Sediment
contaminant concentrations have been measured at most of the RMP
sites since 1991. Samples were collected by the Bay
Protection and Toxic Clean-up Program (BPTCP) Pilot Studies
in 19911992 (Flegal et al., 1994) and by the RMP since 1993.
Combining data from those two programs provides a time-series of
12 sampling periods over 7 years. Averages and ranges of concentrations
for trace elements and trace organics, over time, are shown for
each Estuary reach (Figures 4.17a,
b, c,
d, e,
f, g,
h, i,
& j and 4.18a,
b, c,
d, & e).
Except
for the Rivers, plots for the various Estuary reaches include only
muddy sediment samples (<60% sand). At the River stations, one
or both stations had coarse sediments in each sampling period. A
separate plot is presented showing trends for all samples with coarse
(>60% sand) sediments, including the Rivers when sandy.
For
the trace elements, chromium concentrations
appear to have increased in most reaches (except South Bay) between
1991 and 1997, and nickel appears
to have increased in the northern Estuary (Figure 4.17). Although
silver in the Northern Estuary,
South Bay, and Central Bay was higher in 1991 and 1992 than in subsequent
years, only concentrations in the South Bay appear to have continuously
decreased. There were no obvious seasonal (wet, dry) patterns in
any of the trace element trends. However, the January 1997 floods
noticeably changed concentrations of some trace elements measured
the following month. Cadmium,
mercury, nickel,
and zinc were obviously elevated
in some South Bay samples as evidenced by the large range bars.
Conversely, arsenic appeared to
decrease in the South Bay, and in the Central Bay and Northern Estuary
as well. Similarly, copper and
mercury were elevated in the River
samples. Aside from occasional "spikes" in lead
and selenium concentrations, those
two elements showed no obvious trends or influence of the 1997 floods.
However, both trace elements exhibited elevated concentrations at
the San Joaquin River station (BG30) in February (Figures
4.5 and 4.8).
For
the trace organic contaminants, total
DDTs in the Northern Estuary appear to have increased since
1991, but total PCBs, total
chlordanes, and dieldrin in
the Rivers appear to have decreased (Figure 4.18). PCBs in the Central
Bay and dieldrins in the South and Central bays have also decreased
in concentration. Total PAHs at
the Rivers and other reaches are often higher in concentration in
the wet-sampling period than in the dry-sampling period, but there
was no other obvious seasonal pattern in the trace organic contaminants.
As with some of the trace elements, the 1997 flood apparently caused
increases in some trace organic contaminants. The most obvious increases
were in total PAHs and total DDTs at the River stations. Total chlordanes
and total DDTs also increased at the South Bay sites in February,
1997.
In
considering the trends in these plots, it is important to recognize
that concentrations may be influenced by physical sediment factors
as well as proximity to sources. In general, sediments with more
silt and clay (percent fines) and higher total organic carbon (TOC)
have higher concentrations than sediments with more sand and low
TOC. Therefore, some of the variation represented in the plots could
be attributable to spatial and temporal variations in sediment type
rather than in changes in concentrations per se. Additionally, rigorous
time-series analysis generally requires more than the 10 to 12 samples
available. Further study of the relationships between concentrations
and other sediment factors, and over time, are good candidates for
future RMP Special Studies.
Plots
of Sediment Trends
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Plots
of average trace element concentrations in sediments for
each Estuary reach, 1991-1997:
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Plots
of average trace organic concentrations in sediments for
each Estuary reach, 1991-1997:
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