Open access journal: http://periodicos.uefs.br/ojs/index.php/sociobiology ISSN: 0361-6525 DOI: 10.13102/sociobiology.v65i4.3370Sociobiology 65(4): 603-611 (October, 2018) Special Issue Diversity of Flower Visiting Insects in dry Grasslands and Vineyards Close to the City of Vienna with Special Focus on Wild Bees Introduction Interactions between flowering plants and flower- pollinating insects belong to the most significant in the terrestrial synecology (Richards, 1978; Proctor et al., 1996). Diversity and local distribution resp. commonness or rarity of both plants and insects are strongly dependent on the development and integrity of these relationships (e.g. Fontaine et al., 2006). In the surrounding of the city of Vienna open semi- dry grasslands are one of the most important hot spots of biodiversity for both plants and insects (Adler & Mrkvicka, 2003). But their part in the landscape is comparatively small, and patches of grassland are in most cases strongly isolated from each other by the surrounding forests, settlement Abstract Interactions between flower visiting insects and nectar resp. pollen producing plants belong to the most relevant in terrestrial ecosystems. Their diversity and dominance relationship are important indicators for the stability and functionality of ecosystems and belong to the high ranking ecosystem services. Potential pollinators should be strongly concerned especially regarding anthropogenic impacts on habitats. We studied the diversity and quantities of flower visiting insects with special focus on wild bees (Apiformes) in two locations near the city of Vienna (Austria). Insect sampling occurred from May until July 2015 every two weeks parallel to the vegetation surveys incl. records of the cover of flowering plants. In each location patches of semi-natural grassland as well as flowering strips within vineyards were investigated. We found a significant correlation between the number of insects or insect taxa (especially for Hymenoptera) and the current flower cover. In some cases flowering strips in vineyards harbor higher numbers of insects and higher diversity of bee species than the semi-natural grassland due to temporarily higher values of flower cover. However, grassland patches provide a much more constant supply with nectar producing plants replacing each other in their flowering phase during the season. In contrast, flowering strips are often dominated by one or a few short-lived sown plants, which is of advantage for some oligolectic bees specialized on Brassicaceae or Fabaceae. Flowering strips within organically farmed vineyards are more similar to semi-natural grassland regarding the diversity of flower visiting insects than to conventionally farmed vineyards. Sociobiology An international journal on social insects L Rasran, A Diener, B Pachinger, K-G Bernhardt Article History Edited by Kleber Del Claro, UFU, Brazil Cândida Aguiar, UEFS, Brazil Received 25 April 2018 Initial acceptance 28 June 2018 Final acceptance 13 July 2018 Publication date 11 October 2018 Keywords Organic farming, flower cover, flower strips. Corresponding author Leonid Rasran Institute of Botany University of Natural Resources and Life Sciences Vienna Gregor-Mendel-Str 33, A-1180 Vienna, Austria. E-Mail: leonid.rasran@boku.ac.at infrastructure and agricultural landscapes including arable fields and vineyards. Fragmentation and isolation of biotopes lead to the reduction of their functionality as habitat and dispersal corridors for insects (Tscharntke et al., 2002; Garibaldi et al., 2011). Moreover, intensive agriculture presumes the application of pesticides, which either leads to the reduction of insect diversity and quantity. One of the expected consequences could be pollination limitation (reduction of fruit setting rate due to insufficient pollination, Calvo & Horvitz, 1990; Jennersten & Nilsson, 1993; Larson & Barrett, 2000). Lack of pollinators is relevant not only for plant species diversity and population stability of rare and endangered semi-dry and dry grassland herbs, but also for the entire agricultural production and has a clear economical value (Klein et al., 2007; Neumayer, 2011). University of Natural Resources and Life Sciences Vienna, Austria RESEARCH ARTICLE - BEES mailto:leonid.rasran@boku.ac.at L Rasran; A Diener; B Pachinger; K-G Bernhardt – Pollinator diversity in dry grasslands and vineyards604 Bee species (Apiformes) are especially sensitive to the decline of insect-pollinated plants in the landscape (Biesmeijer et al., 2006) and thus are good indicators for the stability and integrity of plant/pollinator interactions and ecosystem services (Burkle et al., 2013). The cultural landscape of low mountains around the city of Vienna (parts of Vienna Forest, so called Wiener Hausberge - Leopoldsberg, Nussberg, Bisamberg) was significantly changed in the last decades. In some parts agricultural use (mainly in form of vineyards) was strongly intensified, while at the same time formerly moderately used grassland areas became abandoned and are now covered by shrubs or forest. In both cases the attractiveness of areas for pollinators has been reduced. Some authors (see e.g. Haaland et al., 2011) express the expectation, that flower strips within or besides the vineyards could serve as important step-stone biotopes and feeding grounds for bees and other plant pollinating insects. In these functions and ecosystem services flower strips would complete or even replace the species-rich grasslands formerly present in the area in high percentage. However, flowering strips are artificial sites with significant differences to (semi-) natural grasslands. Following critical points can be mentioned in this context: (i) seed mixtures for flower strips usually include only a few dominant, but short-lived species which offer nectar and pollen for a rather narrow, restricted time span (van Elsen et al., 2007; Rundlöf et al., 2014); (ii) the seed mixtures for flower strips often include alien species or genetic varieties, which are either less adapted to local conditions or are potential invaders with a negative impact for the resident biota (Keller et al., 2000); (iii) flower strips are involved in agricultural production and are affected by the application of pesticides and mineral fertilizers together with the wine rows. Mowing of the flower strips is also linked to the demands of crop production, which means that mowing occurs earlier and more frequently than in the grassland and shorten significantly the flowering period of plant species and their offer of nectar and pollen (Bruggisser et al., 2010). Regarding the mowing time, significant differences could be expected between traditional and ecological viticulture, both present in the study area. The present study focuses on the comparison between semi-natural grassland patches and flower strips in vineyards. We recorded the floristic diversity, vegetation structure and flower cover (as a cue for pollen respectively nectar availability). Parallel, we analyze the quantities and species composition of flower-visiting insects with special focus on wild bees. Following research questions can be worded: i. How far does the flower cover correlate with diversity and quantity of flower visiting insects? ii. Are there significant differences in composition of insect communities in general and bee communities in particular between semi-natural grasslands and flower strips? iii. Are there significant differences between flower strips within traditional and ecological viticulture regarding the pollinator communities? Material and Methods Study areas The present study was carried out at two low mountains on the outskirts of the city of Vienna (Austria): Bisamberg north of the Danube (N 48° 18` E 16° 22`, 358 m a. s. l.) and Leopoldsberg/Nussberg south (N 48° 16` E 16 21`, 425 m a. s. l.). These mountains belong to the most NE-part of Vienna Forest and build together the so called “Vienna Gate” of the Danube valley. The south-exposed slopes of both mountains are covered by semi-dry deciduous forests (downy oak forests), different types of semi-dry calcareous grasslands (Mesobromion) and vineyards. We selected ten plots per area (Bisamberg – five grasslands and five vineyard flower strips; Leopoldsberg/Nussberg – three grasslands and seven vineyard flower strips). On Bisamberg all vineyard flower strips and three of five grassland plots were situated within the research farm “Götzhof” (Federal Department of Viti- and Pomiculture), where ecological agricultural methods are tested. The vineyards and associated flower strips on Nussberg are managed in a traditional way. The study areas are about 5 km away from each other and within the area all study plots were situated within the circle of about 1200 m diameter. The study plots were of different shape dependent on the landscape - from 10 x 10 m squares in grassland to 1.5 x 66.6 m strips between vine rows, but of the same size of 100 m². The current management and the composition of seed mixtures for flower strips are listed in Table 1. Vegetation and insect surveys Each study plot was monitored six times from May to July 2015 in a two week interval. The monitoring included an observation of flower-visiting insects performed by one person with a sampling time of 15 minutes by patrolling the plot (linear or zigzag dependent on plot configuration) and capturing the insects with help of an entomological hand-net. All captured insects were immediately counted. Individuals, which could not be easily identified in the field, were killed with ethyl acetate and