Response of true limpet Patella aspera (Patellogastropoda) pediveliger larvae to a range of settlement cues
Diego Castejón A B * , Loreto García A , Natacha Nogueira A B and Carlos A. P. Andrade CA
B
C
Marine and Freshwater Research 74(15) 1296-1313 https://doi.org/10.1071/MF22270
Submitted: 22 December 2022 Accepted: 28 August 2023 Published: 18 September 2023
Abstract
Settlement and metamorphosis are key processes influencing the natural recruitment and aquaculture production of aquatic organisms. Recruitment requirements in limpets (Patellogastropoda) are mostly unknown, because of the lack of reliable settlement inducers.
This study tested the reliability of different cues as settlement inducers for competent larvae of the economically valuable Patella aspera.
Natural crustose coralline algae (CCA) and biofilms of the benthic diatom Navicula salinicola were tested as positive controls. The following four pharmacological agents were tested as chemical inducers in a wide range of concentrations: gamma-aminobutyric acid (GABA), acetylcholine (ACH), 3-isobutyl-1-methylxanthine (IBMX) and potassium chloride (KCl). Settlers were identified by the velum loss and teleoconch development.
CCA were strong settlement cues in all the assays. Contrary to previous hypotheses, GABA was a weak inducer with a peak effect at 10−5 M. Neither the diatom biofilms nor the other pharmacological agents (ACH, IBMX and KCl) promoted the settlement response. All pharmacological agents at high concentrations influenced larval behaviour.
CCA were reliable positive controls and settlement inducers for the production of post-larvae. With regard to pharmacological agents, P. aspera showed restrictive settlement requirements that should be considered for ecological and aquaculture studies in other limpet species.
This method allows the study of the settlement biology of limpets. It provides a positive control and integrates animal monitoring and comparative response to other cues.
Keywords: algae, aquaculture, benthos, biofouling, larval biology, molluscs, post-larval production, recruitment.
References
Alfaro AC, Young T, Ganesan AM (2011) Regulatory effects of mussel (Aulacomya maoriana Iredale, 1915) larval settlement by neuroactive compounds, amino acids and bacterial biofilms. Aquaculture 322–323, 158-168.
| Crossref | Google Scholar |
Alfaro AC, Young T, Bowden K (2014) Neurophysiological control of swimming behaviour, attachment and metamorphosis in black-footed abalone (Haliotis iris) larvae. New Zealand Journal of Marine and Freshwater Research 48(3), 314-334.
| Crossref | Google Scholar |
Barlow LA (1990) Electrophysiological and behavioral responses of larvae of the red abalone (Haliotis rufescens) to settlement-inducing substances. Bulletin of Marine Science 46(2), 537-554.
| Google Scholar |
Bouzaza Z, Mezali K (2019) On the presence of Cymbula safiana (Gastropoda: Patellidae) on the Algerian coast (SW Mediterranean): population structure and new record stations. Ecologia Mediterranea 45(1), 5-13.
| Crossref | Google Scholar |
Branch GM, Odendaal F (2003) The effects of marine protected areas on the population dynamics of a South African limpet, Cymbula oculus, relative to the influence of wave action. Biological Conservation 114(2), 255-269.
| Crossref | Google Scholar |
Bryan PJ, Qian P-Y (1998) Induction of larval attachment and metamorphosis in the abalone Haliotis diversicolor (Reeve). Journal of Experimental Marine Biology and Ecology 223(1), 39-51.
| Crossref | Google Scholar |
Campos EO, Pinto A, Bustos E, Rodriguez SR, Inestrosa NC (1994) Metamorphosis of laboratory-reared larvae of Concholepas concholepas (Mollusca; Gastropoda). Aquaculture 126(3), 299-303.
| Crossref | Google Scholar |
Carballo JL, Yáñez B, Bautista-Guerrero E, García-Gómez JC, Espinosa F, Tortolero-Langarica JJA, Michel-Morfín JE (2020) Decimation of a population of the endangered species Scutellastra mexicana (Broderip & Sowerby, 1829) (Mollusca, Gastropoda) in the Marías Island (Eastern Ocean Pacific) Biosphere Reserve. Aquatic Conservation: Marine and Freshwater Ecosystems 30(1), 20-30.
