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Träfflista för sökning "WFRF:(Ehrlén Johan) ;pers:(Lehtilä Kari)"

Sökning: WFRF:(Ehrlén Johan) > Lehtilä Kari

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1.
  • Lehtilä, Kari, et al. (författare)
  • Forest succession and population viability of grassland plants : long repayment of extinction debt in Primula veris
  • 2016
  • Ingår i: Oecologia. - : Springer Science and Business Media LLC. - 0029-8549 .- 1432-1939. ; 181:1, s. 125-135
  • Tidskriftsartikel (refereegranskat)abstract
    • Time lags in responses of organisms to deteriorating environmental conditions delay population declines and extinctions. We examined how local processes at the population level contribute to extinction debt, and how cycles of habitat deterioration and recovery may delay extinction. We carried out a demographic analysis of the fate of the grassland perennial Primula veris after the cessation of grassland management, where we used either a unidirectional succession model for forest habitat or a rotation model with a period of forest growth followed by a clear-cut and a new successional cycle. The simulations indicated that P. veris populations may have an extinction time of decades to centuries after a detrimental management change. A survey of the current incidence and abundance of P. veris in sites with different histories of afforestation confirmed the simulation results of low extinction rates. P. veris had reduced incidence and abundance only at sites with at least 100 years of forest cover. Time to extinction in simulations was dependent on the duration of the periods with favourable and unfavourable conditions after management cessation, and the population sizes and growth rates in these periods. Our results thus suggest that the ability of a species to survive is a complex function of disturbance regimes, rates of successional change, and the demographic response to environmental changes. Detailed demographic studies over entire successional cycles are therefore essential to identify the environmental conditions that enable long-term persistence and to design management for species experiencing extinction debts.
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2.
  • Boalt, Elin, 1976- (författare)
  • Ecology and evolution of tolerance in two cruciferous species
  • 2008
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Tolerance to herbivory is the ability of plants to maintain fitness in spite of damage. The goal of this thesis is to investigate the genetic variation and expression of tolerance within species, determine whether and in what conditions tolerance has negative side-effects, and how tolerance is affected by different ecological factors. Tolerance is investigated with special focus on the effects of different damage types, competitive regimes, history of herbivory, and polyploidization in plants. Studies are conducted as a literature review and three experiments on two cruciferous species Raphanus raphanistrum and Cardamine pratensis.In the tolerance experiments, plants are subjected to artificial damage solely, or in a combination with natural damage. A literature review was conducted in order to investigate the effects of damage method. We found that traits related to tolerance, such as growth and fitness were not as sensitive in regard to damage method as measures of induced chemical traits, or measures of secondary herbivory.Genetic variation of tolerance was demonstrated within populations of R. raphanistrum and between subspecies of C. pratensis. In R. raphanistrum, traits involved in floral display and male fitness were positively associated with plant tolerance to herbivore damage. A potential cost of tolerance was demonstrated as a negative correlation between levels of tolerance in high and low competitive regimes. I found no evidence of other proposed costs of tolerance in terms of highly tolerant plants suffering of reduced fitness in the absence of herbivores or trade-offs in terms of a negative association between tolerance to apical and leaf damage, or between tolerance and competitive ability. In C. pratensis, higher ploidy level in plants involved higher levels of tolerance measured as clonal reproduction. Furthermore, populations exposed to higher levels of herbivory had better tolerance than populations exposed to lower levels of herbivory. In this thesis, I demonstrate evidence of different components for the evolution of tolerance in plants: genotypic variation, selective factors in terms of costs and ploidization, and selective agents in terms of changing environment or herbivore pressure.
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4.
