Likely Population-Level Effects of Contaminants on a Resident Estuarine Fish Species: Comparing <Emphasis Type="Italic">Gillichthys mirabilis</Emphasis> Population Static Measurements and Vital Rates in San Francisco and Tomales Bays

Gillichthys mirabilis population static measurements (abundance, age, and size class structures) and vital rates (growth, mortality, recruitment) were monitored on an annual basis from 2002 to 2007. Population-level metrics were used to gauge habitat quality at two study sites (a contaminated site and a reference site) in two large northern California estuaries (San Francisco and Tomales Bays). San Francisco Bay populations exhibited slower growth and higher mortality rates and contained higher amounts of contaminants than Tomales Bay. Recruitment rates were highest at contaminated sites (Stege Marsh and Walker Creek) in 3 years out of 5 years, suggesting low adult survival. This study suggests that population-level effects on a residential fish may be attributed to estuarine contamination on the US Pacific coast.     

Rapid and Intense Phosphate Desorption Kinetics When Saltwater Intrudes into Carbonate Rock

It is important to understand how phosphate sorption dynamics of coastal carbonate aquifers are affected by seawater intrusion, because many coastal aquifers are composed of carbonate rocks and subject to an increase in saltwater intrusion during relative sea-level rise. Twelve carbonate rock and unconsolidated sediment specimens were acquired from a test corehole spanning the full thickness of the Biscayne aquifer in southeastern Florida. All 12 samples exhibit low phosphorus content but variable contents of iron. Column leaching experiments were conducted with two carbonate aquifer samples, alternating between freshwater and saltwater flow. With the first influx of saltwater, phosphate concentration in leachate increased rapidly from a freshwater value of approximately 0.2 μM to peaks of between 0.8 and 1.6 μM. The phosphate concentration began to diminish as saltwater continued to flow, but sustained desorption continued for over 2 h. Overall, seawater drove sorption behavior much more than chemical composition for the aquifer rocks and sediment from the seven rock samples for which we did isotherm sorption experiments. Our results indicate that an immediate and intense pulse of phosphate desorption from carbonate rock and sediment with low phosphorus content occurs in response to an influx of seawater and that the duration of desorption will vary by layer within a single aquifer.     

The Cerro los Calvos and La Banderia chondrites

Abstract— The Cerro los Calvos meteorite is a single stone of 68.5 g found in the Nuevo Mercurio strewn field of Zacatecas, Mexico (24°20′N, 102°8′W). It is an unusual H4 chondrite. Its olivine (Fa_12.5) and orthopyroxene (Fs 11.7, Wo 0.8) are reduced relative to typical H chondrites. The La Banderia meteorite of 54.3 g from the same vicinity is an LL5 chondrite of shock classification e.     

Io: Geochemistry of sulfur

The evidence from Voyager imaging, Earth-based spectral reflectivity studies, and thermal emission measurements combine to suggest an extremely fresh, volcanically recycled sulfur-rich crust for Io, with very shallow large-scale melting. Two present styles of volcanism are possible, depending on the thickness of local deposits of sulfur: shallow liquid sulfur magma generation with quiescent flooding, and high-temperature volcanism with violent eruption of a sulfur-iron magma driven by SO₂. Evolutionary considerations preclude direct derivation of Io's lithosphere from any metal-bearing chondritic source material. Metal-free C3V- or C2M-type parent material of either primary or secondary origin is the most plausible direct antecedent of the present sulfur-rich crust. Sulfates are almost certainly important constituents of the mantle, and can participate in the recycling of reduced, dense sulfide species to prevent total extraction of sulfur into the core.     

