Importance of water quality to nekton habitat use in a North Carolina Branch estuary

Nekton abundance and water quality were examined over 8 yr (1986–1993) in Isaac Creek, a small (2.5 km long), shallow (1–2 m), estuarine creek draining to Adams Creek (Neuse River system), North Carolina, United States. Water quality and nekton were sampled at 8 to 12 stations at 2–3 wk intervals from April to October (76 dates). The nekton assemblage, sampled by trawl, included 42 taxa but was dominated by 11 species (7 fish and 4 decapod crustaceans). Nekton and water quality (temperature, salinity, dissolved oxygen [DO], salinity gradient) data were grouped and analyzed by three (upper, middle, and lower) creek zones to determine if estimated abundance was correlated with water quality. Potentially stressful water quality conditions for salinity (<5 ppt), temperature (>30°C in morning), and DO (<2 mg 1⁻¹) mainly occurred in the upper and middle zones. The most frequent occurrence of potentially stressful conditions for salinity was in the spring and for dissolved oxygen and temperature in middle to late summer. The frequency of potentially stressful conditions increased during a 3-yr period following timber harvest of a large portion of the watershed. Canonical correspondence analysis (CCA) suggested little correlation between the top 11 species and water quality and indicated an assemblage with regular seasonal changes. Comparison of nekton use of the middle and upper zones of the creek for 3-yr pre- and post-harvest periods showed an increase in proportion of nekton caught in those zones, despite the higher frequency of potentially stressful water quality conditions. This observation suggests that a complex set of factors, including water quality, influence the pattern of nekton use in Isaac Creek.     

Influence of vegetation change on watershed hydrology: implications for paleoclimatic interpretation of lacustrine δ18O records

Stratigraphic shifts in the oxygen isotopic (¹⁸O) and trace element (Mg and Sr) composition of biogenic carbonate from tropical lake sediment cores are often interpreted as a proxy record of the changing relation between evaporation and precipitation (E/P). Holocene ¹⁸O and Mg and Sr records from Lakes Salpetén and Petén Itzá, Guatemala were apparently affected by drainage basin vegetation changes that influenced watershed hydrology, thereby confounding paleoclimatic interpretations. Oxygen isotope values and trace element concentrations in the two lowland lakes were greatest between ~ 9000 and 6800 ¹⁴C-yr BP, suggesting relatively high E/P, but pollen data indicate moist conditions and extensive forest cover in the early Holocene. The discrepancy between pollen- and geochemically-inferred climate conditions may be reconciled if the high early Holocene ¹⁸O and trace element values were controlled principally by low surface runoff and groundwater flow to the lake, rather than high E/P. Dense forest cover in the early Holocene would have increased evapotranspiration and soil moisture storage, thereby reducing delivery of meteoric water to the lakes. Carbonate ¹⁸O and Mg and Sr decreased between 7200 and 3500 ¹⁴C-yr BP in Lake Salpetén and between 6800 and 5000 ¹⁴C-yr BP in Lake Petén Itzá. This decline coincided with palynologically documented forest loss that may have led to increased surface and groundwater flow to the lakes. In Lake Salpetén, minimum ¹⁸O values (i.e., high lake levels) occurred between 3500 and 1800 ¹⁴C-yr BP. Relatively high lake levels were confirmed by ¹⁴C-dated aquatic gastropods from subaerial soil profiles ~ 1.0–7.5 m above present lake stage. High lake levels were a consequence of lower E/P and/or greater surface runoff and groundwater inflow caused by human-induced deforestation.     

