Current zoological research may benefit in many ways from the study of old collections of shells. These collections may provide materials for the verification of broad zoogeographical and ecological hypotheses on the reproduction of molluscs, as they include records from many areas where sampling is currently impossible or very difficult due to political circumstances. In the present paper we present data on viviparous and embryo-retention reproductive modes in clausiliid land snails (subfamily Phaedusinae) acquired from specimens collected since the nineteenth century in the Pontic, Hyrcanian, and East and Southeast Asian regions. X-ray imaging (micro-CT) enabled relatively quick screening of more than 1,000 individuals classified within 141 taxa, among which we discovered 205 shells containing embryos or eggs. Gravid individuals were found to belong to 55 species, representing, for some of these species, the first indication of brooding reproductive strategy.
Specimens deposited in natural history museums possess huge potential as an almost limitless biodiversity resource. These preserved animals form a basis for fundamental insights into zoological systematics, biogeography, ecology, and evolution. In the past decade, collection-based research has incorporated several technological and methodological advances which have extended the scope of study far beyond alpha taxonomy and taxonomic reviews. Indisputably, the major source of input in the field has been molecular methods, including next-generation sequencing and barcoding1,2. Important additions to knowledge have been made possible by means of isotopic studies, geometric morphometry, and microcomputed tomography (e.g.3,4,5,6). Moreover, the digitisation of collections, in tandem with species modelling, has enhanced our ability to synthesise biogeographical data and our knowledge of the possible responses of species to ongoing climatic or anthropogenic threats7,8. In the present paper, we explore the potential of old malacological collections (Fig. 1) as a source of data for life history studies, including reproductive modes and fecundity. We focus on brooding strategy (the development of embryos within the parental reproductive system) in terrestrial gastropods of the family Clausiliidae. For this purpose, micro-CT scanning was adopted as a screening technique. We also evaluated the usefulness of dry- and ethanol-preserved specimens for this kind of research.
Among terrestrial pulmonate molluscs, several reproductive modes are recognised, among which oviparity (whereby laid eggs contain only a single-celled zygote or the earliest cleavage stages) seems to be the most common9,10,11. However, in a great number of species classified within at least 30 families, developing embryos are retained in the parental reproductive tract for various parts of the embryonic period9,10,11. If the period of embryo retention is very long and hatching occurs in the reproductive tract, the reproductive mode should be classified as live-bearing reproduction, or viviparity12. Formerly, the term ovoviviparity was frequently used for this strategy in malacological literature9,11,13,14,15, despite critical comments from researchers in other fields16. An intermediate strategy between oviparity and viviparity, whereby the first part of embryonic development takes place in the genital tract and the second in the ambient environment, is also widespread. This reproductive mode is referred to here as embryo retention. Strategies involving the development of embryos inside the parental organism, including both embryo retention and viviparity, are referred to in this paper as brooding. During embryo retention, nutrients and calcium for the developing offspring can be derived either from the yolk alone (lecithotrophy) or directly from the parent (matrotrophy); the latter has been proven only in a limited number of land snail taxa17,18.
The strategy of brooding is usually seen as an adaptation which contributes to reducing the level of mortality caused by drought or predators, as well as enhancing competition for food over the young of oviparous animals19,20. Brooding may have evolved in land snails in response to several different selective pressures, such as irregular onset of the rainy season in subtropics, short growing periods in temperate areas, and lack of suitable oviposition sites in habitats with extreme environmental conditions (e.g. exposed rocks)19,20. None of these hypotheses has been tested within a phylogenetic framework (e.g. a gastropod family). In our opinion, such analyses are hindered mainly by the lack of reliable data on the distribution of reproductive modes across taxa, geographical areas, and habitats.
Clausiliidae, probably the largest family of land snails21, has become a model group for studies of diversity in breeding biology in these animals (e.g.14,22,23). Within relatively well-studied species from Europe, several reproductive modes were identified based on long-term breeding experiments and field observations14,23,24,25,26,27,28. For embryo-retaining and viviparous species, it was shown that during the reproductive season (usually late spring/summer in Central Europe) a substantial proportion of adult snails are gravid, with one to several embryos in the genital tract23,25,29,30. Embryos are initially enveloped in the egg membrane, which contains calcium carbonate crystals; prior to parturition, an embryo may develop an embryonic shell with 1–3 whorls. The period of internal development lasts from several days to ca 3 weeks; however, the source of nutrient and calcium provision for embryos has not yet been studied. Embryos found in the genital tract constitute direct evidence of a non-oviparous reproductive strategy (i.e. brooding). In contrast, a typically oviparous species lays eggs within hours of fertilisation; thus it is unusual to find eggs or egg shells in their genital tracts during dissection9.
