Gersberg RoleOfAquaticPlantsInWetlands 1986
Gersberg RoleOfAquaticPlantsInWetlands 1986
Gersberg RoleOfAquaticPlantsInWetlands 1986
00
Printed in Great Britain. All rights reserved Copyright 0 1986 Pergamon Press Ltd
Abstract-This report describes investigations using artificial wetlands which quantitatively assess the role
of each of three higher aquatic plant types, Scirpus validus (bulrush), Phragmites communis (common reed)
and Typha lalifola (cattail), in the removal of nitrogen (via sequential nitrification-denitrification), BOD
and TSS from primary municipal wastewaters. During the period August 1983-December 1984, the mean
ammonia concentration of 24.7mgl-' in the primary wastewater inflow (hydraulic application
rate = 4.7 cm day-') was reduced to mean effluent levels of 1.4 mg 1-' for the bulrush bed, 5.3 mg1-I for
the reed bed and 17.7mg1-I for the cattail bed, as compared to a mean value of 22.1 mgl-I for the
unvegetated (control) bed. For all three vegetated beds, the mean effluent ammonia values were
significantly below that for the unvegetated bed and for the inflow. The bulrushes and reeds (in that order)
proved to be superior at removing ammonia, both with mean effluent levels significantly below that for
the cattail bed. The high ammonia-N (and total N) removal efficiencies shown by the bulrush and reed
beds are attributed to the ability of these plants to translocate 0, from the shoots to the roots. The oxidized
rhizosphere so formed stimulates sequential nitrification-denitrification. Similarly BOD removal
efficiencies were highest in the bulrush and reed beds, both with mean effluent BOD levels (5.3 and
22.2 mg I-', respectively) significantly below that for the unvegetated bed (36.4 mg I-') and equal to or
better than secondary treatment quality (30 mg I-'). Our results demonstrate that higher aquatic plants
can indeed play a significant role in secondary and advanced (N removal) wastewater treatment by wetland
systems, a role that is completely distinct from that associated with their pollutant uptake capacity.
Fig. 1. Photograph of the artificial wetlands site at the Santee Water Reclamation Facility. For scale, note
the person standing in foreground. Each wetland bed is 18.5 m long x 3.5 m wide. From left to right are
the unvegetated beds, the reeds, the cattails (directly to person's right) and the bulrushes (darkly shaded
vegetation).
Role of aquatic plants in wastewater treatment
45 7
Fig. 2. Level of ammonia-N in the inflow (0-0) and effluent of the vegetated and unvegetated beds,
at a primary wastewater application rate of 4.7 cm day-'. Inflow; unvegetated; 0 cattails; V reeds;
0 bulrushes.
2.0mgl-I), levels for any quarter never exceeded 0.7 mg I-' for all beds throughout the period of study.
0.6 mg 1-'. Mean (NO; + NO;)-N concentrations Even the rate of plant growth and associated nutrient
were 0.29 mgl-' for the inflow and 0.99, 0.05, 0.15 uptake could not account for the highly efficient N
and 0.09 mg I-' for bulrush, reed, cattail and un- removal we have observed. With a maximum annual
vegetated beds, respectively. Such low effluent harvestable yield of biomass in the range of 15-20 g
(NO; + NO;)-N levels in all the vegetated beds, dry ~ t m day-'
- ~ (Gersberg et al., 1983) and an N
indicate that nearly all the ammonia that was nitrified content of approx. 1% of the dry weight, then plant
in these wetlands must have subsequently been uptake could only account for about 13u-
denitrified, and lost from the system as gaseous N2 or 200 mgN m-2. This is only 12-16% of the overall
N,O. Indeed, Gersberg et al. (1983) have shown that removal of 1213 mg N m-2 day - ' we measured for
when sufficient dissolved carbon is present, these the bulrush bed which had primary wastewater
artificial wetlands are very efficient at promoting applied at the application rate of 4.7 cm day-'. This
denitrification, with removal efficiencies of greater estimate is also at the upper range of values reported
than 95% of the nitrate present in secondary waste- for the aboveground biomass nitrogen removal
waters at application rates of up to 40 cm day-'. potential of reeds, bulrushes and cattails (27-
Aside from sequential nitrification-denitrification, 190 mg N m-2 day-', Stephenson et al., 1980).
