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1 Department of Geology and Soil Science, Ghent University, Krijgslaan 281 S8, B-9000 Ghent, Belgium
2 Geobound International Ltd, Environmental Research Group and Consultants, Doornstraat 27, B-9550 Herzele, Belgium
* E-mail address of corresponding author: Florias.Mees{at}UGent.be
| Abstract |
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Key Words: Analcime Chabazite Diagenesis Olduvai Phillipsite Tanzania Zeolites
| INTRODUCTION |
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This paper presents the results of a petrographic study of all main stratigraphical units (Beds I to IV; Reck, 1951) sampled in the southeastern part of the basin. In this area, early Pleistocene lake-margin deposits of great significance for paleoanthropological research are exposed. The main objective of this study is an improved understanding of the mechanisms and timing of zeolite diagenesis at Olduvai, based on the nature of zeolite occurrences and their relationship with other (non- zeolitic) diagenetic features.
| GEOLOGICAL SETTING |
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The centre of the Olduvai Basin was occupied by a perennial saline alkaline lake during the early part of its recorded history (2.01.7 my; Hay, 1976). During the next stage (1.71.2 my), the lake progressively shrank and the area of alluvial terrains increased, followed by a period during which sedimentation mainly took place in an alluvial plain environment (1.20.6 my; Beds III and IV). The deposits include a number of mostly trachytic tuff layers, containing variable amounts of non-volcanic material.
Lake water and groundwater have been characterized by high alkalinity at all times, up to the present. This high alkalinity is mainly due to weathering of sodic volcanic rocks within the catchment (Hay, 1963, 1970). Semi-arid climatic conditions, which persisted through- out the Quaternary in this region (Hay, 1976, 1990), resulted in the development of saline alkaline lake and soil water.
| PREVIOUS STUDIES OF ZEOLITE OCCURRENCES IN THE OLDUVAI BASIN |
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In the fluvial deposits of Beds II to IV, analcime is the dominant zeolite mineral in claystone and sandstone, occurring as veins, cements and isolated crystals (Hay, 1970). Chabazite and phillipsite are less common and natrolite is rare. Analcime and chabazite commonly occur together, suggesting that they formed at the same time, whereas natrolite always formed at a later stage. In tuff layers, phillipsite is the dominant zeolite mineral. All zeolites formed at or near an exposed paleosurface, whereby detrital clays acted as the main source of Al and Si (Hay, 1970).
Part of the zeolites in deposits of the Olduvai Basin formed after incision of the gorge. These zeolite occurrences, dominated by phillipsite, are recognized for deposits that post-date gorge incision (Hay, 1963, 1964, 1966, 1980), as well as for exposed older deposits (Hay, 1963, 1964).
| MATERIALS AND METHODS |
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radiation, scan time 1 s per 0.02°2
, range 360°2
). Thin-sections were prepared for 68 samples, after impregnation of air-dried undisturbed fragments with a cold-setting polyester resin. The composition of all zeolite minerals was checked by energy-dispersive analysis, using undisturbed fragments of selected samples (Noran Vantage microanalysis system, Jeol JSM-6400 scanning electron microscope).
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| STRATIGRAPHY AND DEPOSITIONAL ENVIRONMENTS OF THE STUDIED DEPOSITS |
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The Bed III deposits are typically reddish brown (sandy) claystones. These are fluvial sediments which formed after a major change in drainage patterns due to tectonic movements. The detrital fraction is dominated by volcanic detritus from southern and eastern source areas. The deposits of Bed IV largely consist of greyish brown claystones, representing fluvial deposits that were derived from metamorphic basement rocks in the north and northwest. They formed after a northward displacement of the drainageway that marks the boundary between zones with different sediment source areas.
Throughout Beds I to IV, many intervals show indications of subaerial exposure or pedogenesis, including the occurrence of root traces and soil structure development (Hay, 1976; Kafumu, 2000) (Figure 2
).
| RESULTS |
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In the following paragraphs, the nature of zeolite occurrences is described for the lake margin and fluvial deposits. The boundary between these facies is the base of Tuff IIB (see Figure 2
). For every interval, an overview of the zeolite minerals that are present is first given, followed by a description of their mode of occurrence and the relationship between the various zeolite minerals, and then by information about their relationship with other diagenetic features. For associated occurrences of zeolites and Fe/Mn oxides, only intervals where zeolites are covered by Fe/Mn oxides are reported below. The reverse situation is much more common, throughout Beds I to IV.
