Small-scale, nature-based tourism as a pro-poor development intervention: Two examples in Kwazulu-Natal, South Africa

Tourism is widely acknowledged as a key economic sector that has the potential to contribute to national and local development and, more specifically, serve as a mechanism to promote poverty alleviation and pro-poor development within a particular locality. In countries of the global South, nature-based tourism initiatives can make a meaningful impact on the livelihoods of the poor, in particular the subsistence based rural poor. Taking two examples in KwaZulu-Natal Province, South Africa, where small-scale tourism initiatives were developed recently in response to existing natural attractions in the context of coping with local economic crises, this paper broadly assesses the modest benefits to date, as well as drawbacks, in improving conditions of life.     

Mortar coupling and upscaling of pore-scale models

Pore-scale models are becoming increasingly useful as predictive tools for modeling flow and transport in porous media. These models can accurately represent the 3D pore-structure of real media. Currently first-principles modeling methods are being employed for obtaining qualitative and quantitative behavior. Generally, artificial, simple boundary conditions are imposed on a model that is used as a stand-alone tool for extracting macroscopic parameters. However, realistic boundary conditions, reflecting flow and transport in surrounding media, may be necessary for behavior that occurs over larger length scales or including pore-scale models in a multiscale setting. Here, pore-scale network models are coupled to adjacent media (additional pore-scale or continuum-scale models) using mortars. Mortars are 2D finite-element spaces employed to couple independent subdomains by enforcing continuity of pressure and flux at shared boundary interfaces. While mortars have been used in the past to couple subdomains of different models, physics, and meshes, they are extended here for the first time to pore-scale models. The approach is demonstrated by modeling single-phase flow in coupled pore-scale models, but the methodology can be utilized to model dynamic processes and perform multiscale modeling in 3D continuum simulators for flow and transport.     

A note on the bonding,optical spectrum and composition of tetrahedrite

Tetrahedrites of composition (Cu, Ag)₁₀(Cu₂, Fe, Zn)₂(Sb, As)₄S₁₃ or Cu₁₂Sb_14/3S₁₃ have 208 valence electrons per unit cell and are expected to be semiconductors. The bands are full in these cases, whereas compositions towards the classical formula Cu₁₂Sb₄S₁₃ (204 valence electrons per unit cell) have only partially filled bands and are therefore expected to be metallic. These predictions are supported by new optical absorption spectra of tetrahedrites with 205 and 208 valence electrons per unit cell. The gap between valence and conduction bands of the semiconductor is about 1.7 (±0.2) eV. A further prediction based on a nearly-free electron model is that 208 valence electrons per unit cell represent a compositional limit for tetrahedrites, and that the stability increases as compositions approach this limit. Existing data indicate an exponential increase in the number of occurrences as the limit is approached.     

Heavy-mineral concentrates from rocks in exploration for massive sulphide deposits

A number of programs have investigated the use of rock geochemistry in the search for volcanogenic massive sulphide deposits in the Canadian Shield. Regional-scale studies have been successful in differentiating productive from nonproductive volcanic cycles. Wall-rock studies have successfully delineated alteration halos related to the mineralizing event. While an alteration halo has been identified around the South Bay massive sulphide deposit, this halo does not extend far enough from the deposit to be useful for reconnaissance purposes. The authors therefore tested the possibility of enhancing detection of a primary trace-element halo by using the heavy mineral fraction of the rocks.The geochemical dispersion of trace elements in the heavy-mineral fraction of rocks was investigated around the South Bay massive sulphide deposit, in the Superior Province of the Canadian Shield. Approximately 270 samples were ground to 74–500 μm (−35 +200 mesh) and separated using the heavy liquid bromoform. Following removal of the magnetic fraction, the samples were further pulverized, and analyzed by atomic absorption spectrophotometry for Cu, Pb, Zn, Ag, Fe, Mn, Co and Ni. Corresponding whole-rock samples were analyzed to provide for a comparative study with the whole-rock geochemistry.Analysis of the heavy-mineral fraction of rocks revealed strong and extensive halos of Cu, Pb, Zn and Ag persisting in some cases up to 10 km along strike away from the South Bay Deposit. By comparison, in the whole-rock data, halos of Pb, Ag and Zn were detected no farther than 1–2 km away from the deposit. Furthermore, trace-element content in the whole rocks appeared to be dominated by rock type; either multivariate statistical techniques, or separation of the data by rock type, was necessary to distinguish the anomaly related to mineralization. Trace-element content in the heavy-mineral concentrates was dominated by the presence of the sulphide minerals pyrite, chalcopyrite, and sphalerite, thus directly reflecting mineralization.Use of the heavy-mineral fraction of the rock eliminates the dilution effects of quartz and feldspar, allowing enhancement of trace-metal concentrations in sulphide minerals, and the delineation of strong and extensive halos of Cu, Pb, Zn, Ag and Mn around the South Bay massive sulphide deposit. While the cost of preparation of heavy-mineral separates is higher than that for whole-rock samples, the anomaly clearly defined by the trace-element content of the heavy fraction avoids the need for costly major-element and subsequent statistical analysis, and increases target size by an order of magnitude. The heavy-mineral fraction obtained from rocks shows great potential as an exploration guide to volcanogenic massive sulphide deposits.     

