Pecten Maximus Research Articles

Effects of Temperature and Ocean Acidification on the Extrapallial Fluid pH, Calcification Rate, and Condition Factor of the King Scallop Pecten maximus

Increasing anthropogenic carbon dioxide is predicted to cause declines in ocean pH and calcium carbonate saturation state over the coming centuries, making it potentially harder for marine calcifiers to build their shells and skeletons. One mechanism of resilience to ocean acidification is an organism's ability to regulate pH and, thus, calcium carbonate saturation state, at its site of calcification. This mechanism has received detailed study in scleractinian corals but is relatively understudied in other taxonomic groups that are vulnerable to ocean acidification, such as bivalves. Here, the results of a 74-day controlled laboratory experiment investigating the impact of ocean acidification on the extrapallial fluid (EPF; the bivalve calcifying fluid) pH, calcification rate, and condition factor of the king scallop Pecten maximus at their average spring and summer temperatures (362 ppm/9.0°C, 454 ppm/12.3°C; 860 ppm/9.0°C, 946 ppm/12.3°C; 2,639 ppm/8.9°C, 2,750 ppm/12.1°C) are presented. Scallop EPF pH was lower than seawater pH in all treatments and declined with increasing pCO2 under the spring temperature (9°C) but was uncorrelated with pCO2 under the summer temperature (12°C). Furthermore, king scallop calcification rate and EPF pH were inversely correlated at 9°C and uncorrelated at 12°C. This inverse correlation between EPF pH and scallop calcification rate, combined with the observation that scallop EPF pH is consistently lower than seawater pH, suggests that pH regulation is not the sole mechanism by which scallops concentrate carbonate ions for calcification within their EPF. Calcification trends contrasted most other published studies on bivalves, increasing with ocean acidification under spring temperature and exhibiting no response to ocean acidification under summer temperature. Scallop condition factor exhibited no response to ocean acidification under spring temperature but increased with ocean acidification under summer temperature—exactly the opposite of their calcification response to ocean acidification. These results suggest that king scallops are relatively resilient to CO2-induced ocean acidification, but that their allocation of resources between tissue and shell production in response to this stressor varies seasonally.

Comparative study of the culturable microbiota present in two different rearing systems, flow‐through system (FTS) and recirculation system (RAS), in a great scallop hatchery

A comparison of the culturable microbiota present in the different compartments of a great scallop (Pecten maximus) hatchery with two experimental production systems, FTS and RAS, throughout a cycle of larval rearing was carried out. All isolates obtained from broodstock gonads, larvae, tank water, biofilm, microalgae, UV-treated water and biofilter in both systems at three sampling times were characterized by biochemical tests and identified by sequencing of the 16S rRNA gene. Some of the genera were found to be exclusive of broodstock gonads, such as Sinobacterium, Kordia or Microbulbifer, and differences between gonad microbiota before and after spawning were detected. The number of morphotypes obtained in water, larvae and biofilm was similar in both systems, as well as the behaviour of the microbial populations in almost all hatchery compartments, in which Vibrio, Neptuniibacter, Pseudoalteromonas and Shewanella were the most common genera. The diversity obtained was analysed using the principal component analysis (PCA) and Fisher's exact test, showing that the microbial communities present in the common compartments between FTS and RAS did not significantly differ. These results suggest that, at least from a microbiological point of view, the recirculation system could be a good alternative for the production of scallop larvae.

Improving scallop (Pecten maximus and Placopecten magellanicus) spat production by initial larvae size and hydrodynamic cues used in nursery system

