Abstract
Two categories of evolutionary challenges result from escalating human impacts on the planet. The first arises from cancers, pathogens and pests that evolve too quickly, and the second from the inability of many valued species to adapt quickly enough. Applied evolutionary biology provides a suite of strategies to address these global challenges that threaten human health, food security, and biodiversity. This review highlights both progress and gaps in genetic, developmental and environmental manipulations across the life sciences that either target the rate and direction of evolution, or reduce the mismatch between organisms and human-altered environments. Increased development and application of these underused tools will be vital in meeting current and future targets for sustainable development.
Human influence on the biosphere (1,2) has profound consequences for both the rate and direction of evolution (3). Among the consequences are the challenges billions of people face from the effects of cancers, pests and pathogens that adapt quickly to our interventions against them. At the same time, humans and other organisms that we value for economic, ecological or aesthetic reasons are often not able to adapt quickly enough to keep pace with human alterations of the environment. These contemporary dilemmas increasingly threaten human health, food security and biological diversity (4,5,6,7,8,9,10,11,12). For example, the World Health Organization (WHO) warns that microbial resistance to antimicrobial drugs threatens the achievements of modern medicine (13). Likewise, more than 11,000 documented cases of pesticide resistance in nearly 1,000 species of insects, weeds, and plant pathogens jeopardize agricultural economies and food supplies worldwide (14). Failure to adapt may be equally dire and costly, as in the prevalent mismatch between modern human nutritional and lifestyle behaviors and those of our evolutionary past, which generally considered a major contributing factor to the high incidence of obesity and associated illnesses such as type 2 diabetes mellitus and cardiovascular disease (15). Meanwhile, the prospect of earth's sixth mass extinction of species becomes imminent as species are unable to adapt quickly enough to environmental change (16). A growing application of principles from evolutionary biology to challenges such as these may improve our ability to meet many of the most pressing problems of the 21st century (12,17,18,19).
Here we review current and prospective applications of evolutionary biology that may provide solutions for major societal challenges. We examine management approaches that attempt to either improve or undermine adaptation to modern environments by manipulating the relationships between the traits of organisms and the patterns of selection imposed by their environments. These manipulations include tools that may be widely considered evolutionary, such as selective breeding and emerging technologies in genetics, but also manipulations that are often overlooked as evolutionary, specifically manipulations of development that modify traits independent of genetic change, and altering environments in ways that can modulate selection itself. A conceptual framework linking all of these genetic, developmental and environmental manipulations is likely to lead to greater implementation and cross-disciplinary integration of applied evolutionary methods. We highlight how evolutionary strategies may be used to achieve policy targets of sustainable development for improved human health, food production, natural resource use and biodiversity conservation, including how stakeholder conflicts may be reduced to achieve desired outcomes. Throughout, we underscore the merits of building a more unified and integrated field of applied evolutionary biology to address global challenges.
Core evolutionary concepts and their relevance to global challenges
Evolution, defined as the change in genetic makeup of a population over successive generations, requires genetic variation, which arises from mutation and recombination (20). Most important for adaptation is genetic variation that affects variation in functional traits (21), such that alternate genotypes produce alternate phenotypes. Selection increases the frequency of genes that improve fitness – the ability to survive and reproduce. The specific genetic basis for most traits is not known, but trait differences among individuals typically have a significant heritable (genotypic) basis. This basis includes heritable aspects of development, which also may evolve and give rise to adaptive phenotypic plasticity (22). A population with low fitness may experience strong natural selection that favors better- adapted genotypes. However, strong selection will not necessarily ‘rescue’ a population if there are too few adapted individuals or suitable genes for the population to persist (23). Movement of genes between populations (gene flow) and random changes in gene frequency in small populations (genetic drift) can also cause evolution and influence the outcome of natural selection (20). These concepts apply not only to organisms from bacteria to humans, but also to viruses and cancer cells (24).
The core concepts of evolutionary biology are best known for explaining the unity, diversity, and adaptive characteristics of organisms (17). Phylogenetic methods that establish the relatedness of organisms are central to understanding the patterns and processes of evolution underlying the function and diversity of living systems (25). The practical applications of phylogenetic methods have been thoroughly reviewed by others, and include such diverse objectives as reconstructing invasion routes of harmful organisms, conservation planning and combating crime (17,26). Here we focus on the manipulation of processes that determine the adaptedness of individuals, populations and other biological systems in order to meet management objectives (Fig. 1).
