A new species of Bivesiculoides (Digenea: Bivesiculidae) infecting atherinid fishes of the Great Barrier Reef, Queensland, Australia.

We describe a new species of Bivesiculidae, Bivesiculoides maiae n. sp., from Hypoatherina tropicalis (Whitley) (Atherinidae) collected from off Heron Island (southern Great Barrier Reef, Queensland, Australia). Bivesiculoides maiae n. sp. is morphologically consistent with Bivesiculoides Yamaguti, 1938 in the entirely pre-testicular position of its uterus, and the possession of caeca and vitelline fields that extend posteriorly to level with the anterior extremity of the testis. The new species is morphologically distinct from the six known Bivesiculoides species in body size and shape, and shape of the pharynx and testis. Bivesiculoides maiae n. sp. is genetically distinct from the only other sequenced Bivesiculoides species, Bivesiculoides fusiformis Cribb, Bray & Barker, 1994, with which it occurs sympatrically at Heron Island. A review of related species allows two systematic recombinations. In view of the pre-testicular position of its uterus, we recombine Bivesicula hepsetiae Manter, 1947 as Bivesiculoides hepsetiae (Manter, 1947) n. comb. In view of its obtriangular body shape, round pharynx, strongly elongated testis, and the position of its ovary opposite the testis, we recombine Bivesiculoides triangularis Machida & Kuramochi, 2000 as Treptodemoides triangularis (Machida & Kuramochi, 2000) n. comb. Host-specificity of species of Bivesiculoides and their geographic distributions are discussed.

The oceanic pleuston community as a potentially crucial life-cycle pathway for pelagic fish-infecting parasitic worms.

Pleustonic organisms form an important part of pelagic ecosystems by contributing to pelagic trophic chains and supporting connectivity between oceanic habitats. This study systematically analysed the trematode community harboured by pleustonic molluscs and cnidarians from offshore Queensland, Australia. Four mollusc and three cnidarian species were collected from beaches of North Stradbroke Island, Queensland. Two mollusc species and all three cnidarians harboured large numbers of hemiuroid metacercariae (Trematoda: Hemiuroidea). Eight taxa from four hemiuroid families (Accacoeliidae, Didymozoidae, Hemiuridae and Sclerodistomidae) were distinguished via molecular sequencing. Four of those taxa were identified to species. All trematode taxa except one didymozoid were shared by two or more host species; five species occurred in both gastropods and cnidarians. It is hypothesised that the life-cycles of these hemiuroids are highly plastic, involving multiple opportunistic pathways of metacercarial transmission to the definitive hosts. Transmission and the use of pleuston by hemiuroids likely varies with sea surface use and ontogenetic trophic shifts of apex predators. The small number of trematode species found in pleuston is consistent with significant ecological specificity, and the inference that other pelagic trematodes use alternative pathways of transmission that do not involve pleustonic organisms. Such pathways may involve i) pelagic hosts exclusively; ii) benthic or demersal hosts exclusively, consumed by apex predators during their dives; or iii) both benthic and pelagic hosts in transmission chains dependent on vertical migrations of prey. The influence of the connectivity of open-ocean ecosystems on parasite transmission is identified as an area in critical need of research.

Evidence that a lineage of teleost-infecting blood flukes (Aporocotylidae) infects bivalves as intermediate hosts.

The family Aporocotylidae is recognized as having the widest intermediate host usage in the Digenea. Currently, intermediate host groups are clearly correlated with definitive host groups; all known life cycles of marine teleost-infecting aporocotylids involve polychaetes, those of freshwater teleost-infecting aporocotylids involve gastropods, and those of chondrichthyan-infecting aporocotylids involve bivalves. Here we report the life cycle for a marine elopomorph-infecting species, Elopicola bristowi Orélis-Ribeiro & Bullard in Orélis-Ribeiro, Halanych, Dang, Bakenhaster, Arias & Bullard, 2017, as infecting a bivalve, Anadara trapezia (Deshayes) (Arcidae), as the intermediate host in Moreton Bay, Queensland, Australia. The cercaria of E. bristowi has a prominent finfold, distinct anterior and posterior widenings of the oesophagus, a tail with symmetrical furcae with finfolds, and develops in elongate to oval sporocysts. We also report molecular data for an unmatched aporocotylid cercaria from another bivalve, Megapitaria squalida (G. B. Sowerby I) (Veneridae), from the Gulf of California, Mexico, and six unmatched cercariae from a gastropod, Posticobia brazieri (E. A. Smith) (Tateidae), from freshwater systems of south-east Queensland, Australia. Phylogenetic analyses demonstrate the presence of six strongly-supported lineages within the Aporocotylidae, including one of elopomorph-infecting genera, Elopicola Bullard, 2014 and Paracardicoloides Martin, 1974, now shown to use both gastropods and bivalves as intermediate hosts. Of a likely 14 aporocotylid species reported from bivalves, six are now genetically characterised. The cercarial morphology of these six species demonstrates a clear distinction between those that infect chondrichthyans and those that infect elopomorphs; chondrichthyan-infecting aporocotylids have cercariae with asymmetrical furcae that lack finfolds and develop in spherical sporocysts whereas those of elopomorph-infecting aporocotylids have symmetrical furcae with finfolds and develop in elongate sporocysts. This morphological correlation allows predictions of the host-based lineage to which the unsequenced species belong. The Aporocotylidae is proving exceptional in is propensity for major switches in intermediate host use, with the most parsimonious interpretation of intermediate host distribution implying a minimum of three host switches within the family.

