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Nutrient Cycling in Mangrove Ecosystem: A Brief Overview

Gurmeet Singh1 , AL.Ramanathan2 and M. Bala Krishna Prasad3

School of Environmental Sciences
Jawaharlal Nehru University
New Delhi







Mangrove forests are highly productive coastal ecosystems confined to the intertidal
zons. They are considered the major conduits for tidal exchange of dissolved and
particulate matter between the forest environment and adjacent coastal waters as well
as net exporters of organic matter and nutrients to the ocean, caused by biological and
physical processes within the forest ecosystem. Nitrogen Phosphorus and sulfur are
some of the major macronutrient essential for the various biological activities, hence
an effort has been made in present paper to explain their behavior in the mangrove
ecosystem. A brief review of the behavior of heavy metal in the mangrove forest as
well as the capability of scavenging heavy metals has been attempted in present

Key Words: Mangrove, nutrient cycling , nitrogen , phosphorus, heavy metals

Mangroves are intertidal forest ecosystems in sheltered saline to brackish
environments. They are among the most productive coastal ecosystems in the world,
confined to the tropics and subtropics, which dominate approximately 75% of the
worlds coastline between 25o N and 25o S and are estimated to cover an area of 1.7 to
2.0 X 105 Km2 (Borges et al, 2003). Under natural growing conditions mangrove trees
are well adapted to both flooding and saline water. They are regarded not only as
sinks of sediment and nutrients, but also as sources of organic matter of low nutrient
quality (Boto, 1992). Through out welling of leaf litter and dissolved organic matter,
these generally productive wetlands act as detritus sources to the adjacent oligotrophic
marine food webs, supporting valuable estuarine and coastal fisheries (Lee, 1995) The
mangrove sediments are characterized by high organic matter and ammonia contents
but low oxygen content (Morell and Corredor 1993) and, hence, contributions of
nutrients, organic matter and detritus to the nearby coastal ecosystem are high.

The mangrove ecosystem as a whole is net autotrophic, but the water column
and the sediment are largely net heterotrophic, due to three processes (Jennerjahn and
Ittekkot, 2002).:
1. Aquatic primary production is limited by high turbidity in the water column as
well as due to canopy shadow and large changes in salinity;
2. Water column and sediments receive important quantities of leaf and wood
litter from the overlying canopy;
3. Export of labile organic carbon from mangroves to adjacent aquatic systems,
although variable from one site to another, can be low

Recent biogeochemical studies focused on tidal exchange between wetland

vegetation and coastal waters as well as nutrient recycling through sediment-water
interface. Most studies indicate some net export of detritus to the sea from salt
marshes (Nixon 1980; Dame and others 1986) and mangrove forests (Boto and Bunt
1981; Flores-Vergudo and others 1987; Wolanski 1995; Wafar et al, 1997).


Mangrove creeks are generally considered the major conduits for tidal
exchange of dissolved and particulate matter between the forest environment and
adjacent coastal waters; (Rivera - Monroy et al., 1995). Most studies support the
contention that mangrove forests are net exporters of organic matter and nutrients to
the ocean, caused by biological and physical processes within the forest ecosystem
(Robertson, 1986; Dittmer & Lara, 2001). Export of dissolved inorganic nutrients by
tidal water in mangrove forests where the forest floor and creek bottoms are known to
be sinks of these compounds (Kristensen et al., 1995; Alongi, 1996) suggests that
other mechanisms than diffusive flux from sediments are also involved.
Figure 1
There are two interesting sources of nutrient in mangrove:

Seepage of nutrient rich pore-water from creek banks during falling

tides, and


Microbial mineralization of nutrient containing organic matter in the

creek water itself.
Although pore-water seepage from creek banks is a potential source of

nutrients, the volume of water passing through this pathway is generally orders of

magnitude smaller than the tidal transport. This source can therefore only affect the
chemistry of creek water when the interstitial nutrient concentrations in creek banks
are very high. Nevertheless, Lara & Dittmar (1999) suggested that most of the diurnal
nutrient oscillations in a Brazilian mangrove creek are due to dilution of nutrient-rich
pore-water seeping from creek banks by a variable and tidal driven volume of oceanic
water. However, Howes & Goehringer (1994) found that the nutrient levels in the
small amount of water seeping from creek banks in a New England salt marsh are
insufficient to affect the concentration of both dissolved organic carbon and inorganic
nutrients significantly in tidal waters.
Following processes have been shown to regulate the sediment-water
exchange of nutrients:

Molecular diffusion, caused by a nutrient gradient at the

sediment-water interface (Sweerts et al., 1991),


Faunal activity, such as ventilation or excretion (Blackburn and

Henriksen, 1983; Rutgers van der Loeff., 1984; Kristensen, 1985; 1988), and

Benthic algal uptake of nutrients (Rysgaard et al., 1995).

Benthic regeneration in transitional coastal environments is also the potential

source of nutrients to the overlying waters (Hartwig 1976; Zeitschel 1980;). An
intertidal flat region, where the sediment is regularly exposed and sufficient light
penetrates to the sediment, has been reported to have characteristically high levels of
benthic microalgal biomass and productivity (Colijn and de Jonge, 1984; Varela and
Penas, 1985). Photosynthetic processes can result in large diurnal changes and affect
the nutrient cycle near the sediment surface due to algal demand.

Mangrove forests are highly productive ecosystems, with the net primary
production rates reaching as high as 2050 t C ha -1 year-1(Clough1992, 1997). Almost
one third of the net primary production can be lost as plant litter, such as leaves and
twigs, and up to half of this litter is exported from mangrove creeks to adjacent
coastal waters (Robertson et al., 1992). The export of such a large amount of organic
matter has a recognizable effect on the nutrition or biomass of consumer communities
in coastal waters (Odum and Heald, 1975; Alongi 1990), although their quantitative
relationship is still to be established (Daniel and Robertson, 1990; Robertson and
Blaber, 1992). The amount of leaves decomposing in and on the forest floor is a
function of input (litter fall and import from adjacent areas) and output/removal
(export by tides, decomposition and removal by leaf-eating crabs). Decomposition
rates increase with humidity, temperature, and oxygen availability and depend on the
composition of the organic matter (Benner and Hodson, 1985).The export of plant
litter or macro-particulate matter from mangrove creeks is beyond doubt, but no
general consensus has been reached for other materials, such as nutrients and
dissolved and particulate organic matter (Twilley, 1985; Boto and Wellington, 1988;
Wattayakorn et al., 1990; Moran et al., 1991; Simpson et al., 1997). The presence or
absence of freshwater inputs into mangrove creeks seems to be an important factor
affecting the direction and magnitude of material fluxes (Boto and Wellington, 1988;
Robertson et al., 1992). However, inconsistencies amongst the published data may
have resulted from the differences of other characteristics, such as tidal range,
geomorphology, soil chemistry and mangrove plant biomass and community

The decomposition of plant litter typically occurs in three, often-simultaneous

(1) Physical and biological fragmentation,
(2) Microbial oxidation of refractory components such as cellulose and lignin,
(3) Leaching of soluble components (Valiela et al., 1985).
Oxygen penetration and thus aerobic decomposition processes in coastal
marine sediments are usually limited to the upper few millimetres (Revsbech et al.,
1980; Howarth & Jrgensen, 1984). Below the oxic zone, decomposition of organic
matter occurs by a variety of anaerobic processes (e.g. Gambrell & Patrick, 1978;
Mackin & Swider, 1989). Bacterial respiration processes in marine sediments use O 2,
NO-3, MnO2, FeOOH, SO4-2 and CO2 as electron acceptors (Fenchel & Blackburn,
1979). Macrophyte detritus, e.g. from mangrove trees and saltmarsh grasses, typically
has high C:N and C:P ratios (e.g. Kristensen, 1990; Buchsbaum et al., 1991; Wafar et
al., 1997) compared with the demands of

decomposing bacteria (Fenchel &

Blackburn, 1979). Therefore a rapid immobilization of nutrients may occur during

decomposition in mangrove forest sediments (Boto et al., 1989; Alongi, 1991; 1994;
1996; Kristensen et al., 1998), and other sediments as well. Immobilization due to
adsorption reactions in these sediments may further reduce the availability of
phosphorus (e.g. Krom & Berner, 1980; Clough et al., 1983; Sundby et al., 1992) and
ammonium (Mackin & Aller, 1984) in the porewater. Thus, there is an increased
loading of phosphate and ammonium to the sediment. The leaching phase of
mangrove leaf decomposition is characterized by a rapid loss of soluble organic
compounds (sugars, organic acids, proteins, phenolics, etc.) and inorganic minerals

