Luna 20 pyroxenes: exsolution and phase transformation as indicators of petrologic history

Pyroxenes from our sample of Luna 20 soil are predominantly orthopyroxene with subordinate pigeonite. The orthopyroxenes are chromium-rich bronzites and contain submicroscopic lamellae of augite in a twinned orientation exsolved on (100). These lamellae have a composition close to the diopside-hedenbergite join. Asymmetric diffuse streaks parallel to $\text{a}{}^1$ indicate stacking faults parallel to (100) and possibly very thin (10–20 Å) lamellae of clinobronzite parallel to (100). Pigeonite crystals are very complex crystallographically and chemically, with optically visible (001) augite exsolution lamellae and two sets of chromite exsolution lamellae. In addition, there are submicroscopic (100) augite lamellae and a second generation of clinohypersthene lamellae which appear to have exsolved from the (001) augite lamellae. The clinohypersthene host, which has a large number of stacking faults parallel to (100), has partially inverted to hypersthene of the same composition. The hypersthene occurs as very fine lamellae (less than 1000 Å) parallel to the (100) plane of the clinohypersthene. X_D^Fe-Mg values for five host-lamellae pairs in pigeonite K-4 indicate a significant amount of subsolidus readjustment. We tentatively conclude that many of the bronzite and pigeonite crystals were derived from rocks crystallized from a high level magma chamber in the lunar highland crust.     

Transmission electron microscope study of dislocations in orthopyroxene (Mg,Fe)2Si2O6

The orthopyroxene crystal structure can be viewed as the stacking of alternating tetrahedral and octahedral layers parallel to the (100) plane. Easy glide occurs in the (100) plane at the level of the octahedral layer to prevent breakage of the strong Si-O bonds. Dislocations with c and b Burgers vectors have been activated in (100) by room temperature indentation in an orthoenstatite gem quality single crystal. Investigations in transmission electron microscopy show that the b dislocations (b?9 Å) are not dissociated while the c's (c=5.24 Å) are dissociated into four partials. This result is interpreted by considering the oxygen sublattice as a distorted FCC one. The four c partials are thus Shockley partials bounding three stacking faults. For the two outer ones, synchroshear of the cations is necessary to keep unchanged their sixfold coordination; the oxygen sublattice is locally transformed into a HCP lattice. This accounts for the observed low splitting (?100 Å) of these faults as compared to the median one (?500 Å) which does not affect the oxygen sublattice and does not require cation synchroshear. In a Fe rich orthopyroxene (eulite), semi coherent exsolution lamellae have been studied. Either only c edge dislocations or both b and c edge dislocations occur in the phase boundaries depending upon the thickness of the lamellae. Only the c dislocations are dissociated. From the observed spacing between these mismatch dislocations a crude estimate of the exsolution temperature is proposed T _ex ? 700° C.     

