Comparing resident and tourist preferences for public beach access and related amenities

As coastal destinations continue to grow, due to tourism and residential expansion, the demand for public beach access and related amenities will also increase. The issue confronting management agencies responsible for providing and maintaining public beach access and related amenities is the varying needs and preferences of both residents and tourists of coastal destinations. The purpose of this paper is to provide comprehensive information about coastal recreational needs of residents and tourists with regards to public beach access and associated amenities using the stated preference choice method. Overall, the results indicate tourists were more interested in additional public beach access points and commercial development, while residents supported beach rules and regulations but opposed high levels of crowding and noise. Implications of these results for management agencies include the utilization of parking fees to subsidize additional public beach access points, identifying appropriate types and levels of commercial development that moderate the use of coastal resources by tourists and day-trip users, and implementing beach rules and regulations that reduce the potential for conflict between user groups. Providing management agencies with comprehensive information of the preferences of different beach user groups can assist in the development of more effective policies and management programs.     

Photolysis of 2,4-Dinitrotoluene and 2,6-Dinitrotoluene in Seawater

The purpose of this experiment was to determine the rate of photolysis for 2,4-dinitrotoluene (2,4-DNT) and 2,6-dinitrotoluene (2,6-DNT) in salt water and pure water, examine the influence of salt concentration on the photolysis rate, and to identify the products of the photolysis of 2,4-DNT and 2,6-DNT in seawater. For the photolysis of 2,4-DNT in pure water, the half-life was longer than 100 h, whereas the photolysis half-life in salt water was ~15 h. For 2,6-DNT, the pure water photolysis half-life was close to 20 h, but the salt water photolysis half-life was only 5 h. The photolysis rate for 2,6-DNT in seawater was affected by the ionic strength of the parent solution and was independent of the identity of the salt. The photolysis of both DNTs in seawater resulted in a complex mixture of products that exhibit a distinct yellow color. Analysis by gas and liquid chromatography mass spectroscopy (GCMS, LCMS) following liquid–liquid extraction or solid phase extractions resulted in the confirmation of the corresponding dinitrobenzaldhydes and dinitrobenzoic acids as photolysis products and a probable azoxy compound among the photolysis products in seawater.     

A petrogenetic model for the comagmatic origin of chassignites and nakhlites: Inferences from chlorine‐rich minerals,petrology, and geochemistry

Twelve samples belonging to the chassignite and nakhlite subgroups of Martian meteorites were investigated using a variety of micro‐beam analytical techniques to gain insight into the petrogenesis of these two meteorite classes. There are a striking number of geochemical similarities between the chassignites and nakhlites, including mineralogy and petrology, crystallization age, cosmic‐ray exposure age, and radiogenic isotopic compositions. However, there are also geochemical differences, namely in trace element systematics of pyroxenes, that have led some authors to conclude that the nakhlites are comagmatic with each other, but not comagmatic with the chassignites. On the basis of data presented here, we propose a model in which these differences can be reconciled by the addition of an exogenous Cl‐rich fluid to the chassignite‐nakhlite magma body shortly after the formation of the cumulate horizon that was sampled by the Chassigny meteorite. This model is supported by the textural and chemical associations of the volatile‐bearing minerals apatite, amphibole, and biotite, which record a history starting with the addition of a Cl‐ and LREE‐enriched fluid to the magma body. As the magma continued to crystallize, it eventually reached chloride saturation and degassed a Cl‐rich fluid phase. Depending on the provenance of the Cl‐rich fluid, this model could explain how the chassignites and nakhlites originated from an LREE‐depleted source, yet all exhibit LREE‐enriched bulk‐rock patterns. Additionally, the model explains the range in oxygen fugacity that is recorded by the chassignites and nakhlites because eventual exsolution and loss of Cl‐rich fluid phases near the end of crystallization of the nakhlite sequence leads to auto‐oxidation of the magma body due to the preferential partitioning of Fe²⁺ into the fluid phase.     

