Abstract
The reduction in fecundity associated with the evolution of viviparity may have far-reaching implications for the ecology, demography, and evolution of populations. The evolution of a polygamous behaviour (e.g. polyandry) may counteract some of the effects underlying a lower fecundity, such as the reduction in genetic diversity. Comparing patterns of multiple paternity between reproductive modes allows us to understand how viviparity accounts for the trade-off between offspring quality and quantity. We analysed genetic patterns of paternity and offspring genetic diversity across 42 families from two modes of viviparity in a reproductive polymorphic species, Salamandra salamandra. This species shows an ancestral (larviparity: large clutches of free aquatic larvae), and a derived reproductive mode (pueriparity: smaller clutches of larger terrestrial juveniles). Our results confirm the existence of multiple paternity in pueriparous salamanders. Furthermore, we show the evolution of pueriparity maintains, and even increases, the occurrence of multiple paternity and the number of sires compared to larviparity, though we did not find a clear effect on genetic diversity. High incidence of multiple paternity in pueriparous populations might arise as a mechanism to avoid fertilization failures and to ensure reproductive success, and thus has important implications in highly isolated populations with small broods.
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Introduction
The evolution of viviparity entails pronounced changes in individuals’ reproductive biology and behaviour and, by extension, on population dynamics1,2,3. For example, viviparous species often show an increased parental investment compared to oviparous ones because they produce larger and more developed offspring that are protected from external pressures for longer periods within the mother4,5,6,7. Conversely, viviparity is frequently associated with a reduction in clutch size and fecundity4,8, 9. This can affect population effective size (Ne) which ultimately may decrease species genetic diversity10,11, compromising population viability and adaptive potential to respond to changing environmental pressures12,13. Polygamous mating systems, such as polyandry, can minimize the genetic effects resulting from this loss of fecundity. For instance, the ability of females to produce clutches sired by several fathers (i.e. multiple paternity; hereafter MP) may not only increase within-family genetic diversity and Ne, but also increase reproductive success through the avoidance of genetic incompatibilities14,15,16,17.
Amphibians exhibit a great diversity in reproductive strategies18,19, and MP has been detected in most life histories20,21. However, the reduction of fecundity resulting from the emergence of a novel reproductive mode (e.g. viviparity) might alter the patterns of MP (e.g. its frequency and the number of fathers per clutch) compared to the ancestral reproductive strategy (e.g. oviparity). Although viviparity evolved in each of the three extant orders of amphibians8, exploring the relationship between reproductive strategies and patterns of paternity is challenging. This is because reproductive strategies rarely vary at the intra-specific level and comparisons involving phylogenetically distant species may introduce substantial bias and, consequently, prevent robust conclusions. In that sense, the intra-specific polymorphism in reproductive modes exhibited by the fire salamander (Salamandra salamandra Linnaeus, 1758) makes it a good system to investigate the potential changes in MP levels and offspring genetic diversity related to the evolution of a novel reproductive strategy.
Salamandra salamandra exhibits internal fertilization and two discrete modes of viviparity: (1) an ancestral and more geographically and phylogenetically widespread strategy, larviparity, in which females lay free aquatic larvae22; and (2) pueriparity, which is geographically restricted and independently evolved in two subspecies endemic to the Iberian Peninsula (Pleistocene and Holocene origin in S. s. bernardezi and S. s. gallaica, respectively), and in which females give birth fully metamorphosed juveniles22,23,24. As reported in previous studies, larviparous individuals have on average larger brood sizes (ca. 20–80 aquatic larvae) than pueriparous ones, in which females give birth to ca. 1–35 juveniles, which are generally larger and heavier than aquatic larvae25,26,27,28. These differences in the offspring are due to several heterochronic processes related to the shift to pueriparity, such as the incomplete fertilization of ovulated eggs, accelerated and asynchronous rates of embryonic development, and active feeding on unfertilized eggs (oophagy) and less developed siblings (adelphophagy)25.
Previous studies produced evidence that S. salamandra is a polygynandrous species and MP was reported in one larviparous population from Germany of the subspecies S. s. terrestris29,30. Sperm from multiple mates are accumulated in the spermatheca through a topping off mechanism31, in which first mates sire the highest proportion of a female’s clutch30. Contrary to larviparous salamanders, the presence of MP in pueriparous females is yet to be confirmed. However, one may hypothesize that some of the ontogenetic processes exclusive to pueriparous S. salamandra may potentially affect patterns of MP compared to their larviparous counterparts. For example, as shown in other species32,33,34, intrauterine cannibalism occurring exclusively among pueriparous siblings (both oophagy and adelphophagy25) reduces brood sizes26, but it can also decrease the number of contributing fathers, even if they managed to successfully fertilize some of the female’s eggs.
