SAN DIEGO COUNTY ECOSYSTEMS: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
SAN DIEGO COUNTY ECOSYSTEMS: The Ecological Impacts of Climate Change on a Biodiversity Hotspot This magazine serves as a summary of a report included in California's Fourth Climate Change Assessment. The report was prepared by: Megan K. Jennings, Ph.D San Diego State University Dan Cayan, Ph.D Scripps Institution of Oceanography Julie Kalansky, Ph.D Scripps Institution of Oceanography Amber D. Pairis, Ph.D Climate Science Alliance South Coast Dawn M. Lawson, Ph.D Space and Naval Warfare Systems Command
Alexandra D. Syphard, Ph.D Conservation Biology Institute Udara Abeysekera Climate Science Alliance-South Coast Rachel E.S. Clemesha, Ph.D Scripps Institution of Oceanography Alexander (Sasha) Gershunov, Ph.D Scripps Institution of Oceanography
Kristin Guirguis, Ph.D Scripps Institution of Oceanography John M. Randall, Ph.D The Nature Conservancy Eric D. Stein, Ph.D Southern California Coastal Water Research Project Sula E. Vanderplank, Ph.D Terra Peninsular A.C. Horacio de la Cueva, Ph.D Centro de Investigación Científica y de Educación Superior de Ensenada, Baja California
Shasta Gaughen, Ph.D The Pala Band of Mission Indians Janin Guzman-Morales Scripps Institution of Oceanography Laura Hampton Climate Science Alliance-South Coast Hiram Rivera-Huerta, Ph.D Universidad Autónoma de Baja California David W. Pierce, Ph.D Scripps Institution of Oceanography Rob Roy The La Jolla Band of Luiseño Indians
More information and links at: climatesciencealliance.org/sdc-ecosystems-assessment
Designed by Diane Terry Cover photo by Joanna Gilkeson/USFWS of San Miguel Mountain from Flickr.
March 2018
TABLE OF CONTENTS 3-6 Summary Table: Ecological Impacts of 7 - 8 Changing Conditions Temperature and Temperature 9 - 11 Extremes in the San Diego Region
Introduction to San Diego's Climate and Ecosystems
12 - 14
Precipitation and Drought in San Diego County
15 -17
San Diego Wildfires: Drivers of Change and Future Outlook
18 - 20
Impacts and Influences of Coastal Low Clouds and Fog on Biodiversity in San Diego
21 - 23
Conservation and Management for San Diego's Changing Climate
24 - 26 Key Points 27 - 28 Meet the Scientists 29 Why We Did It 30 References and Supporters 31-34
Conclusions and Future Directions
2
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
INTRODUCTION TO SAN DIEGO'S CLIMATE AND ECOSYSTEMS
by Amber D. Pairis, Udara Abeysekera, John M. Randall, Megan K. Jennings, Julie Kalansky, and Dan Cayan
T
he Mediterranean-type ecosystems of California, characterized by warm, dry summers and relatively cool, intermittantly wet winters, are some of the most ecologically diverse systems outside of the tropics (Cowling et al. 1996). The California Floristic Province (CFP), spanning from southwestern Oregon to northwestern Baja California, is largely coincident with this Mediterraneantype climate zone. The CFP is recognized as one of the
world’s biodiversity hotspots (Stein et al. 2000, Burge et al. 2016) with high species richness and diversity among both plants and animals. The focus of our study is the San Diego region’s mountains, foothills, valleys, and coastal zone. The study area encompasses a complex overlay of topography from the Pacific coast to interior mountains. The area is characterized by highly variable precipitation, strong seasonality, and coastal low clouds and fog (CLCF)
34°30'N
Total Native Species Richness 1099 - 1255 1256 - 1358 1359 - 1426 1427 - 1470 1471 - 1499 1500 - 1519 1520 - 1531 1532 - 1550 1551 - 1580 1581 - 1624 Ecoregions Additional Areas Considered
34°0'N
33°30'N
33°0'N
Pacific Ocean
U.S.
- Mexico Border
32°30'N
0
10
20
40 Miles
/
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © 0 12.5 25 and the GIS 50 OpenStreetMap contributors, userKilometers community 117°30'W
3
117°0'W
116°30'W
FIGURE 1: Map of overall species richness for all plant and vertebrate faunal taxa. Ecoregional subsection boundaries are displayed to identify how richness varies in San Diego’s different ecosystems.
Introduction
(Dettinger et al. 2011, Clemesha et al. 2016), which strongly influence the resident biological palette.
March 2018
"In the near term, ecosystems in the region will be most threatened by landscape changes, disturbances, and fragmentation due to development and fire. In the longer term, climate variability will compound those stressors with significantly warmer temperatures, more variable precipitation regimes resulting in occasional high intensity flooding and more frequent and prolonged droughts, and more destructive fires due to drought and increased ignitions/fuel availability."
to even greater variability.
San Diego County’s diverse ecological landscape is also home to a human population estimated at 3.3 million in 2015 (U.S. Census Bureau 2017). Most of the human population lives in the western third of the County, the majority of which falls within the San Diego metropolitan area. Situated immediately to the south is the metropolitan area of Tijuana, Mexico, which is home to another 1.7 million people (Secretaría de Desarrollo Social 2015). According to the decennial U.S. census, San Diego County’s population has increased rapidly for over a century, growing at rates of 30% - 90% in every decade of the 20th century and of over 10% thus far in each of the first two decades of the 21st century.
Ecologically, the County boasts more taxa of plants and mammals than any other in the United States (Rebman and Simpson 2014, Tremor et al. 2017), and is home to thousands of species (Figure 1) including ~200 taxa of plants and animals that are state- or federally-listed as threatened or endangered (California Department of Fish and Wildlife 2017). This high level of diversity is, in part, the result of the complex physiographic and climatic structure within the short distance from the sea to mountain crest. The distances between ecotones, or transitional regions between ecosystems, are relatively short, and modest climate changes could displace entire ecosystem zones. In the near term, ecosystems in the region will be most threatened by landscape changes, disturbances, and fragmentation due to development and fire. In the longer term, climate models indicate that climate change will compound those stressors with significantly warmer temperatures, more variable precipitation resulting in occasional high intensity flooding and more frequent droughts, and more destructive fires due to drought and increased ignitions/fuel availability. Although the region’s species and ecosystems have adapted to a precipitation regime with greater year-to-year variability than nearly anywhere else in the United States (Dettinger et al. 2011), they will be challenged as average temperatures rise and the precipitation regime is propelled
The rapid development and growth in human population in San Diego County has degraded large areas of habitat, shifted land use patterns, and expanded development into San Diego’s backcountry (Figure 2), which has imperiled many of the region’s distinctive and endemic species. As a result, San Diego’s communities of conservation planners, natural resource managers, and developers were among the first in the nation to come together to collaborate on the planning and implementation of a regional habitat conservation plan. This resulted in a strategy to create networks of linked conserved areas through federal Habitat Conservation Plans (HCPs), and state Natural Community Conservation Plans (NCCPs). Since the mid1990s, most new land conservation efforts in San Diego
Recently updated climate models project yearly average temperatures increasing by about:
RCP 4.5
INTERMEDIATE EMISSIONS // Consistent with future intensive efforts to reduce emissions
ºF
4-6
or
ºF
7-9
by the end of the century
RCP 8.5
HIGH EMISSIONS // Consistent with no future policy changes to reduce emissions
4
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
Historic Vegetation Cover
Present Day Vegetation Cover
34°30'N
34°0'N
33°30'N
33°0'N
S .. U U .. S
M ee xx ii cc oo -- M B B oo rr dd ee rr
S .. U U .. S
32°30'N
Pacific Ocean
Pacific Ocean Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community 118°0'W
117°30'W
M ee xx ii cc oo -- M B B oo rr dd ee rr
117°0'W
Coniferous forest Hardwood forest Shrubland Grassland/Meadow
116°30'W
Agriculture Barren Urban Water/Wetland
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community 118°0'W
117°30'W
117°0'W
Assessment Extent Additional Areas Considered 0
15
30
0
25
50
116°30'W
/
60 Miles 100 Kilometers
FIGURE 2: Change in distribution of urbanization, agricultural lands, and natural vegetation between the 1930s and present day.
County have been tied to these plans. Given this history of conservation planning (Table 1), San Diego is uniquely poised to demonstrate how the intersection of monitoring, research, and combined efforts by scientists and planners can promote effective longterm conservation. Building resilience into San Diego’s ecosystems is a challenge that will require collaborative efforts by policy-makers, planners, land managers, and the broader conservation community. Furthermore, it is becoming increasingly important for researchers to play a more prominent role in the dissemination of their research in ways that are actionable given the existing regulatory, economic, and social context in which land managers work (Enquist et al. 2017). In light of this, a group of ecologists and climatologists, under the umbrella of the Climate Science Alliance, undertook this review of regionally-specific climate impacts. The overarching goal 5
of this collaborative effort was to present an assessment of the San Diego region’s ecosystems and natural resource futures, and to take stock of the implications of climate change in combination with other stressors. This review considers historical climate and environmental observations and plausible future climate in the San Diego region from: 1) Relative Concentration Pathway (RCP) 4.5, a moderately mitigated greenhouse gas (GHG) emission scenario, and 2) RCP 8.5, a business as usual scenario. The data presented in this report include those derived from an ensemble of 32 global climate models (GCMs) or those 10 models that have been selected by the California Fourth Climate Change Assessment (Cayan et al. 2018). The output from these models has been downscaled using the Localized Constructed Analogs (LOCA) statistical downscaling method (Pierce et al. 2014).
Introduction
March 2018
Area (mi2)
% Protected
1498.3 / 58.9%
Chaparral
783.0 / 2.4%
Urban Coastal Scrub
546.8 / 16.4%
413.4 / 8.9%
Oak/Hardwood Forest
243.6 / 6.1%
Agriculture
156.1 / 0.7%
Grassland/Meadow
Riparian Forest Coniferous Forest Wetland Barren
71.2 / 2.0%
47.6 / 2.4% 37.6 / 1.9% 20.7 / 0.4%
TABLE 1: Ten major vegetation/land cover types mapped in San Diego County.
The synthesis here is not fine-scale or focused on single-species issues and therefore, not meant to be prescriptive. However, we hope it can be used to help inform management targets and approaches to promote proactive management and planning for a range of climate scenarios. Each section describes future changes of important climate or climate-driven elements, and examines how and why these phenomena and other costressors might affect ecological factors. In gauging these effects, this assessment describes the region's unique diversity of ecosystems (Figure 3), habitats, plants, and animals, as well as their susceptibility to impacts from climate variability and relevant anthropogenic drivers that may be exacerbated by a changing climate (e.g., urban growth, land use shifts, and fire regimes).
FIGURE 3: Photos from top to bottom: Coniferous and shrub habitat, montane chaparral habitat, oak grassland habitat, and riparian habitat. Photo credit: Megan Jennings
6
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
SUMMARY TABLE:
ECOLOGICAL IMPACTS OF CHANGING CONDITIONS
ANTHROPOGENIC OR CLIMATE DRIVERS OF CHANGE
Mean annual temperature
Heat waves
Spring drying Precipitation variability
Droughts Pests and pathogens Land use change + habitat fragmentation
Fire frequency
Santa Ana winds Coastal low level clouds and fog 7
Projected shift
Confidence in shift *
Associated ecological impacts
San Diego or southern CA example
Very high confidence
Species range shifts, novel assemblages
Narrowly endemic, gabbroassociated plants may experience unsuitable temperatures where suitable soil conditions exist
Increase in frequency and severity
Very high confidence
Increased mortality, decreased reproductive success
Potential for exceeding thresholds for some species like the California owl (Strix occidentalis occidentalis) with known temperature thresholds
General increase
High confidence
General increase
Potential to affect biomass
General increase
High confidence
Impacts to ephemeral and riparian environments less stabilizing vegetation and increased erosion can increase allochthonous input
General increase
High confidence
Potential structural shifts in ecosystems
Decreased reproductive success for species that breed in aquatic systems, e.g., arroyo toad (Anaxyrus californicus) Decrease the shredder functional group of macroinverts reducing downstream detritus food sources for zooplankton and fish
Oak tree (Quercus agrifolia) stress and die off during the 2012-2016 drought
Bark beetle caused mortality in coniferous forest and riparian tree dieback caused by shothole borer and fusarium fungal pathogen
Increase for some pests and vectors
Medium confidence
Increased lethal and sub lethal effects
General increase
Very high confidence
Habitat degradation and loss of landscape connectivity
General increase
High confidence depends on urbanization combined with fire
Type conversion to non-native grasses
Reduced habitat for shrubland species like the CA gnatcatcher that has lost nesting habitat to repeated fires
Unknown
More research needed
Plays a role in fire cycle
Longer dryness extending into Santa Ana Wind season may increase fires under dangerous fire weather conditions
Unknown
More research needed
Future decreases in CLCF may result in shrub cover decrease and exotic grass cover increase degrading coastal sage scrub
Future decreases in CLCF could increase shrub seedling mortality during summer
Disconnected habitats for species like the mountain lion leading to lack of gene flow and population declines
Summary Table: Ecological Impacts of Changing Conditions
March 2018
TABLE 2: Summary of biodiversity drivers and climate impacts on San Diego’s ecosystems. Examples are included as well as an assessment of the state of our knowledge about these impacts and management practices available to address each impact.
* Based on IPCC definitions of confidence
Availability of data/ info to understand ecological responses
Existing management options or strategies
Suggestions for future management, research or monitoring?
