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G.B. Pasternack

Publications and source records attributed to G.B. Pasternack.

3 recordsLinked to original sources

The effects of wildfire on the sediment yield of a coastal California watershed

The occurrence of two wildfires separated by 31 yr in the chaparral-dominated Arroyo Seco watershed (293 km ) of California provides a unique opportunity to evaluate the effects of wildfire on suspended-sediment yield. Here, we compile discharge and suspended-sediment sampling data from before and after the fires and show that the effects of the postfire responses differed markedly. The 1977 Marble Cone wildfire was followed by an exceptionally wet winter, which resulted in concentrations and fluxes of both fine and coarse suspended sediment that were ˜35 times greater than average (sediment yield during the 1978 water year was 11,000 t/km 2 /yr). We suggest that the combined 1977–1978 fire and flood had a recurrence interval of greater than 1000 yr. In contrast, the 2008 Basin Complex wildfire was followed by a drier than normal year, and although suspended-sediment fluxes and concentrations were significantly elevated compared to those expected for unburned conditions, the sediment yield during the 2009 water year was less than 1% of the post–Marble Cone wildfire yield. After the first postfire winters, sediment concentrations and yield decreased with time toward prefire relationships and continued to have significant rainfall dependence. We hypothesize that the differences in sediment yield were related to precipitation-enhanced hillslope erosion processes, such as rilling and mass movements. The millennial-scale effects of wildfire on sediment yield were explored further using Monte Carlo simulations, and these analyses suggest that infrequent wildfires followed by floods increase long-term suspended-sediment fluxes markedly. Thus, we suggest that the current approach of estimating sediment yield from sediment rating curves and discharge data—without including periodic perturbations from wildfires—may grossly underestimate actual sediment yields.

California↗

The role of effective discharge in the ocean delivery of particulate organic carbon by small, mountainous river systems

Recent research has shown that small, mountainous river systems (SMRS) account for a significant fraction of the global flux of sediment and particulate organic carbon (POC) to the ocean. The enormous number of SMRS precludes intensive studies of the sort conducted on large systems, necessitating development of a conceptual framework that permits cross‐system comparison and scaling up. Herein, we introduce the geomorphic concept of effective discharge to the problem of source‐to‐sink POC transport. This idea recognizes that transport effectiveness is the product of discharge frequency and magnitude, wherein the latter is quantified as a power‐law relationship between discharge and load (the ‚rating curve’). An analytical solution for effective discharge ( Q e ) identifies two key variables: the standard deviation of the natural logarithm of discharge (Σ q ), and the rating exponent of constituent i ( b i ). Data from selected SMRS are used to show that for a given river Q e ‐POC , Q e ‐sediment, Q e for different POC constituents (e.g., POC fossil vs. POC modern ) differs in predictable ways, and Q e for a particular constituent can vary seasonally. When coupled with the idea that discharge peaks of small rivers may be coincident with specific oceanic conditions (e.g., large waves, wind from a certain direction) that determine dispersal and burial, these findings have potentially important implications for POC fate on continental margins. Future studies of POC transport in SMRS should exploit the conceptual framework provided herein and seek to identify how constituent‐specific effective discharges vary between rivers and respond to perturbations.

Limnology and Oceanography↗

Volcanic lake systematics II. Chemical constraints

A database of 373 lake water analyses from the published literature was compiled and used to explore the geochemical systematics of volcanic lakes. Binary correlations and principal component analysis indicate strong internal coherence among most chemical parameters. Compositional variations are influenced by the flux of magmatic volatiles and/or deep hydrothermal fluids. The chemistry of the fluid entering a lake may be dominated by a high-temperature volcanic gas component or by a lower-temperature fluid that has interacted extensively with volcanic rocks. Precipitation of minerals like gypsum and silica can strongly affect the concentrations of Ca and Si in some lakes. A much less concentrated geothermal input fluid provides the mineralized components of some more dilute lakes. Temporal variations in dilution and evaporation rates ultimately control absolute concentrations of dissolved constituents, but not conservative element ratios. Most volcanic lake waters, and presumably their deep hydrothermal fluid inputs, classify as immature acid fluids that have not equilibrated with common secondary silicates such as clays or zeolites. Many such fluids may have equilibrated with secondary minerals earlier in their history but were re-acidified by mixing with fresh volcanic fluids. We use the concept of 'degree of neutralization' as a new parameter to characterize these acid fluids. This leads to a classification of gas-dominated versus rock-dominated lake waters. A further classification is based on a cluster analysis and a hydrothermal speedometer concept which uses the degree of silica equilibration of a fluid during cooling and dilution to evaluate the rate of fluid equilibration in volcano-hydrothermal systems.

Book↗