DEVELOPMENTS IN SEDIMENTOLOGY 46 Carbonate Diagenesis and Porosity Clyde H. Moore Basin Research Institute, Louisiana State University, Baton Rouge, LA 70903-4701, U.S.A. ELSEVIER Amsterdam - Lausanne - New York - Oxford - Shannon - Singapore - Tokyo ELSEVIER SCIENCE B.V. Sara Burgerhartstraat 25 P.O. Box 21 1, 1000 AE Amsterdam, The Netherlands First edition 1989 Second impression 1997 ISBN 0-444-87415-1 (Vol. 46) (hardbound) ISBN 0-444-87416-X (Vol46) (Paperback) ISBN 0-444-41238-7 (Series) ' 1989 ELSEVIER SCIENCE B.V. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without the prior written permission of the publisher, Elsevier Science B.V., Copyright & Permissions Department, P.O. Box 521, 1000 AM Amsterdam, The Netherlands. 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This book is printed on acid-free paper Printed in The Netherlands PREFACE This book is an outgrowth of an annual seminar delivered to the Industrial Associates of the Applied Carbonate Research Program for the past 12 years here in Baton Rouge, and a number of public short courses given at various localities in the U.S. and Europe under the auspices of Oil and Gas Consultants of Tulsa, Oklahoma. The aim of these courses and the purpose of this book is to provide the working geologist, and the university graduate student, with a reasonable overview of carbonate diagenesis and its influence on the evolution of carbonate porosity. It is an enormously complex subject, incorporating large dollops of petrography, geochemistry, hydrology, mineralogy, and some would say, witchcraft. I do hope that in my effort to make carbonate diagenesis and porosity evolution understandable to the “normal geologist” that I have not damaged the subject by drifting too far toward over-simplification. In the discussion of tools useful for ehe recognition of diagenetic environments, I have stressed the value of basic petrology and geologic setting because of the perceived audience of this book. In the case of geochemical techniques I attempt to give a balanced view concerning the strengths and constraints of each technique at its present state of development, with the purpose of alerting the reader to the pits and traps that abound in modern high tech geoscience, and to help the reader to evaluate modem published studies in carbonate diagenesis. Case histories must be an integral part of any work treating the interrelationships of diagenesis and porosity. The case histories presented here were chosen on the basis of how well the details of porosity evolution could be tied to specific diagenetic evironments, the level of documentation of the case study, the demonstrated economic importance of the sequence, and finally, the familiarity of the author with the area and the rocks. No particular effort was made to ensure that specific regions, or geological ages were represented, because it is strongly felt that the concepts being developed in the book, and dacumented in the case histories are, in generalneither site nor age specific. Nevertheless it is realized, principally because of the author’s experience, that the book is heavily wrinJlted toward the Americas. Perhaps this unintended provincialism can be rectified it be future. Xnumber of people have assisted in the preparation of this work. The manuscript was read in its entirety by Ellen Tye, Emily Stoudt, and Chad McCabe. Their comments a do bservations were very helpful and many found their way into the final version. Jay Banmi read the sections on trace elements and isotopes and his suggestions were VI PREFACE particularly beneficial. Marlene Moore constructed and maintained the bibliographic data base, and together with Brenda Kirkland, produced the reference section. Mary Lee Eggert, Clifford Duplechain, and James Kennedy produced the figures, while Dana Maxwell printed the photos. The manuscript was edited by Lynn Abadie with the able . assistence of Marlene Moore and Brenda Kirkland Dr. Douglas Kirkland served as consulting grammarian. Brenda Kirkland organized the “Index Gang” consisting of Brian Carter, Allison Drew, Pete George, Ezat Heydari, Marilyn Huff, Kasana Pi- takpaivan, Tinka Saxena, Bill Schramm, Chekchanok Soonthornsaratul,B ill Wade, and Paul Wilson. This group