A chronology for glacial Lake Agassiz shorelines along Upham's namesake transect

Four traditionally recognized strandline complexes in the southern basin of glacial Lake Agassiz are the Herman, Norcross, Tintah and Campbell, whose names correspond to towns in west-central Minnesota that lie on a linear transect defined by the Great Northern railroad grade; the active corridor for commerce at the time when Warren Upham was mapping and naming the shorelines of Lake Agassiz (ca.1880–1895). Because shorelines represent static water planes, their extension around the lake margin establishes time-synchronous lake levels. Transitions between shoreline positions represent significant water-level fluctuations. However, geologic ages have never been obtained from sites near the namesake towns in the vicinity of the southern outlet. Here we report the first geologic ages for Lake Agassiz shorelines obtained at field sites along the namesake transect, and evaluate the emerging chronology in light of other paleoclimate records. Our current work from 11 sampling sites has yielded 16 independent ages. These results combined with a growing OSL age data set for Lake Agassiz's southern basin provide robust age constraints for the Herman, Norcross and Campbell strandlines with averages and standard deviations of 14.1 ± 0.3 ka, 13.6 ± 0.2 ka, and 10.5 ± 0.3 ka, respectively.     

Comparison of 105 years of oxygen isotope and insoluble impurity profiles from the Devon Island and Camp Century ice cores

Oxygen-isotope profiles for the Devon Island ice cap and Camp Century Greenland are affected by a number of variables, some of which must have been the same for both sites. The two δ(¹⁸O) records spanning about 120,000 years are brought into relative alignment by comparison of major δ features, and subsequent verification that the insoluble particulate concentration records were also in phase for this alignment. The difference between the δ profiles is shown to be mainly a function of the altitude of the accumulation area for Camp Century. This altitude seems to have been higher than present for the last 100,000 years, suggesting the present flow line through the site has never been shorter. The maximum altitude for the Camp Century accumulation area is 1500 m above the present site and is almost synchronous with the maximum in particulate concentration that occurs at 16,000 yr B.P. The synchronism is likely due to the maximum sea-level lowering that exposed vast areas of continental shelf to wind erosion.     

Detection of Extended Thermal Infrared Emission around the Vega-like Source HD 141569

We report the detection of extended IR emission at 10.8 and 18.2 μm around the Vega-like source HD 141569. Mid-IR imaging with OSCIR on Keck II shows emission from dust extending out to 100 AU from the B9.5 Ve star. Our modeling of the dust places an upper limit of approximately 2 μm on the diameter of the mid-IR-emitting particles if they are Mie spheres of astronomical silicates. Comparison of our mid-IR images to the near-IR (1.1 μm) NICMOS images of HD 141569 (Weinberger et al. 1999) shows that the mid-IR emission originates at smaller distances from the star than the scattered near-IR light, as also previously observed for the archetype Vega-like source beta Pictoris.     

The influence of pH on the kinetics, reversibility and mechanisms of Pb(II) sorption at the calcite-water interface

Pb(II) sorption experiments with calcite powders were conducted in suspensions equilibrated at atmospheric PCO_2(g) and ambient temperature at pH 7.3, 8.2 and 9.4. Pb fractional sorption was low at pH 7.3 and 9.4 relative to pH 8.2, and correlated well with PbCO₃⁰_(aq) speciation. Desorption experiments conducted for initial sorption times ranging from 0.5 h to 12 d reveal an almost completely reversible process at pH 8.2, attributed to the dominance of an adsorption mechanism, with slight and pronounced irreversibility at pH 7.3 and 9.4 respectively. Similarities in X-ray absorption near edge spectra (XANES) for 24 h and 12 d pH 7.3 and 9.4 sorption samples indicate no effect of initial sorption time. Results from linear combination (LC) fits of XANES spectra for samples sorbed at pH 9.4 confirm ∼75% adsorbed and ∼25% coprecipitated components. The coprecipitated fraction was attributed to the non-exchangeable metal observed in desorption experiments. At pH 7.3, ∼95% adsorbed and ∼5% coprecipitated components were obtained. A comparison of results from desorption experiments and LC-XANES alludes to an irreversibly bound adsorbed component for the pH 9.4 12 d sorption sample. Extended X-ray absorption fine structure spectroscopy (EXAFS) analysis of pH 7.3 and 9.4 12 d sorption samples confirms the presence of both adsorbed and coprecipitated metal. At pH 7.3 a first-shell Pb-O bond length of 2.38 Å is intermediate between that of adsorbed (2.34 Å) and coprecipitated (2.51 Å) Pb. At pH 9.4, two first-shell Pb-O distances at 2.35 Å and 2.51 Å were obtained, indicative of the occurrence of both adsorption and coprecipitation and a larger coprecipitated fraction relative to that at pH 7.3, consistent with LC-XANES results. We propose that the disparity in the fraction of coprecipitated metal with pH may be linked to the ability of sorbed Pb to inhibit near-surface dynamic exchange of Ca and CO₃ species, which dictates step advance and retreat. Less effective inhibition of step motion at pH 9.4, due to lower fractional sorption, combined with highest rates of dynamic exchange results in a significant fraction of coprecipitated Pb at this pH. At low pH, though fractional sorption is also low, lower rates of exchange prohibit significant coprecipitation. At pH 8.2, effective inhibition of surface processes due to higher fractional sorption and lower rates of exchange compared to pH 7.3 and 9.4 preclude detectable coprecipitation. Other factors such as changes in surface speciation and solubility of the Pb-Ca solid solution with pH may also come into play. Overall, this study presents evidence for the influence of pH on Pb sorption mechanisms, and addresses the efficiency of Pb immobilization in calcitic systems.     

