Variability and trends in the annual snow‐cover cycle in Northern Hemisphere land areas, 1972–2000

This study investigated variability and trends in the annual snow‐cover cycle in regions covering high‐latitude and high‐elevation land areas in the Northern Hemisphere. The annual snow‐cover cycle was examined with respect to the week of the last‐observed snow cover in spring (WLS), the week of the first‐observed snow cover in autumn (WFS), and the duration of the snow‐free period (DSF). The analysis used a 29‐year time‐series (1972–2000) of weekly, visible‐band satellite observations of Northern Hemisphere snow cover from NOAA with corrections applied by D. Robinson of Rutgers University Climate Laboratory. Substantial interannual variability was observed in WLS, WFS and DSF (standard deviations of 0·8–1·1, 0·7–0·9 and 1·0–1·4 weeks, respectively), which is related directly to interannual variability in snow‐cover area in the regions and time periods of snow‐cover transition. Over the nearly three‐decade study period, WLS shifted earlier by 3–5 days/decade as determined by linear regression analysis. The observed shifts in the annual snow‐cover cycle underlie a significant trend toward a longer annual snow‐free period. The DSF increased by 5–6 days/decade over the study period, primarily as a result of earlier snow cover disappearance in spring. The observed trends are consistent with reported trends in the timing and length of the active growing season as determined from satellite observations of vegetation greenness and the atmospheric CO₂ record. Copyright © 2002 John Wiley & Sons, Ltd.     

The composition of asteroid 2 Pallas and its relation to primitive meteorites

High resolution spectroscopic observations of asteroid 2 Pallas from 1.7-3.5 μm are reported. These data are combined with previous measurements from 0.4-1.7 μm to interpret Pallas' surface mineralogy. Evidence is found for low-Fe²⁺ hydrated silicates, opaque components, and low-Fe²⁺ anhydrous silicates. This assemblage is very similar to carbonaceous chondrite matrix material such as is found in type CI and CM meteorites, but it has been subjected to substantial aqueous alteration and there is a major extraneous anhydrous silicate component. This composition is compared to that of asteroid 1 Ceres. Although there are substantial differences in their broad band spectral reflectances, it appears that both asteroids are genetically related to known carbonaceous chondrites.     

Evaluation of extraction schemes for organic matter in anoxic estuarine sediments

A persistent criticism of studies of organic matter in sediments and soils has been that the extracted products used in these investigations may not resemble the original material, particularly if harsh extractants such as NaOH, Na₄P₂O₇ or HCl are employed. To minimize chemical changes, a mild separation procedure has been developed for obtaining soluble organic matter from anoxic estuarine sediments. The resulting complex mixture of organic compounds can be analyzed by reversed-phase liquid and size-exclusion chromatographic methods, which monitor the relative molecular polarity and size, respectively. The effects of the strong reagents NaOH, Na₄P₂O₇ and HCl, as well as exposure to the atmosphere and bacterial activity on this anoxic sedimentary extract has been investigated. In each instance, significant degradation of anoxic organic matter occurs, producing molecules of increased polarity and reduced molecular weight. These data indicate that extreme care is necessary to avoid artifacts in preparation and handling of samples.     

Production and R&D networks of foreign ventures in China: Implications for technological dynamism and regional development

This paper analyzes the nature of FDI local networks in production and R&D activities in China and discusses their implications for technological dynamism and regional development. We investigate foreign ventures (or foreign-invested enterprises, FIEs) in the information and communication technology (ICT) industry, based on a large-scale survey of ICT firms conducted in three mega-city regions of China: Beijing, Shanghai-Suzhou, and Shenzhen-Dongguan. Our data show that FIEs in China are gradually localizing their production, but the extent of local embeddedness is contingent upon home country effects, local specific contexts and FDI-host region relationships. We have also found significant influence of industrial agglomeration on FDI location and network decisions. Beijing tends to have broader FDI sources and better integrated global-local networks, while in those regions dominated by FDI such as Suzhou and Dongguan, FIEs are thinly embedded with local economies and tend to establish global-local networks among themselves; local embeddedness is limited by a series of technological, institutional, spatial, and structural mismatches. Shanghai and Shenzhen are in between. More efforts are still needed to better integrate FDI with local economies and strengthen China’s local innovative capacities.     

Rapid removal of terrigenous dissolved organic carbon over the Eurasian shelves of the Arctic Ocean

The fate of terrigenous dissolved organic carbon (tDOC) delivered to the Arctic Ocean by rivers remains poorly constrained on both spatial and temporal scales. Early reports suggested Arctic tDOC was refractory to degradation, while recent studies have shown tDOC removal to be an active but slow process. Here we present observations of DOC, salinity, δ¹⁸O, and ²²⁸Ra/²²⁶Ra in the Polar Surface Layer (PSL) over the outer East Siberian/Chukchi shelf and the adjacent Makarov and Eurasian basins of the eastern Arctic Ocean. This off-shelf system receives meteoric water, introduced by rivers, after a few years residence on the shelf. Elevated concentrations of DOC (> 120 μM C) were observed in low salinity (~ 27) water over the Makarov Basin, suggesting inputs of tDOC-enriched river water to the source waters of the Transpolar Drift. The regression of DOC against salinity indicated an apparent tDOC concentration of 315 ± 7 μM C in the river water fraction, which is significantly lower than the estimated DOC concentration in the riverine sources to the region (724 ± 55 μM C). To obtain the timescale of removal, estimates of shelf residence were coupled with measurements of dissolved ²²⁸Ra/²²⁶Ra, an isotopic tracer of time since shelf residence. Shelf residence time coupled with DOC distributions indicates a first order tDOC removal rate constant, λ = 0.24 ± 0.07 yr^-1, for the eastern Arctic, 2.5–4 times higher than rates previously observed in the western Arctic. The observed removal of tDOC in the eastern Arctic occurs over the expansive shelf area, highlighting the initial lability of tDOC upon delivery to the Arctic Ocean, and suggests that tDOC is composed of multiple compartments defined by reactivity. The relatively rapid remineralization of tDOC on the shelves may mitigate the strength of the Arctic Ocean atmospheric CO₂ sink if a projected increase in labile tDOC flux occurs.     