there appear to be no other mechanisms of nitrogen A comparison of ammonia removal efficiencies in
loss which could explain the efficient removal of the vegetated beds versus the unvegetated bed shows
ammonia shown in Fig. 2 for the bulrush and reed that the presence of the plants did indeed make: a
beds. Waters flowing through the wetlands have a pH difference (although not just via N-incorporation into
of near neutrality, and therefore significant losses of plant biomass). We measured 94% removal for the
ammonia by volatilization would not be expected. bulrushes, 78% for the reeds and 28% for the cattails,
Losses of nitrogen as particulate N (PN) were also as compared with only 11% for the unvegetated bed.
low, with mean effluent PN values of less than Clearly, sequential nitrification-denitrification was
Table 2. Mean concentrations of nitrate-N + nitrite-N in the inflow and effluent of the artificial
wetland beds (all values in m e I-')
Summer 1983 Fa11 1983 Winter 1984 Spring 1984 Summer 1984
(Aug.-Sept.) (0ct.-Dec.) (Jan.-March) (April-June) (JulyUct.)
Inflow* 0.02 0.02 0.93 0.16 0.14
Cattails 0.03 0.01 0.59 0.02 0.03
Reeds 0.0 0.01 0.10 0.10 0.04
Bulrushes - - 0.43 2.05 0.19
Unvegetated 0.01 0.04 0.29 0.03 0.03
'Primary wastewater, hydraulic application rate = 4.7 cm day-'.
366 R. M. GER~BERG
et al.
somehow impeded in the cattail bed as compared to cattail has the shallowest root zone, most of its root
the two other plant types. The same situation was biomass being confined to the top 30 cm of substrate.
true for the unvegetated bed which also lacked any N The root zone of the bulrushes and reeds on the other
uptake by the plants. It had a mean effluent ammonia hand, extended to > 60 cm and 76 cm, respectively.
value significantly different (P < 0.05) than that for Therefore oxidized conditions favoring nitrification
the primary wastewater inflow, but only slightly were probably more extensive in these beds. We also
lower (11%). found that after 2-3 months of operation using
The high nitrogen removal efficiencies shown by primary wastewater as sole source of inflow, the
the bulrush and reed beds may be explained by the cattails showed a marked yellowing, and most had
ability of many aquatic macrophytes to transport died after 6 months. We have repeatedly observed
oxygen down to the roots, thereby establishing an this toxic effect whenever primary wastewater (but
oxidized rhizosphere (Armstrong, 1964). Teal and not secondary wastewater) from the Santee Facility
Kanwisher (1966) and Howes et al. (1981) showed was applied to the cattails. Since the Santee Water
that Spartina was able to oxidize the sediment in the Reclamation Facility receives little industrial waste,
rhizosphere and that the redox potential was higher the concentration of toxic heavy metals and organic
in the root zone of the grass than in unvegetated chemicals in the wastewater is very low. The presence
sediments. Sherr and Payne (1979) found that the of high levels (25mgl-') of ammonia-N in the
presence of aquatic plants (Spartina) enhanced the primary but not the secondary wastewater may ex-
formation of oxides of nitrogen in the rhizosphere. plain the toxic effect we observed (Haynes and Goh,
Iizumi et al. (1980) showed that oxygen released by 1978). Jackson and Gould (1981) using Typha sp.
ther roots of the eelgrass (Zostera) sustained a sedi- grown in a synthetic wastewater containing 33 mg I-'
ment nitrification rate of the same order of magnitude of ammonia-N also reported growth inhibition of
as the denitrification rate. Similarly, Hansen and cattail plants and found that when the wastewater
Andersen (1981) showed that the potential nitrifi- strength was reduced by dilution their growth was
cation rate in sediments from a Phragmites (reed) much improved. The bulrushes and reeds remained
swamp was three times higher than for sediments very healthy throughout our study, and indeed have
without plants from deeper waters. All this evidence been shown to grow well even when supplemented
supports the hypothesis that nitrifying bacteria can with raw wastewater in other studies (Seidel, 1976;
be directly stimulated by the oxidizing abilities of the Small, 1976).
