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Coevolutionary interactions are thought to have spurred the evolution of key innovations and driven the diversification of much of life on Earth. However, the genetic and evolutionary basis of the innovations that facilitate such interactions remains poorly understood. We examined the coevolutionary interactions between plants (Brassicales) and butterflies (Pieridae), and uncovered evidence for an escalating evolutionary arms-race. Although gradual changes in trait complexity appear to have been facilitated by allelic turnover, key innovations are associated with gene and genome duplications. Furthermore, we show that the origins of both chemical defenses and of molecular counter adaptations were associated with shifts in diversification rates during the arms-race. These findings provide an important connection between the origins of biodiversity, coevolution, and the role of gene and genome duplications as a substrate for novel traits.

During the last decade azole resistance has increasingly been reported in Aspergillus fumigatus, which is a fungal pathogen involved in the vast majority of invasive aspergillosis infections in humans, and is now a global public health concern. Antifungal azoles, especially triazoles, are the drugs of choice for medical treatment. However, this treatment is hampered by the emergence of multi-azole resistant A. fumigatus isolates, especially the highly resistant variants TR34/L98H and TR46 /Y121F/T289A. Therefore, to control this disease, it is essential to elucidate by what mechanisms resistance emerges, how resistance spreads and how resistant genotypes persist in environments without azoles. The presented thesis shows the relevance of the life cycle of A. fumigatus to the development of azole resistance and possible evolutionary routes that lead to it. The work highlights the importance of fungal biology and evolution towards understanding the development of azole resistance in fungi. We conclude that azole resistance in A. fumigatus is a consequence of selection pressure by azole in the environment on the genetic variation generated via various aspects in the A. fumigatus life cycle. This thesis also introduces an experimental evolution approach to study the dynamics and mechanisms of the evolution of azole resistance. In addition, we investigate what condition can lead an environment to be a possible hotspot for the development of resistance. Finally, we link this to the potential conditions under which resistance can emerge and spread in the lungs of humans and how this depends on the specific azole used.

Sexual selection is an important factor that drives evolution, in which fitness is increased, not by increasing survival or viability, but by acquiring more or better mates. Sexual selection favours traits that increase the ability of an individual to obtain more matings than other individuals that it is in competition with. For many sexually reproducing organisms, obtaining mates is an essential part of the lifecycle, sexual selection can therefore be very strong. A trait that leads to more matings can be selected, even if it strongly reduces other components of fitness, for instance predator escape. Often sexual selection leads to sex specific traits, which can become very extravagant. In animals and plants, it has been well established that this form of selection is an important evolutionary force, but it has not been considered for fungi. This thesis revolves around the idea that in this aspect, fungi are not fundamentally different from animals and plants and that also for species from this kingdom sexual selection influences evolution. Many fungi reproduce sexually and need to find a partner before reproduction can proceed. Furthermore, it is likely that not all individuals that benefit from mating can perform mating, hence a struggle for mate acquisition will occur. In my research I have investigated how likely it is that in fungi such struggles occur and which mechanisms might act during competitions. For these studies I used the mushroom forming basidiomycete fungus Schizophyllum commune as a model organism. I studied the potential for mate competition in natural populations, performed laboratory mating essays to test competition and preference, and experimentally tested if sexual selection can increase competitive ability. Sexual reproduction in fungi is highly regulated. Many molecular mechanisms are known that modulate each step, from meiosis to gamete production and from mate finding to gamete fusion. In most fungi these characteristics are regulated by genes located on the mating type locus or loci. These genes do not only regulate mating, but also define compatibility between the gametes: gametes with the same alleles at a mating type locus cannot fuse. Because of this double function, fungal mating types are potentially very important for sexual selection. Besides that mating types are a target for sexual selection because they affect traits that might increase competitive ability, since the mating types determine compatibility, they also define who competes with whom. Sexual selection describes how within one sex mating occurs for individuals of the other sex and is therefore always intra-sexual. Fungi do not have different sexes, but do have sex roles. Sexual selection will therefore act if there is competition for mating in the male or female role. Compatibility between sex roles is different from compatibility between mating types. The first is defined by the size of the mycelium, and the second by a genetic