Chemical characterization of Lower Devonian vascular plants

Vegetative remains of three coalified Lower Devonian vascular plants (Zosterophyllum, Psilophyton, Renalia) were analyzed using flash pyrolysis-gas chromatography-mass spectrometry. The distributions of pyrolysis products are compared with those from younger vascular plant fossil xylem (Cordaixylon, Callixylon) and cuticle (Pachypteris). The likelihood of the chemical preservation of characteristic higher plant macromolecules (e.g., lignin and cutan) in the Lower Devonian plant fossils is considered in light of this comparison and associated thermal maturity assessments. Reflectance values from vitrinite-like macerals, which may not be vitrinite sensu stricto in the Lower Devonian host rocks for the fossils selected for this study, are shown to provide a reasonable assessment of the thermal maturity of these early vascular plant fossils. Although lignin altered through burial maturation is the most likely source of the prominent alkylphenols and aromatic hydrocarbons in the Lower Devonian tracheophyte flash pyrolysates, a contribution from thermally modified tannins cannot be ruled out. Comparison of the highly aliphatic pyrolysates from the Zosterophyllum and Psilophyton axes with that of a thermally mature fossil gymnosperm leaf revealed that cutan was an important component in the Devonian plant remains. This is the earliest chemical evidence for the presence of cutan in vascular plants.     

Constraining the Late Mesozoic and Early Tertiary Tectonic Evolution of Southern Mexico: Structure and Deformation History of the Tierra Caliente Region

We analyze the structure and assess the deformation history of the Tierra Caliente Metamorphic Complex (TCMC) of southern Mexico, where Laramide accretion of exotic terranes is in debate. The TCMC consists of a south-plunging antiform fault that is bounded on both its eastern and western flanks. Tierra Caliente Metamorphic Complex rocks show at least two phases of compressional deformation. The first and most prominent records a mean tectonic transport direction of 068 degrees. This phase is responsible for east-verging asymmetrical folding and thrusting of both metamorphic and superjacent sedimentary rocks. The second phase has an average transport direction of 232 degrees and is restricted to the western portion of the TCMC. A third phase is responsible for normal faulting. Lack of discernible deformation before Late Cretaceous time indicates that the main deformation phase is coincident with Laramide orogenesis elsewhere in the North American Cordillera. The stratigraphy, structure, and deformational history of the TCMC do not require accretion of exotic terranes. We explain the Mesozoic tectonostratigraphic evolution of the TCMC in terms of deposition and deformation of Mesozoic volcanic and sedimentary strata over the attenuated continental crust of the North American plate.     

Metal-silicate partitioning of cesium: Implications for core formation

Here we present the first set of metal-silicate partitioning data for Cs, which we use to examine whether the primitive mantle depletion of Cs can be attributed to core segregation. Our experiments independently varied pressure from 5 to 15 GPa, temperature from 1900 to 2400 °C, metallic sulfur content from pure Fe to pure FeS, silicate melt polymerization, expressed as a ratio of non-bridging oxygens to tetrahedrally coordinated cations (nbo/t) from 1.26 to 3.1, and fO₂ from two to four log units below the iron-wüstite buffer. The most important controls on the partitioning behavior of alkalis were the metallic sulfur content, expressed as X_S, and the nbo/t of the silicate liquid. Normalization of X_S to 0.5 yielded the following expressions for D-values as a function of nbo/t: log D_Na = −2.0 + 0.44 × (nbo/t), log D_K = −2.4 + 0.67 × ( nbo/t), and log D_Cs = −3.2 + 1.17 × (nbo/t). Normalization of nbo/t to 2.7 resulted in the following equations for D-values as a function of S content: log D_Na = −4.1 + 6.4 × X_S, log D_K = −7.7 + 13.9 × X_S, and log D_Cs = −12.1 + 23.3 × X_S.There appears to be a negative pressure effect up to 15 GPa, but it should be noted that this trend was not present before normalization, and is based on only two measurements. There is a positive trend in cesium’s metal-silicate partition coefficient with increasing temperature. D_Cs exhibits the largest change and increased by a factor of three over 500 °C. The effect of oxygen fugacity has not been precisely determined but in general, lowering fO₂ by two log units resulted in a rise in all D-values of approximately an order of magnitude. In general, the sensitivity of partition coefficients to changing parameters increased with atomic number.The highest D-value for Cs observed in this study is 0.345, which was obtained at nbo/t of 2.7 and a metal phase of pure FeS. This metallic composition has far more S than has been suggested for any credible core-forming metal. We therefore conclude that the depletion of Cs in Earth’s mantle is either caused by radically different behavior of Cs at pressures higher than 15 GPa or is not related to core formation. Even so, we have shown that a planet with a sufficient S inventory may incorporate significant amounts of alkali elements into its core.     