Low: strategic weather monitoring in complex topography and high gradient climatic settings and inconsistent information among species - need trend data
Habitat management for persistence, protection of regfugia, adaptation through connectivity or facilitated migration
Conduct trend monitoring for species of interest
Low: logistical and ethical issues for experimental studies of ecological response of fauna
Maintain adequate habitat to support populations that can persist. Provide connectivity for species to move to refugia.
Determine if analysis of existing data can provide insight into impacts on plant and animal populations. Model climate refugia and focus conservation efforts on those areas.
Monitoring of at-risk species and recovery efforts for those that have or can be hardest hit by spring drying.
Continuous long-term monitoring at a diversity of habitats.
The SWAMP includes targeted monitoring of streams. Existing focus on cataloguing changes to covered species and habitats.
Redesign of current monitoring plants to include indicator sites and species. Improved stream gauge monitoring.
Medium: Information from recent drought show vulnerabilities of a diversity of species. Thresholds that might trigger landscape changes are unknown.
Existing monitoring beyond rainfall tracking, is unknown
Climate-quality precipitation, wind, humidity, solar radiation and soil moisture observations in strategic locations and higher density array of precipitation gauges along topographic gradients in selected ecosystems in conjunction with habitat monitoring.
Medium: Information for some pests and pathogens are somewhat well studied, but potential for novel pathogens is unknown
Surveillance of known pests and pathogens in the region and use of earth detection and rapid response efforts to address outbreaks
Expand surveillance programs to include pathogens with high probability of reaching San Diego or with potential for significant impacts to humans or ecosystems.
High: Information on the effects of fragmentation on many spcies are known and many more are being researched to determine the population-level effects
Identification and preservation of connectivity across landscapes, including aquatic systems.
Low: insufficient long-term data to understand how a prolonged droughts over affect ecosystem structure
Medium: Monitoring data can be synthesized to examine impacts of large interannual precipitation variability by using monitoring data over the last 7-10 years
High: Existing data supports our understanding. The major unknown is degree of future population growth and land use change.
Coordinating of fire management with land management on conserved lands.
Identification of spatially-explicit linkage zones for functional connectivity. Linkages should be prioritized for conservation with multi-agency stakeholders and focus on land acquisition and mitigating barriers.
Increased efforts to track type conversion or areas at risk. Fire suppression and prevention efforts should be focused on these areas.
See fire
See fire
Same as fire
Medium: Knowledge can be gleaned from work in other regions of California (e.g. northern CA and the Channel Islands) but research linking to impact of CLCF to biodiversity is sparse.
Recent remote sensing work has made spatial CLCF data available, thus making investigating the effets of CLCF on San Diego ecosystems much more accessible.
Monitoring to determine if coastal plain with CLCF can act as a climate refugium.
8
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
TEMPERATURE AND TEMPERATURE EXTREMES IN THE SAN DIEGO REGION
by Megan K. Jennings, Kristen Guirguis, Dawn M. Lawson, Eric D. Stein, and Sula E. Vanderplank
S
an Diego County spans starkly different climate zones where desert conditions are found a short distance east of a mild coastal climate. The coastal zone is characterized by relatively cool days and mild nights. During summer, average daily maximum temperatures in the interior valleys are about 15°F hotter than at the coast. In some parts of the interior valleys average summer maximum temperatures exceed 95°F (35°C) while average coastal maximum temperatures are below 80°F (26.6°C). At night, the dry conditions in the interior valleys promote nighttime cooling, whereas coastal cloud marine layer and low clouds intercepts terrestrial radiation which keeps coastal temperatures mild.
Recent climate models project that, by the end of the 21st century, annual average temperatures will increase by about 4-6°F under the RCP 4.5 scenario, or 7-9°F under RCP 8.5 (Figure 4; Cayan et al. 2013, Pierce et al. 2013, Pachauri et al. 2014). Although there is still uncertainty about how individual species might respond to a warmer climate, observations from other settings suggest that warming will shift species to ranges higher in elevation and northward in latitude and shift flowering times and other phenological stages earlier in the year (Hughes 2000, Cayan et al. 2001, Walther et al. 2002, Parmesan and Yohe 2003).
FIGURE 4: Projected shifts in temperature over the annual cycle displayed as minimum and maximum temperatures under RCP 4.5 and RCP 8.5 in three future periods: 2006- 2039 (blue dotted line), 2040-2069 (brown dashed line), 2070-2100 (red solid line).
9
Temperature, particularly mean minimum temperature of the coldest month and mean maximum temperature of the warmest month, has been identified as a key factor in determining the distribution of shrubland community species (Figure 5; Franklin 1998, Riordan and Rundel 2009). Model projections for the coastal sage scrub vegetation types common in coastal San Diego County include large scale declines in species richness (Riordan and Rundel 2009). Increased air temperatures also result in higher water temperatures for streams and estuaries, affecting their biological communities, particularly in regions like San Diego where relatively shallow systems are more susceptible to heating. Many cold-water-dependent species may already be at the limit of their habitat ranges in the study area. Examples include the California newt (Taricha torosa), found only in stream segments with relatively persistent water. Range shifts may lead to changes in biotic interactions that can have synergistic effects that are important to consider (Russell et al. 2012), particularly when individual plants or vegetation communities are altered. Shifts in environmental conditions can change the availability and suitability of habitat for animal species, especially habitat specialists that rely on particular plant species or assemblages. These species may lose habitat, be forced to follow the shifting ranges of the plants they need, or both. Certain life history characteristics will make some
Temperature and Temperature Extremes FIGURE 5: Extent of suitable habitat for four species of manzanita (Arctostaphylos glandulosa ssp. glandulosa, A. g. ssp. adamsii, A. otayensis, and A. rainbowensis) in the San Diego region with respect to the distribution of maximum temperatures during the warmest months
species more susceptible to the negative effects of climatic variability than others. For short-lived plants, reproductive rates may be most impacted, whereas for animals, decreased survival and reproductive rates are expected under extreme climatic variability (Morris et al. 2008). In the San Diego region, this could be particularly significant for rare and federally listed species that are short-lived such as the Laguna Mountains skipper (Pyrgus ruralis lagunae) and Hermes copper butterfly (Lycanea hermes), or annual plants that are narrow endemics such as the San Diego thornmint (Acanthamintha ilicifolia). The impacts to some annual plant species may be buffered by longlived seed, such as the population of Orcutt’s spineflower (Chorizanthe orcuttiana) which was rediscovered on Point Loma after 20 years (Lawson unpublished data).
March 2018
34°0'N
33°30'N
33°0'N
U.S.
-
order Mexico B
32°30'N
Pacific Ocean
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community
Hot temperature extremes are also 118°0'W 117°30'W 117°0'W 116°30'W expected to increase (Gershunov and Average Tmax for Summer (degC) Manzanita species 1981-2010 Guirguis 2012, Gershunov et al. 2013). 45 ! Arctostaphylos glandulosa subsp. adamsii Background climate warming will 34 ! Arctostaphylos glandulosa subsp. crassifolia 0 5 10 20 Miles increase the frequency, duration, and 26 ! Arctostaphylos otayensis ! Arctostaphylos rainbowensis intensity of heat waves, as measured 14 0 12.5 25 50 Kilometers against historical thresholds. Climate model projections indicate that the thresholds for various species have been documented in number of heat wave days will likely increase by more Southern California. For the federally endangered arroyo than three-fold by 2050 and considerably more than toad (Anaxyrus californicus), estivation, or burrowing, that, especially under high greenhouse gas emissions, by is a common response among adults to avoid high 2100. These extreme events (i.e., heat waves) may exceed temperatures and desiccation during hot, dry summers physiological thresholds for temperature tolerance for (Ramirez 2003). However, because the species breeds in some species. Although there is far less evidence about relatively shallow, slow-moving streams, eggs or tadpoles the direct or indirect impacts on plants and animals than may be more susceptible to early heat waves (Perry et al. humans, animal populations are expected to have similar 2012) that can quickly raise the temperature in shallow responses to heat waves. Extreme temperatures can result water beyond lethal levels or cause premature drying of in direct mortality, particularly to more sensitive segments the stream. of populations such as young and old age classes with the former having a greater effect on population trends as Shifts in temperatures and temperature extremes may reproductive rates and survival to reproductive age may also result in altered timing of ecological phenomena like be limited or significantly reduced by these events. flowering, emergence of insects, and onset of breeding for
/
For the big-eared woodrat (Neotoma macrotis), habitat modeling suggest both winter minimum and summer maximum temperatures may severely limit suitability in the future (Lawson unpublished data). The in-stream environment is another location where temperature
many species. Over the last several decades, the arrival of migratory songbirds to breeding habitats and onset of nesting has trended earlier elsewhere in California (Macmynowski et al. 2007, Socolar et al. 2017). For many aquatic species, the onset of breeding is typically
10
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot 34°30'N
Potential Temperature Refugia Avg Tmax: May-Sept
70.88 - 72.50 72.51 - 75.00 75.01 - 77.50 77.51 - 80.00 80.01 - 82.50 82.51 - 85.00 85.01 - 87.50 87.51 - 90.00 90.01 - 92.50 Conserved Lands
34°0'N
Ecoregions
33°30'N
33°0'N
Pacific Ocean U.S.
-
order Mexico B
32°30'N
0
5
10
20 Miles
/
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © 0 contributors, 12.5 and25the GIS user community 50 Kilometers OpenStreetMap 117°30'W
117°0'W
116°30'W
FIGURE 6: Map of potential temperature refugia based on historic records of more localized temperatures as recorded at weather stations across the region. Larger circles indicate areas more likely to act as a temperature refugium.
triggered by warming temperatures that reach a minimum threshold. Advances in spring warming and other timing changes can trigger earlier emergence of insect larvae and more prolonged and extensive algal blooms, both of which can influence overall productivity of instream communities (Poff et al. 2002, Hamilton et al. 2008). Planning for refugia is an oft cited strategy for designing conservation and land management strategies that will be resilient to climate change. Coastal low clouds and fog may buffer warming along the coast, but in inland 11
regions, we can examine past climate records for potential temperature refugia. In Figure 6, we identify potential refugia where microclimates may provide some relief from shifting temperatures. These locations are based on averaged minimum temperature in the coldest period as well as maximum temperature during the warmest period between 1990 and 2015. Identifying such localscale temperature refugia may be beneficial for planning and management efforts.
Precipitation and Drought in San Diego County
March 2018
PRECIPITATION AND DROUGHT IN SAN DIEGO COUNTY
P
by Julie Kalansky, Dan Cayan, Dawn M. Lawson, Eric D. Stein, and David W. Pierce
lant and animal communities of San Diego County are adapted to thrive in highly variable climates. The Mediterranean-style climate is characterized by extreme intra and interannual variability in rainfall. Approximately 80% of rainfall occurs between November and April with the remaining months being hot and dry. In addition to this markedly seasonal structure, the year-to-year variability in Southern California is higher than anywhere else in the continental United States fluctuating between droughts, extremely wet years and periodic floods (Dettinger et al., 2011). The frequency and intensity of rare, extremely high precipitation events determine if a given year will be wet or dry. Large spatial variability adds to the complexity of the climate regime in the region. The mean annual precipitation ranges widely, between approximately 8-36 inches, with most differences resulting from topographic influences. Shrublands, the most common terrestrial community, use both drought avoidance (e.g., deciduous leaves and extensive root systems) and drought tolerance (e.g. stomatal control and post-fire germination) strategies to survive under these constantly changing conditions. Riparian communities rely on seasonal peak flows that can
vary by over 50 fold during the course of a year, and several hundred percent between years, to support breeding and rearing habitat. Periodic scouring flows are important to prevent senescence, clean spawning gravels, and import fresh sediment, and promote habitat complexity. By mid-21st century, climate model simulations indicate the number of dry days will increase, and the occasional periods of rain of higher intensity than current typical conditions. The driest 5 years (also driest 1, 3 and 7 years, not shown) in a 31-year moving window are projected to become drier, especially under the higher RCP 8.5 GHG scenario. The intensification of dry spells is driven by an increase in the number of individual dry years, shown in Figure 7 - Top. Exacerbating the increased dryness caused by changes in precipitation and temperatures are very likely to increase throughout the 21st century and would increase losses of moisture from the land surface (Cayan et al. 2010, Diffenbaugh et al. 2015, Ault et al. 2016). Extreme drought has the potential to change ecological community composition and structure at the landscape scale in part because drought operates at a larger spatial scale than other disturbances such as fire. In addition to shifting habitat suitability to favor deeper rooted and more drought tolerant species, drier conditions may increase susceptibility of plant communities to pests or pathogens. Combined with increased fire frequency, this may result in shifts to early successional and generalist species at the expense of endemic communities. For example, recently observed oak mortality is thought to be a result of drought-induced weakening combined with secondary attack by wood borers and ambrosia beetles (California Forest Pest Council 2015, Lawson et al. 2017a,b). Conversely, many of the annual
FIGURE 7: (Top) The percent of years in a 31year sliding window that are below the 20th and 5th percentile thresholds averaged from a set of 10 RCP 4.5 (blue) and 10 RCP 8.5 (red) climate change simulations. (Bottom) Departure from average of the driest 5-years in a 31-year sliding window for RCP 8.5 (right). The anomaly is based on the average driest 5 years within the historical period.
