污染湖泊生态系统服务净价值评估——以滇池为例

水污染是我国湖泊生态系统面临的主要环境问题,评估污染条件下湖泊生态系统服务价值对认识和恢复污染湖泊生态功能具有重要意义。针对当前湖泊生态系统服务价值评估方法中未体现水污染负面影响的问题,在传统生态系统服务功能价值评估框架的基础上,将水污染造成的经济损失内化到生态系统服务功能价值中,提出了针对污染湖泊的生态系统服务功能价值评估方法。应用该方法核算了滇池生态系统服务净价值。结果表明:2006—2015年滇池年均生态系统服务功能价值为386.55亿元/a,水污染改变了滇池的价值结构,供水价值丧失,气候调节、旅游和蓄水等成为滇池生态系统服务功能价值的主体;滇池水污染对流域内外经济社会发展造成的损失达到15.23亿元/a,主要经济损失体现在生态补水费用和蓝藻去除费用;综合湖泊生态系统服务的正向价值和水污染的负向损失,滇池的净生态系统服务价值为371.33亿元/a,占流域GDP的11.7%。将水污染损失纳入湖泊生态系统服务功能价值评估中增强了评价结果的合理性,能够更加真实地反映湖泊生态系统对人类经济社会发展的综合影响。     

Hearing in laboratory animals: strain differences and nonauditory effects of noise

Hearing in laboratory animals is a topic that traditionally has been the domain of the auditory researcher. However, hearing loss and exposure to various environmental sounds can lead to changes in multiple organ systems, making what laboratory animals hear of consequence for researchers beyond those solely interested in hearing. For example, several inbred mouse strains commonly used in biomedical research (e.g., C57BL/6, DBA/2, and BALB/c) experience a genetically determined, progressive hearing loss that can lead to secondary changes in systems ranging from brain neurochemistry to social behavior. Both researchers and laboratory animal facility personnel should be aware of both strain and species differences in hearing in order to minimize potentially confounding variables in their research and to aid in the interpretation of data. Independent of genetic differences, acoustic noise levels in laboratory animal facilities can have considerable effects on the inhabitants. A large body of literature describes the nonauditory impact of noise on the biology and behavior of various strains and species of laboratory animals. The broad systemic effects of noise exposure include changes in endocrine and cardiovascular function, sleep-wake cycle disturbances, seizure susceptibility, and an array of behavioral changes. These changes are determined partly by species and strain; partly by noise intensity level, duration, predictability, and other characteristics of the sound; and partly by animal history and exposure context. This article reviews some of the basic strain and species differences in hearing and outlines how the acoustic environment affects different mammals.     

Comparisons of ecosystem services among three conversion systems in Yancheng National Nature Reserve

A conceptual framework of internal and external emergy was addressed to integrate ecosystem services evaluation and emergy analysis. Internal emergy yields support the material, structure, and information of the ecosystem, and external emergy is those goods and services related to the outside of the ecosystem. An accounting system was determined from the conceptual framework and applied to the evaluation of ecosystem services of conversion activities in Yancheng National Nature Reserve (YNNR), an international important coastal wetland in Jiangsu Province of China. Three typical conversion systems were selected as study cases: (1) a ragworm culturing system (RCS, located in the core zone of YNNR), (2) a clam culturing system (CCS, located in the buffer zone), and (3) a fishpond system (FCS, located in an experimental zone). Our results showed that the ragworm culturing system was more sustainable than the other two systems; indices of base emergy yield ratio (Beyr), net emergy yield ratio (EYR), eco-services benefits (Bs), emergy sustainable indices (ESI) were more sensitive in the new accounting system; the function of the ragworm culturing system relied more on renewable resources and the other two relied mainly on the economic management; and environmental impact, and external services played a crucial role in the ecological engineering evaluation.     

Effects of Boat Engine Noise on the Auditory Sensitivity of the Fathead Minnow, Pimephales promelas

Fishes are constantly exposed to various sources of noise in their underwater acoustic environment. Many of these sounds are from anthropogenic sources, especially engines of boats. Noise generated from a small boat with a 55 horsepower outboard motor was played back to fathead minnows, Pimephales promelas, for 2 h at 142 dB (re: 1 Pa), and auditory thresholds were measured using the auditory brainstem response (ABR) technique. The results demonstrate that boat engine noise significantly elevate a fish's auditory threshold at 1 kHz (7.8 dB), 1.5 kHz (13.5 dB), and 2.0 kHz (10.5 dB), the most sensitive hearing range of this species. Such a short duration of noise exposure leads to significant changes in hearing capability, and implies that man-made noise generated from boat engines can have far reaching environmental impacts on fishes.     

