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At least 325 records · Page 18Linked to original sources

Tree-ring derived avalanche frequency and climate associations in a high-latitude, maritime climate

Snow avalanches are a natural hazard in mountainous areas worldwide with severe impacts that include fatalities, damage to infrastructure, disruption to commerce, and landscape disturbance. Understanding long-term avalanche frequency patterns, and associated climate and weather influences, improves our understanding of how climate change may affect avalanche activity. We used dendrochronological techniques to evaluate the historical frequency of large magnitude avalanches (LMAs) in the high-latitude climate of southeast Alaska, United States. We collected 434 cross sections throughout six avalanche paths near Juneau, Alaska. This resulted in 2706 identified avalanche growth disturbances between 1720 and 2018, which allowed us to reconstruct 82 years with LMA activity across three sub-regions. By combining this tree-ring-derived avalanche data set with a suite of climate and atmospheric variables and applying a generalized linear model to fit a binomial regression, we found that February and March precipitation and the Oceanic Niño Index (ONI) were significant predictors of LMA activity in the study area. Specifically, LMA activity occurred during winters with substantial February and March precipitation and neutral or negative (cold) ONI values, while years not characterized by LMAs occur more frequently during warm winters (positive ONI values). Our examination of the climate-avalanche relationship in southeast Alaska sheds light on important climate variables and physical processes associated with LMA years. These results can be used to inform long-term infrastructure planning and avalanche mitigation operations in an urban area, such as Juneau, where critical infrastructure is subject to substantial avalanche hazard.

Alaska↗

Climate change

Amphibian ecology and distribution are strongly correlated with climate. Regional patterns of amphibian biodiversity are intimately linked to temperature, evapotranspiration rate, and clines in humidity. While amphibians are and will continue to be adversely affected by recent and projected changes in climate, research suggests that adaptation may happen more slowly than the expected rate of environmental shifts. Here, we review conservation-relevant aspects of both realised and potential impacts of climate change, and outline options for amphibian conservation planning and management. Recent advances in our understanding of climate change impacts on amphibians have primarily stemmed from ecological modelling and direct assessment of climatic tolerances and dispersal capacities through physiological assays, landscape genetics, and dispersal tracking. Anthropogenic climate change has already altered amphibian assemblages and their impacts on ecosystem functioning and services. Because of known and hypothesised ecological tolerances, many amphibians might have reached or exceeded most limits in their ability to adapt to or tolerate further climate change, however the uncertainties are substantial. Implementation of conservation planning and action can help to forestall severe impacts of environmental shifts. Scientific research and science-based decision-making and policy development have already lagged; the current pace of conservation planning and action may not allow for effective identification of threats and mitigation. An increased response rate could help to avert further loss of amphibian biodiversity and decay of ecosystem services. The lack of basic field research in natural habitats continues to be an underlying challenge. We suggest priority areas of research to include the development of biologically realistic predictive models of amphibian response to climate change, field verification of model estimates and key parameters, population monitoring across multiple sites and taxa, and a combination of efforts within and across ecosystems to understand how impacts of climate change can be better mitigated.

Book chapter↗

Environmental settings of selected streams sampled for mercury in Oregon, Wisconsin, and Florida, 2002-06

From 2002 through 2006, the U.S. Geological Survey National Water-Quality Assessment Program conducted studies investigating mercury biogeochemistry and food-web bioaccumulation in eight streams from three distinct geographic areas of the United States. These streams varied greatly in environmental characteristics, including land-cover, hydrologic, climatic, and chemical characteristics. They ranged from a clear-water, high-gradient, low-percentage wetland stream in the Cascade Mountains of Oregon, to an urban stream near Milwaukee, Wisconsin, to a low-gradient, blackwater stream draining the Okefenokee and Pinhook Swamps along the Georgia-Florida border. This report summarizes the environmental settings of these eight streams.

Florida, Oregon, Wisconsin↗

What makes wildfires destructive in California?