Intertidal mudflat properties, currents and sediment erosion in the partially mixed Tamar Estuary, UK

Results are presented from a 1-year campaign to measure the seasonal variability of some key physical and biological properties of intertidal mudflats over a section of the central Tamar Estuary and to relate these to the physical environment. Seasonal variations in physical mudflat properties, such as grain size, density and moisture content were relatively small. With the exception of the particulate organic carbon content in the upper 0.002 m of surface sediment, biological variations were large. Redox potential exhibited considerable seasonal variation and showed that the sediments were less reduced in winter and more reduced in summer. Chlorophyll a and extracellular polymeric substances (EPS) within the surface 0.002 m of sediment (due to the presence of benthic diatoms) were strongly correlated and exhibited a pronounced seasonal pattern, with smallest values during winter and greatest values during late summer and early autumn. EPS had a dominating influence on sediment erosion, as determined from annular flume measurements. Velocity measurements and velocity modelling indicated that during the flood, and for much of the time during benthic diatom bloom conditions of high chlorophyll a and EPS sediment contents, the stresses exerted by tidal currents were too small to cause significant suspension of sediments over much of the middle and upper mudflats. Suspended fine sediment in the turbidity maximum zone was transported down-estuary and deposited in the main channel at low-water (LW) slack. Some of this sediment, in the form of relatively large aggregates, was subsequently transported onto the mudflats during the flooding tide, where slack currents and fast settling velocities may have enhanced sediment deposition there.Responsible Editor: Hans Burchard     

A granite–gabbro complex from Madagascar: constraints on melting of the lower crust

The Ranomandry Complex is a Neoproterozoic, nested intrusion from central Madagascar composed of a gabbroic core within a coeval peraluminous granite ring intruding pelitic metasediments. Although xenocryst entrainment and magma mixing have both contributed to marginal phases of the granite, the primary melt is characterised by steep LREE/HREE ratios and negligible, or slightly positive, Eu anomalies. Both isotopic and trace element systematics preclude an origin from either partial melting of the metapelitic country rock or from fractional crystallisation of the gabbroic magma. However, trace-element modelling suggests an origin from the dehydration melting of a plagioclase-poor, garnet-bearing metagreywacke at temperatures of 850–900 °C and at lower crustal pressures (>10 kbar). Melting of an enriched subcontinental mantle generated gabbroic magmas that caused advective heating and anatexis at the base of thickened continental crust during their ascent. Transport of the resulting granite magma was facilitated by the pre-existing plumbing system that overcame thermal and mechanical problems associated with both diapirism and self-propagating dykes as mechanisms for long-distance transport of granite magmas. The nested geometry of the intrusions is an indication of a structurally homogeneous lower crust that contains no pre-existing shear zones or fault systems.     

Geological setting of the Rapu Rapu gold-rich volcanogenic massive sulfide deposits,Albay Province,Philippines

Gold-rich Fe–Cu–Zn volcanogenic massive sulfide deposits occur within strata of probable Jurassic age on Rapu Rapu Island in Albay Province, Philippines. Massive sulfides at the Ungay Malobago and Hixbar deposits are spatially associated with dacitic volcanic rocks within a highly-deformed sequence of mafic volcanic and quartzofeldspathic sedimentary rocks. The massive sulfide deposits formed at the stratigraphic contact between footwall dacites and hangingwall mafic volcanic and quartzofeldspathic rocks. The deposits and their host strata have undergone regional metamorphism with strong penetrative deformation. Metamorphic mineral assemblages and textural evidence suggest that peak metamorphism was upper-greenschist to lower-amphibolite grade and syn-D₁ deformation. Based on the age of regional metamorphism, deformation is inferred to be mid-Tertiary in age. Deformation at Rapu Rapu resulted in reorientation of the strata into a broad antiform with strong shallow-plunging elongation fabrics, overturning of the volcanic sequence that hosts the Ungay Malobago deposit, and complex folding of the mineralized zones. The present highly linear form of the Ungay Malobago deposit is mainly a product of this ductile strain.Immobile element ratios for a given lithology generally remain constant in saprolitic samples, and thus provide an effective identification tool even in strongly weathered rocks. Lithogeochemical data define a bimodal volcanic suite that is comparable to bimodal assemblages that occur in several modern back-arc basins in the southwestern Pacific Ocean, including those behind the Vanuatu and the New Britain arcs. On Rapu Rapu, the dacitic rocks are enriched in light REE and have high Zr/Y ratios, which indicates a calc–alkaline affinity and suggests a mature island-arc setting. The quartzofeldspathic sedimentary rocks are more widespread than the dacites and have notably lower Zr/Y ratios; they may have been derived from erosion of a distant volcanic arc. The mafic volcanic rocks are dominantly low-K arc tholeiites of basaltic to andesitic composition, but with modest enrichment in the light REE; comparable rocks can be found in the Vanuatu and New Britain back-arc basins.Electronic Supplementary Material Supplementary material is available in the online version of this article at http://dx.doi.org/10.1007/s00126-003-0349-0An erratum to this article can be found at Editorial handling: O. Christensen     

