Eleonora's falcon (Falco eleonorae Géné, 1839) is a well-known long-distance migrant of the Afro-Palaearctic flyway, a summer breeder of the Mediterranean region and North-west Africa and a winter resident of Madagascar and surrounding areas, thus characterized as a double endemic. Within the context of a long-term monitoring and conservation programme on Antikythira Island, Greece, which accommodates one of the largest concentrations of breeding pairs of Eleonora's falcons globally, birds were subjected to regular inspections for the presence of ticks from 2017 to 2023. In total, 104 adults and 149 nymphs (all belonging to Haemaphysalis genus) were collected. All ticks, apart from 2 nymphs, exhibited broadly salient palpi and did not possess the pronounced palpal segment 2 spurs or spur-like angles that are characteristic of adults, nymphs and most larvae of Rhipistoma, thus placed them in the Ornithophysalis subgenus. Following comprehensive morphological assessment and genetic analysis of the mitochondrial genome by means of next-generation sequencing of both adult and nymphal stages of the ticks, our empirical findings substantiate the delineation of a previously unclassified species. This taxonomic assignment situates the newly described species within the Ornithophysalis subgenus and the Haemaphysalis doenitzi group, marking its presence for the first time within the Western Palaearctic region.

The new species Abarenicola wellsi n. sp. from the Falkland Islands is described along with a re-description of Abarenicola brevior n. stat. with which it had previously been confused. The two species are distinguished using both morphological and molecular techniques, new characters are described and previously recognized characters are clarified, all of which support the assignment of species status as opposed to subspecies. Both species are part of the Abarenicola assimilis ‘group’ within which all taxa were originally described as subspecies. The group as a whole is re-evaluated and all members are elevated from subspecies to species status based mainly on the new characters of shape, distribution and pigmentation of the proboscidial papillae. The group now consists of six species: Abarenicola assimilis n. stat., A. brevior n. stat., Abarenicola devia n. stat., Abarenicola haswelli n. stat., Abarenicola insularum n. stat. and A. wellsi n. sp.

The complete larval development of the lobster shrimp Leonardsaxius amurensis (Kobjakova, 1937) (Decapoda: Axiidea: Axiidae) is described and illustrated for the first time. The first zoeae of this species were collected from the plankton samples and reared in the laboratory before moulting to the megalopa. A molecular genetic analysis based on comparison of partial mitochondrial COI, 12S rDNA and 16S rDNA sequence data confirmed the identity of axiid larvae found in the plankton and L. amurensis adults collected in the same area. The larval development of L. amurensis includes five zoeal stages and a single megalopa. Zoeae I of L. amurensis are characterized by the presence of one short posterodorsal spine on the fifth pleonite in contrast to the larvae of related sympatric species Boasaxius princeps having four posterodorsal spines on the pleonites 2–5. Leonardsaxius amurensis occupies an intermediate position between lobster shrimps with abbreviated pelagic development (2–3 zoeal stages) and species with long development (up to eight zoeal stages). Thus, the number of zoeal stages in the family Axiidae varies widely, similarly to that in the families Callianassidae and Upogebiidae.

Analysis of mitochondrial (16S) and nuclear (H3) gene data using phylogenetic and population genetic approaches has revealed some genetic differences between two putative species of western Atlantic Dondice opisthobranchs that feed differentially on hydroids or on up-side-down jellies of the genus Cassiopeia. These results partially support the validity of the species Dondice parguerensis, which was described for the jelly-eating Dondice. However, phylogenetic analyses revealed that the hydroid-feeding species Dondice occidentalis and D. parguerensis are not reciprocally monophyletic and they are identical for the nuclear H3 gene. Although there are morphological and developmental differences between these two nominal species, the molecular data are inconclusive. A possible explanation is that the two putative species are in the process of speciation due to different feeding habits, resulting in the presence of genetic synapomorphies in D. parguerensis, but only in the more variable 16S gene. Because the ranges D. occidentalis and D. parguerensis overlap and there are no obvious barriers to gene flow between the two putative species, this may constitute a possible example of incipient sympatric speciation in benthic marine organisms.

Recent studies have shown that some digenean trematodes previously identified as single species due to the lack of distinguishing morphological characteristics actually consist of a number of genetically distinct cryptic species. We obtained mitochondrial 16S and nuclear ITS1 sequences for the redial stages of Acanthoparyphium sp. and Curtuteria australis collected from snails and whelks at various locations around Otago Peninsula, New Zealand. These two echinostomes are well-known host manipulators whose impact extends to the entire intertidal community. Using phylogenetic analyses, we found that Acanthoparyphium sp. is actually composed of at least 4 genetically distinct species, and that a cryptic species of Curtuteria occurs in addition to C. australis. Molecular data obtained for metacercariae dissected from cockle second intermediate hosts matched sequences obtained for Acanthoparyphium sp. A and C. australis rediae, respectively, but no other species. The various cryptic species of both Acanthoparyphium and Curtuteria also showed an extremely localized pattern of distribution: some species were either absent or very rare in Otago Harbour, but reached far higher prevalence in nearby sheltered inlets. This small-scale spatial segregation is unexpected as shorebird definitive hosts can disperse trematode eggs across wide geographical areas, which should result in a homogeneous mixing of the species on small geographical scales. Possible explanations for this spatial segregation of the species include sampling artefacts, local adaptation by first intermediate hosts, environmental conditions, and site fidelity of the definitive hosts.

The notothenid species Trematomus bernacchii has previously been shown, by allozyme analysis, to be a complex of two cryptic species, one of which being more closely related to T. hansoni than to the other T. bernacchii cryptic species. Two T. bernacchii colour morphs, “white blotch” and “brown”, at McMurdo Sound, may correspond to these cryptic species. In this study, we present mitochondrial DNA sequences of the 12S and 16S ribosomal regions for six “white blotch” morphs, eight “brown” morphs collected in McMurdo Sound, one individual collected off the Antarctic Peninsula, and two T. hansoni individuals from McMurdo Sound. These sequences were compared with those of T. bernacchii and T. hansoni in the literature. Based on 14 phylogenetically informative sequences, no differences were found between “white blotch” and “brown” morphs. Furthermore, only one substitution separated these sequences from the previously published T. hansoni sequence, while 10 substitutions separated them from the previously published T. bernacchii sequence. Misidentified specimens, and sequence misreadings may be at the origin of these discrepancies. However, the presence of cryptic species within T. bernacchii and T. hansoni is not ruled out.