Are landscape structures insurmountable barriers for foraging bees? A mark-recapture study with two solitary pollen specialist species

To investigate whether landscape structures act as insurmountable barriers for foraging bees, we conducted mark-recapture studies with two pollen-specialist solitary species. Foraging options of the bees were confined to host plant stands across different landscape structures. Differences in altitude of more than 130 m were overcome and forests covering a distance of up to 480 m were crossed by Chelostoma florisomne. A broad river and a motorway with intense traffic did not represent insurmountable barriers for Hoplitis adunca. For C. florisomne, total foraging distances of up to 650 m were measured, but foraging females were recorded predominantly on host plant patches available in relatively close vicinity to their nesting site. While landscape structures might impede foraging in endangered bees, the investigated landscape structures clearly did not act as insurmountable physical barriers for the two common solitary bee species tested in our stud

Microbial recovery of metals from solids

A variety of both lithotrophic and organotrophic microorganisms are known to mediate the mobilization of various elements from solids mostly by the formation of inorganic and organic acids. Under appropriate environmental conditions, metals are solubilized and extracted from metal-rich materials in subsurface ecosystems by the action of bacteria and fungi. In mine tailings or landfills microbial metal leaching represents a potential environmental hazard. However, these microbial activities can be successfully applied in the industry for the recovery of metals from solid materials such as ores or incineration residues. Microbial leaching processes are currently used for the winning of gold and copper from low-grade ores (‘bioleaching'). Solid industrial waste materials such as fly ash, sludges, or dust might also be microbially treated to recover metals for the re-use in metal-manufacturing industries. Bioleaching allows the cycling of metals by a process close to natural biogeochemical cycles reducing the demand for resources such as ores, energy, or landfill spac

Is sunlight good for our heart?

Humans evolved being exposed for about half of the day to the light of the sun. Nowadays, exposure to sunlight is actively discouraged for fear of skin cancer, and contemporary lifestyles are associated with long hours spent under artificial light indoors. Besides an increasing appreciation for the adverse effects of these life-style-related behavioural changes on our chronobiology, the balance between the beneficial and harmful effects of sunlight on human health is the subject of considerable debate, in both the scientific and popular press, and the latter is of major public health significance. While there is incontrovertible evidence that ultraviolet radiation (UVR) in the form of sunlight is a significant predisposing factor for non-melanoma and melanoma skin cancers in pale skinned people,1 a growing body of data suggest general health benefits brought about by sunlight.2 These are believed to be mediated either by melatonin or vitamin D. Melatonin is produced from serotonin by the pineal gland located in the centre of the brain during periods of darkness, and its release is suppressed as a function of the visible light intensity sensed through ocular photoreceptors. Vitamin D is formed by ultraviolet B (UVB)-mediated photolysis of 7-dehydrocholesterol in the skin. Both melatonin and vitamin D are pleiotropic hormones that exert a multitude of cellular effects by interacting with membrane and nuclear receptors, and receptor-independent actions. People with more heavily pigmented skin require higher doses of UVB to produce adequate amounts of vitamin D, and this may have been an evolutionary driver to the variation of human skin colour with latitude and intensity of solar irradiation. Our degree of exposure to sunlight is easily modified by behavioural factors such as the use of clothing, sunglasses, and sun-blocking creams, and time spent outdoors. Balancing the carcinogenic risks with the requirement for vitamin D has led to advice on moderating sun exposure, while supplementing food with vitamin D. Guidance on such behaviour is part of the public health campaigns in most countries with Caucasian populations. Following these suggestions, we may, however, be missing out on other health benefits provided by natural sunlight that are less obvious and unrelated to the above classical mediators

Extracting flowering phenology from grassland species mixtures using time-lapse cameras

