Sören NylinProfessor
Om mig
Jag är professor i zoologisk ekologi och f.d. sektionsdekanus vid sektionen för biologi och ordförande för forskarutbildningsberedningen vid Området för Naturvetenskap. Nu ägnar jag mig åt forskning (särskilt på evolution av insekt/växt-interaktioner) och undervisning i vetenskapsteori och evolutionär ekologi.
Undervisning
Jag undervisar i vetenskapsteori samt om artinteraktioner.
Forskning
Jag studerar för närvarande särskilt interaktioner mellan insekter och växter som ett delprojekt i mina övergripande studier av fenotypisk plasticitet hos insekter. Jag strävar efter en syntes mellan insekt/växt-projektet och de andra delprojekten, som berör effekter av temperatur och dagslängd på insekters livshistorier och livscykler, samt hur fenotypisk plasticitet påverkar artbildning och utdöende. För detta behövs fylogenetisk analys, och därför är jag även mycket intresserad av systematik hos fjärilar.
Forskningsprojekt
Publikationer
I urval från Stockholms universitets publikationsdatabas
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Embracing Colonizations
2018. Sören Nylin (et al.). Trends in Ecology & Evolution 33 (1), 4-14
ArtikelParasitehost and insectplant research have divergent traditions despite the fact that most phytophagous insects live parasitically on their host plants. In parasitology it is a traditional assumption that parasites are typically highly specialized; cospeciation between parasites and hosts is a frequently expressed default expectation. Insectplant theory has been more concerned with host shifts than with cospeciation, and more with hierarchies among hosts than with extreme specialization. We suggest that the divergent assumptions in the respective fields have hidden a fundamental similarity with an important role for potential as well as actual hosts, and hence for host colonizations via ecological fitting. A common research program is proposed which better prepares us for the challenges from introduced species and global change.
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HOST PLANT UTILIZATION, HOST RANGE OSCILLATIONS AND DIVERSIFICATION IN NYMPHALID BUTTERFLIES
2014. Sören Nylin, Jessica Slove, Niklas Janz. Evolution 68 (1), 105-124
ArtikelIt has been suggested that phenotypic plasticity is a major factor in the diversification of life, and that variation in host range in phytophagous insects is a good model for investigating this claim. We explore the use of angiosperm plants as hosts for nymphalid butterflies, and in particular the evidence for past oscillations in host range and how they are linked to host shifts and to diversification. At the level of orders of plants, a relatively simple pattern of host use and host shifts emerges, despite the 100 million years of history of the family Nymphalidae. We review the evidence that these host shifts and the accompanying diversifications were associated with transient polyphagous stages, as suggested by the oscillation hypothesis. In addition, we investigate all currently polyphagous nymphalid species and demonstrate that the state of polyphagy is rare, has a weak phylogenetic signal, and a very apical distribution in the phylogeny; we argue that these are signs of its transient nature. We contrast our results with data from the bark beetles Dendroctonus, in which a more specialized host use is instead the apical state. We conclude that plasticity in host use is likely to have contributed to diversification in nymphalid butterflies.
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The oscillation hypothesis of host-plant range and speciation
2008. Niklas Janz, Sören Nylin. Specialization, speciation and radiation, 203-215
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Vestiges of an ancestral host plant: preference and performance in the butterfly Polygonia faunus and its sister species P. c-album
2015. Sören Nylin (et al.). Ecological Entomology 40 (3), 307-315
Artikel1. In the study of the evolution of insect-host plant interactions, important information is provided by host ranking correspondences among female preference, offspring preference, and offspring performance. Here, we contrast such patterns in two polyphagous sister species in the butterfly family Nymphalidae, the Nearctic Polygonia faunus, and the Palearctic P. c-album. 2. These two species have similar host ranges, but according to the literature P. faunus does not use the ancestral host plant clade-the urticalean rosids'. Comparisons of the species can thus test the effects of a change in insect-plant associations over a long time scale. Cage experiments confirmed that P. faunus females avoid laying eggs on Urtica dioica (the preferred host of P. c-album), instead preferring Salix, Betula, and Ribes.3. However, newly hatched larvae of both species readily accept and grow well on U. dioica, supporting the general theory that evolutionary changes in host range are initiated through shifts in female host preferences, whereas larvae are more conservative and also can retain the capacity to perform well on ancestral hosts over long time spans.4. Similar rankings of host plants among female preference, offspring preference, and offspring performance were observed in P. c-album but not in P. faunus. This is probably a result of vestiges of larval adaptations to the lost ancestral host taxon in the latter species. 5. Female and larval preferences seem to be largely free to evolve independently, and consequently larval preferences warrant more attention.
