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To cite this version:

Jean-François Ghiglione, Vincent Laudet. Marine Life Cycle: A Polluted Terra Incognita Is Unveiled.

Current Biology - CB, Elsevier, 2020, 30, pp.R130 - R133. �10.1016/j.cub.2019.11.083�. �hal-02991960�

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Marine Life Cycle: A Polluted Terra Incognita

Is Unveiled

Jean-Franc¸ois Ghiglione1and Vincent Laudet2

1Observatoire Oceanologique de Banyuls-sur-Mer, UMR CNRS 7621 LOMIC, Sorbonne Universite, 1 avenue Pierre Fabre, 66650

Banyuls-sur-Mer, France

2Observatoire Oceanologique de Banyuls-sur-Mer, UMR CNRS 7232 BIOM, Sorbonne Universite, 1 avenue Pierre Fabre, 66650

Banyuls-sur-Mer, France

Correspondence:ghiglione@obs-banyuls.fr(J.-F.G.),vincent.laudet@obs-banyuls.fr(V.L.)

https://doi.org/10.1016/j.cub.2019.11.083

Teleost fishes have a biphasic life cycle, with pelagic larvae dispersing in the open ocean and juveniles or

adults living in reef or coastal environments. A recent study reveals that fish larvae concentrate in a

specific oceanic compartment, the surface slicks, which are polluted by microplastics that can be

ingested by most larvae.

Because we are terrestrial mammals of macroscopic size we very often neglect the incredible diversity of the living world around us. This diversity culminates in the sea, from which most metazoan phyla originate. But we also often forget that the diversity of animal forms must be extended to their ontogenic stages, and, again, this is particularly true for marine animals [1]. The vast majority of marine animals, including teleost fishes,

exhibit a biphasic life cycle with one (or several) larval planktonic stages and juvenile/adult stages that occur in a different ecological niche [2,3]. The existence of two distinct phases during the life cycle ensures the dispersion of individuals due to oceanic currents that convey these pelagic stages. It also reduces the predation level, which could be very high in coastal environments, such as coral reefs, and

ensures access to a large food source in plankton [4].

A large number of studies have addressed the entry of larval fish to their juvenile environments, often called settlement or recruitment [5]. In the case of coral reef fishes, this step is easy to recognize as it corresponds with the passing of the reef crest and the selection of an adequate microhabitat. In pelagic fishes, this step is less easy to follow, but

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it coincides with the transformation of the larvae into active swimmers that often, like tuna, form a shoal. In any case, this step corresponds to a complete

transformation of a larva into a juvenile — a metamorphosis that is triggered by thyroid hormones [2,6].

The distribution of larvae in the open ocean remains almost a complete mystery, a terra incognita. Where are larvae in the ocean? How are they distributed in the water column? We know now that fish in the late larval stage are much more active than anticipated and are certainly not passive propagules following the currents [7]. Thanks to many studies using plankton nets to better understand the vertical distribution of plankton, we have had several glimpses into their presence in different levels of the water column. However, apart from the observation that they follow the regular diel vertical migration of plankton [8] and that some species often use algal rafts floating on the surface [9], we know almost nothing about the life of oceanic fish larvae [10].

A recent and fascinating analysis by Gove et al. [11], however, brings some news and exciting information on fish

larvae in the open ocean and reveals an astonishing complexity. Sadly, this study also reveals that, despite the tremendous dilution power of the oceanic volume of water, fish larvae reside in an extremely polluted compartment.

Let’s start with the fascinating side of the story. In the western portion of Hawai’i, which is the most protected site from winds, Gove et al. [11] have performed an extensive series (>100) of plankton net tows, searching for fish larvae and focusing on the neuston, the compartment of plankton that lives close to the surface. They observed that the density of plankton was variable from one plankton trait to another, and they realized that planktonic animals, including fish larvae, were more frequent in surface slicks than in the neighboring ambient waters.

Sea surface slicks are formed under calm weather conditions by the accumulation of hydrophobic organic compounds that protrude at the surface, thus creating a film referred to as a ‘slick’ when visible that affects the physical and optical properties of the sea surface [12,13] (Figure 1). These structures aggregate the planktonic organisms that

are the base of the marine food web [14]. Gove et al. [11] have carefully mapped the extent of these labile structures close to Hawai’i west shores and have observed that they form a dynamic network roughly parallel to the shore.