Zeolites in lake-margin deposits of Bed I
Chabazite is the most abundant zeolite in the Bed I deposits (Table 2
; Figure 2
). Phillipsite is recognized in many samples as a subordinate phase and occasionally as the dominant zeolite mineral (Z3).
Chabazite occurs, in varying degrees, as (1) the main or sole constituent of altered vitric volcanic rock fragments and glass shards, (2) coatings and infillings of pores, and (3) a major constituent of the groundmass. Occurrences as part of altered rock fragments include chabazite infillings and coatings of vesicles, generally without any glass remaining between these relics (Figure 3a
). The vesicles are generally lined by thin clay coatings with high interference colors (smectite), also in fragments or parts of fragments where no zeolites developed. Chabazite in pores is restricted to channels in several intervals, and it is absent in more recently developed cracks. It commonly occurs as complete infillings (rather than coatings), composed of small euhedral to subhedral crystals with a limited degree of intergrowth (ZA, Z9, Z17, ZK) (Figure 3b
). In intervals with a high chabazite content outside the pore system (Z4, Z10, Z11, Z15, Z19, Z22, ZK, ZL, Z4), the groundmass has a distinctive greyish color in comparison with intervals with a low chabazite content.
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Chabazite and phillipsite occurrences are only rarely associated with other diagenetic features. They are impregnated by Fe/Mn oxides in three intervals (ZA, ZJ, ZK), and phillipsite coatings are locally covered by sparitic carbonates (ZJ). Elsewhere, chabazite coatings and infillings contain intercalations of yellowish fine clay with second-order interference colors (Z4, ZK) which are different from the illuvial clay coatings in other parts of the deposits (Figure 3d
).
Zeolites in lake-margin deposits of Bed II
Deposits below Tuff IIA. The Bed II deposits below Tuff IIA (see Figure 2
) include a central partly diatomaceous interval without any zeolites (RS8 to RS16). Chabazite is by far the most common zeolite outside this interval (Table 2
; Figure 2
). Erionite is also recognized, as well as kenyaite (NaSi11O20.5(OH)4.3H2O). Chabazite only occurs in the intervals with the strongest field indications for subaerial exposure (heterogeneous aspect, dark color) (RS5, RS7, RS17, RS19). It occurs chiefly in pores and only rarely as part of altered volcanic rock fragments. In one interval, vitric fragments are nearly unaltered, with thin clay coatings along the sides of vesicles as the only sign of alteration (RS16). Chabazite is present in many pores in all chabazite-bearing intervals, but not in recent cracks with closely matching sides, which occasionally cross chabazite occurrences. Erionite occurs as crystals that cover chabazite in pores (RS17). Spherulitic kenyaite aggregates are recognized for a few pores with chabazite coatings or infillings (RS5) (Figure 4a
).
Tuff IIA.
Erionite is the only zeolite mineral in Tuff IIA (Figure 4b
). It occurs primarily as small crystals (2035 µm) in pores, and it is also recognized in vesicles of a few glass fragments. All volcanic glass in this interval is nearly unaltered, with only thin clay coatings around vesicles.
Lower augitic sandstone.
The basal part of this interval (RS24) contains chabazite coatings in pores, similar to those in lower parts of Bed II. It also contains clinoptilolite, which occurs as isolated crystals covering chabazite coatings (RS24). A higher interval only contains (abundant) phillipsite, along the sides of pores (RS31).
Zeolites in fluvial deposits of Bed II
Tuff IIB.
The most common zeolite in Tuff IIB is analcime, occurring as coatings in pores (Table 3
; Figure 2
). The interval also contains considerable amounts of phillipsite, which covers any analcime that is present. Chabazite is locally associated with analcime in one interval (RS39). Analcime and phillipsite are commonly covered by sparitic calcite and fine clay coatings (Figure 5a
). Analcime also occurs between coarse and fine clay coatings (RS35, RS38), and phillipsite locally covers sparitic calcite (RS38).
