Fate of nutrients in shallow groundwater receiving treated septage, Malibu, CA.

Ground Water

Water Resources, U.S. Geological Survey, 4165 Spruance Road, Suite 200, San Diego, CA 92101; (619) 225-6131; fax: (619) 225-6101.

Published: September 2014

AI Article Synopsis

  • Treated wastewater from over 400 onsite systems in Malibu contributes significantly, 28%, to a local alluvial aquifer's recharge, with some samples showing more than 70% wastewater presence.
  • Nitrogen levels in groundwater samples varied, indicating substantial removal through two main processes: ammonium sorption in reducing conditions and nitrification followed by denitrification in oxic conditions, with varying dominance based on seasonal temperature changes.
  • Phosphate removal was less effective, largely dependent on pH, with more significant sorption occurring at near-neutral pH levels, while higher pH levels showed minimal phosphate removal.

Article Abstract

Treated wastewater discharged from more than 400 onsite wastewater treatment systems (OWTS) near the Civic Center area of Malibu, California, 40 km west of downtown Los Angeles, composes 28% of the recharge to a 3.4 km(2) alluvial aquifer. On the basis of δ(18) O and δD data, the fraction of wastewater in some samples was >70%. Ammonium and nitrate concentrations in water from 15 water-table wells sampled in July 2009 and April 2010 ranged from <0.01 to 12 milligrams per liter as nitrogen (mg/L as N), and from <0.01 to 11 mg/L as N, respectively. Chemical and isotopic data (δ(15) N of ammonium and nitrate, and δ(18) O of nitrate) show two processes remove nitrogen discharged from OWTS. Where groundwater was reducing, sorption of ammonium resulted in 30 to 50% nitrogen removal. Where groundwater was initially oxic, nitrification with subsequent denitrification as reducing conditions developed, resulted in up to 60% nitrogen removal. Nitrogen removal through sorption dominated during the cooler April sample period, and denitrification dominated during the warmer July sample period. The combination of mixing and nitrogen removal due to denitrification, sorption, and volatilization produces a δ(15) N apparent fractionation factor (εapp = -5), that can be explained using laboratory-derived fractionation factors (ε) for the individual processes. Phosphate concentrations ranged from < 0.04 to 2 mg/L as phosphorous. Sorption to iron oxides on the surfaces of mineral grains at near-neutral pH's removed some phosphate; however, little removal occurred at more alkaline pH's (>7.3).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265202PMC
http://dx.doi.org/10.1111/gwat.12194DOI Listing

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