12
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot FIGURE 8: The percent change in spring (March-May) soil moisture relative to the historical global climate model runs from 1976-2005. The figures on the left are averaged during mid-century (2040-2069) and the figures on the right are averaged at the end of the century (2070-2100). Top figures are under the RCP 4.5 scenario and bottom are the RCP 8.5 scenario. Overlaid are species occurrence data of select rare, threatened, or endangered plants (Acanthomintha ilicifolia [San Diego thorn mint], Acmispon prostratus [Nuttall’s acmispon], Chloropyron maritimum [Salt march bird’s beak], Chorizanthe orcuttiana [San Diego spine flower], Monardella viminea [Willowy monardella]).
on arthropod populations, such as many reptiles and amphibians, may also be negatively impacted by the increases in drought.
plants common to San Diego County, such as some annual grasses and vernal pool species, may be more resilient to changes in precipitation patterns because of their natural adaptation to prolonged drought and variable climatic conditions. Effects on terrestrial animals would be mediated through changes in habitat. A study of four bird species during 2002 and 2003 indicate a strong response to drought. The wrentit (Chamaea fasciata), spotted towhee (Pipilo maculatus), California towhee (P. crissalis), and rufouscrowned sparrow (Aimophila ruficeps), are dependent on coastal sage scrub for habitat. A 2002 drought resulted in a significant decline in reproductive success with only a 1.8% success rate, attributed mainly to low arthropod food availability (Bolger et al., 2005). Although the research was specific to these species, other animals that are dependent 13
Another aspect of projected intensification of droughts is that global climate models (GCMs) indicate seasonal summer drought in Southern California may become more prolonged due to earlier drying in spring, warmer summers and increased dryness in fall. From the GCMs, spring precipitation decreases considerably, by approximately 20% during the mid-century and approximately 25% by the end of the century under RCP 8.5. Fall precipitation decreases by approximately 15% during midcentury and approximately 20% by the end of the century. Under RCP 8.5 the spring precipitation decline, combined with effects of warming, result in progressive declines in spring soil moisture, amounting to 10-15% decreases by late 21st century (Figure 8). The impacts of the change in hydroperiod will have immense effects on intermittent and ephemeral streams in terms of reduced richness and disruption of breeding and dispersal patterns of invertebrates, fish, and amphibians whose life histories are tuned to cues associated with seasonal flow and inundation patterns. Survival, growth, reproduction, and dispersal of aquatic species, such as stream invertebrates, fish, and amphibians would likely be affected by changes in flow patterns, earlier stream drying, and less frequent, but more extreme scouring high flow events. Secondary effects may occur due to proliferation of macroalgae (due to warmer, slower moving water) which can displace habitat and reduce oxygen due to eutrophication.
Precipitation and Drought in San Diego County
March 2018
! !! !! !! !! ! ! ! ! !!! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! !! ! ! ! ! !! ! !! ! ! ! ! ! ! ! !! ! !! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! !! !! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! !!! ! ! ! !! ! ! !! ! ! !! !!!! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! !! ! ! !! !!! ! ! ! ! ! ! ! !! !! ! ! !!! !! ! ! ! ! ! !! !! ! ! ! ! ! ! ! !! ! ! !! !! ! ! ! !! ! ! !! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !!!!! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! !! ! ! ! !! ! ! ! !! ! ! ! !!! ! !! ! !! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! !! ! !! !! ! ! ! !! ! ! ! ! !! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! !! ! !!!! !!! ! ! !! ! ! ! !! ! !! ! ! !! !! ! ! ! ! ! ! ! ! ! !!! ! !! ! ! !! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! !!! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! !! ! ! ! !!! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! !! !! !! ! ! !! ! ! !! ! ! ! !! ! ! !! ! ! ! !!! !!! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! !!!! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! !!!!! !! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! !! ! ! ! ! ! !!! ! ! ! ! !! ! ! ! ! ! ! !! ! !! !!!!! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! !! ! !! ! !! ! ! ! ! ! ! ! ! ! !! ! !! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !! ! !!!! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !!! ! ! ! ! ! ! !!! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! ! ! ! ! ! ! ! !! ! ! ! !! ! !! !! !! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !! ! ! !! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! ! ! ! !! ! !! ! ! ! !!!!! ! ! ! ! ! ! ! ! !! ! ! !!! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! !! ! ! ! ! ! ! !!! ! ! !! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! !! !! ! ! !! ! !! !! ! ! ! ! !!! ! !! ! ! !! !! !! ! ! !!!!! ! ! !! !! !! ! ! ! ! ! ! ! ! ! !! !! ! ! ! !! !! !! ! !!! ! ! !! !! ! ! ! ! ! ! !!! !! ! ! ! ! ! ! !! !! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! !!!!! !! ! ! ! ! ! ! ! ! ! !! !! ! ! ! o ! ! M eexx ii cc o !! ! UU ..!SS .. -- M !! !! ! ! ! ! ! !! ! ! ! ! !! ! !! ! !! !! ! ! !!! ! ! !! BBoo rr ddee rr !! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !
!
!
!
2040-2069, RCP RCP 4.5 4.5 2040-2069,
34°0'N
! ! ! !! !
!
!! ! ! !
! ! ! ! !! !! !
!
!! !! !! ! !! ! ! ! !!! ! ! ! ! ! ! ! ! !! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! !! !
!
2070-2100, RCP 4.5 !
! ! !
! !
33°0'N
! !
! ! ! ! !! !! ! !! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! !! ! ! !! ! ! !! ! ! ! ! ! !!!! ! !!! ! !! ! ! ! !!!! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! !! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! !! ! ! ! !! ! !! !! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! !!!! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !!! !! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! !!!! !! ! ! !! ! ! ! !! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! !! ! !! ! !! !! ! ! ! !! ! ! ! ! ! !! ! !! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! !! ! ! ! ! !! ! !! ! !!! ! ! ! ! !! ! !!! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! !! !! ! ! !! ! ! !! !! ! ! ! ! ! ! ! ! !! ! ! !!! !! ! ! ! ! !! ! ! !! ! ! ! ! ! !! ! ! ! ! ! ! !! !! !! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! !! !! !! ! !! !!! ! !! !! ! ! ! !! !! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! !!! !! ! ! ! ! ! ! ! !! ! ! ! ! !!!!! ! !! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! !!! ! ! ! ! ! ! ! ! !! ! ! !!! ! ! ! ! !! !! ! ! ! ! ! !! ! ! ! ! !! ! !! ! ! ! !! ! !!! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!!!! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! !! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! !!!! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! !!! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! !!! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! !! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !!! ! !! ! ! ! !! !! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! !! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! !! !!! !! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! !! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! !! ! !! ! ! ! ! ! ! !! ! ! ! ! ! !!! ! ! ! ! ! ! ! ! ! !! ! ! !! ! !! !! ! ! ! !! ! ! ! ! !! ! ! ! !!! ! ! !! ! ! !!! !! ! !! !! ! ! !!!!! ! ! ! !! !! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! !! ! ! ! !! ! !!! ! ! ! !! !! ! ! ! ! ! !!! ! !! ! ! ! !! ! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! !!! ! ! ! !! ! ! !!! ! ! ! ! ! !!!!! !! ! ! ! ! ! ! ! ! ! !! ! !! ! o ! ! ! M eexx ii cc o !! ! UU .. SS .. -- M !! !! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! !! !! ! ! ! !!! ! ! ! BBoo rr ddee rr !!! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !
!!! !! ! ! !
32°30'N
Sources: Esri, USGS, NOAA
Sources: Esri, USGS, NOAA
!! ! !
34°30'N!!
! ! !! !! !
!! !! !
!
! !! ! ! !!
! ! ! !! ! !
! ! ! ! !!
!! ! !
! !!
!
!
! ! !
! ! !! ! ! !! !
!
!
!!
! ! !!
!! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! !! ! !! !!! ! ! ! !! ! ! ! !!!! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! !! ! ! !! !!!! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! !! !! ! ! ! ! ! ! !! !! ! ! !! !! ! ! ! !! !! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!!! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! !!!! ! !! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! ! ! ! ! ! ! ! ! !!!! !! ! ! !! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! !! !!! ! ! ! !! ! ! ! ! ! ! !! ! ! !! ! ! ! ! !! ! ! ! ! ! ! ! !! ! !! ! ! !! !! ! ! ! ! !!! ! ! ! ! ! !! ! !! ! ! !! ! !! ! !! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! !! ! ! !! ! ! !! ! ! ! ! ! !! !! ! ! ! !! ! ! !!! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! !! ! !! !! ! !! ! !! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! !!! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! ! ! !! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! !!! ! ! ! ! ! ! !!! ! ! ! ! !! ! !! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !!! ! !! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! !! ! ! !! ! ! ! ! ! !! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !!! ! ! ! ! ! ! !! ! !! ! !! ! ! ! !!!! !! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! !!! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! ! ! ! ! !! !! ! ! !! !!! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! !! !!! !! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! !! ! ! !! ! ! ! ! ! !! ! ! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! !! !! ! !! ! !! !! !! ! ! !! ! !! ! ! ! ! !!! ! ! !! ! ! !! ! ! !! !! ! !! ! ! ! ! ! ! ! ! !! !! ! ! ! !! ! ! ! ! ! !! !! ! ! ! !! !! !! ! !!! ! ! !! !! ! ! !! ! ! ! !!! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! !!!!! !! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! o ! ! !! M eexx ii cc o ! !! !! ! UU!.. SS .. -- M ! ! !! ! !! ! ! ! ! !! !! !! ! ! ! !! ! ! ! ! ! !! !! BBoo rr ddee rr ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !
! !! !! ! ! !
!
Pacific Ocean
! !
! !
!! !! !! ! ! !! ! ! ! ! !!! ! ! ! ! ! ! ! ! !! !! ! ! ! ! !! ! ! ! ! !! ! ! ! ! !! ! ! ! !! !
!
!!! !! ! ! !
!
!! ! ! !
! ! !! ! !!
! !
!
! !!
! !
!
!
!
!! !! ! ! ! ! ! ! !! !
! ! ! ! ! !!! ! ! !! ! !
34°0'N!!
!
2040-2069, RCP 8.5
!! ! !! ! ! ! !! ! ! !!! ! ! ! ! !
!
32°30'N
FIGURE 9: Change in the average wettest day per year at the end of the century, 2070-2100. The top figures are shown as increase, and the bottom figures are shown as percent. The middle panel is under RCP 4.5 and right is under RCP 8.5. Overlay with select sensitive riparian species (Empidonax traillili extimus [SW willow flycatcher], Anaxyrus califoricus [arroyo toad], and Vireo bellii pusillus [least Bell’s vireo]).
Pacific Ocean
Pacific Ocean
33°0'N
!!
!
33°30'N
33°30'N
!
117°0'W
1976-2005 High : 40
Pacific Ocean
Low : 0
!
!!
117°30'W
Empidonax traillii extimus
!
Anaxyrus californicus
!
Vireo bellii pusillus San Diego Streams
The impacts of specific extreme events are most likely to affect intermittent, ephemeral and headwater streams, such as those common to the San Diego region (Dhungel et al. 2016). Habitat shifts may result in less stabilizing streamside vegetation and increased erosion changing the nature of allochthonous input potentially affecting net primary productivity (Archer and Predick 2008, Heino et al. 2009).
Future changes in the amount of annual precipitation are uncertain, however climate 117°0'W 116°30'W models generally agree the Assessment Extent precipitation variability will Additional Areas Considered increase in the future leading 0 12.5 25 50 Miles to more droughts and more extreme storms. The effects of 0 15 30 60 Kilometers a changing precipitation regime are highly uncertain because the difficulty in predicting future rainfall is compounded by uncertainty in how far the inherent resiliency of plants and animals adapted for dry, variable climates can accommodate changing conditions. A benefit of the naturally highly variable climate in the region is that it provides a laboratory to better understand how ecosystems will respond to the more variable climate projected in the future. Therefore, once long-term and continuous monitoring begins, it could provide a wealth of knowledge to understand how an even more variable climate would impact ecosystems in the region. Increased monitoring of sentinel sites and indicator species under programs such as the existing Multiple Species Conservation Plan and the Surface Water Ambient Monitoring Program will be critical for gaining the knowledge necessary to inform future management decisions. Sources: Esri, USGS, NOAA
Sensitive Riparian Species !
! ! ! ! !
! !! !! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! !! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! !! ! !! !! ! !! ! ! ! ! !!! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! !!! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! !!!! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !!! ! !! !! ! ! ! ! ! ! ! ! !! ! ! !! ! !! ! ! !! ! ! ! ! ! ! ! ! ! !!!! ! !! !! ! ! ! ! ! !! ! !! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! !! ! ! !! !! !! ! ! ! !! ! ! ! ! ! ! !! ! ! ! !! ! ! ! ! ! !! ! ! ! ! !! ! !! ! ! ! !! ! ! !! ! !!! ! ! ! !!! !!! ! ! ! !! ! ! ! ! !! !! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! !!! !! ! ! ! ! ! !! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! !! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! !!! !! !! ! !! !! ! !! !! ! ! ! ! ! !! !! ! ! ! !! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !!! ! ! ! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! !!!!! ! ! ! !! !! ! ! ! ! !! ! ! ! ! ! ! !! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !!!!! ! ! ! !! ! ! ! ! ! !! ! ! !! ! ! ! ! !! ! !! ! ! ! !! ! ! !! ! ! ! ! ! ! !! !! ! ! ! ! ! ! ! !! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! !! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! ! !! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! !!! ! ! ! ! ! ! ! ! ! !! !! ! ! !!! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! !! !! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! !! !! ! ! ! ! !! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! !!! ! !! ! !! ! ! !! ! ! ! ! ! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! ! ! ! ! !! !! ! ! ! ! !!!! ! ! ! ! !! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! !! ! ! ! !! !! !! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! !! ! ! ! ! ! ! !! ! ! ! ! ! !!! ! ! ! ! ! ! ! ! ! ! ! ! !! ! !! !! ! ! ! !! ! ! ! !! ! !! ! ! ! ! !!! ! ! ! ! ! ! ! !!! !! !! ! ! ! !!!! ! ! ! !! !! ! ! ! ! ! ! ! ! ! ! !! ! !! ! ! ! !! !! !!! ! ! !! ! !! !! ! ! ! ! ! ! !!! !! ! ! ! ! ! ! ! !! ! ! ! ! ! ! !! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! !! ! ! !! ! ! ! ! ! !!!!! !! ! ! ! ! ! ! ! ! !! ! !!! ! ! o ! ! M eexx ii cc o !! !! ! UU!.. SS .. -- M !! ! ! ! ! ! ! ! !! ! ! ! ! ! !! !! ! ! ! ! ! !! ! ! ! ! BBoo rr ddee rr !!! ! ! ! ! !! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! ! !
