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USGS2010

Phosphorus and iron cycling in deep saprolite, Luquillo Mountains, Puerto Rico

Rapid weathering and erosion rates in mountainous tropical watersheds lead to highly variable soil and saprolite thicknesses which in turn impact nutrient fluxes and biological populations. In the Luquillo Mountains of Puerto Rico, a 5-m thick saprolite contains high microorganism densities at the surface and at depth overlying bedrock. We test the hypotheses that the organisms at depth are limited by the availability of two nutrients, P and Fe. Many tropical soils are P-limited, rather than N-limited, and dissolution of apatite is the dominant source of P. We document patterns of apatite weathering and of bioavailable Fe derived from the weathering of primary minerals hornblende and biotite in cores augered to 7.5 m on a ridgetop as compared to spheroidally weathering bedrock sampled in a nearby roadcut. Iron isotopic compositions of 0.5 N HCl extracts of soil and saprolite range from about δ 56 Fe = 0 to − 0.1‰ throughout the saprolite except at the surface and at 5 m depth where δ 56 Fe = − 0.26 to − 0.64‰. The enrichment of light isotopes in HCl-extractable Fe in the soil and at the saprolite–bedrock interface is consistent with active Fe cycling and consistent with the locations of high cell densities and Fe(II)-oxidizing bacteria, identified previously. To evaluate the potential P-limitation of Fe-cycling bacteria in the profile, solid-state concentrations of P were measured as a function of depth in the soil, saprolite, and weathering bedrock. Weathering apatite crystals were examined in thin sections and an apatite dissolution rate of 6.8 × 10 − 14 mol m − 2 s − 1 was calculated. While surface communities depend on recycled nutrients and atmospheric inputs, deep communities survive primarily on nutrients released by the weathering bedrock and thus are tightly coupled to processes related to saprolite formation including mineral weathering. While low available P may limit microbial activity within the middle saprolite, fluxes of P from apatite weathering should be sufficient to support robust growth of microorganisms in the deep saprolite.

Puerto Rico↗

USGS1996

Appalachian piedmont regolith: Relations of saprolite and residual soils to rock-type

Saprolite is a major product of rock weathering on the Appalachian Piedmont from New Jersey to Alabama. On the Piedmont, it is the primary substrate from which residual soils are developed. Properties of saprolite and residual soils are highly related to their parent rocks. Studies of cores and outcrops illustrate that rock structure and mineralogy control upland regolith zonation. Saprolite develops by in situ chemical alteration of a wide variety of mafic to highly silicic rocks. Thickness of upland saprolite varies from a few meters on mafic rocks to tens of meters on silicic rocks. Saprolite thickness decreases with increasing slope and saprolite is generally thin or absent in valley bottoms. Massive residual subsoils and soils develop by physical and chemical processes that alter the upper few meters of saprolite. The fabric, texture and mineralogy of residual soils are distinctly different from underlying saprolite. The boundary between soil and saprolite is often gradual, and often a zone of low permeability. Geologic maps are useful guides to Piedmont regolith thickness and zonation. In regional design studies, geologic maps and regolith characteristics can be useful in environmental decision-making.

Geotechnical Special Publication↗

USGS1990

Landslide processes in saprolitic soils of a tropical rain forest, Puerto Rico

Shallow soil slips, earth and debris slides appear to be a primary mechanism of hillslope denudation in the rainforest of eastern Puerto Rico. Annual rainfall in excess of 4,000 mm, and thick sequences (up to 20 m) of residual soils (saprolite) combine to produce these landslides. Shear strength testing and observatons of tension cracks indicate that landslides may start as tensile failure of saprolitic material. The tension cracks provide avenues for rapid infiltration of rainwater and saturation of the underlying soil. During or shortly after intense or prolonged precipitation, shear failure then occurs as a result of pore-pressure buildup along zones of low permeability within the saprolite. Tensile stresses in the unsaturated, low-density upper saprolite zone range from 3 to 10 kPa, and mean seismic refraction velocities are 476 +/- 127 m/s. Denser, clay-rich, less permeable saprolitic zones having mean seismic velocities of 1420 +/- 157 m/s represent zones that are commonly associated with perched ground water and are zones where exess pore-water pressure is most likely to trigger movement. These zones of translocated clay show marked density increases. Slickensides are present in the saprolite along relict fractures and joints derived from the parent rock; they are common in quartz-diorite bedrock, and less so in marine-deposited volcaniclastic bedrock. The failure planes of many landslides have exposed these relict fractures and joints as slickensides, and landslides appear to move on these pre-existing planes of weakness in the saprolite. The larges landslides (areas greater than 20,000 m 2 , however, are those that fail along saprolite-bedrock boundaries, which are zones of contrasting density and permeability within or at the base of the weathered profile.

