Abstract
The seagrass beds in the mangrove-fringed shallow coastal waters
of Hinchinbrook Channel, Australia, survive in shallow coastal
waters. They are sheltered from excessive sedimentation and turbidity
by the plankton and vegetative detritus generating a marine snow
that accelerates the settling of fine mud out of suspension.
Introduction
Mangrove-fringed coastal waters in a number of embayments in
tropical Australia are often very turbid, with visibility reduced
to a few cm in inter-tidal waters. Below the mean sea level, sometimes
only tens of meters from the coast, extensive seagrass beds are
found. Such is the case in Hinchinbrook Channel near Cardwell,
Cleveland Bay near Townsville and Trinity Bay near Cairns. At
some sites the seagrass is not found closer inshore for a number
of reasons including occasional desiccation, excessive turbidity
and minimal light, and storm-induced liquefaction of the bottom.
High sedimentation in other locations has damaged or destroyed
seagrass beds (Onuf, 1994; Schoellhamer, 1996). The seagrass
thus survives in a potentially very hostile environment. The
aim of this paper is to identify the physical processes that help
the seagrass to survive.
Methods
The field study site was the mangrove-fringed Hinchinbrook Channel
near Cardwell (Fig. 1). An oceanographic mooring was deployed
at site 1 for 5 weeks in July-August 1996 and January-February
1997. The mooring included an Inter-Ocean model S4 current meter
and 4 nephelometers spread between 0.2 to 1.8 m above the bottom.
The nephelometers were calibrated in-situ to yield the suspended
sediment concentration (SSC). Vertical profiles of temperature,
salinity and SSC were obtained at stations using a SeaBird CTD
equipped with a nephelometer that was also calibrated in-situ.
Microphotographs of the sediment in suspension were obtained
using the technique described by Wolanski and Gibbs (1995).
Results
The shallow coastal waters, especially the inter-tidal areas, were extremely turbid, both in the dry and the wet season but only at spring tides. The mooring data show the near-bottom suspended sediment concentration (SSC) reaching 1 kg m-3 (1000 ppm; Fig. 2), but only during peak tidal currents at spring tides. At such times visibility was less than 2 cm. The rest of the time during spring tides, as well as throughout the neap tides, the SSC values were small and visibility at times exceeded 1 m.
The high turbidity zone, when it was found, was restricted to a narrow band along the coast (Fig. 1). This turbid coastal water was named the coastal boundary layer by Wolanski and Ridd (1990). This water, shared between the mangroves and the ocean, mixes very slowly with offshore waters and thus provides a buffer between the mangroves and offshore waters (Wolanski et al., 1990). The formation of a coastal boundary layer is due to the effect of bottom friction in shallow coastal waters.
The coastal boundary layer was about 800 m wide and was identified by its high turbidity with suspended sediment concentration commonly exceeding 0.04 kg m-3 (Fig. 1) and peaking at 1 kg m-3 (Fig. 2). This layer was parallel to the mangrove-fringed coast without diffusing offshore. In this layer the settling zone was made readily visible by a turbidity front separating clear water offshore from turbid water inshore (Fig. 3), this front was found about 100 m offshore and then only at spring, ebb tides.
The state of the fine sediment in suspension varied greatly from
spring to neap tides. During neap tides, there was practically
no sediment in suspension at that time. Oceanic water was found
throughout the channel. The small amount of fine sediment was
transported in suspension mainly as marine snow, the bacteria,
plankton detritus and mucus acting as a coagulant for the fine
sediment (Ayukai and Wolanski, 1997). In contrast, during spring
tides, mangrove detritus was exported into the coastal boundary
layer; there this organic nucleus aggregated the sediment particles
and the small inorganic flocs into huge flocs (Fig. 4). These
we call "mangrove flocs" and were only found in the
coastal boundary layer.
Discussion
The mangrove-fringed channel is shallow. Seagrass is common at least on the western side and can be found at some sites just below the low tide elevation. Our findings demonstrate that the terrigenous fine sediment in this location is transported in suspension in any quantity only during spring tides. However this material does not extend far offshore under non-storm conditions. In coastal waters the mean diameter of the suspended sediment flocs is several hundreds of microns (Fig. 4) as opposed to a few tens of microns elsewhere. As a result of the increased floc size, the sediment rapidly settles out (Gibbs, 1985). This rapid settling of the sediment is apparent from the time series data of SSC at the mooring site, the sediment clearly settling out in 4 m of water in 1 hour after peak spring tidal currents. This corresponds to a settling velocity of about 0.1 cm s-1. This velocity is 100-1000 times faster than that of the unflocculated mud particles, and 10 times faster than that of the small flocs found elsewhere. Near the coast in the settling zone, the turbidity is the largest. This shelters the waters further offshore from high sedimentation and excessive turbidity.
There are thus two competing gradients of environmental stress for the seagrass. Firstly, the suspended sediment concentration decreases with distance offshore - this would favour seagrass. And secondly, the depth increases with distance offshore, hence light is reduced at the bottom, and this is unfavourable to the seagrass. The location for optimum growth of seagrass can then vary seasonally and from site to site according to the bathymetry and the sediment dynamics.