Argon diffusion domains in K-feldspar I: microstructures in MH-10

Samples of MH-10, a K-feldspar thought to contain discrete diffusion domains for argon, have been examined by light and TEM microsopy to search for domain boudaries. We examined both unheated K-feldspar separates and samples heated in vacuum between 750 and 1150°C in order to characterize the initial microstructure as well as any changes resulting from laboratory heating. The MH-10 rock shows almost no evidence of plastic deformation, and the K-feldspar does not possess networks of dislocations which might define a subgrain structure derived from external stresses. Three classes of substructure are present in the K-feldspar, but only the third appears to have been affected by laboratory heating: (1) Cross-hatched extinction in light microscope is common but variably developed. TEM reveals almost no albite/pericline twinning but tweed microstructure is ubiquitous. (2) Turbid zones occur with about 5 volume % abundance. Micropores, <1 to 2m in diameter, characterize these regions, which often also contain bleds of albite, up to 40 m indiameter, TEM shows these turbid zones to be very complex with intricate twin and tweed structures at the sub-micron scale and numerous dislocation and strain features. (3) Albitic exsolution lamellae (<1 m thick, 20 m long and separated by 1 m) are rarely seen in the light microscope but TEM shows that 0.01 m thick by 0.2–1 m long lamellae, separated by 0.1 to 0.5 m, occur in about 20% of the sample. These lamellae are disk-shaped, have a semi-coherent or coherent relationship to the host K-feldspar, and seem to disappear upon heating to 750°C. Extensive diffusion studies have been conducted on HM-10, and the results analyzed in terms of distribution of sizes of diffusion domains. The preferred result of the analyses was a distribution consisting of three distinct sizes. The largest domain size identified in this way is approximately 50 to 100 m, and this corresponds to blocks of K-feldspar defined by the network of fractured/turbid zones. The smallest domain size inferred from diffusion analysis is 0.1 m which corresponds to the spacing between albite exsolution lamellae that may represent fast diffusion pathways. Alternatively, the modulated argon distribution accompanying the lamellar variation in feldspar composition may result in an overestimation of the initial diffusion coefficients. Even though a promising agreement exists between domain analyses based upon diffusional and microstructural analyses, at least two questions remain unanswered. Firstly, no clear candidate has been identified for a domain of intermediate size. Secondly, the diffusion analysis has been formulated with independent gas release from all domains, whereas the observed structures are likely to be nested (i.e., small domains exist inside bigger domains) with the network of semi-coherent lamellar boundaries having connectivity and permeability which can provide only a modest increase in argon diffusivity over bulk values.     

An electron microscopy study of deformation microstructures in granitic mylonites from southwestern Sweden, with special emphasis on the micas

Summary ¶The lithology, age, geological setting, structural and metamorphic history of the granitic mylonites from the Mylonite Zone (MZ) in southwestern Sweden have been studied extensively. The deformation history, growth of microstructures, intensity of deformation, changes in mineral compositions, and pressure-temperature conditions of deformation have, however, not been addressed. In this study, powder X-ray diffraction, optical microscopy, electron microprobe analysis and transmission electron microscopy of micas, chlorite, and plagioclase are combined to understand the physical and textural changes experienced by the rocks during mylonitization. It is shown that the occurrence of foliated micas in shear bands, recrystallization of quartz and biotite, and undulatory extinction in quartz grains were not uniform throughout the samples studied. Occurrence of dislocations and low-angle grain boundaries confirm that deformation occurred largely by glide dislocations. The low-angle grain boundaries observed are formed by the re-arrangement of these dislocations during grain size reduction processes. The micas show a high degree of spatial stacking order, but spatial stacking disorder in micas and chlorites has also been found.Ordered stacking faults are formed during low strain while disordered stacking faults are formed under high strain conditions. Occurrence of both ordered and disordered stacking faults indicates that the intensity of deformation was not uniform through the entire MZ. Moreover, the chemical composition of plagioclase shows that the exsolution lamellae observed with optical and electron microscopy are due to Ca-subsolidus reactions during low temperature deformation. Several substitution reactions occurring in the micas indicate that deformation took place between 0.3 and 0.4GPa, at a temperature higher than 500°C.Received October 15, 2001; revised version accepted December 25, 2002 Published online June 2, 2003     

An electron microscopic study of amphibole lamellae in augite

Ion-thinned samples of augite from four plutonic igneous rocks have been examined in the electron microscope at 100 kV. Lamellae less than 0.08 m thick were observed parallel to (010) in all four samples. Electron diffraction shows that the lamellae consist of clino-amphibole, space group I2/m, with crystallographic axes parallel to those of the augite. Analytical electron microscopy of the lamellae in one specimen shows that they are a hornblende. The amphibole lamellae have nucleated at the interface between the augite host and exsolution lamellae of orthopyroxene parallel to (100) of the augite. The interface between the amphibole lamellae and the augite is coherent.It is thought that the amphibole lamellae have formed by exsolution from the augite, implying the existence of finite solid solution between members of the pyroxene and amphibole groups of minerals.     

