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Katalin Varga - Academia.edu
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class="u-taCenter"></div><div class="profile--tab_content_container js-tab-pane tab-pane active" id="all"><div class="profile--tab_heading_container js-section-heading" data-section="Papers" id="Papers"><h3 class="profile--tab_heading_container">Papers by Katalin Varga</h3></div><div class="js-work-strip profile--work_container" data-work-id="126077850"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077850/Long_term_response_of_understorey_cover_basal_area_and_diversity_to_stand_density_in_a_mixed_oak_forest_on_the_S%C3%ADkf%C5%91k%C3%BAt_plot_in_Hungary"><img alt="Research paper thumbnail of Long-term response of understorey cover, basal area and diversity to stand density in a mixed oak forest on the Síkfőkút plot in Hungary" class="work-thumbnail" src="https://attachments.academia-assets.com/120010724/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077850/Long_term_response_of_understorey_cover_basal_area_and_diversity_to_stand_density_in_a_mixed_oak_forest_on_the_S%C3%ADkf%C5%91k%C3%BAt_plot_in_Hungary">Long-term response of understorey cover, basal area and diversity to stand density in a mixed oak forest on the Síkfőkút plot in Hungary</a></div><div class="wp-workCard_item"><span>Journal of Forest Science</span><span>, 2013</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The serious oak decline was reported for the 1979–80 period and 63.0% of adult oaks died in a mix...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The serious oak decline was reported for the 1979–80 period and 63.0% of adult oaks died in a mixed oak forest in the Síkfőkút site, Hungary. The data were used to obtain (1) quantitative information on diversity indices of shrub layer and shrub canopy, including foliage cover percentage of the shrub layer, mean cover of shrub species before and after the oak decline and (2) structural information on shrub basal area and shrub foliage arrangement. Since 1972 we have determined diversity indices, cover percentage and basal area of shrubby vegetation on the monitoring and plus plots. A negative relation was detected between Shannon-Wiener and Evenness indices of the shrub layer and living oak tree density. A positive relation was confirmed between basal area and mean cover of dominant woody species (Acer campestre, Acer tataricum and Cornus mas). The mean cover of shrub species except of A. campestre increased non-significantly after the oak decline on the 48 m × 48 m plot. The findin...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="71f055731ceb7acb7cf1a734895962b9" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010724,"asset_id":126077850,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010724/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077850"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077850"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077850; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="126077849"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077849/Reed_management_influences_philopatry_to_reed_habitats_in_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_"><img alt="Research paper thumbnail of Reed management influences philopatry to reed habitats in the Great Reed Warbler (Acrocephalus arundinaceus)" class="work-thumbnail" src="https://attachments.academia-assets.com/120010734/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077849/Reed_management_influences_philopatry_to_reed_habitats_in_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_">Reed management influences philopatry to reed habitats in the Great Reed Warbler (Acrocephalus arundinaceus)</a></div><div class="wp-workCard_item"><span>The Condor</span><span>, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Management of reed beds primarily includes controlling water levels and removing vegetation by mo...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Management of reed beds primarily includes controlling water levels and removing vegetation by mowing, burning, or grazing. Although recent studies have demonstrated increased diversity and abundance of wetland specialists after reed bed management, documenting demographic benefits to individual species would add additional support to the advantages of appropriate management. Here, we explore the effects of reed management on the philopatry of Great Reed Warblers (Acrocephalus arundinaceus) over 7 yr. Reed beds were managed in the winter by occasional burning at mining ponds and large canals, infrequent burning in marshes, and frequent mowing of small canals. Based on resightings and recaptures of 1,243 adult and 1,428 nestlings individually marked at 57 sites in 6 different reed habitats, we built Cormack-Jolly-Seber models to estimate the apparent annual survival and encounter probabilities of birds banded as nestlings or as adults. Apparent survival varied in time for both age groups and both sexes, suggesting annual fluctuations in survival, whereas encounter probability remained constant across years. The encounter probability of birds banded as juveniles was higher in reed beds with shallower water. The encounter probability of birds banded as adults was higher in reed beds with deeper water for females, and strongly increased with variation in reed management and less strongly with variation in water depth for males. We also found that the few returning juveniles displayed strong philopatry to the reed habitat occupied in their first breeding season. Our study provides evidence that reed management influences the return rates of juveniles and adult males and females in different ways. Spatially variable reed management by mowing or burning should be applied and water of varying depths should be maintained to maximize return rates of Great Reed Warblers.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5197a50998ed5166e4b8d8f36009a396" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010734,"asset_id":126077849,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010734/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077849"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077849"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077849; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="126077847"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077847/Wing_size_related_reed_habitat_selection_by_Great_Reed_Warbler_Acrocephalus_arundinaceus_males"><img alt="Research paper thumbnail of Wing size-related reed habitat selection by Great Reed Warbler (Acrocephalus arundinaceus) males" class="work-thumbnail" src="https://attachments.academia-assets.com/120010733/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077847/Wing_size_related_reed_habitat_selection_by_Great_Reed_Warbler_Acrocephalus_arundinaceus_males">Wing size-related reed habitat selection by Great Reed Warbler (Acrocephalus arundinaceus) males</a></div><div class="wp-workCard_item"><span>The Auk</span><span>, 2016</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">In this study we explored the linkage between wing size of Great Reed Warbler males (Acrocephalus...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">In this study we explored the linkage between wing size of Great Reed Warbler males (Acrocephalus arundinaceus) and their habitat selection and relate these linkages to differences in reed habitat quality. We measured the wing sizes of males nesting in 6 different reed habitats. To explain reed habitat selection, we modeled male wing size as a function of 7 predictor variables describing reedbeds: proportion of managed reed; densities of mixed, old, and fresh reed; reed stem diameter; water depth; and fluctuation of water level. Mean wing size was greatest for males at large canals, intermediate at mining ponds and smaller canals, and lowest at marshes and very small canals. The proportion of managed reed and fluctuation of water level were negatively related to wing size, and water depth was positively related to wing size, which suggests that males with larger wings preferred reed habitats with little management in deep water with little fluctuation in water level. We concluded that the availability of stable, deep water and lack of management are primarily important in attracting larger-winged (presumably dominant) males.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="0d1bf5e04da0d87569fd6373172cccb0" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010733,"asset_id":126077847,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010733/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077847"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077847"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077847; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="126077802"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077802/Wing_size_related_habitat_choice_of_Great_Reed_Warbler_females_the_role_of_habitat_quality_and_management"><img alt="Research paper thumbnail of Wing-size related habitat choice of Great Reed Warbler females: the role of habitat quality and management" class="work-thumbnail" src="https://attachments.academia-assets.com/120010714/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077802/Wing_size_related_habitat_choice_of_Great_Reed_Warbler_females_the_role_of_habitat_quality_and_management">Wing-size related habitat choice of Great Reed Warbler females: the role of habitat quality and management</a></div><div class="wp-workCard_item"><span>Avian Conservation and Ecology</span><span>, 2020</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Intersexual differences in habitat choice can arise if males and females differ in morphology, ph...