Elsevier

Marine Pollution Bulletin

Volume 143, June 2019, Pages 24-32
Marine Pollution Bulletin

Marine protected areas are more effective but less reliable in protecting fish biomass than fish diversity

https://doi.org/10.1016/j.marpolbul.2019.04.015Get rights and content

Highlights

  • We develop the Conservation Status Index to test the efficiency of marine protection.

  • The efficiency of marine protection depends on the ecoregion.

  • The CSIbiomass shows the major efficiency in protected areas.

  • The biomass of threatened species presents the highest contribution to the efficiency.

Abstract

Marine protected areas (MPAs) provide multiple conservation benefits, thus raising the question of how good and consistent they are at their roles. Here, we quantified three components, namely, diversity, biomass, and other relevant variables, in numerous protected and unprotected areas across four marine ecoregions in south-western Europe. We created a “global conservation status index” (CSIglobal) as the sum of CSIdiversity, CSIbiomass, and CSIrelevant. We then tested whether CSI and its three components varied as a function of protection and marine ecoregion. MPA efficiency, defined as the effect size of protection on CSIglobal, was unreliable and varied with geography. CSIbiomass and CSIrelevant contributed to the unreliability of MPA efficiency, while CSIdiversity was reliable. CSIbiomass showed the major efficiency in protected areas (60%). Biomass of threatened species was the single largest variable that contributed to MPA efficiency. Our easy-to-use approach can identify high- and low-efficient MPAs and help to clarify their actual roles.

Introduction

Marine protected areas (MPAs) are one of the main management tools for the current human-driven biodiversity crisis. With increasing anthropogenic pressures, MPAs are essential to preserve natural resources, biodiversity, and ecosystem properties (Micheli et al., 2012; Hilborn, 2016; Campbell et al., 2017). MPAs have steadily increased in the last decades to >5% of coastal areas under national jurisdictions and <1% of the high seas (Spalding et al., 2013) figures that keep on increasing with the establishment of some large MPAs, particularly in tropical waters (Devillers et al., 2015). MPAs are pivotal tools for coastal fisheries management and biodiversity conservation (Edgar et al., 2014). Yet, only 10% of the MPA surfaces are no-take zones, free of extraction, or habitat alteration activities, while 94% of MPAs allow fishing and other activities (Thomas et al., 2014; Costello and Ballantine, 2015; Campbell et al., 2017). Certainly, MPAs include a high range of areas, designs, uses, and management goals (Al-Abdulrazzak and Trombulak, 2012; Edgar et al., 2014; Pérez-Ruzafa et al., 2017), which could result in many benefits and varying degrees of protection efficiencies.

Besides MPAs, additional protection measures have been taken to contribute to biodiversity conservation, protection of threatened species, and restoration of fish stocks, including national parks, marine sanctuaries, natural parks, or natural monuments (Al-Abdulrazzak and Trombulak, 2012). Moreover, areas such as military zones can offer protection because of strong surveillance, highly restrictive access, and ban of extractive activities. All these protection measures can lead to the recovery of natural resources and other positive effects on natural communities (Russ et al., 2005; Weeks et al., 2010; Campbell et al., 2017).

The benefits of protection in marine communities are abundant, mostly focused on traits associated with diversity, biomass, or other relevant aspects related to protection. Protected areas are associated with larger species richness (Wantiez et al., 1997; Ciriaco et al., 1998; Edgar and Barrett, 1999; Barrett et al., 2007), larger trophic diversity (Shears and Babcock, 2003; Harmelin-Vivien et al., 2015), and larger functional diversity (Stelzenmüller et al., 2009; Villamor and Becerro, 2012; Guilhaumon et al., 2015) than unprotected areas. Protection also triggers an increase in fish biomass, particularly of commercial fish species (Barrett et al., 2007; Fenberg et al., 2012; Parravicini et al., 2014; Pérez-Ruzafa et al., 2017), likely as a result of decreased fishing pressures (e.g., larger biomass of fish over 20 cm; Edgar and Barrett, 1999; Barrett et al., 2007; Stuart-Smith et al., 2017). However, the biomass of other groups of species such as fish species in the IUCN Red List (Nieto et al., 2015) has received less attention (Willis et al., 2003; Afonso et al., 2011; Harmelin-Vivien et al., 2015). Other relevant variables unevenly used to assess the effects of marine protection include abundance of higher carnivores (Cole, 1994; Harmelin et al., 1995), vulnerability of fish community (Cheung et al., 2007; Stuart-Smith et al., 2017; Vasconcelos et al., 2017), and fish size (Shears and Babcock, 2003; Sciberras et al., 2013). Overall, most available evidence supports for a positive effect of protection on all these traits, providing ample MPA benefits in terms of fish diversity, fish biomass, and relevant traits of the fish community.