preserved for further identification. The focus insect group of bees (Apiformes) and some easily recognizable Coleoptera and Macrolepidoptera were determined down to species level, while at some groups (e.g. Diptera) we had to deal with morphospecies. Bee species were categorized according to their food and nesting preferences following Scheuchl and Willner (2016). Nomenclature of bee species follows Gusenleitner et al. (2012). Insect monitoring took place in the daytime and only in good weather (temperature above 15°C, no precipitation). Subsequent to the insect record a vegetation relevée (scale based on cover percentages of single species) after Londo (Londo, 1976) was performed for the study plot, while besides cover of plant species their contribution to flower cover was estimated. Entomophilous plants with currently open blossoms were seen as relevant Sociobiology 65(4): 603-611 (October, 2018) Special Issue 605 Table 1. Description of the study sites at Bisamberg (B1-B10) and at Leopoldsberg/Nussberg (L1-L10), habitat type (flower strip/grassland), plot shape (length x width; m), vegetation/land use, coordinates and exposition. All plots were of the same size of 100 m². habitat type plot size (m) vegetation/land use coordinates slope angle (°), exposition Bisamberg B1 flower strip 5 x 20 spontaneous re-vegetation, Lepidium draba- dominant cover N48°18´47.7´´ E16°22´18.6´´ 20 S B2 flower strip 1.5 x 66.6 3-component-seed mixture* N48°18´45.7´´ E16°22´24.6´´ 10 S B3 grassland 10 x 10 mown in summer N48°18´45.2´´ E16°22´27.8´´ 8 S B4 flower strip 1.5 x 66.6 3-component-seed mixture* N48°18´45.2´´ E16°22´29.6´´ 8 S B5 flower strip 1.5 x 66.6 seed mixture “Rebenfit”** N48°18´39.0´´ E16°22´28.1´´ 8 - 15 S B6 grassland 10 x 10 mown in summer N48°18´39.5´´ E16°22´26.5´´ 5 S B7 grassland 10 x 10 mown in summer N48°18´39.9´´ E16°22´20.7´´ 6 S B8 flower strip 1.5 x 66.6 seed mixture “Rebenfit”** N48°18´39.7´´ E16°22´18.4´´ 6 S B9 grassland 10 x 10 mown in autumn/abandoned N48°18´45.8´´ E16°21´46.1´´ 2 - 3 S B10 grassland 10 x 10 mown in autumn/abandoned N48°18´46.9´´ E16°21´41.2´´ 15 - 18 S Leopoldsberg/Nussberg L1 grassland 10 x 10 mown in autumn/abandoned N48°16´29.4´´ E16°20´34.2´´ 12 E L2 grassland 10 x 10 mown in autumn/abandoned N48°16´29.6´´ E16°20´31.4´´ 8 E L3 grassland 10 x 10 mown in autumn/abandoned, Orlaya grandiflora-dominant cover N48°16´35.1´´ E16°20´43.4´´ 40 S L4 flower strip 1 x 100 sown Trifolium incarnatum, Phacelia tanacetifolia, Fagopyrum esculentum, Sinapis alba, Raphanus sativus and Vicia sativa N48°16´07.9´´ E16°20´40.9´´ 4 - 10 NE L5 flower strip 10 x 10 sown Trifolium incarnatum, Camelina sativa, Centaurea cyanus, Trifolium repens, Medicago sativa, Medicago lupulina and Plantago lanceolata N48°16´01.9´´ E16°20´54.6´´ 1 - 2 NE L6 flower strip 1.5 x 66.6 sown Sinapis alba, Raphanus sativus subsp. oleiferus, Phacelia tanacetifolia, Melilotus officinalis, Vicia sativa, Vicia pannonica, Calendula officinalis and Malva sylvestris N48°16´00.6´´ E16°20´57.5´´ 0 - 2 S L7 flower strip 1 x 100 sown Melilotus officinalis, Sinapis alba, Raphanus sativus subsp. oleiferus, Trifolium incarnatum, Vicia pannonica, Malva sylvestris, Phacelia tanacetifolia, Trifolium pratense, Trifolium alexandrinum and Cichorium intybus. N48°15´58.8´´ E16°21´03.7´´ 4 - 10 S L8 flower strip 10 x 10 sown Medicago sativa N48°15´56.4´´ E16°21´10.9´´ 8 - 10 S L9 flower strip 1.5 x 66.6 sown Trifolium repens N48°15´47.5´´ E16°21´22.0´´ 2 - 12 S L10 flower strip 1.5 x 66.6 sown Medicago sativa N48°15´48.4´´ E16°21´26.6´´ 2 - 12 S *3-component-seed mixture* includes Phacelia tanacetifolia, Fagopyrum esculentum and Trifolium incarnatum. ** seed mixture "Rebenfit", includes Camelina sativa, Trifolium incarnatum, Trifolium repens, Medicago lupulina, Plantago lanceolata and Centaurea cyanus. L Rasran; A Diener; B Pachinger; K-G Bernhardt – Pollinator diversity in dry grasslands and vineyards606 for flower-visiting insects. Some species, normally seen as wind-pollinated (e.g. Plantago lanceolata (L.)) were counted to the flower cover as well due to the potential importance of their pollen as food for insects (e.g. Sharma et al., 1993). Determination and nomenclature of plant species was according to Fischer et al. (2008). We studied the relationship between species richness respectively quantities of insects and characteristic of study plots (incl. flower cover of different plant groups) applying linear regression and analysis of variances (ANOVA). A Repeated Measurement ANOVA was calculated to study the effect of observation time. Additionally, factor “time” was included in a Three-Way ANOVA together with the factors “area” and “habitat” (grassland vs. flower strips) to study the interactions between them . A canonical correspondence analysis (CCA) was applied