two of the four species (A. rubens and C. papposus) and with temperature in all species, although the effects of temperature were not uniform across life stages. The fastest swimming speeds across all species and temperatures were recorded in lecithotrophic propagules (i.e. max speed 1.2 mm s− 1 in the brachiolaria of C. papposus), whereas propagules of species with planktotrophic development displayed faster relative speeds (body lengths s− 1). Relative speeds increased with temperature in all tested species except C. papposus. Swimming paths typically increased in straightness from early to later developmental stages, and also became straighter with increased temperature in most species, except in C. papposus where they became more circular and complex. In general, planktotrophic and lecithotrophic propagules had similar swimming capacities when tested at the same level of increased temperature, though several stage-specific differences were detected; propagules of species with planktotrophic development had greater relative speeds at the gastrula stage and greater path-corrected speeds at the larval stage. Swimming paths and swimming speeds were similar between propagules of species with planktotrophic development and lecithotrophic development, suggesting that phylogenetically conserved, ontogenetic patterns of swimming capacity (seen here between two sea stars) may supersede the contribution of larval nutritional mode.

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References

  • Abelson A, Denny M (1997) Settlement of marine organisms in flow. Annu Rev Ecol Syst 28:317–339

    Article  Google Scholar 

  • Arshavsky YI, Orlovsky G, Panchin YV, Roberts A, Soffe S (1993) Neuronal control of swimming locomotion: analysis of the pteropod mollusc Clione and embryos of the amphibian Xenopus. Trends Neurosci 16:227–233

    Article  Google Scholar 

  • Barker M (1977) Observations on the settlement of the brachiolaria larvae of Stichaster australis (Verill) and Coscinasterias calamaria (Gray) (Echinodermata: Asteroidea) in the laboratory and on the shore. J Exp Mar Biol Ecol 30:95–108

    Article  Google Scholar 

  • Butman CA, Grassle JP, Buskey EJ (1988) Horizontal swimming and gravitational sinking of Capitella sp. I (Annelida: Polychaeta) larvae: implications for settlement. Ophelia 29:43–57

    Article  Google Scholar 

  • Byrne M, Barker M (1991) Embryogenesis and larval development of the asteroid Patiriella regularis viewed by light and scanning electron microscopy. Biol Bull 180:332–345

    Article  Google Scholar 

  • Byrne M, Soars N, Selvakumaraswamy P, Dworjanyn SA, Davis AR (2010) Sea urchin fertilization in a warm, acidified and high pCO 2 ocean across a range of sperm densities. Mar Environ Res 69:234–239

    Article  CAS  Google Scholar 

  • Chan KY (2012) Biomechanics of larval morphology affect swimming: insights from the sand dollars Dendraster excentricus. Int Comp Biol 52: 458–469. doi:10.1093/icb/ics092

    Article  CAS  Google Scholar 

  • Chan KYK, Grünbaum D, O’Donnell MJ (2011) Effects of ocean-acidification-induced morphological changes on larval swimming and feeding. J Exp Biol 214:3857–3867

    Article  Google Scholar 

  • Chan KYK, Jiang H, Padilla DK (2013) Swimming speed of larval snail does not correlate with size and ciliary beat frequency. PLoS One 8:e82764

    Article  Google Scholar 

  • Chenouard N, Smal I, De Chaumont F, Maška M, Sbalzarini IF, Gong Y, Cardinale J, Carthel C, Coraluppi S, Winter M (2014) Objective comparison of particle tracking methods. Nat Meth 11:281

    Article  CAS  Google Scholar 

  • Chia FS, Buckland J, Young CM (1984) Locomotion of marine invertebrate larvae—a review. Can J Zool 62:1205–1222

    Article  Google Scholar 

  • Childress S, Dudley R (2004) Transition from ciliary to flapping mode in a swimming mollusc: flapping flight as a bifurcation in Re. J Fluid Mech 498:257–288

