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      Recreation effects on wildlife: a review of potential quantitative thresholds

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      Nature Conservation
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          Abstract

          Outdoor recreation is increasingly recognised for its deleterious effects on wildlife individuals and populations. However, planners and natural resource managers lack robust scientific recommendations for the design of recreation infrastructure and management of recreation activities. We reviewed 38 years of research on the effect of non-consumptive recreation on wildlife to attempt to identify effect thresholds or the point at which recreation begins to exhibit behavioural or physiological change to wildlife. We found that 53 of 330 articles identified a quantitative threshold. The majority of threshold articles focused on bird or mammal species and measured the distance to people or to a trail. Threshold distances varied substantially within and amongst taxonomic groups. Threshold distances for wading and passerine birds were generally less than 100 m, whereas they were greater than 400 m for hawks and eagles. Mammal threshold distances varied widely from 50 m for small rodents to 1,000 m for large ungulates. We did not find a significant difference between threshold distances of different recreation activity groups, likely based in part on low sample size. There were large gaps in scientific literature regarding several recreation variables and taxonomic groups including amphibians, invertebrates and reptiles. Our findings exhibit the need for studies to measure continuous variables of recreation extent and magnitude, not only to detect effects of recreation on wildlife, but also to identify effect thresholds when and where recreation begins or ceases to affect wildlife. Such considerations in studies of recreation ecology could provide robust scientific recommendations for planners and natural resource managers for the design of recreation infrastructure and management of recreation activities.

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          Most cited references54

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          Decline in relative abundance of bottlenose dolphins exposed to long-term disturbance.

          Studies evaluating effects of human activity on wildlife typically emphasize short-term behavioral responses from which it is difficult to infer biological significance or formulate plans to mitigate harmful impacts. Based on decades of detailed behavioral records, we evaluated long-term impacts of vessel activity on bottlenose dolphins (Tursiops sp.) in Shark Bay, Australia. We compared dolphin abundance within adjacent 36-km2 tourism and control sites, over three consecutive 4.5-year periods wherein research activity was relatively constant but tourism levels increased from zero, to one, to two dolphin-watching operators. A nonlinear logistic model demonstrated that there was no difference in dolphin abundance between periods with no tourism and periods in which one operator offered tours. As the number of tour operators increased to two, there was a significant average decline in dolphin abundance (14.9%; 95% CI=-20.8 to -8.23), approximating a decline of one per seven individuals. Concurrently, within the control site, the average increase in dolphin abundance was not significant (8.5%; 95% CI=-4.0 to +16.7). Given the substantially greater presence and proximity of tour vessels to dolphins relative to research vessels, tour-vessel activity contributed more to declining dolphin numbers within the tourism site than research vessels. Although this trend may not jeopardize the large, genetically diverse dolphin population of Shark Bay, the decline is unlikely to be sustainable for local dolphin tourism. A similar decline would be devastating for small, closed, resident, or endangered cetacean populations. The substantial effect of tour vessels on dolphin abundance in a region of low-level tourism calls into question the presumption that dolphin-watching tourism is benign.
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            Why behavioural responses may not reflect the population consequences of human disturbance

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              Walk on the Wild Side: Estimating the Global Magnitude of Visits to Protected Areas