Conference Paper↗

USGS2011

Vadose zone controls on weathering intensity and depth: Observations from grussic saprolites

An investigation of vadose zone weathering processes has been undertaken on grussic saprolites developed on Californian granitoids. Preliminary results indicate strong climatic control, through infiltration, on the depth and intensity of weathering. At sites with higher infiltration, the vadose zone is comprehensively altered to grussic saprolite and saprock. Conversely, lower infiltration sites display only thin grussic saprolites, strongly influenced by rock texture. Both vadose zone and weathering depth appear to be governed by local base level, and vadose zone hydrology exerts a fundamental control on the effective operation and relative dominance of the key weathering reactions. In zones of matrix permeability, oxidation of biotite comprehensively disaggregates the rock but results in little mass loss and clay mineral formation. Conversely, the higher transient flow rates that characterize zones of fracture permeability result in plagioclase hydrolysis, significant mass losses and accompanying clay mineral formation. A variable hydrological regime may also contribute to high partial pressures of O 2 in vadose zone pore waters and pore spaces, thereby enhancing the oxidative environment and further predisposing grussic saprolite formation.

Applied Geochemistry↗

USGS1996

Porosity factors that control the hydraulic conductivity of soil-saprolite transitional zones

Slowly permeable transitional horizons separate soil and saprolite, but these horizons cannot be identified easily in the field. The objectives of this study were to determine why the soil-saprolite transitional zone (BC and CB horizons) is slowly permeable, and to evaluate ways for identifying it in the field. Two saprolite deposits were studied in the North Carolina Piedmont. At each site, saturated and unsaturated hydraulic conductivities ( K sat and K unsat ) were measured for major horizons. Volume fractions of water-conducting pores were also compared with the changes in hydraulic conductivity with depth. Horizon mean K sat values at both sites ranged from virtually 0 to approximately 3 cm h -1 . The lowest K sat values (<0.3 cm h -1 ) occurred in or near the transitional horizons that were directly below the Bt horizons. Changes in the volume of pores within or between mineral grains (termed inter/intraparticle pores ) with depth corresponded to changes in both K sat and K unsat . In the transitional horizons, the inter/intraparticle pores were plugged with clay and this caused the horizons to have low K values. In situ measurements of K sat with depth were the most accurate technique to use for identifying transitional zones in the field. Examination of both the soil and rock structures in pits was also an acceptable technique. Texture and consistence were not considered reliable for pin-pointing transitional horizons.

North Carolina↗

USGS2002

Determining mineral weathering rates based on solid and solute weathering gradients and velocities: Application to biotite weathering in saprolites

Chemical weathering gradients are defined by the changes in the measured elemental concentrations in solids and pore waters with depth in soils and regoliths. An increase in the mineral weathering rate increases the change in these concentrations with depth while increases in the weathering velocity decrease the change. The solid-state weathering velocity is the rate at which the weathering front propagates through the regolith and the solute weathering velocity is equivalent to the rate of pore water infiltration. These relationships provide a unifying approach to calculating both solid and solute weathering rates from the respective ratios of the weathering velocities and gradients. Contemporary weathering rates based on solute residence times can be directly compared to long-term past weathering based on changes in regolith composition. Both rates incorporate identical parameters describing mineral abundance, stoichiometry, and surface area. Weathering gradients were used to calculate biotite weathering rates in saprolitic regoliths in the Piedmont of Northern Georgia, USA and in Luquillo Mountains of Puerto Rico. Solid-state weathering gradients for Mg and K at Panola produced reaction rates of 3 to 6 x 10-17 mol m-2 s-1 for biotite. Faster weathering rates of 1.8 to 3.6 ?? 10-16 mol m-2 s-1 are calculated based on Mg and K pore water gradients in the Rio Icacos regolith. The relative rates are in agreement with a warmer and wetter tropical climate in Puerto Rico. Both natural rates are three to six orders of magnitude slower than reported experimental rates of biotite weathering. ?? 2002 Elsevier Science B.V. All rights reserved.