    Article  Google Scholar 

  • Civelek CV, Daigle RM, Metaxas A (2013) Effects of temperature on larval swimming patterns regulate vertical distribution relative to thermoclines in Asterias rubens. J Exp Mar Biol Ecol 445:1–12. doi:10.1016/j.jembe.2013.03.010

    Article  Google Scholar 

  • Clay TW, Grunbaum D (2010) Morphology-flow interactions lead to stage-selective vertical transport of larval sand dollars in shear flow. J Exp Biol 213:1281–1292. doi:10.1242/jeb.037200

    Article  CAS  Google Scholar 

  • Clay TW, Grünbaum D (2011) Swimming performance as a constraint on larval morphology in plutei. Mar Ecol Prog Ser 423:185–196. doi:10.3354/meps08978

    Article  Google Scholar 

  • Collin R, Mobley AS, Lopez LB, Leys SP, Diaz MC, Thacker RW (2010) Phototactic responses of larvae from the marine sponges Neopetrosia proxima and Xestospongia bocatorensis (Haplosclerida: Petrosiidae). Invertebr Biol 129: 121–128 doi:10.1111/j.1744-7410.2010.00196.x

    Article  Google Scholar 

  • Daigle RM, Metaxas A (2012) Modeling of the larval response of green sea urchins to thermal stratification using a random walk approach. J Exp Mar Biol Ecol 438:14–23

    Article  Google Scholar 

  • Dorée M, Guerrier P, Leonard NJ (1976) Hormonal control of meiosis: specificity of the 1-methyladenine receptors in starfish oocytes. Proc Natl Acad Sci USA 73:1669–1673

    Article  Google Scholar 

  • Emlet RB (1983) Locomotion, drag and the rigid skelton of larval echinoderms. Biol Bull 164:433–445

    Article  Google Scholar 

  • Emlet RB (1994) Body form and patterns of ciliation in nonfeeding larvae of echinoderms—functional solutions to swimming in the plankton. Am Zool 34:570–585

    Article  Google Scholar 

  • Epp RW, Lewis WM (1984) Cost and speed of locomotion for rotifers. Oecologia 61:289–292. doi:10.1007/Bf00379624

    Article  Google Scholar 

  • Fenberg PB, Menge BA, Raimondi PT, Rivadeneira MM (2015) Biogeographic structure of the northeastern Pacific rocky intertidal: the role of upwelling and dispersal to drive patterns. Ecography 38:83–95

    Article  Google Scholar 

  • Gemmill JF (1914) The development and certain points in the adult structure of the starfish Asterias rubens. Phil Trans R Soc B 205: 213–294

    Article  Google Scholar 

  • Gemmill JF (1920) The development of the starfish Crossaster papposus. Q J Microsc Sci 64: 155–187

    Google Scholar 

  • Gerritsen J, Strickler JR (1977) Encounter probabilities and community structure in zooplankton: a mathematical model. J Fish Res Board Can 34:73–82

    Article  Google Scholar 

  • Gross TF, Werner FE, Eckman JE (1992) Numerical modeling of larval settlement in turbulent bottom boundary layers. J Mar Res 50:611–642

    Article  Google Scholar 

  • Grunbaum D, Strathmann RR (2003) Form, performance, and trade-offs in swimming and stability of armed larvae. J Mar Res 61:659–691

    Article  Google Scholar 

  • Hamel J-F, Mercier A (1996) Early development, settlement, growth, and spatial distribution of the sea cucumber Cucumaria frondosa (Echinodermata: Holothuroidea). Can J Fish Aquat Sci 53:253–271

    Article  Google Scholar 

  • Harii S, Kayanne H, Takigawa H, Hayashibara T, Yamamoto M (2002) Larval survivorship, competency periods and settlement of two brooding corals, Heliopora coerulea and Pocillopora damicornis. Mar Biol 141:39–46

    Article  Google Scholar 

  • Holst S, Jarms G (2006) Substrate choice and settlement preferences of planula larvae of five Scyphozoa (Cnidaria) from German Bight, North Sea. Mar Biol 151:863–871. doi:10.1007/s00227-006-0530-y