to put the entire species composition of bee communities in relation to land use and flower aspect. The statistical analyses were performed using the software package R 2.15.2 (R Development Core Team, 2015). Multivariate analyses were performed using CANOCO 5 (Smilauer & Leps, 2014). Results Vegetation and flower cover Semi-natural grasslands on both study areas included 28 to 48 species of flowering plants per 100 m² (without Poaceae). The plant species diversity on the flower strips was significantly lower, not above 20 species, in most cases about 10. The estimated flower cover, however, reached similar values for both grassland and flower strips and in some cases was even higher on the last mentioned (Table 2, Fig 1). Most significant for the flower cover of strips was the contribution of sown species such as Phacelia tanacetifolia Benth., Trifolium incarnatum L. or Sinapis alba L., but some spontaneously established ruderal species such as Lepidium draba L. could locally reach a high flower density. The flower cover of grassland plots was mainly polydominant, but strong contribution of one single species in a particular point of time (e.g. Orlaya grandiflora (L.) Hoffm. on one of the plots on Leopoldsberg) was also observed. The temporal variation of the flower cover was especially high at flower strips (Table 2, Fig 1). Generally, the flower cover tended to reduce during the recording period from May to July. Flower strips between vine rows were mown usually once (ecologically managed flower strips on Bisamberg) or twice (traditionally used flower strips on Nussberg) during the observation period. In some cases vegetation could rapidly recover from these effects and developed high flower cover for the second time, but there was a significant time span, where the flower offer for pollinators was lowered. Grassland patches were usually mown in late summer (after the observation period was finished) or remain unmown. dependent Area Time Treatment (grassland vs. flower strips Area x Time Area x Treatment Time x Treatment Area x Time x Treatment No. of plant species 3.6 ns 1.78 ns 41.71*** 0.1 ns 23.81*** 0.07 ns 0.15 ns Sum flower cover 0.01 ns 6.07 *** 2.63 ns 2.77* 6.61* 1.61 ns 4.18** Flower cover Brassicaceae 0.01 ns 5.78*** 7.3** 0.84 ns 0.12 ns 2.14 ns 1.29 ns Flower cover Asteraceae 1.16 ns 0.96 ns 21.54*** 0.69 ns 11.66*** 1.02 ns 2.44* Flower cover Apiaceae 2.23 ns 0.42 ns 8.28 ** 1.32 ns 3.69 ns 0.82 ns 1.98 ns Flower cover Fabaceae 7.9** 1.19 ns 1.29 ns 0.87 ns 4.18* 0.22 ns 0.45 ns No. of insect species 1.64 ns 1.3 ns 6.52* 1.27 ns 28.84*** 1.31 ns 2.15 ns No. of insect ind. 8.17** 2.62* 4.07* 3.39** 12.04*** 2.49* 3.66** Hymenoptera species 0.91 ns 0.24 ns 0.12 ns 1.41 ns 6.65* 1.37 ns 1.46 ns Hymenoptera ind. 6.74* 1.86 ns 5.68* 3.05* 4.78* 2.37* 2.18 ns Coleoptera species 4.33* 1.44 ns 4.98* 1.61 ns 20.44*** 1.27 ns 1.49 ns Coleoptera ind. 4.09* 1.59 ns 0.05 ns 1.27 ns 12.76*** 0.86 ns 2.29 ns Lepidoptera species 0.36 ns 2.07 ns 35.08*** 2.38* 20.27*** 2.72* 1.17 ns Lepidoptera ind. 2.4 ns 1.81 ns 31.38*** 1.74 ns 20.11** 2.59* 2.14 ns Diptera species 2.89 ns 3.89** 0.12 ns 2.38* 22.65*** 2.95* 3.08* Diptera ind. 0.01 ns 2.56* 0.44 ns 3.02* 23.08*** 3.65** 5.92*** Table 2. Differences of plant species diversity, flower cover, flower visiting insects and insect groups between the investigated locations (Bisamberg, Leopoldsberg/Nussberg) and habitats (flower strip and grassland) as well as their interactions. Three-way full factorial ANOVA. Values of Fisher-distribution (F-value) are shown. Significant effects are highlighted and marked as follows: * p<0.05, ** p<0.01 and *** p< 0.001. ns – not significant. Sociobiology 65(4): 603-611 (October, 2018) Special Issue 607 Flower visiting insects in general During the study entirely 201 (morpho-) species of flower-visiting insects were recorded. The most species-rich insect group was Hymenoptera with 62 species (incl. 41 species of Apiformes), followed by Diptera (48), Lepidoptera (45), Coleoptera (31 species), Hemiptera (14) and Neuroptera (1). The number of insect species per record was similar between different sites. The only slight significant differences could be seen between land use forms (Table 2). Semi-natural grassland possessed higher insect diversity, than flower strips. Individual numbers (quantities) of insects recorded on study plots differ both between areas and land use forms and fluctuate strongly in time (repeated measurements ANOVA, F = 2.97 p < 0.05), while these fluctuations have different rhythms in different treatments (Table 2). The quantities of insects were significantly correlated with the flower cover (Ad. R² = 0.325, F = 56.92, p < 0.001), but not with the diversity of plant species (Ad. R² = -0.005, F = 0.35, n.s.). Bee communities We