Agriculture, medicine, and conservation address different challenges, but nonetheless share common strategies to manage evolutionary mismatch and the associated risks to populations experiencing strong selection. Those strategies can be classified as genotypic, developmental, or those related to environmental manipulations (Fig. 2). The potential sustainability of such practices may be assessed by comparing the intensity of selection with the adaptive capacity of a target population (27). For example, the widespread use of antibiotics that exert strong selection on bacteria is typically not sustainable for controlling highly adaptable microbe populations because they rapidly evolve resistance (28). Accordingly, the sustainability of antibiotics use can be increased by either reducing s election, e.g. through regulated use of particularly strong antibiotics, or by attempts to surpass the adaptive capacity of microbes through drug combinations (29). Below, we review successes and emerging methods in applied evolutionary biology, highlighting commonalities across the sectors of health, food and environmental management (Fig. 3).
Successes and prospects in applied evolutionary biology
Applied evolutionary biology encompasses widely different manipulations that may together achieve a broad range of goals. From protecting biodiversity with conventional environmental management that increases fitness in wild environments, to medical recommendations for traditional diets, some methods of applied evolutionary biology have a long history of use even if they are not often seen as evolutionary in nature. In contrast, the synthesis of wholly novel genomes with emerging technologies represents obvious evolutionary manipulation that deliberately adds new organisms to the tree of life, but with little history of application, it involves unknown risks and public controversy. Here we review some of the most recent successes and leading prospects for the application of evolutionary biology, in a progression from relatively well-established methods to underexplored strategies. We first consider manipulations of selection to improve population productivity and individual health, and to delay the emergence of resistance (Fig. 2). We then examine less developed methods for the cultivation of populations inherently pre-adapted to impending environmental changes, and for innovative applications of group selection in crops and wildlife. We end this section with urgent considerations for managing evolutionary factors that span disciplinary boundaries, as in cases of emerging zoonotic disease.
Environmental alignment to secure biodiversity and human health
A common application of evolutionary principles is to manage current environments to be more like the historical habitats in which selection shaped the genetic makeup of humans and other species. Conventional habitat protection and restoration recognize that threatened species often adapt poorly to changing environments in the wild (26,30). Conversely, rapid adaptation to captive rearing programs used to rebuild populations of rare species, contributes to a 50 to 90 percent failure rate of reintroductions (31). Reintroduction success has been improved with enclosures and rearing methods that mimic wild conditions and by limiting the number of captive generations to minimize adaptation to artificial conditions (32).
Some of the most serious non-communicable diseases in humans may be prevented by better aligning current environments with those in which our hunter-gatherer ancestors evolved (33). Sedentary modern lifestyles and diets with high glycemic processed foods are increasingly implicated in the rapidly rising rates of obesity, diabetes and cardiovascular disorders (34). These mismatch disorders are estimated to contribute to about two-thirds of all deaths in Western societies (35) and to a growing proportion of deaths in developing countries (36,37). In 2012, the economic burden of type 2 diabetes alone was estimated at $500 billion globally, nearly 1% of world GDP (38). To restore conditions to which people are better adapted physiologically, while retaining the desired elements of a modern lifestyle (35), public health scientists recommend greater phys ical activity (39) with reduced consumption of refined carbohydrates (36), that is, diets and activity levels closer to those of the past, to which we are better adapted. More generally, a number of evolutionarily-based tools are available to prevent chronic non-communicable diseases, including the 19% of global cancer incidents that the WHO attributes to environmental exposure (40). These tools include life course approaches, which manage the timing and duration of environmental exposures to minimize risks of subsequent chronic disease (41). From a public health standpoint, environmental approaches to disease prevention may often be most cost-effective when applied outside of health care settings and when simultaneously targeting groups of people rather one individual at a time, such as through price regulation on goods, or public information campaigns (42). Further, systematic population scans that associate disease phenotypes with human genotypes (43, 44) are an important tool for determining the genetic basis of lifestyle diseases, and therefore in assessing heritable risk and treatment options. Such assessments however run the risk of identifying false positives and underestimating the complexity of genetic and epigenetic regulation (45, 46). For example, it is estimated that 90% of chronic disease risk cannot currently be directly linked to genetic factors, but is more likely to be understood in the context of human environmental exposures such as diet and toxicants (47). Thus, future prevention and treatment of chronic diseases will combine enhanced genotype-phenotype association scans with improved monitoring of toxic compounds in the surrounding environment and in human tissues (47). Such genotype-phenotype association studies search simultaneously for associations across the hundreds of disease phenotypes included in electronic medical registers (45). This expanded approach reduces the rate of false positives and helps to identify genetic factors that contribute to multiple diseases as well as diseases controlled by multiple genes.