rhizome. Our data are entirely consistent with this The BOD removal efficiencies for the vegetated and
hypothesis. unvegetated beds for the period from August 1983 to
Of the three plant types that we tested, the cattail October 1984 are presented in Fig. 3. The treatment
was the poorest performer with regard to ammonia afforded by the bulrush was superior to the other
removal. This may be attributed to the fact that the plant types, with a mean effluent BOD concentration
A S O N D J F M A M J J A S O N
1983 1984
Fig. 3. Level of BOD, (biochemicaloxygen demand) in the inflow (0-e) and effluent of the vegetated
and unvegetated beds, at a primary wastewater application rate of 4.7cm day-'. Inflow;
unvegetated; 0 cattails; C7 reeds; 0 bulrushes.
Role of aquatic plants in wastewater treatment 367
of 5.3 + 5.2 mg 1-I. This value is significantly lower of constructed wetlands would be required to treat
than values for both the reed and cattail beds and the one million gallons (3785 m') per day.
unvegetated bed ( P < 0.01). Mean effluent BOD Cost estimates (which include the expense of an
+
levels were 22.3 16.6 mg 1-' for reeds, 30.4 + annual biomass harvest) show that artificial wetland
+
21.7 mg 1-' for cattails and 36.4 18.9 mg I-' for the treatment is a lower-cost alternative to conventional
unvegetated bed with all values significantly below secondary treatment processes with regard to both
+
the mean BOD level of 118.3 45.4 mg I-' for the capital, and operation and maintenance (O&M) ex-
primary wastewater inflow. Mean BOD removal pense (Gersberg et al., 1984b). With regard to O&M,
efficiencies (relative to the inflow) were 96, 8 1, 74 and a major cost savings is due to the fact that forced
69%, for the bulrushes, reeds, cattails and un- aeration (as in the activated sludge process) is not
vegetated beds, respectively. The mean effluent value necessary with wetland treatment. Rather, the vegeta-
of 22.3 mg 1-' for the reed bed was also significantly tion translocates oxygen into the underlying substrate
lower ( P < 0.05) than the value for the unvegetated thereby stimulating both nitrification of ammonia
bed. The cattail bed was again the poorest performer and the breakdown of BOD. Such cost and energy
with regard to BOD removal, having a mean effluent savings make artificial wetlands planted with bul-
level not significantly different from the unvegetated rushes or reeds an attractive approach for integrated
bed. Only the reed and bulrush beds showed treat- secondary and advanced (N removal) treatment of
ment equal or better than secondary treatment qual- municipal wastewaters.
ity (30 mg I-'). Since BOD removal (organic carbon
compound degradation) is enhanced under aerobic Acknowledgements-We thank R. Brenner, D. Allen, C.
Loss and I. Cotton for technical support and the Board of
conditions, it is reasonable to assume that the supe- Directors, Manager (E. Houser) and Staff of the Padre Dam
rior treatment afforded by the bulrush (and to a lesser Municipal Water District for providing space and facilities.
extent the reeds) was due to plant translocation of We also thank V. Rosenbrook for help with manuscript
oxygen to an otherwise anaerobic zone, thereby preparation and R. Axler for critical review. The California
Department of Water Resources (Grant B-53459 AM IV; R.
stimulating breakdown of carbonaceous compounds. Lindholm, Project Officer), the U.S. Environmental Protec-
An examination of the data on ammonia-N and tion Agency (Grant CR-807299-03-0; L. Leach, Project
BOD removal in Figs 2 and 3 reveals no definitive Officer) and the members of the San Diego Region Water
seasonal trends. Of course, our studies were carried Reclamation Agency provided financial support.
out in the San Diego region of southern California
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