Abstract
Temporal variability of the genetic structure and connectivity patterns of the blue and red shrimp Aristeus antennatus in the seven most important fishing grounds of the Western Mediterranean Sea, were assessed using twelve microsatellite loci during 2 consecutive years (2016 and 2017), in a total of 1403 adult individuals. A high level of geographical connectivity among groups was observed in the two studied years. In fact, no significant geographical differentiation was found in 2016 (FST = 0.0018, p > 0.05), whereas it was indicated in 2017 (FST = 0.0025, p < 0.05). This small divergence in 2017 was not attributed to the distance among locations nor to the effect of the Ibiza Channel. Significant allele frequency changes were found at local level between the 2 years (FCT = 0.0006, p < 0.05), mainly due to Blanes’ fishing ground. Larval dispersal from the North to the South through the main superficial current supports the high level of connectivity pattern found. The temporal genetic instability detected in the Blanes’ fishing ground could be explained by oceanographic temporary features. Our findings evidence only one biological unit in the study region and establish the baseline for an inter-federal management plan of A. antennatus.
Introduction
The blue and red shrimp Aristeus antennatus (Risso, 1816) has a wide distribution in the Western basin of the Mediterranean Sea1, where it is the most eurybathic species, with a depth range from 80 to nearly 3000 m and a peak of abundance between 400 and 800 m2,3. Aristeus antennatus mainly inhabits the muddy bottoms of the upper and middle slope where it is commercially exploited, but it is found also at the lower slope, non-exploited by fishery4. This species has temporal movements between the open slope and the margins of submarine canyons3,4. Mature males and females form mating aggregations on the middle slope during the reproductive period4, which takes place in late spring and summer5. On the other hand, even though pelagic larval duration is still unknown in A. antennatus, all larval stages found in a few number of studies were in the upper layers of the water column [6 and references therein].
In the Western Mediterranean coast, the species has been intensively exploited by trawling fishery between depths of 400–800 m7,8 in the Catalan-Levantine coast, the Balearic Islands and Alborán Sea (Mediterranean Subareas GSA6, GSA5 and GSA1 respectively), being considered as one of the most important marine resources3,9 included in the priority species list for action by General Fisheries Commission for the Mediterranean Sea10. Nevertheless, the lack of an integral management plan for the species along the North-western Mediterranean coast11 has implied that the management of A. antennatus has been applied locally12,13 without taking into account the genetic diversity and connectivity among populations and without identifying the conservation units, which should be required for a sustainable management of the species14.
Different molecular markers (allozymes, AFLP and mtDNA) have been used to identify population substructure of A. antennatus in the Mediterranean Sea, but they pointed out the Western Mediterranean Sea as a single genetic unit1,15,16,17. Thus, in a fine-scale study, where the differentiation could be relatively small, more highly polymorphic molecular markers are required, such as microsatellites18. Although a set of eight microsatellite loci failed to establish any population structure in the blue and red shrimp in the Central Mediterranean Sea19, microsatellites have successfully been used to identify genetic stock in other marine penaeoid species, such as Penaeus monodon20 and Farfantepenaeus notialis21. The presence of oceanographic discontinuities has been identified as one of the main factors determining the genetic differentiation among populations in marine species, but dispersal by oceanic currents promotes connectivity among them22,23,24. Along the Mediterranean coast of the Iberian Peninsula, the main surface current is the Northern Current, which flows south-westward to at least the Ibiza Channel25, where a part of the flow crosses this channel towards the Alborán Sea, whereas most recirculates north-eastward to the Balearic Islands, forming the Balearic current26. The Ibiza Channel (Fig. 1) is a passage between Ibiza island and the mainland at Cape La Nao, which due to its narrowness (80 km width and 800 m depth)27 has been considered an oceanographic barrier limiting the dispersion of marine species and the genetic connectivity23,28.
Sampling locations for Aristeus antennatus in the Mediterranean Sea used in this study. The dashed line represents the Ibiza Channel oceanographic barrier. Northern and Balearic currents (NC, BC) are shown as blue arrows. For further detail, see Table 1. This map was created from open IGN database (http://www.ign.es/iberpix2/visor/), using FreeHand MX 11.0 version.
Temporal changes in the distribution along the water column, in the diet and the food consumption rates, in the abundance and fishery landings of A. antennatus at regional scale have been reported3,4,29,30. It is particularly interesting to determine whether these changes are related to spatial and temporal variation on the genetic structure of A. antennatus populations, because a federal interest of integral management has been recently stated31 following the Food and Agriculture Organization recommendations32.
The main aim of this study was to describe the temporal stability of the genetic structure and connectivity patterns of A. antennatus among the most important fishing grounds in the North-western Mediterranean Sea, from the Gulf of Lions (France) to Cabo de Palos (Spain), using twelve microsatellite loci. We also analysed the influence of the Ibiza Channel as oceanographic barrier to the dispersion of individuals.
