Literature DB >> 34307807

A dataset of the flowering plants (Angiospermae) in urban green areas in five European cities.

Joan Casanelles-Abella1,2, David Frey1, Stefanie Müller1,3, Cristiana Aleixo4, Marta Alós Ortí5, Nicolas Deguines6,7, Tiit Hallikma5, Lauri Laanisto5, Ülo Niinemets5, Pedro Pinho4, Roeland Samson8, Lucía Villarroya-Villalba1, Marco Moretti1.   

Abstract

This article summarizes the data of a survey of flowering plants in 80 sites in five European cities and urban agglomerations (Antwerp, Belgium; greater Paris, France; Poznan, Poland; Tartu, Estonia; and Zurich, Switzerland). Sampling sites were selected based on a double orthogonal gradient of size and connectivity and were urban green areas (e.g. parks, cemeteries). To characterize the flowering plants, two sampling methodologies were applied between April and July 2018. First, a floristic inventory of the occurrence of all flowering plants in the five cities. Second, flower counts in sampling plots of standardized size (1 m2) only in Zurich. We sampled 2146 plant species (contained in 824 genera and 137 families) and across the five cities. For each plant species, we provide its origin status (i.e. whether the plants are native from Europe or not) and 11 functional traits potentially important for plant-pollinator interactions. For each study site, we provide the number of species, genera, and families recorded, the Shannon diversity as well as the proportion of exotic species, herbs, shrubs and trees. In addition, we provide information on the patch size, connectivity, and urban intensity, using four remote sensing-based proxies measured at 100- and 800-m radii.
© 2021 The Author(s). Published by Elsevier Inc.

Entities:  

Keywords:  Floral traits; Fragmentation; Gardening; Plant traits; Plants; Urban biodiversity; Urban flora; Urban green infrastructure; Urban green spaces

Year:  2021        PMID: 34307807      PMCID: PMC8258796          DOI: 10.1016/j.dib.2021.107243

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table

Value of the Data

The dataset describes the diversity, occurrence, and floral counts of a large number of flowering plant families sampled in a standardized way in different types of public and private green areas in European cities, and with a high taxonomic resolution. The data contribute characterizing European urban floras, derive taxonomic, phylogenetic and trait diversity patterns, and perform comparative studies among different cities, different types of urban green areas and in fragmentation studies. The data can be used to characterize the available food resources of other trophic levels, particularly pollinators, and species interactions. The data on floral counts can be combined with metrics on nectar and pollen content to obtain estimates of resources quality (e.g. as done in [1]) The methodology for collecting the data can be applied in further studies aiming to characterize plant resources in one or more urban ecosystems in a standardized way.

Data Description

The paper presents the data of a plant survey in urban green areas from five European cities and urban agglomerations (Antwerp, Belgium; greater Paris, France; Poznan, Poland; and Zurich, Switzerland). 80 sites were selected (32 in Zurich and 12 in each of the remaining four cities, see Fig. 1) according to an orthogonal gradient of patch size and connectivity (see Section 2.2), representing common public urban green areas such as parks, cemeteries and gardens. To characterize the flowering plants, we sampled plants during four (for Zurich) and three (for Antwerp, Paris, Poznan and Tartu) sampling periods during the year 2018. The sampling was performed in (1) end of April (only for Zurich), (2) end of May, (2) end of June and (3) end of July. The sampling consisted in two methodologies. First, a floristic inventory of the occurrence of all flowering plants inside buffers of 100 m radius (see Fig. 1) in the study sites of the five cities. Second, flower counts of defined floral units (Table 1) in sampling plots of standardized size (1 m2) distributed inside buffers of 100 m radius (see Fig. 1) done only in Zurich. The 100 m radius buffer was defined from existing installed trap-nests place to sample cavity-nesting bees and wasps (Fig. 1).
Fig. 1

Maps of the study sites in each of the five cities (Antwerp, Greater Paris, Poznan, Tartu and Zurich) and an example of how the sampling was conducted. For the site Zu006 (located in Zurich), we show the trap-nest location (green dot), the 100 m radius buffer around it and the 16 cells dividing the buffer.

Table 1

Definition of the flower units and calculation of the floral abundance. For each floral unit type, we show the plant taxa included and how the floral abundance was calculated. For specific floral unit types (i.e. capitula in Dipsacoidae, compound cymes, corymb, panicles, racemes and umbels) we estimated the number of flowers per floral unit by counting all the flowers in seven floral units and computing the mean. Ditto = the same again.

Floral unit definitionPlant taxaEstimation number of flowers within a floral unit (Nf)Floral abundance (Fa)
Single flowersAcanthaceae, Alismataceae, Amaranthaceae, Anacardiaceae, Apocynaceae, Asparagaceae, Balsaminaceae, Begoniaceae, Boraginaceae, Brassicaceae, Campanulaceae (except Phyteuma spp.), Caprifoliaceae (except Dipsacoideae), Caryophyllaceae, Celastraceae, Cistaceae, Cleomaceae, Convolvulaceae, Crassulaceae, Cucurbitaceae, Cytisus spp., Geraniaceae, Hypericaceae, Iridiaceae, Lamiaceae, Lathyrus spp., Linaceae, Lythraceae, Magnoliaceae, Malvaceae, Onargaceae, Orchidaceae, Orobanchaceae, Oxalidaceae,Papaveraceae, Phrymaceae, Plantaginaceae (except Plantago spp.), Polemoniaceae, Polygonaceae, Portulacaceae, Primulaceae, Ranunculaceae, Resedaceae, Rhododendron spp., Rosaceae (except Filipendula ulmaria, Sanguisorba spp., Spiraea spp.), Rutaceae, Saxifragaceae, Spartium spp., Solanaceae, Scrophulariaceae (except Buddleja davidii), Tropeolaceae, Verbenaceae, Violaceae, XanthorrhoeaceaeNot applicableFa=(floralunits)

Single capitulum (in Dipsacoideae)DipsacoideaeEstimation in seven different floral unitsNf = mean of the seven countsFa=((floralunits)×Nf)

Single compound cymeCentranthus spp.DittoDitto

Single corymbAdoxaceae, CornaceaeDittoDitto

Single panicleSapindaceae*, Buddleja davidii, Galium spp., Filipendula ulmaria, Sherardia arvensis, Spiraea spp, Syringa vulgarisDittoDitto
Single racemeFabaceae* (except Cytisus spp., Lathyrus spp., Spartium spp.), Hedera helix, Ligustrum spp., VitaceaeDittoDitto

Single secondary umbellApiaceaeDittoDitto

Single umbellAllium spp.DittoDitto

Single capitulum (in Asteraceae)AsteraceaeNot estimatedFa=(floralunits)

Single catkinBetulaceae*, Fagaceae*, Salicaceae*Not estimatedDitto

Single corymb & single cyme in Hydragea spp.Hydrangea spp.Not estimatedDitto

Single cyme with cyathiaEuphorbia spp.Not estimatedDitto

Single dense clusterSanguisorbaNot estimatedDitto

Single spike (in Plantago spp. & Tamarix spp.)Plantago spp., Tamarix spp.Not estimatedDitto

Observation of the tree canopy and the floral counts of the woody species in these families were done from the ground and are a rough estimate.