Here, we used genetic data (microsatellite genotyping) to address two main objectives: 1) to evaluate the presence of MP in the two known independent origins of pueriparity within S. salamandra (S. s. gallaica and S. s. bernardezi); and 2) to compare levels of MP (i.e. incidence of MP and number of sires) between reproductive modes. We hypothesize that pueriparous populations show smaller levels of MP than larviparous ones due to their smaller brood size26, the topping off mechanism of fertilization30, and the presence of intrauterine cannibalism25. As a reference of MP for larviparity we used the subspecies S. s. terrestris, which occurs throughout central Europe, and is phylogenetically close to S. s. gallaica35. As secondary objectives, we also 3) compared patterns of MP between pueriparous S. s. bernardezi and S. s. gallaica, hypothesizing a higher incidence of MP and number of sires in the latter, as a result of their larger body size and a more recent evolution of pueriparity, and 4) evaluated whether a higher number of siring males increased the fecundity of females and the genetic diversity of their offspring14,36. Finally, and as pilot study, we compared patterns of MP between natural births and dissections at early developmental stages in pueriparous populations, expecting a lower number of sires per clutch in natural births due to the occurrence of intrauterine cannibalism at later stages of pregnancy.
Material and methods
We sampled 18 pueriparous females from two S. s. bernardezi populations (Oviedo, N = 5; Somiedo, N = 5) and one of the two extant pueriparous S. s. gallaica populations (Ons Island; N = 8) (Fig. 1; Table 1 and Supplementary Table S1). During the course of the study we could not observe and collect any gravid females from the rare and small insular pueriparous population of S. s. gallaica in San Martiño37. Between 2015 and 2017 we collected six and four gravid females of S. s. bernardezi (three from each population) and S. s gallaica, respectively, and transported them to laboratory facilities at the University of Oviedo (Spain; in the case of S. s. bernardezi) and to the Research Centre in Biodiversity and Genetic Resources (CIBIO-InBIO, Porto, Portugal; in the case of S. s. gallaica). Individuals were placed in individual terraria (60 × 30 × 40 cm; L × W × H) containing coconut fibre as substrate, a container with water, moss, and shelters (bricks or barks). We fed them twice a week with crickets (Acheta sp.) or flour worms (Tenebrio sp.). After parturition, both females and their offspring were released at their place of capture.
To explore whether the number of siring males varied across gestation stages, we sampled eight more females (two from each S. s. bernardezi population and four from Ons) at the earliest gestation stage possible and sacrificed them by an overdose of anaesthesia (benzocaine; Ethyl 4-aminobenzoate; Sigma-Aldrich, Darmstadt, Germany. Product number: E1501. Ref.: 112909). After dissections, we recorded the uterus (i.e. right or left), clutch size, and the stage of development of each offspring (i.e. embryo, larvae, juvenile). Each individual was stored in pure ethanol for DNA analysis. Salamanders were captured and processed under collection permits provided by regional or national governments (Galicia, Ref. 410/2015 and EB016/2018; Asturias, NºEXPTE: 2017/001208; 2018/007781; 2018/2115), and the study was approved by the ethics committee Research Ethics Committee of the University of Oviedo (PROAE 10/2017). All applicable national and institutional guidelines for the care and use of animals were followed.
We used microsatellite markers to infer patterns of MP (i.e. number of sires and incidence of MP), and characterize within-family genetic diversity. Tissue samples for DNA analysis were collected from a toe-clip in the case of females, and a tail-clip from juveniles. We genotyped 11 microsatellites38,39, following the conditions described in40,41 (see Supplementary Information and Supplementary Table S2 for details). For the larviparous reproductive mode, we used a comprehensive dataset obtained for S. s. terrestris and published by ref.30,42. This dataset includes a total of 591 larvae and 24 females genotyped for a higher number of microsatellite markers. For comparison purposes, we filtered these genotypic profiles to the same 11 loci employed in our study for pueriparous individuals. Although we are aware the optimal design should have included data from nearby larviparous populations of S. s. gallaica, we argue that our comparisons are valid because S. s. gallaica and S. s. terrestris are phylogenetically closely related35. Indeed, phylogenomic analyses show S. s. terrestris as a recent expanded population from S. s. gallaica with very shallow levels of genetic divergence (unpublished genomic data and ref.35).
