U.S. Geological Survey Open-File Report 2004-1098
Version 1.0
Eolian Dust and the Origin of Sedimentary Chert
By C. Blaine Cecil
email: bcecil@usgs.gov
key words: eolian, dust, silica, sedimentary chert
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This paper proposes an alternative model for the primary source of silica contained in bedded sedimentary chert. The proposed model is derived from three principal observations as follows: (1) eolian processes in warm-arid climates produce copious amounts of highly reactive fine-grained quartz particles (dust), (2) eolian processes in warm-arid climates export enormous quantities of quartzose dust to marine environments, and (3) bedded sedimentary cherts generally occur in marine strata that were deposited in warm-arid paleoclimates where dust was a potential source of silica. An empirical integration of these observations suggests that eolian dust best explains both the primary and predominant source of silica for most bedded sedimentary cherts.
The enigmatic source of silica contained in bedded sedimentary cherts is generally inferred from one or more of the following processes: (1) biotic extraction of silica from seawater, (2) silica derived from dissolution of volcanic ash, (3) silica expelled from submarine volcanic vents, or (4) silica deposited by post-burial fluid flow (see reviews by Hesse 1990; Carozzi 1993; and Knauth 1994). It is generally difficult, however, to account for either the temporal and spatial distribution of bedded cherts, or the enormous quantities of silica contained in massive bedded sedimentary cherts by these processes. In particular, biologically mitigated chert formation is especially intractable for Precambrian cherts that were deposited prior to the evolution of silica-secreting organisms (Knauth, 1994).
Except for incidental comments (e.g., Haught
1956; Carozzi 1993; Edgar and Cecil 2003), dust has
not been proposed as the primary source of silica for bedded cherts even though paleogeographic
and paleoclimate reconstructions (e.g., Scotese 1998) indicate that the vast majority of Phanerozoic bedded sedimentary cherts
are associated with strata that were deposited in or near warm-arid to semiarid
paleoclimates.
This paper, therefore, discusses quartzose
dust as the primary source of silica for chert, and
presents selected examples of the empirical relations among chert
occurrences and warm-arid paleoclimates. The postulate developed herein suggests that
quartzose eolian dust best
accounts for the primary and predominant source of silica contained in most
bedded sedimentary cherts.
The chemistry of dust-size particles of quartz (#60 φm) derived from air abrasion provides important clues for dust as a cogent source of silica for chert. The silt-size and smaller particles (#60 φm) of quartz produced by abrasion (Whalley and others, 1987; Wright 2001) are very reactive, in part because of their very small size, high angularity, and the resultant large surface areas and high surface energies. In addition, the surface of abraded quartz particles is composed of a 0.1-φm-thick layer of amorphous silica consisting predominantly of silanol groups (Iller 1955; Kronenberg 1994). Because amorphous silica is an order of magnitude more soluble than quartz (e.g., Iller 1955), the amorphous layer becomes a volumetrically significant source of dissolved silica in particles of fine-grained quartz because of the small size and large surface area.
In addition to the amorphous surface layer, the crystal lattice of abraded quartz particles is disordered to depths of 5 φm and perhaps to depths of 50 to 100 φm (Iller 1955) (Fig. 1). Data on the enthalpy of solution of quartz particles derived from mechanical abrasion in air indicate that the entire lattice of quartz particles less than 30 φm (#medium silt) is disordered and metastable with respect to the ordered core of coarser quartz particles (Hemingway and Nitkiewicz 1995). These data suggest that structural disorder induced by air abrasion is significant to depths of at least 15 φm. As a result of the amorphous outer layer and lattice disorder (to depths of 15 φm), the #-30-φm-size fraction of quartz dust is metastable and relatively soluble. Additionally, water extraction of attrition fragments of quartz derived from air abrasion experiments by Whalley and others, (1987) resulted in concentrations of dissolved silica that ranged from 300 to 1600 ppm (φg/l). They suggested (p. 137) that equally high concentrations of silica in solution could be derived from naturally abraded sand grains. Furthermore, experiments have shown that fine-grained quartz is highly susceptible to pressure solution and diagenetic alteration (Renton and others, 1969). The aforementioned chemical characteristics of fine quartz suggest that quartz dust is highly reactive.
