On biological evolution and environmental solutions
Identifieur interne : 000326 ( Pmc/Corpus ); précédent : 000325; suivant : 000327On biological evolution and environmental solutions
Auteurs : Blake Matthews ; Jukka Jokela ; Anita Narwani ; Katja R S Nen ; Francesco Pomati ; Florian Altermatt ; Piet Spaak ; Christopher T. Robinson ; Christoph VorburgerSource :
- The Science of the Total Environment [ 0048-9697 ] ; 2020.
Abstract
Drawing insights from multiple disciplines is essential for finding integrative solutions that are required to tackle complex environmental problems. Human activities are causing unprecedented influence on global ecosystems, culminating in the loss of species and fundamental changes in the selective environments of organisms across the tree of life. Our collective understanding about biological evolution can help identify and mitigate many of the environmental problems in the Anthropocene. To this end, we propose a stronger integration of environmental sciences with evolutionary biology.
Url:
DOI: 10.1016/j.scitotenv.2020.138194
PubMed: 32251887
PubMed Central: 7118648
Links to Exploration step
PMC:7118648Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">On biological evolution and environmental solutions</title><author><name sortKey="Matthews, Blake" sort="Matthews, Blake" uniqKey="Matthews B" first="Blake" last="Matthews">Blake Matthews</name><affiliation><nlm:aff id="af0005">EAWAG, Department of Fish Ecology and Evolution, Center for Ecology, Evolution, and Biogeochemistry, Seestrasse 79, 6047 Kastanienbaum, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Jokela, Jukka" sort="Jokela, Jukka" uniqKey="Jokela J" first="Jukka" last="Jokela">Jukka Jokela</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Narwani, Anita" sort="Narwani, Anita" uniqKey="Narwani A" first="Anita" last="Narwani">Anita Narwani</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="R S Nen, Katja" sort="R S Nen, Katja" uniqKey="R S Nen K" first="Katja" last="R S Nen">Katja R S Nen</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Pomati, Francesco" sort="Pomati, Francesco" uniqKey="Pomati F" first="Francesco" last="Pomati">Francesco Pomati</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Altermatt, Florian" sort="Altermatt, Florian" uniqKey="Altermatt F" first="Florian" last="Altermatt">Florian Altermatt</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0020">Department of Evolutionary Biology and Environmental Studies, University of Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Spaak, Piet" sort="Spaak, Piet" uniqKey="Spaak P" first="Piet" last="Spaak">Piet Spaak</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Robinson, Christopher T" sort="Robinson, Christopher T" uniqKey="Robinson C" first="Christopher T." last="Robinson">Christopher T. Robinson</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Vorburger, Christoph" sort="Vorburger, Christoph" uniqKey="Vorburger C" first="Christoph" last="Vorburger">Christoph Vorburger</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">32251887</idno><idno type="pmc">7118648</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118648</idno><idno type="RBID">PMC:7118648</idno><idno type="doi">10.1016/j.scitotenv.2020.138194</idno><date when="2020">2020</date><idno type="wicri:Area/Pmc/Corpus">000326</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000326</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">On biological evolution and environmental solutions</title><author><name sortKey="Matthews, Blake" sort="Matthews, Blake" uniqKey="Matthews B" first="Blake" last="Matthews">Blake Matthews</name><affiliation><nlm:aff id="af0005">EAWAG, Department of Fish Ecology and Evolution, Center for Ecology, Evolution, and Biogeochemistry, Seestrasse 79, 6047 Kastanienbaum, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Jokela, Jukka" sort="Jokela, Jukka" uniqKey="Jokela J" first="Jukka" last="Jokela">Jukka Jokela</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Narwani, Anita" sort="Narwani, Anita" uniqKey="Narwani A" first="Anita" last="Narwani">Anita Narwani</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="R S Nen, Katja" sort="R S Nen, Katja" uniqKey="R S Nen K" first="Katja" last="R S Nen">Katja R S Nen</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Pomati, Francesco" sort="Pomati, Francesco" uniqKey="Pomati F" first="Francesco" last="Pomati">Francesco Pomati</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Altermatt, Florian" sort="Altermatt, Florian" uniqKey="Altermatt F" first="Florian" last="Altermatt">Florian Altermatt</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0020">Department of Evolutionary Biology and Environmental Studies, University of Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Spaak, Piet" sort="Spaak, Piet" uniqKey="Spaak P" first="Piet" last="Spaak">Piet Spaak</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Robinson, Christopher T" sort="Robinson, Christopher T" uniqKey="Robinson C" first="Christopher T." last="Robinson">Christopher T. Robinson</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Vorburger, Christoph" sort="Vorburger, Christoph" uniqKey="Vorburger C" first="Christoph" last="Vorburger">Christoph Vorburger</name><affiliation><nlm:aff id="af0010">EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</nlm:aff></affiliation><affiliation><nlm:aff id="af0015">Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</nlm:aff></affiliation></author></analytic><series><title level="j">The Science of the Total Environment</title><idno type="ISSN">0048-9697</idno><idno type="eISSN">1879-1026</idno><imprint><date when="2020">2020</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Drawing insights from multiple disciplines is essential for finding integrative solutions that are required to tackle complex environmental problems. Human activities are causing unprecedented influence on global ecosystems, culminating in the loss of species and fundamental changes in the selective environments of organisms across the tree of life. Our collective understanding about biological evolution can help identify and mitigate many of the environmental problems in the Anthropocene. To this end, we propose a stronger integration of environmental sciences with evolutionary biology.