Monitoring of fire incidences in vegetation types and Protected Areas of India: Implications on carbon emissions

Carbon emissions released from forest fires have been identified as an environmental issue in the context of global warming. This study provides data on spatial and temporal patterns of fire incidences, burnt area and carbon emissions covering natural vegetation types (forest, scrub and grassland) and Protected Areas of India. The total area affected by fire in the forest, scrub and grasslands have been estimated as 48765.45, 6540.97 and 1821.33 km ², respectively, in 2014 using Resourcesat-2 AWiFS data. The total CO ₂ emissions from fires of these vegetation types in India were estimated to be 98.11 Tg during 2014. The highest emissions were caused by dry deciduous forests, followed by moist deciduous forests. The fire season typically occurs in February, March, April and May in different parts of India. Monthly CO ₂ emissions from fires for different vegetation types have been calculated for February, March, April and May and estimated as 2.26, 33.53, 32.15 and 30.17 Tg, respectively. Protected Areas represent 11.46% of the total natural vegetation cover of India. Analysis of fire occurrences over a 10-year period with two types of sensor data, i.e., AWiFS and MODIS, have found fires in 281 (out of 614) Protected Areas of India. About 16.78 Tg of CO ₂ emissions were estimated in Protected Areas in 2014. The natural vegetation types of Protected Areas have contributed for burnt area of 17.3% and CO ₂ emissions of 17.1% as compared to total natural vegetation burnt area and emissions in India in 2014. 9.4% of the total vegetation in the Protected Areas was burnt in 2014. Our results suggest that Protected Areas have to be considered for strict fire management as an effective strategy for mitigating climate change and biodiversity conservation.     

Exploring the impact of diagenesis on (isotope) geochemical and microstructural alteration features in biogenic aragonite

For the Quaternary and Neogene, aragonitic biogenic and abiogenic carbonates are frequently exploited as archives of their environment. Conversely, pre‐Neogene aragonite is often diagenetically altered and calcite archives are studied instead. Nevertheless, the exact sequence of diagenetic processes and products is difficult to disclose from naturally altered material. Here, experiments were performed to understand biogenic aragonite alteration processes and products. Shell subsamples of the bivalve Arctica islandica were exposed to hydrothermal alteration. Thermal boundary conditions were set at 100°C, 175°C and 200°C. These comparably high temperatures were chosen to shorten experimental durations. Subsamples were exposed to different ¹⁸O‐depleted fluids for durations between two and twenty weeks. Alteration was documented using X‐ray diffraction, cathodoluminescence, fluorescence and scanning electron microscopy, as well as conventional and clumped isotope analyses. Experiments performed at 100°C show redistribution and darkening of organic matter, but lack evidence for diagenetic alteration, except in Δ₄₇ which show the effects of annealing processes. At 175°C, valves undergo significant aragonite to calcite transformation and neomorphism. The δ¹⁸O signature supports transformation via dissolution and reprecipitation, but isotopic exchange is limited by fluid migration through the subsamples. Individual growth increments in these subsamples exhibit bright orange luminescence. At 200°C, valves are fully transformed to calcite and exhibit purple‐blue luminescence with orange bands. The δ¹⁸O and Δ₄₇ signatures reveal exchange with the aqueous fluid, whereas δ¹³C remains unaltered in all experiments, indicating a carbonate‐buffered system. Clumped isotope temperatures in high‐temperature experiments show compositions in broad agreement with the measured temperature. Experimentally induced alteration patterns are comparable with individual features present in Pleistocene shells. This study represents a significant step towards sequential analysis of diagenetic features in biogenic aragonites and sheds light on reaction times and threshold limits. The limitations of a study restricted to a single test organism are acknowledged and call for refined follow‐up experiments.     

