282 research outputs found

    UFP-Integrating action for cleaner air and climate protection

    Get PDF
    The background information related to health effects and damage caused to ecosystems by PM atmospheric pollution, particularly by its fine fraction, will be summarisedCurrent international policy instruments for reducing airborne emissions and, consequently, improving air quality, will be reviewed. In particular the EU clean air package and the UN/ECE initiatives under the Long-Range Transboundary Air Pollution Convention (LRTAP), including the recentlyadopted Long-term Strategy, will be considered. The air policy initiatives by EFCA related to improve air quality in relation to PM and its ultrafine fraction/Black Carbon will be described and assessed. Combustion of all kinds produces PM pollution, including its ultrafine fraction (UFP). Carbonaceous particles in form of Black Carbon (BC) and Organic Aerosols (OA) are of particular concern. UFPs are also formed as secondary pollutants. The latter have substantial influence on particle formation and their growth generates half of the cloud condensation nuclei in the atmosphere. Non-CO2 Greenhouse Gases (NCGG), however, are underestimated as pollutants by the climate policy community and deserve to be treated as equally important. UFPs play an important role in policy to reduce toxic air pollution and climate forcers. The series of UFP Symposia has provided strong evidence of impact, and information on sources and effective control techniques. EFCA therefore believes it is now timely to consider policy aspect. It fully supports UFP/BC regulation, including new ceilings in the EU NEC Directive and the revised Gothenburg Protocol under the LRTAP. Moreover, a new metric is urgently needed for UFPs, expressed in weight and by number of particles. Also, dual policy, integrating cleaner air and climate protection criteria, to combat UFPs can be more effective and generate co-benefits for both. The role of integrated policy, as opposed to the current practice of separate sectoral policies in combatting air pollution will be considered with reference to concrete examples, including from the energy system

    Olfactory search at high Reynolds number

    Full text link

    Data-driven honeybee antennal lobe model suggests how stimulus-onset asynchrony can aid odour segregation

    Get PDF
    Insects have a remarkable ability to identify and track odour sources in multi-odour backgrounds. Recent behavioural experiments show that this ability relies on detecting millisecond stimulus asynchronies between odourants that originate from different sources. Honeybees, Apis mellifera , are able to distinguish mixtures where both odourants arrive at the same time (synchronous mixtures) from those where odourant onsets are staggered (asynchronous mixtures) down to an onset delay of only 6 ms. In this paper we explore this surprising ability in a model of the insects' primary olfactory brain area, the antennal lobe. We hypothesize that a winner-take-all inhibitory network of local neurons in the antennal lobe has a symmetry-breaking effect, such that the response pattern in projection neurons to an asynchronous mixture is different from the response pattern to the corresponding synchronous mixture for an extended period of time beyond the initial odourant onset where the two mixture conditions actually differ. The prolonged difference between response patterns to synchronous and asynchronous mixtures could facilitate odour segregation in downstream circuits of the olfactory pathway. We present a detailed data-driven model of the bee antennal lobe that reproduces a large data set of experimentally observed physiological odour responses, successfully implements the hypothesised symmetry-breaking mechanism and so demonstrates that this mechanism is consistent with our current knowledge of the olfactory circuits in the bee brain

    Efficient Olfactory Coding in the Pheromone Receptor Neuron of a Moth

    Get PDF
    The concept of coding efficiency holds that sensory neurons are adapted, through both evolutionary and developmental processes, to the statistical characteristics of their natural stimulus. Encouraged by the successful invocation of this principle to predict how neurons encode natural auditory and visual stimuli, we attempted its application to olfactory neurons. The pheromone receptor neuron of the male moth Antheraea polyphemus, for which quantitative properties of both the natural stimulus and the reception processes are available, was selected. We predicted several characteristics that the pheromone plume should possess under the hypothesis that the receptors perform optimally, i.e., transfer as much information on the stimulus per unit time as possible. Our results demonstrate that the statistical characteristics of the predicted stimulus, e.g., the probability distribution function of the stimulus concentration, the spectral density function of the stimulation course, and the intermittency, are in good agreement with those measured experimentally in the field. These results should stimulate further quantitative studies on the evolutionary adaptation of olfactory nervous systems to odorant plumes and on the plume characteristics that are most informative for the ‘sniffer’. Both aspects are relevant to the design of olfactory sensors for odour-tracking robots