To infer the number of siring males in each family we estimated the most likely number of fathers in COLONY 2.0.6.4.43, a software which implements a maximum likelihood method to infer parentage based on individual multilocus genotypes. We set the species as dioecious and diploid, assumed polygamy for both sexes, no inbreeding, the maternal genotype and maternal sibship was considered known a priori, and no candidate father genotype was included. We applied the maximum likelihood approach with high likelihood precision and two very long runs with different random number seed in each population separately. We provided neither known population allele frequency nor sibship size prior. As we were very conservative during allele scoring and re-amplified a number of samples to check for possible errors (see Supplementary Information), we assumed a minimum error rate of 0.0001. To characterize the genetic diversity of each brood, we calculated the observed heterozygosity (Ho), mean number of alleles (NA), and mean relatedness of offspring per female (Roffsspring) in GenAlex v 6.50344. As NA could be highly affected by differences in brood size, we calculated the unbiased allelic richness (AR) using a rarefaction method implemented in HP-RARE45.
We compared the mean clutch size (Noffspring) and the mean number of fathers (Nfathers) among the studied subspecies, modes of reproduction, and stage of gestation (i.e. natural births vs. dissections) using permutation tests with 1,000 resamplings without replacement (α = 0.05). Additionally, for each subspecies, we used non-parametric Kendall correlations to test the association between MP (Nfathers) and variables related to female’s fecundity (Noffspring), and offspring genetic diversity (Ho, NA, AR, Roffspring). Because the mean number of alleles (NA) is often highly affected by Noffspring, we also tested for the correlation between both variables to enable us to examine whether a putative high correlation between Nfathers and NA is an artefact of the varying Noffspring observed among the studied females. All statistical analyses were performed in R software46.
Results
We obtained 237 offspring from 18 pueriparous females. Four individuals from the original larviparous dataset were excluded due to incongruences with the mother (H04_BT_373) or high presence of missing data (H05_BT_565, H06_BT_566, H07_BT_567), resulting in a final dataset of 587 offspring from the 24 larviparous females. All other individuals were unambiguously assigned to their mothers.
We found evidence for MP in the three study subspecies (S. s. bernardezi, S. s. gallaica, S. s. terrestris), with incidence of MP varying between 54 and 88% (highest in pueriparous S. s. gallaica) and Nfathers ranging between 1 and 7 in pueriparous populations, and 1 and 5 in the larviparous population (Table 1; Fig. 2). In cases where Nfathers > 1, a single male sired on average 71.4% (± 16.4%) of the offspring. The S. s. bernardezi population of Oviedo and the S. s. gallaica population of Ons exhibited the lowest genetic diversity and the highest relatedness among the studied populations (Table 1).
Because they belong to the same subspecies and have reduced sample size, females from both pueriparous S. s. bernardezi populations were pooled (Noffspring = 8.9, Nfathers = 1.7) and compared with both pueriparous S. s. gallaica and larviparous S. s. terrestris. Permutation tests revealed S. s. gallaica (Noffspring = 18.5, Nfathers = 3.8) exhibited a significantly higher Noffspring (P = 0.001) and Nfathers (P = 0.001) than S. s. bernardezi. Comparisons involving different reproductive modes showed that S. s. terrestris (Noffspring = 24.5, Nfathers = 2.0) has a significantly higher Noffspring than S. s. bernardezi (P = 0.001), but not than S. s. gallaica (P = 0.869). The Nfathers was similar between S. s. terrestris and S. s. bernardezi (P = 0.187), while the offspring of S. s. gallaica females appeared to be sired by a higher number of fathers than their larviparous counterparts (P = 0.005) (Table 1; Supplementary Table S3).
All pairwise comparisons involving pueriparous subspecies include data from natural births and dissections because permutation tests did not show differences (P > 0.05) in Noffspring or Nfathers between both sampling methods (Table 1; Supplementary Table S4). The inclusion of females sampled at different stages of pregnancy could affect comparisons involving pueriparous subspecies and the larviparous S. s. terrestris, because the data for the latter were collected only from natural births. However, when excluding dissections, the results from permutation tests do not differ from those including all sampled pueriparous females (Supplementary Table S5).
We did not find a significant relationship between NA and Noffspring among the study subspecies (S. s. bernardezi: τ = − 0.02, P = 0.93; S. s. gallaica: τ = 0.33, P = 0.26; S. s. terrestris: τ = 0.18, P = 0.23), therefore, we also tested the association between Nfathers and NA. Correlation tests revealed a significant positive relationship between Nfathers and female’s fecundity in the larviparous population and the pueriparous S. s. gallaica, but not in pueriparous S. s. bernardezi (Table 2). While heterozygosity in S. s. bernardezi seemed negatively correlated with multiple paternity, NA varied positively with Nfathers in S. s. gallaica and S. s. terrestris. Indeed, in the latter subspecies, relatedness appears to decrease as the number of fathers increases (Table 2).
