Forest Policy and Economics 103 (2019) 17-27
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Forest Policy and Economics
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A simulation-based approach to assess forest policy options under biotic and r®
abiotic climate change impacts: A case study on Scotland's National Forest
Estate^
Duncan Ray 3 ’*, Michal Petr 3 , Martin Mullett , Stephen Bathgate 3 , Maurizio Marchi c ,
Kate Beauchamp 3
a Forest Research, Roslin, Midlothian, Scotland, United Kingdom
b Forest Research, Alice Holt Lodge, Surrey, England, United Kingdom
c Council for Agricultural Research, Forest Research Centre, Arezzo, Italy
ARTICLE INFO
ABSTRACT
Keywords:
Forest policy analysis
Uncertainty
Climate change
Abiotic impacts
Biotic impacts
Ecosystem goods and services
Forest management simulation
The future provision of forest goods and ecosystem services is dependent, among other factors, on climate
change impacts, forest management, and response to forest policies. To assess policy implementation targets for
Scotland's National Forest Estate under climate change, we simulated forest growth through the 21st century -
with and without the abiotic impacts of climate change, and with and without the biotic impacts of an important
fungal disease. Eight different forest management trajectories were simulated under a climate projection, to
assess the future provision of forest ecosystem goods and services. Climate change was represented by the IPCC
RCP 4.5 projection, and the biotic impact of Dothistroma needle blight was predicted using a new vulnerability
matrix. Indicators of three important goods and services: timber production, standing biomass, and biodiversity
were measured in the simulation of forest growth and reported at decadal intervals using dynamically linked
forest models. We found that both a broadleaved species trajectory and a Forest Enterprise Scotland selected
species trajectory would improve standing biomass and biodiversity, but slightly reduce timber volume.
Dothistroma needle blight could reduce standing biomass (by up to 3tha _1 ) and timber volume (by up to
5 m 3 ha -1 ), but the predicted impact is dependent on the type of forest management trajectory. Our findings
show opportunities for diversifying forest management and tree species - and at the same time supporting forest
policy to improve forest resilience under uncertain climate change and Dothistroma impacts. The forest simu¬
lation has been used to demonstrate and evaluate national strategic delivery of multi-purpose forest benefits in
Scotland, and how species and management might be targeted regionally in Forest Districts, to maintain
achievable national targets for timber production, carbon sequestration, and biodiversity under climate change.
1. Introduction
The sustainable multi-purpose management of forests in Europe
involves the assessment of complex inter-related land management is¬
sues covering various aspects of environmental and biodiversity policy,
as summarised in the EU Forestry Strategy (European Commission,
2013). Forests provide multiple benefits to the public. These benefits
relate to the concept of ecosystem goods and services (Millennium
Ecosystem Assessment, 2005) that quantify the goods or benefits people
derive from functioning ecosystems. Forests have attracted much re¬
search and policy interest on the subject of ecosystem goods and
services (e.g. Schroter et al., 2005; Bateman et al., 2013; Quine et al.,
2011). Both managed and unmanaged forests provide a broad range of
goods and services (Quine et al., 2011) compared to more intensive
land management (e.g. intensive agriculture).
Both the UK Government (UK National Ecosystem Assessment, 2011
& 2014) and Scottish Government (Forestry Commission Scotland, 2006)
have stated the need for a more sustainable ecosystems approach to land
management. This requires policy implementation to guide land use and
land management decisions with the aim of providing multiple eco¬
system goods and services now and into the future. Forest management
in Scotland has for several decades considered multi-purpose benefits
^ This article is part of a special issue entitled. “Models and tools for integrated forest management and forest policy analysis”
103C, 2019.
* Corresponding author.
E-mail address: duncan.ray@forestry.gsi.gov.uk (D. Ray).
published at the journal Forest Policy and Economics
http://dx.doi.Org/10.1016/j.forpol.2017.10.010
Received 31 October 2016; Received in revised form 4 October 2017; Accepted 9 October 2017
Available online 06 November 2017
1389-9341/ Crown Copyright © 2017 Published by Elsevier B.V. All rights reserved.
D. Ray, et al
(UK Forestry Standard, 2011) and this has led to a more targeted ap¬
proach in the delivery of goods and services at different geographic scales
(Forestry Commission Scotland, 2013b) through a ‘strategic delivery’
approach of ecosystem services. Testing strategic delivery requires an
assessment of the current and future state of woodlands to understand
how management choices (reflecting direction and ownership objectives)
in different areas will influence forest goods and ecosystem service
provision (Ray et al., 2015). Scotland's publicly owned National Forest
Estate (NFE) is therefore a good case study for assessing the implications
of policy implementation under climate change.
Forestry Commission Scotland's Climate Change Programme
(2013a) outlines how the forest sector can become more resilient to the
impacts of climate change. Approaches to adaptation in the UK and
Scotland include: changes to species choice, increasing the area of na¬
tive woodland, selecting more southerly provenances, conversion to
continuous cover forestry and increasing forest tree species diversity
(Hemery et al., 2015). Changes in forest management will also impact
ecosystem goods and service delivery, including timber production, the
ability to support biodiversity, and carbon sequestration (Ray et al.,
2015; Beauchamp et al., 2016). As identified in Scotland's Adaptation
Programme (Scottish Government, 2014) and in the ‘Low Carbon
Scotland - Second Report on Proposals and Policies’ (Scottish
Government, 2013), adaptation and mitigation strategies must be
considered together. This will ensure that current mitigation efforts are
well adapted to future climates, and that adaptation actions support
mitigation measures; Scotland's forests must be resilient in order to
deliver emissions abatement targets.
Scotland's forest industry has emerged rapidly over the course of a
century (1900-to date), with a change in forest land cover from ap¬
proximately 5% to 17% over the period. Its rapid emergence occurred
in response to phases of forest policy (Harmer et al., 2015). Scotland's
forest industry has been built on a few robust conifer species, e.g. Sitka
spruce ( Picea sitchensis ), Scots pine (Pinus sylvestris ), larch ( Larix decidua
and Larix kaempferi ), and Norway spruce ( Picea abies ) (Quine and Ray,
2010). These were trialled on different sites and monitored with per¬
manent sample plots, where they showed good growth on a range of
often challenging site types.
An emerging issue of increasing concern to forests (Boyd et al., 2013),
and forest managers (Petr et al., 2014), is the increased risk and impact of
pests and pathogens. This is partly due to an increase in global trade
(Pautasso et al., 2012; Roy et al., 2014) and partly climate change (Jung,
2009; Tubby and Webber, 2010) which together have increased the spread
and the risk of colonisation of pests and pathogens. The dynamics of many
host-pathogen interactions are influenced by climate, thus climate change
has the potential to exacerbate or alleviate both the chances of establish¬
ment of new pathogens and the emergence of pre-existing ones (Sturrock
et al., 2011; Pautasso et al., 2012). Foliar fungal pathogens are particularly
sensitive to temperature and water availability for sporulation, spread and
infection and are likely to be effective indicators of environmental change
(Harvell et al, 2002; Garrett et al., 2016). Dothistroma needle blight
(DNB) affects at least 109 Pinaceae taxa, primarily Pinus spp., and is
considered one of the most damaging diseases of pines worldwide, causing
premature defoliation, a reduction in yield, and in extreme cases tree
death (Drenkhan et al., 2016). In Britain, DNB is caused by Dothistroma
septosporum and has been particularly serious on Corsican pine ( Pirtus nigra
ssp. laricio), but also on lodgepole pine ( Pinus contorta var. latifolia) and
Scots pine (Brown and Webber, 2008). It is thought that increasing pre¬
cipitation in the spring and summer months along with warmer tem¬
peratures leads to a greater risk of infection (Woods et al., 2016).
Until recently, Scots pine, lodgepole pine and Corsican pine were
being selected as suitable species for forest stands in the projected fu¬
ture Scottish climate (Ray, 2008). It is therefore of interest to forest
policy and forest practice (Lindner et al., 2010) to consider pest and
pathogen impacts in the context of changing climatic conditions and the
maintenance of resilient forests into the future. This study is concerned
with the potential impacts of climate change impacts, including DNB,
Forest Policy and Economics 103 (2019) 17-27
on the delivery of forest policies and forest management.
