Rivadeneira, M. M. et al. Testing the abundant-centre hypothesis using intertidal porcelain crabs along the Chilean coast: Linking abundance and life-history variation. J. Biogeogr. 37, 486–498 (2010).
Hutchins, L. W. The bases for temperature zonation in geographical distribution. Ecol. Monogr. 17, 325–335 (1947).
Lewis, J. R. Latitudinal trends in reproduction, recruitment and population characteristics of some rocky littoral molluscs and cirripedes. Hydrobiologia 142, 1–13 (1986).
Bernardo, J. The particular maternal effect of propagule size, especially egg size: Patterns, models, quality of evidence and interpretations. Am. Zool. 36, 216–236 (1996).
Thorson, G. Reproductive and larval ecology of marine bottom invertebrates. Biol. Rev. 25, 1–45 (1950).
Google Scholar
Marshall, D. J., Pettersen, A. K. & Cameron, H. A global synthesis of offspring size variation, its eco-evolutionary causes and consequences. Funct. Ecol. 32, 1436–1446 (2018).
Des Roches, S. et al. The ecological importance of intraspecific variation. Nat. Ecol. Evol. 2, 57–64 (2018).
Google Scholar
Violle, C. et al. Let the concept of trait be functional!. Oikos 116, 882–892 (2007).
Sides, C. B. et al. Revisiting Darwin’s hypothesis: Does greater intraspecific variability increase species’ ecological breadth?. Am. J. Bot. 101, 56–62 (2014).
Google Scholar
Moran, E. V., Hartig, F. & Bell, D. M. Intraspecific trait variation across scales: Implications for understanding global change responses. Glob. Change Biol. 22, 137–150 (2016).
Google Scholar
Violle, C. et al. The return of the variance: Intraspecific variability in community ecology. Trends Ecol. Evol. 27, 244–252 (2012).
Google Scholar
Stark, J., Lehman, R., Crawford, L., Enquist, B. J. & Blonder, B. Does environmental heterogeneity drive functional trait variation? A test in montane and alpine meadows. Oikos 126, 1650–1659 (2017).
Stearns, S. C. The Evolution of Life Histories. xii, 249p. No. 575 S81 (Oxford, Oxford University, 1992).
Vance, R. R. On reproductive strategies in marine benthic invertebrates. Am. Nat. 107, 339–352 (1973).
Levitan, D. R. Gamete traits influence the variance in reproductive success, the intensity of sexual selection, and the outcome of sexual conflict among congeneric sea urchins. Evolution 62, 1305–1316 (2008).
Google Scholar
Lavorel, S. & Garnier, E. Predicting changes in community composition and ecosystem functioning from plant traits: revisiting the Holy Grail. Funct. Ecol. 16, 545–556 (2002).
Pineda, M. C. et al. Tough adults, frail babies: An analysis of stress sensitivity across early life-history stages of widely introduced marine invertebrates. PLoS ONE 7, e46672 (2012).
Google Scholar
Harley, C. D. G. et al. The impacts of climate change in coastal marine systems: Climate change in coastal marine systems. Ecol. Lett. 9, 228–241 (2006).
Google Scholar
Stein, A., Gerstner, K. & Kreft, H. Environmental heterogeneity as a universal driver of species richness across taxa, biomes and spatial scales. Ecol. Lett. 17, 866–880 (2014).
Google Scholar
Foo, S. A. & Byrne, M. Marine gametes in a changing ocean: Impacts of climate change stressors on fecundity and the egg. Mar. Environ. Res. 128, 12–24 (2017).
Google Scholar
Dahlhoff, E. P. Biochemical indicators of stress and metabolism: Applications for marine ecological studies. Annu. Rev. Physiol. 66, 183–207 (2004).
Google Scholar
Soudant, P. et al. Comparison of the lipid class and fatty acid composition between a reproductive cycle in nature and a standard hatchery conditioning of the Pacific Oyster Crassostrea gigas. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 123, 209–222 (1999).
Lester, S. E., Gaines, S. D. & Kinlan, B. P. Reproduction on the edge: Large-scale patterns of individual performance in a marine invertebrate. Ecology 88, 2229–2239 (2007).