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Slowed aging during reproductive dormancy is reflected in genome-wide transcriptome changes in Drosophila melanogaster
2016. Lucie Kucerova (et al.). BMC Genomics 17
ArtikelBackground: In models extensively used in studies of aging and extended lifespan, such as C. elegans and Drosophila, adult senescence is regulated by gene networks that are likely to be similar to ones that underlie lifespan extension during dormancy. These include the evolutionarily conserved insulin/IGF, TOR and germ line-signaling pathways. Dormancy, also known as dauer stage in the larval worm or adult diapause in the fly, is triggered by adverse environmental conditions, and results in drastically extended lifespan with negligible senescence. It is furthermore characterized by increased stress resistance and somatic maintenance, developmental arrest and reallocated energy resources. In the fly Drosophila melanogaster adult reproductive diapause is additionally manifested in arrested ovary development, improved immune defense and altered metabolism. However, the molecular mechanisms behind this adaptive lifespan extension are not well understood. Results: A genome wide analysis of transcript changes in diapausing D. melanogaster revealed a differential regulation of more than 4600 genes. Gene ontology (GO) and KEGG pathway analysis reveal that many of these genes are part of signaling pathways that regulate metabolism, stress responses, detoxification, immunity, protein synthesis and processes during aging. More specifically, gene readouts and detailed mapping of the pathways indicate downregulation of insulin-IGF (IIS), target of rapamycin (TOR) and MAP kinase signaling, whereas Toll-dependent immune signaling, Jun-N-terminal kinase (JNK) and Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathways are upregulated during diapause. Furthermore, we detected transcriptional regulation of a large number of genes specifically associated with aging and longevity. Conclusions: We find that many affected genes and signal pathways are shared between dormancy, aging and lifespan extension, including IIS, TOR, JAK/STAT and JNK. A substantial fraction of the genes affected by diapause have also been found to alter their expression in response to starvation and cold exposure in D. melanogaster, and the pathways overlap those reported in GO analysis of other invertebrates in dormancy or even hibernating mammals. Our study, thus, shows that D. melanogaster is a genetically tractable model for dormancy in other organisms and effects of dormancy on aging and lifespan.
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Evolutionary history of host use, rather than plant phylogeny, determines gene expression in a generalist butterfly
2016. Maria de la Paz Celorio-Mancera (et al.). BMC Evolutionary Biology 16
ArtikelBackground: Although most insect species are specialized on one or few groups of plants, there are phytophagous insects that seem to use virtually any kind of plant as food. Understanding the nature of this ability to feed on a wide repertoire of plants is crucial for the control of pest species and for the elucidation of the macroevolutionary mechanisms of speciation and diversification of insect herbivores. Here we studied Vanessa cardui, the species with the widest diet breadth among butterflies and a potential insect pest, by comparing tissue-specific transcriptomes from caterpillars that were reared on different host plants. We tested whether the similarities of gene-expression response reflect the evolutionary history of adaptation to these plants in the Vanessa and related genera, against the null hypothesis of transcriptional profiles reflecting plant phylogenetic relatedness. Result: Using both unsupervised and supervised methods of data analysis, we found that the tissue-specific patterns of caterpillar gene expression are better explained by the evolutionary history of adaptation of the insects to the plants than by plant phylogeny. Conclusion: Our findings suggest that V. cardui may use two sets of expressed genes to achieve polyphagy, one associated with the ancestral capability to consume Rosids and Asterids, and another allowing the caterpillar to incorporate a wide range of novel host-plants.
