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- Dahlgren, Johan, et al.
(författare)
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Linking environmental variation to population dynamics of a forest herb
- 2009
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Ingår i: Journal of Ecology. - : Wiley. - 0022-0477 .- 1365-2745. ; 97:4, s. 666-674
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Tidskriftsartikel (refereegranskat)abstract
- . Although necessary for understanding and predicting population dynamics, abiotic and biotic interactions have only rarely been coupled to demography and population dynamics. 2. We estimated effects of 11 environmental factors on survival, growth and fertility of the perennial herb Actaea spicata and incorporated significant factors into integral projection models to assess their effect on population dynamics. 3. Statistical models suggested that high soil potassium concentration increased individual growth and that seed predation and, to a lesser extent, canopy cover reduced seed production. 4. Demographic models showed that both soil potassium concentration and pre-dispersal seed predation could reverse population growth from positive to negative. The observed range of soil potassium concentration corresponded to growth rates (lambda) between 0.96 and 1.07, at mean observed seed predation intensity. At observed mean potassium concentration, growth rate ranged from 0.99 to 1.02 over observed seed predation intensities. 5. Sensitivity of population growth rate to different vital rates strongly influenced the relative effects of the two factors. Elasticity analysis suggested that proportional changes in soil potassium concentration result in seven times larger effects on population growth rate than changes in seed predation. 6. Synthesis. We conclude that relatively weak associations between environmental factors and vital rates can have substantial long-term effects on population growth. Approaches based on detailed demographic models, that simultaneously assess abiotic and biotic effects on population growth rate, constitute important tools for establishing the links between the environment and dynamics of populations and communities.
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| 5. |
- Arvanitis, Leena, et al.
(författare)
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Butterfly seed predation: effects of landscape characteristics, plant ploidy level and population structure
- 2007
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Ingår i: Oecologia. - : Springer Science and Business Media LLC. - 0029-8549 .- 1432-1939. ; 152:2, s. 275-285
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Tidskriftsartikel (refereegranskat)abstract
- Polyploidization has been suggested as one of the most common mechanisms for plant diversification. It is often associated with changes in several morphological, phenological and ecological plant traits, and therefore has the potential to alter insect–plant interactions. Nevertheless, studies evaluating the effect of plant polyploidy on interspecific interactions are still few. We investigated pre-dispersal seed predation by the butterfly Anthocharis cardamines in 195 populations of two ploidy levels of the herb Cardamine pratensis (tetraploid ssp. pratensis, 2n = 30 vs. octoploid ssp. paludosa, 2n = 56–64). We asked if differences in incidence and intensity of predation among populations were related to landscape characteristics, plant ploidy level and population structure. The incidence of the seed predator increased with increasing plant population size and decreasing distance to nearest population occupied by A. cardamines. The intensity of predation decreased with increasing plant population size and was not affected by isolation. Probability of attack decreased with increasing shading, and intensity of predation was higher in grazed than in non-grazed habitats. The attack intensity increased with increasing mean flower number of plant population, but was not affected by flowering phenology. Individuals in tetraploid populations suffered on average from higher levels of seed predation, had higher mean flower number, were less shaded and occurred more often in grazed habitats than octoploid populations. When accounting for differences in habitat preferences between ploidy levels there was no longer a difference in intensity of predation, suggesting that the observed differences in attack rates among populations of the two ploidy levels are mediated by the habitat. Overall, our results suggest that polyploidization is associated with differentiation in habitat preferences and phenotypic traits leading to differences in interspecific interaction among plant populations. This, in turn, may facilitate further divergence of ploidy levels.
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| 6. |
- Arvanitis, Leena, et al.
(författare)
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Plant ploidy level influences selection by butterfly seed predators
- 2008
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Ingår i: Oikos. ; 117, s. 1020-1025
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Tidskriftsartikel (refereegranskat)abstract
- Polyploidization is a common route to plant diversification. Polyploids often differ from their progenitors in size, flower number, flower size and flowering phenology. Such differences may translate into differences in the intensity of interactions with animals. Here we investigated the impact of the ploidy-related differences in tetraploids and octoploids of the perennial herb Cardamine pratensis on pre-dispersal seed predation by the butterfly Anthocharis cardamines. The probability of escaping attack was lower for octoploids than for tetraploids, even after accounting for the fact that octoploids were larger and had fewer flowers than tetraploids. Flower shoot size was correlated with probability of attack in tetraploids but not in octoploids. Differences in plant traits associated with polyploidization can alter interactions with animals, and animal-mediated differences in trait selection between ploidy types can contribute to their further divergence.