The objective of this study is to demonstrate whether public sector
forestry in Scotland can make a contribution to greenhouse gas abate¬
ment and timber production while maintaining high biodiversity and
other important benefits. The options are simulated by forest models
under the uncertainty of climate change and a forest pathogen. Possible
adjustments to forest management systems and to tree species choice
are tested to ascertain the continued provision of these forest ecosystem
goods and services.
2. Materials and methods
2.1. Study sites
In this study we focus on a forest growth and management simulation
of the National Forest Estate (NFE) in Scotland and four forest districts in
the north (North Highland District), south (Dumfries & Borders District),
east (Moray & Aberdeen District) and west (Lochaber District) - (see Fig.
S2 in online Supplementary material 1). These districts present different
site conditions leading to variations in species composition, and different
future climate change projections. Forestry Commission Scotland's stated
policy of strategic delivery of benefits, plays on the strengths of different
districts. For example, Lochaber and Dumfries & Borders are heavily
focused on timber production, whilst Lochaber and Moray and Aberdeen
have important recreation, biodiversity and community management
interests. The current species composition of Scotland's forests (public
and private sector combined), the NFE, and the four Districts are shown
in Table 1 and Fig. SI (online Supplementary material 1). The NFE re¬
present the public forest managed by the Forestry Commission covering
471,000 ha, approximately 33% of the forested area (Forestry
Commission, 2016), and it is comprised of a broad species selection with
a variety of management systems. The conifer species composition of the
NFE and private sector are similar, but the NFE has a smaller area of
broadleaf forest than the private sector.
2.2. Input data
2.2.1. Spatial Forest inventory and soil data
The dynamically coupled models require spatially explicit forest
inventory data showing the tree species, the age of the stand, and the
current forest management system. This was possible using the Forestry
Commission Sub-Compartment Database (SCDB) of the NFE. We used a
digital soil map, based on a composite of the Soil Survey of Scotland soil
associations mapped at a scale of 1:250,000 (Soil Survey of Scotland,
1981), combined with higher resolution soil type data for areas of
public forest where a digital soil layer mapped at a scale of 1:10,000
was available. These soil data provided information about the soil
quality in terms of soil moisture regime (SMR - soil wetness) and soil
nutrient regime (SNR - soil fertility), where SMR and SNR are two of
the six site quality factors used in the forest classification model, Eco¬
logical Site Classification (Pyatt et al., 2001).
2.2.2. Spatial climate data
To represent the future climate change impact on Scottish forests,
we used the Representative Concentration Pathways (RCP 4.5) climate
change projections of the IPCC Fifth Assessment Report (IPCC, 2014).
The RCP 4.5 was matched to one single variant of the UK 11-member
RCM Regional Climate Model (3Q14) using a Pearson correlation
method (details in online Supplementary material 1). The projected
3Q14 variant provided daily simulated values of temperature, pre¬
cipitation and potential evapotranspiration through the 21st Century.
These were used to calculate monthly values for two of the the four
climatic variables used in the forest model Ecological Site Classifica¬
tion, these were: Accumulated Temperature (AT - day degrees above
5 °C) and Climatic Moisture Deficit (MD - accumulated excess of po¬
tential evapotranspiration over precipitation in mm units).
18
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
Table 1
Current species composition of the four Forest Districts using data from the Forestry Commission Sub-Compartment
Database; Scotland's National Forest Estate (NFE) “Public Sector”, and Scotland's combined public and private forest
“Scotland”(Forestry Commission, 2016). Values in the table are in hectares.
Scotland's National & Regional Forest Composition
U/o
North Highland
Lochaber
Moray &
Aberdeen
Dumfries &
Borders
Public Sector
Scotland
QOther Broadleaves
1083.61
927.18
1309.18
1770.42
15000
73000
R Alder species
37.98
91.69
58.74
21.16
1000
17000
□ Ash
1.54
46.32
25.54
29.17
1000
16000
□ Sycamore
116.28
0.83
33.56
53.58
1000
22000
□ Beech
8.9
14.82
132.77
54.3
1000
15000
ESOak species
33.03
152.44
104.23
156.53
3000
26000
□ Birch species
637
1659
874.7
296.82
11000
128000
H Other Conifers
314.68
157.16
1381.59
298.65
5000
14000
□ Douglas Fir
286.33
167.15
1044.87
613.11
5000
12000
□ Norway Spruce
235.49
684.24
1742.22
1608.54
11000
25000
El Larches
2043.55
1249.88
4431.02
2823.5/
26000
66000
□ Lodgepole Pine
16199.61
3544.64
3783.8
960.75
49000
88000
H Scots Pine
6884.81
1080.73
11621.08
926.06
45000
154000
□ Sitka Spruce
9756.73
12187.81
17345.07
28688.19
225000
507000
Climate data
3Q14 variant (11-RCM)
representing RCP 4.5
Forest soil map
Digital at low to
moderate resolution
Forest inventory
Digital spatially explicit
data on species and age
Forest Management Trajectories
Business as Usual - replace
species and management like for
like
Diversification for Production -
stand replaced with the most
productive species
CCF- transformation from one to
two ages classes in a stand
Short rotation forestry - same
species, rotations at 25 years
Native species - sites are
replaced with native species at
restocking
Broadleaves only - restock with
broadleaved species only
No Sitka spruce - replace SS from
a list of five well suited
alternatives
FES priority species - at
restocking select one of the most
suitable five species from a list of
25 trialed in Scotland
Forest site conditions
Climatic - accumulated temperature, moisture deficit, DAMS
(exposure), continentality
Edaphic - soil moisture regime, soil nutrient regime
Output results for three
indicators of ecosystem goods
and services at decadal
intervals
1. Total biomass
2. Sawlog volume
3. Biodiversity
Annual management cycle
Fig. 1. Schematic diagram of the simulation method of forest management trajectory scenarios on the National Forest Estate of Scotland.
19
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
Table 2
Description of forest management trajectories with assumptions and constraints according rules dictated by site characteristics.
Forest management trajectory (FMT) FMT description, assumptions and constraints
Note: in all FMT types - Norway spruce (Picea abies) and Scots pine ( Pinus sylvestris ) are retained to provide red squirrel habitat.
Business as usual (BAU) No change in species, stands are replanted with the current species.
Thinning in sub-compartments where DAMS < 16. For no thin sub-compartments replace existing species at year 50. For thinning
sub-compartments start at year 20 and then every 5 years to year 50, then fell and replace.
Broadleaves only (BL2) Allows replanting selecting the most suitable broadleaf species.
Continuous cover forestry (CCF) No change in species composition, stands regenerated with the current species. If site conditions suitable, a heavy thinning
intervention is simulated at 25 years.
Sub-compartments DAMS < 14 - marked FMA2 for conversion at year 50 - grow to year 50 thin to half the basal area. DAMS > 14
and < 16 - thin as FMA 4 in BAU. Sub-compartments > 50 years classified as FMA 3 and grown to 100 years before felling.
Diverse species (DIV) Selection of species using high predicted yield class for the site conditions from a selection of available 57 species in ESC. Continue
same FMA allocation as in BAU, only species allowed to change after felling. Most suitable species for the sub-compartment site
conditions for the rotation is chosen. No particular preference made for broadleaved trees or native trees.
Sub-compartments > 50 years old allocated FMA 3 and felled at year 100.
Forest Enterprise Scotland priority species Selection by highest yield class from a management list of 19 priority species suitable for timber production in Scotland. Continue
(FESP) with the same FMA allocation as in BAU, only species allowed to change at time of felling. Broadleaves replace felled broadleaved
stands, and larch and ash are excluded from replanting due to tree health limitations.
Native species (NAT) Native species selected according to the suitability of the site for an NVC woodland type. Continue with the same FMA allocation as
in BAU, only species allowed to change at time of felling. Norway spruce is replaced by Scots pine.
