Broad-Scale Climate Influences on Spring-Spawning Herring (Clupea harengus, L.) Recruitment in the Western Baltic Sea

Climate forcing in complex ecosystems can have profound implications for ecosystem sustainability and may thus challenge a precautionary ecosystem management. Climatic influences documented to affect various ecological functions on a global scale, may themselves be observed on quantitative or qualitative scales including regime shifts in complex marine ecosystems. This study investigates the potential climatic impact on the reproduction success of spring-spawning herring (Clupea harengus) in the Western Baltic Sea (WBSS herring). To test for climate effects on reproduction success, the regionally determined and scientifically well-documented spawning grounds of WBSS herring represent an ideal model system. Climate effects on herring reproduction were investigated using two global indices of atmospheric variability and sea surface temperature, represented by the North Atlantic Oscillation (NAO) and the Atlantic Multi-decadal Oscillation (AMO), respectively, and the Baltic Sea Index (BSI) which is a regional-scale atmospheric index for the Baltic Sea. Moreover, we combined a traditional approach with modern time series analysis based on a recruitment model connecting parental population components with reproduction success. Generalized transfer functions (ARIMAX models) allowed evaluating the dynamic nature of exogenous climate processes interacting with the endogenous recruitment process. Using different model selection criteria our results reveal that in contrast to NAO and AMO, the BSI shows a significant positive but delayed signal on the annual dynamics of herring recruitment. The westward influence of the Siberian high is considered strongly suppressing the influence of the NAO in this area leading to a higher explanatory power of the BSI reflecting the atmospheric pressure regime on a North-South transect between Oslo, Norway and Szczecin, Poland. We suggest incorporating climate-induced effects into stock and risk assessments and management strategies as part of the EU ecosystem approach to support sustainable herring fisheries in the Western Baltic Sea

Long-term dynamics of adaptive evolution in a globally important phytoplankton species to ocean acidification

Marine phytoplankton may adapt to ocean change, such as acidification or warming, because of their large population sizes and short generation times. Long-term adaptation to novel environments is a dynamic process, and phenotypic change can take place thousands of generations after exposure to novel conditions. We conducted a long-term evolution experiment (4 years = 2100 generations), starting with a single clone of the abundant and widespread coccolithophore Emiliania huxleyi exposed to three different CO2 levels simulating ocean acidification (OA). Growth rates as a proxy for Darwinian fitness increased only moderately under both levels of OA [+3.4% and +4.8%, respectively, at 1100 and 2200 μatm partial pressure of CO2 (Pco2)] relative to control treatments (ambient CO2, 400 μatm). Long-term adaptation to OA was complex, and initial phenotypic responses of ecologically important traits were later reverted. The biogeochemically important trait of calcification, in particular, that had initially been restored within the first year of evolution was later reduced to levels lower than the performance of nonadapted populations under OA. Calcification was not constitutively lost but returned to control treatment levels when high CO2–adapted isolates were transferred back to present-day control CO2 conditions. Selection under elevated CO2 exacerbated a general decrease of cell sizes under long-term laboratory evolution. Our results show that phytoplankton may evolve complex phenotypic plasticity that can affect biogeochemically important traits, such as calcification. Adaptive evolution may play out over longer time scales (>1 year) in an unforeseen way under future ocean conditions that cannot be predicted from initial adaptation responses

Using gravel for environmental enrichment in salmonid hatcheries: The effect of gravel size during egg incubation, endogenous and first feeding in rainbow trout

