28 research outputs found

    Water-Borne Cues of a Non-Indigenous Seaweed Mediate Grazer-Deterrent Responses in Native Seaweeds, but Not Vice Versa

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    Plants optimise their resistance to herbivores by regulating deterrent responses on demand. Induction of anti-herbivory defences can occur directly in grazed plants or from emission of risk cues to the environment, which modifies interactions of adjacent plants with, for instance, their consumers. This study confirmed the induction of anti-herbivory responses by water-borne risk cues between adjoining con-specific seaweeds and firstly examined whether plant-plant signalling also exists among adjacent hetero-specific seaweeds. Furthermore, differential abilities and geographic variation in plant-plant signalling by a non-indigenous seaweed as well as native seaweeds were assessed. Twelve-day induction experiments using the non-indigenous seaweed Sargassum muticum were conducted in the laboratory in Portugal and Germany with one local con-familiar (Portugal: Cystoseira humilis, Germany: Halidrys siliquosa) and hetero-familiar native species (Portugal: Fucus spiralis, Germany: F. vesiculosus). All seaweeds were grazed by a local isopod species (Portugal: Stenosoma nadejda, Germany: Idotea baltica) and were positioned upstream of con- and hetero-specific seaweeds. Grazing-induced modification in seaweed traits were tested in three-day feeding assays between cue-exposed and cue-free ( = control) pieces of both fresh and reconstituted seaweeds. Both Fucus species reduced their palatability when positioned downstream of isopod-grazed con-specifics. Yet, the palatability of non-indigenous S. muticum remained constant in the presence of upstream grazed con-specifics and native hetero-specifics. In contrast, both con-familiar (but neither hetero-familiar) native species reduced palatability when located downstream of grazed S. muticum. Similar patterns of grazer-deterrent responses to water-borne cues were observed on both European shores, and were almost identical between assays using fresh and reconstituted seaweeds. Hence, seaweeds may use plant-plant signalling to optimise chemical resistance to consumers, though this ability appeared to be species-specific. Furthermore, this study suggests that native species may benefit more than a non-indigenous species from water-borne cue mediated reduction in consumption as only natives responded to signals emitted by hetero-specifics

    Structure and Composition of Rhodolith Beds from the Sergipe-Alagoas Basin (NE Brazil, Southwestern Atlantic)

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    Rhodolith beds are biogenic benthic habitats mainly formed by unattached, non-geniculate coralline algae, which can be inhabited by many associated species. The Brazilian continental shelf encompasses the largest continuous rhodolith bed in the world. This study was based on samples obtained from seven sites and videos taken by a Remotely Operated Vehicle (ROV) at four transects off the Sergipe-Alagoas Coast on the northeast Brazilian shelf. ROV operations and bottom trawl sampling revealed the occurrence of rhodolith beds between 25 and 54 m depths. At the shallower depths, fruticose (branching) rhodoliths (maërl) appear in troughs of ripples, and other non-branching rhodoliths occur associated with corals and sponge patches surrounded by bioclastic sand. Rhodoliths also occur in patches from 30 to 39 m depth; some are fused, forming larger, complex tridimensional structures. At deeper depths, from 40 to 54 m, the abundance of rhodoliths increases and occur associated with fleshy macroalgae on a smooth seafloor; some rhodoliths are fused into complex structures, locally some are fruticose (maërl), and others are partially buried by fine-grained sediment. The collected rhodoliths vary from fruticose in two sites to encrusting to lumpy, concentric and boxwork nodules in the rest; their size ranges from small (<1.5 cm) to large (~6 cm) and are mostly sub-spheroidal to spheroidal. A total of 16 red algal morpho-taxa were identified in the study sites. Two phases of growth can be distinguished in some rhodoliths by changes in color. The brownish inner cores yielded ages of 1600–1850 cal years before the present, whereas outer layers were much younger (180–50 years BP old). Growth layers appeared to have been separated by a long period of burial in the seafloor sediment. Other rhodoliths have ages of hundreds of years

    AlgaeTraits: a trait database for (European) seaweeds

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    The analysis of biological and ecological traits has a long history in evolutionary and ecological research. However, trait data are often scattered and standardised terminology that transcends taxonomic and biogeographical context are generally missing. As part of the development of a global trait database of marine species, we collated trait information for European seaweeds and structured the data within the standardised framework of the World Register of Marine Species (WoRMS). We collected 45 175 trait records for 21 biologically and ecologically relevant traits of seaweeds. This resulted in a trait database for 1745 European seaweed species of which more than half (56 %) of the records were documented at the species level, while the remaining 44% were documented at a higher taxonomic level and subsequently inherited at lower levels. The trait database for European seaweeds will serve as a foundation for future research on diversity and evolution of seaweeds and their responses to global changes. The data will contribute to developing detailed trait-based ecosystem models and will be an important tool to inform marine conservation policies. The data are publicly accessible through the AlgaeTraits portal, https://doi.org/10.14284/574 (AlgaeTraits, 2022)
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