Metal–organic complexation in the marine environment

We discuss the voltammetric methods that are used to assess metal–organic complexation in seawater. These consist of titration methods using anodic stripping voltammetry (ASV) and cathodic stripping voltammetry competitive ligand experiments (CSV-CLE). These approaches and a kinetic approach using CSV-CLE give similar information on the amount of excess ligand to metal in a sample and the conditional metal ligand stability constant for the excess ligand bound to the metal. CSV-CLE data using different ligands to measure Fe(III) organic complexes are similar. All these methods give conditional stability constants for which the side reaction coefficient for the metal can be corrected but not that for the ligand. Another approach, pseudovoltammetry, provides information on the actual metal–ligand complex(es) in a sample by doing ASV experiments where the deposition potential is varied more negatively in order to destroy the metal–ligand complex. This latter approach gives concentration information on each actual ligand bound to the metal as well as the thermodynamic stability constant of each complex in solution when compared to known metal–ligand complexes. In this case the side reaction coefficients for the metal and ligand are corrected. Thus, this method may not give identical information to the titration methods because the excess ligand in the sample may not be identical to some of the actual ligands binding the metal in the sample.     

Diagenesis and geochemistry of porites corals from Papua New Guinea: Implications for paleoclimate reconstruction

Coral proxy records of sea surface temperature (SST) and hydrological balance have become important tools in the field of tropical paleoclimatology. However, coral aragonite is subject to post-depositional diagenetic alteration in both the marine and vadose environments. To understand the impact of diagenesis on coral climate proxies, two mid-Holocene Porites corals from raised reefs on Muschu Island, Papua New Guinea, were analysed for Sr/Ca, δ¹⁸O, and δ¹³C along transects from 100% aragonite to 100% calcite. Thin-section analysis showed a characteristic vadose zone diagenetic sequence, beginning with leaching of primary aragonite and fine calcite overgrowths, transitional to calcite void filling and neomorphic, fabric selective replacement of the coral skeleton. Average calcite Sr/Ca and δ¹⁸O values were lower than those for coral aragonite, decreasing from 0.0088 to 0.0021 and −5.2 to −8.1‰, respectively. The relatively low Sr/Ca of the secondary calcite reflects the Sr/Ca of dissolving phases and the large difference between aragonite and calcite Sr/Ca partition coefficients. The decrease in δ¹⁸O of calcite relative to coral aragonite is a function of the δ¹⁸O of precipitation. Carbon-isotope ratios in secondary calcite are variable, though generally lower relative to aragonite, ranging from −2.5 to −10.4%. The variability of δ¹³C in secondary calcite reflects the amount of soil CO₂ contributing ¹³C-depleted carbon to the precipitating fluids. Diagenesis has a greater impact on Sr/Ca than on δ¹⁸O; the calcite compositions reported here convert to SST anomalies of 115°C and 14°C, respectively. Based on calcite Sr/Ca compositions in this study and in the literature, the sensitivity of coral Sr/Ca-SST to vadose-zone calcite diagenesis is 1.1 to 1.5°C per percent calcite. In contrast, the rate of change in coral δ¹⁸O-SST is relatively small (−0.2 to 0.2°C per percent calcite). We show that large shifts in δ¹⁸O, reported for mid-Holocene and Last Interglacial corals with warmer than present Sr/Ca-SSTs, cannot be caused by calcite diagenesis. Low-level calcite diagenesis can be detected through X-ray diffraction techniques, thin section analysis, and high spatial resolution sampling of the coral skeleton and thus should not impede the production of accurate coral paleoclimate reconstructions.