Impacts On Marine Life
Impacts On Marine Life
Impacts On Marine Life
a r t i c l e i n f o a b s t r a c t
Article history: Marine debris is listed among the major perceived threats to biodiversity, and is cause for particular con-
Available online 10 February 2015 cern due to its abundance, durability and persistence in the marine environment. An extensive literature
search reviewed the current state of knowledge on the effects of marine debris on marine organisms. 340
Keywords: original publications reported encounters between organisms and marine debris and 693 species. Plastic
Ocean litter debris accounted for 92% of encounters between debris and individuals. Numerous direct and indirect
Garbage consequences were recorded, with the potential for sublethal effects of ingestion an area of considerable
Biodiversity
uncertainty and concern. Comparison to the IUCN Red List highlighted that at least 17% of species affected
Harm
Mortality
by entanglement and ingestion were listed as threatened or near threatened. Hence where marine
Microplastics debris combines with other anthropogenic stressors it may affect populations, trophic interactions and
assemblages.
Ó 2015 Elsevier Ltd. All rights reserved.
http://dx.doi.org/10.1016/j.marpolbul.2014.12.041
0025-326X/Ó 2015 Elsevier Ltd. All rights reserved.
S.C. Gall, R.C. Thompson / Marine Pollution Bulletin 92 (2015) 170–179 171
areas, and also the fragmentation of plastic debris into pieces smal- 2011), in particular coral reefs (Al-Jufaili et al., 1999; Chiappone
ler than those routinely sampled. et al., 2005; Chiappone et al., 2002; Donohue et al., 2001;
The impact of marine debris on marine life is of particular con- Richards and Beger, 2011). Particular concern is associated with
cern, and effects can be wide reaching (Fig. 1), with the conse- species listed on the IUCN Red List as these are at the greatest risk
quences of ingestion and entanglement considered to be harmful. of extinction from a diverse range of impacts.
Reports in the literature began in the 1960s (Brongersma, 1968; The incidence of marine debris and its potential to cause harm
Caldwell et al., 1965; Holgersen, 1961) with fatalities being well has resulted in it being recognised as a global problem (STAP,
documented for birds, turtles, fish and marine mammals (Laist, 2011; Sutherland et al., 2010) and its listing among the major per-
1997; Secretariat of the Convention on Biological Diversity and cieved threats to marine biodiversity (Gray, 1997). The problem
the Scientific and Technical Advisory Panel – GEF, 2012). Debris has been recognised in global and regional agreements such as
has also been shown to provide an additional surface for the rafting the decisions of the 11th Conference of the Parties to the Conven-
of organisms (Aliani and Molcard, 2003; Barnes and Fraser, 2003; tion on Biological Diversity (CBD COP 11 Decision XI/18), the 10th
Barnes and Milner, 2005; Carpenter et al., 1972; Winston et al., Conference of the Parties to the Convention on the Conservation of
1997) which has implications for the transport of non-native spe- Migratory Species of Wild Animals (CMS Resolution 10.4), the
cies, and to provide new habitat for colonisation (Ayaz et al., 2006; International Convention for the Prevention of Pollution From
Carr et al., 1985; Donohue et al., 2001; Goldstein et al., 2012; Good Ships (MARPOL) Annex V, and the EU Marine Strategy Framework
et al., 2010; Pace et al., 2007) which may be particularly important Directive (MSFD). Furthermore, the cumulative impacts of plastic
where it provides hard substrate in areas that are otherwise pre- resins on human health and the environment have led to proposals
dominantly of soft sediment (Pace et al., 2007). It may also cause enacting legislation and policies classifying the most harmful types
physical changes to habitats (Aloy et al., 2011; Carson et al., of plastic debris as hazardous waste (Rochman et al., 2013).
Fig. 1. (A) Debris discarded on the shore near a coral reef, Ta’u Island, American Samoa (Courtesy of Wolcott Henry/Marine Photobank). (B) Debris extracted from the carcass
of a Laysan Albatross chick, Kure Atoll, Hawaii (Courtesy of Claire Fackler, NOAA Marine Sanctuaries/Marine Photobank). (C) Debris incorporated into the nests of a Northern
Gannet (Morus bassanus) on Grasholm, UK (Courtesy of Dr. Stephen Votier, Plymouth University). (D). Marine debris and derelict fishing gear among albatross nesting habitat.
Midway Atoll, Northwestern Hawaiian Islands (Courtesy of Steven Siegel/Marine Photobank). (E) Turtle entangled in plastic rope in Caribbean (photo: UNEP-CAR/RCU, 2008).
172 S.C. Gall, R.C. Thompson / Marine Pollution Bulletin 92 (2015) 170–179
Without sufficient knowledge on the scope of the problem it is, including (where relevant) species name, taxonomic grouping,
however, difficult to develop legislation that is both adequate number of individuals, debris type, type of encounter, and location
and effective. of encounter. Where additional reference was made to specific
Literature to date has highlighted the problems associated with impacts or harm these were also noted, for example lacerations,
the presence of debris in the marine environment and discussed its gut obstruction and death.