Fractional crystallization of the lunar magma ocean: Updating the dominant paradigm

We report results of systematic experimental simulation of fractional crystallization of a lunar magma ocean (LMO) with the Lunar Primitive Upper Mantle bulk composition. These results complement prior work that simulated equilibrium crystallization. In contrast to previous numerical models for investigating magma ocean solidification processes and implications, our combined program simulates these processes directly using petrologic experimentation. Our experiments mimic LMO crystallization that is fractional throughout the process, rather than switching from initially equilibrium to fractional crystallization partway through. To do this, we adopted an iterative approach in which the starting material for each run is synthesized using the composition of the melt phase from the prior run. We compare our results to those from long-standing numerical models of LMO crystallization and show that although some features of those models are broadly reproduced, there are key differences in liquid lines of descent and the cumulate lithologies generated. Our results can be used to estimate the possible thickness of a primordial lunar crust formed from flotation of plagioclase during magma ocean solidification. Our estimate is greater than that from the recent Gravity Recovery and Interior Laboratory (GRAIL) mission, but consistent with the criteria on which the starting bulk composition was originally calculated. It assumes perfectly efficient separation of all plagioclase formed from the crystallizing magma ocean, which is likely not the case. We also demonstrate that a non-chondritic bulk composition, with respect to trace elements, is not required in order to generate a KREEP (potassium, rare earth elements, and phosphorus) signature from magma ocean crystallization.     

Polychlorinated biphenyls (PCBs) and their hydroxylated metabolites (OH-PCBs) in livers of harbor seals (Phoca vitulina) from San Francisco Bay,California and Gulf of Maine

Bioaccumulation of endocrine disruptors in marine mammals positioned at the top of the food chain is of toxicological concern. Livers from four pups and ten adult harbor seals (Phoca vitulina) stranded in San Francisco Bay (SFB) and the Gulf of Maine (GOM) were analyzed for polychlorinated biphenyls (PCBs) and their hydroxylated metabolites (OH-PCBs). We used GC–ECD and GC–NCI/MS to investigate the presence of 28 PCBs and 8 OH-PCB metabolites, respectively. Σ₂₈PCB concentrations (di- to octa-CBs) ranged from 1.81 to 35.9 μg/g lipid with a median of 6.53 for the seal pups and 2.31 to 249 μg/g lipid with a median of 28.9 for the adult seals. Σ₈OH-PCB concentrations (penta- to hepta-OH-PCBs) ranged from 0.02 to 0.69 μg/g lipid with a median of 0.04 for the adult seals, i.e., at much lower concentrations than those for PCBs. Ratios of OH-PCBs to PCBs (0.24% on average) were comparable to those in beluga whale, but were lower than ratios in human livers. The OH-PCB profiles were slightly different between SFB and GOM seal livers, although similar PCB congener patterns were observed. Generally, 4-OH-CB107 was found predominantly in seal livers and was the only OH-PCB detectable in most of seal pup livers. This study provides information on OH-PCBs in seals, adding to the scarce exposure data for these chemicals.     

Something in the Air: Civic science and contentious environmental politics in post-apartheid South Africa

The emergence of an environmental movement in post-apartheid South Africa has involved the reframing of the environment as a ‘brown’ issue, articulating the discourse of social and environmental justice and a rights-based notion of democracy. Environmental movements have pursued a dual strategy of deliberation and activist opposition. Environmental movements have deployed science to pursue the strategic task of democratic opposition and have established networks of environmental knowledge and expertise. Ecological modernization is the dominant approach to environmental governance and adopts a science-based policy approach. In this context the regulation and management of the environment is premised on the need for science, which provides the authoritative basis for a regulatory response. In local environmental movements, there exists a fundamental tension between a cumulative history of lay knowledge about pollution and the lack of official acknowledgement of qualitative narratives. This is accompanied by a lack and suspicion of reliable official data. Environmental movements have thus employed ‘civic science’ strategically to place the issue of air pollution on the political agenda. This paper uses the case of environmental politics in Durban to reflect on the ways in which civic science and lay knowledge, together constituting community hybrid knowledge, are produced and disseminated in order to pressure the state and capital. The three ways in which knowledge is deployed are: to frame environmental problems, in strategies of oppositional advocacy, and in deliberative policy forums. Empirical analysis shows that civic science is produced through knowledge networks, and both lay knowledge and civic science are opportunistically used by environmental movements to engage both inside and outside formal policy making arenas. This deployment of hybrid knowledge by environmental movements represents a broader challenge to the power of science and technology based on increasing evidence of the hazards and risks facing ordinary people in their daily lives.