Abstract
Marine and freshwater ecosystems differ in persistence, size, population connectivity, and the variance in physical and biotic conditions they experience. These differences may select for differing reproductive modes, life histories, dispersal strategies, and chemically cued recruitment behaviors. In marine systems, adults are commonly less mobile, while larvae spend hours to weeks to months dispersing in the plankton and may move over great distances. It is these immature larval stages that must select appropriate recruitment sites in marine environments. In freshwater systems, the fully developed adults more commonly disperse over greater distances, and it is usually adults that determine juvenile recruitment sites via their placement of larvae or fertilized eggs. Thus, in terms of large-scale habitat choices involving chemical cuing, adult stages should be selected to detect and react to habitat cues among most freshwater species, while juveniles should play this role among most marine species. Few studies assess this hypothesis, but adults of freshwater organisms as different as mosquitoes and frogs do key on chemical cues to select sites for depositing eggs or larvae, while chemical cuing of recruitment in marine systems occurs primarily among the larval stages of the numerous fishes and marine invertebrates investigated to date. Cues to general habitat features, to predators or competitors, and to specific prey or hosts have all been shown to affect recruitment. Here, we review chemically mediated recruitment in marine versus freshwater systems, summarizing what is known and suggesting unknowns that may be productive to investigate.
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Aires T, Serebryakova A, Viard F, Serrão EA, Engelen AH (2018) Acidification increases abundances of Vibrionales and Planctomycetia associated to a seaweed-grazer system: potential consequences for disease and prey digestion efficiency. PeerJ 6:e4377. https://doi.org/10.7717/peerj.4377
Almany GR, Berumen ML, Thorrold SR, Planes S, Jones GP (2007) Local replenishment of coral reef fish populations in a marine reserve. Science 316:742–744. https://doi.org/10.1126/science.1140597
Anderson AR, Petranka JW (2003) Odonate predator does not affect hatching time or morphology of embryos of two amphibians. J Herpetol 37:65–71. https://doi.org/10.1670/0022-1511(2003)037[0065:OPDNAH]2.0.CO;2
Anderson JA, Epifanio CE (2009) Induction of metamorphosis in the Asian shore crab Hemigrapsus sanguineus: Characterization of the cue associated with biofilm from adult habitat. J Exp Mar Biol Ecol 382:34–39. https://doi.org/10.1016/j.jembe.2009.10.006
Anger K (1995) The conquest of freshwater and land by marine crabs: adaptations in life-history patterns and larval bioenergetics. J Exp Mar Biol Ecol 193:119–145. https://doi.org/10.1016/0022-0981(95)00114-X
Anger K, Torres G, Giménez L (2006) Metamorphosis of a sesarmid river crab, Armases roberti: stimulation by adult odours versus inhibition by salinity stress. Mar Freshw Behav Physiol 39:269–278. https://doi.org/10.1080/10236240600986183
Arav D, Blaustein L (2006) Effects of pool depth and risk of predation on oviposition habitat selection by temporary pool dipterans. J Med Entomol 43:5. https://doi.org/10.1093/jmedent/43.3.493
Atherton JA, McCormick MI (2015) Active in the sac: damselfish embryos use innate recognition of odours to learn predation risk before hatching. Anim Behav 103:1–6. https://doi.org/10.1016/j.anbehav.2015.01.033
Balian EV, Lévêque C, Segers H, Martens K (eds) (2008) Freshwater animal diversity assessment. Springer, The Netherlands
Banks J, Dinnel P (2000) Settlement behavior of Dungeness crab (Cancer magister Dana, 1852) megalopae in the presence of the shore crab, Hemigrapsus (Decapoda, Brachyura). Crustaceana 73:223–234. https://doi.org/10.1163/156854000504174
Bauer RT (2011) Amphidromy and migrations of freshwater shrimps. II. Delivery of hatching larvae to the sea, return juvenile upstream migration, and human impacts. In: Asakura A (ed) New frontiers in crustacean biology. Brill, pp 157–168
Beatty DS, Clements CS, Stewart FJ, Hay ME (2018) Intergenerational effects of macroalgae on a reef coral: major declines in larval survival but subtle changes in microbiomes. Mar Ecol Prog Ser 589:97–114. https://doi.org/10.3354/meps12465
Benkwitt CE (2017) Predator effects on reef fish settlement depend on predator origin and recruit density. Ecology 98:896–902. https://doi.org/10.1002/ecy.1732
Bjærke O, Andersen T, Titelman J (2014) Predator chemical cues increase growth and alter development in nauplii of a marine copepod. Mar Ecol Prog Ser 510:15–24. https://doi.org/10.3354/meps10918
Blaustein L, Blaustein J, Chase J (2005) Chemical detection of the predator Notonecta irrorata by ovipositing Culex mosquitoes. J Vector Ecol 30:299–301
Blaustein L, Kiflawi M, Eitam A, Mangel M, Cohen JE (2004) Oviposition habitat selection in response to risk of predation in temporary pools: mode of detection and consistency across experimental venue. Oecologia 138:300–305. https://doi.org/10.1007/s00442-003-1398-x
Botello G, Krug PJ (2006) “Desperate larvae” revisited: age, energy and experience affect sensitivity to settlement cues in larvae of the gastropod Alderia sp. Mar Ecol Prog Ser 312:149–159. https://doi.org/10.3354/meps312149
Bouchemousse S, Lévêque L, Viard F (2017) Do settlement dynamics influence competitive interactions between an alien tunicate and its native congener? Ecol Evol 7:200–213. https://doi.org/10.1002/ece3.2655
Boudreau B, Bourget E, Simard Y (1993) Behavioural responses of competent lobster postlarvae to odor plumes. Mar Biol 117:63–69. https://doi.org/10.1007/BF00346426
