Kathryn M. Robinson
Umeå University
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Featured researches published by Kathryn M. Robinson.
Ecology Letters | 2013
Carolina Bernhardsson; Kathryn M. Robinson; Ilka Nacif Abreu; Stefan Jansson; Benedicte R. Albrectsen; Pär K. Ingvarsson
Plant-herbivore interactions vary across the landscape and have been hypothesised to promote local adaption in plants to the prevailing herbivore regime. Herbivores that feed on European aspen (Populus tremula) change across regional scales and selection on host defence genes may thus change at comparable scales. We have previously observed strong population differentiation in a set of inducible defence genes in Swedish P. tremula. Here, we study the geographic patterns of abundance and diversity of herbivorous insects, the untargeted metabolome of the foliage and genetic variation in a set of wound-induced genes and show that the geographic structure co-occurs in all three data sets. In response to this structure, we observe local maladaptation of herbivores, with fewer herbivores on local trees than on trees originated from more distant localities. Finally, we also identify 28 significant associations between single nucleotide polymorphisms SNPs from defence genes and a number of the herbivore traits and metabolic profiles.
PLOS ONE | 2012
Kathryn M. Robinson; Pär K. Ingvarsson; Stefan Jansson; Benedicte R. Albrectsen
We conducted a study of natural variation in functional leaf traits and herbivory in 116 clones of European aspen, Populus tremula L., the Swedish Aspen (SwAsp) collection, originating from ten degrees of latitude across Sweden and grown in a common garden. In surveys of phytophagous arthropods over two years, we found the aspen canopy supports nearly 100 morphospecies. We identified significant broad-sense heritability of plant functional traits, basic plant defence chemistry, and arthropod community traits. The majority of arthropods were specialists, those coevolved with P. tremula to tolerate and even utilize leaf defence compounds. Arthropod abundance and richness were more closely related to plant growth rates than general chemical defences and relationships were identified between the arthropod community and stem growth, leaf and petiole morphology, anthocyanins, and condensed tannins. Heritable genetic variation in plant traits in young aspen was found to structure arthropod community; however no single trait drives the preferences of arthropod folivores among young aspen genotypes. The influence of natural variation in plant traits on the arthropod community indicates the importance of maintaining genetic variation in wild trees as keystone species for biodiversity. It further suggests that aspen can be a resource for the study of mechanisms of natural resistance to herbivores.
BMC Plant Biology | 2014
Kathryn M. Robinson; Nicolas Delhomme; Niklas Mähler; Bastian Schiffthaler; Jenny Önskog; Benedicte Rieber Albrectsen; Pär K. Ingvarsson; Torgeir R. Hvidsten; Stefan Jansson; Nathaniel R. Street
BackgroundEvolutionary theory suggests that males and females may evolve sexually dimorphic phenotypic and biochemical traits concordant with each sex having different optimal strategies of resource investment to maximise reproductive success and fitness. Such sexual dimorphism would result in sex biased gene expression patterns in non-floral organs for autosomal genes associated with the control and development of such phenotypic traits.ResultsWe examined morphological, biochemical and herbivory traits to test for sexually dimorphic resource allocation strategies within collections of sexually mature and immature Populus tremula (European aspen) trees. In addition we profiled gene expression in mature leaves of sexually mature wild trees using whole-genome oligonucleotide microarrays and RNA-Sequencing.ConclusionsWe found no evidence of sexual dimorphism or differential resource investment strategies between males and females in either sexually immature or mature trees. Similarly, single-gene differential expression and machine learning approaches revealed no evidence of large-scale sex biased gene expression. However, two significantly differentially expressed genes were identified from the RNA-Seq data, one of which is a robust diagnostic marker of sex in P. tremula.
