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Saprolite
Saprolite
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This is a diagram and related photograph of soil layers from bedrock to soil.
A represents soil; B represents laterite, a regolith; C represents saprolite, a less-weathered regolith; beneath C is bedrock.

Saprolite is a chemically weathered rock. Saprolites form in the lower zones of soil profiles and represent deep weathering of the bedrock surface. In most outcrops, its color comes from ferric compounds. Deeply weathered profiles are widespread on the continental landmasses between latitudes 35°N and 35°S.

Conditions for the formation of deeply weathered regolith include a topographically moderate relief flat enough to prevent erosion and to allow leaching of the products of chemical weathering. A second condition is long periods of tectonic stability; tectonic activity and climate change can cause erosion. The third condition is humid tropical to temperate climate.

Poorly weathered saprolite grit aquifers are capable of producing groundwater, often suitable for livestock. Deep weathering causes the formation of many secondary and supergene ores: bauxite, iron ores, saprolitic gold, supergene copper, uranium, and heavy minerals in residual accumulations.[1]

Definition, description and locations

[edit]
Saprolite is less weathered than laterite; it is beneath the laterite layer.
Saprolite is not as weathered as laterite; there is a continuum from the upper layer of saprolite to laterite.

Saprolite (from Greek σαπρος (sapros) = putrid + λιθος (lithos) = rock) is a chemically weathered rock (literally, it means "rotten rock"). More intense weathering results in a continuous transition from saprolite to laterite.

Saprolites form in the lower zones of soil horizons[1] and represent deep weathering of the bedrock surface.[2] In lateritic regoliths – regoliths are the loose layer of rocks that rest on the bedrock – saprolite may be overlain by upper horizons of residual laterite; most of the original profile is preserved by residual soils or transported overburden.[1] Weathering formed thin kaolinitic [Al2Si2O5(OH)4] saprolites 1,000 to 500 million years ago; thick kaolinitic saprolites 200 to 66 million years ago; and medium-thick immature saprolites 5 million years ago in Sweden.[2] The general structure of kaolinite has silicate [Si2O5] sheets bonded to aluminium hydroxide [Al2(OH)4] layers.

Saprolite at Arranmore (Ireland). Transition from tectonized quartzite through saprolite to laterite. The weathered section is covered by glacial drift with scattered erratics, Holocene sandy soil and thin bog.

Iron compounds are the primary coloring agents in saprolites.[3] At most outcrops the color comes from ferric compounds; the color relates to the mineralogy and particle size.[3] Submicron-sized goethite [FeO(OH)] is yellow; coarse goethite is brown.[3] Sub-micron-sized hematite [Fe2O3] is red; coarse hematite is gray to black.[3]

Regoliths vary from a few meters to over 150 m (490 ft) thick, depending on the age of the land surface, tectonic activity, climate, climate history and the composition of the bedrock.[1] Although these deeply weathered terrains now occur in a wide variety of climates ranging from warm humid to arid, tropical to temperate, they were formed under similar conditions in the past.[1] In parts of Africa, India, South America, Australia and southeast Asia, regolith has been forming continuously for over 100 million years.[1] Deeply weathered regoliths are widespread in the inter-tropical belt, particularly on the continental landmasses between latitudes 35°N and 35°S.[1] Similar weathered regoliths exist at much higher latitudes – 35–42°S in southeast Australia (Victoria and Tasmania), 40–45°N in the United States (Oregon and Wisconsin) and 55°N in Europe (Northern Ireland, Germany) – although these are not regionally extensive.[1] In some localities it is possible to relatively date saprolite by considering that the saprolite must be younger than the parent material and older than any thick cover unit such a lava or sedimentary rock. This principle is useful in some contexts but in others, like certain parts of Sweden where grus is formed from Precambrian rocks and overlain by Quaternary deposits, it is of little value.[4]

Formation

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The regolith of a region is the product of its long weathering history; leaching and dispersion are dominant during the initial phase of weathering under humid conditions.[1] Saprolites form in high rainfall regions which result in chemical weathering and are characterised by distinct decomposition of the parent rock's mineralogy.[5] Conditions for the formation of deeply weathered regolith include a topographically moderate relief flat enough to allow leaching of the products of chemical weathering.[1] A second condition is long periods of tectonic stability; tectonic activity and climate change partially erode the regolith.[1] Weathering rates of 20 m (66 ft) per million years suggest that deep regoliths require several million years to develop.[1] The third condition is a humid tropical to temperate climate; higher temperatures enable reactions to occur more rapidly.[1] Deep weathering can occur in cooler climates but over longer periods.[1]