Environmental enrichment aims for a deliberate increase in structural complexity in otherwise plain rearing units, helping to reduce aberrant traits and promote welfare of fish kept in captivity. Before putting enrichment protocols into practice, however, practitioners like hatchery managers need clear guidelines on enrichment measures and on the substrates used. In the present study, we used rainbow trout as a model species for salmonid rearing and investigated the use of a single layer of three different gravel types, i.e., small (4–8 mm), medium (8–16 mm) and large (16–32 mm), for environmental enrichment during egg incubation, endogenous and first feeding of rainbow trout and compared this to a barren control. From the egg stage onwards, we determined mortality, fungal prevalence as well as growth of larvae and fingerlings. We found that gravel size significantly affected mortality and fungal prevalence with the smallest gravel size and the control showing the lowest incidents. Growth of larvae and fingerlings was not affected by gravel, both when compared between gravel types and to the barren control. When using gravel for environmental enrichment in salmonid hatcheries, a small gravel size should be used. Small gravel provides the fish with a more natural environment without compromising practical feasibility of enrichment in hatcheries, still allowing for easy visual inspection and manual control of the reared fish

Effect of lure and bait type on catch, size, hooking location, injury and bycatch in the western Baltic Sea recreational cod fishery

Atlantic cod (Gadus morhua) is an important recreational and commercial fisheries target species in the Northern hemisphere. Release rates are high in the recreational fishery due to regulatory and voluntary catch-and-release practice. Although post-release mortality of cod is relatively low, there is potential for further reductions. The most effective way to reduce post-release mortality is to minimize the catch of sublegal fish or non-target species and to reduce hooking injuries by using more selective fishing methods. This study investigated the influence of the lure/bait type on: (1) size of fish, (2) catch and harvest, (3) proportion of bycatch, (4) hooking location, and (5) injury (bleeding) in the western Baltic Sea recreational cod fishery. Data were collected via random onboard sampling of 35 charter vessel angling trips (778 anglers) and during two supplementary studies in the western Baltic Sea. Overall, the median total length was significantly higher for cod caught on artificial lures (39 cm) than for cod caught on natural bait (28 cm), leading to a 43% higher proportion of sublegal (<38 cm) cod for bait than for lure. Median catch-per-unit-efforts (number of captured cod per angling hour) did not differ significantly between lure and bait angling (both: 0.49 cod per hour), whereas the median harvest-per-unit-effort (number of captured cod ≥ minimum landing size (38 cm) per angling hour) was significantly higher for lure (0.24 cod ≥38 cm per hour) than for bait angling (0.06 cod ≥38 cm per hour). The incidence of deep hooking and severe bleeding was significantly higher for bait angling. Furthermore, bait angling significantly increased bycatch of other species dominated by whiting (Merlangius merlangus) and European flounder (Platichthys flesus). Cod anglers can reduce the catch of sublegal cod and non-target species and minimize hooking injuries of released fish by using lures instead of bait in the western Baltic Sea. Thus, voluntary terminal gear recommendations may be an effective tool for anglers and managers to increase selectivity in recreational cod fisheries

Cushing model [Equation (1) – see text] fitted to Rügen herring recruitment data.

<p>(A) Plot of log_e recruitment <i>R</i> (numbers in log_e-thousands) against log_e spawning-stock biomass SSB (log_e-t); the continuous line represents the predicted values of log_e<i>R</i> based on the Cushing model, the open dots connected by a dotted line and annotated by year represent observed log_e values of <i>R</i> at observed log_e SSB, and the light blue area the 95% prediction interval related to the Cushing model. (B) Plot of log_e<i>R</i> over time (years); the continuous line represents the predicted values of log_e<i>R</i> based on the Cushing model, the open dots the observed log_e values of <i>R</i>, and the light blue area the 95% prediction interval related to the Cushing model.</p

Map of the Baltic Sea area surrounded by neighbouring countries.

<p>The inset shows the location of the study area (south-eastern coast of Rügen Island plus the Greifswalder Bodden). The straight broken line connects Oslo (Norway) with Szczecin (Poland) representing the direct geographical distance between the two locations the BSI atmospheric pressure index has been calculated for.</p

Shiftograms of (A) the BSI and (B) the WBSS recruitment time series.

<p>The broken vertical lines indicate years of potential structural breaks (shifts), the open rectangles with broken lines encircle the three major shift detection criteria (AICC, p-joint, power panel).</p