Results
Genetic diversity within samples
After the quality filtering, where individuals with less than eight genotyped loci were eliminated, 1386 out of 1403 individuals were used for further analysis (Table 2).
In all analysed samples, the twelve microsatellite loci were polymorphic, where the number of alleles per locus (NA) ranged from 2 (locus Aa496b in all samples, and locus Aa751 in ROS17) to 23 (locus Aa138 in BLA16 and locus Aa681 in VIG17) (Supplementary Table S1) with a mean of 9.1 alleles per locus per sample. Average allelic richness (AR) ranged from 8.5 (ROS16) to 9.0 (SPO16) in 2016, and from 8.8 (DEN17) to 9.3 (PDS17 and PAL17) in 2017 (Table 2).
Observed heterozygosity (HO) ranged from 0.440 (VIG16) to 0.486 (PAL16) among samples collected in 2016, and from 0.431 (DEN17) to 0.498 (VIG17) among those in 2017. The expected heterozygosity (HE) was higher than HO and ranged from 0.629 (DEN16) to 0.639 (PAL16 and SPO16) in 2016, and from 0.620 (VIG17) to 0.643 (PAL17) in 2017 (Table 2). Significant linkage disequilibrium was only detected in the pair of loci Aa1255 and Aa1061 in PAL16 after Bonferroni correction (p < 0.0001) but not in other locations. Therefore, all loci were included in further analyses.
Significant deviation from the Hardy Weinberg Equilibrium (HWE) occurred at 10 out of 12 loci at least in one sample, related to deficiency of heterozygote individuals (positive FIS values, see Supplementary Table S1). Null alleles were detected in the samples with significant HWE deviations. However, estimated allele frequencies for null alleles were low, only the Aa1255, Aa1444, and Aa818 loci had null allele frequencies higher than 0.2 in four, one and two samples, respectively (Supplementary Table S1). Nevertheless, given the lack of consistency among samples in the presence of null alleles, all loci were included in further analyses.
Geographical and temporal variation
There were no substantial differences in estimated FST values correcting, or not correcting, for the presence of null alleles. In fact, none of the pairwise FST comparisons between samples was significant after Bonferroni correction in year 2016. Among the 2017 samples, pairwise FST values including BLA17 were the highest and significant ones, although only the BLA17 and DEN17 comparison remained significant after Bonferroni correction (Table 3). Genetic and geographical distances were not correlated among 2016 samples (r = −0.403, p = 0.057) nor among the 2017 ones (r = 0.056, p = 0.581), indicating no signal of isolation by distance. For the two temporal collections, migration rates among samples suggested a high level of connectivity, but not related to the geographical proximity among locations (Fig. 2).
Relative migration networks estimated by divMigrate-online. Filter threshold was set to 0.3. Circles represent samples, while arrows indicate the direction and magnitude of relative migration levels using Nm estimator. Thicker arrows indicate stronger migration. Sample codes as in Table 1. (a) Illustrates 2016 collection, (b) illustrates 2017 collection.
Using the Evanno’s approach, the Bayesian clustering analysis revealed the most likely model to be K = 4 for 2016 and K = 3 for 2017. However, the distribution of the clusters across individuals did not show any geographical pattern in both collections (2016 and 2017) (Supplementary Fig. S1). An evaluation of the statistical power estimated a high probability (99.9–100% for chi-square and 99.6–100% for Fisher exact test) of detecting structure for a FST value of 0.0010–0.0025. This result suggests that our test would detect a real population structure if true estimates of FST were at this level. AMOVA results among the 2016 samples (unstructured 2016, Table 4) indicated that more than 99% of genetic diversity was shared among samples and only a small and not significant proportion was allocated to divergence among samples (FST = 0.0018, p > 0.05). Thus, no oceanographic groupings were tested further for 2016 collection. Otherwise, in the 2017 collection a small but significant divergence was detected among samples (FST = 0.0025, p < 0.05). Nevertheless, hierarchical analyses did not give support to the Ibiza Channel as a barrier to A. antennatus dispersal (2017 two regions, Table 4).
The AMOVA analysis for temporal variation (Table 4) assigned a significant percentage of variation to the temporal component (FCT = 0.0006, p < 0.05). However, at the local level, significant differentiation between 2016 and 2017 was restricted to the Blanes’ fishing ground (FST = 0.0048, p < 0.05) (Supplementary Table S2).