Chemical Geology↗

USGS2010

Inferring shallow groundwater flow in saprolite and fractured rock using environmental tracers

The Ridge and Valley Province of eastern Tennessee is characterized by (1) substantial topographic relief, (2) folded and highly fractured rocks of various lithologies that have low primary permeability and porosity, and (3) a shallow residuum of medium permeability and high total porosity. Conceptual models of shallow groundwater flow and solute transport in this system have been developed but are difficult to evaluate using physical characterization or short‐term tracer methods due to extreme spatial variability in hydraulic properties. In this paper we describe how chlorofluorocarbon 12, 3 H, and 3 He were used to infer groundwater flow and solute transport in saprolite and fractured rock near Oak Ridge, Tennessee. In the shallow residuum, fracture spacings are <0.05 m, suggesting that concentrations of these tracers in fractures and in the matrix have time to diffusionally equilibrate. The relatively smooth nature of tracer concentrations with depth in the residuum is consistent with this model and quantitatively suggests recharge fluxes of 0.2 to 0.4 m yr −1 . In contrast, groundwater flow within the unweathered rock appears to be controlled by fractures with spacings of the order of 2 to 5 m, and diffusional equilibration of fractures and matrix has not occurred. For this reason, vertical fluid fluxes in the unweathered rock cannot be estimated from the tracer data.

Water Resources Research↗

USGS1959

Recent saprolite

Thick saprolite has formed in northern New Jersey since the last Pleistocene glacial stage.

New Jersey↗

USGS2024

Imogolite and allophane formed in saprolite of basalt on Maui, Hawaii

Inorganic gel and allophane collected from basaltic saprolite on Maul, Hawaii, and studied by Patterson in I964 were reexamined. The main constituent of the gel is imogolite, and gibbsite and allophane are the minor constituents. Electron and X-ray diffraction patterns, DTA curve, and an infrared spectrum of the gel are characteristic of imogolite. The allophane is virtually noncrystalline to X-rays but contains a small amount of imogolite in relatively short threads. High-resolution electron micrographs indicate differences in structural organization between allophane and imogolite and suggest crystallization of imogolite from allophane. The occurrence of imogolite as a weathering product has been reported in many localities from pyroclastic materials but not from massive rocks. Probably the exceptionally high rainfall, excellent subsurface permeability of the weathered material, and the low pH and high organic content of the leaching solution provide favorable conditions for formation of imogolite from basalt on Maul.

Hawaii↗

USGS2011

Halloysite nanotubes and bacteria at the saprolite-bedrock interface, Rio Icacos watershed, Puerto Rico

Quartz diorite bedrock underlying the Luquillo Mountains of eastern Puerto Rico undergoes weathering at one of the fastest documented rates for granitic rocks in the world. Although tropical temperatures and precipitation promote rapid weathering in this location, increased bacterial densities in the regolith immediately above the bedrock suggest that microorganisms contribute to mineral weathering as well. Deep saprolite and saprock samples were obtained at the bedrock interface in an upland location (Guaba Ridge) in the Rio Icacos watershed for examination by environmental scanning electron microscopy (ESEM). In ESEM images, mineral nanotubes were observed to occur frequently in association with coccus- and rod-shaped structures resembling bacteria. These nanotubes (50–140-nm width and 150–2700-nm length) were identified as halloysite using transmission electron microscopy. Observations of multiple nanotubes on the surfaces of an individual cell are consistent with the cell's exterior functional groups interacting with Si in pore water to facilitate halloysite nucleation. We propose that one mechanism by which bacteria contribute to the rapid weathering of quartz diorite minerals in this regolith is by lowering the free energy for secondary mineral formation. The presence of bacterial surfaces may result in more rapid removal of Si from solution, thereby increasing the dissolution rates of primary minerals.

Puerto Rico↗

USGS1975