The introduced Asian parasitic bopyrid isopod, Orthione griffenis, was first discovered on the Pacific coast of North America in Washington in 1988 and next in California in 1992. The range of Orthione presently extends from British Columbia to Baja California, where it infests at least two species of the native estuary mud shrimp, Upogebia. Intense Orthione infestations are associated with the apparent demise of many local populations of Upogebia pugettensis yet nonindigenous origins of Orthione in North America and thus the ecological significance of its impacts have remained in doubt. Six criteria reveal that Orthione is introduced to North America: its conspecificity with disjunct Asian populations, its earliest (1950s) collections in Asia, its late discovery among symbiotic species associated with Upogebia, its historical absence, and its appearance in North America coincident with extensive new ballast water traffic from Asia. Orthione is the first recognized bopyrid isopod invasion globally. Coexistence of U. pugettensis, which are ecosystem engineers, with its newly acquired parasite cannot be assumed. Orthione threatens eastern Pacific estuary ecosystems where Upogebia were previously abundant.

Ecological, behavioural and anatomical observations of a commensal bivalve, Peregrinamor ohshimai (Mollusca: Galeommatoidea), were carried out in a tidal mudflat in the Seto Inland Sea, Japan. The bivalve attached specifically to the longitudinal groove of the ventral side of the cephalothorax of thalassinidean burrowing shrimps, Upogebia major and Lf. narutensis (Crustacea: Decapoda), singly, dorso-ventrally and longitudinally, using its byssus, with its anterior part towards the head of the host. The mantle of the commensal bivalve has wide anterior (branchio-pedal) and narrow posterior (exhalant) apertures. In the living organism, the extended anterior edges of the mantle protrude from the shell and are inserted into the host's filtering basket, which is formed by the setal rows of the first two pairs of pereiopods and utilized for intercepting suspended matter. By beating its pleopods in a U-shaped burrow, the filter-feeding Upogebia shrimp creates water currents, which are also utilized by the commensal bivalve for filter-feeding. The shell length of the commensal bivalve was in proportion to the host's carapace length. This suggests that the veliger larva attaches to a young host and grows, thus maintaining the host-commensal morphological matching. The bivalve is a hermaphrodite and individuals of >8–5 mm in shell length were already producing eggs. Anatomical observations suggest that P. ohshimai is most closely related to the Montacutidae in Galeommatoidea.

The behaviour of two ectosymbiotic animals, Peregrinamor ohshimai (a bivalve attached to the ventral cephalothorax of the host), and Phyllodurus sp. (a bopyrid isopod attached to the second pleopod of the host), during ecdyses of the host thalassinidean Upogebia shrimps was studied by time-lapse video of infested shrimps. In the intermoult stages of the hosts, both ectosymbionts did not move. However they moved on to the newly emerged body of the host at the time when the host moulted. Peregrinamor ohshimai began to move just after the host started moulting, whereas Phyllodurus sp. moved prior to ecdysis of the host and waited near the fissure from which the newly moulted body emerges first. There are highly correlated morphological relationships between the symbionts and the hosts. It is suggested that both ectosymbionts grow with the same host individuals after infection, keeping morphological affinity with their hosts without being discarded during ecdyses of the hosts.

Two species of grapsid crabs, both of the genus Acmaeopleura, were collected from burrows of a thalassinidean shrimp, Upogebia major, in a tidal flat in Japan. One was Acmaeopleura toriumii, co-habiting in the burrows, and the other was an undescribed species, Acmaeopleura sp., clinging to the abdomen of U. major. Several specimens of A. toriumii were also collected from egg masses of U. major. The field experiment and samplings suggested that A. toriumii is not a burrowing species and depends on Upogebia burrows. Behavioral observations were also made on crabs of the two species maintained in aquaria together with the shrimp. Acmaeopleura toriumii never clung to U. major and seemed to be an omnivorous feeder. In contrast, Acmaeopleura sp. always clung, and almost specifically to the ventral side of the first and second abdominal segments of the host; moreover this crab sometimes migrated to another host individual. A few days after Acmaeopleura sp. was observed clinging to a shrimp, wounds were observed on the abdomen of the host. This ectosymbiotic crab probably feeds on host tissue. In the field, about 13% of the collected U. major had abdominal wounds attributable to Acmaeopleura sp. Symbiotic relationship between Acmaeopleura sp. and U. major will be the first case reported of a crab living ectoparasitically on another decapod.