Maps of the study sites in each of the five cities (Antwerp, Greater Paris, Poznan, Tartu and Zurich) and an example of how the sampling was conducted. For the site Zu006 (located in Zurich), we show the trap-nest location (green dot), the 100 m radius buffer around it and the 16 cells dividing the buffer. Definition of the flower units and calculation of the floral abundance. For each floral unit type, we show the plant taxa included and how the floral abundance was calculated. For specific floral unit types (i.e. capitula in Dipsacoidae, compound cymes, corymb, panicles, racemes and umbels) we estimated the number of flowers per floral unit by counting all the flowers in seven floral units and computing the mean. Ditto = the same again. Observation of the tree canopy and the floral counts of the woody species in these families were done from the ground and are a rough estimate. For each of the 2146 plant species recorded we show in what cities it was recorded (Supplementary material, Table A1). Furthermore, we provide information on 11 traits of potential interest to study plant-pollinator interactions (Table 2) that are the flowering duration, flowering start, growth form, inflorescence type, plant height, floral rewards in the form of nectar, oil and pollen, structural blossom class and floral symmetry based on bibliographic information. Additionally, we documented the origin status of all the sampled plant species, that is, whether or not they are native from Europe. We computed the species, genera, and family richness for each site (Table 3 and Fig. 2) and the composition of plant families of the species sampled in each city (Fig. 3). Moreover, we computed the proportion of exotic species, as well as the proportion of trees, shrubs, and herbs for each site and city (Table 3 and Fig. 4). In addition, we show the frequency distribution of floral counts (Fig. 5) and the composition of plant genera in the flower abundance (Fig. 6) in the city of Zurich.
Table 2

List of the 11 traits included. For each trait together, there is a description, the taken values, and references of the sources used to build the trait table. See also Section 2.7 Traits.

TraitDescriptionValuesReferences
Flowering durationNumber of months a plant species flower.1–12[4], [5], [6], [7], [8]

Flowering startThe month the blossom of a plant species begins to flower.1–12[4], [5], [6], [7], [8]

Growth formClassification of plant species in four broad growth form categories.HerbShrubTreeClimber[6,[9], [10], [11]

Inflorescence typeDetermines whether the blossom is a single flower or an inflorescence.With inflorescenceWithout inflorescence[4], [5], [6],12]

Plant height (m)Measure of the height of a plant species in meters.[4,6,9,10]

Pollination modeDefinition whether a plant species is biotically or abiotically pollinated.BioticAbiotic[6,9]

Rewards: nectarDescribes whether the plant provides nectar resources.AbsentPresent[4,5,10,[13], [14], [15], [16]

Rewards: oilsDescribes whether the plant provides oils.AbsentPresent[4,5,10,[13], [14], [15], [16]

Rewards: pollenDescribes whether the plant provides pollen resources.AbsentPresent[4,5,10,[13], [14], [15], [16]

Structural Blossom ClassDescribing the shape of the blossom of the plant species.Dish-bowlStalk-diskBell trumpetBrushGulletFlagTubeAdapted from [17]

SymmetryDescribes the number of axes of reflection of a flower of a plant species. The value was derived from the structural blossom classNo symmetryZygomorphActinomorph
Table 3

Summary statistics of the plants recorded. For each of the 80 study sites in the five cities, we provide the number of species (N), genera (N), families (N), the value of the Shannon diversity index (H’), and the proportion of herbs (P), shrubs (P), trees (P), and exotic species (P). H’ was calculated using the frequency of each plant species, obtained as the number of cells from the total 16 where the plant was found. The data are based on floristic inventories in the study sites. The data are plotted in Fig. 1-2. Site codes represent the study sites shown in Fig. 1. Note that the statistic does not include species in the families Cyperaceae, Juncaceae and Poaceae. The coordinates of the sites are provided in Table 4.

CitySiteNspeciesNgeneraNfamiliesH'PherbsPshrubsPtreesPexotic
AntwerpAn0119187414.750.720.130.130.34
An0164439223.830.740.170.060.13
An0206157334.30.70.160.120.27
An0565244264.010.860.090.040.15
An0572724153.30.70.110.150.3
An0626553254.160.790.060.090.36
An0686060364.20.610.160.160.48
An0736452294.260.660.170.140.31
An0826156294.160.640.170.140.39
An0884739243.890.650.20.080.33
An0925345244.030.770.110.090.23
An1028573364.550.770.130.080.32

ParisPa013191138515.30.720.180.080.33
Pa191148124515.110.70.170.110.44
Pa24510290404.710.730.140.110.21
Pa2659179394.620.710.190.090.38
Pa269171146565.190.650.220.110.36
Pa2828368344.60.70.070.210.22
Pa295125112544.950.690.190.10.43
Pa39811675551007.070.830.130.020.42
Pa4188575364.480.760.160.050.41
Pa4929174364.580.820.090.090.2
Pa535122110464.910.770.110.10.39
Pa5735251324.080.50.290.170.39

PoznanPo0014543193.910.840.120.040.28
Po0371224163.260.620.150.230.35
Po0595656284.130.760.130.110.24
Po1373729143.640.840.130.030.24
Po1793632193.660.770.050.160.18
Po1837567284.410.740.150.090.28
Po2103533183.690.920.030.050.12
Po2275865324.280.720.10.160.38
Po2673842233.910.80.020.180.16
Po3486352244.20.720.150.110.3
Po4064442183.890.840.060.060.24
Po4237266314.390.790.110.10.2

TartuTa0088773314.530.890.060.030.29
Ta0135948244.140.870.020.080.11
Ta0255145213.950.920.020.060.08
Ta0334840173.850.9800.020.11
Ta04010086354.630.890.040.060.24
Ta0476457294.220.850.030.070.1
Ta0577966294.480.910.020.050.22
Ta0644138203.810.890.020.090.09
Ta1024643183.950.940.020.040.06
Ta1045143193.990.910.040.060.07
Ta1107863284.370.920.050.020.19
Ta1255960304.290.870.030.070.21

ZurichZu006210143575.390.80.120.060.34
Zu007131100354.910.90.040.050.24
Zu015730386996.60.830.110.050.41
Zu018210142535.420.740.130.10.3
Zu033279187585.680.750.120.10.33
Zu039144115455.040.810.090.080.24
Zu057261187625.650.670.150.150.32
Zu062144115474.990.740.160.10.32
Zu067168128505.210.780.10.070.33
Zu08011088404.730.820.090.090.15
Zu082212158565.420.770.090.110.31
Zu08710685324.710.770.130.070.25
Zu094254185625.60.840.080.050.28
Zu10512686324.870.790.10.10.1
Zu113158109445.110.750.150.090.19
Zu11913695364.930.850.050.10.12
Zu126223171565.480.810.120.060.33
Zu133238162575.510.760.150.070.33
Zu141112114415.210.790.120.080.21
Zu154201136485.30.810.10.060.25
Zu15524581274.80.870.070.050.12
Zu158149132455.340.850.060.060.21
Zu173191168515.550.790.120.070.32
Zu179180110455.060.830.130.020.28
Zu904172131455.190.880.040.060.27
Zu905161124465.10.830.090.060.26
Zu906237156535.490.870.070.040.29
Zu907205146465.350.790.130.0010.28
Zu908182122515.260.740.130.110.27
Zu910220159575.470.740.120.090.28
Zu911213136515.40.830.090.060.22
Zu91211386414.760.670.160.140.25
Fig. 2

Flat violin [18] and boxplots representing the Shannon diversity (A) and the number of families (B), genera (C), and species (D) recorded in the study sites in Antwerp, Paris, Poznan, Tartu, and Zurich. Each point in a city represents a measurement in one of the sampling sites (12 in Antwerp, Paris, Poznan and Tartu and 32 in Zurich) and in one of the sampling periods (four periods for Zurich and three periods for the remaining four cities). Note that for Paris and Zurich there are two points with larger richness, which corresponds to the study sites in the botanical gardens of Paris (Jardin des Plantes, National Museum of Natural History) and Zurich (Zurich Botanical Garden). Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling.