Top of Bed II.
Phillipsite, occurring as coatings in pores, is the most abundant zeolite mineral in this part of Bed II (RB2, RB3). Analcime occurs together with phillipsite in the upper part of the interval (RB3) (Figure 5b
). In lower parts, analcime mostly occurs in dissolution cavities in altered volcanic rock fragments and it locally covers phillipsite in pores (RB2). Both minerals cover fine clay coatings in some pores (RB2, RB3), and phillipsite locally covers sparitic calcite (RB2).
Zeolites in fluvial deposits of Bed III
Analcime is the dominant zeolite in the Bed III deposits, occurring as sub/euhedral crystals and xeno- topic isotropic coatings (Table 3
; Figure 2
). Phillipsite is locally present in lower parts of the interval. Chabazite and minor amounts of natrolite occur in the upper half, above a highly calcareous interval with a high micritic carbonate content of the groundmass and a sparitic carbonate cement (RB14).
The zeolites in Bed III occur exclusively as coatings and infillings of pores. In thin-sections of intervals with prominent mottling, there is no difference in zeolite content between parts with a high Fe oxide content and zones with Fe oxide depletion (RB15, RB18, MC1, MC3). In some samples with a high secondary carbonate content, analcime only occurs in parts with a non-calcareous groundmass and without carbonates or clay coatings in pores (RB12, RB14). Pores containing isolated analcime crystals include dissolution cavities in altered volcanic rock fragments. Chabazite occurs as relatively coarse-grained optically anisotropic coatings that are generally xenotopic (see Figure 6a
), in contrast to the fine-grained aggregates of predominantly subhedral crystals in Beds I and II (see Figure 3b, 3d
). Chabazite also occurs around corroded augite grains (RB15, RB18) (Figure 6a
). Some grains of this type are surrounded by calcite instead of chabazite (RB18). Phillipsite occurs together with analcime in the only phillipsite-bearing interval (RB8). Natrolite, occurring as relatively large sub/ euhedral crystals (50100 µm), covers both analcime and chabazite (Figure 6b
).
Analcime commonly covers fine clay coatings (RB5, RB6b, RB10, MC1, MC3), and also occurs along the sides of cracks within these coatings (RB6b, MC1, MC3) (Figure 6c
). Elsewhere, analcime, chabazite or natrolite are covered by fine clay (RB14b, RB21, RB24) (see Figure 6b
). In one interval (RB24), analcime occurs between coarse and fine clay coatings, and it also occurs within the fine clay, partly with associated sparitic calcite and with a pale color of the clay below the zeolite band (Figure 6d
). Chabazite covers coarse clay coatings in an interval in which it is covered by fine clay in other pores (RB21). In several samples, analcime, phillipsite or chabazite are covered by sparitic calcite (RB8, RB10, RB14, RB14b), or they occur together with sparitic calcite without a clear difference in time of development (RB18). A sparitic carbonate cement locally encloses a thin analcime coating parallel to the sides of a pore (RB14b).
Zeolites in fluvial deposits of Bed IV
Analcime is the only zeolite mineral in most parts of Bed IV, occurring in high concentrations in the upper part of this unit (MC12, MC16, MC18, MC19) (Table 3
; Figure 2
). Phillipsite only occurs at the top of Bed IV (MC24).
Analcime occurs exclusively as coatings of pores, which include packing pores (primary pores), channels and cracks. It generally occurs in large parts of the pore system (Figure 7a
), but very seldom as complete infillings of wide pores. Some analcime occurrences are crossed by cracks without zeolites. Nowhere is analcime associated with vitric volcanic rock fragments. At the top of Bed IV (MC24), rock fragments of this type are completely altered to clay, without any associated zeolites (Figure 7b
). In the only phillipsite-bearing interval (MC24), most phillipsite occurs as small crystals (10 µm) in pores, throughout the sample. In this interval, dissolution cavities in volcanic rock fragments and mineral grains contain larger phillipsite crystals (up to 75 µm); analcime occurs together with these phillipsite crystals, representing all analcime that is recognized for this interval (Figure 7c
).