produced the index. The Industrial Associates of the Applied Carbonate Research Program, the Basin Research Institute, and Louisiana State Univer- sity are thanked for support during the project. The manuscript was produced camera ready in house on a Macintosh SE. This book is dedicated to Marlene Mutz Moore, a lady of courage, class, and a ready smile. She has touched us, her friends, family, and compatriots, and we are the better for it. February 16,1989 Clyde H. Moore Baton Rouge, La. Chapter 1 THE NATURE OF CARBONATE DEPOSITIONAL SYSTEMS- COMPARISON OF CARBONATES AND SILICICLASTICS INTRODUCTION While this book is concerned primarily with diagenesis and porosity evolution in carbonate reservoirs, the reader and author must ultimately share a common understand- ing of the fundamental characteristics of the carbonate realm. Therefore, this introduc- tory chapter is designed to compare and contrast carbonates and siliciclastics, and to highlight general concepts unique to the carbonate regime, such as: 1) the biological origin enjoyed by most carbonate sediments; 2) the complexity of carbonate rock clas- sifications; 3) the ubiquitious cyclicity of autochthonous carbonate rock sequences, and their response to sea level fluctuations and global tectonics; and 4) the diagenetic con- sequences of the high chemical reactivity of carbonates. Readers desiring an in-depth review of carbonate depositional environments should read the extensive compilation edited by Scholle, Bebout, and Moore (1983) and the review of carbonate facies by James (1984). CONSEQUENCES OF BIOLOGICAL INFLUENCE OVER CARBONATE SEDIMENTS Introduction The striking differences between carbonate and siliciclastic sediments can gener- ally be traced to the overwhelming biological origin of carbonate sediments, and the influences that this origin exerts on sediment textures, fabrics, and depositional processes such as the ability of certain organisms to build a rigid carbonate framework. The following section outlines these broad influences on carbonate sedimenrs and sedi- mentation. Origin of carbonate sediments Well over 90% of the carbonate sediments found in modern environments are biological in origin and are forming under marine conditions (Milliman, 1974; Wilson, 1975; Sellwood, 1978). Distribution of carbonate sediments is directly controlled by 2 THE NATURE OF CARBONATE DEPOSITIONAL SYSTEMS environmental parameters favorable for the growth of the calcium carbonate organisms. These parameters include temperature, salinity, substrate, and the presence of siliciclas- tics (Lees, 1975). Carbonate sediments generally are deposited near the site of their origin. In contrast, siliciclasticsa re generally formed outside the basin of deposition, and are transported to the basin, where physical processes control their distribution. For siliciclastics,c limate is no constraint,f or they are found worldwide, and are abundant at all depths, in fresh water as well as marine environments. The reef, a unique depositional environment The ability of certain carbonate-secreting organisms to dramatically modify their environment by encrusting, framebuilding, and binding leads to the depositional envi- ronment unique to the carbonate realm--the reef (Fig. 1.1). In this discussion, we shall use the term reef in its genetic sense--a solid organic framework that resists waves (James, 1983). SYMBOLIZED REEF STRUCTURE DETRITAL FILL GREEN ALGAE (Corals, Coralline Algae, Molluscs, Foraminifem, etc.) CEMENT CORALLINE ALGAE (Foraminifera, Hydrocorallines, Bryozoans) FRAME CORALS PRECIPITATED (Aragonite, Mg-Calcite) (Hydrocorallines, Coralline Algae) Fig. I .I.D iagramshowing symbolized reef structure emphasizing interaction betweenf rame, detrital fill, and cement. Modified from Ginsburg and Lowenstam, 1958, Journal of Geology, v.66, p.310. Reprinted with permission of the University of Chicago Press. Copyright (C) 1958, Journal of Geology. In a modern reef, there is an organism-sediment mosaic that sets the pattern for framework ecologic reef sequences. There are four elements: theframework organisms, including encrusting, attached, massive, and branching metazoa; internal sediment, filling primary growth as well as bioeroded cavities; the bioeroders, which