Fig. 3

Barplot of the percentage of the different plant families sampled in all study sites (32 in Zurich and 12 in each of the remaining cities) in each city. Only families containing more than 1% of the species sampled in all the study sites and the sampling periods are shown separately. The remaining families are grouped into the category “Other 103 families” (light gray) and the exact number is provided for each city at the top of each bar (i.e. 29 families in Antwerp, 73 families in Paris, 14 families in Poznan, 18 families in Tartu and 86 families in Zurich). Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling.

Fig. 4

Flat violin [18] and boxplots representing the proportion of exotic plant species (A), trees (B), herbs (C), and shrubs (D) in the study sites in Antwerp, Paris, Poznan, Tartu, and Zurich respectively. Each point in a city represents a measurement in one of the sampling sites (12 in Antwerp, Paris, Poznan and Tartu and 32 in Zurich) and in one of the sampling periods (four periods for Zurich and three periods for the remaining four cities). Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling.

Fig. 5

Histogram of the floral counts in the city of Zurich. Floral abundance, shown in the X axis, is calculated as the sum of all the floral units (see Table 1 for the definitions) in all the quadrats for a given site and sampling period, giving a total N of 128 (32 sites x 4 sampling periods). The dashed vertical line represents the median floral abundance and the straight vertical line the mean floral abundance recorded.

Fig. 6

Barplot of the percentage of plant genera in the floral abundance counted in Zurich. Only genera containing more than 1% of the species sampled in all the study sites are shown separately. The remaining genera are grouped into the category “Other genera” (light gray) and the exact number (272) is provided at the top of the bar. Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling.

List of the 11 traits included. For each trait together, there is a description, the taken values, and references of the sources used to build the trait table. See also Section 2.7 Traits. Summary statistics of the plants recorded. For each of the 80 study sites in the five cities, we provide the number of species (N), genera (N), families (N), the value of the Shannon diversity index (H’), and the proportion of herbs (P), shrubs (P), trees (P), and exotic species (P). H’ was calculated using the frequency of each plant species, obtained as the number of cells from the total 16 where the plant was found. The data are based on floristic inventories in the study sites. The data are plotted in Fig. 1-2. Site codes represent the study sites shown in Fig. 1. Note that the statistic does not include species in the families Cyperaceae, Juncaceae and Poaceae. The coordinates of the sites are provided in Table 4.
Table 4

Site features for each study site based on remote sensing data. For each of the 80 study sites in the five cities, we provide the coordinates where the trap-nest was located, the proximity index (Prox), and patch area (Area) used to select the study sites, and the values of the Second Brightness Index (BI2), Color Index (CI), Urban Index (UI), and Normalized Difference Vegetation Index (NDVI) at 100- and 800-meter radii.

CitySiteXYProx.Area (m2)BI2100BI2800CI100CI800UI100UI800NDVI100NDVI800
AntwerpAn0114.3651.161218.961,085,8540.180.18−0.12−0.10−0.38−0.330.670.55
An0164.4251.18931.4712,4260.160.15−0.13−0.07−0.42−0.310.680.54
An0204.3751.186.8220,1690.150.13−0.060.02−0.28−0.090.490.30
An0564.4851.21247.141,054,8850.200.16−0.21−0.11−0.52−0.340.780.58
An0574.3951.211.5267040.130.100.030.02−0.03−0.100.250.05
An0624.4451.223.3111,1160.140.110.050.04−0.09−0.030.310.22
An0684.4251.222.3193,5420.140.11−0.080.02−0.29−0.020.460.20
An0734.3951.2249.9256,9280.190.13−0.090.00−0.34−0.180.570.14
An0824.4751.244.4860,9430.170.15−0.19−0.02−0.50−0.140.760.33
An0884.4651.257.6914,4010.140.15−0.04−0.05−0.26−0.250.540.47
An0924.4551.2691.9256,1660.180.17−0.06−0.07−0.36−0.310.620.54
An1024.4351.293995.6252,0590.160.170.03−0.03−0.20−0.240.480.50

ParisPa0132.1748.7024.13126,6280.190.18−0.14−0.14−0.45−0.410.660.61
Pa1912.3048.8029.4224,9930.170.16−0.16−0.01−0.46−0.160.670.35
Pa2452.4248.842792.455,933,0640.180.17−0.10−0.07−0.48−0.290.690.46
Pa2652.3748.832.0035530.150.140.030.02−0.01−0.060.220.23
Pa2692.3448.825.39159,6110.160.15−0.110.00−0.42−0.130.620.30
Pa2822.3848.833.8098900.150.14−0.02−0.01−0.100.020.270.10
Pa2952.3748.832.0183390.150.14−0.010.01−0.110.000.280.14
Pa3982.3648.842.98169,3270.210.14−0.11−0.03−0.47−0.040.650.14
Pa4182.2948.849.8346300.140.130.010.010.01−0.010.140.14
Pa4922.2648.8545,794.2891480.150.15−0.07−0.04−0.29−0.210.460.35
Pa5352.3248.8749.76164,1010.180.14−0.07−0.04−0.34−0.030.490.11
Pa5732.3248.881.7946070.130.13−0.01−0.010.040.070.09−0.01
PoznanPo00116.9852.31862.4330,4430.160.17−0.06−0.10−0.29−0.340.560.57
Po03716.9052.3611.6648,7720.170.15−0.22−0.08−0.50−0.300.690.48
Po05916.8852.375.9682000.130.14−0.03−0.04−0.22−0.240.440.40
Po13716.9352.3931.09187,1030.170.15−0.13−0.07−0.44−0.280.680.47
Po17916.9052.403.4656,8860.170.13−0.170.01−0.45−0.090.660.24
Po18316.9552.402136.4510,4230.140.15−0.05−0.04−0.30−0.190.490.35
Po21016.9352.417.9513,2220.150.12−0.080.01−0.24−0.060.440.21
Po22716.8752.4110.5084060.140.15−0.08−0.06−0.33−0.280.530.46
Po26716.9552.43325.971,059,8250.170.16−0.16−0.11−0.44−0.350.680.53
Po34816.9352.4418.6318,7210.160.15−0.09−0.07−0.37−0.290.570.47
Po40616.9252.46468.4756240.150.14−0.04−0.02−0.23−0.190.450.40
Po42316.9352.4712,829.4727,9740.140.15−0.11−0.12−0.32−0.360.560.56

TartuTa00826.7758.3514.2763380.160.16−0.17−0.15−0.40−0.370.660.61
Ta01326.7458.352.74122,8570.170.16−0.23−0.05−0.41−0.160.680.34
Ta02526.7058.372.8733,2370.150.15−0.17−0.08−0.36−0.210.600.44
Ta03326.6858.385.7862250.140.16−0.05−0.06−0.18−0.200.400.42
Ta04026.7358.37314.5636,5900.150.14−0.08−0.07−0.22−0.160.430.35
Ta04726.7258.3857.84131,1000.140.14−0.23−0.10−0.38−0.210.650.43
Ta05726.6958.385.3650660.160.16−0.11−0.08−0.28−0.220.520.44
Ta06426.7458.3714.97183,2270.160.14−0.22−0.10−0.42−0.220.560.39
Ta10226.7058.3922.5413,2360.150.16−0.18−0.14−0.38−0.320.640.56
Ta10426.7658.385.3237,4120.180.17−0.21−0.11−0.41−0.260.670.50
Ta11026.7358.397.0286230.150.15−0.11−0.09−0.27−0.240.530.45
Ta12526.7358.3926.38245,7060.150.15−0.26−0.12−0.45−0.290.730.53

