What is Biodiversity?
Biodiversity is defined as “the
variability among living organisms from all sources and ecosystems and the ecological complexes of which they
are a part this includes diversity within species, between species and
between ecosystems.” (United Nations, 1992). Human factors such as fishing
can influence biodiversity in terms of community
composition, species abundance, species
richness, species biomass as well as the distribution and balance of flora and
fauna within an ecosystem(Forester and Machlist, 1996).
What
is Ecosystem Functioning and Services?
The
function of ecosystems can be quantified
by the services and processes that the ecosystem provides. These processes and services provided by an ecosystem
can be summarised by Provisioning
services, regulating services, cultural services, and supporting services. Ecosystem products such as food, water,
shelter, clothing, or genetic resources are
encompassed under provisioning services. Regulating services are service
that aid in the regulation of the ecosystem such as climate, water, and natural
disasters regulation. Supporting services are required for the rest of the
services and functions to run; these
include biomass production, oxygen production, and
carbon sequestration. As well as nutrient cycling and providing habitats for
organisms. Finally, cultural services are
functions that the ecosystem provides which benefit humans. These include
recreation, spiritual improvement as well as learning and aesthetic services.
The
Impacts of Fishing on Biodiversity and Ecosystem Functioning
Anthropogenic impacts are vital drivers
of change within the marine environment. These influences can create pressure and
even loss of the ecosystem services and biodiversity in the marine environment (Coll et al., 2016; Fu
et al., 2015; Halpern et al., 2008, 2012; Sale, 2008; Worm et al., 2006). Fishing
has been shown to be one of the most significant influencers of marine ecosystems,
and it has been suggested that it is also the greatest pressure on biodiversity
(Coll et al., 2016). Fishing
pressures in marine environments can
significantly alter the community composition, the
abundance of flora and fauna of the area,
in addition to the overall species richness (Russ, 1991). Fishing has also been shown to
decrease the biomass of individual
organisms, specifically apex predators as they are
most commonly targeted due to their high biomass. A decrease in biomass
and abundance of top predators, like piscivorous fish can cause trophic cascades and has been shown to be a dominant
feature in exploited ecosystems (Russ, 1991), for example, due to loss of
predators of cownose rays through
overfishing, there was a consequent increase in cownose ray abundance. This increase caused a dramatic decrease in the
Cownose ray’s prey; North Carolina's bay scallop stock which eventually collapsed
the commercial scallop fishery in that area (Myers et al., 2007). This increase in ray population may have been caused by an Allee effect where there is positive density dependence on personal fitness,
wherein the growth rates of individuals is increased by the increased density of the
population. Overfishing, that is
fishing above a sustainable level, can have a pronounced effect on the
biodiversity of an ecosystem along with its essential
functions and services. Overfishing
causes a direct reduction of targeted species
and can result in trophic cascades which ultimately lead to a decrease in biodiversity. For example, removal
of key species with ecosystems can alter the structure of the habitats (Coleman and Williams, 2002). As most of the time, the largest of the fish are targeted during fishing, the size structure and size diversity
of the community might be altered (Rago et al., 1998).
Unfortunately, the overall impact of fishing on biodiversity
and ecosystem services is hard to quantify, due to many variables such as
differences in the ecosystem, location, habitat, as well as other factors.
Another important boundary to quantifying the impact of fishing on the marine
ecosystem is the illegal, unregulated, and unreported fishing (IUU) which
occurs all around the world.
The IUU means that the true impact
and intensity of the fishing is not
easily quantifiable.
As fishing methods
which physically alter the environment are thought to be the main threats to
ecosystem services (Mak et al., 2005), different methods of fishing and the
various impacts they have on different
organisms, ecosystems and their services will be
examined.
The Effect of Different Fishing
Methods on Biodiversity and Ecosystem Functioning.
Apex Predator Fishing
Apex predators
are predominantly hypercarnivores, which means
that more than 70% of their diet consists of prey items that are at the top of the ecosystem trophic pyramid.
