22 research outputs found

    A legelés léptékfüggő hatásai szikes- és homoki gyepek fajgazdagságára

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    Scale-dependent effects of grazing on the species richness of alkaline and sand grasslands

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    Extensively managed pastures harbour rare and endangered species and have a decisive role in maintaining grassland biodiversity. Traditional herding of local robust cattle breeds is considered as a feasible tool for preserving these habitats. We studied the scale-dependent effects of grazing on the species richness and composition of three dry grassland types in the Great Hungarian Plain: Achilleo setaceae-Festucetum pseudovinae and Artemisio santonici-Festucetum pseudovinae alkaline grasslands, and Potentillo arenariae-Festucetum pseudovinae sand grassland. We asked the following questions: (1) Does extensive grazing have a scale-dependent effect on plant species richness of alkaline and sand grasslands? (2) How does grazing affect the proportion of specialists, generalists and weeds in the three grassland types? We sampled ten sites of each grassland type, including five extensively grazed and five non-grazed sites (altogether we had 30 sites). We used a series of nested plots each consisting of 10 plots from the size of 0.01 m² to 16 m². We revealed that grazing has contrasting effects in the three grassland types, and had a considerable effect on their species richness even at small scales. In both alkaline grassland types, total species richness was overall higher in grazed plots but it increased in a similar manner for both ungrazed and grazed habitats across plot sizes. Small-scale heterogeneity likely due to the uneven distribution of grazing, trampling and defecation together with mitigated rate of competition allowed more species to co-exist even at small scales in grazed alkaline grasslands. Grazing increased the richness of specialists, but likely due to the salt stress, establishment of weeds was hampered. Open gaps formed by trampling likely supported the establishment of several specialist species such as Plantago tenuiflora and Puccinellia limosa which are typical to open alkali grasslands. Contrary, in sand grasslands, we did not detect any effect of grazing on total species richness, likely due to the adverse effect of grazing on the species richness of specialists and weeds. In contrast with the former findings we detected significantly higher species richness in 0.01 m² and 0.0625 m² plots in the grazed sand grasslands, but found no differences at larger scales. Whilst species richness of specialists was significantly decreased, richness of weeds was increased by grazing. Decrease in the specialist species richness was likely due to the lack of their evolutionary adaptation to grazing. Degradation caused by grazing and trampling together with the propagule pressure from the neighbouring anthropo-genic habitats resulted in an increased richness of weeds in the grazed sites

    Co-seeding grasses and forbs supports restoration of species-rich grasslands and improves weed control in ex-arable land

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    Sowing is widely used for the restoration of species-rich grasslands but still there are knowledge gaps regarding the most suitable application of different seed mixtures. We tested the effect of seed mixtures application timing on the establishment of sown forbs and weed control. 36 experimental plots with nine sowing treatments were established in an abandoned cropland in Hungary. Grass-seeds, diverse forb seed mixture and the combination of the two were applied: diverse forb mixture was sown simultaneously or 1, 2 or 3 years after grass sowing, in plots sown previously with grass or in empty plots (fallows). All sowing treatments supported the rapid establishment of the sown species in large cover and hampered weed encroachment. Forbs performed better when sown into fallows than in grass-matrix and forbs establishment was worse in older fallows than in younger ones. Grasses expressed a strong priority effect, especially when forbs were sown at least two years later than grasses. We also investigated the relation between seed germinability, weather parameters and establishment success. Germination rate in the greenhouse could not predict the establishment success of forbs in the field and showed great differences between years, hence we recommend sowing target forbs in multiple years

    Vertical distribution of soil seed bank and the ecological importance of deeply buried seeds in alkaline grasslands

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    Background: Soil seed banks play a central role in vegetation dynamics and may be an important source of ecological restoration. However, the vast majority of seed bank studies examined only the uppermost soil layers (0-10 cm); hence, our knowledge on the depth distribution of seed bank and the ecological significance of deeply buried seeds is limited. The aim of our study was to examine the fine-scale vertical distribution of soil seed bank to a depth of 80 cm, which is one of the largest studied depth gradients so far. Our model systems were alkaline grasslands in East-Hungary, characterised by harsh environmental conditions, due to Solonetz soil reference group with Vertic horizon. We asked the following questions: (1) How do the seedling density and species richness of soil seed bank change along a vertical gradient and to what depth can germinable seeds be detected? (2) What is the relationship between the depth distribution of the germinable seeds and the species traits? Methods: In each of the five study sites, four soil cores (4 cm diameter) of 80 cm depth were collected with an auger for soil seed bank analysis. Each sample was divided into sixteen 5-cm segments by depth (320 segments in total). Samples were concentrated by washing over sieves and then germinated in an unheated greenhouse. Soil penetration resistance was measured in situ next to each core location (0-80 cm depth, 1-cm resolution). We tested the number and species richness of seedlings observed in the soil segments (N= 320), using negative binomial generalized linear regression models, in which sampling layer and penetration resistance were the predictor variables. We ran the models for morphological groups (graminoids/forbs), ecological groups (grassland species/weeds) and life-form categories (short-lived/perennial). We also tested whether seed shape index, seed mass, water requirement or salt tolerance of the species influence the vertical distribution of their seed bank. Results: Germinable seed density and species richness in the seed bank decreased with increasing soil depth and penetration resistance. However, we detected nine How germinable seeds of six species even in the deepest soil layer. Forbs, grassland species and short-lived species occurred in large abundance in deep layers, from where graminoids, weeds and perennial species were missing. Round-shaped seeds were more abundant in deeper soil layers compared to elongated ones, but seed mass and ecological indicator values did not influence the vertical seed bank distribution. Our research draws attention to the potential ecological importance of the deeply buried seeds that may be a source of recovery after severe disturbance. As Vertisols cover 335 million hectares worldwide, these findings can be relevant for many regions and ecosystems globally. We highlight the need for similar studies in other soil and habitat types to test whether the presence of deep buried seeds is specific to soils with Vertic characteristics