Discussion
Our mean observed and expected heterozygosities (HO = 0.468, HE = 0.633) were in accordance with recent studies using the same set of microsatellite loci (HO = 0.443, HE = 0.611 recalculated excluding Aa42133; HO = 0.458, HE = 0.62834). The mean number of alleles per locus and sample (NA = 9.1, Table 2) was slightly higher than reported previously with the same microsatellite loci (NA = 7.9 recalculated excluding Aa42133; NA = 7.834), probably due to the sample size in our study almost doubling the one in those previous studies. Higher diversity levels were observed in Italian and Algerian A. antennatus samples using eight distinct loci (HO = 0.650, HE = 0.80019). Nevertheless, our results were similar to those reported in other shrimp species, such as Acanthephyra pelagica from the Atlantic coast of Canada (NA = 9.3, HO = 0.473, HE = 0.56235), the deep-sea shrimp Rimicaris hybisae from the Caribbean Sea (NA = 8.2, HO = 0.525, HE = 0.58236) and Melicertus kerathurus from the Mediterranean Sea and the North-eastern Atlantic Ocean (NA = 16.0, HO = 0.455, HE = 0.57237).
A common feature of studies on penaeids is a significant deficit of observed heterozygosity38. In the present study the fourteen samples showed a general heterozygote deficit, resulting in the high positive FIS values (Table 2). There are some factors that could be responsible for these deviations from HWE genotypic proportions, such as inbreeding, null alleles or subpopulation structure. According to a recent study about the mating structure of A. antennatus, most of the mating individuals of the spawning groups are not related33, so we did not consider inbreeding to be the cause of the HWE disequilibrium found in our results. Null alleles could explain the heterozygote deficiency, according to our results showed by Micro-checker (Supplementary Table S1). The Wahlund effect cannot be ruled out as one reason for heterozygote deficiency, due to the possibility of having sampled genetically differentiated subpopulations or cohorts simultaneously, as it was pointed out previously for A. antennatus33. Overall, our results from pairwise FST, Isolation by distance, relative migration networks, Bayesian analysis and AMOVAs, showed a high connectivity pattern of A. antennatus fishing grounds (Tables 3, 4, Fig. 2 and Supplementary Fig. S1). A result in accordance with the genetic homogeneity previously reported among the Western Mediterranean Basin red and blue shrimp populations from allozyme15, mitochondrial (16S rDNA, COI and control region1,16,39) and microsatellites diversity19. In a recent study using the same set of microsatellite loci, genetic differentiation between the Alborán Sea and the remainder Western Mediterranean Basin was detected34. However, their results did not point out any significant differentiation among the only three samples of the Spanish Mediterranean coast, whereas our results indicated some degree of differentiation in the 2017 temporal collection (Tables 3, 4). The pelagic life stages are considered the main dispersal mechanism in many marine species including crustaceans40,41. To date, the pelagic larval duration of A. antennatus is still unknown, but extrapolating from other closely related species such as Aristaeomorpha foliacea whose pelagic larval duration could last between 3 and 6 weeks42, A. antennatus may have a long pelagic larval duration, and therefore, high dispersal potential41. The larvae dispersal could be mainly driven by the Northern Current, which flows throughout the North-western Mediterranean coast (Fig. 1) from the Ligurian Sea and continues south of the Ibiza Channel. The Ibiza Channel is considered a seasonal oceanographic barrier because it is thought to have more force in reducing gene flow between populations during spring and early summer25,27. The seasonality is due to the presence of the Western Intermediate Water, which forms an anticyclonic gyre in the northern part of the Ibiza Channel. The gyre reduces or even blocks the southward progression of the Northern Current through this channel, and instead enhances the north-eastward recirculation to the Balearic current25,27. Hence, the Ibiza Channel may restrict the southward dispersal of those species with reproductive time and larval pelagic stages during that period, as it has been observed for the comber fish Serranus cabrilla23, the red gorgonian Paramuricea clavata43 and the swimming crab Liocarcinus depurator28. Instead, for species whose reproductive period is during late summer such as the dusky grouper fish, Epinephelus marginatus, the Ibiza Channel does not seem to prevent gene flow44. Usually, the reproduction of A. antennatus takes place from May until October, being maximum from June to September5, which means that during the last months of the A. antennatus reproductive season, the Ibiza Channel is not acting as a barrier preventing the southward larval transport.
Several factors may explain the temporal genetic instability detected in Blanes’ fishing ground between 2016 and 2017 collections (Table 4 and Supplementary Table S2). One feasible reason could be a variation in the age composition of the samples between years. Aristeus antennatus’ age is inferred by the cephalothorax length (CL), where each modal size class is related to an age class7,45. Our samples are mainly composed of 2-year-old individuals as showed by their mean CL (Supplementary Fig. S2). Besides, unpaired two-sided Student’s t-tests performed at each location to compare the individuals’ CL indicated a widespread variation between temporal collections (Supplementary Table S3), where the CL’s variation found in Palamós’ fishing ground had a similar pattern to the variation in Blanes, however in Palamós the results indicated genetic stability. Therefore, the temporal variation found in Blanes is most likely due to a hydro-biological matter.