There are several factors affecting scallops during the metamorphosis process that could explain the relatively low post-larvae yield observed in hatcheries. Competent bivalve larvae respond to different settlement cues to undergo metamorphosis and without adequate cues, larvae delay their metamorphosis. The objective of this study is to improve the settlement ratio of the two scallop species, Placopecten magellanicus and Pecten maximus by physical cues associated with hydrodynamic conditions, stocking density in settlement units and larval size at time of transfer to settling units. For each treatment, physiological condition was determined by fatty acid analysis to determine the energetic reserves and structural lipids. We observed similar results for the two important commercial pectinid species and validate the hypothesis on the positive effect of increased flow rate and larval size after transfer to settlement systems on settlement success. Increasing flow rate also affects positively the physiological condition of settled post-larvae by a higher accumulation of total fatty acids in neutral lipid fractions. Furthermore, no effect of larval stocking density until 90 larvae cm−2 in the downwelling sieves was observed. To our knowledge this study is the first to characterize the effect of seawater flow rate on settlement success of different pectinid species cultured under similar conditions. The experiments were performed in a close to commercial scale and thus are relevant to industry situations.

Development and In-House Validation of an LC–MS and LC–MS/MS Assay for the Determination of Food Fraud for Different Fish Species

Abstract Background: Fish and fish products are one of the most important food sources of high commercial interest. The global food trade and the associated risks are constantly presenting new challenges to consumer protection and public authorities, which, among other things, demand state-of-the-art analytical methods to ensure food authenticity. Objective: The establishment of MS-based strategies plays a decisive role alongside the (further) development of ELISA- or DNA-oriented methods. Methods: In the present work, therefore, the development and in-house validation of an LC–MS and LC–MS/MS-based assay for authenticity testing of certain fish species is described. Results: Based on the execution of a validated bottom-up LC–electrospray–MS and MS/MS assay and multivariate analysis, the commercially available species Lutjanus malabaricus (red snapper) and Sebastes spp. (redfish) are distinguished from each other, whereas an additional 68 samples [nine additional marine species such as pangasius (Pangasianodon hypophthalmus), salmon (Salmo salar), turbot (Scophthalmus maximus), plaice (Pleuronectes platessa), sole (Solea solea), lemon sole (Glyptocephalus cynoglossus), halibut (Reinhardtius hypoglossoides), red salmon (Oncorhynchus nerka), and great scallop (Pecten jacobaeus)] served as blinded negative controls to ensure the specificity of the assay. Conclusions and Highlights: A promising LC–MS and LC–MSMS based assay has been developed that could enable the detection of fish fraud at the protein level in the future.

Spatio-temporal trace element fingerprinting of king scallops (Pecten maximus) reveals harvesting period and location

A rapidly growing human population is increasingly relying on seafood as a source of protein and other essential nutrients. Bivalve shellfish, both from wild populations and aquaculture, will undoubtedly continue to account for a significant portion of overall seafood production, but consumption of such shellfish carries potential health risks. Biotoxins, disease causing organisms and pollution contribute to this risk, as shellfish are indiscriminate, passive filter feeders. While government bodies, industry regulators and producers are capable of managing this risk, counterfeit produce can risk public safety, in turn damaging the reputation of the entire industry. Traceability tools provide a means to uphold food safety standards and mitigate remaining risk to consumers. Here, we show how the use of trace element (TE) signatures in shells and soft tissues of king scallops combined, can predict geographic origin with 100% accuracy. Importantly, we explore the temporal stability of this method, successfully classifying 100% of individuals correctly between two dates just 42 days apart from the same harvesting location. The most important elements in the trace element signatures of the scallops, discriminating between harvesting sites and dates were barium, boron, chromium, lead, manganese, molybdenum and selenium. The traceability tool described here offers a viable method to trace produce to its source, empowering industry regulators, government authorities, aquaculture practitioners and retailers in terms of tracking shellfish throughout the supply chain, which would comply with legislation and boost consumer confidence.