The variability in MPA traits and benefits also points toward the possibility that MPAs may be inconsistent in their multiple roles, leading to varying degrees and contrasting levels of efficiency (Dichmont et al., 2013; White et al., 2014). In fact, the positive effects of protection are unevenly spread across MPAs, and numerous studies fail to provide evidence for the expected beneficial effects of protection. Literature on the so-called paper parks provides ample evidence that MPAs can be inefficient (Bustamante et al., 2014; Gallacher et al., 2016) due to multiple factors (Rife et al., 2013; Edgar et al., 2014). Often, the protection effects of MPAs, e.g., increase in species richness or abundance, are noticeable after sufficiently long periods together with suitable control sites (Stobart et al., 2009; Chirico et al., 2017). Moreover, many studies that assessed MPA efficiency have focused on one rather than several benefits (McClanahan et al., 1999; Vanderklift et al., 2013), which could account for differences associated with the specifics of each benefit, MPA, or geographic region investigated (Caveen et al., 2015; Fletcher et al., 2015; Hughes et al., 2016).

Studies examining the effects of protection on multiple benefits over large geographic scales can provide opportunities to advance our understanding on how good MPAs are at achieving their multiple benefits and how reliable MPAs are at providing such benefits. In this study, we followed this approach to shed some light on the relationship between protection and their benefits. We used fish communities across south-western Europe to investigate how fish diversity, fish biomass, and other relevant protection-related benefits contributed to the overall differences between fish communities in protected and unprotected areas and tested whether these benefits were consistent or varied as a function of geography. We investigated >20 protected sites distributed in four marine ecoregions of the world (Spalding et al., 2007) in the Atlantic-Mediterranean confluence area. We used species richness, trophic diversity, and functional diversity to evaluate MPA benefits on fish diversity; biomass of commercial fish, biomass of large fish, and biomass of threatened fish species to evaluate MPA benefits on fish biomass; and fish vulnerability, fish size, and abundance of higher carnivores as other MPA benefits on fish communities. Our results showed evidence for a small but consistent protection effect on fish diversity as opposed to larger and geographically variable protection effects on biomass and other relevant variables that resulted in unreliable MPA efficiency in our study area.

Section snippets

Study area and field survey

We sampled a total of 372 sites that are mostly scattered along, but not limited to, the coast of Spain, Portugal, and North Africa (Fig. 1). The locations included 22 MPAs from four marine ecoregions (Alboran Sea; Azores Canaries Madeira, hereafter Canary Is.; South European Atlantic Shelf, hereafter Atlantic; and Western Mediterranean) defined by Spalding et al. (2007) as “areas of relatively homogeneous species composition, clearly distinct from adjacent systems.” The species composition of

Global conservation status index (CSIglobal)

MPA efficiency was unreliable and varied significantly with the ecoregions (Table 3, CSIglobal, p interaction < 0.001, Fig. 3a). We found larger CSI values in protected areas than in unprotected areas in the Canary Is. (4.51 ± 0.42 and 2.70 ± 0.11; t = 5.06, p < 0.001) and Western Mediterranean (2.94 ± 0.19 and 1.87 ± 0.07; t = 3.09, p = 0.002) ecoregions and no CSIglobal differences in the Atlantic (2.57 ± 0.54 and 1.83 ± 0.06; t = 1.39, p = 0.163) and Alboran Sea (2.56 ± 0.12 and 2.27 ± 0.13;

Discussion

MPAs are becoming one of the most prevalent tools to promote biodiversity conservation and sustainable use of marine resources (Gaines et al., 2010; Spalding et al., 2013). Available evidence supports for multiple benefits of protection and points to ineffective MPA management when benefits are missing (Rife et al., 2013). These arguments may lead to believe that MPAs would excel at all their multiple roles under good management practices. Although good management is imperative for effective

Conclusions

The present study showed that MPA efficiency was unreliable and varied with ecoregion, highlighting contrasting differences between effective and ineffective MPAs in multiple geographic areas. Biodiversity conservation, the largest conservation goal present in 17 out of 22 MPAs in our study, is a benefit that MPAs reliably provide in our study area, even though the magnitude of the effect is small. Biomass-related traits were the largest contributors to MPA efficiency, yet the effect of