Rather than conducting time-consuming experiments and field observations, we used shells from museum collections to look for embryo-retaining and viviparous taxa within Clausiliidae (subfamily Phaedusinae). As far as we know, this idea was put forward for the first time by F. E. Loosjes, who provided a foundation for studying the diversity of reproductive modes in clausiliids of East and Southeast Asia31,32,33. The genital anatomy and reproduction of Phaedusinae species were also mentioned in several papers (e.g.34,35,36); however, more detailed studies are scarce37,38,39. The correct identification of reproductive modes in Phaedusinae appears highly significant, as researchers formerly linked life history traits with taxonomically sound characters13,40, or traced them in the molecular phylogeny of this group15. The correlation between shell characters and reproductive strategy in all clausiliids is indisputable, as the delivery of a shell embryo requires the reduction or rearrangement of complex apertural barriers that occur within the ultimate whorl of the shell41. These apertural barriers are believed to provide protection from small predators which enter the shell through the aperture42; on the other hand, they may impose constraints on reproduction, mandating the laying of hard-shelled eggs and viviparity43. The co-existence of viviparity and certain shell characters (e.g. a broad clausilium plate) have been demonstrated for a number of Phaedusinae genera (Table 1, Fig. 2). Oviparous snails require no adaptations to enlarge the capacity of the shell channel, and may be characterised by a narrow clausilium plate13.
On the other hand, previous molecular studies on clausiliids revealed that a complex system of apertural barriers, previously recognised as taxonomically significant, has evolved several times in parallel and may have even undergone reversals15,44,45.
The Phaedusinae subfamily comprises approximately 500 extant species46,47,48, currently classified into 3 tribes: Phaedusini and Synprosphymini, distributed in East and Southeast Asia, and Serrulinini, inhabiting the Pontic and Hyrcanian regions of Asia49,50. Access to substantial parts of their distribution ranges has been cut off for political reasons within the last 80 years, but these areas had been sampled previously and abundant collections have been preserved in natural history museums across Europe and the USA (Fig. 3). These collections provide an opportunity to analyse reproductive modes in Phaedusinae without new field sampling, assuming that snails were collected alive and preserved in ethanol or dried without the removal of soft tissue.
The primary goal of the present paper was to test X-ray screening as a method for studying the reproductive strategies of gastropods kept in museum collections, both ethanol- and dry-preserved. Secondarily, as an introduction to a larger project focusing on the evolution of reproductive modes in land snails, we aimed to reassess the distribution of embryo retention and viviparity across the species-rich group Clausiliidae (Phaedusinae).
Material and Methods
The material included shells on loan from the following museum collections and individual collectors:
MNHN (Museum National d’Histoire Naturelle, Paris, France; dry shells, mostly from the territory formerly known as French Indochina, among them the nineteenth-century collections of A. Bavay, P. Dautzenberg, and L. G. M. Messager);
MCZ (malacology collection; Museum of Comparative Zoology, Harvard University, Cambridge, USA; dry shells, mostly from Japan, among them the collection of Y. Hirase);
NHM (Natural History Museum, London, UK; alcohol-preserved specimens collected in Vietnam and China);
NBC (Naturalis Biodiversity Center, Leiden, the Netherlands; dry- and alcohol-preserved shells, among them samples from Indonesia from the collection of F. Loosjes);
MIIZ (Muzeum i Instytut Zoologii PAN, Warsaw, Poland; alcohol-preserved shells from China, Myanmar, and Thailand);
the private collections of M. Szekeres, E. Stworzewicz, W. Maassen, and A. Drozd.
Altogether, more than 1,000 Phaedusinae shells belonging to 141 taxa (138 species and three subspecies) were analysed (Fig. 3). The majority of material belonged to the species-rich tribe Phaedusini, whereas Serrulinini and Synprosphymini were represented by seven species each. The majority of shells (86%) had been stored dry; the rest were preserved in 70–96% ethanol.
