- Research article
- Open Access
Unprecedented within-species chromosome number cline in the Wood White butterfly Leptidea sinapis and its significance for karyotype evolution and speciation
© Lukhtanov et al; licensee BioMed Central Ltd. 2011
- Received: 7 December 2010
- Accepted: 20 April 2011
- Published: 20 April 2011
Species generally have a fixed number of chromosomes in the cell nuclei while between-species differences are common and often pronounced. These differences could have evolved through multiple speciation events, each involving the fixation of a single chromosomal rearrangement. Alternatively, marked changes in the karyotype may be the consequence of within-species accumulation of multiple chromosomal fissions/fusions, resulting in highly polymorphic systems with the subsequent extinction of intermediate karyomorphs. Although this mechanism of chromosome number evolution is possible in theory, it has not been well documented.
We present the discovery of exceptional intraspecific variability in the karyotype of the widespread Eurasian butterfly Leptidea sinapis. We show that within this species the diploid chromosome number gradually decreases from 2n = 106 in Spain to 2n = 56 in eastern Kazakhstan, resulting in a 6000 km-wide cline that originated recently (8,500 to 31,000 years ago). Remarkably, intrapopulational chromosome number polymorphism exists, the chromosome number range overlaps between some populations separated by hundreds of kilometers, and chromosomal heterozygotes are abundant. We demonstrate that this karyotypic variability is intraspecific because in L. sinapis a broad geographical distribution is coupled with a homogenous morphological and genetic structure.
The discovered system represents the first clearly documented case of explosive chromosome number evolution through intraspecific and intrapopulation accumulation of multiple chromosomal changes. Leptidea sinapis may be used as a model system for studying speciation by means of chromosomally-based suppressed recombination mechanisms, as well as clinal speciation, a process that is theoretically possible but difficult to document. The discovered cline seems to represent a narrow time-window of the very first steps of species formation linked to multiple chromosomal changes that have occurred explosively. This case offers a rare opportunity to study this process before drift, dispersal, selection, extinction and speciation erase the traces of microevolutionary events and just leave the final picture of a pronounced interspecific chromosomal difference.
- Chromosome Number
- Chromosomal Rearrangement
- Male Genitalia
- Chromosomal Race
- Karyotype Variability
Despite the fundamental role of chromosomal change in eukaryotic evolution, the mechanisms related to this process are still poorly known. Main karyotypic features of organisms, such as the number of chromosomes, are usually stable within species [1, 2]. This stability is in good correspondence with the fact that new chromosomal rearrangements usually originate as heterozygotes and are often - although not always - associated with heterozygote disadvantage (=negative heterosis; =underdominance). Therefore, their spread to fixation within a large population has low probability . At the same time, differences in karyotype characters between species, including diploid chromosome number (2n), are extremely common. Numerous cases of extraordinary differences in chromosome number, especially in plants, are due to polyploidy . Even when excluding polyploidy, interspecific variation remains very frequent, and many closely related species often have substantially different chromosome numbers. In metazoan animals, the greatest range of within-genus karyotype variation not related to polyploidy is found in Agrodiaetus blue butterflies, where diploid chromosome number ranges between species from 2n = 20 to 2n = 268 in spite of morphological similarity and very recent time of species divergence . Interestingly, Agrodiaetus also tends to demonstrate the greatest karyotype difference between very closely related species, e.g. sister species A. biruni and A. posthumus have 2n = 20 and 2n = 180 respectively with no intermediates between them.
In vertebrates, the range of chromosome number variation between closely related species is smaller, yet still impressive. For example, the analysis of 11 species of the catfish genus Corydoras revealed that they have karyotypes ranging from 2n = 44 to 2n = 102 . The tuco-tucos, South American rodents of the genus Ctenomys, show chromosomal variation with diploid numbers varying from 2n = 10 to 2n = 70 among the 60 species described . The deer genus Muntiacus includes species with different karyotypes, ranging from 2n = 6 to 2n = 46 . In plants, the greatest range of within-genus karyotype variation not related to polyploidy is found in Carex, where diploid chromosome number ranges from 2n = 12 to 2n = 132 .