A transmission electron microscope study of naturally deformed orthopyroxene

A model is proposed for the production of clinopyroxene lamellae in orthopyroxene by a dislocation mechanism based on simple shear. Four possible shears are described. Two shears apply to each subcell of orthopyroxene, one with =13.3° in one sense, the other with =18.3° in the opposite sense.The senses of shears of the same magnitude in adjacent cells are also opposite. All shears produce the same structure, but in two discrete orientations which can be distinguished from electron diffraction patterns. However, the operative shear cannot be uniquely determined from the diffraction patterns alone. The characteristics of the diffraction contrast fringes and associated partial dislocations observed by transmission electron microscopy in a naturally deformed orthopyroxene are shown to be consistent with the proposed model.     

Formation mechanism of pigeonite lamellae in skaergaard augite

Fine textures of exsolution lamellae and interface boundaries between augite and pigeonite in augite crystals from Skaergaard ferrogabbro 4430 have been studied by high resolution electron microscopy and X-ray methods. Thick pigeonite lamellae have higher densities of (100) stacking faults than thin lamellae. The displacement vector of the faults has been determined as 5/6c from the measured density of faults and the relative rotation of the augite and pigeonite lattices. The augite and pigeonite lattices are apparently coherent, and no growth ledges were observed at the interfaces. The stacking faults are often combined with the antiphase boundary of pigeonite resulting in a total displacement vector of 1/2(a+b)+5/6c. The observation of thick and thin pigeonite lamellae indicated that the thickening of (001) pigeonite lamellae was controlled by coherency strains accumulated at the interfaces between augite and pigeonite.     

Messung des Ultrarot-Pleochroismus von Mineralen VIII. Der Pleochroismus der OH-Streckfrequenz in Andalusit

Zusammenfassung Mikroskopisch Einschluß-freie Andalusite aus Brasilien zeigen im UR-Absorptionsspektrum ein Doppelmaximum bei zirka 2,9 und ein deutlich schwächeres einfaches Maximum bei 3,04 , die OH-Valenzschwingungen zugeordnet werden. Diese Maxima verschwinden nach mehrtägigem Glühen bei 1000° C. In Platten parallel (110) zeigt das Doppelmaximum bei zirka 2,9 einen extrem starken Pleochroismus, wobei die Bande praktisch völlig verschwindet, wenn der elektrische Vektor parallel [001] schwingt. Damit müssen zumindest die OH-Gruppen, die für diese Bande verantwortlich sind, in die Struktur eingebaut sein. Für beide Arten von OH-Gruppen werden die plausiblen Anordnungen diskutiert.

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Measurement of the infrared-pleochroism in minerals. VIII. The pleochroism of the OH-stretching frequency in andalusite

Summary Inclusion-free andalusites from Brazil show in the IR absorption spectrum a double maximum at ca. 2.9 and a much weaker single maximum at 3.04 which are interpreted as belonging to OH-stretching frequencies. The maxima disappear after annealing the specimen at 1000°C for several days. Plates parallel to (110) show a very strong pleochroism for the 2.9 -band, the peak being practically of zero height if the electric vector vibrates parallel [001]. This proves that at least the OH-groups which are responsible for this absorption band are constituents of the crystal structure. For both kinds of OH-groups the probable distributions are discussed.

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Messung des Ultrarot-Pleochroismus von Mineralen. X. Der Pleochroismus der OH-Streckfrequenz in Zoisit

Zusammenfassung Der Pleochroismus der OH-Streckfrequenz (=3,16 ±0,02 ) zeigt sowohl für -Zoisit als auch für -Zoisit, daß die OH-Dipole paralel [001] orientiert sind.

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Measurement of the infrared-pleochroism in minerals. X. The pleochroism of the OH-stretching frequency in zoisite

Summary The pleochroism of the OH-stretching frequency (=3.16 ±0.02 ) proves for - and -zoisite that the OH-dipoles are oriented parallel [001].

