Assessing species richness and diversity on the basis of standardised field sampling effort represents a cost- and time-consuming method. Satellite remote sensing (RS) can help overcome these limitations because it facilitates the collection of larger amounts of spatial data using cost-effective techniques. RS information is hence increasingly analysed to model biodiversity across space and time. Here, we focus on image texture measures as a proxy for spatial habitat heterogeneity, which has been recognized as an important determinant of species distributions and diversity. Using bee monitoring data of four years (2010–2013) from six 4 × 4 km field sites across Central Germany and a multimodel inference approach we test the ability of texture features derived from Landsat-TM imagery to model local pollinator biodiversity. Textures were shown to reflect patterns of bee diversity and species richness to some extent, with the first-order entropy texture and terrain roughness being the most relevant indicators. However, the texture measurements accounted for only 3–5% of up to 60% of the variability that was explained by our final models, although the results are largely consistent across different species groups (bumble bees, solitary bees). While our findings provide indications in support of the applicability of satellite imagery textures for modeling patterns of bee biodiversity, they are inconsistent with the high predictive power of texture metrics reported in previous studies for avian biodiversity. We assume that our texture data captured mainly heterogeneity resulting from landscape configuration, which might be functionally less important for wild bees than compositional diversity of plant communities. Our study also highlights the substantial variability among taxa in the applicability of texture metrics for modelling biodiversity.
Citation: Hofmann S, Everaars J, Schweiger O, Frenzel M, Bannehr L, Cord AF (2017) Modelling patterns of pollinator species richness and diversity using satellite image texture. PLoS ONE 12(10): e0185591. https://doi.org/10.1371/journal.pone.0185591
Editor: Duccio Rocchini, Universita degli Studi di Trento, ITALY
Received: April 18, 2017; Accepted: September 17, 2017; Published: October 3, 2017
Copyright: © 2017 Hofmann et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data are available via PANGAEA: Frenzel M, Preiser C, Creutzburg F. 2016a. Wild bee monitoring in six agriculturally dominated landscapes of Saxony-Anhalt (Germany) in 2010. Helmholtz Centre for Environmental Research UFZ. doi:10.1594/PANGAEA.864790. Frenzel M, Preiser C, Nickels V, Creutzburg F. 2016b. Wild bee monitoring in six agriculturally dominated landscapes of Saxony-Anhalt (Germany) in 2011. Helmholtz Centre for Environmental Research UFZ. doi:10.1594/PANGAEA.864907. Frenzel M, Preiser C, Höhne R, Nickels V, Creutzburg F. 2016c. Wild bee monitoring in six agriculturally dominated landscapes of Saxony-Anhalt (Germany) in 2012. Helmholtz Centre for Environmental Research UFZ. doi:10.1594/PANGAEA.865038. Frenzel M, Preiser C, Dussl F, Höhne R, Nickels V, Creutzburg, F. 2016d. Wild bee monitoring in six agriculturally dominated landscapes of Saxony-Anhalt (Germany) in 2013. Helmholtz Centre for Environmental Research UFZ. doi:10.1594/PANGAEA.865097.
Funding: This work was supported by the Helmholtz long-range strategic research funding (POF III). However, the authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Assessing biodiversity is essential to the effective monitoring of ecosystems and central to the development of sustainable management strategies and conservation plans for both natural and cultivated areas at various spatial scales . However, measuring species richness and diversity on the basis of a standardised field sampling effort represents a cost- and time-consuming method, in particular over broad spatial scales [2, 3]. Therefore, complementary approaches are required to minimize monitoring resources and to maximize a priori knowledge about biodiversity patterns and quality of an area .
