Local permit ownership in Alaska salmon fisheries

Changes in ownership of limited entry permits by “local” residents of the region where a fishery occurs may have significant economic and social implications for fishery-dependent regions. This paper examines changes in local permit ownership in Alaska salmon fisheries, for which a long-term decline in rural local permit ownership is an important policy concern. Theoretically, permit markets allocate permits over time to the individuals who are willing to pay the most for them. Any factors that differentially affect what local and non-local residents are willing to pay for permits may affect the equilibrium share of permits held by local residents. For remote rural fisheries in particular, these may include differences between local and non-local residents with respect to access to and costs of financing permits and boats, costs of travel to the fishery, opportunity costs of participation in the fishery, and many other factors. As a fishery increases in profitability, differences between local and non-local residents in access to financing matter more while differences in costs of travel and opportunity costs matter less in the relative ranking of what local and non-local residents are willing to pay for permits. This tends to increase the share of non-local residents among buyers willing to pay the market price for permits, reducing the equilibrium share of permits held by local residents. This leads to a conflict between two important policy goals: increasing fishery profitability and maintaining rural local permit ownership. Consistent with predictions of this theory, the local share of permit ownership in Alaska salmon fisheries is negatively related to permit prices (an indicator of fishery profitability).     

Orbital-scale record of the late Cenomanian–Turonian oceanic anoxic event (OAE-2) in the Tarfaya Basin (Morocco)

High sedimentation rates (up to 12 cm/kyear) of laminated organic carbon-rich biogenic limestones in the Tarfaya Basin provide an unusually high (millennial) resolution record of the late Cenomanian oceanic anoxic event (OAE-2). The global positive carbon-isotope excursion across the Cenomanian–Turonian corresponds to 11 light/dark sedimentary cycles. We interpret these cycles as a response to orbital obliquity variation and estimate the duration of the complete excursion as 440 kyear or one long eccentricity cycle. On this timescale, the main increase in ¹³C values occurred over a short time interval of less than 20 kyear in the late Cenomanian and reached a first maximum approximately 15 kyear prior to the bulk (mainly coccoliths) ¹⁸O-derived sea surface maximum temperature that occurs coeval to the extinction of Rotalipora cushmani. Organic carbon-accumulation rates follow obliquity cycles, reaching a maximum approximately 10 kyear after the last occurrence of R. cushmani, then slowly decreasing during the early Turonian. Thus, the maximum temperature and the maximum organic carbon accumulation in the Tarfaya Basin lagged by at least 15 kyear behind the global carbon-isotope shift and a proposed reduction of atmospheric CO₂ content. The climate change across the Cenomanian/Turonian boundary probably occurred independent of CO₂ levels and may have been controlled by different greenhouse gases (water vapour and methane) and changes in ocean circulation (i.e., opening of the Equatorial Atlantic gateway)     

Chemical evolution in the high arsenic groundwater of the Huhhot basin (Inner Mongolia,PR China) and its difference from the western Bengal basin (India)

Elevated As concentrations in groundwater of the Huhhot basin (HB), Inner Mongolia, China, and the western Bengal basin (WBB), India, have been known for decades. However, few studies have been performed to comprehend the processes controlling overall groundwater chemistry in the HB. In this study, the controls on solute chemistry in the HB have been interpreted and compared with the well-studied WBB, which has a very different climate, physiography, lithology, and aquifer characteristics than the HB. In general, there are marked differences in solute chemistry between HB and WBB groundwaters. Stable isotopic signatures indicate meteoric recharge in the HB in a colder climate, distant from the source of moisture, in comparison to the warm, humid WBB. The major-ion composition of the moderately reducing HB groundwater is dominated by a mixed-ion (Ca–Na–HCO₃–Cl) hydrochemical facies with an evolutionary trend along the regional hydraulic gradient. Molar ratios and thermodynamic calculations show that HB groundwater has not been affected by cation exchange, but is dominated by weathering of feldspars (allitization) and equilibrium with gibbsite and anorthite. Mineral weathering and mobilization of As could occur as recharging water flows through fractured, argillaceous, metamorphic or volcanic rocks in the adjoining mountain-front areas, and deposits solutes near the center of the basin. In contrast, WBB groundwater is Ca–HCO₃-dominated, indicative of calcite weathering, with some cation exchange and silicate weathering (monosiallitization).     