    Article  Google Scholar 

  • Iyengar EV, Harvell CD (2001) Predator deterrence of early developmental stages of temperate lecithotrophic asteroids and holoturoids. J Exp Mar Biol Ecol 264:171–188

    Article  Google Scholar 

  • Jacobs DK, Nakanishi N, Yuan D, Camara A, Nichols SA, Hartenstein V (2007) Evolution of sensory structures in basal metazoa. Int Comp Biol 47:712–723 doi:10.1093/icb/icm094

    Article  Google Scholar 

  • Kashenko SD (2007) Adaptive responses of embryos and larvae of the heart-shaped sea urchin Echinocardium cordatum to temperature and salinity changes. Russ J Mar Biol 33:381–390. doi:10.1134/s1063074007060041

    Article  Google Scholar 

  • Kelman D, Emlet RB (1999) Swimming and buoyancy in ontogenetic stages of the cushion star Pteraster tesselatus (Echinodermata : Asteroidea) and their implications for distribution and movement. Biol Bull 197:309–314. doi:10.2307/1542784

    Article  CAS  Google Scholar 

  • Kingsford MJ, Leis JM, Shanks A, Lindeman KC, Morgan SG, Pineda J (2002) Sensory environments, larval abilities and local self-recruitment. Bull Mar Sci 70:309–340

    Google Scholar 

  • Koehl M (2007) Mini review: hydrodynamics of larval settlement into fouling communities. Biofouling 23:357–368

    Article  CAS  Google Scholar 

  • Leys SP, Cronin TW, Degnan BM, Marshall JN (2002) Spectral sensitivity in a sponge larva. J Comp Physiol A 188:199–202. doi:10.1007/s00359-002-0293-y

    Article  Google Scholar 

  • Liu W, Pearce C, McKinley R, Forster I (2016) Nutritional value of selected species of microalgae for larvae and early post-set juveniles of the Pacific geoduck clam, Panopea generosa. Aquaculture 452:326–341

    Article  CAS  Google Scholar 

  • Loor A, Ortega D, Lodeiros C, Sonnenholzner S (2016) Early life cycle and effects of microalgal diets on larval development of the spiny rock-scallop, Spondylus limbatus (Sowerby II, 1847). Aquaculture 450:328–334

    Article  Google Scholar 

  • Maldonado M (2006) The ecology of the sponge larva. Can J Zool 84:175–194. doi:10.1139/z05-177

    Article  Google Scholar 

  • Marshall DJ, Keough MJ (2003) Variation in the dispersal potential of non-feeding invertebrate larvae: the desperate larva hypothesis and larval size. Mar Ecol Prog Ser 255:145–153

    Article  Google Scholar 

  • Marshall DJ, Krug PJ, Kupriyanova EK, Byrne M, Emlet RB (2012) The biogeography of marine invertebrate life histories. Annu Rev Ecol Syst 43:97–114. doi:10.1146/annurev-ecolsys-102710-145004

    Article  Google Scholar 

  • McDonald K (2004) Patterns in early embryonic motility: effects of size and environmental temperature on vertical velocities of sinking and swimming echinoid blastulae. Biol Bull 207:93–102

    Article  Google Scholar 

  • McDonald KA (2012) Earliest ciliary swimming effects vertical transport of planktonic embryos in turbulence and shear flow. J Exp Biol 215:141–151

    Article  Google Scholar 

  • McEuen FS, Chia FS (1991) Development and metamorphosis of two psolid sea cucumbers, Psolus chitonoides and Psolidium bullatum, with a review of reproductive patterns in the family Psolidae (Holothuroidea: Echinodermata). Mar Biol 109:267–279. doi:10.1007/BF01319395

    Article  Google Scholar 

  • Meidel SK, Yund PO (2001) Egg longevity and time-integrated fertilization in a temperate sea urchin (Strongylocentrotus droebachiensis). Biol Bull 201:84–94

