Spatio-temporal Variability in Larval-Stage Feeding and Nutritional Sources as Factors Influencing Striped Bass (Morone saxatilis) Recruitment Success

Prey availability and feeding success affect survival of larval striped bass (Morone saxatilis) in Chesapeake Bay and contribute to the >30-fold interannual recruitment variability. Gut contents and stable isotope analyses (δ¹⁵N and δ¹³C) were conducted on striped bass larvae to evaluate sources of nutrition in 2007 and 2008, years of high and poor recruitment, respectively. Ichthyoplankton and zooplankton were surveyed in the upper Chesapeake Bay, in proximity to the estuarine turbidity maximum and associated salt front. Feeding incidence and numbers of prey per gut were similar in both years and varied in relation to the salt front. The primary prey in each year was the estuarine copepod Eurytemora affinis. Substantial consumption of the freshwater cladoceran Bosmina spp. also occurred, especially up-estuary of the salt front in 2007, demonstrating that secondary prey are important to larval diets in some years. Stable isotope analysis of yolk sac and feeding-stage larvae of striped bass revealed an ontogenetic shift from maternal stable isotope signatures to those indicative of prey source. Feeding-stage larvae from up-estuary locations had the most negative δ¹³C values, indicating a relatively high terrestrial carbon source in prey. Spatio-temporal variability in δ¹⁵N signatures of larvae followed similar trends of δ¹⁵N variability in zooplankton prey with the highest δ¹⁵N values up-estuary of the salt front and estuarine turbidity maximum. A stable isotope analysis on archived striped bass larvae collected in 1998 and 2003, years of moderate and high recruitment, respectively, expanded the documented range of isotope signatures but did not clearly distinguish effects of nutritional sources on recruitment.     

FITC‐conjugated lectins as a tool for differentiating between toxic and non‐toxic marine dinoflagellates

FITC‐conjugated lectins proved to be effective probes for differentiating between morphologically similar dinoflagellate species isolated from New Zealand coastal waters. In particular the binding (fluorescence) of peanut (PNA) lectin differentiated G. mikimotoi from Gymnodinium sp. (Waimangu) and G. pulchellum and the non‐binding of Helix pomatia (HPA) and wheat germ (WGA) lectins discriminated between G. mikimotoi and the other Gymnodinium species tested. G. breve (Florida) was differentiated from the New Zealand isolates by binding with soy bean (SBA) lectin. Ulex europeus (UEA) distinguished the toxic species Alexandrium minutum from the morphologically similar, but non‐toxic, Cachonina hallii. Two strains of Prorocentrum lima (Spain and Rangaunu) were not differentiated by the lectins, but P. lima was differentiated from P. compressum.     

Determination of Selenium and Tellurium in Basalt Rock Reference Materials by Isotope Dilution Hydride Generation-Inductively Coupled Plasma-Mass Spectrometry (ID-HG-ICP-MS)

Promising methods have been developed recently for the determination of selenium (Se) and tellurium (Te) in geological materials at ng g⁻¹ and lower levels, using hydride generation-inductively coupled plasma-mass spectrometry. Here we report on a new isotope dilution-hydride generation-inductively coupled plasma-mass spectrometry (ID-HG-ICP-MS) method for the simultaneous determination of Se and Te, which is applied to basalts, and modified compared to previous work. The basalts were attacked and dissolved with hydrofluoric and nitric acid, spiked with enriched isotopes, and passed through a cation exchange column (AG 50-X8 100–200 mesh) to separate the major cations that interfere with Se and Te detection (e.g., Fe). The detection limits of this method were 0.010 ng g⁻¹ for Se and 0.0030 ng g⁻¹ for Te, well below the concentrations of Se and Te expected in basalts. The precision of the method for Se was 12.2 to 15.1% and for Te was 4.6 to 7.2% RSD from replicate analyses of basalt reference samples. The accuracy for Se determinations was 61 to 94% and for Te 28 to 100% of values previously reported in the literature for selected USGS reference materials.     

Controls on Sr/Ca and Mg/Ca in scleractinian corals: The effects of Ca-ATPase and transcellular Ca channels on skeletal chemistry

The Sr/Ca of aragonitic coral skeletons is a commonly used palaeothermometer. However skeletal Sr/Ca is typically dominated by weekly-monthly oscillations which do not reflect temperature or seawater composition and the origins of which are currently unknown. To test the impact of transcellular Ca²⁺ transport processes on skeletal Sr/Ca, colonies of the branching coral, Pocillopora damicornis, were cultured in the presence of inhibitors of Ca-ATPase (ruthenium red) and Ca channels (verapamil hydrochloride). The photosynthesis, respiration and calcification rates of the colonies were monitored throughout the experiment. The skeleton deposited in the presence of the inhibitors was identified (by ⁴²Ca spike) and analysed for Sr/Ca and Mg/Ca by secondary ion mass spectrometry. The Sr/Ca of the aragonite deposited in the presence of either of the inhibitors was not significantly different from that of the solvent (dimethyl sulfoxide) control, although the coral calcification rate was reduced by up to 66% and 73% in the ruthenium red and verapamil treatments, respectively. The typical precision (95% confidence limits) of mean Sr/Ca determinations within any treatment was <±1% and differences in skeletal Sr/Ca between treatments were correspondingly small. Either Ca-ATPase and Ca channels transport Sr²⁺ and Ca²⁺ in virtually the same ratio in which they are present in seawater or transcellular processes contribute little Ca²⁺ to the skeleton and most Ca is derived from seawater transported directly to the calcification site. Variations in the activities of Ca-ATPase and Ca-channels are not responsible for the weekly-monthly Sr/Ca oscillations observed in skeletal chronologies, assuming that the specificities of Ca transcellular transport processes are similar between coral genera.