Artículos

 

Genetic structure and diversity of squids with contrasting life histories in the Humboldt Current System

 

Estructura y diversidad genética de calamares con historias de vida contrastantes en el Sistema de corrientes de Humboldt

 

Christian Marcelo Ibáñez and Elie Poulin*

 

* Instituto de Ecología y Biodiversidad, Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile. Las Palmeras # 3425, Ñuñoa. Chile. e-mail: ibanez.christian@gmail.com

 

Recibido: 2 de febrero de 2012.
Aceptado: 8 de mayo de 2013.

 

ABSTRACT

Dosidiscus gigas and Doryteuthis gahiare the most abundant squids in the Humboldt Current System (HCS). These species have contrasting life histories. To determine the genetic structure and diversity of these species, we collected samples from different places in the HCS and amplified a fragment of the mitochondrial cytochrome C oxidase I gene. The molecular analysis of D. gigas revealed low genetic diversity, absence of population structure and evidence for a demographic expansion during the transition from the last glacial period to the current interglacial. These results suggest that D. gigas is composed of one large population with high levels of gene flow throughout the HCS. In the case of D. gahi, the sequences indicated the presence of two population units in the HCS, one in south-central Chile and one in Peru. The Chilean unit had greater genetic diversity, suggesting that it is an old, relatively stable population. In the Peruvian unit there was less genetic diversity and evidence of a recent demographic expansion. The changes in distribution ranges and population sizes of the squid populations may be related to historical variations in productivity along the HCS. The different dispersion and migration capacities of these species may explain the differences in their structure; however, the genetic diversity of both species appears to be more related to historical variations in their distribution ranges and the biogeographic origin of each.

Key words: Genetic diversity, life histories, population structure, squids.

 

RESUMEN

Dosidiscus gigas y Doryteuthis gahi corresponden a los calamares más abundantes en el Sistema de la Corriente de Humboldt (SCH). Estas especies se caracterizan por tener historias de vida contrastantes. Para determinar la estructura y diversidad genética de ambas especies, se recolectaron muestras de diferentes lugares de SCH, y se amplificó un fragmento del gen mitocondrial citocromo c oxidasa I. Los análisis moleculares de D. gigas mostraron una baja diversidad genética, una ausencia de estructura poblacional y la evidencia de expansión demográfica durante la transición entre el último periodo glacial y el actual interglacial. Estos resultados sugieren que D. gigas corresponde a una única población caracterizada por alto flujo genético. En el caso de D. gahi, las secuencias revelaron la presencia de dos unidades poblacionales correspondientes al centro-sur de Chile y Perú. La unidad chilena mostró niveles más altos de diversidad, lo que sugiere que corresponde a una población antigua y estable. En la unidad peruana se detectó una menor diversidad genética y la evidencia de una reciente expansión demográfica. Los cambios de distribución y abundancia de los calamares podrían estar relacionados a las variaciones históricas de la productividad. Las capacidades diferenciales de dispersión y migración de las dos especies podrían explicar las diferencias en estructura. Sin embargo, la diversidad genética de ambas especies parece relacionarse más con las variaciones históricas de sus rangos de distribución y del origen biogeográfico de cada una de ellas.

Palabras claves: Calamares, diversidad genética, estructura poblacional, historias de vida.

 

INTRODUCTION

The biological and ecological characteristics of organisms affect their dispersal ability and the amount of gene flow among their populations. Thus it is expected that species with little mobility will form genetically distinct populations, while more mobile species will maintain a genetic homogeneity by means of greater gene flow (Futuyma, 2009). However, sessile organisms and those with little vagility have other strategies which allow them to colonize distant sites (e.g., propagules, larvae, spores, seeds; Kinlan & Gaines, 2003; Cowen & Sponaugle, 2009). In the marine environment, invertebrates have a great diversity of life history strategies compared to terrestrial animals (Strathmann, 1990), which is a determining factor in geographic connectivity and genetic diversity. For example, gastropod species with planktonic larvae show lower levels of genetic structure and have greater diversity than those species with direct development (Kyle & Boulding, 2000; Johnson & Black, 2006; Lee & Boulding, 2009). However, this relationship between dispersal capacity and gene flow does not always hold, and oceanographic factors have been described as limiting for the dispersion of larvae or adults (Poulin et al., 2002; Barber etal., 2002). The geographic structure of genetic diversity may reflect historical processes generally associated with geographic breaks, as well as contemporary processes linked to the dispersal capacity of a species (Avise, 2000; Pecl et al., 2009).

