Age and growth of Cape stumpnose Rhabdosargus holubi (Pisces: Sparidae) in the Eastern Cape,South Africa

Rhabdosargus holubi is a small (maximum weight=2.4?kg) yet important fishery species in the estuaries of the south-east coast of South Africa. Little is known of its biology and specifically its growth rate, which is essential for sustainable management of the fishery. We examined and counted the opaque zones in the sectioned otoliths of 134 R. holubi to determine its age and growth parameters. The otoliths from two recaptured fish marked with oxytetracycline confirmed that one opaque zone was deposited annually. The species reached a maximum age of 18 years and growth was adequately described by a von Bertalanffy growth function of the form: L_t = 358.1 (1 – e^{?0.24(t+0.77)}) mm fork length. There were no significant differences between any of the male and female growth parameters (likelihood ratio test: p = 0.3). The growth was slow (omega index: ω = 86.56); however, despite this, the unique life history of R. holubi may provide a degree of resilience to heavy fishing pressure in estuaries.     

Inter‐laboratory Characterisation of Apatite Reference Materials for Chlorine Isotope Analysis

Here we report on a set of six apatite reference materials (chlorapatites MGMH#133648, TUBAF#38 and fluorapatites MGMH#128441A, TUBAF#37, 40, 50) which we have characterised for their chlorine isotope ratios; these RMs span a range of Cl mass fractions within the apatite Ca₁₀(PO₄)₆(F,Cl,OH)₂ solid solution series. Numerous apatite specimens, obtained from mineralogical collections, were initially screened for ³⁷Cl/³⁵Cl homogeneity using SIMS followed by δ³⁷Cl characterisation by gas source mass spectrometry using both dual‐inlet and continuous‐flow modes. We also report major and key trace element compositions as determined by EPMA. The repeatability of our SIMS results was better than ± 0.10‰ (1s) for the five samples with > 0.5 % m/m Cl and ± 0.19‰ (1s) for the low Cl abundance material (0.27% m/m). We also observed a small, but significant crystal orientation effect of 0.38‰ between the mean ³⁷Cl/³⁵Cl ratios measured on three oriented apatite fragments. Furthermore, the results of GS‐IRMS analyses show small but systematic offset of δ³⁷Cl_SMOC values between the three laboratories. Nonetheless, all studied samples have comparable chlorine isotope compositions, with mean 10³δ³⁷Cl_SMOC values between +0.09 and +0.42 and in all cases with 1s ≤ ± 0.25.     

New evidence on the hydrothermal system in Long Valley caldera, California, from wells, fluid sampling, electrical geophysics, and age determinations of hot-spring deposits

Data collected since 1985 from test drilling, fluid sampling, and geologic and geophysical investigations provide a clearer definition of the hydrothermal system in Long Valley caldera than was previously available. This information confirms the existence of high-temperature (> 200°C) reservoirs within the volcanic fill in parts of the west moat. These reservoirs contain fluids which are chemically similar to thermal fluids encountered in the central and eastern parts of the caldera. The roots of the present-day hydrothermal system (the source reservoir, principal zones of upflow, and the magmatic heat source) most likely occur within metamorphic basement rocks beneath the western part of the caldera. Geothermometer-temperature estimates for the source reservoir range from 214 to 248°C. Zones of upflow of hot water could exist beneath the plateau of moat rhyolite located west of the resurgent dome or beneath Mammoth Mountain. Lateral flow of thermal water away from such upflow zones through reservoirs in the Bishop Tuff and early rhyolite accounts for temperature reversals encountered in most existing wells. Dating of hot-spring deposits from active and inactive thermal areas confirms previous interpretations of the evolution of hydrothermal activity that suggest two periods of extensive hot-spring discharge, one peaking about 300 ka and another extending from about 40 ka to the present. The onset of hydrothermal activity around 40 ka coincides with the initiation of rhyolitic volcanism along the Mono-Inyo Craters volcanic chain that extends beneath the caldera's west moat.     