Going West: Nutrient Limitation of Primary Production in the Northern Gulf of Mexico and the Importance of the Atchafalaya River

To investigate controls on phytoplankton production along the Louisiana coastal shelf, we mapped salinity, nutrient concentrations (dissolved inorganic nitrogen (DIN) and phosphorus (P_i), silicate (Si)), nutrient ratios (DIN/P_i), alkaline phosphatase activity, chlorophyll and ¹⁴C primary productivity on fine spatial scales during cruises in March, May, and July 2004. Additionally, resource limitation assays were undertaken in a range of salinity and nutrient regimes reflecting gradients typical of this region. Of these, seven showed P_i limitation, five revealed nitrogen (N) limitation, three exhibited light (L) limitation, and one bioassay had no growth. We found the phytoplankton community to shift from being predominately N limited in the early spring (March) to P limited in late spring and summer (May and July). Light limitation of phytoplankton production was recorded in several bioassays in July in water samples collected after peak annual flows from both the Mississippi and Atchafalaya Rivers. We also found that organic phosphorus, as glucose-6-phosphate, alleviated P limitation while phosphono-acetic acid had no effect. Whereas DIN/P_i and DIN/Si ratios in the initial water samples were good predictors of the outcome of phytoplankton production in response to inorganic nutrients, alkaline phosphatase activity was the best predictor when examining organic forms of phosphorus. We measured the rates of integrated primary production (0.33?C7.01 g C m^?2 d^?1), finding the highest rates within the Mississippi River delta and across Atchafalaya Bay at intermediate salinities. The lowest rates were measured along the outer shelf at the highest salinities and lowest nutrient concentrations (<0.1 ??M DIN and Pi). The results of this study indicate that P_i limitation of phytoplankton delays the assimilation of riverine DIN in the summer as the plume spreads across the shelf, pushing primary production over a larger region. Findings from water samples, taken adjacent the Atchafalaya River discharge, highlighted the importance of this riverine system to the overall production along the Louisiana coast.     

Rare gas abundances in MORB

Data are presented for He, Ar and Xe in a number of MORB glasses and crystalline rocks. The rare gases in the latter group are characterized by atmospheric Ar and Xe, coupled with loss of trapped mantle He, Ar and Xe. The glass data also show clear signs of an atmospheric-like component for Ar and Xe. A reasonably constant world-wide average trapped mantle gas value of ⁴⁰Ar/³⁶Ar ˜15000 ±3000 is suggested. Anomalies are seen in the ¹²⁹Xe/¹³²Xe ratio, but at least part of this might be due to mass fractionation rather than to ¹²⁹I decay. Correlating the data with those from oceanic island basalts in Ar-Xe space indicates that the latter samples are probably also greatly influenced by an atmospheric component rather than (or in addition to) trapping gases from an undepleted mantle source.     

Mainstreaming local perceptions of hurricane risk into policymaking: A case study of community GIS in Mexico

This article suggests a framework for incorporating and communicating local perceptions of hurricane risk into policymaking through a case study conducted at El Zapotito commune in the State of Veracruz, Mexico. The authors constructed a geographical information system (GIS)-based model to quantify and spatially assess specific household-level vulnerabilities from information generated through interviews. This research developed a household vulnerability index applied to a participatory GIS to map vulnerability to hurricane hazard. The results indicate that infrastructural weaknesses are the most important factor contributing to vulnerability, explaining on their own 72.2% of the variation in the vulnerability patterns. These findings are corroborated by a vulnerability and capacity assessment (VCA), which shows that the community lacks strategies to cope with unsafe housing. It is suggested that linking community participation with modern techniques to analyse risk can empower communities and mobilise their capacities to address very specific vulnerabilities.