Abstract

The productivity of the Eastern Baltic cod (EBC) has been severely reduced over the last 25 years, for reasons that remain unclear. The size distribution of EBC has become increasingly truncated, condition and health status have deteriorated, and sexual maturation has started to occur at increasingly smaller sizes. Despite an increasing trend in recruitment during this period, reduced growth or increased mortality rates after the recruitment phase have resulted in decreasing landing levels and low profitability in the cod fishery, whereas the scientific community has difficulties in disentangling the causes of the decline of EBC. We studied changes in metabolic status in EBC between the capture years of 1995 and 2015, by investigating two aspects of fish metabolism that can be extracted retrospectively from otolith (earstone) morphometry and nitrogen content. Changes in relative otolith size to fish size are related to the metabolic history of the individual fish, and the otolith nitrogen content reveals the level of protein synthesis and feeding rate. Because otoliths accrue continuously on their surface and are biological stable (inert), the chemical content of the otolith trajectory reflects the timeline of the fish. We measured the N/Ca ratio as a proxy for protein content in EBC otolith along distal radius traverses from the core to the edge of the otolith by using secondary ion mass spectrometry (SIMS). Here we show that the otoliths were similar or larger at a given fish size, and the ratio of N/Ca has increased over the studied period. These proxies reveal significant metabolic changes during the same period as the condition, and stock productivity has declined. We discuss potential mechanisms behind the metabolic changes, including elevated temperature and compensatory feeding due to nutrient deficiencies. Such changes in food quality may, in turn, relate to still unrecognized but on-going ecosystem shifts, where climate change could be the ultimate driver.

Highlights

  • IntroductionThe Baltic Sea is a large, and in geological terms, young (about 9 KY) brackish watershed (Figure 1)

  • The Baltic Sea is a large, and in geological terms, young brackish watershed (Figure 1)

  • The accuracy of our estimations of the 12C14N−/40Ca− ratios was supported by the fact that the Ca-content over the transverse was stable with a mean coefficient of variation (c.v.) per otolith of 2.7% ± 3.0 (Supplementary Table S3 and Supplementary Figure S2), while the N-estimation showed more than 20 times higher variability

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Summary

Introduction

The Baltic Sea is a large, and in geological terms, young (about 9 KY) brackish watershed (Figure 1). On an intermediate time-scale, the hydrographic development of the Baltic Sea shows large-scale cyclic variation, influenced by the frequency of inflows of saline water from the North Sea (Mohrholz, 2018). Regime shifts due to such climate-induced alternations in the frequency of saltwater inflows from the Atlantic in combination with eutrophication (Savchuk, 2018), may have long-lasting effects on ecosystem structure and function (Österblom et al, 2007; Möllmann et al, 2015). The inflow of salt leads to a stratification of the water column, which may promote the development of hypoxic conditions in the deepwater, as a consequence of organic matter originating from the surface waters sedimenting to the deeper parts of the sea (Fonselius, 1972). Eutrophication has raised primary productivity of phytoplankton in the Baltic Sea over the last century, leading to more widespread hypoxia (Carstensen et al, 2014; Andersen et al, 2017)

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