Formation of corrensite, chlorite and chlorite-mica stacks by replacement of detrital biotite in low-grade pelitic rocks

Transmission and scanning electron microscopy were utilized to investigate the nature and mechanisms of alteration of abundant detrital biotite of volcanic origin and progressive modification of phyllosilicate aggregates in a prograde sequence of pelitic rocks (illite crystallinity index = 0.19–0.58λ2θ) from the Gaspé Peninsula in Quebec.
Detrital biotite has been diagenetically altered to form corrensite and chlorite through two mechanisms; (1) layer-by-layer replacement gave rise to interstratification of packets of layers and complex mixed layering via several kinds of layer transitions between biotite and chlorite, corrensite or smectite; (2) dissolution-transport-precipitation resulted in the formation of relatively coarse-grained aggregates of randomly orientated, corrensite-rich flakes and fine-grained corrensite intergrown with chlorite and illite in the matrix.
The data show that stacks consisting of alternating packets of trioctahedral and dioctahedral phyllosilicates originated during early diagenesis when lenticular fissures in strained altering biotite were filled by dioctahedral clays. Subsequent prograde evolution of dioctahedral clays occurred through deformation, dissolution and crystallization, and overgrowth. Illite evolved to muscovite, with K in part provided through biotite alteration, and corrensite/chlorite to homogeneous chlorite. The alteration of detrital biotite is closely related to the formation of titanite and magnetite in diagenetic rocks, and pyrite, calcite and anatase or rutile in the higher grade rocks.
The observations demonstrate that detrital biotite of volcanic origin may be the principal precursor of chlorite in chlorite-rich metapelites originating in marginal basins. The mineral parageneses suggest that the transitions from corrensite to chlorite and illite to muscovite may be a function of local chemistry and time.     

Architecture and evolution of the Paine channel complex, Cerro Toro Formation (Upper Cretaceous), Silla Syncline, Magallanes Basin, Chile

The Upper Cretaceous Cerro Toro Formation in the Silla Syncline, Parque Nacional Torres del Paine, Magallanes Basin, Chile, includes over 1100 m of mainly thin‐bedded mud‐rich turbidites containing three thick divisions of coarse conglomerate and sandstone. Facies distributions, stacking patterns and lateral relationships indicate that the coarse‐grained sandstone and conglomerate units represent the fill of a series of large south to south‐east trending deep‐water channels or channel complexes. The middle coarse division, informally named the Paine member, represents the fill of at least three discrete channels or channel complexes, termed Paine A, B and C. The uppermost of these, Paine C, represents a channel belt about 3·5 km wide and its fill displays explicit details of channel geometry, channel margins, and the processes of channel development and evolution. Along its northern margin, Paine C consists of stacked, laterally offset channels, each eroded into fine‐grained mudstone and thin‐bedded sandy turbidites. Along its southern margin, the Paine C complex was bounded by a single, deeply incised but stepped erosional surface. The evolution of the Paine C channel occurred through multiple cycles of activity, each involving: (i) an initial period of channel erosion into underlying fine‐grained sediments; (ii) deposition of coarse‐grained pebble to cobble conglomerate and sandstone within the channel; and (iii) waning of coarse sediment deposition and accumulation of a widespread sheet of fine‐grained, thin‐bedded turbidites inside and outside the channel. The thin‐bedded turbidites deposited within, and adjacent to, the channel along the northern margin of the Paine C complex do not appear to represent levée deposits but, rather, a separate fine‐grained turbidite system that impinged on the Paine C channel from the north. The Cerro Toro channel complex in the Silla Syncline may mark either an early axial zone of the Magallanes Basin or a local slope mini‐basin developed behind a zone of slope faulting and folding now present immediately east of the syncline. If the latter, flows moving downslope toward the basin axis further east were diverted to the south by this developing structural high, deposited part of their coarse sediment loads, and exited the mini‐basin at a point located near the south‐eastern edge of the present Silla Syncline.     

Isotopic Studies of Processes in Mafic Magma Chambers: I. The Kiglapait Intrusion, Labrador