identified entirely 41 bee species (Apiformes) during the study, 14 of them occurring only in grassland, 19 only in flower strips within vineyards and 8 in both habitat types (Table 3). Number of bee species was significantly correlated to the plant species diversity per plot (Ad. R² = 0.134, F = 19.42, p < 0.001), while number of individuals was clearly dependent on the entire flower cover (Ad. R² = 0.261, F = 43.00, p < 0.001). Most numerous were Apis mellifera (L.), Bombus lucorum (L.) / Bombus terrestris (L.) and Bombus lapidarius (L.). Honey bees and large earth bumblebees reached the highest individual numbers on Phacelia-dominated flower strips during its flowering time. Regarding their pollen specification, the majority of detected bee species can be considered as polylectic, but there are also some specialists / oligolectic species. As specialists on flower strips species using Brassicaceae (Andrena agilissima (Scop.) and Andrena floricola (Ev.)), Apiaceae (Andrena nitidiuscula Fig 1. Temporal dynamic of total flower cover in percent in relation to the total number of flower visiting insects, separated by location (Bisamberg vs. Leopoldsberg/Nussberg) and habitat type (flower strip/ grassland). Year of recording: 2015. Mean and mean +/- standard error is shown. (Schenck)), Asteraceae (Colletes similis (Schenck)), Fabaceae (Eucera nigrescens (Pérez) and Melitta leporina (Panz.)) as well as Convolvulus-Species (Systropha curvicornis (Scop.)) could be detected. At grassland patches there were mainly specialists feeding on Asteracea (Heriades crenulatus (Nyl.), Hylaeus nigritus (Fab.), Megachile pilicrus (Mor.) and Osmia spinulosa (Kir.)) and on Ranunculaceae (Chelostoma florisomne (L.)). There were also some differences in the bee species composition between habitats regarding their nesting behavior. The most common category were terricolous (ground nesting) species, wide spread on all sites. In contrast, cavity nesting could be mainly found on grassland sites (9 species) and only two of them on flower strips. All three species nesting in snail shells were only found in semi-natural grassland, among them the rare and in Austria endangered species Anthidium septemdentatum (Latr.). L Rasran; A Diener; B Pachinger; K-G Bernhardt – Pollinator diversity in dry grasslands and vineyards608 flower strips grassland Pollen source Nesting behavior Andrena agilissima (Scopoli, 1770) x Brassicaceae t Andrena chrysosceles (Kirby, 1802) x polylectic t Andrena floricola Eversmann, 1852 x Brassicaceae t Andrena haemorrhoa (Fabricius, 1781) x polylectic t Andrena minutula (Kirby, 1802) x polylectic t Andrena minutuloides Perkins, 1914 x polylectic t Andrena nitidiuscula Schenck, 1853 x Apiaceae t Anthidium septemdentatum Latreille, 1809 x polylectic hs Apis mellifera Linnaeus, 1758 x x polylectic Bombus hortorum (Linnaeus, 1761) x polylectic t/h Bombus hypnonum (Linnaeus, 1758) x polylectic t/h Bombus lapidarius (Linnaeus, 1758) x x polylectic t/h Bombus lucorum/Bombus terrestris x polylectic t/h Bombus pascuorum (Scopoli, 1763) x polylectic t/h Chelostoma florisomne (Linnaeus, 1758) x Ranunculus h Colletes similis Schenck, 1853 x Asteraceae t Eucera nigrescens Pérez, 1879 x x Fabaceae t Halictus quadricinctus (Fabricius, 1776) x x polylectic t Halictus rubicundus (Christ, 1791) x polylectic t Halictus sexcinctus (Fabricius, 1775) x polylectic t Halictus simplex Blüthgen, 1923 x x polylectic t Halictus tumulorum (Linnaeus, 1758) x polylectic t Heriades crenulatus Nylander, 1856 x Asteraceae h Hylaeus communis Nylander, 1852 x polylectic h Hylaeus gredleri Förster, 1871 x polylectic h Hylaeus nigritus (Fabricius, 1798) x Asteraceae h Lasioglossum malachurum (Kirby, 1802) x polylectic t Lasioglossum marginatum (Brullé, 1832) x x polylectic t Lasioglossum nigripes (Lepeletier, 1841) x polylectic t Lasioglossum pauxillum (Schenck, 1853) x x polylectic t Lasioglossum politum (Schenck, 1853) x polylectic t Lasioglossum leucozonium (Schrank, 1781) x polylectic t Megachile pilicrus Morawitz, 1877 x Asteraceae h Megachile rotundata (Fabricius, 1787) x polylectic h Melitta leporina (Panzer, 1799) x Fabaceae t Nomada succincta Panzer, 1798 x p p Osmia bicolor (Schrank, 1781) x polylectic hs Osmia spinulosa (Kirby, 1802) x Asteraceae hs Sphecodes gibbus (Linnaeus, 1758) x x p p Systropha curvicornis (Scopoli, 1770) x Convolvulus spp. t Xylocopa violacea (Linnaeus, 1758) x polylectic h Table 3. Distribution of bee species (Apoidea) between the habitats (flower strips in vineyards vs. grassland), pollen source and nesting behavior after Scheuchl & Willner, 2016 (p - cleptoparasite, h - cavity breeder, t - ground-nesting, t/h - ground-nesting and cavity breeder, hs - breeding in snail shells). Sociobiology 65(4): 603-611 (October, 2018) Special Issue 609 The