As human impacts from wildfires mount, there is a pressing need to understand why structures are lost in destructive fires. Despite growing research on factors contributing to structure loss, fewer studies have focused on why some fires are destructive and others are not. We characterized overall differences between fires that resulted in structure loss (“destructive fires”) and those that did not (“non-destructive wildfires”) across three California regions. Then, we performed statistical analyses on large fires only (≥100 ha) to distinguish the primary differences between large destructive large fires and large non-destructive fires. Overall, destructive fires were at least an order of magnitude larger than non-destructive fires, with the largest area burned varying by season in different regions. Fire severity was also significantly higher in destructive than non-destructive fires. The statistical analysis showed that, in the San Francisco Bay Area and the northern Sierra Nevada foothills, proximity to the Wildland Urban Interface (WUI) was by far the most important factor differentiating destructive and non-destructive wildfires, followed by different combinations of short-term weather, seasonal climate, topography, and vegetation productivity. In Southern California, wind velocity on the day of the fire ignition was the top factor, which is consistent with previous assumptions that wind-driven fires tend to be most destructive and most of the destruction occurs within the first 24 h. Additionally, Southern California’s high population density increases the odds that a human-caused wildfire may occur during a severe fire-weather event. The geographical differences among regions and the variation of factors explaining the differences between large destructive and large non-destructive fires reflects the complexity inherent in decision-making for reducing wildfire risk. Land use planning to reduce future exposure of housing development to fire and increased focus on wildfire ignition prevention emerge as two approaches with substantial potential.

California↗

Development of the Wildlife Adaptation Menu for Resource Managers

The Climate Change Response Framework is an example of a collaborative, cross-boundary approach to create a set of tools, partnerships, and actions to support climate-informed conservation and land management. Historically, this effort has focused on the needs of forest managers and forestry professionals. In recent years, however, there has been increasing demand for science and tools to address climate change adaptation in wildlife management and conservation. Not only do wildlife and resource managers need the best available science, it must also be presented in a usable format with feasible options within the purview of an individual manager. The research team is first completing a comprehensive review of peer-reviewed studies to summarize what wildlife-related management actions currently exist in climate change adaptation. They will then develop and test a “menu” of climate change adaptation actions that are suitable for wildlife management in terrestrial ecosystems. This Wildlife Adaptation Menu will be modeled off existing adaptation menus for Forestry and Urban Forestry, and it will be designed to be used in conjunction with the Adaptation Workbook . In addition to a menu of adaption strategies and approaches, the scientists will also identify site-level tactics and develop case studies demonstrating the use and implementation of the menu. To ensure that information and tools meet the needs of managers, the team is involving and integrating input from wildlife managers at every step of the process. Managers will be involved in scoping the project, testing the menu, and implementing the menu.

Final Report↗

Simulating land cover change impacts on groundwater recharge under selected climate projections, Maui, Hawaiʻi

This project developed an integrated land cover/hydrological modeling framework using remote sensing and geographic information systems (GIS) data, stakeholder input, climate information and projections, and empirical data to estimate future groundwater recharge on the Island of Maui, Hawaiʻi, USA. End-of-century mean annual groundwater recharge was estimated under four future land cover scenarios: Future 1 (conservation-focused), Future 2 (status-quo), Future 3 (development-focused), and Future 4 (balanced conservation and development), and two downscaled climate projections: a coupled model intercomparison project (CMIP) phase 5 (CMIP5) representative concentration pathway (RCP) 8.5 “dry climate” future and a CMIP3 A1B “wet climate” future. Results were compared to recharge estimated using the 2017 baseline land cover to understand how changing land management and climate could influence groundwater recharge. Estimated recharge increased island-wide under all future land cover and climate combinations and was dominated by specific land cover transitions. For the dry future climate, recharge for land cover Futures 1 to 4 increased by 12%, 0.7%, 0.01%, and 11% relative to 2017 land cover conditions, respectively. Corresponding increases under the wet future climate were 10%, 0.9%, 0.6%, and 9.3%. Conversion from fallow/grassland to diversified agriculture increased irrigation, and therefore recharge. Above the cloud zone (610 m), conversion from grassland to native or alien forest led to increased fog interception, which increased recharge. The greatest changes to recharge occurred in Futures 1 and 4 in areas where irrigation increased, and where forest expanded within the cloud zone. Furthermore, new future urban expansion is currently slated for coastal areas that are already water-stressed and had low recharge projections. This study demonstrated that a spatially-explicit scenario planning process and modeling framework can communicate the possible consequences and tradeoffs of land cover change under a changing climate, and the outputs from this study serve as relevant tools for landscape-level management and interventions.

