The goose barnacle Conchoderma virgatum is a highly opportunistic epibiont, with observations of attachment to a wide range of marine organisms. Attachment to perciform fishes, however, is rarely observed. Observations of Conchoderma-osteichthyan associations in general are also rare in the southern hemisphere, especially in Australian waters. We present the first record of C. virgatum as an epibiont on an ephippid fish (Platax teira). This is also only the second known record of C. virgatum attached to a perciform fish in the Tasman Sea. We also summarize all previous known observations of C. virgatum in association with perciform fishes.

Sea turtles are partners in commensal relationships with a variety of epibionts, including barnacles. The acorn barnacle Chelonibia testudinaria is one species commonly found associated with sea turtles and other marine fauna throughout temperate to tropical waters including the Indo-Pacific. We conducted a study to assess the occurrence of this barnacle, relative to host life stage and species in a mixed foraging population of green (Chelonia mydas) and hawksbill (Eretmochelys imbricata) turtles (juvenile, sub-adult, adults (female and male)) in Mabul Island, Sabah, Malaysia (Celebes Sea). Expecting similar relative abundance by life stage, we found instead a significant effect between the combined dependent variables (abundance and size of barnacles) and the life stages of sea turtles in Mabul after controlling for the covariates of size and species of sea turtles (F(8, 428) = 5.77, P < 0.001, Pillai = 0.19). Among green turtles with barnacles, though adult males had larger barnacles compared with the female turtles, the mean barnacle abundance on adult females (43.4 individuals ± 5.19 SD) was higher than all other life stages. Most of the barnacles (85.6%; N = 1931) were found on the plastron of the sea turtles. The highest number of barnacle reacquisition was found among the juvenile turtles. In assessing the complemental males of the barnacles, we found they were consistently attached to the shells of the larger of the hermaphrodites from each region of the host's body despite average shell-size differences with each region.

Temnocephala axenos Monticelli, 1898 was described based on specimens from an unidentified host collected in Blumenau, Santa Catarina, Brazil. Information about type locality was imprecise and the host was later identified as Aegla laevis (Latreille, 1818). However, it is known that A. laevis is not present on the eastern side of the Andes. Also, only histological preparations from one specimen studied by Monticelli are currently available in the Museum für Naturkunde Berlin, but it showed none of the taxonomic characters needed for the characterization of the species. Although the updated description of the species based on Uruguayan specimens, neither the author nor the several previous studies about the species showed a search for the type material, a resolution for the misidentification of the type host or the imprecise type locality due to the subsequent geographical division of the municipality cited in the description. The Uruguayan specimens were not even geographically close to the type locality and a neotype was not designed to validate the species’ taxonomic status again. Specimens from Santa Catarina and Paraná States, Brazil, were studied, as well as restudied Argentinean specimens. The new data were compared with the update description of the species. The historical background and the discussion about geographical origins and hosts of the species, as well as a designation of a neotype, allow comparative material of the type locality and type host to exist, eliminating doubts about the identification of T. axenos.

Sea turtles host a diverse array of epibionts, yet it is not well understood what factors influence epibiont community composition. To test whether epibiont communities of sea turtles are influenced by the hosts’ nesting or foraging habitats, we characterized the epibiota of leatherback, olive ridley and green turtles nesting at a single location on the Pacific coast of Costa Rica. We also compared the epibiota of these turtles to conspecific populations nesting elsewhere in the East Pacific. If epibiont communities are influenced by nesting habitats, we predicted that sympatrically nesting turtles would have comparable epibiont taxa. Alternatively, if epibiont communities are influenced by foraging habitats, we predicted the diversity of epibiont taxa should reflect the type and diversity of the hosts’ foraging habitats. We identified 18 epibiont taxa from 18 leatherback, 19 olive ridley and six green turtles. Epibiont diversity was low on leatherbacks (four taxa), but higher for olive ridley and green turtles (12 and nine epibiont taxa respectively). The epibiont communities of olive ridley and green turtles were not statistically different, but both were different from leatherbacks. In addition, conspecific sea turtles from other nesting locations hosted more similar epibiont communities than sympatrically nesting, non-conspecifics. We conclude that epibiont diversity of nesting sea turtles is partially linked to the diversity of their foraging habitats. We also conclude that the surface properties of the skin and carapace of these turtles may contribute to the uniqueness of leatherback turtle epibiont communities and the similarities between olive ridley and green turtle epibiont communities.