The discrepancy between intra- and interspecific variability in chromosome numbers poses a serious evolutionary problem. How can numerous species with extremely diverse karyotypes evolve in a relatively short period of time, if major chromosomal rearrangements changing the number of chromosomes are mostly underdominant and, consequently, intraspecific variations are rare and their range is limited?
One possible explanation is that extremely different chromosome numbers evolve gradually through multiple speciation/raciation events, each involving the fixation of a single (or few) chromosomal rearrangement(s), and followed by the subsequent extinction of species or races with intermediate karyotypes. This step-by-step mechanism of karyotype evolution seems to be common in nature, and its initial phase can be observed in some chromosomally polymorphic organisms such as the mouse Mus musculus domesticus and the shrew Sorex araneus [9–13]. It has been recently demonstrated that the reduction in fertility of hybrids between the house mouse races separated by fixed monobrachial differences is not so pronounced as previously supposed . Nevertheless, this study generally supported the chromosomally-based monobrachial speciation model as a process that accelerates the acquisition of reproductive isolation in the house mouse . In the step-by-step process, the transitional forms are expected to demonstrate a chromosomal fusion/fission polymorphism and, accordingly, numerous examples are known where single or few chromosomal fusions exist in the polymorphic phase, e.g., Robertsonian fusions in Drosophila americana , melanopline grasshoppers  and rodents of the genus Ctenomys [6, 17].
An alternative hypothesis is that dramatic changes in chromosome number appear as a consequence of a within-species accumulation of numerous chromosomal rearrangements, resulting in highly polymorphic systems with the subsequent extinction of intermediate karyomorphs. A necessary precondition for this mechanism is that major chromosomal rearrangements changing the number of chromosomes are not strongly underdominant. This seems to hold true for different groups such as butterflies, flies, grasshoppers, spiders, fishes and mammals [6, 15–25].
While the within-species mechanism of explosive chromosome number evolution is possible in theory, it has been less well documented compared to the evolution through multiple speciation/raciation events. In practice, it is difficult to record such an extensive within-species accumulation for two reasons. First, the transition from one chromosomal form to another may be very fast compared to the species lifespan. The only exception is the chromosomal evolution operated by balancing selection. However, this mechanism seems to be rare, except in the case of inversions [[26, 27], but see ]. Second, even if polymorphism for multiple chromosomal rearrangements is found, it may be difficult to distinguish between a polymorphic system primarily evolved within a species and a polymorphism resulting from hybridization between different, chromosomally diverged species. For example, in the hybridization zones between low and high chromosome number species of the rodent genus Ellobius, there is a so-called "chromosomal fan" including all chromosome numbers from 2n = 31 to 2n = 54 . In fact, this case does not represent evidence for within-species accumulation of chromosomal changes, but simply represents the outcome of secondary parapatry by previously isolated chromosomal races.
Furthermore, the clinal geographical distribution of chromosomal races observed in some organisms [1, 2], apparently compatible with gradual within-species accumulation of chromosomal changes, may be better explained by the multiple speciation mechanism. For example, in butterflies of the Erebia tyndarus complex there are several geographically isolate chromosomal races (chromosome numbers ranging from 2n = 16 to 2n = 102) , and in fossorial mole rats of the Spalax ehrenbergi complex four linearly distributed chromosomal races exist (from 2n = 52 to 2n = 60) . In these cases, intrapopulation chromosomal polymorphism is absent and differences between neighbouring chromosomal races, although minor, are fixed. Detailed molecular and morphological studies provide evidence for non-conspecificity of the E. tyndarus and S. ehrenbergi forms, and several distinct species were identified and formally described [32, 33].