Discussion
This study confirmed the occurrence of MP in pueriparous salamanders, a reproductive strategy restricted to only two urodele genera: Salamandra and Lyciasalamandra47,48,49. While previous studies documented a polygamous mating system in the pueriparous S. atra50,51,52, to the best of our knowledge, the occurrence of MP in any pueriparous species had never been proven.
Contrary to our expectations, the shift to pueriparity seems to maintain, and even increase, the incidence of MP and the number of sires per clutch (Table 1; Fig. 2) despite the smaller brood sizes compared to larviparous salamanders. This result is in agreement with previous studies showing no association between MP and clutch size because similar or even lower levels of MP are known among species of amphibians producing large clutches (e.g. refs.31,53,54,55 ). Moreover, benefits of polyandry may vary among reproductive modes56. In less fecund reproductive modes, female investment per offspring is generally high, and reproductive failures due to genetic incompatibilities imply higher costs compared to more fecund strategies56,57. Within S. salamandra, larviparous progeny rely solely on their yolk provisions, but in pueriparous populations, fecundity is reduced in favour of a lower number of more developed descendants because nutrient provisioning occurs through the availability of both arrested eggs and less developed siblings25,27. Accordingly, reproductive costs due to genetic incompatibilities or mating with sterile males are likely higher in pueriparous females and, therefore, multiple mating (and MP) may be under selection to reduce these costs58. Furthermore, in accordance to previous studies we found a similar pattern of reproductive skew towards a dominant male in polyandrous broods in both reproductive modes, probably resulting from a topping-off mechanism of sperm storage31, in which the first mate fertilizes the majority of eggs30. Although we found no significant differences in clutch size between the larviparous S. s. terrestris and the pueriparous insular S. s. gallaica, the larviparous mainland S. s. gallaica generally have larger clutches26.
Although similar heterochronic processes are thought to mediate pueriparity in both S. s. bernardezi and S. s. gallaica26, clutch size, number of fathers, and incidence of MP are higher in the latter (Table 1). The differences observed between the studied pueriparous subspecies might result from the more recent transition to pueriparity in S. s. gallaica (ca. 8,000 years ago59), which may have led to the retention of some ‘larviparous’ traits associated with reproduction. Additionally, the population-specific traits of this insular population and differences in evolutionary history (e.g. founder effects, isolated, low genetic diversity)37,59,60 may have also contributed to the differences in patterns of paternity observed between insular and continental pueriparous populations. Indeed, the particularly low levels of genetic diversity and higher levels of inbreeding observed in Ons24,60 may increase the risk of reproductive failures and, therefore, MP in Ons may be under selection to increase reproductive success16. Moreover, we found in this population the highest number of males (7) siring a single clutch in S. salamandra, which is remarkable even at the wider taxonomic spectrum of internally fertilizing vertebrates57,61,62. Nonetheless, further research is needed to understand whether MP boosts reproductive success in the fire salamander, and its relationship with other population traits, such as inbreeding.
Salamander males do not provide parental care or extra resources to females or their offspring. However, females may obtain genetic benefits from polyandry. Multiple paternity has been suggested as a mechanism of genetic compensation that helps maintaining high Ne/N ratios and relatively high levels of genetic diversity16,63,64, such as for example, in a small pueriparous population of S. s. bernardezi41,65, and in an overexploited population of rockfish66. Our results appear to corroborate the aforementioned premises; a higher number of fathers appears to be associated not only with an increase in allele diversity within S. s. gallaica and in the larviparous population, but also with a reduction in the offspring genetic relatedness in S. s. terrestris. This potentially suggests MP boosts genetic diversity, though the negative relationship observed between Ho and Nfathers in S. s. bernardezi, together with the reduced sample size, call for caution when interpreting these results.
Another potential benefit of polyandry is an increase in clutch size67. We detected a positive relationship between the number of sires and the number of offspring in the larviparous population (see also ref.30). This pattern holds in the pueriparous S. s. gallaica, but not in S. s. bernardezi, suggesting that small sample size and other factors not considered in this study can be also influencing fecundity, such as the body size of females and offspring8, thus preventing us from making robust predictions about the relationship between polyandry and clutch size. In addition, it is worth considering that in pueriparous systems, the high production of aborted eggs and cannibalistic events reduce brood size68, and thus, this variable likely misrepresents the amount of successful fertilizations.