Special attention should be given to the role of submarine canyons, taking into account the fact that they are considered to serve as nursery, refuge and recruitment grounds for A. antennatus46,47. Furthermore, it has been indicated that submarine canyons provide habitat heterogeneity because hydrodynamics differs between them47,48, so Blanes canyon may have specific physical features which combined with micro-oceanographic characteristics may causing a temporal decrease in gene flow with the surrounding areas. In fact, unlike other nearby submarine canyons such as La Fonera canyon (Palamós) and Cap de Creus canyon (Roses) where water flow has cyclonic vorticity, in Blanes canyon an anticyclonic eddy has been detected, which can cause a northward direction against the main southward water circulation49,50. Indeed, Clavel-Henry et al.48 applying different biophysical models in order to estimate potential connections between North-western Mediterranean fishing grounds of A. antennatus, confirmed that singular features in submarine canyons could have an important role in the species dispersal. For instance, in the open slope at the south of Blanes canyon a northward circulation of particles was detected due to the anticyclonic eddy in Blanes area48. Another explanation could be the cascading event, an intense dense shelf water mass formed in the Gulf of Lions and the subsequent downslope cascade, which occurs periodically during dry and cold winters30. Cascading events have been related to an increase in A. antennatus recruitment inside the North-western Mediterranean submarine canyons in the following years after a cascading event51, including Blanes canyon52. Nevertheless, this could be ruled out not only because the last cascading event (2012–2013) was some years before our collections53,54, but also because it did not have a significant effect in the Blanes canyon55. Additionally, the anthropogenic effects on submarine canyons have been deeply discussed. The bottom trawling activities have a direct effect on the ecological dynamics of the submarine canyons, causing physical disturbances which are variable over time and changes in density and composition of different meiofaunal species, as noticed in Blanes canyon47,55.
In conclusion, despite the temporal differentiation found in Blanes’ fishing ground, in the present study we identified a high level of genetic connectivity of A. antennatus from the Gulf of Lions (France) to Cabo de Palos (Spain). From a fisheries perspective, we advise considering A. antennatus in the North-western Mediterranean coast as one biological unit for stock assessment, and promoting coordinated fishery management plans. Taking the genetic information into account for future management advice would be of significant help to design an effective inter-federal management policy, and therefore a long term sustainability of the fishery resource would be ensured14,22.
Material and methods
Sampling collection and DNA extraction
Sampling was coordinated by the CONECTA-GEN project (Roldán 2014). Locations were chosen because of the large quantity of historical A. antennatus fisheries information and the interest of the Spanish Government to start an integrated management plan11,12,13,31. A total of 1403 adults were collected at seven Mediterranean locations (fishing grounds): Port de la Selva, Roses, Palamós, Blanes, Vilanova i la Geltrú, Dénia, and Santa Pola (Table 1). A sample of 100 adult individuals (~ 50♀: 50♂) was obtained from local fishermen at each location during winter season in 2016 and 2017 years (Table 1; Fig. 1). A portion of about 10 mg of muscle tissue from each individual was preserved in 70% ethanol until DNA extraction was performed using the modified phenol–chloroform protocol outlined in Fernández et al.56.
Molecular markers
A set of twelve polymorphic microsatellite loci split into three multiplex PCRs and one singleplex PCR were used: Aa138, Aa1255, Aa956, Aa496b, Aa123, Aa681, Aa667, Aa1444, Aa751, Aa818, Aa1061, and Aa119533,57. Microsatellite loci were amplified using approximately 30 ng of template DNA in 10 μl final volume, following the methodology described in Planella et al.33. PCR products were analysed in an ABI PRISM 3730xl automatic sequencer (Applied Biosystems, Foster City, CA) at the sequencing unit of the University of Santiago de Compostela (Campus Lugo). Allele scoring was performed with GeneMapper 4.0 software (Applied Biosystems, Foster City, CA), using the LIZ 500 (Applied Biosystems) as size standard.
Genetic analysis
Genetic diversity within each sample was described by the mean number of alleles per locus (NA) and the allelic richness (AR) calculated using FSTAT v. 2.9.358, and the average among loci of the observed and expected heterozygosity (HO, HE) using Genepop v. 4.659. Deviations of observed genotype proportions from expected under HWE were summarized using the inbreeding coefficient FIS60 and its significance was statistically checked using the exact probability test of Guo and Thompson61 implemented in Genepop v. 4.659. Genotypic linkage disequilibrium between all pairs of loci was tested with Genepop v. 4.659, using a Fisher’s exact test with 10,000 dememorizations and 5000 iterations per batch. The Bonferroni correction was used to adjust significance levels for multiple simultaneous comparisons. The presence of null alleles was assessed with the software Micro-Checker v. 2.2.362 by performing 1000 randomizations.