  • Boalt, Elin, et al. (författare)
  • The association among herbivory tolerance, ploidy level, and herbivory pressure in cardamine pratensis
  • 2010
  • Ingår i: Evolutionary Ecology. - : Springer Science and Business Media LLC. - 0269-7653 .- 1573-8477. ; 24:5, s. 1101-1113
  • Tidskriftsartikel (refereegranskat)abstract
    • We tested whether differences in ploidy level and previous exposure to herbivory can affect plant tolerance to herbivory. We conducted a common garden experiment with 12 populations of two ploidy levels of the perennial herb Cardamine pratensis (five populations of tetraploid ssp. pratensis and seven populations of octoploid ssp. paludosa). Earlier studies have shown that attack rates by the main herbivore, the orange tip butterfly Anthocharis cardamines, are lower in populations of octoploids than in populations of tetraploids, and vary among populations. In the common garden experiment, a combination of natural and artificial damage significantly reduced seed and flower production. We measured tolerance based on four plant-performance metrics: survival, growth, seed production and clonal reproduction. For three of these measurements, tolerance of damage did not differ between ploidy levels. For clonal reproduction, the octoploids had a higher tolerance than the tetraploids, although they experience lower herbivore attack rates in natural populations. Populations from sites with high levels of herbivory had higher tolerance, measured by seed production, than populations with low levels of herbivory. We did not detect any significant costs of tolerance. We conclude that high intensity of herbivory has selected for high tolerance measured by seed production in C. pratensis.
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5.
  • Ehrlén, Johan, et al. (författare)
  • How perennial are perennial plants?
  • 2002
  • Ingår i: Oikos. - : Wiley. - 0030-1299 .- 1600-0706. ; 98:2, s. 308-322
  • Tidskriftsartikel (refereegranskat)abstract
    • Trade-offs involving life span are important in the molding of plant life histories. However, the empirical examination of such patterns has so far been limited by the fact that information on life span is mainly available in terms of discrete categories; annuals, semelparous perennials and iteroparous perennials. We used transition matrix models to project continuous estimates of conditional life spans from published information on size- or stage-structured demography for 71 perennial plant species. The projected life span ranged from 4.3 to 988.6 years and more than half of the species had a life span of more than 35 years. Woody plants had on average a projected life span more than four times as long as non-woody plants. Life spans were higher in forests than in open habitats and individuals of non-clonal species tended to have a longer life span than ramets of clonal species. Self-incompatible plants on average lived longer than self-compatible plants. There were no clear relations between life span and geographical region, dispersal syndrome, pollination mode, seed size or the presence of a seed bank. We conclude that accurate estimates of life span are central to understand how longevity is correlated to other traits within the group of perennial plants.
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6.
  • Ehrlén, Johan, et al. (författare)
  • Land use and population growth of Primula veris : an experimental demographic approach
  • 2005
  • Ingår i: Journal of Applied Ecology. - : Wiley. - 0021-8901 .- 1365-2664. ; 42:2, s. 317-326
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. Changes in land use are the primary cause of decline for many plant species. Efficient management actions for such species must be based on knowledge of the key phases of the plant life cycles that respond most to changes in environmental factors. 2. To assess how grazing influences population viability of the perennial rosette herb Primula veris, we applied four experimental treatments to abandoned grasslands and recorded the demographic response in permanent plots and seed sowing experiments over 3 years. 3. Treatments had strong effects on population viability. Transition matrix models showed that cutting the surrounding vegetation had no effect on population growth rate (lambda). However, when this was combined with litter removal lambda increased to 1.46, compared with 1.11 in controls. With disturbance and complete removal of the surrounding vegetation the effect was even stronger, and lambda increased to 1.60. 4. Increases in lambda were primarily a result of increased growth of the smallest rosettes, and increased seedling production. In contrast, the performance of larger P. veris individuals was not affected by experimental treatments. 5. The higher the elasticity of a particular life cycle transition, the less the change in the transition rate caused by treatments. This suggests that plants are able partly to buffer the effects of environmental variation by minimizing changes in the life cycle transitions that are most important to population growth rate. 6. Synthesis and applications. Experimental demographic approaches provide an important tool for assessing how grazing and other types of management influence species viability, and help to unravel the mechanisms underlying such relationships. With such information it is possible to predict the effects of novel types of management and land-use scenarios on population viability. For P. veris, we identified seedling establishment as a key phase in the life cycle, and litter accumulation as a key environmental factor, suggesting that these should be prime targets for management. One practice that is likely to favour as well as seedling establishment preventing litter accumulation is late summer grazing.
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7.