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Planar and line defects in the sapphirine polytypes

Transmission electron microscopy of various natural and synthetic sapphirines shows the existence of extensive polytypic variation in some samples. In addition to the previously described 1Tc and 2M polytypes, 3Tc, 4M and 5Tc structures are observed. The structural principles underlying the polytypism and the associated diffraction behaviour are reviewed, and the correlation between the nature of the observed stacking faults and their origin during crystal growth, in deformation or as a result of solid-state transformation is discussed. Pairs of c/2 partial dislocations observed in synthetic material provide a likely solid-state transformation mechanism, although the evidence suggests that most observed stacking variation arises during growth.A new type of non-conservative planar defect has been found in sapphirine from Finero, Italy, suggestive of unit-cell scale intergrowth with a surinamite- or pyroxene-like structure. A polysomatic model of the sapphirine and surinamite structures as stackings of pyroxene P and spinel S modules is proposed.     

Hydration-induced climb dissociation of dislocations in naturally deformed mantle olivine

Widely dissociated dislocations have been observed in mantle olivine from the Erro-Tobbio peridotite in N.W. Italy. Analysis of diffraction contrast in transmission electron microscopy (TEM) indicates that the dissociation reaction involves the climb dissociation on (001) and {021} planes of b=[001] unit dislocations into partial dislocations with Burgers vectors approximately equal to 1/x 011. In the most extreme case a unit dislocation dissociates into four partials which bound three planar defects. The unusually wide dissociation and the greater extent of dissociation in olivine from amphibole-bearing rocks suggests that the dissociation is related to hydration. The occurrence of fluid inclusions along the dislocations confirms that the partials and planar defects are saturated with volatiles. Analysis of possible planar defect structures in Fo₉₀ shows that; (i) the most likely partial Burgers vectors are b=0 3/11 1/4; (ii) two of the planar defects are cation-deficient and can be stabilised by segregation of H⁺ to produce (Mg, Fe) (OH)₂ layers which are iso-structural with the OH-rich interlayer of the humite group minerals; (iii) the central planar defect is formed by removing a stoichiometric olivine (002) layer so does not produce any local chemical changes. The climb dissociation provides a possible mechanism for the transformation of olivine to a humite group mineral. OH-rich interlayers may nucleate on dislocations and extend into the crystal by climb resulting in a gradual increase of (Mg, Fe) (OH)₂ content. The only addition of material required is hydrogen which can rapidly diffuse into olivine. If the dissociation is stable and occurs at high temperatures and pressures it may significantly influence the nature and kinetics of deformation mechanisms and the olivine — spinel shear transformation mechanism in hydrated olivine.     

TEM study of the transformation of augite to sodic pyroxene in eclogitized ferrogabbro

Transmission and analytical electron microscopy has been used to study relicts of augite that occur in various stages of transformation to sodic pyroxene. The augite relicts are characterized by a hatching produced by two sets of former 001 exsolution lamellae that possess high dislocation densities and were altered completely to sodic pyroxene, even where the augite matrix is still fresh. With further alteration, the sodic pyroxene in these 001 lamellae recrystallized and grew into the augite matrix, resulting in irregular lamellae that consist of subgrains having low dislocation densities. Needles and thin (100) lamellae of sodic pyroxene developed on the 001 lamellae. Alteration of the augite matrix proceeded by growth of areas with defects (dislocations, stacking faults). All sodic pyroxenes in these microstructures have the same orientation as the precursor augite, indicating a topotactic reaction mechanism. The reactions occurred at roughly constant Si and mainly involved replacement of Ca and Mg by Na and Al. Dislocations may have played a prominent role in the transformation by acting as diffusion pathways and by migrating into untransformed augite, leaving sodic pyroxene in their wake. At the grain boundaries of the augite, discrete grains of sodic pyroxene formed without any fixed orientation relation with the augite, consistent with a non-topotactic reaction. The predominance of the topotactic reaction inside the augite over the non-topotactic grain-boundary reaction is attributed to the scarcity of fluids during eclogite metamorphism.     

