Gear selectivity is crucial in fisheries management because it influences the size and species of fish caught, with traditional methods often basing optimal mesh size on the mature length of a target species. However, to ensure sustainable fisheries, both biological aspects of resource protection and fishing operation efficiency must be considered. This study aimed to determine the ideal mesh size for trap fishing of marbled flounder (Pseudopleuronectes yokohamae) in Gyeongsangnam-do, South Korea, by using biological and economic factors for sustainable fisheries management. We sampled fish caught in traps of varying mesh sizes (35, 50, 65, 80, and 100 mm) and developed two models based on fish maturity, bycatch ratio, and CPUE. Model 1 used a maturity criterion of 17.8 cm, and Model 2 used the legal minimum length limit of 20 cm. Net selectivity curves indicated that the optimal mesh size ranged 50–65 mm based only on a minimum mature body length of 17.8 cm. In contrast, the optimal mesh size based on both biological and economic factors ranged 57.5–90 mm. Our findings could guide policymakers in enhancing marble flounder population management strategies through policy adjustments in mesh size and gear restrictions.
Sustainability of natural stocks of crayfish is critical because of their economic and ecological importance. Crayfish (Pontastacus leptodactylus), one of the most important species in Turkish inland fisheries, has been facing serious threats recently. One threat the species faces is high landed bycatch of undersized crayfish because of selective fishing gear, such as fyke nets. We estimated size-selectivity of sorting grids with various bar spacings for crayfish to reduce bycatch. Six bar spacings (15.0, 17.5, 20.0, 22.5, 25.0, and 30.0 mm) were tested alongside commercial crayfish fyke nets. Mean selectivity (L50) (±95% CI) was 6.90 (6.63–6.99) cm for 15.0 mm bar spacing, 7.52 (7.16–8.02) cm for 17.5 mm, 8.52 (8.32–8.71) cm for 20.0 mm, 9.70 (9.28–9.90) cm for 22.5, 10.75 (10.34–11.17) cm for 25.0 mm, 11.80 (11.31–12.24) cm for 30.0 mm, and 8.79 (8.05–9.29) cm for commercial fyke nets. The proportion of undersized specimens caught be reduced from 32.27% for commercial fyke nets to as low as 2.46% by using sorting grids. The codend of 22.5 mm bar spacing was more selective, with significantly lower discard rates, and more effective for individuals above the minimum conservation reference size than commercial fyke nets.
Spatial and temporal distribution of European eel (Anguilla anguilla) during 1967–2020 was used to model European eel distribution in response to climate variability. Modeling integrated predictions from two distinct models for inferences. First, modeling of the relationship between temperature and precipitation and European eel catch values using multiple time-series regression analyses showed that climate variables contributed to eel distribution in Türkiye. Eel catch became restricted to western and southern coasts of Türkiye and total catch decreased between 1967 and 2020. From 1967 to 2020, favorable climatic conditions for European eels in Türkiye were characterized by moderate temperatures. Furthermore, projections for 2050 and 2070 suggested that suitable habitat would be lost in Türkiye. Our findings underscore the urgent need for immediate and widespread implementation of effective conservation policies to mitigate threats to European eel in Türkiye and globally.
Lakes are important in supporting ecosystem services and livelihoods. However, their food webs and ecological functioning are continuously threatened by anthropogenic influences. Food web models have been widely used in studying trophodynamics, fisheries impacts, and ecological functioning of temperate lakes, but less often in Afrotropical lake systems. We used Ecopath mass-balanced trophic models annually in 1999, 2010, and 2020 to assess trends in ecosystem function, and the impact of fisheries on the Lake Baringo Ecosystem, a shallow freshwater lake in Kenya. Pre-balance (PREBAL) and Pedigree analyses supplemented Ecopath models. Model input data were from field sampling, published and gray literature. Food web trophic models indicated a bottom-up grazer and detrital food chains in all 3 years. Odum's ecosystem development indicators (total productivity to total biomass and total respiration ratios; TPP/TB and TPP/TR) showed that the lake was in a low to intermediate developmental stage, with room for bio-manipulation, and a highly reduced mean transfer efficiency (TE) (6.4%–0.49%) indicated low trophic transfer of internal production. System omnivory (SOI) and connectance (CI) indices that varied among years indicated temporal variation in food web complexity. Indices of system resilience (overhead and ascendency) indicated an increasing potential for the lake to recover from perturbations. The mean trophic level of the catch (MTLc) increased from 1999 to 2010 and decreased in 2020, by fishing down the food chain as fishing pressure increased. Oreochromis niloticus, an endemic cichlid, was the keystone species (KSi >0) controlling community structure, while the lungfish Protopterus aethiopicus, the top predator in the lake, was not a keystone species (KSi <0). We recommend an integrated approach to lake management that incorporates watershed regulations, regulates fishing effort on the keystone species (O. niloticus), and monitors water quality for sustainable management of the Lake Baringo ecosystem.
The addition of coarse woody habitat (CWH) is often used to mitigate the loss of natural structure in aging waterbodies. Ecosystem-scale effects of large-scale CWH additions and their influence on fish productivity have been assessed in oligotrophic, natural lakes, but need to be assessed in more ecosystems. Therefore, we tested the effects of an ecosystem-scale addition of CWH to a eutrophic reservoir using a reference reservoir and data from 4 years before and 4 years after habitat enhancement. Zooplankton and benthic macroinvertebrates did not respond to the addition of CWH, but bluegill (Lepomis macrochirus) reproductive productivity and largemouth bass (Micropterus salmoides) size structure increased. Positive fish responses that contrasted with a lack of fish population-level responses after a similar CWH addition in an oligotrophic, natural lake highlight the importance of assessing the efficacy of CWH addition across diverse ecosystems.