break down reef elements by boring, rasping, or grazing, thereby contributing sediment to pen-reef as well as internal reef deposits; and cementation, which actively lithifies, and perhaps contributes to internal sediment (Fig. 1.1). While the reef rock scenario is complex, it is consistent. Chapter 4 presents a comprehensive treatment of marine cementation BIOLOGICAL CONTROL OVER TEXTURE AND FABRIC 3 associated with reef depositional environments. Today, the reef frame is constructed by corals and red algae. Ancillary organisms such as green algae contribute sediment to the reef system. Reef organisms have undergone a progressive evolution through geologic time, so that the reef-formers of the Lower and Middle Paleozoic (i.e., stromatoporoids)a re certainly different from those of the Mesozoic (rudistids and corals) and from those that we observe today (James, 1983). Indeed, there were periods, such as the Upper Cambrian, Mississippian, and Pennsylva- nian, when the reef-forming organisms were diminished, or not present, and major reef development did not occur (James, 1983). Reef complexes, then, while certainly influenced by physical processes, are dominated by a variety of complex, unique, biological, and diagenetic processes that have no siliciclastic counterpart. Unique biological control over the texture and fabric of carbonate sediments The biological origin of most carbonate sedimentary particles places severe constraints on the utility of textural and fabric analysis of carbonate sediments and rocks. Sediment size and sorting in siliciclasticsa re generally indicators of the amount and type of physical energy (such as wind, waves, directed currents and their intensity) influenc- ing sediment texture at the site of deposition (Folk, 1968). Size and sorting in carbonate sediments, however, may be more influenced by the population dynamics of the organism from which the particles were derived, as well as the peculiarities of the organism’s ultrastructure. Folk and Robles (1964) documented the influence of the ultrastructure of coral and Hulimedu on the grain-size distribution of beach sands derived from these organisms at Alacran Reef in Mexico (Fig. 1.2). In certain restricted environments, such as on a tidal flat, it is common to find carbonate grains composed entirely of a single species of gastropod (Shinn and others, 1969). The mean size and sorting of the resulting sediment is controlled by natural size distribution of the gastropod population, and therefore, grain size tells little about the physical conditions at the site of deposition. For example, large conchs are commonly en- countered in and adjacent to mud-dominated carbonate lagoons in the tropics. Upon death, these conchs become incorporated as large clasts in a muddy sediment. This striking textural inversion does not necessitate, as it might in siliciclastics, some unusual transport mechanism such as ice rafting, but simply means that the conch lived and died in the environment of deposition. Other textural and fabric parameters, such as roundness, also suffer biological control. Roundness in siliciclastic grains is generally believed to indicate distance of transport, and/or the intensity of physical processes at the site of deposition (Blatt, 4 "HI? NATURE OF CARBONATE DEPOSITIONAL SYSTEMS g a + & HALIMEDA .:I. .. 4>jy* I) I) :.. - CI w.i.. ., i......i .(.. & 1 COLONY SEGMENTS:WHOLE BROKEN DUST (100) 0 -10 -8 -6 -4 -2 0 2 4 6 8 10 mm 1024 256 64 16 4 1 .25 .06 ,016 ,004 ,001 SIZE Fig. I .2. Bioclast ultrastructural control of grain size in beach sediments from Alacran Reex Mexico. Halimeda breaks down into two main grain-size modes; coarse sand composed of broken segments, and micrite-sized dust composed of the ultimate ultrastructural unit of the organism, single needles of aragonite. Corals also break down into two modes; large gravel-sized joints, and sand-sized particles which represent the main ultrastructural unit of the coral (Fig. 1.3). From Folk and Robles, 1967, Journal of Geology, v.72, p.9. Used with permission of University of Chicago Press. Copyright (C) 1967, Journal of Geology. Middleton, and Murray, 1972). Roundness in carbonate grains, however, may well be controlled by the initial shape of the