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Intersexual differences in habitat choice can arise if males and females differ in morphology, physiology, niche partitioning, or resource use, and can be influenced by variation in habitat structure, quality, and management. To better understand such intersexual differences, we studied habitat choice in female Great Reed Warblers (Acrocephalus arundinaceus), a long-distance migrant flagship species of lowland Palearctic reed (Phragmites australis) habitats. We compared wing length, a widely used proxy for individual quality in passerines, of females nesting in six types of differently managed reed habitats. Our dataset on 391 females nesting in 32 sites over 10 years showed that wing length was significantly greater in mining ponds and medium-sized canals than on large canals. Wing length was negatively related to water level fluctuation and females showed strong philopatry to the habitat type in which they were first captured. In comparison to our previous study on male habitat choice, this study found differences in habitat choice between the sexes. Although long-winged individuals in both sexes preferred habitats with stable water and avoided small canals, longer-winged males preferred large canals with little or no management, whereas long-winged females preferred medium-sized canals with some management. Although these results provide some support for intersexual niche segregation, it is also possible that long-winged females avoid large canals, in which nest parasitism by Cuckoos (Cuculus canorus) is frequent, and/or prefer managed, sparse reed beds with better maneuverability for foraging. Our studies suggest that males may primarily choose habitats with abundant old reed and singing perches, whereas females are less sensitive to environmental variation and may choose nest sites based on male quality or territory quality. For conservation, our studies imply that the maintenance of stable water levels, a low intensity of management and the elimination of Cuckoo perches are likely to benefit both long-winged males and females. Sélection d'habitat lié à la longueur de l'aile chez les Rousserolles turdoïdes femelles : le rôle de la qualité de l'habitat et de l'aménagement RÉSUMÉ. Des différences dans la sélection d'habitat liées au sexe peuvent s'observer si les mâles et les femelles diffèrent en termes de morphologie, de physiologie, de différenciation de niche ou d'utilisation des ressources, et peuvent être influencées par la variation de structure, de qualité et de l'aménagement de l'habitat. Pour mieux comprendre ce type de différences intersexuelles, nous avons étudié la sélection d'habitat chez la femelle Rousserolle turdoïde (Acrocephalus arundinaceus), espèce-phare migratrice de longue distance occupant des milieux paléarctiques de basses terres dominées par le roseau (Phragmites australis). Nous avons comparé la longueur de l'aile, un indicateur très utilisé pour attester de la qualité individuelle des passereaux, de femelles nichant dans six types de milieux de roseaux aménagés de façon différente. Notre jeu de données, comportant 391 femelles nicheuses à 32 sites sur une période de 10 ans, a révélé que la longueur de l'aile était considérablement plus grande chez les femelles occupant les étangs miniers et les canaux de largeur moyenne, comparativement à celles occupant les grands canaux. La longueur de l'aile était négativement liée aux fluctuations du niveau d'eau et les femelles ont montré une forte philopatrie au type de milieu dans lequel elles avaient été capturées la première fois. Comparativement à notre étude précédente portant sur la sélection d'habitat chez les mâles, la présente étude a fait état de différences selon le sexe dans la sélection d'habitat. Même si les individus aux longues ailes chez les deux sexes ont préféré les milieux montrant un niveau d'eau stable et évité les petits canaux, les mâles aux ailes plus longues ont préféré les grands canaux peu ou non aménagés, tandis que les femelles aux ailes longues ont préféré les moyens canaux un peu aménagés. Bien que ces résultats corroborent jusqu'à un certain point une différenciation de niche fondée sur le sexe, il est aussi possible que les femelles aux longues ailes évitent les canaux larges, dans lesquels le parasitisme de nids par les coucous (Cuculus canorus) est fréquent, et/ou préfèrent les îlots de roseaux épars et aménagés, qui permettent de manoeuvrer plus facilement pour chercher la nourriture. Nos études laissent croire que les mâles sélectionnent peutêtre d'abord les milieux comprenant de nombreux vieux roseaux et des perchoirs desquels chanter, tandis que les femelles sont moins sensibles aux variations environnementales et sélectionnent sans doute des sites de nidification en fonction de la qualité du mâle ou du territoire. Aux fins de conservation, nous études indiquent que le maintien d'un niveau d'eau stable, l'aménagement à faible intensité et l'élimination des perchoirs de coucous sont vraisemblablement susceptibles de profiter tant aux mâles qu'aux femelles aux longues ailes.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="9d7423174e35d085e26c62bcf8dc74c6" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010714,"asset_id":126077802,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010714/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077802"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077802"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077802; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794472"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794472/Habitat_use_and_nesting_success_of_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_in_different_reed_habitats_in_Serbia"><img alt="Research paper thumbnail of Habitat use and nesting success of the Great Reed Warbler (Acrocephalus arundinaceus) in different reed habitats in Serbia" class="work-thumbnail" src="https://attachments.academia-assets.com/97153825/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794472/Habitat_use_and_nesting_success_of_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_in_different_reed_habitats_in_Serbia">Habitat use and nesting success of the Great Reed Warbler (Acrocephalus arundinaceus) in different reed habitats in Serbia</a></div><div class="wp-workCard_item"><span>The Wilson Journal of Ornithology</span><span>, 2015</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">We surveyed five reed habitats (mining pond, sand pit, large canal, small canal and lowland river...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">We surveyed five reed habitats (mining pond, sand pit, large canal, small canal and lowland river) in northwestern Vojvodina (Serbia) between 2009-2011 to study habitat use and to estimate nest success in an understudied region of the breeding range of the Great Reed Warbler (Acrocephalus arundinaceus). Data from 174 nests showed that habitat use differed considerably between the habitat types, but was not related to the area of the study site or the reed bed. Higher-than-expected numbers of nests along the small canal and the river suggested that Great Reed Warblers preferred these to other habitats for nesting. Habitat use was closely linked to the availability of reed edges and the quality of the reed stand. Overall Mayfield nest success was 43%, slightly lower than in northern and western Europe. Nest success was low along the small and large canal, where brood parasitism by Common Cuckoos (Cuculus canorus) and nest predation were high due to nearby tree lines providing perching sites to cuckoos and predators. Nest success was intermediate at the mining pond due to very high predation pressure and adverse weather, and nest success was highest in the sand pit (despite high Cuckoo parasitism) and the river (despite relatively high predation). In conclusion, our results suggest that canals can function as ecological traps, which attract edge-preferring Great Reed Warblers but are highly accessible to predators and brood parasites. In contrast, sand pits can be perceptual traps because they provide good resources for nesting but were less attractive to Great Reed Warblers than other habitats. Habitat use in relation to habitat availability thus depends primarily on the availability of reed edges and the quality of the reed stand, whereas nest success also depends on the characteristics of the surroundings and weather conditions.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="8a8698450cd6892fc537010971a053e3" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153825,"asset_id":94794472,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153825/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794472"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794472"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794472; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794471"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794471/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond"><img alt="Research paper thumbnail of Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond" class="work-thumbnail" src="https://attachments.academia-assets.com/97153840/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794471/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond">Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond</a></div><div class="wp-workCard_item"><span>TURKISH JOURNAL OF ZOOLOGY</span><span>, 2014</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Báldi (2001) studied how inundation affected the local breeding passerines at the Kis-Balaton wet...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Báldi (2001) studied how inundation affected the local breeding passerines at the Kis-Balaton wetland. He collected observations in 3 groups (before, immediately after, and years after inundation) and quantified the changes in community structure parameters, community composition, differences between areas and periods, and species and abundances. Savi's Warbler, Locustella luscinioides, declined immediately after inundation, while Reed Bunting, Emberiza schoeniclus, and Sedge Warbler, Acrocephalus schoenobaenus, declined in the long term. However, the Great Reed Warbler (GRW), Acrocephalus arundinaceus, was the only species with a continuous increasing trend. Vadász et al. (2008) reported that the cutting of reed negatively influenced species richness and the abundance of reed passerines on Lake Kolon in Central Hungary. Savi's Warbler, Moustached Warbler Acrocephalus melanopogon, Sedge Warbler, and Reed Warbler Acrocephalus scirpaceus especially avoided cut areas, while GRW did not (Vadász et al., 2008). Báldi and Moskát (1995) and Moga et al. (2010) recorded the presence of GRW in unmanaged, burned, and mowed reed stands. Despite these sporadic observations, our knowledge about the effects of reed management and environmental factors on the breeding success of GRW is weak. Nests of small open-nesting birds are often difficult to detect in the early stages of the breeding season (Mayfield, 1975). Due to the lack of information for the period before nests are found, estimates of mortality, survival, and breeding success can be severely biased. Mayfield (1975) developed a method for estimating breeding success that reduced potential sources of error. The proposed Mayfield estimator has been further recognized as a maximum likelihood estimator (MLE). The asymptotic distribution of the MLE has been calculated, which provides a measure of asymptotic variance (Hensler and Nichols, 1981). MLE and variance can be used to test the significance of daily survival (Hensler and Nichols, 1981). Lloyd and</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="c993a6f41c7f0241284b1cae16b778ed" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153840,"asset_id":94794471,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153840/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794471"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794471"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794471; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794470"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794470/Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW_Vojvodina_Serbia"><img alt="Research paper thumbnail of Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW Vojvodina, Serbia" class="work-thumbnail" src="https://attachments.academia-assets.com/97153824/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794470/Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW_Vojvodina_Serbia">Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW Vojvodina, Serbia</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e. g. clay pits, marsh and fishponds, small canals and large canals) in northwestern Vojvodina (Serbia) between 2009 and 2011 (three breeding seasons). A total of 596 Great Reed Warbler (Acrocephalus arundinaceus) nests were found and monitored. The overall parasitism rate for the study area was 0.127, which was calculated from the number of parasitized nests (76) divided by the total number of Great Reed Warbler nests (596). The parasitism rate did not vary with the total number of Great Reed Warbler nests at a study site. The number of parasitized and successful parasitized nests showed significant negative relationship, which means more parasitized nests resulted with more brood lost. The parasitism rate varied significantly among habitats but not among years while the number of successfully parasitized nests differed among both habitats and years. Parasitized nests found in small and large canals showed the highest reproductive success of Cuckoos. Loss of parasitized nests through predation and bad weather circumstances was relatively high in this study compared to other areas.