- Research article
- Open Access
Population genetic structure in Sabatieria (Nematoda) reveals intermediary gene flow and admixture between distant cold seeps from the Mediterranean Sea
© The Author(s). 2017
Received: 26 January 2017
Accepted: 21 June 2017
Published: 1 July 2017
There is a general lack of information on the dispersal and genetic structuring for populations of small-sized deep-water taxa, including free-living nematodes which inhabit and dominate the seafloor sediments. This is also true for unique and scattered deep-sea habitats such as cold seeps. Given the limited dispersal capacity of marine nematodes, genetic differentiation between such geographically isolated habitat patches is expected to be high. Against this background, we examined genetic variation in both mitochondrial (COI) and nuclear (18S and 28S ribosomal) DNA markers of 333 individuals of the genus Sabatieria, abundantly present in reduced cold-seep sediments. Samples originated from four Eastern Mediterranean cold seeps, separated by hundreds of kilometers, and one seep in the Southeast Atlantic.
Individuals from the Mediterranean and Atlantic were divided into two separate but closely-related species clades. Within the Eastern Mediterranean, all specimens belonged to a single species, but with a strong population genetic structure (ΦST = 0.149). The haplotype network of COI contained 19 haplotypes with the most abundant haplotype (52% of the specimens) shared between all four seeps. The number of private haplotypes was high (15), but the number of mutations between haplotypes was low (1–8). These results indicate intermediary gene flow among the Mediterranean Sabatieria populations with no evidence of long-term barriers to gene flow.
The presence of shared haplotypes and multiple admixture events indicate that Sabatieria populations from disjunct cold seeps are not completely isolated, with gene flow most likely facilitated through water current transportation of individuals and/or eggs. Genetic structure and molecular diversity indices are comparable to those of epiphytic shallow-water marine nematodes, while no evidence of sympatric cryptic species was found for the cold-seep Sabatieria.
The deep sea is one of the largest ecosystems on earth, covering two-thirds of the planet and containing a substantial proportion of the earth’s biodiversity. This ecosystem has long been considered a vast and continuous environment with stable biotic, physicochemical and hydrographical conditions  which enabled widespread distribution of several deep-sea invertebrate species . However, the deep-sea bottom is also characterized by the presence of fragmented and strongly differentiated ecosystems such as seamounts, trenches, hydrothermal vents and cold seeps (e.g., ). The deep sea supports a highly diverse and endemic benthic invertebrate fauna (e.g., [4, 5]). Additionally, molecular evidence suggests the presence of cryptic species complexes (genetically distinct but morphologically identical species; see [4, 6, 7]) of which some are found to be widespread [4, 7, 8] while others appear to be geographically restricted .
While our knowledge on the identity, diversity, and distribution of extant species continues to grow, insights on the evolutionary processes that are at the heart of this diversity in the deep sea are lagging behind. Genetic divergence in the marine environment may result from contemporary and historical processes related to the different oceanic basins , changes in seafloor topography , current regimes [11, 12], depth differences [13, 14], geographic distances  and oxygen levels . For instance, genetic divergence in several benthic species is greater between populations at different depths in the same region than between populations of different regions at the same depth (e.g., [14, 17–19]). Also, bathyal organisms generally exhibit much greater population structure than those from the deeper abyss [6, 14, 20].
Next to hydrothermal vents, cold seeps are among the most widely spread deep-sea reducing environments and are characterized by high levels of methane and sulphide, the latter being toxic to most metazoans. Associated fauna therefore need to be adapted to the complexity of the presence of biogenic structures, geochemical conditions and microbial processes. Active seeps have been reported all over the world, even in the Arctic and Antarctic polar regions [21, 22], and from shallow to hadal depths [22, 23]. Since their discovery in the mid-1980s, one of the most puzzling issues has been the influence of past and present connectivity on the nature of cold-seep species assemblages and their geographical distribution . Within the meiofaunal component of cold-seep biota, free-living nematodes are the most prevailing taxon .