Sulfides are some of the most unstable minerals in humid, oxidizing environments; many cadmium, cobalt, copper, molybdenum, nickel and zinc sulfides are easily leached to deep in the profile.[1] Carbonates are highly soluble, especially in acidic environments; the elements hosted by them – calcium, magnesium, manganese and strontium – are strongly leached.[1] Serpentinite – oxidized and hydrolized low-silicon, iron- and magnesium-rich oxide igneous rocks – are progressively weathered through this zone.[1] Ferromagnesian minerals are the principal hosts for nickel, cobalt, copper, and zinc in sulfide-poor mafic and ultramafic rocks and are retained higher in the profile than sulfide-hosted metals.[1] They are leached from the upper horizons and reprecipitate with secondary iron-manganese oxides in the mid- to lower saprolite.[1]

Uses

[edit]

Aquifers in Western Australia are of saprolite grit.[6] Poorly weathered saprolite grit aquifers are capable of producing groundwater, often suitable for livestock.[6] Yields depend on the texture of the materials and their depth from which the aquifer is derived.[6]

The distributions of gold and calcium carbonate or calcium magnesium carbonates are closely correlated and documented in the southern Yilgarn craton, Western Australia, in the top 1 to 2 m (3.3 to 6.6 ft) of the soil profile and locally as deep as 5 m (16 ft).[1] The gold-carbonate association is also apparent in the Gawler craton, South Australia.[1] Supergene enrichment occurs near the surface and involves water circulation with its resulting oxidation and chemical weathering.[1] Deep weathering causes the formation of many secondary and supergene ores – bauxite, iron ores, saprolitic gold, supergene copper, uranium and heavy minerals in residual accumulations.[1]

See also

[edit]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Saprolite

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Saprolite is a residual, chemically product formed from the decomposition of primarily igneous or metamorphic , retaining the original texture and fabric of the parent rock while undergoing significant alteration. It develops through prolonged chemical processes, often in humid, temperate to tropical climates, where , oxidation, and hydration break down primary minerals into secondary clays and oxides without significant physical . Typically found underlying soils in profiles, saprolite transitions gradually from the above to unweathered below, with thicknesses ranging from a few meters on rocks to tens of meters on silicic ones. Saprolite is commonly divided into two zones based on degree of alteration: the upper massive zone, where relict features like or jointing from the are obliterated, resulting in a more homogeneous, friable material, and the lower structured zone, which preserves these structures. Its porosity increases toward the surface due to volumetric expansion from processes like and root wedging, often exceeding that produced by chemical mass loss alone, with surface porosities up to 0.65 decreasing to 0.35 at depth. correspondingly rises from about 0.96 g/cm³ near the top to 1.71 g/cm³ deeper, reflecting progressive compaction and retention of interlocking grains. The formation and weathering of saprolite play a critical role in landscape evolution, as its breakdown reduces bedrock coherence and enhances physical erosion rates, contributing substantially to overall denudation—often accounting for over 30% of mass loss in regolith-mantled terrains. exerts strong control, with optimal chemical occurring at intermediate elevations where moderate temperatures (9–12°C) and (660–920 mm/year) maximize reaction rates, while extremes limit activity. Ecologically and geotechnically significant, saprolite serves as a key for subsurface water storage, influences and , and poses challenges in due to variable strength and boulder remnants.

Definition and Properties

Definition

Saprolite is a chemically rock that forms through the intense of parent , resulting in a soft, friable material that retains the original rock's fabric and structure. Derived from the Greek words sapros (rotten) and lithos (stone), the term literally means "rotten rock," reflecting its altered, decayed state. This layer typically develops in the lower zones of profiles under humid, tropical, or subtropical conditions, where chemical processes dominate over physical disintegration. Unlike transported soils, saprolite remains in its original position atop unweathered , exhibiting a porous, clay-rich texture due to the and oxidation of primary minerals into secondary clays such as and halloysite. It is characterized by isovolumetric , where the volume of the material does not significantly change during , preserving relict structures like joints and from the parent rock. Saprolite can form from a variety of types, including igneous, metamorphic, and sedimentary rocks, though it is most commonly associated with granitic or compositions in tectonic settings. The distinction between saprolite and overlying horizons is marked by its transitional nature; while the upper layers may involve physical mixing and organic inputs, saprolite represents the C horizon or deeper where chemical alteration is profound yet the rock's identity is still discernible. This material plays a in landscape evolution, acting as a reservoir for and influencing in weathered terrains.