| Crossref | Google Scholar |
Cascales-Soler A, Ramos-Espla AA, Forcada A (2023) Reviewing the knowledge on the genus Patella in the Mediterranean Sea: testing the effect of protection on the mean abundance and size of Patella ferruginea. Frontiers in Marine Science 10, 1158470.
| Crossref | Google Scholar |
Castejón D, Nogueira N, Andrade CAP (2021a) Limpet larvae (Patella aspera Röding, 1798), obtained by gonad dissection and fecundation in vitro, settled and metamorphosed on crustose coralline algae. Journal of the Marine Biological Association of the United Kingdom 101(7), 991-1002.
| Crossref | Google Scholar |
Castejón D, Cañizares JM, Nogueira N, Andrade CAP (2021b) Artificial maturation and larval production of the limpet Patella aspera Röding, 1798 (Patellogastropoda, Mollusca): enhancing fertilization success of oocytes using NAOH-alkalinized seawater. Aquaculture Research 52(5), 1904-1914.
| Crossref | Google Scholar |
Castejón D, García L, Cañizares JM, De Girolamo M, Nunes C, Isidro E, Courtois de Viçose G, Nogueira N, Andrade CAP (2022) Methodologies for patellid limpets’ aquaculture: from broodstock management to juveniles. Frontiers in Marine Science 9, 884262.
| Crossref | Google Scholar |
Castejón D, García L, Nogueira N, Andrade CAP (2023) Improving efficiency of methods for hatchery production of the limpet Patella candei (Patellogastropoda: Patellidae). Journal of the World Aquaculture Society 54(4), 945-964.
| Crossref | Google Scholar |
Cañizares JM, Castejón D, Haroun R, Nogueira N, Andrade CAP (2021) Enhancing oocyte maturation and fertilisation in the black-foot limpet Patella candei d’Orbigny, 1840 (Patellidae, Mollusca). Aquaculture Reports 21, 100856.
| Crossref | Google Scholar |
Colonese AC, Mannino MA, Bar-Yosef Mayer DE, Fa DA, Finlayson JC, Lubell D, Stiner MC (2011) Marine mollusc exploitation in Mediterranean prehistory: an overview. Quaternary International 239(1–2), 86-103.
| Crossref | Google Scholar |
Courtois De Vicose G, Viera M, Bilbao A, Izquierdo M (2010) Larval settlement of Haliotis tuberculata coccinea in response to different inductive cues and the effect of larval density on settlement, early growth, and survival. Journal of Shellfish Research 29(3), 587-591.
| Crossref | Google Scholar |
Courtois de Vicose G, Viera MP, Huchette S, Izquierdo MS (2012) Larval settlement, early growth and survival of Haliotis tuberculata coccinea using several algal cues. Journal of Shellfish Research 31(4), 1189-1198.
| Crossref | Google Scholar |
Daume S, Brand-Gardner S, Woelkerling WJ (1999a) Settlement of abalone larvae (Haliotis laevigata Donovan) in response to non-geniculate coralline red algae (Corallinales, Rhodophyta). Journal of Experimental Marine Biology and Ecology 234(1), 125-143.
| Crossref | Google Scholar |
Daume S, Brand-Gardner S, Woelkerling WJ (1999b) Preferential settlement of abalone larvae: diatom films vs. non-geniculate coralline red algae. Aquaculture 174(3), 243-254.
| Crossref | Google Scholar |
Dobretsov SV, Qian P-Y (2003) Pharmacological induction of larval settlement and metamorphosis in the blue mussel Mytilus edulis L. Biofouling 19(1), 57-63.
| Crossref | Google Scholar | PubMed |
Dodd JM (1957) Artificial fertilisation, larval development and metamorphosis in Patella vulgata L. and Patella caerulea L. Pubblicazioni della Stazione Zoologica di Napoli 29, 172-185.