At Hinchinbrook, this mechanism presumably is the process enabling the existence of seagrass beds immediately offshore from the extremely muddy coast.
The formation of macro-aggregates is important because it accelerates settling. When the macro-aggregates are formed by oceanic plankton, the terrigenous sediment is trapped in a coastal plume which can be several km wide (the Amazon river plume, Berhane et al., 1997; the Fly River plume, Ayukai and Wolanski, 1997; the Dutch coastal zone, Eisma et al., 1990; the North Carolina coastal zone, Wells, 1989). Our study demonstrates that the mangroves accelerate the formation of macro-aggregates. Along a mangrove-fringed coast the width of the fine sediment trapping zone is greatly reduced, occurring over scales of tens to hundreds of meters. Much of the fine, terrigenous sediment does not even reach the 5 m depth contour and is trapped in shallower waters of the settling zone. The mangrove flocs may later be recirculated back into mangroves where they settle (Furukawa and Wolanski, 1996).
Seagrass beds cannot survive in areas of high turbidity (Onuf, 1994; Schoellhamer, 1996). In mangrove-fringed coastal waters the coastal boundary layer acts as a sponge layer for fine terrigenous sediment, the mangrove flocs accelerating the settling of terrigenous sediment. Inshore, high turbidity, desiccation and bottom liquefaction prevent or inhibit seagrass. Offshore, seagrass is found due to the waters being clear or, when turbid, the high turbidity occurs only for a short period (Fig. 5). The width of the sediment settling zone where seagrass is inhibited can vary from location to location as it is likely to depend on a number of parameters such as the mean water depth, the stability of the bed and the stress due to desiccation and/or excessive sedimentation.
In the shallow coastal waters of Hinchinbrook channel the existence of seagrass beds is apparently due to the accelerated settling of fine sediment. Presumably a similar process protects the seagrass in other mangrove-fringed coastal embayments along the tropical coast of Australia, including Cleveland Bay near Townsville and Trinity Bay near Cairns.
The coastal boundary layer in Hinchinbrook Channel is shore-parallel
because the coastline is mostly straight without headlands. As
a result the prevailing currents are also shore-parallel. These
currents will be deflected by engineering structures such as seawalls
or dredged channels. This will bring terrigenous sediment -and
decreased light- further offshore over the offshore seagrass
beds where the light would be limited because of greater depth.
This added sediment will further decrease light and the offshore
seagrass beds may thus become affected. The inshore seagrass
may be influenced by increased settling in the presence of seawalls
and increased turbulence in the presence of a dredged channel.
Acknowledgments
This research was supported by the Australian Institute of Marine
Science, the Kansai Electric Production Corporation - Kansai Environmental
Engineering Company, and the IBM International Foundation.
References
Ayukai, T. & E. Wolanski (1997). Importance of biologically
mediated removal of fine sediments from the Fly River plume, Papua
New Guinea. Estuarine, Coastal and Shelf Science, in press.
Berhane, I., Sternberg, R.W., Kineke, G.C., Milligan & T.G.,
Kranck, K. (1997). The variability of suspended aggregates on
the Amazon continental shelf. Continental Shelf Research,
17, 267-285.
Eisma, D., T. Schuhmacher, H. Boekel, J. van Heerwaarden, H.
Franken, M. Laan, A. Vaars, F. Eugenraam & J. Kalf (1990).
A camera and image analysis system for in situ observations of
flocs in natural waters. Netherlands Journal of Sea Research,
27: 43-56.
Furukawa, K. & E. Wolanski (1996). Sedimentation in mangrove
forests. Mangroves and Salt Marshes, 1: 3-10.
Gibbs, R.J. (1985). Estuarine flocs: Their size, settling velocity
and density. Journal of Geophysical Research, 90: 3249-3251.
Onuf, C.P. (1994). Seagrasses, dredging and light in Laguna Madre,
Texas, U.S.A. Estuarine, Coastal and Shelf Science, 39,
75-92.
Schoellhamer, D.H. (1996). Anthropogenic sediment resuspension
mechanisms in a shallow microtidal estuary. Estuarine, Coastal
and Shelf Science, 43, 533-548.
Wells, J.T. (1989). In-situ measurements of large aggregates
over a fluid-mud bed. Journal of Coastal Research, 5:
75-86.
Wolanski, E. & Ridd, P. (1990). Mixing and trapping in
Australian tropical coastal waters. Coastal and Estuarine
Studies, Springer-Verlag, 38: 165-183.
Wolanski, E. & R.J. Gibbs (1995). Flocculation of suspended
sediment in the Fly River estuary, Papua New Guinea. Journal
of Coastal Research, 11, 754-762.
Wolanski, E., Y. Mazda, B. King & S. Gay (1990). Dynamics,
flushing and trapping in Hinchinbrook channel, a giant mangrove
swamp. Estuarine, Coastal and Shelf Science, 31: 555-580.
Figures






Last updated: 13th May 1997
All contents copyright (C) 1997, AIMS.All rights reserved.