Gear restrictions are an important management tool in small-scale tropical fisheries, improving sustainability and building resilience to climate change. Yet to identify the management challenges and complete footprint of individual gears, a broader systems approach is required that integrates ecological, economic and social sciences. Here we apply this approach to artisanal fish fences, intensively used across three oceans, to identify a previously underrecognized gear requiring urgent management attention. A longitudinal case study shows increased effort matched with large declines in catch success and corresponding reef fish abundance. We find fish fences to disrupt vital ecological connectivity, exploit > 500 species with high juvenile removal, and directly damage seagrass ecosystems with cascading impacts on connected coral reefs and mangroves. As semi-permanent structures in otherwise open-access fisheries, they create social conflict by assuming unofficial and unregulated property rights, while their unique high-investment-low-effort nature removes traditional economic and social barriers to overfishing.
The long-term future of tropical coastal ecosystems and their fisheries will largely be determined by our ability and willingness to address global climate change1,2,3,4,5,6. Yet, addressing localised threats (e.g., unsustainable or damaging fishing practices) can build short-term ecosystem resilience7, improve adaptive capacity of species and ecosystems to changes in climate8, and increase the opportunity for adaptation and acclimation9. However, there are potentially catastrophic impacts in areas where dependence on marine ecosystem services is high. For example, coral reefs provide the majority of protein to over 400 million people10, yet an estimated two-thirds of reef fish are already believed to have been lost11. Developing solutions to slow the degradation of these ecosystems, including identifying the most-damaging practices and understanding what drives them, is therefore among the biggest global challenges facing humanity12.
A range of tools are currently used for sustainable coastal fisheries management. Marine Protected Areas often provide a governance structure for tailored conservation action such as fisheries management and can successfully buffer ecological communities against disturbances13,14,15, especially when optimal reserve size thresholds are met16, manpower and funding are sufficient17, and ecological connectivity is considered18,19. Where strict no-take rules are impractical, fish biomass can be maintained via more tailored fisheries management, including restrictions on gear usage and access20,21, while strengthening fisheries governance at the local-scale best protects ecological processes22. Governance of fishing activities is made more challenging by the multi-gear nature of many tropical small-scale fisheries; it is not uncommon for over 50 distinct gear types to be in use at a single location (including multiple varieties of the same gear class)23,24,25,26. Although on occasion, critical management targets are easily identified, for example, blast fishing with explosives that has received considerable conservation attention27,28, it is often less obvious where effort would be best spent to maximise conservation benefits. Similar to management interventions29, individual gear types express characteristics that span ecological, economic, and social sciences, and to fully understand their true impact they should be viewed beyond the narrow perspective of whether they are visibly destructive. Instead, a multi-directional approach is needed to realise the complete footprint on both the human communities and ecological systems in which they are used.
Artisanal fishing gears are often promoted by managers, based on a widely held perception of smaller footprints compared with more-industrialised or modernised techniques. This is often despite the lack of an holistic understanding of the wide-ranging and far-reaching impacts these gears might pose. Artisanal fish fences (artisanal weirs, static fyke nets), for example, are used frequently and intensively, and their impacts appear severe and far-reaching, making them an ideal gear to test our approach. We show fish fences being used intensively across three ocean basins (Atlantic, Indian, Pacific), before presenting a unique 15-year case study incorporating ecological, fisheries catch and socioeconomic data to examine fish fence impacts across communities (natural and human) and ecosystems (seagrass, coral reef and mangrove), as well as exploring the social and economic drivers underpinning their use. Through such a comprehensive assessment, we are able to highlight otherwise unrecognised threats from this widely used gear type to local stakeholders and across multiple ecosystems, and demonstrate the value of a multi-disciplinary approach in directing evidence-based gear restriction efforts in tropical small-scale fisheries.
Results and discussion
Spatial and temporal patterns in usage and effort
Artisanal fish fences are semi-permanent structures positioned on intertidal and shallow subtidal flats (Fig. 1a) that use fences to funnel fish into a holding structure at the seaward end as the water recedes towards low tide23. They were a common gear type globally before the advent of industrial fishing30, and they remain in use across a wide geographical range as a component of small-scale tropical coastal fisheries. We report the use of artisanal fish fences from the published scientific literature in 19 tropical countries across three oceans; from South America and West Africa through East Africa and the Persian Gulf, to the Indo-Pacific and Pacific Islands (see Methods). Further, image analysis using Google Earth (based on the latest satellite imagery available in July 2018) and the personal observations of the authors, identified their use in three additional countries (Sri Lanka, Thailand and Malaysia), as well as locations in Philippines and Indonesia (Fig. 2). At each location, fence use was shown to not only be present but also in high density.
Long-term data from Kaledupa Island (Wakatobi National Park, Indonesia) show an increase in artisanal fish fence effort over a 15-year period (Fig. 3a; Supplementary Table 1). From just 37 fences in 2002, numbers increased by 450% in only 7 years, peaking at 210 in 2009. Fence length (based on the total length of the central spine) showed a similar trend (analyis of variance; ANOVA, F6 = 9.00, p < 1.25−7), increasing by 69% in 11 years from 106 ± 9 m (mean ± 1SE) in 2005 to 179 ± 9 m in 2016. Finally, mesh size used in the holding structure almost halved (Kruskal–Wallis, H5 = 64.42, p < 1.48−12) from 2.54 ± 0.00 cm in 2005 to only 1.28 ± 0.43 cm in 2016. If all fences were placed end-to-end, they would have stretched for a total of 10.57 km in 2005, and 27.89 km in 2015. Fences are typically arrow-shaped, consisting of a central spine and multiple wings, and those studied here on average incorporated 2.5 times the length of their central spine in total fence length. This means a combined total of 69.73 km of physical barrier was in place around the island in 2015; significantly exceeding the island’s ca. 60 km coastline.
