[1] A remarkable field observation is that landslides of different sizes, from different locations around the globe and triggered by different mechanisms, all seem to follow a single relation, with their volume to surface area ratio following a power law of ∼1.4. This paper presents an analytical examination of the shape of landslides on the basis of limit equilibrium principles involving the exact mathematical solution of the failure mode. The obtained analytical relation between the volume and the surface area of a landslide agrees well with the function obtained from the field observations, and hence a mechanical basis is given to the previously poorly understood field observations. In addition, this paper presents a new graphical interpretation of the factor of safety associated with slope stability analysis and its relation to the probability of failure.

In this study, we present new data on the δ 7 Li values and Li/(Ca+Mg) ratios of carbonate cores from the Great Bahama Bank (Clino, Unda), a deep water core off of the bank top (ODP Leg 166 Site 1007), and the coralline Key Largo Limestone. We use these samples to evaluate the influence of meteoric diagenesis, marine burial diagenesis, and dolomitization on the Li isotope system in carbonates. We find that recrystallization of aragonite to low-Mg calcite in the presence of meteoric fluids results in a systematic decrease of the Li/(Ca+Mg) ratio in Clino, Unda and Key Largo samples, due to the lower Li/(Ca+Mg) ratio in meteoric fluids compared to seawater. For Li isotopes, we observe that the δ 7 Li of meteorically altered low-Mg calcite is +22.0±3.8‰ (n=28, 1σ), which is coincidentally similar to the original aragonite-rich sediments (+22±1‰ in the Bahamas, +18±1‰ in Key Largo), but with a larger variability (from +15 to +27‰). We interpret these features as reflecting the overprinting of primary Li during meteoric alteration with a highly variable isotope signature that may be controlled by a combination of local porewater and/or global climatic conditions; in either case, meteoric diagenesis produces isotopic signatures that are unrelated to seawater composition. In contrast, marine burial diagenesis and dolomitization of Clino and Unda sediments under "fluid-buffered" conditions result in Li isotope composition that is similar (+30.2±1.5‰, n=36, 1σ) to modern seawater (+31‰). For Site 1007, the δ 7 Li values range between +23‰ and +31‰. We interpret this range as reflecting a combination of varying diagenesis style (fluid to sediment-buffered) and varying contribution of calcite derived from pelagic sediments, with distinct isotopic composition due to primary mineralogy. Altogether, our results show that diagenesis does not invalidate the use of bulk carbonates for deriving Li isotope paleo-records, but the reliability of past carbonates as recorders of seawater δ 7 Li values will depend on carefully characterizing their diagenetic history.

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In this study we combine Pb isotopes, Pb, Ni, Cu, Zn, and several major metal concentrations, identification of the aerosol particles, and synoptic and back trajectory analyses to obtain direct evidence for the extent and nature of mixing between Middle Eastern and European sources emissions of metals and aerosols. During the summer months aerosols collected in Israel are highly polluted by metals (EF(Ni) = 120, EF(Cu) = 320, EF(Zn) = 30, EF(Pb) = 540; average values). The fraction of European Pb of mostly industrial sources is 61 +/- 21% in Jerusalem, and the fraction of European Cu, Zn, Ni, and aerosols should be on the same order. Whenever a steep pressure gradient is built between the barometric trough originating from the Persian Gulf and the subtropical ridge along the African coast, stronger westerly winds and cooler temperatures (deep Persian Trough) prevail overthe Middle East, and higher amounts of European pollution are observed in the atmosphere (74 +/- 13%). On the other hand, when the Persian Trough is in its shallow mode, the proportion of European pollution is lower (45 +/- 18%, based on Pb isotopes). This study demonstrates that atmospheric pollution over the East Mediterranean region during the summer is influenced not only by local atmospheric dispersion conditions but also by the ability of the atmosphere to inherit a significant proportion of pollutants from European sources.

The evolution of the global carbon and silicon cycles are thought to have contributed to the long-term stability of the Earth's climate [1][2][3] . Many questions remain, however,

Seawater lithium stable isotope ratios, represented by δ7Lisw (‰), hold key information about the evolution of global climate and the carbon cycle over geologic time. Reconstructions based on foraminifera suggest an ~9‰ increase in δ7Lisw over the past 60 m.y., interpreted as reflecting changes in the silicate weathering regime that may have contributed to global cooling over this time. However, culture experiments suggest that vital effects in foraminifers might cause varied δ7Li fractionation that could have affected past records. Thus, other archives are needed to determine whether the observed rise in foraminifer δ7Li values over the Cenozoic indeed reflects secular changes in δ7Lisw. Such archives would also open possibilities for robust determination of δ7Lisw deeper in geologic time. We analyzed δ7Li compositions in modern brachiopods (n = 34) and found a relatively narrow range of +24.2‰ to +28.8‰ (mean = +26.8‰; 1σ = 0.5‰), similar to the range reported for inorganic calcite precipitated from seawater. These results confirm that brachiopods are good candidates for providing a representative record of δ7Lisw. We present data from fossil specimens dating from 65 Ma to ca. 700 ka, finding that fossilized brachiopods record a similar magnitude of change in δ7Lisw as foraminifers. These results are the first to corroborate the ~9‰ increase in Cenozoic δ7Lisw and open possibilities for generating robust records ofδ7Lisw in deep time, prior to foraminifer evolution.

The pairing of calcium and magnesium isotopes (δ44/40Ca, δ26Mg) has recently emerged as a useful tracer to understand the environmental information preserved in shallow-marine carbonates. Here, we applied a Ca and Mg isotopic framework, along with analyses of carbon and lithium isotopes, to late Tonian dolostones, to infer seawater chemistry across this critical interval of Earth history. We investigated the ca. 735 Ma Coppercap Formation in northwestern Canada, a unit that preserves large shifts in carbonate δ13C values that have been utilized in global correlations and have canonically been explained through large shifts in organic carbon burial. Under the backdrop of these δ13C shifts, we observed positive excursions in δ44/40Ca and δ7Li values that are mirrored by a negative excursion in δ26Mg values. We argue that this covariation is due to early diagenetic dolomitization of aragonite through interaction with contemporaneous seawater under a continuum of fluid- to sediment-buffered conditions. We then used this framework to show that Tonian seawater was likely characterized by a δ7Li value of ~13‰ (~18‰ lower than modern seawater), as a consequence of a different Li cycle than today. In contrast, δ13C values across our identified fluid-buffered interval are similar to modern seawater. These observations suggest that factors other than shifts in global seawater chemistry are likely responsible for such isotopic variation.

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