Apex predators are often targeted during fishing on coral reefs, as their high
biomass often makes their catch a lucrative business. It has been quantified that anthropogenic effects in
the marine environment have led to a
decline in 90% of the apex predator abundance (Myers and Worm, 2003). It has also been suggested that
the most significant influencer on the
apex predators is commercial fishing (Jones et al., 2009). The removal of apex predators
creates instability in the ecosystem food web, as they can affect the behaviour and population dynamics of the organisms
in the lower trophic levels and therefore the biomass of these organisms (Dulvy et al., 2004). In response to fishing pressure
in Coral Reefs, the biomass of critical groups of organisms has been shown to change with
both light and intensive exploitation. Under both light and intense fishing pressures,
the biomass of piscivorous fish (fish which eat other fish) decreases the most,
with the biomass of herbivorous and invertebrate feeding fish also decreasing. Invertebrates
biomass has been shown to increase, probably due to not being directly targeted
during light and intense fishing (Jennings and Polunin, 1996). In unfished coral reef environments
54% of the biomass was comprised of apex predators such as Sharks and Jacks, whereas, in
areas which had increased fishing pressure, apex predators (mainly piscivorous
fish) accounted for only 3% of total biomass (Friedlander and DeMartini, 2002). It was also found that increased fishing pressure, resulted in a 260%
reduction in overall biomass of fish, and fished areas were dominated by herbivores(Friedlander and DeMartini, 2002). The reduction in these large
apex predators can cause a loss in overall ecosystem biomass which is a
reduction in an ecosystem supporting service as biomass production is a crucial ecosystem function although it can
cause an increase in lower trophic biomass production. A decrease in biomass of
top predators, like piscivorous fish can cause trophic cascades, where the
removal of one high trophic species impacts the abundance of the prey species. Another
impact of fishing on coral reef apex predators is bycatch, whereby a non-targeted
species are caught. It is thought that around 50% of the Elasmobranch
bycatch goes unreported, this makes it
hard to quantify the exact pressure
fishing places on apex predators with the estimated landings of apex predators
at around 1.5 million tonnes (Stevens et al., 2000). Bycatch
of apex predators means that even if a sustainable fishing limit is set for these apex predators, the bycatch is
not quantifiable and therefore the sustainable quota is not likely to be met.
Cyanide
Fishing
Cyanide fishing is a method of fishing in
which sodium cyanide is squirted into the
fishes’ habitat to stun the fish. This fishing method is practised in coral reefs to capture fish for the aquarium trade and
occurs most frequently in Asia. It is not a widely discussed fishing method, and although this process of fishing is illegal in most areas, it is thought that it is still widely used.
Approximately 1 million kilograms of cyanide has been used in fishing on the Philippine
reefs (Mak et al., 2005).
It
has been found that cyanide fishing not
only stuns the fish targeted but can also impact the surrounding area, in particular, corals. Exposure to cyanide has
been shown to cause the bleaching ( the dissociation
of symbiotic zooxanthellae ) in corals and therefore affects the photosynthesis of the zooxanthellae (Jones and Hoegh-Guldberg, 1999). Cyanide treated reefs have been
shown to have a 40% reduction in the density of zooxanthellae compared to
control reefs (Jones et al., 1999). Medium doses of cyanide cause
coral bleaching while light treatments
cause discolouration. It has also been found that high doses of cyanide,
comparable to those used in cyanide fishing, caused complete mortality of the
coral. It was also shown that respiration
rates were dramatically reduced by as much as 90% after cyanide exposure (Jones and Steven, 1997). A
reduction in respiration has implications for the supporting ecosystem
services of a coral reef, as loss of the zooxanthellae and reduced respiration mean that less carbon is being sequestered. Coral reefs are an important carbon sink, and around the world account for 111 million tonnes of carbon per year, any reduction in this amount
would be a reduction in vital the ecosystem function of carbon sequestration. The removal of
fish for the aquarium trade through cyanide fishing may also reduce the
biodiversity of the coral reefs, as certain desirable species may be over-taken
from the reef. This will alter the community structure of the reefs.
