REEFS AND SALTS

PART I: REEFS

I. Reef Characteristics:

A. Ecological and Paleoenvironmental Conditions

II. Requirements for Hydrocarbon Accumulation:
A. source beds for petroleum
B. a reservoir
C. a suitable structural setting and a cap rock to "trap" petroleum

Why did reefs and their surrounding environments so often become sites of hydrocarbon accumulation?

III. Major Paleozoic Reef Formers
A. Earliest "Reef" Formers of Cambrian (Not true reefs but mound builders)


IV. Paleozoic Case Histories (to be discussed and illustrated in class)

A. Silurian Reefs of N.Y., Michigan, Ohio, Kentucky, Indiana, Wisconsin.

Middle Silurian barrier reefs circle the Michigan and Illinois Basins, another middle to late Silurian barrier reef in southern Illinois and Indiana.

Patch reefs proliferated throughout e. Iowa, se. Wisconsin, Illinois, Indiana, Ohio and Michigan.

Late Silurian barrier reefs on margins of Michigan, Ohio and New York Basins

B. Devonian Reefs of Williston Basin:

A major calcareous shale basin to north of South Alberta reef complex. Within it were long lines of reef trends - the largest is between Calgary and Edmonton where Canadian oil boom began in 1947.

- Oil in porous reef dolomite, sealed by shales of basinal facies. Most reefs 100' thick, but north of Edmonton > 1000'.

- basin facies extends to Arctic Circle where production occurs from reefs in largely shale facies (MacKenzie R.)

Early Miss. - Madison Sea of western stable interior (Mission Canyon and Livingston Formations of NW states and Alberta). crinoidal limestones and calcarenites Livingston Fm - major cliff formers of Canadian Rockies 2000' in Cordillera 1000' in Front Range 500' in Williston Basin

Mission Canyon leached (increasing porosity) in Williston Basin. Buried by evaporites and Mesozoic shales. Major oil producer in S. Saskatchewan.

- near Front Range, folded and faulted by Laramide orogeny. In late Mississippian, the stable interior was uplifted, interior basins silted up. End of late Ordo - mid Mississippian epeiric seas.

PART II: EVAPORITES

Seawater contains about 3.5% dissolved salts as shown in Table 1.

TABLE 1 PROPORTIONS OF PRINCIPAL SALTS DISSOLVED IN NORMAL SEA WATER

SALTS, AMOUNT DISSOLVED, % THICKNESS IF PRECIPITATED FROM 2,000 m of WATER

NaCl (salt) 2.72 47.5
MgCl2 .38 5.8
MgSO4 .16 3.9
CaSO4 (anhydrite) .12 2.3
K2SO4 .08
CaCO3 (calcite) .01 0.6
MgBr2 .01
3.48 60.1 m

Expected to form in reverse order of their relative solubilities. This not always the case because of changes in basin inflow, dilution of brines, etc.

How much water evaporated to form 750 m of Michigan Basin evaporites?
Equivalent to a sea water column 1000 km deep! Alternatively, reflux in a shallow basin.

TABLE 2 Common Marine Evaporite Minerals

anhydrite CaSO4

NOTE: Anhydrite is dehydrated gypsum. Conversion of gypsum to anhydrite occurs with burial and loss of water which can result in a reduction of solid volume by 38%.

NOTE: Bulk dissolution of evaporite by groundwater is very common. This process may cause collapse structures to form (e.g. New Mexico).

TABLE 3.

Locations, Thicknesses, Types and Ages of some North American Paleozoic Evaporites.

Location Age Thickness Type
Williston Basin Ordovician 25 S
Sil. or Dev. 25 S
Devonian 1000 S,H,B
Mississippian 1000 S
Illinois Basin Ordovician 50 S
Mississippian 200 S
Michigan Basin Sil. or Dev. 3000 S,H
Devonian 1200 H
Mississippian 350 H
Paradox Basin, Co Permian 4000 S,H,B
Gypsum Basin, Co Permian 500 S
N. New Mexico Permian 100 S
S. central N. M. Permian 3000 S,H
S.E. New Mexico Permian 4500 S,H,B
Central Texas Permian 1500 S
Texas Panhandle Permian 2000 S
Western Oklahoma Permian 1500 S
W. central Kansas Permian 800 S,H
Iowa Permian 50 S

S= gypsum and anhrdrite H= halite B= bedded bittern salts of potassium and magnesium