(K, Ca, Mg, Mn, etc.). Regardless of vegetation type, this phase lasts anywhere from a
few days to a few weeks and can be responsible for substantial losses of carbon,
nitrogen, and phosphorus (Parsons et al., 1990; Chale, 1993; Steinke et al., 1993;
Taylor and Barlocher, 1996; France et al., 1997). The biotic contributions in this early
stage of decomposition are usually minimal and are most often limited to microbial
conditioning of the litter (Nykvist, 1959; Cundell et al., 1979; France et al., 1997).
Nitrogen is an essential element for a variety of biological and chemical
processes, both at micro level i.e. organism level as well as macrolevel i.e. at the scale
of ecosystem. It is present in different inorganic (viz. Ammonium, Nitrate, Nitrite) as
well as organic form
Bacterial activity regulates most of the available ammonium pool, particularly
in deeper sediments, devoid of other biota, just like any other aquatic system.
Ammonia immobilization and assimilation by microbes, plants etc. always
accompany and counteracts the mineralization process. The extent these process
balance each other is depended upon the carbon nitrogen(C: N) ratio of the
decomposing organic matter. Substance rich in nitrogen favors net mineralization,
where as those poor in nitrogen favors net immobilization.

Concentration of

ammonium is relatively high and influence by tidal cycle, plant uptake and seasonal
change, microbial decomposition, temperature, rainfall etc. (Boto 1982, 1984, 1985).
The availability of sediment nutrients to microbes and plants is complicated by
geochemical processes, such as the involvement of some nutrients in adsorption

reactions to clay minerals. The ammonium adsorption is low in mangrove sediments

compared to temperate salt marsh sediments, probably due to higher concentration of
competitive cations such as iron (Holmboe & Kristensen, 2003). In mangrove
sediments, ammonium excretion by microfauna, mesofauna and macrofauna must
occur, but rate are almost wholly unknown. Indication of ammonification in the water
column comes mainly from the estimates of ammonium excretion by protozoan and
metazoans grazers. Ikeda et.al.,( In: Alongi et al, 1992 ) suggested the excretion rate
of various organisms ranged from 1 to 415 mg N. animal-1 h-1 over the body sizes,
ranging from ~1 to 10,000 g.animal-1.
The concentration of Dissolved Organic Nitrogen (DON) is low in tropical
mangrove water. DON concentration has been observed decreasing with increase in
salinity (Nixon et al 1984, Wong, 1984). Lowest concentration of DON has been
recorded in the pre-monsoon season due to dilution from rain (Sarala devi et.al 1983).
During a tidal cycle highest concentration occurs at high tide and decreases during
ebb tide (Guerrero et al, 1988, Ovalle et. al., 1990). Similarly the concentration of
DON is also less in mangrove soil as compare to other tropical marine deposits.
High nutrient loading in coastal ecosystems has recently caused serious
eutrophication problems. In a eutrophic shallow environment, oxygen-depleted water
is occasionally generated at the bottom of the water column due to the accumulation
of organic matter (Ochi and Takeoka, 1986; Kemp et al., 1992) and can cause the
death of benthic macro-fauna (Rosenberg and Loo, 1988). Benthic mineralization is
considered as the important nitrogen pathway in shallow ecosystems (e.g., Blackburn
and Henriksen, 1983; Kemp et al., 1992). Nitrification processes occur in sediments
close to the sediment - water interface where there is availability of oxygen, such as at

oxidized line of animal borrows and within the oxidized region of Rhizophora (Boto,
1982). Assimilatory uptake of nitrogen counter balances the oxidation process; where
by the uptake of the nitrate occurs for the growth of mangrove and bacterial cell(Boto
et.al 1985).
Recycled dissolved inorganic nitrogen (DIN) is released from the sediment to
the overlying water through sediment-water exchange processes and can be taken up
by phytoplankton. Therefore, benthic algae in the intertidal flat ecosystems can
control the flux of DIN at the sediment-water interface. Denitrification is also known
to be a significant sink in the coastal ecosystem by the formation of gaseous nitrogen
(e.g., Kaplan et al., 1977; Koike and Hattori, 1978; Nedwell and Trimmer, 1996).
Nitrogen and N2O is the end product following the Michaelis-Menten kinetics.
(Nedwell, 1975; Iuzumi, 1986). The sedimentary denitrification rate is affected by
bacterial processes associated with DIN cycling in marine estuaries in two ways:
(1) Ammonium oxidation by nitrification in the sediment is strongly coupled with
denitrification (Jenkins and Kemp, 1984; Rysgaard et al., 1995; Ogilvie et al.,
1997), and thus nitrification itself indirectly removes nitrogen through these
coupled processes, and
(2) Dissimilatory nitrate reduction to ammonium competes with denitrification for
nitrate as the terminal electron acceptor for respiratory electron transport (Herbert
and Nedwell, 1990).
(3) The competition between the denitrifier and ammonifier under anaerobic
conditions consequently affects the removal of nitrogen by sedimentary
denitrification (Sorensen 1978).



In flooded salt marshes and mangroves, the grass and mangrove trees are able to









microenvironment (Silva et al., 1991; Mendelsshon and Postek, 1982; Mendelsshon et

al., 1981) capable of trapping P as FePO4 following the reaction:
4Fe2+ + O2 + 4H+ 4Fe3+ + 2H2O;
Fe3+ + 3H2O Fe (OH)3 + H+;
Fe (OH)3 + H2PO4 FePO4 + OH- + H2O
In general, the capacity of mangrove soil to immobilize phosphate depends on
the amount of organic matter, its C: P ratio, and the type and amount of clay minerals
present. Dissolution of mineral phosphate also depends on physiochemical
characteristics such as pH, available sulfides, alkalinity and redox state (Boto, 1988).
These factors can, of course, be affected by the activity of microbes and larger
organisms. In comparison with the release rates of phosphorus from mineral
phosphates and refractory organic materials, the turnover time for P uptake, utilization
and excretion by living organisms is very short. Local P cycles can be very efficient in
tropical mangroves, where it has been estimated that up to 88% of the forest P pool is
retained within the system (Boto and Bunt, 1982).
Mangrove trees (Boto and Wellington, 1983; Feller et al., 1999) and microbes
(Alongi, 1994) are often phosphorus (P)-limited in the tropics. The P concentrations in
seawater and porewater of unpolluted mangrove forests are low (Alongi et al., 1992),
and the affinity of the soils for P usually is very high (e.g. Holmboe et al., 2001).
Together with algal growth, leaf litter dynamics have been viewed as important for the
nitrogen cycling of fringe mangrove sediments (Kristensen et al., 1995), and P cycling
is also likely to be influenced by leaf fall and decomposition. The P dynamics in


