Formation and evolution of lateritic profiles in the middle Amazon basin: Insights from radiation-induced defects in kaolinite

The content of radiation-induced defects (RIDs) in kaolinite samples originating from lateritic soils and continental detritic sediments of the middle Amazon Basin (Brazil) is investigated using electron paramagnetic resonance. The paleodose registered by kaolinites ranges from 80 to 900 kGy. Present-day dose rates of radiation, determined from the whole-rock U and Th content, range between 4000 and 40,000 mGy/ka. In most samples, U and Th concentrations are correlated, suggesting that U has not been remobilized by lateritization. This observation is consistent with the fact that ∼80% of the total U content is incorporated in resistant minerals, such as zircon and Ti oxides. The heterogeneous distribution of U, observed by induced fission tracks mapping, makes it possible to neglect the α-radiation contribution of the U decay chains in the dose-rate calculation. The interpretation of the measured content of RIDs in kaolinite is then performed using the calculated present-day dose rate and assuming equilibrium in the radioactive decay chains. For the sedimentary samples, the amount of RIDs is broadly correlated to the dose rate and provides apparent absolute ages older than 20 Ma. The RID contents in kaolinites from the lateritic soils provide apparent ages ranging from 10 to 6 Ma. The high RID content of these lateritic kaolinites shows that their chemical, isotopic, and crystallographic properties are not representative of present-day weathering conditions. Models assuming the “dynamical equilibrium” of kaolinites with local physical-chemical conditions prevailing in lateritic soils are thus questionable. Alternatively, our findings bring strong support for the use of the isotopic composition of kaolinites to decipher continental paleo-climates.     

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.     

Contribution of interstitial OH groups to the incorporation of water in forsterite

Water incorporation in forsterite samples synthesized under low to medium silica-activity conditions mostly occurs via a substitutional mechanism in which a Si vacancy is compensated by four protons. Corresponding IR absorption spectra display a cluster of narrow and weakly anharmonic OH-stretching bands at wavenumbers above 3,500 cm^?1. However, this diagnostic spectrum is often superimposed to one broader absorption band, rarely two, displaying pronounced temperature-dependent properties and tentatively assigned to H atoms in interstitial position (Ingrin et al. in Phys Chem Miner 40:499–510, 2013). Here, we investigate the structural and vibrational properties of selected interstitial H-bearing defects in forsterite using a first-principles modeling approach. We show that the broad bands discussed by Ingrin et al. (Phys Chem Miner 40:499–510, 2013) are most likely related to interstitial OH groups in the vacant octahedral sites alternating with the M2 sites along the c axis of the forsterite structure. The corresponding OH defects lead to the formation of fivefold coordinated Si species. Their peculiar thermal properties stem from the vibrational phase relaxation due to the anharmonic coupling of the high-energy local OH-stretching mode with a low-energy vibrational mode. This “exchange mode” corresponds to the hindered longitudinal translation of the OH group. These results suggest that at high pressure, hydrogen incorporation in forsterite is dominated by coexisting interstitial OH groups and (4H)_Si defects.