Nematodes are among the most numerous multicellular taxa on earth, successfully adapted to nearly every ecosystem, but many species are biologically still poorly understood. Different species feed on materials as varied as algae, fungi, small animals, faecal matter and dead organisms . Most nematode species have separate male and female individuals with males using spicules to transfer sperm into the vulva of females. Most free-living nematodes are egg-laying organisms. Yet, a few species, such as Halomonhystera disjuncta, are known to be ovoviviparous [27, 28]. The eggs then hatch into larvae, which appear essentially identical to the adults, except for an underdeveloped reproductive system.
Compared to more common deep-sea environments, most cold seeps support highly productive ecosystems characterized by poor nematode species richness, high biomass and elevated dominance of a few genera able to withstand the high concentrations of toxic hydrogen sulphide (e.g., [27, 29–33]). Until now, the genetic structure of nematode species inhabiting different isolated reduced deep-sea systems remained largely unknown (but see ). In terms of connectivity and dispersal, nematodes lack a pelagic stage and are therefore considered poor dispersers due to their small size and low swimming ability . However, free-living nematodes and their eggs can become passively suspended and transported in the water column via external forces (e.g., erosion by hydrodynamic forces; ), even by very weak bottom currents . Moreover, some nematode species can actively emerge from the sediment and swim in the water column (e.g., ). Population genetic studies confirmed restricted nematode dispersal in shallow-water environments at large geographical scales (> 100 km) and revealed cryptic diversity in a wide range of marine nematodes [38–40]. Although some of these cryptic species showed restricted geographical distributions, others were widespread and several of them were distributed sympatrically [40, 41]. Widespread and even cosmopolitan species distributions have been reported in several nematode species [41–44].
Here, we investigate the genetic structure and connectivity in species of heterogeneously distributed cold seeps in the deep sea. We sampled the dominant Sabatieria species, S. mortenseni, in one cold seep in the Atlantic and four cold seeps in the Eastern Mediterranean Sea to investigate the genetic diversity patterns within and between reduced cold-seep environments.
The genus Sabatieria is one of the most common nematode genera in marine benthic habitats, especially in muddy and muddy sand sediments , and is one of the dominant deep-dwelling genera in muddy reduced sediments of shallow-water sites all over the world [46–48], including the shelf break and upper slope [25, 49, 50]. The genus can attain high proportions at oxygen minima but gradually disappears almost completely below 2000 m depth [49, 51]. Many of its species are considered eurytopic and tolerant to unstable, highly polluted environments [52, 53]. Currently, 95 Sabatieria species are considered valid  and are found in different localities around the world (e.g., [55–57]). Sabatieria species appear to be divided in five distinct subgroups according to morphological differences related to the type and distribution of precloacal supplements, characteristics of the gubernaculum and apophysis, the number of turns of the amphideal fovea, and the cephalic setae . The specimens investigated in this study belong to the pulchra group, which consists of six species, including S. mortenseni. Species of this group are distinguished by the disposition of the precloacal supplements, which are usually conspicuous and relatively few in numbers (5–9), and by the characteristic gubernaculum median pieces and short paired cervical setae . S. mortenseni has been found in reduced sediments of shallow-water sites in Brazil, USA, Antarctica [58–61] and the Strait of Magellan (Chile) at depths ranging between 8 and 550 m . It is also the dominant species at the REGAB pockmark in the Gulf of Guinea at a depth of more than 3000 m . Based on the particular isolated character of cold seeps and the strong genetic structure in shallow water nematodes, we expected to observe a strong genetic structure between populations of cold seeps located several hundreds of kilometers apart. In addition, based on the presence of substantial cryptic diversity in marine nematodes we also expected to find undiscovered cryptic diversity in these cold seeps.