impacts and implications on marine organisms (Derraik, 2002; Once the data were collated, analyses were undertaken to
Gregory, 2009; Laist, 1997, 1987). The last comprehensive review determine the number of papers reporting encounters, number of
was conducted by Laist (1997) who reported 267 species interact- species involved, number of individuals involved, debris type and
ing with marine debris (becoming entangled or ingesting debris), report location. The paper did not aim to test hypotheses, but to
but provided no synthesis of numbers of individuals impacted, provide summary statistics on mean levels of encounter, including
thus restricting our understanding of the scale of the problem. It means and measures of variability where possible. Species were
is evident that high degrees of uncertainty exist relating to marine included on the species list when in the original publication they
debris data, including, in particular the amount of debris entering were either 1) identified to species level or 2) identified to a lower
the marine environment, what happens to this debris and the taxonomic level but where it could be confirmed that they were
extent of its impact on marine biodiversity. Following this, not included within those already captured. Species were grouped
Derraik (2002) reviewed the pollution of the marine environment taxonomically as appropriate for the ingestion/entanglement and
by plastic debris, in relation to entanglement and ingestion, use rafting categories, with analyses focussing on the groups with
of plastic debris by invasive species, and absorption of pollutants the greatest numbers of species and individuals reported.
by species. Since this time, however, no further review has been The literature review process did not include assessment of the
completed, and it is therefore timely to evaluate the extent to reliability of each report. Literature was screened to ensure that the
which the marine debris problem has changed over time. focus was on the most reliable sources, but the conclusions of the
This paper therefore aims to provide an update to the work of authors regarding whether encounters with marine debris had
Derraik (2002) reviewing and synthesising current knowledge of caused harm to the organisms were not questioned. The objective
the effects of marine debris on marine organisms, presenting data of this work was to present the body of evidence, and it was
on the number of individuals and number of species for which lit- accepted that some subjectivity in different researcher’s assess-
erature exists documenting encounters with marine debris and ment of harm was inherent, but unavoidable. The reference list
also the number of reports that have been published. The opportu- refers only to those references mentioned within this text and is
nity for this work arose from a report the authors were invited to not a full list of all reviewed papers. Those mentioned are charac-
prepare for the CBD and Scientific and Technical Advisory Panel teristic, and indicative of the general trends identified by the
of the Global Environment Facility (STAP). This formed an exten- review.
sive review (61 pages) outlining the impact of marine debris on Some limitations were identified in the data currently available,
biodiversity together with strategies to address the challenge of with a lack of reports considering low trophic level organisms, and
marine debris (Secretariat of the Convention on Biological a geographical reporting bias. Furthermore, the differing aims of
Diversity and the Scientific and Technical Advisory Panel – GEF, studies which have reported encounters result in different infor-
2012). The current paper presents a succinct summary of some mation being provided; hence not all reports provided detail of
of the key messages from that report and builds upon it, providing the size or number of items ingested, the number of individuals
a peer reviewed update on (Derraik, 2002). It is intended that the affected or the impact of the encounters and whether harm was
results will contribute to global understanding of the marine debris caused. It is thought that the impact of microplastic (defined as
problem, providing up to date estimates of the numbers of species plastic material <5 mm (Arthur et al., 2009)) in particular is under-
and individuals affected by marine debris. The results are also represented due to lack of information relating to the size of debris
compared to species conservation status as defined by IUCN to ingested. These limitations are discussed.
provide context for the scale and potential consequences of the
impacts.
3. Results
2. Materials and methods A total of 340 original publications were identified document-
ing encounters between marine debris and marine organisms.
An extensive literature review was conducted, focussing on These reported encounters for a total of 693 species. 76.5% of all
peer reviewed publications and reports in grey literature. Once col- reports listed plastic amongst the debris types encountered by
lated, the literature was divided into four key topics, namely those organisms making it the most commonly reported debris type.
1) documenting ingestion of or entanglement in marine debris by 92% of all encounters between individual organisms and debris
organisms, 2) reporting species rafting on debris, 3) where debris were with plastic.
creates new habitat for colonisation, and 4) where it causes phys- Encounters between organisms and marine debris were first
ical damage to ecosystems. Electronic key word searches were per- reported in the 1960s (Brongersma, 1968; Caldwell et al., 1965;
formed using Web of Science, Google Scholar and Google to Holgersen, 1961). Since that time there has been an increased fre-
identify literature. Key words used for debris included: marine quency of reporting, both for numbers of species and numbers of
debris, floating marine debris, marine litter, debris, plastic, metal, individuals effected (Secretariat of the Convention on Biological
glass and paper, and for effects included: impact, entanglement, Diversity and the Scientific and Technical Advisory Panel – GEF,
ingestion, rafting, habitat, ecosystem, invasive, alien and biodiver- 2012). The average number of documents reporting ingestion and
sity. The reference list from Laist (1997) and papers which refer- entanglement encounters as well as those reporting rafting has
enced other studies that had not already been captured were remained fairly constant since the 1980s (Secretariat of the
also examined and all relevant traceable sources used. Convention on Biological Diversity and the Scientific and
Contact by email was made with key researchers and the Technical Advisory Panel – GEF, 2012).
coordinators of the UNEP Regional Seas Programmes to identify When considering reporting location, regions with the greatest
additional literature, in particular grey literature. Data was com- number of reports included the east coast of North America
piled in terms of the frequency of different types of encounter, (n = 56), Australasia (n = 54), the west coast of North America
S.C. Gall, R.C. Thompson / Marine Pollution Bulletin 92 (2015) 170–179 173
(n = 54) and Europe (n = 52). Regions where reporting was low fragments (37%) (Fig. 2a). When the data are considered according
included Antarctica (n = 6), the east and west coasts of Africa to species, encounters were again most strongly associated with
(n = 7 and n = 5 respectively) the west coast of South America plastic rope and netting for cases of entanglement (55%), and with
(n = 6) and the Arctic (n = 5). plastic fragments (31%) for ingestion (Fig. 2b). Cases of both entan-
glement and ingestion were fewest for the debris types: glass,
3.1. Entanglement and ingestion metal and paper (Fig. 2).
Thirty-five percent more papers reported entanglement
Of the 340 original publications examined, a total of 292 (n = 178) than ingestion (n = 132), and reports were most com-
reported the incidence of ingestion or entanglement encounters monly made for sea turtles, marine mammals and sea birds.