When discussing temporal patterns in total fence effort, it is important to note that, owing to the large spatial footprint and semi-permanent nature of this gear type, both the size and number in use will ultimately be limited by space availability. This could create a false impression to managers that total effort is stabilising, whereas it could simply indicate that spatial saturation is being reached, and that effort may continue to rise through regular mesh size decreases as seen here.
Fishers on the island appear to have changed their main fishing gear preferences, moving from widespread use of low-intensity methods (lines and spears) to a greater reliance on net fishing and fish fences. As part of stratified randomised household interviews throughout Kaledupa, 209 fishers were interviewed in 2005, and 75 interviewed in 2012. The majority of fishers in 2005 used lines as their main gear (54%), with 21% using nets and 7% using fish fences. Ten per cent used small mobile fish traps (bubus) and 5% used spears. By 2012 the majority of fishers used nets (62%) with 30% now using fish fences as their main gear. In 2012, no one reported using spears or lines as their main gear and one fisher reported using a fish attraction device.
Despite this widespread and growing use and large cumulative spatial footprint, fish fences are still only of direct economic benefit to a small proportion of the total fishing community. Each fence is typically owned by a single fisher, and no additional labour is required to maintain their catches unless the owner chooses to employ an assistant to collect catches on their behalf. The widespread negative impacts of fish fence use must be placed in the context of their status as a minority gear type to fully appreciate the mismatch between the economic benefits to a few and the ecological costs suffered by all.
Impacts within and between ecosystems
Local expert workshops and household interviews conducted between 2011 and 2014 revealed the presence of a range of direct physical impacts caused by the construction and use of artisanal fish fences. Considering the importance of habitat in supporting fish stocks31, the loss of habitat from these direct impacts will expand the footprint of fish fence use beyond the simple removal of fish by reducing local carrying capacity and recruitment potential. Fishers commonly remove all seagrass within the immediate vicinity of the fence (Fig. 1d), either through cutting or the use of poison as it is believed that this enhances catch. This creates a patch of habitat loss within the structure of the fence, as well as a halo surrounding it (Fig. 1b), resulting in habitat fragmentation and edge effects, which are known to have negative ecological impacts32,33. Fences also introduce an artificial physical barrier, acting as an obstacle to natural ecosystem functioning, which will interrupt the natural movement of mobile species, but will also impact hydrology, connectivity, and even infochemical processes34, which, in turn, can disrupt benthic community structure. This can lead to a healthy habitat coming abruptly to an end at the seaward side of a fence, to be replaced by a barren seascape on the landward side (Fig. 1c).
Fences are typically constructed using wooden poles harvested in local mangroves, further increasing the ecosystem scale impact of these fisheries. In the Wakatobi, Bruguiera gymnorhiza wood is used35, usually with a 2 m long pole every 0.5 m along the entire length of fence. Based on each structure incorporating on average 2.5 times the length of its central spine in total fence length, this results in ~ 500 poles being used for the construction of a 100 m long fish fence. Using the total number and mean length of fences in 2015, this equates to 139,464 poles being used. Assuming a mean pole radius of 2 cm, and using the average of published wood density values for B. gymnorhiza36, we estimate 268 tonnes of mangrove wood was required to construct the fences present around Kaledupa in 2015, representing a substantial driver of local mangrove deforestation.
Long-term catch monitoring suggests severe and far-reaching ecological impacts from intensive artisanal fish fence use. At the broadest level, catch per unit effort (CPUE) declined by almost 70% between 2005 and 2007 (ANOVA, F8 = 13.53, p < 2−16), from 18.08 ± 6.36 kg fence−1 day−1 to 5.44 ± 0.86 kg fence−1 day−1 (Fig. 3b). This has subsequently stabilised, fluctuating between lows of 3.65 ± 0.22 kg fence−1 day−1 (2012) and 6.29 ± 0.76 kg fence−1 day−1 (2016). The number of individual fish caught showed a similar decline of over 75% (Negative Binomial generalised linear models (GLM), F8 = 478.18, p < 2.2−16), from 713.50 ± 256.67 individuals fence−1 day−1 in 2005 to 172.76 ± 34.32 individuals fence−1 day−1 in 2007. However, unlike CPUE, this downward trend continued, and by 2012 only 36.80 ± 3.10 individuals fence−1 day−1 were being caught. Considering the increases in average fence size and decreases in mesh size during this time, the true extent of decreasing returns from fish fences will be significantly higher than reported here. Stabilised CPUE should not be confused with stable returns. There was also a > 30% decline in the species diversity of catches observed here (ANOVA, F8 = 17.29, p < 2−16), which decreased from 20.00 ± 1.72 species catch−1 in 2005 to 13.69 ± 0.59 in 2016, presumably as species become locally rare or even extirpated.