Physical and Chemical Properties

Saprolite exhibits distinct physical properties that reflect its formation through chemical , retaining the structural fabric of the parent while becoming significantly softer and more friable. It typically appears as a soft, earthy with a porous texture, often displaying relict features such as or from the original . Common colors include red, brown, yellow, or white, resulting from staining or leaching. Thickness can vary from a few meters to over 100 meters in deeply weathered profiles, with generally ranging from 1.0 to 1.95 g/cm³, lower than that of unweathered due to increased from dissolution and mineral alteration. Porosity is high, primarily consisting of interparticle voids, fractures, and channels, but saturated hydraulic conductivity is often low (0.6–98 cm/day), increasing with depth as fractures become more prominent. The texture of saprolite varies by parent rock type; for instance, granitic saprolites are coarser with sand-sized and fragments (52–91% , 1–25% clay), while those derived from are finer and clay-rich (>55% clay). Structurally, it lacks well-developed pedogenic features, appearing massive or crumbly, which contributes to high retention capacity (130–480 mm/m) but limited availability for plant uptake due to dominance of fine pores. Permeability decreases at the soil-saprolite interface, affecting transmission and pollutant , with filtering reducing in coarser materials. Chemically, saprolite is characterized by intense leaching of soluble components, leading to enrichment in insoluble elements such as , aluminum, , iron (as Fe³⁺), and , while bases like sodium, , calcium, and magnesium are depleted. The dominant is , often accompanied by , halloysite, or hydroxy-interlayered minerals in varying proportions depending on the parent ; for example, granitic saprolites may retain and , whereas mafic-derived ones show more pronounced iron and aluminum hydroxides. pH is typically acidic (4.1–5.0), reflecting and base cation loss, with low (typically <4–10 cmol/kg), limiting nutrient retention. These properties underscore saprolite's role as a chemically inert, alumina-silicate-rich zone in weathering profiles.

Formation Processes

Weathering Mechanisms

Saprolite forms primarily through in situ chemical weathering of bedrock, where minerals decompose without significant physical disruption or transport, preserving the original rock structure. This process is dominated by hydrolysis, oxidation, dissolution, and hydration, which progressively alter primary minerals into secondary clays and oxides. Hydrolysis involves the reaction of water and ions with silicate minerals, breaking Si-O bonds and forming hydrated silicates like kaolinite; for instance, feldspars such as plagioclase undergo hydrolysis to produce kaolinite and release soluble ions like sodium and calcium. Oxidation targets iron-bearing minerals, converting Fe(II) to Fe(III) and forming expansive iron oxides like goethite, which can induce fracturing in bedrock and facilitate further weathering; biotite oxidation, for example, expands its lattice spacing from 10.0 Å to 10.5 Å, initiating spheroidal weathering patterns with corestones. Dissolution removes soluble components, creating porosity and enabling deeper fluid penetration; quartz dissolves slowly at rates around 10^{-14.8} mol m^{-2} s^{-1} in saprolite, while more reactive minerals like plagioclase dissolve faster at 90 × 10^{-14} mol m^{-2} s^{-1}, leading to open-system conditions where ions are leached by percolating water acidified by carbonic acid from rainfall. Hydration adds water molecules to minerals, swelling them and promoting breakdown, particularly in mafic minerals like hornblende, which weathers to kaolinite and gibbsite at rates of 1.4 × 10^{-12} mol m^{-2} s^{-1}. These mechanisms often occur anisovolumetrically in saprolite, where chemical mass loss is balanced by secondary mineral precipitation, maintaining volume while increasing porosity up to 50% in granitic profiles. Climate modulates these processes, with warmer temperatures accelerating reaction kinetics per the Arrhenius equation and higher precipitation enhancing solute transport, resulting in chemical denudation rates of 53.5 ± 8.4 t km^{-2} y^{-1} in saprolite compared to 14.7 ± 2.5 t km^{-2} y^{-1} in overlying soils. In tropical settings like Puerto Rico's Luquillo Mountains, these combined mechanisms produce saprolite thicknesses exceeding 35 m at rates of 43–211 m per million years, transforming quartz diorite and volcaniclastic rocks into clay-rich regolith dominated by kaolinite (60–80 wt%). Physical processes, such as microcracking from mineral expansion, interplay with chemical ones to deepen the weathering front, but chemical alteration remains the primary driver of saprolite development.