In this study we describe a chromosomal cline in the Wood White butterfly, Leptidea sinapis (Insecta, Lepidoptera, Pieridae) that provides strong evidence for rapid and extensive within-species chromosome number evolution through accumulation of multiple chromosomal changes. This cline is exceptional in the geographic area that it covers (6000 km) and in its range of within-species chromosome number variation (2n = 56-106). Excluding polyploidy, this is the widest known within-species chromosome number range for any animal or plant, and it is comparable with the highest known level of within-genus karyotype variability.
We analyzed the karyotype, mitochondrial and nuclear genetic markers, and the morphology of the Wood White butterfly L. sinapis. This is a common species widely distributed from Portugal and Spain in the west to Siberia in the east . From this territory different chromosome numbers have been reported in literature ranging from n = 28 to n = 41 . However, these results are impossible to interpret in practice because of the discovery in 1993 of a cryptic sympatric species (L. reali) in Europe and Asia . As all karyotype data for L. sinapis were published before this date, it is unclear whether reported chromosome numbers reflect inter- or intraspecific variability.
In certain species, variation in chromosome number may be caused by the presence of so-called B-chromosomes (=additional chromosomes, =supernumerary chromosomes) . B-chromosomes consist mainly of repetitive DNA and can be usually found in low numbers (one to five) in a percentage of the individuals of a given population. Although they are dispensable, they can sometimes accumulate through processes of mitotic or meiotic drive . B-chromosomes can be distinguished from normal A-chromosomes because they are usually smaller and can be seen as additional chromosomes present in only some of the individuals in a population. The best diagnostic feature is their identity at meiosis, where they may be found as univalents, or in various pairing configurations (bivalents or multivalents), but never pairing with A-chromosomes. Thus, meiotic analysis is critical to distinguish between B-chromosomes and normal A-chromosomes [37, 38]. Although we cannot totally exclude that B-chromosomes can be found in L. sinapis, especially taking into account that they are known in other genera of the family Pieridae , there is good evidence that B-chromosomes are not a valid explanation for the chromosome number cline found in L. sinapis. This is due to the fact that in the Spanish population, where the number of chromosomes is maximal (and correspondingly where the highest number of B-chromosomes would be expected), they seem to be completely absent: the chromosome number is stable within as well as between individuals, and no univalents have been observed during meiosis. Moreover, no univalents have been observed during meiosis in any of the other populations studied. Additionally, the following clear pattern was observed: the higher the chromosome numbers in a population, the smaller the size of chromosomes, and vice versa (Figure 1; Additional file 1, Figure S1). This regularity indicates that chromosomal fusions/fissions (but not B-chromosomes) were the main mechanism of karyotype evolution.
Leptidea sinapis can be distinguished from its closest relative L. reali by the length of the phallus, saccus and vinculum (in male genitalia) or of the ductus bursae (in female genitalia) [36, 40] as well as by molecular markers [41, 42]. Therefore, to exclude the possibility of cryptic species involved in the formation of the extraordinarily high chromosomal variability and to demonstrate the conspecificity of the populations studied, we performed morphological and molecular analysis of each studied individual.
The measured variables of the male genitalia showed no significant difference or apparent trend between chromosomal races according to one-way ANOVA (Figure 2a, b) and to discriminant analysis (DA) (Figure 2c). 100% of the L. reali were correctly classified to species with the DA, but within L. sinapis, between 0 (France and Italy) and 62.5% (Kazakhstan) of specimens were correctly assigned to region (Additional file 1, Table S1).