For the sake of the consistency of the project, classification into genera after Nordsieck46 has been used throughout the text.
For shell examination, the non-destructive method of microcomputed X-ray tomography (micro-CT) was adopted. This technique enables the internal calcareous structure (e.g. embryonic shell) to be examined without destruction of specimens, and thus can be adapted to the study of valuable museum collections51. First, as a screening procedure, a single X-ray projection of each shell, generated by a micro-CT scanner, was obtained. This step alone enabled confirmation of the brooding reproduction mode and indication of the number and size of embryos. Second, gravid individuals were selected for acquisition of a series of X-ray images; subsequently, these projections were used to create three-dimensional models of internal structures of shells.
Depending on temporal availability, the following micro-CT scanners were used to acquire X-ray projections:
Skyscan 1172 micro-CT, Naturalis Biodiversity Center, Leiden, the Netherlands;
Zeiss Xradia MicroXCT-200, Institute of Paleobiology, Polish Academy of Sciences, Warsaw, Poland;
GE Phoenix v|tome|x s, X-ray Microtomography Lab, Faculty of Science and Technology, University of Silesia, Katowice, Poland.
The samples illustrated in the present paper were scanned at the University of Silesia using the following scanner settings: voltage, 90–200 kV; electric current, 100–180 µA; timing, 250 ms; 1000 projections; rotation angle, 360°; voxel size, 10–20 µm, depending on shell size. Finally, the projections were used to reconstruct 3D images of shell interiors with embryos. The 3D models were created in cooperation with Custom Medical Implants Laboratory in Łódź, equipped with Amira software (v. 5.5.0), FEI Visualization Sciences Group, USA, and Geomagic Studio 2014, 3D Systems, USA, and in cooperation with the Institute of Paleobiology, PAS, in Warsaw, equipped with Avizo 7.0 Fire Edition software.
The use of X-ray imaging enabled relatively rapid screening of over a thousand specimens from old collections, as well as the identification of 205 shells containing embryos or egg shells (Fig. 4; Supplementary Material), constituting 19% of X-rayed shells. In dry material, the proportion of gravid snails was 18% (169/936), whereas in alcohol-preserved samples the proportion was 23% (36/155). The difference between the two types of preservation is not significant (χ2, p > 0.05).
Gravid individuals (with embryos or eggs) occurred in 55 species (45 containing embryos, 10 containing egg shells).
Embryos were regularly found in species classified within the East and Southeast Asian genera Phaedusa, Euphaedusa, Reinia, Paraphaedusa, Renschiphaedusa, Parazaptyx, and Metazaptyx, albeit not in all examined individuals (Table 2). The number of embryos ranged from 1 to 12 per individual (usually from 1 to 5) (Fig. 4a–d); the size of embryonic shells reached 1.5–3 whorls (Fig. 5c,d). The greatest numbers of embryos were recorded for Euphaedusa aculus (12), E. digonoptyx (9), and Phaedusa hilberi (9). None of the species classified within the Synprosphymini or Ponto-Caspian Serrulinini tribes retained shelled embryos.
Selected species of other genera, e.g. Oospira javana, O. miranda, O. ferruginea, O. formosensis, O. philippiana, Hemiphaedusa exilis, and H. ooi, contained shelled embryos (Fig. 4e) or egg membranes with calcium crystals (Figs. 4f,h and 5f,h). Our findings proved that these species are capable of retaining fertilised eggs for at least a short time. Among them, O. miranda and O. philippiana (Fig. 5e,g) kept embryos with embryonic shells consisting of more than one whorl. Additionally, we recorded egg membranes/egg shells in Zaptyx dolichoptyx, Z. hirasei (Fig. 4g), Z. kikaiensis, Stereozaptyx exulans, and Serrulina sieversi. For these species, the evaluation of acquired images was not straightforward, as the eggs appeared to be unshaped or damaged, perhaps due to the conservation method.