ZurichZu0068.5247.35104.93104,8710.170.16−0.19−0.12−0.49−0.320.770.59
Zu0078.5647.357.0137170.080.10−0.24−0.28−0.02−0.110.080.16
Zu0158.5647.36167.2339,2580.170.14−0.20−0.06−0.46−0.200.740.51
Zu0188.5347.3656.9757,6660.170.13−0.13−0.11−0.39−0.140.680.36
Zu0338.5647.3628.2410,4000.120.14−0.04−0.07−0.15−0.210.500.52
Zu0398.5447.3610.9636,8830.150.10−0.12−0.18−0.320.010.520.12
Zu0578.5347.376.7413,0400.130.11−0.14−0.01−0.290.010.570.25
Zu0628.5447.376.1618,0370.120.11−0.03−0.02−0.060.040.390.22
Zu0678.5147.3714.78275,3200.180.14−0.18−0.05−0.48−0.170.750.49
Zu0808.5447.388.7526,8550.140.11−0.28−0.02−0.38−0.020.640.27
Zu0828.4947.3817.5113,8540.160.15−0.13−0.06−0.34−0.180.680.49
Zu0878.5247.394.8722,7110.130.12−0.020.01−0.130.000.340.21
Zu0948.4747.39974.6496,1820.200.17−0.17−0.17−0.42−0.400.690.67
Zu1058.5047.4067.9795760.160.14−0.21−0.05−0.36−0.160.670.39
Zu1138.5247.4034,334.0646,4860.180.15−0.11−0.15−0.27−0.340.570.62
Zu1198.5447.4025.45108,0590.160.14−0.15−0.05−0.39−0.190.630.49
Zu1268.5047.4015.6711,7480.170.16−0.10−0.09−0.31−0.260.610.55
Zu1338.5447.4113.9135110.140.14−0.06−0.04−0.21−0.160.520.45
Zu1418.4847.4132.0584210.150.16−0.07−0.12−0.26−0.320.530.58
Zu1548.5147.41750.6157,1500.170.16−0.07−0.17−0.32−0.380.560.65
Zu1558.5547.416.5143460.170.14−0.03−0.01−0.17−0.080.330.35
Zu1588.5347.417.7559360.120.150.00−0.02−0.07−0.130.350.41
Zu1738.5147.4225.0356070.130.16−0.09−0.11−0.26−0.300.560.59
Zu1798.5347.422778.23103,0830.190.17−0.21−0.11−0.46−0.300.760.57
Zu9048.5247.395.0482530.130.130.010.02−0.090.010.280.18
Zu9058.5647.417.0210,9870.140.15−0.03−0.02−0.14−0.110.430.37
Zu9068.5947.409.1010,6290.150.15−0.05−0.07−0.22−0.200.530.48
Zu9078.4947.4025.2122,8940.150.14−0.08−0.06−0.24−0.170.530.40
Zu9088.5847.35262.43102,4010.170.16−0.25−0.16−0.54−0.380.810.65
Zu9108.5347.3414.5053,8980.170.13−0.12−0.14−0.30−0.130.630.34
Zu9118.5047.4318.0932190.150.17−0.05−0.09−0.20−0.280.430.53
Zu9128.5547.358.7189,8600.160.08−0.13−0.30−0.31−0.080.470.09
Flat violin [18] and boxplots representing the Shannon diversity (A) and the number of families (B), genera (C), and species (D) recorded in the study sites in Antwerp, Paris, Poznan, Tartu, and Zurich. Each point in a city represents a measurement in one of the sampling sites (12 in Antwerp, Paris, Poznan and Tartu and 32 in Zurich) and in one of the sampling periods (four periods for Zurich and three periods for the remaining four cities). Note that for Paris and Zurich there are two points with larger richness, which corresponds to the study sites in the botanical gardens of Paris (Jardin des Plantes, National Museum of Natural History) and Zurich (Zurich Botanical Garden). Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling. Barplot of the percentage of the different plant families sampled in all study sites (32 in Zurich and 12 in each of the remaining cities) in each city. Only families containing more than 1% of the species sampled in all the study sites and the sampling periods are shown separately. The remaining families are grouped into the category “Other 103 families” (light gray) and the exact number is provided for each city at the top of each bar (i.e. 29 families in Antwerp, 73 families in Paris, 14 families in Poznan, 18 families in Tartu and 86 families in Zurich). Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling. Flat violin [18] and boxplots representing the proportion of exotic plant species (A), trees (B), herbs (C), and shrubs (D) in the study sites in Antwerp, Paris, Poznan, Tartu, and Zurich respectively. Each point in a city represents a measurement in one of the sampling sites (12 in Antwerp, Paris, Poznan and Tartu and 32 in Zurich) and in one of the sampling periods (four periods for Zurich and three periods for the remaining four cities). Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling. Histogram of the floral counts in the city of Zurich. Floral abundance, shown in the X axis, is calculated as the sum of all the floral units (see Table 1 for the definitions) in all the quadrats for a given site and sampling period, giving a total N of 128 (32 sites x 4 sampling periods). The dashed vertical line represents the median floral abundance and the straight vertical line the mean floral abundance recorded. Barplot of the percentage of plant genera in the floral abundance counted in Zurich. Only genera containing more than 1% of the species sampled in all the study sites are shown separately. The remaining genera are grouped into the category “Other genera” (light gray) and the exact number (272) is provided at the top of the bar. Note that the families Cyperaceae, Juncaceae and Poaceae were not included in the sampling. We provide information on the study site features including the city, their size, connectivity, and urban intensity inferred using a set of remote sensing-based proxies on soil, grey infrastructure, and vegetation, including the Second Brightness Index (BI2), the Color Index (CI), the Urban Index (UI), and the Normalized Difference Vegetation Index (NDVI) within a 100 and 800 m buffer centered in the centroid of the urban green area (Table 4). The data are part of the interdisciplinary research project BioVeins investigating different aspects of urban biodiversity and ecosystem services in urban green areas in European cities (https://www.biodiversa.org/1012). The data can be linked to other taxonomic groups such as nocturnal insects and bats [2], sampled in the same study locations and during the same period. The raw data are available from the repository Envidat [3] with the DOI doi:10.16904/envidat.210. Site features for each study site based on remote sensing data. For each of the 80 study sites in the five cities, we provide the coordinates where the trap-nest was located, the proximity index (Prox), and patch area (Area) used to select the study sites, and the values of the Second Brightness Index (BI2), Color Index (CI), Urban Index (UI), and Normalized Difference Vegetation Index (NDVI) at 100- and 800-meter radii.

Experimental Design, Materials and Methods

Data source

The data was acquired in the European cities of Antwerp, Belgium (51°15′N, 4°24′E), Greater Paris, France (48°51′N, 8°05′E), Poznan, Poland (52°24′N, 16°55′E), Tartu, Estonia (58°22′N, 26°43′E), Zurich, Switzerland (47°22′N, 8°33′E). The climate of Antwerp is oceanic, the climate of Paris is temperate, the climate of Poznan is continental, the climate of Tartu is mild continental boreal and the climate of Zurich is mild continental temperate. The agglomeration of greater Paris is the most populated one in Europe with more than seven million inhabitants (2.18 million inhabitants only in the city of Paris [19]). Antwerp has the second highest population (0.53 million inhabitants [19]) followed by Poznan (0.53 million inhabitants [19]), Zurich (0.4 million inhabitants [19]), and Tartu (0.09 million inhabitants [19]).