In vivo31P-MRS of muscle bioenergetics in marine invertebrates: Future ocean limits scallops' performance

ObjectDynamic in vivo31P-NMR spectroscopy in combination with Magnetic Resonance Imaging (MRI) was used to study muscle bioenergetics of boreal and Arctic scallops (Pecten maximus and Chlamys islandica) to test the hypothesis that future Ocean Warming and Acidification (OWA) will impair the performance of marine invertebrates. Materials & methodsExperiments were conducted following the recommendations for studies of muscle bioenergetics in vertebrates. Animals were long-term incubated under different environmental conditions: controls at 0 °C for C. islandica and 15 °C for P. maximus under ambient PCO2 of 0.039 kPa, a warm exposure with +5 °C (5 °C and 20 °C, respectively) under ambient PCO2 (OW group), and a combined exposure to warmed acidified conditions (5 °C and 20 °C, 0.112 kPa PCO2, OWA group). Scallops were placed in a 4.7 T MR animal scanner and the energetic status of the adductor muscle was determined under resting conditions using in vivo31P-NMR spectroscopy. The surplus oxidative flux (Qmax) was quantified by recording the recovery of arginine phosphate (PLA) directly after moderate swimming exercise of the scallops. ResultsMeasurements led to reproducible results within each experimental group. Under projected future conditions resting PLA levels (PLArest) were reduced, indicating reduced energy reserves in warming exposed scallops per se. In comparison to vertebrate muscle tissue surplus Qmax of scallop muscle was about one order of magnitude lower. This can be explained by lower mitochondrial contents and capacities in invertebrate than vertebrate muscle tissue. Warm exposed scallops showed a slower recovery rate of PLA levels (kPLA) and a reduced surplus Qmax. Elevated PCO2 did not affected PLA recovery further. ConclusionDynamic in vivo31P-NMR spectroscopy revealed constrained residual aerobic power budgets in boreal and Arctic scallops under projected ocean warming and acidification indicating that scallops are susceptible to future climate change. The observed reduction in muscular PLArest of scallops coping with a warmer and acidified ocean may be linked to an enhanced energy demand and reduced oxygen partial pressures (PO2) in their body fluids. Delayed recovery from moderate swimming at elevated temperature is a result of reduced PLArest concentrations associated with a warm-induced reduction of a residual aerobic power budget.

Compound-specific recording of gadolinium pollution in coastal waters by great scallops

Gadolinium-based contrast agents (GBCAs), routinely used in magnetic resonance imaging (MRI), end up directly in coastal seawaters where gadolinium concentrations are now increasing. Because many aquatic species could be sensitive to this new pollution, we have evaluated the possibility of using shellfish to assess its importance. Gadolinium excesses recorded by scallop shells collected in Bay of Brest (Brittany, France) for more than 30 years do not reflect the overall consumption in GBCAs, but are largely controlled by one of them, the gadopentetate dimeglumine. Although its use has been greatly reduced in Europe over the last ten years, gadolinium excesses are still measured in shells. Thus, some gadolinium derived from other GBCAs is bioavailable and could have an impact on marine wildlife.

Deconvolution of the elastic properties of bivalve shell nanocomposites from direct measurement and finite element analysis

Abstract

Shedding and survival of an intracellular pathogenic Endozoicomonas-like organism infecting king scallop Pecten maximus.

The Lyme Bay marine protected area (MPA) hosts a valuable population of king scallop Pecten maximus L. Recently, an Endozoicomonas-like organism (ELO), infecting host gill epithelial tissue, was associated with king scallop mass mortality events within the Lyme Bay MPA. Currently, very little is known about its transmission and survival outside the host. In this investigation, animals collected outside of reported mortality events showed high levels of ELO infection. Gill tissue disruption and the release of bacteria into the interlamellar space was seen histologically, suggesting shedding of ELO from host animals. To investigate pathogen survival outside the host, infected scallops were maintained in static water for a 24 h period, and then removed. Over the subsequent 8 d, water samples were collected and the quantity of ELO 16S rRNA transcript was measured by TaqManTM quantitative PCR (qPCR). The 16S rRNA transcript quantity was stable outside the host for 6 d before bacteria survival declined 2 logs (7.9 × 108 16S rRNA to 2.3 × 106 transcripts), suggesting that ELO can survive independently outside the host organism. The ELO-specific qPCR probe can therefore be used in future field studies of ELO prevalence within the environment and fauna of the Lyme Bay MPA.