There are few studies of the genetic structure of the marine organisms of the Humboldt Current System (HCS). For species with a long-lived planktonic larvae (several weeks) such as the crab Cancer setosus (Molina, 1782), the gastropod Concholepas con-cholepas (Bruguiére, 1789) and the squat lobster Pleuroncodes monodon (H. Milne Edwards, 1837), no spatial genetic structure was detected over at least 2000 km of the coast (Gomez-Uchida et al., 2003; Cárdenas et al., 2009a; Haye et al., 2010). A similar result was found for fishes with a wide geographic range and long larval duration (several weeks) such as the Chilean hake Merluccius gayi(Guichenot, 1848) and the jack mackerel Trachurus murphyi Nichols, 1920 (Galleguillos et al., 2000; Cárdenas et al., 2009b). By contrast, the seaweeds Lessonia nigrescens Bory and Mazzaella laminarioides (Bory de Saint-Vincent) Fredericq and the gastropods Chorus giganteus (Lesson, 1831) and Acanthina monodon (Pallas, 1774) have a significant geographic structure associated with their reduced dispersal potential (F_ST = 0.14-0.99, Faugeron et al., 2001; Gajardo et al., 2002; Faugeron et al., 2005; Tellier et al., 2009; Sánchez et al., 2011). These studies have all dealt with individual species; there have been no comparative studies of sympatric taxa with different life history characters that share the same ecosystem in the HCS. Also, there is no information on the genetic structure of a number of important groups in the HCS such as echinderms, polychaetes and cephalopods.

Within the cephalopods, the squids are a fundamental component of the pelagic ecosystems, due both to their abundance and their trophic role (Boyle & Rodhouse 2005; Thiel et al., 2007). They are also interesting study models in population genetics and phylogeny because of their short life cycles, wide geographic ranges and contrasting life histories (Boyle & Rodhouse, 2005). The most common and abundant squids in the HCS are Dosidi-cus gigas (d'Orbigny, 1835) (Ommastrephidae) and Doryteuthis gahi (d'Orbigny, 1835) (Loliginidae). These species have contrasting body sizes, habitat use, migration patterns and reproductive strategies. In the case of D. gigas, its great dispersal potential associated with its large body size (> 2 m total length) and excellent swimming capacity (> 20 km/h) allows it to migrate actively distances of more than 1,000 km in the HCS, both in latitude and longitude (Nesis, 1970; Nigmatullin et al., 2001; Ibáñez & Cubillos, 2007). Also, D. gigas spawns a large gelatinous mass of millions of eggs in the pelagic environment, which may be transported passively by currents to very distant places (Staaf et al., 2008). Like other ommastrephids, D. gigas haves a short embryonic development (around 6-9 days, Yatsu et al., 1999). In contrast, D. gahi has a small body size (< 50 cm total length), and due to its reduced home range (continental shelf) only makes ontogenetic vertical migrations (Arkhipkin et al., 2004). Additionally, D. gahi spawns on the bottom near the coast, capsules with hundreds of eggs which adhere to seaweeds or soft corals (Arkhipkin et al., 2000; Villegas, 2001). Their embryonic development is completed in around 30-35 days (Guerra et al. 2001), a contrasting strategy compared to D. gigas. These differences between D. gahi and D. gigas could have consequences on their respective dispersal potentials, since only the paralarvae of the loliginids can contribute to passive dispersal, while both eggs and paralarvae of the ommastrephids may be transported by marine currents passively over 600 km from the spawning grounds (Bower, 1996; Boyle & Rodhouse, 2005). This information on the life history of the two squids allows predictions to be made about their spatial structure and genetic diversity. We hypothesize that the squids Dosidicus gigas and Doryteuthis gahi should have different patterns of spatial genetic structure in the Humboldt Current System, given their different life history strategies and migration patterns. D. gigas should show an absence of population genetic structure as a consequence of its large migrations and pelagic spawning, while D. gahishould have a population genetic structure associated with its lower dispersal capacity and benthic spawning.

 

MATERIALS AND METHODS

This study is based upon data already published by Ibanez et al. (2011, 2012), but here reanalyzed in a comparative context; thus the methodological details related to standardized laboratory protocols may be found in these publications. In summary, we collected between 23 and 33 tissue samples of the squids Dosi-dicus gigas and Doryteuthis gahi from several localities of Peru and Chile between 2005 and 2008 (Ibanez et al., 2011, 2012) (Table 1, Fig. 1) and sequenced the mitochondrial Cytochrome Oxidase I gene (COI).

To detect population structure in the squid species we estimated the number of clusters (k) and the posterior probability density (PPD) of belonging to a given cluster by means of Bayes-ian inference, in the software Geneland (Guillot et al. 2005), implemented in R software. We inferred the number of clusters from the modal value of k, running a Markov Chain Monte Carlo (MCMC) with 5x10⁶ iterations, sampling parameters every 1000 iterations. After these runs we burn-in 500 resultant parameters in order to obtain posterior probabilities of population membership for each individual and each spatial domain. Each analysis was run 4 times to check the congruence. Additionally, to compare the levels of population structure in the squid species we calculated the F_ST index for each pair of localities using Arlequin version 3.11 (Excof-fier et al., 2005). Haplotype number and haplotype diversity (Hd) were calculated using Arlequin for each species and location.