Sample locations and characteristics
The four other cold seeps are located in the Eastern Mediterranean area (Fig. 1) at distances that vary from 131 to 405 km. The most northern cold seep, Amsterdam mud volcano (MV), is located on the southern flanks of the Anaximenes seamount (Anaximander Mountains, Southwestern Turkey; ) in the northern Levantine basin. This 2050 m deep MV expels a methane plume of more than 200 m high and harbors methane concentrations of up to 2000 nmol/kg . The other investigated seeps are located at the opposite side of the Eastern Mediterranean sea, at the Nile Deep Sea Fan (NDSF) in the southern Levantine basin. Three major zones of fluid seepage were investigated: the eastern province, the central province (also called the pockmark area) and the Menes caldera. The very active Amon MV, located in the eastern province at ~1118 m depth, is a large volcano of 2.7 km in diameter and 90 m in height . Investigations showed high methane and hydrocarbon emissions (1310 nmol/L) into the water column . In the central province, ship-borne multibeam acoustic images revealed numerous small pockmarks and/or mounds [70, 71]. For this study, the fauna of two major pockmark sites (2A and 2B) and an area close to 2A but located at the lower slope (between ∼ 1650 and 2200 m water depth) were sampled and pooled as PM in the rest of the analyses. Finally, within the Menes caldera, the Cheops MV is an active MV located at 3000 m water depth at the base of the Egyptian continental slope. From the volcanoes flows a mixture of brine, fluids and mud. The brines are expelled through numerous sub-circular vents (a few meters in diameter) which are covered with white sulphidic material produced by sulphate-reducing bacteria .
Sample collection and molecular processing
Overview of the samples used for molecular analysis
For the polymerase chain reaction (PCR), 1 μl of DNA template was used. In this study, 420 base pairs (bp) of the mitochondrial cytochrome c oxidase subunit 1 (COI) gene were amplified using the forward primer JB3 (5′-TTTTTTGGGCATCCTGAGGTTTAT-3′)  and the reverse primer JB5GED (5′-AGCACCTAAACTTAAAACATARTGRAARTG-3′) . Standard PCR amplifications were conducted in 25 μl volumes for 35 cycles, each consisting of 30 s denaturation at 94 °C, 30 s annealing at 50 °C, and 45 s extension at 72 °C, with an initial denaturation step of 5 min at 94 °C and a final extension step of 10 min at 72 °C. Four μl of each PCR product was loaded on a 1% agarose gel to check the strength and size of the amplified product. After electrophoresis, 420 PCR products, each corresponding to a single nematode specimen, were sent to MacroGen (The Netherlands) for bidirectional sequencing with the primers JB3-JB5GED.
After identifying the different COI haplotypes, DNA from each haplotype was used to amplify two nuclear DNA gene regions: the 18S region of the small ribosomal subunit and the D2D3 region of the conserved 28S large ribosomal subunit. 752 bp of the D2D3 region was amplified with the forward primer D2A (5′-ACAAGTACCGTGAGGGAAAGTTG-3′) and the reverse primer D3B (5′-TCCTCGGAAGGAACCAGCTACTA-3′) , while ±950 bp of the 18S region was acquired with the forward primer G18S4 (5′-GCTTGTCTCAAAGATTAAGCC-3′) and the reverse primer 4R (5′-GTATCTGATCGCCKTCGAWC-3′) . PCR conditions were similar to those for COI, except that 40 cycles were applied, and the annealing temperature was augmented to 54 °C. Next to this, an extension time of one minute was applied for the amplification of the 18S gene region. The PCR products of 36 nematodes for 18S and 34 nematodes for D2D3 were sent for sequencing.
Phylogenetic analysis and variation in COI and nuclear markers
COI sequences were checked and trimmed for further phylogenetic analysis in DNASTAR Lasergene Seqman Pro . Primer ends were removed, and sequences which were too short or showed too many uncertain bp were removed from the dataset. The remaining sequences were aligned using CLUSTALW v2 with default parameters as incorporated in MEGA 6.0  and translated using the invertebrate mitochondrial genetic code. A blastx search was performed against the non-redundant protein collection (nr) in GenBank to check the nematode origin of the sequences. Unique haplotypes were identified using a distance matrix based on uncorrected p-distances of untranslated sequences in MEGA. The number of conserved, variable and parsimony informative positions was determined. The best-fit substitution model was selected in jModelTest [80, 81] using the Bayesian Information Criterion (BIC). After that, phylogenetic relationships between haplotypes were constructed in MEGA using Neighbor-Joining (NJ, p-distance model) and Maximum Likelihood (ML, Hasegawa-Kishino-Yano model with gamma distribution as identified by jModelTest; ) tree-constructing algorithms, both with 1000 bootstrap replicates. The nematode species Praeacanthonchus punctatus, Ptycholaimellus carinatus and Odontophora setosa, all from the same subclassis (Chromadoria) as Sabatieria, were added to the dataset as outgroup (Derycke, unpublished data). The same strategy was followed for the two nuclear markers with the exception that a Tamura-Nei + G substitution model  was used in ML tree construction and that outgroups included both unpublished (Odontophora setosa and Praeacanthonchus punctatus) as well as published sequences extracted from GenBank (Ptycholaimellus sp.: accession JN968285-18S; Praeacanthonchus punctatus: accession AF210416-D2D3 and Odontophora sp.: accession DQ077756-D2D3). For D2D3, there were no Ptycholaimellus sequences available. The unique haplotypes found in this study have been submitted to GenBank and are available under accession numbers LT703318-LT703405. Representative DNA samples were deposited in the MoMentuM database of CeMoFe (Centre for Molecular Phylogeny and Evolution), UGent.