recognition mechanism. This difference is of importance to understand how sexual selection can act in fungi and is explained in Chapter 2. Mating in mushroom fungi occurs by reciprocal exchange of nuclei. In the female role nuclei from a compatible mate are incorporated into the haploid mycelium. These nuclei migrate though the mycelium until in each cell of the mycelium two haploid nuclei are present; it becomes a so called dikaryon. Only a dikaryon can produce mushrooms that produce spores. In the male role, a mycelium can donate nuclei to a haploid mycelium. A mycelium can thus be considered hermaphroditic. After fertilize, the dikaryon can still act as a nucleus donor, but not incorporate more nuclei – this type of mating is known as the Buller phenomenon. Also spores can act as male, but as they have no mycelium, not as a female. Due to the presence of more individuals that can mate in the male role than there are female mycelia (monokaryons), competition over fertilizations is expected. Competition can only occur when there are multiple individuals. Fungi are sessile organisms that can only meet other individuals when they are in the same locality. To test whether there is potential for sexual selection in nature, the number of individuals that meet each other needs to be defined. Not much knowledge on numbers of individuals is known, because mushroom fungi generally grow by mycelium expansion inside a substratum and each part of the mycelium can produce mushrooms. Therefore, all mushrooms on a tree can be one genetic individual, but it is also possible that each mushroom is a separate individual. We sampled 24, 12 and 24 mushrooms from the same substrate of three natural populations to analyse how mating occurred (Chapter 3). We determined the identity of the two different nuclei in each mushroom, as well as the mitochondria. Because mitochondria do not migrate during mating, they are specific for each female mycelium. We found that multiple genetic individuals (3, 3 and 8) are present in a small area, and that many matings must have occurred. Even though it is generally assumed that matings occur between two monokaryons, none such matings were found. The data suggest that mating in nature occurs between a monokaryon and a spore, or a monokaryon and a dikaryon. During a dikaryon-monokaryon (di-mon) mating only one of the two nucleus types from the dikaryon is successful in fertilizing the monokaryon. The nucleus type that is successful will likely increase its fitness considerably, as the entire female mycelium becomes colonized. Sexual selection is expected to select for nuclei that are better in performing this fertilization. Furthermore, during mating the receiving monokaryon meets two different nuclei, and might be able to choose between them. We performed crosses between 15 dikaryons and six different monokaryons to test if selection occurs, and whether selection occurs by male-male competition, or by female choice (Chapter 4). When confronting the same dikaryon with different monokaryon, in some of the cases the female mycelium decided which of the two nuclei won. In most cases however, the same nucleus always fertilized the monokaryon, irrespective of which monokaryon. This suggests that nuclei are able to either manipulate the monokaryon in incorporating them into the mycelium and not the other type, or that the nuclei of one type can directly suppress mating by the other nuclei in the dikaryon. Nuclei in a dikaryon have a strict way of cell division in which the different types divide in synchrony. Probably the two nuclei keep each other in check to assure this synchrony. Experiments in which the two nuclei in a dikaryon are separated into monokaryons suggest that the two nuclei suppress each other’s mitotic division, and that one of the two nuclei is better in suppression than the other. Consequently, after de-dikaryotisation more monokaryons of one type are recovered than of the other. We tested if this mechanism of suppression might be responsible for the dominant nuclei in the di-mon matings (Chapter 5). Separating the two nuclei confirmed earlier findings that always one of the two nuclei is dominant and that a hierarchy in dominance exists. This pecking order did not correspond with the results from the winner in the di-mon matings, which suggests that the mechanism of suppressed mitotic division is not responsible for dominance in di-mon matings. Nevertheless, we argue that the hypothesis that a link between the two mechanisms exists should not be completely written off. Because the interactions that take place during di-mon matings are very complex, the functioning of this mechanism might be obscured during mating. The observed variance in mating success described above might lead to sexual selection, however, it does not show that sexual selection actually led to traits that improve increased mate acquisition. To show that traits can evolve that increase fitness by higher mating success, we performed an evolution experiment (Chapter 6). An evolving population of nuclei was continuously mated with a non-evolving monokaryon. This setup selected for novel traits that increase competitive ability over matings. After 20 transfers, four out of twelve evolved lines had increased in competitive fitness and one line had decreased. Different fitness components were measured to investigate which traits had resulted in changed fitness. Fertilization success was mainly determined at the moment of fusion with and in initial migration into the receiving monokaryon. Two strains showed increased spores production, but