The role of fluids in the metamorphism of komatiites,Agnew nickel deposit,western Australia

The Agnew nickel sulfide deposit is spatially associated with a lenticular body of ultramafic rocks which shows a concentric zonation in metamorphic mineralogy. Olivine + tremolite + chlorite + cummingtonite ±enstatite assemblages occur at the margin of the ultramafic lens, giving way to olivine + anthophyllite, olivine + talc and olivine + antigorite assemblages successively inwards. These rocks are interpreted as having crystallized from komatiitic lavas, and exhibit a spectrum of compositions from those of original flow tops to pure olivine adcumulates. The relative modal abundances of metamorphic olivine, tremolite and chlorite reflect original proportions of cumulus olivine and komatiite liquid in the protolith. Peak metamorphic conditions are estimated at 550° C, based on garnet-biotite thermometry, at a maximum pressure of 3 kb. This temperature falls within the narrow range over which metamorphic olivine may co-exist with enstatite, anthophyllite, talc or antigorite depending upon the fugacity of water in the metamorphic fluid. The observed mineralogical zonation is therefore attributed to infiltration by CO₂-rich fluids, generated by decarbonation of talc-carbonate rocks formed during pre-metamorphic marginal alteration of the ultramafic lens. Metamorphic fluids were essentially binary mixtures of water and CO₂, with minor H₂S having a maximum partial pressure less than 1 percent of total pressure. Enstatite-bearing assemblages formed in the presence of CO₂-rich fluids at fluid: rock volume ratios close to one, while anthophyllite, talc and antigorite bearing assemblages formed in the presence of progressively more water-rich fluids at progressively lower fluid-rock ratios.     

Volatile C1C7 organic compounds in an anoxic sediment core from the Pettaquamscutt River (Rhode Island,U.S.A.)

Surface sediments from an anoxic marine environment, the Upper Basin of the Pettaquamscutt River, Rhode Island, were analyzed for volatile organic compounds in the C₁C₇ range. The compounds identified included methane, ethane, alkenes (C₂C₅), carbon disulfide, cyclopentane, 3-methylpentane, methylfuran, aldehydes and ketones. Ethane, methylfuran, and most of the aldehydes and ketones showed maxima at the sediment water interface. Methane levels were very high-10–100 times greater than observed in most other surface sediments examined in this laboratory.     

Mantle-derived volatiles in continental crust: the Massif Central of France

CO₂-rich gases and groundwaters from springs and boreholes originating within the basement of the Massif Central have variable³He/⁴He ratios with correspondingR/R_a values ranging from 0.8 to 5.5 and 0.3 to 2.8 respectively, indicating the presence of a significant component of mantle helium. Molar concentrations of rare gases in the CO₂-rich gases are approximately 5 orders of magnitude greater than in the waters and suggest that a near-surface Henry's Law fractionation has occurred between exsolving CO₂ and water.δ¹³C values of the CO₂-rich gases are in the range −4.2 to −6.1‰, i.e. in that range normally attributed to mantle carbon, but which could also represent an average crustal composition and therefore do not discriminate between mantle and crustal sources.C/³He ratios show 4 orders of magnitude variation from 1.4 × 10¹² to 5 × 10⁸ and, compared to a mantleC/³He ratio of 10⁹, indicate that either a complex fractionation has occurred between mantle helium and mantle CO₂ or more likely that mantle rare gases have been diluted by large quantities of CO₂ with an average crustal carbon isotope composition. The regional distribution of³He and C does not show any obvious relationship to age or proximity of volcanic centres or major faults, suggesting that mantle-derived C and He components decoupled from their silicate melt sources at some depth.The results from this area of active fluid circulation suggest that C-isotope data derived from metamorphic terrains should be interpreted with great caution, but that input of some mantle-derived carbon is expected to accompany crustal extension.     

Exploration of structure and bonding in stishovite with fourier and pseudoatom refinement methods using single crystal and powder X-ray diffraction data

The structure and bonding in stishovite, SiO₂, is explored with Fourier summation and pseudoatom refinement of merged x-ray single crystal and powder diffraction data. Replacement of the 25 lowest-angle, highly extinction-affected, single crystal reflections with structure factors obtained from low-extinction powder diffraction data has resulted in a significant improvement in the analysis compared with earlier studies. The deformation electron density, total electrostatic potential and total and valence electron densities are mapped. Accumulations of electron density are observed in both SiO bonds, together with non-bonding features displayed about the oxygen on both sides of a plane formed by three bonds with Si. Deficits of electron density between O atoms across the shared-edges are rationalized in terms of the Pauli exclusion principle. There is no evidence for strong repulsion of Si atoms across the same ring. The total electrostatic potential has a continuous low value for the vacant channels in the structure along c with localized minima between O atoms on opposite sides of the channel. The sizes of Si and O are related to the electron density and to the electrostatic potential.     

Spherical capacitor hypothesis of the earth's electric field

Summary Stemming from the suggestion that the earth-ionospheric fair weather field arises from the lowest order resonant excitation of the earth-ionosphere cavity by lightning, it is shown that the same field is generated through electrostatic induction by equivalent charge dipoles from thunderclouds in the earth's atmosphere. An electrostatic induction model was used to derive from known worldwide thunderstorm data the magnitude of the expected earth-ionosphere fair weather potential. A value of only approximately one third of the observed potential was obtained. Possible sources of the discrepancy are suggested.     

Survival of sea anemones in Bunker C fuel

Sea anemones (Anthopleura elegantissima) can withstand submersion in Bunker C fuel oil for up to 1 h without visible adverse effects. The wet, mucus-covered tissues of the sea anemones may repel oil. During recovery, the sea anemones expand the column, evert the tentacles and reattach. A dahlia anemone (Tealia lofotensis) withstood immersion in oil for 15 min. The ability to withstand immersion in oil may confer an ecological advantage to sea anemones in contaminated areas.