organism from which the grain is derived (for example, most Foraminifera are round). In addition, an organism's ultrastructure, such as the spherical fiber fascioles characteristic of the coelenterates, may also control the shape of the grains derived from the coral colony (Fig. 1.3). Finally, some grains such as oncoids, rhodoliths, and ooids are round because they originate in an agitated environment where sequential layers are acquired during the grain's traveIs over the bottom, with the final product assuming a distinctly rounded shape (Bathurst, 1971).T herefore, great care must be used when interpretingthe textures and fabrics of carbonate sediments and rocks as a function of physical conditions at the site of deposition. CARBONATE GRAIN COMPOSITION 5 Fig. 1.3. Ultrastructure of a coralseptum composedof sphericalbodiesstackedone on top of the other in inclined rows. Each sphere is about 2 phi sized (grit) and consists of aragonite fibers arranged about a point center. See Fig. 1.2. (Taken from Majeweski, 1969.). Copyright, E. J. Brill, the Netherlands. Used with permission. Carbonate grain composition Since skeletal remains of organisms furnish most of the sediments deposited in carbonate environments, the grain composition of carbonate sediments and rocks often directly reflects their environment of deposition because of the general lack of transport in carbonate regimens and the direct tie to the biological components of the environment. A number of researchersh ave documented the close correlation between biological com- munities, depositional environment, and subsequent grain composition in modern carbonate depositional systems (Ginsburgl956; Swinchatt,l965; Thibodeaux, 1972) (Fig. 1.4). The ability to determine the identity of the organism from which a grain originates by its distinctive and unique ultrastructure (BathurstJ971; MiUiman, 1974; Majewske, 1%9; and Horowitz and Potter, 197 1) is the key to the usefulness of grain composition for environmental reconstruction in ancient carbonate rock sequences. Wilson (1975) and Carrozi and Textoris (1967) based their detailed microfacies studies on the thin sction identification of grain composition, including detailed identification of the biological affinities of bioclasts. In contrast, grain composition in siliciclastics is related to the provenance of the sediment, climate, and stage of tectonic development of the source, rather than to anditions at the site of deposition(Krynine, 1941;F olk, 1954 and 1968; PettiJohn,l957; d Blatt, Middleton and Murray, 1972). 6 THE NATURE OF CARBONATE DEPOSITIONAL SYSTEMS 70 60 50 Y 0 40 z a % 30 8 20 10 n" I REEF I SHELF I FLORIDA BAY Fig. I .4. Graph showing percentage of major grain types in the dominant depositional environments of south Florida (Dataf rom Thibodeaux, 1972). SEDIMENTARY PROCESSES AND DEPOSlTIONAL ENVIRONMENTS COMMON TO BOTH CARBONATES AND SILICICLASTICS Once formed, carbonate sediments not bound by organisms react to physical processes of transport and deposition in the same manner as their siliciclastic counter- parts. Carbonate sands under the influence of directed currents will exhibit appropriate bedforms and cross-stratification as a function of current characteristics (Ball, 1967). Carbonate muds will be winnowed if enough wave or current energy is present in the environment.A carbonate turbidite, under appropriate conditions, will exhibit the classic Bouma sequence of sedimentary structures (Reinhardt, 1977; Rupke, 1978), thus indicating similar processes at the site of deposition regardless of origin of the sediment. It follows that carbonates and siliciclastics share some common marine deposi- tional environments and that general paths to the recognition of these environments in ancient sequences, such as type and sequences of sedimentary structures, textures, and fabrics, will be similar (Inden and Moore, 1983). These analogous environments include: shoreline complexes consisting of beach, dune, tidal flat, tidal channel, and tidal delta environments;s ubmarinet idal barcomplexes; submarine canyon fills and slopedeposits; and basinal turbidites (see Scholle, Bebout, and Moore, 1983 for a comprehensive discussion of these and other carbonate depositional environments).