Boyle PJ, Mitchell R (1981) The function of microorganisms in marine wood-boring processes. OCEANS 81. IEEE, Boston, MA, pp 526–531. https://doi.org/10.1109/OCEANS.1981.1151478
Brooker RM, Hay ME, Dixson DL (2016) Chemically cued suppression of coral reef resilience: Where is the tipping point? Coral Reefs 35:1263–1270. https://doi.org/10.1007/s00338-016-1474-4
Brooker RM, Seyfferth AL, Hunter A, Sneed JM, Dixson DL, Hay ME (2020) Human proximity suppresses fish recruitment by altering mangrove-associated odour cues. Sci Rep 10:21091. https://doi.org/10.1038/s41598-020-77722-7
Brown TA, Fraker ME, Ludsin SA (2019) Space use of predatory larval dragonflies and tadpole prey in response to chemical cues of predation. Am Midl Nat 181:53–62. https://doi.org/10.1674/0003-0031-181.1.53
Bullard SG, Whitlatch RB, Osman RW (2004) Checking the landing zone: Do invertebrate larvae avoid settling near superior spatial competitors? Mar Ecol Prog Ser 280:239–247. https://doi.org/10.3354/meps280239
Burdett-Coutts V, Wahle R, Snelgrove P, Rochette R (2014) Spatial linkages between settling young-of-year and older juvenile lobsters. Mar Ecol Prog Ser 499:143–155. https://doi.org/10.3354/meps10625
Burggren WW, McMahon BR (eds) (1988) Biology of the land crabs. Cambridge University Press, New York, NY
Buxton VL, Sperry JH (2017) Reproductive decisions in anurans: a review of how predation and competition affects the deposition of eggs and tadpoles. Bioscience 67:26–38. https://doi.org/10.1093/biosci/biw149
Cahill AE (2015) Adult density affects larval recruitment in the calyptraeid gastropod Crepidula fornicata. J Exp Mar Biol Ecol 465:77–82. https://doi.org/10.1016/j.jembe.2015.01.013
Cahill AE, Koury SA (2016) Larval settlement and metamorphosis in a marine gastropod in response to multiple conspecific cues. PeerJ 4:e2295. https://doi.org/10.7717/peerj.2295
Campbell JE, Sneed JM, Johnston L, Paul VJ (2017) Effects of ocean acidification and contact with the brown alga Stypopodium zonale on the settlement and early survival of the coral Porites astreoides. Mar Ecol Prog Ser 577:67–77. https://doi.org/10.3354/meps12249
Cayrou J, Céréghino R (2005) Life-cycle phenology of some aquatic insects: implications for pond conservation. Aquat Conserv Mar Freshwat Ecosyst 15:559–571. https://doi.org/10.1002/aqc.739
Chesson J (1984) Effect of notonectids (Hemiptera: Notonectidae) on mosquitoes (Diptera: Culicidae): Predation or selective oviposition? Environ Entomol 13:531–538. https://doi.org/10.1093/ee/13.2.531
Clark TD, Raby GD, Roche DG, Binning SA, Speers-Roesch B, Jutfelt F, Sundin J (2020) Ocean acidification does not impair the behaviour of coral reef fishes. Nature 577:370–375. https://doi.org/10.1038/s41586-019-1903-y
Cobb JS, Booth JD, Clancy M (1997) Recruitment strategies in lobsters and crabs: a comparison. Mar Freshw Res 48:797–806. https://doi.org/10.1071/mf97219
Colman J (1933) The nature of the intertidal zonation of plants and animals. J Mar Biol Assoc UK 18:435. https://doi.org/10.1017/S0025315400043794
Connell JH (1961) Effects of competition, predation by Thais lapillus, and other factors on natural populations of the barnacle Balanus balanoides. Ecol Monogr 31:61–104. https://doi.org/10.2307/1950746
Corallini C, Gaino E (2003) The caddisfly Ceraclea fulva and the freshwater sponge Ephydatia fluviatilis: a successful relationship. Tissue Cell 35:1–7. https://doi.org/10.1016/S0040-8166(02)00086-1
Cowen RK, Paris CB, Srinivasan A (2006) Scaling of connectivity in marine populations. Science 311:522–527. https://doi.org/10.1126/science.1122039
Cragg SM, Pitman AJ, Henderson SM (1999) Developments in the understanding of the biology of marine wood boring crustaceans and in methods of controlling them. Int Biodeterior Biodegrad 43:197–205. https://doi.org/10.1016/S0964-8305(99)00054-2
Cresci A, Paris CB, Durif CMF, Shema S, Bjelland RM, Skiftesvik AB, Browman HI (2017) Glass eels (Anguilla anguilla) have a magnetic compass linked to the tidal cycle. Sci Adv 3:e1602007. https://doi.org/10.1126/sciadv.1602007
Cumberlidge N (1999) The freshwater crabs of West Africa: family Potamonautidae. IRD Editions, France
Davis M, Stoner AW (1994) Trophic cues induce metamorphosis of queen conch larvae (Strombus gigas Linnaeus). J Exp Mar Biol Ecol 180:83–102. https://doi.org/10.1016/0022-0981(94)90081-7
Delgado GA, Glazer RA, Wetzel D (2013) Effects of mosquito control pesticides on competent queen conch (Strombus gigas) larvae. Biol Bull 225:79–84. https://doi.org/10.1086/BBLv225n2p79
Diele K, Simith DJB (2007) Effects of substrata and conspecific odour on the metamorphosis of mangrove crab megalopae, Ucides cordatus (Ocypodidae). J Exp Mar Biol Ecol 348:174–182. https://doi.org/10.1016/j.jembe.2007.04.008
Dixson DL, Abrego D, Hay ME (2014) Chemically mediated behavior of recruiting corals and fishes: a tipping point that may limit reef recovery. Science 345:892–897. https://doi.org/10.1126/science.1255057
Dixson DL, Jones GP, Munday PL, Planes S, Pratchett MS, Srinivasan M, Syms C, Thorrold SR (2008) Coral reef fish smell leaves to find island homes. Proc Royal Soc B Biol Sci. https://doi.org/10.1098/rspb.2008.0876
Dixson DL, Jones GP, Munday PL, Pratchett MS, Srinivasan M, Planes S, Thorrold SR (2011) Terrestrial chemical cues help coral reef fish larvae locate settlement habitat surrounding islands. Ecol Evol 1:586–595. https://doi.org/10.1002/ece3.53
Dixson DL, Munday PL, Jones GP (2010) Ocean acidification disrupts the innate ability of fish to detect predator olfactory cues. Ecol Lett 13:68–75. https://doi.org/10.1111/j.1461-0248.2009.01400.x
Dixson DL, Pratchett MS, Munday PL (2012) Reef fishes innately distinguish predators based on olfactory cues associated with recent prey items rather than individual species. Anim Behav 84:45–51. https://doi.org/10.1016/j.anbehav.2012.04.001
