Estuaries and Coasts

, Volume 32, Issue 4, pp 654–660

Whole Ecosystem Evidence of Eutrophication Enhancement by Wetland Dredging in a Shallow Tropical Lake

  • Humberto Marotta
  • Luiz Bento
  • Francisco de A. Esteves
  • Alex Enrich-Prast
Open Access
Article

DOI: 10.1007/s12237-009-9152-1

Cite this article as:
Marotta, H., Bento, L., Esteves, F.A. et al. Estuaries and Coasts (2009) 32: 654. doi:10.1007/s12237-009-9152-1

Abstract

The purpose of this research was to assess the effects of dredging performed in a marginal wetland colonized by aquatic macrophytes on eutrophication of the adjacent shallow tropical lake (Imboassica Lake, Brazil). The river mouth of the Imboassica River that drains into Imboassica Lake had been densely colonized by aquatic vegetation dominated by Typha domingensis (Pers.) when it was dredged. Total and dissolved nitrogen and phosphorus concentrations were measured monthly over 13 years at four stations in the Imboassica river-lake system. Dredging activities reduced phosphorus and nitrogen retention at the river mouth and subsequently increased these nutrient stocks in the lake waters. Nutrient retention by non-dredged wetland was estimated to be ca. 1,200 kg year−1 (87.3 g m−2 year−1) for nitrogen and 60 kg year−1 (4.5 g m−2 year−1) for phosphorus. Our whole-lake approach suggested that dredging might intensify rather than mitigate eutrophication in shallow tropical lakes when the removal of aquatic macrophytes is coupled to the persistence of anthropogenic nutrient inputs from the watershed.

Keywords

Dredging Nutrient retention Eutrophication Shallow tropical lakes Typha domingensis (Pers.) Wetlands 

Introduction

Lakes are aquatic ecosystems distributed broadly in the terrestrial surface (Downing et al. 2006), constituting an important destination for allochthonous (Lennon 2004; Sobek et al. 2005) and autochthonous (Brevik and Homburg 2004) matter in the watershed. Organic and inorganic inputs into lakes may originate from anthropogenic point and non-point sources (Arbuckle and Downing 2001). One recognizable consequence of pollution by nutrient-enriched effluents is the growth of submerged (Rooney et al. 2003), floating (Kadlec and Knight 1996) and emergent (Gophen 2000) aquatic macrophytes.

Emergent aquatic macrophytes are often abundant in wetlands—transitional habitats between aquatic and terrestrial ecosystems that are inundated or saturated by water during part or all of the year (Neue et al. 1997). Wetlands may mitigate eutrophication at low cost (Verhoeven and Meuleman 1999), showing great potential as complementary sewage treatment systems, even for big cities (Costa-Pierce 1998). Aquatic macrophytes reduce organic matter inputs (Wentz 1987) and contribute to retention of nutrients, mainly nitrogen (Fleischer et al. 1991) and phosphorus (Kadlec 1997), in aquatic ecosystems. This nutrient retention, or the difference between nutrient inputs and outputs, is caused by biological activity, sedimentation and chemical reduction to gases (Saunders and Kalff 2001). The role of emergent aquatic macrophytes in nutrient retention might be especially important in shallow lakes at low latitudes, where tropical conditions favor the colonization of these plants in marginal wetlands (Wetzel 1990).

Eutrophication contributes to silting in lakes because it increases autochthonous primary production and organic matter sedimentation (Brevik and Homburg 2004). The removal of peat sediments through dredging is considered an important intervention to restore the nutrient assimilative capacity of enriched lakes by reducing the internal loading from the sediment to the water column (Ruley and Rusch 2002). Hence, dredging may restore eutrophic aquatic ecosystems, increasing depth and reducing nutrient stocks (Sagehashi et al. 2001). However, this intervention may also remove the aquatic macrophytes that play an important role in nutrient retention in lakes (Rooney et al. 2003).

