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Sökning: LAR1:hh > (2000-2004) > Weisner Stefan E. B.

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1.
  • Strand, John A., et al. (författare)
  • Dynamics of submerged macrophyte populations in response to biomanipulation
  • 2001
  • Ingår i: Freshwater Biology. - Chichester, United Kingdom : Wiley-Blackwell. - 0046-5070 .- 1365-2427. ; 46:10, s. 1397-1408
  • Tidskriftsartikel (refereegranskat)abstract
    • 1. A 6-year study (1992-97) of changes in submerged vegetation after biomanipulation was carried out in the eutrophicated Lake Finjasjon, Southern Sweden. Ten sites around the lake were revisited each year. At each site five samples of above-ground biomass were taken at 10 cm water depth intervals. An investigation of the seed bank at the 10 sites, and a grazing experiment where birds and large fish were excluded was also conducted. 2. Between 1992 and 1996, in shallow areas (water depth < 3 m), vegetation cover 2 increased from < 3 to 75% and above-ground biomass from < 1 to 100 g DW m(-2). Mean outer water depth increased from 0.3 to 2.5 m. Elodea canadensis and Myriophyllum spicatum accounted for > 95% of the increase in biomass and plant cover. The following year (1997), however, cover and above-ground biomass decreased, mainly attributable to the total disappearance of E. canadensis. Secchi depth increased after biomanipulation until 1996, but decreased again in 1997. 3. Total and mean number of submerged species increased after biomanipulation, probably as a result of the improved light climate. However, after the initial increase in species number there was a decrease during the following years, possibly attributed to competition from the rapidly expanding E. canadensis and M. spicatum. The lack of increase in species number after the disappearance of E. canadensis in 1997 implies that other factors also affected species richness. 4. A viable seed bank was not necessary for a rapid recolonization of submerged macrophytes, nor did grazing by waterfowl or fish delay the re-colonization of submerged macrophytes. 5. Submerged macrophytes are capable of rapid recolonization if conditions improve, even in large lakes such as Finjasjon (11 km(2)). Species that spread by fragments will increase rapidly and probably outcompete other species. 6. The results indicate that after the initial Secchi depth increase, probably caused by high zooplankton densities, submerged vegetation further improved the light climate. The decrease in macrophyte biomass in 1997 may have caused the observed increase in phosphorus and chlorophyll a, and the decrease in Secchi depth. We suggest that nutrient competition from periphyton, attached to the macrophytes, may be an important factor in limiting phytoplankton production, although other factors (e.g. zooplankton grazing) are also of importance, especially as triggers for the shift to a clear-water state.
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2.
  • Strand, John A., et al. (författare)
  • Morphological plastic responses to water depth and wave exposure in an aquatic plant (Myriophyllum spicatum)
  • 2001
  • Ingår i: Journal of Ecology. - Oxford, United Kingdom : Wiley-Blackwell. - 0022-0477 .- 1365-2745. ; 89:2, s. 166-175
  • Tidskriftsartikel (refereegranskat)abstract
    • 1 We investigated morphological responses of the submerged macrophyte Myriophyllum spicatum L. to water depth and wave exposure when grown in the same substrate at two sites in two eutrophic lakes. Periphyton production was 4-8 times higher at sheltered than at wave-exposed sites and its influence was further investigated in a glasshouse experiment. Morphological responses in both experiments were compared by allometric analyses, with shoot weight as covariate. 2 In the field study, plants shoots exhibited similar responses (increased plant height and branch length, and decreased branch number) to sheltered conditions as to deep water. The partitioning between above- and below-ground biomass however, differed, with below-ground decreasing with an increasing water depth, but increasing or remaining unaffected at sheltered compared with exposed conditions. 3 In the glasshouse experiment, plant responses to water depth were similar to those in the field study. Furthermore, plant height increased when plants were overgrown with periphyton. 4 High production of periphytic algae at sheltered sites appears to cause light limitation of macrophytes. However, other factors such as nutrient uptake also appears to determine morphological responses. At sheltered sites, where leaf nutrient uptake is reduced by abundant periphyton and thick boundary layers, plants allocate more biomass to roots. At deep and wave-exposed sites, the absence of periphyton allows plants to take up nutrients through their leaves and allocation of biomass to shoots increases photosynthesis. 5 Overall, relative allocation to shoot and root biomass appears to be primarily controlled by nutrient availability, whereas allocation of available shoot biomass to particular structures is controlled by light availability.