The influence of carotid arterial sounds on hearing sensitivity in mammals

Pulsations of the internal carotid and stapedial arteries produce unwanted sounds (noise) in the middle ear cavity which influence hearing in some mammals. 'Noise' pressure levels calculated from pulse rates, volume pulsations of the arteries, and Fourier analysis of arterial waveforms, correlate well with low frequency thresholds of hearing in the Long-eared hedgehog, Tree shrew and Kangaroo rat. In mammals adapted to hear low frequency sounds, such as the Kangaroo rat and fossorial insectivores, the arteries are enclosed in noise attenuating bony tubes. However, most small mammals possess extended high frequency hearing with little sensitivity at the low frequencies of the arterial sounds. In lower tetrapods such as anurans and most lizards, the broad connection between the middle ear cavity and the pharynx creates a leakage pathway which greatly reduces the noise from the stapedial artery. It is probably for these reasons that the large intratympanic arteries did not disturb hearing in early mammals or submammalian forms.     

Noise Reduces Foraging Efficiency in Pallid Bats (Antrozous pallidus)

Anthropogenic noise is an emerging global pollutant. Road networks and energy extraction infrastructure are both spatially extensive and rapidly expanding sources of noise. We predict that predators reliant on acoustic cues for hunting are particularly sensitive to louder environments. Here we examined the foraging efficiency of pallid bats (Antrozous pallidus) when exposed to played‐back traffic and gas compressor station noise in the laboratory. We show that both types of noise at each of five exposure levels (58–76 dBA, 10–640 m from source) and low‐level amplifier noise (35 dBA) increase the time required for bats to locate prey‐generated sounds by twofold to threefold. The mechanism underlying these findings is unclear and, given the potential landscape‐level habitat degradation indicated by our data, we recommend continued research into the effects of noise exposure on acoustically specialized predators.     

200 kHz Commercial Sonar Systems Generate Lower Frequency Side Lobes Audible to Some Marine Mammals

The spectral properties of pulses transmitted by three commercially available 200 kHz echo sounders were measured to assess the possibility that marine mammals might hear sound energy below the center (carrier) frequency that may be generated by transmitting short rectangular pulses. All three sounders were found to generate sound at frequencies below the center frequency and within the hearing range of some marine mammals, e.g. killer whales, false killer whales, beluga whales, Atlantic bottlenose dolphins, harbor porpoises, and others. The frequencies of these sub-harmonic sounds ranged from 90 to 130 kHz. These sounds were likely detectable by the animals over distances up to several hundred meters but were well below potentially harmful levels. The sounds generated by the sounders could potentially affect the behavior of marine mammals within fairly close proximity to the sources and therefore the exclusion of echo sounders from environmental impact analysis based solely on the center frequency output in relation to the range of marine mammal hearing should be reconsidered.     

Assessing the Underwater Acoustics of the World's Largest Vibration Hammer (OCTA-KONG) and Its Potential Effects on the Indo-Pacific Humpbacked Dolphin (Sousa chinensis)

Anthropogenic noise in aquatic environments is a worldwide concern due to its potential adverse effects on the environment and aquatic life. The Hongkong-Zhuhai-Macao Bridge is currently under construction in the Pearl River Estuary, a hot spot for the Indo-Pacific humpbacked dolphin (Sousa chinensis) in China. The OCTA-KONG, the world''s largest vibration hammer, is being used during this construction project to drive or extract steel shell piles 22 m in diameter. This activity poses a substantial threat to marine mammals, and an environmental assessment is critically needed. The underwater acoustic properties of the OCTA-KONG were analyzed, and the potential impacts of the underwater acoustic energy on Sousa, including auditory masking and physiological impacts, were assessed. The fundamental frequency of the OCTA-KONG vibration ranged from 15 Hz to 16 Hz, and the noise increments were below 20 kHz, with a dominant frequency and energy below 10 kHz. The resulting sounds are most likely detectable by Sousa over distances of up to 3.5 km from the source. Although Sousa clicks do not appear to be adversely affected, Sousa whistles are susceptible to auditory masking, which may negatively impact this species'' social life. Therefore, a safety zone with a radius of 500 m is proposed. Although the zero-to-peak source level (SL) of the OCTA-KONG was lower than the physiological damage level, the maximum root-mean-square SL exceeded the cetacean safety exposure level on several occasions. Moreover, the majority of the unweighted cumulative source sound exposure levels (SSELs) and the cetacean auditory weighted cumulative SSELs exceeded the acoustic threshold levels for the onset of temporary threshold shift, a type of potentially recoverable auditory damage resulting from prolonged sound exposure. These findings may aid in the identification and design of appropriate mitigation methods, such as the use of air bubble curtains, “soft start” and “power down” techniques.     