Here, we assessed the effects of dredging in a marginal wetland densely colonized by aquatic macrophytes on the eutrophication of the adjacent shallow tropical lake. This wetland is situated in a small river mouth that drains into the lake. Dredging restored fluvial depth and water flow into the lake by removing a large amount of sediment and aquatic vegetation, growth of which had been encouraged by the shallow depth and input of anthropogenic-generated nutrients. However, nutrient input from sewage into the river remained unchanged, allowing us to assess the role of dredging and removal of aquatic macrophytes on lake eutrophication at an ecosystem scale. We compared nitrogen (N) and phosphorus (P) concentrations in the water column of both river and lake for three periods over 13 years: two before and one after the dredging. Our hypothesis was that dredging with removal of aquatic macrophytes that was not coupled with a reduction in nutrient input would increase eutrophication in a shallow tropical lake.

Materials and Methods

Study Area

The tropical catchment studied here is located in the North region of Rio de Janeiro State, Brazil (Fig. 1). Imboassica River, a fourth order stream of about 14 km in length, is the main tributary of the Imboassica Lake watershed (area = 55 km2; and maximum altitude  120 m). The predominant land use in this watershed is abandoned pasture fields with residual native vegetation. However, the lowlands next to Imboassica Lake are dominated by urban use resulting in domestic sewage discharges directly into this aquatic ecosystem from its margins or from its tributary (Imboassica River), representing two different nutrient sources into the lake. Imboassica Lake (3.26 km2) is a coastal, shallow (mean depth = 1.4 m), and brackish-water (mean salinity = 5 US) ecosystem. Sewage inputs and siltation have increased, mainly since 1995. The marginal area of Imboassica Lake is densely colonized by emergent aquatic macrophytes (especially Southern cattail, Typha domingensis Pers.) at ca. 2,000 g DW m−2 in an area of 0.5 km2 or about 15 % of the total area of this lake (estimated by Palma-Silva 1998). Wetland covering an area of 14,000 m2 (extending for 2 km and with a width of 7 m) in the Imboassica River and its mouth into Imboassica Lake was dredged. This dredging removed aquatic macrophytes and peat sediments during the period from July to September 2002.
Fig. 1

Geographic localization of the Imboassica Lake watershed in Brazil. White circles Sampling stations: RIV, MAC, CEN and BEA (see Materials and Methods for details)

Sampling Stations and Periods

Water samples for N and P measurements were collected monthly from four stations (Fig. 1): RIV—at the Imboassica River, 2 km upstream from the river mouth that drains into Imboassica Lake; MAC—at the Imboassica Lake, in an area close to the Imboassica River mouth; CEN—at the central area of Imboassica Lake; and BEA—located close to the large sandbar that separates the lake from the sea, constituting the station farthest from the river mouth. Water sampling at each station was performed during three periods:
  1. 1

    More Pristine (PRIST)—from May 1992 to December 1994 (32 months): Imboassica Lake and Imboassica River showed more oligotrophic characteristics. The river mouth of the Imboassica river-lake system had a permanent water flow (ca. 5 m3 s−1) and aquatic macrophytes were absent along the river shore.

     
  2. 2

    Before Dredging (BD)—from January 2000 to June 2002 (30 months): the mouth of Imboassica River became densely colonized by T. domingensis due to eutrophication. In this area, a permanent superficial water column persisted only at the RIV station, as the river section from this point to Imboassica Lake no longer flowed superficially because of silting, showing only a groundwater flow. This lake had also been eutrophicated by sewage inputs directly from the margins; the average flow in the main discharge channel was estimated at 82.5 L s−1 (Lopes-Ferreira 1998).

     
  3. 3

    After Dredging (AD)—from May 2003 to October 2005 (28 months): dredging of the river channel restored the water flow between Imboassica River and Imboassica Lake to values similar to those of the PRIST period (ca. 4 m3 s−1). However, comparing the periods before and after dredging, nutrient discharges in the Imboassica River were not enhanced. A marked reduction in the sewage inflow directly from the margins of Imboassica Lake with respect to the BD period was measured, showing mean values of 16 L s−1 in the main discharge channel (Silva 2006).