The X-ray screening method adopted in this study enabled the verification of information concerning embryo retention in many snail taxa. The examined material comprises about 30% of identified Phaedusinae species, and thus should enable the reassessment of the distribution of reproductive modes within this subfamily. However, as we lack a complete phylogenetic framework for the studied group15,49, our conclusions are very cautious. Previously, the taxonomic system of the subfamily was based on shell characters13,52,53,54, some of which are probably related to the reproduction mode and its mechanical constraints. The significance of the reproductive mode in the relevant systematics was expressed explicitly by Nordsieck13, who recognised two tribes, Megalophaedusini and Phaedusini, with the latter characterised by synapomorphies correlated with ovoviviparity (a spirally ascending inferior lamella and a broad clausilium plate). The genera Phaedusa, Parazaptyx, Metazaptyx, Reinia, Renschiphaedusa, Paraphaedusa, and Euphaedusa, listed as members of Phaedusini13, were thus regarded as ovoviviparous. Brooding reproduction in these taxa was assumed based on the shape of the clausilial apparatus13, although findings of embryos have not been documented in all these species (Tables 1 and 2). Contrastingly, genera classified within Megalophaedusini were characterised by a steeply ascending inferior lamella and a narrow clausilium plate in common (Fig. 2). Later, the systematics of Phaedusinae were rearranged: most taxa were classified into Phaedusini, whereas some members of the former Megalophaedusini group were moved to a new tribe, Synprosphymini46. The problematic relationships within Phaedusinae were only partially resolved by the molecular phylogeny of the entire Clausiliidae family49, which showed that East and Southeast Asian Phaedusinae (only 6 species included) formed a single lineage with Ponto-Caspian Serrulininae, which had previously been regarded as a separate subfamily46. The recent molecular phylogeny of Japanese taxa also suggests that the Phaedusinae classification requires profound taxonomical revision15.
The X-ray screening of collections from East and Southeast Asia resulted in the finding of embryo-retaining species among taxa classified within Oospira and Hemiphaedusa (Figs. 4e,f,h and 5e–h) and previously attributed to oviparous Megalophaedusini13. Thus, the classification of Phaedusinae species into ovoviviparous and oviparous genera cannot be sustained. The presence of retained eggs in the uterus of O. javana32 also constituted evidence against this division, although the cited author, having observed egg-laying in his laboratory culture, finally classified the species as oviparous.
In a recent paper on the molecular phylogeny of Japanese clausiliids, the significance of reproductive adaptation in taxonomy was upheld15. The cited authors classified the species into two types of reproduction, ovoviviparity and oviparity. Among six main lineages of Japanese clausiliids, two include only oviparous taxa, two only ovoviviparous taxa; the remaining two include species employing both strategies. Altogether, ovoviviparity was indicated for 77 terminal tips (identified as 47 taxa), oviparity for 184 tips (128 taxa); 12 tips (10 taxa) were left with no reproductive strategy being attributed to them on the tree provided15. Our study overlaps with this dataset for 48 species. Based on museum collections, we confirmed brooding in 13 species classified as ovoviviparous by the Japanese team (Euphaedusa subaculus, E. tau, E. stearnsii, E. digonoptyx, E. digonoptyx comes, Metazaptyx hachijoensis, Phaedusa stereoma, P. sieboldtii, Reinia echo, R. hungerfordiana, R. monelasmus, R. euholostoma, R. variegata). On the other hand, our museum specimens of four species classified as ovoviviparous15 (Phaedusa neniopsis, Hemiphaedusa kanaganensis, Reinia holotrema, Zaptyx hyperoptyx) contained no embryos. It should be understood that the absence of embryos is not always informative. Soft parts may have been intentionally removed by shell collectors55, or snails may have been sampled during an unfavourable season25,28; these factors may explain false negatives in our results. In contrast, the occurrence of shelled embryos in the parental shell always proves the use of the brooding reproductive strategy. We found embryos or egg shells retained in 7 species (Stereozaptyx exulans, Parazaptyx thaumatopoma, Metazaptyx daemonorum, M. pattalus, Zaptyx dolichoptyx, Z. hirasei, and Z. kikaiensis) previously listed as oviparous15. Among these, individuals of P. thaumatopoma, M. daemonorum, and M. pattalus contained embryos with 1.5–2 whorls, which is usually indicative of true viviparous species. The brooding reproductive strategy of these three species was confirmed by Rei Ueshima (personal communication). Other species are likely to retain fertilised eggs only for a short time; their reproductive strategy is of an intermediate character. For the majority of old museum shell collections, information on the month of sampling was missing. Thus, we can draw no conclusions on the duration of the reproductive period in the embryo-retaining clausiliids of East and Southeast Asia, nor can we compare it with previous work on European clausiliids23,24,25. These questions can be addressed in research projects based on regular field sampling.