No Sitka spruce (NOSS) Replacement species is selected at replanting, and available species are restricted to priority species with the addition of lodgepole
pine (Alaskan) (Pinus contorta var. latifolia ) and rowan (Sorbus aucuparia) and grand fir ( Abies grandis ) on moist lowland sites to
ensure sufficient species diversity. Continue with the same FMA allocation as in BAU, only species allowed to change at time of
felling
Short rotation forestry (SRF) No change in species composition, stands are replanted with the current species. SNR > very poor, SMR > Wet, and DAMS <16,
otherwise the site is classed as unthinned FMA4. Sub-compartment stands are felled and replaced at age 25 years.
DAMS - wind exposure, SNR - soil nutrient regime, SMR - soil moisture regime, FMA - Forest Management Alternative stand type.
2.3. Forest simulation using dynamically coupled models
2.3.1. Forest management trajectories under climate change projections
We ran the coupled forest models to simulate tree growth, carbon
sequestration, biomass, timber production and biodiversity on the NFE.
The method builds on previous work described by Ray et al. (2015). A
schematic diagram (Fig. 1) summarizes the simulation method. Three
spatial datasets were used to simulate forest management through the
21st century: climate projections at decadal intervals (2020s, 2030s,
2040s etc); forest soils set as constants for the simulation; forest in¬
ventory data - initialised using the 2016 SCDB. The SCDB inventory
was updated within each annual cycle of the model simulation to reflect
changes in the forest structure and its management under eight dif¬
ferent management trajectories. The forest management trajectories are
comprised of management systems and decision rules designed to im¬
plement different forest policy directions. They were created by ap¬
plying specific forest management systems to forest SCDB data in the
simulation. For example: ‘Broadleaves only’ (Table 2) attempts to
change species choice to broadleaved species when the opportunity
arises at restocking; ‘No Sitka spruce’ attempts to remove and replace
Sitka spruce stands with a mix of suitable alternative high yielding
conifer and/or broadleaved species at the time of restocking. The tra¬
jectories simulated (Table 2) were: business as usual, species diversifi¬
cation for production, continuous cover forestry using a shelterwood
system of two age components, short rotation forestry, native species
selection, broadleaved species selection, species diversification without
Sitka spruce, and finally species selection using Forest Enterprise Sco¬
tland's selected species for diversification.
2.3.2. Forest management alternative simplification of the Forest inventory
data
The eight forest management trajectory types specify rules to si¬
mulate the different forms of forest management applied to the SCDB.
To facilitate the diverse range of silviculture and species described by
the SCDB, we simplified the forest inventory silvicultural descriptions
into Forest Management Alternatives (FMA). Forest Management
Alternatives, described by Duncker et al. (2012), provide a means of
classifying differences in management intensity. They described five
FMA types ranging from FMA type 1 Forest Reserve with no
management, to FMA type 5 intensive single species short rotation
forestry. Production forestry in Scotland is largely described by FMA
types 3 and 4: “combined objective forestry” and “intensive even-aged
forestry”, respectively. “Close to nature forestry”, FMA type 2, is in¬
creasing in Scotland in the form of continuous cover forest manage¬
ment, but has limited potential due Scotland's high wind exposure cli¬
mate. The FMA classification seeks to describe forest management
intensity using criteria such as type of regeneration, level of machine
operation, ground preparation, and size of harvesting coupes. As the
forest model simulation progressed on an annual cycle, rules were ap¬
plied at the appropriate time in the rotation (Table 2) to the FMA types
of the SCDB to maintain the selected forest management trajectory, and
the forest inventory SCDB was updated. Any changes required by the
forest management trajectory (thinning, felling, etc) were controlled by
the rules applied to the SCDB to describe the particular forest man¬
agement trajectory running in the dynamically coupled models.
2.3.3. DNB vulnerability matrix indicator evidence and approach
Our addition of a DNB vulnerability model was based on a body of
literature that associates outbreaks of DNB with spring and summer
rainfall, particularly above average amounts (Watt et al., 2011; Welsh
et al, 2014). Exact values vary but Woods et al. (2016) surmise that
rainfall in excess of 100 mm per month in the warmer months leads to
outbreaks of DNB, which are far less likely to occur when rainfall
is < 50 mm per month. In Britain, high levels of infection were ob¬
served (Murray and Batko, 1962) when total rainfall exceeded 315 mm
from June to September, while no outbreaks were seen when total
rainfall during this period was below 175 mm. Needle wetness is more
important than total seasonal or monthly precipitation in the germi¬
nation and infection of spores. Therefore, extended periods of needle
wetness (e.g. due to frequent low-volume showers or mist) were as¬
sumed to lead to greater levels of disease than heavy downpours fol¬
lowed by long dry spells. The fungus is able to tolerate a wide range of
temperatures, however, 16-20 °C is optimal for both infection and
stomatal development (Gadgil, 1974, 1977). Overall, spring and
summer rainfall along with temperature provide good indicators to
estimate DNB severity.
The vulnerability of a forest to DNB impact depends not only on the
environmental conditions but also the host (e.g. more or less susceptible
20
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
Table 3
Classified values of tree vulnerability to Dothistroma needle blight (DNB) based on a) climatic characteristics of a stand, b) tree species/
provenance type, c) stand Forest Management Alternative (FMA), and d) the total vulnerability class and effect on stand yield, based on the
sum of indices from a, b, & c.
a) Climatic characteristic with DNB vulnerability levels (1 - low, 2 - medium, and 3 - high)
AT Subalpine Cool Warm Very warm
MD
Wet 1
Moist 1
Dry 1
Very dry 1
2
2
2
1
3
3
3
2
3
3
2
1
b) Tree species DNB vulnerability
HIGH MEDIUM LOW
vulnerability vulnerability vulnerability
Species Corsican pine, lodgepole pine Alaskan lodgepole pine, Scots pine Sitka spruce, Douglas-fir
Shift 0 -1 -2
c) FMA DNB vulnerability
FMA1
FMA2
FMA3
FMA4
FMA5
No thin
0
0
+ 1
+ 1
0
Thin
N/A
-1
-1
-1
N/A
d) Total vulnerability index of forest stands to DNB - impact on YC reduction
Final Vulnerability Index DNB Vulnerability Class
0 or < 0
1
2
3 +
VERY LOW
LOW
MODERATE
HIGH
Yield Impact
None
Reduce YC by 10%
Reduce YC by 30%
Reduce YC by 50%
N/A = thinning not performed in FMA 1 (Semi-natural reserve) and FMA5 (Short rotation forestry).
species) and pathogen (e.g. levels of inoculum in the area, virulence of
strains) with the complex interaction between host, pathogen and en¬
vironment. The effect of DNB infection of primary concern to foresters
is a reduction in growth, with radial increment more severely affected
than height, although in extreme cases mortality may follow. Studies
generally agree that at least 25% of foliage must be affected before
losses in growth are measurable (Christensen and Gibson, 1964;
Hocking and Etheridge, 1967; Whyte, 1969). A study on P. radiata in
New Zealand showed that there was a proportional relationship be¬
tween disease level (percentage of foliage infected) and volume loss, so
that, for example, an average disease level of 50% resulted in a volume
loss of 50% after three years (Van der Pas, 1981). Once severely high
levels of infection occur (i.e. 75% of foliage becomes affected) diameter
increment practically ceases (Christensen and Gibson, 1964).
To calculate the DNB impact on forest stands, we used the current
knowledge to modify the yield class (YC) of pine species according to a
classification method based on climatic characteristics (Table 3a),
conifer and pine species vulnerability (Table 3b), and the forest man¬
agement alternative (Duncker et al., 2012) system used (Table 3c). Each
table contains vulnerability values related to the potential DNB impact.
We summed the values in the first three tables to obtain an overall
vulnerability index, listed in the lookup table (Table 3d), which gives
the yield adjustment applicable to the forest stand.
