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Individual niche trajectories in nesting green turtles on Rocas Atoll, Brazil: an isotopic tool to assess diet shifts over time

Trajetórias de nicho individual em tartarugas verdes do Atol das Rocas, Brasil: uma ferramenta isotópica para verificar trocas de dieta ao longo do tempo

Abstract

In this study, multi-tissue (yolk and carapace) stable isotope analysis was used to assess individual isotopic niche trajectories of nesting green turtles on Rocas Atoll, off northeastern Brazil, and to reveal a diet shift in the temporal dimension. The diet trajectories of individual green turtles were highly directional, with a stronger component towards decreasing values of δ15N from carapace to yolk. When the green turtles are in their foraging sites (temporal window measured by the yolk samples), they are more herbivores. Conversely, in a broader temporal window, the green turtles demonstrate a carnivore-omnivore strategy, such as represented by heavier δ15N values in the carapace. This finding confirms a temporal diet shift. This is the first study that applies trophic niche trajectories for sea turtles, adding a new isotopic tool to understand the trophic ecology of these migrant animals.

Keywords:
Chelonia mydas; adult females; stable isotopes; trophic ecology; Atlantic Ocean

Resumo

Neste estudo, a análise de isótopos estáveis em múltiplos tecidos (vitelo e carapaça) foi usada para avaliar as trajetórias individuais de nicho isotópico de tartarugas verdes em nidificação no Atol das Rocas, nordeste do Brasil, e para revelar uma mudança de dieta na dimensão temporal. As trajetórias individuais da dieta de tartarugas verdes foram altamente direcionais, com um componente mais forte na direção de valores decrescentes de δ15N da carapaça ao vitelo. Quando as tartarugas verdes estão em seus locais de forrageamento (janela temporal medida pelas amostras de vitelo), elas são mais herbívoras. Por outro lado, em uma janela temporal mais ampla, as tartarugas verdes demonstram uma estratégia carnívora-onívora, representada por valores mais elevados de δ15N na carapaça. Os resultados confirmam uma mudança temporal na dieta. Este é o primeiro estudo que aplica trajetórias de nicho trófico para tartarugas marinhas, adicionando uma nova ferramenta isotópica para entender a ecologia trófica desses animais migrantes.

Palavras-chave:
Chelonia mydas; fêmeas adultas; isótopos estáveis; ecologia trófica; Oceano Atlântico

Introduction

The green turtle (Chelonia mydas Linnaeus, 1758) is the only sea turtle species known to be herbivore after the individuals’ recruitment from oceanic to coastal waters (Bjorndal 1997BJORNDAL, K.A. 1997. Foraging ecology and nutrition of sea turtles. In The biology of sea turtles (P.L. Lutz & J.A. Musick, eds.). CRC Press, Boca Raton, p.199-231.). However, the contribution of animal matter in its diet can be variable, as demonstrated in the last decade (e.g., Burkholder et al. 2011BURKHOLDER, D.A., HEITHAUS, M.R., THOMSON, J.A. & FOURQUREAN, J.W. 2011. Diversity in trophic interactions of green sea turtles Chelonia mydas on a relatively pristine coastal foraging ground. Mar. Ecol. Prog. Ser. 439: 277-293. ; Carman et al. 2012CARMAN, V.G., FALABELLA, V., MAXWELL, S., ALBAREDA, D., CAMPAGNA, C. & MIANZAN, H. 2012. Revisiting the ontogenetic shift paradigm: The case of juvenile green turtles in the SW Atlantic. J. Exp. Mar. Biol. Ecol. 429: 64-72. ; Veléz-Rúbio et al. 2016; Di Beneditto et al. 2017; Fukuoka et al. 2019FUKUOKA, T., NARAZAKI, T., KINOSHITA, C. & SATO, K. 2019. Diverse foraging habits of juvenile green turtles (Chelonia mydas) in a summer-restricted foraging habitat in the northwest Pacific Ocean. Mar. Biol. 166: 25.). Adult sea turtles are true migrants, moving between foraging and breeding sites thousands of kilometers apart. Comparing satellite telemetry data, Shimada et al. (2020SHIMADA, T., LIMPUS, C.J., HAMANN, M., BELL, I., ESTEBAN, N., GROOM, R. & HAYS, G.C. 2020. Fidelity to foraging sites after long migrations. J. Anim. Ecol. 8: 1008‐1016. ) showed that fidelity to specific foraging sites following breeding migrations is common across several sea turtles species. For the green turtle, the authors stated high and long-term fidelity to specific foraging sites, with feeding activity happening during the migration to-and-from the breeding sites.