between marine debris and organisms. These reported encounters Reports of entanglement in marine debris by species were most
for 44,006 individuals from 395 species, and represented a 49% numerous for the northern right whale (Eubalaena glacialis),
increase over the 267 species reported by Laist (1997). Reports of (n = 38), the green sea turtle (Chelonia mydas), (n = 19), and hawks-
ingestion were made for 13,110 individuals from 208 species and bill turtle (Eretmochelys imbricata), (n = 15), and reports of the inci-
reports of entanglement were made for 30,896 individuals from dence of ingestion of marine debris by species were most
243 species. Plastic was the material for which encounters numerous for the green sea turtle (C. mydas), (n = 20), northern ful-
between individuals and debris were most commonly reported mar (Fulmaris glacialis), (n = 20) and loggerhead turtle (Caretta
for cases of both entanglement and ingestion (92%). When this cat- caretta), (n = 18). Species with the greatest number of individuals
egory was subdivided into debris type it was apparent that the ingesting debris were the northern fulmar (F. glacialis),
majority of entanglement incidents were encounters between the (n = 3444), Laysan albatross (Phoebastria immutabilis), (n = 971)
individual and plastic rope and netting (71%), whereas the majority and greater shearwater (Puffinus gravis), (n = 895), and with the
of ingestion incidents were between the individual and plastic greatest number of individuals becoming entangled in debris were
Fig. 2. Reports of entanglement and ingestion caused by marine debris according to number of (a) individuals, (b) species, and (c) documents/papers per debris type (Rope
and netting, other fishing materials (mainly lines, pots), intact items and packaging, fragments > 5 mm, microplastic < 4.99 mm), glass, metal, paper, other (e.g. rubber) and
unknown. Bars are divided by impact according to taxonomic grouping – marine mammals, birds, fish, sea turtles. The number of species is greater than 395 as it accounts for
species encountering more than one debris type, and total number of papers is greater than 292 as it accounts for papers reporting impacts on more than one species. Data
presented are for all reported encounters identified in the published literature.
174 S.C. Gall, R.C. Thompson / Marine Pollution Bulletin 92 (2015) 170–179
the northern fur seal (Callorhinus ursinus), (n = 3835), Californian and via aquaculture, both of which are known to be substantial
sea lion (Zalophus californianus), (n = 3587), and Atlantic puffin contributors to species dispersal, and also to the transport of inva-
(Fratercula arctica), (n = 1674). sive species (Molnar et al., 2008). Marine debris is now contribut-
Consequences of encounters were considered where docu- ing to the rafting and transport of organisms, with the potential for
mented, suggesting that direct harm or death (defined as where floating debris such as plastic to travel great distances.
the individual was reported to have been injured or killed as a Thirty-four reports were identified reporting organisms rafting
direct result of the encounter with marine debris) is a more com- on debris for 259 species. Numbers of individuals were seldom
mon consequence of entanglement than ingestion, with 79% of reported, so values are not presented. When considering the mate-
cases resulting in direct harm or death for cases of entanglement rials comprising the rafting debris, intact items and packaging
compared to 4% of cases of ingestion (Fig. 3). accounted for 40% of all reported encounters with species, followed
All known species of sea turtle, 54% of all species of marine by fragments (36%), rope and netting (17%), other fishing material
mammal, and 56% of all species of seabird were affected by entan- (1.50%) and microplastics (1.50%), (Fig. 5). Of the species identified,
glement in or ingestion of marine debris and the percentage of only 6 were listed as invasive and were described in a total of 4
encounters has increased for all taxonomic groups since the Laist reports. It is however, expected that this is an underrepresentation
(1997) review (Table 1). Whilst the number of reports of species as the number of reports is low and not all reports identified organ-
of fish encountering marine debris remains low (0.68%), the num- isms to species level.
ber of species affected has almost doubled since 1997.
Data on species that had encountered marine debris were cross
3.4. Assemblage level effects
referenced with species conservation status using the IUCN Red
List to determine how many of those already known to be threa-
Evidence for assemblage level effects were very limited; sug-
tened were encountering debris. From this, it was apparent that
gesting that such effects are difficult to quantify rather than that
approximately 17% of species ingesting or becoming entangled in
they do not exist. A total of eight references were identified. These
marine debris were listed as near threatened, vulnerable, endan-
documented and suggested likely effects on coral reefs (Al-Jufaili
gered or critically endangered (Fig. 3). Reports documenting
et al., 1999; Chiappone et al., 2005; Chiappone et al., 2002;
impacts on critically endangered Hawaiian monk seal (Monachus
Donohue et al., 2001; Richards and Beger, 2011), soft sediment
schauinslandi), (n = 215); endangered loggerhead turtle, (n = 755);
habitats (Uneputty and Evans, 1997) and sandy intertidal sedi-
vulnerable northern fur seal, (n = 3835), and near threatened sooty
ments (Aloy et al., 2011; Carson et al., 2011).
shearwater, (n = 1122) were of particular concern due to the num-
Chiappone et al. (2005) reviewed the consequences of the loss
bers of individuals involved (Fig. 4).
of fishing gear on coral reef and hard bottom sites in the Florida
Keys, finding that hook and line gear was responsible for 84% of
3.2. Potential for debris to provide new habitat
impacts to sponges and cnidarians with tissue abrasion causing
partial or total mortality. They did not attempt to link the quantity
Numerous man made surfaces have been added to the marine
of debris to the damage caused, but it is clear from their assess-
environment, and marine debris contributes to this. These are most
ment that debris had negative impacts on the benthic assemblage.
