A Lagrangian Stochastic Model for Sea-Spray Evaporation in the Atmospheric Marine Boundary Layer

The dispersion of heavy particles subjected to a turbulent forcing is often simulated with Lagrangian stochastic models. Although these models have been employed successfully over land, the implementation of traditional LS models in the marine boundary layer is significantly more challenging. We present an adaptation of traditional Lagrangian stochastic models to the atmospheric marine boundary layer with a particular focus on the representation of the scalar turbulence for temperature and humidity. In this new model, the atmosphere can be stratified and the bottom boundary is represented by a realistic wavy surface that moves and deforms. Hence, the correlation function for the turbulent flow following a particle is extended to the inhomogenous, anisotropic case. The results reproduce behaviour for scalar Lagrangian turbulence in a stratified airflow that departs only slightly from the expected behaviour in isotropic turbulence. When solving for the surface temperature and the radius of evaporating heavy water droplets in the airflow, the modelled turbulent forcing on the particle also behaves remarkably well. We anticipate that this model will prove especially useful in the context of sea-spray dispersion and its associated sensible heat, latent heat, and gas fluxes between spray droplets and the atmosphere.     

Chemical mass balance of calcrete genesis on the Toledo granite (Spain)

The chemical mass balance of calcrete genesis is studied on a typical sequence developed in granite, in the Toledo mountains, Central Spain.

Field evidence and petrographic observations indicate that the texture and the bulk volume of the parent rock are strictly preserved all along the studied calcrete profile.

Microscopic observations indicate that the calcitization process starts within the saprolite, superimposed on the usual mechanisms of granite weathering: the fresh rock is first weathered to secondary clays, mainly smectites, which are then pseudomorphically replaced by calcite. Based on this evidence, chemical mass transfers are calculated, assuming iso-volume transformation from the parent rock to the calcrete.

The mass balance results show the increasing loss of matter due to weathering of the primary phases, from the saprolite towards the calcrete layers higher in the sequence. Zr, Ti or Th, which are classically considered as immobile during weathering, are also depleted along the profile, especially in the calcrete layer. This results from the prevailing highly alkaline conditions, which could account for the simultaneous precipitation of CaCO₃ and silicate dissolution.

The calculated budget suggests that the elements exported from the weathering profile are provided dominantly by the weathering of plagioclase and biotite. We calculate that 8–42% of the original Ca remains in granitic relics, while only 15% of the authigenic Ca released by weathering is reincorporated in the calcite. This suggests that 373 kg/m² of calcium (i.e., three times the original amount) is imported into the calcrete from allochtonous sources, probably due to aeolian transport from distant limestone formations.