Downes BJ, Keough MJ (1998) Scaling of colonization processes in streams: parallels and lessons from marine hard substrata. Aust J Ecol 23:8–26. https://doi.org/10.1111/j.1442-9993.1998.tb00702.x
Duarte CM, Alcaraz M (1989) To produce many small or few large eggs: a size-independent reproductive tactic of fish. Oecologia 80:401–404. https://doi.org/10.1007/BF00379043
Eitam A, Blaustein L (2004) Oviposition habitat selection by mosquitoes in response to predator (Notonecta maculata) density. Physiol Entomol 29:188–191. https://doi.org/10.1111/j.0307-6962.2004.0372.x
Elbourne PD, Clare AS (2010) Ecological relevance of a conspecific, waterborne settlement cue in Balanus amphitrite (Cirripedia). J Exp Mar Biol Ecol 392:99–106. https://doi.org/10.1016/j.jembe.2010.04.013
Ellrich JA, Scrosati RA, Bertolini C, Molis M (2016) A predator has nonconsumptive effects on different life-history stages of a prey. Mar Biol 163:5. https://doi.org/10.1007/s00227-015-2778-6
Endres CS, Putman NF, Ernst DA, Kurth JA, Lohmann CMF, Lohmann KJ (2016) Multi-modal homing in sea turtles: Modeling dual use of geomagnetic and chemical cues in island-finding. Front Behav Neurosci. https://doi.org/10.3389/fnbeh.2016.00019
Fakan EP, McCormick MI (2019) Boat noise affects the early life history of two damselfishes. Mar Pollut Bull 141:493–500. https://doi.org/10.1016/j.marpolbul.2019.02.054
Ferrari MCO, Manassa RP, Dixson DL, Munday PL, McCormick MI, Meekan MG, Sih A, Chivers DP (2012) Effects of ocean acidification on learning in coral reef fishes. PLoS ONE 7:e31478. https://doi.org/10.1371/journal.pone.0031478
Fusari L, Oliveira CN, Hamada N, Roque F (2012) New species of Ablabesmyia Johannsen from the Neotropical region: first report of a sponge-dwelling Tanypodinae. Zootaxa 3239:43–50. https://doi.org/10.13140/RG.2.1.4355.0244
Fusari LM, Roque FO, Hamada N (2014) Systematics of Oukuriella Epler, 1986, including a revision of the species associated with freshwater sponges. Insect Syst Evol 45:117–157. https://doi.org/10.1163/1876312X-04402006
Gara RI, Greulich FE, Ripley KL (1997) Shipworm (Bankia setacea) host selection habits at the port of Everett, Washington. Estuaries 20:441–449. https://doi.org/10.2307/1352356
Garcia TS, Urbina JC, Bredeweg EM, Ferrari MCO (2017) Embryonic learning and developmental carry-over effects in an invasive anuran. Oecologia 184:623–631. https://doi.org/10.1007/s00442-017-3905-5
García-Roger EM, Carmona MJ, Serra M (2005) Deterioration patterns in diapausing egg banks of Brachionus (Müller, 1786) rotifer species. J Exp Mar Biol Ecol 314:149–161. https://doi.org/10.1016/j.jembe.2004.08.023
Gaylord B, Hodin J, Ferner MC (2013) Turbulent shear spurs settlement in larval sea urchins. Proc Natl Acad Sci 110:6901–6906. https://doi.org/10.1073/pnas.1220680110
Gerlach G, Atema J, Kingsford MJ, Black KP, Miller-Sims V (2007) Smelling home can prevent dispersal of reef fish larvae. Proc Natl Acad Sci 104:858–863. https://doi.org/10.1073/pnas.0606777104
Gerlach G, Tietje K, Biechl D, Namekawa I, Schalm G, Sulmann A (2019) Behavioural and neuronal basis of olfactory imprinting and kin recognition in larval fish. J Exp Biol. https://doi.org/10.1242/jeb.189746
Gill DE (1978) The metapopulation ecology of the red-spotted newt, Notophthalmus viridescens (Rafinesque). Ecol Monogr 48:145–166. https://doi.org/10.2307/2937297
Goldstein JS, Butler MJ (2009) Behavioral enhancement of onshore transport by postlarval Caribbean spiny lobster (Panulirus argus). Limnol Oceanogr 54:1669–1678. https://doi.org/10.4319/lo.2009.54.5.1669
Gordon TAC, Harding HR, Wong KE, Merchant ND, Meekan MG, McCormick MI, Radford AN, Simpson SD (2018) Habitat degradation negatively affects auditory settlement behavior of coral reef fishes. Proc Natl Acad Sci 115:5193–5198. https://doi.org/10.1073/pnas.1719291115
Grantham BA, Eckert GL, Shanks AL (2003) Dispersal potential of marine invertebrates in diverse habitats. Ecol Appl 13:108–116. https://doi.org/10.1890/1051-0761(2003)013[0108:DPOMII]2.0.CO;2
Groot C, Margolis L (eds) (1991) Pacific salmon life histories. UBC Press, Vancouver
Grosberg RK (1981) Competitive ability influences habitat choice in marine invertebrates. Nature 290:700–702. https://doi.org/10.1038/290700a0
Groves AB, Collins GB, Trefethen PS (1968) Roles of olfaction and vision in choice of spawning site by homing adult chinook salmon (Oncorhynchus tshawytscha). J Fish Res Board Can 25:867–876. https://doi.org/10.1139/f68-082
Hadfield M, Paul V (2001) Natural chemical cues for settlement and metamorphosis of marine-invertebrate larvae. In: McClintock JB, Baker B (eds) Marine chemical ecology. CRC Press, pp 431–461
Hadfield MG (2011) Biofilms and marine invertebrate larvae: What bacteria produce that larvae use to choose settlement sites. Ann Rev Mar Sci 3:453–470. https://doi.org/10.1146/annurev-marine-120709-142753
Hagiwara A, Hoshi N, Kawahara F, Tominaga K, Hirayama K (1995) Resting eggs of the marine rotifer Brachionus plicatilis Müller: development, and effect of irradiation on hatching. Hydrobiologia 313:223–229. https://doi.org/10.1007/BF00025955
Hairston NG (1996) Zooplankton egg banks as biotic reservoirs in changing environments. Limnol Oceanogr 41:1087–1092. https://doi.org/10.4319/lo.1996.41.5.1087
Hairston NG, Cáceres CE (1996) Distribution of crustacean diapause: micro- and macroevolutionary pattern and process. Hydrobiologia 320:27–44
Harrington L, Fabricius K, D’eath G, Negri A (2004) Recognition and selection of settlement substrata eetermine post-settlement survival in corals. Ecology 85:3428–3437. https://doi.org/10.1890/04-0298
Heiling AM, Herberstein ME (2004) Predator–prey coevolution: Australian native bees avoid their spider predators. Proc R Soc Lond B 271:S196–S198. https://doi.org/10.1098/rsbl.2003.0138