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3.
  • Strand, John A., et al. (författare)
  • Phenotypic plasticity – contrasting species-specific traits induced by identical environmental constraints
  • 2004
  • Ingår i: New Phytologist. - Oxford : Blackwell. - 0028-646X .- 1469-8137. ; 163:3, s. 449-451
  • Tidskriftsartikel (refereegranskat)abstract
    • Can it be assumed that a specific environmental constraint imposed on different species leads to a convergence in, for example, morphology? A phenotype expressed in response to external stimuli (e.g. size-reduction in response to mechanical stress) should be adaptive regardless of species – this is largely intuitive, but has been poorly studied. In this issue (pp. 651–660), Puijalon & Bornette reveal exciting new data that suggest that phenotypic plastic responses to identical environmental constraints may indeed be species-specific (Puijalon & Bornette, 2004).
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4.
  • Svensson, Jonas M., et al. (författare)
  • Rikare mångfald och mindre kväve : Utvärdering av våtmarker skapade med stöd av lokala investeringsprogram och landsbygdsutvecklingsstöd
  • 2004
  • Bok (övrigt vetenskapligt/konstnärligt)abstract
    • På uppdrag av Naturvårdsverket och Jordbruksverket har Våtmarkscentrum, Högskolan i Halmstad, utvärderat svenska våtmarker anlagda med landsbygdsutvecklingsstöd, LBU-stöd (Miva, projektstöd och Lmiva utan projektstöd) respektive våtmarker anlagda inom lokala investeringsprogram (LIP) avseende näringsretention och biologisk mångfald. Resultaten från utvärderingen redovisas separat för de fyra olika grupperna/kategorierna av anlagda våtmarker enligt nedan (fetstil anger kategorihänvisning i text, tabeller och figurer):• Våtmarker anlagda med anläggningsstöd inom Lokala investeringsprogram 1998 - 2002, LIP.• Våtmarker anlagda med anläggningsstöd inom LBU-projektstöd (dessa våtmarker får vanligen även skötselstöd, Lmiva), 2000 - 2002.• Våtmarker anlagda 1996-1999, utan anläggningsstöd men med skötselstöd (Miljöstöd), Miva.• Våtmarker anlagda från år 2000 - , utan anläggningsstöd men med skötselstöd (LBU-våtmarker som endast får skötselersättning), Lmiva.Syftet har främst varit att utvärdera och jämföra hur våtmarksanläggning inom olika stödformer har bidragit till minskad övergödning och ökad biologisk mångfald. Syftet har alltså inte varit att utvärdera enskilda våtmarker utan att ge en helhetsbild för olika stödformer och regioner. Därför har det varit nödvändigt att basera utvärderingen på data för ett stort antal våtmarker. Detta innebär att utförliga mätningar ej kunnat genomföras inom de enskilda objekten. Närsaltsretention har därför beräknats baserat på modeller och biologisk mångfald har undersökts genom att trollsländor använts som indikatorgrupp.Inom uppdraget har, med jordbruksstöd, registrerats information om totalt 908 våtmarksobjekt om totalt 2860 ha ersatt yta fördelat på 1815 ha Miva, 920 ha projektstöd och 125 ha Lmiva utan projektstöd. Totalt registrerade våtmarker med stöd från LIP är 274 st, omfattande 439 ha.Kompletterande fältstudier har utförts i drygt 100 st våtmarker. Främst är det resultaten från dessa våtmarker som sammanfattas nedan...
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5.
  • Tonderski, Karin S., et al. (författare)
  • Våtmarker : Närsaltsfällor och/eller myllrande mångfald?