First elucidation of a didymozoid life cycle: Saccularina magnacetabula n. gen. n. sp. infecting an arcid bivalve.

The first first-intermediate host for a species of Didymozoidae (Trematoda: Hemiuroidea), a bivalve of the family Arcidae, is identified using multi-loci molecular data. First intermediate, (likely) third intermediate, and adult stages of a new didymozoid taxon (Saccularina magnacetabula n. gen. n. sp.) from Moreton Bay, Queensland, Australia were collected from the Sydney cockle Anadara trapezia (Deshayes) (Arcoidea: Arcidae), Sillago sp. (Sillaginidae) and Elops hawaiensis Regan (Elopiformes: Elopidae), respectively, and genetically matched. Infections in A. trapezia were present as sporocysts and cystophorous cercariae, and infected tissue at the base of the gills. Morphologically, S. magnacetabula is distinctive relative to all other didymozoids in the combination of hermaphroditism, mate-pairing, filiform body shape, the presence of a ventral sucker, a single testis, and a saccular excretory vesicle at the posterior extremity. Molecular sequence data were generated for S. magnacetabula and 42 other putative didymozoid species to explore relationships within the Didymozoidae and Hemiuroidea. In molecular phylogenetic analyses of the 28S rDNA region, the new genus forms a clade with an undescribed taxon from the redthroat emperor, Lethrinus miniatus (Bloch & Schneider) (Perciformes: Lethrinidae), from the Great Barrier Reef, and another uncharacterised taxon from E. hawaiensis. This clade is sister to a moderately well-supported clade comprising all other didymozoid species for which sequences are available, including representatives of five of the six presently recognised subfamilies. The infection of a bivalve by a didymozoid is discussed in the context of the overwhelming use of gastropod molluscs as first intermediate hosts by the Hemiuroidea.

Drivers and ecological consequences of dominance in periurban phytoplankton communities using networks approaches.

Evaluating the causes and consequences of dominance by a limited number of taxa in phytoplankton communities is of huge importance in the current context of increasing anthropogenic pressures on natural ecosystems. This is of particular concern in densely populated urban areas where usages and impacts of human populations on water ecosystems are strongly interconnected. Microbial biodiversity is commonly used as a bioindicator of environmental quality and ecosystem functioning, but there are few studies at the regional scale that integrate the drivers of dominance in phytoplankton communities and their consequences on the structure and functioning of these communities. Here, we studied the causes and consequences of phytoplankton dominance in 50 environmentally contrasted waterbodies, sampled over four summer campaigns in the highly-populated Île-de-France region (IDF). Phytoplankton dominance was observed in 32-52% of the communities and most cases were attributed to Chlorophyta (35.5-40.6% of cases) and Cyanobacteria (30.3-36.5%). The best predictors of dominance were identified using multinomial logistic regression and included waterbody features (surface, depth and connection to the hydrological network) and water column characteristics (total N, TN:TP ratio, water temperature and stratification). The consequences of dominance were dependent on the identity of the dominant organisms and included modifications of biological attributes (richness, cohesion) and functioning (biomass, RUE) of phytoplankton communities. We constructed co-occurrence networks using high resolution phytoplankton biomass and demonstrated that networks under dominance by Chlorophyta and Cyanobacteria exhibited significantly different structure compared with networks without dominance. Furthermore, dominance by Cyanobacteria was associated with more profound network modifications (e.g. cohesion, size, density, efficiency and proportion of negative links), suggesting a stronger disruption of the structure and functioning of phytoplankton communities in the conditions in which this group dominates. Finally, we provide a synthesis on the relationships between environmental drivers, dominance status, community attributes and network structure.