Heyward AJ, Negri AP (1999) Natural inducers for coral larval metamorphosis. Coral Reefs 18:273–279. https://doi.org/10.1007/s003380050193
Hinojosa IA, Gardner C, Green BS, Jeffs A (2018) Coastal chemical cues for settlement of the southern rock lobster, Jasus edwardsii. Bull Mar Sci 94:619–633. https://doi.org/10.5343/bms.2017.1136
Hogg R, Stephen MC Jr, Zydlewski J (2013) Anadromous sea lampreys recolonize a Maine coastal river tributary after dam removal. Trans Am Fish Soc 142:1381–1394. https://doi.org/10.1080/00028487.2013.811103
Houde ED (1994) Differences between marine and freshwater fish larvae: implications for recruitment. ICES J Mar Sci 51:91–97. https://doi.org/10.1006/jmsc.1994.1008
Huggett MJ, Williamson JE, de Nys R, Kjelleberg S, Steinberg PD (2006) Larval settlement of the common Australian sea urchin Heliocidaris erythrogramma in response to bacteria from the surface of coralline algae. Oecologia 149:604–619. https://doi.org/10.1007/s00442-006-0470-8
Ituarte RB, Vázquez MG, Bas CC (2019) Chemically induced plasticity in early life history of Palaemon argentinus: Are chemical alarm cues conserved within palaemonid shrimps? J Exp Biol. https://doi.org/10.1242/jeb.199984
Ituarte RB, Vázquez MG, González-Sagrario M de los Á, Spivak ED (2014) Carryover effects of predation risk on postembryonic life-history stages in a freshwater shrimp. Zoology 117:139–145. https://doi.org/10.1016/j.zool.2013.09.004
Jain-Schlaepfer S, Fakan E, Rummer JL, Simpson SD, McCormick MI (2018) Impact of motorboats on fish embryos depends on engine type. Conserv Physiol. https://doi.org/10.1093/conphys/coy014
Jankowski T, Collins AG, Campbell R (2008) Global diversity of inland water cnidarians. In: Balian EV, Lévêque C, Segers H, Martens K (eds) Hydrobiologia. Springer, The Netherlands, pp 35–40
Johnson LE, Strathmann RR (1989) Settling barnacle larvae avoid substrata previously occupied by a mobile predator. J Exp Mar Biol Ecol 128:87–103. https://doi.org/10.1016/0022-0981(89)90094-4
Koehl M, Strother J, Reidenbach M, Koseff J, Hadfield M (2007) Individual-based model of larval transport to coral reefs in turbulent, wave-driven flow: behavioral responses to dissolved settlement inducer. Mar Ecol Prog Ser 335:1–18. https://doi.org/10.3354/meps335001
Koehl MAR, Hadfield MG (2004) Soluble settlement cue in slowly moving water within coral reefs induces larval adhesion to surfaces. J Mar Syst 49:75–88. https://doi.org/10.1016/j.jmarsys.2003.06.003
Koenraadt CJM, Takken W (2003) Cannibalism and predation among larvae of the Anopheles gambiae complex. Med Vet Entomol 17:61–66. https://doi.org/10.1046/j.1365-2915.2003.00409.x
Kotsiri M, Protopapa M, Mouratidis S, Zachariadis M, Vassilakos D, Kleidas I, Samiotaki M, Dedos SG (2018) Should I stay or should I go? The settlement-inducing protein complex guides barnacle settlement decisions. J Exp Biol. https://doi.org/10.1242/jeb.185348
Krug PJ, Manzi AE (1999) Waterborne and surface-associated carbohydrates as settlement cues for larvae of the specialist marine herbivore Alderia modesta. Biol Bull 197:94–103. https://doi.org/10.2307/1543000
Lambert WJ, Todd CD (1994) Evidence for a water-borne cue inducing metamorphosis in the dorid nudibranch mollusc Adalaria proxima (Gastropoda: Nudibranchia). Mar Biol 120:265–271. https://doi.org/10.1007/BF00349687
Lancaster J, Downes BJ (2013) Aquatic entomology. Oxford University Press, United Kingdom
Larson JK, McCormick MI (2005) The role of chemical alarm signals in facilitating learned recognition of novel chemical cues in a coral reef fish. Anim Behav 69:51–57. https://doi.org/10.1016/j.anbehav.2004.04.005
Le Tourneux F, Bourget E (1988) Importance of physical and biological settlement cues used at different spatial scales by the larvae of Semibalanus balanoides. Mar Biol 97:57–66. https://doi.org/10.1007/BF00391245
Lecchini D, Dixson DL, Lecellier G, Roux N, Frédérich B, Besson M, Tanaka Y, Banaigs B, Nakamura Y (2017) Habitat selection by marine larvae in changing chemical environments. Mar Pollut Bull 114:210–217. https://doi.org/10.1016/j.marpolbul.2016.08.083
Lecchini D, Miura T, Lecellier G, Banaigs B, Nakamura Y (2014) Transmission distance of chemical cues from coral habitats: implications for marine larval settlement in context of reef degradation. Mar Biol 161:1677–1686. https://doi.org/10.1007/s00227-014-2451-5
Lecchini D, Osenberg CW, Shima JS, St Mary CM, Galzin R (2007) Ontogenetic changes in habitat selection during settlement in a coral reef fish: ecological determinants and sensory mechanisms. Coral Reefs 26:423–432. https://doi.org/10.1007/s00338-007-0212-3
Lecchini D, Waqalevu VP, Parmentier E, Radford CA, Banaigs B (2013) Fish larvae prefer coral over algal water cues: implications of coral reef degradation. Mar Ecol Prog Ser 475:303–307. https://doi.org/10.3354/meps10094
Leis JM (2006) Are larvae of demersal fishes plankton or nekton? Adv Mar Biol 51:57–141. https://doi.org/10.1016/S0065-2881(06)51002-8
Leis JM (2018) Paradigm lost: ocean acidification will overturn the concept of larval-fish biophysical dispersal. Front Mar Sci. https://doi.org/10.3389/fmars.2018.00047
Leis JM, McCormick MI (2002) The biology, behavior, and ecology of the pelagic, larval stage of coral reef fishes. In: Sale PF (ed) Coral reef fishes: dynamics and diversity in a complex ecosystem. Academic Press, San Diego, pp 171–199
Leis JM, Siebeck U, Dixson DL (2011) How Nemo finds home: the neuroecology of dispersal and of population connectivity in larvae of marine fishes. Integr Comp Biol 51:826–843. https://doi.org/10.1093/icb/icr004
Lema KA, Constancias F, Rice SA, Hadfield MG (2019) High bacterial diversity in nearshore and oceanic biofilms and their influence on larval settlement by Hydroides elegans (Polychaeta). Environ Microbiol 21:3472–3488. https://doi.org/10.1111/1462-2920.14697