mangrove sediments are closely coupled to the activity of Fe- and sulfate-reducing
bacteria, which are the primary microbial decomposers in the normally reduced
sediments (Sherman et al., 1998; Kristensen et al., 2000).
Variations in dissolved P concentrations may mirror changes observed for
dissolved N. For instance, in mangrove estuaries of the wet tropics, dissolved and
total phosphorus concentrations decrease with increasing salinity (Nixon et al., 1984;
Wong,1984; Liebezeit and Rau, 1988; Robertson et al., 1992) Dissolved and
particulate phosphorus concentrates in mangrove sediment are usually generally <40
M for DIP and <4 M for DOP. Concentrations vary over time and intertidal
position, reflecting seasonal effects of plant uptake and microbial growth,
temperature, rainfall, oxygen availability and sediment type (Boto, 1982, 1984).
Dissolved inorganic phosphorus (soluble reactive phosphate) exists mainly as a
nutrient salt (HPO42-) at the pH of seawater. Values in unpolluted mangrove waterways
range from < 0.1 to - 20 M whereas Total P content of mangrove sediments appears
to fall within the range of 100-1600 M g-1 (Boto, 1988)
Soluble reactive phosphate is readily assimilated by bacteria, algae and higher
plants, including mangroves. Most dissolved P in aquatic systems consists of various
organic phosphates (primarily phosphate esters originating from living cells), which
are often resistant to hydrolysis and therefore of limited availability. Mangrove soils
are expected to contain a high proportion of organic P compounds due to their
generally high organic matter content (Boto, 1988). Hesse (1962,1963) for instance,
found that 75-80% of the total extractable P was organic. Boto (1988) has pointed out
that much of this organic P is in the phytate form and bound to humic compounds and
is probably not readily available for microbial and mangrove plant nutrition. .


Although organic P is the major fraction, the inorganic phosphates probably

represent the largest potential pool of plant-available, soluble reactive phosphorus
(Boto, 1988). Most of the inorganic P in mangrove sediments is either bound in the
form of Ca, Fe and Al phosphates or as soluble reactive phosphorus adsorbed onto, or
incorporated into, hydrated Fe and Al sesquioxides . Total organic P concentrations;
proportionally greater in surface (0-25 cm) sediments; reflect the influence of roots,
whereas the inorganic fractions mainly Fe-P, proportionally and in real terms increase
gradually with depth reflecting the influence of increasing anoxia particularly below
the root layer(Boto,1988) Patterns of P in estuaries subjected to heavy monsoonal
rainfall are also nearly identical to those for nitrogen. Lowest P concentrations has
been observed during dry periods (Sarala Devi et al., 1983; Balakrishnan Nair et al.,
Table 2.
Figure 2a & 2b
Sulphur cycling in mangrove sediments can have significant impacts on the benthic
community due to a variety of secondary effects, e.g. associated pH changes. Due to
the high salinity conditions existing in the mangrove ecosystems, sulphate reduction
not expected to be controlled by the concentration of sulphate in the mangrove forest
sediments. It is much more likely that the rates are controlled by the availability of
organic matter and the biological and physical processes acting on the oxidation of the
sediments, e.g. bioturbation, root oxidation and tides. Sulphate reduction appears to be
an important process in mangrove sediments, and relatively high rates have been
found (e.g. Kristensen et a/., 1995; Kristensen, 1997; Alongi et a/., 1998; Holmer et


a/., 1999). This suggests that sulphate reduction may contribute significantly to
mineralization of organic carbon and nutrient availability in tropical mangrove
sediments (Holmer et al., 1994).
The accumulation of sulphur in subtidal marine sediments is primarily
controlled by the rate of sulphate reduction and the oxidation state of the sediment
(Thode-Andersen & Jrgensen, 1989). In tidal environments, however, additional
factors also play an important role. Tidal currents and wave action can affect the
oxidation status of sediments directly by increased advective transport of pore water
and particles. During low tide, the sediment surface desiccates and oxygen can
penetrate deeper into the sediment via burrows and cracks in the surface. The
presence of rooted vegetation also strongly affects the biogeochemical cycling of
sulphur by vertical translocation of organic matter and oxygen (Holmer & Nielsen,
1997; Holmer & Laursen, 2002), and the cycling of sulphur is closely coupled to the
reactive iron pools (Thamdrup, 2000). Reactive iron oxides present in sediments may
efficiently oxidize reduced sulphides. This suggests that the cycling of reduced
sulphur compounds is highly dynamic in mangrove forest sediments. Pyrite appears to
be the most important inorganic sulphur component in mangrove sediments, attaining
pool sizes 50-100 times higher than acid volatile sulfur pools (Kristensen et al., 1991,
1992; Holmer et a!., 1994, 1999; Alongi et al., 1998).
There is quite a significant burial of sulphides in the mangrove forest
sediments in particular in the mid-intertidal sediments, where the oxidation by
bioturbating organisms is low and the sulphate reduction activity high, but also the
high-intertidal sediments show large accumulations below depths of bioturbation
(Holmer et al., 1994). In addition to the burial of inorganic sulphur compounds, an


accumulation of organic sulphur has been found in the deep sediments in the inner
part of mangrove forests (Holmer et al., 1994). A similar accumulation of organic
sulphur has been observed in mangrove peats (Altschuler et al., 1983), but the
underlying mechanisms behind this accumulation are not well understood. However,
the burial of inorganic sulphur appears to be limited by the availability of iron
(Holmer et al., 1994), which may favor formation of organic sulphur compounds.
FIGURE 3a 3b
Elevated concentrations of heavy metals have been recorded in mangrove
sediments all over the world, which often reflects the long-term pollution caused by
human activities (Lacerda et al.,1992; Perdomo et al., 1998; Harris and Santos, 2000;
Tam and Wong, 2000). Due to their Inherent physical and chemical properties,
mangrove muds have an extraordinary capacity to accumulate materials discharged to
the near shore marine environment (Harbison, 1986).The cycling of trace metals in
mangrove ecosystems has been the subject of recent studies, due to the potential role
of mangroves in the abatement of trace metal pollution (Lacerda, 1998).
Trace metals enter mangrove ecosystems with the incoming tide associated
with suspended particles, iron and manganese oxi-hydroxides (Lacerda et al., 1998).
When reaching the reducing conditions, dominant in most mangrove environments,
these oxi-hydroxides are reduced and dissolved, and can release their trace metal load
to the water column. Since mangrove waters can have as much as 10 mg/L of
dissolved sulfide, due to the predominant sulfate reduction metabolism of mangrove
sediments, many trace metals are efficiently precipitated as insoluble sulfides
(Harbinson, 1986a, b; Lacerda et al., 1997; Clark et al., 1997). Due to permanent


anaerobic conditions of mangrove sediments and high sedimentation rates in

mangrove environments, trace metals suffer rapid accumulation and burial in the
sedimentary column. Thus, mangroves can act as biogeochemical barriers to trace
metal transport in coastal waters (Lacerda, 1998). The mechanisms described above
may also hamper trace metal uptake by mangrove plants. However, trace metals
which do not form stable sulfides, will not be affected by this precipitation process
(Lacerda, 1997).
Table 3