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Abdelghani, A A" uniqKey="Abdelghani A">A.A. Abdelghani</name></author><author><name sortKey="Tchounwou, P B" uniqKey="Tchounwou P">P.B. Tchounwou</name></author><author><name sortKey="Anderson, A C" uniqKey="Anderson A">A.C. Anderson</name></author><author><name sortKey="Sujono, H" uniqKey="Sujono H">H. Sujono</name></author><author><name sortKey="Heyer, L R" uniqKey="Heyer L">L.R. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Sci Total Environ</journal-id><journal-id journal-id-type="iso-abbrev">Sci. Total Environ</journal-id><journal-title-group><journal-title>The Science of the Total Environment</journal-title></journal-title-group><issn pub-type="ppub">0048-9697</issn><issn pub-type="epub">1879-1026</issn><publisher><publisher-name>Elsevier B.V.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">32251887</article-id><article-id pub-id-type="pmc">7118648</article-id><article-id pub-id-type="publisher-id">S0048-9697(20)31707-1</article-id><article-id pub-id-type="doi">10.1016/j.scitotenv.2020.138194</article-id><article-id pub-id-type="publisher-id">138194</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>On biological evolution and environmental solutions</article-title></title-group><contrib-group><contrib contrib-type="author" id="au0005"><name><surname>Matthews</surname><given-names>Blake</given-names></name><email>Blake.Matthews@eawag.ch</email><xref rid="af0005" ref-type="aff">a</xref><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0015" ref-type="aff">c</xref><xref rid="cr0005" ref-type="corresp">⁎</xref></contrib><contrib contrib-type="author" id="au0010"><name><surname>Jokela</surname><given-names>Jukka</given-names></name><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0015" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au0015"><name><surname>Narwani</surname><given-names>Anita</given-names></name><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0015" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au0020"><name><surname>Räsänen</surname><given-names>Katja</given-names></name><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0015" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au0025"><name><surname>Pomati</surname><given-names>Francesco</given-names></name><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0015" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au0030"><name><surname>Altermatt</surname><given-names>Florian</given-names></name><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0020" ref-type="aff">d</xref></contrib><contrib contrib-type="author" id="au0035"><name><surname>Spaak</surname><given-names>Piet</given-names></name><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0015" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au0040"><name><surname>Robinson</surname><given-names>Christopher T.</given-names></name><xref rid="af0010" ref-type="aff">b</xref></contrib><contrib contrib-type="author" id="au0045"><name><surname>Vorburger</surname><given-names>Christoph</given-names></name><email>Christoph.Vorburger@eawag.ch</email><xref rid="af0010" ref-type="aff">b</xref><xref rid="af0015" ref-type="aff">c</xref><xref rid="cr0005" ref-type="corresp">⁎</xref></contrib></contrib-group><aff id="af0005"><label>a</label>EAWAG, Department of Fish Ecology and Evolution, Center for Ecology, Evolution, and Biogeochemistry, Seestrasse 79, 6047 Kastanienbaum, Switzerland</aff><aff id="af0010"><label>b</label>EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland</aff><aff id="af0015"><label>c</label>Institute of Integrative Biology, ETH-Zurich, Zurich, Switzerland</aff><aff id="af0020"><label>d</label>Department of Evolutionary Biology and Environmental Studies, University of Zurich, Zurich, Switzerland</aff><author-notes><corresp id="cr0005"><label>⁎</label>Corresponding authors at: EAWAG, Department of Aquatic Ecology, Überlandstr. 133, 8600 Dübendorf, Switzerland. <email>Blake.Matthews@eawag.ch</email><email>Christoph.Vorburger@eawag.ch</email></corresp></author-notes><pub-date pub-type="pmc-release"><day>25</day><month>3</month><year>2020</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><day>1</day><month>7</month><year>2020</year></pub-date><pub-date pub-type="epub"><day>25</day><month>3</month><year>2020</year></pub-date><volume>724</volume><fpage>138194</fpage><lpage>138194</lpage><history><date date-type="received"><day>5</day><month>2</month><year>2020</year></date><date date-type="rev-recd"><day>23</day><month>3</month><year>2020</year></date><date date-type="accepted"><day>23</day><month>3</month><year>2020</year></date></history><permissions><copyright-statement>© 2020 Elsevier B.V. All rights reserved.</copyright-statement><copyright-year>2020</copyright-year><copyright-holder>Elsevier B.V.</copyright-holder><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions><abstract id="ab0005"><p>Drawing insights from multiple disciplines is essential for finding integrative solutions that are required to tackle complex environmental problems. Human activities are causing unprecedented influence on global ecosystems, culminating in the loss of species and fundamental changes in the selective environments of organisms across the tree of life. Our collective understanding about biological evolution can help identify and mitigate many of the environmental problems in the Anthropocene. To this end, we propose a stronger integration of environmental sciences with evolutionary biology.</p></abstract><abstract abstract-type="graphical" id="ab0010"><title>Graphical abstract</title><p><fig id="f0010" position="anchor"><alt-text id="al0015">Unlabelled Image</alt-text><graphic xlink:href="ga1_lrg"></graphic></fig></p></abstract><abstract abstract-type="author-highlights" id="ab0015"><title>Highlights</title><p><list list-type="simple" id="l0025"><list-item id="li0025"><label>•</label><p id="p0050">Evolutionary theory is not widely used to address environmental problems.</p></list-item><list-item id="li0030"><label>•</label><p id="p0055">Evolutionary processes can both ameliorate and exacerbate environmental problems.