116°30'W
Average Wettest Day/Year (% change)
!
!!! !! ! !
Sources: Esri, USGS, NOAA 117°30'W
2070-2100, RCP 8.5
/
The drying that is projected with increased drought intensity and longer seasonal dry periods is offset with a projected increase in the wettest days, representing an increase in precipitation variability. At the end of the 21st century the wettest day of the year is projected to increase by 15-25% percent under RCP 4.5 and 20-30% under RCP 8.5 (Figure 9). Less frequent and occasionally stronger storms might result in more precipitation flushed out to the Pacific and less retained by the soil and biosphere. The future bioavailability of water as a result of this precipitation regime change is a knowledge gap. More research and improved modeling is needed to understand how changes in precipitation regimes will affect the bio-availability of water. Improved observations of soil moisture and stream gauges are needed to track changes and to evaluate and verify hydrological models.
14
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
SAN DIEGO WILDFIRES: DRIVERS OF CHANGE AND FUTURE OUTLOOK
by Alexandra D. Syphard, Alexander Gershunov, Dawn M. Lawson, Hiram Rivera-Huerta, Janin Guzman-Morales, and Megan K. Jennings
W
ildfire is one of the most important yet complex drivers of ecological function and biodiversity in San Diego County. As in other Mediterranean-type ecosystems, fire is a natural ecosystem process that shapes the structure and distribution of the region’s diverse plant communities, and in turn, the habitat for the region’s animal species. Nevertheless, its occurrence, distribution, and ecological and social impact have evolved substantially over time in response to both climatic and anthropogenic factors. Until recently, large, high-intensity fires occurred regularly but infrequently, largely due to the low frequency of natural ignition sources (Keeley 1982, Keeley and Syphard in press). In the 20th century, human population growth skyrocketed, and with it came massive expansion in urban development. As a result, human-caused ignitions have increased dramatically, both in number and in spatial extent, such that much of the landscape is burning at return intervals that are uncharacteristically short relative to pre-Euro-American settlement conditions (Figure 10; Safford and Van de Water 2014). Although the frequency and spatial pattern of fires have changed in response to population growth and urban expansion, the overall seasonality and severity, as well as the mean area
FIGURE 10: Map of study area with mean percent fire-return interval departure (Safford and Van de Water 2014). Values range from 67-99% less frequent fire than historic return intervals for a given vegetation type in dark green to 67-99% more frequent than historic intervals in red where repeated fires have burned in short succession.
15
burned, have remained relatively consistent (Keeley and Syphard 2016). Repeated wildfires, at intervals too short to allow recovery of native vegetation, facilitate the conversion of native shrublands to weedy annual grasses (Figure 11), forming a positive feedback cycle that could irreversibly eliminate some of the region’s rich biodiversity; evidence suggests
San Diego Wildfires: Drivers of Change and Future Outlook
March 2018
FIGURE 11: Examples of shrubland systems that are intact (left), degraded (center), and completely converted to non-native annual grassland vegetation type (right).
that widespread vegetation change has been occurring in recent decades (Syphard et al. in press). Characteristic bird, mammal, and insect communities mostly align with shrub cover, and thus the loss of shrub cover also represents a loss of those associated species (Diffendorfer et al. 2007). Wildfire also threatens human lives and property due to the growing interface between residential communities and wildland vegetation; thousands of structures have been destroyed in recent decades (Keeley et al. 2009, Syphard et al. 2012). Given the unique combination of factors that shape the modern-day fire regime in the region, the potential effect of climate change on fire is nuanced, and different than in other parts of the state. Despite strong relationships between seasonal fluctuations in temperature and precipitation with area burned in higher-elevation forested areas, in lower-elevation coastal and foothill-dominated regions, there has been little or no increase in fire activity associated with hotter and drier conditions, likely because seasonal conditions are already prime for extreme fire behavior every year (Keeley and Syphard 2015, 2016, 2017, Syphard et al. 2017). One climatic variable that has become important in recent years is high prior-year precipitation, likely due to its role in promoting higher abundance of annual grasses that, once dry, become extremely ignitionprone in the subsequent year (Littell et al. 2009, Pilliod et al. 2017, Syphard et al. 2017). The climatic causes of Southern California's unique wildfire regime are the Mediterranean climate with its warm dry summers and the dry, hot and gusty Santa Ana winds, whose season starts in the fall, typically before the first rainstorms of winter. Given that fire activity is predominantly a weather-driven phenomenon, fuel age is not a limiting factor in area burned, as evidenced by the sometimes extraordinarily short intervals that occur between fires (Moritz 2003, Keeley et al. 2004, Moritz et al. 2004, Keeley and Zedler 2009, Price et al. 2012). As such, mechanical fuel treatments and prescription burning in non-forested parts of the landscape play a limited role in reducing area burned, and come at a substantial ecological cost (Syphard et al. 2011, 2012, Penman et al. 2014). As our climate continues to warm, rainstorms will become less frequent in Southern California, particularly so in
the fall and spring, while rare extreme rainfall events will produce more precipitation. Moreover, with less frequent but more extreme rainfall, year-to-year precipitation becomes more volatile. The recent years of historic drought (2012-2016) followed by extremely wet winter 2017 and a bone-dry (record-dry, in fact) fall and early winter, is an example of such volatility, which we expect to see more of in the future. In addition, more frequent, longer, or more intense multi-year droughts could also increase the number of large fires in the region by increasing the proportion of dead fuels in a stand (Figure 12; Keeley and Zedler 2009). Starting in October, but peaking in December and January, Santa Ana winds fan Southern California's most catastrophic wildfires. Santa Ana winds will likely become warmer with climate change, increasing their desiccating potential (Hughes et al. 2011). Also, due to the changing precipitation regime, vegetation will more often remain dry into the traditional wet season when Santa Ana winds peak, lengthening the fire season of Southern California from fall into winter and even spring. The most recent hot and fiery December (2017) {and extreme precipitation from the first significant storm in winter (January 2018) causing mudslides on fire-scarred slopes,} is a perfect example of conditions we expect to occur more frequently in the future. In San Diego County, fire activity is significantly limited by ignitions. That is, despite the fact that Santa Ana winds and extreme fire-weather create ideal fire conditions every year, a resulting large fire will only occur if an ignition coincides in space and time with a wind-driven weather event. More than 95% of the ignitions are caused by humans (Syphard et al. 2007); and because highly flammable shrublands and grasslands are closely juxtaposed with human habitations, fire regimes are and will continue to be most strongly controlled by anthropogenic impacts. Studies show that ignition patterns are non-random in San Diego County; thus, prevention strategies could be customized to target the locations, causes, and timing of the most catastrophic events (Syphard and Keeley 2015). Housing development patterns and proximity to human infrastructure like roads are also significant correlates of fire frequency and area burned, with the highest levels 16
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
2040-2069, RCP 8.5
2070-2100, RCP 4.5
2070-2100, RCP 8.5
34°30'N
34°0'N
33°30'N
33°0'N
S .. U U .. S
32°30'N
M ee xx ii cc oo -- M B B oo rr dd ee rr
Pacific Ocean
S .. U U .. S
117°30'W
117°0'W
116°30'W
% Change in Moisture Deficit High : 20 Low : 0
S .. U U .. S
Pacific Ocean Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community
32°0'N
M ee xx ii cc oo -- M B B oo rr dd ee rr
Pacific Ocean Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community 117°30'W
M ee xx ii cc oo -- M B B oo rr dd ee rr
117°0'W
117°30'W
116°30'W
Shrubland Assessment Extent Additional Areas Considered
0 0
20 40
40
117°0'W
80 Miles 80
116°30'W
/
160 Kilometers
FIGURE 12: Map of climatic water deficit (CWD) in the San Diego region and shrubland vegetation types, where a lack of available moisture during extended droughts is most likely to result in vegetation dieback that will greatly increase fire risk.
of fire activity occurring at low-to-intermediate levels of development which is also where most houses are destroyed by wildfire (Keeley 2005, Syphard et al. 2007, 2009, 2012, Archibald et al. 2010, Mann et al. 2016). The reason for this nonlinear relationship between fire activity and housing density is that, especially in places where most fires are human-caused, there are few people in remote landscapes to start fires, and there is little available fuel to burn in intensely developed areas. At low- to intermediatehousing density, houses are generally more exposed to wildfire, and dispersed housing is more challenging for firefighters to defend (Gude et al. 2013). Research has shown that land use decision-making, either via zoning for housing growth, or through the prioritization of where to purchase private land for conservation, could significantly reduce not only fire risk to humans, but also result in better ecological outcomes (Syphard et al. 2013, 2016, Butsic et al. 2017). The northern portion of the state of Baja California contains similar species and ecosystems as those in San Diego County and thus can be used to contrast the impact of land use on fire regimes (Ojeda-Revah and EspejelCarbajal 2008). Significant vegetation changes have 17
occurred over the last 150 years, in part due to population increases in urban areas, the migration of people to the border zone, and industrial and tourist activities that consume large quantities of water and energy. The state of Baja California has one of the highest incidences of forest fires in Mexico (Sepúlveda-Betancourt et al. 1999). While the causes of these fires are diverse, human activity has been the primary ignition source in recent years, with most incidences of forest fires documented close to urban areas and along roads (Minnich et al. 1993, DelgadilloRodriguez 1998, Rodríguez-Trejo et al. 2011, CONAFOR 2015). In the montane regions of Baja California, in the Sierra de Juárez and the Sierra San Pedro Mártir, natural lightning ignition is common during summer. As we move into the future, extended drought that happens to coincide with Santa Ana winds may lead to increased potential for out-of-season large-fire events. If combined with increasing human-caused ignitions associated with continued urban development, or further type conversion from woody shrubs to flammable herbaceous vegetation, some challenging management decisions will need to be made to allow people and fire to coexist while maintaining the county’s natural heritage.
Impacts and Influences of CLCF on Biodiversity in San Diego
March 2018
IMPACTS AND INFLUENCES OF COASTAL LOW CLOUDS AND FOG ON BIODIVERSITY IN SAN DIEGO
by Dawn M. Lawson, Rachel E.S. Clemesha, Sula E. Vanderplank, Alexander Gershunov, and Dan Cayan
S
an Diego’s Mediterranean climate is characterized by a regular summer drought which, along the coast, can be offset by moisture and shading from coastal low clouds and fog (CLCF) (Figure 13). The commonly used local terms “May Gray” and “June Gloom” attest to the seasonally persistent nature and horizontally uniform appearance of these stratiform (“layer”) clouds. The blanket-like clouds reduce daytime maximum temperatures and when fog occurs (i.e., the cloud base meets Earth’s surface), provide an incremental moisture source. CLCF occurrence responds to a combination of global and regional climate features. Additionally, at the local scale, the inland penetration of these low level marine clouds is limited by distance from the coast and topography. Figure 14 shows the long-term summer average of daily CLCF derived from a satellite record. Within 10 miles (16.5 km) of the coast in San Diego County, low clouds occur more than 30% of each summer day on average. For example, in La Jolla on the coast, CLCF is present about 45% of the time on average for May – September, while less than 30 miles inland of La Jolla this value drops to about 15%. Through reducing solar input, CLCF lowers daytime maximum
temperatures. Thus, if CLCF were to change under climate change, its shading effects upon the modulation of daytime temperatures may be altered. The low cloud cover also modulates heat waves at the coast (Clemesha et al. 2017). A striking recent example occurred on June 20, 2017; during all-time record breaking heat in the San Diego County deserts (reaching 124°F), coastal Del Mar was almost 60 °F cooler. The inland extent of CLCF varies seasonally with a wider swath of San Diego consistently impacted by low clouds in May (Figure 15) and June (the zone covered 30% of the time reaches over 20 miles inland) and, as the summer proceeds, the low cloud cover contracts to the coast. The farthest inland extent of CLCF occurs in the early morning and the cloud deck typically recedes towards the coast later in the day due to daytime warming, drying and mixing processes. Observational records exhibit declines in California CLCF. Johnstone et al. (2010) inferred a 33% reduction in fog for northern California over the last century, but this reduction was not necessarily driven by anthropogenic climate change and may be attributed to natural atmospheric variability (Johnstone and
Figure 13: Fog adapted life forms, Agave sebastiana (lower left) and Pinus radiata var. cedrosensis (upper left). Photo credit: Sula Vanderplank
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot 34°0'N
Mantua 2014). Although observations of declines in southern California fog have been linked to urban warming (Williams et al. 2015), the decreasing trends have not been linked to anthropogenic greenhouse gas induced climate change with certainty. How will CLCF along the San Diego County coast respond to climate change? Definitive answers await more research and continued observations, but it is possible to speculate how some of the major atmospheric and ocean drivers of CLCF (e.g., Schwartz 2015) may change. Thus far, coastal California observations and climate model simulations of marine low cloud cover provide more evidence for future decreases than increases in CLCF. Conversely, theory suggests that the widening subtropical subsidence zone could cause the CLCF season to lengthen. Although the uncertainty in projected changes in CLCF is high, there is much more certainty in projected warming and through their effects on shading and cooling, CLCF, if not substantially reduced, could buffer these warming effects (Williams et al. 2015b, Fischer et al. 2016).
