Archaeological fieldwork at Hjarnø Sund in Horsens Fjord (eastern Jutland, Denmark) has explored an eroding Mesolithic shell midden. Its stratigraphy is characterized by two layers, containing marine mollusk taxa typically collected by Mesolithic hunter-gatherers for food. In the field, the lower layer appeared to be dominated by oysters (Ostrea edulis), while the upper one by cockles (Cerastoderma edule), which was confirmed by our zooarchaeological study. Accelerator mass spectrometry radiocarbon (AMS 14C) dating on shells and paired charcoal samples from the two layers indicate that these are chronologically consecutive (separated by as little as 0–163 yr [95.4%]) and that the oyster-to-cockle shift dated between ~5500–5300 and ~5300–5200 cal BC (around or just after the Kongemose/Ertebølle transition). The shell midden at Hjarnø Sund is, thus, one of the oldest-known in Denmark, demonstrating that intensive shellfish exploitation was a hallmark of the Ertebølle culture from its inception. Oyster-to-cockle shifts, thus, also occurred at times other than the Mesolithic–Neolithic Transition and may have been ultimately caused by local shoreline displacements, resulting from changes in sedimentation, possibly induced by drops in relative sea level.

Fertilization success will determine the rate at which a population can expand and is especially important when considering small, establishing or enduring communities. Introduced species frequently fail to establish reproductively functional populations due to strong Allee effects associated with low densities. The native European oyster, Ostrea edulis broods its fertilized eggs in the pallial cavity for a period of 8–10 days before releasing the larvae. It is considered a partial broadcast spawner and was used as a model species to assess the importance of Allee effects such as inter-individual distance on reproductive success. Distances between individual oysters within test plots in areas of known oyster density were used in conjunction with standardized brood size (n larvae g−1 total wet weight) to assess fertilization success. A significant, positive relationship was observed between brood size and oyster density. Oysters with a nearest neighbour ≤1.5 m were found to brood significantly more larvae than individuals with nearest neighbours ≥1.5 m. Therefore, high density sites need to be maintained to ensure the recovery and enhancement of this OSPAR Convention recognized species in decline.

Marteilia refringens causes marteiliosis in oysters, mussels and other bivalve molluscs. This parasite previously comprised two species, M. refringens and Marteilia maurini, which were synonymized in 2007 and subsequently referred to as M. refringens ‘O-type’ and ‘M-type’. O-type has caused mass mortalities of the flat oyster Ostrea edulis. We used high throughput sequencing and histology to intensively screen flat oysters and mussels (Mytilus edulis) from the UK, Sweden and Norway for infection by both types and to generate multi-gene datasets to clarify their genetic distinctiveness. Mussels from the UK, Norway and Sweden were more frequently polymerase chain reaction (PCR)-positive for M-type (75/849) than oysters (11/542). We did not detect O-type in any northern European samples, and no histology-confirmed Marteilia-infected oysters were found in the UK, Norway and Sweden, even where co-habiting mussels were infected by the M-type. The two genetic lineages within ‘M. refringens’ are robustly distinguishable at species level. We therefore formally define them as separate species: M. refringens (previously O-type) and Marteilia pararefringens sp. nov. (M-type). We designed and tested new Marteilia-specific PCR primers amplifying from the 3’ end of the 18S rRNA gene through to the 5.8S gene, which specifically amplified the target region from both tissue and environmental samples.

Bonamiosis is a parasitic disease (causative agent: Bonamia ostreae) affecting the European flat oyster Ostrea edulis, responsible for a drastic decline in its aquaculture production. Selective breeding programs for resistance to bonamiosis have been undertaken to counter this disease. In the present study, a 6-month cohabitation challenge experiment was performed in order to transmit the disease from wild oysters injected with the parasite to two tested families of oysters (20 and 8-month old at the beginning of the experiment, with different genetic backgrounds) originating from a selective breeding program developed by IFREMER in France. Mortalities were checked daily and ventricular heart smears were performed on dying or moribund oysters to detect the level of infection by B. ostreae. Mortality started after 4 months of cohabitation in the tested oysters. The cumulative mortalities after 6 months were 58% for the wild oysters, 9% for Family 1 (20-month old) and 20% for Family 2 (8-month old). In the dying oysters, the parasite could be detected in 67% of the wild oysters, 68% of Family 1 and 89% of Family 2. It was detected in only 11% of the surviving oysters of Family 2. The mortality and the level of infection by the parasite were significantly higher in Family 2 than in Family 1. Our results demonstrate that prespawning oysters as young as 1 year-old can become infected with the parasite and, most importantly, can die from bonamiosis. This result is inconsistent with the commonly accepted critical age of 2 years-old for the disease development. Additionally, no clear relationship between shell length and level of infection was observed. We also review the different methods for infection of the European flat oyster O. edulis with B. ostreae under experimental conditions and their main results.

