Identification of Winter Flounder (Pseudopleuronectes americanus) Estuarine Spawning Habitat and Factors Influencing Egg and Larval Distributions

A long-term (2002–2011), spatially robust, ichthyoplankton sampling program conducted in the New York/New Jersey Harbor produced 3,033 epibenthic samples from which the relationships between winter flounder egg and larval distributions and environmental parameters were examined. Variations in water temperature, sediment characteristics, and tidal phase were all significantly associated with egg distributions. Inferences about spawning habitats were based on the presence of early-stage eggs (ES1 and ES2). In the Lower Bay (LB), these habitats were primarily non-channel and characterized by more sandy substrates, averaging 96.5 % sand, 2.3 % silt/clay, 0.2 % total organic carbon (TOC), and shallower water (average depths of 5.3 m) compared to LB non-channel stations without ES1 and ES2 eggs (50.2 % sand, 42.0 % silt/clay, 2.1 % TOC, and 7.9 m depths). Occurrences of all stages of eggs in channels were associated with strong tides and severe cold winter water temperatures. These conditions increase the probability of egg transport from shallow spawning sites through increased vertical mixing (strong tides) and delayed development that prolongs the risk of displacement (cold temperatures). Yolk-sac (YS) and Stage-2 larvae were smaller in 2010 when spring water temperatures were highest. Overall, YS larval size decreased with warmer winters (cumulative degree-days for the month preceding peak YS larval collections, r ²?=?0.82, p?<?0.05). In all years, YS larvae collected in LB were smaller and Stage-3 larvae collected in channels were larger and possibly older than those from non-channel habitat. Because estuarine winter flounder populations are highly localized, adverse effects experienced during egg and larval stages are likely to propagate resulting in detrimental consequences for the year class in the natal estuary.     

S-33 constraints on the seawater sulfate contribution in modern seafloor hydrothermal vent sulfides

Sulfide sulfur in mid-oceanic ridge hydrothermal vents is derived from leaching of basaltic-sulfide and seawater-derived sulfate that is reduced during high temperature water rock interaction. Conventional sulfur isotope studies, however, are inconclusive about the mass-balance between the two sources because ³⁴S/³²S ratios of vent fluid H₂S and chimney sulfide minerals may reflect not only the mixing ratio but also isotope exchange between sulfate and sulfide. Here, we show that high-precision analysis of S-33 can provide a unique constraint because isotope mixing and isotope exchange result in different Δ³³S (≡δ³³S-0.515 δ³⁴S) values of up to 0.04‰ even if δ³⁴S values are identical. Detection of such small Δ³³S differences is technically feasible by using the SF₆ dual-inlet mass-spectrometry protocol that has been improved to achieve a precision as good as 0.006‰ (2σ).Sulfide minerals (marcasite, pyrite, chalcopyrite, and sphalerite) and vent H₂S collected from four active seafloor hydrothermal vent sites, East Pacific Rise (EPR) 9-10°N, 13°N, and 21°S and Mid-Atlantic Ridge (MAR) 37°N yield Δ³³S values ranging from −0.002 to 0.033 and δ³⁴S from −0.5‰ to 5.3‰. The combined δ³⁴S and Δ³³S systematics reveal that 73 to 89% of vent sulfides are derived from leaching from basaltic sulfide and only 11 to 27% from seawater-derived sulfate. Pyrite from EPR 13°N and marcasite from MAR 37°N are in isotope disequilibrium not only in δ³⁴S but also in Δ³³S with respect to associated sphalerite and chalcopyrite, suggesting non-equilibrium sulfur isotope exchange between seawater sulfate and sulfide during pyrite precipitation. Seafloor hydrothermal vent sulfides are characterized by low Δ³³S values compared with biogenic sulfides, suggesting little or no contribution of sulfide from microbial sulfate reduction into hydrothermal sulfides at sediment-free mid-oceanic ridge systems. We conclude that ³³S is an effective new tracer for interplay among seawater, oceanic crust and microbes in subseafloor hydrothermal sulfur cycles.     

Can we spot a neighborhood from the air? Defining neighborhood structure in Accra, Ghana

Slums are home to a large fraction of urban residents in cities of developing nations, but little attempt has been made to go beyond a simple slum/non-slum dichotomy, nor to identify slums more quantitatively than through local reputation. We use census data from Accra, Ghana, to create an index that applies the UN-Habitat criteria for a place to be a slum. We use this index to identify neighborhoods on a continuum of slum characteristics and on that basis are able to locate the worst slums in Accra. These do include the areas with a local reputation for being slums, lending qualitative validation to the index. We show that slums also have footprints that can be identified from data classified from satellite imagery. However, variability among slums in Accra is also associated with some variability in the land cover characteristics of slums.     