| Google Scholar |
Espinosa F, Rivera-Ingraham GA, Maestre M, González AR, Bazairi H, García-Gómez JC (2014) Updated global distribution of the threatened marine limpet Patella ferruginea (Gastropoda: Patellidae): an example of biodiversity loss in the Mediterranean. Oryx 48(2), 266-275.
| Crossref | Google Scholar |
Espinosa F, Rivera-Ingraham GA (2017) Chapter three – Biological conservation of giant limpets: the implications of large size. In ‘Advances in marine biology, vol. 76’. (Ed. BE Curry) pp. 105–156. (Academic Press) doi:10.1016/bs.amb.2016.10.002
Espinosa F, Maestre M, García-Gómez JC, Cotaina-Castro MI, Pitarch-Moreno C, Paramio JM, Fort-Santa María P, García-Estévez N (2023) Joining technology and biology to solve conservation problems through translocation in the endangered limpet Patella ferruginea. Frontiers in Marine Science 10, 1100194.
| Crossref | Google Scholar |
Faria J, Pita A, Martins GM, Ribeiro PA, Hawkins SJ, Presa P, Neto AI (2018) Inbreeding in the exploited limpet Patella aspera across the Macaronesia archipelagos (NE Atlantic): implications for conservation. Fisheries Research 198, 180-188.
| Crossref | Google Scholar |
Ferranti MP, Monteggia D, Asnaghi V, Chiantore M (2018) Artificial reproduction protocol, from spawning to metamorphosis, through noninvasive methods in Patella caerulea Linnaeus, 1758. Aquaculture Research 49(10), 3386-3391.
| Crossref | Google Scholar |
Ferranti MP, Monteggia D, Asnaghi V, Dagnino A, Gaino F, Moretto P, Parodi V, Tixi L, Cappanera V, Valerani C, Bava S, Chiantore M (2019) Distribution of the Mediterranean ribbed limpet Patella ferruginea Gmelin, 1791 along the Ligurian coast and implications for conservation actions. Mediterranean Marine Science 20(3), 496-501.
| Crossref | Google Scholar |
Ferranti MP, Guallart J, Fanciulli G, Panzalis PA, Chiantore M (2022) Advancements towards restoration of the endangered limpet Patella ferruginea Gmelin, 1791 through controlled reproduction. Aquaculture Research 53(3), 782-798.
| Crossref | Google Scholar |
Ferranti MP, Guallart J, Asnaghi V, Chiantore M (2023) Update on the current distribution of Patella ferruginea Gmelin, 1791 (Mollusca, Gastropoda) along the Italian coasts. Biologia Marina Mediterranea 27(1), 141-144.
| Google Scholar |
Ferraz RR, Menezes GM, Santos RS (2001) Limpet (Patella spp.) (Mollusca: Gastropoda) exploitation in the Azores, during the period 1993–1998. Arquipélago Life and Marine Sciences 2001(Suppl. 2, Part B), 59-65.
| Google Scholar |
Firth LB (2021) What have limpets ever done for us? On the past and present provisioning and cultural services of limpets. International Review of Environmental History 7(2), 5-45.
| Crossref | Google Scholar |
Gapasin RSJ, Polohan BB (2004) Induction of larval settlement and metamorphosis in the donkey-ear abalone, Haliotis asinina Linnaeus, by chemical cues. Hydrobiologia 519(1), 9-17.
| Crossref | Google Scholar |
Guallart J, Ferranti MP, Bacigalupo L, Chiantore M (2020a) In vivo magnetic resonance imaging to assess the sexual maturity of the endangered limpet Patella ferruginea. Journal of Molluscan Studies 86(4), 422-426.
| Crossref | Google Scholar |
Guallart J, Peña J, Pérez-Larruscaín J, Luque Á, Templado J (2020b) Filling gaps: closing the life cycle of the endangered Mediterranean limpet Patella ferruginea Gmelin, 1791 (Gastropoda, Patellidae). Mediterranean Marine Science 21(2), 400-419.
