Direct impacts
Extraction of maerl
Extraction of maerl, either from beds where live thalli are present or where the maerl
is dead or semi-fossilised, has been carried out in Europe for hundreds of years.
Initially, the quantities extracted were small, being dug by hand from intertidal banks,
but in the 1970s c. 600,000 tonnes of maerl was extracted per annum in France alone
(Briand, 1991). Amounts have declined to c. 500,000 tonnes p.a. since then. Live maerl
extraction is obviously very problematic with regard to growth rates for replacement. Dead
maerl extraction is liable to lead to muddy plumes and excessive sediment load in water
that later settles out and smothers surrounding communities. 'Commercial dredging of maerl deposits is particularly
destructive since this removes the productive surface layer and dumps sediment on any
plants which escape dredging, inhibiting habitat recovery' (Hall-Spencer, 1994).
Case studies UK
In the Fal the Cornish Calcified Seaweed Co. has extracted dead maerl since 1975. Only
the dead maerl is taken, and the most serious danger to the important St Mawes bank has
therefore been thought to be the settling out of the dredge plume (Anon., 1993). The
company has attempted to minimise damage by dredging only on the ebb tide so that the
plume was taken out to sea. Reports on the maerl beds made over the last 15 years (e.g.
Farnham & Bishop, 1985) have indicated that the flora and fauna are very diverse.
However, direct comparisons of the flora with that of maerl in Galway Bay (Rostron, 1988;
see summary table) show that the Fal beds are less species-rich than those in Galway Bay.
It is not known whether this is related specifically to effects of dredging. Perrins et
al. (1995) reported that between 1982 and 1992 the proportion of dead maerl on the St
Mawes bank increased significantly, from 12% to 23%.
Hardiman et al. (1976) attempted to assess the effects of maerl dredging in the
Fal by taking core samples. They found black anaerobic mud under the living maerl, the
amount of mud increasing towards the main river channel. They apparently advocated the
removal of maerl as it provided a poor settlement ground for oysters!
Case studies elsewhere
A report prepared for IFREMER on the maerl beds at Brest, Brittany (Augris &
Berthou, 1990), suggested that due to the very slow rate of growth, maerl beds develop
very slowly. The biological equilibrium is precarious - effectively, maerl extraction is
the exploitation of a non-renewable resource as the slow rate of growth implies a slow
rate of accumulation. Grall & Glémarec (1997) compared various indices of biological
health for exploited and control maerl beds at the isles of Glénan, and found few
significant differences except for a reduction in the number of individuals of each
species counted in samples.
Fish farms
The positioning of cages over a maerl biotope is likely to lead to fish faeces and
partly consumed food pellets contaminating the maerl bed and resulting in anaerobiosis due
to the oxygen demand of the decomposing material. The detrital rain from the cages could
act in a similar way to terrigenous silt, reducing light penetration through the water
column and smothering the maerl surface so that the stabilizing epiphytic algae could no
longer establish themselves. As a minimum impact the increase in nutrient levels might
produce local eutrophication effects.
Case studies UK
SNH reported in Marine Scene (Autumn 1996) that part of Loch Ailort was surveyed
to establish a location where the development of a mussel farm would not affect the maerl
beds present in the area. Monitoring of a salmon farm anchored over a maerl bed in
Shetland has shown a buildup over a 10-year period of Beggiotoa and anoxic
conditions (J. Hall-Spencer, pers. comm.).
Case studies elsewhere
In Ardmore Bay, Kilkieran Bay, Co. Galway, fish cages are anchored over maerl beds in
one area. Current speed seems to be sufficient to clear detrital material and the maerl
has not suffered obvious damage (B. O'Connor,
pers. comm.). However, at a sheltered site at Mweenish Island, also in Co. Galway, Maggs
& Guiry (1987a) noted that maerl under fish cages was covered with Beggiotoa
and fungi.
In the Galician rias, Spain, mussel rafts have affected maerl beds (J. Hall-Spencer,
pers. comm.). Mussel faeces and pseudofaeces rain down onto the maerl surface, altering
sediment structure and compromising the ability of maerl thalli to photosynthesise and
grow - work is ongoing under the BIOMAERL programme to evaluate this damage.
Scallop dredging
The removal of the living maerl thalli from the biotope surface, the loss of the
stabilising algae and the disruption of the structure of both the physical habitat and the
community structure occur. These major changes have been reported from areas where
scallops are dredged from maerl beds (Hily et al., 1992; Hall-Spencer, 1995a,
1998).
Case studies UK
The effects of scallop (Pecten maximus) dredging in the upper Firth of Clyde,
where maerl beds are rare, has been evaluated by Hall-Spencer (1995a, 1998), using video
and direct observation. Passage of the dredges destroyed large animals and algae and
raised particulate sediments into the water, which later settled over a large area,
stressing filter feeders and reducing photosynthesis. Dredge teeth penetrated 10 cm into
the maerl, crushing maerl fragments and killing them by burial. Four months after dredging
there were less than half as many live maerl thalli as in control undredged areas. There
was evidence that the community structure was altered in favour of opportunistic species
such as scavengers. Overall, the effect of scallop dredging on maerl beds was very
serious, with the effects on living maerl compromising habitat integrity and future
recovery.
Case studies elsewhere
In the rade de Brest the maerl beds support populations of the black scallop Chlamys
varia, which are locally abundant and are intensively fished during the winter months.
The dredging activity has been reported to result in severe disruption to the maerl bed
and associated flora and fauna (Hily & Le Fol, 1990).
Suction dredging of bivalves
One of the biggests threats to live and dead maerl beds is suction dredging for large
burrowing bivalves such as Ensis and Venerupis species, which are marketed
in Spain (D. McKay, pers. comm.). Suction dredging not only has major impacts on the
target species, but causes structural damage to the community from which they are being
extracted. The detrimental effects on maerl beds are expected to include impacts of
resuspended sediment settling out over the maerl and reducing photosynthesis.
Case studies UK and elsewhere
Along the west coast of Scotland, sublittoral harvesting of Venerupis has
occurred in the North Sound, Arisaig, and Ensis has been harvested at various
locations including Shetland and Orkney (D. McKay, pers. comm.). Suction dredging for
these species causes disruption of the substratum to considerable depths, creating holes
up to 2 m across and 1 m deep in sandy substrata. Comparable studies have not been made in
maerl habitats, however.
Channel dredging
In order to renew or enlarge navigational channels, extensive dredging may take place.
This involves removing the seabed, which results in the suspension of the fine silt and
clay fractions of the sediment. This fine sediment may be deposited by the inshore
currents either locally or at a considerable distance from the dredging operation. The
additional sediment load will increase local turbidity and may also settle on maerl beds,
burying the calcareous thalli, smothering other algae and animals, possibly destroying the
physical stability of the habitat as well as the ecology of the biotope. Seabed removal
where a maerl bed is present will of course result in the removal of the maerl itself. If
the underlying substratum is altered, it is unlikely that maerl will be able to
re-establish itself at that site, given the probable method of reproduction of the species
involved.
No case studies are known.
Coastal construction and land fill
The results of these activities would be similar to those mentioned above, such as
removal of the seabed, redistribution of mud, and destroying the biotope stability and
viability.
No case studies are known.
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References
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