Altering genomes for improved food security and human health
Climate change and environmental degradation compromise the productivity of agricultural systems that must feed a rapidly growing human population (48). Genetic modification of crops, through enhanced artificial selection methods and perhaps genetic engineering, will likely be important in meeting these challenges. Genetically engineered (GE) crops were first grown on a large scale in 1996, and during 2013, 18 million farmers in 27 countries planted GE crops on approximately 10% of the world's cultivated land (175 million hectares) (49). More than 99% of this area was planted with soybean, corn, cotton or canola into which genes were inserted to confer tolerance to herbicides, protection against insects, or both (50). These engineered varieties are extreme examples of apparently effective genotypic manipulations to reduce mismatch to specific environments. However, societal acceptance is an important factor, and GE crops remain controversial (51,52). They have not been adopted widely in some regions including Europe, where alternative manipulations of evolutionary mismatch, such as use of non-GE lines with some degree of tolerance, pesticide applications and integrated pest management serve as alternative genotypic and environmental manipulations (53).
An alternative to GE is enhanced artificial selection and hybridization of superior cultivated varieties with molecular genetic tools that identify individuals and gene regions conveying preferred traits (54). A priority application, where GE has until now been less successful Carroll et al. 10 (55), is to improve abiotic tolerance due to more frequent weather extremes under climate change. For example, flood tolerant rice, which is grown by two million farmers in Bangladesh and India (49), was developed with marker-assisted breeding using molecular markers of quantitative traits to identify targets for hybridization and selection (56). At the same time, candidate drought tolerance genes for GE crops have also recently been identified in rice as well as corn (57,58), with corn hybrids putatively tolerant to both drought and herbicides brought to market in 2013 (55,59). Regardless, whether produced via artificial selection or genetic engineering, the potential for genetic manipulations of mismatch to improve food security may be greatest when technology allows growers to select or customize crop varieties for adaptation in their local agroecosystems (60).
In contrast to the advances in agriculture, genetic modification to treat human disease is currently in a trial phase. Gene therapy is under development mainly for diseases with high heritability and simple genetic control, in which replacing or complementing parts of a patient’s genome can improve their health (61,62,63). Therapies in advanced trial stages include the targeting of retinal cells to prevent expression of heritable blindness (64,65), and oral administration of p53 gene for tumor suppression (66). However, even as targeted DNA analysis and whole-genome sequencing of patients becomes increasingly routine (67), few efforts have met the promise of their pre-clinical and clinical trials to reach final approval phase of ‘post-marketing’ surveillance trials (68,69).
Using environmental heterogeneity to delay resistance evolution
One of the most costly and widespread outcomes of efforts to limit populations is the rapid evolution of resistance to control measures in insect pests (14), weeds (70), pathogens, and cancers (71). For example, intensive use of the herbicide glyphosate by farmers, particularly those who grow glyphosate-tolerant GE crops, has selected for resistance in 24 weed species in 18 countries since 1996 (72,73). In contrast, strategies that vary selection in space or time have delayed the evolution of resistance in some pests (Fig. 3). For example, scientists and farmers have proactively developed and implemented strategies to slow pest adaptation to GE crops that produce insecticidal proteins from Bacillus thuringiensis (Bt) (74,75). The primary strategy employs ‘refuges’ of host plants that do not produce Bt toxins to promote survival of susceptible pests (74). In principle, the rare resistant pests that survive on Bt crops are more likely to mate with the comparatively abundant, susceptible pests from the nearby refuges. If resistance is inherited as a recessive trait, the heterozygous offspring from such matings will be susceptible and will die on the transgenic plants. The U.S. EPA and regulatory agencies in many other countries have mandated refuges since Bt crops were first commercialized (76,77). Retrospective analysis after more than a decade of monitoring indicates that refuges do indeed delay resistance, particularly when resistance is a recessive trait (77,78).