Frontiers in Plant Science | 2015
Raju Y. Soolanayakanahally; Robert D. Guy; Nathaniel R. Street; Kathryn M. Robinson; Salim N. Silim; Benedicte R. Albrectsen; Stefan Jansson
Populus species with wide geographic ranges display strong adaptation to local environments. We studied the clinal patterns in phenology and ecophysiology in allopatric Populus species adapted to similar environments on different continents under common garden settings. As a result of climatic adaptation, both Populus tremula L. and Populus balsamifera L. display latitudinal clines in photosynthetic rates (A), whereby high-latitude trees of P. tremula had higher A compared to low-latitude trees and nearly so in P. balsamifera (p = 0.06). Stomatal conductance (gs) and chlorophyll content index (CCI) follow similar latitudinal trends. However, foliar nitrogen was positively correlated with latitude in P. balsamifera and negatively correlated in P. tremula. No significant trends in carbon isotope composition of the leaf tissue (δ13C) were observed for both species; but, intrinsic water-use efficiency (WUEi) was negatively correlated with the latitude of origin in P. balsamifera. In spite of intrinsically higher A, high-latitude trees in both common gardens accomplished less height gain as a result of early bud set. Thus, shoot biomass was determined by height elongation duration (HED), which was well approximated by the number of days available for free growth between bud flush and bud set. We highlight the shortcoming of unreplicated outdoor common gardens for tree improvement and the crucial role of photoperiod in limiting height growth, further complicating interpretation of other secondary effects.
Ecology and Evolution | 2015
Kathryn M. Robinson; Céline Hauzy; Nicolas Loeuille; Benedicte R. Albrectsen
Nestedness and modularity are measures of ecological networks whose causative effects are little understood. We analyzed antagonistic plant–herbivore bipartite networks using common gardens in two contrasting environments comprised of aspen trees with differing evolutionary histories of defence against herbivores. These networks were tightly connected owing to a high level of specialization of arthropod herbivores that spend a large proportion of the life cycle on aspen. The gardens were separated by ten degrees of latitude with resultant differences in abiotic conditions. We evaluated network metrics and reported similar connectance between gardens but greater numbers of links per species in the northern common garden. Interaction matrices revealed clear nestedness, indicating subsetting of the bipartite interactions into specialist divisions, in both the environmental and evolutionary aspen groups, although nestedness values were only significant in the northern garden. Variation in plant vulnerability, measured as the frequency of herbivore specialization in the aspen population, was significantly partitioned by environment (common garden) but not by evolutionary origin of the aspens. Significant values of modularity were observed in all network matrices. Trait-matching indicated that growth traits, leaf morphology, and phenolic metabolites affected modular structure in both the garden and evolutionary groups, whereas extra-floral nectaries had little influence. Further examination of module configuration revealed that plant vulnerability explained considerable variance in web structure. The contrasting conditions between the two gardens resulted in bottom-up effects of the environment, which most strongly influenced the overall network architecture, however, the aspen groups with dissimilar evolutionary history also showed contrasting degrees of nestedness and modularity. Our research therefore shows that, while evolution does affect the structure of aspen–herbivore bipartite networks, the role of environmental variations is a dominant constraint.
Physiologia Plantarum | 2018
Ingrid H. Michelson; Pär K. Ingvarsson; Kathryn M. Robinson; Erik Edlund; Maria Eriksson; Ove Nilsson; Stefan Jansson
Autumn senescence in mature aspens, grown under natural conditions, is initiated at almost the same date every year. The mechanism of such precise timing is not understood but we have previously shown that the signal must be derived from light. We studied variation in bud set and autumn senescence in a collection of 116 natural Eurasian aspen (Populus tremula) genotypes, from 12 populations in Sweden and planted in one northern and one southern common garden, to test the hypothesis that onset of autumn senescence is triggered by day length. We confirmed that, although bud set seemed to be triggered by a critical photoperiod/day length, other factors may influence it. The data on initiation of autumn senescence, on the other hand, were incompatible with the trigger being the day length per se, hence the trigger must be some other light-dependent factor.
