This study addresses aspects of the phylogenetic relationships of the commercial Tehuelche scallop, Aequipecten tehuelchus s.l. (Bivalvia: Pectinidae), from southern South America using molecular techniques. The Tehuelche scallop presents two different putative subspecies, A. t. tehuelchus and A. t. madrynensis, and a potentially related sympatric species, Flexopecten felipponei. The Tehuelche scallop is a very important component of ecosystems and is the target of artisanal fisheries in the northern Patagonian gulfs of Argentina. Despite its importance, the systematic relationships of these taxa have not been fully addressed. The main goal of this study is to place the Tehuelche scallop within a partial phylogenetic framework of the family Pectinidae. Scallops were sampled at 10 localities distributed along the south-western Atlantic Ocean. Phylogenetic reconstructions were carried out from two mitochondrial (12S rRNA and 16S rRNA) and two nuclear markers (28S rRNA and H3) using Bayesian, maximum likelihood and maximum parsimony analyses. Our phylogenetic analysis indicates that the two putative subspecies of the Tehuelche scallop together with F. felipponei form a monophyletic clade, without differentiating at the specific level. Observed differences would be the result of phenotypic plasticity, probably caused by environmental factors. However, further analysis using genes with faster evolution rate are needed to corroborate it. Our phylogenetic analysis resolved to Aequipecten as polyphyletic. The Tehuelche scallop has a basal position within the Argopecten group and we recommend that it should be transferred to this genus. The relationship between the hypotheses about the origin of the Tehuelche scallop implicit in the literature and our results are discussed.

The European sea squirt, Ascidiella aspersa was first found as an alien species in 2008 from Funka Bay, Hokkaido, northern Japan, causing serious damage to the scallop aquaculture industry. We investigated A. aspersa on cultured scallops and larval occurrence from July 2010 to June 2014 to clarify life history traits and population dynamics, and consider the relation between the life history of A. aspersa and the process of scallop aquaculture. Larvae of A. aspersa were found from June to December, and recruitment on cultured scallops occurred mainly between July and October. The ascidians grew well and their weights increased until February. We found that 60–80% of A. aspersa that had settled in summer had eggs or sperm in autumn, and 90–100% of A. aspersa matured early the following summer. Maturity size in September was 17–20 mm as male, 22–24 mm as female. Scallops in Funka Bay are hung in the spring and harvested from winter to the next spring. Ascidiella aspersa settle as larvae in early summer, and grow well until winter, resulting in overgrowth on scallops in the harvest season. The linking of the process of scallop aquaculture and the life history of A. aspersa explains why this invasive ascidian has caused serious damage to the aquaculture industry in the bay. In comparison to the earlier descriptions of the native population, A. aspersa in Funka Bay has longer reproductive and growth periods, earlier initiation of reproduction, and possibly smaller maturity size.

Size distribution and swimming activity of the sea scallop, Placopecten magellanicus, were measured in situ from high-definition video recordings collected by a remotely operated vehicle on a fished scallop bed on German Bank, Gulf of Maine in August 2010. Scallop densities ranged from 0.004 to 3.89 m−2 and shell height (SH) ranged from 16.3 to 193.8 mm. The size distribution was bimodal, with high abundance from 20 to 40 mm SH indicating a recent recruitment event in the area. The low abundance of scallops >100 mm SH was likely due to the active fishery in this area. Of 535 observed swims, 200 were characterized for swim distance, time, velocity and distance travelled per adduction. The size of scallops observed to swim ranged from 18.9 to 99.9 mm SH. Both swim time and swim distance increased linearly with SH, and quadratic relationships were observed between velocity and SH, and between distance travelled per adduction and SH. Swimming velocities peaked at ~ 50 cm s−1 for scallops between 60 and 80 mm, and maximum velocity was 103.2 cm s−1observed for an individual of 64.0 mm SH. Our study provided a unique opportunity to investigate size distribution and associated swimming activity of scallops in their natural habitat, rather than in a simulated study in the laboratory, and at depths not reachable by SCUBA diving.