Leonard G, Maie T, Moody KN, Schrank GD, Blob RW, Schoenfuss HL (2012) Finding paradise: cues directing the migration of the waterfall climbing Hawaiian gobioid Sicyopterus stimpsoni. J Fish Biol 81:903–920. https://doi.org/10.1111/j.1095-8649.2012.03352.x
Li K, Brant CO, Huertas M, Hessler EJ, Mezei G, Scott AM, Hoye TR, Li W (2018) Fatty-acid derivative acts as a sea lamprey migratory pheromone. Proc Natl Acad Sci 115:8603–8608. https://doi.org/10.1073/pnas.1803169115
Little EE (1975) Chemical communication in maternal behaviour of crayfish. Nature 255:400–401. https://doi.org/10.1038/255400a0
Little EE (1976) Ontogeny of maternal behavior and brood pheromone in crayfish. J Comp Physiol 112:133–142. https://doi.org/10.1007/BF00606533
Lohmann KJ, Lohmann CMF, Endres CS (2008) The sensory ecology of ocean navigation. J Exp Biol 211:1719–1728. https://doi.org/10.1242/jeb.015792
Malinich TD, Pangle K (2018) Swimming responses of larval and juvenile freshwater fishes to nearshore and offshore water sources. Ecol Freshw Fish 27:933–939. https://doi.org/10.1111/eff.12404
Manríquez PH, Castilla JC (2007) Roles of larval behaviour and microhabitat traits in determining spatial aggregations in the ascidian Pyura chilensis. Mar Ecol Prog Ser 332:155–165. https://doi.org/10.3354/meps332155
Manríquez PH, Jara ME, Opitz T, Castilla JC, Lagos NA (2013) Effects of predation risk on survival, behaviour and morphological traits of small juveniles of Concholepas concholepas (loco). Mar Ecol Prog Ser 472:169–183. https://doi.org/10.3354/meps10055
Marinelli RL, Woodin SA (2002) Experimental evidence for linkages between infaunal recruitment, disturbance, and sediment surface chemistry. Limnol Oceanogr 47:221–229. https://doi.org/10.4319/lo.2002.47.1.0221
Massard JA, Geimer G (2008) Global diversity of bryozoans (Bryozoa or Ectoprocta) in freshwater. In: Balian EV, Lévêque C, Segers H, Martens K (eds) Hydrobiologia. Springer, The Netherlands, pp 93–99
Matson PG, Steffen BT, Allen RM (2010) Settlement behavior of cyphonautes larvae of the bryozoan Membranipora membranacea in response to two algal substrata. Invertebr Biol 129:277–283. https://doi.org/10.1111/j.1744-7410.2010.00203.x
Matsumura K, Nagano M, Fusetani N (1998) Purification of a larval settlement-inducing protein complex (SIPC) of the barnacle, Balanus amphitrite. J Exp Zool 281:12–20. https://doi.org/10.1002/(SICI)1097-010X(19980501)281:1%3c12::AID-JEZ3%3e3.0.CO;2-F
McCollum SA, Leimberger JD (1997) Predator-induced morphological changes in an amphibian: predation by dragonflies affects tadpole shape and color. Oecologia 109:615–621. https://doi.org/10.1007/s004420050124
McCrae AWR (1984) Oviposition by African malaria vector mosquitoes: II. Effects of site tone, water type and conspecific immatures on target selection by freshwater Anopheles gambiae Giles, sensu lato. Ann Trop Med Parasitol 78:307–318. https://doi.org/10.1080/00034983.1984.11811821
Merritt RW, Cummins KW (1996) An introduction to the aquatic insects of North America. Kendall Hunt, United States
Meyer K, Wheeler J, Houlihan E, Mullineaux L (2018) Desperate planktotrophs: decreased settlement selectivity with age in competent eastern oyster Crassostrea virginica larvae. Mar Ecol Prog Ser 599:93–106. https://doi.org/10.3354/meps12653
Minchinton T, McKenzie L (2008) Nutrient enrichment affects recruitment of oysters and barnacles in a mangrove forest. Mar Ecol Prog Ser 354:181–189. https://doi.org/10.3354/meps07178
Missbach C, Vogel H, Hansson BS, Große-Wilde E, Vilcinskas A, Kaiser TS (2020) Developmental and sexual divergence in the olfactory system of the marine insect Clunio marinus. Sci Rep 10:2125. https://doi.org/10.1038/s41598-020-59063-7
Mitchell MD, McCormick MI, Ferrari MCO, Chivers DP (2011a) Coral reef fish rapidly learn to identify multiple unknown predators upon recruitment to the reef. PLoS ONE 6:e15764. https://doi.org/10.1371/journal.pone.0015764
Mitchell MD, McCormick MI, Ferrari MCO, Chivers DP (2011b) Friend or foe? The role of latent inhibition in predator and non-predator labelling by coral reef fishes. Anim Cogn 14:707. https://doi.org/10.1007/s10071-011-0405-6
Moore RD, Newton B, Sih A (1996) Delayed hatching as a response of streamside salamander eggs to chemical cues from predatory sunfish. Oikos 77:331–335. https://doi.org/10.2307/3546073
Morello SL, Yund PO (2016) Response of competent blue mussel (Mytilus edulis) larvae to positive and negative settlement cues. J Exp Mar Biol Ecol 480:8–16. https://doi.org/10.1016/j.jembe.2016.03.019
Müller K (1982) The colonization cycle of freshwater insects. Oecologia 52:202–207
Mumby PJ, Steneck RS (2008) Coral reef management and conservation in light of rapidly evolving ecological paradigms. Trends Ecol Evol 23:555–563. https://doi.org/10.1016/j.tree.2008.06.011
Munday PL, Dixson DL, Donelson JM, Jones GP, Pratchett MS, Devitsina GV, Døving KB (2009) Ocean acidification impairs olfactory discrimination and homing ability of a marine fish. Proc Natl Acad Sci 106:1848–1852. https://doi.org/10.1073/pnas.0809996106
Munday PL, Dixson DL, Welch MJ, Chivers DP, Domenici P, Grosell M, Heuer RM, Jones GP, McCormick MI, Meekan M, Nilsson GE, Ravasi T, Watson S-A (2020) Methods matter in repeating ocean acidification studies. Nature 586:E20–E24. https://doi.org/10.1038/s41586-020-2803-x
Munday PL, Welch MJ, Allan BJM, Watson S-A, McMahon SJ, McCormick MI (2016) Effects of elevated CO2 on predator avoidance behaviour by reef fishes is not altered by experimental test water. PeerJ 4:e2501. https://doi.org/10.7717/peerj.2501