     

Assessment of Dredging Effects on Eutrophication in the Water Column of Imboassica Lake

Dredging effects on eutrophication in the lake were assessed using two approaches: (1) analyzing changes in N and P concentrations (total and dissolved forms) among sampling stations and periods, and (2) comparing N and P standing stocks (mass of total and dissolved forms) in lake water among sampling periods. We assumed that the increase in a given nutrient (N or P) in lake water between PRIST and BD periods was influenced mainly by non-fluvial sources (sewage discharges directly from lake margins). We considered that fluvial nutrient inputs into the lake during this time interval were lower by the initial level of eutrophication in PRIST and due to the strong river mouth silting in BD. The increase in a given nutrient during the time interval just before and after dredging was considered to be due to both non-fluvial and post-dredging fluvial sources. Further, dredging effects on total nutrient standing stock in lake water was assessed by the difference in the increased rate per year of total N and P mass between two time intervals: 5 years from PRIST to BD and 1 year from BD to AD. In this estimate, we estimated conservatively that nutrient inputs directly from the margins into Imboassica Lake by non-fluvial sources between both time intervals were similar, despite an important flow reduction observed in the main sewage discharge channel (see preceding section). Calculations to estimate the effects of dredging on total N or P standing stocks in the lake are described below:
$$\begin{array}{*{20}l}{{{\text{Total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}\,{\text{standing}}} \hfill} \\{{{\text{stocks}}\,{\text{in}}\,{\text{lake}}\,{\text{water}}\,{\left( {\text{t}} \right)}} \hfill} \\\end{array} = \begin{array}{*{20}l}{{{\text{Total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}} \hfill} \\{{{\text{concentrations}}\,{\text{in}}\,{\text{lake}}}\hfill} \\{{{\text{water}}\,{\text{(values}}\,{\text{from}}\,{\text{all}}} \hfill} \\{{{\text{lakes}}\,{\text{stations;}}\,{\text{g}}\,{\text{L}}^{{{\text{ - 1}}}} {\text{)}}} \hfill} \\\end{array} \times \begin{array}{*{20}l}{{{\text{Lake}}} \hfill} \\{{{\text{volume}}\,{\left( {\text{L}} \right)}} \hfill} \\\end{array} \times \begin{array}{*{20}l}{{{\text{10}}^{{{\text{ - 3}}}} } \hfill} \\{{{\text{Correction}}} \hfill} \\{{{\text{factor}}\,{\text{for}}\,{\text{kg}}} \hfill} \\\end{array}$$
(1)
$$\begin{array}{*{20}l}{{{\text{Increase}}\,{\text{rate}}\,{\text{in}}\,{\text{total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}} \hfill} \\{{{\text{standing}}\,{\text{stock}}\,{\text{in}}\,{\text{lake}}\,{\text{water}}} \hfill} \\{{{\text{before}}\,{\text{dredging}}\,{\left( {{\text{kg}}\,{\text{y}}^{{{\text{ - 1}}}} } \right)}} \hfill} \\\end{array} = {\left\{ {\begin{array}{*{20}l}{{{\text{Total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}} \hfill} \\{{{\text{standing}}\,{\text{stocks}}\,{\text{in}}} \hfill} \\{{{\text{lake}}\,{\text{water}}\,{\text{during}}} \hfill} \\{{{\text{BD}}\,{\text{period;}}} \hfill} \\{{{\text{Equation}}{\left( {\text{1}} \right)}} \hfill} \\\end{array} - \begin{array}{*{20}l}{{{\text{Total}}\,{\text{N}}\,{\text{orP}}} \hfill} \\{{{\text{standing}}\,{\text{stocks}}\,{\text{in}}} \hfill} \\{{{\text{lake}}\,{\text{water}}\,{\text{during}}} \hfill} \\{{{\text{PRIST}}\,{\text{period;}}} \hfill} \\{{{\text{Equation}}\,{\left( {\text{1}} \right)}} \hfill} \\\end{array} } \right\}} \times \begin{array}{*{20}c}{{{\text{Time}}}} \\{{{\text{Years}}^{{{\text{ - 1}}}} }} \\{{{\left( {{\text{y}}^{{{\text{ - 1}}}} } \right)}}} \\\end{array}$$
(2)
$$\begin{array}{*{20}l}{{{\text{Increase}}\,{\text{rate}}\,{\text{in}}\,{\text{total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}} \hfill} \\{{{\text{standing}}\,{\text{stock}}\,{\text{in}}\,{\text{lake}}\,{\text{water}}} \hfill} \\{{{\text{after}}\,{\text{dredging}}\,{\left( {{\text{kg}}\,{\text{y}}^{{{\text{ - 1}}}} } \right)}} \hfill} \\\end{array} = {\left\{ {\begin{array}{*{20}l}{{{\text{Total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}} \hfill} \\{{{\text{standing}}\,{\text{stocks}}\,{\text{in}}} \hfill} \\{{{\text{lake}}\,{\text{water}}\,{\text{during}}} \hfill} \\{{{\text{AD}}\,{\text{period;}}} \hfill} \\{{{\text{Equation}}\,{\left( {\text{1}} \right)}} \hfill} \\\end{array} - \begin{array}{*{20}l}{{{\text{Total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}} \hfill} \\{{{\text{standing}}\,{\text{stocks}}\,{\text{in}}} \hfill} \\{{{\text{lake}}\,{\text{water}}\,{\text{during}}} \hfill} \\{{{\text{BD}}\,{\text{period;}}} \hfill} \\{{{\text{Equation}}\,{\left( {\text{1}} \right)}} \hfill} \\\end{array} } \right\}} \times \begin{array}{*{20}l}{{{\text{Time}}\,{\text{in}}} \hfill} \\{{{\text{Years}}^{{{\text{ - 1}}}} } \hfill} \\{{{\left( {{\text{y}}^{{{\text{ - 1}}}} } \right)}} \hfill} \\\end{array}$$
(3)
$$\begin{array}{*{20}l}{{{\text{Dredging}}\,{\text{effects}}\,{\text{on}}} \hfill} \\{{{\text{total}}\,{\text{N}}\,{\text{or}}\,{\text{P}}\,{\text{standing}}} \hfill} \\{{{\text{stocks}}\,{\text{in}}\,{\text{the}}\,{\text{lake}}\,{\text{water}}} \hfill} \\{{{\left( {{\text{kg}}\,{\text{y}}^{{{\text{ - 1}}}} } \right)}} \hfill} \\\end{array} = \begin{array}{*{20}l}{{{\text{Increase}}\,{\text{rate}}\,{\text{in}}\,{\text{total}}\,{\text{N}}} \hfill} \\{{{\text{or}}\,{\text{P}}\,{\text{standing}}\,{\text{stocks}}\,{\text{in}}} \hfill} \\{{{\text{lake}}\,{\text{water}}\,{\text{after}}} \hfill} \\{{{\text{dredging}}\,{\left( {{\text{kg}}\,{\text{y}}^{{{\text{ - 1}}}} } \right)}{\text{;}}} \hfill} \\{{{\text{Equation}}\,{\left( {\text{3}} \right)}} \hfill} \\\end{array} - \begin{array}{*{20}l}{{{\text{Increase}}\,{\text{rate}}\,{\text{in}}\,{\text{total}}\,{\text{N}}} \hfill} \\{{{\text{or}}\,{\text{P}}\,{\text{standing}}\,{\text{stocks}}\,{\text{in}}} \hfill} \\{{{\text{lake}}\,{\text{water}}\,{\text{before}}} \hfill} \\{{{\text{dredging}}\,{\left( {{\text{kg}}\,{\text{y}}^{{{\text{ - 1}}}} } \right)}{\text{;}}} \hfill} \\{{{\text{Equation}}{\left( {\text{2}} \right)}} \hfill} \\\end{array}$$
(4)

