Weathering and weathering rates of natural stone

Physical and chemical weathering were studied as separate processes in the past. Recent research, however, shows that most processes are physicochemical in nature. The rates at which calcite and silica weather by dissolution are dependent on the regional and local climatic environment. The weathering of silicate rocks leaves discolored margins and rinds, a function of the rocks' permeability and of the climatic parameters. Salt action, the greatest disruptive factor, is complex and not yet fully understood in all its phases, but some of the causes of disruption are crystallization pressure, hydration pressure, and hygroscopic attraction of excess moisture. The decay of marble is complex, an interaction between disolution, crack-corrosion, and expansion-contraction cycies triggered by the release of residual stresses. Thin spalls of granites commonly found near the street level of buildings are generally caused by a combination of stress relief and salt action. To study and determine weathering rates of a variety of commercial stones, the National Bureau of Standards erected a Stone Exposure Test Wall in 1948. Of the many types of stone represented, only a few fossiliferous limestones permit a valid measurement of surface reduction in a polluted urban environment.     

Barite deposits of the “Montagne Noire”, Southern France

Several small barite deposits of Devonian age are known in the Monts de Cabrières region, Montagne Noire (southern France). A field and laboratory investigation of these stratabound deposits showed their possible diagenetic origin and a limited economic value.

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Zusammenfassung De petits gisements de barytine du Dévonien dans les Monts de Cabrières (Montagne Noire, France) ont été étudié en détail sur le terrain et au laboratoire. Les observations ont apporté des critères pour une explication génétique de ces gisements «stratiformes». Ils indiquent que les concentrations minérales se sont effectuées par un processus de sécrétion au cours de la diagenèse. L'importance économique de ces gisements est limitée.

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...es ist zwar nicht sinnlos, aber doch etwas unlogisch, wenn man von vornherein nicht versucht, eine Lagerstätte in ihre Umgebung auf die wahrscheinlichste Art einzugliedern, sondern sie unbedingt einem ganz fremden, zunächst nicht von selbst verständlichen Bildungsvorgang zuordnen will. H. Schneiderhöhn (1954)     

The occurrence of bisulfite-aldehyde addition products in fog- and cloudwater

Elevated concentrations of S(IV) and formaldehyde were observed in fog- and cloudwater at sites in California. The highest concentrations (up to 3 mM S(IV) and 0.7 mM CH₂O) were measured at Bakersfield, during a prolonged period of repeated fog. In Bakersfield [S(IV)] generally exceeded [CH₂O], while in the Los Angeles area the reverse was observed. The lowest concentrations of both species were observed at marine and high altitude sites away from local emissions. Equilibrium computations indicate that high concentrations of S(IV) cannot be achieved without the formation of S(IV)-RCHO adducts.     

The Las Chacras-Potrerillos batholith (Pampean Ranges,Argentina): structural evidences,emplacement and timing of the intrusion

Within the southern part of the Sierra Pampeanas (the Sierra de San Luis, Argentina), a series of extensive intrusive bodies are regarded to post-date the Famatinian cycle but were emplaced during the Achalian, a period of heterogeneous deformation along crustal scale fault zones. The largest of those is the Las Chacras-Potrerillos batholith that is situated at the northern end of the transpressive, sinistral Guzmán shear zone. This composite pluton exhibits three sub-domains that comprise two granitoid sub-units each: The southern Potrerillos stock (muscovite-bearing red granite and biotite-bearing red granite) and the central (biotite porphyritic granite and giant porphyritic granite) and northern domain (equigranular granite and porphyritic granite) of the Las Chacras stock. The crystallisation ages of the biotite porphyritic granite is around 381 Ma (U/Pb on zircons and Pb/Pb on sphene), while the host rock was already cooled below 350 °C at 420 Ma. Thermal modelling approaches favour a pulsed intrusion with a duration of 1.5 Ma. The emplacement was followed by rapid cooling below the muscovite cooling temperature. Biotite cooling ages in different sub-units reflect either a long-lasting cooling history of approximately 30 Ma (which is supported by the modelling) or a reheating effect at around 350 Ma. Devonian-age determinations on the fault rocks and granitoids point to a syn-tectonic emplacement of the batholith. The pluton is interpreted to be positioned at the crossover of sinistral shear zones. The origin of this NNE directed extensional setting in a transpressive regime seems to be related to the transfer of displacement along a secondary set of NNW-trending sinistral faults. The final emplacement is due to a subsequent ballooning of the batholith following the direction of space creation. This model is based on the relative timing of the emplacement sequence and macroscopically visible planar fabrics in the field as well as magnetic fabric data. Our results indicate that the emplacement is syn-kinematic with respect to the Achalian deformation event.     