The success of refuge tactics in agriculture is now drawing attention in other management sectors, including fisheries, where refuges may impede costly life history and body size evolution resulting from harvest selection (79). Likewise, in cancer management, portions of tumors with low vascularization and consequently low delivery of chemotoxins may serve as refuges that sustain chemosensitive tumor genotypes (80,81) and slow the evolution of resistance to chemotherapy in metastatic cancer (82,83). Such resistance accounts for a large proportion of current treatment failures (84). Compared w ith typical failures when oncologists try to eradicate a patient's cancer with high drug doses, lower doses could be more successful if they favor survival of chemosensitive cell lines that can outcompete chemoresistant lines (85). Increasingly sophisticated models of tumor evolution may eventually support implementation of such non-eradication therapies (86).
While refuges delay resistance with genetic swamping of resistant lineages by susceptible lineages, another strategy attempts to curb resistance through selection that combines multiple modes of action (also known as “stacking” or “pyramiding”). In many human diseases, including HIV, tuberculosis, malaria and cancer, resistance frequently evolves under selection from individual drugs (87). Combination therapies are based on the evolutionary principle that if genes conferring resistance to each selection pressure are rare and inherited independently, individuals with all of the genes required for full resistance will be rare or even absent in target populations (4,14,88,89). For example, resistance evolved rapidly to potent antiretroviral drugs administered singly in patients with HIV, but combinations of three such drugs have provided long-term efficacy and have become the standard of care (90,91). The potential tradeoffs associated with combining two or more drugs or pesticides to delay resistance include short-term increases in costs (92) and negative side effects (93), as well as the concern that such combinations will also ultimately favor the evolution of multiple resistance (87,94,95,96). For example, incorporating two or more toxins together in GE varieties slows resistance evolution (97,98), but this advantage may diminish when less resistant single-toxin varieties are planted in the same area as multi-toxin varieties, and provide stepping stones for multiple-resistance evolution (99). Combined selection pressures are most likely to be durable when implemented as a facet of more broadly integrated systems, such as integrated pest management (IPM). IPM combines selection pressures from a diverse suite of tactics for pest suppression including various forms of biological control and optimized spatiotemporal cropping schemes (100). By increasing treatment durability, combinatorial strategies are among the most important instruments for the control of highly adaptable pests, pathogens and cancers (Fig. 3).
Choosing population sources to anticipate climate change
While some strategies of applied evolutionary biology are established or rapidly increasing, other rarely used strategies are of interest because of their underexplored potential to replace or complement longstanding management practices. These include using non-local seeding sources for re-planting in environmental restoration and forestry, and the exploitation of group selection-based designs in crop and livestock breeding.
The mismatch of valued plants to new climates is an overarching challenge in forestry, agriculture and conservation biology. A widespread debate concerns whether to use local versus external sources of genetic material for replanting to best anticipate climate change in forestry, agriculture, wildlife and environmental restoration. The massive scale of many replanting efforts – 400,000 ha of production forest is planted each year in Canada alone (101) – plus the long intervals between plantings for many perennial species and restoration projects, means that these choices may have broad economic and ecological consequences. Traditionally, resident stocks have been favored to capture locally valuable adaptations. In forestry this approach is exemplified by established bioclimatic ‘seed-transfer zones’ that steer local seed sourcing for planting of some of the world’s largest production systems (102,103). Evidence from wild plant restoration programs indicates however that local sources are not always best, particularly in altered environments (104,105,106,107,108, 109). This may arise when nearby sources share some of the vulnerabilities responsible for the declines of the original populations (103). In these situations, climate mismatches may be better relieved by translocating genotypes that are pre-adapted to expected conditions (110,111), for example more tolerant to heat, drought or pest stresses (112). When single sources do not show the range of adaptations required at a given site, reintroduction may be improved with propagules pooled from a diversity of sources to increase overall genetic variation, and thus the odds that some individuals will be suited for changing conditions (104,105,113). A recent meta-analysis in restoration ecology underscores shortcomings of the 'local-is-best' dictum (114) and comparable analyses of sourcing successes and failures in forestry and perennial agriculture are needed to find ways to sustain productivity under climate change.