The DNB vulnerability model used the following assumptions: DNB
affects only pines, DNB infection is present in all pine stands (even
though that might not be the case), a change in species choice can be
applied only as a change in forest management system - not as a re¬
sponse to infection, infected stands are retained until the end of the
rotation, and timber quality is unaffected.
2.3.4. Dynamically coupled models and ecosystem goods and services
indicators
The dynamically coupled forest models used in the simulation were:
Ecological Site Classification (Pyatt et al., 2001), ForestGALES
(Gardiner and Quine, 2000), Forest Yield (Matthews, 2008), ASORT
(Rollinson and Gay, 1983) and BSORT (McKay, 2003; Broadmeadow
and Matthews, 2004), and our new DNB vulnerability matrix model
(Section 2.3.3).
1. Ecological Site Classification (ESC) is a forest site classification
model using six site factors: - four climatic factors - accumulated
temperature (AT -degree.days > 5 °C) which describes the growing
season warmth; climatic moisture deficit (MD -mm) describing the
relative wetness or droughtiness of the growing season; wind ex¬
posure (DAMS score); continentality (Conrad index): - and two soil
quality factors - Soil Moisture Regime (SMR) or soil wetness; and
Soil Nutrient Regime (SNR), or soil fertility. ESC predicts the site
potential for a given species in the form of a general yield class.
2. ForestGALES is a wind risk model that calculates the risk of wind
damage, either windthrow, or stem breakage, to forests stands.
3. Forest Yield provides estimates of various aspects of tree growth
(height, diameter at 1.3 m) by stand age, for a range of tree species,
yield classes and management prescriptions.
4. ASORT is an assortment model to provide estimates of potential
timber production volumes.
5. BSORT estimates the tree size class distribution and through allo-
metric equations the biomass per hectare by size components.
The models use the SCDB forest inventory and a set of rules
(Table 2) based on forest management principles to form the eight
forest management trajectories, applied to individual forest stand FMA
types, and described spatially within a Geographic Information System,
with and without both the climate change projections, and the effects of
the DNB vulnerability matrix.
For each of the forest management trajectories, we calculated three
ecosystem goods and services indicators (online Supplementary
21
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
decade
Fig. 2. Change in the provision of standing biomass on the (NFE) under climate change a)
comparing forest management trajectories without DNB impact to business as usual
(BAU) (standing biomass in the 2010 for BAU around 48.6 Mt), and b) changes due to
DNB impact.
material 2): 1) standing biomass (t ha - 1 ), 2) harvested timber volume
(m 3 ha -1 ), and a forest biodiversity index (index ha -1 ). Standing
biomass is a good that stores carbon (regulating service) and when
harvested, can be used as timber in construction (provisioning service),
is used for pulp in making paper (provisioning service), or as biomass
for renewable energy (provisioning service). When used in the latter
way it also substitutes fossil fuel use (regulating service).
Biomass and timber volume were based on a predicted site yield
from Ecological Site Classification and growth using Forest Yield, and
then calculated using ASORT (timber volume) and BSORT (biomass).
The biodiversity index used was based on a method developed by
Humphrey et al. (2002, 2004), based on the age of a stand and its FMA
type. The coupled model outputs have an annual time step, and results
from the models were compiled and reported at decadal intervals.
3. Results
3.1. Changes in ecosystem goods and services on Scotland's National Forest
Estate
The findings highlight changes in the provision of three ecosystem
goods and services under a single climate change scenario, using dif¬
ferent forest management trajectories. In this section we present results
for the NFE in Scotland at decadal intervals between the RCP4.5 climate
projection and the baseline climate, exploring changes in standing
biomass, timber production and biodiversity.
3.1.1. Biomass
The variability in standing biomass provision under different man¬
agement trajectories on the whole NFE (Fig. 2a) shows that in the long
term (50-70 years) an increase from the business as usual management
will occur for native species, broadleaved species, and continuous cover
forest management. This resulted in increases of up to 40 t ha - 1 com¬
pared to business as usual. The continuous cover silviculture showed a
steady increase through the period. However, broadleaves and native
species management trajectories showed a steep increase from 2040 at
which time business as usual (largely fell-restock systems) stands began
to be felled at the age of maximum mean annual increment. In contrast,
the largest reduction of up to 20tha -1 was projected for the short
rotation forestry management, with modelled rotation lengths of only
25 years.
The diverse and small impacts of DNB depend on the type of forest
management trajectory (Fig. 2b). At initialisation of the forest model
simulation, DNB was predicted to reduce standing biomass across the
NFE by approximately 2tha -1 (-1.7%). We see that some forest
management trajectories improved the negative biomass impact of
DNB, especially broadleaved and FE selected species (FESP) in Scot¬
land- since these management trajectories gradually removed high risk
species; Corsican pine and lodgepole pine. Broadleaved management
(with reliance on birch species), was predicted to increase biomass
compared to business as usual management, and may also mitigate DNB
impacts.
In contrast, other management trajectories were projected to con¬
tinue to maintain a reduced standing biomass compared to business as
usual. These include: no Sitka spruce; low impact silviculture; and short
rotation forestry - since these three management trajectories main¬
tained both Corsican and lodgepole pine.
3.1.2. Timber Production
A decrease in timber volume (TDC17 - diameter above 17 cm) was
projected across all management trajectories (Fig. 3a), mainly due to
the currently optimised high timber production of fast growing Sitka
spruce using fell-restock silviculture. Therefore, the current composi¬
tion of tree species and management (business as usual) maintained the
highest provision of timber. On the NFE, we predicted a 50 m 3 ha -1
reduction in timber production, if all stands suitable for short rotation
forestry were transformed by the 2080s. In contrast, a general trans¬
formation to more continuous cover forestry projected little effect on
timber production, since this management trajectory would be possible
on a relatively small proportion of the NFE - forest stands not con¬
strained by wind exposure. Diversifying species selection or selecting
favoured FES species (FESP) would cause a small reduction in pro¬
duction by 2060 (< 10 m 3 ha -1 ). This reduction was predicted to
change to 20-25 nAa' 1 by 2080, as slower growing species compared
to Sitka spruce would become more widespread on sites for which they
were more ecologically suitable. By gradually removing Sitka spruce
from all stands at restocking, the production forecast would reduce by
10 m 3 ha -1 in 2060 and by 50 m 3 ha -1 by 2080, again because of
replacement by lower yielding species.
The impact of DNB on timber volume was projected to be similar
across all forest management trajectories until the 2060s (Fig. 3b), with
the reduction of approximately 4 m 3 ha - 1 (3%). Then, DNB impacts
were shown to diverge with the most negative effects on short rotation
forestry and business as usual and the least negative effects on broad¬
leaved species management trajectories.
For production, all forest management trajectories provided less
timber in the future in contrast to business as usual, but DNB was
projected to have a major impact on the business as usual management.
Comparing the diverse species management (DIV) with the favoured
22
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
bau o div + ccf noss B
bl2 A fesp X nat V srf *
' CD
O
decade
bau o
3 bl2 A
div
fesp X
ccf
nat V
noss B
srf *
=)
<
m
E
o
c/)
(/)
CD
E
o
_c
0
O)
c
03
150
100
50
0
150
100
50
0
Moray&Aberdeenshire
North Hiqhland
*
/2k
* * * * * h
Dumfries&Borders
Lochaber
, m a j ■ jf t?
A t
t m + —- 5? m -TF ->i
> • *■ —4^ — • '
2020 2040 2060
2020 2040 2060
decade
b
bau
b!2
o
A
div + ccf
fesp X nat V
noss B
srf *
b
bau
b!2
o
A
div
fesp X
ccf
nat V
noss B
srf *
03
decade
Fig. 3. Change in the timber volume production on the National Forest Estate (NFE)
under climate change a) from BAU to other forest management trajectories without DNB
impact (timber volume in the 2010 for BAU around 4.4 mil m 3 ), and b) due to DNB
impact.
bau o div + ccf noss B
^ b!2 A fesp x nat V srf *
03
O
decade
Fig. 5. Changes in the provision of standing biomass in four Forest Districts (Moray &
Aberdeen (standing biomass in 2010 around 5.4 Mt), North Highland (standing biomass
in 2010 around 3.2 Mt), Dumfries & Borders (standing biomass in 2010 around 4.8 Mt),
and Lochaber (standing biomass in 2010 around 3.7 Mt)) under climate change a) from
BAU to other forest management trajectories without DNB impact, and b) due to DNB
impact.
species selection (FESP), the forest simulation showed the former would
be impacted more severely by DNB as the latter FESP selection does not
include Corsican pine or lodgepole pine.