species composition and quantity of bee communities have a good explanatory value between the studied habitats (CCA, Aj. expl. variation was 39.26 %, Axis 1 – 18.09 %, Axis 2 – 16.68 %, Pseudo-F on all axes =1.8, p = 0.013). In the ordination diagram bee communities clustered mainly in three groups corresponding to semi-natural grasslands (upper left part), flower strips in traditionally managed vineyards (right-hand part) and ecologically managed vineyards together with regularly mown grasslands (downer left part; Fig 2). Indeed, our study showed that semi-natural Pannonian grasslands remain a higher diversity and higher quality habitat for insects, especially bee species, in comparison to farmland. Even under pollinator-friendly conditions flower strips include a narrow selection of nectar- and pollen-offering plant species, not including those relevant for foraging specialists (see Wood et al., 2015). In our case flower strip sown mixtures contained no Ranunculaceae and only a little amount of Asteraceae-species, while these plant families were strongly represented in grassland patches. Also wild growing Apiaceae (O. grandiflora) and Brassicaceae (Lepidium draba) dominated locally some grassland patches and were important attractors for various insect species. Seed mixtures showed higher cover of Fabaceae (especially T. incarnatum, Medicago sativa (L.)) and P. tanacetifolia, a plant not present in grassland. These species together with Brassicaceae (S. alba) led flower strips within vineyards to provide very high values of flower cover. The entire number of insects, mainly generalists foraging on these species, was comparable or even higher, than on grasslands, especially mown (traditionally used) ones (see also Aviron et al., 2011). Generally, due to high quantities of flower visiting insects flower strips should be able to provide ecosystem (pollination) services for the surrounding landscape (Korpela et al., 2013). Further differences between grasslands and flower strips for bee species were manifested regarding the structure of microhabitats. This include the effects of nesting behavior (availability of cavity including snail shells) or in general the flower-richness of the surrounding and landscape heterogeneity (Rundlöf et al., 2008; Spiesman, 2017). Cultivation of vine rows and associated flower strips destroy small cavities, necessary as nesting habitats for bees. Semi-natural grasslands for their part are more suitable habitats for small snails, than flower strips. Bee species dependent on these structures occur mainly or solely at undisturbed dry grasslands. Differences between flower strips in traditional and organic vineyards are manifested in significant effects of area x treatment interaction, as vineyards of Bisamberg were organic ones and of Nussberg/Leopoldsberg the traditional ones. Flower cover of the strips differed only slightly between the two agricultural forms. But temporal dynamics (due to 2x cut of intensively used strips vs. 1x cut in ecological farming) differed more clearly. Similar to Holzschuh et al. (2007) we also found that the differences in insect (and especially bee) diversities and quantities could be to a significant part explained by the differences in flower cover. Remarkable are the similarities between moderately used grasslands and flower strips in organic managed vineyards (compare Holzschuh et al., 2010). Besides the similarities in management (1x mowing in mid-summer) avoidance of pesticide use could be a good explanation for the high species diversity there compared to traditional farming (e.g. Thompson, 2001, 2003). Attraction of wild bee species and further pollinators (e.g. hoverflies) is an important improvement of pollination services of flower strips for the neighbored crops (Campbell et al., 2017). Fig 2. Constrained ordination (CCA) of studied plots (without consideration of time dynamics). Vegetation cover (veg_cov), total flower cover (flo_cov) as well as flower cover of single plant groups: Ranunculaceae (Ran), Lamiaceae (Lam), Asteraceae (Ast), Apiaceae (Api), Fabaceae (Fab), Convolvulus (Conv) & Phacelia (Pha) were plotted as passive variables. B - location Bisamberg, L – location Leopoldsberg/Nussberg, seminat – semi-natural grassland, mown – intensively used grassland, ecol – flower strips in organic vineyards, int - flower strips in traditional vineyards. Bee species with the highest explanatory values are shown (see Table 3). Following species names are shortened: And_mino - Andrena minutuloides, Bom_hyp - Bombus hypnonum, Che_flo - Chelostoma florisomne, Hali_tum - Halictus tumulorum, Las_pol - Lasioglossum politum. Discussion As expected, the flower cover was the most significant predictor for quantities of insects in general and for the most common / generalist