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Gaston, K.J.; Bennie, J.; Davies, T.W.; Hopkins, J. |

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Title |
The ecological impacts of nighttime light pollution: a mechanistic appraisal |
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Journal Article |
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Year |
2013 |
Publication  |
Biological Reviews of the Cambridge Philosophical Society |
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Biol Rev Camb Philos Soc |
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88 |
Issue |
4 |
Pages |
912-927 |
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Keywords |
dark; information; light; moonlight; night; pollution; resources; rhythms; time |
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Abstract |
The ecological impacts of nighttime light pollution have been a longstanding source of concern, accentuated by realized and projected growth in electrical lighting. As human communities and lighting technologies develop, artificial light increasingly modifies natural light regimes by encroaching on dark refuges in space, in time, and across wavelengths. A wide variety of ecological implications of artificial light have been identified. However, the primary research to date is largely focused on the disruptive influence of nighttime light on higher vertebrates, and while comprehensive reviews have been compiled along taxonomic lines and within specific research domains, the subject is in need of synthesis within a common mechanistic framework. Here we propose such a framework that focuses on the cross-factoring of the ways in which artificial lighting alters natural light regimes (spatially, temporally, and spectrally), and the ways in which light influences biological systems, particularly the distinction between light as a resource and light as an information source. We review the evidence for each of the combinations of this cross-factoring. As artificial lighting alters natural patterns of light in space, time and across wavelengths, natural patterns of resource use and information flows may be disrupted, with downstream effects to the structure and function of ecosystems. This review highlights: (i) the potential influence of nighttime lighting at all levels of biological organisation (from cell to ecosystem); (ii) the significant impact that even low levels of nighttime light pollution can have; and (iii) the existence of major research gaps, particularly in terms of the impacts of light at population and ecosystem levels, identification of intensity thresholds, and the spatial extent of impacts in the vicinity of artificial lights. |
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Environment and Sustainability Institute, University of Exeter, Penryn, Cornwall, TR10 9EZ, U.K |
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0006-3231 |
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PMID:23565807 |
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IDA @ john @ |
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14 |
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Fonken, Laura K; Weil, Zachary M; Nelson, Randy J |

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Title |
Mice exposed to dim light at night exaggerate inflammatory responses to lipopolysaccharide |
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Journal Article |
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Year |
2013 |
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Brain, Behavior, and Immunity |
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34 |
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159-163 |
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animals; rodents; metabolism; health |
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The mammalian circadian system regulates many physiological functions including inflammatory responses. Appropriately timed light information is essential for maintaining circadian organization. Over the past ∼120 years, urbanization and the widespread adoption of electric lights have dramatically altered lighting environments. Exposure to light at night (LAN) is pervasive in modern society and disrupts core circadian clock mechanisms. Because microglia are the resident macrophages in the brain and macrophages contain intrinsic circadian clocks, we hypothesized that chronic exposure to LAN would alter microglia cytokine expression and sickness behavior following LPS administration. Exposure to 4 weeks of dim LAN elevated inflammatory responses in mice. Mice exposed to dimly lit, as compared to dark, nights exaggerated changes in body temperature and elevated microglia pro-inflammatory cytokine expression following LPS administration. Furthermore, dLAN mice had a prolonged sickness response following the LPS challenge. Mice exposed to dark or dimly lit nights had comparable sickness behavior directly following the LPS injection; however, dLAN mice showed greater reductions in locomotor activity, increased anorectic behavior, and increased weight loss than mice maintained in dark nights 24 h post-LPS injection. Overall, these data suggest that chronic exposure to even very low levels of light pollution may alter inflammatory responses. These results may have important implications for humans and other urban dwelling species that commonly experience nighttime light exposure. |
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LoNNe @ schroer @ |
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1588 |
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Fritschi, L.; Erren, T.C.; Glass, D.C.; Girschik, J.; Thomson, A.K.; Saunders, C.; Boyle, T.; El-Zaemey, S.; Rogers, P.; Peters, S.; Slevin, T.; D'Orsogna, A.; de Vocht, F.; Vermeulen, R.; Heyworth, J.S. |

