The family Moitessieriidae includes minute dioecious gastropods exclusively inhabiting subterranean waters, including thermal ones. Only empty shells were collected in most species, the vast majority of them are described from their gross shell morphology alone. Several visits to a site are usually required to obtain at least some living individuals. High variability in shell morphology and the lack of diagnostic features, coupled with anticipated high levels of endemism, has resulted in a long list of nominal moitessierid species. Type specimens stored as empty shells omit unambiguous identification and delimitation of species boundaries. Due to inaccessibility of cave animals and consequent lack of material suitable for molecular analysis, the phylogenetic relationships, as well as the taxonomy of the family at genus/species level, are far from being understood. The anatomy of the family is also poorly known and provided only for a few taxa. The distinctness of the Moitessieriidae has sometimes been questioned, and their monophyly not proved. Twelve species of the Balkan Moitessieriidae are considered: two species of Paladilhiopsis, two species of Bythiospeum, six species of Iglica, Costellina turrita and Lanzaia bosnica. The shell morphology of each species, as well as the reproductive system of Paladilhiopsis and Iglica, were analysed. DNA sequences of nuclear histone H3, ribosomal 18S, ribosomal 28S and mitochondrial cytochrome oxidase subunit I (COI) were applied to infer phylogenetic relationships among the taxa. The sequences of Bythiospeum from GenBank have been used to infer relationships between Bythiospeum and Paladilhiopsis that were recently synonymized. Paladilhiopsis and Iglica are distinct, but closely related genera, as is the genus Bythiospeum, which does not occur in the Balkans. Its relationships with both former taxa remain unresolved. The Moitessieriidae are clearly distinct from all other families of the Truncatelloidea, however, their monophyly remains doubtful.

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Freshwater truncatelloidean gastropods include numerous minute cryptic species, displaying simple morphologies, all of which hampers their taxonomic research based on morphology. Phylogenetic relationships among all but one extant species of the genus Kerkia from five localities in Croatia and one in Slovenia were therefore analysed based on one mitochondrial (cytochrome c oxidase subunit I) and three nuclear markers (18S, 28S and H3). Kerkia kusceri (Bole, ), K. jadertina Kuščer, 1933, K. j. sinjana (Kuščer, 1933), and K. kareli Beran, Bodon et Cianfanelli, 2014, were collected from their type localities. Our analysis confirmed their distinctness, recovering two additional clades that may represent yet undescribed species from Croatia. Apart from Kerkia, Hauffenia media Bole, , H. subpiscinalis (Kuščer, 1932) and H. erythropomatia (Hauffen, 1856) from Slovenia were analysed. Their distinctness together with the rejection of the eligibility for separate genus Erythropomatiana for the latter species was proven. Interestingly, its sequence divergence exceeded all previous estimates for species‐level divergence within the Truncatelloidea, implying a species‐level separation both for the COI and for nuclear loci. High p‐distances for the COI/nuclear loci (0.128/0.027, respectively) confirmed also the uniqueness of both genera. A comparison of their COI sequences with the reference sequences of Alzoniella Giusti et Bodon, 1984, Avenionia Nicolas, 1882, Fissuria Boeters, 1981, and Agrafia Szarowska et Falniowski, 2011, has shown that Kerkia and Hauffenia are not sister clades. The most striking, however, was the apparent introgression of the ‘Hauffenia’ mtDNA type from central Slovenia (cave Babja luknja) into two Kerkia clades from central (Ljubač) and southern (Podgrađe) Croatia, that are located 210 km and 360 km away, respectively. The introduced ‘Hauffenia’ mtDNA type and the closest Hauffenia erythropomatia COI differed by 0.8%. Secondary loss of isolating mechanisms between phylogenetically distant organisms and the severe lack of information on distribution of these underground taxa were postulated as possible explanations of this interesting phenomenon.

Eisenia andrei (Ea) and E. fetida (Ef) lumbricid earthworms are simultaneous hermaphrodites potentially capable of self-fertilization and hybridization. We have shown previously that reproductive isolation in these species is incomplete in Ea and Ef earthworms of French provenance, as viable offspring appeared in inter-specific pairs. Fertile asymmetric hybrids developed from Ea-derived ova fertilized by Ef-derived spermatozoa, as well as Ea or Ef specimens derived after self-fertilization (resulting from admixture of endogenously produced spermatozoa with sperm from a partner), but never Ef-hybrids from Ef-ova fertilized by Ea-spermatozoa. The latter appeared only in backcrosses of Ea-hybrids with the Ef. Here we show that these phenomena are not unique for French Ea/Ef earthworms, but are shared by earthworms from French, Hungarian, and Polish laboratory cultures. Semi-quantitative studies on fertility of Ea-derived hybrids revealed gradually decreasing numbers of offspring in three successive generations, more rapid in backcrosses with Ef than with Ea, and the absence of progeny in pairs of hybrids, despite the presence of cocoons in almost all pairs. Based on species specific mitochondrial and nuclear DNA sequences, we provide the first examples of two unique sterile hybrids with mitonuclear mismatch and potential mitonuclear incompatibility among offspring of one of the hybrid+Ef pairs. Earthworms from the investigated populations did not reproduce when kept from hatching in isolation or with representatives of Dendrobaena veneta but started reproducing upon recognition of a related partner, such as Ea, Ef or their hybrids. The existence of Ea or Ef specimens among offspring of hybrid+Ea/Ef pairs might be explained either by partner-induced self-fertilization

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