Isotopic mapping of groundwater perchlorate plumes

Analyses of stable isotope ratios of chlorine and oxygen in perchlorate can, in some cases, be used for mapping and source identification of groundwater perchlorate plumes. This is demonstrated here for large, intersecting perchlorate plumes in groundwater from a region having extensive groundwater perchlorate contamination and a large population dependent on groundwater resources. The region contains both synthetic perchlorate derived from rocket fuel manufacturing and testing activities and agricultural perchlorate derived predominantly from imported Chilean (Atacama) nitrate fertilizer, along with a likely component of indigenous natural background perchlorate from local wet and dry atmospheric deposition. Most samples within each plume reflect either a predominantly synthetic or a predominantly agricultural perchlorate source and there is apparently a minor contribution from the indigenous natural background perchlorate. The existence of isotopically distinct perchlorate plumes in this area is consistent with other lines of evidence, including groundwater levels and flow paths as well as the historical land use and areal distribution of potential perchlorate sources.     

Geochemistry of reduced gas related to serpentinization of the Zambales ophiolite, Philippines

Methane-hydrogen gas seeps with mantle-like C and noble gas isotopic characteristics issue from partially serpentinized ultramafic rocks in the Zambales ophiolite, Philippines. New measurements of noble gas and ¹⁴C isotope abundances, rock/mixed-volatile equilibrium calculations, and previous chemical and isotopic data suggest that these reduced gases are products of periodotite hydration. The gas seeps are produced in rock-dominated zones of serpentinization, and similar gases may be ubiquitous in ultramafic terranes undergoing serpentinization.     

Effect of graded levels of dietary carbohydrate on growth,feed utilisation and intestinal microbial community structure in dusky kob Argyrosomus japonicus fed a pelleted diet

The ability to utilise carbohydrates is limited for many predatory marine fishes. Graded levels of dietary carbohydrate (4.1–24.6%) were formulated using pregelatinised maize starch, to determine optimal levels for dusky kob Argyrosomus japonicus, an emerging mariculture finfish for which pelleted feeds are being developed. Specific growth rate increased with an increase in the carbohydrate level up to 16.72%, after which it declined. Feed utilisation followed a similar trend, with the best feed conversion ratio (1.28) and protein efficiency ratio (1.76) recorded at 16.4% carbohydrate. Lipid vacuolisation of the hepatocytes was evident in all livers examined, with melano-macrophage aggregates in those of fish fed 24.6% carbohydrate suggesting starvation. Gut bacterial community profiles were variable but were not influenced by dietary carbohydrate level and differed mostly between fish fed trout feed prior to the trial and those fed experimental diets containing starch. The dusky kob were able to clear glucose from their blood when fed up to 16.4% carbohydrate, but glucose removal was not achieved at 24.6% carbohydrate. In conclusion, dusky kob has a limited ability to utilise cooked starch as a carbohydrate source, which may be included in pelleted feed at 16.4% without adverse effects. For this species, levels of dietary carbohydrate above this may result in symptoms consistent with physiological breakdown, including reduced growth, reduced feed intake and feed conversion efficiency, prolonged hyperglycaemia, liver pathology and altered microbial communities in the foregut.     

Kinetic isotopic fractionation during diffusion of ionic species in water

Experiments specifically designed to measure the ratio of the diffusivities of ions dissolved in water were used to determine . The measured ratio of the diffusion coefficients for Li and K in water (D_Li/D_K = 0.6) is in good agreement with published data, providing evidence that the experimental design being used resolves the relative mobility of ions with adequate precision to also be used for determining the fractionation of isotopes by diffusion in water. In the case of Li, we found measurable isotopic fractionation associated with the diffusion of dissolved LiCl (D_⁷Li/D_⁶Li=0.99772±0.00026). This difference in the diffusion coefficient of ⁷Li compared to ⁶Li is significantly less than that reported in an earlier study, a difference we attribute to the fact that in the earlier study Li diffused through a membrane separating the water reservoirs. Our experiments involving Mg diffusing in water found no measurable isotopic fractionation (D_²⁵Mg/D_²⁴Mg=1.00003±0.00006). Cl isotopes were fractionated during diffusion in water (D_³⁷Cl/D_³⁵Cl=0.99857±0.00080) whether or not the co-diffuser (Li or Mg) was isotopically fractionated. The isotopic fractionation associated with the diffusion of ions in water is much smaller than values we found previously for the isotopic fractionation of Li and Ca isotopes by diffusion in molten silicate liquids. A major distinction between water and silicate liquids is that water surrounds dissolved ions with hydration shells, which very likely play an important but still poorly understood role in limiting the isotopic fractionation associated with diffusion.     