Population genetic structure in COI
Analysis of Molecular Variance (AMOVA) was performed in ARLEQUIN version 188.8.131.52  and used to analyze the population genetic structure of Sabatieria COI sequence variation across the different seeps. Population pairwise ΦST-statistics were calculated (10,000 permutations, 0.05 significance level) to determine which seeps were significantly differentiated from each other. Because the HKY model given by jModelTest is not available in ARLEQUIN, the more inclusive Tamura-Nei (TrN) model  with gamma distribution was used to calculate ΦST and other relevant statistics. Significance levels of the obtained p-values were corrected according to the sequential Bonferroni method . Next to this, standard measures of genetic variation within populations, such as nucleotide diversity (π)  and haplotype diversity (h) [86, 87], and their standard deviation were calculated per cold seep. Tajima’s D  and Fu’s Fs  neutrality tests were performed to infer whether sequence evolution was neutral and whether geographical groups showed signs of deviations from neutrality. Significantly negative values for Tajima’s D and Fu’s Fs reflect an excess of rare polymorphisms in a population, which indicates either positive selection or an increase in population size . These tests were performed both on the haplotype distribution of the separate seeps as well as on the whole dataset as one, with the number of simulated samples set at 1000.
To test whether genetic divergence between populations increased with geographic distance (i.e. isolation-by-distance IBD; ), geographic and genetic distances were compared using a Mantel test (1000 permutations; ). Both untransformed and log-transformed distances were used to test the IBD model. The geographic distance between populations was measured as the shortest continuous water-surface distance (Fig. 1). To explore the intraspecific relationships between observed haplotypes, a TCS network was constructed with the PopART software (http://popart.otago.ac.nz).
Phylogenetic analysis of COI
Phylogenetic analysis of the nuclear markers
Similarly, since 5% COI sequence divergence is commonly observed between different nematode species , and because of the congruence between mitochondrial and nuclear markers, the REG clade was considered as an independently evolving lineage, and was omitted from the dataset to investigate population genetic structure within the Eastern Mediterranean clade.
Population genetic structure of COI
Overview of the frequency of the different haplotypes found in Eastern Mediterranean cold seeps
0.598 ± 0.049
0.011 ± 0.006
0.576 ± 0.045
0.002 ± 0.002
0.616 ± 0.052
0.010 ± 0.006
0.773 ± 0.022
0.012 ± 0.007
The TCS network further indicated the dominance of haplotype A, which was found in all four seeps (Fig. 4). Two groups of haplotypes differing in only one mutation with the closest related haplotype could be identified, and both groups had haplotypes in all four cold seeps (group 1 and group 2 in Fig. 4). Group 1 contained 14 haplotypes, of which 5 were only found in Amsterdam MV, 4 only in Cheops and 1 only in Amon. Group 2 contained 5 haplotypes, with Cheops, PM and Amon each having one private haplotype. In addition to these two groups of haplotypes, haplotypes E and N showed 6 and 8 mutational differences with the closest (missing) haplotype.
