L. Fan, Chang‐Po Chen, Mingqiu Yang, Guanglong Qiu, Yong-Yan Liao, H. Hsieh
{"title":"西南地区两种共生马蹄蟹日粮碳源及营养地位的个体发生变化","authors":"L. Fan, Chang‐Po Chen, Mingqiu Yang, Guanglong Qiu, Yong-Yan Liao, H. Hsieh","doi":"10.3354/AB00670","DOIUrl":null,"url":null,"abstract":"Understanding which food sources are nutritionally important at nursery grounds is critical in the conservation of the dwindling populations of horseshoe crabs in Asia. We used δ13C and δ15N values to define life-stage changes in dietary carbon sources and trophic position of 2 co-occurring horseshoe crab species, Tachypleus tridentatus and Carci no scorpius rotundicauda, in a mangroveand seagrass-vegetated estuary, Pearl Bay, in Guangxi, China. δ13C signatures in tissues of T. tridentatus and C. rotundicauda varied between species and among life stages within species, with the greatest differences occurring among earlier life stages (instars 5−7; 20−30 mm prosomal width). Life-stage specific diets were consistent with known habitat use by the 2 horseshoe crab species, with T. tridentatus reflecting slightly enriched seagrass carbon sources and C. ro tun di cauda reflecting influences of lighter sediment particulate organic matter (POM; −15.1 vs. ~ −15.8‰). Overall, seagrass contributed most to dietary carbon of both species (~60%), followed by sediment POM (35%). δ15N signatures were similar between species (~11.6‰), with C. rotundicauda adults exhibiting a slightly more enriched signal than juveniles (12.7 vs. 11.6‰), and all horseshoe crabs occupied secondary consumer trophic levels. The δ15N signatures in horseshoe crabs at Pearl Bay were lighter than those from more urbanized waters, likely due to lower anthropogenic nitrogen loading. Our data and those of previous studies suggest that effective international and national strategies for conserving threatened Asian horseshoe crabs would benefit from incorporating efforts to protect seagrass and mangrove habitats. Newly molted juvenile horseshoe crab (left) and its old shell (right) on a tidal flat adjacent to mangroves in the Pearl Bay estuary (Guangxi, China). Photo: Chang-Po Chen","PeriodicalId":8111,"journal":{"name":"Aquatic Biology","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2017-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":"{\"title\":\"Ontogenetic changes in dietary carbon sources and trophic position of two co-occurring horseshoe crab species in southwestern China\",\"authors\":\"L. Fan, Chang‐Po Chen, Mingqiu Yang, Guanglong Qiu, Yong-Yan Liao, H. Hsieh\",\"doi\":\"10.3354/AB00670\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Understanding which food sources are nutritionally important at nursery grounds is critical in the conservation of the dwindling populations of horseshoe crabs in Asia. We used δ13C and δ15N values to define life-stage changes in dietary carbon sources and trophic position of 2 co-occurring horseshoe crab species, Tachypleus tridentatus and Carci no scorpius rotundicauda, in a mangroveand seagrass-vegetated estuary, Pearl Bay, in Guangxi, China. δ13C signatures in tissues of T. tridentatus and C. rotundicauda varied between species and among life stages within species, with the greatest differences occurring among earlier life stages (instars 5−7; 20−30 mm prosomal width). Life-stage specific diets were consistent with known habitat use by the 2 horseshoe crab species, with T. tridentatus reflecting slightly enriched seagrass carbon sources and C. ro tun di cauda reflecting influences of lighter sediment particulate organic matter (POM; −15.1 vs. ~ −15.8‰). Overall, seagrass contributed most to dietary carbon of both species (~60%), followed by sediment POM (35%). δ15N signatures were similar between species (~11.6‰), with C. rotundicauda adults exhibiting a slightly more enriched signal than juveniles (12.7 vs. 11.6‰), and all horseshoe crabs occupied secondary consumer trophic levels. The δ15N signatures in horseshoe crabs at Pearl Bay were lighter than those from more urbanized waters, likely due to lower anthropogenic nitrogen loading. Our data and those of previous studies suggest that effective international and national strategies for conserving threatened Asian horseshoe crabs would benefit from incorporating efforts to protect seagrass and mangrove habitats. Newly molted juvenile horseshoe crab (left) and its old shell (right) on a tidal flat adjacent to mangroves in the Pearl Bay estuary (Guangxi, China). 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Ontogenetic changes in dietary carbon sources and trophic position of two co-occurring horseshoe crab species in southwestern China