It is known that in some systems, variation in chromosome number may be a result of ongoing hybridization between different, chromosomally diverged species . Therefore, the chromosome number variability discovered may be a consequence of hybridization between L. sinapis and its sibling species L. reali. This explanation may seem possible given that the presence of putative F1 hybrids between L. sinapis and L. reali was suggested . However, these results  were based on some apparent mismatches between DNA-based identifications (which were congruent for RAPD markers and COI) and morphometry of the male genitalia. The classification of the sequenced specimens based on their genitalia was made by employing a bivariate plot, which took into account only the lengths of the phallus and saccus. A recent comprehensive morphometrical study on L. sinapis and L. reali from Central Italy  highlighted the limitation of the "phallus and saccus" approach, which can lead to ambiguous classifications. The same study showed that this limitation can be corrected when using additional genitalic characters (especially the vinculum width) and performing multivariate analyses. Therefore, the report of possible hybrids between L. reali and L. sinapis requires confirmation since it may actually represent an artifact caused by the interpretation of insufficient morphological traits. Moreover, in case of interspecific hybridization we can expect that some individuals would be heterozygous for species-specific nuclear molecular markers and specimens with intermediate morphology of genitalia should be found. None of the specimens studied in our work has shown these characteristics (see above). Due to genitalic morphological constraints between the two species, introgression is likely to be unidirectional with female L. sinapis potentially inseminated by male L. reali [36, 44]. Finally, several studies dealing with the mating behaviour of L. sinapis and L. reali reported that females of both species exclusively mated with conspecific males, suggesting the presence of strong precopulatory barriers [36, 45, 46]. Therefore, we can conclude that interspecific hybridization is an unlikely explanation for the origin of the discovered chromosomal cline.
Several other cases of broad intraspecific chromosomal polymorphism have been described in animals [6, 18–21, 23, 24, 48–56] and plants [8, 57]. However, all these cases differ from the cline found in L. sinapis by the essentially smaller range of karyotype variability and by the possible existence of two or more cryptic species involved in the formation of the polymorphic chromosomal system. In order to demonstrate the intraspecific nature of karyotype variability, the following three criteria should be met simultaneously: 1) segregating chromosomal polymorphism within a population should be demonstrated, 2) molecular markers should not suggest the presence of potential cryptic species, and 3) species-diagnostic morphological differences should be lacking. To our knowledge, only studies on the common shrew and the house mouse have met all these criteria, but chromosomal races within these mammals have essentially smaller differences in chromosome number and apparently evolved through a step-by-step accumulation of single chromosomal rearrangements [9–13] rather than through wide intraspecific and intrapopulation chromosome number polymorphism.
Given that (a) chromosomal races of L. sinapis belong to the same species, (b) intrapopulation chromosome number polymorphism exists, (c) the chromosome number range overlaps between some populations separated by hundreds of kilometers, (d) the species has broad ecological preferences and is widely distributed, (e) the species has a rather homogenous genetic structure, and (f) chromosomal heterozygotes are abundant, this represents a clearly documented case of rapid and massive within-species accumulation of multiple chromosomal rearrangements affecting the number of chromosomes.
The chromosomal rearrangements discovered in our investigation display segregating polymorphism that seems not to strongly affect reproductive fitness within the populations studied. However, these rearrangements are not necessarily irrelevant to the process of formation of reproductive isolation (i.e. to speciation). It is well known that Robertsonian rearrangements (i.e. nonreciprocal translocations involving fission and fusion at or near a centromere), have the potential to limit gene flow and drive speciation [58, 59]. The Wood White butterfly, like other Lepidoptera and some other insects, has holokinetic chromosomes in which the centromere is not localized and centromeric activity is distributed along the length of the chromosome [35, 60–62]. It has been recently demonstrated that fusions/fissions of holokinetic chromosomes restrict gene flow too, and that this effect is cumulative (i.e. increases proportionally with the level of chromosomal differences) . In the case of L. sinapis all evidence suggests that neighbour populations with relatively low differences in chromosome number are reproductively compatible. We cannot exclude that geographically distant and chromosomally divergent populations would display reduced fertility if crossed, although they are connected by a chain of compatible populations that should allow gene flow. Therefore, the discovered system opens the possibility to study clinal speciation, a process that is theoretically possible but difficult to document [, pages 113-123].
Chromosomal rearrangements are known to limit introgression in parapatry or sympatry with regard to isolation genes, thus facilitating the maintenance of incipient species boundaries [64, 65], and serving as regions where isolation genes can accumulate [15, 27, 66–68]. The preservation and/or accumulation of isolation genes protected by chromosomal rearrangements could represent a prerequisite for speciation by means of suppressed-recombination mechanisms [15, 27, 64–68].