The European, native or flat oyster, Ostrea edulis, has been the subject of human-mediated translocation and aquaculture in Europe for centuries and may have diluted or masked natural population genetic structure. Samples of O. edulis from 10 sites in Scotland and The Netherlands, Brittany and Norway were collected and genotyped at up to six microsatellite loci. Numbers of alleles and heterozygosity per locus were high in all populations and were consistent with previous microsatellite studies. There is no evidence that extensive traditional oyster aquaculture has led to loss of allelelic diversity. Deficiencies of heterozygotes against Hardy-Weinberg predictions were common and were probably mainly due to the presence of null alleles. Overall, population differentiation (F st = 0.05) was estimated to be higher than previous studies and could be resolved into four main genetic groups (1) Norway, (2) The Netherlands and Brittany, (3) Scotland apart from (4) Skye. The genetic distinctness of Norway oysters agrees with previous findings. The distinctiveness of the Skye population could be partly due to an artefact of small sample sizes and partly due to the founder effect of importation of Brittany oysters in the 1950s. Further studies are required to ascertain whether the Skye population may be deserving of special conservation status. The results suggest that human aquaculture activities over recent centuries have probably diluted any original local genetic differentiation within Scotland, but that potentially important genetic differentiation still exists at the wider scale across Europe

Throughout much of the UK and in Europe generally the native oyster is in a severely depleted state in the wild. In order to address and potentially to reverse this situation Ostrea edulis was designated as a named species in the UK Biodiversity Action Plan as part of a national commitment to the International Convention on Biodiversity. Amongst other initiatives, some of which are summarised in this paper, a feasibility study was carried out to evaluate all the factors, including an economic assessment, relevant to a programme of stock restoration in the UK. The study showed that there is a considerable body of data on the biology, ecology and distribution of O. edulis to inform restoration projects. Appropriate legislation is in place to allow for restoration. Non-marketable costs and benefits were estimated. They provide an idea of the high value that may be placed on biodiversity aspects. Nevertheless, this study also shows that stock restoration can be commercially viable if fishery prices and yields are sufficiently high. Restoration efforts and associated studies elsewhere have shown the potential for success of native oyster stock regeneration, especially in disease-free areas. For these, there is a very strong element of re-creating and conserving an ecological resource. The relaying of cultch is seen as an essential component of a successful oyster restoration programme and the use of sanctuaries is generally considered beneficial. The loss of the standing stock is a limiting factor and re-stocking is an effective strategy. There is a basic genetic similarity of wild European O. edulis populations such that the source of stocks is not critical. There are some problems with hatchery rearing from these, but using breeding ponds or importing part-grown oysters are viable alternatives.

Marteilia refringens is a paramyxean parasite which infects the flat oyster Ostrea edulis and mussels (Mytilus galloprovincialis), where it has been attributed to a separate species, Marteilia maurini, by several authors. Doubts persist though as to the existence or not of two species of Marteilia in Europe. We have devised a molecular method for the diagnosis of M. refringens based on 358 bp nested-PCR of the rDNA intergene spacer (rDNA IGS) which is capable of detecting 0·5 fg of M. refringens DNA. Molecular characterization of this spacer indicates that the Marteilia parasites which infect oysters and mussels are two different strains of the same species.

Marteilia refringens is a major pathogen of the European flat oyster, Ostrea edulis Linnaeus. Since its description, the life-cycle of this protozoan parasite has eluded discovery. Attempts to infect oysters experimentally have been unsuccessful and led to the hypothesis of a complex life-cycle involving several hosts. Knowledge of this life-cycle is of central importance in order to manage oyster disease. However, the exploration of M. refringens life-cycle has been previously limited by the detection tools available and the tremendous number of species to be screened in enzootic areas. In this study, these two restrictions were circumvented by the use of both molecular detection tools and a mesocosm with low biodiversity. Screening of the entire fauna of the pond for M. refringens DNA was systematically undertaken using PCR. Here, we show that the copepod Paracartia(Acartia) grani is a host of M. refringens. Not only was DNA of M. refringens consistently detected in P. grani but also the presence of the parasite in the ovarian tissues was demonstrated using in situ hybridization. Finally, successful experimental transmissions provided evidence that P. grani can be infected from infected flat oysters.

A study of the growth and mortality of the European oyster Ostrea edulis, including the effects of Marteilia refringens and Bonamia ostreae, was carried out in three oceanic areas in the Bay of Areachon from May 1989 to February 1991. One-year-old spat, free from discase were used for the trials. Six months after beginning the trials, Marteilia refringens had severely infested the cultures. Although Bonamia ostreae was found during the first year, the rate of infestation was low. In the second year Bonamiasis increased and high mortality (>60%) occurred in Ostrea edulis populations. Although the growth of the oysters was good, their condition index was generally poor. Moreover, shell perforations by Polydora sp. were observed. In spring 1990, a low glycogen storage was notedwhich may have been related to the Marteilia refringens infestation although no relationship with the carbohydrate content and mortality was detected. The influence of different rearing procedures on Ostrea edulis survival and development in four commercial batches of oysters, free of discase, was also studied. The growth of Ostrea edulis in single culture was better than in cultures mixed with Crassostrea gigas. However, infestation by Marteilia refringens and Bonamia ostreae in the laid cultures was quite similar to that of the experimental cultures (bags). Due to the persistence of these two parasites, the culture of Ostrea edulis on a commercial scale is not advisable in the Bay of Arcachon.

Murine monoclonal and polyclonal antibodies to antigens of Bonamia ostreae were assessed for serological comparison of parasites associated with different geographical origins of flat oysters, Ostrea edulis, and with Tiostrea lutaria. All Bonamia isolates from O. edulis reacted similary with polyclonal and monoclonal antibodies. The parasite associated with Tiostrea lutaria which lacks reactivity with 20 B2 MAB must be considered as a serologically distinct form of B. ostreae.