this did not add to the increased fitness caused by fusion and initial migration. Little fitness change occurred during migration or in the dikaryon phase. We observed no clear trade-offs between the competitive ability of fertilizing in the male role, and female characteristics. This experiment showed that sexual selection can act in mushroom fungi. Sexual selection can also play a role in other groups of fungi than the mushroom forming fungi. So far this has not been considered, and little research has been done to show how mate competition might influence evolution. We reinterpreted the current knowledge on mating in fungi and assessed whether and when sexual selection might play a role (Chapter 7). Sexual selection is most likely to occur when sex roles can be observed during mating, as this can lead to skewed sex ratios. Also when there is large difference in quality between potential mates sexual selection might lead to evolution of choice. Directions are given where sexual selection is expected to function in fungal mating. Examples are given of how sexual selection might have led to for instance the evolution of micro-conidia in ascomycetes and pheromone redundancy in basidiomycetes. Furthermore, the existence of different sex roles in fungi, can lead to sexual conflict between the genomes derived from the paternal and the maternal gametes of which examples are given. The realization that sexual selection can also act in fungi gives great opportunity to test how universal general theories of sexual selection are in another important group of organisms. Additionally, because fungi are easy to manipulate, predictions on sexual selection can be tested experimentally using fungi. Mushroom forming fungi have a life history which differs from animals and plants. Sexual selection will therefore affect mushroom fungi in a different manner than it would animals and plants. In the general discussion of this thesis (Chapter 8) I will assess how mating influences fungal fitness, teasing apart the benefits and costs of mating in the male and female roles. I give directions for future research and discuss a setup to directly measure the effect of pheromones on female choice in mushroom fungi. There are still many unanswered fundamental questions about sexual selection. Adding knowledge from a third important kingdom can help increase the understanding of the principles that drive evolution by sexual selection. Furthermore, applying sexual selection theory to fungi might elucidate the functioning of the sometimes very complex mechanisms that have evolved for fungal mating.

Sexual selection is an important factor that drives evolution, in which fitness is increased, not by increasing survival or viability, but by acquiring more or better mates. Sexual selection favours traits that increase the ability of an individual to obtain more matings than other individuals that it is in competition with. For many sexually reproducing organisms, obtaining mates is an essential part of the lifecycle, sexual selection can therefore be very strong. A trait that leads to more matings can be selected, even if it strongly reduces other components of fitness, for instance predator escape. Often sexual selection leads to sex specific traits, which can become very extravagant. In animals and plants, it has been well established that this form of selection is an important evolutionary force, but it has not been considered for fungi. This thesis revolves around the idea that in this aspect, fungi are not fundamentally different from animals and plants and that also for species from this kingdom sexual selection influences evolution. Many fungi reproduce sexually and need to find a partner before reproduction can proceed. Furthermore, it is likely that not all individuals that benefit from mating can perform mating, hence a struggle for mate acquisition will occur. In my research I have investigated how likely it is that in fungi such struggles occur and which mechanisms might act during competitions. For these studies I used the mushroom forming basidiomycete fungus Schizophyllum commune as a model organism. I studied the potential for mate competition in natural populations, performed laboratory mating essays to test competition and preference, and experimentally tested if sexual selection can increase competitive ability. Sexual reproduction in fungi is highly regulated. Many molecular mechanisms are known that modulate each step, from meiosis to gamete production and from mate finding to gamete fusion. In most fungi these characteristics are regulated by genes located on the mating type locus or loci. These genes do not only regulate mating, but also define compatibility between the gametes: gametes with the same alleles at a mating type locus cannot fuse. Because of this double function, fungal mating types are potentially very important for sexual selection. Besides that mating types are a target for sexual selection because they affect traits that might increase competitive ability, since the mating types determine compatibility, they also define who competes with whom. Sexual selection describes how within one sex mating occurs for individuals of the other sex and is therefore always intra-sexual. Fungi do not have different sexes, but do have sex roles. Sexual selection will therefore act if there is competition for mating in the male or female role. Compatibility between sex roles is different from compatibility between mating types. The first is defined by the size of the mycelium, and the second by a genetic recognition mechanism. This