Site selection

We selected patches among urban green areas mapped and defined in the European Urban Atlas [see 20], which includes mostly public urban green areas in the form of parks, cemeteries, and ruderal patches. We used an orthogonal gradient of patch size (area in m2) and connectivity. Connectivity was calculated using the Proximity Index (PI) which considers the area and the distance to all nearby patches with a favorable habitat, within a given search radius (in our case 5000 m), and is defined as:Where a is the area (m2) of a patch ijs within specified neighbourhood (m) of a patch ij, and is the distance (m) between the patch ijs, based on patch edge-to-edge distance. Thus, the PI measures the degree of patch isolation, with highest values given to less isolated patches. We considered as favourable habitat all patches with high probability of having trees (besides urban green areas, also forest and low density urban, with less than 30% impervious surface, see [20]). The search radius was set to 5 km from each focal patch, the maximum possible with the available cartography. In fact, lower buffer values (from 500 m onwards) did not greatly change the PI values, because the distances are squared, thus greatly limiting the impact of patches beyond a certain distance. To select patches using the orthogonal design, all possible patches were classified in six size classes and six classes of the PI (36 possible combinations). Within these combinations, patches were selected randomly (random stratified sampling design). Due to resource limitations, we only used 1⁄3 of the possible combinations in Antwerp, Paris, Poznan, and Tartu (maximizing the gradient) and the full range of combinations in Zurich (32 combinations, the other combinations were not available in the city). This resulted in the final selection of 80 sites (Fig. 1): 32 in Zurich and 12 in each of the remaining cities. Sites were selected keeping a minimum distance of 500 m (except for two sites in Zurich selected by their position in the patch and connectivity gradient, separated by 260 m). Median distance to the nearest site was 6610 m in Antwerp (minimum = 966 m, maximum = 15,375 m), 7852 m in Paris (minimum = 721 m, maximum = 31,891 m), 3912 m in Poznan (minimum = 1630 m, maximum = 17,189 m), 3913 m in Tartu (minimum = 788 m, maximum = 10,520 m), and 4299 m in Zurich (minimum = 371 m, maximum = 10,560 m). Furthermore, pairwise distances among sites were in 99% of the cases larger than 750 m.

Remote sensing indices

Urban intensity has been inferred using remote sensing indices on soil, impervious surfaces and vegetation. Particularly, we used the BI2, CI, UI, and NDVI. The BI2 results from the following equation:Where ρRED, ρGREEN and ρNIR are the responses in red, green, and near-infrared bands, respectively. This index is sensitive to the brightness of soils, which in turn is influenced by soil moisture, presence of salts and organic matter content on the soil surface. Thus, brightness values greater than 0.3 are an indicator of soil problems with less decomposed organic materials, which can be reflected in a lower development of trees. In turn, low values of brightness are associated with soils with high moisture content and decomposed organic materials, favoring the growth of tree plants. The Colour Index (CI) was introduced by Pouget et al. [21] and results from the following equation:Where ρRED and ρGREEN are the responses in the red and green bands, respectively. Although this index was developed to differentiate various types of soils in arid environments, it can help to compute better vegetation indices for incomplete canopies. In most cases, the CI provides complementary information with the BI2 and the NDVI, allowing to differentiate plants and soil more effectively, especially in study areas with less than 10% vegetation [21]. Typically, low CI values have been shown to be correlated with the presence of a high concentration of carbonates or sulfates, nutrients that can serve as fertilizers for plant growth. Meanwhile, higher values have been correlated with crusty and sandy soils and with a low content of organic matter. Thus, this index seems to be a good indicator of soil degradation. The Urban Index (UI) was developed by Kawamura et al. [22] to effectively detect the structural details of urban cores. The UI was calculated using the following equation:Where ρMIR2 and ρNIR are the responses in the second short wave and near-infrared bands, respectively. Thus, it is a good index for detecting built and non-built areas and can also be used to identify building densities. The built-up area tends to have UI values greater than 0, while negative values close to −1 tend to be green areas. Finally, the NDVI was developed by Tucker [23] and is the one of the most common indices widely applied for monitoring vegetation dynamics. This index results from the following equation:Where ρNIR and ρRED are the responses in near infrared and red bands, respectively. This index indicates the photosynthetic capacity, or the energy absorbed by plant canopies, hence, the amount of healthy vegetation. Thus, higher NDVI values indicate a higher density of green vegetation. Specifically, in urban environments, NDVI values greater than 0.5 correspond to vigorous green areas, while NDVI values between 0.2 to 0.5 indicate moisture-stressed vegetation, such as natural meadows. NDVI values near zero and decreasing negative values indicate non-vegetated features, such as artificial and barren surfaces, water bodies, snow, and clouds. These four indices can be used to charecterize the existing vegetation and urban infrastructure in the vicinity of sampling sites. Remotely sensed data can be used to improve research on biodiversity and ecosystem services, being a valuable tool to support more sustainable urban planning and management.

Floristic inventories

Between April and July 2018, we sampled all available plants of potential interest for pollinators (i.e. we excluded the families Cyperaceae, Juncaceae and Poaceae) in a buffer of 100 m radius around each trap nest on green areas both public and private within the defined radius in three sampling periods. Each buffer was divided in 16 cells (see Fig. 1). In each buffer, we documented all the plant species found, in order to obtain an estimate of both plant richness and frequency (as the number of cells inside a buffer each species was found). To identify plant species, we used identification guides for European [14,15,24] and Swiss flora [25], as well as specialized guides for ornamental plants [13,16,26] and previous species inventories, e.g. [9] in Zurich. The total duration of each sampling in a site was restricted to about 2.5 h to standardize sampling effort. Note that the late winter and early spring flowers were missed (e.g. Crocus spp., Galanthus spp.). The species, genus, and family richness of each sampling site are given in Table 3. The list of all taxa and the number of observations per taxon are given in the Supplementary material, Table A1.

Floral counts on standardized plots

We calculated the floral abundance in a site and sampling period by using 1 m2 quadrats randomly distributed inside the 100 m buffer. The number of quadrats was determined according to the amount of green areas in each buffer, with a minimum of seven quadrats, when less than 20% of the buffer was covered by green areas, and a maximum of 15 quadrats, when more than 90%. To obtain the floral abundance, we first defined a set of floral units on where we classified the different plant species (see Table 1). The floral abundance of each floral unit type was calculated in the following way. For single flowers, the floral abundance was obtained by summing all the individual flowers (Table 1). For single capitula (in Dipsacoideae species), single compound cymes, single corymbs, single panicles, single racemes, single umbels, we took seven different floral units, counted all the flowers and computed a mean number of flowers per floral unit. The mean number of flowers per floral unit was calculated separately for each site and sampling period. The floral abundance was then obtained by multiplying the number of floral units and the mean number of flowers per floral unit (see Table 1). Finally, for single capitula (in Asteraceae), single catkins, single corymbs or cymes in the Euphorbia genus, single dense clusters (including only Sangisorba spp.) and single spikes (including the genus Plantago spp. and Tamarix spp.) the floral abundance was computed by summing only the number of floral units, that is, we did not estimate a mean number of flowers per floral unit.

Taxonomic treatment

Taxonomy assignment largely followed the criteria of Checklist of the National Data and Information Centre of the Swiss Flora [27], together with The World Flora Online database [28], and other resources, e.g. RHS Dictionary of Gardening [16]. Varieties, taxa within species complexes, and cultivars were mostly grouped into aggregates (e.g. Taraxacum officinale aggr.) or left at the genus level (e.g. Leucanthemum sp.) without further distinction.

