Abstract:In dioecious species with both sexual and asexual reproduction, the spatial distribution of individual clones affects the potential for sexual reproduction and local adaptation. The seaweed Fucus radicans, endemic to the Baltic Sea, has separate sexes, but new attached thalli may also form asexually. We mapped the spatial distribution of clones (multilocus genotypes, MLGs) over macrogeographic (>500 km) and microgeographic (<100 m) scales in the Baltic Sea to assess the relationship between clonal spatial stru… Show more
“…In the northern Baltic Sea, by contrast, adventitious branches form, fall off and develop rhizoids that reattach them to the substratum, and from there they grow clonal copies of the mother thallus. Formation of adventitious branches was most frequent in F. radicans , less frequent in the Baltic Sea F. vesiculosus , and least common or absent in North Sea F. vesiculosus in our experiments, which correlates to the prevalence of clones in these populations (this study and [32]). Asexual reproduction by means of re-attaching adventitious branches seems to be a unique trait to the Baltic Sea that in itself has promoted the spread and establishment in a new area.…”
BackgroundEstablishing populations in ecologically marginal habitats may require substantial phenotypic changes that come about through phenotypic plasticity, local adaptation, or both. West-Eberhard’s “plasticity-first” model suggests that plasticity allows for rapid colonisation of a new environment, followed by directional selection that develops local adaptation. Two predictions from this model are that (i) individuals of the original population have high enough plasticity to survive and reproduce in the marginal environment, and (ii) individuals of the marginal population show evidence of local adaptation. Individuals of the macroalga Fucus vesiculosus from the North Sea colonised the hyposaline (≥2–3‰) Baltic Sea less than 8000 years ago. The colonisation involved a switch from fully sexual to facultative asexual recruitment with release of adventitious branches that grow rhizoids and attach to the substratum. To test the predictions from the plasticity-first model we reciprocally transplanted F. vesiculosus from the original population (ambient salinity 24‰) and from the marginal population inside the Baltic Sea (ambient salinity 4‰). We also transplanted individuals of the Baltic endemic sister species F. radicans from 4 to 24‰. We assessed the degree of plasticity and local adaptation in growth and reproductive traits after 6 months by comparing the performance of individuals in 4 and 24‰.ResultsBranches of all individuals survived the 6 months period in both salinities, but grew better in their native salinity. Baltic Sea individuals more frequently developed asexual traits while North Sea individuals initiated formation of receptacles for sexual reproduction.ConclusionsMarine individuals of F. vesiculosus are highly plastic with respect to salinity and North Sea populations can survive the extreme hyposaline conditions of the Baltic Sea without selective mortality. Plasticity alone would thus allow for an initial establishment of this species inside the postglacial Baltic Sea at salinities where reproduction remains functional. Since establishment, the Baltic Sea populations have evolved adaptations to extreme hyposaline waters and have in addition evolved asexual recruitment that, however, tends to impede local adaptation. Overall, our results support the “plasticity-first” model for the initial colonisation of the Baltic Sea by Fucus vesiculosus.Electronic supplementary materialThe online version of this article (doi:10.1186/s12898-017-0124-1) contains supplementary material, which is available to authorized users.
“…In the northern Baltic Sea, by contrast, adventitious branches form, fall off and develop rhizoids that reattach them to the substratum, and from there they grow clonal copies of the mother thallus. Formation of adventitious branches was most frequent in F. radicans , less frequent in the Baltic Sea F. vesiculosus , and least common or absent in North Sea F. vesiculosus in our experiments, which correlates to the prevalence of clones in these populations (this study and [32]). Asexual reproduction by means of re-attaching adventitious branches seems to be a unique trait to the Baltic Sea that in itself has promoted the spread and establishment in a new area.…”
BackgroundEstablishing populations in ecologically marginal habitats may require substantial phenotypic changes that come about through phenotypic plasticity, local adaptation, or both. West-Eberhard’s “plasticity-first” model suggests that plasticity allows for rapid colonisation of a new environment, followed by directional selection that develops local adaptation. Two predictions from this model are that (i) individuals of the original population have high enough plasticity to survive and reproduce in the marginal environment, and (ii) individuals of the marginal population show evidence of local adaptation. Individuals of the macroalga Fucus vesiculosus from the North Sea colonised the hyposaline (≥2–3‰) Baltic Sea less than 8000 years ago. The colonisation involved a switch from fully sexual to facultative asexual recruitment with release of adventitious branches that grow rhizoids and attach to the substratum. To test the predictions from the plasticity-first model we reciprocally transplanted F. vesiculosus from the original population (ambient salinity 24‰) and from the marginal population inside the Baltic Sea (ambient salinity 4‰). We also transplanted individuals of the Baltic endemic sister species F. radicans from 4 to 24‰. We assessed the degree of plasticity and local adaptation in growth and reproductive traits after 6 months by comparing the performance of individuals in 4 and 24‰.ResultsBranches of all individuals survived the 6 months period in both salinities, but grew better in their native salinity. Baltic Sea individuals more frequently developed asexual traits while North Sea individuals initiated formation of receptacles for sexual reproduction.ConclusionsMarine individuals of F. vesiculosus are highly plastic with respect to salinity and North Sea populations can survive the extreme hyposaline conditions of the Baltic Sea without selective mortality. Plasticity alone would thus allow for an initial establishment of this species inside the postglacial Baltic Sea at salinities where reproduction remains functional. Since establishment, the Baltic Sea populations have evolved adaptations to extreme hyposaline waters and have in addition evolved asexual recruitment that, however, tends to impede local adaptation. Overall, our results support the “plasticity-first” model for the initial colonisation of the Baltic Sea by Fucus vesiculosus.Electronic supplementary materialThe online version of this article (doi:10.1186/s12898-017-0124-1) contains supplementary material, which is available to authorized users.