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5d9e1e5c24e98b0bb95a6dec8721b911" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153824,"asset_id":94794470,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153824/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794470"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794470"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794470; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794469"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794469/Improved_land_cover_mapping_using_aerial_photographs_and_satellite_images"><img alt="Research paper thumbnail of Improved land cover mapping using aerial photographs and satellite images" class="work-thumbnail" src="https://attachments.academia-assets.com/97153826/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794469/Improved_land_cover_mapping_using_aerial_photographs_and_satellite_images">Improved land cover mapping using aerial photographs and satellite images</a></div><div class="wp-workCard_item"><span>Open Geosciences</span><span>, 2014</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Manual Land Cover Mapping using aerial photographs provides sufficient level of resolution for de...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Manual Land Cover Mapping using aerial photographs provides sufficient level of resolution for detailed vegetation or land cover maps. However, in some cases it is not possible to achieve the desired information over large areas, for example from historical data where the quality and amount of available images is definitely lower than from modern data. The use of automated and semiautomated methods offers the means to identify the vegetation cover using remotely sensed data. In this paper automated methods were tested on aerial photographs and satellite images to extract better and more reliable information about vegetation cover. These testswere performed by using automated analysis of LANDSAT7 images (with and without the surface model of the Shuttle Radar Topography Mission (SRTM)) and two temporally similar aerial photographs. The spectral bands were analyzed with supervised (maximum likelihood) methods. In conclusion, the SRTM and the combination of two temporally similar aeria...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="3b14662d8daffa8c5bd1145700c6b875" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153826,"asset_id":94794469,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153826/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794469"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794469"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794469; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "3b14662d8daffa8c5bd1145700c6b875" } } $('.js-work-strip[data-work-id=94794469]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":94794469,"title":"Improved land cover mapping using aerial photographs and satellite images","internal_url":"https://www.academia.edu/94794469/Improved_land_cover_mapping_using_aerial_photographs_and_satellite_images","owner_id":36347448,"coauthors_can_edit":true,"owner":{"id":36347448,"first_name":"Katalin","middle_initials":null,"last_name":"Varga","page_name":"KatalinVarga2","domain_name":"independent","created_at":"2015-10-16T06:43:49.681-07:00","display_name":"Katalin Varga","url":"https://independent.academia.edu/KatalinVarga2"},"attachments":[{"id":97153826,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/97153826/thumbnails/1.jpg","file_name":"10.1515_geo-2015-0002.pdf","download_url":"https://www.academia.edu/attachments/97153826/download_file","bulk_download_file_name":"Improved_land_cover_mapping_using_aerial.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/97153826/10.1515_geo-2015-0002-libre.pdf?1673478360=\u0026response-content-disposition=attachment%3B+filename%3DImproved_land_cover_mapping_using_aerial.pdf\u0026Expires=1741042744\u0026Signature=gKAWpYQNI32iDqjkPgGWHoCX3xf9WL5h97cfV4Pho4g6-HD8jckx23b-b4qvZCL~veJk~PObN6~Se7MDovU~lMGIwQMXr5tNI9ITZ1E2IydoQcj8MoPItQnEvGFp~Ps4lk6rkhd0xhto3EHITyAdCLYkS1MHTB8vfNJCNAtIbY-t7D50KYf1IyapUVrAc-V3GiznTZNJTaASP5l6jSTwRVL2lZGaaRfoPp6dYwFt-JB0xPDsh4a44PpMyp6VGtZCxpJflXgRWFcWVCgL8i4UMKVALbkX9LYOP7kFGdWUQZZlk-AnWoWiv8zAGx1PkNMUD1dNEUHr77h02hKJ5z5XYA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794468"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794468/Grassland_restoration_to_conserve_landscape_level_biodiversity_a_synthesis_of_early_results_from_a_large_scale_project"><img alt="Research paper thumbnail of Grassland restoration to conserve landscape-level biodiversity: a synthesis of early results from a large-scale project" class="work-thumbnail" src="https://attachments.academia-assets.com/97153827/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794468/Grassland_restoration_to_conserve_landscape_level_biodiversity_a_synthesis_of_early_results_from_a_large_scale_project">Grassland restoration to conserve landscape-level biodiversity: a synthesis of early results from a large-scale project</a></div><div class="wp-workCard_item"><span>Applied Vegetation Science</span><span>, 2012</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Question: European landscapes have long been influenced by intensifying use by humans. Although h...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Question: European landscapes have long been influenced by intensifying use by humans. Although habitat restoration can reverse this process, it is often limited in scope by socioeconomic constraints. Here we present a grassland restoration project that is exceptional in spatial scale in Europe. Location: A total area of 760 ha of arable land was restored in the Egyek-Pusztakó cs unit (50 km 2) of Hortobágy National Park, east Hungary, between 2005 and 2008. Methods: Restoration targeted alkali steppes and loess grasslands by sowing seeds of either two (alkali) or three (loess) foundation grass species. In 2009, we surveyed the vegetation in restored and target grasslands and quantified the factors influencing restoration success in a space-for-time substitution design. Results: We recorded 100 species of flowering plants, of which 37 species were non-weed, 'target' species. Annual weeds dominated 1-yr-old fields but had decreased dramatically by the third year due to a developing perennial grass cover. Former alfalfa fields had proportionally fewer weeds than former cereal and sunflower fields. The diversity of common species and the cover of target species increased from 1-to 4-yr-old restored fields. Alkali-restored fields had more heterogeneous vegetation and more species than loess-restored fields. Distance to the target vegetation did not directly affect vegetation variables. There was significant spatial variability in vegetation development, possibly suggesting several local pathways of succession. Conclusions: Grassland restoration was generally successful in accelerating secondary succession towards alkali steppes and loess grasslands. However, further management is necessary to counter the homogenizing effects of litter accumulation, to reduce perennial weeds and to enhance the colonization of target species. Our project provides useful practical insights into grassland restoration and in applying restoration at a number of sites within a larger area to conserve biodiversity at the landscape scale.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5923031315cbe267600a932aa1aefabe" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153827,"asset_id":94794468,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153827/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794468"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794468"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794468; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794357"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794357/Nest_site_characteristics_and_breeding_density_of_Magpie_Pica_pica_in_Sombor_NW_Serbia_"><img alt="Research paper thumbnail of Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia)" class="work-thumbnail" src="https://attachments.academia-assets.com/97153804/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794357/Nest_site_characteristics_and_breeding_density_of_Magpie_Pica_pica_in_Sombor_NW_Serbia_">Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia)</a></div><div class="wp-workCard_item"><span>Acrocephalus</span><span>, 2010</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia) In March...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia) In March 2009, active Magpie Pica pica nests were censused in the town of Sombor (Vojvodina, NW Serbia) to study nest-site characteristics, breeding density and spatial distribution. The area of the town can be divided into two parts according to different urban landscapes, i.e. the town centre (150 ha) and the residential area (2,224 ha). In total, 222 Magpie nests were found and their height, tree species and nest-site type determined. Nests were found in 25 tree and two shrub species, the most of them (31.1%) being placed in the commonest tree species in the town, the Common Hackberry Celtis occidentalis. The majority of the nests were found in tree avenues (39.6%) and groups of trees (31.5%). Nests in the town centre with a mean height (± SD) of 15.2 ± 4.05 m were significantly higher than those in the residential area with a mean height (± SD) of 11.4 ± 5.13 m. The mean distance of nests fr...