Finally, we inferred the demographic history of both squids from the HCS using Bayesian skyride (Minin et al., 2008) analyses implemented in BEAST version 1.7.2 (Drummond et al. 2012). The Bayesian skyride uses Gaussian Markov random fields to achieve temporal smoothing of the effective population size (Ne) by means of a MCMC sampling of sequence data, to estimate a posterior distribution of Ne through time and its highest posterior density intervals (95% HPD) (Minin et al., 2008). Bayesian skyride analyses were run using the Hasegawa-Kishino-Yano substitution model (HKY85), which was identified as the best fitting model by Bayesian decision criteria implemented in jModelTest (Posada, 2008). The relaxed molecular clock with uncorrelated exponential distribution was the model used. In this set of runs, the mean mutation rate was set with a prior normal distribution (0.02 x 10^-6, 10% SD). We ran 20 x 10⁶ iterations, sampling every 1000 generations, while the first 10% were discarded as burn in. The Bayesian skyride plots were generated with the program Tracer version 1.5 (Rambaut & Drummond, 2009).

 

RESULTS

The Bayesian analysis of genetic structure georeferenced showed a maximum posterior probability of one group or population (K = 1) which is constituted D. gigas along its distribution range (Fig. 2a). This mean that the spatial configuration of the posterior probability map is constituted by individuals assigned to no more of one cluster (Fig. 2b), because this squids do not have spatial population structure. In the case of D. gahi the mode of number of clusters showed two genetic units in the HCS (k = 2, Fig. 3a). These units are located in Peru (PP = 0.9) and Southern Chile (PP = 0.9) (Fig. 3b). These results confirm the absence of geographic structure in D. gigas (Fig. 2), while in D. gahi the analysis showed two populations, corresponding to the Peruvian and Chilean locations (Fig. 3). The F_ST values of D. gahi (mean = 0.199 ± 0.15) were several orders of magnitude greater than in D. gigas (mean = 0.000261± 0.02).

A total of 15 haplotypes were found in the 683 bp fragment of COI among the 116 individuals of D. gahi examined, while in D. gigas there were 23 haplotypes in the 657 pb fragment of COI in the 169 individuals examined. The number of haplotypes in each location was similar, ranging between 4 and 8 (Table 1). The haplotype diversity of D. gahi was lower in the northern Humboldt (Hd = 0.34-0.50) than in the southern Humboldt (Hd = 0.75-0.80). For D. gigas the genetic diversity was low in all locations (Hd = 0.20-0.54) (Table 1). In general the haplotype diversity was greater in D. gahi than in D. gigas (Table 1).

Bayesian skyride analyses indicated that population growth of D. gigas initiated approximately 37,000 years ago in the HCS, increasing mean population size from around 10,000 individuals to a mean of 2 million individuals (Fig. 4). The mean Time to the Most Recent Common Ancestor (TMRCA) was estimated at 37,136 years ago (95% HPD 29,843 to 44,734 years). Bayesian skyride analyses of the Peruvian population of D. gahi indicated that population growth initiated approximately 35,000 years ago in the northern HCS and the mean time of TMRCA was estimated at 38,620 years (HPD 95% 30, 762-45, 995 years). The effective population size increased from 10,000 to 1,000,000 individuals in the last 35,000 years (Fig. 5a). The Chilean population showed a low increase of population size through time in the southern HCS from a mean population size of 10, 000 to 100,000 individuals (Figure 5b). In this population the TMRCA was estimated at 96,956 years (HPD 95% 77, 021-116, 400 years).

 

DISCUSSION

This study found contrasting patterns of genetic structure in the two species. The neritic squid D. gahi had high values of genetic differentiation between populations collected in south-central Chile and Peru (> 2,500 km), while D. gigas showed low values of structure in these same zones. However, both species showed an absence of genetic differentiation within the geographic zones (< 1,000 3m).