The initial Nd and Sr isotopic ratios of cumulate rocks andminerals of the Kiglapait intrusion are pertinent as indicatorsof the processes that affected the Kiglapair magma while itwas resident in the crust. A Sm–Nd mineral isochron indicatesthat the crystallization age of the intrusion is 1305?22 millionyears. The initial _Nd values range from—1?6 in the LowerZone to 6 in the Upper Zone and correlate with the anorthitecontent of plagioclase. The initial ₈₇Sr/⁸⁶Sr ratios are 0.70407to 0.70433 in the Lower Zone, and increase monotonically up-section(decreasing plagioclase anorthite content) to 0.7068 in theUpper Zone. These variations are attributed to assimilationof roof rock concurrently with crystallization. It is evidentthat replenishment of the chamber with uncontaminated magmawas important during the accumulation of the lower zone rocks,but did not occurduring crystallization of the Upper Zone. Amathematical model relating isotope ratio shifts to the relativerates of crystallization, assimilation, and replenishment ispresented. It is estimated that the rate of assimilation wasbetween 0.01 and 0.04 of the crystallization rate, and thatduring the accumulation of the Lower Zone, the rate of replenishmentwas about half of the crystallization rate. A formulation for‘assimilation efficiency’is presented that relatedthe actual amount of assimilation (determined from the isotopedata) to the thermodynamic maximum allowable amount. The assimilationefficiency of the Kiglapait intrusion is not tightly constrained,but appears to be of the order of 0.01 near the end of crystallizationand perhaps as high as 0.07 near the beginning. Further quantitativeestimates of assimilation efficiency in different intrusionsemplaced under different conditions may aid in understandingassimilation mechanisms and in assessing the role of assimilationin magmatic evolution in general. Many layered intrusions studiedto date have initial Nd isotope ratios close to the chondriticvalue (_Nd= 0), suggestive of mantle magma sources that are chemicallyundepleted, and thus different from the sources of mid-oceanridge basalt and island-arec basalt.     

An Example of Consequent Mantle Metasomatism in Peridotite Inclusions from Nunivak Island, Alaska

Many of the coarse-grained peridotite inclusions in basanitesfrom Nunivak Island, Alaska, contain amphibole and a smallerfraction also contain phlogopite and apatite. All of these peridotiteshave light REE/heavy REE abundance ratios greater than chondritesand many have abundances of K, Rb, Sr, Ba and light REE whichexceed estimates for primitive mantle. On the basis of mineraltextures and compositions we infer that the clinopyroxene, amphibole,phlogopite and apatite equilibrated with a metasomatic fluid.Isotopic (Sr and Nd) ratios and parent-daughter abundance datafor the coarse-grained peridotites constrain the age of themetasomatism to be less than 200 million years. Associated amphibole pyroxenite inclusions are not metasomatized;these inclusions probably formed as crystal segregates froman alkalic magma. Both pyroxenites and coarse-grained peridotitesare isotopically similar to basalts from Nunivak Island. Usingthese data, we propose a model in which the metasomatized peridotiteswere wallrocks located adjacent to the pyroxenites, and thatmetasomatism of these peridotites was caused by the infiltrationof a residual silicate melt or volatile-rich fluid derived fromthe parental magma of the pyroxenites; i.e. the metasomatismwas a consequence of basaltic magmatism. Furthermore, the parentalmagma of the pyroxenites was probably petrogenetically relatedto the Nunivak volcanism. REE modelling of fluids in equilibriumwith clinopyroxenes from the coarse-grained peridotites is consistentwith this model.     

Late Quaternary glaciation and environmental change on St. Kilda, Scotland, and their palaeoclimatic significance

On Hirta, the largest island of the St. Kilda archipelago near the western edge of the Scottish continental shelf, evidence has been found for four cold periods and one intervening mild period. During the most recent cold period (the Loch Lomond Stadial), two protalus ramparts were formed. Prior to this there occurred two periods of valley glaciation separated by a mild interval during which the local vegetation was dominated by grasses and sedges. For the most recent valley glaciation (= Late Devensian glacial maximum) a mean July temperature of 4°C is inferred. At this time intensive periglacial processes were operative down to present sea level. At some earlier, pre-Dcvensian, time St. Kilda was invaded by the Scottish ice sheet.     

Nitrogen fluxes in a high elevation colorado rocky mountain basin

Measured, calculated and simulated values were combined to develop an annual nitrogen budget for Loch Vale Watershed (LVWS) in the Colorado Front Range. Nine-year average wet nitrogen deposition values were 1·6 (s=0·36) kg NO₃-N ha⁻¹, and 1·0 (s=0·3) kg NH₄-N ha⁻¹. Assuming dry nitrogen deposition to be half that of measured wet deposition, this high elevation watershed receives 3·9 kg N ha⁻¹. Although deposition values fluctuated with precipitation, measured stream nitrogen outputs were less variable. Of the total N input to the watershed (3·9 kg N ha⁻¹ wet plus dry deposition), 49% of the total N input was immobilized. Stream losses were 2·0 kg N ha⁻¹ (1125 kg measured dissolved inorganic N in 1992, 1–2 kg calculated dissolved organic N, plus an average of 203 kg algal N from the entire 660 ha watershed). Tundra and aquatic algae were the largest reservoirs for incoming N, at approximately 18% and 15% of the total 2574 kg N deposition, respectively. Rocky areas and forest stored the remaining 11% and 5%, respectively. Fully 80% of N losses from the watershed came from the 68% of LVWS that is alpine. © 1997 John Wiley & Sons, Ltd.     