Finally, we did not detect substantial differences in clutch sizes or the number of sires between natural births and dissections, although it should be acknowledged that most dissections were performed at a relatively advanced stage of pregnancy. Thus, sampling more females at earlier stages of pregnancy, where most arrested eggs were not yet cannibalized, will be crucial to clarify how ontogenetic processes associated with pueriparity affect the incidence and frequency of MP. For instance, in the polygamous pueriparous S. atra species, discordances between the number of mating males and sires are expected because only one or two completely developed offspring are delivered after a long period of gestation over which the main source of nourishment consists on aborted eggs50,52,69.
The present study constitutes the first step towards the understanding of the potential relationship between MP and alternative life histories in S. salamandra. Specifically, we showed pueriparous populations of S. salamandra exhibit identical or higher rates of multipaternity, even though their fecundity is lower. Nevertheless, we cannot rule out that some other factors may have also influenced our results. The lack of replicates for both larviparous populations and the pueriparous S. s. gallaica limit our ability in disentangling the effects of population-specific traits and reproductive mode in the observed patterns of multipaternity. Specifically, our data do not allow us to evaluate accurately whether other ecological, geographical and demographic traits influence MP70,71,72. Indeed, despite the potential benefits that MP entails in an isolated and inbred population, the high rates of MP observed in the insular population of Ons can reflect a relaxation of the potential constraints determining the acquisition of mates (e.g. population density, rates of individuals encounters, territoriality)37,62,73,74. Hence, future studies should extend sampling to cover as much diversity within the species as possible and consider the potential effects of geographic and populational variability on MP.
Overall, this study constitutes a relevant contribution to the understanding on how reproductive strategies evolve to account for the trade-off between offspring quality and quantity. Although other factors might be involved, our results appear to suggest the evolution of a derived reproduction mode may affect other traits to compensate the loss of fecundity and ensure reproductive success.
Data availability
Datasets used in the present study can be found in Figshare (https://doi.org/10.6084/m9.figshare.12014580).
References
Blackburn, D. G. Viviparity and oviparity: evolution and reproductive strategies. In Encyclopedia of Reproduction (eds Knobil, T. E. & Neill, J. D.) 994–1003 (Academic Press, Cambridge, 1999).
Blackburn, D. G. Evolution of vertebrate viviparity and specializations for fetal nutrition: a quantitative and qualitative analysis. J. Morphol. 276, 961–990 (2015).
Shine, R. The evolution of oviparity in squamate reptiles: an adaptationist perspective. J. Exp. Zool. Part B 324, 487–492 (2015).
Wourms, J. P. & Lombardi, J. Reflections on the evolution of piscine viviparity. Am. Zool. 32, 276–293 (1992).
Andrews, R. M. Evolution of viviparity in squamate reptiles (Sceloporus spp): a variant of the cold-climate model. J. Zool. 250, 243–253 (2000).
Shine, R. Reconstructing an adaptationist scenario: what selective forces favor the evolution of viviparity in montane reptiles?. Am. Nat. 160, 582–593 (2002).
While, G. M., Uller, T. & Wapstra, E. Offspring performance and the adaptive benefits of prolonged pregnancy: experimental tests in a viviparous lizard. Funct. Ecol. 23, 818–825 (2009).
Wells, K. D. The Ecology and Behavior of Amphibians (The University of Chicago Press, Chicago, 2007).
Meiri, S., Feldman, A., Schwarz, R. & Shine, R. Viviparity does not affect the numbers and sizes of reptile offspring. J. Anim. Ecol. 89, 360–369 (2020).
Romiguier, J. et al. Comparative population genomics in animals uncovers the determinants of genetic diversity. Nature 515, 261 (2014).
Ellegren, H. & Galtier, N. Determinants of genetic diversity. Nat. Rev. Genet. 17, 422 (2016).
Jump, A. S., Marchant, R. & Peñuelas, J. Environmental change and the option value of genetic diversity. Trends Plant Sci. 14, 51–58 (2009).
Hughes, A. R., Inouye, B. D., Johnson, M. T. J., Underwood, N. & Vellend, M. Ecological consequences of genetic diversity. Ecol. Lett. 11, 609–623 (2008).
Taylor, M. L., Price, T. A. R. & Wedell, N. Polyandry in nature: a global analysis. Trends Ecol. Evol. 29, 376–383 (2014).
Slatyer, R. A., Mautz, B. S., Backwell, P. R. Y. & Jennions, M. D. Estimating genetic benefits of polyandry from experimental studies: a meta-analysis. Biol. Rev. 87, 1–33 (2012).
Tregenza, T. & Wedell, N. Polyandrous females avoid costs of inbreeding. Nature 415, 71 (2002).
Jennions, M. D. & Petrie, M. Why do females mate multiply? A review of the genetic benefits. Biol. Rev. 75, 21–64 (2000).