Spatial heterogeneity of habitats, i.e. the variation of the area in spatial scale, has been recognized as an important determinant of species distributions and diversity as regions with higher heterogeneity typically provide greater numbers of ecological niches and therefore can potentially host more co-existing species (e.g. [5, 6]). Spatial heterogeneity can be estimated from available satellite remote sensing (RS) data, e.g. through relationships with categorical land-cover information  or through indicators of spectral variability (SV) following the spectral variation hypothesis . The latter hypothesis states that spectral heterogeneity of a RS image correlates well with landscape structure and complexity, which are directly related to spatial habitat heterogeneity. Hence, RS information is increasingly used to model and understand species distributions in space and time and to predict biodiversity-rich sites (see [4, 8, 9] and references therein). However, the commonly used land-cover classification data ignore subtle variations within a given class and gradients between classes, i.e. variation in vegetation structure [10, 11], which, in turn, influences the distribution of biodiversity . Moreover, land-cover information is typically limited in both spatial and temporal grain, and, therefore, may not be the most pertinent for different species. The use of spatial heterogeneity in the spectral signal can overcome some of the limits of land-cover classifications (e.g. thematic constraints), and can therefore be a suitable proxy for species diversity estimates (reviewed in ). Yet, there are other challenges associated with this approach. For example, the strength of relationships between SV and biodiversity can vary considerably with spatial scales, diversity indices used, locations, and the imagery type [12, 13].
Similar to spectral radiance information, RS-based texture measures provide spatially continuous and temporally consistent observations of the land surface and render within-class vegetation structure. The use of these metrics has been recognized as an important method for quantifying spatial heterogeneity in terms of the spatial distribution [14, 15]. Image texture, considered as a function of the spatial variation in pixel brightness, is commonly measured as first-order (occurrence) and second-order (co-occurrence) statistics . The first-order measures are summary computations, such as mean and standard deviation. They describe the frequency distribution of pixel values in a defined neighbourhood (commonly implemented as kernel or a moving window), while second-order statistics are based on the probability of joint occurrence of two pixel-intensity values which are in certain inter-pixel distance and orientation. Many of these texture metrics have been successfully explored to assess biodiversity. However, studies are biased towards certain species group (mainly vascular plants and birds; [11, 17–19]). For insect communities, the applicability of satellite-derived texture metrics for modelling patterns of local biodiversity is poorly understood. However, other remote-sensing techniques, e.g. airborne and terrestrial laser scanning, have been successfully, although barely, applied for modelling composition and diversity of spiders and beetles [20, 21].
Here, we focussed on wild bees, which are one of the most important groups of pollinators in most terrestrial ecosystems and economic crops [22, 23]. Bees are highly sensitive to floral resource abundance and diversity and probably also to the presence of nesting sites , and have frequently been shown to respond strongly to landscape heterogeneity and management [25–27]. For example, many wild bees nest or hibernate in semi-natural habitats and visit agricultural fields mainly for foraging. Consequently, pollinator species richness decrease with increasing distance from natural or semi-natural habitats, such as field margins, species-rich grasslands or forests edges . Thus, bees are assumed to profit from complex landscapes within their foraging distance, making this group particular useful for our purposes.
The objective of our study was to examine the utility of RS texture information for indicating patterns of pollinator diversity across small spatial extents. We particularly aimed to explore the ability of texture features based on the Normalized Differenced Vegetation Index (NDVI) derived from 30-m resolution Landsat imagery to capture spatial habitat heterogeneity and model local pollinator species richness and diversity. While our results indicate some support to satellite-derived texture metrics as indicators for patterns of biodiversity, they underline the high level of variation among taxa in terms of the predictability of diversity measures by RS texture metrics.
Material and methods
Bee data were collected in accordance with German law. The study was approved and annual sampling permissions were provided by the local nature conservation authorities (RL-0174-V; issued by Federal Agency for Environmental Protection Saxony-Anhalt).