Munga S, Minakawa N, Zhou G, Barrack O-OJ, Githeko AK, Yan G (2006) Effects of larval competitors and predators on oviposition site selection of Anopheles gambiae sensu stricto. J Med Entomol 43:221–224. https://doi.org/10.1093/jmedent/43.2.221
Negri A, Webster N, Hill R, Heyward A (2001) Metamorphosis of broadcast spawning corals in response to bacteria isolated from crustose algae. Mar Ecol Prog Ser 223:121–131. https://doi.org/10.3354/meps223121
Nishizaki MT, Ackerman JD (2005) A secondary chemical cue facilitates juvenile-adult postsettlement associations in red sea urchins. Limnol Oceanogr 50:354–362. https://doi.org/10.4319/lo.2005.50.1.0354
Nunes AL, Richter-Boix A, Laurila A, Rebelo R (2013) Do anuran larvae respond behaviourally to chemical cues from an invasive crayfish predator? A community-wide study. Oecologia 171:115–127. https://doi.org/10.1007/s00442-012-2389-6
O’Connor JJ, Lecchini D, Beck HJ, Cadiou G, Lecellier G, Booth DJ, Nakamura Y (2016) Sediment pollution impacts sensory ability and performance of settling coral-reef fish. Oecologia 180:11–21. https://doi.org/10.1007/s00442-015-3367-6
O’Connor NJ, Gregg AS (1998) Influence of potential habitat cues on duration of the megalopal stage of the fiddler crab Uca pugnax. J Crustac Biol 18:700–709
O’Connor NJ, Judge ML (1999) Cues in salt marshes stimulate molting of fiddler crab Uca pugnax megalopae: more evidence from field experiments. Mar Ecol Prog Ser 181:131–139. https://doi.org/10.3354/meps181131
Olsen K, Sneed JM, Paul VJ (2016) Differential larval settlement responses of Porites astreoides and Acropora palmata in the presence of the green alga Halimeda opuntia. Coral Reefs 35:521–525. https://doi.org/10.1007/s00338-015-1394-8
Olson RR (1985) The consequences of short-distance larval dispersal in a sessile marine invertebrate. Ecology 66:30–39. https://doi.org/10.2307/1941304
Pasternak Z, Blasius B, Abelson A (2004a) Host location by larvae of a parasitic barnacle: larval chemotaxis and plume tracking in flow. J Plankton Res 26:487–493. https://doi.org/10.1093/plankt/fbh040
Pasternak Z, Blasius B, Achituv Y, Abelson A (2004b) Host location in flow by larvae of the symbiotic barnacle Trevathana dentata using odour–gated rheotaxis. Proc R Soc Lond B 271:1745–1750. https://doi.org/10.1098/rspb.2004.2765
Pawlik JR (1992) Chemical ecology of the settlement of benthic marine invertebrates. Oceanogr Mar Biol Annu Rev 30:273–335
Pawlik JR (1988) Larval settlement and metamorphosis of sabellariid polychaetes, with special reference to Phragmatopoma lapidosa, a reef-building species, and Sabellaria floridensis, a non-gregarious species. Bull Mar Sci 43:41–60
Pawlik JR, Faulkner DJ (1986) Specific free fatty acids induce larval settlement and metamorphosis of the reef-building tube worm Phragmatopoma californica (Fewkes). J Exp Mar Biol Ecol 102:301–310. https://doi.org/10.1016/0022-0981(86)90183-8
Pawlik JR, Hadfield MG (1990) A symposium on chemical factors that incluence the settlement and metamorphosis of marine invertebrate larvae: introduction and perspective. Bull Mar Sci 46:450–454
Petersen JH (1984) Larval settlement behavior in competing species: Mytilus californianus Conrad and M. edulis L. J Exp Mar Biol Ecol 82:147–159. https://doi.org/10.1016/0022-0981(84)90100-X
Pinceel T, Buschke F, Weckx M, Brendonck L, Vanschoenwinkel B (2018) Climate change jeopardizes the persistence of freshwater zooplankton by reducing both habitat suitability and demographic resilience. BMC Ecol 18:2. https://doi.org/10.1186/s12898-018-0158-z
Pires A, Hadfield MG (1993) Responses of isolated vela of nudibranch larvae to inducers of metamorphosis. J Exp Zool 266:234–239. https://doi.org/10.1002/jez.1402660310
Pistevos JCA, Nagelkerken I, Rossi T, Connell SD (2017) Ocean acidification alters temperature and salinity preferences in larval fish. Oecologia 183:545–553. https://doi.org/10.1007/s00442-016-3778-z
Prince DJ, Saglam IK, Hotaling TJ, Spidle AP, Miller MR (2017) The evolutionary basis of premature migration in Pacific salmon highlights the utility of genomics for informing conservation. Sci Adv 3:e1603198. https://doi.org/10.1126/sciadv.1603198
Pronzato R, Manconi R (1994) Adaptive strategies of sponges in inland waters. Bollettino Di Zoologia 61:395–401. https://doi.org/10.1080/11250009409355912
Pruett J, Weissburg M (2019) Eastern oysters use predation risk cues in larval settlement decisions and juvenile inducible morphological defenses. Mar Ecol Prog Ser 621:83–94. https://doi.org/10.3354/meps12998
Qian P-Y (1999) Larval settlement of polychaetes. In: Dorresteijn AWC, Westheide W (eds) Reproductive strategies and developmental patterns in annelids. Springer, Netherlands, Dordrecht, pp 239–253
Rao D, Webb JS, Holmström C, Case R, Low A, Steinberg P, Kjelleberg S (2007) Low densities of epiphytic bacteria from the marine alga Ulva australis inhibit settlement of fouling organisms. AEM 73:7844–7852. https://doi.org/10.1128/AEM.01543-07
Relyea RA (2001) Morphological and behavioral plasticity of larval anurans in response to different predators. Ecology 82:523–540. https://doi.org/10.1890/0012-9658(2001)082[0523:MABPOL]2.0.CO;2
Relyea RA (2007) Getting out alive: how predators affect the decision to metamorphose. Oecologia 152:389–400. https://doi.org/10.1007/s00442-007-0675-5
Rengefors K, Karlsson I, Hansson L-A (1998) Algal cyst dormancy: a temporal escape from herbivory. Proc Royal Soc B Biol Sci 265:1353–1358. https://doi.org/10.1098/rspb.1998.0441
Rodríguez A, Cuesta JA (2011) Morphology of larval and first juvenile stages of the kangaroo shrimp Dugastella valentina (Crustacea, Decapoda, Caridea), a freshwater atyid with abbreviated development and parental care. Zootaxa 2867:43. https://doi.org/10.11646/zootaxa.2867.1.3
Roe AW, Grayson KL (2008) Terrestrial movements and habitat use of juvenile and emigrating adult Eastern Red-Spotted Newts, Notophthalmus viridescens. J Herpetol 42:22–30. https://doi.org/10.1670/07-040.1