MIXTURE ANALYSIS USING FACTOR ANALYSIS.Ⅱ:SELF-MODELING CURVE RESOLUTION

One of the major applications of factor analysis in the chemical literature,self-modeling curve resolution(SMCR),is covered in this review,including a historical account of the inethods derived from Lawtonand Sylvestre's original method.Papers treating the theory or applications of SMCR are included.Qualitative and quantitative applications are described where appropriate.     

Competitive adsorption of strontium and fulvic acid at the muscovite-solution interface observed with resonant anomalous X-ray reflectivity

Molecular-scale distributions of Sr²⁺ and fulvic acid (FA) adsorbed on the muscovite (0 0 1) surface were investigated using in situ specular X-ray reflectivity (XR) and resonant anomalous X-ray reflectivity (RAXR). The total amount of Sr²⁺ adsorbed from a 1 × 10⁻² mol/kg SrCl₂ and 100 mg/kg Elliott Soil Fulvic Acid II (ESFA II) solution at pH 5.5 compensated 81 ± 5% of the muscovite surface charge, less than previously measured (118 ± 5%) in an ESFA II-free solution with the same Sr concentration and pH. Inner-sphere (IS) and outer-sphere (OS) Sr²⁺ constituted 87% of the total adsorbed species in IS:OS proportions of 19:81 compared to 42:58 in the solution without FA, suggesting that adsorbed FA competes with the IS Sr²⁺ for surface sites. The coverage of both IS and OS Sr²⁺ decreased even more in a pH 3.5 solution containing the same concentration of FA and 0.5 × 10⁻² mol/kg Sr(NO₃)₂, whereas a significant amount of Sr²⁺ accumulated farther from the surface in the FA layer. The amount of Sr²⁺ incorporated in the ∼10 Å thick FA layer decreased by 79% with decreasing FA concentration (100 → 1 mg/kg) and increasing Sr²⁺ concentration (0.5 × 10⁻² → 1 × 10⁻² mol/kg) and pH (3.5 → 3.6). These results indicate not only that adsorbed FA molecules (and perhaps also H₃O⁺) displace Sr²⁺ near the muscovite surface, but also that the sorbed FA film provides binding sites for additional Sr²⁺ away from the surface. When a muscovite crystal pre-coated with FA after reaction in a 100 mg/kg ESFA II solution for 50 h was subsequently reacted with a 0.5 × 10⁻² mol/kg Sr(NO₃)₂ and 100 mg/kg ESFA II solution at pH 3.7, a significant fraction of Sr²⁺ was distributed in the outer part of the FA film similar to that observed on fresh muscovite reacted at pH 3.5 with a pre-mixed Sr-FA solution at the same concentrations. However, this Sr²⁺ sorbed in the pre-adsorbed organic film was more widely distributed and had a lower coverage, suggesting that pre-sorbed FA may undergo fractionation and/or conformational changes that diminish its capacity, and that of the muscovite (0 0 1) surface, for adsorbing the aqueous Sr cation.     

Assessment of the likely sensitivity to climate change for the key marine species in the southern Benguela system

Climate change is altering many environmental parameters of coastal waters and open oceans, leading to substantial present-day and projected changes in the distribution, abundance and phenology of marine species. Attempts to assess how each species might respond to climate change can be data-, resource- and time-intensive. Moreover, in many regions of the world, including South Africa, species may be of vital socioeconomic or ecological importance though critical gaps may exist in our basic biological or ecological knowledge of the species. Here, we adapt and apply a trait-based sensitivity assessment for the key marine species in the southern Benguela system to estimate their potential relative sensitivity to the impacts of climate change. For our analysis, 40 priority species were selected based on their socioeconomic, ecological and/or recreational importance in the system. An extensive literature review and consultation with experts was undertaken concerning each species to gather information on their life history, habitat use and potential stressors. Fourteen attributes were used to estimate the selected species’ sensitivity and capacity to respond to climate change. A score ranging from low to high sensitivity was given for each attribute, based on the available information. Similarly, a score was assigned to the type and quality of information used to score each particular attribute, allowing an assessment of data-quality inputs for each species. The analysis identified the white steenbras Lithognathus lithognathus, soupfin shark Galeorhinus galeus, St Joseph Callorhinchus capensis and abalone Haliotis midae as potentially the most sensitive species to climate-change impacts in the southern Benguela system. There were data gaps for larval dispersal and settlement and metamorphosis cues for most of the evaluated species. Our results can be used by resource managers to determine the type of monitoring, intervention and planning that may be required to best respond to climate change, given the limited resources and significant knowledge gaps in many cases.