Over the course of this study, the proportion of juvenile fish in individual catch averages increased by > 400%, from 9.72 ± 3.33% in 2005 to 40.27 ± 1.92% in 2016 (ANOVA, F8 = 19.81, p < 2−16). For species that mature > 15 cm, 81.37 ± 1.73% were caught as juveniles in 2016 compared to 40.79 ± 9.02% in 2005 (Quasibinomial GLM, F8 = 148.47, p < 2.2−16), and those that mature at > 20 cm were caught at 89.73 ± 1.58% in 2016 compared with 57.63 ± 9.82% in 2005 (Quasibinomial GLM, F8 = 96.12, p < 2.2−16). When all catches are combined, the proportion of juveniles caught each year increased from 4.15% to 36.38% (all species), 13.25% to 81.41% (species that mature > 15 cm) and 61.23% to 90.54% (species that mature > 15 cm) (Fig. 3c). Minimising the removal of juvenile fish is a core principle of the ecosystem approach to fisheries management37, whereas larger species tend to be the most ecologically and commercially valuable. Their loss can have significant detrimental impacts, including cascade effects from predator declines38 and macroalgal overgrowth from large herbivore loss39, and so the removal of almost exclusively juveniles will likely have a devastating impact on their survival prospects, and potentially on ecosystem resilience as a whole40.
Analysis of the 10 most abundant species found in catches across years showed an overall decrease in median lengths from the start to the end of this study for seven species; two of these decreases were significant (Moods Median Test; Supplementary Table 2). Interestingly, 2 of the 10 species showed significant increases in median length over the course of the study: Lethrinus rubrioperculatus and Siganus canaliculatus. On one hand this could indicate that, in such a complex multi-species fishery, no individual species were caught in sufficient numbers to accurately detect the true length distributions at a single time point. Alternatively, if these changes are indeed accurate, it could suggest that some species are benefiting from the intensive removal of competitors/predators elsewhere in the system (e.g., from other gear types), or they represent potential winners of environmental change. For example, S. canaliculatus feeds on epiphytic algae, which tends to proliferate with habitat degradation.
Fish surveys via underwater visual census (UVC) on adjacent coral reefs show a corresponding decline in overall abundance. When all sites and depths are combined, fish densities (individuals 250 m−2) almost halved in 10 years, from 910 ± 88 in 2002 to 498 ± 31 in 2012 (Supplementary Figure 1). This was largely driven by a loss in upper outliers, representing the most-pristine reef areas, with maximum densities encountered falling over the same time from 2437 to 1196 individuals 250 m−2, and range declining from 2214 to 969. Whereas reef fish density decreased negatively with the number of fish fences in use (Supplementary Figure 1), this was found not to be statistically significant (linear regression p = 0.08), although in a complex multi-gear fishery this is unsurprising. However, there is evidence to suggest that fish fences are an important, and under-appreciated, driver of these ecosystem wide declines, namely (i) their high exploitation of vulnerable life stages, (ii) their non-selective nature and subsequent exploitation across a diverse fish community, and (iii) their inherent purpose of disrupting the natural movements of fish populations that limits vital connectivity.
Owing to the semi-permanent nature of artisanal fish fences, combined with their large dimensions and small mesh size (1.28 ± 0.43 cm in 2016), they are highly non-selective (i.e., they remove a large proportion of the available community including early life stages). When this is framed within the hyperdiverse marine ecosystems of the Indo-Pacific12, the footprint of such non-selective gears across the entire fish community can be huge. Fish community composition around Kaledupa is well known, thanks to over two decades of intensive research combining visual surveys and fishery catch monitoring (see Methods). A total of 575 fish species have been recorded by visual surveys of local reef, seagrass, and mangrove habitats historically. Of these, 251 (44%) have also been recorded in fish fence catches (Fig. 4). However, a further 263 species have been recorded in fish fence catches that have not also featured in local surveys, meaning these fences are known to exploit at least 514 fish species to some extent at a single location. This includes charismatic species such as sharks and rays, which were observed as by-catch during this study in addition to non-fish species including turtles and various invertebrates. Although discarding of by-catch was minimal during this study, it has recently been recorded in other parts of the Indo-Pacific41, suggesting further sustainability concerns for artisanal fisheries.
Fish fences are designed to take advantage of the natural movements of fish, by forming a barrier from which they are unable to escape as the water recedes towards low tide. This causes disruption to the well-described, and ecologically important, natural connectivity between coastal marine habitats42,43. When the cumulative extent of this barrier is equivalent to ca. 50% of the coastline, as seen here around Kaledupa Island, this disruption is likely to be extreme. When the species recorded in local surveys are categorised into habitat associations based on the specific visual surveys in which they have been recorded locally, the proportion of which are known to be exploited by fish fences increased in those communities occupying multiple habitats (Fig. 4). For example, 90% of the species observed in “reef + seagrass + mangrove” and 85% of species observed in “reef + mangrove” have been recorded in fence catches. This is compared with only 38% of species observed only on reefs. Natural connectivity enhances fish abundance and protects ecological processes19, as well as preserving resilience18, and so any activity that acts to disrupt this connectivity will be counter-productive to conservation efforts. Considering reef fish have been shown to migrate over 30 km44 even local fish fence use can have far-reaching implications across a wide geographical area.