These results corroborate previous studies in these two squid families. The majority of the species of ommastrephids show an absence of genetic structure at scales of thousands of kilometers in the same biogeographic zone (e.g., Adcock et al., 1999; Sandoval-Castellanos et al., 2007, 2010; Ibanez et al., 2011). For these species, only major biogeographical breaks on the order of 10,000 km appear to be able to generate a spatial structure in their genetic diversity (e.g. Brierley et al., 1993; Aoki et al., 2008; Katugin, 2002; Sandoval-Castellanos et al., 2007, 2010). In contrast, loliginid squids generally show genetic structure at a smaller geographic scale and appear to be influenced by local barriers such as the mouths of large rivers or abrupt changes in the sea floor (Brierley eta/., 1995; Shaw etal., 1999; Herke & Foltz, 2002; Semmens et al., 2007). In the absence of such barriers, these species are genetically homogenous up to a scale of hundreds of kilometers (e.g. Carvalho & Loney, 1989; Brierley etal., 1995; Reichow & Smith, 2001; Shaw et al., 2004; Buresch et al., 2006; Shaw et al., 2010).

This difference in patterns of genetic structure at the family level may be the consequence of the different life history strategies which characterize them, in particular those elements related to the dispersal potential of individuals (Shaw et al. 2010). The ommastrephids, which have little genetic structuring, are characterized by pelagic spawning and long migrations. According to the classification proposed by Rocha et al. (2001), the squids of the family Ommastrephidae are essentially monocyclic (animals reproduce once and then die), and some species such as D. gigas may spawn in batches (repeatedly). By contrast, squids of the family Loliginidae such as D. gahi have terminal spawning. Loliginid squids are neritic and spawn on the ocean floor, depositing their eggs in seaweeds or soft corals, while ommastrpehids are oceanic and spawn masses of pelagic eggs (O'Dor, 1998).

Just as proposed in the literature (Boyle & Rodhouse, 2005; Shaw et al. 2010), these different life history strategies appear to have direct consequences on the patterns of gene flow and thus on the spatial structuring of the genetic diversity of these squids.

In terms of genetic diversity, both species had low numbers of recovered haplotypes, both in the northern and southern zones of the HCS. However, there were clear differences in the patterns of haplotype diversity (Hd) between the species, as well as between geographic zones within each species. Low levels of genetic diversity generally occur in populations that have undergone drastic fluctuations in population sizes, bottlenecks or founder events, while high levels of genetic diversity are indicative of population stability or metapopulation dynamics (Grant & Bowen, 1998; Carvalho & Nigmatullin, 1998; Hoelzel, 1999; Lecomte etal., 2004; Freeland, 2005). The spatial variation in Hd observed in this study may thus be related to past climatic changes in each geographic area and the way each species has responded locally, as the demographic analysis showed.

In the case of D. gigas, although there was low genetic diversity both in Peru and in Chile, the locations of the northern HCS had more diversity compared to the south. This low diversity, decreasing towards the south, may be due to a recent demographic expansion inferred by demographic analysis. Although the evidence at an ecological time scale shows latitudinal variations of D. gigas, usually attributed to El Niño Southern Oscillation (ENSO) or the Pacific Decadal Oscillation (PDO) (Keyl et al., 2008), the genetic evidence shows signs of an older demographic process (37,000 years), probably linked to the drastic variations in the productivity of the eastern Pacific during the last glacial cycle (Hebbeln et al., 2002). Based on our results we propose that D. gigas extended its distribution range towards the south during the transition between the last glacial maximum and the current interglacial period when the environmental conditions were more favorable. A similar phenomenon appears to have occurred in the California Current, in which its distribution was extended to more northern latitudes (Key etal., 2008). In fact, the divergence of the northern and southern populations of D. gigas along the Pacific coast is estimated to have been 39,000 years ago (Staaf et al., 2010).

The demographic history of D. gahi appears to have followed a completely different trajectory. In contrast to D. gigas, the highest diversity values were found in the southern HCS; only the population of Peru showed signals of a recent population expansion around 35,000 years ago. The greater genetic diversity and the low population growth estimated by demographic analysis in the southern HCS suggest that this population of D. gahi did not undergo major demographic fluctuations during the last glacial cycle. On the contrary, we suggest that it increased northward from the south of the South American continent to the northern zone of the HCS at the end of the last glacial period around 40,000 years ago when environmental conditions were more favorable.

The patterns of genetic diversity and effective population sizes do not appear to be linked to the life history strategies of these squids, and may reflect past demographic processes associated with climatic changes over long time scales. However, these two species showed different responses to the changes which characterized the transition from the last glacial period to the current interglacial period. Changes in the productivity of the HCS over the last 30,000 years may be associated with the northward movement and intensification of the winds from the west which control the upwellings and practically all the climate in these latitudes (Lamy et al., 1999; Hebbeln et al., 2002). These environmental fluctuations may be responsible for the changes in the distribution and abundance of marine populations in the past, and the current observed patterns of genetic diversity are the result of processes of demographic expansion or bottlenecks inferred by means of the events of coalescence in the genetic lineages.