</p></list-item><list-item id="li0035"><label>•</label><p id="p0060">Evolution can be informative about disease dynamics, biofuel production, adaptation to pollution, and harmful algal blooms.</p></list-item><list-item id="li0040"><label>•</label><p id="p0065">We propose a stronger integration of evolutionary biology with environmental sciences to help solve environmental problems.</p></list-item></list></p></abstract><kwd-group id="ks0005"><title>Keywords</title><kwd>Biological evolution</kwd><kwd>Environmental science</kwd><kwd>Biofuels</kwd><kwd>Pollution</kwd><kwd>Disease</kwd><kwd>Harmful algal blooms</kwd></kwd-group></article-meta><notes><p id="mi0005">Editor: Sergei Sabater</p></notes></front><body><sec id="s0005"><label>1</label><title>Introduction</title><p id="p0070">All ecosystems, be they natural or engineered, contain biological organisms that are bound by the principles of biological evolution. As such, biological evolution is often a central feature of many problems that are currently being tackled by environmental scientists. Yet fundamental principles from the discipline of evolutionary biology are rarely used in the analysis and mitigation of environmental problems, even when evolutionary processes are closely linked to their manifestation (<xref rid="bb0080" ref-type="bibr">Carroll et al., 2014</xref>; <xref rid="bb0235" ref-type="bibr">Jørgensen et al., 2019</xref>). Environmental scientists are particularly adept at reaching across disciplines to ensure that they have the knowledge and tools necessary to tackle complex environmental problems. Here we propose that a wider application of principles of evolutionary biology would help us achieve more sustainable solutions to environmental problems.</p><p id="p0075">In brief, evolution is a process of heritable change in the phenotype of a population of organisms (<xref rid="b0005" ref-type="boxed-text">Box 1</xref>). While evolution can result from random genetic drift (representing “neutral” evolution), here we focus on adaptive evolution, defined as a change in population mean fitness in response to natural selection (<xref rid="b0005" ref-type="boxed-text">Box 1</xref>). Genetic and trait variation, and how such variation changes over time and space, are fundamental properties of living systems. There is mounting evidence that evolution is sufficiently fast in natural populations to be highly relevant for understanding how populations will respond to human-mediated environmental change (<xref rid="bb0190" ref-type="bibr">Hendry and Kinnison, 1999</xref>; <xref rid="bb0185" ref-type="bibr">Hendry, 2017</xref>).</p><p id="p0080">Applying evolutionary principles to understand environmental problems is not a novel idea (<xref rid="bb0170" ref-type="bibr">Gunderson and Holling, 2002</xref>, <xref rid="bb7000" ref-type="bibr">Santamaria and Mendez, 2012</xref>), but widespread application is still limited (<xref rid="bb0235" ref-type="bibr">Jørgensen et al., 2019</xref>). In the context of the biodiversity crisis ecologists are increasingly using evolutionary theory to help mitigate the loss of genetic and species diversity due to climate change and environmental pollution (<xref rid="bb0020" ref-type="bibr">Bell and Gonzalez, 2009</xref>; <xref rid="bb0280" ref-type="bibr">Kristensen et al., 2018</xref>). Evolutionary theory is also critical to understanding the emergence of antibiotic resistance in microbes (<xref rid="bb0390" ref-type="bibr">Palmer and Kishony, 2013</xref>) and chemical resistance in pests (<xref rid="bb0145" ref-type="bibr">Fisher et al., 2018</xref>). Plainly, evolutionary theory can be highly relevant to pertinent environmental problems, but it is not broadly applied. There is a frequent use of methods and technologies originating from evolutionary biology. In particular, molecular genetic methods are often used to characterise microbial community composition (<xref rid="bb0130" ref-type="bibr">Das and Dash, 2019</xref>), and the patterns of gene expression of individual organisms and communities (<xref rid="bb0380" ref-type="bibr">Oziolor et al., 2017</xref>). While such methods are undeniably useful to gain functional insights, they are rarely used in environmental science to study evolutionary <italic>processes</italic>. The potential for evolutionary applications in environmental sciences is far reaching, and in the next sections we focus on core concepts of evolution and exemplify how they can be applied to a range of environmental problems in aquatic ecosystems.</p><sec id="s0010"><label>1.1</label><title>The structure of evolutionary processes</title><p id="p0085">The structure and rate of change of heritable trait variation in living systems are particularly relevant for understanding environmental problems. Living systems are hierarchically structured, where the traits of individuals arise from the interpretation of the environment by genes (so called genotype-phenotype maps; (<xref rid="bb0210" ref-type="bibr">Houle et al., 2010</xref>)). Individuals interact within populations, where average trait values change through evolutionary and environmental processes (<xref rid="bb0070" ref-type="bibr">Burns, 1992</xref>; <xref rid="bb0155" ref-type="bibr">Frank, 2011</xref>; <xref rid="bb0405" ref-type="bibr">Pedersen and Tuomi, 1995</xref>), and populations interact and evolve within multi-species communities (<xref rid="bb0500" ref-type="bibr">Weber et al., 2017</xref>). As a result of this hierarchical structure, human activities affecting one level of biological organization can have unanticipated outcomes at another level (<xref rid="bb0170" ref-type="bibr">Gunderson and Holling, 2002</xref>; <xref rid="bb0360" ref-type="bibr">Melián et al., 2018</xref>). For example, human activities that affect gene flow among populations can lead to the introduction of either beneficial alleles that help populations adapt to changing environments, or deleterious alleles that contribute to maladaptation of natural populations and thereby can potentially hinder conservation efforts (<xref rid="bb0300" ref-type="bibr">Leitwein et al., 2019</xref>). Despite the long held view that evolution is a slow process, it is now well established that the pace of heritable trait change can be sufficiently fast to affect population dynamics, species interactions, and ecosystem processes - i.e. evolution can act at ecological time scales (<xref rid="bb0175" ref-type="bibr">Hairston et al., 2005</xref>; <xref rid="bb0470" ref-type="bibr">Stockwell et al., 2003</xref>). The dynamics of species interactions in natural communities are hence not simply a product of past evolution. Rather, evolutionary processes can shape trait distributions of populations (i.e. mean and variance) at a pace that is highly relevant for many environmental problems.