Bioeconomic controls and social conflict
Indonesian fishers will typically invest ca. USD 400 (correct as of 2018) of capital to construct a new fence, and typically no further financial outlay is required for at least 1 year, after which there will be small costs associated with maintenance and repair. This level of capital investment is similar to other gear types used on coral reefs, e.g., gill nets45, but while these alternatives are also typically associated with high regular effort (labour at sea and on land), fish fence use requires little regular effort from the fisher for as long as the structural integrity of the fence is maintained (at which point they can choose whether to repair, replace or exit the fishery). Fish fences are generally moved up to four times per year. Daily effort is restricted to a single trip to empty the fence at low tide and return the catch to land. This makes artisanal gears an example of a highly efficient gear, which are known to impact fish stocks46, but also means fence owners are forced (by the need to recover capital investments) and incentivised (by long-term cost neutrality and low regular effort) to operate their fences for as long as possible. Once a fence is constructed, there exists a lack of any economic or energetic barriers to overfishing. This is coupled to a lack of any technical barrier in the form of gear availability, access to fishing grounds, and required expertise. Thus, fishing pressure is maintained in the face of diminishing returns and habitat damage, satisfying the criteria of Malthusian overfishing when framed alongside continued high human population growth in the tropics47,48.
From a bioeconomic perspective, increasing the cost of fishing (for example, via high capital investment) should theoretically improve sustainability by reducing the total effort at which open-access equilibrium is reached49. However, conversely, a reduction in regular unit cost/effort should have an opposite effect, exacerbating overfishing beyond the original open-access equilibrium. The passive nature of fish fences could therefore negate the potential benefit of capital investment as a control mechanism against overfishing, and could even accelerate fishery collapse (Fig. 5). This impact is worsened by the privatisation of fish fences in recent decades, having evolved from cooperative to single ownership. This concentrates the benefits of fence use within a narrow group of people, and displaces others into other gear types to maintain livelihoods, thus intensifying overall fishing pressure. It is also likely an important contributing factor toward the increase in fence numbers documented during this study as former cooperative members switch to individual ownership.
Many tropical marine habitats, including those studied here around Kaledupa Island, are open-access50. Fisheries governance can be strengthened by the addition of property rights such as territorial user rights fisheries22, or via catch shares in the form of quotas51, in order to avoid a tragedy of the commons scenario52. However, fish fence owners assume perceived property rights while excluding other stakeholders from accessing traditionally open-access fishing grounds. Fish fence owners then assume an unofficial (and unregulated) exclusive spatial harvest right, while undermining the catches of the wider stakeholder community through previously discussed disruption of ecological connectivity and high juvenile removal. The fences surveyed as part of this study averaged a 5:1 length to width ratio, meaning that in 2015 (the most recent year in which all effort metrics are available), a mere 160 fishers (one fisher per fence) assumed dedicated access privileges over an estimated 0.97 km2 of fishing grounds in addition to the ca. 70 km of physical barrier limiting the natural movement of fish stocks.
Fish fences also create social conflict in Indonesia owing to perceived social hierarchy between Pulo (islander) and Bajo (sea nomad) communities. Informal restrictions mean only Pulo fishers are socially permitted to own fences, therefore excluding not only based on economic status but also on ethnicity. To our knowledge, this is locally unique to fish fence ownership, with no other gear types restricting Bajo involvement based on social hierarchy alone, although they are often marginalised by a lack of financial capacity to utilise more technology-driven fishing techniques. When combined with the issues surrounding assumed property rights and privatisation, fish fences undermine co-management efforts, which rely on buy-in across the stakeholder group53. Our interviews with local fishers also reveal evidence of increasing levels of conflict between fishers over space, as catches decline and fishers look to move into new areas.
A new management priority?
Considering the widespread shortfalls in resources impacting the performance of marine conservation interventions17, it is crucial that management effort is directed to maximise positive change via evidence-based recommendations54. In the case of complex tropical multi-gear fisheries, a better understanding of the impact and extent of individual gear types will help identify those having a disproportionate impact and make more informed decisions. For example, it can help ensure that no-take areas (NTA) are matched by evidence-based management of gear types used outside of them15,16,20,55. Fish fences are used where fish protein forms a major part of people’s diets;10 thus maintaining sustainable fisheries is a high priority to protect human health, livelihoods and culture. Yet, they disrupt vital ecological connectivity, remove high quantities of juveniles, exploit hundreds of species, lack traditional economic and social barriers to overfishing and create social conflict among wider stakeholder groups, whilst only benefiting a minority of the overall stakeholder community. This suggests a worrying, and disproportionately high, impact on both fisheries sustainability and the multiple ecosystems on which they depend.
Restricting fish fence use would represent a low-effort—high-reward conservation strategy as they are semi-permanent and thus easily detectable, making them far easier to police than many other gears. This effort would result in direct and immediate benefits to the health and extent of three distinct ecosystems (coral reefs, seagrass beds, and mangrove forests), would remove a significant sink for large numbers of juvenile fish across many hundreds of species, and would benefit the wider fishing community by removing an important source of social conflict whilst re-opening large areas of currently inaccessible fishing ground and restoring natural fish movement/migrations. There would likely be displacement into alternative gear types, but owing to the wide-ranging threats from fish fence use outlined here, we would anticipate this to have an overall net benefit to the fishery as a whole. Without restriction, the low regular effort required to maintain operation combined with the economic need to recover initial investment will likely mean their widespread and intensive use persists regardless of further declines in fish stocks. We therefore call on managers to target gear restrictions toward fish fences as an urgent priority in achieving sustainability in these vital fisheries, while improving our understanding of the hidden threats of artisanal fisheries by applying our approach to a broader suite of gear types.