Stable isotopes are chemical proxies applied as a tool to analyse animals’ trophic niches because they allow inferences on food resource use over many temporal scales (Newsome et al. 2007NEWSOME, S.D., MARTINEZ DEL RIO, C., BEARHOP, S. & PHILLIP, D.L. 2007. A niche for isotopic ecology. Front. Ecol. Environ. 5: 429-436. ). The stable isotope of carbon (δ13C) represents the food resource origin, with more enriched values (less negative) in coastal than in oceanic waters and in benthic than in pelagic environments. The stable isotope of nitrogen (δ15N) tracks the animals’ trophic position and it is more enriched at higher trophic levels, i.e. carnivore and omnivore consumers usually have more enriched δ15N values in their tissues than herbivore consumers (Fry 2008FRY, B. 2008. Stable Isotope Ecology. Springer Science Business Media, New York, 316 p.).

Since each tissue has a specific metabolic rate, its turnover time, i.e. the time within which stable isotopes in tissues are replaced by stable isotopes derived from the food sources, is different (Auerswald et al. 2010AUERSWALD, K., WITTMER, M.H.O., ZAZZO, A., SCHÄUFELE, R. & SCHNYDER, H. 2010. Biases in the analysis of stable isotope discrimination in food webs. J. Appl. Ecol. 47:936-941. ). Keratinous tissues, like hair and carapace scutes, are metabolically inert and maintain an isotopic record from the location where they were synthesized, representing the dietary information over a longer period (e.g. several months or years) (Hobson 1999HOBSON, K. 1999. Tracing origins and migration of wildlife using stable isotopes: a review. Oecologia 120: 314-326. ). In metabolically active tissues, such as liver, this information refers to a shorter time, such as a few weeks (Hobson 1999). The vitellogenesis process of sea turtles happens 4 to 6 months before the female’s migration to the breeding site, when she is still at the feeding site (Rostal et al. 1998ROSTAL, D.C., OWENS, D.W., GRUMBLES, J.S., MACKENZIE, D.S. & AMOSS Jr, M.S. 1998. Seasonal reproductive cycle of the Kemp’s ridley sea turtle (Lepidochelys kempi). Gen. Comp. Endocrinol. 109: 232-243. ). Thus, the egg yolk represents the dietary information in a narrower temporal window when compared to carapace scutes. By comparing the isotopic profile from different tissues, it is possible to analyse the temporal consistency of individual diet through isotopic niche trajectories (Costa-Pereira et al. 2019). The assumption is that individuals with temporally consistent diets have more similar isotope values across tissues than individuals with temporally variable diets (Martínez del Rio et al. 2009).

Individuals from the same population do not necessarily have temporally consistent foraging strategies, undergoing diet shifts over time, while others may have a more constant diet (Bearhop et al. 2004BEARHOP, S., ADAMS, C.E., WALDRON, S., FULLER, R.A. & MACLEOD, H. 2004. Determining trophic niche width: A novel approach using stable isotope analysis. J. Animal. Ecol. 73:1007-1012. ; Martínez del Rio et al. 2009). Fukuoka et al. (2019FUKUOKA, T., NARAZAKI, T., KINOSHITA, C. & SATO, K. 2019. Diverse foraging habits of juvenile green turtles (Chelonia mydas) in a summer-restricted foraging habitat in the northwest Pacific Ocean. Mar. Biol. 166: 25.) demonstrated by stable isotope analysis and biologging experiments the seasonal diet shift in a juvenile green turtle population from Japanese Pacific waters. The temporal dimension of individual foraging strategies allows for an understanding of habitat use as a whole (Costa-Pereira et al. 2019), which is especially important for true migrant species, such as the sea turtles.