</p><p id="p0090">Evolutionary processes can either ameliorate or exacerbate environmental problems. Evolutionary adaptation, for example, can drive the recovery of populations, or even multi-species communities, from decline, in a process known as “evolutionary rescue” (<xref rid="bb0020" ref-type="bibr">Bell and Gonzalez, 2009</xref>; <xref rid="bb0340" ref-type="bibr">Low-Décarie et al., 2015</xref>). In natural populations, evolution has rescued killifish from chemical pollution (<xref rid="bb6000" ref-type="bibr">Whitehead et al., 2017</xref>) and amphibians from acidification (<xref rid="bb5000" ref-type="bibr">Hangartner et al., 2012</xref>). In these cases, genetic adaptation has allowed for the persistence of populations in environments that would otherwise be unsuitable. Evolutionary novelty can also emerge in populations exposed to synthetic environments created by humans, and, in doing so, perform essential evosystem services (<xref rid="bb0435" ref-type="bibr">Rudman et al., 2017</xref>). For example, the artificial sweetener acesulfame (ACE) is a persistent compound in aquatic environments because it is resistant to microbial-mediated biodegradation both in natural and wastewater treatment environments (<xref rid="bb0245" ref-type="bibr">Kahl et al., 2018</xref>). Recent work suggests that the catabolism of this compound has evolved repeatedly in multiple wastewater treatment plants in Germany (<xref rid="bb0245" ref-type="bibr">Kahl et al., 2018</xref>), possibly associated with a microbial consortium of proteobacterial species (<xref rid="f0005" ref-type="fig">Fig. 1</xref>). Identifying the evolutionary processes governing such bioremediation dynamics could help address the persistence of chemicals in our natural environments for which engineering solutions are lacking. On the other hand, evolutionary processes can also create novel environmental problems, or worsen existing ones. For example, the emergence and amplification of antibiotic resistance genes is a global problem, caused by the widespread overuse of antibiotics (<xref rid="bb0390" ref-type="bibr">Palmer and Kishony, 2013</xref>). In wastewater treatment plants, the concentration of antibiotic resistance genes may be amplified by evolution prior to water discharge into natural aquatic environments (<xref rid="bb0240" ref-type="bibr">Ju et al., 2019</xref>) (<xref rid="f0005" ref-type="fig">Fig. 1</xref>). Understanding and monitoring the evolutionary process in wastewater treatment plants could improve our ability to limit the release of antibiotic resistance genes into natural environments (<xref rid="bb0125" ref-type="bibr">Czekalski et al., 2015</xref>).<fig id="f0005"><label>Fig. 1</label><caption><p>Two scenarios illustrating how microbial evolution within a wastewater treatment plant (WWTP) can either cause a beneficial reduction in a pollutant concentration (ACE: the artificial sweetener Acesulfame) due to the evolution of catabolism of novel/synthetic compounds, or an unwanted increase in resistance genes in a microbial population due to positive selection in the treatment plant (Figure design by Peter Penicka, EAWAG).</p></caption><alt-text id="al0005">Fig. 1</alt-text><graphic xlink:href="gr1_lrg"></graphic></fig></p></sec></sec><sec id="s0015"><label>2</label><title>Case studies</title><p id="p0095">In this section, we illustrate how a broader application of evolutionary theory can enable environmental scientists to craft better solutions for environmental problems. To this end, we use four examples from aquatic systems: (i) emergence and epidemiology of disease, (ii) renewable production of biofuels, (iii) chemical pollution, and (iv) outbreaks of algal blooms.</p><sec id="s0020"><label>2.1</label><title>Disease dynamics in natural populations: when evolution kills or cures</title><p id="p0100">Diseases are among the most severe environmental problems. They are a threat to biodiversity (<xref rid="bb0145" ref-type="bibr">Fisher et al., 2018</xref>; <xref rid="bb0320" ref-type="bibr">Lips et al., 2006</xref>), to food production (<xref rid="bb0475" ref-type="bibr">Strange and Scott, 2005</xref>) and to human health (<xref rid="bb0230" ref-type="bibr">Jones et al., 2008</xref>). Disease outbreaks are often caused by pathogens that have undergone a recent host shift or expansion of their geographic range (<xref rid="bb0135" ref-type="bibr">Engering et al., 2013</xref>; <xref rid="bb0330" ref-type="bibr">Longdon et al., 2014</xref>). Most disease-causing organisms have large populations and short generation times, which generally facilitates rapid evolution. Consequently, disease emergence typically involves rapid co-evolutionary dynamics that stem from natural selection on both pathogen infectivity and host defense (<xref rid="bb0410" ref-type="bibr">Penczykowski et al., 2016</xref>). Rapid evolutionary dynamics are expected to take place at the onset of disease emergence, governed by the pathogens' and the hosts' evolutionary history.</p><p id="p0105">Disease emergence is often a consequence of human activities. Transport between continents can bring pathogens into naïve host populations that are, at least initially, defenseless; they can lack sufficient genetic variation for resistance because they do not have coevolutionary history with these pathogens. The crayfish plague provides a good example. <italic>Aphanomyces astaci</italic>, a pathogen of freshwater crayfish native to North America came to Europe with introduced American crayfish (<xref rid="bb0485" ref-type="bibr">Svoboda et al., 2017</xref>). American crayfish species had evolved a high tolerance of the pathogen, due to their long evolutionary history, but the pathogen proved devastating to stocks of European freshwater crayfish species (<xref rid="bb0205" ref-type="bibr">Holdich et al., 2009</xref>). Likewise, human activities that modify ecosystems for food production can promote the emergence of locally highly virulent pathogens (<xref rid="bb0480" ref-type="bibr">Stukenbrock and McDonald, 2008</xref>). For example, large monocultures of genetically homogenous plants can facilitate the evolution of host specialization (<xref rid="bb0355" ref-type="bibr">McDonald and Stukenbrock, 2016</xref>), leading to evolutionary dynamics that are not commonly observed in natural ecosystems.