The habitat-heterogeneity hypothesis predicts that biodiversity increases with increasing habitat heterogeneity due to greater niche dimensionality. However, recent studies have reported that richness can decrease with high heterogeneity due to stochastic extinctions, creating trade-offs between area and heterogeneity. This suggests that greater complexity in heterogeneity-diversity relationships (HDRs) may exist, with potential for group-specific responses to different facets of heterogeneity that may only be partitioned out by a simultaneous test of HDRs of several species groups and several facets of heterogeneity. Here, we systematically decompose habitat heterogeneity into six major facets on ~500 temperate forest plots across Germany and quantify biodiversity of 12 different species groups, including bats, birds, arthropods, fungi, lichens and plants, representing 2600 species. Heterogeneity in horizontal and vertical forest structure underpinned most HDRs, followed by plant diversity, deadwood and topographic heterogeneity, but the relative importance varied even within the same trophic level. Among significant HDRs, 53% increased monotonically, consistent with the classical habitat-heterogeneity hypothesis, but 21% were humped-shaped, 25% had a monotonically decreasing slope and 1% showed no clear pattern. Overall, we found no evidence of a single generalizable mechanism determining HDR patterns.
Aim The observed decrease in insect colour lightness with increasing latitude has been explained in earlier macroecological studies by the increased solar absorption of dark coloration, which allows extended periods of activity. However, melanin‐based dark coloration also protects against pathogens and ultraviolet radiation, which select for dark coloration at low latitudes where these selection pressures intensify. In nocturnal insects, the relative importance of these protective functions of dark coloration is expected to surpass thermoregulatory functions, as nocturnal species cannot benefit from extended periods of activity during the daytime. Hence, we expected that diurnal and nocturnal insects show contrasting geographical patterns of colour lightness. We tested these predictions using geometrid moths, which comprise both diurnal and nocturnal species. Location Western Palearctic. Time period Contemporary. Major taxa studied Geometridae (Lepidoptera). Methods We used digital image analysis to assess the colour lightness of 637 species, compiled their distribution across 3,777 grid cells of 50 km × 50 km and calculated the assemblage‐based average colour lightness. We used multiple regressions, autoregressive error models and randomizations to test for relationships between colour lightness and environmental variables associated with the thermal environment, putative pathogen pressure and ultraviolet radiation. Results We found a clear decrease in colour lightness of assemblages of both diurnal and nocturnal moth species with increasing latitude. In every model, solar radiation was the most important predictor of colour lightness; that is, colour lightness consistently increased with increasing solar radiation. Main conclusions These results indicate that the thermal environment is the most influential climatic driver of insect colour lightness—independent of thermoregulatory strategy and nocturnal or diurnal activity. This challenges the view that extended periods of activity are the main selection pressure for geographical variation in insect colour lightness. Consequently, the relationship between insect colour lightness and the thermal environment might be more general than previously thought.
Recent progress in remote sensing provides much-needed, large-scale spatio-temporal information on habitat structures important for biodiversity conservation. Here we examine the potential of a newly launched satellite-borne radar system (Sentinel-1) to map the biodiversity of twelve taxa across five temperate forest regions in central Europe. We show that the sensitivity of radar to habitat structure is similar to that of airborne laser scanning (ALS), the current gold standard in the measurement of forest structure. Our models of different facets of biodiversity reveal that radar performs as well as ALS; median R² over twelve taxa by ALS and radar are 0.51 and 0.57 respectively for the first non-metric multidimensional scaling axes representing assemblage composition. We further demonstrate the promising predictive ability of radar-derived data with external validation based on the species composition of birds and saproxylic beetles. Establishing new area-wide biodiversity monitoring by remote sensing will require the coupling of radar data to stratified and standardized collected local species data.
The high diversity of insects has limited the volume of long-term community data with a high taxonomic resolution and considerable geographic replications, especially in forests. Therefore, trends and causes of changes are poorly understood. Here we analyse trends in species richness, abundance and biomass of nocturnal macro moths in three quantitative data sets collected over four decades in forests in southern Germany. Two local data sets, one from coppiced oak forests and one from high oak forests included 125K and 48K specimens from 559 and 532 species, respectively. A third regional data set, representing all forest types in the temperate zone of central Europe comprised 735K specimens from 848 species. Generalized additive mixed models revealed temporal declines in species richness (−38%), abundance (−53%) and biomass (−57%) at the regional scale. These were more pronounced in plant host specialists and in dark coloured species. In contrast, the local coppiced oak forests showed an increase, in species richness (+62%), while the high oak forests showed no clear trends. Left and right censoring as well as cross validation confirmed the robustness of the analyses, which led to four conclusions. First, the decline in insects appears in hyper diverse insect groups in forests and affects species richness, abundance and biomass. Second, the pronounced decline in host specialists suggests habitat loss as an important driver of the observed decline. Third, the more severe decline in dark species might be an indication of global warming as a potential driver. Fourth, the trends in coppiced oak forests indicate that maintaining complex and diverse forest ecosystems through active management may be a promising conservation strategy in order to counteract negative trends in biodiversity, alongside rewilding approaches.
Previous macroecological studies have suggested that larger and darker insects are favored in cold environments and that the importance of body size and color for the absorption of solar radiation is not limited to diurnal insects. However, whether these effects hold true for local communities and are consistent across taxonomic groups and sampling years remains unexplored. This study examined the variations in body size and color lightness of the two major families of nocturnal moths, Geometridae and Noctuidae, along an elevational gradient of 700 m in Southern Germany. An assemblage‐based analysis was performed using community‐weighted means and a fourth‐corner analysis to test for variations in color and body size among communities as a function of elevation. This was followed by a species‐level analysis to test whether species occurrence and abundance along an elevation gradient were related to these traits, after controlling for host plant availability. In both 2007 and 2016, noctuid moth assemblages became larger and darker with increasing elevation, whereas geometrids showed an opposite trend in terms of color lightness and no clear trend in body size. In single species models, the abundance of geometrids, but not of noctuids, was driven by habitat availability. In turn, the abundance of dark‐colored noctuids, but not geometrids increased with elevation. While body size and color lightness affect insect physiology and the ability to cope with harsh conditions, divergent trait–environment relationships between both families underline that findings of coarse‐scale studies are not necessarily transferable to finer scales. Local abundance and occurrence of noctuids are shaped by morphological traits, whereas that of geometrids are rather shaped by local habitat availability, which can modify their trait–environment‐relationship. We discuss potential explanations such as taxon‐specific flight characteristics and the effect of microclimatic conditions.
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