    Airborne chemical sensing with mobile robots

    Get PDF
    Airborne chemical sensing with mobile robots has been an active research areasince the beginning of the 1990s. This article presents a review of research work in this field,including gas distribution mapping, trail guidance, and the different subtasks of gas sourcelocalisation. Due to the difficulty of modelling gas distribution in a real world environmentwith currently available simulation techniques, we focus largely on experimental work and donot consider publications that are purely based on simulations

    Use of habitat odour by host-seeking insects

    Get PDF
    Locating suitable feeding or oviposition sites is essential for insect survival. Understanding how insects achieve this is crucial, not only for understanding the ecology and evolution of insect–host interactions, but also for the development of sustainable pest-control strategies that exploit insects' host-seeking behaviours. Volatile chemical cues are used by foraging insects to locate and recognise potential hosts but in nature these resources usually are patchily distributed, making chance encounters with host odour plumes rare over distances greater than tens of metres. The majority of studies on insect host-seeking have focussed on short-range orientation to easily detectable cues and it is only recently that we have begun to understand how insects overcome this challenge. Recent advances show that insects from a wide range of feeding guilds make use of ‘habitat cues’, volatile chemical cues released over a relatively large area that indicate a locale where more specific host cues are most likely to be found. Habitat cues differ from host cues in that they tend to be released in larger quantities, are more easily detectable over longer distances, and may lack specificity, yet provide an effective way for insects to maximise their chances of subsequently encountering specific host cues. This review brings together recent advances in this area, discussing key examples and similarities in strategies used by haematophagous insects, soil-dwelling insects and insects that forage around plants. We also propose and provide evidence for a new theory that general and non-host plant volatiles can be used by foraging herbivores to locate patches of vegetation at a distance in the absence of more specific host cues, explaining some of the many discrepancies between laboratory and field trials that attempt to make use of plant-derived repellents for controlling insect pests

    Trends in extreme weather events in Europe: implications for national and European Union adaptation strategies

    Get PDF
    This report, based on a comprehensive collection of scientific data from the last 20 years, provides a rallying call for Europe’s policy makers to come together to devise common strategies to help mitigate the physical, human and economic costs of the rising number of extreme weather events in Europe, such as extreme heat and cold, extremes of precipitation, storms, winds and surges, and drought. Highlights refer to the nature of the evidence for climate-driven changes in extreme weather in the past, the potential impact of further climate change in altering the pattern of these extremes, and possible adaptation strategies for dealing with extreme weather impacts. It first provides information on extreme weather events and trends in recent decades as well as related impacts upon society. It is followed by an introduction to the scientific background on global warming and weather extremes, and the projections of future trends of meteorological extreme events that emerge from climate models under various scenarios of future greenhouse gas emissions. Finally, approaches to adaptation are introduced and recommendations provided. Readers wishing to obtain full source details for the figures, tables and references are recommended to consult the full report, which also includes more detailed analyses of the climatic conditions in various sub-regions of the EU