Google Scholar
Helmuth, B., Mieszkowska, N., Moore, P. & Hawkins, S. J. Living on the edge of two changing worlds: Forecasting the responses of rocky intertidal ecosystems to climate change. Annu. Rev. Ecol. Evol. Syst. 37, 373–404 (2006).
Sagarin, R. D., Barry, J. P., Gilman, S. E. & Baxter, C. H. Climate-related change in an intertidal community over short and long time scales. Ecol. Monogr. 69, 465–490 (1999).
Dubois, S., Retière, C. & Olivier, F. Biodiversity associated with Sabellaria alveolata (Polychaeta: Sabellariidae) reefs: Effects of human disturbances. J. Mar. Biol. Assoc. UK 82, 817–826 (2002).
Jones, A. G., Dubois, S. F., Desroy, N. & Fournier, J. Interplay between abiotic factors and species assemblages mediated by the ecosystem engineer Sabellaria alveolata (Annelida: Polychaeta). Estuar. Coast. Shelf Sci. 200, 1–18 (2018).
Google Scholar
Bonifazi, A. et al. Macrofaunal biodiversity associated with different developmental phases of a threatened Mediterranean Sabellaria alveolata (Linnaeus, 1767) reef. Mar. Environ. Res. 145, 97–111 (2019).
Google Scholar
Holt, T. J., Biogenic Reefs. An Overview of Dynamic and Sensitivity Characteristics for Conservation Management of Marine SACs. UK Marine SACs Project (1998).
Crisp, D. The effects of the severe winter of 1962–1963 on marine life in Britain. J. Anim. Ecol. 33, 165–210 (1964).
Firth, L. B. et al. Historical comparisons reveal multiple drivers of decadal change of an ecosystem engineer at the range edge. Ecol. Evol. 5, 3210–3222 (2015).
Google Scholar
Firth, L. B. et al. Specific niche requirements underpin multidecadal range edge stability, but may introduce barriers for climate change adaptation. Divers. Distrib. 27, 668–683 (2021).
Wethey, D. S. et al. Response of intertidal populations to climate: Effects of extreme events versus long term change. J. Exp. Mar. Biol. Ecol. 400, 132–144 (2011).
Sagarin, R. D. & Gaines, S. D. Geographical abundance distributions of coastal invertebrates: Using one-dimensional ranges to test biogeographic hypotheses. J. Biogeogr. 29, 985–997 (2002).
Rahman, M. A., Henderson, S., Miller-Ezzy, P., Li, X. X. & Qin, J. G. Immune response to temperature stress in three bivalve species: Pacific oyster Crassostrea gigas, Mediterranean mussel Mytilus galloprovincialis and mud cockle Katelysia rhytiphora. Fish Shellfish Immunol. 86, 868–874 (2019).
Google Scholar
Osada, M., Nishikawa, M. & Nomura, T. Involvement of prostaglandins in the spawning of the scallop, Patinopecten yessoensis. Comp. Biochem. Physiol. C 94, 595–601 (1989).
Stanley, D. W. & Howard, R. W. The biology of prostaglandins and related eicosanoids in invertebrates: Cellular, organismal and ecological actions. Am. Zool. 38, 369–381 (1998).
Google Scholar
Pernet, F., Tremblay, R., Comeau, L. & Guderley, H. Temperature adaptation in two bivalve species from different thermal habitats: Energetics and remodelling of membrane lipids. J. Exp. Biol. 210, 2999–3014 (2007).
Google Scholar
Muir, A. P., Nunes, F. L. D., Dubois, S. F. & Pernet, F. Lipid remodelling in the reef-building honeycomb worm, Sabellaria alveolata, reflects acclimation and local adaptation to temperature. Sci. Rep. 6, 35669 (2016).
Google Scholar
Hulbert, A. & Else, P. L. Membranes as possible pacemakers of metabolism. J. Theor. Biol. 199, 257–274 (1999).
Google Scholar
Brokordt, K. B., Himmelman, J. H., Nusetti, O. A. & Guderley, H. E. Reproductive investment reduces recuperation from exhaustive escape activity in the tropical scallop Euvola zizac. Mar. Biol. 137, 857–865 (2000).
