This paper was presented at the International Workshop "Microorganisms - Water and Aquifers", organized by the Zuckerberg Institute For Water Research, J. Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, held on September 20-21, 2005 in the Sede Boqer Campus, Israel.
Introduction
Most studies designed to delineate the transport behavior of bacteria in drinking-water aquifers are performed in the laboratory. Flow-through column studies provide a greater degree of control and, consequently, are useful in providing detailed, mechanistic information about specific processes affecting the subsurface movement of bacteria. Also, columns can be designed to more nearly meet initial boundary conditions for bacterial transport models and avoid the release of potentially harmful bacteria into drinking water aquifers. However, many processes that govern transport of bacteria in drinking-water aquifers are operative on spatial- and temporal-scales not conducive to laboratory studies. In-situ injection and recovery tests involving bacterial surrogates can provide additional information about the potential for substantive advective migration of pathogenic bacteria in the vicinity of wells. Because of the time, expense, and technical difficulties involved in conducting natural-gradient bacterial transport studies in the field, in situ bacterial tests involving granular aquifers usually are conducted over relatively short travel distances, e.g., <30 m (e.g., harvey and garabedian, 1991; johnson et al., 2001; fuller et al., 2004).
It is often beneficial to combine laboratory experiments that allow better delineation of individual processes and model calibration with field studies that provide a framework in which the applicability of laboratory-derived results can be evaluated under natural conditions. In general, considerably more information can be derived from an iterative approach that combines both column- and small-scale field investigations. However, even a coupled, iterative approach using both column- and small-scale field studies may not account for the combined effects of the various controls that govern microbial transport on an environmentally relevant field scale. There are many factors in addition to the hydrological characteristics of the aquifer itself, which control the movement of bacteria in the vicinity of drinking-water wells. These biotic and abiotic factors include growth, predation by protists, possible parasitism by bacteriophages, motility, lyses under unfavorable conditions, changes in cell size and propensity for attachment to solid surfaces in response to alterations in nutrient conditions, spore formation in the case of some gram-positive species, reversible and irreversible attachment to solid surfaces, detachment from surfaces, and straining (Fig. 1). Many of these processes are inter-related through other factors, poorly understood, and (or) difficult to describe mathematically.
Figure 1. Factors that affect the subsurface transport of bacteria in the vicinity of drinking-water wells.
Results and Discusion
Column-scale studies
Laboratory-scale studies have resulted in useful and detailed information on a number of processes governing bacterial transport behavior in granular media (Harvey and Harms, 2001). For example, it has been demonstrated that bacterial attachment/transport studies involving core material from the aquifer can allow differentiation between physical and chemical controls (Dong et al., 2002). However, in general, even when subsurface core material is employed results of flow-through, bench-scale studies are generally difficult to extrapolate to the field-scale. There are several reasons for this. The unavoidable alteration of the secondary pore structure caused by repacking, handling, and (or) shipping of the core material typically diminishes bacterial transport (Smith et al., 1985; Harvey et al., 1993). Although generally negligible at the column-scale (Unice and Logan, 2000), hydrodynamic dispersion is quite large (e.g., meters) in field-scale transport studies (Leblanc et al., 1991). Finally, the elevated flow velocities typically used in flow-through columns relative to most granular aquifers can affect the degree of bacterial immobilization (Hendry et al., 1997; Camesano and Logan, 1998).
Field studies
Small-scale injection and recovery studies in which labeled, non-pathogenic bacterial populations are added to and tracked downgradient in an aquifer have yielded valuable site-specific information about the role of local-scale physical heterogeneities (Mailloux et al., 2003), aquifer removal characteristics for pathogens (Schijven et al., 2000), and in-situ bacterial growth (Mailloux and Fuller, 2003). However, small-scale injection and recovery tests have not elucidated the effect of groundwater protists, which can be abundant and very active in drinking water aquifers (Kinner et al., 1998, 2002), upon the fate of bacterial pathogens. Many drinking water aquifers are limited with respect to readily-degraded organic carbon and very little information is available regarding the environmental carrying capacity of these systems. Evidence collected from large-scale surveys (Harvey and Barber, 1992) and from recent down-well incubations in a sole-source aquifer in Cape Cod, Massachusetts suggests that the downgradient abundances of bacteria intentionally or unintentionally introduced to certain groundwater environments may, at least for bacteria capable of in situ growth, be determined more by a site-specific “carrying capacity” than by predation and (or) sorptive losses (Harvey et al., in preparation). The abundance of bacteria at substantive distances downgradient in such systems would be difficult to predict a priori from any existing transport models. This has important implications for transport of certain pathogens in drinking water aquifers and for the practices of aquifer storage and recover and riverbank filtration.
References
- Camesano T.A. and Logan B.E. (1998). Influence of fluid velocity and cell concentration on the transport of motile and non-motile bacteria in porous media. Environ. Sci. Technol., 32(11), 1699-1708.