    Effect of sex pheromone emission on the attraction of Lobesia botrana

    Full text link
    Since the discovery of Lobesia botrana Denis & Schiffermüller (Lepidoptera: Tortricidae) sex pheromone, it has played an important role in the control and detection of this pest, for example, through the use of pheromone-baited traps and mating disruption techniques. Rubber septa are the most common pheromone dispensers used in monitoring traps, but often dispenser performance is not optimized. The key to improve methods based on pheromones as attractants (monitoring, mass trapping, or ‘attract and kill’) is to know the optimum emission interval, because release rates can strongly affect the attraction. In this work, five levels of pheromone load with different release rates were compared in traps using mesoporous pheromone dispensers to investigate the optimum release rate maximizing L. botrana catches. Residual pheromone loads of the dispensers were extracted and quantified by gas chromatography, to study release profiles and to estimate the various emission levels. The efficacy of pheromone emission was measured in field trials as number of moths caught. A quadratic model was fitted to relate the numbers caught vs. the daily emission rates. The resulting quadratic term was statistically significant, confirming the existence of a relative maximum for L. botrana catches. Taking into account that the trial was carried out only in one location, an optimum emission value of ca. 400 μg per day could be considered to enhance the attraction of L. botrana under West-Mediterranean weather conditions.© 2011 The Authors. Entomologia Experimentalis et Applicata © 2011 The Netherlands Entomological Society.Vacas González, S.; Alfaro Cañamás, C.; Zarzo Castelló, M.; Navarro-Llopis, V.; Primo Millo, J. (2011). Effect of sex pheromone emission on the attraction of Lobesia botrana. Entomologia Experimentalis et Applicata. 139(3):250-257. doi:10.1111/j.1570-7458.2011.01124.xS2502571393Anshelevich, L., Kehat, M., Dunkelblum, E., & Greenberg, S. (1994). Sex Pheromone Traps for Monitoring the European Vine Moth,Lobesia botrana: Effect of Dispenser Type, Pheromone Dose, Field Aging of Dispenser, and Type of Trap on Male Captures. Phytoparasitica, 22(4), 281-290. doi:10.1007/bf02980529Arn, H., Rauscher, S., Guerin, P., & Buser, H.-R. (1988). Sex pheromone blends of three tortricid pests in European vineyards. Agriculture, Ecosystems & Environment, 21(1-2), 111-117. doi:10.1016/0167-8809(88)90143-0Bradley, S. J., Suckling, D. M., McNaughton, K. G., Wearing, C. H., & Karg, G. (1995). A temperature-dependent model for predicting release rates of pheromone from a polyethylene tubing dispenser. Journal of Chemical Ecology, 21(6), 745-760. doi:10.1007/bf02033458Branco, M., Jactel, H., Silva, E. B., Binazzi, A., & Mendel, Z. (2004). Effect of trap design, trap size and pheromone dose on male capture of two pine bast scales species (Hemiptera: Matsucoccidae): implications for monitoring and mass-trapping. Agricultural and Forest Entomology, 6(3), 233-239. doi:10.1111/j.1461-9555.2004.00219.xCork, A., Alam, S. N., Das, A., Das, C. S., Ghosh, G. C., Farman, D. I., … Srinivasan, K. (2001). Journal of Chemical Ecology, 27(9), 1867-1877. doi:10.1023/a:1010416927282Corma A Muñoz-Pallares J Primo-Yufera E 1999 Production of semiochemical emitters having a controlled emission speed which are based on inorganic molecular sievesCorma A Muñoz-Pallares J Primo-Yufera E 2000 Emitter of semiochemical substances supported