In conclusion, the L. sinapis chromosomal cline seems to represent a narrow time-window of the very first steps of species formation linked to multiple chromosomal changes that have occurred explosively. This case offers a rare opportunity to study this process before drift, dispersal, selection, extinction and speciation erase the traces of microevolutionary events and just leave the final picture of a pronounced interspecific chromosomal difference.
Note: During the publication process of this paper it has been shown that the Romanian specimens of L. reali used here as outgroup actually belong to a new cryptic species named Leptidea juvernica .
Fresh male Leptidea specimens (Additional file 1, Table S2) were collected with the insect net and were kept alive in glassine envelopes. In the laboratory, butterflies were killed by pressing the thorax and testes were removed from the abdomen and immediately placed into a 0.5 ml vial with freshly prepared Carnoy fixative (ethanol and glacial acetic acid, 3:1). Bodies were placed into a 2 ml plastic vial with 100% ethanol for DNA analysis and wings were stored in glassine envelopes. Each sample has been assigned a unique sample ID. All the samples are stored in Roger Vila's DNA and Tissues Collection in Barcelona, Spain.
Genitalia preparation and morphometric analyses
Male genitalia were prepared according to the following protocol: maceration for 15 minutes at 95°C in 10% potassium hydroxide, dissection and cleaning under a stereomicroscope and storage in tubes with glycerin. Genitalia were photographed laterally (Figure 2c), without being pressed, in a thin layer of distilled water under a Carl Zeiss Stemi 2000-C stereomicroscope equipped with a DeltaPix Invenio 3S digital camera. Measurements were performed based on the digital photographs by using AxioVision software. A total of 73 specimens of L. sinapis were included in the morphometrical analyses (Additional file 1, Table S3). These included 35 of the karyotyped samples, and 38 individuals collected in the same locality and moment for which the cytogenetic studies did not produce results. In addition, five specimens of the sibling L. reali were added as outgroup. Three elements of the male genitalia were measured: phallus, saccus and vinculum width. These are the best diagnostic characters to separate L. sinapis from L. reali . The vinculum width was used to normalize the size of the specimen.
StatView 5.0.1 (SAS Institute Inc., 1992-1998) was used to perform one-way ANOVA in order to test for differences in the length of the phallus and saccus, each normalized by the width of the vinculum, between regions for L. sinapis, and between L. sinapis and L. reali. All variables were normally distributed (Kolmogorov-Smirnov Test, p > 0.05). The software SPSS 14.0 was used to perform a discriminant analysis by employing the stepwise method. The Box's M test was used to evaluate the homogeneity of covariance assumption (p > 0.05). The variables were selected with the Wilks' lambda statistic, which measures how each function separates cases into groups. In order to test the obtained classification a cross validation was carried out.
Gonads were stored in Carnoy fixative (ethanol and glacial acetic acid, 3:1) for 2-6 months at 4ï‚°C and then stained with 2% acetic orcein for 30 days at 20ï‚°C as it was previously described [70, 71].
Chromosomes of butterflies (Lepidoptera) are small, numerous and uniform in both shape and size . They lack a distinct primary constriction (the centromere) and are regarded as holokinetic with kinetochores extended over a large portion of the chromosome surface . The uniformity of lepidopteran chromosomes, the absence of morphological markers such as the centromeres and the lack of convenient differential banding techniques  make difficult the identification of individual chromosomes by standard cytogenetic methods. Although new approaches to individual identification of the Lepidoptera chromosomes based on the fluorescent in situ hybridization (FISH) technique have been recently elaborated [72–74], they are applicable only for studying species bred in the laboratory. For this reason, the chromosome number remains the most commonly used karyotypic character in Lepidoptera cytogenetics and karyosystematics. In our study we counted the diploid chromosome numbers (2n) in mitotic spermatogonial cells and the haploid chromosome numbers (n) in metaphase II of male meiosis. We also counted the number of chromosomal elements (n) (bivalents + multivalents) in metaphase I of male meiosis. In the last case, the number of chromosomal elements was equal to the haploid number (n) if all the elements were represented by bivalents, or less if some elements were represented by multivalents. To distinguish between bivalents and multivalents, we used a special method . Briefly, by varying the pressure on the coverslip, we were able to manipulate chromosomes, e.g. change their position and orientation in intact (not squashed) spermatocyte cells, and consequently to analyze the structure of the bivalents and multivalents.