| Google Scholar |
Hadfield MG (2011) Biofilms and marine invertebrate larvae: what bacteria produce that larvae use to choose settlement sites. Annual Review of Marine Science 3(1), 453-470.
| Crossref | Google Scholar |
Hadfield MG, Paul VJ (2001) Natural chemical cues for settlement and metamorphosis of marine invertebrate larvae. Marine Chemical Ecology 13, 431-461.
| Google Scholar |
Inestrosa NC, Gonzalez M, Campos EO (1992) Metamorfosis de larvas planctonicas de Concholepas concholepas (‘loco’) (Mollusca, Gastropoda, Muricidae). [Metamorphosis of planktonic larvae of Concholepas concholepas (‘loco’) (Mollusca, Gastropoda, Muricidae).]. Revista de Biología Marina y Oceanografía 27(2), 249-263 [In Spanish].
| Google Scholar |
Kay M (2002) Recruitment in the intertidal limpet Lottia digitalis (Patellogastropoda: Lottiidae) may be driven by settlement cues associated with adult habitat. Marine Biology 141(3), 467-477.
| Crossref | Google Scholar |
Kay MC, Emlet RB (2002) Laboratory spawning, larval development, and metamorphosis of the limpets Lottia digitalis and Lottia asmi (Patellogastropoda, Lottiidae). Invertebrate Biology 121(1), 11-24.
| Crossref | Google Scholar |
Klein RG (1979) Stone Age Exploitation of Animals in Southern Africa: Middle Stone Age people living in southern Africa more than 30,000 years ago exploited local animals less effectively than the Later Stone Age people who succeeded them. American Scientist 67(2), 151-160.
| Google Scholar |
Lasiak T (1993a) The shellfish-gathering practices of indigenous coastal people in transkei: patterns, preferences and perceptions. South African Journal of Ethnology 16(4), 115-120.
| Google Scholar |
Lasiak T (1993b) Temporal and spatial variations in exploited and non-exploited populations of the intertidal limpet Cellana capensis. Journal of Molluscan Studies 59(3), 295-307.
| Crossref | Google Scholar |
Li H, Wei L, Zhang G, Cai Z, Cai G, Chang Y, Xing K (2006) Enhancement of larval settlement and metamorphosis through biological and chemical cues in the abalone Haliotis diversicolor supertexta. Aquaculture 258(1), 416-423.
| Crossref | Google Scholar |
Lozano-Bilbao E, Herranz I, González-Lorenzo G, Lozano G, Hardisson A, Rubio C, González-Weller D, Paz S, Gutiérrez ÁJ (2021) Limpets as bioindicators of element pollution in the coasts of Tenerife (Canary Islands). Environmental Science and Pollution Research 28(31), 42999-43006.
| Crossref | Google Scholar | PubMed |
López C, Poladura A, Hernández JC, Martín L, Concepción L, Sangil C, Clemente S (2012) Contrasting effects of protection from harvesting in populations of two limpet species in a recently established marine protected area. Scientia Marina 76(4), 799-807.
| Google Scholar |
Martins GM, Jenkins SR, Hawkins SJ, Neto AI, Medeiros AR, Thompson RC (2011) Illegal harvesting affects the success of fishing closure areas. Journal of the Marine Biological Association of the United Kingdom 91(4), 929-937.
| Crossref | Google Scholar |
Martins GM, Faria J, Furtado M, Neto AI (2014) Shells of Patella aspera as ‘islands’ for epibionts. Journal of the Marine Biological Association of the United Kingdom 94(5), 1027-1032.
| Crossref | Google Scholar |
Martins GM, Borges CDG, Vale M, Ribeiro PA, Ferraz RR, Martins HR, Santos RS, Hawkins SJ (2017) Exploitation promotes earlier sex change in a protandrous patellid limpet, Patella aspera Röding, 1798. Ecology and Evolution 7(10), 3616-3622.