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="66169ab9d61c6b3e85eccd8705ed9d66" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153804,"asset_id":94794357,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153804/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794357"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794357"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794357; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="16874617"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/16874617/Early_changes_of_orthopteran_assemblages_after_grassland_restoration_a_comparison_of_space_for_time_substitution_versus_repeated_measures_monitoring"><img alt="Research paper thumbnail of Early changes of orthopteran assemblages after grassland restoration: a comparison of space-for-time substitution versus repeated measures monitoring" class="work-thumbnail" src="https://attachments.academia-assets.com/39231692/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/16874617/Early_changes_of_orthopteran_assemblages_after_grassland_restoration_a_comparison_of_space_for_time_substitution_versus_repeated_measures_monitoring">Early changes of orthopteran assemblages after grassland restoration: a comparison of space-for-time substitution versus repeated measures monitoring</a></div><div class="wp-workCard_item"><span>Biodiversity and Conservation</span><span>, 2013</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Although grasslands harbour significant biodiversity and their restoration is common in 26 biodiv...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Although grasslands harbour significant biodiversity and their restoration is common in 26 biodiversity conservation, we know very little about how such interventions influence arthropod 27 groups. Here we compared orthopteran assemblages in croplands, natural grasslands and one to 28 four-year-old grasslands restored in a large-scale programme in Hortobágy National Park (East 29 Hungary). We sampled orthopterans by standardized sweep-netting both in a repeated measures 30 design from year 0 (croplands) to 4 and in a space-for-time substitution (chronosequence) design 31 in 2009. Species richness, abundance and Shannon diversity of orthopterans decreased in year 1 32 following restoration, but increased afterwards. By year 4, species richness doubled and 33 abundance increased almost ten-fold in restored grasslands compared to croplands. Species 34 composition diversified compared to croplands and progressed towards natural grasslands. Local 35 restoration conditions (last crop, seed mixture) and landscape configuration (proportion of 36 natural grasslands) did not influence the above patterns in either study design, whereas time 37 since restoration affected almost all community variables. We found that ubiquitous generalist 38 species were the first to appear in restored grasslands and that species characteristic to the target 39 natural grasslands colonised gradually in later years. The qualitative and quantitative properties 40 of the orthopteran assemblages in restored fields did not yet reach those of natural grasslands, 41 therefore, our study suggests that the full regeneration of the orthopteran assemblages takes more 42 than four years. We also concluded that the repeated-measures design was more sensitive to 43 subtle changes and was thus more effective than the chronosequence design at detecting post-44 restoration changes in orthopteran assemblages. 45 46 47 3</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="30e917ba2d2711996e4e7c5cfdf04ccb" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":39231692,"asset_id":16874617,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/39231692/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="16874617"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="16874617"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 16874617; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "30e917ba2d2711996e4e7c5cfdf04ccb" } } $('.js-work-strip[data-work-id=16874617]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":16874617,"title":"Early changes of orthopteran assemblages after grassland restoration: a comparison of space-for-time substitution versus repeated measures monitoring","internal_url":"https://www.academia.edu/16874617/Early_changes_of_orthopteran_assemblages_after_grassland_restoration_a_comparison_of_space_for_time_substitution_versus_repeated_measures_monitoring","owner_id":36347448,"coauthors_can_edit":true,"owner":{"id":36347448,"first_name":"Katalin","middle_initials":null,"last_name":"Varga","page_name":"KatalinVarga2","domain_name":"independent","created_at":"2015-10-16T06:43:49.681-07:00","display_name":"Katalin Varga","url":"https://independent.academia.edu/KatalinVarga2"},"attachments":[{"id":39231692,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/39231692/thumbnails/1.jpg","file_name":"02e7e517be17596190000000.pdf","download_url":"https://www.academia.edu/attachments/39231692/download_file","bulk_download_file_name":"Early_changes_of_orthopteran_assemblages.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/39231692/02e7e517be17596190000000-libre.pdf?1445003129=\u0026response-content-disposition=attachment%3B+filename%3DEarly_changes_of_orthopteran_assemblages.pdf\u0026Expires=1741042744\u0026Signature=EIWyGn6B06ANrkycnLv4QlLF3n3gySHANHuIgWvcEvza4BURv6KaMDfG7O8LjbcUrqvAqARvjBANz6DK5dP6fBOScyzGAH8h82w2ZPGAgR0dUSEKMbSUgVBNceJeUghUYJ7vZTL~d5sybDoBxxHG0T68tTqlruQi2G7F1YrJNY8kBCf1vuUeXlyncSd9hG6uScGHRjfWfd0HOs6mfJc5VurozfKaj4Xzg7r3II~E289ffGDksnE0uvtoKSzXeHBOtnWeJ7hc8GeHHNNBixPNZcnigH5FoqJMymY1wuZoPaLCv6SL~RGrj4zpJ8iXfM5WcW63yrxjoXeFSJx1IXaf7A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="6183746"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/6183746/original_scientific_paper_izvorni_znanstveni_rad_BREEDING_OF_THE_BROOD_PARASITIC_COMMON_CUCKOO_CUCULUS_CANORUS_IN_REED_HABITATS_IN_NW_VOJVODINA_SERBIA_Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW"><img alt="Research paper thumbnail of original scientific paper/izvorni znanstveni rad BREEDING OF THE BROOD PARASITIC COMMON CUCKOO (CUCULUS CANORUS) IN REED HABITATS IN NW VOJVODINA, SERBIA: Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW" class="work-thumbnail" src="https://attachments.academia-assets.com/33065667/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/6183746/original_scientific_paper_izvorni_znanstveni_rad_BREEDING_OF_THE_BROOD_PARASITIC_COMMON_CUCKOO_CUCULUS_CANORUS_IN_REED_HABITATS_IN_NW_VOJVODINA_SERBIA_Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW">original scientific paper/izvorni znanstveni rad BREEDING OF THE BROOD PARASITIC COMMON CUCKOO (CUCULUS CANORUS) IN REED HABITATS IN NW VOJVODINA, SERBIA: Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/KatalinVarga2">Katalin Varga</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://unideb.academia.edu/ThomasOliverM%C3%A9r%C5%91">Thomas Oliver Mérő</a>, and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/AntunZuljevic">Antun Zuljevic</a></span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e. g. clay pits, marsh and fishponds, small canals and large canals) in northwestern Vojvodina (Serbia) between 2009 and 2011 (three breeding seasons). A total of 596 Great Reed Warbler (Acrocephalus arundinaceus) nests were found and monitored. The overall parasitism rate for the study area was 0.127, which was calculated from the number of parasitized nests (76) divided by the total number of Great Reed Warbler nests (596). The parasitism rate did not vary with the total number of Great Reed Warbler nests at a study site. The number of parasitized and successful parasitized nests showed significant negative relationship, which means more parasitized nests resulted with more brood lost. The parasitism rate varied significantly among habitats but not among years while the number of successfully parasitized nests differed among both habitats and years. Parasitized nests found in small and large canals showed the highest reproductive success of Cuckoos. Loss of parasitized nests through predation and bad weather circumstances was relatively high in this study compared to other areas.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="60ae0a8e7be2a468b9049fb4b780b5ae" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":33065667,"asset_id":6183746,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/33065667/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="6183746"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="6183746"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 6183746; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="9916187"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/9916187/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond"><img alt="Research paper thumbnail of Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond" class="work-thumbnail" src="https://attachments.academia-assets.com/36070423/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/9916187/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond">Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/Ren%C3%A1taBocz">Renáta Bocz</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://unideb.academia.edu/ThomasOliverM%C3%A9r%C5%91">Thomas Oliver Mérő</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/KatalinVarga2">Katalin Varga</a>, and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/AntunZuljevic">Antun Zuljevic</a></span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">In this study, we present the effects of reed burning and precipitation on the breeding success o...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">In this study, we present the effects of reed burning and precipitation on the breeding success of Great Reed Warblers on a mining pond (2008–2011). Breeding success, i.e. the probability that an egg would produce a fledgling, was 0.43. Clutch survival was lowest in 2010, due to the precipitation and high water level during the season. Breeding success was higher in the second half of the breeding season, although in 2008 and 2011 precipitation was also higher in the second half than in the first half of the breeding season. During the first half of the breeding season, daily egg and nestling survival did not differ. However, in the second half of the breeding season, daily egg survival was higher than daily chick survival. In years when reed was burned, breeding density varied between 7.7 and 12.3 pairs ha–1, which was not significantly lower than in years when reed was not managed (average: 13.2 pairs ha–1). Despite the<br />availability of fresh reed in large areas, birds placed their nests mainly in mixed reed stands. Breeding success in fresh and mixed reed did not differ. Generally, breeding success and density were not affected by reed burning, but water level affected breeding success and density.