Die Glaukophangesteine,ihre stofflichen Äquivalente und Uniwandlungsprodukte in Nordcalabrien (Süditalien)

In the southern Apennin (= northern part of the region dealt with) and the Coasta Chain (= southern part) there are metabasalts wich are classified in the northern part as:

1. Glaucophane rocks of the albite-lawsonite-glaucophane-subfacies with the assemblage glaucophane + pumpellyite + lawsonite ±albite ±aragonite ±muscovite (7 rock analyses, 8 mineral analyses). These rocks are conceived as relics of an older burial metamorphism.
2. Rocks with pumpellyite and chlorite or also chlorite alone, that are interpreted as reaction rims between the metastable glaucophane rocks and the country rock (phyllites, quartzites). The assemblages pumpellyite + chlorite and chlorite alone are to be found (2 rock analyses and 2 mineral analyses).
3. Rocks with lawsonite and/or epidote belong to the same mineral facies as the country rock: a facies similar to the greenschist facies (called “lawsonite-albite-chlorite-subfacies”) which is characterized by the assemblages lawsonite + albite + chlorite ±calcite and also epidote ±lawsonite + albite + chlorite ± muscovite. These types are attributed to a younger dynamo-metamorphism (2 rock analyses).

In the southern part, the metabasalts can be found only as rocks with epidote and/or lawsonite, a metamorphism with more than one event cannot be proved petrologically (3 rock analyses). Equations of the observed mineral reactions are given. The transitions of one facies into another are represented in the pseudo-quaternary system Al₂O₃-CaO-Na₂O · Al₂O₃-2 Fe₂O₃ + FeO + MnO + MgO-(H₂O). The pressure-temperature conditions are estimated on the basis of published experimental data (300° C and 6–7 kb for the glaucophane rocks; 400° C and about 6 kb for the rocks with lawsonite and/or epidote) and are compared with geologic facts.     

北京东郊722土壤垂向剖面重金属污染的磁学响应及其统计意义

对北京城东附近某苗圃内典型的土壤污染剖面进行了环境磁学和地球化学分析,发现某些重金属(Pb、Zn、Sr、Ba、Cu)和磁性参数呈现相同的垂向变化趋势,都在37cm以上显示高值区,磁化率均值达到192.02×10-8m3/kg,如Pb含量达到67.62mg/kg,而在37cm以下,明显属低值区,磁化率均值只有18.38×10-8m3/kg,Pb含量也只有23.43mg/kg.借助于指标聚类分析和主成分分析方法,揭示出各种指标之间的内在联系,表明磁参数与Pb、Zn、Sr、Ba、Cu等元素显著相关,彼此的相关系数都达到0.90以上,属于同一类别的隶属度在80%以上,说明磁指标可以作为这些重金属污染的一种代用指标.利用模糊C均值聚类分析分辨出了土壤上部污染物堆积层和下部未污染土壤背景2种不同的特征段.     

Mollusc and brachiopod skeletal hard parts: Intricate archives of their marine environment

The biogenic carbonate hard parts of fossil bivalves, cephalopods and brachiopods are among the most widely exploited marine archives of Phanerozoic environmental and climate dynamics research. The advent of novel analytical tools has led many workers to explore non‐traditional geochemical and petrographic proxies, and work performed in neighbouring disciplines sheds light on the complex biomineralization strategies applied by these organisms. These considerations form a strong motivation to review the potential and problems related to the compilation and interpretation of proxy data from bivalve, cephalopod and brachiopod hard parts from the viewpoint of the sedimentologist and palaeoceanographer. Specific focus is on the complex biomineralization pathways of a given dissolved ion or food particle from its aquatic environment via the digestion and biomineralization apparatus in molluscs and brachiopods and its incorporation into a biomineral. Given that molluscs and brachiopods do not secrete their hard parts from seawater but rather from their mantle and periostracum, this paper evaluates differences and similarities of seawater versus that of body fluids. Cephalopods, bivalves and brachiopods exert a strong biological control on biomineralization that, to some degree, may buffer their shell geochemistry against secular changes in seawater chemistry. Disordered (amorphous) calcium carbonate precursor phases, later transformed to crystalline biominerals, may be significant in carbonate archive research due to expected geochemical offset relative to the direct precipitation of stable phases. A reasonable level of understanding of the related mechanisms is thus crucial for those who use these skeletal hard parts as archives of the palaeo‐environment. The impact of what is commonly referred to as ‘biological factors’ on the geochemistry of mollusc and brachiopod hard parts is explored for conventional isotope systems such as carbon, oxygen, strontium and traditionally used element to calcium ratios. In particular, the often used δ¹³C_carb or the Mg/Ca and Sr/Ca elemental proxies are fraught with problems. An interesting new research field represents the analysis, calibration and application of non‐traditional proxies to mollusc and brachiopod hard parts. Examples include the carbonate clumped isotope (Δ₄₇) approach and the analysis of the isotopes of Ca, Mg, N, Li, S or element to Ca ratios such as Li/Ca or B/Ca and rare earth elements. Based on considerations discussed here, a series of “do's and don'ts” in mollusc and brachiopod archive research are proposed and suggestions for future work are presented. In essence, the suggestions proposed here include experimental work (also field experiments) making use of recent archive organisms or, where possible, a reasonable recent analogue in the case of extinct groups. Moreover, the detailed understanding of the architecture of mollusc and brachiopod hard parts and their ultra‐structures must guide sampling strategies for geochemical analyses. Where feasible, a detailed understanding of the diagenetic pathways and the application of multi‐proxy and multi‐archive approaches should form the foundation of fossil carbonate archive research. The uncritical compilation of large data sets from various carbonate‐shelled organisms collected at different locations is not encouraged.