An island arc origin for the Canyon Mountain ophiolite complex,eastern Oregon,U.S.A.

The Canyon Mountain ophiolite, Oregon, is exceptional in lacking sheeted dikes, basaltic pillow lavas, and sediments that are characteristic of many other ophiolites. Instead, the uppermost portion of the complex consists of a significant volume of plagiogranites, which, in addition to minor basalts, intrude a large section of keratophyres believed to be of volcanic origin. The trend of intrusive rocks and of bedding in the keratophyres is mostly parallel to layering in the underlying gabbroic cumulates and to contacts between units in the remainder of the ophiolite. It is suggested that the plagiogranites, basalts, and keratophyres comprise a sill complex. Both the plagiogranites and the keratophyres are similar, respectively, to low-K₂O plutonic and extrusive rocks of island arcs. The mineralogy and penetrative deformation structures of the ultramafic and some of the gabbroic rocks of the ophiolite indicate greater depth of formation, related to magmatism and diapirism above a Benioff zone. Radiometric age dates of plagiogranites confine the minimum age of the complex to the Early Permian. The Canyon Mountain ophiolite may thus be correlative with other fragments of a Lower Permian arc terrane throughout northeastern Oregon which were chaotically mixed during renewed subduction in middle to late Triassic time.     

Late Wisconsinan glaciation models of northern Maine and adjacent Canada

Surficial stratigraphic units of Aroostook County, Maine, have been mapped and formal stratigraphic names for these units are proposed. Evidence exists for at least two distinct glacial phases which are represented by three tills. Two of these tills were deposited penecontemporaneously either as the result of coalescing ice sheets or as the result of the thermal regime existing within a single ice sheet. The oldest till is named the St. Francis and is correlated with the Chaudière Till of southeastern Quebec. The other tills are named the Mars Hill and Van Buren tills, respectively, and are correlated with the Lennoxville till of southeastern Quebec. Interbedded stratified sediments associated with the St. Francis till are correlated with the Gayhurst Formation. Stratified sediments associated with Van Buren and Mars Hill tills are correlated with post Lennoxville sediments of Quebec. Granite-gneiss erratics of Canadian Shield provenance in the Van Buren till indicate advance of the Laurentide ice into northern Maine during late Wisconsinan time. Moraines in southern Aroostook County with associated outwash and eskers record general recession from coastal Maine. Recession occurred after the formation of the Pineo Ridge moraine in Maine and the St. Antonin-Highland Front moraine complex in Quebec. The Caribou-Winterville moraine complex in northern Maine marks the boundary between the penecontemporaneously deposited Van Buren and Mars Hill surface tills and is correlated with the Grand Falls moraine at Grand Falls, New Brunswick.     

Dynamical formulation of Broecker''s model for marine cycles of biologically incorporated elements

Broecker presented a steady-state, two-box model which emphasizes the role of kinetic factors in determining the chemical composition of sea water. Unlike thermodynamic models, Broecker's model suggests that sizable temporal variation in the composition of sea water and rates of sedimentation may have taken place in the past 100 million years. To describe the evolution of the ocean's chemical system and interpret variations observed in the sedimentary record, we have formulated a dynamical model. Mass-balance consideration leads to a set of coupled nonlinear differential equations. The equations are linearized and solved for step function changes in the rate of river input and in the rate of vertical mixing. This simple model of the ocean's chemical system is shown to be stable against oscillations. Using data for the modern ocean, the response times for P, C, Si, Ca, and Ba are calculated to be of the order of 10⁴ to 10⁶ yr for changes in river and other inputs and of the order 10¹ to 10² yr for a change in the rate of vertical mixing. Analog-simulation techniques, discussed for the situation of the two-box model, provide a powerful tool for treating nonlinearities and systems with more than two components. In the final section, consequences of the dynamical formulation are compared with parameters appearing in Broecker's steady-state formulation.     

Greatlakean Substage: A replacement for Valderan Substage in the Lake Michigan basin

New evidence from recent field and seismic investigations in the Lake Michigan basin and in the type areas of the Valders, Two Creeks and Two Rivers deposits necessitates revision of late-glacial ice-front positions, rock- and time-stratigraphic nomenclature and climatic interpretations and deglaciation patterns for the period ca. 14,000–7,000 radiocarbon years B.P. The previously reported and long accepted pattern of deglaciation for the Lake Michigan basin started with a regular retreat from the Lake Border Morainic System, with a minor oscillation marked by the Port Huron moraine(s) and then an extensive Twocreekan deglaciation followed by a major (320 km) post-Twocreekan advance (Valders). However, we now record a major retreat between the times of the Lake Border and Port Huron moraines, followed by a gradual retreat from the Port Huron limit and interrupted by a minor standstill (deposition of Manitowoc Till), a retreat (Twocreekan) and a readvance (Two Rivers Till). No Woodfordian or younger readvance was as extensive as had been the preceding one. This sequence argues for a normal, climatically controlled, progressive deglaciation rather than one interrupted by a major post-Twocreekan (formerly Valderan) surge. This revision appears finally to harmonize the geologic evidence and the palynological record for the Great Lakes region. Our investigations show that Valders Till from which the Valderan Substage was named is late-Woodfordian in age. We propose the term “Greatlakean” as a replacement for the now misleading time-stratigraphic term “Valderan”. The type section and the definition of the upper and lower boundaries of the Greatlakean Substage remain the same as those originally proposed for the Valderan Substage but the name is changed.     

