Sustainable Tourism Policy Frameworks

Author(s):  
Alexandra Coghlan

Having looked at the external and internal challenges facing the move towards more sustainable tourism, and the impacts of tourism, you should now be wondering how sustainability in tourism can be turned into more than an ideal. Perhaps one of the most obvious way to achieve this is simply to regulate the sector. After all regulation worked for the ozone layer: scientists raised the alarm in the 1970s that a hole was appearing in the atmosphere’s ozone layer, caused by Ozone Depleting Substances or ODS (most notably CFCs) and resulting in adverse effects on human health and the environment. By 1987 the Montreal Protocol was established to phase out the use of ODS, and by June 2015, all countries in the United Nations, the Cook Islands, Holy See, Niue and the supranational European Union had ratified the original Protocol. The result was a 98% drop in ODS since ratification, and the hole is expected to have fully repaired itself by 2050. A significant achievement in terms of international cooperation, based on scientific advice.

2016 ◽  
Author(s):  
Peter G. Simmonds ◽  
Matthew Rigby ◽  
Archibold McCulloch ◽  
Simon O'Doherty ◽  
Dickon Young ◽  
...  

Abstract. High frequency, in situ global observations of HCFC-22 (CHClF2), HCFC-141b (CH3CCl2F), HCFC-142b (CH3CClF2) and HCFC-124 (CHClFCF3) and their main HFC replacements HFC-134a (CH2FCF3), HFC-125 (CHF2CF3), HFC-143a (CH3CF3), and HFC-32 (CH2F2) have been used to determine their changing global growth rates and emissions in response to the Montreal Protocol and its recent amendments. The 2007 adjustment to the Montreal Protocol required the accelerated phase-out of HCFCs with global production and consumption capped in 2013, to mitigate their environmental impact as both ozone depleting substances and important greenhouse gases. We find that this change has coincided with a reduction in global emissions of the four HCFCs with aggregated global emissions in 2015 of 444 ± 75 Gg/yr, in CO2 equivalent units (CO2 e) 0.75 ± 0.1 Gt/yr, compared with 483 ± 70 Gg/yr (0.82 ± 0.1 Gt/yr CO2 e) in 2010. (All quoted uncertainties in this paper are 1 sigma). About 80 % of the total HCFC atmospheric burden in 2015 is HCFC-22, where global HCFC emissions appear to have been relatively constant in spite of the 2013 cap on global production and consumption. We attribute this to a probable increase in production and consumption of HCFC-22 in Montreal Protocol Article 5 (developing) countries and the continuing release of HCFC-22 from the large banks which dominate HCFC global emissions. Conversely, the four HFCs all show increasing annual growth rates with aggregated global HFCs emissions in 2015 of 329 ± 70 Gg/yr (0.65 ± 0.12 Gt/yr CO2 e) compared to 2010 with 240 ± 50 Gg/yr (0.47 ± 0.08 Gt/yr CO2 e). As HCFCs are replaced by HFCs we investigate the impact of the shift to refrigerant blends which have lower global warming potentials (GWPs). We also note that emissions of HFC-125 and HFC-32 appear to have increased more rapidly during the 2011–2015 5-yr period compared to 2006–2010.


2018 ◽  
Vol 18 (9) ◽  
pp. 6567-6584 ◽  
Author(s):  
Johannes Staehelin ◽  
Pierre Viatte ◽  
Rene Stübi ◽  
Fiona Tummon ◽  
Thomas Peter

Abstract. Climatic Observatory (LKO) in Arosa (Switzerland), marking the beginning of the world's longest series of total (or column) ozone measurements. They were driven by the recognition that atmospheric ozone is important for human health, as well as by scientific curiosity about what was, at the time, an ill characterised atmospheric trace gas. From around the mid-1950s to the beginning of the 1970s studies of high atmosphere circulation patterns that could improve weather forecasting was justification for studying stratospheric ozone. In the mid-1970s, a paradigm shift occurred when it became clear that the damaging effects of anthropogenic ozone-depleting substances (ODSs), such as long-lived chlorofluorocarbons, needed to be documented. This justified continuing the ground-based measurements of stratospheric ozone. Levels of ODSs peaked around the mid-1990s as a result of a global environmental policy to protect the ozone layer, implemented through the 1987 Montreal Protocol and its subsequent amendments and adjustments. Consequently, chemical destruction of stratospheric ozone started to slow around the mid-1990s. To some extent, this raises the question as to whether continued ozone observation is indeed necessary. In the last decade there has been a tendency to reduce the costs associated with making ozone measurements globally including at Arosa. However, the large natural variability in ozone on diurnal, seasonal, and interannual scales complicates the capacity for demonstrating the success of the Montreal Protocol. Chemistry-climate models also predict a super-recovery of the ozone layer at mid-latitudes in the second half of this century, i.e. an increase of ozone concentrations beyond pre-1970 levels, as a consequence of ongoing climate change. These factors, and identifying potentially unexpected stratospheric responses to climate change, support the continued need to document stratospheric ozone changes. This is particularly valuable at the Arosa site, due to the unique length of the observational record. This paper presents the evolution of the ozone layer, the history of international ozone research, and discusses the justification for the measurements in the past, present and into future.