Pairwise genetic differentiation between samples (FST) were calculated using the software Arlequin v. 3.563 with 10,000 permutations to test significance. We applied the Bonferroni correction for multiple comparisons. FST values corrected for the presence of null alleles and its significance were estimated using the FreeNA software64. Hierarchical analyses of molecular variance (AMOVA65) as implemented in Arlequin v.3.563 were performed to assess oceanographic and temporal divergence among samples. The oceanographic grouping considers the Ibiza Channel as an oceanographic barrier isolating fishing areas located northward and southward (Fig. 1). As the Dénia’s fishing ground is the closest location to the Ibiza Channel, we performed two hierarchical oceanographic groupings, the first one included Dénia in the southward region of the channel, and the second grouping included Dénia in the northward region. The hierarchical temporal grouping was used to check whether geographical structure was maintained over time. The significance of the tests was assessed by permutation with 10,000 replicates. A Bayesian clustering analysis was performed applying the admixture model implemented in STRUCTURE v. 2.3.466 to infer the underlying population structure. Ten independent runs were made for each number of genetic clusters (K = 1–8) where each run consisted of a burn-in period length of 50,000 iterations followed by 200,000 Markov chain Monte Carlo iterations. The most likely number of K was selected according to the Evanno’s method67 implemented in STRUCTURE HARVESTER68.
The software POWSIM v. 4.169 was used to assess the statistical power of our set of loci to detect significant genetic differentiation for the present sample sizes, number of loci and their allele frequencies, by both Pearson’s chi-square and Fisher exact tests (1000 dememorizations, 100 batches, and 1000 iterations) and 1000 replicates. We explored a range of different values for FST by varying the number of generation of drift (t). The percentage of significant outcomes was interpreted as the power of the tests for detecting the defined level of genetic divergence. The effective population size (Ne) was estimated for each sample using the bias-corrected version of the method based on linkage disequilibrium70,71 as implemented in NeEstimator v. 2.172. Ten out of the fourteen samples had an infinite Ne, so the selected Ne to assess the statistical power of our loci to detect genetic differentiation was 10,000.
Isolation by distance (IBD) among fishing grounds was assessed from the correlation between genetic and geographical distance matrices among studied locations. Pairwise genetic differentiation was linearized as FST/(1 − FST)73. The geographical distances were measured as the shortest coastline between locations in kilometres. The statistical significance was assessed by Mantel tests with 10,000 permutations using the software NTSYSpc v. 2.174.
Using divMigrate-online75, the relative direction and magnitude of migration between samples for each temporal collection were summarized as a network from the estimated effective number of migrants (Nm).
Data availability
All data are included in the article.
References
Fernández, M. V., Heras, S., Maltagliati, F., Turco, A. & Roldán, M. I. Genetic structure in the blue and red shrimp Aristeus antennatus and the role played by hydrographical and oceanographical barriers. Mar. Ecol. Prog. Ser. 421, 163–171 (2011).
Campillo, A. Bio-ecology of Aristeus antennatus in the French Mediterranean. in Proceedings of the International Workshop on Life Cycles and Fisheries of the Deep-water Red Shrimps Aristaeomorpha foliacea and Aristeus antennatus (ed. Bianchini, M. L. & Ragonese, S.) 25–26 (I.T.P.P. Spec. Publ., Mazara del Vallo, Italy, 1994).
Sardà, F. et al. An introduction to Mediterranean deep-sea biology. Sci. Mar. 68, 7–38 (2004).
Sardà, F., Company, J. B. & Castellón, A. Intraspecific aggregation structure of a shoal of a Western Mediterranean (Catalan coast) deep-sea shrimp, Aristeus antennatus (Risso, 1816), during the reproductive period. J. Shellfish Res. 22, 569–579 (2003).
García-Rodriguez, M. & Esteban, A. On the biology and fishery of Aristeus antennatus (Risso, 1816), (Decapoda, Dendrobranchiata) in the Ibiza Channel (Balearic Islands, Spain). Sci. Mar. 63, 27–37 (1999).
Carreton, M. et al. Morphological identification and molecular confirmation of the deep-sea blue and red shrimp Aristeus antennatus larvae. PeerJ 7, e6063 (2019).
Carbonell, A., Carbonell, M., Demestre, M., Grau, A. & Monserrat, S. The red shrimp Aristeus antennatus (Risso, 1816) fishery and biology in the Balearic Islands, Western Mediterranean. Fish. Res. 44, 1–13 (1999).
Maynou, F. Environmental causes of the fluctuations of red shrimp (Aristeus antennatus) landings in the Catalan Sea. J. Mar. Syst. 71, 294–302 (2008).
Massutí, E. et al. The influence of oceanographic scenarios on the population dynamics of demersal resources in the western Mediterranean; hypothesis for hake and red shrimp off Balearic Islands. J. Mar. Syst. 71, 421–438 (2008).
Food and Agriculture Organization. General Fisheries Commission for the Mediterranean; Report of the ninth session of the Scientific Advisory Committee. FAO Fish. Rep. 814, 1–106 (2006).
Boletín Oficial del Estado. Orden AAA/2808/2012, de 21 de diciembre, por la que se establece un Plan de Gestión Integral para la conservación de los recursos pesqueros en el Mediterráneo afectados por las pesquerías realizadas con redes de cerco, redes de arrastre y artes fijos y menores, para el período 2013–2017. BOE 313, 89468–89475 (2012).