3.1.3. Biodiversity
Fig. 4 shows changes (compared to the business as usual manage¬
ment system) in the provision of biodiversity - using a relative indicator
(1 = low and 10 high). The main increase in biodiversity by up to
0.6 units was shown to occur for continuous cover management. In
contrast, the main decrease, by up to 0.4 units, occurred for short ro¬
tation forestry, while other management trajectories ensured a similar
provision of biodiversity to business as usual. DNB would have no im¬
pact on biodiversity using the remaining management trajectories, as
the index is not sensitive to species changes in pine forests.
3.2. Changes in ecosystem goods and services for individual districts
Fig. 4. Change in the provision of biodiversity on the NFE under climate change from
BAU to other forest management trajectories without DNB impact.
In this section we present results showing changes in standing bio¬
mass, timber production and biodiversity index under climate change
and for different management trajectories for four Forest Districts of the
NFE (see Fig. S2 - online Supplementary material). The districts are
Moray and Aberdeen in the east, North Highland in the north, Dumfries
23
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
and Borders in the south, and Lochaber in the west of Scotland.
a
bau
bl2
o
A
div
fesp X
ccf
nat V
noss E)
srf *
3.2.1. Biomass
As in Fig. 2a on the NFE, biomass provision was shown to increase
gradually in all four districts (Fig. 5a) under the continuous cover for¬
estry management trajectory, slightly more in Lochaber and Moray &
Aberdeen than in North Highland and Dumfries & Borders due to a
greater proportion of suitable sites for CCF in the former two districts.
In Moray & Aberdeen, Dumfries & Borders and Lochaber the changes in
biomass production among management trajectories were very similar
to the NFE national results. In North Highland there was a large in¬
crease in biomass provision for native species selection and broadleaved
species, largely because of the availability of suitable sites for native
birch species under warmer climatic conditions, which is expected to
improve the yield.
Three districts (Lochaber, Moray & Aberdeen, and Dumfries &
Borders) showed a smaller proportion of lodgepole pine than North
Highland, leading to an initial DNB impact reducing biomass provision
by approximately 4 t ha - 2 (Fig. 5b). In North Highland, a much larger
reduction in biomass due to DNB was predicted for the business as
usual, continuous cover and short rotation forestry (up to 12 tha -1 ).
For these management trajectories the species present at initialisation
was maintained through to 2080, leading to the continuation of large
areas of lodgepole pine, and larger impacts from DNB. In Moray &
Aberdeen, Scots pine is widely distributed, and the results showed a
medium impact of DNB reducing biomass provision by approximately
4 tha -1 which decreased slightly from 2060 and then increased
slightly by 2080.
3.2.2. Timber production
Compared to business as usual, the forest simulation showed re¬
ductions in timber production volume for all management trajectories
in Moray & Aberdeen, Lochaber, and Dumfries & Borders districts, with
the largest reductions (50-100 m 3 ha - 2 ) in the latter district by 2080
(Fig. 6a). Lochaber and Dumfries & Borders have large proportions of
Sitka spruce, and the results showed spatial differences in the way
climate change and management trajectories interact between the south
of Scotland (drier summers) and western Scotland (wetter summers),
which caused the variation in the production volumes. Compared to
business as usual, results for the FESP preferred species selection
showed similar production targets as business as usual in Lochaber by
2070 and 2080 (20-25 m 3 ha - 2 ), but greater reductions in production
in Dumfries and Borders in 2070 and 2080 (50 m 3 ha -1 ). Similarly,
results for the native species management trajectory showed production
losses of 75-100 m 3 ha -1 in Dumfries & Borders, and < 50 m 3 ha - 1 in
Lochaber.
Changes in Moray & Aberdeen followed a similar pattern to
Lochaber, but in North Highland the results showed production benefits
to be gained over business as usual in moving to FE preferred species
(FESP), native species, species diversity, and broadleaved species
management trajectories. DNB impacts were shown to be greater in
Moray & Aberdeen, and North Highland (Fig. 6b) where Scots pine,
Corsican pine and lodgepole pine are currently more extensively
planted than in the other two districts. Unsurprisingly, in both districts
a change to broadleaved species and/or native species was shown to
reduce DNB impacts. Dumfries & Borders currently has much less pine
and is largely unaffected by DNB.
3.2.3. Biodiversity
The same changes in biodiversity as described for the NFE (see
Fig. 4) were shown to occur in each of the four districts (Fig. 7). Con¬
tinuous cover systems produced increases in the biodiversity index and
the short rotation forestry trajectory reduced the biodiversity index.
The DNB vulnerability matrix model had no impact on the biodiversity
index.
03
-C
co
^E
ID
<
CD
E
o
0
^ 50 -
O
>
i—
0
-Q
E
0
O)
c
03
50 -
0
-50 -
0
-50 -
Moray&Aberdeenshire
North Highland
>-*-*-A - ft -m -~ .
J
Dumfries&Borders
Lochaber
h—■ 9 - 9 - # y - ? -
+
m
4^
2020 2040 2060
2020 2040 2060
decade
bau
bl2
div
fesp
+
X
ccf
nat
noss
srf
03
SZ
00
JE
0
V
-5
E
-10
o
>
-15
0
_Q
E
0
c
o
-5
CD
Z
-10
O
u—
-15
o
o
03
Q-
E
Morav&Aberdeenshire
North Highland
- * * * • I !
' •
• i
Dumfries&Borders
Lochaber
- ► •- 9 * ,
\ i i i i i i
1 1 1 1 1 1
2020 2040 2060 2020 2040 2060
decade
Fig. 6. Change in timber volume production in four Forest Districts (Moray & Aberdeen
(timber volume in 2010 around 0.55 mil m 3 ), North Highland (timber volume in 2010
around 0.28 mil m 3 ), Dumfries & Borders (timber volume in 2010 around 0.43 mil m 3 ),
and Lochaber (timber volume in 2010 around 0.39 mil m 3 )) under climate change a) from
BAU to other forest management trajectories without DNB impact, and b) due to DNB
impact.
bau o div + ccf noss 8
b!2 A fesp X nat V srf *•
0
7D
c
=)
<
CD
E
o
£
0
>
~o
o
0
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c
03
_C
o
Morav&Aberdeenshire
North Highland
0.5 -
o.o -
> — » ^1; 9 — * — 9—t^
-0.5 -
- * - h
Dumfries&Borders
Lochaber
0.5 -
# - 9 -•-• - 9 & ~~ '
0.0 -
‘ * t z • *
* ^
-0.5 -
-#-1
^— 9 h
—i-1-1-1-1-1--1-1-1-1-1-r
2020 2040 2060 2020 2040 2060
decade
Fig. 7. Change in the provision of biodiversity in four Forest Districts (Moray & Aberdeen,
North Highland, Dumfries & Borders and Lochaber) under climate change a) from BAU to
other forest management trajectories without DNB impact, and b) due to DNB impact.
24
D. Ray, et al
4. Discussion
4.1. Sensitivity of ecosystem goods and service delivery to changes in
management choices, climate and disease
This study investigated ways in which the public sector forestry in
Scotland can make a contribution to greenhouse gas abatement and
timber production while maintaining high biodiversity and other im¬
portant benefits. Scottish forest policy encourages species and forest
management diversity, and the use of strategic targeting to meet mul¬
tiple objectives. The results show the National Forest Estate's im¬
plementation of policy will deliver these intended benefits. In parti¬
cular, given an RCP4.5 climate projection, with associated abiotic and
DNB impacts, the production forecast could be maintained, or would
suffer only small reductions. This outcome could be achieved by in¬
creasing the use of continuous cover forestry systems and by introdu¬
cing more Forest Enterprise Scotland favoured species (FESP). Such a
change would also maintain the forest biodiversity index. The com¬
bined abiotic and biotic analysis is an example case study that will help
policy developers assess the sensitivity of forest ecosystem goods and
services to changes in climate and pathogens (Lindner et al., 2010), and
improve understanding of trade-offs resulting from different policy and
practice decisions (Seidl and Lexer, 2013).
