Abstract
Marine litter is a global challenge that has recently received policymakers' attention, with new environmental targets in addition to changes to old legislation. There are no global estimates of benthic litter because of the scarcity of data and only patchy survey coverage. However, estimates of baseline abundance and composition of litter are vital in order to implement litter reduction policies and adequate monitoring schemes. Two large-scale surveys of submarine geomorphological features in the Indian and Atlantic Oceans reveal that litter was found at all locations, despite their remoteness. Litter abundance was patchy, but both surveyed oceans had sites of high litter density. There was a significant difference in the type of litter found in the two oceans, with the Indian Ocean sites being dominated by fishing gear, whereas the Atlantic Ocean sites displayed a greater mix of general refuse. This study suggests that seabed litter is ubiquitous on raised benthic features, such as seamounts. It also concludes that the pattern of accumulation and composition of the litter is determined by a complex range of factors both environmental and anthropogenic. We suggest that the tracing of fishing effort and gear type would be an important step to elucidate hotspots of litter abundance on seamounts, ridges and banks.
Introduction
Marine litter has been identified as a significant and growing global problem (UNEP, 2009; UNGA, 2012; GOC, ). Estimates suggest 6.4 million tons of litter enter the marine ecosystem annually (UNEP, 2009). Litter items, defined as; persistent, manufactured or processed solids that have been disposed of or abandoned, deliberately or unintentionally (UNEP, 2005), are present in all marine environments, including remote locations such as Antarctica (Barnes et al., ; Ivar Do Sol et al., ) and in the deep sea (Galgani et al., ; Ramirez-Llodra et al., ; Pham et al., ). However, the source and fate of marine litter is little understood (Derraik, ). Observations of litter have revealed direct impacts on megafauna through entanglement and ingestion, and on habitats through smothering, transporting alien species, and altering benthic community structure (Gregory, ). In addition, plastics can fragment to microplastics which also have potential impacts on the environment and biota, both physical and biochemical (Teuten et al., 2009; Andrady, ; Wright et al., 2013; Bakir et al., ).
A plethora of studies have reported on abundance and composition of debris in surface water and on beaches (e.g., Ryan et al., 2009). The deep sea, however, is logistically challenging and expensive to survey, therefore few studies have been conducted. Most of these have concentrated on small areas of the seabed, mostly on the continental shelf (Ramirez-Llodra et al., ), but there are a few studies that have reported deep-sea litter in more extreme locations e.g., the Ryukyu Trench; [7216 m depth (Miyake et al., )], Molloy Hole; [up to 5500 m; (Galgani and Lecornu, )], and Kuril-Kamchatka Trench (Fischer et al., ) and have assessed trends in litter composition and abundance (Bergmann and Klages, ; Schlining et al., 2013). To date, records have shown that deep-sea litter is not evenly distributed, with environmental and anthropogenic factors both influencing litter abundance (Schlining et al., 2013; Pham et al., ). More specifically, near-shore canyons may accumulate more litter than expected (Pham et al., ), and some regions of these canyons can have greater litter abundance than others e.g., more rugose parts of the Monterey Canyon had greater litter densities (Schlining et al., 2013), and thus marine litter assessments may have underestimated the true figure.
The main constituent of beach, seabed and surface water litter is plastic (Derraik, ). This is because it has a low degeneration and degradation rate, and production has increased annually since the 1950's (Thompson et al., 2009). Studies suggest litter items arrive in the deep sea from the shore, offshore installations, shipping and fisheries activities (Pham et al., ). The proportional contribution of different litter sources is likely to result from the complex interactions of oceanographic processes, geography and local anthropogenic activity (Ramirez-Llodra et al., ). Some submarine features are disproportionately affected by some types of litter. For example, in Europe, fishing gear contributes over 70% of the litter found on seamounts, banks and mounds and is also the greatest constituent of litter found in one ocean ridge study (Pham et al., ). This large contribution of fishing gear is not unexpected as, seamounts and other geomorphological features are often a focus for fisheries (Clark and Koslow, ).
To date, there have been no studies, using a consistent methodology, that survey multiple seamounts or other submarine features within the same ocean basin. The objective of this study was 3-fold; (1) to determine the amount and composition of litter on remote Atlantic Ocean and south-west Indian Ocean submarine features (seamounts, banks and a ridge), and to compare litter within and between the regions; (2) to infer the relative importance of geographical, geomorphological, biological and anthropogenic factors on the patterns of litter abundance and composition (e.g., distance from land, benthic rugosity, and shipping activity) and (3) to discuss results in the context of current legislation.
