Researchers: Thomas Harter, Rob Atwill
Recently, several large
waterborne outbreaks of human cryptosporidiosis
have raised concern about the occurrence of the
protozoal pathogen, Cryptosporidium parvum,
in drinking water. C. parvum has also
been found in groundwater samples. In reaction
to widespread public attention, state and federal
health and environmental agencies have begun to
require increased monitoring of C. parvum
in drinking water systems. High levels of
C. parvum have been associated with
the occurrence of livestock and concentrated animal
facilities among others. Municipal and rural water
suppliers are becoming increasingly aware of potential
sources of C. parvum in their watersheds.
In recent decisions, they have begun to take measures
to control or even eliminate known potential sources
from entire watersheds. However, research and
knowledge on the fate of C. parvum in
the environment is widely lacking. In particular,
there is almost no systematic research regarding
the transport mechanisms of C. parvum
in soil and groundwater. Neither has there been
a systematic effort to provide evidence on whether
and where the organism is likely to occur in groundwater.
We have implemented bench-scale experiments
(see figure) to better understand the transport
properties of C. parvum and to provide
preliminary data for the development of a more
extensive research program.. Outside its mammal
host, C. parvum occurs in form of an
oocyst (see figure) that is approximately 5 µm
in diameter (5,000 oocysts need to be lined up
in a chain measuring 1 inch). The results indicate
that the transport behavior of the infectious
C. parvum oocyst is similar to that of
other colloids (colloids are small particles that
are larger than molecules but smaller than approximately
10 µm. Examples of colloids are clay particles,
protozoa, bacteria, and viruses). The experiments
were conducted with different sands (fine, medium,
and coarse sand) and at different water filtration
velocity (fast to immitate infiltration during
a rain, and slow to immitate water movement in
an aquifer). In the coarse sand (sand particles
with a diameter of approximately 1/12 of an inch),
approximately 70% of the oocysts passed through
the sand column (see figure), during rapid infiltration,
whereas only 10% passed through the column with
the slower groundwater velocity. The finer the
sand particles, the fewer oocysts passed through
the sand column. In the fine sand (sand particles
with a diameter of approximately 1/100 of an inch)
less than one percent passed through the column
with the rapid infiltration velocity. The remainder
of the oocysts were filtrated and sorbed within
the sand column. We made several interesting observations
that we will be looking at closer: in the coarse
sand, the oocysts travelled approximately 20%
faster than the average water molecule, because
their tortuous travel path through the sand column
is restricted to the coarsest pores where the
water travels faster. This phenomenon is referred
to as "velocity enhancement" and is well-known
in colloid science. standard colloid filtration
theory with a "sticking coefficient" of 1 predicts
the breakthrough concentrations of oocysts within
an order of magnitude. in contrast to predictions
by the colloid filtration model, we observed low,
but measurable concentrations of oocysts long
after we had begun flushing the column with uncontaminated
water. In the fine sand, oocyst concentrations
at levels near the initial peak persisted for
over 100 pore volumes of column flushing indicating
a slow release of oocysts trapped in the fine
sand.
Table 1: Average relative velocity enhancement
and mass retained in the soil column for each
experiment. The relative total recovery is the
sum % mass eluted (equal to the relative steady-state
concentration at the bottom of the column) and
the % mass retained. The sticking coefficient,
, is computed after determining all other parameters
independently. CS: coarse sand, MS: medium sand,
FS: fine sand. ()* indicates questionable value
due to experimental difficulties.
| Experiment |
CS fast |
CS slow |
MS fast |
MS slow |
FS fast |
| velocity enhancement
[%] |
16 |
27 |
8 |
10 |
0 |
| mass retained [%] |
15 |
40 |
92 |
74 |
40 |
| % total recovery |
84 |
50 |
93 |
74 |
41 |
| sticking coefficient,
|
4.8 |
2.6 |
(6.6)* |
1.8 |
0.8 |
Also see:
Harter, T., S. Wagner, E. R. Atwill, Colloid transport
and filtration of Cryptosporidium parvum in
sandy soils and aquifer sediments, Env. Science
and Technology, 34(1), 62-70, 2000. (pdf file
and
supplement
for personal use only).
Atwill, E. R., L. Hou, B. M. Karle, T. Harter,
K. W. Tate, R. A. Dahlgren. Transport of Cryptosporidium
parvum oocysts through vegetated buffer strips
and estimated filtration efficiency, Applied
and Environmental Microbiology 68(11),
pp. 5517-5527, 2002.(pdf
file for personal use only).
Searcy, K. E., A. Packman, E. R. Atwill,
and T. Harter, 2005. Association of Cryptosporidium
parvum with Suspended Particles: Impact on Oocyst
Sedimentation, Applied
and Environmental Microbiology 71(2):1072-1078.(pdf
file for personal use only).
Discussion
of C. parvum removal in bank filtration
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