 

ACKNOWLEDGEMENTS

We thank a number of people who helped with different aspects of this research. For laboratory techniques we thank Angie Díaz, Claudio González and Marcela Espinoza of the Universidad de Chile (UCHILE). For sample collections we thank Carmen Yamashiro, Juan Arguelles, Juan Rubio, María Inés Sanjinés and Ricardo Tafur of IMARPE, Peru; Luis Adasme and Renato Céspedes of IFOP, Chile; Karin Lohrmann of UCN, Chile, Luis Cubillos, UDEC, Chile and Miguel Araya UNAP, Chile. For ideas in the writing and revising of the manuscript we thank Friedemann Keyl (UNI-BREMEN, Germany) and María Cecilia Pardo (UCHILE). This research was financed by CONICYT AT24080021, ICM P05-002, PFB-23 and "Becas de estadías cortas de investigación destinadas a estudiantes tesistas de doctorado y magister de la Universidad de Chile".

 

REFERENCES

Adcock, G. J., P. W. Shaw, P. G. Rodhoüse & G. R. Carvalho. 1999. Microsatellite analysis of genetic diversity in the squid Illex argentinus during a period of intensive fishing. Marine Ecology Progress Series 187: 171-178.         [ Links ]

Aoki, M., H. Imai, T. Narüse & Y. Keda. 2008. Low genetic diversity of oval squid, Sepioteuthis cf. lessoniana (Cephalopoda: Loliginidae), in Japanese Waters Inferred from a Mitochondrial DNA Non-coding Region. Pacific Science 62: 403-412.         [ Links ]

Arkhipkin, A. I., R. Grzebielec, A. M. Sirota, A. V. Remeslo, I. A. Polishchük & A. J. Middleton. 2004. The influence of seasonal environmental changes on ontogenetic migrations of the squid Loligo gahi on the Falkland shelf. Fisheries Oceanography 13: 1-9.         [ Links ]

Arkhipkin, A. I., V. V. Laptikhovsky & D. A. J. Middleton. 2000. Adaptations for cold water spawning in loliginid squid: Loligo gahi in Falkland waters. Journal of Molluscan Studies 66: 551-564.         [ Links ]

Avise, J. C. 2000. Phylogeography. Massachusetts, Harvard University Press. 447 p.         [ Links ]

Barber, P. H., S. R. Palümbi, M. V. Erdmann & M. K. Moosa. 2002. Sharp genetic breaks among populations of Haptosquilla pulchella (Stomatopoda) indicate limits to larval transport: patterns, causes, and consequences. Molecular Ecology 11: 659-674.         [ Links ]

Bower, J. R. 1996. Estimated paralarval drift and inferred hatching sites for Ommastrephes bartrami (Cephalopoda, Ommastrephidae) near the Hawaiian Archipelago. Fishery Bulletin 94: 398-411.         [ Links ]

Boyle, P. R. & P. G. Rodhoüse. 2005. Cephalopods: ecology and fisheries. Blackwell Science Ltd, Oxford. 438 p.         [ Links ]

Brierley, A. S., P. G. Rodhoüse, J. P. Thorpe & M. R. Clarke. 1993. Genetic evidence of population heterogeneity and cryptic speciation in the ommastrephid squid Martialia hyadesi from the Patagonian Shelf and the Antarctic Polar Frontal Zone. Marine Biology 116: 593-602.         [ Links ]

Brierley, A. S., J. P. Thorpe, G. J. Pierce, M. R. Clarke & P. R. Boyle. 1995. Genetic variation in the neritic squid Loligo forbesi (Myopsida: Loliginidae) in the northeast Atlantic Ocean. Marine Biology 122: 79-86.         [ Links ]

Buresch, K. C., G. Gerlach & R. T. Hanlon. 2006. Multiple genetic stocks of longfin squid Loligo pealeii in the NW Atlantic: stocks segregate inshore in summer, but aggregate offshore in winter. Marine Ecology Progress Series 310: 263-270.         [ Links ]

Cárdenas, L., A. X. Silva, A. Magoulas, J. Cabezas, E. Poulin & F. P. Ojeda. 2009b. Genetic population structure in the Chilean jack mackerel, Trachurus murphyi (Nichols) across the South-eastern Pacific Ocean. Fisheries Research 100: 109-115.         [ Links ]

Cárdenas, L., J. C. Castilla & F. Viard. 2009a. A phylogeographical analysis across three biogeographical provinces of the south-eastern Pacific: the case of the marine gastropod Concholepas concholepas. Journal of Biogeography 36: 969-981.         [ Links ]

Carvalho, G. R. & Ch. M. Nigmatullin. 1998. Stock structure analysis and species identifcation. FAO Fisheries Technical Paper 376: 199-232.         [ Links ]

Carvalho, G. R. & K. H. Loney. 1989. Biochemical genetic studies on the Patagonian squid, Loligo gahi d' Orbigny. I. electrophoretic survey of genetic variability. Journal of Experimental Marine Biology and Ecology 126: 231-241.         [ Links ]