commonly coastal structures such as harbour walls and coastal
Richards and Beger (2011) identified similar consequences from
defences, and artificial reefs which result from purposeful intro-
the presence of marine debris in a lagoon in the Republic of the
duction of additional surfaces. Whilst the contribution of marine
Marshall Islands, finding that coral cover significantly decreased
debris to this is slim, it does represents the addition of hard sub-
as debris cover increased, again suggesting assemblage level
strata into the sea, providing new surfaces for colonisation by
effects.
microorganisms and macrobiota (Harrison et al., 2011; Whal,
In soft sediment habitats, Uneputty and Evans (1997) found
1989; Ye and Andrady, 1991), and influencing the relative abun-
that marine debris accumulating on the seabed in Ambon Bay,
dance of organisms within local assemblages (Secretariat of the
Indonesia increased the abundance of meiofauna and decreased
Convention on Biological Diversity and the Scientific and
that of diatoms when compared to areas without debris, although
Technical Advisory Panel – GEF, 2012). The impact of this will
no change was noted for macrofauna.
likely be more substantial in areas away from the coastal zone
Not all studies were able to directly link their findings to assem-
where other man made habitats are scarce.
blage level effects, however, but instead identified the potential for
Six papers were identified that described this, listing a total of
these to occur. Aloy et al. (2011) determined experimentally that
85 taxa (both mobile and sessile) using marine debris as habitat
when plastic cover was 50% the efficiency of the gastropod
from 12 taxonomic groups (Table 2). Number of individuals was
Nassarius pullus in locating and moving towards a food source sig-
not commonly reported, often as organisms were colonial. Four
nificantly decreased, but the maximum cover of plastic that they
of the papers reported colonisation of derelict fishing gear by
found on the shore was only 0.77%. Similarly, Carson et al. (2011)
mobile and sessile species (Ayaz et al., 2006; Carr et al., 1985;
determined that the quantity of plastic fragments in beach sedi-
Donohue et al., 2001; Good et al., 2010), highlighting an effect
ments altered the sediment’s thermal properties, and although
aside from the destructive ‘ghost fishing’ with which they are usu-
they did not identify an assemblage level impact they hypothesised
ally associated.
that this could have significant consequences for beach organisms,
particularly those such as sea turtles whose eggs have temperature
3.3. Dispersal via rafting, including transport of invasive species
dependent sex determination. Hence, rather than identifying a
current assemblage level effect, both authors have identified the
The dispersal of species in the marine environment largely
potential for this to be the case in the future.
depends on oceanic currents, but, increasingly the range of species
with no pelagic larval stage has expanded, suggesting that rafting
on man-made objects is playing a role in their spread (Thiel and 4. Discussion
Gutow, 2005). Species have always rafted on natural materials
such as wood, sargassum and volcanic pumice (Thiel and Gutow, It is apparent that a wide range of species are affected by inges-
2005), but increased industrialisation has opened new pathways tion and entanglement in marine debris and that the frequency of
such as the transport of organisms in the ballast water of ships encounters has increased over time. While it seems inevitable that
S.C. Gall, R.C. Thompson / Marine Pollution Bulletin 92 (2015) 170–179 175
Table 1
Number of species with records of entanglement and ingestion documented in Laist (1997), the number reported here and the total number of species identified worldwide. The
percentage of the total number of known species that are reported entangled or ingesting is given in brackets. NB This value will also be affected by the number of species within a
taxonomic group. For groups with fewer species less sampling effort would be required to demonstrate that all or a large percentage of the species were affected. Sources for total
number of identified species: Laist (1997), First Census of Marine Life (2010).
Species group Number of known species Number of species with Number of species with Total number of species with either
entanglement records ingestion records entanglement or ingestion records
Laist (1997) This study Laist (1997) This study Laist (1997) This study
Marine mammals 115 32 (28%) 52 (45%) 26 (23%) 30 (26%) 49 (43%) 62 (54%)
Fish 16,754 34 (0.20%) 66 (0.39%) 33 (0.20%) 50 (0.30%) 60 (0.36%) 114 (0.68%)
Seabirds 312 51 (16%) 79 (25%) 111 (36%) 122 (39%) 138 (44%) 174 (56%)
Sea turtles 7 6 (86%) 7 (100%) 6 (86%) 6 (86%) 6 (86%) 7 (100%)
Fig. 4. Number of species listed as near threatened, vulnerable, endangered or critically endangered on the IUCN Red List for which impacts of marine debris through
entanglement or ingestion effects have been recorded. Species are listed in order of number of impacted individuals from largest to smallest. E denotes that the species has
been impacted by entanglement, and I that it has been impacted by ingestion. For critically endangered species, 1 represents entanglement, 1 ingestion and 3 both
entanglement and ingestion; for endangered species, 6 represent entanglement, 6 ingestion, and 3 both entanglement and ingestion; for vulnerable species, 9 represent
entanglement, 18 ingestion, and 5 both entanglement and ingestion; and for near threatened species, 5 represent entanglement, 7 ingestion, and 2 both entanglement and
ingestion. Data presented are for all reported encounters identified in the published literature.