“…Within‐season genetic differences at herring spawning sites are interpreted as genetically different populations using the same spawning grounds (spawning waves; Jørgensen, Hansen, Bekkevold, Ruzzante, & Loeschcke, ; Jørgensen, Hansen, & Loeschcke, ). Short‐term genetic changes indicating drift have been observed in the species with low effective sizes (Table ) and also in turbot and narrow wrack (Ardehed et al, ; Florin & Höglund, ).…”
Abstract1. The Baltic Sea has a rare type of brackish water environment which harbours unique genetic lineages of many species. The area is highly influenced by anthropogenic activities and is affected by eutrophication, climate change, habitat modifications, fishing and stocking. Effective genetic management of species in the Baltic Sea is highly warranted in order to maximize their potential for survival, but shortcomings in this respect have been documented. Lack of knowledge is one reason managers give for why they do not regard genetic diversity in management.2. Here, the current knowledge of population genetic patterns of species in the Baltic Sea is reviewed and summarized with special focus on how the information can be used in management. The extent to which marine protected areas (MPAs) protect genetic diversity is also investigated in a case study of four key species.
| INTRODUCTIONGenetic diversity is the foundation for all biological diversity; the persistence and evolutionary potential of species rely on it for adaptation to natural and human-induced selective pressures (Allendorf, Luikart, & Aitken, 2013). Research during the past decade has shown links between variation at the DNA level within species (genetic diversity) and biological productivity and viability (Lindley et al., 2009;Reusch, Ehlers, Hammerli, & Worm, 2005), resilience to environmental stressors (Frankham, 2005;Hellmair & Kinziger, 2014) * These authors contributed equally to this work.
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“…The genotype diversity (>1,000 genotypes) observed in this study is the highest ever documented for terrestrial or marine populations. Most studies assessing genetic variation in partially clonal organisms are not spatially explicit (Arnaud‐Haond et al., ; Gorospe, Donahue, & Karl, ; Schwartz & McKelvey, ), are based on sampling few individuals (~50) (Adjeroud et al., ; Ardehed et al., ; Becheler, Benkara, Moalic, Hily, & Arnaud‐Haond, ) or involve sampling of a single habitat (Gorospe & Karl, ). Such studies may therefore underestimate genotype diversity in clonal populations.…”
Clonal populations are often characterized by reduced levels of genotypic diversity, which can translate into lower numbers of functional phenotypes, both of which impede adaptation. Study of partially clonal animals enables examination of the environmental settings under which clonal reproduction is favoured. Here, we gathered genotypic and phenotypic information from 3,651 georeferenced colonies of the fire coral Millepora platyphylla in five habitats with different hydrodynamic regimes in Moorea, French Polynesia. In the upper slope where waves break, most colonies grew as vertical sheets ("sheet tree") making them more vulnerable to fragmentation. Nearly all fire corals in the other habitats are encrusting or massive. The M. platyphylla population is highly clonal (80% of the colonies are clones), while characterized by the highest genotype diversity ever documented for terrestrial or marine populations (1,064 genotypes). The proportion of clones varies greatly among habitats (≥58%-97%) and clones (328 clonal lineages) are distributed perpendicularly from the reef crest, perfectly aligned with wave energy. There are six clonal lineages with clones dispersed in at least two adjacent habitats that strongly demonstrate phenotypic plasticity. Eighty per cent of the colonies in these lineages are "sheet tree" on the upper slope, while 80%-100% are encrusting or massive on the mid slope and back reef. This is a unique example of phenotypic plasticity among reef-building coral clones as corals typically have wave-tolerant growth forms in high-energy reef areas.
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