Cowen, R. K. & S. Sponaugle. 2009. Larval dispersal and marine population connectivity. Annual Review of Marine Science 1: 443-466.         [ Links ]

Drummond, A. J., M. A. Suchard, D. Xie & A. Rambaut. 2012. Bayesian phylogenetics with BEAUti and the BEAST 1.7. Molecular Biology and Evolution 29 (8): 1969-1973.         [ Links ]

Excoffier, L., G. Laval & S. Schneider. 2005. Arlequín ver. 3.0: An integrated software package for population genetics data analysis. Evolutionary Bioinformatics Online 1: 47-50.         [ Links ]

Faugeron, S., E. A. Martínez, J. A. Correa & C. Billot. 2005. Long-term copper mine waste disposal in northern Chile associated with gene flow disruption of the intertidal kelp Lessonia nigrescens. Marine Ecology Progress Series 288: 129-140.         [ Links ]

Faugeron, S., M. Valero, C. Destombe, E. A. Martínez & J. A. Correa. 2001. Hierarchical spatial structure and discriminant analysis of genetic diversity in the red alga Mazzaella laminarioides (Gigartinales, Rhodophyta). Journal of Phycology 37: 705-716.         [ Links ]

Freeland, J. R. 2005. Molecular Ecology. John Wiley & Sons, Ltd., West Sussex. 388 p.         [ Links ]

Futuyma, D. J. 2009. Evolution. 2nd Ed. Sinauer Associates, Sunderland, Massachusetts. 603 p.         [ Links ]

Gajardo, G., J. M. Cancino & J. M. Navarro. 2002. Genetic variation and population structure in the marine snail Chorus giganteus (Gastropoda: Muricidae), an overexploited endemic resource from Chile. Fisheries Research 55: 329-333.         [ Links ]

Galleguillos, R., L. Troncoso, C. Oyarzún, M. Astorga & M. Peñaloza. 2000. Genetic differentiation in Chilean hake Merluccius gayi gayi (Pisces: Merlucciidae). Hydrobiologia 420: 49-54.         [ Links ]

Gomez-Uchida, D., D. Weetman, L. Hauser, R. Galleguillos & M. Retamal. 2003. Allozyme and AFLP analyses of genetic population structure in the hairy edible crab Cancer setosus from the Chilean coast. Journal of Crustacean Biology 23: 486-494.         [ Links ]

Grant, W. S. & B. W. Bowen. 1998. Shallow population histories in deep evolutionary lineage of marine fishes: insights for sardines and anchovies and lesson for conservation. Journal of Heredity 89: 415426.         [ Links ]

Guerra, A., F. Rocha & A. F. González. 2001. Embryonic stages of the pa-tagonian squid oligo gahi(Mollusca: Cephalopoda). The Veliger 44: 109-115.         [ Links ]

Guillot, G., F. Mortier & A. Estoup. 2005. Geneland: A program for landscape genetic. Molecular Ecology Notes 5: 712-715.         [ Links ]

Haye, P. A., P. Salinas, E. Acuña & E. Poulin. 2010. Heterochronic phenotypic plasticity with lack of genetic differentiation in the southeastern Pacific squat lobster Pleuroncodes monodon. Evolution and Development 12: 627-633.         [ Links ]

Hebbeln, D., M. Marchant & G. Wefer. 2002. Paleoproductivity in the southern Peru-Chile current through the last 33000 yr. Marine Geology 186: 487-504.         [ Links ]

Herke, S. W. & D. W. Foltz. 2002. Phylogeography of two squid (Loligo pealei and L. plei) in the Gulf of Mexico and northwestern Atlantic Ocean. Marine Biology 140: 103-115.         [ Links ]

Hoelzel, A. R. 1999. Impact of population bottlenecks on genetic variation and the importance of life-history; a case study of the northern elephant seal. Biological Journal of the Linnean Society 68: 23-39.         [ Links ]

Ibáñez, C. M. & L. A. Cubillos. 2007. Seasonal variation in the length structure and reproductive condition of the jumbo squid Dosidicus gigas (d' Orbigny, 1835) off central-south Chile. Scientia Marina 71: 123-128.         [ Links ]

Ibáñez, C. M., J. Arguelles, C. Yamashiro, L. Adasme, R. Céspedes & E. Poulin. 2012. Spatial genetic structure and demographic inference of the Patagonian squid Doryteuthis gahi in the Southeastern Pacific Ocean. Journal of the Marine Biological Association of the United Kingdom 92: 197-203.         [ Links ]