Many studies on trace metals in mangrove plants have shown concentration

factors (leaf concentration to sediment concentration ratio) lower than 1.0 for most
trace metals, the only exception being Mn, which always has concentration factors
higher than 1.0. Of all trace elements studied, Mn generally, shows a significant
correlation between sediment and leaf concentrations (Lacerda, 1997).
Mangrove sediments are anaerobic and reduced, as well as being rich in
sulphide and organic matter. They therefore favor the retention of water-borne heavy
metals and the subsequent oxidation of sulphides between tides allows metal
mobilization and bioavailability (Silva et al., 1990; Tam and Wong, 2000).
Concentrations of heavy metals in sediments usually exceed those of the overlying
water by 35 orders of magnitude (Zabetoglou et al., 2002) and, with such high
concentrations, the bioavailability of even a minute fraction of the total sediment
metal content assumes considerable importance with respect to bioaccumulation
within both animal and plant species living in the mangrove environment. Since
heavy metals cannot be degraded biologically, they are transferred and concentrated
into plant tissues from soils and pose long-term damaging effects on plants. However
Tam and Wang (1993) suggested that the mangrove soil component has a large


capacity to retain heavy metals, and the role of mangrove plants in retaining metals
will depend on plant age and their biomass production.
Many mangrove ecosystems are close to urban development areas (Shriadiah,
1999, Tam and Wong, 2000; MacFarlane, 2002; Preda and Cox, 2002) and are
impacted by urban and industrial runoff, which contains trace and heavy metals in the
dissolved or particulate form.
Mangrove ecosystems are one of the major types of natural wetlands in
tropical and subtropical regions, flooded by fresh river water as well as by salty
seawater. Similar to other estuarine zones, mangrove ecosystems also receive a large
amount of waste from their related drainage and rivers and have become a massive
pollution sink. Recent studies have also questioned the importance of mangroves as a
source of inorganic nutrients and have shown that certain mangrove ecosystems may
not be as significant sources as accepted before and may even represent sinks of
inorganic nutrients The use of a mangrove ecosystem, the same as other natural
wetlands, as an alternative low cost sewage treatment facility has been proposed by a
number of researchers (Henley, 1978; Clough et al., 1983; Richardson and Davis,
1987; Tam and Wong, 1993; Breaux and Day, 1994; Corredor and Morell, 1994,
Tam., 1996; Wong et al., 1995) especially in coastal regions with pressing needs for
wastewater treatment.

Like other trees, mangrove trees absorb nutrients and

pollutants from the inerstitial waters or sediment solution in the vicinity of the roots
hairs (Sadiq, 1992). However, there seems to be a knowledge gap as to the role of
these cations for phytoplankton dynamics in mangrove ecosystems. For seawater,
these cations are usually treated as conservative, yet relatively little is known about


their sources or sinks in mangrove creeks and the biotic and/or abiotic processes
controlling their concentrations (Cohen et al 1999).
The effectiveness of a wetland system to remove the input pollutants is highly
dependent on the chemical, biological and/or physical processes, and the entire soilplant-water system is important in the reduction of pollutants from wastewater
(Dunbabin and Bowmer, 1992; Gale et al., 1993). The performance of a natural
wetland wastewater treatment system therefore depends very much on the wetland
characteristics, which are extremely variable. It is difficult, if not impossible, to
translate results from one geographical area to another, or from one type of wetland to
another (Trattner & Woods, 1989). Despite their significance in purifying wastewater,
natural wetlands in many countries including the United States are legally limited to
providing only tertiary treatment of secondary waste (Breaux & Day, 1994). Most
studies were focused on the removal mechanisms of suspended solids, organic matter
and nutrients from domestic or livestock wastewater by wetlands (Corredor and
Morell, 1994)..
Mangroves ecosystem demonstrate close link between vegetation assemblage
and geomorphologic defined habitats. However despite of their close link, the
prevailing geomorphologic and ecomorppholgical view are quite contrary the
ecologist view mangrove as highly productive source of organic matter from where,
there is a net out welling of energy supporting complex estuarine and near shore food
wave. Geologists, however, view mangrove sediments as a sink for nutrients
characterized by long term import of sediments. Though a lot work has been done in
order to get a clear picture of nutrient cycling in mangrove ecosystem, but still the


dynamics is not completely understood. It is also felt that there is an urgent need of
establishment of the detailed database in order to have a more cleare picture of the
cycling of nutrients


Alongi D.M., 1990 a Effects of mangrove detrital outwelling on nutrient regeneration
and oxygen fluxes in coastal sediments of the central Great Barrier Reef
lagoon. Estuarine Coastal Shelf Science, 31 : 581598
Alongi, D. M. 1994, The role of bacteria in nutrient recycling in tropical mangrove
and other coastal benthic ecosystems. Hydrobiologia 285: 1932.
Alongi, D. M., 1996,. The dynamics of benthic nutrient pools and fluxes in tropical
mangrove forests. J. Marine. Research, 54: 123148.
Alongi, D.M., 1990 b., Abundances of benthic microfauna in relation to outwelling of
mangrove detritus in a tropical coastal lagoon. Marine Ecology Progress
Series 63: 5363.
Alongi, D.M., 1991, The role of intertidal mudbanks in the diagenesis and export of
dissolved and particulate materials from the Fly Delta, Papua New Guinea.
Journal of Experimental Marine Biology and Ecology 149: 81-107
Alongi, D.M., Boto, K.G., Robertson, A.I., 1992. Nitrogen and phosphorus cycles. In:
Robertson, A.I., Along, D.M. (Eds.), Tropical Mangrove Ecosystems. Coastal
and Estuarine Studies, vol. 41. American Geophysical Union, Washington DC,
pp. 251 292.
Alongi, D.M., Sasekumar, A., Tirendi, F. and Dixon, P..1998, The influence of stand
age on benthic decomposition and recycling of organic matter in managed
mangt0ve forests of Malaysia. Journal of Experimental Marine Biology and
Ecology, 225: 197-218.
Altschuler, Z.S., Schnepfe, M.M., Silber, C.C. and Simon, F.O., 1983, Sulfur
diagenesis in Everglades peat and origin of pyrite in coal. Science, 221, 221227.
Attiwill P.M., and Clough B.F., 1978, Productivity and Nutrient recycling in the
mangrove and sea grass communities of Westernport Bay., Report to Ministry
for conservation Victoria, Australia 86 pp.
Balakrishnan Nair, N., Abdul Azis, P.K., Krishna Kumar, K., Dharmaraj, K., and
Arunachalam, M., 1984, Ecology of Indian estuaries: Part VI - Physico-


Chemical conditions in Kadinamkulam backwater, SW coast of India. Indian

Journal of Marine Sciences, 13:69-74.
Blackburn, T.H. and Henriksen, K. 1983. Nitrogen cycling in different types of
sediments from Danish waters. Limnology and Oceanography 28: 477493.
Borges.,A.V. S.Djenidi, G. Lacroix, J. Theate, B. Delille, and M. Frankignoule.2003.
Atomspheric CO2 fluxes from mangrove surrounding waters, Geophysical
Research Letter 30(11): 12-1-4
Boto K.G. ., Saffigna , P. and Clough B.F., 1985, Role of nitrate in the nitrogen
nutrition of the mangrove Avecinia marina Marine Ecology Progress Series
Boto KG, Bunt JS, 1981, Tidal export of particulate organic matter from a northern
Australian mangrove system. Estuarine Coastal Shelf Science 13 : 247255
Boto, K. G. 1992.,

Nutrients and mangroves. In Pollution in Tropical Aquatic

Systems (Connell, D. W. & Hawker D. W., eds). CRC Press, Boca Raton, pp.
Boto, K.G. and Wellington, J., 1983., Phosphorus and nitrogen nutritional status of a
northern Australian mangrove forest. Marine Ecology Progress Series 11: 63
Boto, K.G. and Wellington, J., 1988, Seasonal variations in concentration. And fluxes
of dissolved organic nad inorganic materials in a tropica, tidally dominated
mangrove waterway,. Marine Ecology Progress Series 50: 151160
Boto, K.G., Alongi, D.M., and Nott, A.L.l., 1989. Dissolved organic carbon-bacteria
interactions at sedimentwater interface in a tropical mangrove system. Marine
Ecology Progress Series 51:243-251.
Boto, KG., 1982., Nutrient and organic fluxes in mangroves. In: Clough, B.F. (Ed.).
Mangrove Ecosystems in Australia, Australian National University Press,
Canberra, pp. 239-257.
Boto, KG., 1984., Waterlogged saline soils. In: Snedaker, S.c. and Snedaker, J.G.
(Eds). The Mangrove Ecosystem: Research Methods. pp. 114-130, UNESCO,


Boto, KG., 1988., The phosphorus cycle. In: Agate, A.D., Subramanian, C.V. and
Vannucci, M. (Eds). Mangrove Microbiology, pp. 85-100, UNLPIUNESCO
Regional Project (RAS/86/1988), New Delhi
Boto, KG., and Bunt, I.S. 1982., Carbon export from mangroves. In: Galba1ly, I.E.
and Freney, l.R. (Eds). The cycling of carbon, nitrogen, sulfur and phosphorus
in terrestrial and aquatic ecosystems, Australian Academy of Science,
Canberra. pp. 105-110,
Breaux, A. M .and

& J. W. Day Jr, 1994. Policy considerations for


wastewater treatment in the coastal zone: a case study for Louisiana. Coast.
Mgmt 22: 285307.
Buchsbaum, R., Valiela, I., Swain, T., Dzierzeski, M. & Allen, S. 1991 Available and
refractory nitrogen in detritus of coastal vascular plants and macroalgae.
Marine Ecology Progress Series 72, 131143.
Chale, F.M., 1993. Degradation of mangrove leaf litter under aerobic conditions.
Hydrobiologia 257, 177183.
Clark, M.W., McConchie, D., Saenger, P. and Pillsworth, M. 1997. Hydrological
controls on copper, cadmium, lead and zinc concentrations in an



ecosystem, Wynnum,


Australia. Journal of Coastal Research 13: 11501158.