Glycol Ethers As Groundwater Contaminants

Ether derivatives of dihydroxy alcohols, which are formed from ethylene or propylene, comprise an important group of groundwater contaminants known as glycol ethers. Compounds in this group are used as solvents, cleaning agents, and emulsifiers in many chemical products and manufacturing operations. Glycol ethers have been associated with a variety of toxic effects, and some compounds in the group are relatively potent teratogens. The limited information available suggests that glycol ethers are contaminants in groundwater, especially in anaerobic plumes emanating from disposal of mixed industrial and household waste. Most methods used to analyze groundwater samples cannot adequately detect 7g/’ (ppb) concentrations of glycol ethers, and the existing methods perform worst for the most widely used and toxic species. A new method capable of analyzing 7g/’ concentrations of glycol ethers was recently developed, and its use is recommended for groundwater samples where glycol ethers are likely to be present. Résumé. Les éthers glycol, polluants des eaux souterraines. Les dérivés d'éther de dihydroxy-alcool, formés à partir de l'éthylène ou du propylène, constituent un important groupe de polluants des eaux souterraines connus sous le nom d'éthers glycol. Les composés de ce groupe sont utilisés comme solvants, comme agents de nettoyage et comme émulsifiants dans de nombreux produits chimiques et dans de nombreux processus de fabrication. Des effets toxiques variés ont été attribués aux éthers glycol et certains des composés sont des agents tératogènes relativement puissants. Les données disponibles, qui sont limitées, indiquent que les éthers glycol sont des polluants communs dans les eaux souterraines, particulièrement dans les panaches anaéorobies émis par les décharges mixtes de déchets industriels et domestiques. La plupart des méthodes d'analyse d'échantillons d'eau souterraine ne sont pas capables de détecter convenablement des concentrations en éthers glycol de l'ordre du 7g/l (ppb); les méthodes actuelles sont médiocres pour doser les espèces toxiques les plus courantes. Une nouvelle méthode permettant de doser des concentrations en éthers glycol de l'ordre du 7 g/l a été récemment mise au point; son utilisation est préconisée pour les échantillons d'eau souterraine contenant des éthers glycol.     

Cadmium distribution in coastal sediments and mollusks of the US

Cadmium (Cd) concentrations in the coastal United States were assessed using the National Status and Trends (NS&T) Mussel Watch dataset, which is based on the analysis of sediments and bivalves collected from 280 sites since 1986. Using the 1997 sediment data, Pearson correlation (r = 0.44, p < 0.0001) suggested that Cd distributions in sediment can, be to some extent, explained by the proximity of sites to population centers. The 2003 tissue data indicated that “high” Cd concentrations (greater than 5.6 μg/g dry weights [dw] for mussel and 5.4 μg/g dw for oysters) were related to salinity along the East and Gulf coasts. Along the West coast, however, these “high” sites appeared to be related to upwelling phenomenon. Additionally, sedimentary diagenesis was found to be the most likely explanation of why sediment and mollusk Cd content were not well correlated.     

Emission of aliphatic amines from animal husbandry and their reactions: Potential source of N2O and HCN

We measured the emissions of volatile aliphatic amines and ammonia produced by the manure of beef cattle, dairy cows, swine, laying hens and horses in livestock buildings. The amine emissions consisted almost exclusively of the three methylamines and correlated with those of ammonia. The molar emission ratios of the methylamines to ammonia, and data on NH₃ emissions from animal husbandry in Europe, together with global statistics on domestic animals, were used to estimate the global emissions of amines. Annual global methylamine-N input to the atmosphere from animal husbandry in 1988 was 0.15±0.06 TgN (Tg=10¹² g). Almost 3/4 of these emissions consisted of trimethylamine-N. This represents about half of all methylamine emissions to the atmosphere. Other sources are marine coastal waters and biomass burning.Possible reaction pathways for atmospheric methylamines are shown. Among various speculative but possible products N₂O and HCN are of interest because the emission of methylamines could contribute to the global budgets of these compounds. Maximum atmospheric N₂O production from methylamines are below 0.4 Tg N/year, which is less than 10% of the annual N₂O growth rate. Although we do not expect the methylamine emissions to contribute in a major way to the atmospheric N₂O budget, more studies are needed to establish this conclusion beyond doubt. Similar conclusions hold for HCN.     

Spatial and temporal temperature trends in Nigeria, 1901–2000

Trends and periodicity analyses can provide information on climate variability inherent in a particular variable. In this study, trend tests and spectral analysis are used to examine the existence of trends and cycles in temperature series (1901–2000) of Nigeria. Periods 1901–1929 and 1942–1980 exhibited cooling trends while 1930–1941 and 1981–2000 showed warming trends. The warmest years in Nigeria were 1941, 1935, 1931 and 1987. The coldest years were 1929, 1975, 1925 and 1974. Whereas no significant trends were detected for 1901–1930 period, the standard period 1931–1960 was marked by significant cooling while 1961–1990 was marked with significant warming. Annual temperature has risen by 0.03?°C/decade during the last century. The overall warming was mostly confined to the south of 12°N especially during April and June. Changes in minimum temperature are higher than that of maximum temperature. The quasi-biennial oscillation was found in annual data for all the six zones with periods of about 2–4?years. Nigeria landscape is under strong North Atlantic Oscillation influence in dry season and under ENSO influence during wet season. Annual temperature series was also found to exhibit significant negative correlation with SOI.