difference is of importance to understand how sexual selection can act in fungi and is explained in Chapter 2. Mating in mushroom fungi occurs by reciprocal exchange of nuclei. In the female role nuclei from a compatible mate are incorporated into the haploid mycelium. These nuclei migrate though the mycelium until in each cell of the mycelium two haploid nuclei are present; it becomes a so called dikaryon. Only a dikaryon can produce mushrooms that produce spores. In the male role, a mycelium can donate nuclei to a haploid mycelium. A mycelium can thus be considered hermaphroditic. After fertilize, the dikaryon can still act as a nucleus donor, but not incorporate more nuclei – this type of mating is known as the Buller phenomenon. Also spores can act as male, but as they have no mycelium, not as a female. Due to the presence of more individuals that can mate in the male role than there are female mycelia (monokaryons), competition over fertilizations is expected. Competition can only occur when there are multiple individuals. Fungi are sessile organisms that can only meet other individuals when they are in the same locality. To test whether there is potential for sexual selection in nature, the number of individuals that meet each other needs to be defined. Not much knowledge on numbers of individuals is known, because mushroom fungi generally grow by mycelium expansion inside a substratum and each part of the mycelium can produce mushrooms. Therefore, all mushrooms on a tree can be one genetic individual, but it is also possible that each mushroom is a separate individual. We sampled 24, 12 and 24 mushrooms from the same substrate of three natural populations to analyse how mating occurred (Chapter 3). We determined the identity of the two different nuclei in each mushroom, as well as the mitochondria. Because mitochondria do not migrate during mating, they are specific for each female mycelium. We found that multiple genetic individuals (3, 3 and 8) are present in a small area, and that many matings must have occurred. Even though it is generally assumed that matings occur between two monokaryons, none such matings were found. The data suggest that mating in nature occurs between a monokaryon and a spore, or a monokaryon and a dikaryon. During a dikaryon-monokaryon (di-mon) mating only one of the two nucleus types from the dikaryon is successful in fertilizing the monokaryon. The nucleus type that is successful will likely increase its fitness considerably, as the entire female mycelium becomes colonized. Sexual selection is expected to select for nuclei that are better in performing this fertilization. Furthermore, during mating the receiving monokaryon meets two different nuclei, and might be able to choose between them. We performed crosses between 15 dikaryons and six different monokaryons to test if selection occurs, and whether selection occurs by male-male competition, or by female choice (Chapter 4). When confronting the same dikaryon with different monokaryon, in some of the cases the female mycelium decided which of the two nuclei won. In most cases however, the same nucleus always fertilized the monokaryon, irrespective of which monokaryon. This suggests that nuclei are able to either manipulate the monokaryon in incorporating them into the mycelium and not the other type, or that the nuclei of one type can directly suppress mating by the other nuclei in the dikaryon. Nuclei in a dikaryon have a strict way of cell division in which the different types divide in synchrony. Probably the two nuclei keep each other in check to assure this synchrony. Experiments in which the two nuclei in a dikaryon are separated into monokaryons suggest that the two nuclei suppress each other’s mitotic division, and that one of the two nuclei is better in suppression than the other. Consequently, after de-dikaryotisation more monokaryons of one type are recovered than of the other. We tested if this mechanism of suppression might be responsible for the dominant nuclei in the di-mon matings (Chapter 5). Separating the two nuclei confirmed earlier findings that always one of the two nuclei is dominant and that a hierarchy in dominance exists. This pecking order did not correspond with the results from the winner in the di-mon matings, which suggests that the mechanism of suppressed mitotic division is not responsible for dominance in di-mon matings. Nevertheless, we argue that the hypothesis that a link between the two mechanisms exists should not be completely written off. Because the interactions that take place during di-mon matings are very complex, the functioning of this mechanism might be obscured during mating. The observed variance in mating success described above might lead to sexual selection, however, it does not show that sexual selection actually led to traits that improve increased mate acquisition. To show that traits can evolve that increase fitness by higher mating success, we performed an evolution experiment (Chapter 6). An evolving population of nuclei was continuously mated with a non-evolving monokaryon. This setup selected for novel traits that increase competitive ability over matings. After 20 transfers, four out of twelve evolved lines had increased in competitive fitness and one line had decreased. Different fitness components were measured to investigate which traits had resulted in changed fitness. Fertilization success was mainly determined at the moment of fusion with and in initial migration into the receiving monokaryon. Two strains showed increased spores production, but this did not add to the