Results of the AMOVA analysis for the COI marker
Source of variation
Sum of squares
% of variation
Φ ST = 0.149
AMOVA pairwise Φst-values for COI
Our results show that Sabatieria mortenseni is present in all samples in cold seeps from the East Mediterranean. The continuous character and the presence of currents as a large-scale transportation mechanism of organisms are likely to facilitate dispersal and gene flow in the marine environment and may result in wide species distributions (e.g., deep-sea foraminifera in Arctic and Antarctic sediments [93, 94]; see also ). Also for nematodes, widespread distributions have been reported. For example, the nematode Litoditis marina maintains trans-Atlantic populations, and specimens have been found floating in macroalgae rafts in the North Sea . Bik and co-authors  found evidence for cosmopolitan marine Oncholaimid species with identical gene sequences (18S, 28S and COI) at trans-Atlantic sample sites. Bhadury and co-workers  revealed that the majority of the morphologically defined Terschellingia longicaudata specimens shared a single 18S rRNA sequence and apparently belonged to a single species distributed from the British Isles to Malaysia in a wide range of marine habitats and ecological ranges. The high similarity of the T. longicaudata from Amon MV in this study with the shallow-water specimens described in  (98% similarity; Accession No.: AM941225, AM941226 and AM234716) is indicative of a wide distribution for this species. Nematodes can become passively suspended and transported in the water column by currents [35, 36]. This might not only apply to the organism itself, but also to the eggs, although this latter possibility has not been investigated yet. Next to passive transport, some nematode species can actively swim in the water column, with widespread species distributions as a result [41–43].
For Sabatieria, community analysis of the cold-seep environments analyzed in this study revealed that the genus (with S. mortenseni) was abundantly present in all reduced sediments sampled (relative abundances 10.6–88.6%; personal observation). The species was also present in the surrounding oxidized sediments, albeit in much lower abundances (0.0–6.4%; personal observation), indicating its preference for hypoxic or anoxic conditions. These data suggest a widespread distribution in the area under study. However, the extent of genetic similarity between Sabatieria mortenseni from the non-reduced environment and the cold seeps is not clear, since specimens from the non-reduced environment were preserved in formalin.
Genetic structure of Sabatieria mortenseni shows intermediate gene flow between cold seeps
The strong genetic structure revealed by AMOVA and the high pairwise Φst values suggest that suspension and transport by currents are not enough to establish extensive gene flow between the Sabatieria populations of the different cold seeps. Instead, several haplotypes are shared between seeps, the number of mutations between haplotypes is low and private haplotypes are present in each cold seep, all indicating that intermediate gene flow is occurring without long-term barriers to dispersal between cold seeps (cf. pattern V in ). The presence of S. mortenseni in the surrounding environment may indicate that the distribution of this species in the deep sea is much more homogeneous than anticipated. Evidently, widely distributed species that are not restricted to certain habitat types may have a larger capacity to disperse than narrowly distributed, specialized species. Even though the abundances of S. mortenseni in the surrounding sediment are low, such small local units may form part of a source-sink system facilitating gene flow between distant populations.
The East Mediterranean is one of two sub-basins of the Mediterranean Sea and hosts a complex array of current systems, including deep-water formation in the Adriatic Sea (Eastern Mediterranean Deep Water EMDW; ), cyclonic and anticyclonic gyres, and small energetic eddies [97, 98]. Main deep-water currents flow from west to east, along the North African coastline in the southern Ionian and Levantine basin (passing the Nile Deep Sea Fan, i.e. location of Cheops, PM and Amon MV) towards the northern Levantine basin (i.e. location of Amsterdam MV) . Therefore, physical connections between the different cold seep environments of this study are theoretically possible and can explain the presence of several shared haplotypes between the cold seeps.
