The world's biodiversity is in peril. The major threats to biodiversity globally are habitat change, overexploitation, climate change, invasive species and pollution. Not only do these stressors impact free-living organisms, but they affect parasitic ones as well. Herein, this perspective examines the potential consequences of these anthropogenic perturbations on helminth populations and communities, with emphasis on significant developments over the past decade. Furthermore, several case studies are examined in more detail for each of these threats to biodiversity. While effects are widespread and diverse, for the most part all these environmental stressors have negative effects on parasite populations and communities. Those parasites with complex life cycles that are trophically transmitted are often more at risk, although larval parasites with a wide host spectrum, and directly transmitted ectoparasites, appear less threatened and may even benefit. However, differential effects on hosts and parasites, on parasite life cycle stages and on host–parasite interactions made specific predictions difficult and context-dependent. Experimental laboratory and mesocosm studies on specific parasites that test effects on the different life cycle stages, hosts and host–parasite interactions, permitting the determination of net effects of an environmental stressor, yield insightful and sometimes counterintuitive results, although they remain a simplification of real-world complexity. Recent advances in the use of parasites as bioindicators of effects also are discussed.

The best way to study digenean diversity combines molecular genetic methods, life-cycle studies and elaborate morphological descriptions. This approach has been barely used for one of the most widespread digenean taxa parasitizing fish – the superfamily Hemiuroidea. Here, we applied the integrative approach to the hemiuroideans from the family Derogenidae parasitizing fish at the White and Barents Seas. Analysis of 28S, 18S, 5.8S rDNA, ITS2 and cox1 gene sequences from sexually adult worms (maritae) showed genetic heterogeneity for 2 derogenid species known from this area: Derogenes varicus and Progonus muelleri. Thus, 2 pairs of genetic lineages were found: DV1 and DV2, PM1 and PM2, respectively. Data from other regions indicate that 2 more lineages of D. varicus probably exist. Based on previous records from the White and Barents Seas, we hypothesized that the cercariae found in the moonsnails (family Naticidae) belong to the Derogenidae and may help to differentiate these lineages as species. According to our results, Cercaria appendiculata from Cryptonatica affinis matched DV1, similar nameless cercariae from Euspira pallida and Amauropsis islandica matched DV2, and Cercaria octocauda from C. affinis matched PM1. We provide new data on the structure of these cercariae and discuss the life-cycle pattern of the studied digeneans.

Morphological discrimination of species is problematic in many digenean taxa. Parasites of marine fish from the genus Lecithaster Lühe, 1901 are a good example of this. Our goal was to understand which species of Lecithaster infect fish in the White Sea, and reveal their life cycles. We collected specimens of maritae from nine fish species, analysed their morphology and sequenced 28S ribosomal DNA and internal transcribed spacer 2 (ITS2). Contrary to previous accounts, all of them belong to a single species, Lecithaster salmonis Yamaguti, 1934, which was previously only recorded from the Pacific. Morphologically, our maritae specimens were highly variable, sharing characters of L. salmonis, Lecithaster confusus Odhner, 1905 and Lecithaster gibbosus (Rudolphi, 1802) Lühe, 1901. This variability did not correlate with the moderate differences in ITS2 among the specimens, and neither did the fish host species. Members of the subfamily Salmoninae appear to be the best suited definitive hosts, judging from the intensity rates. The intermediate hosts were also discovered: the first is Cryptonatica affinis (Gmelin, 1791) and the second are planktonic copepods. These lifecycle data from the White Sea are consistent with L. salmonis species identification and with the distribution of this species in the North Pacific. The geographical range of L. salmonis seems to be interrupted, and we discuss possible ways of L. salmonis expansion.

Of over 250 species of Monorchiidae Odhner, 1911, just four are known from gerreid fishes. Here, we report adult specimens of a new species infecting Gerres oyena (Forsskål) and Gerres subfasciatus Cuvier from off Heron Island and North Stradbroke Island, Queensland, Australia. The species is morphologically most similar to the concept of Lasiotocus Looss, 1907, which currently comprises eight species, in the possession of an unspined genital atrium, bipartite terminal organ, round oral sucker and unlobed ovary. However, phylogenetic analyses of the 28S ribosomal DNA gene region shows the species to be distantly related to the two sequenced species of Lasiotocus – Lasiotocus mulli (Stossich, 1883) Odhner, 1911 and Lasiotocus trachinoti Overstreet & Brown, 1970 – and that it clearly requires a distinct genus; thus, we propose Gerricola queenslandensis n. g., n. sp. Morphologically, G. queenslandensis n. g., n. sp. differs significantly from L. mulli and L. trachinoti only in the possession of distinctly longer caeca, which terminate in the post-testicular region, and in the absence of a distinct gap in the terminal organ spines. The remaining species of Lasiotocus possess caeca that also terminate in the post-testicular region, which might warrant their transfer to Gerricola n. g. However, doubt about their monophyly due to a combination of significant morphological variation, a lack of information on some features and infection of a wide range of hosts, lead us to retain these taxa as species of Lasiotocus until molecular sequence data are available to better inform their phylogenetic and taxonomic positions. Sporocysts and cercariae of G. queenslandensis n. g., n. sp. were found in a lucinid bivalve, Codakia paytenorum (Iredale), from Heron Island. Sexual adult and intramolluscan stages were genetically matched with the ITS2 ribosomal DNA and cox1 mitochondrial DNA regions. This is the second record of the Lucinidae as a first intermediate host for the Monorchiidae. Additionally, we report sporocysts and cercariae of another monorchiid infection in a tellinid bivalve, Jactellina clathrata (Deshayes), from Heron Island. Molecular sequence data for this species do not match any sequenced species and phylogenetic analyses do not suggest any generic position.