Hawaii↗

Estimating spatially and temporally varying recharge and runoff from precipitation and urban irrigation in the Los Angeles Basin, California

A daily precipitation-runoff model, referred to as the Los Angeles Basin watershed model (LABWM), was used to estimate recharge and runoff for a 5,047 square kilometer study area that included the greater Los Angeles area and all surface-water drainages potentially contributing recharge to a 1,450 square kilometer groundwater-study area underlying the greater Los Angeles area, referred to as the Los Angeles groundwater-study area. The recharge estimates for the Los Angeles groundwater-study area included spatially distributed recharge in response to the infiltration of precipitation, runoff, and urban irrigation, as well as mountain-front recharge from surface-water drainages bordering the groundwater-study area. The recharge and runoff estimates incorporated a new method for estimating urban irrigation, consisting of residential and commercial landscape watering, based on land use and the percentage of pervious land area. The LABWM used a 201.17-meter gridded discretization of the study area to represent spatially distributed climate and watershed characteristics affecting the surface and shallow sub-surface hydrology for the Los Angeles groundwater study area. Climate data from a local network of 201 monitoring sites and published maps of 30-year-average monthly precipitation and maximum and minimum air temperature were used to develop the climate inputs for the LABWM. Published maps of land use, land cover, soils, vegetation, and surficial geology were used to represent the physical characteristics of the LABWM area. The LABWM was calibrated to available streamflow records at six streamflow-gaging stations. Model results for a 100-year target-simulation period, from water years 1915 through 2014, were used to quantify and evaluate the spatial and temporal variability of water-budget components, including evapotranspiration (ET), recharge, and runoff. The largest outflow of water from the LABWM was ET; the 100-year average ET rate of 362 millimeters per year (mm/yr) accounted for 66 percent of the combined water inflow of 551 mm/yr, including 488 mm/yr from precipitation and 63 mm/yr from urban irrigation. The simulated ET rate varied from a minimum of 0 mm/yr for impervious areas to high values of more than 1,000 mm/yr for many areas, including the south-facing slopes of the San Gabriel Mountains, stream channels underlain by permeable soils and thick root zones, and pervious locations receiving inflows both from urban irrigation and surface water. Runoff was the next largest outflow, averaging 145 mm/yr for the 100-year period, or 26 percent of the combined precipitation and urban-irrigation inflow. Recharge averaged 45 mm/yr, or about 8 percent of the combined inflow from precipitation and urban irrigation. Simulation results indicated that recharge in response to urban irrigation was an important component of spatially distributed recharge, contributing an average of 56 percent of the total recharge to the eight LABWM subdomains containing the Los Angeles groundwater study area. The 100‑year average recharge rate for the eight subdomains was 41 mm/yr, or 8,473 hectare-meters per year (ha-m/yr), with urban irrigation included in the simulation compared to a recharge rate of 18 mm/yr, or 3,741 ha-m/yr, with urban irrigation excluded. In contrast to recharge, the effect of urban irrigation on runoff was slight; runoff was 72,667 ha-m/yr with urban irrigation included compared to 72,618 ha-m/yr with urban irrigation excluded, an increase of only 48 ha-m/yr (about 0.1 percent). Simulation results also indicated that potential recharge from hilly drainages outside of, but bordering and tributary to, the lower-lying area of the Los Angeles groundwater study area, in this study referred to as mountain-front recharge, could provide an important contribution to the total recharge for the groundwater basins. The time-averaged recharge rate was similar to the combined direct and mountain-front recharge components estimated in a previous study and used as input for a calibrated groundwater model. The annual (water year) recharge estimates simulated in this study, however, indicated much greater year-to-year variability, which was dependent on year-to-year variability in the magnitude and distribution of daily precipitation, compared to the previous estimates.

California↗

Magnitude and frequency of floods in rural and urban basins of North Carolina

The applicability of the nationwide urban flood relations in the Piedmont and Coastal Plain provinces is evaluated. Data for 254 gaging stations on rural streams with 10 or more years of record were used in multiple linear regression analyses with basin and climatic variables, to derive regional relations for estimating flood discharges having recurrence intervals of 2- to 100-years. Rural relations are presented for three hydrologic areas: (1) Blue Ridge-Piedmont, (2) Coastal Plain, and (3) Sand Hills. Drainage area is the only basin characteristic in the relations. The average standard error of estimate of the relations for the Blue Ridge-Piedmont, Coastal Plain, and Sand Hills hydrologic areas is 44, 39, and 24%, respectively. Flood discharges for the 2-, 5-, 10-, 25-, 50-, and 100-year recurrence intervals for the 254 streamflow stations used in the regionalization study are also presented. Flood frequency distributions of simulated annual maximum discharges for four urban basins in the Coastal Plain indicate that the nationwide relations are applicable in the province. The root mean squared error for the 10- and 100-year flood discharges, using the nationwide relations, is 44% and 49%, respectively. Simulated data for six sites in the Piedmont were used to analyze the applicability of the nationwide urban relations in the province. The root mean squared error is 64% for the 10-year flood and 42% for the 100-year flood. No recommendation is made concerning use of the nationwide relations in the Piedmont.