In total, preparations from 209 males were analyzed. As cell divisions are extremely rare in Leptidea during imago stage , metaphase plates were observed in only 35 individuals (Additional file 1, Table S2). These individuals were also used for morphological and molecular analysis.
Geographical longitude vs. chromosome number
Pearson correlation coefficients were used to assess the degree of association between haploid karyotype and geographical longitude. Longitude was measured in decimal degrees and only 23 samples with unambiguous chromosome number counts were included (see Additional file 1, Table S4). If the specimen showed different chromosome numbers in different cells, the average between the different chromosome numbers was used.
Total genomic DNA was extracted using Chelex 100 resin, 100-200 mesh, sodium form (Biorad), under the following protocol: one leg was removed and introduced into 100 μl of Chelex 10% and 5 μl of Proteinase K (20 mg/ml) were added. The samples were incubated overnight at 55°C, afterwards were incubated at 100°C for 15 minutes and were subsequently centrifuged for 10 seconds at 3000 rpm.
A 676 bp fragment at the 5' end of the mitochondrial gene cytochrome oxidase subunit I (COI) was amplified by polymerase chain reaction using the primers LCO 1490 (5'-GGTCAACAAATCATAAAGATATTGG-3')  and Nancy (5'-CCCGGTAAAATTAAAATATAAACTTC-3') . When these primers failed, we used the primers LepF1 (5'-ATTCAACCAATCATAAAGATATTGG-3') and LepR1 (5'-TAAACTTCTGGATGTCCAAAAAATCA-3') , which amplified a 658 bp fragment of COI. Double-stranded DNA was amplified in 25 μl volume reactions: 13.22 μl ultra pure (HPLC quality) water, 2.5 μl 10× buffer, 4.5 μl 25 mM MgCl2, 0.25 μl 100 mM dNTP, 1.2 μl of each primer (10 mM), 0.13 μl Taq DNA Gold Polymerase (Qiagen) and 2 μl of extracted DNA. The typical thermal cycling profile was: 95°C for 60 seconds, 44°C for 60 seconds and 72°C for 90 seconds, for 40 cycles. A total of 70 L. sinapis samples were successfully sequenced for this marker. These included 34 of the karyotyped samples, and 36 individuals collected in the same locality as the karyotyped samples. Five L. reali and two L. morsei specimens were also sequenced and used as outgroup.
A 571 bp fragment at the 5' end of the nuclear gene CAD was amplified by polymerase chain reaction using the primers CADFa (5'-GDATGGTYGATGAAAATGTTAA-3') and CADRa (5'- CTCATRTCGTAATCYGTRCT-3') (designed by A. Kaliszewska). Double-stranded DNA was amplified in 25 μl volume reactions: 16.65 μl ultra pure (HPLC quality) water, 2.5 μl 10× buffer, 1 μl 100 mM MgCl2, 0.25 μl 100 mM dNTP, 1.2 μl of each primer (10 mM), 0.2 μl Taq DNA Polymerase (Bioron, GmbH) and 2 μl of extracted DNA. The typical thermal cycling profile was: 95°C for 60 seconds, 48°C for 60 seconds and 72°C for 90 seconds, for 40 cycles. A total of 14 samples (all karyotyped) were sequenced for this marker. Three L. reali and two L. morsei specimens were also sequenced and used as outgroup.