increased fitness caused by fusion and initial migration. Little fitness change occurred during migration or in the dikaryon phase. We observed no clear trade-offs between the competitive ability of fertilizing in the male role, and female characteristics. This experiment showed that sexual selection can act in mushroom fungi. Sexual selection can also play a role in other groups of fungi than the mushroom forming fungi. So far this has not been considered, and little research has been done to show how mate competition might influence evolution. We reinterpreted the current knowledge on mating in fungi and assessed whether and when sexual selection might play a role (Chapter 7). Sexual selection is most likely to occur when sex roles can be observed during mating, as this can lead to skewed sex ratios. Also when there is large difference in quality between potential mates sexual selection might lead to evolution of choice. Directions are given where sexual selection is expected to function in fungal mating. Examples are given of how sexual selection might have led to for instance the evolution of micro-conidia in ascomycetes and pheromone redundancy in basidiomycetes. Furthermore, the existence of different sex roles in fungi, can lead to sexual conflict between the genomes derived from the paternal and the maternal gametes of which examples are given. The realization that sexual selection can also act in fungi gives great opportunity to test how universal general theories of sexual selection are in another important group of organisms. Additionally, because fungi are easy to manipulate, predictions on sexual selection can be tested experimentally using fungi. Mushroom forming fungi have a life history which differs from animals and plants. Sexual selection will therefore affect mushroom fungi in a different manner than it would animals and plants. In the general discussion of this thesis (Chapter 8) I will assess how mating influences fungal fitness, teasing apart the benefits and costs of mating in the male and female roles. I give directions for future research and discuss a setup to directly measure the effect of pheromones on female choice in mushroom fungi. There are still many unanswered fundamental questions about sexual selection. Adding knowledge from a third important kingdom can help increase the understanding of the principles that drive evolution by sexual selection. Furthermore, applying sexual selection theory to fungi might elucidate the functioning of the sometimes very complex mechanisms that have evolved for fungal mating.

Birds, in particular poultry and ducks, are a source of many infectious diseases, such as those caused by influenza viruses. These viruses are a threat not only to the birds themselves but also to poultry farming and human health, as forms that can infect humans are known to have evolved. It is believed that migratory birds in general play an important role in the global spread of avian influenza (AI). However, it is still debated how large this role precisely is and whether other modes of spread may be more important. The mallard (Anas platyrhynchos) is the world’s most abundant and well-studied waterfowl species. Besides being an important game and agricultural species, it is also a flagship species in wetland conservation and restoration. Waterfowl (Anseriformes: Anatidae) and especially ducks currently are the focal bird group in long distance dispersal of Avian Influenza in the wild, and the mallard has been identified as the most likely species to transport this virus. In my thesis I report aspects of the biology of this important host species of AI by molecular ecological means. As molecular marker system I established a genome-wide set of more than 100,000 SNPs of which I developed a subset of 384 SNPs into an assay to genotype about 1,000 ducks. This subset was employed to study the evolutionary history and speciation processes in the Anas genus. Further investigations into the world-wide mallard population structure on a species level were based not only on this set of 384 SNPs but also on mitochondrial DNA sequences. Last but not last, I investigated an option of AI sampling and detection from duck faeces by technology that is safe from a biohazard perspective, and solves transportation issues related to cold chains. The main results of my thesis include the development of a generally applicable improved analysis pipeline to develop genome-wide SNP sets for non-model organisms. Further, my results show that, from a migration system perspective, mallard flyways/populations can hardly be delineated from a biological point of view. Detailed phylogenetic, population genetic and coalescent analyses of a data set of samples spanning the whole northern hemisphere leads me to conclude that the only firm population boundaries that I can draw are between Eurasia and North America, within which panmixia is almost achieved. Mallards’ and other Anas-ducks’ whole continental to global distribution brings them together in sympatry. I can show that a combination of sympatric distribution, conflicting genetically determined and learned mate recognition mechanisms, and genomic compatibility between species helps to explain the long-standing puzzle of waterfowl hybridisation and introgression of genes from one duck species into another. Besides obvious management implications I propose that this fact can be part of the explanation why ducks are so well adaptable and successful, as well as why they show extraordinary abilities to withstand AI infections, or its consequences for health status.