Study area and bee monitoring data
Bee monitoring data were used from six sites (Fig 1) across Saxony-Anhalt, Germany, generated in four consecutive years (2010–2013). The study sites are monitored on a regular basis as part of the TERENO project (Terrestrial Environmental Observatories; www.tereno.net) and of the German-European Long-Term Ecological Research network (LTER-D; http://www.ufz.de/lter-d/). They are representative for the dominating agricultural land use in a wider landscape and largely differ in terms of landscape structure and altitude (for details see Table 1). In particular, the region is characterized by a high variation in land-use intensity (from flat regions with up to 98% agriculture and large fields to regions with high levels of altitudinal heterogeneity, high cover of forests or other semi-natural habitats, less agriculture and smaller fields) and some variation in climatic conditions. The main crops are winter cereals, oilseed rape, maize and to some extent potato, sugar beet and peas . Each site covers an area of 4 × 4 km and is divided in a grid of 1 × 1 km, containing one combined flight trap (a combination of yellow funnel and window panel; ) per grid cell. The traps were placed randomly within each square with the constraint that all traps had to be located at ecotones (i.e. transition zone between two habitat types, usually between an agricultural and a semi-natural area). Trapping efficiency was proofed extremely high and confirmed by local experts [30, 31]. Pollinator species were collected in two periods per year, extending from May to June (early summer) and from August to September (late summer), comprising 42.5 trapping days on average per period (41–50 days). Traps were active for two weeks before being emptied. Collected bees were identified to species level. Honeybees were excluded from the analyses to avoid potential anthropogenic effects caused by honeybee management. For an overview of the workflow of the study see S1 Fig.
The TERENO study locations are indicated by black frames (FBG: Friedeburg, GFH: Greifenhagen, HAR: Harsleben, SIP: Siptenfelde, SST: Schafstaedt, Wan: Wanzleben), and trapping points are given as yellow filled circles.
Remote sensing data sources and image metrics processing
The red (band 3) and near-infrared (band 4) from a 30-m resolution Landsat-5 TM scene acquired on May 08, 2011 (path 194, row 24) were used to calculate the NDVI as implemented in ENVI 5.0 software (Research Systems Inc., Boulder, CO). Atmospheric correction of the Landsat data was performed using the Landsat Ecosystem Disturbance Adaptive Processing System (LEDAPS; ). The Landsat image was captured during a time that matches the early sampling period of the pollinators at the TERENO sites. Previously published research has been shown that NDVI texture is superior to the texture of any individual Landsat TM band for modelling biodiversity . Based on this NDVI image a set of first- and second-order texture measures was computed in ENVI 5.0, except evenness (see below), including metrics that have been recently proven to be particular suitable to capture spatial habitat heterogeneity : mean, evenness, entropy and variance (first-order textures) as well as contrast, dissimilarity, entropy and homogeneity (second-order textures); see Table 2. Evenness was calculated with the r.diversity module using GRASS GIS 7.2.0 [34, 35]. Second-order texture measures were extracted from a grey-level co-occurrence matrix (GLCM), a tabulation of how often different combinations of pixel brightness values occur in the image [16, 36]. Since this matrix is sensitive to rotation we varied the directions for texture calculations by four different rotational angels (0°, 45°, 90° and 135°), and averaged the results . All image texture analyses were computed from a window of 3 × 3 pixels (90 m × 90 m), which was considered an adequate size for measuring neighbour conditions relevant to pollinators. In addition to the mean of the textures, we selected the measure of first-order standard deviation due to its 'intuitive appeal' for characterizing levels of heterogeneity . In order to relate our measures to the different foraging distances of the various pollinator groups we derived different-sized ring buffers around each sample site (100–1000 m, 100 m intervals). For each buffer area we then calculated the mean and standard deviation of each of the metrics using Hawth’s tool , as well the mean and coefficient variation (cv) of the NDVI. Moreover, we derived a microtopography-based 'terrain roughness' metric from a local 10 m digital elevation model (DGM 10, GeoBasis-DE/BKG 2012), that used the same coordinate system as the other layers (ETRS89/UTM zone 32N). Roughness is a measure of spatial configuration or landscape heterogeneity, as it is correlated with other terrain attributes (e.g. relief, standard deviation of elevation, slope and standard deviation of slope). We generated this metric as the amount of elevation difference between adjacent cells according to  and  using the Geomorphometry and Gradient Metrics Toolbox v2.0  and applying a moving window size of 9 × 9 (i.e. 90 × 90 m). Hawth’s tool was again used to summarize roughness values (mean, standard deviation) within the different buffer areas around each sample point.