Blast
Fishing
Blast fishing is a fishing method whereby
explosives such as dynamite are used to stun the fish, using shockwaves so that
they can be easily retrieved. Although this practice is illegal in many places,
it is thought that blast fishing still
occurs in around 40 countries. It is a particular problem in Tanzania where
explosives are cheap, easy to obtain, and
it provides a lucrative income (Slade and Kalangahe, 2015). However, the blast fishing is altering
the structure of the coral reefs which are a key
source of revenue for Tanzania in the form of tourism. Tourism is a crucial cultural ecosystem service, so by
altering the reef this essential ecosystem service may be impacted. A
FAO and NGO led team was
implemented in 2015 to bring awareness to the issues of blast fishing in Tanzania. However, some studies have shown that there
has not been a reduction in the
occurrence of blast fishing even with this scheme in place (Katikiro and Mahenge, 2016).
Dynamite
or blast fishing not only stuns the fish but also physically changes the
habitat, primarily when used in the vicinity
of coral reefs. The dynamite blast causes parts
of the calcium carbonate skeletons of coral to shatter. Which, often causes
mortality of the hard coral. The main source of restoration is larval supply
from other corals in the vicinity as long as they have not been impacted. Recovery
depends on many factors including the intensity of the blast fishing (Roberts, 1997). Blast fishing is particularly detrimental
to corals as many coral species are not able to recover very well from disturbance which physically alters the habitat
compared to disturbance which does not change the physical environment(Connell, 1997). The disturbance caused by blast fishing can cause a
significant alteration in the community
structure in coral reefs, communities which were
once dominated by calcium carbonate hard coral structures shift to a
composition dominated by algae and soft-bodied
corals such as Xenia spp. (Roberts, 1995).
This shift may be because soft corals
have higher fecundity and more modes of larval dispersion than hard corals. Once
soft corals have colonised an area, it is unlikely to shift back to its
original composition as soft corals hinder the colonisation
of hard-bodied corals(Maida et al., 1995).
This change in structure leads to a
reduction in biodiversity as the soft corals do not provide the same level of
protection and habitat as hard corals(Inoue et al., 2013).
Also, it can cause a reduction in the
biomass of coral reef fishes in the area as reef fish numbers and size is influenced by the coral cover and reef
complexity among other things (Roberts, 1995).
Trawling
Trawling is
the process of pulling a net through the water column often with a beam or
other mechanism to keep the net open, being
dragged across the sea floor. Trawling can impact the marine environment
in multiple ways and have impacts on the biodiversity of the benthos and the ecosystem
functions it provides. The effects of
trawling with equipment like otter trawls and beam trawls have been a cause for
concern since 1376 when the changes to the seabed caused by trawling were brought before the British Parliament (De Groot, 1984). Some of the major issues with trawling; include the capture of non-target species, the ploughing of the substrate, alteration of the
benthos and sediment resuspension. Trawling has also been shown to drive long-term changes to the composition and structure
of the benthos (Jones, 1992). Direct impacts of trawling have been shown to influence the abundance,
biomass and species richness as well as other indicators of biodiversity.
Sedentary fauna such as anemones, sponges, and
bryozoans were found at higher abundances
in areas of un-trawled benthos compared to trawled areas due to the lack of
physical disturbance in un-trawled areas, which could damage these organisms.
Biodiversity and number of niches were found to be greatest in un-trawled regions (McConnaughey et al., 2000). It has also been found that species richness was higher in
un-trawled areas were as species evenness
(similarity) was higher in trawled sites. These finding may be due to un-trawled
zones providing a more complex habitat
compared to trawled areas (Collie et al., 1997).