Understanding the impacts of climate change on plant phenology is crucial for predicting ecosystem responses. However, accurately tracking the flowering phenology of individual plant species in grassland species mixtures is challenging, hindering our ability to study the impacts of biotic and abiotic factors on plant reproduction and plant-pollinator interactions. Here, we present a workflow for extracting flowering phenology from grassland species mixtures using near-surface time-lapse cameras. We used 89 image series acquired in plots with known species composition at the Jena trait-based experiment (Germany) to develop random forest classifiers, which were used to classify images and compute time series of flower cover for each species. The high temporal resolution of time-lapse cameras allowed to select images in proper light conditions, and to extract vegetation indices and texture metrics to improve discrimination among flowering species. The random forest classifiers showed a high accuracy in predicting the cover of Leucanthemum vulgare, Ranunculus acris, and Knautia arvensis flowers, whereas graminoid flowers were harder to predict due to their green-to-brownish colours. The proposed workflow can be applied in climate change studies, ecosystem functioning, plant community ecology, and biodiversity change research, including the investigation of effects of species richness on individual species' flowering phenology. Our method could be a valuable tool for understanding the impacts of climate change on plant reproduction and ecosystem dynamic

Interactive effects of tree species mixture and climate on foliar and woody trait variation in in a widely distributed deciduous tree

Despite increasing reports of severe drought and heat impacts on forest ecosystems, community-level processes, which could potentially modulate tree responses to climatic stress, are rarely accounted for. While numerous studies indicate a positive effect of species diversity on a wide range of ecosystem functions and services, little is known about how species interactions influence tree responses to climatic variability. We quantified the intraspecific variation in 16 leaf and wood physiological, morphological, and anatomical traits in mature beech trees (Fagus sylvatica L.) at six sites located along a climatic gradient in the French Alps. At each site, we studied pure beech and mixed stands with silver fir (Abies alba Mill.) or downy oak (Quercus pubescens Willd.). We tested how functional traits differed between the two species mixtures (pure vs. mixed stands) within each site and along the climatic gradient. We found significant changes in many traits along the climatic gradient as conditions progressively got drier and warmer. Independent of the mixture, reduced leaf-level CO2 assimilation, stomatal size, and thicker leaf cuticles, consistent with a more conservative resource use strategy, were found. At the drier sites, higher foliar stable carbon isotopic composition (δ13C), thicker mesophyll tissues, and lower specific leaf area (SLA) in pure stands suggests that beech had more acquisitive traits there compared to mixed stands. At the wetter sites, trees in beech-silver fir mixtures had higher chlorophyll concentration, lower δ13C, larger xylem vessels, and higher SLA, suggesting a more acquisitive resource use strategy in mixed stands than in pure stands. Our work revealed that species interactions are significant modulators of functional traits, and that they can be just as important drivers of intraspecific trait variation as climatic conditions. We show that downy oak mixtures lead to an adaptive drought response by common beech in dry environments. In contrast, in milder climates, interactions with silver fir seem to increase beech’ resource acquisition and productivity. These findings highlight a strong context-dependency and imply that incorporating local interspecific interactions in research on climate impacts could improve our understanding and predictions of forest dynamics.MD and CG were supported by the Swiss National Science Foundation SNF (PZ00P3_174068). CG is supported by the Sandoz Family Foundation. The plot design used in this study is part of the GMAP plot network (https://oreme.org/observation/foret/gmap/), partly funded by the OSU OREME in Montpellier, France

Анализ минеральных равновесий термальных вод Байкальской рифтовой зоны с использованием программных пакетов Hydrogeo и PHREEQC

В работе изложены результаты сравнительного анализа значений индекса насыщения термальных вод Байкальской рифтовой зоны к ряду породообразующих минералов. Получены интересные, но в то же время спорные, результаты расчетов с применением современных программных продуктов HydroGeo и PHREEQC. В первом случае было выявлено равновесие некоторых терм к кварцу, арагониту, кальциту, доломиту, флюориту, тогда как во втором - в основном к силикатам (кварцу, халцедону, хризотилу, сепиолиту и др.) и так же к флюориту. The paper presents the results of the comparative analysis index values of saturation of the thermal waters of the Baikal rift zone to some rock-forming minerals. Interesting, but at the same time controversial, the results of calculations with the use of modern software products HydroGeo and PHREEQC. In the first case revealed a certain equilibrium therm to quartz, aragonite, calcite, dolomite, fluorite, whereas the second is mostly silicates (quartz, chalcedony chrysotile, sepiolite, etc.) and fluorite

Bachofen-Shoot-and-Root-measurements

This file contains all measurements: shoot and root biomass, shoot height, vertical root length. All other variables (root biomass fraction, specific shoot height, specific vertical root length) are derived from this data as described in the publication