Satellite imagery visual analysis to determine extent of artisanal fish fence use
Owing to the large and semi-permanent nature of artisanal fish fences, their structures are easily visible from satellite imagery30. Artisanal fish fences have previously been mentioned within the scientific literature as being used in 19 countries within the tropics: Indonesia;23,25,56 French Polynesia;57 Micronesia;58 Samoa;59,60 Tonga;61 Mozambique;62 Tanzania;25,63 Kuwait/Saudi Arabia/Qatar/United Arab Emirates/Iran/Bahrain;30 Brazil/Mauritania/India/Singapore/Philippines/Australia25. Here, we use Google Earth to identify their widespread use at locations in three additional countries (Malaysia, Thailand and Sri Lanka), plus new locations in Indonesia and Philippines, to better highlight the geographical scale of their use. These locations were selected based on personal field observations of the authors, and for each location visual scans were performed, with the GPS co-ordinates of each visible fence recorded (Fig. 2). Visual scans were repeated twice by the same researcher to ensure accurate counts.
Longitudinal case study location
The Wakatobi Marine National Park, Southeast Sulawesi, was designated in 1996 and covers 1.39 million hectares. Kaledupa is the second largest island in the park, with a human population of around 17,000 distributed among 27 villages with a high reliance on artisanal fisheries23. There are two distinct ethnic groups present on and around Kaledupa: the land-based Butonese descendents (Pulo) and a nomadic sea people (Bajo) who settled in permanent villages built on artificial platforms over the reef flats during the 20th Century64. Owing to assumed ownership rights over fishing grounds locally, they are only constructed and owned by Pulo fishers.
Local effort assessment
To estimate the effort allocated to artisanal fence use by the local fishing community during the course of this study, three values were quantified. First, island-wide visual censuses of fences were conducted by circumnavigating Kaledupa and its outlying islands by boat. A similar pre-study census from 2002 was also included as a historical time point (unpublished). Second, the total length of each fence monitored in this study was measured along the central spine (Panaju) to provide an approximate mean total fence length for Kaledupa. The mesh size in use in each fence was also measured in the collection end (typically, the finest mesh size in use within the structure). Census and fence length data are unavailable for all years owing to logistical constraints, specifically adverse weather conditions prohibiting island-wide access.
Household surveys and workshops
To understand marine and coastal resource use patterns around Kaledupa Island, a series of stratified randomised and semi-quantitative household interviews were conducted around the Island (spread across 17 villages) in both 2005 and 2012 (see ref. 65). Within these interviews 209 fishers were interviewed in 2005 and 75 interviewed in 2012, and the data specific to fishers were examined in both years with respect to fisheries gear use.
In order to gain detailed insights into the methods and broader environmental context of fish fence use, we ran two local expert focus discussion workshops (see ref. 66) during 2012. One of these was with the local government, NGO, and village-level officials who had involvement in fishery activity. The second workshop was with fishers from the local indigenous Bajo communities. Discussions focussed on perceived impacts on the local marine environment and long-term ecological change. Ethical approval for working with human participants was obtained from Swansea University (SU-Ethics-Staff-250319/134), and informed consent was obtained.
Catches from artisanal fish fences were monitored around the northeast coast of Kaledupa, in 5-week-long intensive sampling periods between July and August in 2003, 2005, 2007, 2009, and annually between 2011 and 2016. During each sampling period a locally run fish fence cooperative (known locally as a Kelompok), comprising between 7 and 20 individual fences and their owners, was selected at random and their owners approached informally to discuss participation in the study. Each fence was emptied daily, as usual at low tide, and the catch returned by the owner to a centralised location (typically an owner’s home) in the village of Laulua (5°29’56.08”S 123°44’52.97”E) for analysis.
On arrival, the total catch was weighed to provide CPUE, reported as kg fence−1 day−1. All fish were subsequently identified to species level, and length measurements taken of all individuals. Where > 20 individuals of a species appeared in a single catch, a random sub-sample of 20 individuals were chosen for length measurements and mean values applied to the total number caught. Length data were used to quantify the proportion of each species and total catch caught as juveniles using published species-specific size of maturation values67. Where these values were not available, a value one-third of the species-specific maximum size was used to estimate minimum size of maturation68,69. To explore trends in the length of caught species, 10 species were chosen that were caught in the highest numbers throughout the study (excluding the smallest shoaling species, e.g. sardines). The median length of each of these species was then calculated from the catch monitoring data.
Over the nine sampling seasons, 995 catches were surveyed comprising 70,967 individual fish. As no animals were harmed for the purposes of this study (normal daily catches of a working fishery were observed), ethical approval was not sought.
Fish surveys of adjacent reefs
Densities of fish on adjacent coral reefs were determined via a reef monitoring programme between 2002 and 2012. During this time, six reef sites were visited between June-August in 2002–03, 2005, 2007–09, and 2011–2012. UVC70 was performed along 50 × 5 × 5 m belt transects, with all fish identified to species level. At each site and year, triplicate transects were completed on three reef zones: reef flat (0–3 m), reef crest (3–8 m), and reef slope (8–15 m).
Species lists from fish fence catch and reef fish surveys were combined with similar lists from published surveys of Kaledupan seagrass and mangrove habitats43,71,72,73. Each species was then assigned a particular habitat association (e.g., reef + seagrass + mangrove), based on the surveys in which it was recorded. These data provided a casual estimate of the inter-habitat connectivity present for each species locally, and the proportion of each community known to be exploited by fish fences.