| Crossref | Google Scholar | PubMed |
Mau A, Jha R (2018a) Aquaculture of two commercially important molluscs (abalone and limpet): existing knowledge and future prospects. Reviews in Aquaculture 10(3), 611-625.
| Crossref | Google Scholar |
Mau A, Jha R (2018b) Effects of dietary protein to energy ratios on growth performance of yellowfoot limpet (Cellana sandwicensis Pease, 1861). Aquaculture Reports 10, 17-22.
| Crossref | Google Scholar |
McCoy MD (2008) Hawaiian limpet harvesting in historical perspective: a review of modern and archaeological data on Cellana spp. from the Kalaupapa Peninsula, Moloka‘i Island. Pacific Science 62(1), 21-38.
| Crossref | Google Scholar |
McCoy SJ, Kamenos NA (2015) Coralline algae (Rhodophyta) in a changing world: integrating ecological, physiological, and geochemical responses to global change. Journal of Phycology 51(1), 6-24.
| Crossref | Google Scholar | PubMed |
Mesías-Gansbiller C, Silva A, Maneiro V, Pazos A, Sánchez JL, Pérez-Parallé ML (2013) Effects of chemical cues on larval settlement of the flat oyster (Ostrea edulis L.): a hatchery approach. Aquaculture 376-379, 85-89.
| Crossref | Google Scholar |
Moss GA (1999) Factors affecting settlement and early post-settlement survival of the New Zealand abalone Haliotis australis. New Zealand Journal of Marine and Freshwater Research 33(2), 271-278.
| Crossref | Google Scholar |
Muñoz-Colmenero M, Turrero P, Horreo JL, Garcia-Vazquez E (2012) Evolution of limpet assemblages driven by environmental changes and harvesting in North Iberia. Marine Ecology Progress Series 466, 121-131.
| Crossref | Google Scholar |
Nakano T, Nakayama R, Takahashi Y (2020) Artificial fertilisation and early development of a limpet Lottia tenuisculpta (Patellogastropoda: Lottiidae). Molluscan Research 40(1), 52-59.
| Crossref | Google Scholar |
Nhan HT, Ako H (2014) Reproductive biology and effect of arachidonic acid level in broodstock diet on final maturation of the Hawaiian limpet Cellana sandwicensis. Journal of Aquaculture Research & Development 5(5), 256-264.
| Google Scholar |
Nhan HT, Ako H (2016) Dietary protein and carbohydrate requirement of juvenile Hawaiian limpet (Cellana sandwicensis Pease, 1861) fed practical diet. International Aquatic Research 8, 323-332.
| Crossref | Google Scholar |
Nhan HT, Ako H (2019) Reproductive biology, seed production, and culture of the Hawaiian limpet Cellana sandwicensis (Pease, 1861). Invertebrates Ecophysiology and Management 1-19.
| Google Scholar |
Nunes C, Ramirez A, Rodeia J, De Girolamo M, Isidro E (2021) Invasive vs. non-invasive methods of reproduction in Patella candei (d’Orbigny, 1840): from fertilization to settlement. In ‘Aquaculture Europe 2021 – oceans of opportunity’. pp. 892–893. (European Aquaculture Society: Funchal, Madeira, Portugal)
Orton JH, Southward AJ, Dodd JM (1956) Studies on the biology of limpets: II. The breeding of Patella vulgata L. in Britain. Journal of the Marine Biological Association of the United Kingdom 35(1), 149-176.
| Crossref | Google Scholar |
Pechenik JA, Heyman WD (1987) Using KCl to determine size at competence for larvae of the marine gastropod Crepidula fornicata (L.). Journal of Experimental Marine Biology and Ecology 112(1), 27-38.
| Crossref | Google Scholar |
Pereira F, Piló D, Carvalho AN, Rufino M, Moura P, Vasconcelos P, Gaspar MB (2022) Epibiont assemblages on limpet shells: biodiversity drivers in intertidal rocky shores. Marine Environmental Research 174, 105556.