Studies of sea turtle epibiosis have focused on the diversity and ecology of facultative commensalisms and less attention has been given to parasitic associations, in which the epibiont species derives nutrients from the tissue of the host turtle. We present the first description and quantitative survey of the parasitic isopods Excorallana costata, Excorallana bicornis and Excorallana oculata on loggerhead (N = 79) and hawksbill turtles (N = 23), and E. costata on olive ridley turtles (N = 9), nesting on Praia do Forte, Bahia, Brazil during the 2009–2010 season. Excorallana costata was the most common isopod species (N = 651), followed by E. bicornis (N = 77) and E. oculata (N = 20). Patterns include: (1) E. costata exhibited a higher frequency and intensity of parasitism than E. bicornis and E. oculata and (2) loggerheads hosted parasitic isopods at a higher frequency and intensity than hawksbills and olive ridleys. We also detected temporal shifts in the occurrence and intensity of parasitism across the nesting season, which strongly suggests that turtles were parasitized by all three isopod species during their internesting periods. Because parasitic isopods were observed only rarely prior to the 2009–2010 turtle-nesting season and have continued to be common in subsequent seasons, it is important to gain a better understanding of the basic biology of these interactions, the reasons for their recent emergence, and the potential biological impacts on turtle, as well as isopod, populations.

This study reports for the first time on the whole epibiont fauna of loggerhead marine turtles, Caretta caretta, in the western Mediterranean, analysing the factors that account for the predictability and composition of the assemblage. A total of 104 loggerhead turtles stranded along the coasts of eastern Spain during 1995–2006 were surveyed for epibionts. A total of 39 epibiont taxa were identified, three of them being new records for loggerhead turtles: Bittium sp., Idotea metallica and Jassa sp. The assemblage was composed of a group of 27 facultative taxa that use turtles as any inanimate buoyant substrate, and 12 taxa that have developed more specific associations to marine turtles, including six species that occur in marine turtles exclusively, two that dwell also on other hosts, and four that can also survive as free-living forms but have developed a strong association with marine turtles. Hierarchical clustering and Similarity Profile Analysis based on the occurrence of 166 epibiont taxa from nine available surveys indicated that the epibiont assemblages from loggerhead turtles in the western Mediterranean (WM) are similar to those from Central Mediterranean (CM), but significantly different from turtles surveyed in the eastern Mediterranean and the Atlantic. The subset of epibionts occurring on WM and CM turtles is defined by a combination of geographic factors (exclusive Mediterranean epibiont taxa) and ecological factors (relative absence of littoral-benthic taxa). Loggerhead turtles from WM and CM apparently exploit both pelagic and benthic habitats in similar fashion, representing a homogeneous unit for epibiont recruitment.

The galatheid crab Shinkaia crosnieri, is the sole member of the subfamily Shinkaiinae. It is abundant and forms dense beds around active hydrothermal vents in the Okinawa Trough. Thousands of filamentous bacteria attached to the plumose setae on the ventral surface of this crab were observed using field-emission scanning electron microscopy and transmission electron microscopy. Nucleic acids were extracted from the filamentous bacteria, and the phylotypes of 16S rRNA genes were identified from 81 clones. These phylotypes were divided into three groups: Epsilonproteobacteria (74%); Gammaproteobacteria (20%); and Bacteroidetes (6%). Gamma- and major phylotypes of Epsilonproteobacteria were also detected using fluorescence in situ hybridization analysis. These Epsilon- and Gammaproteobacteria were closely related to cultured and uncultured bacteria from hydrothermal vent fields including episymbionts of vent-associated invertebrates such as Rimicaris exoculata, Alvinella pompejana, the scaly-foot snail, Kiwa hirsuta etc. The carbon isotopic compositions of the muscle of S. crosnieri and in filamentous bacteria were similar. The muscle of S. crosnieri contained monounsaturated C16 and C18 fatty acids, which are known to be characteristic of sulphur-oxidizing bacteria in H2S-rich marine habitats. Through the video images transmitted by a submersible and a remotely operated vehicle, S. crosnieri was observed to comb out its ventral setae using the third maxilliped and appeared to consume the contents. These evidences suggest the epibiotic association between S. crosnieri and the filamentous bacteria attached to the ventral setae of the crab, but the details of role and function are still unclear at the present study.