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="e29f0d0d0af7729c99833ef61d20cad3" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":36070423,"asset_id":9916187,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/36070423/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="9916187"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="9916187"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 9916187; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="3765826" id="papers"><div class="js-work-strip profile--work_container" data-work-id="126077850"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077850/Long_term_response_of_understorey_cover_basal_area_and_diversity_to_stand_density_in_a_mixed_oak_forest_on_the_S%C3%ADkf%C5%91k%C3%BAt_plot_in_Hungary"><img alt="Research paper thumbnail of Long-term response of understorey cover, basal area and diversity to stand density in a mixed oak forest on the Síkfőkút plot in Hungary" class="work-thumbnail" src="https://attachments.academia-assets.com/120010724/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077850/Long_term_response_of_understorey_cover_basal_area_and_diversity_to_stand_density_in_a_mixed_oak_forest_on_the_S%C3%ADkf%C5%91k%C3%BAt_plot_in_Hungary">Long-term response of understorey cover, basal area and diversity to stand density in a mixed oak forest on the Síkfőkút plot in Hungary</a></div><div class="wp-workCard_item"><span>Journal of Forest Science</span><span>, 2013</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The serious oak decline was reported for the 1979–80 period and 63.0% of adult oaks died in a mix...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The serious oak decline was reported for the 1979–80 period and 63.0% of adult oaks died in a mixed oak forest in the Síkfőkút site, Hungary. The data were used to obtain (1) quantitative information on diversity indices of shrub layer and shrub canopy, including foliage cover percentage of the shrub layer, mean cover of shrub species before and after the oak decline and (2) structural information on shrub basal area and shrub foliage arrangement. Since 1972 we have determined diversity indices, cover percentage and basal area of shrubby vegetation on the monitoring and plus plots. A negative relation was detected between Shannon-Wiener and Evenness indices of the shrub layer and living oak tree density. A positive relation was confirmed between basal area and mean cover of dominant woody species (Acer campestre, Acer tataricum and Cornus mas). The mean cover of shrub species except of A. campestre increased non-significantly after the oak decline on the 48 m × 48 m plot. The findin...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="71f055731ceb7acb7cf1a734895962b9" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010724,"asset_id":126077850,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010724/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077850"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077850"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077850; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="126077849"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077849/Reed_management_influences_philopatry_to_reed_habitats_in_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_"><img alt="Research paper thumbnail of Reed management influences philopatry to reed habitats in the Great Reed Warbler (Acrocephalus arundinaceus)" class="work-thumbnail" src="https://attachments.academia-assets.com/120010734/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077849/Reed_management_influences_philopatry_to_reed_habitats_in_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_">Reed management influences philopatry to reed habitats in the Great Reed Warbler (Acrocephalus arundinaceus)</a></div><div class="wp-workCard_item"><span>The Condor</span><span>, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Management of reed beds primarily includes controlling water levels and removing vegetation by mo...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Management of reed beds primarily includes controlling water levels and removing vegetation by mowing, burning, or grazing. Although recent studies have demonstrated increased diversity and abundance of wetland specialists after reed bed management, documenting demographic benefits to individual species would add additional support to the advantages of appropriate management. Here, we explore the effects of reed management on the philopatry of Great Reed Warblers (Acrocephalus arundinaceus) over 7 yr. Reed beds were managed in the winter by occasional burning at mining ponds and large canals, infrequent burning in marshes, and frequent mowing of small canals. Based on resightings and recaptures of 1,243 adult and 1,428 nestlings individually marked at 57 sites in 6 different reed habitats, we built Cormack-Jolly-Seber models to estimate the apparent annual survival and encounter probabilities of birds banded as nestlings or as adults. Apparent survival varied in time for both age groups and both sexes, suggesting annual fluctuations in survival, whereas encounter probability remained constant across years. The encounter probability of birds banded as juveniles was higher in reed beds with shallower water. The encounter probability of birds banded as adults was higher in reed beds with deeper water for females, and strongly increased with variation in reed management and less strongly with variation in water depth for males. We also found that the few returning juveniles displayed strong philopatry to the reed habitat occupied in their first breeding season. Our study provides evidence that reed management influences the return rates of juveniles and adult males and females in different ways. Spatially variable reed management by mowing or burning should be applied and water of varying depths should be maintained to maximize return rates of Great Reed Warblers.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5197a50998ed5166e4b8d8f36009a396" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010734,"asset_id":126077849,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010734/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077849"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077849"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077849; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="126077847"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077847/Wing_size_related_reed_habitat_selection_by_Great_Reed_Warbler_Acrocephalus_arundinaceus_males"><img alt="Research paper thumbnail of Wing size-related reed habitat selection by Great Reed Warbler (Acrocephalus arundinaceus) males" class="work-thumbnail" src="https://attachments.academia-assets.com/120010733/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077847/Wing_size_related_reed_habitat_selection_by_Great_Reed_Warbler_Acrocephalus_arundinaceus_males">Wing size-related reed habitat selection by Great Reed Warbler (Acrocephalus arundinaceus) males</a></div><div class="wp-workCard_item"><span>The Auk</span><span>, 2016</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">In this study we explored the linkage between wing size of Great Reed Warbler males (Acrocephalus...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">In this study we explored the linkage between wing size of Great Reed Warbler males (Acrocephalus arundinaceus) and their habitat selection and relate these linkages to differences in reed habitat quality. We measured the wing sizes of males nesting in 6 different reed habitats. To explain reed habitat selection, we modeled male wing size as a function of 7 predictor variables describing reedbeds: proportion of managed reed; densities of mixed, old, and fresh reed; reed stem diameter; water depth; and fluctuation of water level. Mean wing size was greatest for males at large canals, intermediate at mining ponds and smaller canals, and lowest at marshes and very small canals. The proportion of managed reed and fluctuation of water level were negatively related to wing size, and water depth was positively related to wing size, which suggests that males with larger wings preferred reed habitats with little management in deep water with little fluctuation in water level. We concluded that the availability of stable, deep water and lack of management are primarily important in attracting larger-winged (presumably dominant) males.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="0d1bf5e04da0d87569fd6373172cccb0" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010733,"asset_id":126077847,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010733/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077847"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077847"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077847; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="126077802"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/126077802/Wing_size_related_habitat_choice_of_Great_Reed_Warbler_females_the_role_of_habitat_quality_and_management"><img alt="Research paper thumbnail of Wing-size related habitat choice of Great Reed Warbler females: the role of habitat quality and management" class="work-thumbnail" src="https://attachments.academia-assets.com/120010714/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/126077802/Wing_size_related_habitat_choice_of_Great_Reed_Warbler_females_the_role_of_habitat_quality_and_management">Wing-size related habitat choice of Great Reed Warbler females: the role of habitat quality and management</a></div><div class="wp-workCard_item"><span>Avian Conservation and Ecology</span><span>, 2020</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Intersexual differences in habitat choice can arise if males and females differ in morphology, ph...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Intersexual differences in habitat choice can arise if males and females differ in morphology, physiology, niche partitioning, or resource use, and can be influenced by variation in habitat structure, quality, and management. To better understand such intersexual differences, we studied habitat choice in female Great Reed Warblers (Acrocephalus arundinaceus), a long-distance migrant flagship species of lowland Palearctic reed (Phragmites australis) habitats. We compared wing length, a widely used proxy for individual quality in passerines, of females nesting in six types of differently managed reed habitats. Our dataset on 391 females nesting in 32 sites over 10 years showed that wing length was significantly greater in mining ponds and medium-sized canals than on large canals. Wing length was negatively related to water level fluctuation and females showed strong philopatry to the habitat type in which they were first captured. In comparison to our previous study on male habitat choice, this study found differences in habitat choice between the sexes. Although long-winged individuals in both sexes preferred habitats with stable water and avoided small canals, longer-winged males preferred large canals with little or no management, whereas long-winged females preferred medium-sized canals with some management. Although these results provide some support for intersexual niche segregation, it is also possible that long-winged females avoid large canals, in which nest parasitism by Cuckoos (Cuculus canorus) is frequent, and/or prefer managed, sparse reed beds with better maneuverability for foraging. Our studies suggest that males may primarily choose habitats with abundant old