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Unifying host-associated diversification processes using butterfly-plant networks
2018. Mariana P. Braga (et al.). Nature Communications 9
ArtikelExplaining the exceptional diversity of herbivorous insects is an old problem in evolutionary ecology. Here we focus on the two prominent hypothesised drivers of their diversification, radiations after major host switch or variability in host use due to continuous probing of new hosts. Unfortunately, current methods cannot distinguish between these hypotheses, causing controversy in the literature. Here we present an approach combining network and phylogenetic analyses, which directly quantifies support for these opposing hypotheses. After demonstrating that each hypothesis produces divergent network structures, we then investigate the contribution of each to diversification in two butterfly families: Pieridae and Nymphalidae. Overall, we find that variability in host use is essential for butterfly diversification, while radiations following colonisation of a new host are rare but can produce high diversity. Beyond providing an important reconciliation of alternative hypotheses for butterfly diversification, our approach has potential to test many other hypotheses in evolutionary biology.
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Selective attention by priming in host search behavior of 2 generalist butterflies
2019. Gabriella Gamberale-Stille (et al.). Behavioral Ecology 30 (1), 142-149
ArtikelWe show that females of 2 generalist butterflies improve their search efficacy after previous encounters of the same host in a way similar to search-image formation, especially if the butterfly-host relationship is historically old. Thus, by targeting a single host at a time, host search efficacy may be improved and constitute a selection pressure for specialization. This result can help explain the evolutionary trend toward host specialization in phytophagous insects that is not well understood. Abstract In phytophagous insects such as butterflies, there is an evolutionary trend toward specialization in host plant use. One contributing mechanism for this pattern may be found in female host search behavior. Since search attention is limited, generalist females searching for hosts for oviposition may potentially increase their search efficacy by aiming their attention on a single host species at a time, a behavior consistent with search image formation. Using laboratory reared and mated females of 2 species of generalist butterflies, the comma, Polygonia c-album, and the painted lady, Vanessa cardui (Lepidoptera: Nymphalidae), we investigated the probability of finding a specific target host (among nonhost distractors) immediately after being primed with an oviposition experience of the same host as compared with different host in indoor cages. We used species-specific host plants that varied with respect to growth form, historical age of the butterfly-host association, and relative preference ranking. We found improved search efficacy after previous encounters of the same host for some but not all host species. Positive priming effects were found only in hosts with which the butterfly has a historically old relationship and these hosts are sometimes also highly preferred. Our findings provides additional support for the importance of behavioral factors in shaping the host range of phytophagous insects, and show that butterflies can attune their search behavior to compensate for negative effects of divided attention between multiple hosts.
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Phylogenetic reconstruction of ancestral ecological networks through time for pierid butterflies and their host plants
2021. Mariana P. Braga (et al.). Ecology Letters 24 (10), 2134-2145
ArtikelThe study of herbivorous insects underpins much of the theory that concerns the evolution of species interactions. In particular, Pieridae butterflies and their host plants have served as a model system for studying evolutionary arms races. To learn more about the coevolution of these two clades, we reconstructed ancestral ecological networks using stochastic mappings that were generated by a phylogenetic model of host-repertoire evolution. We then measured if, when, and how two ecologically important structural features of the ancestral networks (modularity and nestedness) evolved over time. Our study shows that as pierids gained new hosts and formed new modules, a subset of them retained or recolonised the ancestral host(s), preserving connectivity to the original modules. Together, host-range expansions and recolonisations promoted a phase transition in network structure. Our results demonstrate the power of combining network analysis with Bayesian inference of host-repertoire evolution to understand changes in complex species interactions over time.
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Evolution of butterfly seasonal plasticity driven by climate change varies across life stages
2023. Matthew Nielsen (et al.). Ecology Letters 26 (9), 1548-1558
ArtikelPhotoperiod is a common cue for seasonal plasticity and phenology, but climate change can create cue-environment mismatches for organisms that rely on it. Evolution could potentially correct these mismatches, but phenology often depends on multiple plastic decisions made during different life stages and seasons that may evolve separately. For example, Pararge aegeria (Speckled wood butterfly) has photoperiod-cued seasonal life history plasticity in two different life stages: larval development time and pupal diapause. We tested for climate change-associated evolution of this plasticity by replicating common garden experiments conducted on two Swedish populations 30 years ago. We found evidence for evolutionary change in the contemporary larval reaction norm-although these changes differed between populations-but no evidence for evolution of the pupal reaction norm. This variation in evolution across life stages demonstrates the need to consider how climate change affects the whole life cycle to understand its impacts on phenology.
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