CPUE and reef fish survey data were log-transformed and data on species diversity and the total proportion of juveniles square-root-transformed to allow parametric statistical testing. Significant variations in the means of the above variables over time, along with untransformed data on fence length, were tested for using one-way ANOVA, with the specific source of significance explored using post hoc Tukey–Kramer testing. Variations in mesh size were tested for using non-parametric Kruskal–Wallis with pairwise Mann–Whitney U with Bonferroni correction. Data on the number of individuals per catch, as well as the proportion of juveniles amongst species that mature over either 15 cm or 20 cm body size failed to conform to the assumptions of linear regression, and so negative binomial (individuals) and quasibinomial (proportion of juveniles among larger species) GLM were performed alongside post hoc Tukey–Kramer testing. Differences in fish length for individual species between the start and end of the study were performed using Moods Median Test. All statistical analyses were performed using R74.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Hughes, T. P. et al. Coral reefs in the anthropocene. Nature 546, 82–90 (2017).
Eyre, B. D. et al. Coral reefs will transition to net dissolving before end of century. Science 359, 908–911 (2018).
Hoegh-Guldberg, O., Kennedy, E. V., Beyer, H. L., McClennen, C. & Possingham, H. P. Securing a long-term future for coral reefs. Trends Ecol. Evol. 33, 936–944 (2018).
Arias-Ortiz, A. et al. A marine heatwave drives massive losses from the world’s largest seagrass carbon stocks. Nat. Clim. Chang 8, 338–344 (2018).
Harborne, A. R., Rogers, A., Bozec, Y.-M. & Mumby, P. J. Multiple stressors and the functioning of coral reefs. Ann. Rev. Mar. Sci. 9, 445–468 (2017).
Rogers, A., Blanchard, J. L. & Mumby, P. J. Fisheries productivity under progressive coral reef degradation. J. Appl. Ecol. 55, 1041–1049 (2018).
Graham, N. A. J., Jennings, S., MacNeil, M. A., Mouillot, D. & Wilson, S. K. Predicting climate-driven regime shifts versus rebound potential in coral reefs. Nature 518, 94–97 (2015).
Gattuso, J. P. et al. Contrasting futures for ocean and society from different anthropogenic CO2emissions scenarios. Science. 349, aac4722 (2015).
Hoegh-Guldberg, O. Coral reef sustainability through adaptation: Glimmer of hope or persistent mirage? Curr. Opin. Environ. Sustain 7, 127–133 (2014).
Dulvy, N. K. & Allison, E. H. A place at the table? Nat. Clim. Chang. 3, 68–70 (2009).
Edgar, G. J. et al. Global conservation outcomes depend on marine protected areas with five key features. Nature 506, 216–20 (2014).
Barlow, J. et al. The future of hyperdiverse tropical ecosystems. Nature 559, 517–526 (2018).
Eastwood, E. K., López, E. H. & Drew, J. A. Population connectivity measures of fishery-targeted coral reef species to inform marine reserve network design in Fiji. Sci. Rep. 6, 1–10 (2016).
Mellin, C., Macneil, M. A., Cheal, A. J., Emslie, M. J. & Caley, M. J. Marine protected areas increase resilience among coral reef communities. Ecol. Lett. 19, 629–637 (2016).
Roberts, C. M. et al. Marine reserves can mitigate and promote adaptation to climate change. Proc. Natl Acad. Sci. 114, 6167–6175 (2017).
Krueck, N. C. et al. Reserve sizes needed to protect coral reef fishes. Conserv. Lett. 00, 1–9 (2017).
Gill, D. A. et al. Capacity shortfalls hinder the performance of marine protected areas globally. Nature 543, 665–669 (2017).
McCook, L. J. et al. Management under uncertainty: Guide-lines for incorporating connectivity into the protection of coral reefs. Coral Reefs 28, 353–366 (2009).
Olds, A. D., Connolly, R. M., Pitt, K. A. & Maxwell, P. S. Habitat connectivity improves reserve performance. Conserv. Lett. 5, 56–63 (2012).
MacNeil, M. A. et al. Recovery potential of the world’s coral reef fishes. Nature 520, 341 (2015).
McClanahan, T. R., Graham, N. A. J., MacNeil, M. A. & Cinner, J. E. Biomass-based targets and the management of multispecies coral reef fisheries. Conserv. Biol. 29, 409–417 (2015).
Cinner, J. E. et al. Bright spots among the world’s coral reefs. Nature 535, 416–419 (2016).
Exton, D. A. Nearshore fisheries of the Wakatobi. in Marine Research and Conservation in the Coral Triangle (eds Clifton, J., Unsworth, R. K. F. & Smith, D. J.) Nova Science Publishers, New York 1–15 (2010).
Selgrath, J. C., Gergel, S. E. & Vincent, A. C. J. Incorporating spatial dynamics greatly increases estimates of long-term fishing effort: a participatory mapping approach. ICES J. Mar. Sci. 75, 210–220 (2018).
Nordlund, L. M., Unsworth, R. K. F., Gullström, M. & Cullen-Unsworth, L. C. Global significance of seagrass fishery activity. Fish Fish. 19, 399–412 (2018).
Selgrath, J. C., Gergel, S. E. & Vincent, A. C. J. Shifting gears: diversification, intensification, and effort increases in small-scale fisheries (1950–2010). PLoS ONE 13, e0190232 (2018).