</p><p id="p0110">Evolutionary theory can be instrumental in helping to understand the origin and spread of diseases through populations. Increasingly, researchers can track disease dynamics over time by comparing genetic variation among isolates, and such data can help inform policy decision and management of viral diseases, such as COVID-19 (<xref rid="bb0015" ref-type="bibr">Andersen et al., 2020</xref>, <xref rid="bb0055" ref-type="bibr">Brüssow, 2020</xref>) and Ebola (<xref rid="bb0350" ref-type="bibr">Mbala-Kingebeni et al., 2019</xref>). Drug treatment is often the default approach used to control emergent bacterial and fungal diseases, but in some cases a single new drug can cause strong natural selection, and, combined with the high evolutionary potential of pathogens, this means that the expected time until drug resistance evolves can be short (<xref rid="bb0145" ref-type="bibr">Fisher et al., 2018</xref>; <xref rid="bb0255" ref-type="bibr">Kennedy and Read, 2018</xref>). For such scenarios, we need to develop evolution-aware strategies to avoid and control emergent diseases. For example, in the case of chemical treatments, combination therapy or the sequential application of different drugs can delay resistance evolution (<xref rid="bb0390" ref-type="bibr">Palmer and Kishony, 2013</xref>; <xref rid="bb0430" ref-type="bibr">Roemhild et al., 2018</xref>), and the development of ‘evolution-proof’ drugs is a particularly attractive idea (<xref rid="bb0025" ref-type="bibr">Bell and MacLean, 2018</xref>). Alternative strategies include fighting the disease with agents that are able to evolve themselves, such as microbial symbionts that provide protection against the disease (<xref rid="bb0285" ref-type="bibr">Kueneman et al., 2016</xref>).</p></sec><sec id="s0025"><label>2.2</label><title>Renewable biofuels: when evolution fills our tanks</title><p id="p0115">The dwindling supply and the negative environmental impact of fossil fuels have spurred substantial research and investment into using biofuels as a renewable and sustainable source of energy (<xref rid="bb0445" ref-type="bibr">Sheehan et al., 1998</xref>). Among the many potential sources of biomass for biofuels, phytoplankton or “algal” biofuels are among the most efficient in terms of land-use and energy production per unit biomass (Y. <xref rid="bb0100" ref-type="bibr">Chisti, 2008</xref>; Yusuf <xref rid="bb0095" ref-type="bibr">Chisti, 2007</xref>). Until now, algal biomass production for biofuel has heavily focused on the production of single species with desirable properties, namely high lipid content, fast growth rates, and resistance to disease and grazers. However, farming monocultures is notoriously difficult because individual species or strains, be they algae or crops, can never possess all of the desirable traits for long-term stable crop production at high yields (<xref rid="bb0460" ref-type="bibr">Smith et al., 2010</xref>). The ideal species for maximum production would be unconstrained by the trade-offs inherent to all living systems. Yet such omnipotent organisms, known in evolutionary biology as Darwinian demons (<xref rid="bb0275" ref-type="bibr">Krakauer, 2011</xref>; <xref rid="bb0290" ref-type="bibr">Law, 1979</xref>), do not exist and cannot be engineered. Nevertheless, sustainable yield of biofuels could be optimized by understanding the biochemical and biophysical basis of the fundamental trade-offs between growth rate, lipid production and traits that make better competitors, confer resistance to parasites, and are resistant to grazers (<xref rid="bb0450" ref-type="bibr">Shurin et al., 2013</xref>, <xref rid="bb0455" ref-type="bibr">Shurin et al., 2016</xref>; T. <xref rid="bb0520" ref-type="bibr">Yoshida et al., 2004</xref>). Understanding the evolution of ecologically relevant traits, under different biotic and abiotic contexts, may improve the stability and efficiency of biofuel production.</p><p id="p0120">The application of evolutionary theory to algal biofuel production is in its infancy, but holds immense potential. Algal populations are large and have short generation times. Usually the populations maintain high phenotypic and genetic diversity (<xref rid="bb0040" ref-type="bibr">Brandenburg et al., 2018</xref>; <xref rid="bb0090" ref-type="bibr">Chen and Rynearson, 2016</xref>; <xref rid="bb0295" ref-type="bibr">Lebret et al., 2012</xref>; <xref rid="bb0345" ref-type="bibr">Masseret et al., 2009</xref>; <xref rid="bb0440" ref-type="bibr">Rynearson and Armbrust, 2000</xref>). Evolution in such populations can be fast if selection is strong (<xref rid="bb0490" ref-type="bibr">Thibodeau et al., 2015</xref>; Takehito <xref rid="bb0515" ref-type="bibr">Yoshida et al., 2003</xref>). Harnessing the adaptive evolutionary potential of algal populations could help us explore the range of feasible trait space to obtain desirable trait combinations. For example, researchers are currently trying to simultaneously improve the yield of triacylglycerols in culture (used to produce fatty acid methyl esters needed used in biodiesel production), while concurrently maximizing population growth rates. Such trait combinations are normally mutually exclusive. Approaches include genetic engineering (<xref rid="bb0525" ref-type="bibr">Zeng et al., 2011</xref>), directed evolution via successive rounds of mutagenesis and selection (<xref rid="bb0225" ref-type="bibr">Johnson et al., 2016</xref>; <xref rid="bb0305" ref-type="bibr">Lewin et al., 2016</xref>), and selection on the existing levels of genetic variation in a population (<xref rid="bb0370" ref-type="bibr">Mooij et al., 2013</xref>; <xref rid="bb0455" ref-type="bibr">Shurin et al., 2016</xref>).