Traffic noise impacts on urban forest soundscapes in south‐eastern Australia

While the negative impacts of road infrastructure on faunal diversity and abundance have been extensively studied, many traffic noise studies have been conducted in the presence of confounding factors. Therefore, the extent to which traffic noise alone is responsible for impacts is not well known and a better understanding is required to inform urban planning and management decisions. We examined the impact of traffic noise on soundscape patterns at road edges in urban forests. Acoustic sensors were deployed at road and powerline edges, as well as within interior habitat, at three sites in south‐east Queensland, Australia. Powerline edges were included to separate edge effects from traffic noise impacts. We used soundscape power (normalized watts per kHz) of technophony (traffic noise in the 1–2 kHz range) and biophony (animal sounds in the 3–11 kHz range) to investigate soundscape patterns. The results showed that biophony was consistently lower at road edges and was negatively correlated with traffic noise and positively correlated with distance to road edge. Technophony was higher at road edges and was found to correlate negatively with distance to road edge and positively with traffic noise. Technophony and biophony at powerline edges generally exhibited values comparable to interior habitat. These results indicate that traffic noise affects urban forest soundscape patterns at road edges in south‐eastern Australia.     

Pollinators and Other Flying Insects inside and outside the Fukushima Evacuation Zone

Following the accident at the Fukushima Daiichi nuclear power plants in 2011, a large evacuation zone was imposed in an area where residents had historically managed forests and farmlands. Thus, the human activities that had maintained biodiversity and ecosystem services in the zone were discontinued. Such change can affect insects, a biodiversity component that is relatively tolerant to radiation exposure. In this study, we investigated flying insects, including pollinators, important ecosystem providers inside and outside the zone, using Malaise traps. The results showed that the number of individuals of Xylocopa appendiculata, the largest Apidae species in the region, was significantly lower inside the evacuation zone than outside it, whereas those of other insects were not lower significantly. Although we suggest that flying insects and their ecosystem services (i.e., benefits from them such as pollination) 3 years after the disaster were not critically impacted, it is important to monitor the long-term effects of the evacuation in the future.     

Threshold for onset of injury in Chinook salmon from exposure to impulsive pile driving sounds

The risk of effects to fishes and other aquatic life from impulsive sound produced by activities such as pile driving and seismic exploration is increasing throughout the world, particularly with the increased exploitation of oceans for energy production. At the same time, there are few data that provide insight into the effects of these sounds on fishes. The goal of this study was to provide quantitative data to define the levels of impulsive sound that could result in the onset of barotrauma to fish. A High Intensity Controlled Impedance Fluid filled wave Tube was developed that enabled laboratory simulation of high-energy impulsive sound that were characteristic of aquatic far-field, plane-wave acoustic conditions. The sounds used were based upon the impulsive sounds generated by an impact hammer striking a steel shell pile. Neutrally buoyant juvenile Chinook salmon (Oncorhynchus tshawytscha) were exposed to impulsive sounds and subsequently evaluated for barotrauma injuries. Observed injuries ranged from mild hematomas at the lowest sound exposure levels to organ hemorrhage at the highest sound exposure levels. Frequency of observed injuries were used to compute a biological response weighted index (RWI) to evaluate the physiological impact of injuries at the different exposure levels. As single strike and cumulative sound exposure levels (SEL(ss), SEL(cum) respectively) increased, RWI values increased. Based on the results, tissue damage associated with adverse physiological costs occurred when the RWI was greater than 2. In terms of sound exposure levels a RWI of 2 was achieved for 1920 strikes by 177 dB re 1 μPa(2)?s SEL(ss) yielding a SEL(cum) of 210 dB re 1 μPa(2)?s, and for 960 strikes by 180 dB re 1 μPa(2)?s SEL(ss) yielding a SEL(cum) of 210 dB re 1 μPa(2)?s. These metrics define thresholds for onset of injury in juvenile Chinook salmon.     