reed and singing perches, whereas females are less sensitive to environmental variation and may choose nest sites based on male quality or territory quality. For conservation, our studies imply that the maintenance of stable water levels, a low intensity of management and the elimination of Cuckoo perches are likely to benefit both long-winged males and females. Sélection d'habitat lié à la longueur de l'aile chez les Rousserolles turdoïdes femelles : le rôle de la qualité de l'habitat et de l'aménagement RÉSUMÉ. Des différences dans la sélection d'habitat liées au sexe peuvent s'observer si les mâles et les femelles diffèrent en termes de morphologie, de physiologie, de différenciation de niche ou d'utilisation des ressources, et peuvent être influencées par la variation de structure, de qualité et de l'aménagement de l'habitat. Pour mieux comprendre ce type de différences intersexuelles, nous avons étudié la sélection d'habitat chez la femelle Rousserolle turdoïde (Acrocephalus arundinaceus), espèce-phare migratrice de longue distance occupant des milieux paléarctiques de basses terres dominées par le roseau (Phragmites australis). Nous avons comparé la longueur de l'aile, un indicateur très utilisé pour attester de la qualité individuelle des passereaux, de femelles nichant dans six types de milieux de roseaux aménagés de façon différente. Notre jeu de données, comportant 391 femelles nicheuses à 32 sites sur une période de 10 ans, a révélé que la longueur de l'aile était considérablement plus grande chez les femelles occupant les étangs miniers et les canaux de largeur moyenne, comparativement à celles occupant les grands canaux. La longueur de l'aile était négativement liée aux fluctuations du niveau d'eau et les femelles ont montré une forte philopatrie au type de milieu dans lequel elles avaient été capturées la première fois. Comparativement à notre étude précédente portant sur la sélection d'habitat chez les mâles, la présente étude a fait état de différences selon le sexe dans la sélection d'habitat. Même si les individus aux longues ailes chez les deux sexes ont préféré les milieux montrant un niveau d'eau stable et évité les petits canaux, les mâles aux ailes plus longues ont préféré les grands canaux peu ou non aménagés, tandis que les femelles aux ailes longues ont préféré les moyens canaux un peu aménagés. Bien que ces résultats corroborent jusqu'à un certain point une différenciation de niche fondée sur le sexe, il est aussi possible que les femelles aux longues ailes évitent les canaux larges, dans lesquels le parasitisme de nids par les coucous (Cuculus canorus) est fréquent, et/ou préfèrent les îlots de roseaux épars et aménagés, qui permettent de manoeuvrer plus facilement pour chercher la nourriture. Nos études laissent croire que les mâles sélectionnent peutêtre d'abord les milieux comprenant de nombreux vieux roseaux et des perchoirs desquels chanter, tandis que les femelles sont moins sensibles aux variations environnementales et sélectionnent sans doute des sites de nidification en fonction de la qualité du mâle ou du territoire. Aux fins de conservation, nous études indiquent que le maintien d'un niveau d'eau stable, l'aménagement à faible intensité et l'élimination des perchoirs de coucous sont vraisemblablement susceptibles de profiter tant aux mâles qu'aux femelles aux longues ailes.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="9d7423174e35d085e26c62bcf8dc74c6" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":120010714,"asset_id":126077802,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/120010714/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="126077802"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="126077802"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 126077802; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794472"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794472/Habitat_use_and_nesting_success_of_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_in_different_reed_habitats_in_Serbia"><img alt="Research paper thumbnail of Habitat use and nesting success of the Great Reed Warbler (Acrocephalus arundinaceus) in different reed habitats in Serbia" class="work-thumbnail" src="https://attachments.academia-assets.com/97153825/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794472/Habitat_use_and_nesting_success_of_the_Great_Reed_Warbler_Acrocephalus_arundinaceus_in_different_reed_habitats_in_Serbia">Habitat use and nesting success of the Great Reed Warbler (Acrocephalus arundinaceus) in different reed habitats in Serbia</a></div><div class="wp-workCard_item"><span>The Wilson Journal of Ornithology</span><span>, 2015</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">We surveyed five reed habitats (mining pond, sand pit, large canal, small canal and lowland river...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">We surveyed five reed habitats (mining pond, sand pit, large canal, small canal and lowland river) in northwestern Vojvodina (Serbia) between 2009-2011 to study habitat use and to estimate nest success in an understudied region of the breeding range of the Great Reed Warbler (Acrocephalus arundinaceus). Data from 174 nests showed that habitat use differed considerably between the habitat types, but was not related to the area of the study site or the reed bed. Higher-than-expected numbers of nests along the small canal and the river suggested that Great Reed Warblers preferred these to other habitats for nesting. Habitat use was closely linked to the availability of reed edges and the quality of the reed stand. Overall Mayfield nest success was 43%, slightly lower than in northern and western Europe. Nest success was low along the small and large canal, where brood parasitism by Common Cuckoos (Cuculus canorus) and nest predation were high due to nearby tree lines providing perching sites to cuckoos and predators. Nest success was intermediate at the mining pond due to very high predation pressure and adverse weather, and nest success was highest in the sand pit (despite high Cuckoo parasitism) and the river (despite relatively high predation). In conclusion, our results suggest that canals can function as ecological traps, which attract edge-preferring Great Reed Warblers but are highly accessible to predators and brood parasites. In contrast, sand pits can be perceptual traps because they provide good resources for nesting but were less attractive to Great Reed Warblers than other habitats. Habitat use in relation to habitat availability thus depends primarily on the availability of reed edges and the quality of the reed stand, whereas nest success also depends on the characteristics of the surroundings and weather conditions.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="8a8698450cd6892fc537010971a053e3" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153825,"asset_id":94794472,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153825/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794472"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794472"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794472; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794471"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794471/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond"><img alt="Research paper thumbnail of Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond" class="work-thumbnail" src="https://attachments.academia-assets.com/97153840/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794471/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond">Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond</a></div><div class="wp-workCard_item"><span>TURKISH JOURNAL OF ZOOLOGY</span><span>, 2014</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Báldi (2001) studied how inundation affected the local breeding passerines at the Kis-Balaton wet...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Báldi (2001) studied how inundation affected the local breeding passerines at the Kis-Balaton wetland. He collected observations in 3 groups (before, immediately after, and years after inundation) and quantified the changes in community structure parameters, community composition, differences between areas and periods, and species and abundances. Savi's Warbler, Locustella luscinioides, declined immediately after inundation, while Reed Bunting, Emberiza schoeniclus, and Sedge Warbler, Acrocephalus schoenobaenus, declined in the long term. However, the Great Reed Warbler (GRW), Acrocephalus arundinaceus, was the only species with a continuous increasing trend. Vadász et al. (2008) reported that the cutting of reed negatively influenced species richness and the abundance of reed passerines on Lake Kolon in Central Hungary. Savi's Warbler, Moustached Warbler Acrocephalus melanopogon, Sedge Warbler, and Reed Warbler Acrocephalus scirpaceus especially avoided cut areas, while GRW did not (Vadász et al., 2008). Báldi and Moskát (1995) and Moga et al. (2010) recorded the presence of GRW in unmanaged, burned, and mowed reed stands. Despite these sporadic observations, our knowledge about the effects of reed management and environmental factors on the breeding success of GRW is weak. Nests of small open-nesting birds are often difficult to detect in the early stages of the breeding season (Mayfield, 1975). Due to the lack of information for the period before nests are found, estimates of mortality, survival, and breeding success can be severely biased. Mayfield (1975) developed a method for estimating breeding success that reduced potential sources of error. The proposed Mayfield estimator has been further recognized as a maximum likelihood estimator (MLE). The asymptotic distribution of the MLE has been calculated, which provides a measure of asymptotic variance (Hensler and Nichols, 1981). MLE and variance can be used to test the significance of daily survival (Hensler and Nichols, 1981). Lloyd and</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="c993a6f41c7f0241284b1cae16b778ed" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153840,"asset_id":94794471,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153840/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794471"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794471"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794471; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794470"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794470/Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW_Vojvodina_Serbia"><img alt="Research paper thumbnail of Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW Vojvodina, Serbia" class="work-thumbnail" src="https://attachments.academia-assets.com/97153824/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794470/Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW_Vojvodina_Serbia">Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW Vojvodina, Serbia</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e. g. clay pits, marsh and fishponds, small canals and large canals) in northwestern Vojvodina (Serbia) between 2009 and 2011 (three breeding seasons). A total of 596 Great Reed Warbler (Acrocephalus arundinaceus) nests were found and monitored. The overall parasitism rate for the study area was 0.127, which was calculated from the number of parasitized nests (76) divided by the total number of Great Reed Warbler nests (596). The parasitism rate did not vary with the total number of Great Reed Warbler nests at a study site. The number of parasitized and successful parasitized nests showed significant negative relationship, which means more parasitized nests resulted with more brood lost. The parasitism rate varied significantly among habitats but not among years while the number of successfully parasitized nests differed among both habitats and years. Parasitized nests found in small and large canals showed the highest reproductive success of Cuckoos. Loss of parasitized nests through predation and bad weather circumstances was relatively high in this study compared to other areas.