Clough, B. F., K. G. Boto & P. M. Attiwill, 1983. Mangrove and sewage: a reevaluation. In Teas, H. J. (ed.), Biology and Ecology of Mangroves. Tasks for
Vegetation Science Series, Vol. Dr W. Junk Publishers, Lancaster: 151162.
Cohen M.C.L., Lara R.J., Ramos J.F.F. and Dittmar T. 1999.Factors influencing the
variability of magnesium, calcium and potassium in waters of a mangrove
creek in Braganca, North Brazil. Mang. Salt Marsh. 3: 915.
Colijn, F. and de Jonge, V.N. 1984. Primary production of microphytobenthos in the
Ems-Dollard estuary. Marine Ecology Progress Series 14: 185196.
Corredor, J. E.&J. M. Morell, 1994. Nitrate depuration of secondary sewage effluents
in mangrove sediments. Estuaries 17: 295300.


Cundell, A.M., Brown, M.S., Stanford, R., Mitchell, R., 1979. Microbial degradation
of Rhizophora mangle leaves immersed in the sea. Estuarine Coastal Shelf
Science. 9, 281286
Dame R, Chrzanowski T, Bildstein K, Kjerfve B, McKeller H, Nelson D, Spurrier T,
Stancyk S, Stevenson H, Vernberg J, Zingmark R (1986) The outwelling
hypothesis and north inlet South Carolina. Marine Ecological Progress Series
33: 217229
Daniel, P.A. and Robertson, A.I. 1990. Epibenthos of mangrove waterways and open
embayments: community structure and the relationship between exported
mangrove detritus and epifaunal standing stocks. Estuarine, Coastal and Shelf
Sciences 31: 599619.
Davis S. E., D. L. Childers, J. W. Day, Jr , D. T. Rudnick and F. H. Sklar 2001
Nutrient Dynamics in Vegetated and Unvegetated Areas of a Southern
Everglades Mangrove Creek Estuarine, Coastal and Shelf Science, Volume
52, Issue 6, Pages 753-768
Dittmar, T. & Lara, R. J. 2001 Do mangroves rather than riversprovide nutrients to
coastal environments south of the AmazonRiver? Evidence from long-term
flux measurements. Marine Ecology Progress Series. 49: 21-29
Dittmar, T. 1999 Outwelling of organic matter and nutrients from a mangrove in north
Brazil: Evidence from organic tracers and flux measurements. Centre for
Tropical Marine Ecology, Bremen .ZMT-contribution pp 5-.
Dunbabin, J. S. & K. H. Bowmer, 1992. Potential use of constructed wetland for
treatment of industrial wastewaters containingmetals. Sci. tot. Envir. 111: 151
Feller, I.C., Whigham, D.F., ONeill, J.P., McKee, K.L., 1999. Effects of nutrient
enrichment on within-stand cycling in a mangrove forest. Ecology 80, 2193
Fenchel, T. & Blackburn, T. H. 1979 Bacteria and Mineral Cycling. Academic Press,
London, 225 pp.


Flores-Vergudo FJ, Day JW, Briseno-Duenas R (1987) Structure, litter fall,

decomposition and detritus dynamics of mangroves in a Mexican coastal
lagoon with an ephemeral inlet. Marine Ecology Progress Series 35 :8390
France, R., Culbert, H., Freeborough, C., Peters, R., 1997. Leaching and early mass
loss of boreal leaves and wood in oligotrophic water. Hydrobiologia 345, 209
Gale, P. M., K. R. Reddy & D. A. Graetz, 1993. Nitrogen removal from reclaimed
water applied to constructed and natural wetland microcosms. Water.
Environmetal. Research. 65: 162168.
Gambrell, R. P. & Patrick, W. H. Jr. 1978 Chemical and microbiological properties of
anaerobic soils and sediments. In Plant life in anaerobic environments (Hook,
D. D. & Crawford, R. M. M., (eds) Ann Arbor Science Publishers, Michigan,
(13), 375410.
Guerrero, G.R., Cervantes, D.R., and Jimenez, LA., 1988. Nutrient variation during a
tidal cycle at the mouth of a coastal lagoon in the northwest of Mexico. Indian
Journal of Marine Science 17:235-237.
Guzman, H.M., Jimenez, C.E., 1992. Contamination of coral reefs by heavy metals
along the Caribbean coast of Central America (Costa Rica and Panama).
Marine Pollution Bulletin 24, 554561.
Harbinson, P. 1986 a. Diurnal variations in the chemical environment of a shallow
tidal inlet, Gulf of St Vincent, South Australia: implications for water quality
and trace metal migration. Marine Environmental Research 20: 161195.
Harbison, P., 1986 b. Mangrove muds: a sink or source for trace metals. Marine
Pollution Bulletin 17, 246250.
Harris, R.R, and Santos, M.C.F., 2000. Heavy metal contamination and physiological
variability in the Brazilian mangrove crabs, Ucides cordatus and Callinectes
danoe (Crustacea: Decapoda). Marine Biology 137, 691703.
Hartwig EO (1976) The impact of nitrogen and phosphorus release from siliceous
sediment on the overlying water. In:Wiley M (ed) Estuarine Processes, vol 1.
Acad Press, London, 103117


Henley, D. A., 1978. An investigation of proposed effluent discharge into a tropical

mangrove estuary. In Proceedings of International Conference onWater
Pollution Control in Developing Countries. Sept. 1978, Thailand: 4364.
Herbert, R.A. and Nedwell, D.B., 1990. Role of environmental factors in regulating
nitrate respiration in intertidal sediments. pp. 7790. In: Revsbech, N.P. and
Srensen, J. (eds), Denitrification in soil and sediment. Plenum Press, New
Hesse, P.R., 1963. Phosphorus relationships in a mangrove swamp mud with
particular reference to aluminium toxicity. Plant and Soil 19:205-218.
Holmboe ,N. Kristensen E. 2003, Ammonium adsorption in sediments from a tropical
mangrove forest (Thailand ) and a temperate Wadden Sea area (Denmark),
Wetland Ecology and Management 10(6:453-460).
Holmboe, N., Kristensen, E., Andersen, F.., 2001. Anoxic decomposition in
sediments from a tropical mangrove forest and the temperate Wadden Sea:
impacts of N and P addition experiments. Estuarine Coastal Shelf Science.
53, 125 140.
Holmer, M. and Laursen, L. (2002) Effect of shading of Zostera marina (eelgrass) on
sulfur cycling in sediments with contrasting organic matter and sulfide pools.
Journal of Experimental Marine Biology and Ecology, 270, 25-37
Holmer, M. and Nielsen, S.L. (1997) Sediment sulfur dynamics related to biomassdensity patterns in Zostera marina (seagrass) beds. Marine Ecology Progress
Series, 146, 163-171.
Holmer, M., Andersen, F.O., Holmboe, N., Kristensen, E. and Thongtham, N. (1999)
Transformation and exchange processes in the Bangrong mangrove forest-sea
grass bed system, Thailand. Seasonal and spatial variations in benthic
metabolism and sulfur biogeochemistry. 'Aquatic Microbial Ecology, 20, 203212.
Holmer, M., Kristensen, E., Banta, G., Hansen, K., Jensen, M.H. and Bussawarit, N.
(1994) Biogeochemical cycling of sulfur and iron in sediments of a south-east
Asian mangrove, Phuket Island, Thailand. Biogeochemistry, 26, 145-161.