Role of cage material, working style and hearing sensitivity in perception of animal care noise

During daily care, laboratory animals are exposed to a variety of sounds which may have effects on welfare and also cause physiological and behavioural changes. So far, almost no attention has been paid to individual sounds or the sound level caused by animal care or the sound level inside the animal cage. In this study, sounds from selected rat care procedures were recorded: pulling cage out of the rack, placing it onto a table and replacing the cage back into the rack; with measurements made inside the rat cage and in the adjacent cage. Diet was poured into the food hopper and sounds were recorded inside the cage and also the adjacent cage. The work was repeated in a calm and also in a hurried style, using stainless steel and polycarbonate cages. Finally, the sounds produced by running tap water were recorded. Differences between rat and human hearing were compared using novel species-specific sound level weightings: R-weighting for rats dB(R) and H-weighting for human dB(H). Hurried work with steel caused sound exposure levels exceeding 90 dB(R) when the cages were placed into the rack and about 80 dB(R) when pulling them out of the rack or placing onto a table. With polycarbonate, the levels were 10-15 dB(R) lower. Unhurried calm working produced lower sound exposure levels than hurried working in many procedures. When the procedures were repeated with measurements in the adjacent cage, the sound exposure levels were lower, but the results were similar. Pouring food pellets into a hopper above the rat's head caused 15 dB(R) higher sound exposure levels than pouring food to an adjacent cage. In general, humans hear these sounds about 10-15 dB louder than rats. In conclusion, cage material, working style and hearing sensitivity all have an impact on the sound exposure level in the rodent cage. With correct working methods, high sound levels can be efficiently avoided in most cases.     

Commercialization of wild medicinal plants from Southwest Puebla,Mexico

This paper describes the trade of dry medicinal plants in the southwestern area of the state of Puebla, Mexico. Gatherers who collect medicinal plants represent the poorest economic link in the trade chain. The critical socioeconomic situation of the human population is reflected in the state of the wild plants at the zone, as a result of an increase in their use for economic survival. The stock of medicinal plants handled by regional traders is an indicator of the abundance and diversity of the flora present in the zone, and permits a dynamic exchange of these products with regional traders from outside. Tracing the commercial path of six medicinal plants from the field to the market, only 6.17% of the consumer price, on average, was returned to the collectors. Most of the medicinal plants marketed and used in Mexico are wild plants. This fact, combined with the increasing demand that exists for medicinal plants in this region, create a potential environmental threat. Since this threat is a multifactorial one, involving the complex socioeconomic conditions in which rural workers and their families live, conservation programs for the wild flora (including reassessed gathering methods, production of selected medicinal species and protection of wild populations and market regulations of quality and equity) have to be applied within an organizational framework of the gatherers and peasants in the zone.     

Fin Whale Sound Reception Mechanisms: Skull Vibration Enables Low-Frequency Hearing

Hearing mechanisms in baleen whales (Mysticeti) are essentially unknown but their vocalization frequencies overlap with anthropogenic sound sources. Synthetic audiograms were generated for a fin whale by applying finite element modeling tools to X-ray computed tomography (CT) scans. We CT scanned the head of a small fin whale (Balaenoptera physalus) in a scanner designed for solid-fuel rocket motors. Our computer (finite element) modeling toolkit allowed us to visualize what occurs when sounds interact with the anatomic geometry of the whale’s head. Simulations reveal two mechanisms that excite both bony ear complexes, (1) the skull-vibration enabled bone conduction mechanism and (2) a pressure mechanism transmitted through soft tissues. Bone conduction is the predominant mechanism. The mass density of the bony ear complexes and their firmly embedded attachments to the skull are universal across the Mysticeti, suggesting that sound reception mechanisms are similar in all baleen whales. Interactions between incident sound waves and the skull cause deformations that induce motion in each bony ear complex, resulting in best hearing sensitivity for low-frequency sounds. This predominant low-frequency sensitivity has significant implications for assessing mysticete exposure levels to anthropogenic sounds. The din of man-made ocean noise has increased steadily over the past half century. Our results provide valuable data for U.S. regulatory agencies and concerned large-scale industrial users of the ocean environment. This study transforms our understanding of baleen whale hearing and provides a means to predict auditory sensitivity across a broad spectrum of sound frequencies.     