Birds, in particular poultry and ducks, are a source of many infectious diseases, such as those caused by influenza viruses. These viruses are a threat not only to the birds themselves but also to poultry farming and human health, as forms that can infect humans are known to have evolved. It is believed that migratory birds in general play an important role in the global spread of avian influenza (AI). However, it is still debated how large this role precisely is and whether other modes of spread may be more important. The mallard (Anas platyrhynchos) is the world’s most abundant and well-studied waterfowl species. Besides being an important game and agricultural species, it is also a flagship species in wetland conservation and restoration. Waterfowl (Anseriformes: Anatidae) and especially ducks currently are the focal bird group in long distance dispersal of Avian Influenza in the wild, and the mallard has been identified as the most likely species to transport this virus. In my thesis I report aspects of the biology of this important host species of AI by molecular ecological means. As molecular marker system I established a genome-wide set of more than 100,000 SNPs of which I developed a subset of 384 SNPs into an assay to genotype about 1,000 ducks. This subset was employed to study the evolutionary history and speciation processes in the Anas genus. Further investigations into the world-wide mallard population structure on a species level were based not only on this set of 384 SNPs but also on mitochondrial DNA sequences. Last but not last, I investigated an option of AI sampling and detection from duck faeces by technology that is safe from a biohazard perspective, and solves transportation issues related to cold chains. The main results of my thesis include the development of a generally applicable improved analysis pipeline to develop genome-wide SNP sets for non-model organisms. Further, my results show that, from a migration system perspective, mallard flyways/populations can hardly be delineated from a biological point of view. Detailed phylogenetic, population genetic and coalescent analyses of a data set of samples spanning the whole northern hemisphere leads me to conclude that the only firm population boundaries that I can draw are between Eurasia and North America, within which panmixia is almost achieved. Mallards’ and other Anas-ducks’ whole continental to global distribution brings them together in sympatry. I can show that a combination of sympatric distribution, conflicting genetically determined and learned mate recognition mechanisms, and genomic compatibility between species helps to explain the long-standing puzzle of waterfowl hybridisation and introgression of genes from one duck species into another. Besides obvious management implications I propose that this fact can be part of the explanation why ducks are so well adaptable and successful, as well as why they show extraordinary abilities to withstand AI infections, or its consequences for health status.

Dit rapport behandelt de evolutionaire consequenties van visserij en de implicaties hiervan voor het duurzaam beheer. Visserij verhoogt de kans dat vissen worden weggevangen voordat ze volwassen worden en zich kunnen voortplanten. Dit betekent dat de dieren die genetisch geprogrammeerd zijn om op jongere leeftijd volwassen te meer nakomelingen zullen produceren dan dieren die pas op latere leeftijd volwassen worden. Een andere eigenschap die beïnvloed kan worden is de voortplantingsinspanning (aantal eieren) en de groeisnelheid. Dieren die meer eieren produceren zijn in het voordeel. Een verlaging van de geslachtsrijpe leeftijd en een verhoging van de voortplantingsinspanning resulteert in een afname van de groeisnelheid. Visserij leidt dus tot verschuivingen in de genetische eigenschappen (evolutionaire veranderingen) van de geëxploiteerde bestanden. In dit rapport wordt een overzicht gegevens van de huidige wetenschappelijk inzichten in de door de visserijgeïnduceerde evolutie en de implicaties die dit heeft voor het visserijbeheer. Speciale aandacht wordt gegeven aan de beschikbare kennis over Noordzee platvis en de mogelijkheden die er zijn om op basis van deze kennis tot een Evolutionair Impact Assessment voor deze bestanden te komen.

Dit rapport behandelt de evolutionaire consequenties van visserij en de implicaties hiervan voor het duurzaam beheer. Visserij verhoogt de kans dat vissen worden weggevangen voordat ze volwassen worden en zich kunnen voortplanten. Dit betekent dat de dieren die genetisch geprogrammeerd zijn om op jongere leeftijd volwassen te meer nakomelingen zullen produceren dan dieren die pas op latere leeftijd volwassen worden. Een andere eigenschap die beïnvloed kan worden is de voortplantingsinspanning (aantal eieren) en de groeisnelheid. Dieren die meer eieren produceren zijn in het voordeel. Een verlaging van de geslachtsrijpe leeftijd en een verhoging van de voortplantingsinspanning resulteert in een afname van de groeisnelheid. Visserij leidt dus tot verschuivingen in de genetische eigenschappen (evolutionaire veranderingen) van de geëxploiteerde bestanden. In dit rapport wordt een overzicht gegevens van de huidige wetenschappelijk inzichten in de door de visserijgeïnduceerde evolutie en de implicaties die dit heeft voor het visserijbeheer. Speciale aandacht wordt gegeven aan de beschikbare kennis over Noordzee platvis en de mogelijkheden die er zijn om op basis van deze kennis tot een Evolutionair Impact Assessment voor deze bestanden te komen.