Coastal Low Cloudiness and Fog (CLCF) 1996 - 2014 May - September Daily Mean High : 50 Low : 0
33°30'N
Diegan CSS Riversidian CSS Venturan CSS Assessment Extent
33°0'N
U.S.
- Mexico Border
32°30'N
32°0'N
31°30'N
Pacific Ocean 31°0'N
30°30'N
30°0'N
/
0
15
30
60 Miles
0
25
50
100 Kilometers
29°30'N
118°0'W
117°30'W
117°0'W
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community 116°30'W
116°0'W
115°30'W
115°0'W
FIGURE 14: Average summer (May-September) coastal low clouds and fog. Coastal
sage scrub (CSS) data from Axelrod 1978. Through effects on water balance, low clouds and fog are important drivers of species dynamics and ecosystem function (Dawson 1998, D’Antonio et al. 2002, Fog drip supports a diverse range of taxa including Vasey et al. 2012, Fischer et al. 2016). In arid systems, plants, animals and microbes (Manzoni et al. 2012) and low clouds and fog during the regular dry season or ecosystem processes including nutrient mineralization prolonged drought can be particularly influential to and carbon cycling (Carbone et al. 2013). In addition to ecological communities due to their contribution to the fog drip, direct foliar uptake of fog water is important even hydrological regime and effects on ambient temperature where fog water is insufficient to change soil moisture when moisture is most limiting (Breshears et al. 2008, (Breshears et al. 2008). Shading reduces solar input and Fischer et al. 2009). CLCF influences the water budget thus thermal loading and ultimately evapotranspirative by water addition through uptake of fog drip by shallow stress on plants (Fischer et al. 2009) and heat stress on roots, foliar uptake of fog water and reduction in water animals (Henschel and Seely 2008). loss by shading.
19
Impacts and Influences of CLCF on Biodiversity in San Diego 34°0'N
March 2018
Coastal Low Cloudiness and Fog (CLCF) 1996 - 2013 May Average High : 50 Low : 0
33°30'N
!
Ceanothus verrucosus Assessment Extent
33°0'N
- Mexico Border
U.S. ! 32°30'N
!
! !!! ! !! ! ! !! ! ! !
32°0'N
! !
!!!
! ! ! !!
31°30'N
!
!
! ! !! !! ! ! ! !
!
Pacific Ocean
!
31°0'N
! !
!!!
!
!! 30°30'N
! ! !!
!
30°0'N
Ceanothus verrucosus
/
0
15
30
60 Miles
0
25
50
100 Kilometers
29°30'N
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community
season (Burgess and Dawson 2004, Fischer et al. 2016, Oladi et al. 2017). Further, CLCF can have significant effects on plant demographics including survival, growth and consequent recruitment to larger size classes, reproduction, and overall population size (Baguskas et al. 2014, Baguskas et al. 2016, Allen et al. 2010, Corbin and D’Antonio 2004). A number of species are limited to areas with CLCF including the narrow range endemic wart-stemmed ceanothus (Ceanothus verrucosus) (Figure 15). Based on physiological and biogeographical evidence this restricted range may be due to the effect of CLCF on winter low temperatures (Lawson et al. 2010). High floristic diversity in both coastal sage scrub and maritime chaparral has been linked to CLCF (Axelrod 1978, Vasey et al. 2014). In coastal sage scrub this is reflected in the diversity of the three coastal sage subtypes within the study region where the coastal sub-types Diegan and Venturan have higher diversity than the inland Riversidian Scrub type (Figure 14).
Less is known about the effects of CLCF on fauna, but a review of the literature reveals FIGURE 15: Distribution of wart-stemmed ceanothus (Ceanothus verrucosus) and May longterm mean CLCF. Wart-stemmed ceanothus is a highly visible component of chaparral collection of aerosolized water when flowering around February of each year (inset picture). Distrubution data from San by a number of different Diego Natural History Museum (2017), California Department of Fish and Wildlife (2017), mechanisms and reduction of Lawson (2009). heat stress, and shows a wide range of effects from flight The effects of CLCF on plants are varied and include behavior in birds, to timing of nesting, nesting success, phenology, productivity, and demographics. Vanderplank and behavior in different taxa. and Ezcurra (2015) showed that coastal sites in the Individual species’ ability and effectiveness at utilizing fog California Floristic Province (CFP) of Baja California water is highly variable (Emery and Lesage 2015) with with a stronger influence of CLCF showed lower variances many trade-offs. This combined with high spatial and in timing of flowering than sites further inland. While temporal variation in the presence and intensity of CLCF there are trade-offs in light that supports photosynthesis results in a complex web of effects across the landscape. and shade that reduces evapotranspirative stress, a This variation influences interspecific interactions and number of studies have found higher growth rates in species distributions, species assemblages, and ultimately woody species that experience CLCF during the dry biodiversity (Fischer et al. 2009). 118°0'W
117°30'W
117°0'W
116°30'W
116°0'W
115°30'W
115°0'W
20
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
CONSERVATION AND MANAGEMENT FOR SAN DIEGO'S CHANGING CLIMATE
by Megan K. Jennings, Amber D. Pairis, John M. Randall, Dawn M. Lawson, Eric D. Stein, Shasta Gaughen, Udara Abeysekera, and Horacio de la Cueva
photo by Lisa Cox / USFWS
S
outhern California is a biodiversity hotspot situated in a highly urbanized landscape with a growing population. The most immediate threats to the region’s ecosystems and rich biodiversity are urbanization, land use change, and changing water management practices. However, climate change will act synergistically to exacerbate existing stressors and bring new impacts to a landscape already compromised by habitat loss and fragmentation. San Diego County has a long history
of landscape-scale conservation and management, yet current management paradigms are not necessarily conducive to addressing and minimizing climate impacts. In addition, management goals and approaches that are required to address near-term, regulatory requirements for single-species management may hamper the ability to build resilience to climate change and increased climate variability into the future.
NCCP Planning Areas Stage Implementation Planning Assessment Extent Additional Areas Considered 34°0'N
OC Coastal OC Transportation Authority
Western Riverside MSHCP
OC Southern 33°30'N
SD North County MSCP SD County MHCP SD East County MSCP
33°0'N
SD County MSCP SDGE Subregional
Pacific Ocean
SD Water Authority
U.S.
- Mexico Border
32°30'N
0 4.5 9
18 Miles
/
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © 0 10 20 40 Kilometers OpenStreetMap contributors, and the GIS user community 118°0'W
117°30'W
117°0'W
116°30'W
Since the mid-1990s, most new land preservation efforts in San Diego County have resulted from efforts to develop regional conservation networks through federal Habitat Conservation Plans (HCPs) and state Natural Community Conservation Program (NCCP) Plans (Figure 16). The unifying theme in these conservation planning efforts in San Diego County, and across much of the West, has been protection of the large number of state and federally protected species in these ecosystems. This approach has conserved lands with habitat for listed species which has also served to benefit populations of many other species. These protected lands form the foundation from which a regional network or series of networks can be built. Such a network, rather than isolated preserves, will be necessary to strengthen the region's ecosystems' ability to resist the impacts of climate change in the short-term (decades), and to ensure the region’s ecosystems can accommodate and transform in the face of continuing climate change over the longterm (multiple decades and centuries). Climate change projections make it clear, however, that more will need to be done to improve resilience and adaptive capacity to the threats and stressors while also FIGURE 16: Map of NCCP and HCP planning areas. Completed plans that are in the implementation phase are shaded green. Plans that are in progress are identified with gray shading.
Conservation and Management for San Diego's Changing Climate
March 2018
34°0'N
33°30'N
33°0'N
32°30'N
U.S.
Pacific Ocean
- Mexico Border
Sources: Esri, USGS, NOAA, Esri, HERE, DeLorme, MapmyIndia, © OpenStreetMap contributors, and the GIS user community 118°0'W
117°30'W
117°0'W
Statewide Missing Linkages San Diego's Highway 67 Connectivity Planning South Coast Missing Linkages California Essential Habitat Connectivity Areas
116°30'W
Conserved Lands Assessment Extent 0 0
5 10
10 20
/
20 Miles
40 Kilometers
FIGURE 17: Map of existing connectivity plans for the San Diego region. Conserved lands are depicted in gray. Green sticks represent proposed linkage zones from the Statewide Missing Linkages Project (Penrod et al. 2001). Spatiallyexplicit corridors mapped in yellow are the South Coast Missing Linkages Project (South Coast Wildlands 2008), brown are California Essential Habitat Connectivity Plan linkages (Spencer et al. 2010), and blue for San Diego’s Highway 67 Connectivity Plan (Jennings and Zeller 2017).
22
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
mitigating those impacts. Increasing the attention given to maintaining functional diversity at the community or ecosystem level will also be necessary. Integrating climate smart conservation strategies into planning and management activities will help facilitate adaptation, or transformation, of those communities to the greater changes in climate expected over the long term. Management approaches that allow flexibility and target the three categories of adaptation — resistance, accommodation, and transformation (Fisichelli et al. 2016) — are key to facilitating climate adaptation in natural systems. To promote resistance, we may choose to intensively manage to retain certain species or systems although the climate conditions are no longer suitable habitat for the species or system such as high profile species with isolated populations, like Cuyamaca cypress (Hesperocyparis stephensonii) or Tecate cypress (Hesperocyparis forbesii). To both resist and accommodate change in natural ecosystems management efforts may focus on ameliorating compounding stressors that may reduce resilience of populations and communities. For example, habitat connectivity (Figure 17) is essential to climate-smart landscape strategies (Heller and Zavaleta 2009) and strengthens ecosystem resilience to
additional stressors such as habitat fragmentation (Beier and Gregory 2012), and other disturbances (Noss 1991, Hilty et al. 2006). Finally, at either preserve or regional management levels, we may choose to guide systems in their transformation to novel states that can be maintained and persist on their own. This management approach requires careful consideration of potential future states and a thoughtful process for setting goals and management targets. Adaptive management and an active monitoring program to inform it will be critical to the success of managing for altered states. For any of the above strategies, adaptation and scenario planning are the primary approaches to facilitate the preservation of natural systems under uncertain and likely increasing climate variability. Adaptation planning is the process of assessing the risks and opportunities in a changing climate and taking actions to address climate change impacts by targeting those risks and leveraging the opportunities (Füssel 2007). Given that the general trajectories of climate change projected for the region are known (i.e., hotter, drier, more fires, less water), these adaptation planning efforts should begin without delay. This would involve identifying regions, habitats, and species that are conducive to supporting
TABLE 3: The key knowledge and information gaps in San Diego's preserve system that need to be filled and targeted with adaptation and scenario planning A cohesive strategy to understanding how species and watersheds will respond to the new projected precipitation regime. Spatially explicit landscape linkages designed at the regional level that provide functional connectivity under shifting climate regimes and increased urbanization. A connectivity plan and linkage design that focuses on cross-border connectivity and addresses the challenge of facilitating movement and migration for species across fenced sections of the international border. Defined thresholds or triggers for changes in management action and monitoring programs designed to deliver the necessary data to respond accordingly. Identification of the elements of San Diego's ecosystems that make them more or less accomodating to change. Management actions can then preserve and promote those elements that support resilience.
resistance, accommodation, and transformation and focusing planning strategies on these targets accordingly. Scenario planning is a type of adaptation planning focused on the process of identifying several plausible futures and exploring the consequences of a management or conservation decision in each of those scenarios. Scenario planning offers a framework for deciding on when, how, and where to act in an uncertain future (Peterson et al. 2003) and is particularly useful in informing adaptation strategies because individual climate event timelines are difficult to predict. The spatial and temporal scales at which climate impacts 23
must be considered to build resilience into our natural systems require landscape-scale planning that is best addressed in a cooperative, cross-jurisdictional approach. Long-term monitoring and adaptive management will be critical to managing species and ecosystems into the future, and adaptation and scenario planning will also play a role. In light of projected growing impacts of climate change, it is likely that management goals may warrant re-evaluation, recognizing that managing for the near-term, particularly single-species management, may hamper abilities to build resilience into vulnerable ecosystems (Boitani et al. 2007).