Rothfuss AH, Heilveil JS (2018) Distribution of Sisyridae and freshwater sponges in the upper-Susquehanna watershed, Otsego County, New York with a new locality for Climacia areolaris (Hagen). Am Midl Nat 180:298–305. https://doi.org/10.1674/0003-0031-180.2.298
Schindler DE, Hilborn R, Chasco B, Boatright CP, Quinn TP, Rogers LA, Webster MS (2010) Population diversity and the portfolio effect in an exploited species. Nature 465:609–612. https://doi.org/10.1038/nature09060
Schmitt TM, Hay ME, Lindquist N (1995) Constraints on chemically mediated coevolution: multiple functions for seaweed secondary metabolites. Ecology 76:107–123. https://doi.org/10.2307/1940635
Schmitt TM, Lindquist N, Hay ME (1998) Seaweed secondary metabolites as antifoulants: effects of Dictyota spp. diterpenes on survivorship, settlement, and development of marine invertebrate larvae. Chemoecology 8:125–131. https://doi.org/10.1007/s000490050017
Schockaert ER, Hooge M, Sluys R, Schilling S, Tyler S, Artois T (2008) Global diversity of free living flatworms (Platyhelminthes, ‘“Turbellaria”’) in freshwater. In: Balian EV, Lévêque C, Segers H, Martens K (eds) Hydrobiologia. Springer, The Netherlands, pp 41–48
Schulte LM, Yeager J, Schulte R, Veith M, Werner P, Beck LA, Lötters S (2011) The smell of success: choice of larval rearing sites by means of chemical cues in a Peruvian poison frog. Anim Behav 81:1147–1154. https://doi.org/10.1016/j.anbehav.2011.02.019
Scott A, Dixson DL (2016) Reef fishes can recognize bleached habitat during settlement: sea anemone bleaching alters anemonefish host selection. Proc Royal Soc B Biol Sci 283:20152694. https://doi.org/10.1098/rspb.2015.2694
Sebesvari Z, Neumann R, Brinkhoff T, Harder T (2013) Single-species bacteria in sediments induce larval settlement of the infaunal polychaetes Polydora cornuta and Streblospio benedicti. Mar Biol 160:1259–1270. https://doi.org/10.1007/s00227-013-2178-8
Segev O, Verster R, Weldon C (2017) Testing the link between perceived and actual risk of predation: mosquito oviposition site selection and egg predation by native and introduced fish. J Appl Ecol 54:854–861. https://doi.org/10.1111/1365-2664.12789
Shanks AL (2009) Pelagic larval duration and dispersal distance revisited. Biol Bull 216:373–385. https://doi.org/10.1086/BBLv216n3p373
Shanks AL, Grantham BA, Carr MH (2003) Propagule dispersal distance and the size and spacing of marine reserves. Ecol Appl 13:159–169. https://doi.org/10.1890/1051-0761(2003)013[0159:PDDATS]2.0.CO;2
Silberbush A, Blaustein L (2008) Oviposition habitat selection by a mosquito in response to a predator: Are predator-released kairomones air-borne cues? J Vector Ecol 33:208–211. https://doi.org/10.3376/1081-1710(2008)33[208:OHSBAM]2.0.CO;2
Simith D de J de B, Abrunhosa FA, Diele K (2017) Metamorphosis of the edible mangrove crab Ucides cordatus (Ucididae) in response to benthic microbial biofilms. J Exp Marine Biol Ecol 492:132–140. https://doi.org/10.1016/j.jembe.2017.01.022
Simpson S, Yan H, Wittenrich M, Meekan M (2005) Response of embryonic coral reef fishes (Pomacentridae: Amphiprion spp.) to noise. Mar Ecol Prog Ser 287:201–208. https://doi.org/10.3354/meps287201
Slattery M, Hines GA, Starmer J, Paul VJ (1999) Chemical signals in gametogenesis, spawning, and larval settlement and defense of the soft coral Sinularia polydactyla. Coral Reefs 18:75–84. https://doi.org/10.1007/s003380050158
Snell TW (1998) Chemical ecology of rotifers. Hydrobiologia 387:267–276. https://doi.org/10.1023/A:1017087003334
Stav G, Blaustein L, Margalith J (1999) Experimental evidence for predation risk sensitive oviposition by a mosquito, Culiseta longiareolata. Ecol Entomol 24:202–207. https://doi.org/10.1046/j.1365-2311.1999.00183.x
Stoner DS (1994) Larvae of a colonial ascidian use a non-contact mode of substratum selection on a coral reef. Mar Biol 121:319–326. https://doi.org/10.1007/BF00346740
Swanson R, de Nys R, Huggett M, Green J, Steinberg P (2006) In situ quantification of a natural settlement cue and recruitment of the Australian sea urchin Holopneustes purpurascens. Mar Ecol Prog Ser 314:1–14. https://doi.org/10.3354/meps314001
Swanson RL, Byrne M, Prowse TAA, Mos B, Dworjanyn SA, Steinberg PD (2012) Dissolved histamine: a potential habitat marker promoting settlement and metamorphosis in sea urchin larvae. Mar Biol 159:915–925. https://doi.org/10.1007/s00227-011-1869-2
Swanson RL, Williamson JE, De Nys R, Kumar N, Bucknall MP, Steinberg PD (2004) Induction of settlement of larvae of the sea urchin Holopneustes purpurascens by histamine from a host alga. Biol Bull 206:161–172. https://doi.org/10.2307/1543640
Tamburri MN, Luckenbach MW, Breitburg DL, Bonniwell SM (2008) Settlement of Crassostrea ariakensis larvae: Effects of substrate, biofilms, sediment and adult chemical cues. J Shellfish Res 27:601–608. https://doi.org/10.2983/0730-8000(2008)27[601:SOCALE]2.0.CO;2
Tapia-Lewin S, Pardo LM (2014) Field assessment of the predation risk - food availability trade-off in crab megalopae settlement. PLoS ONE 9:e95335. https://doi.org/10.1371/journal.pone.0095335
Taris N, Comtet T, Stolba R, Lasbleiz R, Pechenik JA, Viard F (2010) Experimental induction of larval metamorphosis by a naturally-produced halogenated compound (dibromomethane) in the invasive mollusc Crepidula fornicata (L.). J Exp Mar Biol Ecol 393:71–77. https://doi.org/10.1016/j.jembe.2010.07.001
Tebben J, Motti CA, Siboni N, Tapiolas DM, Negri AP, Schupp PJ, Kitamura M, Hatta M, Steinberg PD, Harder T (2015) Chemical mediation of coral larval settlement by crustose coralline algae. Sci Rep 5:10803. https://doi.org/10.1038/srep10803
