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Sökning: WFRF:(Ramula Satu)

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1.
  • Arias, M. C., et al. (författare)
  • Permanent Genetic Resources added to Molecular Ecology Resources Database 1 February 2013-31 March 2013
  • 2013
  • Ingår i: Molecular Ecology Resources. - : Wiley. - 1755-098X .- 1755-0998. ; 13:4, s. 760-762
  • Tidskriftsartikel (refereegranskat)abstract
    • This article documents the addition of 142 microsatellite marker loci to the Molecular Ecology Resources database. Loci were developed for the following species: Agriophyllum squarrosum, Amazilia cyanocephala, Batillaria attramentaria, Fungal strain CTeY1 (Ascomycota), Gadopsis marmoratus, Juniperus phoenicea subsp. turbinata, Liriomyza sativae, Lupinus polyphyllus, Metschnikowia reukaufii, Puccinia striiformis and Xylocopa grisescens. These loci were cross-tested on the following species: Amazilia beryllina, Amazilia candida, Amazilia rutila, Amazilia tzacatl, Amazilia violiceps, Amazilia yucatanensis, Campylopterus curvipennis, Cynanthus sordidus, Hylocharis leucotis, Juniperus brevifolia, Juniperus cedrus, Juniperus osteosperma, Juniperus oxycedrus, Juniperus thurifera, Liriomyza bryoniae, Liriomyza chinensis, Liriomyza huidobrensis and Liriomyza trifolii.
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2.
  • Buckley, Yvonne M., et al. (författare)
  • Causes and consequences of variation in plant population growth rate : a synthesis of matrix population models in a phylogenetic context
  • 2010
  • Ingår i: Ecology Letters. - : Wiley. - 1461-023X .- 1461-0248. ; 13:9, s. 1182-1197
  • Forskningsöversikt (refereegranskat)abstract
    • Explaining variation in population growth rates is fundamental to predicting population dynamics and population responses to environmental change. In this study, we used matrix population models, which link birth, growth and survival to population growth rate, to examine how and why population growth rates vary within and among 50 terrestrial plant species. Population growth rates were more similar within species than among species; with phylogeny having a minimal influence on among-species variation. Most population growth rates decreased over the observation period and were negatively autocorrelated between years; that is, higher than average population growth rates tended to be followed by lower than average population growth rates. Population growth rates varied more through time than space; this temporal variation was due mostly to variation in post-seedling survival and for a subset of species was partly explained by response to environmental factors, such as fire and herbivory. Stochastic population growth rates departed from mean matrix population growth rate for temporally autocorrelated environments. Our findings indicate that demographic data and models of closely related plant species cannot necessarily be used to make recommendations for conservation or control, and that post-seedling survival and the sequence of environmental conditions are critical for determining plant population growth rate.
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3.
  • Burns, Jean H., et al. (författare)
  • Empirical tests of life-history evolution theory using phylogenetic analysis of plant demography
  • 2010
  • Ingår i: Journal of Ecology. - : Wiley. - 0022-0477 .- 1365-2745. ; 98:2, s. 334-344
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. A primary goal of evolutionary ecology is to understand factors selecting for the diversity of life histories. Life-history components, such as time-to-reproduction, adult survivorship and fecundity, might differ among species because of variation in direct and indirect benefits of these life histories in different environments or might have lower-than-expected variability because of phylogenetic constraints. Here, we present a phylogenetic examination of demography and life histories using a data base of 204 terrestrial plant species. 2. Overall, statistical models without phylogeny were preferred to models with phylogeny for vital rates and elasticities, suggesting that they lacked phylogenetic signal and are evolutionarily labile. However, the effect of phylogeny was significant in models including sensitivities, suggesting that sensitivities exhibit greater phylogenetic signal than vital rates or elasticities. 3. Species with a greater age at first reproduction had lower fecundity, consistent with a cost of delayed reproduction, but only in some habitats (e.g. grassland). We found no evidence for an indirect benefit of delayed reproduction via a decrease in variation in fecundity with age to first reproduction. 4. The greater sensitivity and lower variation in survival than in fecundity was consistent with buffering of more important vital rates, as others have also found. This suggests that studies of life-history evolution should include survival, rather than only fecundity, for the majority of species. 5. Synthesis. Demographic matrix models can provide informative tests of life-history theory because of their shared construction and outputs and their widespread use among plant ecologists. Our comparative analysis suggested that there is a cost of delayed reproduction and that more important vital rates exhibit lower variability. The absolute importance of vital rates to population growth rates (sensitivities) exhibited phylogenetic signal, suggesting that a thorough understanding of life-history evolution might require an understanding of the importance of vital rates, not just their means, and the role of phylogenetic history.
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4.