Conclusions and Future Directions
March 2018
CONCLUSIONS AND FUTURE DIRECTIONS
S
by Amber D. Pairis, Udara Abeysekera, Julie Kalansky, Dan Cayan, and Megan K. Jennings
an Diego County is part of a biologically diverse and unique landscape that will be impacted in multifold ways due to current and future climatic variability (Table 2). This assessment serves as an important first step in understanding the state of the science which is critical to evaluating the vulnerability of systems, communities, and populations. Conducting the assessment has provided a summary of a wealth of known information, and a better appreciation of the large number of unknowns that will impact the region under a changing climate. In addition, we have highlighted the information needed to move
forward with management and decision-making. While there is still uncertainty about exactly how some of these changes will play out across the landscape, the findings from this assessment indicate enough knowledge exists to offer insights into managing natural resources throughout the ecoregion and across jurisdictional boundaries in the face of a changing climate. The characteristics that make San Diego unique with respect to climate and ecosystems include its remarkable variability of precipitation, coastal low clouds and fog, the region’s human population and associated development,
FIGURE18: Cross-cutting issues and impacts on ecosystems and biodiversity
24
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
TABLE 4 Climate Ecological Monitoring Monitoring
Summary of knowledge gaps that are identified throughout the report. The category that the gap best fits under is highlighted. Analyses using existing data
Collaborations
TARGETED ACTIONS TO FILL KNOWLEDGE GAPS Enhance our understanding of the interaction between climate, habitat elements, populations, and interspecific interactions through modeling of biotic interactions for a broader range of the region’s species. Build enhanced spatial resolution of temperature observations to inform ecological modeling and to determine key elements of local refugia (e.g., extent, location). Study the impacts of temperature shifts, particularly temperature extremes, on demographic parameters and population dynamics by tracking populations and species with range limits within or adjacent to the region. Utilize phenology and population trend monitoring to identify when asynchrony is likely to lead to cascading ecological impacts (e.g., timing of resource availability, loss of pollination services). Evaluate how changes in precipitation regime will affect bioavailability of water. Improved observational soil moisture and hydrologic data in the region can be used to refine and validate regional hydrological modeling, which can then be used to examine future impacts. Identify drought thresholds that can lead to structural changes in regional ecosystems as specific functional groups are more severely impacted. This includes field studies of the potential for drought to impede recovery of native shrublands after disturbance, particularly fire. Gather data to evaluate the effects of an extended and more extreme dry season over several years on individual species as well as ecosystem structure and function. Generate a cost-benefit analysis and prioritization of where and when to conduct fire management strategies to optimize fire-risk reduction and biodiversity conservation. Assess the role of extended drought in vegetation die-back, and how that may lead to increased area burned under Santa Ana wind conditions. Investigate the interaction between drought and vegetation-type conversion through quantification of the extent and rate of conversion across the region, and the primary drivers of this vegetation change. Improve tracking and availability of data on ignition sources of wildland fires to evaluate unknown sources and better design prevention programs. One area of needed research is the weather conditions under which powerline-caused fires are most likely to occur and how effective vegetation clearing is for mitigating that risk. Gather data on species’ responses to low clouds and fog. Studies of individual species or groups of organisms will greatly inform our understanding of local ecosystem dynamics. Encourage land managers to incorporate CLCF into management planning and adaptive management (e.g., restoration efforts, out-plantings and projecting natural disturbance and project effects on conservation targets) by using spatial data sets derived from remote sensing. Establish a cohesive strategy to monitor how species and watersheds will respond to the new projected climatic conditions. Delineate and conserve spatially-explicit landscape linkages at the regional level, including across the U.S-Mexico border. Linkages should provide for functional connectivity under shifting climate regimes and increased urbanization. These linkages should then be integrated into reserve design and regional planning and management. Define thresholds or triggers for changes in management action and refine or design monitoring programs to deliver the necessary data to respond accordingly. Identify the elements of San Diego’s ecosystems that make them more or less resilient to change. Target management actions that preserve and promote those elements that support resilience (e.g., restoration using palettes of plant species resistant to increased temperatures and variable precipitation). Make monitoring data and the interpretation of those data readily available to decision makers and the public to encourage engagement and ongoing dialogue on adaptive management.
Conclusion and Future Directions
March 2018
This review, combining the knowledge of climatologists and ecologists with regional expertise and embedded in regional conservation and planning efforts, is a demonstration of what boundary spanning organizations and projects can do to inform actions that advance realistic climate adaptation planning."
and a histor y of conservation planning and action to protect the region’s rich biodiversity. How these key features interact to either exacerbate or dampen impacts of climatic shifts and non-climate stressors has been woven throughout the report. Here, we highlight the interactions among these key characteristics, projected climate shifts, associated ecological impacts, and the ecological variables that are likely to be affected (Figure 18). We have also broadly summarized the knowledge and monitoring gaps that have been identified throughout the report (Table 4). In general, these questions and research gaps cannot be fully addressed by conducting experiments or mobilizing to collect data during indivdual climate events. Instead, ongoing monitoring to gather baseline and trend data for comparison can allow for analyses when environmental conditions create the opportunity to learn from natural experiments as they arise. The distinction between new monitoring and new research can become blurred as monitoring supports and informs research. As such, we do not try to separate these two gaps in the table. Instead, we identify the category (or categories) that the research falls under: more ecological monitoring, more climate monitoring, research using existing data, and need to improve collaborations. All of the gaps would benefit from enhancements in all categories, but by identifying the most critical, we hope to provide a path forward. Numerous scientists and natural resource entities are working to address different forms of climate impacts on natural resources in the San Diego region. However, this science does not always reach the communities that are the most affected by these impacts. This means there may be
missed opportunities for the public to understand the need for climate action and/or to build trust in science coming from local researchers. The continued involvement of researchers, managers, and community members in organizations like the Climate Science Alliance is vital in developing the co-produced knowledge that is transferable and actionable to decision makers and managers. This review, combining the knowledge of climatologists and ecologists with regional expertise and embedded in regional conservation and planning efforts, is a demonstration of what boundary spanning organizations and projects can do to inform actions that advance realistic climate adaptation planning. In this assessment, researchers have not limited themselves to the role of producing knowledge but instead are intent on working hand-in-hand with other disciplines and professions, and within communities where citizens will have a real stake in the welfare of the ecosystems that contribute richly to our society, economy, and values. Recognizing that people are at the center of our climate adaptation decisions requires that research needs to be actionable and delivered in a timely manner. Actionable science, or science that is intentionally created to serve society (Palmer 2012), includes activities that take into account the existing regulatory, economic, legal, and social context that decision makers work within. Most decision makers do not have the luxury to wait for data to be published and instead need findings communicated in real-time to the greatest extent possible. This kind of dialogue can help encourage proactive and adaptive management and help to leverage and coordinate regionally specific adaptation projects.
26
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
KEY POINTS • San Diego County is part of a biologically diverse and unique landscape that will be impacted in multifold ways due to current and future climatic variability.
• This assessment of the state of the science, is critical to understanding the vulnerability of systems, and allowing partners to take stock of the state of knowledge about potential climate impacts at the regional level. • Climate warming superimposed upon the pronounced spatially-varying temperature in the San Diego region will likely be associated with range shifts for many species resulting in novel community assemblages and biotic interactions. • More frequent and more intense heat waves may disproportionately affect younger age classes and reduce reproductive and survival rates of species sensitive to temperature extremes. Warming temperatures may also create phenological mismatches. • The region’s precipitation regime is projected to become more variable with more dry days and more dry years. However, the few extremely heavy precipitation events, increased over historical levels could result in increased flooding and occasional wet years.
• Drought may occur more frequently due to increased occurrence of dry days and could
intensify because of warmer temperatures. Since drought disproportionately affects some species, these projected changes may cause structural changes to ecosystems.
• Annually, the occurrence of Santa Ana winds during increasingly dry fall months would create ideal fire conditions. Longer dry spells and decreased precipitation in fall may extend fire season into the winter, increasing the risk of Santa Ana wind-driven fires. Regardless of climatic shifts, people will remain the major driver of fires in San Diego.
• Coastal low clouds and fog buffer warming and drying along the coast through shading
and cooling. Although these marine stratus clouds will remain a presence, future changes in this phenomenon are uncertain, so the degree to which this will ameliorate the impacts of warming and drying is unknown.
Photo of San Miguel Mountain by Joanna Gilkeson/USFWS
Key Points
March 2018
• San Diego is a biologically diverse region that has been the focus of more than 20 years of conservation planning, investment, and innovation. However, much remains to be done to complete a network of protected habitats that is necessary to ensure the survival of the region’s biodiversity, and through allowing for adaptability to future climate change. • The spatial and temporal scales at which climate impacts must be considered to build resilience into natural systems require the integration of complementary approaches at multiple scales. Landscape-scale planning can build on single-species approaches that have historically driven conservation action in the region. • Building resilience into San Diego’s ecosystems is a challenge to be addressed in a crossjurisdictional, multidisciplinary fashion by scientists, policy-makers, planners, land managers, and the broader conservation community. • Conservation management goals and approaches need to be updated to balance addressing near-term, regulatory requirements for single-species management with landscape-level actions necessary to build resilience and adaptability for the future under climate change.
• Long-term monitoring and adaptive management will be critical to managing species and ecosystems into the future. This includes adaptation and scenario planning.
• Future research and planning to build resilience to climate impacts will need to focus on identifying and protecting climate refugia, understanding weather, climate, and hydrologic characteristics along protected corridors, and stronger and sustained collaborations of science, planning, policy, and implementation communities.
• Boundary spanning organizations like the Climate Science Alliance can advance climate
adaptation planning by providing opportunities to translate science into actions, forge new and expanded partnerships, and catalyze innovative, large-scale actions needed to build long-term resilience to climate change.
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
MEET THE SCIENTISTS The Authors 1
The Contributors
2
5
8
3
6
12
16
7
10
9
14
4
15
17
18
11
13
19
20
1. Megan K. Jennings, Ph.D
11. John M. Randall, Ph.D
Conservation Ecologist and Co-Director of San Diego State University's Institute for Ecological Monitoring and Management
Lead Scientist for the Nature Conservancy's California Chapter
2. Dan Cayan, Ph.D
Research Meteorologist at Scripps Institution of Oceanography, UC San Diego
3. Julie Kalansky, Ph.D
Climate Scientist and Program Manager of California Nevada Climate Application Program at Scripps Institution of Oceanography
4. Amber D. Pairis, Ph.D
Director of the Climate Science Alliance
5. Dawn M. Lawson, Ph.D
Plant Ecologist working primarily with the Navy and Marine Corps in southern California
6. Alexandra D. Syphard, Ph.D
Senior Research Ecologist with the Conservation Biology Institute
7. Udara Abeysekera
Project Lead for Conservation Planning at the Climate Science Alliance
8. Rachel E.S. Clemesha, Ph.D
Project Scientist at Scripps Institution of Oceanography, UC San Diego
9. Alexander (Sasha) Gershunov, Ph.D
Research Meteorologist at Scripps Institution of Oceanography, UC San Diego
10. Kristen Guiguis, Ph.D
Project Scientist at Scripps Institution of Oceanography, UC San Diego
12. Eric D. Stein, Ph.D
Principal Scientist at the Southern California Coastal Water Research Project
13. Sula E. Vanderplank, Ph.D
Field Botanist with Terra Peninsular A.C. of Mexico
14. Horacio de la Cueva, Ph.D
Senior Researcher at the Ecology Department of CICESE in Mexico
15. Shasta Gaughen, Ph.D
Environmental Director for The Pala Band of Mission Indians
16. Janin Guzman-Morales
PhD Student at Scripps Institution of Oceanography, UC San Diego
17. Laura Hampton
Program Manager for Innovative Community Engagement at the Climate Science Alliance
18. Hiram Rivera-Huerta, Ph.D
Visiting Professor in Digital Cartography/GIS at Universidad Autónoma de Baja California
19. David W. Pierce, Ph.D
Programmer Analyst at CASPO, Scripps Institution of Oceanography, UC San Diego
20. Rob Roy
Environmental Director for The La Jolla Band of Luiseño Indians
Meet the Scientists / Why we did it
March 2018
WHY WE DID IT S
ustained, long-term collaboration is needed to conserve biodiversity and allow species and habitats to adapt to climate change and shift over time. However, the smallto-large spatial and temporal scales at which climate impacts must be considered to build resilience into natural systems require landscape-scale planning rather than the single-species approaches which have historically driven conservation action in the region. Increasing the resilience of San Diego’s ecosystems in the face of climate change is a challenge that will require multidisciplinary assessments, scenario evaluations, and other comprehensive sciencebased strategies to inform management and conservation actions. The Climate Science Alliance created a space for these ecologists and climatologists to interact and gather regionally specific climate information and assess the impacts on local species and habitats caused by climate variability as well as other stressors. This collaboration is unusual in that the project was conducted without a mandate or funding, but solely out of a desire to articulate risks that had not previously been made available to conservation planners and land managers.
Researchers taking part in this assessment are committed to the creation of actionable science that is applicable to the myriad challenges that land managers and conservation practitioners face. From the onset of this effort, all participants made an intentional effort to consider how the results of this assessment will play out across different jurisdictional boundaries within the study region and how to present the science in ways that would be most accessible to inform natural resource planning, decision-making, and management. This review, combining the knowledge of climatologists and ecologists with regional expertise and embedded in regional conservation and planning efforts, is a demonstration of what boundary spanning organizations and projects can do to inform actions that advance realistic climate adaptation planning. In this assessment, researchers have stepped outside of their more familiar roles as knowledge producers to work hand-in-hand with other disciplines and professions. We think this is an example of how diverse experts can participate within communities where citizens will have a real stake in the welfare of the ecosystems that contribute richly to our societies, economies, and values.