Disequilibrium for Ca during growth of pelitic garnet

Compositional zoning in hundreds of almandine-rich garnets in amphibolite by facies micaceous quartzites from the Picuris Range, north-central New Mexico USA, indicates that although Mn, Mg and Fe achieve chemical equilibrium at hand-sample scale during garnet growth, Ca does not. Instead, Ca concentrations at the surface of growing garnets appear to depend strongly on kinetic factors that govern the local chemical environment, yielding disequilibrium for Ca at scales larger than the region immediately surrounding an individual porphyroblast. Detailed zoning profiles were obtained for 371 garnet crystals in a small volume of a single sample of garnetiferous quartzite, and core analyses were made of 97 additional crystals. Each analysis was made on a section that passed precisely through the morphological centre of the crystal, located by means of 3-D imagery from computed X-ray tomography. The data reveal strong correlations between crystal size and concentrations of Mn, Mg and Fe (but not Ca) in garnet cores; a relationship between crystal size and isolation; rigorous cross-correlations among concentrations of Mn, Mg and Fe (but not Ca); and systematic variations in Ca concentrations as a function of crystal size and core composition that are anomalous in comparison to the behaviour of the other divalent cations. We interpret these observations as the result of thermally accelerated diffusion-controlled garnet growth, in circumstances that promoted rapid intergranular diffusion and thus rock-wide equilibration of Mn, Mg and Fe, but that prevented equilibration at similar scale for Ca because of its more sluggish intergranular diffusion. The anomalous behaviour of Ca is made evident in these garnets by the presence of sharp spikes in Ca concentration, which are demonstrably not a consequence of any simultaneous rock-wide event, such as a change in pressure, temperature, or some other intensive parameter. Instead, Ca concentrations probably reflect the local extent of reaction in the immediate vicinity of each porphyroblast. To the degree that such kinetic factors introduce departures from chemical equilibrium for Ca, thermobarometric estimates that involve grossular contents of pelitic garnet will be in error.     

A Preliminary Study of the Self-Directed Photography of Middle-Class,Homeless, and Mobility-Impaired Children*

Understanding the ways in which children with different life experiences come to terms with day-to-day contexts and constraints has become an important topic of social science research. This study applies the technique of auto-photography to the study of children-environment transactions. How children apprehend their environments is described through a leitmotif analysis and an interpretation of photographs taken by children from middle-class families, homeless children, and children whose mobility is impaired by cerebral palsy. We speculate upon the social and physical contexts of these children based upon the images that they selected to photograph. Although impressionistic, our findings suggest the importance of auto-photography as a method for uncovering children-environment transactions.     

Time-dependent stress change during failure of rocks

The energy balance of a solid subject to fracture has been explored using heat and mass transfer equations with regard to the volumetric and superficial components. In the suggested model, brittle fracture of a cracked solid considered as a heterogeneous two-phase medium is described by an equation analogous to the Griffith’s criterion for propagation of a single crack. The derived equation is used, together with estimates of relative change in specific interface area, to study the respective change of free strain energy and pressure in rocks associated with failure.     

Rugose corals from the Upper Ordovician Sholeshook Limestone of southwest Wales with an assessment of the coral affinities and biofacies

Limestone horizons of Upper Ordovician (Katian) age in southwest Wales contain diverse fossil faunas including rugose corals. The existence of Ordovician Rugosa in Wales was first reported by Murchison in the 1830s, but since then hardly any specimens have been documented systematically until this present study. Newly collected material from the area around Llanddowror (Carmarthenshire) has now confirmed the diversity of rugose corals in the Sholeshook Limestone (Katian age), an arenaceous limestone originating from the shelf edge of the palaeocontinent Avalonia. The majority of the specimens are preserved as moulds. This means that in many instances preservation of the fossils was insufficient for specific identification; nevertheless, it was possible to document a diverse rugose coral fauna, including Helicelasma, probable Grewingkia and Kenophyllum, and a potential early mucophyllid. While associated with considerable difficulties, as some diagnostic features of Rugosa are not visible in moulds, it is demonstrated here that the work with such specimens can result in faunal information which would otherwise be unobtainable. An assemblage of rugose and tabulate corals in the Sholeshook Limestone can be differentiated from a similar assemblage in the neighbouring Robeston Wathen Limestone which has a slightly different lithology. The fauna has strong similarities with other Avalonian (Irish, English, Belgian) as well as Baltic (Estonian and Norwegian) rugose coral faunas. Copyright © 2012 John Wiley & Sons, Ltd.