Analytical Methods

Water samples were collected with a Van Dorn bottle, transported to a field laboratory, filtered through 1.2 µm glass fiber filters (GF/C Whatman) for dissolved forms analyses and frozen. Total and dissolved N concentrations were obtained by the sum of Kjeldahl nitrogen (Mackereth et al. 1978) and nitrate (Golterman et al. 1978) concentrations. Total and dissolved P concentrations were determined by the blue molybdenum method (Golterman et al. 1978).

Statistical Analysis

Transformed data did not meet the assumptions of parametric tests (Zar 1996); the data were not normally distributed (Kolmogorov-Smirnov, P < 0.05) and variances were heterogeneous (Bartlett, P < 0.05). Medians and a non-parametric test were used to compare sampling groups (Kruskal-Wallis, P < 0.05; Zar, 1996). Statistical tests were carried out using GraphPad Prism 4.0. After this step, pair-to-pair differences were assessed with False Discovery Rate (FDR; P < 0.05), considering P-values from Mann-Whitney tests and a specific lambda equal to zero (Benjamini and Hochberg 1995). FDR was calculated using the software Q-VALUE, as this approach may be more powerful than traditional Bonferroni corrections and deserves more frequent use in ecological field studies, especially in those involving a relatively large number of multiple comparisons (Garcia 2004).

Results

N and P concentrations in all sampling stations were significantly lower in the PRIST period with respect to after dredging (FDR; P < 0.05; Figs. 2, 3, 4, 5). Nutrient concentrations at the river station increased strongly between the periods PRIST and BD (FDR; P < 0.05), but no significant differences were observed comparing these periods at the lake station next to the river (MAC) and for dissolved forms at other lake stations (CEN and BEA; FDR; P > 0.05; Figs. 2, 3, 4, 5). Before dredging, the river station showed the maximum difference of N and P concentrations in relation to lake stations, with median values between 6 and 10 times higher. Comparing the periods before and after dredging, nutrient concentrations decreased significantly at the river station and increased in all lake stations (FDR; P < 0.05, Figs. 2, 4, 5), except total N in CEN and BEA (FDR; P > 0.05, Fig. 3).
Fig. 2

Dissolved phosphorus (P) concentrations in the three study periods: more pristine (PRIST; n = 32 months from 1992 to 1994), before dredging (BD; n = 30 months from 2000 to 2002), and after dredging (n = 28 months from 2003 to 2005). Black squares and error bars represent the median and 25–75 % interquartile interval, respectively. The same lower case letters represent no significant difference among sampling stations and periods [P > 0.05; false discovery rate (FDR)]. Note break in scale on the y-axis

Fig. 3

Dissolved nitrogen (N) concentrations in the three study periods. Descriptions of sampling stations and statistics as in Fig. 2

Fig. 4

Total P concentrations in the three study periods. Descriptions of sampling stations and statistics as in Fig. 2

Fig. 5

Total N concentrations in the three study periods. Descriptions of sampling stations and statistics as in Fig. 2

Standing stocks of dissolved and total N and dissolved P in the water column of Imboassica Lake showed no significant changes between the two first periods, PRIST and BD (FDR; P > 0.05, Fig. 6), and a significant increase (ca. 108, 37 and 165 %, respectively) comparing the periods BD and AD (FDR; P < 0.05, Fig. 6). The standing stock of total P was characterized by a significant increase in both time intervals between study periods (FDR; P < 0.05), about 80 % in the 5 years from PRIST to BD, and about 50 % in only 1 year from BD to AD (Fig. 6). The increased rate due to dredging activities in the studied wetland was estimated as 1,222 kg year−1 for total N and 63 kg year−1 for total P (Table 1). Considering the area of 14,000 m2 of dredged wetland, the nutrient retention per area was estimated as 87.3 g N m−2 year−1 and 4.5 g P m−2 year−1.
Fig. 6

Standing stocks of P (white bars) and N (grey bars) in the water column of Imboassica Lake. a Dissolved, b total. Sampling periods as in Fig. 2. The same lower case letters for each variable represents no significant difference among periods (P > 0.05; FDR)

Table 1

Dredging effects on standing stock of total nitrogen (N) and phosphorus (P) in the waters of Imboassica Lake

Standing stock of total nutrients

Time intervals

Absolute increase (kg)

Increase rate (kg year−1)

Dredging effects in water (kg year−1)

Nitrogen

Between BD and PRIST

nsa

ns

1,222

Between AD and BD

1,222

1,222

Phosphorus

Between BD and PRIST

66

13

63

Between AD and BD

76

76

aNo significant increase

Discussion

Nutrient inputs from the watershed over 13 years resulted in a general enrichment of N and P at all sampling stations. The highest N and P concentrations observed at the river station when the river mouth was silted up (before dredging) might be attributed to factors other than just increases in sewage discharges. The very low water flow also influenced this result, as this would reduce nutrient dilution and contribute to eutrophication in natural waters (Schindler 2006).