    Article  CAS  Google Scholar 

  • Meidel SK, Scheibling RE, Metaxas A (1999) Relative importance of parental and larval nutrition on larval development and metamorphosis of the sea urchin Strongylocentrotus droebachiensis. J Exp Mar Biol Ecol 240:161–178

    Article  Google Scholar 

  • Mercier A, Hamel J-F (2010) Synchronized breeding events in sympatric marine invertebrates: role of behavior and fine temporal windows in maintaining reproductive isolation. Behav Ecol Sociobiol 64:1749–1765. doi:10.1007/s00265-010-0987-z

    Article  Google Scholar 

  • Mercier A, Doncaster EJ, Hamel J-F (2013a) Contrasting predation rates on planktotrophic and lecithotrophic propagules by marine benthic invertebrates. J Exp Mar Biol Ecol 449:100–110. doi:10.1016/j.jembe.2013.09.007

    Article  Google Scholar 

  • Mercier A, Sewell MA, Hamel J-F (2013b) Pelagic propagule duration and developmental mode: reassessment of a fading link. Glob Ecol Biogeogr 22:517–530. doi:10.1111/geb.12018

    Article  Google Scholar 

  • Metaxas A (2001) Behaviour in flow: perspectives on the distribution and dispersion of meroplanktonic larvae in the water column. Can J Fish Aquat Sci 58:86–98

    Article  Google Scholar 

  • Metaxas A, Saunders M (2009) Quantifying the “bio-” components in biophysical models of larval transport in marine benthic invertebrates: advances and pitfalls. Biol Bull 216:257–272

    Article  Google Scholar 

  • Mileikovsky SA (1973) Speed of active movement of pelagic larvae of marine bottom invertebrates and their ability to regulate their vertical position. Mar Biol 23:11–17

    Article  Google Scholar 

  • Mogami Y, Oobayashi C, Yamaguchi T, Ogiso Y, Baba SA (1988) Negative geotaxis in sea urchin larvae: a possible role of mechanoreception in the late stages of development. J Exp Biol 137:141–156

    Google Scholar 

  • Moore SW (2003) Scrambled eggs: mechanical forces as ecological factors in early development. Evol Dev 5:61–66

    Article  Google Scholar 

  • Morgan SG (2014) Behaviorally mediated larval transport in upwelling systems. Adv Oceanog 2014:1–18

    Article  Google Scholar 

  • Mos B, Cowden KL, Nielsen SJ, Dworjanyn SA (2011) Do cues matter? Highly inductive settlement cues don’t ensure high post-settlement survival in sea urchin aquaculture. PLoS One 6:e28054

    Article  CAS  Google Scholar 

  • Myksvoll MS, Jung K-M, Albretsen J, Sundby S (2014) Modelling dispersal of eggs and quantifying connectivity among Norwegian coastal cod subpopulations. ICES J Mar Sci 71:957–969

    Article  Google Scholar 

  • North EW, Schlag Z, Hood R, Li M, Zhong L, Gross T, Kennedy VS (2008) Vertical swimming behavior influences the dispersal of simulated oyster larvae in a coupled particle-tracking and hydrodynamic model of Chesapeake Bay. Mar Ecol Prog Ser 359:99–115

    Article  Google Scholar 

  • Pawlik JR (1992) Chemical ecology of the settlement of benthic marine invertebrates. Oceanog Mar Biol 30:273–335

    Google Scholar 

  • Pearce CM, Williams SW, Yuan F, Castell JD, Robinson S (2005) Effect of temperature on somatic growth and survivorship of early post-settled green sea urchins, Strongylocentrotus droebachiensis (Müller). Aquac Res 36:600–609

    Article  Google Scholar 

  • Pechenik JA (1999) On the advantages and disadvantages of larval stages in benthic marine invertebrate life cycles. Mar Ecol Prog Ser 177:269–297

    Article  Google Scholar 

  • Pizarro V, Thomason J (2008) How do swimming ability and behaviour affect the dispersal of coral larvae Proceedings of the 11th International Coral Reef Symposium, Fort Lauderdale, Florida, 7, pp 464–467