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5d9e1e5c24e98b0bb95a6dec8721b911" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153824,"asset_id":94794470,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153824/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794470"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794470"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794470; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794469"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794469/Improved_land_cover_mapping_using_aerial_photographs_and_satellite_images"><img alt="Research paper thumbnail of Improved land cover mapping using aerial photographs and satellite images" class="work-thumbnail" src="https://attachments.academia-assets.com/97153826/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794469/Improved_land_cover_mapping_using_aerial_photographs_and_satellite_images">Improved land cover mapping using aerial photographs and satellite images</a></div><div class="wp-workCard_item"><span>Open Geosciences</span><span>, 2014</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Manual Land Cover Mapping using aerial photographs provides sufficient level of resolution for de...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Manual Land Cover Mapping using aerial photographs provides sufficient level of resolution for detailed vegetation or land cover maps. However, in some cases it is not possible to achieve the desired information over large areas, for example from historical data where the quality and amount of available images is definitely lower than from modern data. The use of automated and semiautomated methods offers the means to identify the vegetation cover using remotely sensed data. In this paper automated methods were tested on aerial photographs and satellite images to extract better and more reliable information about vegetation cover. These testswere performed by using automated analysis of LANDSAT7 images (with and without the surface model of the Shuttle Radar Topography Mission (SRTM)) and two temporally similar aerial photographs. The spectral bands were analyzed with supervised (maximum likelihood) methods. In conclusion, the SRTM and the combination of two temporally similar aeria...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="3b14662d8daffa8c5bd1145700c6b875" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153826,"asset_id":94794469,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153826/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794469"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794469"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794469; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "3b14662d8daffa8c5bd1145700c6b875" } } $('.js-work-strip[data-work-id=94794469]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":94794469,"title":"Improved land cover mapping using aerial photographs and satellite images","internal_url":"https://www.academia.edu/94794469/Improved_land_cover_mapping_using_aerial_photographs_and_satellite_images","owner_id":36347448,"coauthors_can_edit":true,"owner":{"id":36347448,"first_name":"Katalin","middle_initials":null,"last_name":"Varga","page_name":"KatalinVarga2","domain_name":"independent","created_at":"2015-10-16T06:43:49.681-07:00","display_name":"Katalin Varga","url":"https://independent.academia.edu/KatalinVarga2"},"attachments":[{"id":97153826,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/97153826/thumbnails/1.jpg","file_name":"10.1515_geo-2015-0002.pdf","download_url":"https://www.academia.edu/attachments/97153826/download_file","bulk_download_file_name":"Improved_land_cover_mapping_using_aerial.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/97153826/10.1515_geo-2015-0002-libre.pdf?1673478360=\u0026response-content-disposition=attachment%3B+filename%3DImproved_land_cover_mapping_using_aerial.pdf\u0026Expires=1741042744\u0026Signature=gKAWpYQNI32iDqjkPgGWHoCX3xf9WL5h97cfV4Pho4g6-HD8jckx23b-b4qvZCL~veJk~PObN6~Se7MDovU~lMGIwQMXr5tNI9ITZ1E2IydoQcj8MoPItQnEvGFp~Ps4lk6rkhd0xhto3EHITyAdCLYkS1MHTB8vfNJCNAtIbY-t7D50KYf1IyapUVrAc-V3GiznTZNJTaASP5l6jSTwRVL2lZGaaRfoPp6dYwFt-JB0xPDsh4a44PpMyp6VGtZCxpJflXgRWFcWVCgL8i4UMKVALbkX9LYOP7kFGdWUQZZlk-AnWoWiv8zAGx1PkNMUD1dNEUHr77h02hKJ5z5XYA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794468"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794468/Grassland_restoration_to_conserve_landscape_level_biodiversity_a_synthesis_of_early_results_from_a_large_scale_project"><img alt="Research paper thumbnail of Grassland restoration to conserve landscape-level biodiversity: a synthesis of early results from a large-scale project" class="work-thumbnail" src="https://attachments.academia-assets.com/97153827/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794468/Grassland_restoration_to_conserve_landscape_level_biodiversity_a_synthesis_of_early_results_from_a_large_scale_project">Grassland restoration to conserve landscape-level biodiversity: a synthesis of early results from a large-scale project</a></div><div class="wp-workCard_item"><span>Applied Vegetation Science</span><span>, 2012</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Question: European landscapes have long been influenced by intensifying use by humans. Although h...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Question: European landscapes have long been influenced by intensifying use by humans. Although habitat restoration can reverse this process, it is often limited in scope by socioeconomic constraints. Here we present a grassland restoration project that is exceptional in spatial scale in Europe. Location: A total area of 760 ha of arable land was restored in the Egyek-Pusztakó cs unit (50 km 2) of Hortobágy National Park, east Hungary, between 2005 and 2008. Methods: Restoration targeted alkali steppes and loess grasslands by sowing seeds of either two (alkali) or three (loess) foundation grass species. In 2009, we surveyed the vegetation in restored and target grasslands and quantified the factors influencing restoration success in a space-for-time substitution design. Results: We recorded 100 species of flowering plants, of which 37 species were non-weed, 'target' species. Annual weeds dominated 1-yr-old fields but had decreased dramatically by the third year due to a developing perennial grass cover. Former alfalfa fields had proportionally fewer weeds than former cereal and sunflower fields. The diversity of common species and the cover of target species increased from 1-to 4-yr-old restored fields. Alkali-restored fields had more heterogeneous vegetation and more species than loess-restored fields. Distance to the target vegetation did not directly affect vegetation variables. There was significant spatial variability in vegetation development, possibly suggesting several local pathways of succession. Conclusions: Grassland restoration was generally successful in accelerating secondary succession towards alkali steppes and loess grasslands. However, further management is necessary to counter the homogenizing effects of litter accumulation, to reduce perennial weeds and to enhance the colonization of target species. Our project provides useful practical insights into grassland restoration and in applying restoration at a number of sites within a larger area to conserve biodiversity at the landscape scale.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5923031315cbe267600a932aa1aefabe" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153827,"asset_id":94794468,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153827/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794468"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794468"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794468; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="94794357"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/94794357/Nest_site_characteristics_and_breeding_density_of_Magpie_Pica_pica_in_Sombor_NW_Serbia_"><img alt="Research paper thumbnail of Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia)" class="work-thumbnail" src="https://attachments.academia-assets.com/97153804/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/94794357/Nest_site_characteristics_and_breeding_density_of_Magpie_Pica_pica_in_Sombor_NW_Serbia_">Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia)</a></div><div class="wp-workCard_item"><span>Acrocephalus</span><span>, 2010</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia) In March...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Nest-site characteristics and breeding density of Magpie Pica pica in Sombor (NW Serbia) In March 2009, active Magpie Pica pica nests were censused in the town of Sombor (Vojvodina, NW Serbia) to study nest-site characteristics, breeding density and spatial distribution. The area of the town can be divided into two parts according to different urban landscapes, i.e. the town centre (150 ha) and the residential area (2,224 ha). In total, 222 Magpie nests were found and their height, tree species and nest-site type determined. Nests were found in 25 tree and two shrub species, the most of them (31.1%) being placed in the commonest tree species in the town, the Common Hackberry Celtis occidentalis. The majority of the nests were found in tree avenues (39.6%) and groups of trees (31.5%). Nests in the town centre with a mean height (± SD) of 15.2 ± 4.05 m were significantly higher than those in the residential area with a mean height (± SD) of 11.4 ± 5.13 m. The mean distance of nests fr...