Despite the strong eutrophication in Imboassica River, the lake station closest to this river (MAC) did not show a significant nutrient enrichment before dredging, probably due to dense colonization by aquatic macrophytes in the Imboassica river–lake system during this sampling period. Wetlands colonized by aquatic macrophytes can remove significant amounts of P (Kadlec 1997) and N (Saunders and Kalff 2001) from aquatic ecosystems. In our study, the removal of aquatic macrophytes with decreases in water residence time by dredging was related to a strong increase in N and P standing stocks in Imboassica Lake.

Retention of N and P per area in this tropical wetland, which is densely colonized by aquatic macrophytes, was estimated as about two orders of magnitude lower than often described for N (Arheimer and Wittgren 2002; Jiang et al. 2007; Blankenberg et al. 2008) and P (Uusi-Kamppa et al. 2000; Jiang et al. 2007) in highly nutrient-enriched constructed wetlands (effluent treatment systems). However, nutrient retention in the Imboassica river–lake system before dredging was comparable or higher than one currently described in natural or more oligotrophic constructed wetlands for N (Jansson et al. 1998; Fisher and Acreman 2004; Silvan et al. 2004) and P (Mitsch and Reeder 1991; Fisher and Acreman 2004; Silvan et al. 2004). Therefore, our results confirm the potential role of aquatic macrophytes in retaining excess nutrients (Hutchinson 1970; Demars and Harper 1998), and in reducing nutrient pollution of eutrophic lakes (Steinmann et al. 2003).

The removal of internal nutrient loading in the water–sediment interface by dredging with increases in the water flow can contribute to the restoration of aquatic ecosystems (Lohrer and Wetz 2003; Jiang and Shen 2006), but this intervention was related positively to nutrient enrichment in the studied lake. Many studies have independently assessed the role of dredging (Sagehashi et al. 2001) and aquatic vegetation (Steinmann et al. 2003) on the mitigation of aquatic eutrophication. On the other hand, the effects of drastic removal of large stands of aquatic macrophytes by dredging are still not well known. Our results suggest that eutrophication in a shallow tropical lake was significantly enhanced after dredging, confirming the proposed hypothesis. In conclusion, dredging may be considered an effective engineering technology for restoration of lakes (Jiang and Shen 2006), but might intensify rather than mitigate eutrophication when the removal of aquatic macrophytes is coupled with continued anthropogenic nutrient input. Dredging needs integrated planning related to decreases in nutrient inputs from the watershed, especially in tropical shallow lakes where aquatic macrophytes may be important players in nutrient cycling.

Acknowledgments

The authors would like to acknowledge PETROBRAS for financial support of the ECOLagoas Project and logistic support in NUPEM/UFRJ. We wish to thank Dr. David Bastviken for useful advice, and the two anonymous reviewers for valuable comments on an earlier draft of this manuscript. We are also grateful to the Brazilian funding agencies FAPERJ, CAPES and CNPq for scholarships and financial support.

Copyright information

© Coastal and Estuarine Research Federation 2009

Authors and Affiliations

  • Humberto Marotta
    • 1
    • 2
  • Luiz Bento
    • 1
    • 2
  • Francisco de A. Esteves
    • 3
  • Alex Enrich-Prast
    • 1
  1. 1.Laboratório de Biogeoquímica, Inst. de Biologia, Depto. de EcologiaUniversidade Federal do Rio de Janeiro (UFRJ)Rio de JaneiroBrazil
  2. 2.Programa de Pós-Graduação em Ecologia (PPGE) Prédio CCSUniversidade Federal do Rio de Janeiro (UFRJ)Rio de JaneiroBrazil
  3. 3.Laboratório de Limnologia, Inst. de Biologia, Depto. de EcologiaUniversidade Federal do Rio de Janeiro (UFRJ)Rio de JaneiroBrazil

Personalised recommendations