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A new species of Myxobolidae, Henneguya cardii n. sp., is described infecting the European seabass Dicentrarchus labrax, a fish of high commercial value intensively cultivated in southern Europe. Henneguya cardii n. sp. was found in the bulbus arteriosus and spleen with a prevalence of infection of 13.5%. In the heart, it forms irregular whitish plasmodia measuring 1 mm in size. Mature myxospores are broadly obovoid in frontal view and ellipsoidal in lateral view, with 2 equal caudal appendages. Polar capsules are ovoid and symmetric, with 3–4 polar tubule coils. Myxospores measure 10.2 ± 0.6 (8.8–11.6) μm in length, 8.0 ± 0.7 (5.3–8.8) μm in width and 5.6 ± 0.2 (5.1–6.4) μm in thickness. Caudal appendages are 36.6 ± 3.2 (27.4–42.9) μm long. Total spore length is 47.6 ± 3.2 (41.2–53.2) μm. Polar capsules measure 4.0 ± 0.2 (3.4–4.6) by 2.2 ± 0.1 (1.9–2.6) μm. Small subunit ribosomal RNA-based tree topologies position H. cardii n. sp. within a lineage of marine myxobolids that is mostly comprised of other Henneguya species. Host-relatedness is reinforced as the main evolutionary driver for myxobolids, with the positioning of H. cardii n. sp. further suggesting tissue tropism as another important evolutionary driver for marine heart infecting Henneguya. Nonetheless, the inner complexity of this lineage suggests that identification of the evolutionary patterns driving its phylogeny will require discovery of the true diversity of marine myxobolids.
We herein investigated the influence of temperature on the embryonic development (from fertilisation to hatching) of Mugil liza larvae. For this purpose, oocytes (>600 μm) and sperm were obtained from breeding stock at the laboratory of marine fish culture (LAPMAR). After fertilisation, 1200 eggs were distributed in 12 cylindrical experimental units of 400 mL under four different temperatures 18, 22, 26 and 30 ºC, all in triplicate. Every 15 min until hatching, about 10 eggs were randomly sampled in each treatment. The eggs were visualized and photographed, and the classification of embryonic stages was performed. Temperature influenced the main events of the embryonic development of M. liza. More accelerated development was observed according to the increase in temperature until the gastrula phase. At temperatures of 22 and 26 °C, embryonic development occurred from fertilisation to hatching of the larvae. In the 18 °C treatment, it was verified that most of the embryos ceased development during the final phase of cleavage and the beginning of blastula formation, while in the 30 °C treatment patterns of embryo malformation were also verified, with erratic divisions of the blastomeres, resulting in irregular cells. Unlike what was observed at a temperature of 18 °C, none of the embryos incubated at 30 °C reached the blastopore closure phase, stopping in the gastrula. The larvae hatched in the treatments at 22 and 26 °C were viable and exhibited intense swimming, with a large amount of reserve material (yolk) and an evident drop of oil.
We have developed probabilistic models to estimate the likelihood of harmful algae presence and outbreaks along the Norwegian coast, which can help optimization of the national monitoring program and the planning of mitigation actions. We employ support vector machines to calibrate probabilistic models for estimating the presence and harmful abundance (HA) of eight toxic algae found along the Norwegian coast, including Alexandrium spp., Alexandrium tamarense, Dinophysis acuta, Dinophysis acuminata, Dinophysis norvegica, Pseudo-nitzschia spp., Protoceratium reticulatum, and Azadinium spinosum. The inputs are sea surface temperature, photosynthetically active radiation, mixed layer depth, and sea surface salinity. The probabilistic models are trained with data from 2006 to 2013 and tested with data from 2014 to 2019. The presence models demonstrate good statistical performance across all taxa, with R (observed presence frequency vs. predicted probability) ranging from 0.69 to 0.98 and root mean squared error ranging from 0.84% to 7.84%. Predicting the probability of HA is more challenging, and the HA models only reach skill with four taxa (Alexandrium spp., A. tamarense, D. acuta, and A. spinosum). There are large differences in seasonal and geographical variability and sensitivity to the model input of different taxa, which are presented and discussed. The models estimate geographical regions and periods with relatively higher risk of toxic species presence and HA, and might optimize the harmful algae monitoring. The method can be extended to other regions as it relies only on remote sensing and model data as input and running national programs of toxic algae monitoring.