In an interval with a high sand content (MC 9 to MC14), analcime is only present in pores that contain clay coatings or secondary carbonates, occurring within coarse or fine clay coatings (MC11b, MC12) or as crystals that are covered or enclosed by sparitic calcite (MC11b, MC14) (Figure 7d
). In the only phillipsite-bearing interval (MC24), phillipsite covers clay coatings throughout the sample, and it is covered by a thick paler clay coating in one pore. Phillipsite is also covered by Fe/Mn oxides in some pores.
| DISCUSSION |
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Part of the zeolites in the lake-margin deposits formed by interaction of volcanic material with saline alkaline solutions, as recorded by the common occurrence of chabazite as an alteration product of vitric volcanic rock fragments. The first step in their alteration was the development of thin smectite coatings, which were commonly preserved when chabazite formed during continued alteration of the glass. During a final stage, glass dissolution often proceeded without local zeolite formation, as shown by the common absence of glass between isolated chabazite occurrences that represent coatings and infillings of vesicles in the original glass fragments.
Interaction between volcanic material and alkaline solutions can also account for high chabazite concentrations in the groundmass, when glass dissolution and zeolite formation take place in different parts of the sediments instead of representing local replacement reactions. Another possible mechanism for the development of a zeolite-rich groundmass is replacement of fine-grained detrital Al silicates (e.g. Remy and Ferrell, 1989; Renaut, 1993). Both types of zeolite formation within the groundmass, in contrast to mineral formation in macropores, require continuous contact with saline alkaline solutions that pervade the deposits. It will generally take place in subaqueous settings, or at or near water saturation in subaerial settings, rather than within or above the vadose zone of a soil profile.
Chabazite was formed or redistributed extensively within the pore system during periods of subaerial exposure. It commonly occurs as complete infillings consisting of loosely stacked crystals, rather than dense intergrowths that may have formed by continued growth of coatings along the sides of a pore. The development of loose infillings generally requires conditions resulting in mineral formation in water-filled pores, at or above the groundwater table. The nature of these chabazite occurrences therefore suggests that zeolite formation in pores at this stage took place under conditions with a shallow groundwater table below a subaerially exposed surface.
Zeolites are largely absent in an interval that includes abundant diatom remains (RS10, RS11) and unaltered glass (RS16). Lake-water salinity and alkalinity must have been too low to allow zeolite formation, which is compatible with the persistence of freshwater conditions with relatively low pH due to decaying organic matter in wetlands around springs (Deocampo and Ashley, 1999). Zeolites only occur at a few levels in this part of Bed II, representing thin surface horizons affected by zeolite formation during periods of subaerial exposure with very shallow groundwater depths.
Chabazite in altered volcanic rock fragments may, in principle, have formed at a different stage than chabazite in pores, e.g. at an earlier stage by subaqueous diagenesis. If the times of development were different, both periods of zeolite formation were characterized by similar chemical environments, producing the same mineral phase. Phillipsite, which always covers chabazite where both minerals occur together and which occurs in larger numbers of pores than chabazite, mainly formed at a later stage, after further development of the pore system. In contrast to chabazite in this part of the deposits, it never formed under conditions that resulted in the development of loose zeolite infillings. Zeolite formation was only locally followed by a period of frequent water saturation with Fe/Mn oxide redistribution or the development of sparitic calcite infillings.
The overall predominance of chabazite suggests a relatively early stage of inflow water evolution, with relatively low salinity and alkalinity. This is also indicated by the occurrence of associated intercalations of authigenic smectite, which generally forms from less evolved solutions than zeolite minerals. The formation of phillipsite after a period of chabazite formation records a change in chemical environment. This change may, in principle, have taken place during a single period of zeolite development (e.g. Brey and Schmincke, 1980), but there are no indications of this in the studied deposits. Phillipsite forms in conditions with a higher pH (Brey and Schmincke, 1980) or higher K+ activities (Chipera and Apps, 2001) than chabazite. It can therefore be expected to have formed during drier periods, from more evolved highly alkaline solutions with high relative K+ concentrations following a stage with formation of Na-dominated authigenic minerals. The formation of erionite and clinoptilolite after chabazite requires a significant increase in Si/Al activity ratios, which can be caused by a decrease in pH (Mariner and Surdam, 1970) or by the removal of Al by zeolite formation (e.g. Sheppard and Gude, 1969). An influence of local sediment composition on zeolite mineral assemblages is suggested by aberrant (non-chabazitic) zeolite occurrences in a number of tuff beds (phillipsite predominance in Tuff IC and IF, erionite in Tuff IIA).