RAD sequencing sheds new light on the genetic structure and local adaptation of European scallops and resolves their demographic histories

Recent developments in genomics are advancing our understanding of the processes shaping population structure in wild organisms. In particular, reduced representation sequencing has facilitated the generation of dense genetic marker datasets that provide greater power for resolving population structure, investigating the role of selection and reconstructing demographic histories. We therefore used RAD sequencing to study the great scallop Pecten maximus and its sister species P. jacobeus along a latitudinal cline in Europe. Analysis of 219 samples genotyped at 82,439 single nucleotide polymorphisms clearly resolved an Atlantic and a Norwegian group within P. maximus as well as P. jacobeus, in support of previous studies. Fine-scale structure was also detected, including pronounced differences involving Mulroy Bay in Ireland, where scallops are commercially cultured. Furthermore, we identified a suite of 279 environmentally associated loci that resolved a contrasting phylogenetic pattern to the remaining neutral loci, consistent with ecologically mediated divergence. Finally, demographic inference provided support for the two P. maximus groups having diverged during the last glacial maximum and subsequently expanded, whereas P. jacobeus diverged around 95,000 generations ago and experienced less pronounced expansion. Our results provide an integrative perspective on the factors shaping genome-wide differentiation in a commercially important marine invertebrate.

Development and In-House Validation of an LC-MS and LC-MS/MS Assay for the Determination of Food Fraud for Different Fish Species.

Background: Fish and fish products are one of the most important food sources of high commercial interest. The global food trade and the associated risks are constantly presenting new challenges to consumer protection and public authorities, which, among other things, demand state-of-the-art analytical methods to ensure food authenticity. Objective: The establishment of MS-based strategies plays a decisive role alongside the (further) development of ELISA- or DNA-oriented methods. Methods: In the present work, therefore, the development and in-house validation of an LC-MS and LC-MS/MS-based assay for authenticity testing of certain fish species is described. Results: Based on the execution of a validated bottom-up LC-electrospray-MS and MS/MS assay and multivariate analysis, the commercially available species Lutjanus malabaricus (red snapper) and Sebastes spp. (redfish) are distinguished from each other, whereas an additional 68 samples [nine additional marine species such as pangasius (Pangasianodon hypophthalmus), salmon (Salmo salar), turbot (Scophthalmus maximus), plaice (Pleuronectes platessa), sole (Solea solea), lemon sole (Glyptocephalus cynoglossus), halibut (Reinhardtius hypoglossoides), red salmon (Oncorhynchus nerka), and great scallop (Pecten jacobaeus)] served as blinded negative controls to ensure the specificity of the assay. Conclusions and Highlights: A promising LC-MS and LC-MSMS based assay has been developed that could enable the detection of fish fraud at the protein level in the future.

Incorporation of Feed and Fecal Waste From Salmon Aquaculture in Great Scallops (Pecten maximus) Co-fed by Different Algal Concentrations

Juvenile scallops of Pecten maxiumus were studied to see the capability to clear out and incorporate salmon feed and feces (30 µg L-1). Algae were also given, in a low and high concentration in addition to feed and faeces, to mimic a winter and summer situation in Norwegian waters. Rhodomonas baltica and Chaetoseris muelleri were provided in a concentration of 50 µg L-1 and 300 µg L-1. The feeding trial lasted for 27 days. Clearance rate was measured to study filtration characteristics, while fatty acid profiling and stable isotopes of nitrogen and carbon were used to trace the uptake of salmon feed and feces in the digestive gland and muscle of juvenile scallops (30–35 mm shell height). The results show that the scallops could clear out and retain both salmon feed and feces particles, although at a statistically lower clearance rate than the algae. Fatty acid profiling revealed that the scallops assimilated and incorporated the consumed salmon feed and feces, given with either high or low algae concentrations, in their tissues, where the fatty acid C18:1n9 was used as a tracer fatty acid. The digestive gland of the scallops that were fed salmon feed and feces contained a higher share of C18:1n9 than those that were only fed algae. The digestive gland reflected the fatty acid composition of the diet, while the fatty acid composition of the muscle, which also changed, reflected a more complex relation between diet and metabolic processes in the tissue. The use of stable isotopes of carbon and nitrogen to trace food sources was inconclusive in this study due to low differences between samples fed different feeds. Fatty acid profiling was a more sensitive method for tracing low concentrations of salmon feed and feces in the algae diet of scallops. Our results suggest that P. maximus could be a candidate for integrated multi trophic aquaculture (IMTA) and that scallops have the potential to utilize small particles of wasted salmon feed and feces during a winter situation with low phytoplankton concentration and during an algal bloom in Norwegian waters.