Google Scholar
Levitan, D. R. & Roitberg, B. D. Optimal egg size in marine invertebrates: Theory and phylogenetic analysis of the critical relationship between egg size and development time in echinoids. Am. Nat. 156, 175–192 (2000).
Google Scholar
Moran, A. L. & McAlister, J. S. Egg size as a life history character of marine invertebrates: Is it all it’s cracked up to be?. Biol. Bull. 216, 226–242 (2009).
Google Scholar
Marshall, D. J. & Burgess, S. C. Deconstructing environmental predictability: Seasonality, environmental colour and the biogeography of marine life histories. Ecol. Lett. 18, 174–181 (2015).
Google Scholar
Racault, M.-F., Le Quéré, C., Buitenhuis, E., Sathyendranath, S. & Platt, T. Phytoplankton phenology in the global ocean. Ecol. Indic. 14, 152–163 (2012).
Henson, S., Cole, H., Beaulieu, C. & Yool, A. The impact of global warming on seasonality of ocean primary production. Biogeosciences 10, 4357–4369 (2013).
Google Scholar
Morim, J. et al. Robustness and uncertainties in global multivariate wind-wave climate projections. Nat. Clim. Change 9, 711–718 (2019).
Google Scholar
Stillman, J. H. Heat waves, the new normal: Summertime temperature extremes will impact animals, ecosystems, and human communities. Physiology 34, 86–100 (2019).
Google Scholar
McCarthy, D., Young, C. & Emson, R. Influence of wave-induced disturbance on seasonal spawning patterns in the sabellariid polychaete Phragmatopoma lapidosa. Mar. Ecol. Prog. Ser. 256, 123–133 (2003).
Google Scholar
Aviz, D., Pinto, A. J. A., Ferreira, M. A. P., Rocha, R. M. & Rosa Filho, J. S. Reproductive biology of Sabellaria wilsoni (Sabellariidae: Polychaeta), an important ecosystem engineer on the Amazon coast. J. Mar. Biol. Assoc. UK https://doi.org/10.1017/S0025315416001776 (2016).
Google Scholar
Bowman, R. S. & Lewis, J. Annual fluctuations in the recruitment of Patella vulgata L. J. Mar. Biol. Assoc. U. K. 57, 793–815 (1977).
Sagarin, R. D. & Somero, G. N. Complex patterns of expression of heat-shock protein 70 across the southern biogeographical ranges of the intertidal mussel Mytilus californianus and snail Nucella ostrina. J. Biogeogr. 33, 622–630 (2006).
Wernberg, T. et al. An extreme climatic event alters marine ecosystem structure in a global biodiversity hotspot. Nat. Clim. Change 3, 78–82 (2013).
Google Scholar
Firth, L. B., Knights, A. M. & Bell, S. S. Air temperature and winter mortality: Implications for the persistence of the invasive mussel, Perna viridis in the intertidal zone of the south-eastern United States. J. Exp. Mar. Biol. Ecol. 400, 250–256 (2011).
Seabra, R., Wethey, D. S., Santos, A. M. & Lima, F. P. Side matters: Microhabitat influence on intertidal heat stress over a large geographical scale. J. Exp. Mar. Biol. Ecol. 400, 200–208 (2011).
Meneghesso, C. et al. Remotely-sensed L4 SST underestimates the thermal fingerprint of coastal upwelling. Remote Sens. Environ. 237, 111588 (2020).
Google Scholar
Marshall, D. J. & Keough, M. J. The evolutionary ecology of offspring size in marine invertebrates. in Advances in Marine Biology, 1–60. https://doi.org/10.1016/S0065-2881(07)53001-4 (Elsevier, 2007).
Albert, C. H. et al. A multi-trait approach reveals the structure and the relative importance of intra- vs. interspecific variability in plant traits: Intra- vs. interspecific variability in plant traits. Funct. Ecol. 24, 1192–1201 (2010).
Olofsson, H., Ripa, J. & Jonzén, N. Bet-hedging as an evolutionary game: The trade-off between egg size and number. Proc. R. Soc. B Biol. Sci. 276, 2963–2969 (2009).