  • König, Malin A. E., et al. (författare)
  • Among-Population Variation in Tolerance to Larval Herbivory by Anthocharis cardamines in the Polyploid Herb Cardamine pratensis
  • 2014
  • Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 9:6, s. e99333-
  • Tidskriftsartikel (refereegranskat)abstract
    • Plants have two principal defense mechanisms to decrease fitness losses to herbivory: tolerance, the ability to compensate fitness after damage, and resistance, the ability to avoid damage. Variation in intensity of herbivory among populations should result in variation in plant defense levels if tolerance and resistance are associated with costs. Yet little is known about how levels of tolerance are related to resistance and attack intensity in the field, and about the costs of tolerance. In this study, we used information about tolerance and resistance against larval herbivory by the butterfly Anthocharis cardamines under controlled conditions together with information about damage in the field for a large set of populations of the perennial plant Cardamine pratensis. Plant tolerance was estimated in a common garden experiment where plants were subjected to a combination of larval herbivory and clipping. We found no evidence of that the proportion of damage that was caused by larval feeding vs. clipping influenced plant responses. Damage treatments had a negative effect on the three measured fitness components and also resulted in an earlier flowering in the year after the attack. Tolerance was related to attack intensity in the population of origin, i.e. plants from populations with higher attack intensity were more likely to flower in the year following damage. However, we found no evidence of a relationship between tolerance and resistance. These results indicate that herbivory drives the evolution for increased tolerance, and that changes in tolerance are not linked to changes in resistance. We suggest that the simultaneous study of tolerance, attack intensity in the field and resistance constitutes a powerful tool to understand how plant strategies to avoid negative effects of herbivore damage evolve.
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9.
  • Lehtilä, Kari, et al. (författare)
  • Habitat change and demography of Primula veris : Identification of management targets
  • 2006
  • Ingår i: Conservation Biology. - : Wiley. - 0888-8892 .- 1523-1739. ; 20:3, s. 833-843
  • Tidskriftsartikel (refereegranskat)abstract
    • Although the effects of deterministic factors on population viability often are more important than stochasticity, few researchers have dealt with the effect of deterministic habitat changes on plant population demography We assessed population viability for the perennial herb Primula veris L. and identified targets for management based on demographic data from five different habitat types representing different degrees of canopy closure. We conducted replicate studies at the border of the distribution area and in more central parts. Demographic patterns were similar between the two regions. Most study populations had a positive population growth, and only populations in late phases of forest succession showed consistently negative trends. The populations of open habitats had high seedling recruitment, and the populations of early and middle forest succession had high seed production. The importance of survival for population growth rate increased with increasing habitat closure, whereas the importance of growth and reproduction decreased. Results of the elasticity analysis suggested that the best method to manage decreasing late-successional populations is to increase survival of the largest individuals. The life-table response experiment (LTRE) analysis, however, showed that survival of the largest individuals contributed little to differences in population growth rates of different habitats, whereas seed production and growth of small individuals were more important. Moreover, direct perturbation of the performance of the largest stages showed that late-successional populations would not attain positive population growth even if the largest stages had no mortality at all. We conclude that restoration of recruitment is the only possibility for positive population growth in late-successional populations of P. veris, although the elasticities of recruitment transitions are low. Our results also suggest that retrospective demographic methods such as LIRE constitute an important and necessary complement to prospective methods such as elasticities in identifying management targets.
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10.
  • Lehtilä, Kari, et al. (författare)
  • Seed size as an indicator of seed quality : a case study of Primula veris
  • 2005
  • Ingår i: Acta Oecologica. - : Elsevier BV. - 1146-609X .- 1873-6238. ; 28:3, s. 207-212
  • Tidskriftsartikel (refereegranskat)abstract
    • Seed size is a widely accepted measure of seed quality, because many earlier studies have shown that large seeds have high seedling survival, growth and establishment. We tested whether ovule loss increases size of the remaining seeds and whether such size increase affects seedling establishment. We removed all except one flower from inflorescences of Primula veris L. (Primulaceae), a perennial hemicryptophyte herb, at a late stage of flowering. Flower removal (FR) increased seed size by 33% compared to the control plants. We then divided the seeds within each treatment to small, middle-sized and large seeds and carried out a sowing experiment in the field, Within each experimental group, seedling establishment was positively associated with seed size. However, despite size differences, seeds from the FIR and control groups had the same seedling establishment probability. Seeds from FR plants had a higher seedling emergence in May than those from control plants, but the number of seedlings alive per sowing plot in the late summer was the same in both experimental groups. Increase in seed mass after partial FR thus did not enhance seedling performance, although seed size variation due to other causes was positively correlated with seedling establishment. Further studies are needed to show whether plastic changes of seed size are usually adaptive or not.
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