High temperature,high strain rate deformation in the lower crustal Kalka Intrusion,central Australia

Mafic and ultramafic gneisses (blastomylonites) characterised by a strongly developed planar lenticular foliation-layering are developed in lower crustal (high pressure) cumulates of the stratiform Kalka Intrusion in central Australia. The gneisses occur in two distinct zones, the Numbunja and West Kalka Gneissic Belts, parallel to or at low angles to igneous layering. They developed during and shortly after the final stages of crystallization of the intrusion at temperatures between about 1000 and 1200 ° C, and represent an incipient thrusting deformation probably with associated high strain rates. The most deformed textures in the centre of the belts typically consist of megacrysts of orthopyroxene, clinopyroxene, olivine and plagioclase showing abundant features of extreme ductile flow within a finegrained syntectonically recrystallized matrix of the same material. Mineral elongation, kink band orientation and matrix petrofabrics indicate that the maximum principal elongation and the maximum principal shortening occurred parallel to the lineation and normal to the foliation respectively.Single crystal deformation features (some unique to these rocks) include flow elongation of orthopyroxene and plagioclase (up to at least 400% elongation without recrystallization), kinking of orthopyroxene, clinopyroxene, olivine and plagioclase, production of rare clinoenstatite in orthopyroxene, and an unusual fingerprint texture in clinopyroxene. The occurrence of either flow elongation or kinking of orthopyroxene is dependent on crystal orientation relative to the maximum principal elongation/shortening directions. Detailed analysis shows that the flow orthopyroxenes and possibly the flow plagioclases deformed by simple shear. The results have relevance in studies of possible deformation mechanisms in the upper mantle, and in alpine peridotites.     

Relationship of Water Chemistry to Serum ThyroidHormones in Captive Sharks with Goitres

Captive whitetip reef sharks, Triaenodon obesus,at Sea Life Park (SLP) Hawaii, Waimanalo, Hawaii develop goitre, whereas, T. obesus at the Waikiki Aquarium (WAQ), Honolulu,Hawaii do not develop goitre. To determine theeffects of natural concentrations of iodine on thereduction of goitre, two sharks from SLP with goitrewere placed in an enclosed coastal lagoon with naturalseawater. Using ultrasound measurements the twogoitres were initially 11.4 cm and 14.6 cm in depthand after 3 months decreased to 4.7 cm and 5.7 cm. Radioimmunoassay analysis of the thyroid hormoneT3 sera concentrations were initially 0.22 ng/mland 0.33 ng/ml and increased to 1.84 ng/ml after beingplaced in the lagoon. Sera T4 were initially0.93 ng/ml and 0.99 ng/ml and increased dramaticallyto 17 ng/ml and 56 ng/ml. Over the six month samplingperiod, two resident sharks in the lagoon with normalthyroids had sera T3 concentrations from 0.89ng/ml to 1.1 ng/ml, and sera T4 concentrationsfrom 3.1 ng/ml to 7.9 ng/ml. The hypothyroidcondition in the SLP goitred-sharks is likely linkedto the low environmental iodide (<0.005 M), andhigh nitrate (111 M) of SLP water. The WAQwell-water facility was characterized by anoxic waterwith high iodide (0.60 M), total iodine (1.90M), and typical nitrate (24.6 M)concentrations of interstitial groundwater. Thedifference of iodide concentration of SLP and WAQ tankwater (<0.005 M versus 0.60 M) wasdirectly related to the hydrogeology of the well-watersources. To avoid goitre in marine aquarium systems,we recommend maintaining iodide concentrations of atleast 0.15 M.     

Study of the distribution of Trace elements in soils in and around Mysore city,Karnataka

Soil samples collected from various places in and around Mysore were analyzed for the total trace elements such as Fe, Mn, Cu, Zn, Pb, and Cd. The results of the analysis indicate that the concentration of lead and cadmium in soils is below 2.5 g ml^–1 and 0.2 g ml^–1, respectively, which are the minimum detection levels, whereas the concentration of iron, manganese, copper, and zinc in most of the samples is within the global average ranges of 3%, 500–1000 g g^–1, 15–40 g g^–1, and 50–100 g g^–1, respectively. The investigated area has the presence of gneisses and schists, in which partly there are igneous intrusions and pegmatitic intrusions. There are amphibolite enclaves in gneisses that account for the higher concentration of trace elements. The lower concentration may be attributed to the presence of silicic type of rock.     