In this study, multi-tissue (yolk and carapace) stable isotopes were used to assess the consistency of trophic niches of nesting green turtles over time. This approach was adapted from Costa-Pereira et al. (2019), whose study with dozens of populations and hundreds of individuals from tropical frogs’ species demonstrated the reliability of the trophic niche trajectories to measure the trophic consistency of individuals in a temporal scale. The carapace represents a comprehensive assimilation, integrating diet from several months to years ago, whereas the yolk represents the food assimilation from a few months before oviposition, while the nesting females are still at the feeding sites. If the hypothesis of a consistent dietary pattern over time is supported, yolk and carapace isotope values will be similar, and variation in the individual trophic niche trajectories (lengths and angles) is not expected to differ from a random pattern of changes.

Material and Methods

1. Sampling

The sampling of green turtles on Rocas Atoll (03°51’S; 33°49’W) was authorized by the Brazilian Government by the license number 59809. This area is the second largest nesting site for the green turtles in Brazilian waters (Bellini et al. 2013BELLINI, C., SANTOS, A.J., GROSSMAN, A., MARCOVALDI, M.A. & BARATA, P.C. 2013. Green turtle (Chelonia mydas) nesting on Atol das Rocas, north-eastern Brazil, 1990-2008. J.Mar. Biol. Assoc. UK 93:1117-1132. ). It is the only atoll in the South Atlantic Ocean, with 7.5 km2 and located 266 km off the northeastern Brazilian coast. Rocas Atoll is a marine biological reserve; therefore, a pristine area. Bellini et al. (2013) conducted a comprehensive survey to monitor the nesting females in this site from 1990 to 2008. The nesting season occurs from December (beginning, with few nests) to May, with peak from February to April. The average number of nesting females per season is 73, with five nests per individual. The mean remigration period is 3.5 years. The authors estimated that 255 reproductively active females nested on the Rocas Atoll between 1990 to 2008. The authors observed a high site fidelity for the reproductive females in the Rocas Atoll nesting site, confirming its demographic independence in relation to a close reproductive site (Fernando de Noronha Island, 03°51’S; 32°25’W).

In the 2019 nesting season, 22 female individuals were sampled in Rocas Atoll, and sampling began as soon as each female initiated the first egg laying. All females had a healthy appearance, i.e. no visible tumours (Jones et al. 2016JONES, K., ARIEL, E., BURGESS, G., & READ, M. 2016. A review of fibropapillomatosis in green turtles (Chelonia mydas). Vet. J. 212: 48-57.). During sampling, each female was measured for curved carapace length, from the nuchal notch to the tip of the longest posterior marginal scute (cm), and microchipped for individual identification (to avoid resampling). Two fresh eggs were sampled during the first laying, rinsed in filtered water, and the yolk separated from other egg fractions. The bulk sample with two yolks (from the same female) was stored in a clean transparent plastic bag and kept frozen (-20°C) until analyses. A carapace fragment (5 cm2) was sampled from the margin of the anterior scute, close to the nuchal notch. Each fragment was immersed in pure acetone to dissolve any incrustation. Then, it was rinsed in filtered water, dried at room temperature, grounded into a homogeneous powder and stored in a clean plastic vial until analyses. The fragment does not represent the oldest tissue in the carapace, as indicated in Lopéz-Castro et al. (2014), but since all samples were collected in the same way, bias is not expected.

2. Stable isotopes analysis

One gram of wet weight of yolk (bulk sample) was freeze-dried for 96 hours and ground into a homogeneous powder. Since yolk has a large amount of lipids (>50% in freeze-dried samples) (Carpentier et al. 2015CARPENTIER, A.S., BOOTH, D.T., ARTHUR, K.E. & LIMPUS, C.J. 2015. Stable isotope relationships between mothers, eggs and hatchlings in loggerhead sea turtles Caretta caretta. Mar. Biol. 162: 783-797. ), the samples were treated using a 2:1 solvent mixture of chloroform and methanol prior to lipid extraction (Bligh and Dyer 1959BLIGH, E.G. & DYER, W.J. 1959. A rapid method of total lipid extraction and purification. Can.J. Biochem. Physiol. 37: 911-917.). The samples were dried at 60°C in an oven for 48 hours to remove the residual solvent. This procedure minimizes bias in δ13C data interpretation (Post et al. 2007POST, D.M., LAYMAN, C.A., ARRINGTON, D.A., TAKIMOTO, G., QUATTROCHI, J. & MONTAÑA, C.G. 2007. Getting to the fat of the matter: models, methods and assumptions for dealing with lipids in stable isotope analyses. Oecologia 152: 179-189. ). Since the extraction of lipids can interfere with the δ15N values (Petitet & Bugoni 2017PETITET, R. & BUGONI, L. 2017. High habitat use plasticity by female olive ridley sea turtles (Lepidochelys olivacea) revealed by stable isotope analysis in multiple tissues. Mar. Biol. 164: 134. ); the yolk samples were analyzed twice: with and without lipid extraction. For δ13C, the mean values in yolk with and without lipid extraction were -17.9 ± 1.7‰ and -20.0 ± 1.7 ‰, respectively; and for δ15N they were 7.2 ± 1.3‰ and 6.9 ± 1.3 ‰, respectively.