Scallops seasoned with nanoplastics

Plastic Pollution![Figure][1] The great scallop ( Pecten maximus ) reveals details about the uptake of nanoplastics by marine organisms. PHOTO: NATURE PICTURE LIBRARY/ALAMY STOCK PHOTO Microplastics are present in marine environments worldwide. As these particles break down further, they form nanoplastics, which are harder to detect. Nanoplastics also can enter the environment directly from commercial products such as paints and cosmetics. Al-Sid-Cheikh et al. investigate the uptake of such nanoplastics by scallops at predicted environmental concentrations. The authors use radiocarbon labeling to track the nanoplastics within the scallop tissues. Uptake differs depending on particle size: Larger nanoparticles accumulate in the intestine, whereas smaller nanoparticles are dispersed through the entire scallop body. After exposure to nanoplastics ceased, smaller nanoparticles were no longer detected after 14 days, but some larger nanoparticles persisted for more than 48 days. The presence of the smaller nanoparticles in muscle tissue suggests that the particles can cross epithelial membranes. Environ. Sci. Technol. 52 , 14480 (2018). [1]: pending:yes

Estudio taxonómico y arqueológico de la colección de malacofauna procedente de la Colonia "Augusta Emerita" (Mérida) con especial atención al uso de "Pecten maximus" en el tocador de la mujer romana

This paper presents a taxonomic analysis of the collection of malacofauna of the National Museum of Roman Art of Mérida, an interesting collection from the historical point of view, since practically in its totality it is unpublished. This work also focuses its analysis on the specific case of the specimens of Pecten maximus (L, 1758), whose use seems to be associated in a recurrent way with the toilette of the Roman woman, with very outstanding examples of noble materials such as silver or amber.

Uptake, Whole-Body Distribution, and Depuration of Nanoplastics by the Scallop Pecten maximus at Environmentally Realistic Concentrations.

Previous studies of uptake and effects of nanoplastics by marine organisms have been conducted at what may be unrealistically high concentrations. This is a consequence of the analytical challenges in tracking plastic particles in organisms at environmentally relevant concentrations and highlights the need for new approaches. Here, we present pulse exposures of 14C-radiolabeled nanopolystyrene to a commercially important mollusk, Pecten maximus, at what have been predicted to be environmentally relevant concentrations (<15 μg L-1). Uptake was rapid and was greater for 24 nm than for 250 nm particles. After 6 h, autoradiography showed accumulation of 250 nm nanoplastics in the intestine, while 24 nm particles were dispersed throughout the whole-body, possibly indicating some translocation across epithelial membranes. However, depuration was also relatively rapid for both sizes; 24 nm particles were no longer detectable after 14 days, although some 250 nm particles were still detectable after 48 days. Particle size thus apparently influenced the biokinetics and suggests a need for chronic exposure studies. Modeling extrapolations indicated that it could take 300 days of continued environmental exposure for uptake to reach equilibrium in scallop body tissues although the concentrations would still below 2.7 mg g-1. Comparison with previous work in which scallops were exposed to nonplastic (silver) nanomaterials of similar size (20 nm), suggests that nanoparticle composition may also influence the uptake tissue distributions somewhat.