Exsolution of Ca-amphibole from glaucophane and the miscibility gap between sodic and calcic amphiboles

Transmission and analytical electron microscopy (TEM/AEM) of glaucophane from glaucophane + Ca-amphibole-bearing blueschist and eclogite from two Vermont localities (Ecologite Brook and Tillotson Peak) and one California locality (Cazadero) has revealed the first evidence from exsolution for the miscibility gap between sodie and calcic amphiboles. The Tillotson Peak samples and the Cazadero samples contain coarsegrained glaucophane—actinolite pairs, while the Eclogite Brook samples contain coexisting glaucophane and actinolitic hornblende. Ca-rich glaucophanes contain abundant fine-scale lamellae of Ca-rich amphibole. These lamellae are usually oriented near (100) and . High-resolution TEM (HRTEM) images show them to be coherent. The exsolution lamellae are so narrow, beyond the resolution of AEM, that their true Ca contents are obscured by analytical contributions from the surrounding host. The AEM data suggest that the lamellae are either winchite or actinolite, depending on the true Ca concentration. In most cases, the exsolution lamellae have very curved interfaces and show variable orientation. This is attributed to the close similarity of unit-cell parameters for the two amphiboles. Three-dimensional optimal phase-boundary calculations using EPLAG (Fleet 1982) show that the observed 100 and orientations are consistent with the minimization of area strain between the two lattices along the interface. Some samples show evidence for incipient exsolution in the form of homogeneously distributed, fine-scale precipitates. These results suggest that Ca-rich glaucophanes from other glaucophane—actinolite assemblages may be exsolved at the TEM scale. The coexisting amphiboles from Eclogite Brook also have been studied using the electron microprobe (EMP). The compositional gap defined by the Eclogite Brook pairs is consistent with previously reported results, but shows a wider break along the glaucophane—actinolite pseudobinary join, suggesting very limited solid solution up to temper-atures of about 500–550°C. The glaucophanes are relatively poor in Ca, except for one anomalous grain containing Ca-amphibole lamellae. Ferric iron, estimated by normalization to fixed cation numbers, is strongly partitioned into the actinolitic hornblende and the glaucophanes are very poor in the riebeckite component.     

The effect of aluminum and water on the development of deformation fabrics of orthopyroxene

The effect of alumina and water solubility on the development of fabric in orthopyroxene in response to simple shear deformation has been investigated at a pressure of 1.5 GPa and a temperature of 1,100 °C using the D-DIA apparatus. The microstructure observations at these conditions indicate that dislocation glide is the dominant deformation mechanism. In MgSiO₃ enstatite and hydrous aluminous enstatite, partial dislocations bounding the stacking faults in [001] glide parallel to the (100) (or) the (100) [001] slip system. Electron backscattered diffraction analysis of anhydrous aluminous enstatite, however, indicates operation of the (010) [001] slip system, and microstructure analysis indicates dislocation movement involving [001] on both (100) and {210} planes. The strong covalent bonding induced by the occupation of M1 and T2 sites by Al could have restricted the glide on (100), activating slip on {210}. The resulting seismic anisotropies (~2 %) in orthopyroxene are weaker compared to olivine (~9.5 %), and reduced anisotropy can be expected if orthopyroxene coexists with olivine. Weak anisotropy observed in stable cratonic regions can be explained by the relatively high abundance of orthopyroxene in these rocks.     