North Carolina↗

Coastal wetlands in the Anthropocene

We review the functioning and sustainability of coastal marshes and mangroves. Urbanized humans have a 7,000-year-old enduring relationship to coastal wetlands. Wetlands include marshes, salt flats, and saline and freshwater forests. Coastal wetlands occur in all climate zones but are most abundant in deltas. Mangroves are tropical, whereas marshes occur from tropical to boreal areas. Quantification of coastal wetland areas has advanced in recent years but is still insufficiently accurate. Climate change and sea-level rise are predicted to lead to significant wetland losses and other impacts on coastal wetlands and the humans associated with them. Landward migration and coastal retreat are not expected to significantly reduce coastal wetland losses. Nitrogen watershed inputs are unlikely to alter coastal marsh stability because watershed loadings are mostly significantly lower than those in fertilization studies that show decreased belowground biomass and increased decomposition of soil organic matter. Blue carbon is not expected to significantly reduce climate impacts. The high values of ecosystem goods and services of wetlands are expected to be reduced by area losses. Humans have had strong impacts on coastal wetlands in the Holocene, and these impacts are expected to increase in the Anthropocene.

Annual Review of Environment and Resources↗

Minnesota and Landsat

Landsat land-imaging satellites underpin public and private sector decisions in the Minnesota and across the Nation for effective adaptation to changing landscapes. Those decisions often lead to enhanced agricultural productivity, smart urban development, and sustainable forest management. Landsat also enables more accurate inland lake water-quality monitoring, increased disaster resilience and risk assessment, effective water use, more-informed climate research, and other applications.

Minnesota↗

Effects of climate change on freshwater ecosystems of the south-eastern United States and the Gulf Coast of Mexico

The south-eastern United States and Gulf Coast of Mexico is physiographically diverse, although dominated by a broad coastal plain. Much of the region has a humid, warm temperate climate with little seasonality in precipitation but strong seasonality in runoff owing to high rates of summer evapotranspiration. The climate of southern Florida and eastern Mexico is subtropical with a distinct summer wet season and winter dry season. Regional climate models suggest that climate change resulting from a doubling of the pre-industrial levels of atmospheric CO2 may increase annual air temperatures by 3-4??C. Changes in precipitation are highly uncertain, but the most probable scenario shows higher levels over all but the northern, interior portions of the region, with increases primarily occurring in summer and occurring as more intense or clustered storms. Despite the increases in precipitation, runoff is likely to decline over much of the region owing to increases in evapotranspiration exceeding increases in precipitation. Only in Florida and the Gulf Coast areas of the US and Mexico are precipitation increases likely to exceed evapotranspiration increases, producing an increase in runoff. However, increases in storm intensity and clustering are likely to result in more extreme hydrographs, with larger peaks in flow but lower baseflows and longer periods of drought. The ecological effects of climate change on freshwaters of the region include: (1) a general increase in rates of primary production, organic matter decomposition and nutrient cycling as a result of higher temperatures and longer growing seasons: (2) reduction in habitat for cool water species, particularly fish and macroinvertebrates in Appalachian streams; (3) reduction in water quality and in suitable habitat in summer owing to lower baseflows and intensification of the temperature-dissolved oxygen squeeze in many rivers and reservoirs; (4) reduction in organic matter storage and loss of organisms during more intense flushing events in some streams and wetlands; (5) shorter periods of inundation of riparian wetlands and greater drying of wetland soils, particularly in northern and inland areas; (6) expansion of subtropical species northwards, including several non-native nuisance species currently confined to southern Florida; (7) expansion of wetlands in Florida and coastal Mexico, but increase in eutrophication of Florida lakes as a result of greater runoff from urban and agricultural areas; and (8) changes in the flushing rate of estuaries that would alter their salinity regimes, stratification and water quality as well as influence productivity in the Gulf of Mexico. Many of the expected climate change effects will exacerbate current anthropogenic stresses on the region's freshwater systems, including increasing demands for water, increasing waste heat loadings and land use changes that alter the quantity and quality of runoff to streams and reservoirs. Research is needed especially in several critical areas: long-term monitoring of key hydrological, chemical and biological properties (particularly water balances in small, forested catchments and temperature-sensitive species); experimental studies of the effects of warming on organisms and ecosystem processes under realistic conditions (e.g. in situ heating experiments); studies of the effects of natural hydrological variation on biological communities; and assessment of the effects of water management activities on organisms and ecosystem processes, including development and testing of management and restoration strategies designed to counteract changes in climate.