Environmental Influences

The formation of saprolite is profoundly shaped by climatic conditions, particularly temperature and precipitation patterns, which drive chemical weathering rates. In humid tropical and subtropical environments, high temperatures (typically 15–25°C) and abundant rainfall (over 1000 mm annually) accelerate hydrolysis and dissolution of primary minerals, leading to thick saprolite profiles exceeding 10–20 meters in depth. For instance, in the Luquillo Mountains of Puerto Rico, rapid weathering under these conditions produces highly leached saprolite that isolates subsurface biogeochemical cycles from surface processes. Conversely, in cooler, drier climates such as high-elevation sites (e.g., 3000 m with 3–5°C mean temperatures and 1000 mm precipitation), weathering rates decline to about 25–40 t km⁻² y⁻¹, resulting in thinner saprolite layers due to reduced water availability and slower reaction kinetics. Topography exerts significant control over saprolite development through variations in drainage, slope stability, and water flux. On ridge tops and stable hillslopes with low gradients (around 10–15°), water percolates deeply, promoting isovolumetric weathering that preserves rock structure while increasing porosity, often yielding saprolite thicknesses of 10–15 m. In contrast, steep slopes or valley bottoms enhance physical erosion, limiting saprolite accumulation to less than 5 m by removing weathered material before full alteration occurs. Hillslope aspect further modulates this process; north-facing slopes in temperate mountains retain snowmelt longer, sustaining soil moisture levels up to 31 cm effective recharge over two years, which fosters deeper chemical weathering compared to south-facing slopes with only 13 cm recharge and intermittent drying. Biological activity, including vegetation and microbial processes, enhances saprolite formation by supplying organic acids and elevating carbon dioxide levels in soil pore water. Decaying plant matter and root respiration increase CO₂ concentrations, lowering pH and intensifying mineral dissolution, particularly of feldspars and ferromagnesian silicates, in the upper saprolite zones. In forested tropical settings, bioturbation from tree roots and soil fauna mixes regolith, doubling sediment transport rates (to 0.28 cm² y⁻¹) and exposing fresh surfaces to weathering agents. Microbial communities, such as iron-oxidizing bacteria, couple biological iron cycling with mineral alteration, accelerating biotite oxidation and porosity development in granitic saprolite. These effects are most pronounced in humid climates where dense vegetation cover (e.g., 96% in low-elevation oak grasslands) contrasts with sparse high-elevation communities, influencing weathering intensity by up to 50%.

Distribution and Occurrence

Global Patterns

Saprolite primarily forms and is preserved in tropical and subtropical regions characterized by high temperatures and abundant rainfall, which promote intense chemical weathering over long periods. These conditions are most prevalent in stable continental interiors, such as Precambrian shields and Phanerozoic basins, where tectonic stability allows for deep regolith development without significant erosion. Globally, extensive saprolite profiles are documented across Africa, South America, India, Southeast Asia, and Australia, often reaching depths of hundreds of meters in low-relief, slowly eroding landscapes. In these humid tropical environments, saprolite develops from a variety of parent rocks, including granites, basalts, and ultramafics, resulting in thick, in situ weathered layers that retain relict structures. Climatic patterns, including seasonal humidity and well-drained settings, control the thickness and mineralogy, with saprolite zones often underlying lateritic caps in profiles up to 100 meters deep. For instance, in equatorial belts within approximately 26° latitude, saprolite is integral to Ni-Co laterite deposits, reflecting the interplay of warm, wet climates and ultramafic protoliths. Occurrences diminish in arid, high-latitude, or tectonically active zones, where physical weathering or rapid erosion limits preservation; remnants exist in buried forms in parts of Europe and North America, but these are exceptions rather than widespread patterns. Overall, saprolite's global distribution underscores the dominance of chemical weathering in humid tropics, covering significant portions of continental surfaces in stable cratons, though exact extents vary with local geology and paleoclimate history.