New insights into the reproductive cycle of two Great Scallop populations in Brittany (France) using a DEB modelling approach

The present study aimed to improve understanding of the environmental conditions influencing the reproductive cycle of the great scallop Pecten maximus in two locations in Brittany (France). We also evaluated potential consequences of future climate change for reproductive success in each site.We simulated reproductive traits (spawning occurrences and synchronicity among individuals) of P. maximus, using an existing Dynamic Energy Budget (DEB) model. To validate and test the model, we used biological and environmental datasets available for the Bay of Brest (West Brittany, France) between 1998 and 2003. We also applied the scallop DEB model in the Bay of Saint-Brieuc (North Brittany, France) for the same period (1998–2003) to compare the reproductive cycle in different environmental conditions. In order to accurately model the P. maximus reproductive cycle we improved the scallop DEB model in two ways: through (1) energy acquisition, by incorporating microphytobenthos as a new food source; and (2) the reproductive process, by adding a new state variable dedicated to the gamete production. Finally, we explored the effects of two contrasting IPCC climate scenarios (RCP2.6 and RCP8.5) on the reproductive cycle of P. maximus in these two areas at the 2100 horizon.In the Bay of Brest, the simulated reproductive cycle was in agreement with field observations. The model reproduced three main spawning events every year (between May and September) and asynchronicity in the timing of spawning between individuals. In the Bay of Saint-Brieuc, only two summer spawning events (in July and August) were simulated, with a higher synchronicity between individuals. Environmental conditions (temperature and food sources) were sufficient to explain this well-known geographic difference in the reproductive strategy of P. maximus. Regarding the forecasting approach, the model showed that, under a warm scenario (RCP8.5), autumnal spawning would be enhanced at the 2100 horizon with an increase of seawater temperature in the Bay of Brest, whatever the food source conditions. In the Bay of Saint-Brieuc, warmer temperatures may impact reproductive phenology through an earlier onset of spawning by 20 to 44 days depending on the year.

HISTOPATHOLOGICAL CHANGES IN THE STOMACH MUCOSA OF RATS FED WITH GREAT SCALLOP (Pecten maximus)

Heavy metals, industrial and household wastes and pesticides are threats for the aquatic ecosystem. Polluted water sources are streaming into the seas and cause pollution in these systems. Dardanelles is exposed to pollution from the Marmara and Black Sea. Our previous studies demonstrated that the water and mollusc from certain regions of the Dardanelles contained heavy metal salts. The purpose of the study is to demonstrate the histopathologic changes in the gastric tissues of rats which are fed with great scallop (Pecten maximus) that are collected from the Çardak region of the Dardanelles. Four groups of rats are included in the study, group 1 (n=6), control group fed with standard rat food, group 2 (n=6), 75% great scallop and 25% standard rat food daily, group 3 (n=6), 75% great scallop and 25% standard rat food every two days, group 4 (n=6), 75% great scallop and 25% standard rat food every three days. After the routine histopathologic processing all gastric tissue samples are evaluated in terms of 8-hydroxy-2' -deoxyguanosine (8-OHdG) immunoreactivity with light microscopy and image analysis software. No histopathologic differences found in standard hematoxylin-eosin (H.E.) stained gastric tissue samples of the control group. Second group showed active chronic gastritis, third group showed less inflamation and chronic gastritis compared with the second group and fourth group showed less mononuclear inflammation compared to the second and third groups. In immunohistochemical staining, 8-OHdG immunoreactivity in gastric epithelial cells. 8-OHdG immunoreactivity was negative in stomach tissues in all groups. There was no statistically significant difference between the groups that were fed every day, every other day and every three days with great scallop (p&gt;0.05). The results of our studies showed that rats fed more with great scallops could produce gastritis in the stomach

Understanding the mechanisms involved in the high sensitivity of Pecten maximus larvae to aeration

