ALBERT

Description: 〈jats:title〉Abstract〈/jats:title〉〈jats:p〉Numerous policy and international frameworks consider that “destructive fishing” hampers efforts to reach sustainability goals. Though ubiquitous, “destructive fishing” is undefined and therefore currently immeasurable. Here we propose a definition developed through expert consultation: “Destructive fishing is any fishing practice that causes irrecoverable habitat degradation, or which causes significant adverse environmental impacts, results in long‐term declines in target or nontarget species beyond biologically safe limits and has negative livelihood impacts.” We show strong stakeholder support for a definition, consensus on many biological and ecological dimensions, and no clustering of respondents from different sectors. Our consensus definition is a significant step toward defining sustainable fisheries goals and will help interpret and implement global political commitments which utilize the term “destructive fishing.” Our definition and results will help reinforce the Food and Agricultural Organization's Code of Conduct and meaningfully support member countries to prohibit destructive fishing practices.〈/jats:p〉

Description: Low-temperature (〈100 °C) alteration of oceanic crust plays an important role in determining the chemical composition of the oceans. Although a major sink of seawater potassium, little is known about the effects of low-temperature basalt alteration on the potassium isotopic composition of seawater (K∼0‰), which is ∼0.50‰ enriched relative to bulk silicate Earth (BSE, K= -0.54‰). Here, we present a suite of isotopic systems (K, Mg, Li, 87Sr/86Sr) and major/minor elements in bulk rock, veins and mineral separates from the upper volcanic section of Cretaceous (Troodos ophiolite) and Jurassic (Ocean Drilling Program Hole 801C) oceanic crust. We use these data to estimate the K isotopic fractionation associated with low-temperature oceanic crust alteration and provide new constraints on the role of this process in the global geochemical cycles of Mg and K in seawater. We find that hydrothermally altered basalts from the Troodos ophiolite and ODP Hole 801C, most of which are enriched in K relative to the unaltered glass compositions, have K values both higher and lower than BSE, ranging from +0.01‰ to -1.07‰ (n=83) and +0.04‰ to -0.88‰ (n=17), respectively. Average K values of bulk-rock samples from Troodos and Hole 801C are indistinguishable from each other at ∼-0.50‰, indicating that low-temperature basalt alteration is a sink of 39K from seawater, and explaining, in part, why seawater has a higher 41K/39K than BSE. In contrast to K, average Mg values for both Troodos (∼0.00‰) and Hole 801C (∼0.20‰) indicate that altered oceanic crust (AOC) is a sink of 26Mg from seawater, likely contributing to the light Mg composition of seawater (∼-0.8‰) relative to BSE (∼-0.2‰). We observe isotopically heavy Mg values in basalt samples characterized by small to no changes in bulk Mg content, consistent with extensive isotopic exchange of Mg between seawater and oceanic crust during low-temperature oceanic crust alteration. Finally, we find that variability in Li and K across three sites in the Troodos ophiolite can be explained by different styles of alteration that appear to be related to the timing of sedimentation and its effects on chemical and isotopic exchange between seawater and oceanic crust.