Figure 1. – Diagrammatic cross section of an angular silt-sized grain of quartz analogous to the maximum grain size in aerosols. Eolian abrasion induces silica structures that progressively grade inward as follows: 1) an outer amorphous layer, 2) an underlying structurally disordered layer, 3) an ordered core of α-quartz.
In a thorough review of silica in chert, Knauth (1994) pointed out that most cherts are predominantly composed of α-quartz in the form of granular microcrystalline quartz and megaquartz, with minor amounts of fibrous silica. According to Knauth (1994), silica particles in chert range in size from less than 1 to 60 µm, but they are generally on the order of 8-10 µm. The particle sizes of silica particles in chert are remarkably similar to the particle sizes of quartz in aerosols (airborne dust) derived from warm deserts. Furthermore, partial or total diagenetic dissolution of the metastable outer layers of air-abraded α-quartz particles in dust would significantly diminish the size of detrital particles and also change particle shape (Fig. 1).
Conclusions.-- The thermodynamic data of Hemingway and Nitkiewicz (1995), the amounts of dissolved silica derived from experimentally abraded quartz particles (Whalley and others, 1987), and the susceptibility of fine-quartz to pressure solution (Renton and others, 1969) suggest that quartzose dust is very reactive and highly susceptible to diagenetic alteration. Following dissolution of the metastable outer layers, the residual inter core approximates the size of much of the megaquartz found in chert (Fig. 1). Furthermore, the thermodynamic data indicate that the microquartz and fibrous silica in chert may be the product of precipitation of silica from solutions that were supersaturated with respect to α-megaquartz. Diagenesis of quartzose dust, therefore, may best explain the source of silica and the petrology of most bedded cherts.
Dust as a precursor for chert is likely restricted to
aerosols derived from warm-arid deserts where fine-grained quartz is the
predominant mineral component.
Significant quantities of quartzose eolian dust are exported from modern
terrestrial warm-arid environments. For
example, 130 to 760 million tonnes of dust are blown from the
Although upwelling has been suggested as the source of
silica for some chert (e.g., Hesse 1990), the
offshore surface winds from modern warm-arid deserts that deposit dust in
marine environments (Sarnthein and others, 1981; Goudie and Middleton 2001) commonly contribute to
upwelling. As a result, both eolian dust
and upwelling are plausible sources of nutrients and silica for chert offshore
of warm arid high-pressure belts. Although
upwelling may serve as a source of dissolved silica for silica secreting organisms,
dust also has the potential to supply both soluble silica for biogenic
productivity as well as fine particles of α-quartz that approximate the size of megaquartz in chert.
Eolian processes, therefore, provide an alternative to upwelling as the
source of silica for chert and nutrients for biological productivity,
particularly in ancient epeiric seas.
This observation is supported by data from Kolla
and others, (1981) who report greater than 30 percent biogenic opaline silica in recent carbonate-free sediment off the
eastern coast of the Arabian Peninsula in an area known to receive significant
amounts of dust (Gulf of Oman, Fig. 2).
Areas of upwelling to the south in the
Increases
in silica concentrations in the world’s oceans during Pleistocene glacial
intervals have been documented and attributed to variations in the amount of
silica supplied by rivers (Froelich and others, 1992). In contrast, Kurtz and
Figure 2. – Northeasterly winds from Iran and Pakistan
transport dust plums over the eastern Persian Gulf (left center), Gulf of Oman (lower center)
and northern Arabian Sea (lower right) (photo credit: Jeff Schmaltz, MODIS Rapid Response Team, NASA/GSFC 11-16-2003). Periodically, winds from the west and
southwest also bring dust from the
Conclusions.--- Copious influxes of dust to marine environments during periods of aridity in warm climates is likely to be conducive to the formation of bedded cherts, whereas humid periods limit or preclude eolian dust transport and chert formation. In addition, marine evaporative conditions associated with variations in the degree of aridity also may play an important role in silica equilibrium. Periods of highly evaporative conditions could trigger silica precipitation, probably as gels, along with evaporites, which may explain the common association of chert with evaporties. Furthermore, massive influxes of quartzose dust are likely to produce major increases in the productivity of silica-secreting organisms in response to increases in dissolved silica and nutrients.