Tar ball frequency data and analytical results from a long-term beach monitoring program

Following the spill of fuel oils from the New Carissa in February 1999, approximately 300 km of beaches on the Pacific coast of North America were surveyed. A long-term observation program focused on the documentation of stranded tar balls in the vicinity of the spill site. Systematic beach surveys which were conducted over the period March 1999 to April 2001 and semi-logarithmic scale, time-series plots proved the most useful format for identifying trends. Beach monitoring continued through to August 2001. by which time 212 tar balls had been analyzed by GC/MS for their chemical characteristics. The samples of tar balls collected between February 1999 and August 2001 were qualitatively compared with New Carissa source oils (NCSO) and 101 (48%) were not consistent with NSCO. The presence of tar balls that are not related to an incident can confound attempts to define cleanup or endpoint criteria and to assess possible injury to natural resources.     

The relation between rigorous and Helmert’s definitions of orthometric heights

Following our earlier definition of the rigorous orthometric height [J Geod 79(1-3):82–92 (2005)] we present the derivation and calculation of the differences between this and the Helmert orthometric height, which is embedded in the vertical datums used in numerous countries. By way of comparison, we also consider Mader and Niethammer’s refinements to the Helmert orthometric height. For a profile across the Canadian Rocky Mountains (maximum height of ~2,800 m), the rigorous correction to Helmert’s height reaches ~13 cm, whereas the Mader and Niethammer corrections only reach ~3 cm. The discrepancy is due mostly to the rigorous correction’s consideration of the geoid-generated gravity disturbance. We also point out that several of the terms derived here are the same as those used in regional gravimetric geoid models, thus simplifying their implementation. This will enable those who currently use Helmert orthometric heights to upgrade them to a more rigorous height system based on the Earth’s gravity field and one that is more compatible with a regional geoid model.     

ARGO upper salinity measurements: perspectives for L-band radiometers calibration and retrieved sea surface salinity validation

With the view of preparing the strategy for the calibration/validation of future L-band satellite radiometers, we examine the salinity variability recorded by Array for Real-Time Geostrophic Oceanography (ARGO) floats in the upper 10-m layer of the surface ocean. Using one year of ARGO measurements,we show that the surface salinity variability at ten days and 200-km scales is above /spl plusmn/0.1 psu for 30% of the drifters and that this variability is larger than 0.2 psu in tropical regions affected by strong river discharges and by precipitations, and in frontal areas characterized by strong mesoscale activity. Vertical gradient observed between 5-10-m depth is much lower than the horizontal variability but leads to systematic biases in the tropics. The South Pacific Ocean appears to be the less variable both vertically and horizontally.     

Doppler radar observation, CG lightning activity and aerial survey of a multiple downburst in southern Germany on 23 March 2001

Two downburst events from one thunderstorm are investigated, which occurred on 23 March 2001, in Germany's climatologic annual minimum of downburst activity. Observations by two Doppler radars are combined with hail reports, ground lightning detection and an aerial survey conducted after the event. The downburst-producing storm had formed at a synoptic convergence line within the warm sector of a cyclone. It had a remarkably high propagation speed of up to 31 m s^− 1 corresponding to the mid-tropospheric flow. Thus, by superposition with the storm motion, even two weak downbursts were sufficient to cause the observed damage of F1 and F2 intensity, respectively. While in its late stages, the storm was dynamically characterized by lower- and mid-tropospheric divergence; at about the time of the first downburst, a mesocyclonic vortex signature was verified. Aside from mid-tropospheric dry air entrainment, a thermodynamic explanation for the triggering of the two downbursts by melting of small hail according to recent findings by Atlas et al. [Atlas, D., Ulbrich, C.W., Williams, C.R., 2004. Physical origin of a wet microburst: observations and theory. J. Atmos. Sci. 61, 1186–1196] appears probable. Despite the lack of warnings to the public, the storm's potential for hail and strong straight-line winds was detected by the German weather service radar software CONRAD more than a half hour before the downbursts occurred.     