Materials and methods
Study areas
Data were collected during two research cruises aboard R.R.S. James Cook during 2011 and 2013. During each cruise, 16 remotely operated vehicle (ROV) dives were conducted. Submarine features (seamounts and banks) along the south-west Indian Ocean ridge were observed during JC66 using the ROV Kiel 6000. Later, an east-west transect of the equatorial Atlantic Ocean was conducted as part of JC94, observing seamounts and a fracture zone area using the ROV ISIS. Ten submarine features were surveyed in total, five on each cruise (Table 1 and Figure 1).
Table 1
| Region | Location | Feature type | ROV Dives | Area covered (ha) | Depth range surveyed (m) | Distance from land (km) | Shipping activity proxy | Items (ha−1) |
|---|---|---|---|---|---|---|---|---|
| Atlantic | Carter | Seamount | 5 | 2.78 | 200–2800 | 630 | 0.12 | 12.23 |
| Atlantic | Knipovich | Seamount | 3 | 2.18 | 600–2800 | 1360 | 0.23 | 2.29 |
| Atlantic | VEMA | Fracture zone | 3 | 1.80 | 600–3000 | 1040 | 0.07 | 5.56 |
| Atlantic | Vayda | Seamount | 3 | 3.10 | 400–2300 | 1170 | 0.01 | 1.94 |
| Atlantic | Gramberg | Seamount | 2 | 1.70 | 900–2200 | 940 | 0.21 | 0.59 |
| Indian | Coral | Seamount | 5 | 2.04 | 500–1500 | 1610 | 0.01 | 1.47 |
| Indian | Melville | Bank | 4 | 1.35 | 100–1300 | 1440 | 0.00 | 13.33 |
| Indian | Middle of What | Seamount | 3 | 0.41 | 1000–1400 | 1460 | 0.00 | 2.44 |
| Indian | Sapmer | Seamount | 1 | 0.46 | 300–700 | 1390 | 0.00 | 17.39 |
| Indian | Atlantis | Bank | 3 | 1.34 | 700–1200 | 1320 | 0.10 | 0.75 |
Sampling data including geomorphological feature surveyed, number of remotely operated vehicle (ROV) dives, area of ROV survey, depth range surveyed, distance from land, shipping activity proxy and litter abundance.
Figure 1
All submarine topographic features had different morphologies (Rogers and Taylor, 2012; Hoy et al.,
Data recording
The primary purposes of the ROV dive transects were to video benthic habitat and sample specific megafauna. Dives always started at depth and progressed to shallower water. Typically three dives were performed on each submarine feature, but this varied from five to one (Table 1). ROV geographic position and depth were recorded using Ocean Floor Observation Protocol (OFOP) software (Huetten and Grienert,
Video analysis
Video transects from the main color HD camera were played in real-time through Video Annotation and Reference System software (VARS; Schlining and Jacobsen Stout, 2006), which recorded time, geographic location and depth when the observer noted a litter item. All videos were watched twice by the same observer to ensure no objects were missed. The other HD video recordings (downward looking and pan and tilt) were used when possible to confirm the identity of litter items. In addition, the OFOP observer text, made onboard ship during the ROV dives, was queried for annotations that may relate to marine litter such as “trash,” “anthropogenic,” “fishing,” and “plastic” and the video footage was checked. Litter items (Figure 2) were placed into five broad categories which included: “fishing gear,” “plastic,” “metal,” “glass” or “other.” Unidentified objects, as well as those made from material that were not plastic, metal or glass, were classified as “other” (Table S1). The fishing gear was mainly made from plastic, but the separate designation of “fishing gear” was retained to ensure that the source of these items was recorded in order to determine if there was any correlation between litter type and habitat, this also follows other studies (Miyake et al.,
Figure 2

Six examples of benthic litter items observed during surveys in the Atlantic Ocean and Indian Ocean: (A) fishing gear from the Indian Ocean; (B) plastic object, possible plumbing item from the Indian Ocean; (C) glass bottle from the Atlantic Ocean; (D) glass bottle from the Atlantic Ocean; (E) engine head gasket, categorized as “other” from the Indian Ocean (F) work glove, categorized as “other” from the Atlantic Ocean.