Duellman, W. E. & Trueb, L. Biology of Amphibians (JHU Press, Baltimore, 1986).
Crump, M. L. Anuran reproductive modes: evolving perspectives. J. Herpetol. 49, 1–16 (2015).
Sandberger-Loua, L., Feldhaar, H., Jehle, R. & Rödel, M. O. Multiple paternity in a viviparous toad with internal fertilisation. Sci. Nat. 103, 51 (2016).
Byrne, P. G. & Roberts, J. D. Evolutionary causes and consequences of sequential polyandry in anuran amphibians. Biol. Rev. 87, 209–228 (2012).
Velo-Antón, G. & Buckley, D. Salamandra común–Salamandra salamandra. In Enciclopedia Virtual de los Vertebrados Españoles (eds Salvador, A. & Martínez-Solano, I.) (Museo Nacional de Ciencias Naturales, Madrid, 2015).
García-París, M., Alcobendas, M., Buckley, D. & Wake, D. B. Dispersal of viviparity across contact zones in Iberian populations of fire salamanders (Salamandra) inferred from discordance of genetic and morphological traits. Evolution 57, 129–143 (2003).
Velo-Antón, G., Zamudio, K. R. & Cordero-Rivera, A. Genetic drift and rapid evolution of viviparity in insular fire salamanders (Salamandra salamandra). Heredity 108, 410 (2012).
Buckley, D., Alcobendas, M., García-París, M. & Wake, M. H. Heterochrony, cannibalism, and the evolution of viviparity in Salamandra salamandra. Evol. Dev. 9, 105–115 (2007).
Velo-Antón, G., Santos, X., Sanmartín-Villar, I., Cordero-Rivera, A. & Buckley, D. Intraspecific variation in clutch size and maternal investment in pueriparous and larviparous Salamandra salamandra females. Evol. Ecol. 29, 185–204 (2015).
Dopazo, H. J. & Korenblum, M. Viviparity in Salamandra salamandra (Amphibia: Salamandridae): adaptation or exaptation?. Herpetologica 56, 144–152 (2000).
Dopazo, H., Boto, L. & Alberch, P. Mitochondrial DNA variability in viviparous and ovoviviparous populations of the urodele Salamandra salamandra. J. Evol. Biol. 11, 365–378 (1998).
Steinfartz, S., Stemshorn, K., Kuesters, D. & Tautz, D. Patterns of multiple paternity within and between annual reproduction cycles of the fire salamander (Salamandra salamandra) under natural conditions. J. Zool. 268, 1–8 (2006).
Caspers, B. A. et al. The more the better–polyandry and genetic similarity are positively linked to reproductive success in a natural population of terrestrial salamanders (Salamandra salamandra). Mol. Ecol. 23, 239–250 (2014).
Jones, A. G., Adams, E. M. & Arnold, S. J. Topping off: a mechanism of first-male sperm precedence in a vertebrate. Proc. Natl. Acad. Sci. USA 99, 2078–2081 (2002).
Gilmore, R. G., Putz, O. & Dodrill, J. W. Oophagy, intrauterine cannibalism and reproductive strategy in lamnoid. In Reproductive Biology and Phylogeny of Chondrichthyes: Sharks, Batoids and Chimaeras (ed. Hamlett, W. C.) 435–462 (Science Publishers, London, 2005).
Exbrayat, J.-M. Reproductive Biology and Phylogeny of Gymnophiona (Caecilians) (Science Publishers Incorporated, London, 2006).
Chapman, D. D. et al. The behavioural and genetic mating system of the sand tiger shark, Carcharias taurus, an intrauterine cannibal. Biol. Lett. 9, 20130003 (2013).
Steinfartz, S., Veith, M. & Tautz, D. Mitochondrial sequence analysis of Salamandra taxa suggests old splits of major lineages and postglacial recolonizations of Central Europe from distinct source populations of Salamandra salamandra. Mol. Ecol. 9, 397–410 (2000).
Calsbeek, R., Bonneaud, C., Prabhu, S., Manoukis, N. & Smith, T. B. Multiple paternity and sperm storage lead to increased genetic diversity in Anolis lizards. Evol. Ecol. Res. 9, 495–503 (2007).
Velo-Antón, G. & Cordero-Rivera, A. Ethological and phenotypic divergence in insular fire salamanders: diurnal activity mediated by predation?. Acta Ethol. 20, 243–253 (2017).
Steinfartz, S., Kuesters, D. & Tautz, D. Isolation and characterization of polymorphic tetranucleotide microsatellite loci in the Fire salamander Salamandra salamandra (Amphibia: Caudata). Mol. Ecol. Notes 4, 626–628 (2004).