Howarth, R. W. & Jrgensen, B. B. 1984 Formation of 35Slabelled elemental sulfur

and pyrite in coastal marine sediments (Limfjorden and Kysing Fjord,
Denmark) during short-term 35SO42- reduction measurements. Geochemica et
Cosmochimica Acta 48, 18071818.
Howes, B. L. & Goehringer, D. D. 1994. Porewater drainage and dissolved organic
carbon and nutrient losses through the intertidal creekbanks of a New England
salt marsh. Marine Ecology Progress Series. 114: 289301.
Iizumi, H., 1986. Soil nutrient dynamics. In: Cragg, S. and Polunin, N. (Eds).
Workshop on Mangrove Ecosystem Dynamics, UNDP/UNESCO Regional
Project (RAS/79/002) New Delhi, pp.171-180.
Jenkins, M.C. and Kemp, W.M. 1984. The coupling of nitrification and denitrification
in two estuarine sediments. Limnology and Oceanography 29: 609619.
Jennerjahn, T. C., and V. Ittekkot, Relevance of mangroves for the production and
deposition of organic matter along tropical continental margins,
Kaplan, W.A., Teal, J.M. and Valiela, I. 1977. Denitrification in saltmarsh sediments:
evidence for seasonal temperature selection among populations of denitrifiers.
Microbial Ecology 3: 193204.
Kemp, W.M., Sampou, P.A., Garber, J., Tuttle, J. and Boynton, W.R. 1992. Seasonal
depletion of oxygen from bottom waters of Chesapeake Bay: roles of benthic
and planktonic respiration and physical exchange processes. Marine Ecology
Progress Series 85: 137152.
Koike, I. and Hattori, A. 1978. Simultaneous determinations of nitrification and
nitrate reduction in coastal sediments by a 15N dilution technique. Applied
and Environmental Microbiology 35: 853857.
Kristensen, E. (1997) Carbon, sulfur, and nitrogen biogeochemistry of tropical
mangrove sediments, in Coastal Zone Management Imperative for Maritime
Developing Nations (eds B.U. Haq, S.M. Haq,G. Kullenberg and J.H. Stel),
Kluwer Academic Publishers, The Netherlands, pp. 199-232.


Kristensen, E. 1985. Oxygen and inorganic nitrogen exchange in a Nereis virens

(Polychaeta) bioturbated sediment-water system. Journal of Coastal Research
1: 109116.
Kristensen, E. 1990 Characterization of biogenic organic matter by stepwise
thermogravimetry (STG). Biogeochemistry 9, 135159.
Kristensen, E., 1988. Benthic fauna and biogeochemical processes

in marine

activities and fluxes. In: Blackburn, T.H. and Srensen, J. (eds), Nitrogen
cycling in coastal marine environments. John Wiley and Sons, New York. pp.
Kristensen, E., Andersen, F.., Holmboe, N., Holmer, M., Thongtham, N., 2000.
Carbon and nitrogen mineralization in sediments of the Bangrong mangrove
area, Phuket, Thailand. Aquatic. Microbial Ecology 22, 199 213.
Kristensen, E., Devol, A.H., Ahmed, S.l. and Saleem, M. (1992) Preliminary study of
benthic metabolism and sulfate reduction in a mangrove svamp of the Indus
Delta, Pakistan. Marine Ecology Progress Series, 90, 287-297.
Kristensen, E., Holmer, M. and Bussawarit, N. (1991) Benthic metabolism and sulfate
reduction in a south-east Asian mangrove svamp. Marine Ecology Progress
Series, 73, 93-103.
Kristensen, E., Holmer, M., Banta, G.T., Jensen, M.H., Hansen, K., 1995. Carbon,
nitrogen and sulfur cycling in sediments of the Ao Nam Bor mangrove forest,
Phuket, Thailand: a review. Res. Bull.-Phuket Mar. Biol. Cent. 60, 37 64.
Kristensen, E., Jensen, M. H., Banta, G. T., Hansen, K., Holmer, M. & King, G. M.
1998 Transformation and transport of inorganic nitrogen in sediments of a
southeast Asian mangrove forest. Aquatic Microbial Ecology 15, 165175.
Krom, M. D. & Berner, R. A. 1980 Adsorption of phosphate in anoxic marine
sediments. Limnology and Oceanography 25, 797806.
Lacerda, I.D., Fernandez, M.A., Calazans, C.F., Tanizaki, K.F., 1992.Bioavailability
of heavy metals in sediments of two coastal lagoons in Rio de Janeiro, Brazil.
Hydrobiologia 228, 6570.


Lacerda, L.D. 1997. Trace metals in mangrove plants, why such low concentrations?
pp. 7178. In: Kjerfve, B., Lacerda, L.D. and Diop, E.S. (eds), Mangrove
Ecological Studies in Latin America and Africa. UNESCO, Paris.
Lacerda, L.D. 1998. Biogeochemistry of trace metals and diffuse pollution in
mangrove ecosystems. ISME occasional papers 2. International Society for
Mangrove Ecosystems, Okinawa.
Lacerda, L.D., C.E., Rezende, D.M.V. Jose, and M.C.F. Francisco, 1986. Metal
composition of mangrove leaves from the southeastern Brazilian coast. Rev.
Braz. Biol., 46: 395-399.
Lara, R.J., and Dittmar, T. (1999) Nutrient dynamics in a mangrove creek (North Brazil)
during the dry season. Mangroves and Salt Marshes, 3, 185-195

Li M. S. 1997 Nutrient Dynamics of a Futian Mangrove Forest in Shenzhen, South

China Estuarine, Coastal and Shelf Science 45, 463472
Li, M. S., Wong, Y. S., Tam, N. F. Y. et al. 1997 Litter production and return of
nutrient elements in Futian mangrove swamp, Shenzhen, China. In:
proceeding of the international Workshopn on the Mangrove Ecosytem of the
Mai Po Marshes and Deep Bay, (Eds) Lee S.Y. Hongkong University press,
Hong Kong :128-141
Liebeziet, G., and Rau, M.T., 1988. Nutrient chemistry of two Papua New Guinean
mangrove systems.In: Field, C.D. and Vannucci, M. (Eds.), Symposium on
New Perspectives in Research and ManaRement of Mangrove Ecosystems, pp.
37-48, UNDP/UNESCO Regional Project RAS/86/120, New Delhi.
Lin, P., Wang, W., 2001. Changes in the leaf composition, leaf mass and leaf area
during leaf senescence in three species of mangroves. Ecol. Eng. 16, 415424.
MacFarlane, G.R. 2002 Potential biological indicators of heavy metal stress in
mangrove ecosystems. Wetlands 20(1), 29-42.
MacFarlane, G.R., and Burchett, M.D., 2002. Toxicity, growth and accumulation
relationships of copper, lead and zinc in the Grey Mangrove Avicennia marina
(Forsk.) Veirh. Marine Environmental Research 54, 6584.