Pollinator data: Rarefaction and diversity analyses
Data preparation and all analyses were performed in R version 3.2.5 . Because we did not expect all pollinator species to respond uniformly to measures of textures, we performed all analyses on (i) the whole community of wild bees (dataset 'nohb') and the community split in two subsets; ii) bumble bees (data set 'bb') and iii) remaining wild bees (data set 'sb'). This roughly separates the community in large eusocial bees and smaller bees that are mostly solitary. Although the second subset is not a 'pure' trait group, this separation is often used to identify differences relating to foraging distance (body size) and food requirements (whole colony at once, or individual, solitary, foragers) [47, 48]. In addition to the number of bees (bee count, BC; normalized to trapping days), we estimated abundance-independent species richness (SpR) by rarefaction with the iNext package [49, 50]. Species richness was interpolated to three times the minimum abundance of individuals in the dataset. Shannon’s diversity (SD)  was estimated using the 'Hs' function in the DiversitySampler package .
Although BC, SD and SpR were partly positively correlated (S1 Table), we analysed them separately following the same procedure. The three data sets were initially explored through descriptive analysis. Pollinator data (BC, SD, SpR) was assessed per season and year in all three datasets (see above) for normal distribution using Shapiro-Wilk tests and Q-Q plot analyses. Annual, seasonal and location-associated differences were tested within each biodiversity measurement using the Kruskal-Wallis test . Finally, we used Pearson’s correlation coefficients (r) of the season classes 'early' and 'late' to determine whether there was a strong relationship between them, which would provide additional evidence for a fixed seasonal effect.
To eliminate predictor collinearity prior to generating the models, we first calculated Pearsons’s correlation coefficients for all pairs of distance classes per variable to remove classes with coefficients │c│> 0.7 (S2 Fig). We eliminated all data of correlated distance classes and all variables that showed a correlation across all distance classes. Secondly, we computed the correlation between the remaining variables and excluded the variable of a correlated pair with │c│> 0.7 that we considered to be the less biologically important of the two (S3A and S3B Fig). The resulting dataset contained two distance classes (100 m and 1000 m) each with five potentially predictive variables (cvNDVI, roughness, entropy [1st order], contrast and homogeneity [2nd order]; Fig 2). Further potential correlations between variables within distance classes were addressed during model building.
Light blue dots correspond to the trapping points.
To investigate the potential relations of biodiversity to image texture indices, we applied linear models (LM). We used the R-packages car , MASS , MuMln , ncf  and nlme . For each dataset (bb, sb, nohb) and response variable (BC, SD, SpR) we first built a full model by including all texture metrics as fixed effects test predictors as well as the location site, season and year as fixed effects control predictors. Control predictors were not pertinent to our hypotheses but have known effects that needed to be controlled for to allow valid conclusions about our test predictors . We calculated the variance inflation factors (vif) for each of the full models and excluded predictors with a square root of the vif > 2 . Due to their high vif the metrics homogeneity, entropy and roughness for the 1000 m distance class as well as contrast for the 100 m distance class were excluded from the full model (Table 3 for an overview of all predictors throughout the models, and S4 Fig). Model residuals were inspected to assess model fit. We ensured that model residuals were not spatially autocorrelated by creating spline correlograms  using the ncf package in R. The significance of correlograms was tested for distance classes increasing by 100 m using randomization test with 500 times of permutation at the 0.05 level.
1st = first order texture; 2nd = second order texture; bb = bumble bees; cv = coefficient of variance; con = contrast; ent = entropy; hom = homogeneity; nohb = all wild bees; rough = roughness; sb = solitary bees; BC = bee count; SD = Shannon’s diversity; SpR = Species richness.