</p><p id="p0125">While evolution might help us improve biofuel production (<xref rid="bb0250" ref-type="bibr">Kazamia et al., 2014</xref>), it might also culminate in undesirable outcomes. For example, engineering solutions based on evolutionary trade-offs might be eroded over time due to mutation, horizontal gene transfer, and recombination. Custom designed biofuel production systems should also consider the evolutionary consequences of rapid harvesting. For example, rare beneficial mutations arising during population expansion, might be periodically lost before they sweep to dominance in the populations (<xref rid="bb0060" ref-type="bibr">Bull and Collins, 2012</xref>; <xref rid="bb0455" ref-type="bibr">Shurin et al., 2016</xref>). In short, evolution offers both promises and pitfalls for biofuel production.</p></sec><sec id="s0030"><label>2.3</label><title>Chemical pollutants: when evolution is, and is not, the solution to pollution</title><p id="p0130">Chemical pollution is a global problem with a local character (<xref rid="bb0165" ref-type="bibr">Grimm et al., 2008</xref>; <xref rid="bb0180" ref-type="bibr">Halpern et al., 2008</xref>; <xref rid="bb0495" ref-type="bibr">Vörösmarty et al., 2010</xref>). Chemical pollution often stems from chemical pest control applied in agricultural production, as well as from the unwanted waste produced by human population growth and industrial activities. Wastewater treatment plants can only remove and target compounds that pass through the sewage system; many other compounds still enter the natural environment in a diffuse manner, especially from agriculture. These chemical compounds can have toxic effects on individual organisms and these effects can be enhanced when they occur in mixtures (<xref rid="bb0005" ref-type="bibr">Abdelghani et al., 1997</xref>; <xref rid="bb0110" ref-type="bibr">Connon et al., 2012</xref>). For instance, pest control requires highly biologically active substances to target unwanted algae, fungi and arthropods. When pesticides then leak into ecosystems that are not the target of the application, this can change food web structure and influence ecosystem function (<xref rid="bb0465" ref-type="bibr">Stamm et al., 2016</xref>).</p><p id="p0135">Because pollution and the ecological context in which pollution occurs is often highly local, we can expect pollution to have many different evolutionary consequences in natural ecosystems. However, the biological effects of pollutants are typically studied using a limited number of model species and strains, usually in oversimplified ecological contexts that might underestimate their effects in nature (<xref rid="bb0425" ref-type="bibr">Relyea and Hoverman, 2006</xref>). Furthermore, many of the approaches used in environmental science and ecotoxicology to assess the environmental effects of pollutants only test a few selected genetic lineages of organisms (e.g., single strains of <italic>Daphnia</italic>), and often ignore both within-population variation in sensitivity to pollutants and the effects of mixtures of pollutants on organisms. For example, morphologically similar but genetically distinct lineages of amphipods, within the <italic>Gammarus fossarum</italic> cryptic species complex, vary in their sensitivity to the fungicide tebuconazole and the insecticide thiacloprid (<xref rid="bb0140" ref-type="bibr">Feckler et al., 2012</xref>). Such lineage diversity within species is rarely accounted for in typical assessments of pollutants on organisms (<xref rid="bb0425" ref-type="bibr">Relyea and Hoverman, 2006</xref>). Synthetic chemicals present a particular challenge because the exposed organisms may lack the exposure history necessary for the emergence of an evolutionary adaptation. Synthetic chemicals can also act as mutagens that disrupt the homeostasis of organisms (<xref rid="bb0030" ref-type="bibr">Bickham et al., 2000</xref>).</p><p id="p0140">Chemical toxicity can rapidly drive populations to such small sizes that their persistence over time becomes threatened (<xref rid="bb0505" ref-type="bibr">Williams and Oleksiak, 2008</xref>). Interestingly many classic studies about rapid evolution involve chemical pollution, such as the evolution of resistance to pesticides, resistance to antibiotics or mining-related metal pollution (<xref rid="bb0200" ref-type="bibr">Hoffmann and Parsons, 1997</xref>; <xref rid="bb0395" ref-type="bibr">Palumbi, 2009</xref>) and, more recently, pollutant induced elevated mutation rates and rapid adaptation (<xref rid="bb0035" ref-type="bibr">Brady et al., 2017</xref>; <xref rid="bb0120" ref-type="bibr">Coutellec and Barata, 2013</xref>; <xref rid="bb0265" ref-type="bibr">Kimberly and Salice, 2012</xref>; <xref rid="bb0335" ref-type="bibr">Loria et al., 2019</xref>; <xref rid="bb0395" ref-type="bibr">Palumbi, 2009</xref>). Evolutionary adaptation to chemical pollution can also rescue populations from extinction caused by demographic decline. For example, experimental <italic>Daphnia</italic> populations that were initially highly sensitive to metal contamination recovered rapidly via genetic adaptation (<xref rid="bb0195" ref-type="bibr">Hochmuth et al., 2015</xref>). In another example, natural killifish populations inhabiting urban estuaries adapted to lethal levels of pollutants with genetic adaptations (<xref rid="bb0380" ref-type="bibr">Oziolor et al., 2017</xref>; <xref rid="bb0420" ref-type="bibr">Reid et al., 2016</xref>). Unsurprisingly, adaptation of a population can also be an unwanted outcome of management, such as when the evolution of resistance reduces the sensitivity of a species used in ecological risk assessment (<xref rid="bb0375" ref-type="bibr">Morgan et al., 2007</xref>). Evolution's ability to alter the direction of responses to environmental change, such as that brought by chemical pollution, is one of the main arguments for including evolutionary concepts in environmental research. Finally, potential for evolutionarily based solutions to pollution comes from implementing bioremediation, such as designing microbial communities that have evolved the ability of biodegradation of chemicals (<xref rid="bb0325" ref-type="bibr">Liu and Suflita, 1993</xref>).