Most importantly, Gove et al. [11] found that the densities of phytoplankton (measured by chlorophyll content), zooplankton and fish larvae are effectively higher (1.7-, 3.7- and, strikingly 8.1-fold, respectively) in surface slicks than in ambient waters. Clearly, larval fish would benefit from the accumulation of planktonic organisms. Interestingly, they observed that the overall distance between two such surface slicks is 500 m, a distance that can easily be crossed by a fish larva that is capable of actively swimming [7]. In total, they observed that the surface slick

represented 8.3% of all nearshore waters at the time of their observations, and that they contained 42% of all surface fish larvae. The authors therefore suggest that the convergence of surface waters underlying the surface slicks aggregates the marine organisms that are at the base of the oceanic food chain, creating a gradient of plankton which is, of course,

(CO2’ O2’ CH4’ N2) Hydrophobic surfactant Phyto-plankton Zoo-plankton Fish larvae EF = 1.7 EF = 3.7 Bacteria and viruses Hydrophobic persistant organic pollutants (POPs) and antibiotics Current Biology

Sea surface layer

1m depth Current EF = 8.1 Turbulence Bubble production Gas exchanges Solar radiation

Wind Sea surface slicks

Aerosols

Evaporation

Microplastic EF = 126

Precipitation

Figure 1. Natural sea water slicks.

These structures formed under calm weather conditions are enriched in phytoplankton, zooplankton and fish larvae, but also in microplastic that may have adverse effects on the entire trophic chain. EF: enrichment factor in surface slick as compared with ambient water, with indicated values coming from [11].

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converge passively and actively in these structures. As the surface is also the vital ‘skin’ of the ocean, linking the water and the atmosphere, these structures may also have other specific features in terms of oxygen content, organic matter content, light filtering, or UV ray penetrance that provide selective advantage [12,13].

Gove et al. [11] have carefully studied the taxonomic composition of the fish larvae encountered in those slicks and have observed that they belong to a wide variety of fish taxa whose adults live in a variety of habitats. They found larvae of large pelagic fish such as swordfish, mahi-mahi or flying fish at an astonishing 28-fold higher density but they also found more demersal species such as jacks, goatfish, as well as deep-water

mesopelagic fish such as lanternfish and even some coral reef fishes such as triggerfish.

It is clear from their data that there is a hidden complexity here since the authors observed a difference in the respective amount of the various types of fish in the surface slicks versus the ambient waters. For example, they observed that slicks contain 50% pelagic fishes and 45% of coral reef fishes, whereas the ambient waters contain mostly (73.6%) coral reef fishes and only 15.3% of pelagic fishes. Coupled with the observation that surface slicks contain more fish larvae of more than 8 mm of size, this suggests that fish larvae choose the compartment that they prefer. Are coral fish larvae avoiding these surface slicks because of a higher predation level? Are pelagic fish larvae, especially the older, and therefore bigger ones, more active and therefore more able to fully exploit the opportunity offered by the concentration of plankton in the slicks? Could these differences be linked to a difference in maturity between waves of larvae produced by spawning events in coral reefs or in the pelagic ocean? How are these concentrations of organisms in surface slicks formed, and what happens to them during periods of strong winds that disrupt these structures? Do the fish smell the concentration of organic matters and plankton to actively swim toward those slicks? All these questions are still unresolved and are exciting avenues to explore in future studies. Once again, this reinforces the notion that fish

own behavior and have constantly vital choices to make.

This fascinating story also has, however, an upsetting aspect. Indeed, Gove et al. [11] show that the processes forming the surface slicks and

concentrating phytoplankton and zooplankton also concentrate buoyant microplastic particles present in the ocean. They observed that microplastics were present at a 126-fold higher concentration in surface slicks than in ambient water. Overall, their results suggest that 91% of the plastic particles present in the surface area were found in the sea surface slicks, probably due to their low density and hydrophobic properties. Microplastics in sea surface slicks were mainly composed of polyethylene (77%) and polypropylene (20%) with 41% being of the size of fish larval prey (<1 mm). Overall, the ratio between microplastics and fish larvae was inverted between surface slicks (7:1) and ambient water (1:2), fish larvae thus being more likely to ingest microplastics in surface slicks.

Microplastics are not passively concentrated in surface slicks — they also more heavily contaminate the fish larvae present in these structures. After dissecting 658 larval fishes, Gove et al. [11] observed that larval fish captured in surface slicks are 2.3-fold more contaminated than larvae coming from ambient water. The authors observed mostly blue or translucent microfibers in the ingested plastics, suggesting that the fish larvae confuse the microplastic particles with their zooplanktonic prey items.

These observations are really disturbing. Indeed, the fact that surface slicks host a large proportion of fish larvae suggests that these structures have a role as nurseries and are therefore critical for the replenishment of adult fish populations. This is likely to be of major importance since it concerns species critical in the food chain, such as flying fish, and most of them, such as swordfish or mahi-mahi (common dolphinfish), are consumed by humans. This critical compartment is also, however, heavily contaminated by microplastic particles that will not only dramatically obstruct the digestive tracts of the larvae but also contaminate

their surface. This is particularly the case in surface slicks where persistent organic pollutants (POPs) and antibiotics accumulate [15,16]. This is even more disquieting, as it is known that larval stages are very often the life stages most sensitive to endocrine disruptors known to be part of the composition of many plastic additives [17]. It has been shown that the thyroid hormone-controlled transformation of fish larvae into juveniles is effectively sensitive to endocrine disruption by pollutants [6] and that this step influences post-metamorphosis animal condition [18]. Microplastics are also known to host bacteria, the so-called ‘plastisphere’, which may cause diseases when ingested [19]. Many of us were expecting that plastic pollution would only affect fish living near the shore, owing to the immense dilution effect of the ocean. The analysis of Gove et al. [11], however, suggests that even in the pelagic realm the level of pollution by microplastics may be sufficient to affect a very sensitive, and vital, component of the marine ecological network.