To assess the impact of individual image metrics, we generated models with all possible combinations of predictors of the global model, as we did not have any a priori hypotheses on the subsets of predictors in question. We did not fit interactions between any of the factors, as this would require a large number of coefficients and would be difficult to interpret. All test predictors were scaled to allow comparing their relative effects. Models on the different biodiversity variables (BC, SD, SpR) were compared using Akaike’s information criterion (AIC; [59, 62]). Statistical differences between models were based on ΔAIC scores larger than 2 . Parameter estimates and standard errors were obtained as model-averaged estimates from the top model set (ΔAIC ≤ 2), and their p‐values with likelihood ratio tests (LRT) of the full model against the model without the effect in question. Finally, we constructed the null model (including only the control predictors) and compared it to the global model to assess the amount of variance that is explained by the test and the control predictors, respectively.
Pollinator data characteristics
During four years of monitoring, more than 20.000 individual bees of 260 bee species were collected. 238 out of these taxa were solitary bee and 22 bumble bee species. In most of the subsets, the data showed a significant deviation from a normal distribution for seasons, except for the log-transformed bee count and species richness of the full data and the solitary bees (data not shown). Highly significant differences in biodiversity were present between seasons and locations in the bumble bees, solitary bees and wild bees data set (S5 and S6 Figs). Again, bee count and species richness showed no differences between years in the full and solitary-bee data sets but in the bumble-bee data. Pearson’s correlation coefficients (r) of the season classes 'early' and 'late' ranged between 0.14 and 0.42 with p-values lower than 0.01, providing indications for a systematic seasonal effect on bee diversity (S7 Fig).
According to the spline correlograms the fitted residuals of the global LMs showed no evidence for significant spatial structure among the traps (S8 Fig). This was supported by the randomization tests that did not show any significant autocorrelation whatever the distance lag considered (data not shown). Therefore, we considered the residuals as spatially independent.
Species richness and diversity models
For each of the three data sets (BC, SD, SpR), the LM explained at least 15% of the variability of biodiversity with an R2 ranging from 0.149 (species-richness model of solitary bees) to 0.596 (bumble bee count model; Table 4). Five of the image measures (roughness, cv of NDVI, 1st order entropy and 2nd order homogeneity within 100 m radius as well as cv of the NDVI within 1000 m radius), were included in seven of the nine optimal models selected by AIC. Although most of the variability was captured by the control predictors (location, year, season), the texture metric entropy (1st order) and/or the roughness of the surface contributed significantly to each of the models (Table 4). Notably, surface roughness remained in every model used for model averaging, while entropy remained in every model except for the species richness of bumble bees (S2 Table). Regardless of the data set, our image metrics performed slightly better in the Shannon’s-diversity and species-richness models (ΔR2- R2NULL = 0.031 to 0.048) compared to the bee count models (ΔR2- R2NULL = 0.01 to 0.036). However, the overall model performance of the species-richness model in solitary bees (R2 = 0.206) and the full data set (0.149) was substantial lower than for the Shannon’s diversity (R2 = 0.46 and 0.49) and bee count models (0.52 and 0.60).
The R2 corresponds to the global model including all predictors that remained after model selection, while the R2 of the Null model (R2NULL) refers to the model including only the fixed effects control predictors. Δ = R2- R2NULL. IMP = relative importance; SD = Standard deviation; nmodel = number of models averaged; P = P-values. con2 = 2nd order contrast; ent1 = 1st order entropy; hom2 = 2nd order homogeneity; NDVI_cv = coefficient of variance of the NDVI; rough = surface roughness; 100/1000 = 100 m or 1000 m scale.
Our models revealed that texture metrics derived from Landsat imagery played a significant but minor role in explaining local pollinator biodiversity, with the first-order entropy texture and terrain roughness being the most relevant indicators. The results are in striking contrast to the high predictive power of texture metrics reported previously for avian communities.