For more information and links, visit www.climatesciencealliance.org/sdc-ecosystems-assessment 30
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
REFERENCES Allen, C. D., A. K. Macalady, H. Chenchouni, D. Bachelet, N. McDowell, M. Vennetier, T. Kitzberger, A. Rigling, D. D. Breshears, E. H. Hogg, P. Gonzalez, R. Fensham, Z. Zhang, J. Castro, N. Demidova, J. H. Lim, G. Allard, S. W. Running, A. Semerci, and N. Cobb. 2010. A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests. Forest Ecology and Management 259:660–684. Archer, S. R., and K. I. Predick. 2008. Climate Change and Ecosystems of the Southwestern United States. Rangelands 30:23–28. Archibald, S., R. J. Scholes, D. P. Roy, G. Roberts, and L. Boschetti. 2010. Southern African fire regimes as revealed by remote sensing. International Journal of Wildland Fire 19:861–878. Ault, T. R., J. S. Mankin, B. I. Cook, and J. E. Smerdon. 2016. Relative impacts of mitigation, temperature, and precipitation on 21st-century megadrought risk in the American Southwest. Science Advances 2(10):e1600873. Axelrod, D. I. 1978. The Origin of Coastal Sage Vegetation , Alta and Baja California. American Journal of Botany 65:1117–1131. Baguskas, S. A., S. H. Peterson, B. Bookhagen, and C. J. Still. 2014. Evaluating spatial patterns of drought-induced tree mortality in a coastal California pine forest. Forest Ecology and Management 315:43–53. Baguskas, S. A., C. J. Still, D. T. Fischer, C. M. D’Antonio, and J. Y. King. 2016. Coastal fog during summer drought improves the water status of sapling trees more than adult trees in a California pine forest. Oecologia 181:137–148. Beier, P., and A. J. Gregory. 2012. Desperately seeking stable 50-year-old landscapes with patches and long, wide corridors. PLoS Biology 10. Boitani, L., A. Falcucci, L. Maiorano, and C. Rondinini. 2007. Ecological networks as conceptual frameworks or operational tools in conservation. Conservation Biology 21:1414–1422. Bolger, D. T., M. A. Patten, and D. C. Bostock. 2005. Avian reproductive failure in response to an extreme climatic event. Oecologia 142:398–406. Breshears, D. D., N. G. McDowell, K. L. Goddard, K. E. Dayem, S. N. Martens, C. W. Meyer, and K. M. Brown. 2008. Foliar absorption of intercepted rainfall improves woody plant water status most during drought. Ecology 89:41–47. Burge, D. O., J. H. Thorne, S. P. Harrison, B. C. O’Brien, J. P. Rebman, J. R. Shevock, E. R. Alverson, L. K. Hardison, J. D. RodrÍguez, S. A. Junak, T. A. Oberbauer, H. Riemann, S. E. Vanderplank, and T. Barry. 2016. Plant Diversity and Endemism in the California Floristic Province. Madroño 63:3–206. Burgess, S. S. O., and T. E. Dawson. 2004. The contribution of fog to the water relations of. Environment:1023–1034. Butsic, V., A. Syphard, J. Keeley, and A. Bar-Massada. 2017. Modeling the impact of private land conservation on wildfire risk in San Diego County, CA. Landscape and Urban Planning 157:161–169. California Department of Fish and Wildlife. 2017. California Natural Diversity Database 2017. https://www.wildlife.ca.gov/Data/CNDDB. California Forest Pest Council. 2015. 2015 California Forest Pest Conditions. Carbone, M. S., A. Park Williams, A. R. Ambrose, C. M. Boot, E. S. Bradley, T. E. Dawson, S. M. Schaeffer, J. P. Schimel, and C. J. Still. 2013. Cloud shading and fog drip influence the metabolism of a coastal pine ecosystem. Global Change Biology 19:484–497. Cayan, D., D. W. Pierce, and J. Kalansky. 2018. Climate, Drought, and Sea Level Rise Scenarios for the Fourth California Climate Assessment. Cayan, D. R., T. Das, D. W. Pierce, T. P. Barnett, M. Tyree, and A. Gershunov. 2010. Future dryness in the southwest US and the hydrology of the early 21st century drought. Proceedings of the National Academy of Sciences 107:21271–21276. Cayan, D. R., S. A. Kammerdiener, M. D. Dettinger, J. M. Caprio, and D. H. Peterson. 2001. Changes in the Onset of Spring in the Western United States. Bulletin of the American Meteorological Society 82:399–415. Cayan, D. R., M. Tyree, K. E. Kunkel, C. Castro, A. Gershunov, J. Barsugli, A. J. Ray, J. Overpeck, M. Anderson, J. Russell, B. Rajagopalan, I. Rangwala, P. Duffy, and M. Barlow. 2013. Future Climate: Projected Average. Pages 101–125 in Assessment of Climate Change in the Southwest United States. Island Press/Center for Resource Economics, Washington, DC. Clemesha, R. E. S., K. Guirguis, A. Gershunov, I. J. Small, and A. Tardy. 2017. California heat waves: their spatial evolution, variation, and coastal modulation by low clouds. Climate Dynamics. Clemesha, R. E. S., A. Gershunov, S. F. Iacobellis, A. P. Williams, and D. R. Cayan. 2016. The northward March of summer low cloudiness along the California coast. Geophysical Research Letters 43:1287–1295. CONAFOR. 2015. Reporte semanal de resultados de incendios forestales 2015. Corbin, J. D., and C. M. D’Antonio. 2004. Competition between native perennial and exotic annual grasses: Implications for an historical invasion. Ecology 85:1273–1283. Cowling, R. M., P. W. Rundel, B. B. Lamont, M. K. Arroyo, and M. Arianoutsou. 1996. Plant diversity in mediterranean-climate regions. Trends in Ecology and Evolution 11:362–366. D’Antonio, C. M., S. Bainbridge, C. Kennedy, J. Bartolome, and S. Reynolds. 2002. Ecology and restoration of California grasslands with special emphasis on the influence of fire and grazing on native grassland species. University of California, Berkeley. Dawson, T. E. 1998. Fog in the California redwood forest: Ecosystem inputs and use by plants. Oecologia 117:476–485. Delgadillo-Rodriguez, J. 1998. Florística y ecología del norte de Baja California. Universidad Autónoma de Baja California, Mexicali. Dettinger, M. D., F. M. Ralph, T. Das, P. J. Neiman, and D. R. Cayan. 2011. Atmospheric Rivers, Floods and the Water Resources of California. Water 3:445–478. Dhungel, S., D. G. Tarboton, J. Jin, and C. P. Hawkins. 2016. Potential Effects of Climate Change on Ecologically Relevant Streamflow Regimes. River Research and Applications 32:1827–1840. Diffenbaugh, N. S., D. L. Swain, and D. Touma. 2015. Anthropogenic warming has increased drought risk in California. Proceedings of the National Academy of Sciences 112:3931–3936. Diffendorfer, J. E., G. M. Fleming, J. M. Duggan, R. E. Chapman, M. E. Rahn, M. J. Mitrovich, and R. N. Fisher. 2007. Developing terrestrial, multi-taxon indices of biological integrity: An example from coastal sage scrub. Biological Conservation 140:130–141. Emery, N., and J. Lesage. 2015. Late Summer Fog Use In The Drought Deciduous Shrub, Artemisia californica (Asteraceae). Madrono 62:150–157. Enquist, C. A. F., S. T. Jackson, G. M. Garfin, F. W. Davis, L. R. Gerber, J. A. Littell, J. L. Tank, A. J. Terando, T. U. Wall, B. Halpern, J. K. K. Hiers, T. L. T. L. Morelli, E. McNie, N. L. N. L. Stephenson, M. A. M. A. Williamson, C. A. C. A. Woodhouse, L. Yung, M. W. M. W. Brunson, K. R. K. R. Hall, L. M. L. M. Hallett, D. M. D. M. Lawson, M. A. M. A. Moritz, K. Nydick, A. Pairis, A. J. A. J. Ray, C. Regan, H. D. H. D. Safford, M. W. M. W. Schwartz, and M. R. R. Shaw. 2017. Foundations of translational ecology. Frontiers in Ecology and the Environment 15:541–550. Fischer, D. T., C. J. Still, C. M. Ebert, S. A. Baguskas, and A. P. Williams. 2016. Fog drip maintains dry season ecological function in a California coastal pine forest. Ecosphere 7:1– 21. Fischer, D. T., C. J. Still, and A. P. Williams. 2009. Significance of summer fog and overcast for drought stress and ecological functioning of coastal California endemic plant species. Journal of Biogeography 36:783–799. Fisichelli, N. A., G. W. Schuurman, and C. H. Hoffman. 2016. Is “Resilience” Maladaptive? Towards an Accurate Lexicon for Climate Change Adaptation. Environmental Management 57:753–758. Franklin, J. 1998. Predicting the distribution of shrub species in southern California from climate and terrain-derived variables. Journal of 31 Vegetation Science 9:733–748.
References
March 2018
Füssel, H.-M. 2007. Adaptation planning for climate change: concepts, assessment approaches, and key lessons. Sustainability Science 2:265–275. Gershunov, A., and K. Guirguis. 2012. California heat waves in the present and future. Geophysical Research Letters 39(18). Gershunov, A., B. Rajagopalan, J. Overpeck, K. Guirguis, D. Cayan, M. Hughes, M. Dettinger, C. Castro, R. E. Schwartz, M. Anderson, A. J. Ray, J. Barsugli, T. Cavazos, M. Alexander, and F. Dominguez. 2013. Future climate: Projected extremes. Pages 126–147 in Assessment of Climate Change in the Southwest United States: A Report Prepared for the National Climate Assessment. Gude, P. H., K. Jones, R. Rasker, and M. C. Greenwood. 2013. Evidence for the effect of homes on wildfire suppression costs. International Journal of Wildland Fire 22:537–548. Hamilton, A., M. Barbour, J. Gerritsen, and M. Paul. 2008. Climate change effects on stream and river biological indicators: A preliminary analysis. Washington, DC. Heino, J., R. Virkkala, and H. Toivonen. 2009. Climate change and freshwater biodiversity: detected patterns, future trends and adaptations in northern regions. Biological Reviews 84:39–54. Heller, N. E., and E. S. Zavaleta. 2009. Biodiversity management in the face of climate change: A review of 22 years of recommendations. Biological Conservation 142:14–32. Henschel, J. R., and M. K. Seely. 2008. Ecophysiology of atmospheric moisture in the Namib Desert. Atmospheric Research 87:362–368. Hilty, J. A., W. Z. Lidicker, and A. M. Merenlender. 2006. Corridor ecology : The science and practice of linking landscapes for biodiversity conservation. Island Press. Hughes, L. 2000. Biological consequences of global warming: is the signal already apparent? Trends in Ecology & Evolution 15:56–61. Hughes, M., A. Hall, and J. Kim. 2011. Human-induced changes in wind, temperature and relative humidity during Santa Ana events. Climatic Change 109:119–132. Jennings, M. K., and K. A. Zeller. 2017. Comprehensive multi-species connectivity assessment and planning for the Highway 67 region of San Diego County, California. San Diego, CA. Johnstone, J. A., T. E. Dawson, and I. Y. Fung. 2010. Climatic context and ecological implications of summer fog decline in the coast redwood region. Proceedings of the National Academy of Sciences 107:4533–4538. Johnstone, J. A., and N. J. Mantua. 2014. Atmospheric controls on northeast Pacific temperature variability and change, 1900–2012. Proceedings of the National Academy of Sciences of the United States of America 111:14360–14365. Keeley, J. E. 1982. Distribution of lightning-and man-caused wildfires in California. Page 431– 437 in Proceedings of the International Symposium on the Dynamics and Management of Mediterranean Type Ecosystems. GTR-PSW-58. Keeley, J. E. 2005a. Fire as a threat to biodiversity in fire-type shrublands. Pages 97–106 in Planning for biodiversity: bringing research and planning together. Gen. Tech. Rep. GTR- PSW- 195. US Department of Agriculture. Keeley, J. E. 2005b. Fire history of the San Francisco East Bay region and implications for landscape patterns. International Journal of Wildland Fire 14. Keeley, J. E., C. J. Fotheringham, and M. A. Moritz. 2004. Lessons from the October 2003. Wildfires in Southern California. Journal of Forestry 102:26–31. Keeley, J. E., H. D. Safford, C. J. Fotheringham, J. Franklin, and M. A. Moritz. 2009. The 2007 southern California wildfires-Lessons in complexity. Journal of Forestry 107:287–296. Keeley, J. E., and A. D. Syphard. 2015. Different fire–climate relationships on forested and non- forested landscapes in the Sierra Nevada ecoregion. International Journal of Wildland Fire 24:27. Keeley, J. E., and A. D. Syphard. 2016. Climate Change and Future Fire Regimes: Examples from California. Geosciences 6:37. Keeley, J. E., and A. D. Syphard. 2017. Different historical fire–climate patterns in California. International Journal of Wildland Fire 26(4):253. Keeley, J. E., and A. D. Syphard. 2018. South coast bioregion. In J. W. van Wagtendonk, N. G. Sugihara, S. L. Stephens, A. E. Thode, K. E. Shaffer, and J. Fites-Kaufman, editors. Fire in California’s Ecosystems. Second Edi. University of California Press, Berkeley, CA, USA. Keeley, J. E., and P. H. Zedler. 2009. Large, high-intensity fire events in southern California shrublands: debunking the fine-grain age patch model. Ecological Applications 19:69–94. Lawson, D. M. 1993. The Effects of Fire on Stand Structure of Mixed Quercus agrifolia and Q. engelmannii woodlands. San Diego State Universtiy. Lawson, D. M. 2009. Examination of habitat fragmentation and effects on species persistence in the vicinity of Naval Base Pt. Loma and Marine Corps Air Station Miramar, San Diego, CA 2008 Annual Report. San Diego. Lawson, D. M., D. A. Marschalek, and L. R. Ordonez. 2017a. Goldspotted Oak Borer Monitoring Report and Early Detection Rapid Response Plan Review, 2016 Flight Season. Camp Pendleton. Lawson, D. M., L. Ordonez, and G. GS. 2017b. Wildland fuel moisture trends 2012-2016, Annual Report Marine Corps Installations West. Lawson, D. M., H. M. Regan, P. H. Zedler, and J. Franklin. 2010. Cumulative effects of land use, altered fire regime and climate change on persistence of Ceanothus verrucosus, a rare, fire-dependent plant species. Global Change Biology 16:2518–2529. Littell, J. S., D. McKenzie, D. L. Peterson, and A. L. Westerling. 2009. Climate and wildfire area burned in western U.S. ecoprovinces, 1916–2003. Ecological Applications 19:1003–1021. Macmynowski, D. P., T. L. Root, G. Ballard, and G. R. Geupel. 2007. Changes in spring arrival of Nearctic-Neotropical migrants attributed to multiscalar climate. Global Change Biology 13:2239–2251. Mann, M. L., E. Batllori, M. A. Moritz, E. K. Waller, P. Berck, A. L. Flint, L. E. Flint, and E. Dolfi. 2016. Incorporating Anthropogenic Influences into Fire Probability Models: Effects of Human Activity and Climate Change on Fire Activity in California. PLoS One 11. Moritz, M. A. 2003. Spatiotemporal analysis of controls on shrubland fire regimes: age dependency and fire hazard. Ecology 84:351–361. Moritz, M. A., J. E. Keeley, E. A. Johnson, and A. A. Schaffner. 2004. Testing a basic assumption of shrubland fire management: how important is fuel age? Frontiers in Ecology and the Environment 2:67–72. Morris, W. F., C. A. Pfister, S. Tuljapurkar, C. V Haridas, C. L. Boggs, M. S. Boyce, E. M. Bruna, D. R. Church, T. Coulson, D. F. Doak, S. Forsyth, J.-M. Gaillard, C. C. Horvitz, S. Kalisz, B. E. Kendall, T. M. Knight, C. T. Lee, and E. S. Menges. 2008. Longevity can buffer plant and animal populations against changing climate variability. Ecology 89:19–25. Noss, R. F. 1991. Landscape connectivity: different functions at different scales. Pages 27–39 in W. E. Hudson, editor. Landscape linkages and biodiversity. Island Press. Ojeda-Revah, L., and M. I. Espejel-Carbajal. 2008. La cuenca binacional del río Tijuana : Un enfoque biohistórico. Economía, Sociedad y Territorio VIII:517–548. Oladi, R., M. Emaminasab, and D. Eckstein. 2017. The dendroecological potential of shrubs in north Iranian semi-deserts. Dendrochronologia 44:94–102. Pachauri, R., M. Allen, V. Barros, and J. Broome. 2014. Climate Change 2014: Synthesis Report. Contribution of Working Groups I, II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Parmesan, C., and G. Yohe. 2003. A globally coherent fingerprint of climate change impacts across natural systems. Nature 421:37–42. Penman, T. D., R. A. Bradstock, and O. F. Price. 2014. Reducing wildfire risk to urban developments: Simulation of cost-effective fuel treatment solutions in south eastern Australia. Environmental Modelling and Software 52:166–175.