Bee Threat Elicits Alarm Call in African Elephants

Unlike the smaller and more vulnerable mammals, African elephants have relatively few predators that threaten their survival. The sound of disturbed African honeybees Apis meliffera scutellata causes African elephants Loxodonta africana to retreat and produce warning vocalizations that lead other elephants to join the flight. In our first experiment, audio playbacks of bee sounds induced elephants to retreat and elicited more head-shaking and dusting, reactive behaviors that may prevent bee stings, compared to white noise control playbacks. Most importantly, elephants produced distinctive “rumble” vocalizations in response to bee sounds. These rumbles exhibited an upward shift in the second formant location, which implies active vocal tract modulation, compared to rumbles made in response to white noise playbacks. In a second experiment, audio playbacks of these rumbles produced in response to bees elicited increased headshaking, and further and faster retreat behavior in other elephants, compared to control rumble playbacks with lower second formant frequencies. These responses to the bee rumble stimuli occurred in the absence of any bees or bee sounds. This suggests that these elephant rumbles may function as referential signals, in which a formant frequency shift alerts nearby elephants about an external threat, in this case, the threat of bees.     

Invasion of the acoustic niche: variable responses by native species to invasive American bullfrog calls

Biological invasions are a major threat to biodiversity. Invasive species that use acoustic communication can affect native species through interference in the acoustic niche. The American Bullfrog Lithobates catesbeianus is a highly invasive anuran that is widely distributed in the Brazilian Atlantic Rainforest. Adult male bullfrogs emit loud advertisement calls at frequencies that overlap with the calls of several native species of frogs. Given that spectral overlap is a major factor in acoustic masking, the purpose of this study was to test the effects of the acoustic invasion of L. catesbeianus on native frogs that have calls with and without spectral overlap with the invader. In field experiments, we exposed calling males of two overlapping species and two non-overlapping species to recorded bullfrog vocalizations, white noise, and the vocalization of another native frog species. To identify effects, we compared calls recorded before, during, and after exposure. Our results showed that native species altered their calls in response to the bullfrog calls. However, we also observed similar responses to white noise and heterospecific native calls. Both the invasive and heterospecific calls were emitted at low frequencies, which suggests that the observed responses might be specific to low-frequency calls. Our results provide evidence that the introduction of new sounds can cause native species to modify their calls, and that responses to exogenous sounds are species- and stimulus-specific.     

Learned or innate production of acoustic signals in fishes: a test using a cyprinid

No information on the inheritance of the ability to produce sounds exists for fishes. In birds, which usually provide extensive post-hatching parental care, acoustic signals are learned in some species but are innate in others. Almost no fishes provide extensive post-hatching parental care and, consequently, the offspring have little opportunity to hear and learn sounds produced by the parents (usually the male in fishes); they may, however, be exposed to acoustic signals of conspecifics in the same habitat. We used a cyprinid, Codoma ornata, to test whether sound production is learned from the parents or whether it is innate. Fertilized eggs of this species were raised in isolation from adults. Upon maturity, these fish were tested for sound production in aggressive and reproductive contexts. Fish which had no contact with adults, and therefore no opportunity to hear the acoustic signals of their species, produced sounds that were similar to those produced by their parents, and they produced these in the same contexts. Significant differences were observed in dominant frequency for one context, with the smaller F₁ fish having signals of higher frequency than parental fish. Since no opportunity for learning existed, this provided evidence that the ability to produce sounds is innate in this minnow species.     

Acoustic noise induces attention shifts and reduces foraging performance in three-spined sticklebacks (Gasterosteus aculeatus)

Acoustic noise is known to have a variety of detrimental effects on many animals, including humans, but surprisingly little is known about its impacts on foraging behaviour, despite the obvious potential consequences for survival and reproductive success. We therefore exposed captive three-spined sticklebacks (Gasterosteus aculeatus) to brief and prolonged noise to investigate how foraging performance is affected by the addition of acoustic noise to an otherwise quiet environment. The addition of noise induced only mild fear-related behaviours--there was an increase in startle responses, but no change in the time spent freezing or hiding compared to a silent control--and thus had no significant impact on the total amount of food eaten. However, there was strong evidence that the addition of noise increased food-handling errors and reduced discrimination between food and non-food items, results that are consistent with a shift in attention. Consequently, noise resulted in decreased foraging efficiency, with more attacks needed to consume the same number of prey items. Our results suggest that acoustic noise has the potential to influence a whole host of everyday activities through effects on attention, and that even very brief noise exposure can cause functionally significant impacts, emphasising the threat posed by ever-increasing levels of anthropogenic noise in the environment.     