Fluvial deposits
Analcime is the dominant zeolite in the fluvial deposits of Beds II to IV, in agreement with earlier reports (e.g. Hay, 1966, 1970). Analcime typically forms at rather high salinity and alkalinity, in more central parts of saline alkaline lake basins than other zeolite minerals (e.g. Sheppard and Gude, 1969, 1973; Gude and Sheppard, 1988). In such environments, analcime formation is favored by high Na+/H+ ratios, low Si/Al ratios and low H2O activities. There are no clear indications that a change in sediment composition contributed to the abrupt shift from chabazite to analcime predominance.
Phillipsite occurs in the lower part of the sequence of fluvial deposits, representing a transition to the zeolite assemblage that is recognized for the lake-margin deposits. The common co-occurrence of phillipsite and analcime (RB3, RB8, MC24), without indications of differences in time of development, shows that they formed in conditions that allow their co-precipitation (see e.g. La Iglesia et al., 1991). Chabazite is recognized in thin-sections for the upper part of Bed III, above an interval with a high secondary carbonate content (RB14). The re-appearance of relatively abundant chabazite seems to be related to a temporary change in water chemistry, associated with a period of subaerial exposure that is recorded by that calcareous interval. A change in zeolite mineralogy following a period of exposure with carbonate enrichment is also recorded at the top of Bed IV, where the base of a phillipsite- dominated section coincides with the top of an interval with an upward increase in (nodular) carbonate content. Natrolite, which has an even lower Si/Al ratio and higher extra-framework cation content than analcime (see Table 1
), formed under conditions of higher salinity and alkalinity than this more common phase.
Zeolites in the fluvial deposits occur nearly exclusively in pores. In contrast to chabazite in parts of the lake-bed deposits, nowhere do they occur as loose complete infillings of macropores, which would imply a lower degree of water saturation. Zeolites in the fluvial deposits are not associated with volcanic rock fragments, 670 Mees et al. Clays and Clay Minerals except locally at the top of Bed IV. Analcime and phillipsite occur in dissolution cavities in some rock fragments, but this is not necessarily related to their dissolution. Similarly, chabazite around corroded augite grains can be infillings of dissolution cavities rather than replacement products. Only the formation of analcime and phillipsite associated exclusively with altered rock fragments at the top of Bed IV (MC24) is clearly related to local dissolution. The presence of analcime as part of the groundmass is not recognized in thin-sections (in contrast to chabazite in Bed I), and XRD results indicate that submicroscopic analcime is not a major constituent. An absence of submicroscopic zeolites would not exclude the possibility that zeolites formed to a large extent by an interaction of saline alkaline pore water with clay minerals or amorphous Al silicates. There are no indications, in any case, that analcime formed by transformation of a zeolite precursor as has been inferred for several other analcime occurrences (e.g. Sheppard and Gude, 1969, 1973; Ratterman and Surdam, 1981).
No clear relationship exists between zeolite content or mineralogy and the presence of indications for soil development or subaerial exposure. Significant changes do occur around some lithological discontinuities, including levels which represent paleosurfaces: (1) the lower boundary of the fluvial deposits marks an abrupt change to an analcime-dominated zeolite assemblage; (2) the common occurrence of phillipsite ends abruptly at the boundary between Beds II and III; (3) a paleosurface level marks the base of a chabazite-rich interval in the middle of Bed III; (4) a significant increase in analcime content occurs above the top of a sandy interval in the middle of Bed IV; and (5) a paleosurface is recognized for the lower boundary of the phillipsite-dominated upper part of Bed IV. These examples show that breaks or major changes in sedimentation have an impact on zeolite mineralogy, but not through zeolite formation in deposits below an exposed surface. Vertical variations compatible with zeolite enrichment by groundwater evaporation along an exposed surface, which was subsequently covered by deposits with a relatively low zeolite content, are only recognized for the top of both Bed III intervals with reddish deposits (RB4 to RB6b, and RB15 to MC4).