Even in the presence of currents able to mediate long-distance dispersal of organisms and eggs in relatively homogeneous habitats, dispersal success tends to decrease with increasing distance, resulting in larger genetic dissimilarity between populations that are more distant from each other (i.e. stepping-stone model; ). Given the scattered distribution of deep-sea cold seeps and hydrothermal vents, such distance effects have frequently been invoked to explain genetic divergence in chemosynthetic invertebrate species with pelagic larvae [100–103]. For the passively dispersing nematodes which lack such a larval stage, the isolation-by-distance effect might be even more pronounced. However, no significant isolation-by-distance for the Sabatieria populations of the East Mediterranean cold seeps was observed (see Mantel test results). This was also evident from the COI phylogenetic tree where populations did not cluster according to their geographic location (Fig. 2). Instead, genetic distances between closely located seeps (e.g., Amon MV and PM) were sometimes larger than between seeps further apart (e.g., Amsterdam MV and PM; Table 4). Such a pattern where genetic structuring does not correlate with geographic distance (i.e. chaotic genetic patchiness) is quite common in the marine environment for organisms with larval development [104–108], but also for nematodes , and can be explained by the multidirectional movement of organisms due to turbulent and nonlinear water currents, as well as by other ecological factors (e.g., variable local natural selection on settling larvae; ).
Few mutations between haplotypes point to the absence of long-term geographic barriers between cold seeps
Besides contemporary physical drivers for genetic population differentiation (currents, distance), historical events often leave their mark on current species distributions. On an evolutionary timescale, the Mediterranean deep-sea environment and its fauna are relatively young compared to that of other oceans. Our results show a significant population genetic structuring between the cold seeps within the Eastern Mediterranean sea which may reflect past isolation and (re-) colonization events. The haplotype network for COI consisted of a few central widespread and abundant haplotypes (A and B) surrounded by multiple private haplotypes (Fig. 4, group 1 and 2). Such a pattern is characteristic for population expansion, but statistical confirmation of such an event was limited: Tajima’s D was only significantly negative for Cheops MV. Instead, the two haplotype groups were separated by 2 or 3 mutations suggesting recent admixture between previously isolated populations (see also [95, 110]). The higher number of haplotypes in group 1 and the high abundance of the central haplotype A in all cold seeps indicate that this cluster of haplotypes has a longer evolutionary history in the four cold seeps than haplotypes from group 2, which was much less abundant and diverse than group 1 (Fig. 4). The high number of mutations in haplotypes E and N, their very low abundance and their restriction to the Amon cold seep (and PM for E) in the south suggest that individuals harboring these haplotypes most likely originated in locations outside our sampling area, in the southern part of the Mediterranean. In this scenario, the Amon cold seep has been colonized by four independent events (one event containing haplotypes from group 1, one containing haplotypes from group 2, one containing haplotype N and one containing haplotype E), whereas the other cold seeps were colonized by two (Cheops and Amsterdam MV) or three (PM) separate events. Overall, haplotype and nucleotide diversity for Sabatieria populations were similar to values reported for shallow-water nematodes (e.g., [38, 111]) and generally low (especially nucleotide diversity).
Finally, the genetic structure present in S. mortenseni may result from a strong adaptation to the particular local conditions at the different cold seep habitats. Such a scenario of differentiation by adaptation seems plausible considering the environmental heterogeneity typically found in chemosynthetic habitats . In this case, local selective pressures could prevent the successful exchange of individuals (e.g., ), leading to isolation of the gene pools of the different populations. However, based on the data at hand it is difficult to assess whether such a mechanism can be invoked in the case of Sabatieria in the East Mediterranean.
Our results show the presence of cryptic species within Sabatieria mortenseni from seeps located in different ocean basins: genetic evidence pointed towards two independently evolving lineages, one in the Eastern Mediterranean and one in the Southeast Atlantic region. Yet, no differences in diagnostic morphological features were observed and morphometric characters overlapped with those of S. mortenseni reported in [45, 74] (Additional file 1: Table S1). In general, cryptic species are common in the marine environment (e.g., ). Numerous cryptic species exist among the vesicomyid clams [115, 116] and lepetodrilid limpets  that dominate vents and seeps worldwide. Cryptic species have also frequently been detected in free-living marine nematodes from intertidal environments with sympatric distributions [38, 39, 118]. In contrast, populations of the marine nematode Paracanthonchus gynodiporata living on macroalgae were genetically homogeneous across more than 1000 km Brazilian coastline but showed substantial phenotypic plasticity . Cryptic species have also been reported in deep-sea nematodes: Halomonhystera disjuncta from the Håkon Mosby mud volcano is genetically distinct from the intertidal Halomonhystera disjuncta  and two cryptic species have recently been discovered in Sabatieria from the continental shelf in Antarctica . The current study shows that cryptic diversity is also present in nematodes dominating cold seeps in the deep-sea floor, but apparently only at a larger geographic scale. Although morphometric characters overlapped with S. mortenseni from [45, 74], specimens from the REGAB cold seep have a larger body size than S. mortenseni reported from the literature (Additional file 1: Table S1). Yet, the body size of the REGAB specimens overlaps with that of specimens from Amon and Amsterdam. We measured a large number of males (18–28 per cold seep in the Mediterranean Sea) and find a much larger morphological plasticity in S. mortenseni from the cold seeps than observed in S. mortenseni from the subtidal area near Rio de Janeiro . Unfortunately, no sequence data are available from specimens from Rio de Janeiro to verify the extent of genetic differentiation between S. mortenseni from both areas.