Osovitz, C. J. & Hofmann, G. E. Marine macrophysiology: Studying physiological variation across large spatial scales in marine systems. Comp. Biochem. Physiol. A. Mol. Integr. Physiol. 147, 821–827 (2007).
Google Scholar
Clarke, A. Reproduction in the cold: Thorson revisited. Invertebr. Reprod. Dev. 22, 175–183 (1992).
Hawkins, S. J. et al. Distinguishing globally-driven changes from regional- and local-scale impacts: The case for long-term and broad-scale studies of recovery from pollution. Mar. Pollut. Bull. 124, 573–586 (2017).
Google Scholar
Dahlhoff, E. P., Stillman, J. H. & Menge, B. A. Physiological community ecology: Variation in metabolic activity of ecologically important rocky intertidal invertebrates along environmental gradients. Integr. Comp. Biol. 42, 862–871 (2002).
Google Scholar
Nunes, F. L. D., Rigal, F., Dubois, S. F. & Viard, F. Looking for diversity in all the right places? Genetic diversity is highest in peripheral populations of the reef-building polychaete Sabellaria alveolata. Mar. Biol. 168, 63 (2021).
Bush, L. E. Stability and Variability of the Ecosystem Engineer Sabellaria alveolata on Differing Temporal and Spatial Scales (Bangor University, 2016).
Lourenço, C. R., Nicastro, K. R., McQuaid, C. D., Krug, L. A. & Zardi, G. I. Strong upwelling conditions drive differences in species abundance and community composition along the Atlantic coasts of Morocco and Western Sahara. Mar. Biodivers. 50, 15 (2020).
Ritchie, H. & Marshall, D. J. Fertilisation is not a new beginning: Sperm environment affects offspring developmental success. J. Exp. Biol. 216, 3104–3109 (2013).
Google Scholar
Dubois, S., Comtet, T., Retière, C. & Thiébaut, E. Distribution and retention of Sabellaria alveolata larvae (Polychaeta: Sabellariidae) in the Bay of Mont-Saint-Michel, France. Mar. Ecol. Prog. Ser. 346, 243–254 (2007).
Google Scholar
Costello, D. P., Henley, C., & Marine Biological Laboratory (Woods Hole, Mass.). Methods for obtaining and handling marine eggs and embryos [by] Donald P. Costello and Catherine Henley. ([s.n.], 1971). https://doi.org/10.5962/bhl.title.1020.
Gruet, Y. Aspects morphologiques et dynamiques de constructions de l’Annélide polychete Sabellaria alveolata (Linne). Rev. Trav. Inst. Pêch. Marit. 36, 131–161 (1972).
Saulquin, B., Gohin, F. & Garrello, R. Regional objective analysis for merging high-resolution MERIS, MODIS/Aqua, and SeaWiFS Chlorophyll-a data from 1998 to 2008 on the European Atlantic Shelf. IEEE Trans. Geosci. Remote Sens. 49, 143–154 (2011).
Google Scholar
Gohin, F. Annual cycles of chlorophyll-a, non-algal suspended particulate matter, and turbidity observed from space and in-situ in coastal waters. Ocean Sci. 7, 705–732 (2011).
Google Scholar
Seabra, R., Wethey, D. S., Santos, A. M. & Lima, F. P. Understanding complex biogeographic responses to climate change. Sci. Rep. 5, 12930 (2015).
Google Scholar
Schlegel, R. W., Darmaraki, S., Benthuysen, J. A., Filbee-Dexter, K. & Oliver, E. C. J. Marine cold-spells. Progress Oceanogr. 198, 102684 (2021).
Hobday, A. J. et al. A hierarchical approach to defining marine heatwaves. Prog. Oceanogr. 141, 227–238 (2016).
Google Scholar
Schlegel, R. W., Oliver, E. C., Hobday, A. J. & Smit, A. J. Detecting marine heatwaves with sub-optimal data. Front. Mar. Sci. 6, 737 (2019).
Egbert, G. D., Erofeeva, S. Y. & Ray, R. D. Assimilation of altimetry data for nonlinear shallow-water tides: Quarter-diurnal tides of the Northwest European Shelf. Cont. Shelf Res. 30, 668–679 (2010).