Exploiting group versus individual performance in crops and livestock
In most agriculture and aquaculture, productivity is measured at the level of groups (e.g., field or herd) rather than in individual performance. More attention to traits that improve group performance may thus offer a broader suite of tactics to increase production while demanding fewer resources, including pesticides, to meet basic human needs (115) (Fig. 3). In the majority of natural systems, group selection is considered weak relative to selection among individuals (116). Consequently, past natural selection in the ancestors of domesticated species may have favored traits that promote individual performance but are costly to group productivity. One important consequence may be greater current opportunities for artificial selection of individual traits that improve group performance while avoiding inadvertent evolution of ‘uncooperative’ individuals (8), such as those with competitive root structures in dryland field crops (117). Artificial selection for group yield in maize has produced lines with reduced male function and that bear more-vertical leaves, which reduce the shading of neighbors. Both of these traits decrease individual plant performance while enhancing group productivity (118,119), but in the absence of strategic breeding to favor these changes directly, they have evolved only slowly, requiring 60 years to appear as unplanned responses to selection on group yield alone (120). Weiner and colleagues (121) have proposed a proactive evolutionary design for wheat production that selects for traits that increase collective shading of weeds within specific planting configurations, in order to increase overall crop yield while reducing herbicide use. Similar group-based perspectives apply in animal husbandry, where traits like reduced aggressiveness favor group productivity under domestication, but might have been selected against in the wild (122). By combining agronomy and environmental physiology with evolutionary modeling, group-based agricultural systems may offer new and more sustainable paths to meet global production goals.
Addressing evolution across management sectors
One of the most significant outcomes of the scale of human activity is that evolutionary concerns in one management sector often spill over into, or depend on, others (Fig. 4). These connections result from novel biotic interactions due to natural, intentional or inadvertent transport of organisms and their genes by trade, infrastructure, and waste streams (123,124). Further coordination of prevention, control and monitoring will be required to address growing interdependencies among management sectors. Increased exchange of emerging pathogens between health, agricultural and natural systems is a key case in point (125,126,127,128). For example, while domestic pigs are the principal reservoir of ‘swine influenza’ (H1N1), they simultaneously host other influenza strains, including those associated with human hosts and domestic and migratory avian hosts (129). The intensive communal raising of pigs and poultry for food therefore encourages virus strains to exchange genes and adapt to more host species (130). One overarching concern is that pigs hosting highly pathogenic wild avian strains (H5N1) could contribute to selection for the direct mammal-to-mammal transmission that underlies human epidemics. The consequences of such evolution (131) are foreshadowed by the recent global outbreaks of H5N1 in 2004 and H1N1 in 2009 (132). These events underscore the need for initiatives in prevention and control that cross traditional disciplinary boundaries, including coordinated surveillance of viral evolution and the monitoring of pathogen reservoir species across the food, health and environment spectrum (127,133).
The unresolved problem of rapidly evolving antimicrobial resistance is another pressing example of interdependence among management sectors, particularly between systems managed for food production and human health. Annual estimated costs of combatting multidrug resistant microbes in the US alone total $35 billion (134,135), and the failure to produce new antimicrobials as quickly as their predecessors lose efficacy (136,137) places a premium on stewardship of the few drugs that remain broadly effective (138,139). Although overprescribing of antibiotics for human treatment is a very real concern, the major use of antimicrobial drugs in many parts of the world is to promote the health and growth of livestock (140,141). This use selects for antimicrobial resistant microbes that may infect humans (Fig. 4) (141,142). Antibiotic-treated animals that are raised to feed people are now implicated in the origins of the most extensively resistant Escherichia coli encountered in human sepsis (143). Particularly worrisome is that once free in the environment, resistance genes do not dissipate with distance like many abiotic environmental pollutants. Resistance genes can replicate, and thus they can transfer horizontally among bacterial taxa, travel intact over great distances via hosts, and rise to new abundances in the presence of antimicrobials with similar modes of action. As pools of resistance genes become more prevalent and disseminated through human activities, they are likely to become increasingly important in new regions and management sectors (144). Because coupled evolutionary dynamics operate over such large spatial scales and multiple management sectors, their management requires political coordination, as exemplified by the Transatlantic Taskforce on Antimicrobial Resistance (145). Regulatory bodies have also taken the first steps to restrict use of some antibiotics to single management sectors (146,147). Broader and more rigorous implementation of such restrictions will be needed to sustain the most critical public benefits of our modern antibiotic era.