Trawling
has been shown to have an indirect effect on the length at age of certain
species such as Pleuronectes platessa or the European
Plaice. Plaice were found to be smaller in areas of gravel than in areas of
sand; it is suggested that this is because Plaice in gravel habitats are more
likely to feed on echinoderms and molluscs which are negatively impacted by
trawling. Therefore, leading to a decrease in prey and hence a decrease in growth of these Plaice. Whereas, sand-living Plaice feed
predominantly on polychaetes which are
positively impacted by medium intensity trawling, therefore their growth is
enhanced. This suggests that trawling may
influence an ecosystems biomass production either negatively or positively
depending on the substrate. This may have a severe
consequence for crucial
ecosystem services such as food production (a
key ecosystem product) and may lead to a decline or increase in commercial
fish production (Shephard et al., 2010). Discards from trawling constitute a
significant driver of change in the marine environment (Dayton et al., 1995). Non- targeted
species, which are caught as bycatch are
sometimes used as alternative food sources but are very often thrown back into
the sea. It has been calculated that for some areas, just under 80% of discard would
not survive (Hill and Wassenberg, 2000) and therefore the discard of this dead material can impact the
ecosystem in several ways (Dayton et al., 1995). One impact of trawling discard may be an increase in the abundance of Elasmobranchs and other scavengers
such as seabirds which learn to associate
trawlers with food as they scavenge on the “free food”(Furness et al., 1992). This behaviour may impact the marine food web
in the area as increased predator abundance could decrease the abundance and
biomass of organisms of the lower trophic
levels, this may influence the fisheries landings of that area and therefore
the key ecosystem function of food
production. Almost all the continental margins are now being trawled, however, the
range of trawling is being expanded as
new technology is developed. Increasingly
trawling is occurring in the deep sea. Trawling has been shown to reduce
overall biodiversity by half as well as impacting many ecosystem services such as the organic carbon turnover which
showed a 37% decrease in areas that had been
trawled as well as a decrease of over a half of organic matter. The
abundance of fauna has been shown to decrease up to 82% when the pressure of
deep sea trawling is present (Pusceddu et al., 2014). Some deep-water
fish stocks are being exploited to collapse, so much, so that deep sea fishing (in its
current form) is considered by some as unmaintainable (Davies et al., 2007).
Dredging
Dredges have similar effects to trawls
as they also create physical disturbance
to the seabed by either digging the
sediment or by using jets of water to lift the substrate. The largest dredges can leave 1 by 0.4 m grooves in the sediment, and
some boats can dredge upwards of 30
dredges at the same time, therefore creating a
large impact on the benthos. Dredges are more
effective at slower speeds than trawls, therefore, spending more time in
contact with the seabed.(Kaiser et al., 1996)
Conclusion
Fishing is a major
driver for change within different marine habitats, with fishing having a significant impact on the biodiversity, in terms of reducing the species richness and increasing the
species evenness. Fishing has also been
shown to change the community structure and even the genetic resources of an environment
by the removal or change in essential
species. Fishing also has an impact on
the abundance and biomass of individual species which are both supporting
ecosystem functions. This variation in
biomass of certain species can have a knock-on
effect further down the food web. Thus, fishing can be responsible for altering
the entire community structure. Fishing can also influence other ecosystem
functions such as carbon sequestration and nutrient cycling. Fishing can also
physically modify an environment such as coral reefs, which not only impacts the
fauna and flora inhabiting that area but also on humans who use some marine
habitats to fulfil cultural and social
function such as recreation. Some fishing methods can alter the environment so
much that these cultural services are no longer viable.
References
Coleman, F.C., and Williams, S.L.
(2002). Overexploiting marine ecosystem engineers: potential consequences for
biodiversity. Trends in Ecology &
Evolution 17, 40–44.
Coll, M.,
Shannon, L.J., Kleisner, K.M., Juan-Jordá, M.J., Bundy, A., Akoglu, A.G.,
Banaru, D., Boldt, J.L., Borges, M.F., and Cook, A. (2016). Ecological indicators to capture the effects of
fishing on biodiversity and conservation status of marine ecosystems. Ecological Indicators 60, 947–962.
Collie,
J.S., Escanero, G.A., and Valentine, P.C. (1997). Effects of bottom fishing on the benthic megafauna of Georges Bank.
Marine Ecology Progress Series 155, 159–172.