In the absence of a standardized reporting system, the coverage extent of the litter item on the benthos was recorded using two parameters, shape and size. For the first of these, shape, items were classified as either elongate or oblate; for example rope was classified as elongate and bottles as oblate. Objects were grouped by size into four categories that increase by an order of magnitude <20 cm, 20 cm–2 m, 2 m–20 m, and >20 m for the elongate objects, and <10 cm2, 10 cm2–1 m2, 1 m2–10 m2 and >10 m2 for oblate objects. These size categories were chosen to make the measurement simple, using the width between the two lasers (10 cm) and average field of view during the dives (2 m). The impact of the item was then represented by size category with litter type subdivided into either elongate or oblate. When both elongate and oblate items were present e.g., fishing nets (net and the top and bottom ropes), both types of impact were reported separately. Finally any interactions of litter with benthic fauna were recorded, be they through entanglement or use of the litter as substratum.
Spatial analysis
Litter location was plotted using ArcGIS v10.2 (ERSI,
To calculate rugosity, bathymetry raster files for the 10 surveyed features were combined in ArcGIS, using the “mosaic to raster” function. Rugosity was then determined using the terrain ruggedness feature in the Benthic Terrain Modeler (BTM) extension set at five (Wright et al., 2012). This measure of rugosity relies on the resolution of the bathymetry survey and thus the rugosity had 50 and 100 m resolution of both the Indian and Atlantic Oceans, respectively. This rugosity was then assigned to six categories (0–0.9, 1–1.9, 2–2.9, 3–3.9, 4–4.9, 5+). The habitat where the litter was found was used as a proxy for rugosity at finer resolution. The habitat was assigned to one of five categories that increased in rugosity from sand/silt flat areas, to deep rock crags (Figure S1).
Commercial shipping activity was calculated using a proxy derived from the World Meteorological Organization Voluntary Observing Ships Scheme data Oct 2004–Oct 2005 with 1 km resolution (Halpern et al.,
Data analysis
Abundance of litter was calculated for each seamount per hectare surveyed (items ha−1). Non-parametric tests were applied as data were not normally distributed (Ryan-Joiner, p < 0.05), but variances were not significantly different (Levene's test p > 0.05). Litter patchiness was computed using Lloyd's index implemented in Passage v2, where n > 1 means aggregation (Lloyd,
Results
Litter abundance and ubiquity
Litter was found on every one of the 10 submarine features surveyed in the Indian and Atlantic Oceans. A total of 56 items were found in the Atlantic Ocean over a survey area of 11.6 ha, and 31 items in the Indian Ocean over 5.6 ha (Figure 1). Litter was present in depths ranging from 209 to 2318 m in the Atlantic Ocean, and 112–1278 m in the Indian Ocean. The differences in the depth at which litter was observed reflected the bathymetry of the features surveyed (Table 1). In the Indian Ocean litter items, of all size categories, were seen for both shape categories (elongate and oblate), whereas the litter from the Atlantic Ocean was just from the smallest three size categories for both shape types. The greatest amount of litter was found on Sapmer Seamount in the Indian Ocean (17.39 items ha−1), and the least (0.59 items ha−1) on Gramberg Seamount in the Atlantic Ocean. It was not possible to compare litter between different types of topographic features, i.e., bank, ridge, seamount, as the sample size was too small.
There was great variation in the abundance of items between submarine features within the same ocean, with one seamount, Carter, in the Atlantic Ocean and two features (Melville and Sapmer) in the Indian Ocean having a high density of litter (12.23–17.39 items ha−1), while the rest of the sites had much lower densities (0.59–5.56 items ha−1). The mean litter abundance was greatest in the Indian Ocean, but the oceans had similar variance (Atlantic: 4.52 items ha−1 SE ± 2.09; Indian: 7.07 items ha−1 SE ± 3.45) (Table 1). However, the litter had a patchy distribution across all locations (P = 3.4) according to Lloyd's index.
There was no significant difference between the number of items ha−1 found in each ocean (Mann-Whitney: W = 25.0, η1 = −15.1 η2 = 9.8, p = 0.8). There was also no significant difference between the amount of litter observed on flanks compared with summits of the topographic features (W = 6, η1 = −8.0 η2 = −29.0 p = 0.7). But because of sample size it was not possible to compare litter abundance between types of submarine features.
Rugosity, as calculated by BTM and habitat both negatively correlate with litter abundance [BTM: ρ = −0.9, p < 0.01; habitat: ρ = −1.0, p < 0.01]. Most litter items were found in areas with the flattest rugosity ratings (77% Atlantic Ocean, 69% Indian Ocean). In addition we explored the data to determine if there was correlation of litter abundance with distance from land and shipping activity, however, probably because of the low level of replication these test results were not significant and are not presented.