The evaluation of the effects of early starvation and feeding on survival and growth in the early stages of the life cycle of ornamental marine caridean shrimp species is fundamental to establish adequate feeding protocols in their culture. In this study, we determine the nutritional vulnerability in the early larval stages of ornamental shrimp Lysmata ankeri exposed to different periods of starvation or feeding. The larvae were separated into three groups (zoea I-ZI, zoea II with ZI fed, and zoea II with ZI unfed) and subjected to two experiments: (1) point-of-no-return (PNR), comprising one or two days of initial starvation followed by feeding; and (2) point-of-reserve-saturation (PRS), comprising one or two days of initial feeding followed by starvation. Each experiment was still composed of two control groups: continuous feeding and continuous starvation. Larvae tolerated some periods of starvation, with a high PNR value (2.00) and low PRS (0.50). Longer periods of starvation influenced both growth and survival rates in zoea II stages. The nutritional vulnerability index for zoea I was 0.25, which represents a low dependence on food supply. In this study, it was observed that ornamental shrimp L. ankeri larvae hatch with energy reserves, presenting facultative primary lecithotrophy, in which they are able to moult from zoea I to zoea II using such reserves in the absence of food. In this sense, the early larvae stages (zoeas I and II) can tolerate a certain period of starvation, indicating the great potential of this species for aquaculture.
Sustainability and sustainable development are the buzzwords of our era. Nowhere is this clearer than in primary production/extraction industries, such as aquaculture and fisheries. Yet in the seafood sector (as with many others), the term continues to be used most commonly in relation to the environmental dimension; much less is known about social and economic sustainability. In this review, we explore what is known about social sustainability in the seafood sector. We identify seven key thematic areas: livelihoods and human development; human rights; social, psychological, and cultural needs; equitable access to resource and benefit sharing; a voice in public issues; flow-on benefits for local and regional economies and improved infrastructure and access. We reveal that while there has been a clear focus on developing social sustainability indicators, this has largely missed more relational and subjective aspects of social sustainability. We also show that some thematic areas of social sustainability also remain underdeveloped. Overall, we argue that it is imperative that we address the knowledge gaps and incorporate what we already know about social sustainability into existing industry and governance processes. If we do not, not only risk not achieving the Sustainable Development Goals, but we also risk moving closer towards environmental and societal collapse.
As the Middle Ages drew to a close, however, a rising share of Europeans were eating fish from systems other than their natural local waters. By 1500 around Paris, for instance, elite menus featured carp and headless codfish, while lesser folk made do with herring and haddock. Beside the Mediterranean, Valencia was receiving millions of Atlantic sardines and hake, while Romans could get herring from the North Sea, Norwegian cod, and tuna from Sicily. Both cultured carp and fishes from Europe’s economic frontiers changed Europeans’ relations with aquatic nature.
Carp aquaculture colonized nature, creating artificial habitats to rear an organism alien to western Europe. Late fifteenth- and early sixteenth-century financial records and instructional manuals from east-central Europe detail an original and distinctive European mode for farming fish. Those practices provide a benchmark to identify and trace their creation in twelfth- to thirteenth-century France – where the carp was a late invader – and subsequent spread eastwards of the innovation. Human-controlled aquaculture created thousands of local ecological revolutions across interior Europe, providing inland elites with a steady source of live fresh fish, serving as a vehicle of elite power over subjected nature and people, and replacing indigenous ecosystems with private anthropogenic habitats tailored for domesticated, soon also feral, invaders. For contemporary writers fish had become objects of human agency.
In the coming decades, promoting the production of ecosystem service provisioning will become increasingly important in the U.S. Northeast, which is expected to experience a number of impacts as a result of climate change, including rising temperatures, changes in precipitation and seasonality, and sea-level rise, among others (U.S. Global Change Research Program 2020). Incentives have been shown to motivate the adoption of sustainable production practices that provision ecosystem services across different types of working landscapes. Using data from a recent landscape assessment in the Northeast, this paper finds an incredible breadth of programs available to producers across a variety of working landscapes (e.g., agricultural lands and working forests) and for different production practices. These data also point to critical gaps in current programming and also highlight important opportunities for programmatic synergy and more holistic program design going forward. This paper concludes by discussing the results in the context of four main themes of particular relevance to the U.S. Northeast which include (1) working landbase and infrastructure, (2) livelihood provisioning, (3) scale, and (4) resilience.
Brazilian basslet Gramma brasiliensis is a fish highly appreciated by the marine ornamental industry. There is an increasing interest in the development of a breeding protocol for this species. However, descriptions of the reproductive biology, eggs and larval development are scarce. This study was the first to describe the spawning, eggs and larvae of G. brasiliensis in captivity, including mouth size information. Six spawning events produced egg masses with 27, 127, 600, 750, 850, and 950 eggs. Larger egg masses showed embryos with at least two different developmental stages. Eggs are spherical (∼1.0 mm diameter), held together by filaments entangling chorionic projections. Larvae with fewer than 12 hph (hours post-hatch) presented 3.55 mm standard-length, well developed eyes, fully absorbed yolk sac, an inflated swim bladder and mouth opened. Exogenous feeding on rotifers began within 12 hph. The average mouth width at first feeding was 0.38 mm. The first settled larva was noted by day 21. This information should help to determine appropriate diets and prey-shift time during the larviculture of the species.