Ibáñez, C. M., L. A. Cubillos, R. Tafur, J. Arguelles, C. Yamashiro & E. Poulin. 2011. Genetic diversity and demographic history of Dosidicus gigas (Cephalopoda: Ommastrephidae) in the Humboldt Current System. Marine Ecology Progress Series 431: 163-171.         [ Links ]

Johnson, M. S. & R. Black. 2006. Effects of mode of reproduction on genetic divergence over large spatial and temporal scales in intertidal snails of the genus Bembicium Philippi (Gastropoda: Littorinidae). Biological Journal of the Linnean Society 89: 689-704.         [ Links ]

Katugin, 0. N. 2002. Patterns of genetic variability and population structure in the North Pacific squids Ommastrephes bartramii, Todarodes pacificus, and Berryteuthis magister. Bulletin of Marine Science 71: 383-420.         [ Links ]

Keyl, F., J. Argüelles, L. Mariátegui, R. Tafur, M. Wolff & C. Yamashiro. 2008. A hypothesis on range expansion and spatio-temporal shifts in size-at-maturity of jumbo squid (Dosidicus gigas) in the eastern Pacific Ocean. California Cooperative Oceanic Fisheries Investigations Reports 49: 119-128.         [ Links ]

Kinlan, B. P. & S. D. Gaines. 2003. Propagule dispersal in marine and terrestrial environments: a community perspective. Ecology 84: 2007-2020.         [ Links ]

Kyle, C. & E. G. Boulding. 2000. Comparative population genetic structure of marine gastropods (Littorina spp.) with and without pelagic larval dispersal. Marine Biology 137: 835-845.         [ Links ]

Lamy, F., D. Hebbeln & G. Wefer. 1999. High resolution marine record of climatic change in mid-latitude Chile during the last 28 ka based on terrigenous sediment parameters. Quaternary Research 51: 83-93.         [ Links ]

Lecomte, F., W. S. Grant, J. J. Dodson, R. Rodriguez-Sanchez & B. W. Bowen. 2004. Living with uncertainty: genetics imprints of climate shifts in East Pacific anchovy (Engraulis mordax) and sardine (Sardinops sagax). Molecular Ecology 13: 2169-2182.         [ Links ]

Lee, H. J. & E. G. Boulding. 2009. Spatial and temporal population genetic structure of four northeastern Pacific littorinid gastropods: the effect of mode of larval development on variation at one mitochondrial and two nuclear DNA markers. Molecular Ecology 18: 2165-2184.         [ Links ]

Minin, V. N., E. W. Bloomquist & M. A. Suchard. 2008. Smooth Skyride through a Rough Skyline: Bayesian Coalescent-Based Inference of Population Dynamics. Molecular Biology and Evolution 25: 1459-1471.         [ Links ]

Nesis, K. N. 1970. The biology of the giant squid of Peru and Chile, Dosidicus gigas. Okeanology 10: 140-152.         [ Links ]

Nigmatullin, Ch. M., K. N. Nesis & A. I. Arkhipkin. 2001. A review of the biology of the jumbo squid Dosidicus gigas (Cephalopoda: Ommastrephidae). Fisheries Research 54: 9-19.         [ Links ]

O'Dor, R. K. 1998. Squid life-history strategies. FAO Fisheries Technical Paper 376: 233-254.         [ Links ]

Pecl, R. A., R. R. Warner & S. D. Gaines. 2009. Geographical patterns of genetic structure in marine species with contrasting life histories. Journal of Biogeography 36: 1881-1890.         [ Links ]

Posada, D. 2008. jModelTest: phylogenetic model averaging. Molecular Biology and Evolution 25: 1253-1256.         [ Links ]

Poulin, E., A. T. Palma, G. Leiva, D. NarvAez, R. Pacheco, S. A. Navarrete & J. C. Castilla. 2002. Avoiding offshore transport of competent larvae during upwelling events: the case of the gastropod Concholepas concholepas in Central Chile. Limnology and Oceanography 47: 1248-1255.         [ Links ]

Rambat, A. & A. J. Drummond. 2009. Tracer v 1.5. Available at http://tree.bio.ed.ac.uk/software/tracerLinks ]tree.bio.ed.ac.uk/software/tracer" target="_blank">

Reichow, D. & M. J. Smith. 2001. Microsatellites reveal high levels of gene flow among populations of the California squid Loligo opalescens. Molecular Ecology 10: 1101-1110.         [ Links ]

Rocha, F., A. Guerra & A. F. González. 2001. A review of reproductive strategies in cephalopods. Biological Review 76: 291-304.         [ Links ]

Sánchez, R., R. D. Sepúlveda, A. Brante & L. Cárdenas. 2011. Spatial pattern of genetic and morphological diversity in the direct developer Acanthina monodon (Gastropoda: Mollusca) Marine Ecology Progress Series 434: 121-131.         [ Links ]