Stress induced transformation of pigeonites from achondritic meteorites

A transmission electron microscopic (TEM) study was conducted to investigate the stress-induced transformation mechanisms of pigeonites from two achondrites. In pigeonites from the Allan Hills 77257 ureilite, abundant lamellae of orthopyroxene-pigeonite intergrowth accompanied by minor amounts of blebby augite precipitates were observed. In pigeonites from the Juvinas eucrite, some stacking faults running through the (001) augite lamellae were observed although most of the stacking faults terminated at the host-lamella interface. High resolution TEM observation shows the fringe offset produced by the stacking fault in the Juvinas pigeonites. The magnitude of the mismatch parallel to [001] is approximately c/4, which is related to the formation of the partial edge dislocation near the host-lamella interface. The partial dislocation is imaged as an edge dislocation with an (002) extra-plane. Three partial dislocation mechanisms with distinct displacement vectors are proposed in order to explain the stress-induced transformation textures observed in the achondritic pyroxenes. Further study will be required to determine unequivocally the mechanism of atomic displacements during stress-induced transformation. However, regardless of the actual mechanism of transformation, it is not difficult to convert orthopyroxene to clinopyroxene or vice versa by this transformation from the structural point of view. Low-Ca pyroxenes are deformed without a stress-induced transformation by slip at high temperature and geologically reasonable strain rates. However, meteoritic pyroxenes can be deformed by stress-induced transformation even at high temperature because preterrestrial impact processes will produce a deformation condition with high strain rates. Deformation at high strain rates and high temperature is very important when we interpret the microtexture of meteoritic pyroxenes.     

Analysis of high-voltage,high-resolution images of lattice defects in experimentally-deformed dolomite

Deformation-induced stacking defects in dolomite have been characterised following examination at the cation sublattice level using high-resolution electron microscopy at 500kV. Slip on c (≡{0001}) is observed to produce stacking faults, often de-localised laterally, which are terminated by partial dislocations with Burgers vectors of the form 1/3 [1 \(\overline 1 \) 00]: a model for the faulted dolomite lattice has been constructed which agrees with the image appearance. Slip on f (≡{10 \(\overline 1 \) 2}) produces long planar faults which are established as not being stacking faults, in the normal sense, since there appear to be no offsets of the cation sublattice across the faults, nor any general indication of any terminating partial dislocations: it is proposed that the contrast arises from rotational disorder in CO₃ groups which has resulted from the prior passage of partial dislocations during deformation.     

Trace elements in the shallow ground water of The Netherlands. A geochemical and statistical interpretation of the national monitoring network data

Concentration levels of the trace elements Al, As, B, Ba, Be, Cd, Co, Cr, Cu, Li, Mo, Ni, Pb, Sr, V, Y, and Zn in the shallow Dutch ground water were studied. Data were extracted from the data base of the Dutch National Ground Water Quality Monitoring Network, a network set up to monitor the diffuse contamination. The network contains over 350 sites at a low density of about 1 per 100 km². The sites are sampled once a year at two depths (approx. 10 and 25 m below surface). A two-step multivariate statistical approach was used, in which the major element chemistry was used to define water types. Within each water type, trace element behavior could be coupled to distinct geochemical processes: dilution, acidification and weathering, carbonate dissolution, oxidation/reduction, and ion exchange. In recently infiltrated acid rain water in low buffering capacity sands, the anthropogenic influence indirectly caused mobilization of Al (median 430 g/l), Cd (0.6 g/l), Co (14 g/l), Cu (2.7 g/l), Ni (16 g/l), Y (11 g/l), and Zn (50 mg/l). In carbonate bearing sediments the acidification is neutralized, and the mentioned trace elements remain immobile. Arsenic and Cr have higher concentrations levels in ground waters with a slightly reducing character and are possibly governed by the dissolution of iron-manganese hydroxides. Boron, Li, and Sr have high concentrations (respectively 875, 80, 2700 g/l) in the water type related to a seawater source. Strontium is related to carbonate dissolution in all other water types (medians ranging from 100 to 1000 g/l). Barium shows a complex behaviour. It is concluded that the high Al, Cd, Co, Cr, Ni, and Zn concentrations are anthropogenically induced. High Ba and Cr concentrations are inferred to be due to natural processes.