that marine debris may be contributing to the potential for species level effects. For example van Franeker et al. (2011) who have stud-
extinction. ied the northern fulmar population in the North Sea over than last
The main focus of the literature to date has been on entangle- 33 years determined that approximately 95% of individuals
ment and ingestion of marine debris. The provision of an additional washed ashore dead contained plastic debris, and that of these,
source of rafting material for species may, however, also have neg- 58% contained quantities exceeding the OSPAR Ecological Quality
ative consequences, with Barnes (2002) estimating that debris Objective critical level of 0.1 g per individual. Whilst they did not
might have substantially increased the propagation of fauna in identify specific negative impacts on the fulmars resulting from
subtropical and high latitudes. Where species are invasive this the ingestion of plastic debris, it seems likely that they are occur-
could be problematic, and whilst unlikely to be a major pathway ring. The strength of this data has led to the suggestion that plastic
for transport, rafting on marine debris may provide an additional content in this population could be used as a monitoring indicator
and in some locations, substantial method for the spread of to assess spatial and temporal changes in surface debris concentra-
invasive species (Gregory, 2009). tions on a regional basis within the north-eastern Atlantic. Simi-
Despite lack of solid evidence to confirm it, for species where larly, due to the finding that plastic was retained in the stomachs
there is a clear record of marine debris encounters affecting sub- of petrels for months, (Furness, 1985; Ryan and Jackson, 1987), it
stantial numbers of individuals there is concern for population has been suggested that these species could be a useful proxy for
S.C. Gall, R.C. Thompson / Marine Pollution Bulletin 92 (2015) 170–179 177
5. Conclusions
the marine environment, however, the benefits to society associ- Ayaz, A., Acarli, D., Altinagac, U., Ozekinci, U., Kara, A., Ozen, O., 2006. Ghost fishing
by monofilament and multifilament gillnets in Izmir Bay, Turkey. Fish. Res. 79,
ated with items typically found as marine debris can be fully rea-
267–271.
lised without the need for end of life material to accumulate in Baltz, D., Morejohn, G., 1976. Evidence from seabirds of plastic particle pollution off
the oceans. Whilst a broad range of instruments are used to central California. Western Bird 7, 111–112.
address the problem from sectoral land or sea based perspectives Barnes, D.K.A., 2002. Invasions by marine life on plastic debris. Nature 416, 808–
809.
it is evident from the current trends that their effectiveness is rel- Barnes, D.K.A., Fraser, K.P.P., 2003. Rafting by five phyla on man-made flotsam in the
atively low considering the global scale of the marine debris chal- Southern Ocean. Mar. Ecol. Prog. Ser. 262, 289–291.
lenge (Goldstein et al., 2012; Rochman et al., 2013; STAP, 2011; Barnes, D.K.A., Galgani, F., Thompson, R.C., Barlaz, M., 2009. Accumulation and
fragmentation of plastic debris in global environments. Philos. Trans. Roy. Soc. B
Thompson et al., 2009; UNEP Year Book, 2011). There is wide rec- 364, 1985–1998.
ognition that marine debris does not belong, nor does it need to be Barnes, D.K.A., Milner, P., 2005. Drifting plastic and its consequences for sessile
in the marine environment. Finding effective solutions requires a organism dispersal in the Atlantic Ocean. Mar. Biol. 146, 815–825.
Bjorndal, K.A., Bolten, A.B., Lagueux, C.J., 1994. Ingestion of marine debris by
holistic approach, considering the entire life cycle of items that juvenile sea turtles in coastal Florida habitats. Mar. Pollut. Bull. 28, 154–158.
become marine debris including green chemistry and design and Bourne, W., Imber, M., 1980. Plastic pellets collected by a prion on Gough Island,
manufacturing as well as effective waste management and preven- central south Atlantic Ocean. Mar. Pollut. Bull. 13, 20–21.
Brongersma, L., 1968. Notes upon some turtles from the Canary Islands and from
tion and removal of marine debris (Secretariat of the Convention Madeira. Proc. K. Ned. Akad. Wet. Ser. C Biol. Med. Sci. 71, 128–136 (In: Balazs,
on Biological Diversity and the Scientific and Technical Advisory G. (1985) Impact of ocean debris on marine turtles: entanglement and
Panel – GEF, 2012). Hence finding ways to ensure greater engage- ingestion. In: Shomura, R., Yoshida, H. (Eds.). Proceedings of the workshop on
the fate and impact of marine debris, 1927–1929 November 1984, Honolulu, US
ment and effectiveness of solutions perhaps requires a higher pri-
Department of Commerce (1985), pp. 1387–1429 NOAA Technical
ority than additional research to further the evidence about the Memorandum NMFS SWFC-1954).
impacts of the debris itself. Caldwell, D., Caldwell, M., Rice, D., 1965. Observations on captive and wild Atlantic
bottlenosed dolphins, Tursiops truncates, in the northeastern Gulf of Mexico. Los
Angeles City Museum Contrib. Sci. 91, 2–10. In: Walker, W., Coe, J. 1990. Survey
of marine debris ingestion by Odontocete cetaceans. In: Shomura, R., Godfrey, M.
Acknowledgements (Eds.). Proceedings of the second international conference on marine debris.
1990 U.S. Department of Commerce, NOAA Technical Memorandum. NMFS.
NOAA-TM-NMFS-SWFSC-1154. pp. 1747-1774.
GEF-STAP for funding this work. Carpenter, E.J., Anderson, S.J., Harvey, G.R., Miklas, H.P., Peck, B.B., 1972. Polystyrene
The authors also wish to thank all those who have contributed spherules in coastal waters. Science 178, 749–750.
data or comments on the text. Carr, A., Amaral, E., Hulbert, A., Cooper, R., 1985. Underwater survey of simulated
lost demersal and lost commercial gill nets off New England. In: Shomura, R.,
In particular: Lev Neretin, Thomas Hammond & Christine Wel-
Yoshlda, H., (Eds.). Proceedings of the workshop on the fate and impact of
lington-Moore, Secretariat of the Scientific and Technical Advisory marine debris, 27–29 November 1984, Honolulu, Hawaii, pp. 439–447. U.S.