Google Scholar
Burrows, M., Harvey, R. & Robb, L. Wave exposure indices from digital coastlines and the prediction of rocky shore community structure. Mar. Ecol. Prog. Ser. 353, 1–12 (2008).
Google Scholar
Wessel, P. & Smith, W. H. F. A global, self-consistent, hierarchical, high-resolution shoreline database. J. Geophys. Res. Solid Earth 101, 8741–8743 (1996).
Seers, B. fetchR: Calculate Wind Fetch. R Package Version 2-1 (2017).
Guillaume, A. S., Monro, K. & Marshall, D. J. Transgenerational plasticity and environmental stress: Do paternal effects act as a conduit or a buffer?. Funct. Ecol. 30, 1175–1184 (2016).
Curd, A. et al. Connecting organic to mineral: How the physiological state of an ecosystem-engineer is linked to its habitat structure. Ecol. Indic. 98, 49–60 (2019).
Google Scholar
Gruet, Y. & Lassus, P. Contribution a l’etude de la biologie reproductive d’une population naturelle de l’Annelide Polychete, Sabellaria alveolata (Linnaeus). Ann. Inst. Oceanogr. Monaco 59, 127–140 (1983).
Hazel, J. The role of alterations in membrane lipid composition in enabling physiological adaptation of organisms to their physical environment. Prog. Lipid Res. 29, 167–227 (1990).
Google Scholar
Hochachka, P. W. & Somero, G. N. Biochemical Adaptation: Mechanism and Process in Physiological Evolution (Oxford University Press, 2002).
Abele, D. & Puntarulo, S. Formation of reactive species and induction of antioxidant defence systems in polar and temperate marine invertebrates and fish. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 138, 405–415 (2004).
Google Scholar
Folch, J., Lees, M. & Stanley, G. H. S. A simple method for the isolation and purification of total lipides from animal tissues. J. Biol. Chem. 226, 497–509. http://www.jbc.org/content/226/1/497 (1957).
Google Scholar
Sieracki, C., Sieracki, M. & Yentsch, C. An imaging-in-flow system for automated analysis of marine microplankton. Mar. Ecol. Prog. Ser. 168, 285–296 (1998).
Google Scholar
Pasteels, J. J. Etude au microscope électronique de la réaction corticale. II. La réaction corticale de l’oeuf vierge de Sabellaria alveolata. J. Embryol. Exp. Morphol. 13, 327–339 (1965).
Google Scholar
Doledec, S. & Chessel, D. Co-inertia analysis: An alternative method for studying species-environment relationships. Freshw. Biol. 31, 277–294 (1994).
Robert, P. & Escoufier, Y. A unifying tool for linear multivariate statistical methods: The RV-coefficient. J. R. Stat. Soc. Ser. C Appl. Stat. 25, 257–265 (1976).
Google Scholar
Legendre, P. & Legendre, L. Ecological resemblance. in Developments in Environmental Modelling Chapter 7, Vol. 24, 265–335 (Elsevier, 2012).
Borcard, D., Legendre, P. & Drapeau, P. Partialling out the spatial component of ecological variation. Ecology 73, 1045–1055 (1992).
Peres-Neto, P. R., Legendre, P., Dray, S. & Borcard, D. Variation partitioning of species data matrices: Estimation and comparison of fractions. Ecology 87, 2614–2625 (2006).
Google Scholar
Dormann, C. F. et al. Collinearity: A review of methods to deal with it and a simulation study evaluating their performance. Ecography 36, 27–46 (2013).
Messier, J., McGill, B. J. & Lechowicz, M. J. How do traits vary across ecological scales? A case for trait-based ecology: How do traits vary across ecological scales?. Ecol. Lett. 13, 838–848 (2010).
Google Scholar
Rao, C. R. The use and interpretation of principal component analysis in applied research. Sankhyā Indian J. Stat. Ser. A (1961-2002) 26, 329–358 (1964).
R Core Team: A language and environment for statistical computing. Available from: https://www.R-project.org/ (2018).
Oksanen, J. et al. Package ‘vegan’. Commun. Ecol. Package Version 2, 1–295 (2013).
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