The man in-the-street who frequently asks the question “Why am I here?” finds even more difficulty with the question “Why are parasites here?” The public's distaste for parasites (and by implication, for parasitologists!) is therefore understandable, as maybe was the feeling of early 20th century biologists that parasites were a puzzle because they did not conform to the then widely held association between evolution and progress, let alone the reason why a benevolent Creator should have created them. In mid-century, the writer, contemplating a career in parasitology was taken aback when he found that extolled contemporary biologists disdained parasites or thought little of parasitology as an intellectual subject. These attitudes reflected a lack of appreciation of the important role of parasites in generating evolutionary novelty and speciation, also unawareness of the value of parasite life-cycle studies for formulating questions of wider significance in biology, deficiencies which were gratifyingly beginning to be remedied in the latter half of the century.

The infestation of Weddell seals and several fish species by the anisakid nematodes Contracaecum osculatum and C. radiatum was compared. Nematode numbers in Weddell seal stomachs ranged from 30 560 to 122 640. Third stage larvae from seals and fish were separated into a short and a long type. The short type was related to C. radiatum and the long type to C. osculatum. The short type was more abundant in pelagic fish species, whereas the long type prevailed in benthic fish species. Fish-feeding channichthyids Cryodraco antarcticus and Chionodraco myersi seemed to play an important role as paratenic hosts for the third stage larvae of both Contracaecum species. Different advantageous and detrimental features of a benthic versus a pelagic life cycle under high Antarctic ecological conditions are discussed. Varying abundance of the two nematode species in hosts may be controlled by differences in their life cycles, which follow either a pelagic or a benthic food web. Crucial importance is thus given to the local availability of pelagic versus benthic food resources for Weddell seals.

Time series (1965-1985) of Illex illecebrosus catch and morphometric data from the Northwest Atlantic were analysed to describe geographic variability in population structure. The areas studied were NAFO sub-areas 3 to 6, which range from Newfoundland to the northeastern USA shelf. Population components, reflecting seasonal spawning groups, were identified based on analysis of length frequency data. Components 3 and 4 represent two prominent life cycles: the summer spawners and winter spawners respectively. Components 1, 2, and 5 do not represent different life cycles, but result from the capacity to shift between life cycles by prolonging (or shortening) the life span. The presence of up to five components in the southern area illustrates a life history strategy involving protracted spawning and complex population structure. There was clear geographic variability in annual catch, with fluctuations being most extreme in the most northern area. Annual catch levels in all areas were significantly correlated with the abundance of the winter-spawning component, as represented by the number of squid within samples which belong to component 4. Population structure in the most northem area was simplest and catch levels therefore were most dependent on the highly migratory winter-spawning component. This leads to greater catchvariability in the most northern area than in the other areas. The advantages of good feeding conditions may compensate for the risks associated with long-range migrations, especially recruitment failure. Life history strategies involving migratory and non-migratory population components limit the risk of recruitment failure. The overall resultant life history strategy for Illex illecebrosus is one that ensures survival of the species by stabilizing recruitment in at least one (southern) area through protracted spawning, complex population structure and interaction of spawning components.

The band-legged ground cricket group comprises a pair of very closely related species; Dianemobius fascipes occurs widely over tropical and subtropical regions of Southeast Asia, while D. nigrofasciatus is restricted to temperate regions. A similar situation is found in the lawn ground cricket group; the tropical/subtropical species D. taprobanensis is replaced by D. mikado in temperate regions. In both southern species, tropical strains were almost homodynamic, but they produced a few delayed eggs independently of photoperiod and a variable proportion of macropters in response to photoperiod; subtropical strains showed clearer responses. Both northern species controlled egg diapause, nymphal development and wing form by various photoperiodic responses. The two species groups showed parallel geographical profiles of size variation, and the adults and eggs were smaller in the southern than in the northern species. In the absence of strong climatic selection for larger growth rate, size increase in tropical regions would be counteracted by predation pressure. The optimal adult size thus seems to be smaller in tropical than in temperate regions, being determined by the geographically variable balance between counteracting selecting forces.