Our dynamically coupled forest model predicts that DNB could re¬
duce standing biomass (by up to 3 t ha - *) and timber volume (by up to
5 m 3 ha -1 ). The impact is dependent on the type of forest management
systems applied and introducing FESP would reduce this impact.
We demonstrated how interactions between management systems
and abiotic and biotic climate impacts differ among regions in Scotland.
In North Highland and in Moray & Aberdeen particular changes in
species and silvicultural management (less pine more broadleaved
species; more continuous cover systems) would improve biomass pro¬
vision and timber production, and at the same time relieve the current
impact of DNB, and improve biodiversity in forests.
4.2. Use of simulation tools in understanding forest policy implementation
There are relatively few models that can examine policy options and
forest management scenarios together. Notable examples include the
European Forest Information Scenario model (EFISCEN) (Schelhaas
et al., 2015), which has been used to analyse large scale applications of
climate change abiotic effects (Hanewinkel et al., 2012; Verkerk et al.,
2014) and also regional forest biotic disturbances (Seidl et al., 2009)
with the patch-based model PICUS (Lexer and Honninger, 2001). For
national and district analyses where detailed FMA descriptions, soil
types, and climate scenarios are available, our dynamically coupled
model approach can examine the effects of implementing forest policy
in different ways, in different places and at different times into the
future. The approach can accommodate the effects of forest planning on
policy targets, by accumulating goods and services to regional and
national scales.
The decision support tool used in this study is not intended to be
used by forestry professionals alone, but jointly with forest scientists to
assess scenarios and future implications of current policy and practice.
This will enable capacity building (Grainger, 2012) and help manage
uncertainty (Petr et al., 2014) within the National Forest Estate and,
with modifications, within private forests.
The novelty of the forest model simulation is the multi-scale tem¬
poral view of forest policy implementation and future outcomes. The
decision support tool uses ecosystem service indicators to appraise the
combinations of forest management, and climate change abiotic and
biotic impacts and can explore the notion of resilient forests meeting
their intended delivery of ecosystem goods and services into the future
(Ray et al., 2015).
It has been argued (Buizer and Lawrence, 2014), that re¬
commendations for mitigation have used a more quantitative approach
Forest Policy and Economics 103 (2019) 17-27
than recommendations for adaptation. This is because adaptation is
concerned more with changing forestry professional's frames on tree
species selection and/or silvicultural systems. Our approach uses high
resolution spatial data in a multi-scale analysis which can provide re¬
commendations tailored to forest regions and ecosystem services. Such
results can be used in novel action expiration charts (Petr et al., 2016)
for knowledge exchange with forestry professionals. The combination
of simulations with the action expiration chart methodology also partly
answers the Buizer and Lawrence (2014) recommendation to “engage
with both the social and ecological complexity and value conflicts” in
climate change adaptation discourse, through a dynamic spatial and
temporal scenario assessment.
4.3. Opportunities for stakeholder involvement in simulation assessment
The mix of policy, management objectives, economic benefits and
natural science is very much a multidisciplinary complex system
(Costanza, 2001) involving forest policy makers, practitioners and sci¬
entists. It is in this area of uncertainty and mixed objectives that the
simulation approach shows much potential. Our results have been used
in discussions at the national level on forest policy, and at the forest
district level regarding maintaining the multiple objectives of forestry.
This has helped show how Forestry Commission Scotland's ‘strategic
directions’ policy can target regional resources to provide particular
benefits at the national level (Forestry Commission Scotland, 2013b),
rather than each district being expected to deliver on ‘aspirational
targets’ for all ‘key commitments’. The work has helped inform the
potential of alternate land management plans at the district scale to
deliver recreation and biodiversity benefits (Beauchamp et al., 2016)
requested in community discussions.
5. Conclusions
If large forestry enterprises, ignore information on likely abiotic and
biotic impacts of climate change, and ignore policy recommendations,
there is a risk of loss of production and a reduced resilience of forest
stands. Scotland's National Forest Estate delivers important forest eco¬
system goods and services (Ray et al., 2016; Sing et al., 2015), and we
have shown under the uncertainty of climate change, how spatio-tem¬
poral scenario forest model simulations can inform solutions for the
targeted delivery of benefits (Forestry Commission Scotland, 2013b).
Furthermore, we have shown how forest model simulations can explore
scenarios and show differences in the interactions between forest
management trajectories, species choice, abiotic and biotic impacts.
Our results support the policy of targeted delivery, and this leads us to
believe that better informed decisions will improve future forestry ob¬
jectives and strategic delivery, compared to trial and error manage¬
ment.
Our decision support tool currently extends to Scotland's National
Forest Estate, which covers one third of Scotland's forest area. The
principles of our findings can not be extended to the remaining area,
due differences in species composition between the public and private
ownerships (see Supplementary material) due to the underlying dif¬
ferences in soil and climatic conditions; so we plan to develop private
sector case studies. In addition, other pest/pathogen models could be
developed and incorporated to test combined abiotic/biotic climate
change impacts.
Our approach applied single forest management trajectories across
the National Forest Estate to assess and compare the impact of one
trajectory with others. In practice, the forest simulation would test land
management plans and strategic plans where different forest manage¬
ment trajectories could/should be spatially targeted to meet forest ob¬
jectives and ecosystem goods and service provision.
25
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
Funding and acknowledgements
The study was funded by Forestry Commission GB within the re¬
search programmes of the Forest Research Science and Innovation
Strategy (ISBN:978-0-85538-903-l). The work was completed as a case
study for Working Group 2 of the European COST Action FP1207
(Orchestra) - Orchestrating forest policy implementation in Europe. We
are grateful for comments from two reviewers and the editor, and to
Professor Chris Quine for helpful comments on an earlier draft.
Appendix A. Supplementary data
Supplementary data to this article can be found online at https://
doi.org/10.1016/j.forpol.2017.10.010.
References
Bateman, I.J., Harwood, A.R., Mace, G.M., Watson, R.T., Abson, D.J., Andrews, B., Binner,
A., Crowe, A., Day, B.H., Dugdale, S., Fezzi, C., Foden, J., Hadley, D., Haines-Young,
R. , Hulme, M., Kontoleon, A., Lovett, A.A., Munday, P., Pascual, U., Paterson, J.,
Perino, G., Sen, A., Siriwardena, G., van Soest, D., Termansen, M., 2013. Bringing
ecosystem services into economic decision-making: land use in the United Kingdom.
Science 341, 45-50. http://dx.doi.org/10.1126/science.1234379.
Beauchamp, K., Bathgate, S., Nicoll, B., Ray, D., 2016. Forest Ecosystem Service Delivery
under Future Climate Scenarios and Adaptation Management Options: A Case Study
in central Scotland, Scottish Forestry, December 2016. Royal Scottish Forestry
Society, Edinburgh.
Boyd, I.L., Freer-Smith, P.H., Gilligan, C.A., Godfray, H.C.J., 2013. The consequence of
tree pests and diseases for ecosystem services. Science (New York, N.Y.) 342,
1235773. http://dx.doi.org/10.1126/science. 1235773.
Broadmeadow, M.S.J., Matthews, R.W., 2004. Survey Methods for Kyoto Protocol
Monitoring and Verification of UK Forest Carbon Stocks. In: DEFRA report.
Brown, A.V., Webber, J., 2008. Red band needle blight of conifers in Britain. In: Res. Note
- For. Comm, (8 pp.).
Buizer, M., Lawrence, A., 2014. The politics of numbers in forest and climate change
policies in Australia and the UK. Environ. Sci. Pol. 35, 57-66. http://dx.doi.org/10.