Surprisingly, there was no evidence for cryptic speciation within the East Mediterranean despite the fact that geographical distances were much larger than those in previous studies in marine nematodes . Because of the young age of the Mediterranean Sea (5.3–2 Myr), speciation of the Sabatieria populations may not have been completed yet. As a reference, cryptic species found in the shallow-water nematode Litoditis marina are at least 6.5 Myr old . Nevertheless, the high variability of local cold-seep conditions (e.g., heterogeneity in fluid composition of sulphide and methane; see Methods section) and low exchange between cold seeps could induce perfect conditions for ecological speciation. We therefore expected cryptic speciation in disjunct cold-seep areas. However, Sabatieria species are known to withstand fluctuations in environmental chemistry as they regularly are the dominant genus in various reduced ecosystems (e.g., [27, 30–33]). The lack of cryptic species in these Mediterranean cold seeps can thus be due to the fact that this species, after spreading in the Mediterranean area, still shows sufficient gene flow to homogenize gene pools.
The populations of the marine nematode Sabatieria mortenseni inhabiting cold seeps from the bathyal East Mediterranean Sea and Atlantic Ocean are genetically structured. The presence of shared haplotypes and the low number of mutations between haplotypes indicate that barriers to dispersal between these cold seep populations are relatively recent. The low abundances of S. mortenseni in the surrounding sediment together with water currents in the area may form part of a source-sink system facilitating gene flow between distant populations. Our results further show the presence of cryptic species within S. mortenseni from seeps located in different ocean basins: genetic evidence pointed towards two independently evolving lineages, one in the Eastern Mediterranean and one in the Southeast Atlantic region but no differences in diagnostic morphological features were observed. Our results expand our knowledge on genetic diversity in marine nematodes and confirm that a single nematode species can be widely distributed despite the lack of pelagic larval stages.
The authors wish to thank the captain and crew of the RV Pourqoui Pas?, RV Merian and RV Meteor, as well as the scientific crew onboard all expeditions for their help and support in sample acquisition. Special thanks go to the pilots of the ROV Quest and ROV Victor 6000 for their technical support during sampling. We are grateful to Annelien Rigaux for the molecular support in the CeMoFE lab, Ghent University. We thank two anonymous reviewers for their critical and constructive remarks.
This work was funded by the BOF-project No. 01 J14909 and by the project ‘Hotspot Ecosystem Research and Man’s Impact on European Seas’ (HERMIONE), funded by the European Commission under the Framework Program VII (Contract No. 226354).
Availability of data and materials
Sequences of the different genetic markers have been deposited to the European Nucleotide Archive (ENA: http://www.ebi.ac.uk/ena) and GenBank and can be found under accession numbers LT703318-LT703405. All other data are included in this published article.
ADG, AV and SD conceived the ideas and concept for this study; ADG performed the laboratory analyses; ADG, FH, AV and SD analyzed the data; ADG, FH, AV and SD contributed to the writing. All authors read and approved the final version of the manuscript.
Ethics approval and consent to participate
The manuscript does not report on or involve the use of any vertebrate or human data or tissue, therefore this section is not applicable.
Consent for publication
The authors declare that they have no competing interests.
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