Variations in the type and distribution of organic matter in some Carboniferous sediments from northern England

The organic content of a number of sediments from the Carboniferous of northern England have been examined as a function of their depositional environment. Extraction of the sediments yielded the soluble organic matter whilst microscopic examination of polished blocks of shales enabled the detection of particles of organic detritus. A relationship between the amount of extract and the quantity of terrestrial plant material in the sediments has been established. However, the yield of extract (mg/g org. C) is higher in the more marine environment than the nonmarine environment. The proportion of saturated hydrocarbons in the extract appears to be related to the amount of identifiable organic matter (coal macerals) in the sediment. The n-alkane distribution patterns have been compared with these obtained from coal macerals. The suggestion that the pristane to phytane ratios may reflect the source material of the organic matter has been examined.     

Experiments in reconstructing twentieth-century sea levels

One approach to reconstructing historical sea level from the relatively sparse tide-gauge network is to employ Empirical Orthogonal Functions (EOFs) as interpolatory spatial basis functions. The EOFs are determined from independent global data, generally sea-surface heights from either satellite altimetry or a numerical ocean model. The problem is revisited here for sea level since 1900. A new approach to handling the tide-gauge datum problem by direct solution offers possible advantages over the method of integrating sea-level differences, with the potential of eventually adjusting datums into the global terrestrial reference frame. The resulting time series of global mean sea levels appears fairly insensitive to the adopted set of EOFs. In contrast, charts of regional sea level anomalies and trends are very sensitive to the adopted set of EOFs, especially for the sparser network of gauges in the early 20th century. The reconstructions appear especially suspect before 1950 in the tropical Pacific. While this limits some applications of the sea-level reconstructions, the sensitivity does appear adequately captured by formal uncertainties. All our solutions show regional trends over the past five decades to be fairly uniform throughout the global ocean, in contrast to trends observed over the shorter altimeter era. Consistent with several previous estimates, the global sea-level rise since 1900 is 1.70 ± 0.26 mm yr⁻¹. The global trend since 1995 exceeds 3 mm yr⁻¹ which is consistent with altimeter measurements, but this large trend was possibly also reached between 1935 and 1950.     

Consistency of temporal and habitat-related differences among assemblages of fish in coastal lagoons

The consistency of habitat-related differences in coastal lagoon fish assemblages was assessed across different spatial and temporal scales. Multimesh gillnets were used to sample assemblages of fish on a monthly basis for 1-year in three habitats (shallow seagrass, shallow bare and deep substrata) at two locations (>1 km apart), in each of two coastal lagoons (approximately 500 km apart), in southeastern Australia. A total of 48 species was sampled with 34 species occurring in both lagoons and in all three habitats; species caught in only one lagoon or habitat occurred in low numbers. Ten species dominated assemblages and accounted for more than 83% of all individuals sampled. In both lagoons, assemblages in the deep habitat consistently differed to those in the shallow strata (regardless of habitat). Several species were caught more frequently or in larger numbers in the deep habitat. Assemblages in the two shallow habitats did not differ consistently and were dominated by the same species and sizes of fish, possibly due to habitat heterogeneity and the scale and method of sampling. Within each lagoon, very few between location differences in assemblages within each habitat were observed. Consistent differences in assemblages were detected between lagoons for the shallow bare and deep habitats, indicating there were some intrinsic differences in ichthyofauna between lagoons. Assemblages in spring differed to those in summer, which differed to those in winter for the shallow bare habitat in both lagoons, and the deep habitat in only one lagoon. Fish-habitat relationships are complex and differences in the fish fauna between habitats were often temporally inconsistent. This study highlights the need for greater testing of habitat relationships in space and time to assess the generality of observations and to identify the processes responsible for structuring assemblages.     

Coupled North Atlantic slope water forcing on Gulf of Maine temperatures over the past millennium

To investigate ocean variability during the last millennium in the Western Gulf of Maine (GOM), we collected a 142-year-old living bivalve (Arctica islandica L.) in 2004, and three fossil A. islandica shells (calibrated ¹⁴C_AMS = 1030 ± 78 ad; 1320 ± 45 ad; 1357 ± 40 ad) for stable isotope and growth increment analysis. A statistically significant relationship exists between modern GOM temperature records [shell isotope-derived (30 m) (r = ?0.79; P < 0.007), Prince 5 (50 m) (r = ?0.72; P < 0.019), Boothbay Harbor SST (r = ?0.76; P < 0.011)], and Labrador Current (LC) transport data from the Eastern Newfoundland Slope during 1993–2003. In all cases, as LC transport increased, GOM water temperatures decreased the following year. Decadal trends in the North Atlantic Oscillation (NAO) and the Atlantic Multidecadal Oscillation (AMO) influence GOM water temperatures in the most recent period, with water temperatures decreasing during NAO and AMO negative modes most likely linked to LC transport and Gulf Stream interaction. Mean shell-derived isotopic changes (δ¹⁸O_c) during the last 1,000 years were +0.47‰ and likely reflect a 1–2°C cooling from 1000 ad to present. Based on these results, we suggest that observed cooling in the GOM during the last millennium was due to increased transport and/or cooling of the LC, and decreased Gulf Stream influence on the GOM.