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1.
Sci Rep ; 11(1): 10633, 2021 05 20.
Artigo em Inglês | MEDLINE | ID: mdl-34017032

RESUMO

The feeding biology of deep-sea octocorals remains poorly understood, as attention is more often directed to reef building corals. The present study focused on two common deep-water octocoral species in the Azores Archipelago, Dentomuricea aff. meteor and Viminella flagellum, aiming at determining their ability to exploit different food sources. We adopted an experimental approach, with three different food sources, including live phytoplankton, live zooplankton and dissolved organic matter (DOM), that were artificially enriched with 13C and 15N (C and N tracers). The presence of tracers was subsequently followed in the coral tissue, C respiration and particulate organic C and N (POC and PON) release. In both species, feeding with zooplankton resulted in significantly higher incorporation of tracers in all measured variables, compared to the other food sources, highlighting the importance of zooplankton for major physiological processes. Our results revealed contrasting metabolic strategies between the two species, with D. aff. meteor acquiring higher amounts of prey and allocating higher percentage to respiration and release of POC and PON than V. flagellum. Such metabolic differences can shape species fitness and distributions and have further ecological implications on the ecosystem function of communities formed by different octocoral species.


Assuntos
Antozoários/metabolismo , Oceanos e Mares , Animais , Carbono/análise , Modelos Biológicos , Nitrogênio/análise , Consumo de Oxigênio
2.
Mar Pollut Bull ; 64(3): 602-13, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22240204

RESUMO

Cages and fertilizers were used at Glover's Atoll, Belize to test the relative importance of nitrogen (N) and phosphorus (P) to microbial euendolithic communities (bacteria, algae and fungi) and their bioerosion rates of Strombus gigas shells after 56-days of exposure. By the end of the experiment, the abundance of green algae was higher than cyanobacteria and fungi in N and N+P treatments, although green algae did not increase proportionally with increasing N concentrations, suggesting that green algae were co-limited by P and N. In contrast, cyanobacteria abundance increased with increasing P concentration, suggesting that cyanobacteria were P-limited. Fungi were not significantly affected by the addition of nutrients. Microbioerosion rates in the N and N+P treatments were 2-times greater than rates in the P treatment and 15-times greater than the control treatment. Results demonstrate that increased nutrient concentrations on coral reefs may increase microbioerosion rates, and variations in nutrient ratios can modify microborers community composition.


Assuntos
Nitrogênio/farmacologia , Fósforo/farmacologia , Poluentes Químicos da Água/farmacologia , Exoesqueleto , Animais , Bactérias/efeitos dos fármacos , Bactérias/crescimento & desenvolvimento , Belize , Biodegradação Ambiental/efeitos dos fármacos , Ecossistema , Monitoramento Ambiental , Eutrofização , Fungos/efeitos dos fármacos , Fungos/crescimento & desenvolvimento , Fungos/fisiologia , Microalgas/efeitos dos fármacos , Microalgas/crescimento & desenvolvimento , Microalgas/fisiologia , Nitrogênio/análise , Fósforo/análise , Água do Mar/química , Poluentes Químicos da Água/análise
3.
Mar Pollut Bull ; 54(12): 1947-57, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17963793

RESUMO

Nitrogen and phosphorous fertilizers were used to determine their short-term summer effects on algal colonization, abundance, and species composition in moderate herbivory treatments. Secondary succession of algae on coral skeletons was examined in four treatments: an untreated control, a pure phosphate fertilizer, a pure nitrogen fertilizer, and an equal mix of the two fertilizers. Turf algae cover was the only measure of algae abundance to respond significantly to fertilization. Turf cover was three times higher in treatments with added nitrogen when compared with the pure phosphorus treatment. These turfs were dominated by green and cyanobacteria taxa, namely Enteromorpha prolifera, Lyngbya confervoides, and two species of Cladophora. The phosphate treatment was dominated by encrusting corallines and the cyanobacteria L. confervoides, while the controls had the highest cover of frondose brown algae, namely Padina sanctae-crucis and two species of Dictyota. Results indicate that turf algae were co-limited by nitrogen and phosphorus but enrichment appeared to inhibit brown frondose algae that currently dominate these reefs. Number of species was lowest on the pure phosphorus and nitrogen treatments, highest in the controls and intermediate in the mixed treatments, which suggests that diversity is reduced most by an imbalanced nutrient ratio.