Sandoval-Castellanos, E., M. Uribe-Alcocer & P. Díaz-Jaimes. 2007. Population genetic structure of jumbo squid (Dosidicus gigas) evaluated by RAPD analysis. Fisheries Research 83: 113-118.         [ Links ]

Sandoval-Castellanos, E., M. Uribe-Alcocer & P. Díaz-Jaimes. 2010. Population genetic structure of Humboldt squid (Dosidicus gigas) inferred by mitochondrial DNA analysis. Journal of Experimental Marine Biology and Ecology 385: 73-78.         [ Links ]

Semmens, J. M., G. T. Pecl, B. M. Gillanders, C. M. Waluda, E. k. Shea, D. Jouffre, T. Ichii, k. Zumholz, 0. N. Katugin, S. C. Leporati & P. W. Shaw. 2007. Approaches to resolving cephalopod movement and migration patterns. Review in Fish Biology and Fisheries 17: 401 -423.         [ Links ]

Shaw, P. W., G. J. Adcock, W. J. Burnett, G. R. Carvalho & A. I. Arkhipkin. 2004. Temporally distinct spawning cohorts and geographically distinct spawning aggregations within the Patagonian squid Loligo gahi do not represent genetically differentiated sub-populations. Marine Biology 144: 961-970.         [ Links ]

Shaw, P. W., G. J. Pierce & P. R. Boyle. 1999. Subtle population structuring within a highly vagile marine invertebrate, the Veined Squid Loligo forbesi, demonstrated with microsatellite DNA markers. Molecular Ecology 8: 407-417.         [ Links ]

Shaw, P. W., L. Hendrickson, L. J. McKeown, T. Stonier, M. J. Naud & W. H. H. Sauer. 2010. Discrete spawning aggregations of loliginid squid do not represent genetically distinct populations. Marine Ecology Progress Series 408: 117-127.         [ Links ]

Staaf D. J., R. I. Ruiz-Cooley, C. Elliger, Z. Lebaric, B. Campos, U. Markaida & W. F. Gilly. 2010. Ommastrephid squids Sthenoteuthis oualaniensis and Dosidicus gigas in the eastern Pacific show convergent biogeographic breaks but contrasting population structures. Marine Ecology Progress Series 418: 165-178.         [ Links ]

Staaf, D. J., S. Camarillo-Coop, H. D. Haddock, A. C. Nyack, J. Payne, C. A. Salinas-Zavala, B. A. Seibel, l. Trueblood, C. Widmer & W. F. Gilly. 2008. Natural egg mass deposition by the Humboldt squid (Dosidicus gigas) in the Gulf of California and characteristics of hatchlings and paralarvae. Journal of the Marine Biological Association of the United Kingdom 88: 759-770.         [ Links ]

Strathmann, R. R. 1990. Why life histories evolve differently in the sea. American Zoologist 30: 197-207.         [ Links ]

Tellier, F., A. P. Meynard, J. A. Correa, S. Faugeron & M. Valero. 2009. Phylogeographic analyses of the 30 °S south-east Pacific biogeographic transition zone establish the occurrence of a sharp genetic discontinuity in the kelp Lessonia nigrescens: Vicariance or parapatry?. Molecular Phylogenetics and Evolution 53: 679-693.         [ Links ]

Thiel, M., E. Macaya, E. Acuña, W. Arntz, H. Bastías, K. Brokordt, P. Camus, J. C. Castilla, L. R. Castro, M. Cortés, C. P. Dumont, R. Escribano, M. Fernández, D. Lancelloti, J. A. Gajardo, C. F. Gaymer, I. Gomez, A. E. González, H. E. González, P. A. Haye, J. E. Illanes, J. L. Iriarte, G. Luna-Jorquera, C. Luxoro, P. H. Manríquez, V. Marín, P. Muñoz, S. A. Navarrete, E. Pérez, E. Poulin, J. Sellanes, A. Sepúlveda, W. Stotz, F. Tala, A. Thomas, C. A. Vargas, J. A. Vásquez & A. Vega. 2007. The Humboldt Current System of northern and central Chile. Oceanographic processes, ecological interactions and socioeconomic feedback. Oceanography and Marine Biology: An Annual Review 45: 195-344.         [ Links ]

Villegas, P. 2001. Growth, life cycle and fishery biology of Loligo gahi (d'Orbigny 1835) off the Peruvian coast. Fisheries Research 54: 123-131.         [ Links ]

Yatsu, A., R. Tafur & C. Maravi. 1999. Embryos and rhynchoteuthion paralarvae of the jumbo flying squid Dosidicus gigas (Cephalopoda) obtained through artificial fertilization from Peruvian waters. Fisheries Science 65: 904-908.         [ Links ]