MacFarlane, G.R., Burchett, M.D., 2000. Cellular distribution of Cu, Pb and Zn in the
Grey Mangrove Avicennia marina (Forsk.) Vierh. Aquatic Botany 68, 4559.
Mackin, J. E. & Aller, R. C. 1984 Ammonium adsorption in marine sediments.
Limnology and Oceanography 29, 250257.
Mackin, J. E. & Swider, K. T. 1989 Organic matter decomposition pathways and
oxygen consumption in coastal marine sediments. Journal of Marine Research
47, 681716.
Mendelssohn, I.A. and Postek, M.T. 1982. Elemental analysis of deposit on the roots
of Spartina alterniflora Loisel. American Journal of Botany 69: 904912.
Mendelssohn, I.A., McKee, K.L., Patrick, W.H., Jr. 1981. Oxygen deficiency in
Spartina alterniflora roots: metabolic adaptation to anoxia. Science 214: 439
Moran, M.A., Wicks, R.J., Hodson, R.E., 1991. Export of dissolved organic matter
from a mangrove swamp ecosystem: evidence from natural fluorescence,
dissolved lignin phenols, and bacterial secondary productivity. Marine
Ecology Progress Series. 76: 175184.
Morell JM, Corredor JE , 1993, Sediment nitrogen trapping in a mangrove lagoon.
Estuar Coast Shelf Sci 37 : 203212
Nedwell D.B., 1975. Inorganic nitrogen metabolism in a eutrophicated tropical
mangrove estuary. Water Research 9:221-231.
Newell, S.Y., 1984. Carbon and nitrogen dynamics in decomposing leaves of three
coastal marine vascular plants of the subtropics. Aquatic Botany 19: 183-192.
Nielsen Thomas, and Frede Andersen, 2003, Phosphorus dynamics during
decomposition of mangrove (Rhizophora apiculata) leaves in sediments
Journal of Experimental Marine Biology and Ecology 293: 73 88
Nixon SW (1980) Between coastal marshes and coastal waters. A review of twenty
years of speculation and research in the role of salt marshes in estuarine
productivity and water chemistry. In: Hamilton P, McDonald KB (eds)
Estuarine and wetland Processes. Plenum Publication Corporation, New York,
pp 437525


Nixon, S.W., Furnas, B.N., Lee, V., Marshall, N., Ong, 1.-E., Wong, C.-H., Gong, W.K., and Sasekumar, A., 1984. The role of mangroves in the carbon and nutrient
dynamics of Malaysia estuaries. In: Soepandmo, E., Rao, A.N., Macintosh,
D.l. (Eds). Proceedings of the Asian Symposium on Mangrove Environments:
Research and Management, pp. 496-513, University of Malaya and UNESCO,
Kuala Lumpur.
Nykvist, N., 1959. Leaching and decomposition of litter. I. Experiments on leaf litter
of Fraxinus excelsior. Oikos 10, 190211.
Odum,W.E. and Heald, E.J. 1975. The detritus-based food web of an estuarine
mangrove community. pp. 265286. In: Cronin, L.E. (ed.), Estuarine
Research, Volume 1. Academic Press, New York.
Oglivie, B., Nedwell, D.B., Harrison, R.M., Robinson, A. and Sage, A. 1997. High
nitrate, muddy estuarine as nitrogen sinks: the nitrogen budget of the River
Colne estuary (United Kingdom). Marine Ecology Progress Series 150: 21
Ohowa, B. O. Mwashote, B.M Mwashote, B. M. And Shirmabora W.S. 1997
Dissolved Inorganic nutrient fluxes from two seasonal rivers into Gazi Bay,
Estuarine, Coastal, and Shelf Science 45 189-195.
Onuf, C. P., Teal, J. M. & Valiela, I. 1977 Interaction of nutrients, plant growth and
herbivory in a mangrove ecosystem. Ecology 58, 514526.
Ovalle ARC, Rezende CE, Lacerda LD, Silva CAR, 1990, Factors affecting the
hydrochemistry of a mangrove tidal creek, Sepetiba Bay, Brazil. Estuar Coast
Shelf Sci 31 : 639650
Ovalle, A.R.C., Rezende, C.E., Lacerda, L.D. and Silva, C.A.R. 1991.
Hydrochemistry of a mangrove tidal creek in Sepetiba Bay, Rio de Janeiro,
Brazil. Estuarine, Coastal and Shelf Science 31: 639650.
Parsons,W., Taylor, B.R., Parkinson, D., 1990. Decomposition of aspen (Populus
tremuloides) leaf litter modified by leaching. Can. J. For. Res. 20, 943951.
Patrick, Wm. H., Jr. and I.C. Mahapatra. 1968. Transformation and availability to rice
of nitrogen and phosphorus in waterlogged soils. Adv. Agron. 20: 323-359


Perdomo, L., Ensminger, I., Espinos, L.F., Elsters, C., Wallner-Kersanach, M.,
Schnetters, M.L., 1998. The mangrove ecosystem of the Cienaga Grande de
Santa Marta (Colombia): Observations on regeneration and trace metals in
sediment. Marine Pollution Bulletin 37, 393403.
Preda, M., and

Cox, M.E., 2002. Trace metal occurrence and distribution in

sediments and mangroves, Pumicestone region, southeast Queensland,

Australia. Environment International 28, 433449.
Ramanathan AL 1998 Mangrove forest: A Brief Overview. In: Recent trends in
Environmental Biogeochemistry (Ed.), Subranamian V., ENVIS publication,
New Delhi, India pp 195-205.
Ramanathan AL 1999 Environmental geochemistry of Pichavaram Mangrove
ecosystem(tropical), southeastcoast of India, Environmental Geology 37(3)
Revsbech, N. P., Sorensen, J., Blackburn, T. H. & Lomholt, J. P. 1980 Distribution of
oxygen in marine sediments measured with microelectrodes. Limnology and
Oceanography 25, 403411.
Richardson, C. J. & J. A. Davis, 1987. Natural and artificial wetland ecosystems:
Ecological opportunities and limitations. In Reddy, K. R. & W. H. Smith (eds),
Aquatic Plants for Water Treatment and Resource Recovery. Magnolia
Publishing, Florida: 819854.
Rivera-Monroy, V.H. , J.W. Day, R. Twilley, F. Vera-Herrera And C. CoronadoMolina. 1995. Flux Of Nitrogen And Sediments In A Fringe Mangrove Forest
In Terminos Lagoon, Mexico. Estuarine, Coastal and Shelf Science 40: 139160
Robertson, A.I. and Blaber, S.J.M. 1992. Plankton, epibenthos and fish communities.
pp. 173224. In: Robertson, A.I. and Alongi, D.M. (eds), Tropical Mangrove
Ecosystems Coastal and Estuarine Series 41. American Geophysical Union,
Robertson, A.I., 1986. Leaf-burying crabs: their influence on energy flow and export
from mixed mangrove forests (Rhizophora spp.) in northeastern Australia.
Journal ofExperimental Marine Biology and Ecology 102:237-248.


Robertson, A.I., Alongi, D.M. and Boto, K.G. 1992. Food chains and carbon fluxes.
pp. 293326. In: Robertson, A.I. and Alongi, D.M. (eds), Tropical Mangrove
Ecosystems Coastal and Estuarine Series 41. American Geophysical Union,
Washington. Alongi, D.M. 1998. Coastal Ecosystem Processes. CRC Press,
Boca Raton, Florida.