Part of the zeolites in the fluvial deposits formed at an early stage, after the development of secondary pores but before the formation of (fine) clay coatings or sparitic carbonates. For one interval, early analcime formation is also suggested by indications that it was partly dissolved before or during a period with secondary carbonate enrichment and clay illuviation (RB12, RB14). In several intervals, zeolites occur between or within other diagenetic features in pores. Analcime locally occurs between a coarse-clay coating, which typically forms at a relatively short distance from the soil surface, and a fine-clay coating, formed at greater depths within the vadose zone. Zeolites occurring within fine-clay coatings show that zeolite formation occasionally continued during periods of fine clay illuviation, under conditions of alternating wetting and drying. Analcime associated with sparitic calcite formed under rather stable conditions with a high degree of water saturation, which is generally required for the development of a sparitic carbonate cement. Iron oxide depletion below intercalations of analcime and sparitic calcite is compatible with this, because it indicates reducing conditions which can be related to water saturation. Conditions required for the development of these associated zeolite and carbonate occurrences are encountered in the lower part of the capillary fringe above the water table, where zeolite enrichment can be strong (Bernhard and Barth-Wirsching, 2002).
Although some zeolites in the fluvial deposits formed at an early stage, most zeolites formed at a late stage, after a period of clay illuviation and locally after the development of sparitic calcite coatings or infillings. It also generally postdates Fe/Mn oxide redistribution under conditions with a fluctuating groundwater table, recorded by the presence of analcime coatings in pores with Fe/Mn oxide impregnation of the sediment along their sides. Zeolite formation after a period of Fe/Mn oxide redistribution is also suggested by the lack of variations in zeolite content with Fe/Mn oxide content in mottled intervals. Other features recording late-stage development include the presence of analcime in cracks that formed within illuvial clay coatings. It is also recorded by the occurrence of analcime in large parts of the pore system, including planar pores formed by shrinkage, instead of being confined to channels as in large parts of the lake-margin deposits. Some of these zeolites could have formed after the deposits became exposed to the atmosphere along the sides of the gorge. However, there are various indications that zeolites did not form extensively after incision of the gorge, which was eroded to its present level prior to deposition of the Naisiusiu Beds (Hay, 1976) (62 ky BP; Skinner et al., 2003). Indications against zeolite formation after exposure along the sides of the gorge include the absence of late-stage zeolites in all intervals in which zeolites are covered by clay coatings or secondary carbonates and the mentioned changes in zeolite content or mineralogy around lithological discontinuities.
| CONCLUSIONS |
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Some of the zeolites may have formed in a subaqueous setting, but they certainly formed extensively during periods of subaerial exposure, resulting in their common occurrence in pores. The recognition of paleosurfaces that were exposed during periods of zeolite formation is difficult. A detailed study of vertical trends would be needed, but their interpretation will be complicated by the superposition of zeolite occurrences that formed during successive stages of subaerial exposure. In addition, studies of vertical variations might essentially produce a record of groundwater levels during periods of zeolite formation (English, 2001; Bernhard and Barth-Wirsching, 2002).
Establishing the timing of zeolite formation must be done with care for deposits with intervals showing indications of subaerial exposure and for deposits susceptible to zeolite enrichment or redistribution in present-day exposures. The present study illustrates the use of several criteria to obtain information about this aspect of zeolite formation, such as the relationship between zeolite occurrences and illuvial clay coatings or sparitic carbonate infillings.
Variations in zeolite mineralogy reflect changes in water composition. Within the study area, the water had a relatively low salinity and alkalinity during deposition and early diagenesis of the lake-margin deposits of Bed I and the lower part of Bed II, replaced by pore water with higher K/Na ratios during later stages of diagenesis. In the younger fluvial deposits, zeolites formed under conditions with more highly saline, Na-rich solutions. This type of sequence, whereby an analcime-dominated facies is succeeded by a facies dominated by other zeolite minerals, is more commonly recognized as a lateral trend. Its occurrence at Olduvai is related to a fairly abrupt basin-wide change in depositional environments rather than to a gradual change in patterns of variation in water composition.
| Footnotes |
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(Received 17 September 2004; revised 10 June 2005)
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