  • Podolsky RD, Emlet RB (1993) Separating the effects of temperature and viscosity on swimming and water movement by sand dollar larvae (Dendraster excentricus). J Exp Biol 176:207–222

    Google Scholar 

  • Poulin E, Boletzky SV, Feral J-P (2001) Combined ecological factors permit classification of developmental patterns in benthic marine invertebrates: a discussion note. J Exp Mar Biol Ecol 257:109–115

    Article  CAS  Google Scholar 

  • Pringle JM, Byers JE, Pappalardo P, Wares JP, Marshall D (2014) Circulation constrains the evolution of larval development modes and life histories in the coastal ocean. Ecology 95:1022–1032

    Article  Google Scholar 

  • Puvanendran V, Brown JA (1998) Effect of light intensity on the foraging and growth of Atlantic cod larvae: interpopulation difference. Mar Ecol Prog Ser 167:207–214

    Article  Google Scholar 

  • Rebolledo AP, Emlet RB (2015) The parachute function of the hull in eggs of Mopalia kennerleyi (Chitonida: Mopaliidae), and swimming of its larvae through ontogeny. Invertebr Biol 134: 31–37

    Article  Google Scholar 

  • Reitzel AM, Miner BG, McEdward LR (2004) Relationships between spawning date and larval developmental time for benthic marine invertebrates: a modelling approach. Mar Ecol Prog Ser 280:13–23

    Article  Google Scholar 

  • Robins PE, Neill SP, Giménez L, Jenkins SR, Malham SK (2013) Physical and biological controls on larval dispersal and connectivity in a highly energetic shelf sea. Limnol Oceanogr 58:505–524

    Article  Google Scholar 

  • Roller RA, Stickle WB (1994) Effects of adult salinity acclimation on larval survival and early development of Strongylocentrotus droebachiensis and Strongylocentrotus pallidus (Echinodermata: Echinoidea). Can J Zool 72:1931–1939

    Article  Google Scholar 

  • Roy A, Metaxas A, Daigle RM (2012a) Changes in vertical distribution and aggregative behaviour in response to population density for larval sea urchins (Strongylocentrotus droebachiensis) and sea stars (Asterias rubens). Mar Ecol 33:194–204 doi:10.1111/j.1439-0485.2011.00480.x

    Article  Google Scholar 

  • Roy A, Metaxas A, Ross T (2012b) Swimming patterns of larval Strongylocentrotus droebachiensis in turbulence in the laboratory. Mar Ecol Prog Ser 453:117–127

    Article  Google Scholar 

  • Salama N, Collins C, Fraser J, Dunn J, Pert C, Murray A, Rabe B (2013) Development and assessment of a biophysical dispersal model for sea lice. J Fish Dis 36:323–337

    Article  CAS  Google Scholar 

  • Sameoto JA, Ross T, Metaxas A (2010) The effect of flow on larval vertical distribution of the sea urchin, Strongylocentrotus droebachiensis. J Exp Mar Biol Ecol 383:156–163. doi:10.1016/j.jembe.2009.11.014

    Article  Google Scholar 

  • Saranchova OL, Flyachinskya LP (2001) The influence of salinity on early ontogeny of the mussel Mytilus edulis and the starfish Asterias rubens from the White Sea. Russ J Mar Biol 27:87–93

    Article  Google Scholar 

  • Scheltema RS (1986) On dispersal and planktonic larvae of benthic invertebrates: an eclectic overview and summary of problems. Bull Mar Sci 39:290–322

    Google Scholar 

  • Staver JM, Strathmann RR (2002) Evolution of fast development of planktonic embryos to early swimming. Biol Bull 203:58–69

    Article  Google Scholar 

  • Strathmann RR (1971) The feeding behaviour of planktotrophic echinoderm larvae: mechanisms, regulation, and rates of suspension feeding. J Exp Mar Biol Ecol 6:109–160