Pet-Soede, C., Cesar, H. & Pet, J. An economic analysis of blast fishing on Indonesian coral reefs. Environ. Conserv. 26, 83–93 (1999).
Fox, H. & Caldwell, R. Recovery from blast fishing on coral reefs: a tale of two scales. Ecol. Appl. 16, 1631–1635 (2006).
Harvey, B. J., Nash, K. L., Blanchard, J. L. & Edwards, D. P. Ecosystem-based management of coral reefs under climate change. Ecol. Evol. (2018). https://doi.org/10.1002/ece3.4146.
Al-abdulrazzak, D. & Pauly, D. Managing fisheries from space: Google Earth improves estimates of distant fish catches. ICES J. Mar. Sci. 71, 450–454 (2014).
Brown, C. J. et al. The assessment of fishery status depends on fish habitats. Fish Fish. (2018). https://doi.org/10.1111/faf.12318.
Smith, T. M., Hindell, J. S., Jenkins, G. P. & Connolly, R. M. Edge effects on fish associated with seagrass and sand patches. Mar. Ecol. Prog. Ser. 359, 203–213 (2008).
Fletcher, R. J. et al. Is habitat fragmentation good for biodiversity? Biol. Conserv. 226, 9–15 (2018).
Exton, D. A., Mcgenity, T. J., Steinke, M., Smith, D. J. & Suggett, D. J. Uncovering the volatile nature of tropical coastal marine ecosystems in a changing world. Glob. Chang. Biol. 21, 1383–1394 (2015).
Cragg, S. M. & Hendy, I. W. Mangrove forests of the Wakatobi National Park. in Marine Research and Conservation in the Coral Triangle: The Wakatobi National Park (eds Clifton, J., Unsworth, R. K. F. & Smith, D.). Nova Science Publishers, New York 67–83 (2010). ISBN- 9781616684730.
Chave, J. et al. Towards a worldwide wood economics spectrum. Ecol. Lett. 12, 351–366 (2009).
Graham, N., Ferro, R. S. T., Karp, W. A. & MacMullen, P. Fishing pratice, gear design, and the ecosystem approach - three case studies demonstrating the effect of management strategy on gear selectivity and discards. ICES J. Mar. Sci. 64, 744–750 (2007).
Estes, J., Terborgh, J. & Brashares, J. Trophic downgrading of planet Earth. Science 333, 301–306 (2011).
Fox, R. J. & Bellwood, D. R. Herbivores in a small world: network theory highlights vulnerability in the function of herbivory on coral reefs. Funct. Ecol. 28, 642–651 (2014).
Pratchett, M. S., Hoey, A. S. & Wilson, S. K. Reef degradation and the loss of critical ecosystem goods and services provided by coral reef fishes. Curr. Opin. Environ. Sustain. 7, 37–43 (2014).
Jones, B. L., Unsworth, R. K. F., Udagedara, S. & Cullen-Unsworth, L. C. Conservation concerns of small-scale fisheries: by-catch impacts of a shrimp and finfish fishery in a Sri Lankan lagoon. Front. Mar. Sci. 5, 1–13 (2018).
Mumby, P. J. et al. Mangroves enhance the biomass of coral reef fish communities in the Caribbean. Nature 427, 533–536 (2004).
Unsworth, R. K. F. et al. High connectivity of Indo-Pacific seagrass fish assemblages with mangrove and coral reef habitats. Mar. Ecol. Prog. Ser. 353, 213–224 (2008).
McMahon, K. W., Berumen, M. L. & Thorrold, S. R. Linking habitat mosaics and connectivity in a coral reef seascape. Proc. Natl Acad. Sci. 109, 15372–15376 (2012).
Mangi, S. C., Roberts, C. M. & Rodwell, L. D. Financial comparisons of fishing gear used in Kenya’s coral reef lagoons. Source. AMBIO A J. Hum. Environ. 36, 671–676 (2007).
Brewer, T. D., Cinner, J. E., Green, A. & Pressey, R. L. Effects of human population density and proximity to markets on coral reef fishes vulnerable to extinction by fishing. Conserv. Biol. 27, 443–452 (2013).
Pauly, D. From growth to Malthusian overfishing: stages of fisheries resource misuse. Tradit. Mar. Resour. Manag. Knowl. Inf. Bull. 3, 7–14 (1994).
McClanahan, T. R., Hicks, C. C. & Darling, E. S. Malthusian overfishing and efforts to overcome it on Kenyan coral reefs. Ecol. Appl. 18, 1516–1529 (2008).
McManus, J. W. Tropical marine fisheries and the future of coral reefs: a brief review with emphasis on Southeast Asia. Coral Reefs 16, S121–S127 (1997).
Newton, K., Côté, I. M., Pilling, G. M., Jennings, S. & Dulvy, N. K. Current and future sustainability of island coral reef fisheries. Curr. Biol. 17, 655–658 (2007).
Costello, C., Gaines, S. D. & Lynham, J. Can catch shares prevent fisheries collapse? Science 321, 1678–1681 (2008).
Berkes, F. et al. Globalization, roving bandits, and marine resources. Science 311, 1557–1558 (2006).
Cinner, J. E. et al. Comanagement of coral reef social-ecological systems. Proc. Natl Acad. Sci. 109, 5219–5222 (2012).