on a sepiolite, preparation process and applicationsCritchley, B. R., Hall, D. R., Farman, D. I., McVeigh, L. J., Mulaa, M. A. O. A., & Kalama, P. (1997). Monitoring and mating disruption of the maize stalkborer, Busseola fusca, in Kenya with pheromones. Crop Protection, 16(6), 541-548. doi:10.1016/s0261-2194(97)00026-4Cross, J. V., Hesketh, H., Jay, C. N., Hall, D. R., Innocenzi, P. J., Farman, D. I., & Burgess, C. M. (2006). Exploiting the aggregation pheromone of strawberry blossom weevil Anthonomus rubi Herbst (Coleoptera: Curculionidae): Part 1. Development of lure and trap. Crop Protection, 25(2), 144-154. doi:10.1016/j.cropro.2005.04.002Domínguez-Ruiz, J., Sanchis, J., Navarro-Llopis, V., & Primo, J. (2008). A New Long-Life Trimedlure Dispenser for Mediterranean Fruit Fly. Journal of Economic Entomology, 101(4), 1325-1330. doi:10.1603/0022-0493(2008)101[1325:anltdf]2.0.co;2El-Sayed, A., Gödde, J., Witzgall, P., & Arn, H. (1999). Journal of Chemical Ecology, 25(2), 389-400. doi:10.1023/a:1020811200054Evenden, M. L., Borden, J. H., Van Sickle, G. A., & Gries, G. (1995). Development of a Pheromone-Based Monitoring System for Western Hemlock Looper (Lepidoptera: Geometridae): Effect of Pheromone Dose, Lure Age, and Trap Type. Environmental Entomology, 24(4), 923-932. doi:10.1093/ee/24.4.923Franklin, A. J., & Grégoire, J.-C. (2001). Journal of Chemical Ecology, 27(12), 2425-2435. doi:10.1023/a:1013619313415Groot, P., & DeBarr, G. L. (1998). Factors affecting capture of the white pine cone beetle,Conophthorus coniperda(Schwarz) (Col., Scolytidae) in pheromone traps. Journal of Applied Entomology, 122(1-5), 281-286. doi:10.1111/j.1439-0418.1998.tb01498.xHowse, P. E., Stevens, I. D. R., & Jones, O. T. (1998). Insect Pheromones and their Use in Pest Management. doi:10.1007/978-94-011-5344-7Ideses, R., Klug, J. T., Shani, A., Gothilf, S., & Gurevitz, E. (1982). Sex pheromone of the European grapevine moth,Lobesia botrana Schiff. (Lepidoptera: Tortricidae): Synthesis and effect of isomeric purity on biological activity. Journal of Chemical Ecology, 8(1), 195-200. doi:10.1007/bf00984016Ifoulis, A. A., & Savopoulou-Soultani, M. (2006). Use of Geostatistical Analysis to Characterize the Spatial Distribution ofLobesia botrana(Lepidoptera: Tortricidae) Larvae in Northern Greece. Environmental Entomology, 35(2), 497-506. doi:10.1603/0046-225x-35.2.497Jacobson, M., & Beroza, M. (1964). Insect Attractants. Scientific American, 211(2), 20-27. doi:10.1038/scientificamerican0864-20Jactel, H., Menassieu, P., Vétillard, F., Barthélémy, B., Piou, D., Frérot, B., … Battisti, A. (2006). Population monitoring of the pine processionary moth (Lepidoptera: Thaumetopoeidae) with pheromone-baited traps. Forest Ecology and Management, 235(1-3), 96-106. doi:10.1016/j.foreco.2006.08.002Kawazu, K., Kamimuro, T., Kamiwada, H., Nagata, K., Matsunaga, T., Sugie, H., … Tatsuki, S. (2004). Effective pheromone lures for monitoring the rice leaffolder moth, Cnaphalocrocis medinalis (Lepidoptera: Crambidae). Crop Protection, 23(7), 589-593. doi:10.1016/j.cropro.2003.11.009Kehat, M., Anshelevich, L., Dunkelblum, E., Fraishtat, P., & Greenberg, S. (1994). Sex pheromone traps for monitoring the codling moth: effect of dispenser type, field aging of dispenser, pheromone dose and type of trap on male captures. Entomologia Experimentalis et Applicata, 70(1), 55-62. doi:10.1111/j.1570-7458.1994.tb01758.xKnutson, A. E., Harris, M. K., & Millar, J. G. (1998). Effects of Pheromone Dose, Lure Age, and Trap Design on