Understanding which food sources are nutritionally important at nursery grounds is critical in the conservation of the dwindling populations of horseshoe crabs in Asia. We used δ13C and δ15N values to define life-stage changes in dietary carbon sources and trophic position of 2 co-occurring horseshoe crab species, Tachypleus tridentatus and Carci no scorpius rotundicauda, in a mangroveand seagrass-vegetated estuary, Pearl Bay, in Guangxi, China. δ13C signatures in tissues of T. tridentatus and C. rotundicauda varied between species and among life stages within species, with the greatest differences occurring among earlier life stages (instars 5−7; 20−30 mm prosomal width). Life-stage specific diets were consistent with known habitat use by the 2 horseshoe crab species, with T. tridentatus reflecting slightly enriched seagrass carbon sources and C. ro tun di cauda reflecting influences of lighter sediment particulate organic matter (POM; −15.1 vs. ~ −15.8‰). Overall, seagrass contributed most to dietary carbon of both species (~60%), followed by sediment POM (35%). δ15N signatures were similar between species (~11.6‰), with C. rotundicauda adults exhibiting a slightly more enriched signal than juveniles (12.7 vs. 11.6‰), and all horseshoe crabs occupied secondary consumer trophic levels. The δ15N signatures in horseshoe crabs at Pearl Bay were lighter than those from more urbanized waters, likely due to lower anthropogenic nitrogen loading. Our data and those of previous studies suggest that effective international and national strategies for conserving threatened Asian horseshoe crabs would benefit from incorporating efforts to protect seagrass and mangrove habitats. Newly molted juvenile horseshoe crab (left) and its old shell (right) on a tidal flat adjacent to mangroves in the Pearl Bay estuary (Guangxi, China). Photo: Chang-Po Chen
期刊介绍:
AB publishes rigorously refereed and carefully selected Feature Articles, Research Articles, Reviews and Notes, as well as Comments/Reply Comments (for details see MEPS 228:1), Theme Sections, Opinion Pieces (previously called ''As I See It'') (for details consult the Guidelines for Authors) concerned with the biology, physiology, biochemistry and genetics (including the ’omics‘) of all aquatic organisms under laboratory and field conditions, and at all levels of organisation and investigation. Areas covered include:
-Biological aspects of biota: Evolution and speciation; life histories; biodiversity, biogeography and phylogeography; population genetics; biological connectedness between marine and freshwater biota; paleobiology of aquatic environments; invasive species.
-Biochemical and physiological aspects of aquatic life; synthesis and conversion of organic matter (mechanisms of auto- and heterotrophy, digestion, respiration, nutrition); thermo-, ion, osmo- and volume-regulation; stress and stress resistance; metabolism and energy budgets; non-genetic and genetic adaptation.
-Species interactions: Environment–organism and organism–organism interrelationships; predation: defenses (physical and chemical); symbioses.
-Molecular biology of aquatic life.
-Behavior: Orientation in space and time; migrations; feeding and reproductive behavior; agonistic behavior.
-Toxicology and water-quality effects on organisms; anthropogenic impacts on aquatic biota (e.g. pollution, fisheries); stream regulation and restoration.
-Theoretical biology: mathematical modelling of biological processes and species interactions.
-Methodology and equipment employed in aquatic biological research; underwater exploration and experimentation.
-Exploitation of aquatic biota: Fisheries; cultivation of aquatic organisms: use, management, protection and conservation of living aquatic resources.
-Reproduction and development in marine, brackish and freshwater organisms