Do birds differentiate between white noise and deterministic chaos?

Noisy, unpredictable sounds are often present in the vocalizations of fearful and stressed animals across many taxa. A variety of structural characteristics, called nonlinear acoustic phenomena, that include subharmonics, rapid frequency modulations, and deterministic chaos are responsible for the harsh sound quality of these vocalizations. Exposure to nonlinear sound can elicit increased arousal in birds and mammals. Past experiments have used white noise to test for effects of deterministic chaos on perceivers. However, deterministic chaos differs structurally from white noise (i.e., random signal with equal energy at all frequencies), and unlike white noise, may differ dramatically depending on how it is produced. In addition, the subtle structural variation of chaos may not be distinguishable in the environment due to the attenuation and degradation of sound over distance and different habitat types. We designed two experiments to clarify whether American robins (Turdus migratorius) and warbling vireos (Vireo gilvus) discriminate between white noise and deterministic chaos. We broadcast and re‐recorded white noise and two exemplars of deterministic chaos—one generated with a Chua oscillator and the other generated using a logistic equation—at 1, 10, 20, 30, 40, and 80 m across open and forested habitat and used spectrogram correlations to compare stimuli along this degradational gradient. We found that sounds degraded similarly in both habitats when compared to a reference distance of 1 m. Comparing pairs of stimuli across distances suggested that Chua chaos was more easily distinguishable from noise and logistic chaos. In addition, all stimuli became more distinctive over increased distance. The second experiment tested behavioral responses of robins and warbling vireos to control sounds of tropical kingbird (Quiscalus mexicanus), white noise, and two exemplars of deterministic chaos (Chua and logistic). Neither American robins nor warbling vireos responded differently to at least two types of deterministic chaos and white noise, validating previous playback studies that used white noise as a surrogate for deterministic chaos. Uniform responses to a variety of nonlinear features in these birds possibly reflect error management in alarm signal detection.     

A method to include in lca road traffic noise and its health effects

Background, Aims and Scope  Transport noise represents an environmental problem that is perceived by humans more directly than the usual chemical emissions or resource uses. In spite of this, traditional LCA applications still exclude noise — probably due to the unavailability of an appropriate assessment method. In order to fill the gap, this article presents a study proposing a new computational procedure for the determination of health impairment resulting from noise emissions of road vehicles. Main Features  The magnitude of health impairment due to noise is determined separately for each vehicle class (cars, trucks,..) and is calculated per vehicle-kilometre driven during the day or at nighttime on the Swiss road network. This health impairment is expressed in cases of sleep disturbance or communication disturbance, and furthermore aggregated in DALY (Disability Adjusted Life Years) units representing the number, duration and severity of the health cases. The method is modelling the full cause-effect chain from the noise emissions of a single vehicle up to the health damage. As in some other modern concepts of environmental damage assessment, the analysis is subdivided into the four modules of fate analysis, exposure analysis, effect analysis and damage analysis. The fate analysis yielding the noise level increment due to an additional road transport over a given distance is conducted for transports with known or with unknown routing, the latter case being more important in LCA practice. The current number of persons subject to specific background levels of noise is determined on the basis of the road traffic noise model, LUK, developed by the Swiss canton of Zurich. The number of additional cases of health impairment due to incremental noise is calculated with data out of the Swiss Noise Study 90. An assessment of the severity of sleep disturbance and communication disturbance, in comparison to other types of health impairment, was performed by a panel consisting of physicians experienced in the field of severity weighting of disabilities. Results and Discussion  The quantities of health cases and of DALY units are given per 1′000 truck or car kilometres on Swiss roads, and the range of the confidence interval is estimated. A plausibility check is made by a quantitative comparison of the results with health damage due to traffic accidents in Switzerland, and with health damage due to traffic noise in the Netherlands. Conclusions and Oudook  The method is ready for use in LCA practice. However, the temporary solution for transports outside of Switzerland should be replaced by feeding country specific data into the fate and exposure model. Further, a comparable assessment for rail transport would facilitate decisions on road or rail transport. A decisive element of transport noise assessment is the availability of robust links between noise level and medical conditions. Whilst the number of the corresponding studies is sufficiendy large, a design for better pooling of study results is desirable.