Connell,
J.H. (1997). Disturbance and recovery of coral assemblages. Coral Reefs 16,
S101–S113.
Davies,
A.J., Roberts, J.M., and Hall-Spencer, J. (2007). Preserving deep-sea natural
heritage: Emerging issues in offshore
conservation and management. Biological Conservation 138, 299–312.
Dayton,
P.K., Thrush, S.F., Agardy, M.T., and Hofman, R.J. (1995). Environmental effects of marine fishing.
Aquatic Conserv: Mar. Freshw. Ecosyst. 5, 205–232.
De Groot,
S.J. (1984). The impact of bottom trawling on benthic
fauna of the North Sea. Ocean Management 9, 177–190.
Dulvy,
N.K., Freckleton, R.P., and Polunin, N.V.C. (2004). Coral reef cascades and the indirect effects of predator removal by
exploitation. Ecology Letters 7, 410–416.
Forester,
D.J., and Machlist, G.E. (1996). Modeling Human
Factors That Affect the Loss of Biodiversity. Conservation Biology 10,
1253–1263.
Friedlander,
A.M., and DeMartini, E.E. (2002). Contrasts in
density, size, and biomass of reef fishes between the northwestern and the main
Hawaiian islands:: the effects of fishing down apex predators. Marine
Ecology Progress Series 230, 253–264.
Fu, C.,
Large, S., Knight, B., Richardson, A.J., Bundy, A., Reygondeau, G., Boldt, J.,
Van Der Meeren, G.I., Torres, M.A., and Sobrino, I. (2015). Relationships among fisheries exploitation,
environmental conditions, and ecological indicators across a series of marine
ecosystems. Journal of Marine Systems 148, 101–111.
Furness,
R.W., Ensor, K., and Hudson, A.V. (1992). The use of fishery waste by gull
populations around the British Isles. Ardea 80, 105–113.
Halpern,
B.S., Walbridge, S., Selkoe, K.A., Kappel, C.V., Micheli, F., D’Agrosa, C.,
Bruno, J.F., Casey, K.S., Ebert, C., Fox, H.E., et al. (2008). A Global Map of Human Impact on Marine Ecosystems. Science 319,
948–952.
Halpern,
B.S., Longo, C., Hardy, D., McLeod, K.L., Samhouri, J.F., Katona, S.K., Kleisner,
K., Lester, S.E., O’Leary, J., and Ranelletti, M. (2012). An index to assess the health and benefits of the global ocean.
Nature 488, 615–620.
Hill,
B.J., and Wassenberg, T.J. (2000). The probable fate of discards from prawn
trawlers fishing near coral reefs: A study in the northern Great Barrier Reef,
Australia. Fisheries Research 48, 277–286.
Inoue,
S., Kayanne, H., Yamamoto, S., and Kurihara, H. (2013). Spatial community shift
from hard to soft corals in acidified water. Nature Climate Change 3, 683.
Jennings,
S., and Polunin, N.V. (1996). Impacts of fishing on tropical reef ecosystems.
Ambio 44–49.
Jones,
J.B. (1992). Environmental impact of trawling on the seabed: A review. New
Zealand Journal of Marine and Freshwater Research 26, 59–67.
Jones, R.J.,
and Hoegh-Guldberg, O. (1999). Effects of cyanide on coral photosynthesis:
implications for identifying the cause of coral bleaching and for assessing the
environmental effects of cyanide fishing.
Marine Ecology Progress Series 83–91.
Jones,
R.J., and Steven, A.L. (1997). Effects of cyanide on corals in relation to cyanide fishing on reefs. Marine
and Freshwater Research 48, 517–522.
Jones,
E., Gray, T., and Umponstira, C. (2009). The impact of artisanal fishing on
coral reef fish health in Hat Thai Mueang, Phang-nga Province, Southern
Thailand. Marine Policy 33, 544–552.
Jones,
R.J., Kildea, T., and Hoegh-Guldberg, O. (1999). PAM chlorophyll fluorometry: a
new in situ technique for stress assessment in scleractinian corals, used to
examine the effects of cyanide from cyanide fishing. Marine Pollution Bulletin 38,
864–874.