Traits

We aimed to select important determinants of plant-pollinator interactions. We developed a data set of 11 traits (see Table 2) for 2313 plant species. We used 11 functional traits including start and duration of the flowering period, growth type, inflorescence type, pollination mode, blossom class, symmetry, plant height and the presence of rewards in the form of pollen, nectar and oils. Additionally, we included the origin of the plant species, which are no functional traits per se. For functional traits, we used as main sources the TRY plant trait database [10], the national data, and information centre for the Swiss flora [6], the Bundesamt für Naturschutz (BfN) [7], Faegri and van der Pijl [17], Frey and Moretti [9], Missouri Botanical Garden Plant Finder [5], Plants For A Future [4], Plants of the World Online [12], and BiolFlor [8]. Regarding the origin status of the plant species, a species was considered to be native when its origin was Europe and exotic if it originated elsewhere. To document the origin status of each plant species, we used the Global Biodiversity Information System [29]. Cultivar groups not derived from native plants were considered to be alien. The start and duration of the flowering period are given in months. For exotic plants from the Southern hemisphere, we do not provide information on the phenology. We defined the pollination mode for each species, based on Frey and Moretti [9]. Here, we distinguished whether a species is biotically or abiotically pollinated, i.e., mainly either by insects (entomophilous) or by wind (anemophilous). Concerning growth form, we defined four broad categories, that is, tree, shrub, herb, and climber. Trees included woody species typically classified as phanaerophytes, including species described as small trees or tall shrubs (e.g. Crataegus spp., Ligustrum spp.). Shrubs included mostly chamaephytes. Herbs included all herbaceous plants regardless of their height or growth form. Finally, climbers included woody and non-woody epyphites such as lianas and vines. The inflorescence types considered are the same as the ones in the floral counts (see Supplementary material, Table A1). We considered the type of structural blossom classes according to Faegri and van der Pijl [17]. Concerning symmetry, each plant was classified in three main categories of actinomorphy (two or more axis of symmetry), zygomorphy (one axis of symmetry) or without symmetry. Finally, for the rewards, we reported whether the plant species had been shown to provide floral resources in the form of nectar, oil and pollen.

CRediT Author Statement

Joan Casanelles-Abella: Conceptualisation, Methodology, Investigation, Validation, Data curation, Writing Original draft, Writing Review & Editing, Formal analysis, Project administration; David Frey: Methodology, Validation, Resources, Data curation, Writing Review & Editing; Stefanie Müller: Conceptualisation, Methodology, Investigation, Data curation, Writing Review & Editing; Cristiana Aleixo: Investigation, Data curation, Resources, Writing Review & Editing; Marta Alós Ortí: Investigation, Writing Review & Editing; Nicolas Deguines: Investigation, Validation, Writing Review & Editing; Tiit Hallikma: Investigation, Validation, Writing Review & Editing; Lauri Laanisto: Methodology, Writing Review & Editing; Ülo Niinemets: Funding acquisition, Writing Review & Editing; Pedro Pinho: Funding acquisition, Methodology, Investigation, Data curation, Resources, Writing Review & Editing; Roeland Samson: Funding acquisition, Methodology; Lucía Villarroya-Villalba: Investigation, Validation, Writing Review & Editing; Marco Moretti: Funding acquisition, Conceptualisation, Methodology, Writing Review & Editing, Supervision, Project administration.

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships which have or could be perceived to have influenced the work reported in this article.
SubjectEcology, Nature, and Landscape Conservation.
Specific subject areaUrban ecology
Type of dataTableFig.
How data were acquiredFloristic inventories and standardized floral counts. Satellite data.
Data formatRaw and aggregated
Parameters for data collectionSites were selected from the European Urban Atlas, using the features mapped as green areas. Sites were chosen following an orthogonal gradient of patch size and connectivity inferred with the proximity index. We selected 32 sites in Zurich, Switzerland, and 12 sites in each of the remaining four cities (i.e. Antwerp, Paris, Poznan and Tartu).
Description of data collectionWe applied two sampling methodologies inside of buffers of 100 m radius: 1) a floristic inventory of the occurrence of all flowering plants of potential interest for pollinators performed in the five cities, and 2) flower counts in sampling plots of standardized size (1 m2) done only in Zurich. Sites were visited on three occasions between April and July 2018. The duration of each visit was restricted to a maximum of 2.5 h.
Data source locationCity of Antwerp, Belgium; 51°15′N, 4°24′EGreater Paris, France; 48°51′N, 8°05′ECity of Poznan, Poland; 52°24′N, 16°55′ECity of Tartu, Estonia; 58°22′N, 26°43′ECity of Zurich, Switzerland; 47°22′N, 8°33′E
Data accessibilityRepository name: EnvidatData identification number: doi:10.16904/envidat.210Direct URL to data: https://www.envidat.ch/dataset/flowering-plants-angiospermae-in-urban-green-areas-in-five-european-citiesFile 1: Floral_1_occurrence.csv contains the list of plant species sampled in the five cities during the different sampling periods.File 2: Floral_2_counts.csv contains the floral units, mean number of flowers per floral units and the floral abundance of the different plants counted in quadrats in the study sites in Zurich during four sampling periods.File 3: Floral_traits.csv contains the trait values extracted from the literature for the sampled plants.
  3 in total