ASSESSMENT OF CLIMATE CHANGE AND FRESHWATER ECOSYSTEMS OF THE ROCKY MOUNTAINS,USA AND CANADA

The Rocky Mountains in the USA and Canada encompass the interior cordillera of western North America, from the southern Yukon to northern New Mexico. Annual weather patterns are cold in winter and mild in summer. Precipitation has high seasonal and interannual variation and may differ by an order of magnitude between geographically close locales, depending on slope, aspect and local climatic and orographic conditions. The region's hydrology is characterized by the accumulation of winter snow, spring snowmelt and autumnal baseflows. During the 2–3-month ‘spring runoff’ period, rivers frequently discharge > 70% of their annual water budget and have instantaneous discharges 10–100 times mean low flow. Complex weather patterns characterized by high spatial and temporal variability make predictions of future conditions tenuous. However, general patterns are identifiable; northern and western portions of the region are dominated by maritime weather patterns from the North Pacific, central areas and eastern slopes are dominated by continental air masses and southern portions receive seasonally variable atmospheric circulation from the Pacific and the Gulf of Mexico. Significant interannual variations occur in these general patterns, possibly related to ENSO (El Niño–Southern Oscillation) forcing. Changes in precipitation and temperature regimes or patterns have significant potential effects on the distribution and abundance of plants and animals. For example, elevation of the timber-line is principally a function of temperature. Palaeolimnological investigations have shown significant shifts in phyto- and zoo-plankton populations as alpine lakes shift between being above or below the timber-line. Likewise, streamside vegetation has a significant effect on stream ecosystem structure and function. Changes in stream temperature regimes result in significant changes in community composition as a consequence of bioenergetic factors. Stenothermic species could be extirpated as appropriate thermal criteria disappear. Warming temperatures may geographically isolate cold water stream fishes in increasingly confined headwaters. The heat budgets of large lakes may be affected resulting in a change of state between dimictic and warm monomictic character. Uncertainties associated with prediction are increased by the planting of fish in historically fishless, high mountain lakes and the introduction of non-native species of fishes and invertebrates into often previously simple food-webs of large valley bottom lakes and streams. Many of the streams and rivers suffer from the anthropogenic effects of abstraction and regulation. Likewise, many of the large lakes receive nutrient loads from a growing human population. We concluded that: (1) regional climate models are required to resolve adequately the complexities of the high gradient landscapes; (2) extensive wilderness preserves and national park lands, so prevalent in the Rocky Mountain Region, provide sensitive areas for differentiation of anthropogenic effects from climate effects; and (3) future research should encompass both short-term intensive studies and long-term monitoring studies developed within comprehensive experimental arrays of streams and lakes specifically designed to address the issue of anthropogenic versus climatic effects. © 1997 John Wiley & Sons, Ltd.     

CONTROLS ON SURFACE WATER CHEMISTRY IN THE UPPER MERCED RIVER BASIN,YOSEMITE NATIONAL PARK,CALIFORNIA

Surface water draining granitic bedrock in Yosemite National Park exhibits considerable variability in chemical composition, despite the relative homogeneity of bedrock chemistry. Other geological factors, including the jointing and distribution of glacial till, appear to exert strong controls on water composition. Chemical data from three surface water surveys in the upper Merced River basin conducted in August 1981, June 1988 and August 1991 were analysed and compared with mapped geological, hydrological and topographic features to identify the solute sources and processes that control water chemistry within the basin during baseflow. Water at most of the sampling sites was dilute, with alkalinities ranging from 26 to 77 μequiv. l⁻¹. Alkalinity was much higher in two subcatchments, however, ranging from 51 to 302 μequiv. l⁻¹. Base cations and silica were also significantly higher in these two catchments than in the rest of the watershed. Concentrations of weathering products in surface water were correlated to the fraction of each subcatchment underlain by surficial material, which is mostly glacial till. Silicate mineral weathering is the dominant control on concentrations of alkalinity, silica and base cations, and ratios of these constituents in surface water reflect the composition of local bedrock. Chloride concentrations in surface water samples varied widely, ranging from <1 to 96 μequiv. l⁻¹. The annual volume-weighted mean chloride concentration in the Merced River at the Happy Isles gauge from 1968 to 1990 was 26 μequiv. l⁻¹, which was five times higher than in atmospheric deposition (4–5 μequiv. l⁻¹), suggesting that a source of chloride exists within the watershed. Saline groundwater springs, whose locations are probably controlled by vertical jointing in the bedrock, are the most likely source of the chloride. Sulphate concentrations varied much less than most other solutes, ranging from 3 to 14 μequiv. l⁻¹. Concentrations of sulphate in quarterly samples collected at the watershed outlet also showed relatively little variation, suggesting that sulphate may be regulated to some extent by a within-watershed process, such as sulphate adsorption.