R., Loo L., 1988, Marine eutrophication induced oxygen deficiency:effects on soft bottom fauna,

western Sweden, Ophelia, 29, 213225

Rosenberg, R. and Loo, L.O. 1988. Marine eutrophication induced oxygen deficiency:
effects on soft bottom fauna, western Sweden. Ophelia 29: 213225
Rosenfeld, J. F. 1979 Ammonium adsorption in near-shore anoxic sediments.
Limnology and Oceanography 24, 356364.
Rutgers van der Loeff, 1984. The asphyxiation technique: an approach to
distinguishing between molecular diffusion and biologically mediated
transport at the sediment-water interface. Limnology and Oceanography
29: 675686.
Rysgaard, S., Christensen, P.B. and Nielsen, L.P. 1995. Seasonal variation in
nitrification and denitrification in estuarine sediment colonized by benthic
microalgae and bioturbating infauna. Marine Ecology Progress Series 126:
Sadiq Muhammad and

Zaidi T.H. 1994 Sediment composition and metal

concentrations in mangrove leaves from the Saudi coast of the Arabian Gulf ,
The Science of the Total Environment 155 1-8
Sadiq, M.1992. Toxic Metal Chemistry in Marine Environ- ments. Marcel Dekkar,
Inc., New York.
Sarala Devi, K., Venugopal, P., Remani, K., Zacharias. D.. and Unnithan, R.V., 1983.
Nutrients in some estuaries of Kerala. Mahasagar 16: 161-173
Schories, D. Kadler, S. Meeben I. and Mehling U. Phytoplankton Chlorophyll a and
seston variability in a small mangrove tidal creek near Braganca(PA, North
Brazil) Wetland Ecology and Management (submitted).


Seitzinger, S.P. and C. Kroeze. 1998. Global distribution of nitrous oxide production
and N inputs in freshwater and coastal marine ecosystems. Global
Biogeochemical Cycles 12(1): 93-113.
Sherman, R.E., Fahey, T.J., Howarth, R.W., 1998. Soilplant interactions in a
neotropical mangrove forest: iron, phosphorus and sulfur dynamics. Oecologia
115, 553563.
Shriadah ,M.M.A.1999, Heavy Metals in mangrove Sediments of the United Arab
Emirates Shoreline (Arabain Gulf) Water Air and Soil Pollution 116:523-534
Silva, C.A.R. 1992. Formas e taxas de ciclagem do fosforo no ecossistema
manguezal de Itacurussa, Baia de Sepetiba, RJ. PhD thesis. Universidade
Federal de Sao Carlos, 100 pp.
Silva, C.A.R. andMozeto, A.A. 1997. Release and retention of phosphorus in
mangrove sediments: Sepetiba Bay, Brazil. 179190. In: Kjerfve, B., Lacerda,
L.D. and Diop, E.H.S. (eds), Mangrove Ecosystem Studies in Latin America
and Africa. United Nations Educational Publisher, The Hague.
Silva, C.A.R., Lacerda, L.D., Rezende, C.E., 1990. Heavy metal reservoirs in a red
mangrove forest. Biotropica 22, 339345. Clark, M.W., McConchie, D.,
Lewis, D.W., Saenger, P., 1998. Redox stratification and heavy metal
partitioning in Avicennia-dominated mangrove sediments: a geochemical
model. Chemical Geology 149, 147171.
Silva, C.A.R., Lacerda, L.D., Silva, L.F.F. and Rezende, C.E. 1991. Forest structure
and biomass distribution in a redmangrove stand, Sepetiba Bay, Rio de
Janeiro. Revista Brasileira de Botanica 14: 2125.
Silva, M.L.N., Curi, N., Blancaneaux, P., Lima, J.M. and Carvalho, A.M. 1977. Rotac
ao adubo verde: milho e adsorc ao de fosforo em latossolo vermelhoescuro.
Pesquisa Agropecuaria brasileira, Brasilia 32: 649654.
Simpson, J.H., Gong, W.K. and Ong, J.E. 1997. The determination of the net fluxes
from a mangrove estuary system. Estuaries 20: 103109.
Sorensen, J. 1978. Denitrification rates in a marine sediment as measured by the
acetylene inhibition technique. Appl. Environ. Microbial. 36: 139-143.


Steinke, T.D., Holland, A.J., Singh, Y., 1993. Leaching losses during decomposition of
mangrove leaf litter. S. Afr. J. Bot. 59, 2125.
Sundby, B., Gobeil, C., Silverberg, N. & Mucci, A. 1992 The phosphorus cycle in
coastal marine sediments. Limnology and Oceanography 37, 11291145.
Sweerts, J.P.R.A., Kelly, C.A., Rudd, J.W.M., Hesslein, R. and Cappenberg, T.E.
1991. Similarity of whole-sediment molecular diffusion coefficients in
freshwater sediments of low and high porosity. Limnology and Oceanography
36: 335342.
Tam N.F.Y 1996 Retention and distribution of heavy metals in mangrove soils
receiving wastewater., Environmental Pollution, 94 (3):283-291,
Tam, N. F. Y. & Y. S.Wong, 1993. Retention of nutrients and heavy metals in
mangrove sediment receiving wastewater of different strengths. Envir.
Technol. 14: 719729.
Tam, N.F.Y., Wong, W.S., 2000. Spatial variation of heavy metals in surface
sediments of Hong Kong mangrove swamps. Environmental Pollution 110,
Taylor, B.R., Barlocher, F., 1996.Variable effects of air-drying on leaching losses from
tree leaf litter. Hydrobiologia 325, 173182.
Thamdrup, B., 2000, Bacterial manganese and iron reduc:ion in 3.quatic sediments, in

in Microbial Ecology, vol. 16 (ed. B. Schink), Kluwer

Academic /Plenum Publishers, New York, pp.41-84

Thode-Andersen, S. and Jrgensen, B.B., 1989, Sulfate reduction and the formation
of 35S-labeled FeS, FeS2, and So in coastal marine sediments. Limnology and
Oceanography, 34, 793-806.
Trattner, R. B. & S. J. E. Woods, 1989. The use of wetlands systems for municipal
wastewater treatment. In Cheremisinoff, P. N. (ed.), Encyclopedia of
Environmental Control Technology Vol. 3, Wastewater Treatment Technology.
Gulf Publishing Co., Houston: 591622.


Twilley, R. R., Lugo, A. E. & Patterson-Zucca, C. 1986a Litter production and

turnover in basin mangrove forests in southwest Florida. Ecology 67, 670
Twilley, R.R. 1985., The exchange of organic carbon in basin mangrove forests in a
southwest Florida estuary. Estuarine, Coastal and Shelf Science 20: 543557.
Twilley, R.R., Ejdung, G., Romare, P., Kemp, W.M., 1986 b. A comparative study of
decomposition, oxygen consumption, and nutrient release for selected aquatic
plants occuring in an estuarine environment. Oikos 47, 190198.
Varela, M. and Penas, E., 1985. Primary production of benthic microalgae in an
intertidal sand flat of the Ria de Arosa, NW Spain. Marine Ecology Progress
Series 25: 111119.
Wafar, S., Untwale, A. G. & Wafar, M., 1997, Litter fall and energy flux in a
mangrove ecosystem. Estuarine, Coastal and Shelf Science 44, 111124.
Wattayakorn, G., Wolanski, E. and Kjerfve, B. 1990. Mixing, trapping and outwelling
in the Klong Ngao mangrove swamp, Thailand. Estuarine, Coastal and Shelf
Sciences 31: 667688.
Wolanski, E., King, B. and Galloway, D. 1995. Dynamics of the turbidity maximum
in the Fly River estuary, Papua New Guinea. Estuarine, Coastal and Shelf
Science 40: 321337.
Wong, C. H. 1984: Mangrove aquatic nutrients. InProductivity of Mangrove
Ecosystem: Management Implications, ed. by J. E. Ong and W.-K. Gong,
Universiti Sains Malaysia, Penang. . p. 6068
Wong, Y. S., C. Y. Lan, G. Z. Chen, S. H. Li, X. R. Chen, Z. P. Liu & N. F. Y. Tam,
1995. Effect of wastewater discharge on nutrient contamination of mangrove
soils and plants. Hydrobiologia 295: 243254.
Zabetoglou, K., Voutsa, D., Samara, C., 2002. Toxicity and heavy metal
contamination of sur.cial sediments from Bay of Thessaloniki (Northwestern
Aegean Sea) Greece. Chemosphere 49, 1726.


Zeitschel B (1980) Sediment-water interactions in nutrient dynamics.In: Tenore KR,

Coull BC (eds) Marine enthic dynamics. Univ. South Carolina Press, pp195