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="66169ab9d61c6b3e85eccd8705ed9d66" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":97153804,"asset_id":94794357,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/97153804/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="94794357"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="94794357"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 94794357; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="16874617"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/16874617/Early_changes_of_orthopteran_assemblages_after_grassland_restoration_a_comparison_of_space_for_time_substitution_versus_repeated_measures_monitoring"><img alt="Research paper thumbnail of Early changes of orthopteran assemblages after grassland restoration: a comparison of space-for-time substitution versus repeated measures monitoring" class="work-thumbnail" src="https://attachments.academia-assets.com/39231692/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/16874617/Early_changes_of_orthopteran_assemblages_after_grassland_restoration_a_comparison_of_space_for_time_substitution_versus_repeated_measures_monitoring">Early changes of orthopteran assemblages after grassland restoration: a comparison of space-for-time substitution versus repeated measures monitoring</a></div><div class="wp-workCard_item"><span>Biodiversity and Conservation</span><span>, 2013</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Although grasslands harbour significant biodiversity and their restoration is common in 26 biodiv...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Although grasslands harbour significant biodiversity and their restoration is common in 26 biodiversity conservation, we know very little about how such interventions influence arthropod 27 groups. Here we compared orthopteran assemblages in croplands, natural grasslands and one to 28 four-year-old grasslands restored in a large-scale programme in Hortobágy National Park (East 29 Hungary). We sampled orthopterans by standardized sweep-netting both in a repeated measures 30 design from year 0 (croplands) to 4 and in a space-for-time substitution (chronosequence) design 31 in 2009. Species richness, abundance and Shannon diversity of orthopterans decreased in year 1 32 following restoration, but increased afterwards. By year 4, species richness doubled and 33 abundance increased almost ten-fold in restored grasslands compared to croplands. Species 34 composition diversified compared to croplands and progressed towards natural grasslands. Local 35 restoration conditions (last crop, seed mixture) and landscape configuration (proportion of 36 natural grasslands) did not influence the above patterns in either study design, whereas time 37 since restoration affected almost all community variables. We found that ubiquitous generalist 38 species were the first to appear in restored grasslands and that species characteristic to the target 39 natural grasslands colonised gradually in later years. The qualitative and quantitative properties 40 of the orthopteran assemblages in restored fields did not yet reach those of natural grasslands, 41 therefore, our study suggests that the full regeneration of the orthopteran assemblages takes more 42 than four years. We also concluded that the repeated-measures design was more sensitive to 43 subtle changes and was thus more effective than the chronosequence design at detecting post-44 restoration changes in orthopteran assemblages. 45 46 47 3</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="30e917ba2d2711996e4e7c5cfdf04ccb" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":39231692,"asset_id":16874617,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/39231692/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="16874617"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="16874617"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 16874617; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "30e917ba2d2711996e4e7c5cfdf04ccb" } } $('.js-work-strip[data-work-id=16874617]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":16874617,"title":"Early changes of orthopteran assemblages after grassland restoration: a comparison of space-for-time substitution versus repeated measures monitoring","internal_url":"https://www.academia.edu/16874617/Early_changes_of_orthopteran_assemblages_after_grassland_restoration_a_comparison_of_space_for_time_substitution_versus_repeated_measures_monitoring","owner_id":36347448,"coauthors_can_edit":true,"owner":{"id":36347448,"first_name":"Katalin","middle_initials":null,"last_name":"Varga","page_name":"KatalinVarga2","domain_name":"independent","created_at":"2015-10-16T06:43:49.681-07:00","display_name":"Katalin Varga","url":"https://independent.academia.edu/KatalinVarga2"},"attachments":[{"id":39231692,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/39231692/thumbnails/1.jpg","file_name":"02e7e517be17596190000000.pdf","download_url":"https://www.academia.edu/attachments/39231692/download_file","bulk_download_file_name":"Early_changes_of_orthopteran_assemblages.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/39231692/02e7e517be17596190000000-libre.pdf?1445003129=\u0026response-content-disposition=attachment%3B+filename%3DEarly_changes_of_orthopteran_assemblages.pdf\u0026Expires=1741042744\u0026Signature=EIWyGn6B06ANrkycnLv4QlLF3n3gySHANHuIgWvcEvza4BURv6KaMDfG7O8LjbcUrqvAqARvjBANz6DK5dP6fBOScyzGAH8h82w2ZPGAgR0dUSEKMbSUgVBNceJeUghUYJ7vZTL~d5sybDoBxxHG0T68tTqlruQi2G7F1YrJNY8kBCf1vuUeXlyncSd9hG6uScGHRjfWfd0HOs6mfJc5VurozfKaj4Xzg7r3II~E289ffGDksnE0uvtoKSzXeHBOtnWeJ7hc8GeHHNNBixPNZcnigH5FoqJMymY1wuZoPaLCv6SL~RGrj4zpJ8iXfM5WcW63yrxjoXeFSJx1IXaf7A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="6183746"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/6183746/original_scientific_paper_izvorni_znanstveni_rad_BREEDING_OF_THE_BROOD_PARASITIC_COMMON_CUCKOO_CUCULUS_CANORUS_IN_REED_HABITATS_IN_NW_VOJVODINA_SERBIA_Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW"><img alt="Research paper thumbnail of original scientific paper/izvorni znanstveni rad BREEDING OF THE BROOD PARASITIC COMMON CUCKOO (CUCULUS CANORUS) IN REED HABITATS IN NW VOJVODINA, SERBIA: Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW" class="work-thumbnail" src="https://attachments.academia-assets.com/33065667/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/6183746/original_scientific_paper_izvorni_znanstveni_rad_BREEDING_OF_THE_BROOD_PARASITIC_COMMON_CUCKOO_CUCULUS_CANORUS_IN_REED_HABITATS_IN_NW_VOJVODINA_SERBIA_Breeding_of_the_brood_parasitic_Common_Cuckoo_Cuculus_canorus_in_reed_habitats_in_NW">original scientific paper/izvorni znanstveni rad BREEDING OF THE BROOD PARASITIC COMMON CUCKOO (CUCULUS CANORUS) IN REED HABITATS IN NW VOJVODINA, SERBIA: Breeding of the brood parasitic Common Cuckoo (Cuculus canorus) in reed habitats in NW</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/KatalinVarga2">Katalin Varga</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://unideb.academia.edu/ThomasOliverM%C3%A9r%C5%91">Thomas Oliver Mérő</a>, and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/AntunZuljevic">Antun Zuljevic</a></span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">We monitored the breeding success of the Common Cuckoo (Cuculus canorus) in four reed habitats (e. g. clay pits, marsh and fishponds, small canals and large canals) in northwestern Vojvodina (Serbia) between 2009 and 2011 (three breeding seasons). A total of 596 Great Reed Warbler (Acrocephalus arundinaceus) nests were found and monitored. The overall parasitism rate for the study area was 0.127, which was calculated from the number of parasitized nests (76) divided by the total number of Great Reed Warbler nests (596). The parasitism rate did not vary with the total number of Great Reed Warbler nests at a study site. The number of parasitized and successful parasitized nests showed significant negative relationship, which means more parasitized nests resulted with more brood lost. The parasitism rate varied significantly among habitats but not among years while the number of successfully parasitized nests differed among both habitats and years. Parasitized nests found in small and large canals showed the highest reproductive success of Cuckoos. Loss of parasitized nests through predation and bad weather circumstances was relatively high in this study compared to other areas.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="60ae0a8e7be2a468b9049fb4b780b5ae" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":33065667,"asset_id":6183746,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/33065667/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="6183746"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="6183746"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 6183746; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="9916187"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/9916187/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond"><img alt="Research paper thumbnail of Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond" class="work-thumbnail" src="https://attachments.academia-assets.com/36070423/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/9916187/Effect_of_reed_burning_and_precipitation_on_the_breeding_success_of_Great_Reed_Warbler_Acrocephalus_arundinaceus_on_a_mining_pond">Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/Ren%C3%A1taBocz">Renáta Bocz</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://unideb.academia.edu/ThomasOliverM%C3%A9r%C5%91">Thomas Oliver Mérő</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/KatalinVarga2">Katalin Varga</a>, and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/AntunZuljevic">Antun Zuljevic</a></span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">In this study, we present the effects of reed burning and precipitation on the breeding success o...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">In this study, we present the effects of reed burning and precipitation on the breeding success of Great Reed Warblers on a mining pond (2008–2011). Breeding success, i.e. the probability that an egg would produce a fledgling, was 0.43. Clutch survival was lowest in 2010, due to the precipitation and high water level during the season. Breeding success was higher in the second half of the breeding season, although in 2008 and 2011 precipitation was also higher in the second half than in the first half of the breeding season. During the first half of the breeding season, daily egg and nestling survival did not differ. However, in the second half of the breeding season, daily egg survival was higher than daily chick survival. In years when reed was burned, breeding density varied between 7.7 and 12.3 pairs ha–1, which was not significantly lower than in years when reed was not managed (average: 13.2 pairs ha–1). Despite the<br />availability of fresh reed in large areas, birds placed their nests mainly in mixed reed stands. Breeding success in fresh and mixed reed did not differ. Generally, breeding success and density were not affected by reed burning, but water level affected breeding success and density.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="e29f0d0d0af7729c99833ef61d20cad3" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":36070423,"asset_id":9916187,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/36070423/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="9916187"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="9916187"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 9916187; 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