Among the numerous examples of bedded cherts occurring in
strata that were deposited under warn-arid climatic conditions, five specific
examples are briefly discussed herein.
These examples include both shallow water epeiric sea and deep water
trough depositional systems. Shallow epeiric sea examples include Early and
early Middle Devonian cherts in the Appalachian Basin, Mississippian cherts
across the North American craton, and unnamed Pennsylvanian cherts and cherty
limestones in southeastern
Although deposition of Early and early Middle Devonian chert was widespread across
Conclusions.--- The source of silica for the Shriver and Huntersville cherts (and equivalent cherty limestones) has previously been attributed to the biotic extraction of silica from seawater derived from the dissolution of volcanic ash (Dennison 1961; Sheppard and Heald 1984). Although minor amounts of biotic components have been recognized in the cherts, and volcanic ash (bentonite) occurs near the top of the Huntersville, the lithologies of the stratigraphic interval considered herein appear to be best explained by eolian sand and dust as the predominant source of silica. The coarsest silt fraction accounts for the quartz silt noted in the cherts as well as the quartz silt in interbedded limestone, whereas the finer size fraction of quartz dust readily provided an ample supply of soluble silica and residual particles that are equivalent in size to quartz crystallites in chert. Thus, the Early and early Middle Devonian sequence in the Appalachian Basin can be readily explained by temporal and spatial variations in eolian processes in a warm arid climate. In contrast, it is unclear how the enormous amounts of Devonian chert can be accounted for by either silica derived from dissolution of volcanic ash or biotic extraction of silica from normal seawater.
Relatively high sea level resulted in flooding of much of
the North American craton during the late Osagean and early Meramecian
(Mississippian) (Gutschick and Sandberg
1983) when aridity was widespread across the North American craton. Aridity is indicated by the presence of evaporites
in
Conclusions.--- The Osagean-Meramecian epeiric seas of North American were situated in an arid belt in the vicinity of 20E to 30E S. lat (Scotese 1998). Aridity is indicated by widespread occurrences of evaporites. The paleogeography of the time is consistent with atmospheric high pressure, an arid climate, and the export of large volumes of dust from exposed areas of aridity upwind of the chert-bearing Osagean-Meramecian units. Thus, the primary source of the enormous quantities of silica contained in shallow water Osagean-Meramecian cherts appears to be better explained by an eolian source rather than by any of the other sources that are traditionally inferred.
Cecil and others, (2003) traced a Middle Pennsylvanian
(Desmoinsian) cyclothem (fourth-order sequence) from the Appalachian Basin across
the craton to southeastern Nevada (Arrow Canyon), where Pennsylvanian strata
were deposited in a shallow-shelf environment inboard of the western margin of
Pangea. Detailed investigations of the
fourth-order sequence in Arrow Canyon revealed that a quartzose siltstone with
calcite cement, interpreted as a continental dust deposit, overlies a paleoexposure surface (unconformity) that delineates the
lower fourth-order sequence boundary (Cecil and others, 2003). The siltstone is overlain by transgressive cherty limestone and impure chert, which were
interpreted as peritidal in origin. An
open marine limestone with chert nodules overlies the cherty peritidal
carbonates, and the open marine limestone is capped by a paleoexposure
surface that represents the upper unconformable fourth-order sequence
boundary. Fourth-order sequences are
very repetitive in
Interpreted paleowind directions
(Parrish and Peterson 1988) in Pennsylvanian sand seas in
Conclusions.---
Eolian dust appears to best explain the detrital quartz silt and silica contained within the
Pennsylvanian siltstones, bedded cherts, impure limestones, and dolomites in
Protracted periods of continental-scale deposition of cherts in shallow-water epeiric
seas of
Caballos Novaculite.--- McBride and Thomson (1970) provided a comprehensive review and summary of the various postulates regarding the origin of the Caballos Novaculite. They described five members of the Caballos from bottom to top as follows: (1) lower chert member, (2) lower novaculite member, (3) lower chert and shale member, (4) upper novaculite member, and (5) upper chert and shale member. They pointed out that the novaculite members are white and consist of nearly pure microquartz, similar to the Arkansas Novaculite, whereas the cherts and shales are variable in composition. They also noted that red shales in the chert members are the result of primary deposition of clay and unaltered iron oxide minerals. McBride and Thomson (1970) concluded that the Caballos is the product of biogenic precipitation, although they pointed out that it could not be demonstrated that more than 12 percent of the silica is the result of biotic processes.