Johnson, A. E. et al. Trends, current understanding and future research priorities for artisanal coral reef fisheries research. Fish Fish. 14, 281–292 (2013).
McCauley, D. J. et al. Marine defaunation: Animal loss in the global ocean. Science 347, 6219 (2015).
Unsworth, R. K. F. & Cullen, L. C. Recognising the necessity for Indo-Pacific seagrass conservation. Conserv. Lett. 3, 63–73 (2010).
Clua, E. et al. Towards multidisciplinary indicator dashboards for coral reef fisheries management. Aquat. Living Resour. 18, 199–213 (2005).
Takeda, J. The Progress Report of the 1999 Survey of the Research Project ‘Social Homeostasis of Small Islands in an Island-Zone. Kagoshima University Research Center for the Pacific Islands, Occasional Papers No. 34. 117–127. (2001).
Fa’asili, U. & Kelokolo, L. The use of village by-laws in marine conservation and fisheries management. Pacific Sci. Assoc. Intercongress 9–13 (1997).
Johannes, R. E. The renaissance of community-based marine resource management in Oceania. Annu. Rev. Ecol. Syst. 33, 317–340 (2002).
King, M., Faasili, U. & Ropeti, E.. Management strategies for inshore fisheries in tropical Pacific Islands. in South Pacific Comm. Forum Fish. Agency Work. Manag. 606 South Pacific Inshore Fish. Manuscr. Collect. Ctry. Statements Backgr. Pap. 2, 507–519 (1995).
de Boer, W. F., van Schie, A. M. P., Jocene, D. F., Mabote, A. B. P. & Guissamulo, A. The impact of artisanal fishery on a tropical intertidal benthic fish community. Environ. Biol. Fishes 61, 213–229 (2001).
Torre-Castro, De. La, Rönnbäck, M. & Links, P. between humans and seagrasses - an example from tropical East. Afr. Ocean Coast. Manage. 47, 361–387 (2004).
Clifton, J. Refocusing conservation through a cultural lens: Improving governance in the Wakatobi National Park, Indonesia. Mar. Policy 41, 80–86 (2013).
Cullen-Unsworth, L. C., Pretty, J. & Smith, D. J. Developing community-derived indicators of economic status in the coral triangle: a management support tool. Ocean Coast. Manage. 54, 446–454 (2011).
Nyumba, T. O., Wilson, K., Derrick, C. J. & Mukherjee, N. The use of focus group discussion methodology: insights from two decades of application in conservation. Methods Ecol. Evol. 9, 20–32 (2018).
Froese, R. & Pauly, D. FishBase. http://www.fishbase.org. (2018).
Dorenbosch, M., Grol, M., Nagelkerken, I. & van der Velde, G. Different surrounding landscapes may result in different fish assemblages in ast african seagrass beds. Hydrobiologia 563, 45–60 (2006).
Nagelkerken, I. & van der Velde, G. Do non-estuarine mangroves harbour higher densities of juvenile fish than adjacent shallow-water and coral reef habitats in Curacao (Netherlands Antilles)? Mar. Ecol. Prog. Ser. 245, 191–204 (2002).
Samoilys, M. A. & Carlos, G. Determining methods of underwater visual census for estimating the abundance of coral reef fishes. Environ. Biol. Fishes 57, 289–304 (2000).
Green, B., Smith, D. J. & Underwood, G. J. Habitat connectivity and spatial complexity differentially affect mangrove and salt marsh fish assemblages. Mar. Ecol. Prog. Ser. 466, 177–192 (2012).
Unsworth, R. K. F. et al. Structuring of Indo-Pacific fish assemblages along the mangrove-seagrass continuum. Aquat. Biol. 5, 85–95 (2009).
Unsworth, R. K. F., Wylie, E., Smith, D. J. & Bell, J. J. Diel trophic structuring of seagrass bed fish assemblages in the Wakatobi Marine National Park, Indonesia. Estuar. Coast. Shelf Sci. 72, 81–88 (2007).
Core Team, R. R: A language and environment for statistical computing. R. Found. Stat. Comput. 1, 409 (2013).
Caddy, J. F. & Mahon, R. Reference points for fisheries management. FAO Fisheries Technical Paper No 347. Rome. (1995). ISBN92-5-103733-7.
This research was funded by Operation Wallacea in partnership with Hasanuddin University, Makassar, with permission from RISTEK. We thank all field scientists and student volunteers who helped with data collection, and thank the local communities of Kaledupa Island, in particular the fish fence owners themselves, for allowing their daily routines to be disrupted in order for our surveys to be conducted. We are particularly grateful to Beloro and his team at the local Kaledupan fisheries NGO FORKANI, who provided invaluable local knowledge and facilitation; this project would not have been possible without them. We also thank Pippa Mansell for logistical assistance and fish fence census data collection.
The authors declare no competing interests.
Journal peer review information: Nature Communications thanks Laurent Vigliola and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Exton, D.A., Ahmadia, G.N., Cullen-Unsworth, L.C. et al. Artisanal fish fences pose broad and unexpected threats to the tropical coastal seascape. Nat Commun 10, 2100 (2019). https://doi.org/10.1038/s41467-019-10051-0
This article is cited by
Suppressed recovery of functionally important branching Acropora drives coral community composition changes following mass bleaching in Indonesia
Coral Reefs (2022)
The ecological importance of habitat complexity to the Caribbean coral reef herbivore Diadema antillarum: three lines of evidence
Scientific Reports (2021)