Regional Examples

Saprolite formations are particularly prominent in tropical and subtropical regions where intense chemical weathering has developed extensive laterite profiles over ultramafic and mafic rocks, leading to nickel-enriched deposits. These occurrences are often associated with stable cratons or shields that have experienced prolonged exposure to humid climates, resulting in deep weathering profiles up to tens of meters thick. In Africa, notable examples include the Nkamouna and Mada nickel laterite deposits in central Cameroon, where saprolite forms a significant layer within the weathering profile, typically 10-20 meters thick, overlying bedrock and underlying limonite zones. The saprolite here is dominated by nickeliferous serpentine and hydrous magnesium silicates, with average nickel grades of 0.8-1.2% and associated cobalt and manganese enrichment, making it economically viable for mixed sulfide production through hydrometallurgical processing. These deposits developed on peridotite intrusions within the Congo Craton, illustrating how tectonic stability facilitates deep saprolitization in equatorial Africa. In Australia, saprolite is widespread in the Yilgarn Craton, as exemplified by the Murrin Murrin deposit in Western Australia, one of the largest nickel-cobalt operations globally. The saprolite horizon, reaching thicknesses of 20-30 meters, hosts nickel in smectite and other clay minerals, with grades up to 2.5% Ni in high-grade zones. As of 2024, the deposit has Mineral Resources of 205 million tonnes at 1.00% Ni and 0.08% Co, processed via high-pressure acid leaching to recover metals from the hydrous silicate matrix. This region's ancient, low-relief landscapes have allowed continuous weathering since the Mesozoic, preserving thick saprolite blankets over komatiitic ultramafics. Brazil's Amazonian and central cratons feature prominent saprolite in the Niquelandia complex, Goiás state, where weathering of mafic-ultramafic intrusions has produced nickel-enriched saprolite up to 15-25 meters deep, characterized by vermiculite and serpentine derived from pyroxene alteration. Nickel concentrations average 1-1.5%, often with cobalt byproducts, supporting open-pit mining and ferronickel smelting; the profile's development is linked to Cenozoic humid conditions on the stable São Francisco Craton. In Southeast Asia, the Soroako deposit in Sulawesi, Indonesia, represents a classic hydrous silicate subtype, with saprolite layers 10-20 meters thick containing garnierite rims on serpentine relics, yielding nickel grades up to 2.67% and magnesium oxide contents of 16-35%. This occurrence, part of the Sula Spur microcontinent, benefits from the region's tropical monsoon climate, enabling rapid supergene enrichment; it has been exploited since the 1970s via selective mining of high-grade saprolite for nickel matte production. Similar profiles extend to the Philippines and New Caledonia, underscoring the arc-related ultramafic belts of the Southwest Pacific as prime saprolite terrains. In North America, saprolite remnants occur as exceptions in temperate regions, such as the Appalachian Piedmont in the southeastern United States, where profiles up to 30 meters thick have developed on granitic and metamorphic bedrock under humid subtropical conditions, often buried or eroded by Quaternary events. These non-economic examples highlight saprolite's preservation in stable, low-relief areas outside the tropics.

Uses and Significance

Economic Applications

Saprolite, as a deeply weathered residual rock, plays a crucial role in the extraction of from lateritic deposits, which constitute approximately 60% of the world's nickel resources and are the dominant source for future production. These deposits form through intense chemical weathering in tropical and subtropical environments, concentrating in the saprolite horizon, typically with grades ranging from 1.3% to 2.5% Ni. Mining operations target this layer for its relatively high nickel content compared to overlying limonite zones, enabling efficient open-pit extraction followed by processing methods such as pyrometallurgical smelting to produce ferronickel alloys used in stainless steel and battery production. Major producing regions include Indonesia, which accounted for over 50% of global nickel mine production in 2023 (approximately 54%) and about 58% in 2024, much of it from saprolite ores processed in high-pressure acid leaching (HPAL) or rotary kiln-electric furnace (RKEF) facilities, generating significant economic value through exports and downstream industries like electric vehicle batteries. In New Caledonia, saprolite comprised about 78% of nickel ore mined in 2020, supporting a vital export sector that contributes substantially to the local economy. The economic viability of saprolite mining is enhanced by its soft, friable nature, which reduces drilling and blasting costs compared to hard-rock sulfide ores, though challenges include high moisture content and variable grades requiring beneficiation. Saprolite-sourced nickel is important for industrial applications, particularly stainless steel production. However, saprolite nickel mining has raised environmental concerns, including significant deforestation and water pollution in major producing regions like , where operations have impacted over 100,000 hectares of forest as of 2023, prompting stricter regulations and moratoriums on new permits. Beyond nickel, saprolite hosts economic concentrations of , often as a byproduct in laterite profiles, with grades up to 0.1-0.2% Co, contributing to supplies for rechargeable batteries and superalloys. In bauxite mining contexts, saprolite underlies many deposits and, while typically siliceous and subeconomic for direct alumina extraction, serves as overburden or low-grade feed in some operations; for instance, in and , it forms part of the weathering sequence essential for identifying viable bauxite reserves exceeding 30% Al2O3. Saprolite's association with in lateritic profiles also supports artisanal and small-scale mining in West Africa and South America, where supergene enrichment in the saprolite zone yields recoverable placer-style deposits. In non-metallurgical applications, processed saprolite emerges as a low-cost raw material for refractory aggregates, substituting for scarce calcined clays in high-temperature industries like steelmaking furnaces. Studies on saprolite from Indian bauxite mines demonstrate that sintering at optimized temperatures yields granules with bulk densities of 1.8-2.2 g/cm³, porosities under 25%, and pyrometric cone equivalents (PCE) of 30-32 (refractoriness >1650°C), meeting standards for basic refractory bricks and reducing reliance on imported materials. This valorization of mining waste enhances economic sustainability in bauxite-producing regions by diverting subeconomic saprolite from disposal to value-added products.