When data on viviparous or embryo-retaining taxa were plotted on the available molecular tree of Phaedusini49, it appeared that brooding must have evolved more than once in this tribe. The cited authors suggested that Euphaedusa (brooding) forms a clade with Megalophaedusa martensi (oviparous), from which Oospira miranda (brooding) and subsequently O. swinhoei (oviparous) branch off basally (Fig. 6). The cited paper did not resolve the relationships between O. miranda, O. swinhoei, and the remaining taxa49. It was also suggested that Oospira, as defined by Nordsieck46, is not monophyletic15. Phylogenetic analysis covering more Phaedusini taxa is needed in order to test the hypothesis on the repeated evolution of reproductive modes in this group. Concerning the tribes Serrulinini and Synprosphymini, no evidence for brooding was found in X-rayed shells, with the exception of an egg-like structure in Serrulina sieversi. The number of scanned individuals from these tribes and the records in the literature concerning their reproductive biology34,37 were too limited for the purpose of drawing a final conclusion. Moreover, Synprosphymini were not included in the cited molecular analysis49. A multilocus molecular phylogeny of Phaedusinae, based on sampling of a much wider range of taxa, is currently being prepared by the authors of the present paper.
The number of embryos found in the reproductive tract in Phaedusini was usually small and reached maxima of six for Phaedusa corticina, eleven for P. paviei and Euphaedusa tau31,32,36,38,39,56,57,58. The number of embryos found in X-rayed shells is in accord with the data from the literature given above. A single brood kept in the genital tract of some European clausiliids may contain even twice as many embryos14,23,29.
It has been widely accepted that the loss or significant reduction of apertural barriers in some clausiliids (e.g. in Balea perversa, Reinia variegata, and Macroptychia africana) is an adaptation to viviparous reproduction34,36,59. As a trade-off, the apertural barriers of these species ceased to perform a protective function. However, viviparity and embryo retention also occur among species with well-developed apertural barriers in several genera and subgenera occurring in Europe, namely among Alinda, Vestia, Pseudalinda, Cochlodina, Ruthenica, and Idyla14,23,28,30,60. Recent biometric studies based on X-ray microcomputed tomography demonstrated the existence of adaptive changes in apertural barriers in these taxa which involved the widening of the shell channel41. This suggests that the greater patency of the shell channel and aperture in viviparous clausiliids must have evolved as a convergence in taxonomically distant species to enable the delivery of shelled embryos41. Consequently, the patency of the shell channel (and the shape of the clausilium plate which mirrors its shape) should not be of taxonomical significance. Similarly, other shell characters, such as a neck keel and a clausilium with a calcar, originated via parallel evolution in several groups of Clausiliidae13.
The evolution of brooding reproductive adaptation within clausiliids requires further investigation, including analysis of molecular phylogeny and in-depth histological study of the reproductive tract and pattern of embryo provision. We have shown that micro-CT screening of museum collections is a reliable method which may yield the necessary data and enhance our ability to select species for further research on reproductive strategies in land snails.
Micro-CT screening of shell collections is an efficient method for testing evolutionary hypotheses concerning reproductive diversity in gastropods. We found that 1) the number of species characterised by viviparity or embryo retention in highly diversified clades of terrestrial pulmonates had been underestimated, and 2) clausiliid taxonomy based on shell characters related to viviparous reproduction should be carefully revised.
The datasets analysed during the current study are available from the corresponding author on reasonable request.
Buerki, S. & Baker, W. J. Collections-based research in the genomic era. Biol. J. Linn. Soc. 117, 5–10 (2016).
McLean, B. S. et al. Natural history collections-based research: progress, promise, and best practices. J. Mammal. 97, 287–297 (2016).
Lawing, A. M. & Polly, P. D. Geometric morphometrics: recent applications to the study of evolution and development. J. Zool. 280, 1–7 (2010).
Faulwetter, S., Vasileiadou, A., Kouratoras, M., Dailianis, T. & Arvanitidis, C. Micro-computed tomography: Introducing new dimensions to taxonomy. ZooKeys 263, 1–45 (2013).