Hendrix, R., Hauswaldt, J. S., Veith, M. & Steinfartz, S. Strong correlation between cross-amplification success and genetic distance across all members of ‘True Salamanders’(Amphibia: Salamandridae) revealed by Salamandra salamandra-specific microsatellite loci. Mol. Ecol. Resour. 10, 1038–1047 (2010).
Lourenço, A., Antunes, B., Wang, I. J. & Velo-Antón, G. Fine-scale genetic structure in a salamander with two reproductive modes: Does reproductive mode affect dispersal?. Evol. Ecol. 32, 699–732 (2018).
Álvarez, D., Lourenço, A., Oro, D. & Velo-Antón, G. Assessment of census (N) and effective population size (Ne) reveals consistency of Ne single-sample estimators and a high Ne/N ratio in an urban and isolated population of fire salamanders. Conserv. Genet. Resour. 7, 705–712 (2015).
Caspers, B. A. et al. Data from: The more the better—polyandry and genetic similarity are positively linked to reproductive success in a natural population of terrestrial salamanders (Salamandra salamandra). Mol. Ecol. 23, 239–250. https://doi.org/10.5061/dryad.jp203 (2014).
Jones, O. R. & Wang, J. COLONY: a program for parentage and sibship inference from multilocus genotype data. Mol. Ecol. Resour. 10, 551–555 (2010).
Peakall, R. & Smouse, P. E. GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research-an update. Bioinformatics 28, 2537–2539 (2012).
Kalinowski, S. T. hp-rare 1.0: a computer program for performing rarefaction on measures of allelic richness. Mol. Ecol. Notes 5, 187–189 (2005).
R Development Core Team. R: A language and environment for statistical computing (R Development Core Team, Vienna, 2016).
Dinis, M. & Velo-Antón, G. How little do we know about the reproductive mode in the north African salamander, Salamandra algira? Pueriparity in divergent mitochondrial lineages of S. a. tingitana. Amphibia-Reptilia 38, 540–546 (2017).
Veith, M. et al. Seven at one blow: the origin of major lineages of the viviparous Lycian salamanders (Lyciasalamandra Veith and Steinfartz, 2004) was triggered by a single paleo-historic event. Amphibia-Reptilia 37, 373–387 (2016).
Buckley, D. Evolution of Viviparity in Salamanders (Amphibia, Caudata). ELS https://doi.org/10.1002/9780470015902.a0022851 (2011).
Häfeli, H. P. Reproductive biology of the alpine salamander (Salamandra atra Laur). Rev. Suisse Zool. 78, 235–293 (1971).
Helfer, V., Broquet, T. & Fumagalli, L. Sex-specific estimates of dispersal show female philopatry and male dispersal in a promiscuous amphibian, the alpine salamander (Salamandra atra). Mol. Ecol. 21, 4706–4720 (2012).
Trochet, A. et al. A database of life-history traits of European amphibians. Biodivers. Data J. 2, e4123. https://doi.org/10.3897/BDJ.2.e4123 (2014).
Gopurenko, D., Williams, R. N., McCormick, C. R. & DeWoody, J. A. Insights into the mating habits of the tiger salamander (Ambystoma tigrinum tigrinum) as revealed by genetic parentage analyses. Mol. Ecol. 15, 1917–1928 (2006).
Rovelli, V. et al. She gets many and she chooses the best: polygynandry in Salamandrina perspicillata (Amphibia: Salamandridae). Biol. J. Linn. Soc. 116, 671–683 (2015).
Liebgold, E. B., Cabe, P. R., Jaeger, R. G. & Leberg, P. L. Multiple paternity in a salamander with socially monogamous behaviour. Mol. Ecol. 15, 4153–4160 (2006).
Zeh, J. A. & Zeh, D. W. Reproductive mode and the genetic benefits of polyandry. Anim. Behav. 61, 1051–1063 (2001).
Liu, J.-X. & Avise, J. C. High degree of multiple paternity in the viviparous Shiner Perch, Cymatogaster aggregata, a fish with long-term female sperm storage. Mar. Biol. 158, 893–901 (2011).
Stockley, P. Female multiple mating behaviour, early reproductive failure and litter size variation in mammals. Proc. R. Soc. Lond. B 270, 271–278 (2003).
Velo-Antón, G., García-París, M., Galán, P. & Cordero-Rivera, A. The evolution of viviparity in holocene islands: ecological adaptation versus phylogenetic descent along the transition from aquatic to terrestrial environments. J. Zool. Syst. Evol. Res. 45, 345–352 (2007).