Silver in the subarctic northeast Pacific Ocean: Explaining the basin scale distribution of silver

Five vertical profiles of silver (Ag) in the subarctic northeast Pacific are presented. Dissolved (< 0.2 μm) Ag concentrations within the surface mixed layer range from 6–25 pM, with the highest observed values at the most coastal site. Elevated Ag concentrations at this station are most likely attributable to the estuarine circulation in the Juan de Fuca Strait. One open-ocean station (P20) exhibited a strong surface Ag maximum. The station was located at the edge of a Haida eddy which raises the possibility that such eddies transport Ag seaward from the coastal zone. Ag concentrations in the deep waters ranged from 60–80 pM. These measurements are consistent with other recent Ag data collected in the Pacific. Ag profiles throughout the Pacific Ocean yield a strong positive correlation between Ag concentration and dissolved silicic acid concentration. However, Ag is depleted relative to silicic acid at intermediate depths where dissolved O₂ concentrations are low, implying a possible removal of Ag from oxygen-depleted waters by scavenging and/or precipitation.     

A comparison of ozone and chlorine toxicity to three life stages of the American oyster Crassostrea virginica

The effects of ozone-produced oxidants (OPO) on three developmental stages of the American oyster, Crassostrea virginica, were evaluated. Both straight-hinge (48-h post fertilisation) and setting pediveliger larvae were exposed to a series of OPO concentrations ranging from 0·05 to 0·30 mg/litre OPO (as total residual chlorine) at 25°C for 96 h. Mortality was used as the response parameter and results were quantitatively compared with the effects of chlorine-produced oxidants (CPO) obtained from the literature on these same developmental stages. Adult oysters (2- to 4-year class) were exposed to OPO concentrations ranging from 0·01 to 0·50 mg/litre at 15°C for 5 days and to the same concentration range at 25°C for two consecutive 6-day periods. Shell deposition and faecal matter accumulation were used as the response parameters for this stage.Straight-hinge larvae were significantly more sensitive to OPO than setting pediveliger larvae. Both larval stages were significantly more sensitive to CPO than to OPO. Shell deposition was significantly inhibited at all OPO concentrations for both 15°C and 25°C acclimated adult oysters. No significant differences were found between the shell deposition response of oysters at the two acclimation temperatures. Faecal matter accumulation was significantly reduced at OPO concentrations ≥ 0·05 mg/litre at both 15°C and 25°C. It was significantly (p < 0·05) greater for 25°C acclimated oysters than for 15°C acclimated oysters at OPO concentrations < 0·10 mg/litre but not at higher concentrations.     

Nutrient and carbon removal ratios and fluxes in the Ross Sea, Antarctica

Net community production (NCP) and nutrient deficits (Def(X)) were calculated using decreases in dissolved CO₂ and nutrient concentrations due to biological removal in the upper 200 m of the water column during four cruises in the Ross Sea, Antarctica along 76°30′S in 1996 and 1997. A comparison to excess dissolved and particulate organic carbon showed close agreement between surplus total organic carbon (TOC) and NCP during bloom initiation and productivity maximum; however, when TOC values had returned to low wintertime values NCP was still significantly above zero. This seasonal NCP, 3.9±1 mol C m⁻², must be equivalent to the particle export to depths greater than 200 m over the whole productive season. We estimate that the annual export was 55±22% of the seasonal maximum in NCP. The fraction of the seasonal maximum NCP that is exported through 200 m is significantly higher than that measured by moored sediment traps at a depth of 206 m. The removal of carbon, nitrate and phosphate (based on nutrient disappearance since early spring) and their ratios showed significant differences between regions dominated by diatoms and regions dominated by the haptophyte Phaeocystis antarctica. While the ΔC/ΔN removal ratio was similar (7.8±0.2 for diatoms and 7.2±0.1 for P. antarctica), the ΔN/ΔP and ΔC/ΔP removal ratios for diatoms (10.1±0.3 and 80.5±2.3) were significantly smaller than those of P. antarctica (18.6±0.4 and 134.0±4.7). The similarity in ΔC/ΔN removal ratios of the two assemblages suggests that preferential uptake of phosphate by diatoms caused the dramatic differences in ΔC/ΔP and ΔN/ΔP removal ratios. In contrast to low ΔC/ΔP and ΔN/ΔP removal ratio in diatom-dominated areas early in the growing season, deficit N/P and C/P ratios in late autumn indicate that the elemental stochiometry of exported organic matter did not deviate significantly from traditional Redfield ratios. Changes in biologically utilized nutrient and carbon ratios over the course of the growing season indicated either a substantial remineralization of phosphate or a decrease in phosphate removal relative to carbon and total inorganic nitrogen over the bloom period. The species dependence in C/P ratios, and the relative constancy in the C/N ratios, makes N a better proxy of biological utilization of CO₂.