  • Eckstein, Rolf Lutz, 1965-, et al. (författare)
  • Biological flora of Central Europe– Lupinus polyphyllus Lindley
  • 2023
  • Ingår i: Perspectives in plant ecology, evolution and systematics. - : Elsevier. - 1433-8319 .- 1618-0437. ; 58
  • Tidskriftsartikel (refereegranskat)abstract
    • The invasive herb Lupinus polyphyllus has been focus of a number of fact sheets worldwide but a comprehensive summary of the species’ taxonomy and morphology, distribution, habitat requirements, and biology has been lacking. This paper gives a thorough account of the species’ systematic position and taxonomy, highlighting the difficulties to delimit taxa, which is related to interbreeding among members of this genus. However, L. polyphyllus var. polyphyllus is apparently the taxon that has naturalized and is regionally invasive in temperate-humid climates worldwide. We also present an updated distribution map of L. polyphyllus in the native and invaded ranges, which highlights seven regions in the world where the species has been established. We show that the climatic niche of L. polyphyllus in the invaded range shifts towards higher summer precipitation and lower isothermality, probably because the invaded range includes subcontinental regions of eastern Europe and western Siberia. The habitats of L. polyphyllus range from rather dry to wet, have moderately acidic to strongly acidic soils, and the species’ indicator values across Europe suggest that it occurs along a gradient from very nutrient poor sites to intermediate to rich sites from northern to southern Europe. The species shows high resistance to both drought and frost. In Central Europe, the species has a stronghold in alpic mountain hay meadows, abandoned meadows and pastures, low and medium altitude hay meadows, anthropogenic herb stands and temperate thickets and scrubs. In northern Europe, the species occurs in anthropogenic herb stands along roads and railroads as well as in abandoned pastures and fields. We also found some doubtful information about L. polyphyllus in the literature. This refers to its description as “rhizomatous perennial” although it lacks rhizomes; an apparently very high longevity of its seeds, which may only be true under artificial conditions in an ex situ seed repository; and a very deep rooting depth, which may not represent the average rooting depth but rather an extreme value. Knowledge about the interrelationships between the species’ future population dynamics and spread and ongoing climate warming is lacking. Finally, our review points out that there is currently no evidence-based strategy for a cost-efficient management of L. polyphyllus although it is among the most problematic non-native plant species in Europe due to its environmental and socio-economic impacts. 
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5.
  • Jakalaniemi, A., et al. (författare)
  • Variability of important vital rates challenges the demographic buffering hypothesis
  • 2013
  • Ingår i: Evolutionary Ecology. - : Springer Science and Business Media LLC. - 1573-8477 .- 0269-7653. ; 27:3, s. 533-545
  • Tidskriftsartikel (refereegranskat)abstract
    • Selection is assumed to eliminate life-histories showing high variability in vital rates that have the greatest influence on population performance. Therefore, an inverse variability-importance relationship of vital rates is believed to be a universal pattern for diverse life-histories. We tested for such a relationship using multi-year demographic data on a large number of populations of two perennial plant species. Applying different approaches, we first examined the overall variability-importance relationship for the average main vital rates (survival, growth, retrogression, fecundity) per species, and then separately for each population. We found an overall inverse relationship between temporal variation and importance of the average main vital rates for both study species, but these negative species-level correlations were mainly caused by different scales of the examined vital rates. When variability-importance relationships were examined across individual demographic transitions within populations, the abundance of positive and negative correlations depended largely on the method used, and positive correlations were more common after correcting vital rates for sampling variation than when using uncorrected vital rates. Our results cast doubt on the generality of the demographic buffering hypothesis, suggesting that the inverse variability-importance relationship may not be a universal pattern when vital rates are examined for multiple populations of the same plant species.
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6.
  • Kourantidou, Melina, et al. (författare)
  • The economic costs, management and regulation of biological invasions in the Nordic countries
  • 2022
  • Ingår i: Journal of Environmental Management. - : Elsevier BV. - 0301-4797 .- 1095-8630. ; 324
  • Tidskriftsartikel (refereegranskat)abstract
    • A collective understanding of economic impacts and in particular of monetary costs of biological invasions is lacking for the Nordic region. This paper synthesizes findings from the literature on costs of invasions in the Nordic countries together with expert elicitation. The analysis of cost data has been made possible through the InvaCost database, a globally open repository of monetary costs that allows for the use of temporal, spatial, and taxonomic descriptors facilitating a better understanding of how costs are distributed. The total reported costs of invasive species across the Nordic countries were estimated at $8.35 billion (in 2017 US$ values) with damage costs significantly outweighing management costs. Norway incurred the highest costs ($3.23 billion), followed by Denmark ($2.20 billion), Sweden ($1.45 billion), Finland ($1.11 billion) and Iceland ($25.45 million). Costs from invasions in the Nordics appear to be largely underestimated. We conclude by highlighting such knowledge gaps, including gaps in policies and regulation stemming from expert judgment as well as avenues for an improved understanding of invasion costs and needs for future research.