1016/j.envsci.2012.12.003.
Christensen, P.S., Gibson, I.A.S., 1964. Further observations in Kenya on a foliage disease
of pines caused by Dothistroma pini Hulbary, 1: effect of disease on height and
diameter increment in three and four-years-old Pinus Radiata. Commonw. For. Rev.
43, 326-331.
Costanza, R., 2001. Visions, values, valuation, and the need for an ecological economics.
Bioscience 51, 459-468. http://dx.doi.org/10.1043/0006-3568C2001)
051 (0459: WVATN)2.0.CO;2.
Drenkhan, R., Tomesova-Haataja, V., Fraser, S., Bradshaw, R.E., Vahalik, P., Mullett,
M.S., Martin-Garcia, J., Bulman, L.S., Wingfield, M.J., Kirisits, T., Cech, T.L., Schmitz,
S. , Baden, R., Tubby, K., Brown, A., Georgieva, M., Woods, A., Ahumada, R.,
Jankovsky, L., Thomsen, I.M., Adamson, K., Mar^ais, B., Vuorinen, M., Tsopelas, P.,
Koltay, A., Halasz, A., La Porta, N., Anselmi, N., Kiesnere, R., Markovskaja, S.,
Kacergius, A., Papazova-Anakieva, I., Risteski, M., Sotirovski, K., Lazarevic, J.,
Solheim, H., Boron, P., Braganga, H., Chira, D., Musolin, D.L., Selikhovkin, A.V.,
Bulgakov, T.S., Keca, N., Karadzic, D., Galovic, V., Pap, P., Markovic, M., Poljakovic
Pajnik, L., Vasic, V., Ondruskova, E., Piskur, B., Sadikovic, D., Diez, J.J., Solla, A.,
Millberg, H., Stenlid, J., Angst, A., Queloz, V., Lehtijarvi, A., Dogmu§-Lehtijarvi, H.T.,
Oskay, F., Davydenko, K., Meshkova, V., Craig, D., Woodward, S., Barnes, I., 2016.
Global geographic distribution and host range of Dothistroma species: a compre¬
hensive review. For. Pathol, http://dx.doi.org/10.llll/efp.12290.
Duncker, P.S., Barreiro, S.M., Hengeveld, G.M., Lind, T., Mason, W.L., Ambrozy, S., 2012.
Classification of Forest Management Approaches: A New Conceptual Framework and
Its Applicability to European Forestry 17.
European Commission, 2013. Communication From The Commission To The European
Parliament, The Council, The European Economic And Social Committee And The
Committee Of The Regions. A New EU Forest Strategy: For Forests and the Forest-
based Sector Brussels. 20.9.2013; COM(2013) 659 final, http://eur-lex.europa.eu/
legal-content/EN/TXT/PDF/?uri = CELEX:52013DC0659.
Forestry Commission, 2016. Forestry Statistics. Edinburgh, www.forestry.gov.uk/
forestry/infd-7aqdgc.
Forestry Commission Scotland, 2006. Scottish Forestry Strategy, Edinburgh, Scotland.
http://scotland.forestry.gov.uk/images/corporate/pdf/scottish-forestry-strategy-
2006 pdf.
Forestry Commission Scotland, 2013a. Climate Change Programme. www.Scotland.
forestry. gov. uk/images/corporate/pdf/climate-change-programme. pdf.
Forestry Commission Scotland, 2013b. The role of Scotland's National Forest Estate and
strategic directions 2013-2016.
Gadgil, P.D., 1974. Effect of temperature and leaf wetness period on infection of Pinus
radiata by Dothistroma pini. N. Z. J. For. Sci. 4, 495-501.
Gadgil, P.D., 1977. Duration of leaf wetness periods and infection of Pinus radiata by
Dothistroma pini. N. Z. J. For. Sci. 7, 83-90.
Gardiner, B.A., Quine, C.P., 2000. Management of forests to reduce the risk of abiotic
damage - a review with particular reference to the effects of strong winds. For. Ecol.
Manag. 135, 261-277.
Garrett, K.A., Nita, M., De Wolf, E.D., Gomez, L., Sparks, A.H., 2016. Plant pathogens as
indicators of climate change. In: Climate Change, Chapter 21. Elsevier, B.V.
Grainger, A., 2012. Forest sustainability indicator systems as procedural policy tools in
global environmental governance. Glob. Environ. Chang. 22, 147-160. http://dx.doi.
org/10.1016/j. gloenvcha.2011.09.001.
Hanewinkel, M., Cullmann, D.A., Schelhaas, M., Nabuurs, G.-J., Zimmermann, N.E.,
2012. Climate change may cause severe loss in the economic value of European forest
land. Nat. Clim. Chang. 2, 1-5.
Harmer, R., Watts, K., Ray, D., 2015. A hundred years of woodland restoration in Britain:
changes in the drivers that influenced the increase in woodland cover. In: Stanturf,
John A. (Ed.), Restoration of Boreal and Temperate Forests, Second edition. CRC
Press.
Harvell, C.D., Mitchell, C.E., Ward, J.R., Altizer, S., Dobson, A.P., Ostfeld, R.S., Samuel,
M.D., 2002. Climate warming and disease risks for terrestrial and marine biota.
Science 296, 2158-2162. http://dx.doi.org/10.1126/science.1063699.
Hemery, G., Petrokofsky, G., Ambrose-Oji, B., Atkinson, G., Broadmeadow, M., Edwards,
D., Harrison, C., Lloyd, S., Mumford, J., O'Brien, L., Reid, C., Seville, M., Townsend,
M. , Weir, J., Yeomans, A., 2015. Awareness, action and aspiration among Britain's
forestry community relating to environmental change: Report of the British
Woodlands Survey 2015. www.sylva.org.uk/forestryhorizons/bws2015.
Hocking, D., Etheridge, D.E., 1967. Dothistroma needle blight of pines. I. Effect and
etiology. Ann. Appl. Biol. 59, 133-141.
Humphrey, J.W., Ferris, R., Jukes, M., Peace, A., 2002. Biodiversity of planted forests. In:
Claridge, J. (Ed.), Forest Research Annual Report and Accounts 2000-2001. Forestry
Commission, Edinburgh.
Humphrey, J.W., Sippola, A.-L., Lemperiere, L.G., Dodelin, B., Alexander, K.N.A., Butler,
J.E., 2004. Deadwood as an indicator of biodiversity in European forests: from theory
to operational guidance. In: Marchetti, M. (Ed.), Monitoring and Indicators of Forest
Biodiversity in Europe - From Ideas to Operationality. European Forest Institute,
Joensuu, pp. 193-206.
IPCC, 2014. Climate Change 2014: Impacts, Adaptation, and Vulnerability. Part A: Global
and Sectoral Aspects. Contribution of Working Group II to the Fifth Assessment
Report of the Intergovernmental Panel on Climate Change.
Jung, T., 2009. Beech decline in Central Europe driven by the interaction between
Phytophthora infections and climatic extremes. For. Pathol. 39, 73-94.
Lexer, M.J., Honninger, K., 2001. A modified 3D-patch model for spatially explicit si¬
mulation of vegetation composition in heterogeneous landscapes. For. Ecol. Manag.
144, 43-65. http://dx.doi.org/10.1016/S0378-l 127(00)00386-8.
Lindner, M., Maroschek, M., Netherer, S., Kremer, A., Barbati, A., Garcia-Gonzalo, J.,
Seidl, R., Delzon, S., Corona, P., Kolstrom, M., Lexer, M.J., Marchetti, M., 2010.
Climate change impacts, adaptive capacity, and vulnerability of European forest
ecosystems. For. Ecol. Manag. 259, 698e709.
Matthews, R.W., 2008. Forest Yield, 4 edition. Forestry Commission, Edinburgh.
McKay, H., 2003. Woodfuel Resource in Britain. In: Final Report to DTI, Scottish
Enterprise, WAG and FC. Forestry Contracting Association.
Millennium Ecosystem Assessment, 2005. Ecosystems and Human Well-being: Synthesis.