1.  TRY plant trait database - enhanced coverage and open access.

Authors:  Jens Kattge; Gerhard Bönisch; Sandra Díaz; Sandra Lavorel; Iain Colin Prentice; Paul Leadley; Susanne Tautenhahn; Gijsbert D A Werner; Tuomas Aakala; Mehdi Abedi; Alicia T R Acosta; George C Adamidis; Kairi Adamson; Masahiro Aiba; Cécile H Albert; Julio M Alcántara; Carolina Alcázar C; Izabela Aleixo; Hamada Ali; Bernard Amiaud; Christian Ammer; Mariano M Amoroso; Madhur Anand; Carolyn Anderson; Niels Anten; Joseph Antos; Deborah Mattos Guimarães Apgaua; Tia-Lynn Ashman; Degi Harja Asmara; Gregory P Asner; Michael Aspinwall; Owen Atkin; Isabelle Aubin; Lars Baastrup-Spohr; Khadijeh Bahalkeh; Michael Bahn; Timothy Baker; William J Baker; Jan P Bakker; Dennis Baldocchi; Jennifer Baltzer; Arindam Banerjee; Anne Baranger; Jos Barlow; Diego R Barneche; Zdravko Baruch; Denis Bastianelli; John Battles; William Bauerle; Marijn Bauters; Erika Bazzato; Michael Beckmann; Hans Beeckman; Carl Beierkuhnlein; Renee Bekker; Gavin Belfry; Michael Belluau; Mirela Beloiu; Raquel Benavides; Lahcen Benomar; Mary Lee Berdugo-Lattke; Erika Berenguer; Rodrigo Bergamin; Joana Bergmann; Marcos Bergmann Carlucci; Logan Berner; Markus Bernhardt-Römermann; Christof Bigler; Anne D Bjorkman; Chris Blackman; Carolina Blanco; Benjamin Blonder; Dana Blumenthal; Kelly T Bocanegra-González; Pascal Boeckx; Stephanie Bohlman; Katrin Böhning-Gaese; Laura Boisvert-Marsh; William Bond; Ben Bond-Lamberty; Arnoud Boom; Coline C F Boonman; Kauane Bordin; Elizabeth H Boughton; Vanessa Boukili; David M J S Bowman; Sandra Bravo; Marco Richard Brendel; Martin R Broadley; Kerry A Brown; Helge Bruelheide; Federico Brumnich; Hans Henrik Bruun; David Bruy; Serra W Buchanan; Solveig Franziska Bucher; Nina Buchmann; Robert Buitenwerf; Daniel E Bunker; Jana Bürger; Sabina Burrascano; David F R P Burslem; Bradley J Butterfield; Chaeho Byun; Marcia Marques; Marina C Scalon; Marco Caccianiga; Marc Cadotte; Maxime Cailleret; James Camac; Jesús Julio Camarero; Courtney Campany; Giandiego Campetella; Juan Antonio Campos; Laura Cano-Arboleda; Roberto Canullo; Michele Carbognani; Fabio Carvalho; Fernando Casanoves; Bastien Castagneyrol; Jane A Catford; Jeannine Cavender-Bares; Bruno E L Cerabolini; Marco Cervellini; Eduardo Chacón-Madrigal; Kenneth Chapin; F Stuart Chapin; Stefano Chelli; Si-Chong Chen; Anping Chen; Paolo Cherubini; Francesco Chianucci; Brendan Choat; Kyong-Sook Chung; Milan Chytrý; Daniela Ciccarelli; Lluís Coll; Courtney G Collins; Luisa Conti; David Coomes; Johannes H C Cornelissen; William K Cornwell; Piermaria Corona; Marie Coyea; Joseph Craine; Dylan Craven; Joris P G M Cromsigt; Anikó Csecserits; Katarina Cufar; Matthias Cuntz; Ana Carolina da Silva; Kyla M Dahlin; Matteo Dainese; Igor Dalke; Michele Dalle Fratte; Anh Tuan Dang-Le; Jirí Danihelka; Masako Dannoura; Samantha Dawson; Arend Jacobus de Beer; Angel De Frutos; Jonathan R De Long; Benjamin Dechant; Sylvain Delagrange; Nicolas Delpierre; Géraldine Derroire; Arildo S Dias; Milton Hugo Diaz-Toribio; Panayiotis G Dimitrakopoulos; Mark Dobrowolski; Daniel Doktor; Pavel Dřevojan; Ning Dong; John Dransfield; Stefan Dressler; Leandro Duarte; Emilie Ducouret; Stefan Dullinger; Walter Durka; Remko Duursma; Olga Dymova; Anna E-Vojtkó; Rolf Lutz Eckstein; Hamid Ejtehadi; James Elser; Thaise Emilio; Kristine Engemann; Mohammad Bagher Erfanian; Alexandra Erfmeier; Adriane Esquivel-Muelbert; Gerd Esser; Marc Estiarte; Tomas F Domingues; William F Fagan; Jaime Fagúndez; Daniel S Falster; Ying Fan; Jingyun Fang; Emmanuele Farris; Fatih Fazlioglu; Yanhao Feng; Fernando Fernandez-Mendez; Carlotta Ferrara; Joice Ferreira; Alessandra Fidelis; Bryan Finegan; Jennifer Firn; Timothy J Flowers; Dan F B Flynn; Veronika Fontana; Estelle Forey; Cristiane Forgiarini; Louis François; Marcelo Frangipani; Dorothea Frank; Cedric Frenette-Dussault; Grégoire T Freschet; Ellen L Fry; Nikolaos M Fyllas; Guilherme G Mazzochini; Sophie Gachet; Rachael Gallagher; Gislene Ganade; Francesca Ganga; Pablo García-Palacios; Verónica Gargaglione; Eric Garnier; Jose Luis Garrido; André Luís de Gasper; Guillermo Gea-Izquierdo; David Gibson; Andrew N Gillison; Aelton Giroldo; Mary-Claire Glasenhardt; Sean Gleason; Mariana Gliesch; Emma Goldberg; Bastian Göldel; Erika Gonzalez-Akre; Jose L Gonzalez-Andujar; Andrés González-Melo; Ana González-Robles; Bente Jessen Graae; Elena Granda; Sarah Graves; Walton A Green; Thomas Gregor; Nicolas Gross; Greg R Guerin; Angela Günther; Alvaro G Gutiérrez; Lillie Haddock; Anna Haines; Jefferson Hall; Alain Hambuckers; Wenxuan Han; Sandy P Harrison; Wesley Hattingh; Joseph E Hawes; Tianhua He; Pengcheng He; Jacob Mason Heberling; Aveliina Helm; Stefan Hempel; Jörn Hentschel; Bruno Hérault; Ana-Maria Hereş; Katharina Herz; Myriam Heuertz; Thomas Hickler; Peter Hietz; Pedro Higuchi; Andrew L Hipp; Andrew Hirons; Maria Hock; James Aaron Hogan; Karen Holl; Olivier Honnay; Daniel Hornstein; Enqing Hou; Nate Hough-Snee; Knut Anders Hovstad; Tomoaki Ichie; Boris Igić; Estela Illa; Marney Isaac; Masae Ishihara; Leonid Ivanov; Larissa Ivanova; Colleen M Iversen; Jordi Izquierdo; Robert B Jackson; Benjamin Jackson; Hervé Jactel; Andrzej M Jagodzinski; Ute Jandt; Steven Jansen; Thomas Jenkins; Anke Jentsch; Jens Rasmus Plantener Jespersen; Guo-Feng Jiang; Jesper Liengaard Johansen; David Johnson; Eric J Jokela; Carlos Alfredo Joly; Gregory J Jordan; Grant Stuart Joseph; Decky Junaedi; Robert R Junker; Eric Justes; Richard Kabzems; Jeffrey Kane; Zdenek Kaplan; Teja Kattenborn; Lyudmila Kavelenova; Elizabeth Kearsley; Anne Kempel; Tanaka Kenzo; Andrew Kerkhoff; Mohammed I Khalil; Nicole L Kinlock; Wilm Daniel Kissling; Kaoru Kitajima; Thomas Kitzberger; Rasmus Kjøller; Tamir Klein; Michael Kleyer; Jitka Klimešová; Joice Klipel; Brian Kloeppel; Stefan Klotz; Johannes M H Knops; Takashi Kohyama; Fumito Koike; Johannes Kollmann; Benjamin Komac; Kimberly Komatsu; Christian König; Nathan J B Kraft; Koen Kramer; Holger Kreft; Ingolf Kühn; Dushan Kumarathunge; Jonas Kuppler; Hiroko Kurokawa; Yoko Kurosawa; Shem Kuyah; Jean-Paul Laclau; Benoit Lafleur; Erik Lallai; Eric Lamb; Andrea Lamprecht; Daniel J Larkin; Daniel Laughlin; Yoann Le Bagousse-Pinguet; Guerric le Maire; Peter C le Roux; Elizabeth le Roux; Tali Lee; Frederic Lens; Simon L Lewis; Barbara Lhotsky; Yuanzhi Li; Xine Li; Jeremy W Lichstein; Mario Liebergesell; Jun Ying Lim; Yan-Shih Lin; Juan Carlos Linares; Chunjiang Liu; Daijun Liu; Udayangani Liu; Stuart Livingstone; Joan Llusià; Madelon Lohbeck; Álvaro