Hydrological Processes↗

The Detroit River, Michigan: an ecological profile

A part of the connecting channel system between Lake Huron and Lake Erie, the Detroit River forms an integral link between the two lakes for both humans and biological resources such as fish, nutrients, and plant detritus. This profile summarizes existing scientific information on the ecological structure and functioning of this ecosystem. Topics include the geological history of the region, climatic influences, river hydrology, lower trophic-level biotic components, native and introduced fishes, waterfowl use, ecological interrelationships, commercial and recreational uses of the river, and current management issues. Despite urbanization, the river still supports diverse fish, waterfowl, and benthic populations. Management issues include sewer overflows; maintenance dredging for navigation and port activities; industrial discharges of potentially hazardous materials; and wetland, fishery, and waterfowl protection and enhancement.

Biological Report↗

Loss and modification of habitat

Amphibians live in a wide variety of habitats around the world, many of which have been modified or destroyed by human activities. Most species have unique life history characteristics adapted to specific climates, habitats (e.g., lentic, lotic, terrestrial, arboreal, fossorial, amphibious), and local conditions that provide suitable areas for reproduction, development and growth, shelter from environmental extremes, and predation, as well as connectivity to other populations or habitats. Although some species are entirely aquatic or terrestrial, most amphibians, as their name implies, lead a dual life and require a mosaic of habitats in both aquatic and terrestrial ecosystems. With over 6 billion people on Earth, most species are now persisting in habitats that have been directly or indirectly influenced by human activities. Some species have disappeared where their habitats have been completely destroyed, reduced, or rendered unsuitable. Habitat loss and degradation are widely considered by most researchers as the most important causes of amphibian population decline globally (Barinaga 1990; Wake and Morowitz 1991; Alford and Richards 1999). In this chapter, a background on the diverse habitat requirements of amphibians is provided, followed by a discussion of the effects of urbanization, agriculture, livestock grazing, timber production and harvesting, fire and hazardous fuel management, and roads on amphibians and their habitats. Also briefly discussed is the influence on amphibian habitats of natural disturbances, such as extreme weather events and climate change, given the potential for human activities to impact climate in the longer term. For amphibians in general, microhabitats are of greater importance than for other vertebrates. As ectotherms with a skin that is permeable to water and with naked gelatinous eggs, amphibians are physiologically constrained to be active during environmental conditions that provide appropriate body temperatures and adequate water balance (Thorson and Svihla 1943; Brattstrom 1963; Tracy 1976). Hence, individuals require and seek specific microhabitats that maintain their preferred body temperature while at the same time reducing water loss or allowing individuals to re-hydrate. Amphibians also possess relatively few physical attributes that protect them from predators. Although they may avoid predators behaviourally or deter them by skin toxins, amphibians lack defensive shells or hardened cuticles, do not have protective teeth or claws, and most are insufficiently fast to escape predators. Hence, they are relatively dependent on sites that conceal or protect them from predation. Most amphibians also differ significantly from other vertebrates in possessing a complex two-phase life cycle: the pre-metamorphic larval (tadpole) stage and the post-metamorphic juvenile and adult stage (Wilbur 1980, 1984). Most amphibian species have two distinct econes (Heatwole 1989), each with different habitat requirements, the larvae being aquatic and the post-metamorphic animals more terrestrial. The habitats required by the two phases can differ greatly, but both are essential to the survival of a species. However, amphibian diversity is great and exceptions to this general pattern exist. For example, some species have direct development without going through a larval stage and are fully terrestrial, whereas the larvae of other species can reach sexual maturity without going through metamorphosis (i.e., neoteny) and are fully aquatic.