α-Emitting mineral inclusions in apatite, their effect on (U-Th)/He ages, and how to reduce it

U-Th rich mineral inclusions in apatite are often held responsible for erroneously old (U-Th)/He ages, because they produce “parentless” He. Three aspects associated with this problem are discussed here. First, simple dimensional considerations indicate that for small mineral inclusions, the parentless helium problem might not be as serious as generally thought. For example, a mineral inclusion that is 10% the length, width and height of its host apatite needs to be a thousand times more concentrated in U and Th to produce an equal amount of He. Therefore, single isolated inclusions smaller than a few μm are unlikely to contribute significant helium. For larger or more abundant inclusions, the parentless helium problem can be solved by dissolution of the apatite and its inclusions in hot HF. Second, besides creating parentless helium, inclusions also complicate α-ejection corrections. Mathematical exploration of this latter problem for spherical geometries reveals that for randomly distributed inclusions, the probability distribution of single-grain ages is predicted to have a sharp mode at the mean age, with tails towards younger and older ages. Multiple-grain measurements will yield accurate and precise age estimates if 10 or more randomly distributed α-emitting mineral inclusions are present in a sample. Third, thermal modeling indicates that mineral inclusions have a non-trivial but minor (<5 °C) effect on the closure temperature. These predictions were tested on apatites from rapidly cooled migmatites of Naxos (Greece) which contain abundant U-rich zircon inclusions. Thirty-seven samples were subjected to two kinds of treatment. The “pooled” age (i.e., the synthetic multi-grain age computed from a number of single-grain analyses) of four inclusion-free samples (13 apatites), prepared in HNO₃ is 10.9 Ma, close to apatite and zircon fission-track ages from the same rock. (U-Th)/He ages of 14 inclusion-bearing samples dissolved in HNO₃ range between 9 and 45 Ma, with a pooled age of 22.6 Ma. The ages of 19 HF-treated samples range between 5 and 16 Ma, with 10 of 14 single-grain samples between 9 and 13 Ma and a pooled age of 10.9 Ma. These observations agree with the theoretical predictions and support the addition of HF-treated apatite (U-Th)/He dating to the thermochronological toolbox.     

Changes in size distribution of fresh water nanoscale colloidal matter and associated elements on mixing with seawater

Changes in size distribution and elemental composition of 0.5-50 nm fresh water colloids during estuarine mixing have been studied by in-laboratory mixing of natural creek water and synthetic seawater, followed by size fractionation with Asymmetrical Flow Field-Flow Fractionation, and online elemental quantification by High-Resolution ICPMS. At least two types of colloids were present in the studied size region; 0.5-3 nm fluorescent dissolved organic matter (FDOM), and >3 nm colloids that were rich in Fe and colored dissolved organic matter (CDOM). Most trace elements were associated in different proportions to these two populations of colloids. Following mixing with synthetic seawater, the >3 nm Fe-rich colloids and CDOM were extensively removed from the studied size region by salt induced aggregation. The degree of removal with increasing salinity was greatest below 2.5‰ salinity, continued to a lesser degree between 2.5‰ and 15‰ salinity, above which only very small additional removal could be distinguished. At 25‰ salinity, the Fe concentration in the 0.5-50 size region had been reduced down to 15% of its original value in freshwater, while the amount of CDOM had been reduced to 55%. On the contrary, the concentration of the 0.5-3 nm FDOM was unchanged by the increased concentration of sea salt. Therefore, colloidally associated Al, P, Co, Cu, Zn, Ce, Lu and Pb were removed from the 0.5-50 nm size region according to their relative distributions between the FDOM and the Fe-rich colloids. Consequently, at 25‰ salinity, the 0.5-50 nm concentrations of Al, Mn, P and Pb, (mainly associated with the Fe-rich colloids) had been reduced down to 13-26 % of their values in freshwater, while the concentrations of Co and Cu (with higher preferences for FDOM) were less reduced, down to 46% and 57%, respectively. Changes in the elemental composition of the remaining colloidal matter were observed, the most pronounced were increased contents of P, Al and Pb in Fe-rich colloidal matter of medium size (∼3-15 nm) and increased Pb content in Fe-rich colloidal matter of larger size (∼5-50 nm).