Mechanisms Controlling Porosity in Red River (Upper Ordovician) Carbonate Reservoir, Cabin Creek Field, Montana: ABSTRACT

AAPG Bulletin ◽  
1980 ◽  
Vol 64 ◽  
Author(s):  
Kenneth Ruzyla, Gerald M. Friedma
1982 ◽  
Vol 22 (03) ◽  
pp. 429-444 ◽  
Author(s):  
Kenneth Ruzyla ◽  
Gerald M. Friedman

Abstract Several different pore systems are present in dolomite reservoir rocks of the Red River formation (Upper Ordovician) at Cabin Creek field, MT. Each system is associated with particular depositional environments and diagenetic regimes. Pore geometry is mostly a function of the size and shape of the dolomite crystals composing the rock matrix. Mean pore-throat size, a statistical measure of pore geometry, increases as porosity percent increases, depending on the type of dolomite. This relationship permits prediction of reservoir pore geometry and a better assessment of recovery efficiency once lithofacies distribution, porosity origin, and diagenetic history have been determined for the reservoir by study of cores and rock thin-sections. Introduction The reservoir characteristics of any rock type depend on the arrangement of the pore space and how the pores are interconnected. The pore-system geometry of a reservoir rock must be understood to determine fully its response to primary or enhanced recovery. To predict pore geometry trends, it is necessary to establish relationships between measures of pore geometry and petrophysical parameters. which are measurable by electric-log surveys of boreholes. This is because cores, which are necessary for pore geometry determination, are usually available for select wells of any given field. Pore geometry is mostly a function of depositional environment and diagenetic processes such as cementation, recrystallization, mineralogical alterations, and selective leaching of rock components. This study presents an approach for determining heterogeneities of carbonate-reservoir pore geometry and for delineating pore geometry throughout the reservoir. The application to future enhanced recovery also is discussed. The formation under study is the Red River formation (Upper Ordovician) of Cabin Creek field, a producing oil field located in southeast Montana (Fig. 1). The Red River formation is a major producing reservoir in the area, and Cabin Creek is a potential candidate for tertiary recovery. Structurally, Cabin Creek is on the Cedar Creek anticline, a long asymmetrical feature on the southwest margin of the Williston basin (Fig. 1). Fig. 2 is a structure contour map of Cabin Creek field. The Red River formation averages about 500 ft (153 m) in thickness and consists of a sequence of alternating limestones and dolostones (Fig. 3). Production is from the U2, U4, and U6 dolostone units in the upper 150 ft (46 m) of the formation. The interstratified U1, U3, and US limestone units are nonproductive and nonporous (Fig. 4). Lateral and vertical variations in degree of dolomitization are mostly responsible for variations of reservoir properties. Commingled Ordovician and Silurian oil production was 61,570,000 bbl as of Sept. 1979, with reserves of 13,425,000 bbl (2 134 405 m ). The field has been on waterflood since April 1964. Approximately 1,450 ft (444 m) of core from 12 different wells was studied to delineate field stratigraphy, distribution of lithofacies, and depositional environments. Core slabs were ground with abrasive grit, then etched in diluted hydrochloric acid to enhance sedimentary structures and aid in identification of carbonate grains and matrix material. Staining methods were used to aid mineralogical identification. Diagenesis, porosity types, and origin of porosity were determined by petrographic analysis of thin-sections. Values of porosity percentage, permeability, and saturations are from core-plug analyses. Size and shape of pore throats were determined from mercury capillary-pressure data and from scanning-electron micrographs of resin pore casts, respectively. Plots were made of porosity percentage vs. parameters of pore geometry for producing zones within the Red River formation. SPEJ P. 429^


1989 ◽  
Vol 26 (1) ◽  
pp. 74-87 ◽  
Author(s):  
Charles E. Mitchell ◽  
Walter C. Sweet

Ten samples from a 160 m section through the lower Whittaker Formation yielded Red River Province conodonts as well as a shelly macrofossil assemblage representing the "Arctic Ordovician fauna." Both the microfossils and macrofossils have strong affinities with taxa represented in strata of Cincinnatian age in the western Midcontinent Province of North America.Conodont-based graphic correlation of section W-1 with a Composite Standard Section developed for midcontinental United States indicates that the lower Whittaker Formation on the east flank of the Redstone Arch represents nearly the entire Cincinnatian Series. Trilobites of the Ceraurus mackenziensis Zone occur in strata correlative with the upper Edenian and those of the Whittakerites planatus Zone first appear at or just below the projected base of the Maysvillian Stage. The age of the Ceraurinella necra Zone is still uncertain but is likely to be early Edenian.Thaerodonta recedens (Sardeson) and other elements of the Bighornia – Thaerodonta fauna also debut in uppermost Edenian or lowermost Maysvillian strata. The morphology of Sowerbyella redstonensis n.sp. and Thaerodonta recedens from the lower Whittaker Formation indicates that the common ancestor of early Thaerodonta species may have arisen during latest Edenian time. The first appearance of Thaerodonta may constitute a useful biostratigraphic datum throughout the Red River Province. The strongly Thaerodonta-like species, Sowerbyella redstonensis n.sp., is described from silicified material of mid-Edenian age.