The morphology of burrows constructed by the eel goby Taenioides cirratus was studied using resin castings of burrows in situ as well as aquarium observations. Burrows had several openings, one of which was associated with a crateriform mound. The structure of the burrows consisted of the mound, gently sloping interconnected tunnels, and many short cul-de-sac side branches. The presence of the mound suggests that the fish actively process sediment.

The burrow morphology of the mud shrimp Upogebia yokoyai was investigated on a tidal flat in the Nanakita River mouth in north-eastern Japan using in situ resin casting. A total of 26 burrow casts were recovered, including those of 16 large shrimps and 10 small shrimps. Burrows of large shrimp were relatively simple and Y-shaped with depth exceeding 1.2 m. Although burrow diameter was related to shrimp size, correlation with other burrow measurements was low. Three large casts were connected to others via a narrow horizontal portion potentially reflecting mating behaviour of the shrimp. Burrows of small shrimp were more complex than those of the other upogebiids and were connected to large burrows. In 6.7% of cases, bopyrid isopods were present in the branchial chamber. Three species of gobies were found in the burrows. These data show that burrows of U. yokoyai serve not only as a recruitment site for conspecific shrimp, but also as habitat for other animals in the tidal flat.

Zoanthids (Cnidaria, Hexacorallia) of the genus Epizoanthus are often found in association with other marine invertebrates, including gastropods and hermit crabs. However, little information exists on the specificity and nature of these associations due to a lack of investigation into Epizoanthus species diversity, and the taxonomy of Epizoanthus is therefore confused. In this study, analyses of morphological data (tentacle number, polyp size, etc) and molecular data (mitochondrial cytochrome oxidase subunit 1 = COI, 16S ribosomal DNA = 16S rDNA) were used to examine Epizoanthus specimens from Tosa Bay, Kochi, Japan. The Epizoanthus specimens were found on both live gastropods (Gemmula unedo) and hermit crabs (Paguristes palythophilus) inhabiting G. unedo and G. cosmoi shells. While morphological analyses did not show clear differences between examined specimens, both COI and mt 16S rDNA clearly divided the specimens into two groups, one associated only with hermit crabs (= Epizoanthus sp. C), and another associated only with living gastropods (= Epizoanthus sp. S). Unexpectedly, DNA sequences from both groups did not match with two previously reported Epizoanthus species from Japan (E. indicus, E. ramosus), indicating they both may be undescribed species. These results highlight the utility of DNA "barcoding" of unknown zoanthids, and will provide a foundation for re-examinations of Epizoanthus species diversity and specificity, which will be critical in understanding the evolution of these unique marine invertebrates.

The morphology of burrows constructed by the upogebiid mud shrimps Austinogebia narutensis and Upogebia issaeffi was studied using resin castings of burrows in situ on Mukaishima Island, Seto Inland Sea, Japan, where the two species occurred sympatrically. The burrow structure of both shrimps is a relatively simple Y-shaped pattern, which is typical of the family Upogebiidae. Total burrow length, and length and overall width of the U-shaped section of A. narutensis were greater than those of U. issaeffi, possibly because A. narutensis is the larger species. When the ratios of the burrow measurements to the mean burrow diameter were compared to exclude possible size effects, the burrows of A. narutensis had a wider and shallower U-shaped section than those of U. issaeffi. Because the casts were made where the two species occurred sympatrically, the differences in the burrow morphology were not due to the differences in environmental factors but to the difference in the shrimp species, whether they are adaptive or not.