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| 7. |
- Ehrlén, Johan, et al.
(författare)
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Land use and population growth of Primula veris : an experimental demographic approach
- 2005
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Ingår i: Journal of Applied Ecology. - : Wiley. - 0021-8901 .- 1365-2664. ; 42:2, s. 317-326
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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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| 9. |
- Herben, T, et al.
(författare)
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Longterm spatial dynamics of Succisa pratensis in a changing rural landscape : linking dynamical modelling with historical maps
- 2006
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Ingår i: Journal of Ecology. - : Wiley-Blackwell. - 0022-0477 .- 1365-2745. ; 94:1, s. 131-143
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Tidskriftsartikel (refereegranskat)abstract
- We attempt to explain the current distribution of a long-lived perennial plant, Succisa pratensis, in a rural landscape in southern Sweden by linking its population biology with documented changes in the landscape, using a dynamical, spatially explicit model incorporating population dynamics and spatial spreading of the plant. Changes in the landscape were inferred from historical maps (1850 and 1900) and aerial photographs (1945 and 2001). We tested whether predictions for the current species distribution are affected by assumptions about its early 19th century distribution, to determine whether recent history and current processes are dominant, and how past landscape changes determine current distributions. Initial conditions influence predictions of current distribution, suggesting that the current distribution still partly reflects the distribution of the species in the early 19th century. A period of 150 years is too short for Succisa to have spread extensively if dispersal parameters are given realistic values. Simulations in which present-day land-use patterns were imposed at earlier dates showed that changes in landscape structure over the past 175 years also had a strong effect on the present-day habitat occupancy and population sizes of Succisa. The dominant process for Succisanow is extinction from marginal habitats. It is therefore likely that the (relatively) high present-day occupation patterns are still due to much larger areas having been available in the past rather than to successful dispersal. Although the species has responded to landscape changes, there is little evidence of population sizes reaching equilibrium. Our approach shows that the wealth of landscape information available from historical maps can be linked with data on population biology by means of dynamical models that can make predictions about species dynamics.
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| 10. |
- Jonsson, Magnus, et al.
(författare)
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Genetic divergence of climatically marginal populations of Vicia pisiformis on the Scandinavian Peninsula
- 2008
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Ingår i: Hereditas. - : Springer Science and Business Media LLC. - 0018-0661 .- 1601-5223. ; 145:1, s. 1-8
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Tidskriftsartikel (refereegranskat)abstract
- Vicia pisiformis L. is a perennial leguminous plant with a main distribution in broadleaved forest-steppes of eastern Europe. The species is classified as endangered (EN) according to the IUCN red-lists in both Norway and Sweden, due to severe fragmentation, small population sizes and continuing population decline. The populations on the Scandinavian Peninsula constitute the northern limit of the species distribution and are mostly restricted to warm stony slopes with predominantly southern aspects. In this study we used the AFLP method, which is a high-resolution genetic fingerprint method. Samples were collected from 22 Scandinavian populations. The overall genetic structure was analysed in an AMOVA, in a Mantel test and through constrained correspondence analysis (CCA). The ordination scores representing non-geographic genetic divergence were extracted from the CCA and analysed in a linear model using habitat variables and population size as explanatory variables. We found (i) a strong geographic structure, (ii) significant genetic divergence between populations, (iii) that this genetic divergence remained significant even after removing the effect of geography in a partial CCA and (iv) that the remaining non-geographic part of genetic divergence (distance from the ordination centre) was associated with aspect, populations with a northern aspect were more genetically divergent. Aspect explains more variation than population size and is the only variable retained in the minimal adequate model. We suggest that local adaptation has caused this divergence from an expected geographical pattern of genetic variation. This explanation