Swimming activity of the Antarctic scallop at a temperature of c. −1.4°C was analysed using in situ video recordings obtained from a remotely operated vehicle (ROV) in Terra Nova Bay, Ross Sea. Data are presented on swimming trajectories, distance travelled and velocity during a swimming bout, adduction frequency, shell gape angle, and the angular opening and closing velocities of shell. This scallop is an effective swimmer although swimming bouts in response to the ROV were generally short, consisting of 2–5 adduction cycles in the take-off phase followed by 1–4 (exceptionally 14) adductions during level swimming. The maximum velocity during each adduction cycle ranged from 19.4–43.1 cm s−1 and the mean velocity during a swimming bout from 12.0–23.5 cm s−1. Each adduction cycle consists of opening, closing and glide phases of approximately equal duration. Adduction frequency during swimming averaged 1.5 adductions s−1.

Several molluscs that have been introduced world-wide have become economically important for coastal communities. As far as it is known, at least four scallop species (Argopecten irradians, Argopecten purpuratus, Patinopecten yessoensis, Pecten maximus) have been moved between different biological provinces and it is possible there will be further such movements. Making an introduction involves responsibilities and so requires careful consideration. This is because there have been several unwanted impacts with movements of molluscs in the past. The International Council for the Exploration of the Sea's (ICES) 1995 Code of Practice on the Introductions and Transfers of Marine Organisms and recent revision provides a basis for undertaking such an action wisely. In this review, scallops that may be used in future cultivation or in fisheries as potential candidates are examined in relation to the first phase of an introduction—the prospectus. This prospectus should take account of the purposes and objectives of the introduction, including relevant biological, pathological and ecological conditions in the donor region and the potential impacts of the species in the expected range occupied in the recipient region. This may require a study visit to the donor region to evaluate concerns relating to potential hazards. The ecomorphology of five different scallop shell morphs is discussed in relation to their behaviour and occupied habitat. Such information may provide an indication of their interaction with native scallop species in advance of their introduction.

The digestive gland of Pecten maximus consists, as in other lamellibranchs, of numerous blindending tubules which communicate with the stomach by partially ciliated main ducts and non ciliated secondary ducts. The non-ciliated cells of the main ducts are characterized by a well developed brush border constituted by high and dense microvilli and a strong pinocytotic activity. Ciliated and non ciliated cells have a very similar fine structure. The digestive tubules have a large lumen and contain digestive cells at different stages of absorption, digestion and excretion, one part of the tubules being functional while the other is disintegrating. The dark crypts contain the flagellated secretory cells, characterized by a well developed granular endoplasmic reticulum, and the young immature cells which may replace both the secretory and digestive cells. The numerous lipid droplets occurring in the digestive duct cells and in the digestive cells reveal the lipid storage function of the digestive gland. Several enzyme activities involved in digestion have been localized in the digestive gland. High amylase activity and cellulase and lysozyme activities have been found in the ducts and in the tubules, whereas no proteolytic activity could be detected histochemically. Some intracellular peptidases and glycosidases have been localized in the cells of the digestive gland, especially in the brush-border cells of the ducts and in the functional part of the tubules. High alkaline and acid phosphatase activities are displayed by the duct brush-border cells and the digestive and secretory cells. These results show the main role of the digestive gland, both in extracellular digestion (secretion of the digestive enzymes) and in absorption and intracellular digestion and provide information on the respective functions of the different cells within these processes.

This paper presents a summary of information on reproduction biology in the scallop, Pecten maximus, which is required for the successful reseeding and intensive aquaculture programs developed in France since 1982. Data are presented on the following subjects: environmental factors that sustain gametogenic activity and the time of year this activity occurs; biochemical changes that are associated with gametogenesis; the consistency of egg quality; and development of a simple test to predict egg quality.