Caro, A., Gomez-Moliner, B. J. & Madeira, M. J. Integrating multilocus DNA data and 3D geometric morphometrics to elucidate species boundaries in the case of Pyrenaearia (Pulmonata: Hygromiidae). Mol. Phylogent. Evol. 132, 194–206 (2019).
Jochun, A., Yu, T. & Neubauer, T. A. First record of the Paleozoic land snail family Anthracopupidae in the Lower Jurassic of China and the origin of Stylommatophora. J. Paleontol. https://doi.org/10.1017/jpa.2019.68 (2019).
Vo, A.-T. E., Bank, M. S., Shine, J. P. & Edwards, S. V. Temporal increase in organic mercury in an endangered pelagic seabird assessed by century-old museum specimens. PNAS 108, 7466–7471 (2011).
Hallmann, N., Burchell, M., Brewster, N., Martindale, A. & Schöne, B. R. Holocene climate and seasonality of shell collection at the Dundas Islands Group, northern British Columbia, Canada - A bivalve sclerochronological approach. Palaeogeogr. Palaeocl. 373, 163–172 (2013).
Tompa, A. S. Oviparity, egg retention and ovoviviparity in Pulmonates. J. Moll. Stud. 45, 155–160 (1979).
Tompa, A. S. Studies on the reproductive biology of gastropods: Part 1. The systematic distribution of egg retention in the subclass Pulmonata (Gastropoda). J. Malacol. Soc. Austral. 4, 113–120 (1979).
Heller, J. Life history strategies in The biology of terrestrial molluscs (ed. Barker, G. M.) 413–445 (CABI Publishing, 2001).
Blackburn, D. G. Viviparity and oviparity: evolution and reproductive strategies in Encyclopedia of reproduction (ed. Knobil, T. E. & Neill, J. D.) 994–1003 (Academic Press, 1999).
Nordsieck, H. Revision of the system of the Phaedusinae from mainland China with the description of new taxa. Arch. Molluskenkd. 129, 25–63 (2001).
Maltz, T. K. & Sulikowska-Drozd, A. Life cycles of clausiliids of Poland – knowns and unknowns. Ann. Zool. 58, 857–880 (2008).
Motochin, R., Wang, M. & Ueshima, R. Molecular phylogeny, frequent parallel evolution and new system of Japanese clausiliids land snails (Gastropoda: Stylommatophora). Zool. J. Linn. Soc. 181, 795–845 (2017).
Blackburn, D. G. Review: discrepant usage of the term “ovoviviparity” in the herpetological literature. Herpetol. J. 4, 65–72 (1994).
Solem, A. Tekoulina, a new viviparous tornatellinid land snail from Raratonga, Cook Islands. Proc. Malacol. Soc. Lond. 40, 93–114 (1972).
Ostrovsky, A. N. et al. Matrotrophy and placentation in invertebrates: a new paradigm. Biol. Rev. Camb. Philos. Soc. 91, 673–711 (2016).
Tompa, A. S. Land snails (Stylommatophora) in The Mollusca, vol. 7, Reproduction (eds. Tompa, A. S., Veronk, N. H. & van den Biggelaar, J. A. M.) 47–140 (Academic Press, 1984).
Baur, B. Parental care in terrestrial gastropods. Experientia 50, 5–14 (1994).
Schileyko, A. A. Treatise on Recent Terrestrial Pulmonate Molluscs. Ruthenica, Suppl. 2 (2003).
Uit de Weerd, D. R., Groenenberg, D. S. J., Schilthuizen, M. & Gittenberger, E. Reproductive character displacement by inversion of coiling in clausiliid snails (Gastropoda, Pulmonata). Biol. J. Linn. Soc. 88, 155–164 (2006).
Sulikowska-Drozd, A. Egg-retention and ovoviviparity in clausiliids of the genus Vestia P. Hesse (Gastropoda: Clausiliidae). J. Mollus. Stud. 75, 351–359 (2009).
Mamatkulov, A. L. Breeding biology of some East European Clausiliidae species (Mollusca, Pulmonata). Zool. Zh. 86, 403–414 (2007).
Sulikowska-Drozd, A., Maltz, T. K. & Kappes, H. Brooding in temperate zone land snail: seasonal and regional patterns. Contrib. Zool. 82, 85–94 (2013).
Szybiak, K., Gabala, E. & Lesniewska, M. Reproduction and shell growth in two clausiliids with different reproductive strategies. Biologia 70, 625–631 (2015).