Next Steps
Applied evolutionary biology in international policy
Applied evolutionary biology addresses both the rapidly evolving and the mismatched biological systems that underlie many global challenges (148). Meeting international objectives for sustainable development (Millennium Development Goals and the anticipated Sustainable Development Goals (149)) and biodiversity conservation (the Convention for Biological Diversity’s 2020 ‘Aichi’ targets (150)) will require much greater integration of evolutionary principles into policy than has been widely acknowledged. Box 1 summarizes potential policy contributions of cases reviewed here. For example, we must implement resistance management strategies for pesticides and antibiotics to meet newly proposed Sustainable Development Goals for human health, food and water security (149). Likewise, choices of adaptable source populations will improve the resilience of restored habitats (Aichi target 15: ‘restore 15 percent of degraded habitats before 2020’) and increase the reliability of crop supplies. Further, sustainable harvest strategies (151,152) and early warning signs of unsustainable harvest (153) will help to achieve lasting stocks of fish and aquatic invertebrates (Aichi target 6: all stocks should be harvested sustainably). The identification and protection of diverse genotypes is also critical to the future of crop improvement and for the discovery of chemical compounds such as new therapeutics. In this realm, the international Nagoya protocol on Access and Benefit-Sharing of genetic resources (154) may assist in securing public access to resources for adaptation to local conditions while coordinating with global research and development efforts (155,156,157).
Box 1: Recommended contributions of applied evolutionary biology to proposed themes of new international sustainable development goals (149), based on examples presented in this review.
Goal 1: Thriving lives and livelihoods
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Reduce chronic lifestyle disease through environmental alignment of human lifestyle.
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Reduce environmental levels of human toxicants through application of reduced selection response techniques* to pesticides/biocides.
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Apply reduced selection response techniques to maintain long-term efficacy of antimicrobials and avert the anbiotics crisis.
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Reconcile individual and group incentives in health systems to reduce virulence and resistance of emerging and re-emerging pathogens.
Goal 2: Sustainable food security
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Increase crop yield through continued selection of varieties and improved access to these.
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Prolong efficacy of pesticides and artificially selected or GE crops through reduced selection response techniques.
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Improve yields through integration of group selection in production of novel crop varieties.
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Reduce climate change impact by choosing crop varieties resilient to drought, flooding and other extremes.
Goal 3: Secure sustainable water
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Increase water security through use of reduced selection response techniques to water polluting pesticides/biocides
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Use genetic manipulation to produce crop varieties with improved water economy.
Goal 4: Universal clean energy
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Improve biofuels through genetic manipulation with the aim to reduce CO2 emissions and land area for energy production.
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Assess risks and benefits of synthetic organisms for biofuel production taking taking gene flow, land use and property rights issues into account.
Goal 5: Healthy and productive ecosystems
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Reduce biodiversity extinction rates through environmental alignment and genetic manipulation of fitness.
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Retain naturalness of captive biodiversity through environmental alignment.
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Choose pre-adapted or high diversity sources for increased habitat restoration success.
Goal 6: Governance for sustainable societies
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Incorporate externalities from rapid evolution as well as the loss of evolutionary history and potential into green accounting for sustainable governance of the earth system.
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Coordinate strategies of SDG’s in a coupled systems framework to reduce conflicts from inadvertent contemporary evolution and phenotype-environment mismatch.
* Reduced selection response techniques refer to the four tactics in Figure 3 that slows evolution by varying selection in space and time, diversifying selection, and targeting of specific traits, and additionally adoption of alternatives to strong selection agents such as toxins.
The extensive and targeted genetic manipulations permitted through recent advances in biotechnology are setting the stage for novel biological functions for which we either lack an understanding of potential risks, or knowledge of how best to assess them (158). Thus, perhaps the area of applied evolutionary biology where development of international policy is most urgent is the area of synthetic biology. Synthesizing wholly or partially novel organisms offers tremendous opportunities in many areas such as biofuels, medicine, environmental restoration and conservation (159,160,161), but national and international guidelines are needed to avert potentially harmful outcomes (158,162). Segments of medicine and agriculture include social scientists and economists in systematic risk assessment (76,163). Similar practices would benefit conservation biology and natural resource management, as increasingly proactive and intensive manipulations appear on the horizon. These prospects include resurrected species and wild populations genetically engineered for resistance to lethal diseases such as chytrid fungus in frogs and white-nose syndrome in bats (161,162).