Panel of the Global Environment Facility (STAP). Department of Commerce, NOAA Technical Memorandum, NMFS. NOAA-TM-
NMFSSWFC., Laist, D. Overview of the biological effects of lost and discarded
Also Francoise Galgani, IFREMER, Jan van Franeker, IMARES,
plastic debris in the marine environment. Mar. Pollut. Bull. 18, pp. 319–326.
Monika Thiele, CMS, Chris Corbin, Caribbean Environmental Pro- Carson, H.S., Colbert, S.L., Kaylor, M.J., McDermid, K.J., 2011. Small plastic debris
gramme, Heidi Savelli, UNEP and Henk Bouwman, STAP for provid- changes water movement and heat transfer through beach sediments. Mar.
ing comments, and: Ellik Adler, Coordinating Body on the Seas of Pollut. Bull. 62, 1708–1713.
Chiappone, M., Dienes, H., Swanson, D.W., Miller, S.L., 2005. Impacts of lost fishing
East Asia; Courtney Arthur, NOAA Marine Debris Program; Chris gear on coral reef sessile invertebrates in the Florida Keys National Marine
Carroll, Seas at Risk; Françoise Claro, Groupe Tortues Marine Sanctuary. Biol. Conserv. 121, 221–230.
France; David Michael Fleet, The Schleswig-Holstein Agency for Chiappone, M., White, A., Swanson, D.W., Miller, S.L., 2002. Occurrence and
biological impacts of fishing gear and other marine debris in the Florida Keys.
Coastal Defence, National Park and Marine Conservation; Riki Mar. Pollut. Bull. 44, 597–604.
Gunn, Ghost Nets Australia; Seong-Gil Kang, Marine Environmen- Coe, J.M., Rogers, D. (Eds.), 1997. Marine Debris: Sources, Impacts and Solutions.
tal Emergency Preparedness and Response Regional Activity Cen- Springer, New York.
Cole, M., Lindeque, P., Halsband, C., Galloway, T.S., 2011. Microplastics as
tre; Loïc Kerambrun, Centre de documentation, de recherché et contaminants in the marine environment: a review. Mar. Pollut. Bull. 62,
d’expérimentations sur les pollutions accidentelles des eaux; Sue 2588–2597.
Kinsey, Marine Conservation Society; Kara Lavender Law, Sea Derraik, J.G.B., 2002. The pollution of the marine environment by plastic debris: a
review. Mar. Pollut. Bull. 44, 842–852.
Education Association; Keith Reid, Commission for the Conserva-
Donohue, M.J., Boland, R.C., Sramek, C.M., Antonelis, G.A., 2001. Derelict fishing gear
tion of Antarctic Marine Living Resources; Seba Sheavly, Sheavly in the northwestern Hawaiian Islands: diving surveys and debris
Consultants; Thomas Kirk Sørensen, DTU Aqua; Monika Stan- removal in 1999 confirm threat to coral reef ecosystems. Mar. Pollut. Bull. 42,
1301–1312.
kiewicz, Helsinki Commission; Hideshige Takada, Tokyo University
First Census of Marine Life, 2010. First census of marine life 2010: Highlights of a
of Agriculture and Technology; Joana Mira Veiga, Coastal and decade of discovery. In: Ausubel, J.H., Crist, D.T., Waggoner, P.E. (Eds.). Census of
Marine Union and Rei Yamashita, Tokyo University of Agriculture Marine Life International Secretariat, United States of America.
and Technology. Furness, R.W., 1985. Ingestion of plastic particles by seabirds at Gough Island, south
Atlantic Ocean. Environ. Pollut. A 38, 261–272.
Galgani, F., Fleet, D., Van Franeker, J., Katsanevakis, S., Maes, T., Mouat, J.,
Oosterbaan, L., Poitou, I., Hanke, G., Thompson, R., Amato, E., Birkun, A.,
References Janssen, C., 2010. Marine strategy framework directive, task group 10 report:
Marine Litter. In: Zampoukas, N. (Ed.), JRC Scientific and Technical Reports.
European Commission Joint Research Centre, Ispra.
Al-Jufaili, S., Al-Jabri, M., Al-Baluchi, A., Baldwin, R.M., Wilson, S.C., West, F.,
Gaylor, M.O., Harvey, E., Hale, R.C., 2012. House crickets can accumulate
Matthews, A.D., 1999. Human impacts on coral reefs in the sultanate of oman.
polybrominated diphenyl ethers (PBDEs) directly from polyurethane foam
Estuar. Coast. Shelf Sci. 49 (Suppl. 1), 65–74.
common in consumer products. Chemosphere 86, 500–505.
Aliani, S., Molcard, A., 2003. Hitch-hiking on floating marine debris: macrobenthic
Gibbs, P., Bryan, G., Pascoe, P., Burt, G., 1987. The use of the dog-whelk, Nucella
species in the Western Mediterranean Sea. Hydrobiologia 503, 59–67.
lapillus, as an indicator of tributyltin (TBT) contamination. J. Mar. Biol. Assoc. U.
Aloy, A.B., Vallejo Jr, B.M., Juinio-Meñez, M.A., 2011. Increased plastic litter cover
K. 67, 507–523.
affects the foraging activity of the sandy intertidal gastropod Nassarius pullus.
Goldstein, M.C., Rosenberg, M., Cheng, L., 2012. Increased oceanic microplastic
Mar. Pollut. Bull. 62, 1772–1779.
debris enhances oviposition in an endemic pelagic insect. Biol. Lett. 8, 817–820.