In nematodes, the structure of male copulatory organs is a significant taxonomic distinguisher and includes the morphometry of the spicules. The description of these structures mainly relies on the study of whole mounts using light microscopy. In rare instances, protruding spicules have been described with scanning electron microscopy. Even fewer studies have described the ultrastructure of isolated spicules following their isolation. In the present study, two different methods of spicule isolation were performed on two parasitic camallanid nematodes, Procamallanus (Procamallanus) pseudolaeviconchus Moravec & van As, 2015 and Paracamallanus cyathopharynx (Baylis, 1923), from African sharptooth catfish to determine the practicality and efficiency of the methodologies. The first method involved using sharpened tungsten needles and microdissection of the spicule pouch to free the spicules, followed by soft tissue digestion if necessary. Alternatively, the spicules were isolated through mechanical release instead of dissection in a method developed in the current study. This involved freeing the spicules from surrounding soft tissue by placing live specimens between a coverslip and a glass slide in a drop of water and exerting pressure with small rotational movements. Both methods yielded favourable results, but Method 2 is recommended for future studies due to the many advantages.
Global farmed finfish production increased from 9 to 56 million tonnes between 1990 and 2019. Although finfishes are now widely recognised as sentient beings, production is still being quantified as biomass rather than number of individuals (in contrast to farmed mammals and birds). Here, we estimate the global number of farmed finfishes slaughtered using FAO aquaculture production tonnages (1990–2019 data) and estimates of individual weight at killing (determined from internet searches at species and country level where possible). We relate these numbers to knowledge on humane slaughter, animal welfare law, and certification schemes. Since 1990, farmed finfish numbers killed annually for food have increased nine-fold, to 124 billion (1.24 × 1011, range 78–171 billion) in 2019. This figure does not represent the total number farmed (due to mortalities during rearing and non-food production) and is expected to increase as aquaculture expands. Our estimates indicate that farmed finfishes now outnumber the 80 billion farmed birds and mammals killed globally each year for food. The majority are produced in Asia. Inhumane slaughter practices cause suffering for most farmed finfishes. Most, 70–72%, have no legal welfare protection, and less than 1% have any fish-specific legal protection, at slaughter. The main global certification schemes in 2013–2015 accounted for 2% of slaughtered farmed finfishes. Fishes for which species-specific parameters for automated humane stunning are published comprise 20–24%. As the dominant taxa of farmed vertebrates, finfishes would benefit from better welfare if species-specific humane slaughter was defined and incorporated into laws and certification schemes.
Fish parasitological research associated with fisheries and aquaculture has expanded remarkably over the past century. The application of parasites as biological tags has been one of the fields in which fish parasitology has generated new insight into fish migration and stock assessments worldwide. It is a well-established discipline whose methodological issues are regularly reviewed and updated. Therefore, no concepts or case-studies will be repeated here; instead, we summarize some of the main recent findings and achievements of this methodology. These include the extension of its use in hosts other than bony fishes; the improvements in the selection of parasite tags; the recognition of the host traits affecting the use of parasite tags; and the increasingly recognized need for integrative, multidisciplinary studies combining parasites with classical methods and modern techniques, such as otolith microchemistry and genetics. Archaeological evidence points to the existence of parasitic problems associated with aquaculture activities more than a thousand years ago. However, the main surge of research within aquaculture parasitology occurred with the impressive development of aquaculture over the past century. Protozoan and metazoan parasites, causing disease in domesticated fish in confined environments, have attracted the interest of parasitologists and, due to their economic importance, funding was made available for basic and applied research. This has resulted in a profusion of basic knowledge about parasite biology, physiology, parasite–host interactions, life cycles and biochemistry. Due to the need for effective control methods, various solutions targeting host–parasite interactions (immune responses and host finding), genetics and pharmacological aspects have been in focus.