  • 2003
  • Ingår i: Vatten: tidskrift för vattenvård. - Nykvarn : Föreningen Vatten. - 0042-2886. ; 59:4, s. 259-270
  • Tidskriftsartikel (refereegranskat)abstract
    • This paper summarizes the state-of-the-art with respect to wetlands for nutrient removal and biodiversity enhancement, as expressed at a research workshop in December 2002. In the end of 2002, 260 and 884 wetlands had been constructed in Sweden with subsidies from LIP and the European Union, respectively. Most frequently, the aims were to remove nutrients from water and enhance biodiversity. The question raised is if we know how to design multifunctional wetlands. Should a wetland be deep or shallow, with or without macrophytes to be an efficient nutrient sink? Diverging opinions are presented, but generally it appears that fairly shallow wetlands at least partly covered by emergent macrophytes are favourable. The importance of extreme high flows and hydraulic short-circuiting is highlighted, and Danish and Norwegian approaches to wetlands construction are presented. Also, there is a risk that nutrient retaining wetlands develop a fairly trivial flora and fauna unless special care is taken. Intentional establishment of desirable and less common species, as well as creation of a variation of depth gradients to favour such species are such measures. Others are allowing for water level variations, as well as vegetation management such as grazing and harvesting.
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6.
  • Vretare Strand, Viveka, et al. (författare)
  • Interactive effects of pressurized ventilation, water depth and substrate conditions on Phragmites australis
  • 2002
  • Ingår i: Oecologia. - Berlin : Springer. - 0029-8549 .- 1432-1939. ; 131:4, s. 490-497
  • Tidskriftsartikel (refereegranskat)abstract
    • Pressurized ventilation acts to increase the oxygen supply to roots and rhizomes in some species of emergent plants. In a greenhouse experiment, we investigated how pressurized ventilation affected growth, biomass allocation and mineral content of Phragmites australis in two water depths (15 cm or 75 cm) and two substrates (organic sediment or sand). Through perforating each stem above the water surface, pressurized ventilation was inhibited without affecting oxygen diffusion. In controls, 10-20% of the stems were perforated to make certain that lack of efflux sites would not limit pressurized ventilation. Plants with inhibited pressurized ventilation had lower oxygen concentrations in their stem bases than control plants. Growth was lower in plants with inhibited pressurized ventilation compared to controls except when plants grew in a combination of sand and shallow water. In plants grown in an organic sediment, but not in those grown in sand, inhibition of pressurized ventilation resulted in decreased biomass allocation to soil roots but increased allocation to aquatic roots. Stem perforation affected the tissue concentrations of nitrogen, phosphorus, magnesium, manganese and aluminium but not of calcium or iron. We suggest that the lower growth in plants with inhibited pressurized ventilation was caused by decreased mineral uptake, which may have resulted from the decreased proportional allocation to soil root weight, from decreased mineral availability or from impaired root function. In plants grown in sand in shallow water, diffusion seemed to cover the oxygen demand, as pressurized ventilation did not affect growth.
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7.
  • Vretare, Viveka, et al. (författare)
  • Influence of pressurized ventilation on performance of an emergent macrophyte (Phragmites australis)
  • 2000
  • Ingår i: Journal of Ecology. - Oxford, United Kingdom : Wiley-Blackwell. - 0022-0477 .- 1365-2745. ; 88:6, s. 978-987
  • Tidskriftsartikel (refereegranskat)abstract
    • 1 Pressurized ventilation, which increases gas exchange between aerial and submerged plant parts, has been found in various emergent macrophyte species. We investigated the potential for this mechanism to affect growth, morphology and biomass allocation in Phragmites australis in glasshouse experiments. 2 Inhibition of pressurized ventilation by perforation of stems above the water surface resulted in decreased oxygen concentrations in stem bases and rhizomes. Perforation caused little mechanical damage. 3 Allometric methods were used to evaluate treatment effects on biomass allocation and morphology. 4 Inhibition of pressurized ventilation resulted in decreased allocation to belowground weight and decreased rhizome penetration into the substrate in two of three experiments. Treatment also decreased growth rate, rhizome length and number of rhizomes when substrate had a high organic content. In the third experiment, growth clearly decreased in deep water, although inhibition of pressurized ventilation did not affect growth, biomass allocation or morphology at either of the water depths tested. 5 Decreased allocation to below-ground parts and decreased rhizome lengths may be adaptations to allow the oxygen concentration in roots and rhizomes to be maintained above a critical level when the oxygen supply is low. 6 Pressurized ventilation may improve the performance of P. australis but only under certain conditions (e.g. not when growth rate is low or the substrate has a high redox potential).