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7.
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8.
  • Ramula, Satu, et al. (författare)
  • Demographic consequences of pollen limitation and inbreeding depression in a gynodioecious herb
  • 2007
  • Ingår i: International journal of plant sciences. - : University of Chicago Press. - 1058-5893 .- 1537-5315. ; 168:4, s. 443-453
  • Tidskriftsartikel (refereegranskat)abstract
    • In a gynodioecious plant population, where female and hermaphroditic plants co- occur, females must produce more seeds or better- quality offspring than hermaphrodites to be maintained. Further, differences in the magnitude of pollen limitation and inbreeding depression between females and hermaphrodites may affect the relative fitness of the gender morphs and consequently population dynamics. We integrated demographic data into data on pollen limitation and inbreeding depression in a gynodioecious herb. Using a matrix model approach, we then examined the effects of pollen limitation and inbreeding depression on population growth rate and sex ratio. Hermaphrodites tended to contribute more to population growth rates than females. Because of the insensitivity of population growth rates to variation in annual fecundity, pollen limitation of either females or hermaphrodites had a negligible effect on population sex ratio. Inbreeding depression expressed simultaneously in three fitness components of the offspring produced by hermaphrodites reduced stochastic population growth rate and increased female frequency. Given that population growth rates are insensitive to fecundity transitions and that hermaphrodites have moderate selfing rates, our results suggest that inbreeding depression plays a larger role in the maintenance of females in gynodioecious populations than pollen limitation.
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9.
  • Ramula, Satu, et al. (författare)
  • Importance of correlations among matrix entries in stochastic models in relation to number of transition matrices
  • 2005
  • Ingår i: Oikos. - : Wiley. - 0030-1299 .- 1600-0706. ; 111:1, s. 9-18
  • Tidskriftsartikel (refereegranskat)abstract
    • Stochastic matrix models are used to predict population viability and the risk of extinction. Different stochastic methods require different amounts of estimation effort and may lead to divergent estimates. We used 16 transition matrices collected from ten populations of the perennial herb Primula veris to compare population estimates produced by different stochastic methods, such as selection of matrices, selection of vital rates, selection of matrix elements, and Tuljapurkar's approximation. Specifically, we tested the reliability of the methods using different numbers of transition matrices, and examined the importance of correlations among matrix entries. When correlations among matrix entries were included in the models, selection of vital rates produced the lowest and Tuljapurkar's approximation produced the highest estimates of mean population growth rates. Selection of matrices and matrix elements often produced nearly similar population estimates. Simulations based on incompletely estimated correlations among matrix entries considerably differed from those based on all correlations estimated, particularly when correlations were strong. The magnitude of correlations among matrix entries depended on the number of matrices, which made it difficult to generalize correlations within a species. Given that selection of vital rates or matrix elements is used, correlations among matrix entries should usually be included in the model, and they should preferably be estimated from the present data rather than according to other information of the species.
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10.
  • Ramula, Satu, et al. (författare)
  • Linking phenological shifts to demographic change
  • 2015
  • Ingår i: Climate Research. - : Inter-Research Science Center. - 1616-1572 .- 0936-577X. ; 63:2, s. 135-144
  • Forskningsöversikt (refereegranskat)abstract
    • Climate-induced phenological shifts may have serious consequences for organisms and populations, but it is challenging to link such shifts to demographic change. Here, we present an overview of current methodological approaches for studying the demographic consequences of phenological shifts, based on a literature survey of 62 studies on diverse taxa. The majority of these studies (66%) were conducted using an approach that linked phenological shifts to demography through the measurement of vital rates (survival, growth, and fecundity). About 18% of the studies used a population-based approach that linked the phenological shifts to changes in population size, and 16% took a combined approach by considering changes in both vital rates and population size. Birds and mammals were overrepresented in studies of the demographic consequences of phenological shifts, compared to their occurrence in nature, while insects were heavily underrepresented. The effects of phenological shifts often varied according to the particular vital rate under consideration, in many cases even within a single species. In the few studies that examined changes in phenology together with both vital rate and population data, the changes in vital rates did not always predict changes in population size. To better understand the ultimate causes of population-level effects we argue that further study is needed on density-dependent aspects of population dynamics and on the sensitivity of population dynamics to perturbations in vital rates. We encourage re searchers to observe multiple vital rates throughout organisms' life-cycles in order to enable more meaningful examination of the consequences of phenological shifts for population dynamics.
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