1998 ◽  
Vol 5 (3) ◽  
pp. 176-179 ◽  
Author(s):  
Louis-Philippe Boulet

The stratospheric ozone layer plays a crucial role in protecting living organisms against ultraviolet radiation. Chlorofluorocarbons (CFC) contained in metered-dose inhalers (MDIs) contribute to ozone depletion and in accordance with theMontreal Protocol on Substances That Deplete the Ozone Layerestablished 10 years ago, phase-out strageies have been developed worldwide for this category of agents. Alternatives to CFC-containing inhalers have been developed, such as powder inhalers and those using hydrofluoroalkanes (HFAs) as propellants, which have been shown to be as safe and effective as CFC-containing inhalers and even offer interesting advantages over older inhalers. The transition to non-CFC MDIs requires a major effort to make the new products available and to ensure adequate comparision with the previous ones. It also requires a harmonization of actions taken by industry, government, licencing bodies and patients or health professional associations to ensure adequate information and education to the public and respiratory care providers.


2017 ◽  
Vol 17 (7) ◽  
pp. 4641-4655 ◽  
Author(s):  
Peter G. Simmonds ◽  
Matthew Rigby ◽  
Archie McCulloch ◽  
Simon O'Doherty ◽  
Dickon Young ◽  
...  

Abstract. High-frequency, in situ global observations of HCFC-22 (CHClF2), HCFC-141b (CH3CCl2F), HCFC-142b (CH3CClF2) and HCFC-124 (CHClFCF3) and their main HFC replacements, HFC-134a (CH2FCF3), HFC-125 (CHF2CF3), HFC-143a (CH3CF3) and HFC-32 (CH2F2), have been used to determine their changing global growth rates and emissions in response to the Montreal Protocol and its recent amendments. Global mean mole fractions of HCFC-22, -141b, and -142b have increased throughout the observation period, reaching 234, 24.3 and 22.4 pmol mol−1, respectively, in 2015. HCFC-124 reached a maximum global mean mole fraction of 1.48 pmol mol−1 in 2007 and has since declined by 23 % to 1.14 pmol mol−1 in 2015. The HFCs all show increasing global mean mole fractions. In 2015 the global mean mole fractions (pmol mol−1) were 83.3 (HFC-134a), 18.4 (HFC-125), 17.7 (HFC-143a) and 10.5 (HFC-32). The 2007 adjustment to the Montreal Protocol required the accelerated phase-out of emissive uses of HCFCs with global production and consumption capped in 2013 to mitigate their environmental impact as both ozone-depleting substances and important greenhouse gases. We find that this change has coincided with a stabilisation, or moderate reduction, in global emissions of the four HCFCs with aggregated global emissions in 2015 of 449 ± 75 Gg yr−1, in CO2 equivalent units (CO2 eq.) 0.76 ± 0.1 Gt yr−1, compared with 483 ± 70 Gg yr−1 (0.82 ± 0.1 Gt yr−1 CO2 eq.) in 2010 (uncertainties are 1σ throughout this paper). About 79 % of the total HCFC atmospheric burden in 2015 is HCFC-22, where global emissions appear to have been relatively similar since 2011, in spite of the 2013 cap on emissive uses. We attribute this to a probable increase in production and consumption of HCFC-22 in Montreal Protocol Article 5 (developing) countries and the continuing release of HCFC-22 from the large banks which dominate HCFC global emissions. Conversely, the four HFCs all show increasing mole fraction growth rates with aggregated global HFC emissions of 327 ± 70 Gg yr−1 (0.65 ± 0.12 Gt yr−1 CO2 eq.) in 2015 compared to 240 ± 50 Gg yr−1 (0.47 ± 0.08 Gt yr−1 CO2 eq.) in 2010. We also note that emissions of HFC-125 and HFC-32 appear to have increased more rapidly averaged over the 5-year period 2011–2015, compared to 2006–2010. As noted by Lunt et al. (2015) this may reflect a change to refrigerant blends, such as R-410A, which contain HFC-32 and -125 as a 50 : 50 blend.