Boletín Oficial del Estado. Orden AAA/923/2013, de 16 de mayo, por la que se regula la pesca de gamba rosada (Aristeus antennatus) con arte de arrastre de fondo en determinadas zonas marítimas próximas a Palamós. BOE 126, 40016–40022 (2013).
Boletín Oficial del Estado. Orden APM/532/2018, de 25 de mayo, por la que se regula la pesca de gamba rosada (Aristeus antennatus) con arte de arrastre de fondo en determinadas zonas marítimas próximas a Palamós. BOE 128, 55045–55051 (2018).
Waples, R. S., Punt, A. E. & Cope, J. M. Integrating genetic data into management of marine resources: how can we do it better?. Fish. Fish. 9, 423–449 (2008).
Sardà, F., Bas, C., Roldán, M. I., Pla, C. & Lleonart, J. Enzymatic and morphometric analyses in mediterranean populations of the rose shrimp, Aristeus antennatus (Risso, 1816). J. Exp. Mar. Biol. Ecol. 221, 131–144 (1998).
Roldán, M. I., Heras, S., Patellani, R. & Maltagliati, F. Analysis of genetic structure of the red shrimp Aristeus antennatus from the Western Mediterranean employing two mitochondrial regions. Genetica 136, 1–4 (2009).
Lo Brutto, S., Maggio, T., Delana, A. M., Cannas, R. & Arculeo, M. Further investigations on populations of the Deep-water blue and red shrimp Aristeus antennatus (Risso, 1816) (Decapoda, Dendrobranchiata), as inferred from amplified fragment length polymorphism (AFLP) and mtDNA analyses. Crustaceana 85, 1393–1408 (2012).
Wright, J. M. & Bentzen, P. Microsatellites: genetic markers for the future. Rev. Fish. Biol. Fish. 4, 384–388 (1994).
Cannas, R. et al. Genetic variability of the blue and red shrimp Aristeus antennatus in the Western Mediterranean Sea inferred by DNA microsatellite loci. Mar. Ecol. 33, 350–363 (2012).
You, E.-M. et al. Microsatellite and mitochondrial haplotype diversity reveals population differentiation in the tiger shrimp (Penaeus monodon) in the Indo-Pacific region. Anim. Genet. 39, 267–277 (2008).
Robainas-Barcia, A. et al. Spatiotemporal genetic differentiation of Cuban natural populations of the pink shrimp Farfantepenaeus notialis. Genetica 133, 283–294 (2008).
Hauser, L. & Carvalho, G. R. Paradigm shifts in marine fisheries genetics: ugly hypotheses slain by beautiful facts. Fish. Fish. 9, 333–362 (2008).
Schunter, C. et al. Matching genetics with oceanography: directional gene flow in a Mediterranean fish species. Mol. Ecol. 20, 5167–5181 (2011).
Vera, M. et al. Current genetic status, temporal stability and structure of the remnant wild European flat oyster populations: conservation and restoring implications. Mar. Biol. 163, 239 (2016).
García-Ladona, E. Currents in the Western Mediterranean basin. In Atlas of Bedforms in the Western Mediterranean (eds Guillén, J. et al.) 41–47 (Springer, Cham, 2017).
Fernández, V., Dietrich, D. E., Haney, R. L. & Tintoré, J. Mesoscale, seasonal and interannual variability in the Mediterranean Sea using a numerical ocean model. Prog. Oceanogr. 66, 321–340 (2005).
Pinot, J.-M., López-Jurado, J. L. & Riera, M. The Canales experiment (1996–1998). Interannual, seasonal and mesoscale variability of the circulation in the Balearic Channels. Prog. Oceanogr. 55, 335–370 (2002).
García-Merchán, V. H. et al. Phylogeographic patterns of decapod crustaceans at the Atlantic-Mediterranean transition. Mol. Phylogenet. Evol. 62, 664–672 (2012).
Cartes, J. E., Madurell, T., Fanelli, E. & López-Jurado, J. L. Dynamics of suprabenthos-zooplankton communities around the Balearic Islands (western Mediterranean): influence of environmental variables and effects on the biological cycle of Aristeus antennatus. J. Mar. Syst. 71, 316–335 (2008).
Company, J. B. et al. Climate influence on deep sea populations. PLoS ONE 3, e1431 (2008).
Direcció General d’Agricultura, Ramadería, Pesca i Alimentació. Programa d’Acció Marítima. Estratègia marítima de Catalunya 2030—Pla Estratègic 2018–2021 (2018).
Food and Agriculture Organization. General Fisheries Commission for the Mediterranean; Report of the nineteenth session of the Scientific Advisory Committee on Fisheries. FAO Fish. Rep. 1209, 1–174 (2017).
Planella, L., Vera, M., García-Marín, J.-L., Heras, S. & Roldán, M. I. Mating structure of the blue and red shrimp, Aristeus antennatus (Risso, 1816) characterized by relatedness analysis. Sci. Rep. 9, 7227 (2019).