The ratios of stable isotopes were determined in 0.3-0.4 mg of dry weight of each sample (yolk and carapace) using an organic elemental analyzer (Flash 2000, Thermo Scientific) coupled with a mass spectrometer (Delta V Advantage Isotope Ratio Mass Spectrometer, Thermo Scientific) through the ConFlo-VI interface (Model BR30140, Thermo Scientific) in the Laboratório de Ciências Ambientais at Universidade Estadual do Norte Fluminense Darcy Ribeiro. Reference values were Pee Dee Belemnite (PDB) and atmospheric nitrogen. Samples were analyzed using analytical blanks and urea analytical standards (IVA Analysentechnik-330802174). Analytical control was performed for every 10 samples using a certified isotopic standard (Elemental Microanalysis Protein Standard OAS). The reproducibility was based on triplicates for every 10 samples (±0.2‰, δ13C; ±0.3‰, δ15N).

3. Individual niche trajectories

Individual niche trajectories between isotope values of carapace and yolk quantified the temporal consistency of individual diets (Schmidt et al. 2007SCHMIDT, S.N., OLDEN, J.D., SOLOMON, C.T. & VANDER ZANDEN, M.J.V. 2007. Quantitative approaches to the analysis of stable isotope food web data. Ecology 88: 2793-2802. ; Costa-Pereira et al. 2019). The length of trajectories in the bivariate isotopic space (δ15N-δ13C) was calculated by the Euclidean distance between starting points (carapace) and endpoints (yolk) for each individual. The trajectory direction was determined by the (counter clockwise) angle of the line connecting carapace and yolk values in relation to the x-axis (δ13C). The yolk and carapace are dependent measures because part of the dietary information integrated into one tissue is hierarchically integrated to another tissue. Differences between tissues regarding stable isotope values may emerge by temporal variation in environmental baselines and/or differential isotopic route, and not necessarily due to diet variation over time. Since these potential biases should be homogeneous across individuals, they are not expected to bias the results (Schmidt et al. 2007).

The vectors representing the niche trajectory between carapace and yolk for each green turtle individual in the isotopic space represent a dietary shift from the more general life pattern to the period of vitellogenesis. Differences in the angle of change indicate whether and in which direction individuals’ isotopic values shift vertically (δ15N or trophic level shift) and/or horizontally (δ13C or base carbon sources) over time. The magnitude of the diet shift can be measured by the trajectory length. To compare the observed circular distribution of trajectories with the expected null distribution of random changes, we calculated three statistics: mean trajectory length, standard deviation of trajectory length (as a measure of variability) and Rao’s spacing statistic (U). The spacing statistic measures the sum of differences of arc-lengths between adjoining points (ranked by angle) and the regularly spaced arc-lengths expected for the null hypothesis of uniformity (2π/n) (Pewsey et al. 2013PEWSEY, A., NEUHAUSER, M. & RUXTON, G.D. 2013. Circular statistics in R. Oxford University Press, Oxford, 192 p.). The U values become larger as directionality increases, with less deviation between individuals’ trajectories. The circular statistics were calculated in the R package circular (Agostinelli & Lund 2017AGOSTINELLI, C. & LUND, U. 2017. R package “circular”: Circular Statistics (version 0.4-93). URLhttps://r-forge.r-project.org/projects/circular/URL https://r-
https://r-forge.r-project.org/projects/c...
; R Core Team 2020).