| Crossref | Google Scholar | PubMed |
Pombo OA, Escofet A (1996) Effect of exploitation on the limpet Lottia gigantea: a field study in Baja California (Mexico) and California (USA). Pacific Science 50(4), 393-403.
| Google Scholar |
Riera R, Pérez Ó, Álvarez O, Simón D, Díaz D, Monterroso Ó, Núñez J (2016) Clear regression of harvested intertidal mollusks. A 20-year (1994–2014) comparative study. Marine Environmental Research 113, 56-61.
| Crossref | Google Scholar | PubMed |
Rivera-Ingraham GA, Espinosa F, García-Gómez JC (2011a) Present status of the endangered limpet Cymbula nigra (Gastropoda, Patellidae) in Ceuta: how do substrate heterogeneity and area accessibility affect population structure? Animal Biodiversity and Conservation 34(2), 319-330.
| Crossref | Google Scholar |
Rivera-Ingraham GA, Espinosa F, Garcia-Gomez JC (2011b) Effect of γ-amino butyric acid on limpet populations: towards the future management and conservation of endangered patellid species. Journal of Chemical Ecology 37(1), 1-9.
| Crossref | Google Scholar | PubMed |
Rivera-Ingraham GA, Espinosa F, Krock B (2015) Presence of gamma-aminobutyric acid (GABA) in the pedal mucus of the critically endangered species Patella ferruginea. Journal of Chemical Ecology 41(5), 501-504.
| Crossref | Google Scholar | PubMed |
Roberts RD, Nicholson CM (1997) Variable response from abalone larvae (Haliotis iris, H. virginea) to a range of settlement cues. Molluscan Research 18(2), 131-141.
| Crossref | Google Scholar |
Roberts RD, Kaspar HF, Barker RJ (2004) Settlement of abalone (Haliotis iris) larvae in response to five species of coralline algae. Journal of Shellfish Research 23(4), 975-988.
| Google Scholar |
Roberts RD, Barker MF, Mladenov P (2010) Is settlement of Haliotis iris larvae on coralline algae triggered by the alga or its surface biofilm? Journal of Shellfish Research 29(3), 671-678.
| Crossref | Google Scholar |
Rodríguez SR, Ojeda FP, Inestrosa NC (1993) Settlement of benthic marine invertebrates. Marine Ecology Progress Series 97(2), 193-207.
| Crossref | Google Scholar |
Sagarin RD, Ambrose RF, Becker BJ, Engle JM, Kido J, Lee SF, Miner CM, Murray SN, Raimondi PT, Richards D, Roe C (2007) Ecological impacts on the limpet Lottia gigantea populations: human pressure over a broad scale on island and mainland intertidal zones. Marine Biology 150(3), 399-413.
| Crossref | Google Scholar |
Seabra MI, Cruz T, Fernandes JN, Silva T, Hawkins SJ (2019) Recruitment of the limpet Patella ulyssiponensis and its relationship with crustose coralline algae: patterns of juvenile distribution and larval settlement. Journal of the Marine Biological Association of the United Kingdom 99(8), 1787-1796.
| Crossref | Google Scholar |
Searcy-Bernal R, Anguiano-Beltrán C (1998) Optimizing the concentration of gamma-aminobutyric acid (GABA) for inducing larval metamorphosis in the red abalone Haliotis rufescens (Mollusca: Gastropoda). Journal of the World Aquaculture Society 29(4), 463-470.
| Crossref | Google Scholar |
Sousa R, Delgado J, Pinto AR, Henriques P (2017) Growth and reproduction of the north-eastern Atlantic keystone species Patella aspera (Mollusca: Patellogastropoda). Helgoland Marine Research 71(1), 8.
| Crossref | Google Scholar |
Sousa R, Vasconcelos J, Henriques P, Pinto AR, Delgado J, Riera R (2019a) Long-term population status of two harvested intertidal grazers (Patella aspera and Patella candei), before (1996–2006) and after (2007–2017) the implementation of management measures. Journal of Sea Research 144, 33-38.
