Mobulid rays have a conservative life history and are caught in direct fisheries and as by-catch. Their subsequent vulnerability to overexploitation has recently been recognized, but fisheries management can be ineffective if it ignores habitat and prey preferences and other trophic interactions of the target species. Here, we assessed the feeding ecology of four mobulids (Manta birostris, Mobula tarapacana, M. japanica, M. thurstoni) in the Bohol Sea, Philippines, using stomach contents analysis of fisheries specimens landed between November and May in 2013–2015. We show that the mobulids feed heavily on euphausiid krill while they are in the area for approximately six months of the year. We found almost no trophic separation among the mobulid species, with Euphausia diomedeae as the major prey item for all species, recorded in 81 of 89 total stomachs (91%). Mobula japanica and M. thurstoni almost exclusively had this krill in their stomach, while M. tarapacana had a squid and fish, and Ma. birostris had myctophid fishes and copepods in their stomachs in addition to E. diomedeae. This krill was larger than prey for other planktivorous elasmobranchs elsewhere and contributed a mean of 61 364 kcal per stomach (±105 032 kcal s.e., range = 0–631 167 kcal). Our results show that vertically migrating mesopelagic species can be an important food resource for large filter feeders living in tropical seas with oligotrophic surface waters. Given the conservative life history of mobulid rays, the identification of common foraging grounds that overlap with fishing activity could be used to inform future fishing effort.
Mobulid rays, a group of closely related filter-feeders, are threatened globally by bycatch and targeted fisheries. Their habitat use and feeding ecology are not well studied, and most efforts have focused on temporally limited stomach content analysis or inferences from tagging data. Previous studies demonstrate a variety of different diving behaviors across species, which researchers have interpreted as evidence of disparate foraging strategies. However, few studies have examined feeding habitats and diets of multiple mobulid species from a single location, and it is unclear if the proposed differences in diving and inferred foraging behavior are examples of variability between species or regional adaptations to food availability. Here, we use stable isotope data from mobulids landed in fisheries to examine the feeding ecology of 5 species at 3 sites in the Indo-Pacific. We use Bayesian mixing models and analyses of isotopic niche areas to demonstrate dietary overlap between sympatric mobulid species at all of our study sites. We show the degree of overlap may be inversely related to productivity, which is contrary to prevailing theories of niche overlap. We use isotope data from 2 tissues to examine diet stability of Manta birostris and Mobula tarapacana in the Philippines. Finally, we observe a significant but weak relationship between body size and isotope values across species. Our findings highlight challenges to bycatch mitigation measures for mobulid species and may explain the multi-species mobulid bycatch that occurs in a variety of fisheries around the world.
In light of the global decline of mobulid populations and the necessity for sustainable fisheries management, baseline data for population dynamics were collected from a targeted fishery in the Bohol Sea, Philippines. This study focused on life-history parameters and reproductive cycles of four mobulid rays (Mobula thurstoni, Mobula japanica, Mobula tarapacana, and Manta birostris), and re-estimated their intrinsic population growth rates. Size and reproductive data were collected from 1,509 specimens (30% of catch) landed in two fishing seasons in 2015 and 2016. Size-at-birth was reviewed, and analysis of the embryos and follicles did not show any clear seasonality in the reproductive cycle, but supported an interbreeding interval. Females of all species matured at a larger size than males, and exhibited a larger size-at-pregnancy than -at-maturity. This delay in reproduction resulted in population growth rates lower than the actual r max when based on size-at-pregnancy (r mat = r max = 0.016-0.055 year −1 and r preg = 0.008-0.044 year −1 ), and a population doubling time of 15.8-86.6 years. This study suggests that population growth rates previously reported were overestimated. In light of the Convention on International Trades of Endangered Species (CITES) and Convention on Migratory Species (CMS) assessments, while fisheries management should reflect the delayed maturation of these species and the slower population growth potential, at the current status of these population, the sustainability of any exploitation level seems unrealistic and strongly discouraged.
Diet studies provide base understanding of trophic structure and are a valuable initial step for many fields of marine ecology, including conservation and fisheries biology. Considerable complexity in marine trophic structure can exist due to the presence of highly mobile species with long life spans. Mobula rays are highly mobile, large, planktivorous elasmobranchs that are frequently caught either directly or as bycatch in fisheries, which, combined with their conservative life history strategy, makes their populations susceptible to decline in intensely fished regions. Effective management of these iconic and vulnerable species requires an understanding of the diets that sustain them, which can be difficult to determine using conventional sampling methods. We use three DNA metabarcode assays to identify 44 distinct taxa from the stomachs ( n = 101) of four sympatric Mobula ray species ( Mobula birostris , Mobula tarapacana , Mobula japanica , and Mobula thurstoni ) caught over 3 years (2013–2015) in a direct fishery off Bohol in the Philippines. The diversity and incidence of bony fishes observed in ray diets were unprecedented. Nevertheless, rays showed dietary overlap, with krill ( Euphausia ) dominating their diet. Our results provide a more detailed assessment of sympatric ray diets than was previously described and reveal the complexity that can exist in food webs at critical foraging habitats.
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