1985 ◽  
Vol 59 (S16) ◽  
pp. 1-58 ◽  
Author(s):  
Robert J. Elias

The Upper Ordovician (middle Edenian to upper Richmondian) Montoya Group of southern New Mexico and westernmost Texas comprises, in ascending order, the Second Value Dolomite, Aleman Formation, and Cutter Dolomite. Solitary rugose corals in the Second Value are Grewingkia robusta (Whiteaves, 1896), Bighornia sp. cf. B. patella (Wilson, 1926), Streptelasma divaricans (Nicholson, 1875), a new species of Neotryplasma, and Salvadorea? spp. A and B. Salvadorea kingae kingae Nelson, 1981, G. franklinensis n. sp., and G. crassa alemanensis n. subsp. occur in the Aleman. Taxa found in the Cutter are S. kingae cutterensis n. subsp., G. sp. cf. G. franklinensis, and B. sp. cf. B. patella.Grewingkia robusta is the most abundant species in the solitary rugosan assemblage that is present within the Second Value. This assemblage apparently inhabited comparatively deep-water environments. Most of the corals lived in relatively high-energy conditions, but epizoic forms favored low-energy niches. Salvadorea kingae is the most common taxon in the assemblage that characterizes the Aleman-Cutter. This is probably a comparatively shallow-water assemblage. The dominant taxon inhabited relatively low-energy environments, while less common species lived in higher energy conditions. If the distribution of solitary rugose corals in the area of Montoya deposition was related primarily to water depth, a paleobathymetric gradient from relatively deep in the west to predominantly shallow in the southeast existed through Second Value–Aleman time. During Cutter time, water was relatively deep in the southwest and northeast, and predominantly shallow in the southeast. If the degree of environmental restriction was the principal factor limiting the distribution of Montoya solitary Rugosa, open normal marine environments were predominant in the southeast and uncommon in the north and west.Montoya representatives of Grewingkia, Bighornia, and Salvadorea indicate that the area of deposition was situated within the Red River–Stony Mountain Solitary Coral Province, which occupied most of North America during Late Ordovician time. All species of these genera are typical “epicontinental” forms. Neotryplasma, the only “continental margin” taxon, reflects a cratonic margin paleoposition. The discovery of Streptelasma divaricans within Edenian-Maysvillian strata in the Montoya is consistent with an hypothesis that solitary Rugosa were introduced to the Richmond Solitary Coral Province of eastern North America during an early Richmondian transgression.Within the Red River–Stony Mountain Province, geographic speciation and dispersion seem to have been important factors in the evolution and diversification of Grewingkia robusta and related taxa, including G. haysii selkirkensis n. subsp. from the Selkirk Member of the Red River Formation in southern Manitoba. In Salvadorea, speciation events within the New Mexico–Texas area and Williston Basin were apparently rapid, and coincided with onsets of clastic deposition. Evolutionary change within this genus has not been recognized in the Hudson Bay Basin, where there were no clastic influxes.In the Aleman-Cutter sequence of the Montoya Group, recognition of specific intervals bearing solitary rugose corals may permit detailed biostratigraphic, and possibly chronostratigraphic, correlation. The change from a Grewingkia-dominated assemblage to a Salvadorea-dominated assemblage was not synchronous throughout the Red River–Stony Mountain Province, and the ranges of widely distributed species such as G. robusta and S. kingae cannot be considered isochronous from basin to basin. Within particular basins, endemic taxa having restricted stratigraphic ranges, such as G. crassa alemanensis, can be useful biostratigraphic markers. Streptelasma divaricans remains useful as a Richmondian index fossil in strata within the area occupied by the Richmond Province.


2006 ◽  
Vol 89 (1-3) ◽  
pp. 179-182 ◽  
Author(s):  
D.K. Khan ◽  
B.J. Rostron ◽  
Z. Margitai ◽  
D. Carruthers

1980 ◽  
Vol 17 (2) ◽  
pp. 272-277 ◽  
Author(s):  
Robert J. Elias

Borings occur in solitary rugose corals from the Selkirk Member of the late Middle or Upper Ordovician Red River Formation in southern Manitoba. They are assigned to Dictyoporus garsonensis n. ichnosp., which was produced by algae, and Trypanites weisei Mägdefrau 1932, made by spionid polychaete annelids. Most, and possibly all, boring occurred while the host corals were alive and in life position. The location and relative abundance of borings support interpretations that unattached curved solitary corals lay with the convex cardinal side in the sediment and the concave counter side facing upward during life, whereas straight conical forms were oriented upright in the sediment. These ichnospecies suggest that host corals lived in very shallow marine environments.


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