Litter type
The relative litter composition of the two oceans was significantly different [1-way ANOSIM R = 0.242, p < 0.05]; litter in the Indian Ocean was dominated by fishing gear (84%) whereas in the Atlantic Ocean, the litter was a mix of fishing gear, glass and other debris, each comprising about 25% of the total litter, with metal and plastic objects making up the final quarter (Figure 3). Objects classed as “other items” in the Atlantic Ocean were as diverse as a pottery urn and machinery gaskets. In the Indian Ocean, this category also included gaskets as well as a work glove. Fishing gear was seen at the most number of different sites, with all locations in the Indian Ocean and three of the five sites in the Atlantic Ocean having at least one occurrence. Plastic items were only seen in two sites in each ocean (Carter and Vayda - Atlantic Ocean; Coral and Sapmer - Indian Ocean) and were of low abundance. The pattern of plastic litter distribution differed from that of glass debris which was seen at three Atlantic sites and was highly abundant at one site (Carter), but less so at the other two (Knipovitch, VEMA) (Figure 1).
Figure 3

Composition of benthic litter estimated from seabed observations. Circles represent studies on raised features such as seamounts, stars represent canyon studies and other topography is represented by a square. Filled symbols are the summary data from the current study and labeled Indian and Atlantic Ocean. Open symbols are data from previous studies and references are given. Watters et al. (2010) data is given for two areas along the California coast. European data, reviewed by Pham et al. (
Multivariate analyses were not successful in elucidating patterns of correlation as a result of the small sample sizes at some sites. The litter was reanalyzed by re-categorizing it as fishing gear or non-fishing litter. Subsequent analyses were conducted to determine correlation between distance from shore, shipping activity, depth category and rugosity; the only significant relationship was a negative one between fishing gear items and shipping activity [Spearman's rank order ρ −0.72, p < 0.05].
Litter coverage extent
There was a significant difference in the coverage extent of the litter items between oceans and between areas according to their shipping activity [1-way ANOSIM Ocean R = 0.27, P < 0.01; Shipping activity R = 0.95 p < 0.01], but not between seamounts or distance from shore. SIMPER analysis showed that the difference between the oceans was mainly driven by the dissimilarity between the coverage extent of fishing gear (elongate 33.7% and oblate 20.2%).
When this litter coverage extent was re-categorized as either fishing gear or non-fishing litter, there was no significant correlation between litter coverage extent and rugosity calculated by habitat, however, there is a significant negative correlation between coverage extent of litter and habitat calculated by BTM [Spearman's rank-order ρ = −0.94, p < 0.01].
Associated organisms
Very few faunal associations were seen, with most being associated with items from the Indian Ocean. Encrusting organisms were observed on 18% of litter items, all of which were fishing gear, these items were often entirely covered and heavily encrusted (Figure 2A). The identification of associated taxa was difficult as most litter items were not brought up to the surface, and often the ROV was unable to get close to fishing gear for operational and safety reasons. However, where identification was possible, coral and hydroids were seen encrusting the gear, whilst fish, crinoids, anemones, sea urchins, and brittle stars were seen using the items as habitat. Entanglement was obvious in four fishing gear items; two of these were also encrusted. These entangled organisms comprised the broadest range of taxa, including coral, sponge, fish and crustacea. Finally, a further three items were used as substrata for organisms to hide under (Figure 2F), to lay eggs on, or to use as a holdfast.