              Enjoyment of nature, much of it in protected areas (PAs), is recognised as the most prominent cultural ecosystem service [1–3], yet we still lack even a rough understanding of its global magnitude and economic significance. Large-scale assessments have been restricted to regional or biome-specific investigations [4–8] (but see [9]). There are good reasons for this. Information on visit rates is limited, widely scattered, and confounded by variation in methods [10,11]. Likewise, estimates of the value of visits vary greatly—geographically, among methods, and depending on the component of value being measured [12–14]. Until now, these problems have prevented data-driven analysis of the worldwide scale of nature-based recreation and tourism. But with almost all the world’s governments committed (through the Aichi Biodiversity Targets [15]) to integrating biodiversity into national accounts, policymakers require such gaps in our knowledge of natural capital to be filled. We tackled this shortfall in our understanding of a major ecosystem service by focusing on terrestrial PAs, which cover one-eighth of the land [16] and are a major focus of nature-based recreation and tourism. We compiled data on visit rates to over 500 PAs and built region-specific models, which predicted variation in visitation in relation to the properties of PAs and to local socioeconomic conditions. Next, we used these models to estimate visit rates to all but the smallest of the world’s terrestrial PAs. Last, by summing these estimates by region and combining the totals with region-specific medians for the value of nature visits obtained from the literature, we derived approximate estimates of the global extent and economic significance of PA visitation. Given the scarcity of data on visits to PAs, our approach was to use all available information (although we excluded marine and Antarctic sites, and International Union for Conservation of Nature (IUCN) Category I PAs where tourism is typically discouraged; for further details of data collection and analysis see Materials and Methods). This generated a database of visitor records for 556 PAs spread across 51 countries and included 2,663 records of annual visit numbers over our best-sampled ten-year period (1998–2007) (S1 Table). Mean annual visit rates for individual PAs in this sample ranged from zero to over 10 million visits/y, with a median across all sampled PAs of 20,333 visits/y. We explored this variation by modelling it in relation to a series of biophysical and socioeconomic variables that might plausibly predict visit rates (after refs [6,7,17]): PA size, local population size, PA remoteness, a simple measure of the attractiveness of the PA’s natural features, and national income (see Materials and Methods for a priori predictions). For each of five major regions, we performed univariate regressions (S2 Table) and then built generalised linear models (GLMs) in an effort to predict variation in observed visit rates. While the GLMs had modest explanatory power within regions (S3 Table), together they accounted for 52.9% of observed global variation in visit rates. Associations with individual GLM variables—controlling for the effects of other variables—differed regionally in their strength but broadly matched our predictions (S1 Fig.). Visit rates increased with local population size (in Europe), decreased with remoteness (everywhere apart from Asia/Australasia), increased with natural attractiveness (in North and Latin America), and increased with national income (everywhere else). Controlling for these variables, visit rates were highest in North America, lower in Asia/Australasia and Europe, and lowest in Africa and Latin America. To quantify how often people visit PAs as a whole, we used our region-specific GLMs to estimate visit rates to 94,238 sites listed in the World Database on Protected Areas (WDPA) [18]). We again excluded marine, Antarctic, and Category I PAs, as well as almost 40,000 extremely small sites which were below the size (10 ha) of the smallest PA in our sample (S2 Fig.). The limited power of our GLMs and significant errors in the WDPA mean our estimates of visit rates should be treated with caution for individual sites or (when aggregated to national level) for smaller countries. However, the larger-scale patterns they reveal are marked. Estimated median visit rates per PA (averaged within countries) are lowest in Africa (at around 3,000/y) and Latin America (4,000/y), and greatest in North America (350,000/y) (S3 Table). When visit rates are aggregated across all PAs within a country, pronounced regional differences in the numbers of PAs (with relatively few in Africa and Latin America) magnify these patterns and indicate that while many African countries have 1 billion visits/y (albeit many of them cultural rather than nature-based) to China’s National Parks in 2006 [19], and 3.2–3.9 billion visits/y to all British “ecosystems” (most of which are not in PAs) in 2010 [7]. Finally, what can be inferred about the economic significance of visits on this scale? Economists working on tourism distinguish two main, non-overlapping components of value [12]: direct expenditure by visitors (an element of economic impact, calculated from spending on fees, travel, accommodation, etc.); and consumer surplus (a measure of economic value which arises because many visitors would be prepared to pay more for their visit than they actually have to, and which is defined as the difference between what visitors would be prepared to pay for a visit and what they actually spend; consumer surplus is typically quantified using travel cost or contingent valuation methods). We conducted an extensive literature search to derive median (but conservative) figures for each type of value for each region (S4 Table). Applying these to our corresponding estimates of visit rates and summing across regions yields an estimate of global gross direct expenditure associated with PA visits (within-country only, and excluding indirect and induced expenditure) of ~US $600 billion/y worldwide (at 2014 prices). The corresponding figure for global consumer surplus is ~US $250 billion/y. Such numbers are unavoidably imprecise. Uncertainty in our modelled visit rates and the wide variation in published estimates of expenditure and consumer surplus mean that they could be out by a factor of two or more. However, comparison with calculations that visits to North American PAs alone have an economic impact of $350–550 billion/y [4] and that direct expenditure on all travel and tourism worldwide runs at $2,000 billion/y [20] suggests our figures are of the correct order of magnitude, and that the value of PA visitation runs into hundreds of billions of dollars annually. These results quantify, we believe for the first time, the scale of visits to the world’s PAs and their approximate economic significance. We currently spend <$10 billion/y in safeguarding PAs [21]—a figure which is widely regarded as grossly insufficient [21–25]. Even without considering the many other benefits which PAs provide [22], our estimates of the economic impact and value of PA visitation dwarf current expenditure—highlighting the risks of underinvestment in conservation, and suggesting substantially increased investments in protected area maintenance and expansion would yield substantial returns. Supporting Information S1 Fig Visit rates plotted against each predictor variable. Plots show observed visit rates (adjusted for every other predictor variable) against each predictor variable (top to bottom) for each region (left to right). Values for mean visit rate, PA size, local population size, remoteness, and national income are all log10-transformed (after adding one to all values of mean visit rate and local population size and remoteness). Red lines show the relationships summarised in part A of S3 Table. In the Europe plots, blue symbols and lines show the data (and relationships) for the United Kingdom National Parks. (TIF) Click here for additional data file. S2 Fig The representativeness of our sample PAs. Histograms show the values of each of our predictor variables (top to bottom) for all terrestrial PAs in each region (left to right; excluding marine and IUCN Category I PAs), compared with the range represented in our sample of PAs (red vertical lines). For each predictor, the range of observed values is well covered by our sample, except for PA size, where we sampled no PAs <10 ha in area (black vertical lines); we therefore excluded these extremely small PAs from further analysis. Values for PA size, local population size, remoteness, and national income are all log10-transformed (after adding one to all values of mean visit rate, local population size, and remoteness). (TIF) Click here for additional data file. S1 Table Annual visit data for PAs, 1998–2007. (DOCX) Click here for additional data file. S2 Table Univariate regressions between observed visit rates and potential predictor variables for each region. (DOCX) Click here for additional data file. S3 Table Results of GLMs of PA visit rates in each region. (DOCX) Click here for additional data file. S4 Table Empirically-derived estimates of the values of visits to terrestrial PAs or similar natural sites. (DOCX) Click here for additional data file. S1 Text Materials and methods. (DOCX) Click here for additional data file.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Nature Conservation
                NC
                Pensoft Publishers
                1314-3301
                1314-6947
                May 28 2021
                May 28 2021
                : 44
                : 51-68
                Article
                10.3897/natureconservation.44.63270
                cdcd0d72-d09f-4e58-a649-81e8d618db5f
                © 2021

                http://creativecommons.org/licenses/by/4.0/

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