Following the procedure delineated in Costa-Pereira et al. (2019), we used a randomization process to generate stochastic individual niche trajectories in the isotopic space. For each individual, the observed isotopic starting point was kept constant (carapace isotopic values) and the isotopic endpoint was assigned by drawing randomly (without replacement) a pair of yolk isotopic values from the distribution of observed yolk isotope values in the sample of 22 individuals. For each resampling, the endpoint of random trajectories could therefore, assume isotope values observed in the conspecific individuals. The null model tested whether the mean length and standard deviation of observed niche trajectories are compatible with a random expectation, and whether the distribution of trajectory angles support a uniform circular distribution. The null distribution of trajectory statistics was based on 10,000 replicates. Probability values were calculated by the sum of permuted statistics that were equal to or more extreme than the observed, divided by 10,000. The stable isotope values used in this study, as well as the R script to calculate trajectory statistics and the randomization procedure are available as Supplementary material.

Results and Discussion

The multi-tissue isotopes explored the individual trophic consistency of nesting green turtles over the foraging period while individuals stay in the foraging sites (yolk samples), and in a broader temporal scale (carapace samples). Trajectory angles showed directionality towards lighter δ15N values and heavier δ13C values (Figure 1). The observed mean and standard deviation of niche trajectory length were smaller than expected by chance (p < 0.0001) (Figure 2). The observed sample was more directional than expected under a uniform circular distribution (U = 176.568, p = 0.0083) (Figure 2). The curved carapace length was very homogeneous across the sample (n = 22 individuals; 112.5 ± 5.0 cm; 107 to 123 cm) and not associated with any isotopic or descriptive variable of the niche trajectory.

Figure 1
Individual niche trajectories represented by vectors between carapace (black circle) and yolk (black arrow) isotope values, for nesting green turtles on Rocas Atoll, Brazil. The inset represents the observed circular distribution of niche trajectory angles.

Figure 2
Null distributions of niche trajectory statistics: mean and standard deviation of trajectory length, the Euclidean distance between carapace and yolk stable isotope values from a given green turtle individual, and Rao's spacing statistic, quantifying the degree of directionality in niche trajectories. Red vertical lines indicate observed values.

The results highlighted that most individuals vary in the consistency of their feeding strategies over time, following a similar pattern. Therefore, a temporal diet shift was noted for the reproductive females that nested at Rocas Atoll during the nesting season of 2019, and this shift was similar within the sample. When the green turtles are in their foraging sites (temporal window measured by the yolk samples), they are more herbivore with stronger association with coastal-benthic waters. Lighter δ15N values represent lower trophic level, typical in herbivore strategy, whereas heavier δ13C values are usually associated with coastal-benthic environments (Fry 2008FRY, B. 2008. Stable Isotope Ecology. Springer Science Business Media, New York, 316 p.). Conversely, in a broader temporal window, the green turtles demonstrate a carnivore-omnivore strategy, such as represented by heavier δ15N values in the carapace. Heavier δ15N values usually represent a greater contribution of animal matter to the consumer diet (Fry 2008), but they could represent variations in isotopic baseline across turtles’ habitat. Different sources of nitrogen in turtles foraging sites influence the isotopic profile of turtles from the same trophic level (Ceriani et al. 2012CERIANI, S.A., ROTH, J.D., EVANS, D.R., WEISHAMPEL, J.F., & EHRHART, L.M. 2012. Inferring foraging areas of nesting loggerhead turtles using satellite telemetry and stable isotopes. Plos One 7: e45335. ; Pajuelo et al. 2012PAJUELO, M., BJORNDAL, K., REICH, K., ARENDT, M. & BOLTEN, A. 2012. Distribution of foraging habitats of male loggerhead turtles (Caretta caretta) as revealed by stable isotopes and satellite telemetry. Mar. Biol. 159. https://doi.org/10.1007/s00227-012-1906-9.
https://doi.org/10.1007/s00227-012-1906-...
). However, if the δ15N values represented the habitat baseline instead of the ingestion of animal matter, we would expect closer δ15N values between yolk and carapace in the same turtle, which was noted for only three individuals (Figure 1).