Conclusions.---
In contrast to earlier postulates for the origin of the
With more accurate age control on the various novaculite members, it should be possible to relate chert-novaculite lithologies to long-term climate variations. For example, it appears that deposition of the lower member of the Arkansas Novaculite was contemporaneous with the Devonian cherts and quartzarenites in the Appalachian Basin and elsewhere across the craton, whereas deposition of the middle member of the Arkansas Novaculite (impure chert and shale) was coeval with a pluvial event in the Appalachian Basin that spans the Late Devonian-Early Mississippian transition (Cecil and others, 1998; Cecil and others, 2002). The upper member of the Arkansas Novaculite is contemporaneous with chert deposition on the craton and the major Osagean-Meramecian period of aridity.
The general associations of Paleozoic cherts and cherty limestones in North American strata that were deposited within or near warm-arid climates appear to be too numerous to be purely coincidental. Although volcanic ash, volcanic vents, and upwelling may contribute to the origin of some sedimentary chert, these processes do not satisfactorily reconcile either the predominant source of silica (volume required) or the stratigraphy of most bedded sedimentary cherts. In contrast, the temporal and spatial distribution of the vast majority of bedded sedimentary cherts appears to be readily explained by dissolution, reprecipitation, and diagenesis of eolian dust. The enigmas of silica supply, chemistry of silica dissolution, and abiotic precipitation of silica are resolved with an eolian source of silica, the metastable portions of which will dissolve and reprecipitate in accordance with the thermodynamic properties of amorphous silica and quartz. Furthermore, dust is a cogent source of dissolved silica and nutrients for the production of biogenic silica.
In addition to the temporal and spatial association of bedded cherts with warm-arid paleoclimate settings, the experimental data of Whalley et al (1987) indicate that dissolution of massive influxes of eolian dust results in silica saturation or even supersaturation of seawater as well as sediment pore waters. Furthermore, the dissolved silica concentrations reported by Whalley et al (1987) far exceed silica concentrations in normal seawater, silica in upwelling waters, and dissolved silica delivered to the world’s oceans by rivers, which rarely if ever exceeds the solubility of quartz. Quartzose dust, therefore, could have been the predominant source of silica for chert including biotic precipitates, abiotic precipitates of microquartz and fibrous silica, and residual fine-grained particles of α-quartz (megaquartz).
As with all the other inferred sources of silica in chert, the warm-arid dust hypothesis may be equally difficult to prove. For example, primary oxygen isotope signatures of quartz dust are likely to be obscured by the complexity of reactions involved in dissolution, reprecipitation, and diagenesis of silica in aqueous environments. In addition, diagenesis and chert formation are also likely to obliterate much of the physical evidence for silica provenance and for eolian transport. In contrast, however, diagenetic alteration and chert formation may account for the paucity of demonstrable deposits of dust currently documented in marine strata.
Although the distribution of chert throughout the geologic
record appears to be secular, individual occurrences probably recorded periodic
influxes of dust. The periodicity is
likely to be highly variable and range from relatively short-term, such as the
cyclicity of chert beds in the Cretaceous chalks of
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For questions about the scientific content of this report, contact C. Blaine Cecil.
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