Marzec, M. Life cycle and growth of Bulgarica cana (Held, 1836) under laboratory and natural conditions. J. Conch. 43, 149–166 (2018).
Sulikowska-Drozd, A., Apostolopoulou, K., Giokas, S. & Schilthuizen, M. Viviparous reproduction in the land snail Idyla (Pulmonata: Clausiliidae) from Greece: a disadvantageous inheritance? J. Moll. Stud. 85, 262–270 (2019).
Sulikowska-Drozd, A., Maltz, T. K. & Stachyra, P. Egg retention in the clausiliid Balea (Pseudalinda) fallax (Rossmässler, 1836) from Roztocze (S. E. Poland). Folia Malacol. 20, 35–38 (2012).
Sulikowska-Drozd, A. & Maltz, T. K. Reproductive strategy in rock-dwelling snail Cochlodina orthostoma (Gastropoda: Pulmonata: Clausiliidae). Biologia 71, 1353–1360 (2016).
Loosjes, F. E. & Loosjes-van Bemmel, A. C. W. On Phaedusa paviei Morlet and an allied new species. Basteria 13, 31–35 (1949).
Loosjes, F. E. Monograph of the Indo-Australian Clausiliidae. Beaufortia 31, 1–226 (1953).
Loosjes, F. E. & Loosjes-van Bemmel, A. C. W. Some anatomical and systematic data on Asiatic Clausiliidae (Gastropoda, Pulmonata). Ann. Zool. 30, 1–32 (1973).
Likharev, I. M. Klauziliidy (Clausiliidae). Fauna SSSR, N. S. 83, Mollyuski III, 4. (Moskva-Leningrad, 1962).
Nishi, K. The oviparity and ovoviviparity of clausilids. The Reports of the Kyushu Mollusk Study. Society 14, 19–22 (1980).
Minato, H. Genital Studies of the Japanese land Snails – XXI. Clausiliidae (7): The Genus Pictophaedusa. Venus 42, 331–343 (1983).
Páll-Gergely, B. & Nemeth, L. Observation on the breeding habits, shell development, decollation and reproductive anatomy of Pontophaedusa funiculum (Mousson 1856) (Gastropoda, Pulmonata, Clausiliidae, Phaedusinae). Malacol. Bohemosl. 7, 11–14 (2008).
Sulikowska-Drozd, A., Chiżyńska, A. & Maltz, T. K. The reproductive strategies of clausiliid land snails from Northern Vietnam (Gastropoda: Stylommatophora). J. Nat. Hist. 52, 1785–1799 (2018).
Sulikowska-Drozd, A., Hirano, T., Wu, S. P. & Páll-Gergely, B. High fecundity, rapid development and selfing ability in three species of viviparous land snails Phaedusinae (Gastropoda: Stylommatophora: Clausiliidae) from East Asia. Zool. Stud. 57, 38, https://doi.org/10.6620/ZS.2018.57-38 (2018).
Nordsieck, H. Annotated check-list of the South East Asian Phaedusinae, with the description of new taxa (Gastropoda, Pulmonata, Clausiliidae). Basteria 66, 85–100 (2002).
Sulikowska-Drozd, A., Walczak, M. & Binkowski, M. Evolution of shell apertural barriers in viviparous land snails (Gastropoda: Pulmonata: Clausiliidae). Can. J. Zool. 92, 205–213 (2014).
Gittenberger, E. Adaptation of the aperture in terrestrial gastropod-pulmonate shells. Neth. J. Zool. 46, 191–205 (1996).
Pokryszko, B. M. Land snail apertural barriers – adaptation or hindrance? (Gastropoda: Pulmonata). Malakol. Abh. Staatl. Mus. Tierkd. Dresden 18, 239–248 (1997).
Moorsel, V. C. H. M., Dijkstra, E. G. M. & Gittenberger, E. Molecular evidence for repetitive parallel evolution of shell structure in Clausiliidae (Gastropoda, Pulmonata). Mol. Phylogenet. Evol. 17, 200–208 (2000).
Uit de Weerd, D., Piel, D. R. & Gittenberger, E. Widespread polyphyly among Alopiinae snail genera: when phylogeny mirrors biogeography more closely than morphology. Mol. Phylogent. Evol. 33, 533–548 (2004).