is further supported by the association between aspect and specific AFLP fragments. Many plant populations are relics of a different climate (Aguirre-Planter et al. 2000; Despres et al. 2002; Pico and Riba 2002). In response to long-term climate change, populations can either migrate towards a more favourable climate or adapt to the new conditions (delaVega 1996; Jump et al. 2006). Species with limited dispersal ability are at risk of reaching isolated dead-ends of decreasingly suitable habitat, without any suitable habitat within dispersal distance (Colas et al. 1997). Isolated populations have to use their inherent evolutionary potential and adapt to changes in environmental conditions, or they will go extinct. As population fragments go extinct, those that remain will become increasingly isolated from each other both spatially and also genetically as the level of gene flow declines with increasing distance. Such correlation between genetic dissimilarities and geographic distances, known as isolation by distance (Slatkin 1993; Wright 1943), when found, suggests a history of geographically limited gene flow (Kimura and Weiss 1964). On top of an isolation by distance pattern there might be other genetic structures to be found. Occasional long-distance dispersal events for example may disturb geographic patterns with puzzling allele distributions as a result (Nichols and Hewitt 1994). Genetic drift is a process that will affect any pattern of genetic variation in a random fashion. Local adaptation through natural selection is a process that, if sufficiently strong in comparison with gene flow and genetic drift, will create patterns where genetic differentiation is associated with certain environmental conditions (Wright 1951). Several studies have shown the importance of local adaptation of populations (reviewed by Kawecki and Ebert 2004) (see also Bonin et al. 2006; Knight and Miller 2004; Kolseth and Lönn 2005; Lönn et al. 1998). Local adaptation can be strong also at small spatial scales (Snaydon and Davies 1976; Lönn 1993) even though it is sometimes very limited in terms of the number of genes involved (Kärkkainen et al. 2004) Environmental variability provides a base for biological variation by imposing differentiated selection pressures resulting in local adaptation. Topography provides large environmental variation within a relatively small area and thereby provides a basis for small-scale local adaptations. Depending on the local topographic possibilities populations can either migrate up and down slopes or along the same altitude to a different aspect to find a suitable microclimate. The dispersal distance will be much shorter per degree of temperature change during altitudinal migration (Hewitt 1996), than during simple latitudinal migration across a flat landscape. Slope and aspect are two important topographic parameters that determine the influx level of solar radiation, especially towards the poles where the total global radiation decreases (Larcher 2003). Vicia pisiformis is an endangered poorly-dispersed long-lived forest herb with its main distribution across the semi-open broadleaved forest steppes of eastern Europe. The Scandinavian populations are believed to be climate relict populations from warmer times. Earlier genetic studies of V. pisiformis using allozymes, RAPD:s and morhology, have found low to very low levels of genetic variation (Gustafsson and Gustafsson 1994; Black-Samuelsson et al. 1997; Black-Samuelsson and Lascoux 1999). Therefore we used AFLP (amplified fragment length polymorphism) markers, which detect even very small genetic differences between individuals. AFLP mainly analyse neutral variation, as the major fraction of most genomes is assumed to be neutral. However, since the AFLP-fragments are distributed randomly throughout the whole genome some fragments may be situated so close to regions under selection that they become more or less linked to them. This linkage disequilibrium between molecular markers and regions under selection, often referred to as quantitative trait loci (QTL), forms the basis for both QTL-mapping and marker assisted selection (MAS), reviewed by Dekkers and Hospital (2002). Gardner and Latta (2006) for example, found QTL under selection in both natural environments and in the greenhouse. Markers have been found to be connected to biomass production (Cavagnaro et al. 2006) and environmental variation (Bonin et al. 2006; Jump et al. 2006; Porcher et al. 2006). In this study we examine 22 Swedish and Norwegian populations of Vicia pisiformis and ask (i) if there is genetic differentiation between these populations, (ii) if there is can it be explained in its entirety by geographic location or (iii) can it partly be explained by habitat characteristics, suggesting local adaptation, or population size, suggesting genetic drift. We show that populations are differentiated geographically and that genetic variation in addition to the geographical pattern is associated with habitat.
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