Washington, DC.
Murray, J.S., Batko, S., 1962. Dothistroma pini Hulbary: a new disease on pine in Britain.
Forestry 34, 57-65.
Pautasso, M., Doring, T.F., Garbelotto, M., Pellis, L., Jeger, M.J., 2012. Impacts of climate
change on plant diseases—opinions and trends. Eur. J. Plant Pathol. 133, 295-313.
http://dx. doi. org/10.1007/sl 0658-012-9936-1 .
Petr, M., Boerboom, L., Ray, D., van der Veen, A., 2014. An uncertainty assessment fra¬
mework for forest planning adaptation to climate change. For. Policy Econ. 41, 1-11.
http://dx.doi.Org/10.1016/j.forpol.2013.12.002.
Petr, M., Boerboom, L.G.J., Ray, D., van der Veen, A., 2016. New climate change in¬
formation modifies frames and decisions of decision makers: an exploratory study in
forest planning. Reg. Environ. Chang. 16, 1161-1170. http://dx.doi.org/10.1007/
slOl 13-015-0827-9.
Pyatt, G., Ray, D., Fletcher, J., 2001. An ecological site classification for forestry in Great
Britain. In: Forestry Commission Bulletin 124. HMSO, Edinburgh.
Quine, C., Ray, D., 2010. Sustainable forestry - which species for which site for which
world. In: Species Management: Challenges and Solutions for the 21st Century, pp.
417-434.
Quine, C., Cahalan, C., Hester, A., Humphrey, J., Kirby, K., Moffat, A., 2011. Woodlands.
In: UK National Ecosystem Assessment: Technical Report. UNEP-WCMC, Cambridge,
UK, pp. 1-53.
Ray, D., 2008. Impacts of climate change on forests in Scotland - a preliminary synopsis
of spatial modelling research. In: Forestry Commission Research Note 001.
Edinburgh, Forestry Commission Scotland, Edinburgh.
Ray, D., Bathgate, S., Moseley, D., Taylor, P., Nicoll, B., Pizzirani, S., Gardiner, B., 2015.
Comparing the provision of ecosystem services in plantation forests under alternative
climate change adaptation management options in Wales. Reg. Environ. Chang. 15
(8), 1501-1513.
Ray, D., Sing, L., Nicoll, B., 2016. Forest Ecosystem Services & Climate Change,
Agriculture and Forestry Climate Change Report Card. Technical Paper 9. pp. 1-34.
Rollinson, T.J.D., Gay, J.M., 1983. An Assortment Forecasting Service. Forestry
Commission Research Information Note 77/83/MENS. Forestry Commission,
Edinburgh.
Roy, B.A., Alexander, H.M., Davidson, J., Campbell, F.T., Burdon, J.J., Sniezko, R.,
Brasier, C., 2014. Increasing forest loss worldwide from invasive pests requires new
trade regulations. Front. Ecol. Environ. 12, 457-465. http://dx.doi.org/10.1890/
130240.
Schelhaas, M.J., Nabuurs, G.J., Hengeveld, G., Reyer, C., Hanewinkel, M., Zimmermann,
N. E., Cullmann, D., 2015. Alternative forest management strategies to account for
26
D. Ray, et al
Forest Policy and Economics 103 (2019) 17-27
climate change-induced productivity and species suitability changes in Europe. Reg.
Environ. Chang. 15, 1581-1594. http://dx.doi.org/10.1007/sl0113-015-0788-z.
Schroter, D., Cramer, W., Leemans, R., Prentice, I.C., Araujo, M.B., Arnell, N.W., Bondeau,
A., Bugmann, H., Carter, T.R., Gracia, C.A., de la Vega-Leinert, A.C., Erhard, M.,
Ewert, F., Glendining, M., House, J.I., Kankaanpaa, S., Klein, R.J.T., Lavorel, S.,
Lindner, M., Metzger, M.J., Meyer, J., Mitchell, T.D., Reginster, I., Rounsevell, M.,
Sabate, S., Sitch, S., Smith, B., Smith, J., Smith, P., Sykes, M.T., Thonicke, K., Thuiller,
W., Tuck, G., Zaehle, S., Zierl, B., 2005. Ecosystem service supply and vulnerability to
global change in Europe. Science 80 (310), 1333-1337. http://dx.doi.org/10.1126/
science.il 15233.
Scottish Government, 2013. Low Carbon Scotland: Meeting the Emissions Reduction
Targets 2013-2027, The Second Report on Proposals and Policies (RPP2). http://
www.gov.scot/Resource/0042/00426134.pdf.
Scottish Government, 2014. Climate Ready Scotland: Scottish Climate change Adaptation
Programme. http://www.gov.scot/Resource/0045/00451392.pdf.
Seidl, R., Lexer, M.J., 2013. Forest management under climatic and social uncertainty:
trade-offs between reducing climate change impacts and fostering adaptive capacity.
J. Environ. Manag. 114, 461-469. http://dx.doi.Org/10.1016/j.jenvman.2012.09.
028.
Seidl, R., Schelhaas, M.J., Lindner, M., Lexer, M.J., 2009. Modelling bark beetle dis¬
turbances in a large scale forest scenario model to assess climate change impacts and
evaluate adaptive management strategies. Reg. Environ. Chang. 9, 101-119. http://
dx.doi.org/10.1007/sl0113-008-0068-2.
Sing, L., Ray, D., Watts, K., 2015. Ecosystem services and forest management. In: Forestry
Commission Research Note 20. Scotland, Forest Research, Roslin.
Soil Survey of Scotland, 1981. Sheets at 1:250000 Scale. James Hutton Institute,
Aberdeen, Scotland, UK.
Sturrock, R.N., Frankel, S.J., Brown, A.V., Hennon, P.E., Kliejunas, J.T., Lewis, K.J.,
Worrall, J.J., Woods, A.J., 2011. Climate change and forest diseases. Plant Pathol. 60,
133-149.
Tubby, K.V., Webber, J.F., 2010. Pests and diseases threatening urban trees under a
changing climate. Forestry 83 (4).
UK Forestry Standard, 2011. Forestry Commission, Edinburgh, Scotland.
UK National Ecosystem Assessment, 2011. The UK National Ecosystem Assessment:
Synthesis of the Key Findings. Cambridge.
UK National Ecosystem Assessment, 2014. The UK National Ecosystem Assessment -
Follow On: Synthesis of the Key Findings. UK.
Van der Pas, J.B., 1981. Reduced early growth rates of Pinus radiata caused by
Dothistroma pini. N. Z. J. For. Sci. 11, 210-220.
Verkerk, P.J., Mavsar, R., Giergiczny, M., Lindner, M., Edwards, D., Schelhaas, M.J.,
2014. Assessing impacts of intensified biomass production and biodiversity protec¬
tion on ecosystem services provided by European forests. Ecosyst. Serv. 1-11. http://
dx.doi.org/10.1016/j.ecoser.2014.06.004.
Watt, M.S., Palmer, D.J., Bulman, L.S., 2011. Predicting the severity of Dothistroma on
Pinus radiata under current climate in New Zealand. For. Ecol. Manag. 261,
1792-1798.
Welsh, C., Lewis, K.J., Woods, A.J., 2014. Regional outbreak dynamics of Dothistroma
needle blight linked to weather patterns in British Columbia, Canada. Can. J. For.
Res. 44, 212-219. http://dx.doi.org/10.1139/cjfr-2013-0387.
Whyte, A.G.D., 1969. Tree growth in the presence of Dothistroma pini. Rep. For. Res. Inst.
1968 N. Z. For. Serv. Wellingt. NZ. pp. 51-53.
Woods, A.J., Martin-Garcia, J., Bulman, L., Vasconcelos, M.W., Boberg, J., La Porta, N.,
Peredo, H., Vergara, G., Ahumada, R., Brown, A., Diez, J.J., 2016. Dothistroma
needle blight, weather and possible climatic triggers for the disease's recent emer¬
gence. For. Pathol, http://dx.doi.org/10.llll/efp.12248.
27