Nordsieck, H. Worldwide door snails (Clausiliidae), recent and fossil. (ConchBooks, 2007).
Hunyadi, A. & Szekeres, M. New taxa and distribution data of Clausiliidae (Gastropoda: Pulmonata) from Southeastern China. J. Conch. 42, 129–150 (2016).
Páll-Gergely, B. & Szekeres, M. New and little-known Clausiliidae (Gastropoda: Pulmonata) from Laos and Southern Vietnam. J. Conch. 42, 507–521 (2017).
Uit de Weerd, D. & Gittenberger, E. Phylogeny of the land snail family Clausiliidae (Gastropoda: Pulmonata). Mol. Phylogent. Evol. 67, 201–216 (2013).
Bouchet, P. et al. Revised Classification, Nomenclator and Typification of Gastropod and Monoplacophoran Families. Malacologia 61, 1–526 (2017).
Sutton, M. D. Tomographic techniques for the study of exceptionally preserved fossils. Proc. R. Soc. B 275, 1587–1593 (2008).
Zilch, A. Die Typen und Typoide des Natur-Museums Senckenberg, 12: Mollusca, Clausiliidae (1): Phaedusinae, Neniinae. Arch. Molluskenkd. 83, 1–63 (1954).
Minato, H. Taxonomy and Distribution of the Land Snail Family Clausiliidae (Gastropoda: Pulmonata) of Japan. Venus, Suppl. 2, 1–212 (1994).
Nordsieck, H. Critical revision of the system of the Japanese Phaedusinae, proposed by Minato (1994). Arch. Molluskenkd. 127, 21–32 (1998).
Fukuda, H., Haga, T. & Tatara, Y. Niku-nuki: a useful method for anatomical and DNA studies on shell bearing molluscs. Zoosymposia 1, 15–38 (2008).
Chang, K. M. Reinia (Proreinia) eastlakeana tayalis Kuroda, 1941 from the mountain side of Urai, Northern Taiwan (Pulmonata: Clausiliidae). Bull. Malacol. ROC. 8, 19–25 (1981).
Azuma, M. Colored illustrations of the land snails of Japan. (Hoikusha Publishing Co., LTD, 1982).
Chen, D. Three new species of the genus Phaedusa from China (Pulmonata: Stylommatophora: Clausiliidae). Acta Zootaxon. Sin. 19, 412–418 (1994).
Neubert, E. The non-Alopiine Clausiliidae of Africa, with a note on Clausilia giraudi Bourguignat (Mollusca, Stylommatophora: Clausiliidae) in Collectanea Malacologica, Festschrift fur Gerhard Falkner (eds. Falkner, M., Groh, K. & Speight, M. C. D.) 253–275 (Conchbooks, 2002).
Szybiak, K. Ruthenica filograna (Rossmässler, 1836) (Gastropoda: Pulmonata: Clausiliidae). Structure, variation, life cycle, ecology and distribution (Kontekst, 2010).
The research was founded by Polish National Science Centre (NCN project no. 2016/21/B/NZ8/03086). We are grateful for collections’ managers: Jeroen Goud (NBC), Adam Baldinger (MCZ), Virginie Heros and Phillipe Maestri (MNHN), Jonathan Ablett (NHM), and Dominika Mierzwa-Szymkowiak (MIIZ) for the access to the material. Microtomography analyses were performed: 1. at Naturalis Biodiversity Centre, Leiden, during a Synthesis Scholarship (NL-TAF-5042) granted to A.S.-D., with Menno Schilthuizen as a host, 2. in the NanoFun laboratories at the Institute of Paleobiology, PAS Warsaw, co-financed by the European Regional Development Fund within the Innovation Economy Operational Programme POIG.02.02.00-00-025/09, 3. At the Faculty X-ray Microtomography Lab, Faculty of Science and Technology, University of Silesia in Katowice, Poland. 3D visualization were performed by Ms. Michalina Urbaniak from Custom Medical Implants Lab, Molecular and Nanostructural Biophysics Laboratory, Lodz Regional Science and Technology Park.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Sulikowska-Drozd, A., Duda, P. & Janiszewska, K. Micro-CT screening of old shell collections helps to understand the distribution of viviparity in the highly diversified clausiliid clade of land snails. Sci Rep 10, 60 (2020). https://doi.org/10.1038/s41598-019-56674-7