REFERENCES

1.Nielsen, C. (2012). Animal Evolution: Interrelationships of the Living Phyla, 3rd ed. (Oxford University Press).

2.Laudet, V. (2011). The origins and evolution of vertebrate metamorphosis. Curr. Biol. 21, R726–R737.

3.McMenamin, S.K., and Parichy, D.M. (2013). Metamorphosis in teleosts. Curr. Top. Dev. Biol. 103, 127–165.

4.Jones, G.P., Almany, G.R., Russ, G.R., Sale, F., Steneck, R.S., van Oppen, M.J.H., and Willis, B.L. (2009). Larval retention and connectivity among populations of corals and reef fishes: history, advances and challenges. Coral Reefs 28, 307–325.

5.Sponaugle, S. (2015). Recruitment of coral reef fishes: linkage across stages. In Ecology of Fishes on Coral Reefs, C. Mora, ed. (Cambridge Univ. Press), pp. 28–33.

6.Holzer, G., Besson, M., Lambert, A., Franc¸ois, L., Barth, P., Gillet, B., Hughes, S., Piganeau, G., Leulier, F., Viriot, L., et al. (2017). Fish larval recruitment to reefs is a thyroid hormone-mediated metamorphosis sensitive to the pesticide chlorpyrifos. Elife 6, e27595. 7.Leis, J.M. (2006). Are larvae of demersal fishes

plankton or nekton? Adv. Mar. Biol. 51, 57–141.

8.Neilson, J.D., and Perry, R.I. (1990). Diel vertical migration of marine fishes: An obligate or facultative process? Adv. Mar. Biol. 26, 115–168.

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rafting in the marine environment. II. The rafting organisms and community. Oceano. Mar. Biol. Annu. Rev. 43, 279–418.

10.Llopiz, J.K., Cowen, R.K., Hauff, M.J., Ji, R., Munday, P.L., Muhling, B.A., Peck, M.A., Richardson, D.E., Sogard, S., and Sponaugle, S. (2014). Early life history and fisheries oceanography: New questions in a changing world. Oceanography 27, 26–41.

11.Gove, J.M., Whitney, J.L., McManus, M.A., Lecky, J., Carvalho, F.C., Lynch, J.M., Li, J., Neubauer, P., Smith, K.A., Phipps, J.E., et al. (2019). Prey-size plastics are invading larval fish nurseries. Proc. Natl. Acad. Sci. USA 116, 24143–24149.

12.Zhang, Z., Liu, L., Liu, C., and Cai, W. (2003). Studies on the sea surface microlayer II. The layer of sudden change of physical and

264, 148–159.

13.Engel, A., Bange, H.W., Cunliffe, M., Burrows, S.M., Friedrichs, G., Galgani, L., Herrmann, H., Hertkorn, N., Johnson, M., Liss, P.S., et al. (2017). The ocean’s vital skin: Toward an integrated understanding of the sea surface microlayer. Front. Mar. Sci. 4, 165.

14.Kingsford, M.J., and Choat, J.H. (1986). Influence of surface slicks on the distribution and onshore movements of small fish. Marine Biol. Mar. Biol. 91, 161–171.

15.Ziccardi, L.M., Edgington, A., Hentz, K., Kulacki, K.J., and Kane Driscoll, S. (2016). Microplastics as vectors for bioaccumulation of hydrophobic organic chemicals in the marine environment: A state-of-the-science review. Env. Tox. Chem. 35, 1667–1676.

Adsorption of antibiotics on microplastics. Env. Poll. 237, 460–467.

17.Groh, K.J., Backhaus, T., Carney-Almroth, B., Geueke, B., Inostroza, P.A., Lennquist, A., Leslie, H.A., Maffini, M., Slunge, D., Trasande, T., et al. (2019). Overview of known plastic packaging-associated chemicals and their hazards. Sci. Total Env. 651, 3253–3268. 18.Hamilton, S.L. (2008). Larval history influences

post-metamorphic condition in a coral-reef fish. Oecologia 158, 449–461.

19.Jacquin, J., Cheng, J., Odobel, C., Pandin, C., Conan, P., Pujo-Pay, M., Barbe, V., Meistertzheim, A.L., and Ghiglione, J.F. (2019). Microbial ecotoxicology of marine plastic debris: a review on colonization and biodegradation by the ‘plastisphere’. Front. Microbiol. 10, 865.

Figure

Figure 1. Natural sea water slicks.

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