    Vertical distribution of soil seed bank and the ecological importance of deeply buried seeds in alkaline grasslands

    Get PDF
    Background: Soil seed banks play a central role in vegetation dynamics and may be an important source of ecological restoration. However, the vast majority of seed bank studies examined only the uppermost soil layers (0-10 cm); hence, our knowledge on the depth distribution of seed bank and the ecological significance of deeply buried seeds is limited. The aim of our study was to examine the fine-scale vertical distribution of soil seed bank to a depth of 80 cm, which is one of the largest studied depth gradients so far. Our model systems were alkaline grasslands in East-Hungary, characterised by harsh environmental conditions, due to Solonetz soil reference group with Vertic horizon. We asked the following questions: (1) How do the seedling density and species richness of soil seed bank change along a vertical gradient and to what depth can germinable seeds be detected? (2) What is the relationship between the depth distribution of the germinable seeds and the species traits? Methods: In each of the five study sites, four soil cores (4 cm diameter) of 80 cm depth were collected with an auger for soil seed bank analysis. Each sample was divided into sixteen 5-cm segments by depth (320 segments in total). Samples were concentrated by washing over sieves and then germinated in an unheated greenhouse. Soil penetration resistance was measured in situ next to each core location (0-80 cm depth, 1-cm resolution). We tested the number and species richness of seedlings observed in the soil segments (N= 320), using negative binomial generalized linear regression models, in which sampling layer and penetration resistance were the predictor variables. We ran the models for morphological groups (graminoids/forbs), ecological groups (grassland species/weeds) and life-form categories (short-lived/perennial). We also tested whether seed shape index, seed mass, water requirement or salt tolerance of the species influence the vertical distribution of their seed bank. Results: Germinable seed density and species richness in the seed bank decreased with increasing soil depth and penetration resistance. However, we detected nine How germinable seeds of six species even in the deepest soil layer. Forbs, grassland species and short-lived species occurred in large abundance in deep layers, from where graminoids, weeds and perennial species were missing. Round-shaped seeds were more abundant in deeper soil layers compared to elongated ones, but seed mass and ecological indicator values did not influence the vertical seed bank distribution. Our research draws attention to the potential ecological importance of the deeply buried seeds that may be a source of recovery after severe disturbance. As Vertisols cover 335 million hectares worldwide, these findings can be relevant for many regions and ecosystems globally. We highlight the need for similar studies in other soil and habitat types to test whether the presence of deep buried seeds is specific to soils with Vertic characteristics

    Hamvas rétihéják (Circus pygargus) fészkelőhelyválasztása Magyarországon

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    Az elmúlt évszázadban a hamvas rétihéják számára alkalmas természetes és természetközeli élőhelyek jelentős negatív változásokon mentek át, főként a mezőgazdaság terjeszkedése, intenzifikálódása, a területek beépítése és a folyószabályozások miatt. Ebből kifolyólag a párok elkezdtek kultúrnövényzetben költeni, mely több okból is veszélyezteti a fészekaljakat. Dolgozatomban archív fészkelési adatok, mezei pocok állománysűrűségek és éves átlagos csapadákösszegek hatását vizsgálom a hamvas rétihéják költési sikere kapcsán. Amely tényezők hatással vannak a költési sikerre, befolyásolják a madarak fészkelőhelyválasztását.MSc/MABiológusg

    Owl-mediated Diploendozoochorous Seed Dispersal Increases Dispersal Distance and Supports Seedling Establishment

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    Seed dispersal is an essential process contributing to the maintenance of plant populations. Zoochory is a widespread way of plant dispersal in every terrestrial ecosystem that can ensure the long-distance dispersal of seeds. Secondary seed dispersal (SSD) by far-ranging raptors is a special type of zoochory, which might have a role in colonizing new habitats. We used the barn owl (Tyto alba) as model species to test the effectivity and seasonality of SSD in open semi-natural landscapes. We collected 582 pellets from six sites in East-Hungary throughout one year. We identified prey items in the pellets and determined the viable seed content of the pellets by germination experiments. We found that herbivorous Microtus arvalis L. was the most abundant prey item through which most of the seeds spread. Owls dispersed the seeds of generalist and disturbancetolerant plants, indicating the habitat type where small mammals occur abundantly. In another experiment we tested the effect of the pellet material on the seedling survival and found that prey remains enhanced establishment of seedlings. Our study suggests that SSD by barn owl is occasional but important event in long-distance seed dispersal. Since the studied owl species uses several habitat types and has larger mobility than the rodents, the revealed dispersal mechanism can considerably increase seed dispersal distance and seed exchange between habitat types
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