Capture of Male Pecan Nut Casebearer (Lepidoptera: Pyralidae) in Pheromone-Baited Traps. Journal of Economic Entomology, 91(3), 715-722. doi:10.1093/jee/91.3.715Kovanci, O. B., Schal, C., Walgenbach, F., & Kennedy, G. G. (2006). Effects of pheromone loading, dispenser age, and trap height on pheromone trap catches of the oriental fruit moth in apple orchards. Phytoparasitica, 34(3), 252-260. doi:10.1007/bf02980952Leonhardt, B. A., Cunningham, R. T., Rice, R. E., Harte, E. M., & Hendrichs, J. (1989). Design, Effectiveness, and Performance Criteria of Dispenser Formulations of Trimedlure, an Attractant of the Mediterranean Fruit Fly (Diptera: Tephritidae). Journal of Economic Entomology, 82(3), 860-867. doi:10.1093/jee/82.3.860Leonhardt, B. A., Mastro, V. C., Paszek, E. C., Schwalbe, C. P., & Devilbiss, E. D. (1990). Dependence of Gypsy Moth (Lepidoptera: Lymantriidae) Capture on Pheromone Release Rate from Laminate and Other Dispensers. Journal of Economic Entomology, 83(5), 1977-1981. doi:10.1093/jee/83.5.1977Mason, L. J., Jansson, R. K., & Heath, R. R. (1990). Sampling range of male sweetpotato weevils (Cylas formicarius elegantulus) (Summers) (Coleoptera: Curculionidae) to pheromone traps: Influence of pheromone dosage and lure age. Journal of Chemical Ecology, 16(8), 2493-2502. doi:10.1007/bf01017472Millar, J. G., Knudson, A. E., McElfresh, J. S., Gries, R., Gries, G., & Davis, J. H. (1996). Sex attractant pheromone of the pecan nut casebearer (Lepidoptera: Pyralidae). Bioorganic & Medicinal Chemistry, 4(3), 331-339. doi:10.1016/0968-0896(96)00010-7Murlis, J., Elkinton, J. S., & Cardé, R. T. (1992). Odor Plumes and How Insects Use Them. Annual Review of Entomology, 37(1), 505-532. doi:10.1146/annurev.en.37.010192.002445ROEHRICH, R., CARLES, J.-P., DREUILHE, A., & VONDERHEYDEN, F. (1983). Captures de Lobesia botrana Den. & Schiff. (Lepidoptera, Tortricidae) au piège sexuel en relation avec la dose en phéromone du diffuseur. Agronomie, 3(9), 925-930. doi:10.1051/agro:19830915Roelofs, W. L., & CardÉ, R. T. (1974). Oriental Fruit Moth 1 and Lesser Appleworm 1 Attractant Mixtures Refined 2. Environmental Entomology, 3(4), 586-588. doi:10.1093/ee/3.4.586ROELOFS, W. L., GIESELMANN, M. J., CARDÉ, A. M., TASHIRO, H., MORENO, D. S., HENRICK, C. A., & ANDERSON, R. J. (1977). Sex pheromone of the California red scale, Aonidiella aurantii. Nature, 267(5613), 698-699. doi:10.1038/267698a0Vacas, S., Alfaro, C., Navarro-Llopis, V., Zarzo, M., & Primo, J. (2009). Study on the Optimum Pheromone Release Rate for Attraction of Chilo suppressalis (Lepidoptera: Pyralidae). Journal of Economic Entomology, 102(3), 1094-1100. doi:10.1603/029.102.0330Witzgall, P., Tasin, M., Buser, H.-R., Wegner-Kiß, G., Marco Mancebón, V. S., Ioriatti, C., … Francke, W. (2005). New Pheromone Components of the Grapevine Moth Lobesia botrana. Journal of Chemical Ecology, 31(12), 2923-2932. doi:10.1007/s10886-005-8404-1Witzgall, P., Kirsch, P., & Cork, A. (2010). Sex Pheromones and Their Impact on Pest Management. Journal of Chemical Ecology, 36(1), 80-100. doi:10.1007/s10886-009-9737-yWyman, J. A. (1979). Effect of Trap Design and Sex Attractant Release Rates on Tomato Pinworm Catches1. Journal of Economic Entomology, 72(6), 865-868. doi:10.1093/jee/72.6.865Zhang, A., & Amalin, D. (2005). Sex Pheromone of the Female Pink Hibiscus Mealybug,Maconellicoccus hirsutus(Green) (Homoptera: Pseudococcidae): Biological Activity Evaluation. Environmental Entomology, 34(2), 264-270. doi:10.1603/0046-225x-34.2.26
    corecore