Geological and Environmental Roles

Saprolite plays a pivotal role in geological processes by facilitating the transition from to through chemical , which influences evolution and dynamics. In eroding landscapes, saprolite formation involves both chemical mass loss and physical volumetric strain, often resulting in anisovolumetric where strain exceeds mass loss, particularly in granitic terrains. This process is controlled by factors such as and rates, with studies across global sites showing that over 98% of Earth's land surface supports such patterns, leading to increased and reduced coherence. Saprolite rates, averaging 53.5 t km⁻² y⁻¹, frequently surpass those in overlying , enhancing soil production rates from 31 to 136 t km⁻² y⁻¹ and correlating strongly with physical (r² = 0.65), thereby shaping hillslope morphology and in upland environments. Environmentally, saprolite occupies the deepest section of the Critical Zone, acting as a critical interface for hydrological and biogeochemical cycles. Its porous structure enables significant infiltration, retention, and , supporting perched water tables in dense basal layers and influencing in tropical and subtropical regions. As a nutrient reservoir, saprolite releases essential elements like and metals through alteration, fostering growth and while contributing to the silicate by consuming CO₂ during . Additionally, it aids in retention and gas flux regulation, impacting productivity and long-term environmental over geological timescales.

References

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  9. https://www.usgs.gov/publications/appalachian-piedmont-regolith-relations-saprolite-and-residual-soils-rock-type
  10. https://www.researchgate.net/publication/287485743_Physical_chemical_and_morphological_properties_of_some_regoliths_in_North_Carolina
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  14. https://website.whoi.edu/gfd/wp-content/uploads/sites/14/2018/10/Dixon_et_al_Geology_09_79144.pdf
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  18. https://pubs.usgs.gov/sir/2010/5070/h/pdf/SIR10-5070-H.pdf
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  22. https://www.sciencedirect.com/science/article/pii/S2096519225000114
  23. https://pubs.usgs.gov/myb/vol3/2023/myb3-2023-indonesia.pdf
  24. https://pubs.usgs.gov/periodicals/mcs2025/mcs2025-nickel.pdf
  25. https://pubs.usgs.gov/myb/vol3/2020-21/myb3-2020-21-new-caledonia.pdf
  26. https://pubs.usgs.gov/of/2011/1259/OF11-1259.pdf
  27. https://ieefa.org/resources/indonesias-nickel-boom-built-environmental-cost
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  29. https://www.sciencedirect.com/science/article/pii/S0169136824002798
  30. https://www.researchgate.net/publication/350910010_Converting_Saprolite_a_Low-Grade_Unutilized_Material_into_Refractory_Aggregates_A_Viable_Substitute_for_Calcined_Clay_in_the_Refractory_Industry
  31. https://www.researchgate.net/publication/332835543_19_A_process_for_development_of_refractory_aggregates_from_Saprolite
  32. https://www.sciencedirect.com/science/article/pii/B9780444635228000036
  33. https://doi.org/10.1073/pnas.1315667111
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