Anastasopoulou, A., Mytilineou, C., Smith, C.J., Papadopoulou, K.N., 2013. Plastic
Good, T.P., June, J.A., Etnier, M.A., Broadhurst, G., 2010. Derelict fishing nets in Puget
debris ingested by deep-water fish of the Ionian Sea (Eastern Mediterranean).
Sound and the Northwest Straits: patterns and threats to marine fauna. Mar.
Deep Sea Res. Part I 74, 11–13.
Pollut. Bull. 60, 39–50.
Andrady, A.L., 2011. Microplastics in the marine environment. Mar. Pollut. Bull. 62,
Gray, J., 1997. Marine biodiversity: patterns, threats and conservation needs.
1596–1605.
Biodivers. Conserv. 6, 153–175.
Arthur, C., Baker, J., Bamford, H., (Eds.), 2009. Proceedings of the international
Gregory, M.R., 1991. The hazards of persistent marine pollution: drift plastics and
research workshop on the occurrence, effects and fate of microplastic marine
conservation islands. J. Roy. Soc. NZ. 21, 83–100.
debris. NOAA Technical Memorandum NOS-OR&R-30. September 9–11
S.C. Gall, R.C. Thompson / Marine Pollution Bulletin 92 (2015) 170–179 179
Gregory, M.R., 2009. Environmental implications of plastic debris in marine settings Secretariat of the Convention on Biological Diversity and the Scientific and
– entanglement, ingestion, smothering, hangers-on, hitch-hiking and alien Technical Advisory Panel – GEF, 2012. Impacts of marine debris on
invasions. Philos. Trans. Roy. Soc. B 364, 2013–2025. biodiversity: current status and potential solutions. Montreal Technical Series
Harper, P.C., Fowler, J.A., 1987. Plastic pellets in New Zealand storm-killed prions No. 67, 61.
(Pachyptila spp.), 1958–1977. Notornis 34, 65–70. Spear, L.B., Ainley, D.G., Ribic, C.A., 1995. Incidence of plastic in seabirds from the
Harrison, J.P., Sapp, M., Schratzberger, M., Osborn, A.M., 2011. Interactions between tropical Pacific, 1984–91: relation with distribution of species, sex, age, season,
microorganisms and marine microplastics: a call for research. Mar. Technol. year and body weight. Mar. Environ. Res. 40, 123–146.
Soc. J. 45, 12–20. STAP, 2011. Marine Debris as a Global Environmental Problem: Introducing a
Holgersen, H., 1961. Norske lomviers vandringer. Sterna 4, 229–240Bourne, W., solutions based Framework Focused on Plastic. A STAP Information Document.
Nylon netting as a hazard to birds. Mar. Pollut. Bull. 1978, 1975–1976. Global Environment Facility, Washington, DC, p. 40.
Holmes, L.A., Turner, A., Thompson, R.C., 2012. Adsorption of trace metals to plastic Sutherland, W.J., Clout, M., Côté, I.M., Daszak, P., Depledge, M.H., Fellman, L.,
resin pellets in the marine environment. Environ. Pollut. 160, 42–48. Fleishman, E., Garthwaite, R., Gibbons, D.W., De Lurio, J., Impey, A.J., Lickorish, F.,
Laist, D., 1997. Impacts of marine debris: entanglement of marine life in marine Lindenmayer, D., Madgwick, J., Margerison, C., Maynard, T., Peck, L.S., Pretty, J.,
debris including a comprehensive list of species with entanglement and Prior, S., Redford, K.H., Scharlemann, J.P.W., Spalding, M., Watkinson, A.R., 2010.
ingestion records. In: Marine Debris. Springer, New York, pp. 99–139. A horizon scan of global conservation issues for 2010. Trends Ecol. Evol. 25, 1–7.
Laist, D.W., 1987. Overview of the biological effects of lost and discarded plastic Teuten, E.L., Rowland, S.J., Galloway, T.S., Thompson, R.C., 2007. Potential for plastics
debris in the marine environment. Mar. Pollut. Bull. 18, 319–326. to transport hydrophobic contaminants. Environ. Sci. Technol. 41, 7759–7764.
Lithner, D., Larsson, Å., Dave, G., 2011. Environmental and health hazard ranking Teuten, E.L., Saquing, J.M., Knappe, D.R., Barlaz, M.A., Jonsson, S., Björn, A., Rowland,
and assessment of plastic polymers based on chemical composition. Sci. Total S.J., Thompson, R.C., Galloway, T.S., Yamashita, R., 2009. Transport and release of
Environ. 409, 3309–3324. chemicals from plastics to the environment and to wildlife. Philos. Trans. Roy.
Lusher, A.L., McHugh, M., Thompson, R.C., 2013. Occurrence of microplastics in the Soc. B 364, 2027–2045.
gastrointestinal tract of pelagic and demersal fish from the English Channel. Thiel, M., Gutow, L., 2005. The ecology of rafting in the marine environment. I. The
Mar. Pollut. Bull. 67, 94–99. floating substrata. Oceanogr. Mar. Biol. Annu. Rev. 42, 181–264.
Mato, Y., Isobe, T., Takada, H., Kanehiro, H., Ohtake, C., Kaminuma, T., 2001. Plastic Thompson, R.C., Moore, C.J., vom Saal, F.S., Swan, S.H., 2009. Plastics, the
resin pellets as a transport medium for toxic chemicals in the marine environment and human health: current consensus and future trends. Philos.
environment. Environ. Sci. Technol. 35, 318–324. Trans. Roy. Soc. B 364, 2153–2166.
Molnar, J.L., Gamboa, R.L., Revenga, C., Spalding, M.D., 2008. Assessing the global Thompson, R.C., Olsen, Y., Mitchell, R.P., Davis, A., Rowland, S.J., John, A.W.G.,
threat of invasive species to marine biodiversity. Front. Ecol. Environ. 6, 485– McGonigle, D., Russell, A.E., 2004. Lost at sea: where is all the plastic? Science
492. 304, 838.