Tebben J, Tapiolas DM, Motti CA, Abrego D, Negri AP, Blackall LL, Steinberg PD, Harder T (2011) Induction of larval metamorphosis of the coral Acropora millepora by tetrabromopyrrole isolated from a Pseudoalteromonas bacterium. PLoS ONE 6:e19082. https://doi.org/10.1371/journal.pone.0019082
Toth G, Lindeborg M (2008) Water-soluble compounds from the breadcrumb sponge Halichondria panicea deter attachment of the barnacle Balanus improvisus. Mar Ecol Prog Ser 354:125–132. https://doi.org/10.3354/meps07275
Toth GB, Larsson AI, Jonsson PR, Appelqvist C (2015) Natural populations of shipworm larvae are attracted to wood by waterborne chemical cues. PLoS ONE 10:e0124950. https://doi.org/10.1371/journal.pone.0124950
Toth GB, Norén F, Selander E, Pavia H (2004) Marine dinoflagellates show induced life-history shifts to escape parasite infection in response to water–borne signals. Proc R Soc Lond B 271:733–738. https://doi.org/10.1098/rspb.2003.2654
Turner B, Trekels H, Vandromme M, Vanschoenwinkel B (2020) Prey colonization in freshwater landscapes can be stimulated or inhibited by the proximity of remote predators. J Anim Ecol 89:1766–1774. https://doi.org/10.1111/1365-2656.13239
Uno H, Power ME (2015) Mainstem-tributary linkages by mayfly migration help sustain salmonids in a warming river network. Ecol Lett 18:1012–1020. https://doi.org/10.1111/ele.12483
Vogt G (2013) Abbreviation of larval development and extension of brood care as key features of the evolution of freshwater Decapoda. Biol Rev 88:81–116. https://doi.org/10.1111/j.1469-185X.2012.00241.x
Voight JR (2007) Experimental deep-sea deployments reveal diverse Northeast Pacific wood-boring bivalves of Xylophagainae (Myoida: Pholadidae). J Molluscan Stud 73:377–391. https://doi.org/10.1093/mollus/eym034
Waldman J, Grunwald C, Wirgin I (2008) Sea lamprey Petromyzon marinus: an exception to the rule of homing in anadromous fishes. Biol Lett 4:659–662. https://doi.org/10.1098/rsbl.2008.0341
Wallace RL, Edmondson WT (1986) Mechanism and adaptive significance of substrate selection by a sessile rotifer. Ecology 67:314–323. https://doi.org/10.2307/1938575
Walsh EJ (1989) Oviposition behavior of the littoral rotifer Euchlanis dilatata. Hydrobiologia 186:157–161. https://doi.org/10.1007/BF00048908
Webster NS, Smith LD, Heyward AJ, Watts JEM, Webb RI, Blackall LL, Negri AP (2004) Metamorphosis of a scleractinian coral in response to microbial biofilms. Appl Environ Microbiol 70:1213–1221. https://doi.org/10.1128/AEM.70.2.1213-1221.2004
Weersing K, Toonen R (2009) Population genetics, larval dispersal, and connectivity in marine systems. Mar Ecol Prog Ser 393:1–12. https://doi.org/10.3354/meps08287
Welch J, Rittschof D, Bullock T, Forward R Jr (1997) Effects of chemical cues on settlement behavior of blue crab Callinectes sapidus postlarvae. Mar Ecol Prog Ser 154:143–153. https://doi.org/10.3354/meps154143
Wenger AS, McCormick MI, McLeod IM, Jones GP (2013) Suspended sediment alters predator–prey interactions between two coral reef fishes. Coral Reefs 32:369–374. https://doi.org/10.1007/s00338-012-0991-z
Whalan S, Webster NS, Negri AP (2012) Crustose coralline algae and a cnidarian neuropeptide trigger larval settlement in two coral reef sponges. PLoS ONE 7:e30386. https://doi.org/10.1371/journal.pone.0030386
Wheeler JD, Chan KYK, Anderson EJ, Mullineaux LS (2016) Ontogenetic changes in larval swimming and orientation of pre-competent sea urchin Arbacia punctulata in turbulence. J Exp Biol 219:1303–1310. https://doi.org/10.1242/jeb.129502
Whitear AK, Wang X, Catling P, McLennan DA, Davy CM (2016) The scent of a hatchling: intra-species variation in the use of chemosensory cues by neonate freshwater turtles. Biol J Lin Soc. https://doi.org/10.1111/bij.12855
Williams DD, Hynes HBN (1976) The recolonization mechanisms of stream benthos. Oikos 27:265–272. https://doi.org/10.2307/3543905
Williamson JE, De Nys R, Kumar N, Carson DG, Steinberg PD (2000) Induction of metamorphosis in the sea urchin Holopneustes purpurascens by a metabolite complex from the algal host Delisea pulchra. Biol Bull 198:332–345. https://doi.org/10.2307/1542689
Woodin SA, Marinelli RL, Lincoln DE (1993) Allelochemical inhibition of recruitment in a sedimentary assemblage. J Chem Ecol 19:517–530. https://doi.org/10.1007/BF00994322
Woodin SA, Marinelli RL, Lindsay SM (1998) Process-specific cues for recruitment in sedimentary environments: Geochemical signals? J Mar Res 56:535–558. https://doi.org/10.1357/002224098321822410
Wright J, Boxshall A (1999) The influence of small-scale flow and chemical cues on the settlement of two congeneric barnacle species. Mar Ecol Prog Ser 183:179–187. https://doi.org/10.3354/meps183179
Yonge CM (1937) The biology of Aporrhais pes-pelecani (L) and A. serresiana (Mich.). J Mar Biol Assoc UK 21:687–703
Young CM, Chia F-S (1981) Laboratory evidence for delay of larval settlement in response to a dominant competitor. Int J Invertebr Reprod 3:221–226. https://doi.org/10.1080/01651269.1981.10553397
Acknowledgements
Financial support came from the US National Science Foundation (grant no. OCE 1947522) and the Anna and Harry Teasley Gift Fund. We thank Alicia Caughman for aiding the literature search and Nolan Barrett, Emily Brown, and Bhuwan Chhetri for help with chemical structures.
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Support was provided by the Anna and Harry Teasley Gift Fund to the Georgia Institute of Technology and by NSF-OCE 1947522.
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Bilodeau, S.M., Hay, M.E. Chemical cues affecting recruitment and juvenile habitat selection in marine versus freshwater systems. Aquat Ecol 56, 339–360 (2022). https://doi.org/10.1007/s10452-021-09905-x
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DOI: https://doi.org/10.1007/s10452-021-09905-x