Pollinator biodiversity, texture metrics and habitat heterogeneity
The results of the present study indicate some support for existing evidence that texture metrics represent a potential tool for modelling biodiversity. We found that on small spatial scale (within 100 m) first order entropy and surface roughness explained a substantial proportion (up to 5%) of the variability in pollinator count, species richness and Shannon’s diversity, with our final models explaining between 15% and 60% of the variability. Our findings are largely consistent with each other, regardless of the defined taxa group, suggesting that the methods we used and the results we present are robust. Similar low but likewise significant levels (4%) of explained variance by texture information were recently reported for biodiversity models of Arctiinae moths .
In previous studies, various texture features have been proposed as best predictor for biodiversity at different spatial scales and for different habitat types, such as mean summary of NDVI values for ovenbird density and occurrence , the angular second moment for species richness and diversity of shrub and tree nesting bird species , and second order homogeneity for avian species richness in diverse habitat types . Entropy, however, hasn’t attracted much attention so far, although in most of the studies using texture metrics for the analyses of biodiversity patterns, first-order entropy is among the set of 'standard' measurements . In our study, this metric accounted for a significant amount of variance in all biodiversity indices within the different datasets, except for species richness of bumble bees. Species richness typically does not consider species abundances, but rather the number of species in a particular area. As the number of bumble bee species present on our sites was considerably lower than in solitary bees, their variance might have been too small to be captured to some degree by texture metrics.
Entropy in any system represents uncertainty, where in the case of texture analysis it characterizes spatial ‘disorderliness’ of an image  and is inversely related to measures of local homogeneity (e.g. the angular second moment or energy). Our study sites are dominated by agricultural land use, but differ largely in terms of altitude and landscape structure (e.g. 2–17% cover of semi-natural areas; Table 1). Farmland fields usually occur as homogeneous patches of similar grey values in the image, while any discontinuity would increase heterogeneity among grey values, leading a priori to a higher number of distinct tone levels within the moving window during analyses, and, thus, higher entropy. Ultimately, the metric relates significantly to our underlying hypothesis that biodiversity can be modelled by local heterogeneity. Our results line up with previous findings showing that entropy is among the most sensitive texture metric to map farmland field size and as such the degree of local heterogeneity . Consistently, entropy statistics of the NDVI have been shown to depict the diversity of vegetation types, which is assumed to be directly related to structural complexity, thus, may support more coexisting species . Since wild bees’ abundance and species richness have been shown to be enhanced by landscape heterogeneity (percentage of semi-natural habitats) , it is not surprising that the entropy texture measurement was able to explain some of the variance in our models.
Similar to first-order entropy, surface roughness accounted for a significant proportion of the variance of bee count, diversity and richness (with the only exception being the abundance of solitary bees). The linkage between topographic characteristics and species distribution across different spatial scales is a well-known fact ([67, 68] and references therein) that has been used for modelling and monitoring biodiversity, especially in plants (e.g. [68–71]), but also in birds [28, 72]. Moreover, relief roughness has been demonstrated to be strongly related to land-use intensity. The latter decreases rapidly with an increasing variability of the surface area, which is accompanied by increasing landscape heterogeneity that, in turn, impacts biodiversity [73, 74]. Again, pollinator communities have been shown to benefit from heterogeneous landscapes because of both their structural as well as plant mediated positive effects on bee diversity . For example, nesting sites are almost exclusively found in (semi-)natural habitats, underlining the importance of a heterogeneous agri-environment . We assume that plain and smooth surfaces are characteristic for larger homogeneous agricultural segments that are intensively managed, providing less complex environments and therefore harbour less diverse communities where generalist species dominate. In contrast, landscapes characterized by a hilly surface are likely to have smaller agricultural patches and a mixture of different land cover types, associated with lower land use intensity and higher natural heterogeneity .