Discussion
Distribution and abundance
The most notable finding of this study is that litter was found at all deep-sea sites surveyed. The ubiquity of the litter on seamounts, banks and ridges has previously not been as explicit because the features were focused on individually. Litter abundance on these submarine features was patchy, with high and low densities of litter reported within each ocean. However, all litter abundances were within those previously reported in the North Atlantic Ocean for seamounts, banks, mounds and ridges (Pham et al.,
The surveyed area on each geomorphic feature was limited. This is common in the deep-sea, even when a region is well-studied e.g., Monterey Bay (Schlining et al., 2013). Even though this current study sampled multiple sites, the survey area for each separate feature was within the range that others had reported (0.9–5.6 ha) (Pham et al.,
To extrapolate our data to provide global estimates of litter on seamounts is challenging, as we only surveyed <1% of each submarine feature, the depth ranges we surveyed are not typical of seamounts generally, and we focused on remote locations. However, we have extrapolated from existing data (Yesson et al., 2011) on non-overlapping seamounts that are within 500 km of our study locations and that have similar depths (summits > 3000 m). We estimate that over 32 million and 38 million litter items are present on the seamounts of the Atlantic and south-west Indian Oceans, respectively. These figures are derived from the mean abundance (2.15 items ha−1) when the three outlier sites with greatest abundance are removed, and using the seamount data of Yesson et al. (2011). The areas on which this extrapolation is based are about 10% of the seamount area calculated for the FAO regions that contain the areas of interest in our study (Yesson et al., 2011). These extrapolations take account of all data currently available, however, this dataset comes from a very small area compared with the size of the ocean and so our estimates should be used as a guide. Specifically we show that the accumulation of litter on the seabed is patchy, therefore further surveys are required to confirm the average litter abundance on the ocean floor. In addition we have not taken into account the impact of tides, currents and the morphology of the topographic features. Future studies to model the desposition and accumulation of litter would be an important contribution to this field of study, but paucity of data currently prevents this analysis.
Previous studies reveal that certain geomorphological features accumulate more litter than others, with canyons having the highest litter loads (Galgani et al.,
The survey sites in this study were outside the subtropical gyres which accumulate surface litter (Moore et al.,
Type and impact of litter
A clear difference in the composition of the litter items was found between the two oceans surveyed (Figure 3). Fishing gear, the predominant litter type on Indian Ocean submarine features, is also the most abundant litter type on seamounts and other deep-sea features in European waters (Pham et al.,
In this study few associations between litter and organisms were recorded as (1) most litter was not sampled by the ROV and therefore small encrusting organisms were not seen, and (2) because of the challenges of navigating the ROV close to litter in the most rugged terrain, especially when loose fishing gear was present. However, the variety of taxa, either encrusting or entangled in fishing gear, was diverse and congruent with previous studies (Laist,
Conclusion
There are few legal instruments that regulate waste being dumped at sea. Commercial shipping dumping is regulated by the London Protocol and the recently revised International Convention for the Prevention of Pollution from Ships (MARPOL 73/78), Annex V, and particular regions are covered by specific agreements (NE Atlantic; OSPAR Convention) and reviewed by UNEP (2005). However, legislation is not a panacea for positive change as fishing gear debris rates did not fall when MARPOL was initially implemented in 1989 (Henderson,
Strandline litter and accumulation of debris in surface water are well-reported in the media, and citizens actively monitor and lobby about these issues. The issue of the un-seen benthic litter has recently attracted more attention (Galgani et al.,
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Statements
Acknowledgments
This work was funded by NERC grant NE/F005504/1, ERC grant 278705 and the Philip Leverhulme Trust. We would like to thank participants of JC66 and JC94, especially E. Muller, S. Hoy, and V. Huvenne for bathymetry data, L. Marsh, M. Taylor, N. Serpetti, and M. Packer for their support at sea and the ROV teams and captain and crew of the R.R.S. James Cook for their assistance.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary material
The Supplementary Material for this article can be found online at: http://www.frontiersin.org/journal/10.3389/fmars.2015.00003/abstract
Figure S1Photographs of habitat categories increasing from smooth (A) to most rugose (E).
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Summary
Keywords
litter, debris, seamount, benthic, fishing gear
Citation
Woodall LC, Robinson LF, Rogers AD, Narayanaswamy BE and Paterson GLJ (2015) Deep-sea litter: a comparison of seamounts, banks and a ridge in the Atlantic and Indian Oceans reveals both environmental and anthropogenic factors impact accumulation and composition. Front. Mar. Sci. 2:3. doi: 10.3389/fmars.2015.00003
Received
27 November 2014
Accepted
16 January 2015
Published
02 February 2015
Volume
2 - 2015
Edited by
Alex Ford, University of Portsmouth, UK
Reviewed by
Adolphe Debrot, Institute for Marine Research and Ecosystem Studies Wageningen University and Research Center, Netherlands; Francois Galgani, Institut Français de Recherche pour l'Exploitation de la Mer, France; Christopher Kim Pham, IMAR-Institute of Marine Research, Portugal
Copyright
© 2015 Woodall, Robinson, Rogers, Narayanaswamy and Paterson.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Lucy C. Woodall, Department of Life Sciences, The Natural History Museum, Cromwell Road, London SW7 5BD, UK e-mail: l.woodall@nhm.ac.uk
This article was submitted to Marine Pollution, a section of the journal Frontiers in Marine Science.
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