Genome Biology | 2018
Jing Wang; Jihua Ding; Biyue Tan; Kathryn M. Robinson; Ingrid H. Michelson; Anna Johansson; Björn Nystedt; Douglas G. Scofield; Ove Nilsson; Stefan Jansson; Nathaniel R. Street; Pär K. Ingvarsson
BackgroundThe initiation of growth cessation and dormancy represent critical life-history trade-offs between survival and growth and have important fitness effects in perennial plants. Such adaptive life-history traits often show strong local adaptation along environmental gradients but, despite their importance, the genetic architecture of these traits remains poorly understood.ResultsWe integrate whole genome re-sequencing with environmental and phenotypic data from common garden experiments to investigate the genomic basis of local adaptation across a latitudinal gradient in European aspen (Populus tremula). A single genomic region containing the PtFT2 gene mediates local adaptation in the timing of bud set and explains 65% of the observed genetic variation in bud set. This locus is the likely target of a recent selective sweep that originated right before or during colonization of northern Scandinavia following the last glaciation. Field and greenhouse experiments confirm that variation in PtFT2 gene expression affects the phenotypic variation in bud set that we observe in wild natural populations.ConclusionsOur results reveal a major effect locus that determines the timing of bud set and that has facilitated rapid adaptation to shorter growing seasons and colder climates in European aspen. The discovery of a single locus explaining a substantial fraction of the variation in a key life-history trait is remarkable, given that such traits are generally considered to be highly polygenic. These findings provide a dramatic illustration of how loci of large-effect for adaptive traits can arise and be maintained over large geographical scales in natural populations.
bioRxiv | 2017
Jing Wang; Jihua Ding; Biyue Tan; Kathryn M. Robinson; Ingrid H. Michelson; Anna Johansson; Björn Nystedt; Douglas G. Scofield; Ove Nilsson; Stefan Jansson; Nathaniel R. Street; Pär K. Ingvarsson
Background: The initiation of growth cessation and dormancy represent critical life-history trade-offs between survival and growth, and have important fitness effects in perennial plants. Such adaptive life history traits often show strong local adaptation along environmental gradients but despite their importance, the genetic architecture of these traits remains poorly understood. Results: We integrate whole genome re-sequencing with environmental and phenotypic data from common garden experiments to investigate the genomic basis of local adaptation across a latitudinal gradient in European aspen (Populus tremula). We discover a single genomic region containing the PtFT2 gene that mediates local adaptation in the timing of bud set and that explains 65% of the observed genetic variation in bud set. This locus is the likely target of a recent selective sweep that originated right before or during colonization of northern Scandinavia following the last glaciation. Field and greenhouse experiments confirm that variation in PtFT2 gene expression affect the phenotypic variation in bud set that we observe in wild natural populations. Conclusions: Our results reveal a major effect locus that determine the timing of bud set and that have facilitated rapid adaptation to shorter growing seasons and colder climates in European aspen. The discovery of a single locus explaining a substantial fraction of the variation in a key life history trait is remarkable given that such traits are generally considered to be highly polygenic. These findings provide a dramatic illustration of how loci of large-effect for adaptive traits can arise and be maintained over large geographical scales in natural populations.The timing of growth and dormancy represent critical life-history trade-offs in perennial plants and often show strong local adaptation. Despite their importance, the genetic architecture of phenological traits remains poorly understood. Here we identify a ∼700 Kbp region mediating local adaptation in the timing of bud set in Populus tremula across a latitudinal gradient (∼56-66°N) in Sweden, where extensive gene flow has removed almost all traces of population structure. The strongest genomic associations with bud set are centered on a P. tremula homolog of FLOWERING LOCUS T2 (PtFT2) and explain 32-52% of the variation in bud set across sites and years. This region also shows multiple signs of a recent selective sweep restricted to the northernmost populations. Under field and greenhouse conditions, variation in bud set among accessions originating from different latitudes is strongly associated with variation in PtFT2 gene expression. Finally, transgenic down-regulation of PtFT2 yields a phenotype that, under field conditions, closely mimics variation observed between phenotypic extremes in natural populations. Our results thus provide evidence of one genomic region in P. tremula, centered on PtFT2, with major effects on adaptation to shorter growing seasons and colder climates following post-glacial colonization.
Ecography | 2009
Benedicte R. Albrectsen; Johanna Witzell; Kathryn M. Robinson; Sören Wulff; Virginia Luquez; Rickard Ågren; Stefan Jansson
New Phytologist | 2018
Åsa Grimberg; Ida Lager; Nathaniel R. Street; Kathryn M. Robinson; Salla Marttila; Niklas Mähler; Pär K. Ingvarsson; Rishikesh P. Bhalerao