Lourenço, A., Sequeira, F., Buckley, D. & Velo-Antón, G. Role of colonization history and species-specific traits on contemporary genetic variation of two salamander species in a Holocene island-mainland system. J. Biogeogr. 45, 1054–1066 (2018).
Uller, T. & Olsson, M. Multiple paternity in reptiles: patterns and processes. Mol. Ecol. 17, 2566–2580 (2008).
Avise, J. C. & Liu, J.-X. Multiple mating and its relationship to brood size in pregnant fishes versus pregnant mammals and other viviparous vertebrates. Proc. Natl. Acad. Sci. USA 108, 7091–7095 (2011).
Pearse, D. E. & Anderson, E. C. Multiple paternity increases effective population size. Mol. Ecol. 18, 3124–3127 (2009).
Michalczyk, Ł et al. Inbreeding promotes female promiscuity. Science 333, 1739–1742 (2011).
Lourenço, A., Álvarez, D., Wang, I. J. & Velo-Antón, G. Trapped within the city: Integrating demography, time since isolation and population-specific traits to assess the genetic effects of urbanization. Mol. Ecol. 26, 1498–1514 (2017).
Gao, T., Ding, K., Song, N., Zhang, X. & Han, Z. Comparative analysis of multiple paternity in different populations of viviparous black rockfish, Sebastes schlegelii, a fish with long-term female sperm storage. Mar. Biodivers. 48, 2017–2024 (2018).
Fitze, P. S., Le Galliard, J. F., Federici, P., Richard, M. & Clobert, J. Conflict over multiple-partner mating between males and females of the polygynandrous common lizards. Evolution 59, 2451–2459 (2005).
Greven, H. & Guex, G. D. Structural and physiological aspects of viviparity in Salamandra salamandra. Mertensiella 4, 139–160 (1994).
Guex, G.-D. & Chen, P. S. Epitheliophagy: Intrauterine cell nourishment in the viviparous alpine salamander, Salamandra atra (Laur). Experientia 42, 1205–1218 (1986).
Kelly, C. D., Godin, J.-G.J. & Wright, J. M. Geographic variation in multiple paternity within natural populations of the guppy (Poecilia reticulata). Proc. R. Soc. Lond. B. 266, 2403–2408 (1999).
Lodé, T., Holveck, M.-J. & Lesbarreres, D. Asynchronous arrival pattern, operational sex ratio and occurrence of multiple paternities in a territorial breeding anuran, Rana dalmatina. Biol. J. Linn. Soc. 86, 191–200 (2005).
Dobson, F. S., Abebe, A., Correia, H. E., Kasumo, C. & Zinner, B. Multiple paternity and number of offspring in mammals. Proc. R. Soc. B 285, 20182042 (2018).
Soucy, S. & Travis, J. Multiple paternity and population genetic structure in natural populations of the poeciliid fish, Heterandria formosa. J. Evol. Biol. 16, 1328–1336 (2003).
Sztatecsny, M., Jehle, R., Burke, T. & Hödl, W. Female polyandry under male harassment: the case of the common toad (Bufo bufo). J. Zool. 270, 517–522 (2006).
Acknowledgements
We are thankful to Kevin Mulder, Bernardo Antunes and Marco Dinis for their help during fieldwork and Patrícia Ribeiro for laboratory assistance. We thank the National Park staff that facilitated our trip and lodging in Ons Island. This work was funded by the Ministerio de Economía Competitiviad (Spain) (grants no. CGL2012-40246-C02-02 and CGL2017-86924-P); by FEDER funds (Operational Programme for Competitiveness Factors – COMPETE, FCOMP-01-0124-FEDER-028325 and POCI-01-0145-FEDER-006821); and by National Funds through Fundação para a Ciência e a Tecnologia (FCT, Portugal) (EVOVIV: PTDC/BIA-EVF/3036/2012; SALOMICS: PTDC/BIA-EVL/28475/2017). L.A.-R. was supported by a FPU grant (FPU14/03015) from the Ministerio de Educación, Cultura y Deporte (Spain). A.L. and G.V.A. are supported by FCT (PD/BD/106060/2015 and IF/01425/2014, respectively).
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L.A.-R., A.G.N. and G.V.-A. designed the study and carried out fieldwork to collect females. L.A.-R. and A.L. carried out molecular lab work and analyses. L.A.-R. led the writing, to which all authors contributed.
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Alarcón-Ríos, L., Nicieza, A.G., Lourenço, A. et al. The evolution of pueriparity maintains multiple paternity in a polymorphic viviparous salamander. Sci Rep 10, 14744 (2020). https://doi.org/10.1038/s41598-020-71609-3
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DOI: https://doi.org/10.1038/s41598-020-71609-3
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