flower visitors in particular (Potts et al., 2003; Holland et al., 2015). Fluctuations of flower cover caused immediately changes at insect numbers. L Rasran; A Diener; B Pachinger; K-G Bernhardt – Pollinator diversity in dry grasslands and vineyards610 Conclusions Flower strips in vineyards are able to provide food for high quantities of flower-visiting insects, comparable to semi- natural grasslands of the surrounding. Especially strips within ecologically managed vineyards are comparable to moderately used (mown) grassland patches. The diversity of insect and explicitly of bee species was however higher at grassland sites due to food and nesting specialists, dependent on them. The development of ecologically managed flower strips can thus provide the important ecosystem service of pollination in the landscape, but protection of grassland patches is either crucial for the preservation of biodiversity. Acknowledgments We would like to thank Dr. Reinhard Eder and Stefan Lassl from the research farm “Götzhof” for their help and important information. Dr. Kati Vogt and two anonymous reviewers helped us with their remarks to improve the manuscript. The research was supported by the University Foundation of the City of Vienna (Hochschuljubiläumsstiftung der Stadt Wien). References Adler, W. & Mrkvicka, A.Ch. (2003). Die Flora Wiens gestern und heute. Wien: Verlag des NHM, 831 p. Aviron, S., Herzog, F., Klaus, I., Schüpbach, B. & Jeanneret, P. (2011). Effects of wildflower strip quality, quantity, and connectivity on butterfly diversity in a Swiss arable landscape. Restoration Ecology, 19: 500-508. doi: 10.1111/j.1526-100X. 2010.00649.x Biesmeijer, J.C., Roberts, S.P., Reemer, M., Ohlemüller, R., Edwards, M., Peeters, T., Schaffers, A.P., Potts, S.G., Kleukers, R., Thomas, C.D., Kunin, W.E. & Settele, J. (2006). Parallel declines in pollinators and insect-pollinated plants in Britain and the Netherlands. Science, 313: 351-354. doi: 10.1126/science.1127863 Bruggisser, O.T., Schmidt-Entling, M.H. & Bacher, S. (2010). Effects of vineyard management on biodiversity at three trophic levels. Biological Conservation 143: 1521-1528. doi: 10.1016/j.biocon.2010.03.034 Burkle, L.A., Marlin, J.C. & Knight, T.M. (2013). Plant- pollinator interactions over 120 years: loss of species, co- occurrence, and function. Science, 339: 1611-1615. doi: 10. 1126/science.1232728 Calvo, R.N. & Horvitz, C.C. (1990). Pollinator limitation, cost of reproduction, and fitness in plants: a transition-matrix demographic approach. American Naturalist, 136: 499-516. doi: 10.1086/285110 Campbell, A.J., Wilby, A., Sutton, P. & Wäckers, F.L. (2017). Do sown flower strips boost wild pollinator abundance and pollination services in a spring-flowering crop? A case study from UK cider apple orchards. Agriculture, Ecosystems & Environment, 239: 20-29. doi: 10.1016/j.agee.2017.01.005 Fischer, M.A., Oswald, K. & Adler, W. (2008). Exkursionsflora für Österreich, Lichtenstein und Südtirol, 3. Aufl. Biologiezentrum der Oberösterreichischen Landesmuseen, Linz, 1392 p. Fontaine, C., Dajoz, I., Meriguet, J. & Loreau, M. (2006). Functional Diversity of Plant–Pollinator Interaction Webs Enhances the Persistence of Plant Communities. PLoS Biology, 4: 129-135. doi: 10.1371/journal.pbio.0040001 Garibaldi, L.A., Steffan-Dewenter, I., Kremen, C., Morales, J.M., Bommarco, R., Cunningham, S.A., Carvalheiro, L.G., Chacoff, N.P., Dudenhöffer J.H., Greenleaf, S., Holzschuh, A., Isaacs, R., Krewenka, K., Mandelik, Y., Mayfield, M.M., Morandin, L.A., Potts, S.G., Ricketts, T.H., Szentgyörgyi, H., Viana, B.F., Westphal, C., Winfree, R. & Klein, A.M. (2011). Stability of pollination services decreases with isolation from natural areas despite honey bee visits. Ecology Letters, 14: 1062–1072. doi: 10.1111/j.1461-0248.2011.01669.x Gusenleitner, F., Schwarz, M., Mazzucco, K. (2012). Apidae (Insecta: Hymentoptera). In R. Schuster (Ed.), Biosystematics and Ecology Series No. 29: Checkliste der Fauna Österreichs (pp. 1-129), No. 6 ÖAW-Verlag der Österreichischen Akademie der Wissenschaften, Vienna. Haaland, C., Naisbit, R.E. & Bersier, L. F. (2011). Sown wildflower strips for insect conservation: a review. Insect Conservation and Diversity, 4: 60-80. doi: 10.1111/j.1752- 4598.2010.00098.x Holland, J.M., Smith, B.M., Storkey, J., Lutman, P. J. & Aebischer, N.J. (2015). Managing habitats on English farmland for insect pollinator conservation. Biological Conservation, 182: 215-222. doi: 10.1016/j.biocon.2014.12.009 Holzschuh, A., Steffan-Dewenter, I., Kleijn, D. & Tscharntke, T. (2007). Diversity of flower-visiting bees in cereal fields: effects of farming system, landscape composition and regional context. Journal of Applied Ecology, 44: 41-49. doi: 10.111 1/j.1365-2664.2006.01259.x