Heras, S., Planella, L., García-Marín, J.-L., Vera, M. & Roldán, M. I. Genetic structure and population connectivity of the blue and red shrimp Aristeus antennatus. Sci. Rep. 9, 13531 (2019).
Jorquera, E., Anstey, L., Paterson, I., Kenchington, E. & Ruzzante, D. E. Isolation and characterization of 26 novel microsatellite loci in the deep-sea shrimp Acanthephyra pelagica. Conserv. Genet. Resour. 6, 731–733 (2014).
Jacobson, A., Plouviez, S., Thaler, A. D. & Van Dover, C. L. Characterization of 13 polymorphic microsatellite loci in Rimicaris hybisae, a shrimp from deep-sea hydrothermal vents. Conserv. Genet. Resour. 5, 449–451 (2013).
Arculeo, M., Pellerito, R. & Bonhomme, F. Isolation and use of microsatellite loci in Melicertus kerathurus (Crustacea, Penaeidae). Aquat. Living Resour. 23, 103–107 (2010).
Benzie, J. A. H. Population genetic structure in penaeid prawns. Aquac. Res. 31, 95–119 (2000).
Maggio, T., Lo Brutto, S., Cannas, R., Deiana, A. M. & Arculeo, M. Environmental features of deep-sea habitats linked to the genetic population structure of a crustacean species in the Mediterranean Sea. Mar. Ecol. 30, 354–365 (2009).
Palumbi, S. R. Marine reserves and ocean neighbourhoods: the spatial scale of marine populations and their management. Annu. Rev. Environ. Resour. 29, 31–68 (2004).
Anger, K. Contributions of larval biology to crustacean research: a review. Invertebr. Reprod. Dev. 49, 175–205 (2006).
Palmas, F., Olita, A., Addis, P., Sorgente, R. & Sabatini, A. Modelling giant red shrimp larval dispersal in the Sardinian seas: density and connectivity scenarios. Fish. Oceanogr. 26, 364–378 (2017).
Mokhtar-Jamaï, K. et al. From global to local genetic structuring in the red gorgonian Paramuricea clavata: the interplay between oceanographic conditions and limited larval dispersal. Mol. Ecol. 20, 3291–3305 (2011).
Schunter, C. et al. Genetic connectivity patterns in an endangered species: The dusky grouper (Epinephelus marginatus). J. Exp. Mar. Biol. Ecol. 401, 126–133 (2011).
Carbonell, A. Evaluación de la gamba rosada, Aristeus antennatus (Risso, 1816), en el Mar Balear. (University of the Balearic Islands, Mallorca, Spain, 2005).
Sardà, F., Company, J. B., Rotllant, G. & Coll, M. Biological patterns and ecological indicators for Mediterranean fish and crustaceans below 1,000 m: a review. Rev. Fish. Biol. Fish. 19, 329–347 (2009).
Paradis, S. et al. Spatial distribution of sedimentation-rate increases in Blanes Canyon caused by technification of bottom trawling fleet. Prog. Oceanogr. 169, 241–252 (2018).
Clavel-Henry, M. et al. Influence of the summer deep-sea circulations on passive drifts among the submarine canyons in the northwestern Mediterranean Sea. Ocean. Sci. 15, 1745–1759 (2019).
Masó, M. & Tintoré, J. Variability of the shelf water off the northeast Spanish coast. J. Mar. Syst. 1, 441–450 (1991).
Ahumada-Sempoal, M.-A., Flexas, M. M., Bernardello, R., Bahamon, N. & Cruzado, A. Northern Current variability and its impact on the Blanes Canyon circulation: a numerical study. Prog. Oceanogr. 118, 61–70 (2013).
Fernandez-Arcaya, U. et al. Ecological role of submarine canyons and need for canyon conservation: a review. Front. Mar. Sci. 4, 1–26 (2017).
Zúñiga, D. et al. Particle fluxes dynamics in Blanes submarine canyon (Northwestern Mediterranean). Prog. Oceanogr. 82, 239–251 (2009).
Durrieu de Madron, X. et al. Interaction of dense shelf water cascading and open-sea convection in the northwestern Mediterranean during winter 2012. Geophys. Res. Lett. 40, 1379–1385 (2013).
Cisneros, M. et al. Deep-water formation variability in the north-western Mediterranean Sea during the last 2500 yr: a proxy validation with present-day data. Glob. Planet. Change 177, 56–68 (2019).
Román, S. et al. High spatiotemporal variability in meiofaunal assemblages in Blanes Canyon (NW Mediterranean) subject to anthropogenic and natural disturbances. Deep. Sea Res Part I Oceanogr. Res. Pap. 117, 70–83 (2016).
Fernández, M. V., Heras, S., Maltagliati, F. & Roldán, M. I. Deep genetic divergence in giant red shrimp Aristaeomorpha foliacea (Risso, 1827) across a wide distributional range. J. Sea. Res. 76, 146–153 (2013).