32
San Diego County Ecosystems: The Ecological Impacts of Climate Change on a Biodiversity Hotspot
33
Penrod, K., R. Hunter, and M. Marrifield. 2001. Missing Linkages: Restoring connectivity to theCalifornia landscape. Perry, L. G., D. C. Andersen, L. V Reynolds, S. M. Nelson, and P. B. Shafroth. 2012. Vulnerability of riparian ecosystems to elevated CO2 and climate change in arid and semiarid western North America. Global Change Biology 18:821–842. Peterson, G. D., G. S. Cumming, and S. R. Carpenter. 2003. Scenario Planning: a Tool for Conservation in an Uncertain World. Conservation Biology 17:358–366. Pierce, D. W., D. R. Cayan, and B. L. Thrasher. 2014. Statistical Downscaling Using Localized Constructed Analogs (LOCA)*. Journal of Hydrometeorology 15:2558–2585. Pierce, D. W., T. Das, D. R. Cayan, E. P. Maurer, N. L. Miller, Y. Bao, M. Kanamitsu, K. Yoshimura, M. A. Snyder, L. C. Sloan, G. Franco, and M. Tyree. 2013. Probabilistic estimates of future changes in California temperature and precipitation using statistical and dynamical downscaling. Climate Dynamics 40:839–856. Pilliod, D. S., J. L. Welty, and R. S. Arkle. 2017. Refining the cheatgrass-fire cycle in the Great Basin: Precipitation timing and fine fuel composition predict wildfire trends. Ecology and Evolution:8126–8151. Poff, N. L. R., M. M. Brinson, and J. W. Day. 2002. Aquatic ecosystems and global climate change: potential impacts on inland freshwater and coastal wetland ecosystems in the United States. Price, O. F., R. A. Bradstock, J. E. Keeley, and A. D. Syphard. 2012. The impact of antecedent fire area on burned area in southern California coastal ecosystems. Journal of Environmental Management 113:301–307. Ramirez, R. 2003. Arroyo toad (Bufo californicus) hydrogeomorphic habitat baseline analysis/radio telemetry study - Rancho Las Flores San Bernardino County, California. Final report to Rancho Las Flores Limited Partnership by Cadre Environmental, Carlsbad, California. Carlsbad. Rebman, J. P., and M. G. Simpson. 2014. Checklist of Vascular Plants of San Diego County. Riordan, E. C., and P. W. Rundel. 2009. Modelling the distribution of a threatened habitat: The California sage scrub. Journal of Biogeography 36:2176–2188. Rodríguez-Trejo, D. A., P. A. Martínez-Hernández, H. Ortiz-Contla, M. R. Chavarría-Sánchez, and F. Hernández-Santiago. 2011. The present status of fire ecology, traditional use of fire, and fire management in Mexico and Central America. Fire Ecology 7:40–56. Russell, B. D., C. D. G. Harley, T. Wernberg, N. Mieszkowska, S. Widdicombe, J. M. Hall-Spencer, and S. D. Connell. 2012. Predicting ecosystem shifts requires new approaches that integrate the effects of climate change across entire systems. Biology Letters 8:164– 166. Safford, H. D., and K. M. Van de Water. 2014. Using Fire Return Interval Departure (FRID) analysis to map spatial and temporal changes in fire frequency on National Forest lands in California. Pacific Southwest Research Station - Research Paper PSW-RP-266:1–59. San Diego Natural History Museum. 2017. San Diego County Plant Atlas. http://www.sdplantatlas.org/. Schwartz, R. 2015. California coastal low clouds: Variability and influences across climate to weather and continental to local scales. University of California, San Diego. Secretaría de Desarrollo Social (SEDESOL). 2015. Catálogo de Localidades, “Tijuana.” SEMARNAT and SAGARPA. 2009. NOM-015-SEMARNAT/SAGARPA-2007. Métodos de uso del fuego. Dof 20090116:23. Sepúlveda-Betancourt, J. I., W. R. Zúñiga-Castillo, M. Olguín-Espinoza, and A. Gomero-Portilla. 1999. Implementación de un sistema de información geográfica para la prevención de incendios forestales en Baja California. Ensenada. Socolar, J. B., P. N. Epanchin, S. R. Beissinger, and M. W. Tingley. 2017. Phenological shifts conserve thermal niches in North American birds and reshape expectations for climate-driven range shifts. Proceedings of the National Academy of Sciences 114:12976–12981. South Coast Wildlands. 2008. South coast missing linkages : A wildland network for the southcoast ecoregion. Spencer, W. D., P. Beier, K. Penrod, K. Winters, C. Paulman, H. Rustigian-Romsos, J. Strittholt, M. Parisi, and A. Pettler. 2010. California Essential Habitat Connectivity Project : A strategy for conserving a connected California. Stein, B., L. Kutner, and J. Adams. 2000. Precious Heritage:The Status of Biodiversity in the United States. Syphard, A. D., A. Bar Massada, V. Butsic, and J. E. Keeley. 2013. Land Use Planning and Wildfire: Development Policies Influence Future Probability of Housing Loss. PLoS One 8. Syphard, A. D., T. J. Brennan, and J. E. Keeley. 2018. Chaparral Landscape Conversion in Southern California. Page in E. C. Underwood, H. D. Safford, J. E. Keeley, and N. A. Molinari, editors. Valuing Chaparral: Ecological, Socio-Economic, and Management Perspectives Springer. Syphard, A. D., V. Butsic, A. Bar-Massada, J. E. Keeley, J. A. Tracey, and R. N. Fisher. 2016. Setting priorities for private land conservation in fire- prone landscapes: Are fire risk reduction and biodiversity conservation competing or compatible objectives? Ecology and Society 21. Syphard, A. D., and J. E. Keeley. 2015. Location, timing and extent of wildfire vary by cause of ignition. International Journal of Wildland Fire 24:37–47. Syphard, A. D., J. E. Keeley, and T. J. Brennan. 2011. Comparing the role of fuel breaks across southern California national forests. Forest Ecology and Management 261:2038–2048. Syphard, A. D., J. E. Keeley, A. B. Massada, T. J. Brennan, and V. C. Radeloff. 2012. Housing Arrangement and Location Determine the Likelihood of Housing Loss Due to Wildfire. PLoS ONE 7. Syphard, A. D., J. E. Keeley, A. H. Pfaff, and K. Ferschweiler. 2017. Human presence diminishes the importance of climate in driving fire activity across the United States. Proceedings of the National Academy of Sciences 114(52):13750–13755. Syphard, A. D., V. C. Radeloff, T. J. Hawbaker, and S. I. Stewart. 2009. Conservation Threats Due to Human-Caused Increases in Fire Frequency in Mediterranean-Climate Ecosystems. Conservation Biology 23:758–769. Syphard, A. D., V. C. Radeloff, J. E. Keeley, T. J. Hawbaker, M. K. Clayton, S. I. Stewart, and R. B. Hammer. 2007. Human influence on California fire regimes. Ecological Applications 17:1388–1402. Tremor, S., D. Stokes, W. Spencer, J. Diffendorfer, H. Thomas, S. Chivers, and P. Unitt, editors. 2017. San Diego County Mammal Atlas. 46th edition. Proceedings of the San Diego Society of Natural History, San Diego, CA. U.S. Census Bureau. 2017. Population and Housing Unit Estimates. Vanderplank, S. E., and E. Ezcurra. 2015. Marine influence controls plant phenological dynamics in Mediterranean Mexico. Journal of Plant Ecology 9:410–420. Vasey, M. C., M. E. Loik, and V. T. Parker. 2012. Influence of summer marine fog and low cloud stratus on water relations of evergreen woody shrubs (Arctostaphylos: Ericaceae) in the chaparral of central California. SpringerInternational Association for Ecology. Vasey, M. C., T. T. Parker, K. D. Holl, M. E. Loik, and S. Hiatt. 2014. Maritime climate influence on chaparral composition and diversity in the coast range of central California. Ecology and Evolution 4:3662–3674. Walther, G., E. Post, and A. Menzel. 2002. Ecological responses to recent climate change. Nature 416:389–395. Williams, A. P., R. E. Schwartz, S. Iacobellis, R. Seager, B. I. Cook, C. J. Still, G. Husak, and J. Michaelsen. 2015a. Urbanization causes increased cloud base height and decreased fog in coastal Southern California. Geophysical Research Letters 42:1527–1536. Williams, A. P., R. Seager, J. T. Abatzoglou, B. I. Cook, J. E. Smerdon, and E. R. Cook. 2015b. Contribution of anthropogenic warming to California drought during 2012–2014. Geophysical Research Letters 42:6819–6828.
March 2018
The mission of the Climate Science Alliance is to safeguard natural and human communities in the face of a changing climate. We do this through leading activities and creating partnerships which promote increased awareness and action on climate change related issues. Learn more about the Alliance at www.climatesciencealliance.org The development of this magazine would not have been possible without the financial support of: center for
Climate Change Impacts and Adaptation at Scripps Institution of Oceanography UC San Diego
Acknowledgements: The San Diego region has a diverse community of land managers, consultants, researchers and policy makers and we thank those who contributed throughts and insights to this work both as we developed this report and over our careers. The wealth of citations of local work throughout this document is a testament to the vibrant research community addressing basic and applied science on a multitude of projects driven by the need to solve complex resource conservation and management problems. We thank the institutions of each of the authors that provided in-kind support for our time to contribute to this unfunded collaboration. This includes San Diego State University, Scripps Institution of Oceanography, Climate Science Alliance, CA Department of Fish and Wildlife, Space and Naval Warfare Systems Center Pacific, Conservation Biology Institute, the CA Chapter of the Nature Conservancy, and the Southern Coastal Water Research Project. Further, our additional contributors represented Centro de Investigación Científica y de Educación Superior de Ensenada, Universidad Autónoma de Baja California, the Pala Band of Mission Indians, and the La Jolla Band of Luiseño Indians.
This magazine serves as a summary of a technical report included in California's Fourth Climate Change Assessment. To read the full report, please visit: http://www.climateassessment.ca.gov/techreports/ CITATION: Jennings, Megan K., Dan Cayan, Julie Kalansky, Amber D. Pairis, Dawn M. Lawson, Alexandra D. Syphard, Udara Abeysekera, Rachel E.S. Clemesha, Alexander Gershunov, Kristen Guirguis, John M. Randall, Eric D. Stein, and Sula Vanderplank. (San Diego State University). 2018. San Diego County Ecosystems: Ecological Impacts Of Climate Change On A Biodiversity Hotspot. California’s Fourth Climate Change Assessment, California Energy Commission. Publication number: EXT-CCC4A-2018-010.
34
Supporting Climate Resilience in our Communities and Natural Areas www.climatesciencealliance.org
For more information and links, visit www.climatesciencealliance.org/sdc-ecosystems-assessment