This study aimed to evaluate the ploidy and survival of larvae resulting from crosses between tetraploid females and diploid males of yellowtail tetra Astyanax altiparanae, both females (three diploids and three tetraploids) and males (n = 3 diploids). Breeders were subjected to hormonal induction with pituitary gland extract from common carp fish (Cyprinus carpio). Females received two doses at concentrations of 0.3 and 3.0 mg/kg −1 body weight and at intervals of 6 h. Males were induced with a single dose of 3.0 mg/kg −1 applied simultaneously with the second dose in females. Oocytes from each diploid and tetraploid female were fertilized with semen from the same male, resulting in two crosses: cross 1 (diploid male and diploid female) and cross 2 (diploid male and tetraploid female). The procedures were performed with separate females (diploid and tetraploid) and diploid males for each repetition (n = 3). For ploidy determination, 60 larvae from each treatment were analyzed using flow cytometry and cytogenetic analyses. As expected, flow cytometry analysis showed that progenies from crosses 1 and 2 presented diploid and triploid individuals, respectively, with a 100% success rate. The same results were confirmed in the cytogenetic analysis, in which the larvae resulting from cross 1 had 50 metaphase chromosomes and those from cross 2 had 75 chromosomes. The oocytes have a slightly ovoid shape at the time of extrusion. Diploid oocytes had a size of 559 ± 20.62 μm and tetraploid of 1025.33 ± 30.91 μm. Statistical differences were observed between eggs from crosses 1 and 2 (P = 0.0130). No significant differences between treatments were observed for survival at the 2-cell stage (P = 0.6174), blastula (P = 0.9717), gastrula (P = 0.5301), somite (P = 0.3811), and hatching (P = 0.0984) stages. In conclusion, our results showed that tetraploid females of the yellowtail tetra A. altiparanae are fertile, present viable gametes after stripping and fertilization using the ‘dry method’, and may be used for mass production of triploids. This is the first report of these procedures within neotropical characins, and which can be applied in other related species of economic importance.
Atlantic salmon (Salmo salar) are an economically and ecologically important fish species that interact with humans during farming, fishing and research operations. Routine handling in nets exposes fish to mesh and causes scale loss. To promote welfare and experimental refinement, a study was performed in a controlled environment to investigate the effect of net mesh type (rubber-coated or standard knotless, both bag volumes circa 7 l; mesh size: 6 mm) and the number of fish per net (capture density) on scale loss. Up to three large adult salmon (mean weight: 900 g) or 15 small smolts (mean weight: 145 g) were briefly captured in hand-nets during routine immersed-stock movement between tanks. Scales were recovered and counted from transportation containers, to establish a simple and rapid methodology. For both size grades, scale loss was generally proportional to capture density. For large adult salmon, scale loss significantly increased with capture density when knotless mesh was used, however the increase was less marked and not statistically significant for adults handled in rubber mesh. Small smolts also demonstrated significantly reduced scale loss when handled with rubber mesh, which increased gradually with capture density. In contrast, small smolts handled in knotless mesh showed greater scale loss as capture density increased. An overall reduction in scale loss with increased capture density was not shown, although the biomass loading per net used in this study were intentionally low (< 3.5 kg). This method suggests a low-tech and rapid approach to quantitatively compare net types and husbandry techniques and suggests a fundamental but simple improvement to salmonid handling in recreational and commercial operations. However, any correlation to conventional stress assays or behavioural observations remains to be established.
In the expanding salmon industry, many farmers use production methods that could result in poor welfare of the fish at various points of their lifecycle. We have reviewed methods used for producing salmon for food with the aim of identifying and drawing attention to factors likely to affect farmed Atlantic salmon (Salmo salar) welfare. In addition to water conditions and high stocking density at sea, other issues are important for fish welfare. Handling and transport of salmon between fresh- and seawater phases and before slaughter can have severe negative effects and research should continue to seek improved methods. Stocking densities in fresh- or seawater have substantial effects on the welfare of salmon and a reduction in densities should be considered in order to reduce fin damage in particular. Currently used feeding systems result in starvation for some fish and fin damage for others, hence new systems should be developed. Some on-demand feeding systems improve welfare. All farmed fish should be stunned prior to slaughter, not left to die of asphyxia. Carbon dioxide and electrical stunning methods do not always stun salmon humanely. The widely used methods of percussive stunning, manual or automatic, must be precise to effectively stun large numbers of fish. Welfare outcome indicators, such as fin damage, morbidity and mortality rate, should be used in standards and laws relating to salmon welfare.