Heras, S. et al. Development and characterization of novel microsatellite markers by Next Generation Sequencing for the blue and red shrimp Aristeus antennatus. PeerJ 4, e2200 (2016).
Goudet, J. FSTAT, a program to estimate and test gene diversities and fixation indices (version 2.9.3). Accessed 20 Nov 2019; https://www2.unil.ch/popgen/softwares/fstat.htm (2001).
Rousset, F. GENEPOP´007: a complete re-implementation of the GENEPOP software for Windows and Linux. Mol. Ecol. Resour. 8, 103–106 (2008).
Weir, B. S. & Cockerham, C. C. Estimating F-statistics for the analysis of population structure. Evolution 38, 1358–1370 (1984).
Guo, S. W. & Thompson, E. A. Performing the exact test of Hardy–Weinberg proportion for multiple alleles. Biometrics 48, 361–372 (1992).
Van Oosterhout, C., Hutchinson, W. F., Wills, D. P. M. & Shipley, P. Micro-Checker: software for identifying and correcting genotyping errors in microsatellite data. Mol. Ecol. Notes 4, 535–538 (2004).
Excoffier, L. & Lischer, H. E. L. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol. Ecol. Resour. 10, 564–567 (2010).
Chapuis, M.-P. & Estoup, A. Microsatellite null alleles and estimation of population differentiation. Mol. Biol. Evol. 24, 621–631 (2007).
Excoffier, L., Smouse, P. E. & Quattro, J. M. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131, 479–491 (1992).
Pritchard, J. K., Stephens, M. & Donnelly, P. Inference of population structure using multilocus genotype data. Genetics 155, 945–959 (2000).
Evanno, G., Regnaut, S. & Goudet, J. Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Mol. Ecol. 14, 2611–2620 (2005).
Earl, D. A. & vonHoldt, B. M. STRUCTURE HARVESTER: a website and program for visualizing STRUCTURE output and implementing the Evanno method. Conserv. Genet. Resour. 4, 359–361 (2012).
Ryman, N. & Palm, S. POWSIM: a computer program for assessing statistical power when testing for genetic differentiation. Mol. Ecol. Notes 6, 600–602 (2006).
Hill, W. G. Estimation of effective population size from data on linkage disequilibrium. Genet. Res. 38, 209–216 (1981).
Waples, R. S. A bias correction for estimates of effective population size based on linkage disequilibrium at unlinked gene loci. Conserv. Genet. 7, 167–184 (2006).
Do, C. et al. NeEstimator V2: re-implementation of software for the estimation of contemporary effective population size (Ne) from genetic data. Mol. Ecol. Resour. 14, 209–214 (2014).
Rousset, F. Genetic differentiation and estimation of gene flow from F-statistics under isolation by distance. Genetics 145, 1219–1228 (1997).
Rohlf, F. J. NTSYS-pc. Numerical Taxonomy and Multivariate Analysis System, Version 2.1. Setauket, New York (1993).
Sundqvist, L., Keenan, K., Zackrisson, M., Prodöhl, P. & Kleinhans, D. Directional genetic differentiation and relative migration. Ecol. Evol. 6, 3461–3475 (2016).
Acknowledgements
We gratefully thank the ship-owners Francisco Torné (Eli-Hermi II), Manel Noguera (Port de Roses), Conrad Masseguer (Nova Gasela), Pere Pérez (Peret II), Marc Pons (Avi Salvador), Rafael Montoya (Avi Pau), Juan Antonio Sepulcre (La androna) and Jorge Castejón (Isabel y Andrés) for assistance in sampling collection. This work was supported by a grant from Spanish Ministerio de Economia y Competitividad (CTM2014-54648-C2-2-R) to MIR. LP and MA benefited from predoctoral fellowship from the Universitat de Girona (BR2014 and IFUdG2018, respectively). A. antennatus image in Fig. 1 was taken by Francesc Rabat.
Author information
Authors and Affiliations
Contributions
All authors conceived the ideas and designed the study. M.A. Collected the data, analysed the data and wrote the original manuscript draft. All authors revised the manuscript for significant intellectual content and approved the final version.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Agulló, M., Heras, S., García-Marín, JL. et al. Genetic analyses reveal temporal stability and connectivity pattern in blue and red shrimp Aristeus antennatus populations. Sci Rep 10, 21505 (2020). https://doi.org/10.1038/s41598-020-78634-2
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-020-78634-2
This article is cited by
-
An evaluation of the genetic connectivity and temporal stability of the blue and red shrimp Aristeus antennatus: a case study of spawning females’ grounds in the Western Mediterranean Sea
Hydrobiologia (2022)
-
Genetic diversity and population structure analysis of Lateolabrax maculatus from Chinese coastal waters using polymorphic microsatellite markers
Scientific Reports (2021)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.