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The association between different night shiftwork factors and breast cancer: a case-control study |
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Journal Article |
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2013 |
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British Journal of Cancer |
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Br J Cancer |
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109 |
Issue |
9 |
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2472-2480 |
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Adult; Aged; Aged, 80 and over; Breast Neoplasms/*epidemiology/etiology; Case-Control Studies; Female; Humans; Life Style; Middle Aged; Questionnaires; Risk; Risk Factors; Western Australia/epidemiology; *Work Schedule Tolerance; Young Adult; oncogenesis |
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BACKGROUND: Research on the possible association between shiftwork and breast cancer is complicated because there are many different shiftwork factors, which might be involved including: light at night, phase shift, sleep disruption and changes in lifestyle factors while on shiftwork (diet, physical activity, alcohol intake and low sun exposure). METHODS: We conducted a population-based case-control study in Western Australia from 2009 to 2011 with 1205 incident breast cancer cases and 1789 frequency age-matched controls. A self-administered questionnaire was used to collect demographic, reproductive, and lifestyle factors and lifetime occupational history and a telephone interview was used to obtain further details about the shiftwork factors listed above. RESULTS: A small increase in risk was suggested for those ever doing the graveyard shift (work between midnight and 0500 hours) and breast cancer (odds ratio (OR)=1.16, 95% confidence interval (CI)=0.97-1.39). For phase shift, we found a 22% increase in breast cancer risk (OR=1.22, 95% CI=1.01-1.47) with a statistically significant dose-response relationship (P=0.04). For the other shiftwork factors, risks were marginally elevated and not statistically significant. CONCLUSION: We found some evidence that some of the factors involved in shiftwork may be associated with breast cancer but the ORs were low and there were inconsistencies in duration and dose-response relationships. |
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Western Australian Institute for Medical Research, The University of Western Australia, Nedlands, Western Australia, Australia |
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0007-0920 |
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PMID:24022188; PMCID:PMC3817316 |
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IDA @ john @ |
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153 |
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Shimose, T.; Yokawa, K.; Tachihara, K. |

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Title |
Higher Catch Rates Around the Full Moon for Blue Marlin, Makaira Nigricans, in a Diurnal Trolling Fishery |
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Journal Article |
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2013 |
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Bulletin of Marine Science |
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Bms |
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89 |
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3 |
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759-765 |
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fish; blue marlin; Makaira nigricans; Moon; moonlight; Feeding Behavior |
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The relationship between lunar phase and catch rates of blue marlin, Makaira nigricans Lacépède, 1802, in a diurnal trolling fishery at Yonaguni Island, southwestern Japan, was investigated. The mean catch per unit effort of blue marlin to lunar day was expressed by a periodic regression and significantly increased around the full moon. The stomach content index also significantly increased around the full moon in small blue marlin (<200 cm lower jawâfork length), indicating that diurnal feeding activities of blue marlin increased around the full moon, especially for smaller individuals. The diurnal feeding activity is thought to be influenced by the nighttime activities of blue marlin and/or prey movements. |
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0007-4977 |
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IDA @ john @ |
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63 |
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Author |
Shimmura, Tsuyoshi; Yoshimura, Takashi |

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Title |
Circadian clock determines the timing of rooster crowing |
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Journal Article |
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2013 |
Publication  |
Current Biology |
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23 |
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6 |
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R231âR233 |
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animals; rooster; bird |
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Crowing of roosters is described by onomatopoetic terms such as âcock-a-doodle-dooâ (English), âki-ke-ri-kiâ (German), and âko-ke-kok-kohâ (Japanese). Rooster crowing is a symbol of the break of dawn in many countries. Indeed, crowing is frequently observed in the morning [1] . However, people also notice that crowing is sometimes observed at other times of day. Therefore, it is yet unclear whether crowing is under the control of an internal biological clock, or is simply caused by external stimuli. Here we show that predawn crowing is under the control of a circadian clock. Although external stimuli such as light and crowing by other individuals also induce roostersâ crowing, the magnitude of this induction is also regulated by a circadian clock. |
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LoNNe @ schroer @ |
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1600 |
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