Acknowledgements

This work was supported by the Spanish Ministry of Economy grant MARINERES [grant number CGL2013-49122-C3-1-R], and Josu G. Alday was supported by Ramón y Cajal fellowships (RYC-2016-20528). Besides, we are deeply grateful to the Spanish Ministry of Defense, specifically to “Grupo de Regulares de Melilla n52” and “Regimiento Mixto de Artillería n32” for the strong support to access remote military locations including Peñón Vélez de la Gomera and Archipiélago de Alhucemas. Additional thanks to

References (66)

  • T.R. McClanahan et al.

    The effects of marine parks and fishing on coral reefs of northern Tanzania

    Biol. Conserv.

    (1999)
  • A. Pérez-Ruzafa et al.

    Modelling spatial and temporal scales for spill-over and biomass exportation from MPAs and their potential for fisheries enhancement

    J. Nat. Conserv.

    (2008)
  • C. Sangil et al.

    No-take areas as an effective tool to restore urchin barrens on subtropical rocky reefs

    Estuar. Coast. Shelf Sci.

    (2012)
  • A. Villamor et al.

    Species, trophic, and functional diversity in marine protected and non-protected areas

    J. Sea Res.

    (2012)
  • R.C. Babcock et al.

    Decadal trends in marine reserves reveal differential rates of change in direct and indirect effects

    Proc. Natl. Acad. Sci.

    (2010)
  • A.E. Bates et al.

    Resilience and signatures of tropicalization in protected reef fish communities

    Nat. Clim. Chang.

    (2013)
  • Brown, C., Parker, B., Ahmadia, G.N., Ardiwijaya, R., Purwanto, P., Game, E.T., 2017. The Cost of Enforcing Marine...
  • G. Bustamante et al.

    Marine protected areas management in the Caribbean and Mediterranean seas: making them more than paper parks

    Aquat. Conserv. Mar. Freshwat. Ecosyst.

    (2014)
  • S.J. Campbell et al.

    Fishing-gear restrictions and biomass gains for coral reef fishes in marine protected areas

    Conserv. Biol.

    (2017)
  • A. Caveen et al.

    The Controversy over Marine Protected Areas

    (2015)
  • W.W.L. Cheung et al.

    Intrinsic vulnerability in the global fish catch

    Mar. Ecol. Prog. Ser.

    (2007)
  • A.A.D. Chirico et al.

    Community- and government-managed marine protected areas increase fish size, biomass and potential value

    PLoS One

    (2017)
  • S. Ciriaco et al.

    Monitoring the Miramare Marine Reserve: assessment of protection efficiency

    Ital. J. Zool.

    (1998)
  • J. Claudet et al.

    Marine reserves: size and age do matter

    Ecol. Lett.

    (2008)
  • S. Clemente et al.

    Evidence of the top-down role of predators in structuring sublittoral rocky-reef communities in a marine protected area and nearby areas of the Canary Islands

    ICES J. Mar. Sci.

    (2009)
  • R. Devillers et al.

    Reinventing residual reserves in the sea: are we favouring ease of establishment over need for protection?

    Aquat. Conserv. Mar. Freshwat. Ecosyst.

    (2015)
  • C.M. Dichmont et al.

    Evaluating marine spatial closures with conflicting fisheries and conservation objectives

    J. Appl. Ecol.

    (2013)
  • G.J. Edgar et al.

    Systematic global assessment of reef fish communities by the Reef Life Survey program

    Sci. Data

    (2014)
  • G.J. Edgar et al.

    Global conservation outcomes depend on marine protected areas with five key features

    Nature

    (2014)
  • W.J. Fletcher et al.

    Large-scale expansion of no-take closures within the Great Barrier Reef has not enhanced fishery production

    Ecol. Appl.

    (2015)
  • S.D. Gaines et al.

    Designing marine reserve networks for both conservation and fisheries management

    Proc. Natl. Acad. Sci. U. S. A.

    (2010)
  • A.M. García-Mederos et al.

    The structure of a nearshore fish assemblage at an oceanic island: insight from small scale fisheries through bottoms traps at Gran Canary Island (Canary Islands, eastern Atlantic)

    Aquat. Living Resour.

    (2015)
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