| Crossref | Google Scholar |
Sousa R, Vasconcelos J, Riera R, Pinto AR, Delgado J, Henriques P (2019b) Potential impact of harvesting management measures on the reproductive parameters of the limpets Patella aspera and Patella candei from Madeira Island. Estuarine, Coastal and Shelf Science 226, 106264.
| Crossref | Google Scholar |
Sousa R, Henriques P, Vasconcelos J, Pinto AR, Delgado J, Riera R (2020a) The protection effects of marine protected areas on exploited molluscs from an oceanic archipelago. Aquatic Conservation: Marine and Freshwater Ecosystems 30(4), 717-729.
| Crossref | Google Scholar |
Sousa R, Pinto AR, Vasconcelos J, Riera R (2020b) Does harvesting affect the relative growth in Patella aspera Röding, 1798? The European Zoological Journal 87(1), 395-401.
| Crossref | Google Scholar |
Stewart P, Soonklang N, Stewart MJ, Wanichanon C, Hanna PJ, Poomtong T, Sobhon P (2008) Larval settlement of the tropical abalone, Haliotis asinina Linnaeus, using natural and artificial chemical inducers. Aquaculture Research 39(11), 1181-1189.
| Crossref | Google Scholar |
Sánchez-Lazo C, Martínez-Pita I (2012) Induction of settlement in larvae of the mussel Mytilus galloprovincialis using neuroactive compounds. Aquaculture 344–349, 210-215.
| Crossref | Google Scholar |
Terradas-Fernández M, Zubcoff J, Ramos-Esplá AA (2019) Early succession patterns in a Mediterranean vermetid reef. Journal of Sea Research 152, 101768.
| Crossref | Google Scholar |
Trapido-Rosenthal HG, Morse DE (1986) Regulation of receptor-mediated settlement and metamorphosis in larvae of a gastropod mollusc (Haliotis rufescens). Bulletin of Marine Science 39(2), 383-392.
| Google Scholar |
Valdez-Cibrián A, Michel-Morfín JE, Gómez-Torres M, Landa-Jaime V, Gómez-Gastelum L, Carballo JL (2021) Population status of the endangered giant Mexican limpet Scutellastra mexicana in the central Mexican Pacific. Aquatic Conservation: Marine and Freshwater Ecosystems 31(3), 531-542.
| Crossref | Google Scholar |
Vasconcelos J, Sousa R, Ferro J, Pinto AR, Freitas M, Riera R (2023) Fecundity, an overlooked life-history trait for coastal management of commercial molluscs? Frontiers in Marine Science 10, 1173629.
| Crossref | Google Scholar |
Yang J-L, Li S-H, Li Y-F, Liu Z-W, Liang X, Bao W-Y, Li J-L (2013) Effects of neuroactive compounds, ions and organic solvents on larval metamorphosis of the mussel Mytilus coruscus. Aquaculture 396–399, 106-112.
| Crossref | Google Scholar |
Young T, Alfaro AC, Robertson J (2011) Effect of neuroactive compounds on the settlement of mussel (Perna canaliculus) larvae. Aquaculture 319(1), 277-283.
| Crossref | Google Scholar |
Yu X, He W, Gu J-D, He M, Yan Y (2008) The effect of chemical cues on settlement of pearl oyster Pinctada fucata martensii (Dunker) larvae. Aquaculture 277(1), 83-91.
| Crossref | Google Scholar |
Yu X, Yan Y, Li H (2010) The effect of chemical cues on larval settlement of the abalone, Haliotis diversicolor supertexta. Journal of the World Aquaculture Society 41(4), 626-632.
| Crossref | Google Scholar |
Zhao B, Zhang S, Qian P-Y (2003) Larval settlement of the silver- or goldlip pearl oyster Pinctada maxima (Jameson) in response to natural biofilms and chemical cues. Aquaculture 220(1), 883-901.
| Crossref | Google Scholar |