2019 ◽  
pp. 304-322
Author(s):  
Frederike Albrecht ◽  
Charles F. Parker

The Montreal Protocol—the regime designed to protect the stratospheric ozone layer—has widely been hailed as the gold standard of global environmental governance and is one of few examples of international institutional cooperative arrangements successfully solving complex transnational problems. Although the stratospheric ozone layer still bears the impacts of ozone depleting substances (ODSs), the problem of ozone depletion is well on its way to being solved due to the protocol. This chapter examines how the protocol was designed and implemented in a way that has allowed it to successfully overcome a number of thorny challenges that most international environmental regimes must face: how to attract sufficient participation, how to promote compliance and manage non-compliance, how to strengthen commitments over time, how to neutralize or co-opt potential ‘veto players’, how to make the costs of implementation affordable, how to leverage public opinion in support of the regime’s goals, and, ultimately, how to promote the behavioural and policy changes needed to solve the problems and achieve the goals the regime was designed to solve. The chapter concludes that while some of the reasons for the Montreal Protocol’s success, such as fairly affordable, available substitutes for ODSs, are not easy to replicate, there are many other elements of this story that can be utilized when thinking about how to design solutions to other transnational environmental problems.


2018 ◽  
Vol 18 (2) ◽  
pp. 1379-1394 ◽  
Author(s):  
William T. Ball ◽  
Justin Alsing ◽  
Daniel J. Mortlock ◽  
Johannes Staehelin ◽  
Joanna D. Haigh ◽  
...  

Abstract. Ozone forms in the Earth's atmosphere from the photodissociation of molecular oxygen, primarily in the tropical stratosphere. It is then transported to the extratropics by the Brewer–Dobson circulation (BDC), forming a protective ozone layer around the globe. Human emissions of halogen-containing ozone-depleting substances (hODSs) led to a decline in stratospheric ozone until they were banned by the Montreal Protocol, and since 1998 ozone in the upper stratosphere is rising again, likely the recovery from halogen-induced losses. Total column measurements of ozone between the Earth's surface and the top of the atmosphere indicate that the ozone layer has stopped declining across the globe, but no clear increase has been observed at latitudes between 60° S and 60° N outside the polar regions (60–90°). Here we report evidence from multiple satellite measurements that ozone in the lower stratosphere between 60° S and 60° N has indeed continued to decline since 1998. We find that, even though upper stratospheric ozone is recovering, the continuing downward trend in the lower stratosphere prevails, resulting in a downward trend in stratospheric column ozone between 60° S and 60° N. We find that total column ozone between 60° S and 60° N appears not to have decreased only because of increases in tropospheric column ozone that compensate for the stratospheric decreases. The reasons for the continued reduction of lower stratospheric ozone are not clear; models do not reproduce these trends, and thus the causes now urgently need to be established.


2010 ◽  
Vol 10 (8) ◽  
pp. 19005-19029 ◽  
Author(s):  
J. A. Mäder ◽  
J. Staehelin ◽  
T. Peter ◽  
D. Brunner ◽  
H. E. Rieder ◽  
...  

Abstract. The release of man-made ozone depleting substances (ODS, including chlorofluorocarbons and halons) into the atmosphere has lead to a near-linear increase in stratospheric halogen loading since the early 1970s, which started to level off after the mid-1990s and then to decline, in response to the ban of many ODSs by the Montreal Protocol (1987). We developed a multiple linear regression model to test whether this has already a measurable effect on total ozone values observed by the global network of ground-based instruments. The model includes explanatory variables describing the influence of various modes of dynamical variability and of volcanic eruptions. In order to describe the anthropogenic influence a first version of the model contains a linear trend (LT) term, whereas a second version contains a term describing the evolution of equivalent effective stratospheric chlorine (EESC). By comparing the explained variance of these two models we evaluated which of the two terms better describes the observed ozone evolution. For a significant majority of the stations, the EESC proxy fits the long term ozone evolution better than the linear trend term. Therefore, we conclude that the Montreal Protocol has started to show measurable effects on the ozone layer about twenty years after it became legally binding.