</p></sec><sec id="s0035"><label>2.4</label><title>Algal blooms: when evolution muddies the waters</title><p id="p0145">Harmful algal blooms are often associated with eutrophication, pollution and climate change (<xref rid="bb0215" ref-type="bibr">Huisman et al., 2018</xref>; <xref rid="bb0365" ref-type="bibr">Monchamp et al., 2018</xref>). Harmful algal blooms, which can persist for weeks or months, may foul drinking water, turn lakes anoxic and kill fish, and render lakes unacceptable for recreational use (<xref rid="bb0310" ref-type="bibr">Lewitus et al., 2012</xref>; <xref rid="bb0385" ref-type="bibr">Paerl et al., 2011</xref>). Ecological theory suggests that blooms develop when nutrient input releases phytoplankton from control by grazers (<xref rid="bb0010" ref-type="bibr">Abrams and Walters, 1996</xref>; <xref rid="bb0160" ref-type="bibr">Gragnani et al., 1999</xref>; <xref rid="bb0400" ref-type="bibr">Pančić and Kiørboe, 2018</xref>). Additionally, evolutionary processes are also relevant to the emergence, volume and toxicity of blooms. Indeed, we postulate that trying to manage harmful blooms without Darwin, is like trying to fly to the moon without Newton (modifying Andrew Read's concluding remark on his TEDMED talk on importance of evolutionary medicine: <ext-link ext-link-type="uri" xlink:href="https://www.tedmed.com/talks/show?id=7286" id="ir0005">https://www.tedmed.com/talks/show?id=7286</ext-link>).</p><p id="p0150">The trade-off between resource uptake and grazing resistance is at the root of the ecological and evolutionary causes of bloom biomass (<xref rid="bb0105" ref-type="bibr">Cloern, 2018</xref>). Selective grazing by zooplankton will deplete edible algae and, subsequently, increase the abundance of well-defended algae (<xref rid="bb0175" ref-type="bibr">Hairston et al., 2005</xref>; Takehito <xref rid="bb0515" ref-type="bibr">Yoshida et al., 2003</xref>). Harmful algal blooms are characterised by an array of defense traits that are favored by natural selection. Some algae produce compounds that are toxic to grazers, such as the neurotoxins, saxitoxins and domoic acid produced by dinoflagellates, cyanobacteria, and diatoms, respectively (<xref rid="bb0400" ref-type="bibr">Pančić and Kiørboe, 2018</xref>; <xref rid="bb0510" ref-type="bibr">Xu and Kiørboe, 2018</xref>). Remarkably, toxin production varies widely both within and among populations. For example, some lineages entirely lack the genes for toxin production (<xref rid="bb0040" ref-type="bibr">Brandenburg et al., 2018</xref>; <xref rid="bb0050" ref-type="bibr">Briand et al., 2009</xref>). The evolutionary dynamics of different toxic/non-toxic genotypes during algal blooms is likely driven by physiological trade-offs between costs of toxin production and resource uptake for growth (<xref rid="bb0040" ref-type="bibr">Brandenburg et al., 2018</xref>; <xref rid="bb0075" ref-type="bibr">Cadier et al., 2019</xref>; <xref rid="bb0085" ref-type="bibr">Chakraborty et al., 2019</xref>; <xref rid="bb0270" ref-type="bibr">Kiørboe and Andersen, 2019</xref>). Such defense-growth trade-offs are likely important for the emergence of harmful algal blooms (<xref rid="bb0065" ref-type="bibr">Burford et al., 2019</xref>; <xref rid="bb0220" ref-type="bibr">Jankowiak et al., 2019</xref>; <xref rid="bb0260" ref-type="bibr">Kim et al., 2010</xref>; <xref rid="bb0315" ref-type="bibr">Li et al., 2012</xref>), but the selective factors that favor toxic variants in bloom forming algae are not fully understood. Identifying the evolutionary processes involved in algal blooms would likely help us predict which algal blooms might turn toxic. In a first step, reliable prediction would enable the avoidance of risks associated with toxic algal blooms (e.g. by timely establishment of exclusion zones), and in a second step, it could inform mitigation measures to reduce the occurrence of algal blooms (e.g. by influencing relevant selective forces such as nutrient input).</p></sec></sec><sec id="s0040"><label>3</label><title>Evolving the environmental sciences</title><p id="p0155">Evolutionary processes are often an inescapable and critical component of both understanding and solving environmental problems. The evolution of resistance genes will continually challenge our efforts to halt diseases through the development of new drugs, highlighting the need to complement efforts in drug discovery with the development of evolution-aware application strategies. A better appreciation of evolution's limits and, in particular, the impossibility of Darwinian demons, is critical to meeting our energy demands by matching algal genotypes with optimal environmental conditions for biofuel production. In a similar vein, choosing strains that have evolved tolerance to pollutants might help sustain populations in deteriorating environments, while strains naive to pollution might be a more conservative option when assessing ecological risk to chemical pollutants. Engineering solutions in waste-water treatment plants might be improved if we could harness evolution's power to help biodegrade persistent compounds (<xref rid="bb0045" ref-type="bibr">Brenner et al., 2008</xref>). Other environmental problems with limited engineering-oriented solutions could be tackled with evolutionary perspectives. For example, biocides may be applied to combat algal blooms, but it is notoriously difficult to predict the timing, duration and toxicity of algal blooms. A better understanding of the evolutionary dynamics of such systems, gained, for example, by tracking environmental change in real-time and linking those changes with environmental sources of natural selection, could help us predict the outbreaks of toxic algae.