The present study investigated the operational feasibility of the recently developed Salmon Welfare Index Model (SWIM 1.0) designed for Atlantic salmon (Salmo salar L) in production cages. Ten salmon farms containing spring smolts were visited twice, first between May and June the first year in sea cages, and secondly 2-3 months later. On each farm the SWIM 1.0 assessments were carried out for the two cages assumed by the farmer to represent the best and worst welfare status. The applied welfare indicators (WIs) were water temperature, salinity, stocking density, lighting, disturbance, daily mortality rate, appetite, sea lice infestation ratio, condition factor, emaciation state, vertebral deformation, maturation stage, smoltification state, fin condition and skin condition. The effective time to carry out the welfare evaluation was about 1.5 h per farm. The results showed some marked differences between visits; relatively larger proportions of emaciated fish were sampled during the first compared to the second visit, and more homogeneous scores of skin and fin damage were found on the second visit. The overall welfare index scores were generally in accordance with the farmers’ ranking of the ‘best’ and the ‘worst’ sea cage during the first visit. Together, the findings of this study suggest that the SWIM model may be employed for documentation of animal welfare over the salmon marine production cycle. The results call attention towards re-assessment of some of the welfare indicators, improved sampling methods, and a more user-friendly interface. All-in-all, the current SWIM model is regarded as a promising candidate tool towards welfare assessment of farmed salmon.
As the harvesting of fish through commercial fisheries becomes both harder and less economically viable, the world is becoming increasingly dependent on aquaculture to provide fish for human consumption. The closely related activity of stock enhancement, whereby large numbers of fish are reared and then released, is a common practice aimed at increasing the numbers of fish in rivers and along coasts. Aquaculture and stock enhancement practices raise a number of welfare and conservation issues both for fish that are reared within captivity, and for the local populations and habitats that are influenced by fish-rearing activities. In this review, we illustrate how fish farms and hatcheries have directly affected fish welfare. Examples cover on-farm fish husbandry and healthcare, the interactions between farmed and wild fish, and survival of fish released for stock enhancement. These aspects are often intertwined with important conservation issues. Thus, we also review direct effects that aquaculture-generated pollution can have on local habitats, issues associated with feeding reared fish, and problems created by alien fish (either escapees or intentionally released fish). While awareness of fish welfare is certainly growing, so is the rate at which fish are reared. There is, therefore, a pressing need to understand the welfare and conservation issues that are affected by aquaculture and stock enhancement.
Fish welfare is a key factor in ensuring successful cultures. Farmed fish that are stressed have been shown to be susceptible to pathologies and present lower growth rates. The present work seeks to check the efficacy of faecal cortisol as a non-invasive method of assessing acute stress in a commercial cultured fish, the gilthead seabream (Sparus aurata). Typical stress markers (plasma cortisol, glucose and lactate) and faecal cortisol were measured in basal and post-stress (air exposure) state. Plasma and faecal cortisol, and plasma lactate after acute stress varied significantly compared to basal levels. Moreover, faecal cortisol showed a significant correlation with plasma cortisol and lactate. In conclusion, this work describes an easy, non-invasive and practical technique to assess acute stress in farmed fish. Further studies are needed to focus on other practical procedures for chronic stress measurements in sea-farms in order to improve the welfare of these animals.
Fish (Elasmobranchia and Actinopterygii) inhabit the majority of aquatic habitats globally. They are crucial for human nutrition but they may be negatively affected by parasitic protists and metazoan parasites. Fish parasites are also an extraordinary group of animals because of their ecological and evolutionary importance and unique adaptations to parasitism. They also play a key role in ecosystem functioning. In the present special issue, 13 review and research articles on major groups of fish parasites are provided to document the current advancement in our understanding of different aspects of their biology, ecology and associations with their fish hosts. The existing gaps in our knowledge of these peculiar animals are mapped and future trends in their research outlined.
U.S. per capita seafood consumption is historically high due to population and income growth and consumer preference shifts toward healthy protein options. Despite this expansion, U.S. fisheries, especially those in the Great Lakes region, no longer fulfill domestic demand due to pressure on fish stocks and regulatory constraints. Instead, aquaculture and imports fill the gap. Rainbow trout, yellow perch, and walleye—three species historically produced in the North Central Region (NCR)—exemplify such trends. To expand marketing opportunities for NCR aquaculture producers, this study estimates willingness to pay (WTP) for these species and several search and credence fish attributes. We designed and distributed a survey instrument to collect hypothetical choice experiment responses from U.S. seafood consumers. Using a random utility framework, we estimate mean total WTP for trout, yellow perch, and walleye of $19.99/lb., $15.89/lb., and $17.37/lb., respectively. Further, we identify average price premia of $1.64/lb., $1.97/lb., and $0.84/lb. for NCR-sourced, wild-caught, and fresh fillet attributes. Our analysis also captures regional preferences. Mean WTP estimates for yellow perch and walleye, which are native to the Great Lakes, are significantly higher inside the NCR. Further, trout commands a higher premium outside the NCR than within, suggesting potential market segmentation for the analyzed species.