- Dong H., Onstott T.C., Deflaun M.F., Fuller M.E., Scheibe T.D., Streger S.H., Rothmel R.K. and Mailloux B.J. (2002). Relative dominance of physical versus chemical effects on the transport of adhesion-deficient bacteria in intact cores from South Oyster, Virginia. Environ. Sci. Technol., 36(5), 891-900.
- Fuller M.E., Mailloux B.J., Streger S.H., Hall J.A., Zhang P., Kovacik W.P., Vainberg S., Johnson W.P., Onstott T.C. and DeFlaun M.F. (2004). Application of a vital fluorescent staining method for simultaneous, near-real-time concentration monitoring of two bacterial strains in an Atlantic coastal plain aquifer in Oyster, Virginia. Appl. Environ. Microbiol., 70(3), 1680-1687.
- Harvey R.W. and Barber L.B. (1992). Associations of free-living bacteria and dissolved organic compounds in a plume of contaminated groundwater. J. Contam. Hydrol., 9(1-2), 91-103.
- Harvey R.W. and Garabedian S.P. (1991). Use of colloid filtration theory in modeling movement of bacteria through a contaminated sandy aquifer. Environ. Sci. Technol., 25(1), 178-185.
- Harvey R.W., Gruden C.L., Aiken G., Kinner N.E., Metge D.W. and Lisle J.T. (in preparation). DOM-determined “carrying capacity” for unattached subsurface bacterial populations: Implications for biodegradation and bacterial transport in carbon-limited groundwater environments. Water Resour. Res.
- Harvey R.W. and Harms H. (2001). Transport of microorganisms in the terrestrial subsurface: in-situ and laboratory methods. In: Manual of Environmental Microbiology, 2nd edn., C.J. Hurst, M.J. McInerney, L.D. Stetzenbach and R.L. Crawford (eds.), ASM Press, Washington, DC, pp. 753-776.
- Harvey R.W., Kinner N.E., Macdonald D., Metge D.W. and Bunn A. (1993). Role of physical heterogeneity in the interpretation of small- scale laboratory and field observations of bacteria, microbial-sized microsphere, and bromide transport through aquifer sediments. Water Resour. Res., 29(8), 2713-2721.
- Hendry M.J., Lawrence J.R. and Maloszewski P. (1997). The role of sorption in the transport of Klebsiella oxytoca through saturated silica sand. Ground Water 35(4), 574-584.
- Johnson W.P., Zhang P., Fuller M.E., Scheibe T.D., Mailloux B.J., Onstott T.C., Deflaun M.F., Hubbard S.S., Radtke J., Kovacik W.P. and Holben W. (2001). Ferrographic tracking of bacterial transport in the field at the narrow channel focus area, Oyster, VA. Environ. Sci. Technol., 35(1), 182-91.
- Kinner N.E., Harvey R.W., Blakeslee K., Novarino G. and Meeker L.D. (1998). Size-selective predation on groundwater bacteria by nanoflagellates in an organic-contaminated aquifer. Appl. Environ. Microbiol., 64(2), 618-625.
- Kinner N.E., Harvey R.W., Shay D.M., Metge D.W. and Warren A. (2002). Field evidence for a protistan role in an organically-contaminated aquifer. Environ. Sci. Technol., 36(20), 4312-8.
- Leblanc D.R., Garabedian S.P., Hess K.M., Gelhar L.W., Quadri R.D., Stollenwerk K.G. and Wood W.W. (1991). Large-scale natural gradient tracer test in sand and gravel, cape-cod, massachusetts.1. Experimental-design and observed tracer movement. Water Resour. Res., 27(5), 895-910.
- Mailloux B.J. and Fuller M.E. (2003). Determination of in situ bacterial growth rates in aquifers and aquifer sediments. Appl. Environ. Microbiol., 69(7), 3798-3808.
- Mailloux B.J., Fuller M.E., Onstott T.C., Hall J., Dong H., Deflaun M.F., Streger S.H., Rothmel R.K., Green M., Swift D.J.P. and Radke J. (2003). The role of physical, chemical, and microbial heterogeneity on the field-scale transport and attachment of bacteria. Water Resour. Res., 39(6), 1142-1158.
- Schijven J.F., Medema G., Vogelaar A.J. and Hassanizadeh S.M. (2000). Removal of microorganisms by deep well injection. J. Contam. Hydrol., 44, 301-327.
- Smith M.S., Thomas G.W., White R.E. and Ritonga D. (1985). Transport of Escherichia coli through intact and disturbed soil columns. Journal of Environmental Quality, 14(1), 87-91.
- Unice K.M. and Logan B.E. (2000). Insignificant role of hydrodynamic dispersion on bacterial transport. J. Environ. Eng.-ASCE, 126(6), 491-500.
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