Holzschuh, A., Steffan-Dewenter, I. & Tscharntke, T. (2010). How do landscape composition and configuration, organic farming and fallow strips affect the diversity of bees, wasps and their parasitoids? Journal of Animal Ecology, 79: 491- 500. doi: 10.1111/j.1365-2656.2009.01642.x Jennersten, O. & Nilsson, S.G. (1993). Insect flower visitation frequency and seed production in relation to patch size of Viscaria vulgaris (Caryophyllaceae). Oikos, 68: 283–292. doi: 10.2307/3544841 Keller, M., Kollmann, J. & Edwards, P.J. (2000). Genetic introgression from distant provenances reduces fitness in local weed populations. Journal of Applied Ecology, 37: 647- Sociobiology 65(4): 603-611 (October, 2018) Special Issue 611 659. doi: 10.1046/j.1365-2664.2000.00517.x Klein, A.M., Vaissiere, B.E., Cane, J.H., Steffan-Dewenter, I., Cunningham, S.A., Kremen, C. & Tscharntke, T. (2007). Importance of pollinators in changing landscapes for world crops. Proceedings of the Royal Society of London B: Biological Sciences, 274(1608): 303-313. doi: 10.1098/rspb.2006.3721 Korpela, E.L., Hyvönen, T., Lindgren, S. & Kuussaari, M. (2013). Can pollination services, species diversity and conservation be simultaneously promoted by sown wildflower strips on farmland? Agriculture, Ecosystems & Environment, 179: 18-24. doi: 10.1016/j.agee.2013.07.001 Larson, B.M.H. & Barrett, S.C.H. (2000). A comparative analysis of pollen limitation in flowering plants. Biological Journal of the Linnean Society, 69: 503–520. doi: 10.1111/ j.1095-8312.2000.tb01221.x Londo, G. (1976). The decimal scale for relevés of permanent quadrats. Plant Ecology, 33(1): 61-64. doi: 10.1007/BF00055300 Neumayer, J. (2011). Bestäubung - Warum wir Bienen & Co brauchen. Natur & Land, 2: 4–9. Potts, S.G., Vulliamy, B., Dafni, A., Ne’eman, G. & Willmer P. (2003). Linking bees and flowers: how do floral communities structure pollinator communities? Ecology, 84: 2628-2642. doi: 10.1890/02-0136 Proctor, M., Yeo, P. & Lack, A. (1996). The natural history of pollination. London: Harper Collins Publishers New Naturalist, 487 p. R Development Core Team. (2015). R: a language and environment for statistical computing, version 3.3.1. R Foun- dation for Statistical Computing, Computer Program, Vienna. Richards, A.J. (1978). The pollination of flowers by insects. London: Academic Press for the Linnean Society xi (Linnean Society Symposium Series 20. 6.), 213 p. Rundlöf, M., Nilsson, H. & Smith, H.G. (2008). Interacting effects of farming practice and landscape context on bumble bees. Biological Conservation, 141: 417-426. doi: 10.1016/j. biocon.2007.10.011 Rundlöf, M., Persson, A.S., Smith, H.G. & Bommarco, R. (2014). Late-season mass-flowering red clover increases bumble bee queen and male densities. Biological Conservation, 172: 138-145. doi: 10.1016/j.biocon.2014.02.027 Scheuchl, E. & Willner, W. (2016). Taschenlexikon der Wildbienen Mitteleuropas: Alle Arten im Porträt. Quelle & Meyer Verlag, Wiebelsheim, 920 p. Sharma, N., Koul, P. & Koul, A.K. (1993). Pollination biology of some species of genus Plantago L. Botanical Journal of the Linnean Society, 111: 129-138. doi: 10.1111/j.1095-8339. 1993.tb01895.x Smilauer, P. & Leps, J. (2014). Multivariate analysis of ecological data using CANOCO 5. Cambridge: Cambridge University Press, 2nd ed., 362 p. Spiesman, B.J., Bennett, A., Isaacs, R. & Gratton, C. (2017). Bumble bee colony growth and reproduction depend on local flower dominance and natural habitat area in the surrounding landscape. Biological Conservation, 206: 217-223. doi: 10.1016/ j.biocon.2016.12.008 Thompson, H.M. (2001). Assessing the exposure and toxicity of pesticides to bumblebees (Bombus sp.). Apidologie, 32: 305-321. doi: 10.1051/apido:2001131 Thompson, H.M. (2003). Behavioural effects of pesticides in bees–their potential for use in risk assessment. Ecotoxicology, 12: 317-330. doi: 10.1023/A:1022575315413 Tscharntke, T., Steffan-Dewenter, I., Kruess, A. & Thies, C. (2002). Contribution of small habitat fragments to conservation of insect communities of grassland–cropland landscapes. Ecological Applications, 12: 354-363. doi: 10.1890/1051-0761 van Elsen, T., Godt, J., Haase, T., Fricke, T., Wachendorf, M., Saucke, H., Möller, D., Quintern, M., Otto, M., Kölsch, E., Baars, T. & Heß, J. (2007). E+ E-Projekt, Integration von Naturschutzzielen in den Ökologischen Landbau am Beispiel der Hessischen Staatsdomäne Frankenhausen “-Maßnahmen in der bewirtschafteten Fläche. 9. Wissenschaftstagung Ökologischer Landbau, Universität Hohenheim, Stuttgart, Deutschland. http://orgprints.org/view/projects/wissenschaftsta gung-2007.html Wood, T. J., Holland, J. M. & Goulson, D. (2015). Pollinator- friendly management does not increase the diversity of farmland bees and wasps. Biological Conservation, 187: 120- 126. doi: 10.1016/j.biocon.2015.04.022