Book chapter↗

Loss and modification of habitat

Amphibians live in a wide variety of habitats around the world, many of which have been modified or destroyed by human activities. Most species have unique life history characteristics adapted to specific climates, habitats (e.g., lentic, lotic, terrestrial, arboreal, fossorial, amphibious), and local conditions that provide suitable areas for reproduction, development and growth, shelter from environmental extremes, and predation, as well as connectivity to other populations or habitats. Although some species are entirely aquatic or terrestrial, most amphibians, as their name implies, lead a dual life and require a mosaic of habitats in both aquatic and terrestrial ecosystems. With over 6 billion people on Earth, most species are now persisting in habitats that have been directly or indirectly influenced by human activities. Some species have disappeared where their habitats have been completely destroyed, reduced, or rendered unsuitable. Habitat loss and degradation are widely considered by most researchers as the most important causes of amphibian population decline globally (Barinaga 1990; Wake and Morowitz 1991; Alford and Richards 1999). In this chapter, a background on the diverse habitat requirements of amphibians is provided, followed by a discussion of the effects of urbanization, agriculture, livestock grazing, timber production and harvesting, fire and hazardous fuel management, and roads on amphibians and their habitats. Also briefly discussed is the influence on amphibian habitats of natural disturbances, such as extreme weather events and climate change, given the potential for human activities to impact climate in the longer term. For amphibians in general, microhabitats are of greater importance than for other vertebrates. As ectotherms with a skin that is permeable to water and with naked gelatinous eggs, amphibians are physiologically constrained to be active during environmental conditions that provide appropriate body temperatures and adequate water balance (Thorson and Svihla 1943; Brattstrom 1963; Tracy 1976). Hence, individuals require and seek specific microhabitats that maintain their preferred body temperature while at the same time reducing water loss or allowing individuals to re-hydrate. Amphibians also possess relatively few physical attributes that protect them from predators. Although they may avoid predators behaviourally or deter them by skin toxins, amphibians lack defensive shells or hardened cuticles, do not have protective teeth or claws, and most are insufficiently fast to escape predators. Hence, they are relatively dependent on sites that conceal or protect them from predation. Most amphibians also differ significantly from other vertebrates in possessing a complex two-phase life cycle: the pre-metamorphic larval (tadpole) stage and the post-metamorphic juvenile and adult stage (Wilbur 1980, 1984). Most amphibian species have two distinct econes (Heatwole 1989), each with different habitat requirements, the larvae being aquatic and the post-metamorphic animals more terrestrial. The habitats required by the two phases can differ greatly, but both are essential to the survival of a species. However, amphibian diversity is great and exceptions to this general pattern exist. For example, some species have direct development without going through a larval stage and are fully terrestrial, whereas the larvae of other species can reach sexual maturity without going through metamorphosis (i.e., neoteny) and are fully aquatic.

Book chapter↗

The influence of climatic variability on local population dynamics of Cercidium microphyllum (foothill paloverde)

This study investigated correlations among climatic variability, population age structure, and seedling survival of a dominant Sonoran Desert tree, Cercidium microphyllum (foothill paloverde), at Tucson, Arizona, USA. A major goal was to determine whether wet years promote seedling establishment and thereby determine population structure. Plant age was estimated from basal circumference for a sample of 980 living and dead trees in twelve 0.5-ha plots. Ages ranged from 1 to 181 years. Age frequency distribution showed that the population is in decline. Most (51.2%) of the 814 living trees were 40–80 years old; only 6.5% were younger than 20 years. The average age of the 166 dead trees was 78 years. Fifty-nine percent of dead trees were aged 60–100 years. Survival of newly emerged seedlings was monitored for 7 years in a 557-m 2 permanent plot. Mean survival in the 1st year of life was 1.7%. Only 2 of 1,008 seedlings lived longer than 1 year. Length of survival was not correlated with rainfall. Residual regeneration, an index of the difference between predicted and observed cohort size, showed that regeneration was high during the first half of the twentieth century and poor after the mid-1950s. Trends in regeneration did not reflect interannual variation in seasonal temperature or rain before 1950, that is, in the years before urban warming. Taken together, the seedling study and the regeneration analysis suggest that local population dynamics reflect biotic factors to such an extent that population age structure might not always be a reliable clue to past climatic influences.

Oecologia↗

The influence of tree canopy cover data choices on urban ecosystem accounting

Because urban landscapes are heterogeneous, the methods and spatial resolution used to depict the land surface greatly influence the representation of urban features. Land cover products such as tree canopy cover (TCC) are particularly sensitive to the methodology and resolution used in their creation. Differences in TCC mapping have implications on the outcomes of ecosystem service (ES) models, including those underlying natural capital accounting. Here, we quantify the sensitivity of physical rainfall interception and local climate regulation ES models for 189 U.S. cities to TCC inputs from four TCC products: a) National Land Cover Database (NLCD), b) Enhanced NLCD TCC, c) aggregated city-specific composite, and d) global tree canopy height dataset. We find both city-level and aggregate differences in TCC estimates, from a 38% decrease to a 3% increase relative to an aggregated high-resolution product. These differences result in up to 3% overestimations and 27% underestimation of rainfall interception and 2–56% underestimation of local climate regulation ES. City size, population, and greenness in addition to climatic variation drove differences between TCC products, and this variation requires users to carefully consider the choice of input data for any planned analysis. Though high-resolution data can offer greater nuance and accuracy, more limited spatiotemporal availability can hinder their usefulness for long-term monitoring applications such as natural capital accounting. The differences found in this study provide valuable insights for making informed decisions on data inputs for use in urban ecosystem research and for contextualizing model outcomes.

