Patrick Reynolds

This study aimed to expand knowledge on lumpfish stress physiology by investigating the effects of acute stress on primary (i.e., cortisol) and secondary (e.g., metabolites) stress responses, as well as oxidative stress biomarkers, from stress exposure to a recovery phase. The results showed that the lumpfish physiological response to 1 min air exposure is mild, in line with recent studies, and comparable to that described for white sturgeons. Cortisol seems to be the most reliable acute stress biomarker in lumpfish, with a significant increase in plasma 30 min after stress exposure, returning to resting levels 2 h after exposure. In contrast, glucose and lactate were not significantly altered by short-term air exposure. Effects on hepatic energy mobilisation were also detected following the acute stress. This study showed that acute 1 min air exposure seems tolerable, allowing a swift recovery. However, more studies on the impacts of air exposure and repeated acute stressors on lumpfish stress and immune responses are required to develop industry standards for lumpfish health and welfare monitoring.

Aquaculture of the lumpfish (Cyclopterus lumpus L.) has become a large, lucrative industry owing to the escalating demand for “cleaner fish” to minimise sea lice infestations in Atlantic salmon mariculture farms. We used over 10K genome-wide single nucleotide polymorphisms (SNPs) to investigate the spatial patterns of genomic variation in the lumpfish along the coast of Norway and across the North Atlantic. Moreover, we applied three genome scans for outliers and two genotype–environment association tests to assess the signatures and patterns of local adaptation under extensive gene flow. With our ‘global’ sampling regime, we found two major genetic groups of lumpfish, i.e., the western and eastern Atlantic. Regionally in Norway, we found marginal evidence of population structure, where the population genomic analysis revealed a small portion of individuals with a different genetic ancestry. Nevertheless, we found strong support for local adaption under high gene flow in the Norwegian lumpfish and identified over 380 high-confidence environment-associated loci linked to gene sets with a key role in biological processes associated with environmental pressures and embryonic development. Our results bridge population genetic/genomics studies with seascape genomics studies and will facilitate genome-enabled monitoring of the genetic impacts of escapees and allow for genetic-informed broodstock selection and management in Norway.

Data from research and commercial use of lumpfish were collected from the research facilities of Gifas (Inndyr, Northern Norway, 67.0° N, 14.0° E). The data were sourced from 12 main lumpfish groups subdivided into 66 subgroups (N = 160,729) delivered to Gifas between 2013 and 2020 and used in cleaner-fish research in (a) land-based facilities, (b) small-scale, or (c) large-scale sea pens. The data were standardised and organised into three main headings. Firstly, background information included transfer time, point of origin, mean starting weight and population size on arrival. Other information included to which site the lumpfish were transferred, volume of cage/tank, whether in the presence of salmon or not, stocking density, days at each site and water quality parameters. Causes of mortality were recorded, when possible, for each group, along with calculated mortality rates, patterns, and analytical information, along with imaging where available. Results show that causes of mortality varied within and between research sites. For lumpfish in hatcheries as well as for those deployed at small-scale sea pens, the primary cause of mortality was identified as pathogenic, while for lumpfish deployed at large-scale sea pens, transporting, grading and mechanical delousing were the primary causes of mortality. The results indicate that more research is required to clarify best practices both in commercial hatcheries and salmon cages and further understanding on lumpfish biological requirements and stress physiology is necessary to develop better methods that safeguard lumpfish welfare and meet their needs.

In this review, we have systematized current knowledge about the effect of stocking lumpfish (Cyclopterus lumpus) as cleaner fish to control Lepeophtheirus salmonis infestations on farmed Atlantic salmon (Salmo salar L.). The review was prompted by recent reports in which the usefulness of lumpfish has been doubted, and the urgent need to investigate whether common lumpfish can be used to reduce L. salmonis numbers on farmed Atlantic salmon by active grazing on this species. Available published data clearly indicate that lumpfish graze on L. salmonis, and can significantly lower the lice burden in Atlantic salmon farming. It is possible to enhance the lice grazing behavior of lumpfish with the assistance of live feed conditioning prior to sea pen transfer, and with selective breeding. Data indicate that lice grazing of lumpfish is size dependent, and grazing effect is low for lumpfish larger than 200–250 g. Observations from large-scale rearing of Atlantic salmon in open sea cages in Norway, Iceland, the Faroe Islands, and Scotland also indicate that lumpfish can be effective in lowering infestations of L. salmonis on salmon. Overall, this present review reveals that lumpfish can actively contribute to lower numbers of L. salmonis on farmed Atlantic salmon.