Assuntos
Antozoários , Eucariotos/efeitos dos fármacos , Fertilizantes , Nitrogênio/farmacologia , Fósforo/farmacologia , Animais , Belize , Biomassa , Cianobactérias/efeitos dos fármacos , Cianobactérias/crescimento & desenvolvimento , Interações Medicamentosas , Ecossistema , Eucariotos/classificação , Eucariotos/crescimento & desenvolvimento , Dinâmica Populacional , Fatores de Tempo
4.
J Exp Mar Biol Ecol ; 262(2): 133-153, 2001 Jul 30.
Artigo em Inglês | MEDLINE | ID: mdl-11445084

RESUMO

During feeding, echinoids remove a large proportion of calcium carbonate in addition to the algae growing on dead coral and are consequently of importance in estimating the turnover of organic and inorganic carbon in coral reefs. Rates of herbivory and the erosion of dead coral substratum, referred to as bioerosion, by the most abundant echinoid species in Kenyan reefs, Echinothrix diadema (Linnaeus), Diadema setosum (Leske), D. savignyi (Michelin) and Echinometra mathaei (de Blainville), were compared in three different reef categories with different histories of fishing and its exclusion. These were reefs: (i) protected within Marine National Parks, which exclude all forms of fishing, coral and shell collection for more than 25 years; (ii) one reef within a Marine Park, which has received protection from fishing activities for 8 years (referred to as 'newly protected' reef); and (iii) unprotected reefs, which experience heavy fishing and some coral collection. The aim was to investigate the grazing and bioerosion activity by the above echinoid species in these reef categories. We surveyed sea urchin population densities and determined their rates of bioerosion and herbivory per individual and square meter. Individual rates of bioerosion and herbivory, of the species D. setosum, D. savignyi and E. diadema were estimated from laboratory gut content analysis and gut evacuation experiments in the field, using elevated underwater cages. Individual rates of bioerosion and herbivory of E. mathaei were obtained from a previous field study [J. Exp. Mar. Biol. Ecol. 147 (1991) 121]. Sea urchin bioerosion was greater than herbivory for all studied species and proportional to the body size of the sea urchin species. The large-bodied E. diadema exhibited the highest bioerosion and herbivory rates (5.5+/-0.9 and 2.2+/-0.3 g individual(-1) day(-1), respectively) followed by D. setosum (1.8+/-0.3 and 1.1+/-0.2 g individual(-1) day(-1)) and D. savignyi (0.7+/-0.2 and 0.4+/-0.1 g individual(-1) day(-1)). Highest sea urchin densities were recorded at unprotected reefs (6.2+/-1.5 individual m(-2)), and therefore, bioerosion and herbivory by sea urchins were also highest in this reef category (1180+/-230 g CaCO(3) m(-2) year(-1) and 450+/-77 g algae m(-2) year(-1)). Protected reefs recorded 20 times lower sea urchin bioerosion and herbivory rates (50.3+/-25.8 g CaCO(3) m(-2) year(-1) and 20.7+/-10.4 g algae m(-2) year(-1)), due to the low sea urchin population densities in these reefs (0.06+/-0.01 individual m(-2)). The newly protected reef, with intermediate number of sea urchins (1.2+/-0.1 individual m(-2)), had intermediate rates of sea urchin bioerosion and herbivory (711+/-157 g CaCO(3) m(-2) year(-1) and 299+/-63 g algae m(-2) year(-1)). These findings suggest that echinoids are important in the carbon cycle and reef development, and that fishing can influence these ecological processes.

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