Contiguous United States↗

Coastal systems and low-lying areas

Since the IPCC Third Assessment Report (TAR), our understanding of the implications of climate change for coastal systems and low-lying areas (henceforth referred to as ‘coasts’) has increased substantially and six important policy-relevant messages have emerged. Coasts are experiencing the adverse consequences of hazards related to climate and sea level (very high confidence). Coasts are highly vulnerable to extreme events, such as storms, which impose substantial costs on coastal societies [6.2.1, 6.2.2, 6.5.2]. Annually, about 120 million people are exposed to tropical cyclone hazards, which killed 250,000 people from 1980 to 2000 [6.5.2]. Through the 20th century, global rise of sea level contributed to increased coastal inundation, erosion and ecosystem losses, but with considerable local and regional variation due to other factors [6.2.5, 6.4.1]. Late 20th century effects of rising temperature include loss of sea ice, thawing of permafrost and associated coastal retreat, and more frequent coral bleaching and mortality [6.2.5]. Coasts will be exposed to increasing risks, including coastal erosion, over coming decades due to climate change and sea-level rise (very high confidence). Anticipated climate-related changes include: an accelerated rise in sea level of up to 0.6 m or more by 2100; a further rise in sea surface temperatures by up to 3°C; an intensification of tropical and extra-tropical cyclones; larger extreme waves and storm surges; altered precipitation/run-off; and ocean acidification [6.3.2]. These phenomena will vary considerably at regional and local scales, but the impacts are virtually certain to be overwhelmingly negative [6.4, 6.5.3]. Corals are vulnerable to thermal stress and have low adaptive capacity. Increases in sea surface temperature of about 1 to 3°C are projected to result in more frequent coral bleaching events and widespread mortality, unless there is thermal adaptation or acclimatisation by corals [Box 6.1, 6.4]. Coastal wetland ecosystems, such as saltmarshes and mangroves, are especially threatened where they are sediment starved or constrained on their landward margin [6.4.1]. Degradation of coastal ecosystems, especially wetlands and coral reefs, has serious implications for the well-being of societies dependent on the coastal ecosystems for goods and services [6.4.2, 6.5.3]. ncreased flooding and the degradation of freshwater, fisheries and other resources could impact hundreds of millions of people, and socio-economic costs on coasts will escalate as a result of climate change [6.4.2, 6.5.3]. The impact of climate change on coasts is exacerbated by increasing human-induced pressures (very high confidence). Utilisation of the coast increased dramatically during the 20th century and this trend is virtually certain to continue through the 21st century. Under the SRES scenarios, the coastal population could grow from 1.2 billion people (in 1990) to 1.8 to 5.2 billion people by the 2080s, depending on assumptions about migration [6.3.1]. Increasing numbers of people and assets at risk at the coast are subject to additional stresses due to land-use and hydrological changes in catchments, including dams that reduce sediment supply to the coast [6.3.2]. Populated deltas (especially Asian megadeltas), low-lying coastal urban areas and atolls are key societal hotspots of coastal vulnerability, occurring where the stresses on natural systems coincide with low human adaptive capacity and high exposure [6.4.3]. Regionally, South, South- East and East Asia, Africa and small islands are most vulnerable [6.4.2]. Climate change therefore reinforces the desirability of managing coasts in an integrated manner [6.6.1.3]. Adaptation for the coasts of developing countries will be more challenging than for coasts of developed countries, due to constraints on adaptive capacity (high confidence). While physical exposure can significantly influence vulnerability for both human populations and natural systems, a lack of adaptive capacity is often the most important factor that creates a hotspot of human vulnerability. Adaptive capacity is largely dependent upon development status. Developing nations may have the political or societal will to protect or relocate people who live in low-lying coastal zones, but without the necessary financial and other resources/capacities, their vulnerability is much greater than that of a developed nation in an identical coastal setting. Vulnerability will also vary between developing countries, while developed countries are not insulated from the adverse consequences of extreme events [6.4.3, 6.5.2]. Adaptation costs for vulnerable coasts are much less than the costs of inaction (high confidence). Adaptation costs for climate change are much lower than damage costs without adaptation for most developed coasts, even considering only property losses and human deaths [6.6.2, 6.6.3]. As post-event impacts on coastal businesses, people, housing, public and private social institutions, natural resources, and the environment generally go unrecognised in disaster cost accounting, the full benefits of adaptation are even larger [6.5.2, 6.6.2]. Without adaptation, the high-end sea-level rise scenarios, combined with other climate changes (e.g., increased storm intensity), are as likely as not to render some islands and lowlying areas unviable by 2100, so effective adaptation is urgently required [6.6.3]. The unavoidability of sea-level rise, even in the longer-term, frequently conflicts with present-day human development patterns and trends (high confidence). Sea-level rise has substantial inertia and will continue beyond 2100 for many centuries. Irreversible breakdown of the West Antarctica and/or Greenland ice sheets, if triggered by rising temperatures, would make this long-term rise significantly larger, ultimately questioning the viability of many coastal settlements across the globe. The issue is reinforced by the increasing human use of the coastal zone. Settlement patterns also have substantial inertia, and this issue presents a challenge for long-term coastal spatial planning. Stabilisation of climate could reduce the risks of ice sheet breakdown, and reduce but Chapter 6 Coastal systems and low-lying areas 317 not stop sea-level rise due to thermal expansion [Box 6.6]. Hence, it is now more apparent than it was in the TAR that the most appropriate response to sea-level rise for coastal areas is a combination of adaptation to deal with the inevitable rise, and mitigation to limit the long-term rise to a manageable level [6.6.5, 6.7].