López-García; Gabriela Lopez-Gonzalez; Zdeňka Lososová; Frédérique Louault; Balázs A Lukács; Petr Lukeš; Yunjian Luo; Michele Lussu; Siyan Ma; Camilla Maciel Rabelo Pereira; Michelle Mack; Vincent Maire; Annikki Mäkelä; Harri Mäkinen; Ana Claudia Mendes Malhado; Azim Mallik; Peter Manning; Stefano Manzoni; Zuleica Marchetti; Luca Marchino; Vinicius Marcilio-Silva; Eric Marcon; Michela Marignani; Lars Markesteijn; Adam Martin; Cristina Martínez-Garza; Jordi Martínez-Vilalta; Tereza Mašková; Kelly Mason; Norman Mason; Tara Joy Massad; Jacynthe Masse; Itay Mayrose; James McCarthy; M Luke McCormack; Katherine McCulloh; Ian R McFadden; Brian J McGill; Mara Y McPartland; Juliana S Medeiros; Belinda Medlyn; Pierre Meerts; Zia Mehrabi; Patrick Meir; Felipe P L Melo; Maurizio Mencuccini; Céline Meredieu; Julie Messier; Ilona Mészáros; Juha Metsaranta; Sean T Michaletz; Chrysanthi Michelaki; Svetlana Migalina; Ruben Milla; Jesse E D Miller; Vanessa Minden; Ray Ming; Karel Mokany; Angela T Moles; Attila Molnár; Jane Molofsky; Martin Molz; Rebecca A Montgomery; Arnaud Monty; Lenka Moravcová; Alvaro Moreno-Martínez; Marco Moretti; Akira S Mori; Shigeta Mori; Dave Morris; Jane Morrison; Ladislav Mucina; Sandra Mueller; Christopher D Muir; Sandra Cristina Müller; François Munoz; Isla H Myers-Smith; Randall W Myster; Masahiro Nagano; Shawna Naidu; Ayyappan Narayanan; Balachandran Natesan; Luka Negoita; Andrew S Nelson; Eike Lena Neuschulz; Jian Ni; Georg Niedrist; Jhon Nieto; Ülo Niinemets; Rachael Nolan; Henning Nottebrock; Yann Nouvellon; Alexander Novakovskiy; Kristin Odden Nystuen; Anthony O'Grady; Kevin O'Hara; Andrew O'Reilly-Nugent; Simon Oakley; Walter Oberhuber; Toshiyuki Ohtsuka; Ricardo Oliveira; Kinga Öllerer; Mark E Olson; Vladimir Onipchenko; Yusuke Onoda; Renske E Onstein; Jenny C Ordonez; Noriyuki Osada; Ivika Ostonen; Gianluigi Ottaviani; Sarah Otto; Gerhard E Overbeck; Wim A Ozinga; Anna T Pahl; C E Timothy Paine; Robin J Pakeman; Aristotelis C Papageorgiou; Evgeniya Parfionova; Meelis Pärtel; Marco Patacca; Susana Paula; Juraj Paule; Harald Pauli; Juli G Pausas; Begoña Peco; Josep Penuelas; Antonio Perea; Pablo Luis Peri; Ana Carolina Petisco-Souza; Alessandro Petraglia; Any Mary Petritan; Oliver L Phillips; Simon Pierce; Valério D Pillar; Jan Pisek; Alexandr Pomogaybin; Hendrik Poorter; Angelika Portsmuth; Peter Poschlod; Catherine Potvin; Devon Pounds; A Shafer Powell; Sally A Power; Andreas Prinzing; Giacomo Puglielli; Petr Pyšek; Valerie Raevel; Anja Rammig; Johannes Ransijn; Courtenay A Ray; Peter B Reich; Markus Reichstein; Douglas E B Reid; Maxime Réjou-Méchain; Victor Resco de Dios; Sabina Ribeiro; Sarah Richardson; Kersti Riibak; Matthias C Rillig; Fiamma Riviera; Elisabeth M R Robert; Scott Roberts; Bjorn Robroek; Adam Roddy; Arthur Vinicius Rodrigues; Alistair Rogers; Emily Rollinson; Victor Rolo; Christine Römermann; Dina Ronzhina; Christiane Roscher; Julieta A Rosell; Milena Fermina Rosenfield; Christian Rossi; David B Roy; Samuel Royer-Tardif; Nadja Rüger; Ricardo Ruiz-Peinado; Sabine B Rumpf; Graciela M Rusch; Masahiro Ryo; Lawren Sack; Angela Saldaña; Beatriz Salgado-Negret; Roberto Salguero-Gomez; Ignacio Santa-Regina; Ana Carolina Santacruz-García; Joaquim Santos; Jordi Sardans; Brandon Schamp; Michael Scherer-Lorenzen; Matthias Schleuning; Bernhard Schmid; Marco Schmidt; Sylvain Schmitt; Julio V Schneider; Simon D Schowanek; Julian Schrader; Franziska Schrodt; Bernhard Schuldt; Frank Schurr; Galia Selaya Garvizu; Marina Semchenko; Colleen Seymour; Julia C Sfair; Joanne M Sharpe; Christine S Sheppard; Serge Sheremetiev; Satomi Shiodera; Bill Shipley; Tanvir Ahmed Shovon; Alrun Siebenkäs; Carlos Sierra; Vasco Silva; Mateus Silva; Tommaso Sitzia; Henrik Sjöman; Martijn Slot; Nicholas G Smith; Darwin Sodhi; Pamela Soltis; Douglas Soltis; Ben Somers; Grégory Sonnier; Mia Vedel Sørensen; Enio Egon Sosinski; Nadejda A Soudzilovskaia; Alexandre F Souza; Marko Spasojevic; Marta Gaia Sperandii; Amanda B Stan; James Stegen; Klaus Steinbauer; Jörg G Stephan; Frank Sterck; Dejan B Stojanovic; Tanya Strydom; Maria Laura Suarez; Jens-Christian Svenning; Ivana Svitková; Marek Svitok; Miroslav Svoboda; Emily Swaine; Nathan Swenson; Marcelo Tabarelli; Kentaro Takagi; Ulrike Tappeiner; Rubén Tarifa; Simon Tauugourdeau; Cagatay Tavsanoglu; Mariska Te Beest; Leho Tedersoo; Nelson Thiffault; Dominik Thom; Evert Thomas; Ken Thompson; Peter E Thornton; Wilfried Thuiller; Lubomír Tichý; David Tissue; Mark G Tjoelker; David Yue Phin Tng; Joseph Tobias; Péter Török; Tonantzin Tarin; José M Torres-Ruiz; Béla Tóthmérész; Martina Treurnicht; Valeria Trivellone; Franck Trolliet; Volodymyr Trotsiuk; James L Tsakalos; Ioannis Tsiripidis; Niklas Tysklind; Toru Umehara; Vladimir Usoltsev; Matthew Vadeboncoeur; Jamil Vaezi; Fernando Valladares; Jana Vamosi; Peter M van Bodegom; Michiel van Breugel; Elisa Van Cleemput; Martine van de Weg; Stephni van der Merwe; Fons van der Plas; Masha T van der Sande; Mark van Kleunen; Koenraad Van Meerbeek; Mark Vanderwel; Kim André Vanselow; Angelica Vårhammar; Laura Varone; Maribel Yesenia Vasquez Valderrama; Kiril Vassilev; Mark Vellend; Erik J Veneklaas; Hans Verbeeck; Kris Verheyen; Alexander Vibrans; Ima Vieira; Jaime Villacís; Cyrille Violle; Pandi Vivek; Katrin Wagner; Matthew Waldram; Anthony Waldron; Anthony P Walker; Martyn Waller; Gabriel Walther; Han Wang; Feng Wang; Weiqi Wang; Harry Watkins; James Watkins; Ulrich Weber; James T Weedon; Liping Wei; Patrick Weigelt; Evan Weiher; Aidan W Wells; Camilla Wellstein; Elizabeth Wenk; Mark Westoby; Alana Westwood; Philip John White; Mark Whitten; Mathew Williams; Daniel E Winkler; Klaus Winter; Chevonne Womack; Ian J Wright; S Joseph Wright; Justin Wright; Bruno X Pinho; Fabiano Ximenes; Toshihiro Yamada; Keiko Yamaji; Ruth Yanai; Nikolay Yankov; Benjamin Yguel; Kátia Janaina Zanini; Amy E Zanne; David Zelený; Yun-Peng Zhao; Jingming Zheng; Ji Zheng; Kasia Ziemińska; Chad R Zirbel; Georg Zizka; Irié Casimir Zo-Bi; Gerhard Zotz; Christian Wirth
Journal:  Glob Chang Biol       Date:  2019-12-31       Impact factor: 10.863

2.  Raincloud plots: a multi-platform tool for robust data visualization.

Authors:  Micah Allen; Davide Poggiali; Kirstie Whitaker; Tom Rhys Marshall; Rogier A Kievit
Journal:  Wellcome Open Res       Date:  2019-04-01

3.  A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens.

Authors:  David Frey; Marco Moretti
Journal:  Data Brief       Date:  2019-05-23
  3 in total

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