    Article  Google Scholar 

  • Strathmann RR (1993) Hypotheses on the origins of marine larvae. Annu Rev Ecol Syst 24:89–117

    Article  Google Scholar 

  • Strathmann RR, Grunbaum D (2006) Good eaters, poor swimmers: compromises in larval form. Int Comp Biol 46:312–322. doi:10.1093/icb/icj031

    Article  Google Scholar 

  • Strathmann RR, Grünbaum D (2006) Good eaters, poor swimmers: compromises in larval form. Int Comp Biol 46:312–322

    Article  Google Scholar 

  • Tamburri MN, Finelli CM, Wethey DS, Zimmer-Faust RK (1996) Chemical induction of larval settlement behavior in flow. Biol Bull 191:367–373

    Article  CAS  Google Scholar 

  • Thorson G (1949) Reproductive and larval ecology of marine bottom invertebrates. Biol Rev 25:1–45

    Article  Google Scholar 

  • Uthicke S, Schaffelke B, Byrne M (2009) A boom-bust phylum? Ecological and evolutionary consequences of density variations in echinoderms. Ecol Monogr 79:3–24

    Article  Google Scholar 

  • Villalobos FB, Tyler PA, Young CM (2006) Temperature and pressure tolerance of embryos and larvae of the Atlantic seastars Asterias rubens and Marthasterias glacialis (Echinodermata: Asteroidea): potential for deep-sea invasion. Mar Ecol Prog Ser 314:109–117

    Article  CAS  Google Scholar 

  • Visser AW, Kiørboe T (2006) Plankton motility patterns and encounter rates. Oecologia 148:538–546

    Article  Google Scholar 

  • Walker G (2004) Swimming speeds of the larval stages of the parasitic barnacle, Heterosaccus lunatus (Crustacea: Cirripedia: Rhizocephala). J Mar Biol Assoc UK 84:737–742

    Article  Google Scholar 

  • Walters LJ, Miron G, Bourget E (1999) Endoscopic observations of invertebrate larval substratum exploration and settlement. Mar Ecol Prog Ser 182:95–108

    Article  Google Scholar 

  • Webb CM (1989) Larval swimming and substrate selection in the brittle star O. brevispinum Reproduction, Genetics and Distributions of Marine Organisms: 23rd European Marine Biology Symposium. Olsen & Olsen, School of Biological Sciences, University of Wales, Swansea, pp 217

  • Wendt DE (2000) Energetics of larval swimming and metamorphosis in four species of Bugula (Bryozoa). Biol Bull 198:346–356

    Article  CAS  Google Scholar 

  • Wood S, Paris C, Ridgwell A, Hendy E (2014) Modelling dispersal and connectivity of broadcast spawning corals at the global scale. Glob Ecol Biogeogr 23:1–11

    Article  Google Scholar 

  • Wray GA, Kitazawa C, Miner B (2004) Culture of echinoderm larvae through metamorphosis. Methods Cell Biol 74:75–86

    Article  Google Scholar 

  • Young CM, Sewell MA, Tyler PA, Metaxas A (1997) Biogeographic and bathymetric ranges of Atlantic deep-sea echinoderms and ascidians: the role of larval dispersal. Biodivers Conserv 6:1507–1522. doi:10.1023/a:1018314403123

    Article  Google Scholar 

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Acknowledgements

The authors wish to thank Memorial University Field Services for animal collections. The authors also wish to thank two anonymous reviewers and K. Gamperl (Memorial University) for constructive comments on the manuscript.

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This work was completed with funding from Natural Sciences and Engineering Research Council Discovery Grant (#311,406) and Canadian Foundation for Innovation Grant (#11,231) issued to A. Mercier and an NSERC CGS-D Award to E. Montgomery.

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Montgomery, E.M., Hamel, JF. & Mercier, A. Ontogenetic shifts in swimming capacity of echinoderm propagules: a comparison of species with planktotrophic and lecithotrophic larvae. Mar Biol 164, 43 (2017). https://doi.org/10.1007/s00227-017-3072-6

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