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8.
  • Vretare, Viveka, et al. (författare)
  • Phenotypic plasticity in Phragmites australis as a functional response to water depth
  • 2001
  • Ingår i: Aquatic Botany. - Amsterdam, Netherlands : Elsevier. - 0304-3770 .- 1879-1522. ; 69:2-4, s. 127-145
  • Tidskriftsartikel (refereegranskat)abstract
    • We have performed investigations to see if the emergent macrophyte Phragmites australia (Cav.) Trin. ex Steud. exhibits phenotypic plasticity as a response to water depth and if such responses in biomass allocation pattern and morphology are functional responses, improving the performance of the plant. In greenhouse experiments plants were grown in deep or shallow water to evaluate plastic responses. Allometric methods were used to handle effects caused by size differences between treatments. To evaluate if phenotypic responses to water depth are functional, the relative growth rate (RGR) of plants acclimatised to shallow or deep water, respectively, were compared in deep water, and the growth of plants in fluctuating and constant water level were compared. When grown in deep (70 or 75 cm), compared to shallow (20 or 5 cm) water, plants allocated proportionally less to below-ground weight, made proportionally fewer but taller stems, and had rhizomes that were situated more superficially in the substrate. Plants acclimatised to shallow water had lower RGR than plants acclimatised to deep water, when they were grown in deep water, and plants in constant water depth (40 cm) grew faster than plants in fluctuating water depth (15/65 cm). In an additional field study, the rhizomes were situated superficially in the sediment in deep, compared to shallow water. We have shown that P. australis acclimatises to deep water with phenotypic plasticity through allocating more resources to stem weight, and also by producing fewer but taller stems, which will act to maintain a positive carbon balance and an effective gas exchange between aerial and below-ground parts. Furthermore, the decreased proportional allocation to below-ground parts probably results in decreased nutrient absorption, decreased anchorage in the sediment and decreased carbohydrate reserves. Thus, in deep water, plants have an increased risk of becoming uprooted and experience decreased growth and dispersal rates. (C) 2001 Elsevier Science B.V. All rights reserved.
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9.
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10.
  • Weisner, Stefan E. B., et al. (författare)
  • Ecology and management of plants in aquatic ecosystems
  • 2002
  • Ingår i: Handbook of ecological restoration. - Cambridge : Cambridge University Press. - 0521791286 ; , s. 242-256
  • Bokkapitel (refereegranskat)abstract
    • The central role of macrophytes for the functioning of aquatic systems means that the most effective way to manage these systems is often through vegetation management. For this we need to understand the mechanisms regulating vegetation distribution. Submerged macrophyte distribution is mainly related to water depth, water transparency and epiphytic growth. The distribution of emergent vegetation can largely be predicted from water depth and substrate characteristics. Also, in both submerged and emergent macrophytes, the effects on the vegetation of grazing can be dramatic. Management should aim at providing environmental conditions favouring the desired ecosystem state, rather than methods directly aimed at the vegetation. For example, the best method for promoting establishment of emergent vegetation is often lowering of the water level. To establish submerged vegetation, water transparency can be increased through biomanipulation (the removal of zooplanktivorous fish leading to increased zooplankton grazing pressure on phytoplankton). Changes in water depth and introduction of grazers are often effective measures to control growth of aquatic weeds.
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