Methane consumption in Cariaco Trench waters and sediments

Detailed measurements of CH₄ in the water column and sediments of the Cariaco Trench show that CH₄ is non-conservative in both environments. Concentration differences between the sediments and adjacent overlying water suggest that the sediments are the source of the water column CH₄. Co-metabolism of CH₄ by sulfate reducers appears to be the CH₄ sink in anoxic environments.     

Transfer functions under no-analog conditions: Experiments with Indian Ocean planktonic Foraminifera

This paper documents and investigates an important source of inaccuracy when paleoecological equations calibrated on modern biological data are applied downcore: fossil assemblages for which there are no modern analogs. Algebraic experiments with five calibration techniques are used to evaluate the sensitivity of the methods with respect to no-analog conditions. The five techniques are: species regression; principal-components regression [e.g., Imbrie, J., and Kipp, N. G. (1971). In “The Late Cenozoic Ages,” 71–181]; distance-index regression [Hecht, A. D. (1973). Micropaleontology19, 68–77]; diversity-index regression (Williams, D. F., and Johnson, W. C. (1975). Quaternary Research5, 237–250]; weighted-average method [Jones, J. I. (1964). Unpublished Ph. D. Thesis, Univ. of Wisconsin]. The experiments indicate that the four regression techniques extrapolate under no-analog conditions, yielding erroneous estimates. The weighted-average technique, however, does not extrapolate under no-analog conditions and consequently is more accurate than the other techniques. Methods for recognizing no-analog conditions downcore are discussed, and ways to minimize inaccuracy are suggested. Using several equations based on different calibration techniques is recommended. Divergent estimates suggest that no-analog conditions occur and that estimates are unreliable. The value determined by the weighted-average technique, however, may well be the most accurate.     

Biostratigraphic usefulness of stromatolitic precambrian microbiotas: A preliminary analysis

Diverse, cellularly preserved microbial communities are now known from stromatolitic sediments of at least twenty-eight Precambrian formations. These fossiliferous deposits, principally cherts and cherty portions of carbonate units, range in age from Early Proterozoic (Transvaal Dolomite, ca. 2250 Ma old) to Vendian (Chichkan Formation, ca. 650 Ma old) and include units from Australia, India, Canada, South Africa, Greenland, the United States and the Soviet Union. More than three-quarters of these microbiotas have been discovered since 1970. Although few, therefore, have as yet been studied in detail, virtually all of the assemblages are known to be dominated by prokaryotic (bacterial and blue-green algal) microorganisms and to contain three major categories of microfossils: spheroidal unicells, cylindrical tube-like sheaths, and cellular trichomic filaments. Analyses of data now available (including measurements of more than 7800 fossil unicells) indicate that each of these three types of microfossils exhibited a gradual, but marked, increase in mean diameter and size range during the Proterozoic and that taxonomic diversity apparently also increased, especially beginning about 1400 Ma ago. Thus, it now seems evident that (i) the microbial components of Proterozoic stomatolitic assemblages have varied systematically as a function of geologic age and that (ii) such communities are both more abundant and more widespread than had previously been recognized. These observations augur well for the future use of such assemblages in Precambrian biostratigraphy. At present, however, data are sufficient to warrant the provisional establishment of only a few microfossil-based subdivisions of the Proterozoic. Such zones, necessarily relatively long-ranging, are here tentatively defined; it is of interest to note that boundaries between certain of these microfossil-based subdivisions appear to coincide, at least approximately, with previously suggested stromatolite-based boundaries. To some extent, therefore, results of this study seem consistent with, and may be supportive of, the concept of stromatolite-based biostratigraphy. At the same time, however, the study seems to indicate that stromatolites of markedly differing age, whether of similar or of dissimilar morphology, were probably formed by distinctly differing microbiotas. Data are as yet insufficient to indicate whether differing types of coetaneous, stratigraphically useful, stromatolites were formed by differing microbial communities and two what extent the “evolution” of stromatolite morphology was a result of the biologic evolution of stromatolite-building microorganisms. There is thus continued need for investigation of the potential biostratigraphic usefulness of stromatolitic microbiotas and, especially, for more effective integration of results of such studies with those available from studies of stromatolites without preserved microbiotas and from studies of the acritarchs preserved in Proterozoic shales.