Among reared bivalves, some “novel species”, such as the great scallop, Pecten maximus, have experienced more difficulty with routine reproduction due to their high sensitivity to biological, chemical, and physical stress during stages of early development. Working with high larval densities requires the use of aeration systems to provide optimal larval suspension and feed distribution. The high susceptibility of the great scallop to aeration in small-volume systems may impose an important limitation in hatchery-based practices. The present study aimed to investigate the processes impacted by aeration in P. maximus veliger larvae exposed to continuous aeration in small-volume tanks (10 L). Aeration appeared as major stressor that was responsible for early mortality among exposed animals (at 96 h after aeration started, haa) when exposure started 13 days after fertilization. Exposed larvae and controls were collected at 12, 24 and 72 haa, and a total of 18 cDNA libraries, each representing a pool of approximately 7,500 larvae, were sequenced, obtaining 358,817,016 raw reads. RNA-seq data were first used to build a de novo transcriptome assembly, and differential transcript abundance was assessed in exposed and control groups; thus, the molecular mechanisms involved in high sensitivity to aeration were deciphered. More than 2,000 transcripts were differentially expressed between exposed and control larvae across the entire time series (logFC > 1, FDR < 5%). Functional analysis revealed that transcriptional changes in larvae exposed to aeration mainly involved the genes that regulate digestive activity and energy metabolism, immune defense, inflammation, apoptosis, larval growth, and development. The results of this study demonstrate that, overall, aeration affects the feeding capacity and energy metabolism of larvae, with expected consequences on the animal's fitness, including its swimming efficiency. Aeration also triggered immune responses and apoptosis, which then increased through opportunistic infections. Notably, infections may be a consequence of a bacterial bloom triggered by the first mortality events that occurred in the culture. This study provides insights into the interactions between environmental variables and great scallop larvae physiology, and the results may contribute to the development of strategies for improving larval rearing practices and ensuring long-term sustainability of P. maximus aquaculture.

Reconstructing physiological history from growth, a method to invert DEB models

Dynamic Energy Budget (DEB) models rely on measurements of food availability to describe the rates at which organisms assimilate and use energy from food for maintenance, growth, maturation and reproduction. Although crucial, the determination of appropriate and accurate energy input variables can be problematic. We developed an inverted DEB model to reconstruct the food intake from temperature and growth trajectories. The method makes use of a reformulation of the DEB model dynamics into a second order linear equation. This formula not only allows the reconstruction of the scaled functional response but also gives access to reserve dynamics, mobilization, and somatic maintenance fluxes. The shell of the great scallop, Pecten maximus, providing high resolution records of incremental growth, was used to explore the potential of this approach to reconstruct the functional response from daily shell growth rates data. In a theoretical case, we investigated the resolution and sensitivity limits of the method. In a validation process, predictions were used to re-simulate growth that was compared to the initial growth trajectory. Moreover, as growth data used in the reconstruction process usually show high-frequency variability, we also developed a smoothing method, based on DEB theory assumptions, to filter growth data time series.

Rapid analysis of paralytic shellfish toxins and tetrodotoxins by liquid chromatography-tandem mass spectrometry using a porous graphitic carbon column

Although paralytic shellfish toxins (PSTs) have traditionally been analyzed by liquid chromatography with either pre- or post-column derivatization, and these methods have been validated successfully through inter-laboratory studies, mass spectrometry methods have also been described in literature for use in monitoring programs. However, methods using liquid chromatography coupled with mass spectrometry (LC-MS) need to be improved in terms of sensitivity, analyte recovery and retention time stability because of undesirable matrix effects. Furthermore, tetrodotoxin (TTX) has been found in northern European bivalves, so it is important to analyze TTX compounds alongside PSTs because characteristics of their toxicity are similar. This paper describes, for the first time, a chemical method that allows determination of PSTs, both hydrophilic and hydrophobic, alongside TTX and its analogue 4,9-anhydro tetrodotoxin (4,9-anhTTX) with LC-MS/MS using a Hypercarb® column. The method was validated for 13 hydrophilic PSTs and TTXs and was able to discriminate six hydrophobic PSTs in 20 min. The method was developed for four shellfish matrices: mussel (Mytillus galloprovincialis), clam (Ruditapes decussatus), scallop (Pecten maximus) and oyster (Ostrae edulis). Clean-up procedure used in this work allowed us to obtain good results for validation parameters for both PSTs and TTXs. No standards were available so strains of Gymnodinium catenatum (G. catenatum) were used instead.