</p><p id="p0160">Indeed, there is a growing need in many areas of environmental science to efficiently forecast ecosystem change across natural and human-induced gradients (<xref rid="bb0415" ref-type="bibr">Petchey et al., 2015</xref>) and to understand the consequences of such changes for ecosystem (and evosystem) services (<xref rid="bb0115" ref-type="bibr">Costanza et al., 1997</xref>; <xref rid="bb0435" ref-type="bibr">Rudman et al., 2017</xref>). This is particularly relevant for ecosystems that provide vital services to society, but are also sensitive to anthropogenic impacts. Predictions about complex ecological systems are challenging and require solid understanding of ecological and evolutionary mechanisms behind population growth, genetic and trait diversity, trait-environmental relationships, trade-offs, and community dynamics. Such principles are present in the environmental science literature, but are only sporadically applied to solve environmental issues.</p><p id="p0165">It is possible that prevailing misconceptions about the pace and prevalence of evolution may be blocking the integration of evolution into the environmental sciences. First, the pace of evolutionary adaptation is not only set by the rate of mutations and the subsequent rate of increase of novel alleles in the population. Instead, the rate of adaptation, i.e. the increase in mean population fitness over time, is directly proportional to the genetic variance in a population that can respond to natural selection (<xref rid="bb0150" ref-type="bibr">Fisher, 1930</xref>). Evolution from existing levels of heritable trait variation in a population can be much quicker and more predictable than expected based on evolution driven via new variants in the population that arise solely by mutation. Second, evolution is neither rare nor a special case. The challenge for environmental science is to determine the relative importance of evolution, either for causing or for ameliorating a particular environmental problem.</p><p id="p0170">Overall, we argue that evolutionary principles are a useful resource for coming up with solutions to environmental problems. On the one hand, seemingly rational solutions might require some ‘evolution proofing’ to effectively anticipate and limit any potential negative impacts of evolution on the expected outcomes of our interventions. On the other hand, evolution itself can be a powerful design strategy for solving environmental problems. Design by directed evolution, for example, has made considerable progress developing novel enzymes (<xref rid="bb9000" ref-type="bibr">Arnold, 1998</xref>), and configuring communities to perform specific functions that improve environmental conditions (<xref rid="bb8000" ref-type="bibr">Ghoul and Mitri, 2016</xref>). Natural selection is a powerful force that can efficiently explore the combinatorial trait space that organisms could theoretically occupy. The trait space of living systems is replete with opportunities to solve environmental problems, and natural selection might often outpace our own ability to find these solutions. Perhaps a way forward is to relinquish our engineering hubris in favor of a problem solving strategy that is either informed by, or directed by, evolution. Environmental science has a rich history of interdisciplinarity. A stronger integration with evolutionary biology would improve our ability to address global societal challenges in general (<xref rid="bb0080" ref-type="bibr">Carroll et al., 2014</xref>), and environmental challenges in particular.</p><p id="p0175"><boxed-text id="b0005"><label>Box 1</label><caption><title>The four forces of evolution.</title></caption><p id="p0005"><list list-type="simple" id="l0005"><list-item id="li0005"><p id="p0010">Mutation</p></list-item></list></p><p id="p0015">Mutations are random, heritable changes in the sequence or structure of a gene. They include substitutions of individual bases in the DNA sequence, insertions and deletions of DNA fragments, and structural rearrangements of chromosomes. New variants of the same gene generated by mutation are referred to as alleles. Mutations can be neutral, meaning they do not affect the phenotype of their carrier, advantageous in specific environments, meaning they affect the phenotype such that it increases survival and/or reproduction, i.e. fitness, or deleterious in specific environments. For example, a mutation that confers resistance to a pesticide may be beneficial in an environment where the pesticide is present but detrimental in an environment where the pesticide is absent. Mutations are the ultimate source of genetic variation and provide the original resource for adaptive evolution and biological innovation.<list list-type="simple" id="l0010"><list-item id="li0010"><p id="p0020">Natural selection</p></list-item></list></p><p id="p0025">Natural selection is the process of unequal survival and reproduction among individuals due to differences in phenotype. Some individuals of the population are more likely to survive and reproduce because they have trait combinations that make them better at coping with the current environment than other individuals. Assuming that the phenotypic traits under selection are heritable, i.e. trait values are transmitted across generations, the favorable traits, which represent ‘good genes’, will be passed to the offspring. In this way, the frequency of the ‘good’ gene variants will increase in the population, leading to evolutionary adaptation.<list list-type="simple" id="l0015"><list-item id="li0015"><p id="p0030">Gene flow</p></list-item></list></p><p id="p0035">Gene flow is the exchange of genetic material between populations. It occurs when individuals or their gametes migrate into a new population and reproduce. Gene flow can bring new alleles (i.e. genetic variants) into the receiving population and thereby influence the potential for this population to evolve. Gene flow can be maladaptive, and reduce the fitness of the local population, or adaptive. If migration is sufficiently high and migrant genes are not selected against, gene flow will homogenize allele frequencies and reduce genetic differences in the genetic composition of populations.<list list-type="simple" id="l0020"><list-item id="li0020"><p id="p0040">Genetic drift</p></list-item></list></p><p id="p0045">Genetic drift is the stochastic change in allele frequencies over generations. It occurs because allele frequencies in populations can deviate by chance from those of the parental generation, due to the random sampling of gametes. It affects particularly small populations. 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