A 684 bp fragment at the 5' end of the nuclear internal transcribed spacer 2 (ITS2) was amplified by polymerase chain reaction using the primers ITS3 (5'-GCATCGATGAAGAACGCAGC-3') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3') . Double-stranded DNA was amplified in 25 μl volume reactions: 16.7 μl ultra pure (HPLC quality) water, 2.5 μl 10× buffer, 1 μl 100 mM MgCl2, 0.25 μl 100 mM dNTP, 1.2 μl of each primer (10 mM), 0.15 μl Taq DNA Polymerase (Bioron, GmbH) and 2 μl of extracted DNA. The typical thermal cycling profile was: 95°C for 45 seconds, 47°C for 60 seconds and 72°C for 60 seconds, for 40 cycles. A total of 14 samples (all karyotyped) were sequenced for this marker. Three L. reali and two L. morsei specimens were also sequenced and used as outgroup. PCR products were purified and sequenced by Macrogen Inc. (Seoul, Korea). Sequences obtained specifically for this study were deposited in GenBank (accession numbers indicated in Additional file 1, Table S2).
Sequence alignment and phylogenetic inference
COI, ITS2 and CAD sequences were edited and aligned using Geneious Pro 4.7.5 . These resulted in three final alignments of 658 bp and 77 specimens for COI, 571 bp and 19 specimens for CAD, and 684 bp and 19 specimens for ITS2. For COI, duplicate haplotypes were removed using Collapse 1.2 . Maximum Likelihood (ML) phylogenetic trees were inferred for CAD, ITS2 and COI using Phyml 2.4.4 , with the nucleotide substitution model HKY  for nuclear markers and HKY+I for COI, as suggested by jModeltest 0.1 , and 100 bootstrap replicates.
In order to examine relationships among haplotypes, a maximum parsimony haplotype network was constructed using TCS 1.21 . The haplotype network was built with a 99% parsimony connection limit. The network presented one loop, which was broken according to frequency and geographic criteria .
Estimation of TMRCA
Time to the most recent common ancestor (TMRCA) of L. sinapis was inferred with BEAST v.1.5.3  independently for COI, ITS2 and CAD haplotypes under a Coalescent model with constant population size. Duplicate haplotypes were removed from the matrix using Collapse 1.2 . A lognormal distribution (Mean = 0.15, Stdev = 0.798) was used assuming a maximum possible limit of 405000 years as the 95% HPD of the distribution, trying to let the maximum exploratory space to MCMC runs. To estimate this prior, we used the maximum COI intraspecific divergence for L. sinapis under a rather slow invertebrate mitochondrial substitution rate: 1.5% uncorrected pairwise distance per million years . Since substitution rates are known to overestimate ages for recent lineages still under the coalescence process, we are certain that 405000 years is a good maximum estimate for the TMRCA of this species. The dataset was analyzed using the HKY model and applying a strict molecular clock along the branches. Base frequencies were estimated and a randomly generated initial tree was used. Parameters were estimated using two independent runs of 10 million generations each (with a pre-run burn-in of 100,000 generations) to ensure convergence, checked with the program Tracer v1.4.
A multi-locus approach with *BEAST  was also employed to check the results with a smaller set of 12 samples, including those with most divergent COI haplotypes. In order to study the effect of the outgroup, COI and multilocus analyses were conducted by both including and excluding L. reali haplotypes (Additional file 1, Table S5).
We thank L. Dapporto, A.-M. Hereș, J. Martínez-Vilalta and C. Sañudo for advice on the statistical analyses and to I.Y. Bakloushinskaya and V.G. Kuznetsova for suggestions on the manuscript. A. Kaliszewska designed the primers for CAD. Support for this research was provided by the Russian Foundation for Basic Research (grants RFFI 09-04-01234, 11-04-00734 and 11-04-01119), by grant NSH-3332.2010.4 (Leading Scientific Schools) and by the programs of the Presidium of Russian Academy of Science 'Gene Pools and Genetic diversity' and 'Origin of biosphere and evolution of geo-biological systems' to V.A.L.; by the Spanish Ministerio de Ciencia e Innovación (project CGL2007-60516/BOS to V.D., G.T. and R.V., and predoctoral fellowship BES-2008-002054 to G.T.); and by a predoctoral fellowship from Universitat Autònoma de Barcelona to V.D.
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