The global spread of artificial light is eroding the natural night-time environment. The estimation of the pattern and rate of growth of light pollution on multi-decadal scales has nonetheless proven challenging. Here we show that the power of global satellite observable light emissions increased from 1992 to 2017 by at least 49%. We estimate the hidden impact of the transition to solid-state light-emitting diode (LED) technology, which increases emissions at visible wavelengths undetectable to existing satellite sensors, suggesting that the true increase in radiance in the visible spectrum may be as high as globally 270% and 400% on specific regions. These dynamics vary by region, but there is limited evidence that advances in lighting technology have led to decreased emissions.
The nighttime environment of much of Earth is being changed rapidly by the introduction of artificial lighting. While data on spatial and temporal variation in the intensity of artificial lighting have been available at a regional and global scale, data on variation in its spectral composition have only been collected for a few locations, preventing variation in associated environmental and human health risks from being mapped. Here, we use imagery obtained using digital cameras by astronauts on the International Space Station to map variation in the spectral composition of lighting across Europe for 2012–2013 and 2014–2020. These show a regionally widespread spectral shift, from that associated principally with high-pressure sodium lighting to that associated with broad white light-emitting diodes and with greater blue emissions. Reexpressing the color maps in terms of spectral indicators of environmental pressures, we find that this trend is widely increasing the risk of harmful effects to ecosystems.
The nighttime environment is being altered rapidly over large areas worldwide through introduction of artificial lighting, from streetlights and other sources. This is predicted to impact the visual ecology of many organisms, affecting both their intra- and interspecific interactions. Here, we show the effects of different artificial light sources on multiple aspects of hawkmoth visual ecology, including their perception of floral signals for pollination, the potential for intraspecific sexual signalling, and the effectiveness of their visual defences against avian predators. Light sources fall into three broad categories: some that prevent use of chromatic signals for these behaviours, others that more closely mimic natural lighting conditions, and, finally, types whose effects vary with light intensity and signal colour. We find that Phosphor Converted (PC) amber LED lighting – often suggested to be less harmful to nocturnal insects – falls into this third disruptive group, with unpredictable consequences for insect visual ecology depending on distance from the light source and the colour of the objects viewed. The diversity of impacts of artificial lighting on hawkmoth visual ecology alone argues for a nuanced approach to outdoor lighting in environmentally sensitive areas, employing intensities and spectra designed to limit those effects of most significant concern.
Urban species and habitats provide important ecosystem services such as summertime cooling, recreation, and pollination at a variety of scales. Many studies have assessed how biodiversity responds to urbanization, but little work has been done to try and create recommendations that can be easily applied to urban planning, design and management practice. Urban planning often operates at broad spatial scales, typically using relatively simplistic targets for land-cover mix to influence biodiversity and ecosystem service provision. Would more complicated, but still easily created, prescriptions for urban vegetation be beneficial? Here we assess the importance of vegetation measures (percentage vegetation cover, tree canopy cover and variation in canopy height) across four taxonomic groups (bats, bees, hoverflies and birds) at multiple spatial scales (100, 250, 500, 1000 m) within a major urban area (Birmingham, the United Kingdom). We found that small-scale (100-250-m radius) measures of vegetation were important predictors for hoverflies and bees, and that bats were sensitive to vegetation at a medium spatial-scale (250-500 m). In contrast, birds responded to vegetation characteristics at both small (100 m) and large (1000 m) scales. Vegetation cover, tree cover and variation in canopy height were expected to decrease with built surface cover; however, only vegetation cover showed this expected trend. The results indicate the importance of relatively small patches of vegetationfor supporting urban biodiversity, and show that relatively simple measures of vegetation characteristics can be useful predictors of species richness (or activity density, in the case of bats). They also highlight the danger of relying upon percentage built surface cover as an indicator of urban biodiversity potential.
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