The temporal diet shift demonstrated for the green turtles that nest on Rocas Atoll had a directional pathway, albeit some individual tendencies are noted (Figure 1, Supplementary material). In the four individuals with the highest δ15N values in the carapace (> 9‰), both oceanic and coastal foraging habitats are represented (δ13C range), indicating isotopic enriched in different areas. In three individuals, yolk and carapace samples have similar δ15N values and the temporal diet shift is not evident. Similarities between tissues regarding δ15N values could represent habitat baseline. Individuals from the same population can vary in their foraging strategies over time, while others may have a more constant diet (Bearhop et al. 2004BEARHOP, S., ADAMS, C.E., WALDRON, S., FULLER, R.A. & MACLEOD, H. 2004. Determining trophic niche width: A novel approach using stable isotope analysis. J. Animal. Ecol. 73:1007-1012. ; Martínez del Rio et al. 2009). The nesting populations of sea turtles represent a mix of individuals from several foraging sites, and satellite telemetry reveals high fidelity to specific sites following breeding migrations (Meylan et al. 2011MEYLAN, P.A., MEYLAN, A.B. & GRAY, J.A. 2011. The ecology and migrations of sea turtles. 8. Tests of the developmental habitat hypothesis. Bull. Am. Mus. Nat. Hist. 357: 1-70. ; Shimada et al. 2020SHIMADA, T., LIMPUS, C.J., HAMANN, M., BELL, I., ESTEBAN, N., GROOM, R. & HAYS, G.C. 2020. Fidelity to foraging sites after long migrations. J. Anim. Ecol. 8: 1008‐1016. ). For the green turtle, Shimada et al. (2020) stated high and long-term fidelity to specific foraging sites, with feeding activity also happening during the migration to-and-from the breeding sites. These features support the individual tendencies described above.

Herbivory is recognized as the predominant feeding habit in adult green turtles (Bjorndal 1997BJORNDAL, K.A. 1997. Foraging ecology and nutrition of sea turtles. In The biology of sea turtles (P.L. Lutz & J.A. Musick, eds.). CRC Press, Boca Raton, p.199-231.; Burgett et al. 2018BURGETT, C.M., BURKHOLDER, D.A., COATES, K.A., FOURQUREAN, V.L., KENWORTHY, W.J., MANUEL, S.A., OUTERBRIDGE, M.E. & FOURQUREAN, J.W. 2018. Ontogenetic diet shifts of green sea turtles (Chelonia mydas) in a mid-ocean developmental habitat. Mar. Biol. 165:33.), but the adult individuals have enough feeding plasticity to take advantage of other food resources when necessary and available, allowing them to behave temporally like carnivores-omnivores (Burkholder et al. 2011BURKHOLDER, D.A., HEITHAUS, M.R., THOMSON, J.A. & FOURQUREAN, J.W. 2011. Diversity in trophic interactions of green sea turtles Chelonia mydas on a relatively pristine coastal foraging ground. Mar. Ecol. Prog. Ser. 439: 277-293. ). Agostinho et al. (2020AGOSTINHO, K.F.F., LACERDA, D., TOSTES, E.C.L., BALDASSIN, P., DI BENEDITTO, A.P.M. & CARVALHO, C.E.V. 2020. Trace elements in green turtles (Chelonia mydas) from Rocas Atoll, NE Brazil: Baseline reference from a pristine nesting site. Mar. Poll. Bull. 157: 111-271. ) mentioned the possible foraging activity of nesting green turtles while stay at Rocas Atoll for breeding due to the high diversity of food items locally. Indeed, this area is a foraging site for juvenile green and hawksbill turtles (Bellini et al. 2013BELLINI, C., SANTOS, A.J., GROSSMAN, A., MARCOVALDI, M.A. & BARATA, P.C. 2013. Green turtle (Chelonia mydas) nesting on Atol das Rocas, north-eastern Brazil, 1990-2008. J.Mar. Biol. Assoc. UK 93:1117-1132. ). The Rocas Atoll biodiversity includes 143 taxa of macroalgae (Villaça et al., 2010VILLAÇA, R., FONSECA, A.C., JENSEN, V.K. & KNOPPERS, B. 2010. Species composition and distribution of macroalgae on Atol das Rocas, Brazil, SW Atlantic. Botan. Marin. 53: 113-122.) and a range of zoobenthos and fish species (Moraes et al. 2003MORAES, F.C., VILANOVA, E.P. & MURICY, G. 2003. Distribuição das esponjas (Porifera) na Reserva Biológica do Atol das Rocas, nordeste do Brasil Arq. Mus. Nac. 61: 13-22.; Paiva et al. 2007PAIVA, P.C., YOUNG, P.S. & ECHEVERRÍA, CA. 2007. The Rocas Atoll, Brazil: a preliminary survey of the Crustacea and Polychaete fauna. Arq Mus Nac 65:241-250; Batista et al. 2012BATISTA, H., ZILL, J., VERAS, D., HAZIN, F., OLIVEIRA, P., MARINS, Y., OLIVEIRA, D., PEREIRA, R., TOLOTTI, M. & SILVA, M. 2012. New records of reef fishes (Teleostei: Perciformes) in the Rocas Atoll Biological Reserve, off northeastern Brazil. Check List 8: 584-588.; Paiva et al. 2015). The higher δ15N values for oceanic habitats (more negative δ13C values) noted in two nesting individuals (Figure 1) could be related to the animal matter ingested around the nesting site, that is an oceanic habitat; or even during the migration to-and-from the nesting site.