Implementing applied evolutionary biology locally and globally
Reconciliation of individual and group stakeholder interests plays a central role in the effort to achieve sustainability through applied evolutionary biology (164,165,166,167). Anthropogenic evolutionary change often has consequences that extend beyond the immediate vicinity of the causal agents and pose dilemmas in achieving cooperation from local to global scales (168). Thus, in some applied evolutionary strategies, individuals must exchange their private short-term gains for the long-term public good. In managing pest resistance to transgenic Bt crops, farmers who plant refuges of conventional crops contribute to the long-term public good of sustained pest susceptibility to Bt toxin, but may incur the short-term private cost of pest damage to their refuges. For example, farmers that planted only non-Bt corn in five midwestern states of the U.S. accrued nearly two-thirds of the estimated $6.8 billion in Bt corn benefits between 1996 and 2009 (169). This benefit arose from a combination of less expensive non-Bt corn and because widespread adoption of Bt corn caused regional suppression of the major target pest (169). Perhaps in part due to the latter, farmer compliance with the refuge strategy for Bt corn in the U.S. has steadily declined and threatens the sustainability of resistance management (170). Such conflicts between individual and public good may be the rule rather than the exception in the implementation of applied evolutionary biology.
The economic theories of public choice provide tools for reconciling individual and group conflicts (171) (Box 1). Governments can tax undesirable actions, subsidize desirable ones, regulate activities (146,147), and create tradable property rights. For example, subsidies and regulated access to public schools can increase participation in vaccination programs that benefit public health but may increase risks to unvaccinated individuals (172). Theoretical modeling suggests that an unregulated vaccination market will yield too little advance vaccination and too much vaccination at the time of infection, which could select for increased virulence (163). With pathogen resistance, both the relative fitness of resistant genotypes in untreated environments (173,174) and the prevalence of resistance in natural environments (175) may increase the cost of lost susceptibility to a drug. Improved policies that reduce public costs may emerge from better accounting of the causes and consequences of such evolutionary externalities (163,176).
Toward a unified discipline
As demonstrated by many of the examples above, applied evolutionary biology uses principles common to all areas of biology, and because of this, progress in one area may often enable solutions in others. New approaches in this developing field may best be generated and assessed through collaborations that span disciplinary boundaries (177) (Fig. 3). Promoting greater adoption and consistency in the use of evolutionary terminology, which is inconsistent across disciplines (178), will therefore be an important first step toward a more unified field of applied evolutionary biology.
The global scale of human impacts is now more widely appreciated than ever before. Successful governance of living systems requires understanding evolutionary history as well as contemporary and future evolutionary dynamics. Our current scientific capacity for evolutionarily-informed management does not match the need, but it can be increased through new and more widespread training and collaboration, monitored experimentation, and context-sensitive implementation. Like engineering, which is a multifaceted applied science with common core principles, shared vocabulary and coordinated methods, applied evolutionary biology has the potential to serve society as a predictive and integrative framework for addressing practical concerns in applied biology which share at their core the basic evolutionary principles governing life.
Supplementary Material
Acknowledgements
M.T.K., R.F.D., S.P.C., S.Y.S., and T.B.S. were supported by grants from NSF. C.T.B. is supported by NIGMS grant number U54GM088558. M.T.K., is supported by Maine Agricultural and Forest Experiment Station; P.D.G. by the National Research Centre for Growth and Development; S.P.C. by CSIRO and the Australian-American Fulbright Commission; S.Y.S. by grants from the College of Biological Sciences, UC Davis; T.B.S. by grants from NIH, and B.E.T. by USDA Biotechnology Risk Assessment Grant 2011-33522-30729. P.S.J. acknowledges the Danish National Research Foundation for support to the Center for Macroecology, Evolution and Climate, and the American-Scandinavian Foundation. Sonal Singhal, Jacobus Boomsma, Carsten Rahbek, Niels Strange and Trevon Fuller provided useful comments on previous versions of the manuscript.
Footnotes
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