Mouat, J., Lopez Lozano, R., Bateson, H., 2010. Economic impacts of marine litter. Tourinho, P.S., Ivar do Sul, J.A., Fillmann, G., 2010. Is marine debris ingestion still a
Kommunenes Internasjonale Miljøorganisasjon (KIMO International), UK. problem for the coastal marine biota of southern Brazil? Mar. Pollut. Bull. 60,
Murray, F., Cowie, P.R., 2011. Plastic contamination in the decapod crustacean 396–401.
Nephrops norvegicus (Linnaeus, 1758). Mar. Pollut. Bull. 62, 1207–1217. UNEP-CAR/RCU, 2008. Marine Litter in the Wider Caribbean Region: A Regional
Oehlmann, J., Schulte-Oehlmann, U., Kloas, W., Jagnytsch, O., Lutz, I., Kusk, K.O., Overview. United Nations Environment Programme, Nairobi, p. 81.
Wollenberger, L., Santos, E.M., Paull, G.C., Van Look, K.J.W., Tyler, C.R., 2009. A UNEP, 2005. Marine Litter an Analytical Overview. United Nations Environment
critical analysis of the biological impacts of plasticizers on wildlife. Philos. Programme, Kenya, p. 47.
Trans. Roy. Soc. B 364, 2047–2062. UNEP, 2009. Marine Litter: A Global Challenge. UNEP, Nairobi, p. 232.
OSPAR, 2007. OSPAR Pilot Project on Monitoring Marine Beach Litter: Monitoring of UNEP Year Book, 2011. Emerging Issues in our Global Environment, United Nations
marine litter on beaches in the OSPAR region. OSPAR Commission, London. Environment Programme, Nairobi. Published February 2011 <http://www.unep.
Pace, R., Dimech, M., Camilleri, M., 2007. Litter as a source of habitat islands on deep org/yearbook/2011>.
water muddy bottoms. Rapport Commission International pour l’ exploration Uneputty, P., Evans, S.M., 1997. The impact of plastic debris on the biota of tidal flats
scientifique de la Mer Mediterranee 38, 567. in Ambon Bay (eastern Indonesia). Mar. Environ. Res. 44, 233–242.
PlasticsEurope, 2012. Plastics – The Facts 2012. PlasticsEurope, Belgium. van Franeker, J.A., Blaize, C., Danielsen, J., Fairclough, K., Gollan, J., Guse, N., Hansen,
Richards, Z.T., Beger, M., 2011. A quantification of the standing stock of macro- P.-L., Heubeck, M., Jensen, J.-K., Le Guillou, G., Olsen, B., Olsen, K.-O., Pedersen, J.,
debris in Majuro lagoon and its effect on hard coral communities. Mar. Pollut. Stienen, E.W.M., Turner, D.M., 2011. Monitoring plastic ingestion by the
Bull. 62, 1693–1701. northern fulmar Fulmarus glacialis in the North Sea. Environ. Pollut. 159,
Rochman, C.M., Browne, M.A., Halpern, B.S., Hentschel, B.T., Hoh, E., Karapanagioti, 2609–2615.
H.K., Rios-Mendoza, L.M., Takada, H., Teh, S., Thompson, R.C., 2013. Policy: Whal, M., 1989. Marine epibiosis 1. Fouling and antifouling: some basic aspects.
classify plastic waste as hazardous. Nature 494, 169–171. Mar. Ecol. Prog. Ser. 58, 175–205.
Rochman, C.M., Hoh, E., Hentschel, B.T., Kaye, S., 2012. Long-term field Winston, J., Gregory, M., Stevens, L., 1997. Encrusters, epibionts and other biota
measurement of sorption of organic contaminants to five types of plastic associated with pelagic plastics: a review of biogeographical, environmental,
pellets: implications for plastic marine debris. Environ. Sci. Technol. 47, 1646– and conservation issues. In: Coe, J., Rogers, D. (Eds.), Marine Debris, Sources,
1654. Impacts, Solutions. Springer-Verlag New York Inc., pp. 81–97.
Ryan, P., Jackson, S., 1987. The lifespan of ingested plastic particles in seabirds and Woodall, L.C., Sanchez-Vidal, A., Canals, M., Paterson, G.L.J., Coppock, R., Sleight, V.,
their effect on digestive efficiency. Mar. Pollut. Bull. 18, 217–219. Calafat, A., Rogers, A.D., Narayanaswamy, B.E., Thompson, R.C., 2014. The deep
Ryan, P.G., 1988. Effects of ingested plastic on seabird feeding: evidence from sea is a major sink for microplastic debris. R. Soc. Open Sci. 1, 140317.
chickens. Mar. Pollut. Bull. 19, 125–128. Wright, S.L., Rowe, D., Thompson, R.C., Galloway, T.S., 2013. Microplastic ingestion
Ryan, P.G., 2008. Seabirds indicate changes in the composition of plastic litter in the decreases energy reserves in marine worms. Curr. Biol. 23, R1031–R1033.
Atlantic and south-western Indian Oceans. Mar. Pollut. Bull. 56, 1406–1409. Ye, S., Andrady, A.L., 1991. Fouling of floating plastic debris under Biscayne Bay
Ryan, P.G., Connell, A.D., Gardner, B.D., 1988. Plastic ingestion and PCBs in seabirds: exposure conditions. Mar. Pollut. Bull. 22, 608–613.
is there a relationship? Mar. Pollut. Bull. 19, 174–176.