Relevance of the results and limitations of the study
Although the consistency of our results in the different data sets provides indications in support of the potential of the two metrics (entropy, roughness) for modelling pollinator diversity and richness, the relatively low amount of variability explained by textures in our models differs considerably to previous findings in bird communities. Measures of image texture were highly effective in modelling spatial patterns of avian biodiversity in multiple habitat types, accounting for over 50% (7–51%) or even for up to 82% (31.5–82.3%) of the variability in species richness [15, 17]. These variations in the ability of texture metrics to predict biodiversity corroborate recent contributions, showing that the applicability of indicators developed from texture analysis differ significantly among taxa .
Bees respond very differently to landscape features compared to birds, and textures information probably depict only minor parts of features that bees are responding to. For example, (foraging) plant species composition and flower abundance [26, 76] might be functionally more important for wild bees than geometric complexity of spatial patterning of vegetation cover types . In addition, wild bees are assumed to respond more strongly to specific habitat features at local scale than to landscape configuration at larger spatial scales . However, the resolution of most sensors currently employed for RS derived texture analyses has so far prevented the examination of the internal heterogeneity of plant communities, as the size of commonly-used pixels is too large to detect such small-scale variation . Hence, the grain of Landsat data may not be sufficient for echoing the (most) relevant habitat components of pollinator species (e.g. nesting sites, flower diversity). In contrast, many birds respond strongly to vegetation/habitat structure, while plant species composition is often less or equally important, particularly over large spatial scale (landscape level) [79–81]. Therefore, avian communities represent a biological group that seems to be far more pertinent compared to pollinators to be modelled by image textures in terms of species richness, diversity and abundance. In pollinators, image texture parameters alone appear to be less applicable for the predictability of diversity measures. Yet, they may improve predictions of species diversity in more sophisticated models .
Knowing whether image texture information are differently useful in different taxonomic groups, and which metrics are more useful than others in modelling biodiversity is important for a number of reasons. From a practical perspective these insights will help guiding researchers as to which metrics and which (meaningful) taxa they should focus on when assessing biodiversity by texture information. Also, this knowledge will add to a better understanding at which scale relevant biological properties, to which the respective species community is responding, can be depicted by textural attributes.
Our results provide some support for previous findings that texture metrics derived from Landsat and DEM data can indicate patterns of species diversity and richness by reflecting spatial heterogeneity. However, the limited performance of the texture metrics in our models (in particular in comparison to similar studies in avian biodiversity) underlines both the substantial variation among taxa in terms of the applicability of these measures and an insufficient spatial resolution. Other, for pollinator species potentially more relevant information, such as compositional heterogeneity of ground vegetation, was possibly not reflected by textural attributes at the given resolution. It is hoped, that recently launched sensors (e.g. Sentinel-2) will provide habitat data with higher spatial and temporal resolution (compared to Landsat) that will probably greatly facilitate analyses as in the study at hand.
S2 Fig. Pearsons’s correlation coefficients for all pairs of distance classes per test variable.
Pearsons’s correlation coefficients between the test variables (a) and remaining variables after removing variables with coefficients │c│≥ 0.7 (b).
S4 Fig. Pearsons’s correlation coefficients for all pairs of remaining test variable and distance class (100 and 1000 m).
S5 Fig. Differences between trapping seasons (2010–23013) within the biodiversity variables per data set (df).
S6 Fig. Differences between years (upper two rows) and locations (lower two rows) within the biodiversity variables per data set (df).
S7 Fig. Pearson’s correlation of the early and late trapping season for the biodiversity variables per data frame (df).
Spline correlograms for the global fitted models as per model selection for each response variable of (a) the bumble-bees data set (bb), (b) the solitary-bees data set (sb), and (c) the wild bee data set (nohb).
S1 Table. Correlation between bee count (BC), Shannon’s diversity (SD) and species richness (SpR) variables.
We are grateful to Mick Wu (UFZ) for providing statistical support. We thank Aliénor Jeliazkov and Annegret Grimm-Seyfarth for their constructive comments on the study. This work was part of the Integrated Projects of the long-range strategic research program (POF III) of the Helmholtz Association.
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