Book chapter↗

Water-quality, biological, and physical-habitat conditions at fixed sites in the Cook Inlet Basin, Alaska, National Water-Quality Assessment Study Unit, October 1998-September 2001

The Cook Inlet Basin study unit of the U.S. Geological Survey National Water-Quality Assessment Program comprises 39,325 square miles in south-central Alaska. Data were collected at eight fixed sites to provide baseline information in areas where no development has taken place, urbanization or logging have occurred, or the effects of recreation are increasing. Collection of water-quality, biology, and physical-habitat data began in October 1998 and ended in September 2001 (water years 1999-2001). The climate for the water years in the study may be categorized as slightly cool-wet (1999), slightly warm-wet (2000), and significantly warm-dry (2001). Total precipitation was near normal during the study period, and air temperatures ranged from modestly cool in water year 1999 to near normal in 2000, and to notably warm in 2001. Snowmelt runoff dominates the hydrology of streams in the Cook Inlet Basin. Average annual flows at the fixed sites were approximately the same as the long-term average annual flows, with the exception of those in glacier-fed basins, which had above-average flow in water year 2001. Water temperature of all streams studied in the Cook Inlet Basin remained at 0 oC for about 6 months per year, and average annual water temperatures ranged from 3.3 to 6.2 degrees Celsius. Of the water-quality constituents sampled, all concentrations were less than drinking-water standards and only one constituent, the pesticide carbaryl, exceeded aquatic-life standards. Most of the stream waters of the Cook Inlet Basin were classified as calcium bicarbonate, which reflects the underlying geology. Streams in the Cook Inlet Basin draining areas with glaciers, rough mountainous terrain, and poorly developed soils have low concentrations of nitrogen, phosphorus, and dissolved organic carbon compared with concentrations of these same constituents in streams in lowland or urbanized areas. In streams draining relatively low-lying areas, most of the suspended sediment, nutrients, and dissolved organic carbon are transported in the spring from the melting snowpack. The urbanized stream, Chester Creek, had the highest concentrations of calcium, magnesium, chloride, and sodium, most likely because of the application of de-icing materials during the winter. Several volatile organic compounds and pesticides also were detected in samples from this stream. Aquatic communities in the Cook Inlet Basin are naturally different than similar sites in the contiguous United States because of the unique conditions of the northern latitudes where the Cook Inlet Basin is located, such as extreme diurnal cycles and long periods of ice cover. Blue-green algae was the dominant algae found at all sites although in some years green algae was the most dominant algae. Macroinvertebrate communities consist primarily of Diptera (true flies), Ephemeroptera (mayflies), and Plecoptera (stoneflies). Lowland areas have higher abundance of aquatic communities than glacier-fed basins. However, samples from the urbanized stream, Chester Creek, were dominated by oligochaetes, a class of worms. Most of the functional feeding groups were collector-gatherers. The number of taxa for both algae and macroinvertebrates were highest in water year 2001, which may be due to the relative mild winter of 2000?2001 and the above average air temperatures for this water year. The streams in the Cook Inlet Basin typically are low gradient. Bank substrates consist of silt, clay, or sand, and bed substrate consists of coarse gravel or cobbles. Vegetation is primarily shrubs and woodlands with spruce or cottonwood trees. Canopy angles vary with the size of the stream or river and are relatively low at the smaller streams and high at the larger streams. Suitable fish habitat, such as woody debris, pools, cobble substrate, and overhanging vegetation, is found at most sites. Of the human activities occurring in the fixed site basins ? high recreational use, logging, and urbanizat

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