Figgener et al. (2019FIGGENER, C., BERNARDO, J. & PLOTKIN, P.T. 2019. Data from: MarTurtSI, a global database of stable isotope analyses of marine turtles. Sci. Data 6: 16. ) organized an isotopic database for sea turtles species worldwide, demonstrating the variability of isotopic signatures among them, both inter- and intraspecifically, as well as similarities in the isotopic profile. The green turtle is the second most studied species, with 40% of the available stable isotope studies until November 2018 (Figgener et al. 2019). Meanwhile, data on the isotopic profile of nesting green turtles are still scarce, limited to five studies until the above period (Godley et al. 1998GODLEY, B.J., THOMPSON, D.R., WALDRON, S. & FURNESS, R.W. 1998. The trophic status of marine turtles as determined by stable isotope analysis. Mar. Ecol. Prog. Ser. 166: 277-284. ; Hatase et al. 2006HATASE, H., SATO, K., YAMAGUCHI, M., TAKAHASHI, K. & TSUKAMOTO, K. 2006. Individual variation in feeding habitat use by adult female green sea turtles (Chelonia mydas): are they obligately neritic herbivores? Oecologia 149: 52-64. ; Vander Zanden et al. 2013a; 2013b; Bradshaw et al. 2017BRADSHAW, P.J., BRODERICK, A.C., CARRERAS, C., INGER, R., FULLER, W., SNAPE, R., STOKES, K.L. & GODLEY, B.J. 2017. Satellite tracking and stable isotope analysis highlight differential recruitment among foraging areas in green turtles. Mar. Ecol. Prog. Ser. 582: 201-214. ). Thus, this study also contributes to the database on δ13C and δ15N values in this species (Supplementary material).

Despite the small sample size (n = 22), the isotopic niche trajectories had strong statistical support to demonstrate the temporal diet shift for most green turtle individuals that nest on Rocas Atoll, off northeastern Brazil, during 2019 nesting season. To our knowledge, this is the first study that presents this approach for sea turtles, adding a new isotopic tool to understand the trophic ecology of these migrant animals. This approach has potential to be applied in other green turtle populations and/or in other sea turtle species. Since the adult green turtles can feed in the full extent of the habitat (foraging sites, breeding sites and to-and-from), changes in the food availability in these sites and over their migratory routes might compromise the health of the reproductive population. In a global scenario of rapid environmental changes, it deserves concern because sea turtles are long-lived endangered animals, and most species, like the green turtles, have high site fidelity for both feeding and breeding sites.

Acknowledgments

We are indebted to Dr. Marcelo Gomes de Almeida for the stable isotopes analysis, to Jarian Dantas for helping during field activities and to Maurizélia de Brito Silva, coordinator of Biological Reserve of Rocas Atoll, for logistic support in the field campaigns. The Instituto Chico Mendes de Conservação da Biodiversidade (ICMBio), Fundação SOS Mata Atlântica and FUNBIO/Banco Mundial (GEFMAR project) support the field campaigns. The Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq (grant 301.259/2017-8), Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro - FAPERJ (grants E-26/202.770/2017, E-26/210.883/2016 and E-26/210.064/2018) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES (Finance Code 001) contribute with financial support.

Supplementary Material

The following online material is available for this article:

Stable isotopes data of nesting green turtles on Rocas Atoll, Brazil (2019 nesting season)

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Publication Dates

  • Publication in this collection
    14 Dec 2020
  • Date of issue
    2021

History

  • Received
    06 Aug 2020
  • Reviewed
    19 Oct 2020
  • Accepted
    09 Nov 2020
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