2010 ◽  
Vol 10 (24) ◽  
pp. 12161-12171 ◽  
Author(s):  
J. A. Mäder ◽  
J. Staehelin ◽  
T. Peter ◽  
D. Brunner ◽  
H. E. Rieder ◽  
...  

Abstract. The release of man-made ozone depleting substances (ODS, including chlorofluorocarbons and halons) into the atmosphere has led to a near-linear increase in stratospheric halogen loading since the early 1970s, which levelled off after the mid-1990s and then started to decline, in response to the ban of many ODS by the Montreal Protocol (1987). We developed a multiple linear regression model to test whether this already had a measurable effect on total ozone values observed by the global network of ground-based instruments. The model includes explanatory variables describing the influence of various modes of dynamical variability and of volcanic eruptions. In order to describe the anthropogenic influence a first version of the model contains a linear trend (LT) term, whereas a second version contains a term describing the evolution of Equivalent Effective Stratospheric Chlorine (EESC). By comparing the explained variance of these two model versions we evaluated, which of the two terms better describes the observed ozone evolution. For a significant majority of the stations, the EESC proxy fits the long term ozone evolution better than the linear trend term. Therefore, we conclude that the Montreal Protocol has started to show measurable effects on the ozone layer about twenty years after it became legally binding.


2018 ◽  
Author(s):  
Dimitrios K. Papanastasiou ◽  
Allison Beltrone ◽  
Paul Marshall ◽  
James B. Burkholder

Abstract. Hydrochlorofluorocarbons (HCFCs) are ozone depleting substances and potent greenhouse gases that are controlled under the Montreal Protocol. However, the majority of the 274 HCFCs included in Annex C of the protocol do not have reported global warming potentials (GWPs) that are used to guide the phase-out of HCFCs and the future phase-down of hydrofluorocarbons (HFCs). In this study, GWPs for all C1-C3 HCFCs included in Annex C are reported based on estimated atmospheric lifetimes and theoretical methods used to calculate infrared absorption spectra. Atmospheric lifetimes were estimated from a structure activity relationship (SAR) for OH radical reactivity and estimated O(1D) reactivity and UV photolysis loss processes. The HCFCs display a wide range of lifetimes and GWPs dependent on their molecular structure and H-atom content of the individual HCFC. The results from this study provide reliable policy relevant GWP metrics for the HCFCs included in the Montreal Protocol in the absence of experimentally derived metrics.


2019 ◽  
Author(s):  
William T. Ball ◽  
Gabriel Chiodo ◽  
Marta Abalos ◽  
Justin Alsing

Abstract. The stratospheric ozone layer shields surface life from harmful ultraviolet radiation. Following the Montreal Protocol ban of long-lived ozone depleting substances (ODSs), rapid depletion of total column ozone (TCO) ceased in the late 1990s and ozone above 32 km now enjoys a clear recovery. However, there is still no confirmation of TCO recovery, and evidence has emerged that ongoing quasi-global (60° S–60° N) lower stratospheric ozone decreases may be responsible, dominated by low latitudes (30° S–30° N). Chemistry climate models (CCMs) used to project future changes predict that lower stratospheric ozone will decrease in the tropics by 2100, but not at mid-latitudes (30°–60°). Here, we show that CCMs display an ozone decline similar to that observed in the tropics over 1998–2016, likely driven by a increase of tropical upwelling. On the other hand, mid-latitude lower stratospheric ozone is observed to decrease, while CCMs show an increase. Despite opposing lower stratospheric ozone changes, which should induce opposite temperature trends, CCM and observed temperature trends agree; we demonstrate that opposing model-observation stratospheric water vapour (SWV) trends, and their associated radiative effects, explain why temperature changes agree in spite of opposing ozone trends. We provide new evidence that the observed mid-latitude trends can be explained by enhanced mixing between the tropics and extratropics. We further show that the temperature trends are consistent with the observed mid-latitude ozone decrease. Together, our results suggest that large scale circulation changes expected in the future from increased greenhouse gases (GHGs) may now already be underway, but that most CCMs are not simulating well mid-latitude ozone layer changes. The reason CCMs do not exhibit the observed changes urgently needs to be understood to improve confidence in future projections of the ozone layer.


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