Kaiser,
M.J., Hill, A.S., Ramsay, K., Spencer, B.E., Brand, A.R., Veale, L.O., Prudden,
K., Rees, E.I.S., Munday, B.W., and Ball, B. (1996). Benthic disturbance by fishing gear in the Irish Sea: a comparison of beam
trawling and scallop dredging. Aquatic Conservation: Marine and
Freshwater Ecosystems 6, 269–285.
Katikiro,
R.E., and Mahenge, J.J. (2016). Fishers’ Perceptions of the Recurrence of
Dynamite-Fishing Practices on the Coast of Tanzania. Frontiers in Marine Science 3, 233.
Maida,
M., Sammarco, P.W., and Coll, J.C. (1995). Effects
of soft corals on scleractinian coral recruitment. I: Directional allelopathy
and inhibition of settlement. Marine Ecology Progress Series 191–202.
Mak,
K.K., Yanase, H., and Renneberg, R. (2005). Cyanide fishing and cyanide
detection in coral reef fish using chemical tests and biosensors. Biosensors
and Bioelectronics 20, 2581–2593.
McConnaughey,
R.A., Mier, K.L., and Dew, C.B. (2000). An
examination of chronic trawling effects on soft-bottom benthos of the eastern Bering Sea. ICES J Mar Sci 57,
1377–1388.
Myers,
R.A., and Worm, B. (2003). Rapid worldwide depletion of predatory fish communities.
Nature 423, 280–283.
Myers,
R.A., Baum, J.K., Shepherd, T.D., Powers, S.P., and Peterson, C.H. (2007). Cascading effects of the loss of apex predatory
sharks from a coastal ocean. Science 315, 1846–1850.
Pusceddu,
A., Bianchelli, S., Martín, J., Puig, P., Palanques, A., Masqué, P., and
Danovaro, R. (2014). Chronic and intensive bottom trawling impairs deep-sea
biodiversity and ecosystem functioning. PNAS 111, 8861–8866.
Rago,
P.J., Sosebee, K.A., Brodziak, J.K.T., Murawski, S.A., and Anderson, E.D.
(1998). Implications of recent increases
in catches on the dynamics of Northwest Atlantic spiny dogfish (Squalus
acanthias). Fisheries Research 39, 165–181.
Roberts, C.M. (1995). Effects of Fishing on the Ecosystem
Structure of Coral Reefs.
Conservation Biology 9, 988–995.
Roberts,
C.M. (1997). Connectivity and management of Caribbean coral reefs. Science 278,
1454–1457.
Russ,
G.R. (1991). Coral reef fisheries: effects and yields. In The Ecology of Fishes on Coral Reefs, (Elsevier), pp. 601–635.
Sale, P.F.
(2008). Management of coral reefs: where we have gone wrong and what we can do
about it. Marine Pollution Bulletin 56, 805–809.
Shephard,
S., Brophy, D., and Reid, D.G. (2010). Can bottom trawling indirectly diminish carrying capacity in a
marine ecosystem? Mar Biol 157, 2375–2381.
Slade,
L.M., and Kalangahe, B. (2015). Dynamite fishing in Tanzania. Marine Pollution
Bulletin 101, 491–496.
Stevens,
J.D., Bonfil, R., Dulvy, N.K., and Walker, P.A. (2000). The effects of fishing on sharks, rays, and chimaeras
(chondrichthyans), and the implications for marine ecosystems. ICES J
Mar Sci 57, 476–494.
United
Nations (1992). UN Conference on Environment and Development, Rio de Janerio
1992, Convention on Biodiversity, Aricle 2. p.
Worm, B.,
Barbier, E.B., Beaumont, N., Duffy, J.E., Folke, C., Halpern, B.S., Jackson,
J.B.C., Lotze, H.K., Micheli, F., Palumbi, S.R., et al. (2006). Impacts of Biodiversity Loss on Ocean Ecosystem
Services. Science 314, 787–790.
No comments:
Post a Comment