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At least 1,261 records · Page 70Linked to original sources

Persistence of native and exotic plants 10 years after prairie reconstruction

Prairie reconstructions are a critical component of preservation of the imperiled tallgrass prairie ecosystem in the Midwestern United States. Sustainability of this endeavor depends on establishment of persistent cover of planted native species and resistance to noxious weeds. The goal of this study was to understand the influence of early reconstruction practices on long-term outcomes. Twelve replicates of three planting methods (dormant-season broadcast, growing-season broadcast, and growing-season drill) and three seed mix richness levels (10, 20, or 34 species), fully crossed in a completely randomized design were planted in 2005 on nine former agricultural fields located in Iowa and Minnesota. Cover by species was estimated in 2005–2007, 2010, and 2015. In 2015, cover of planted species, native nonplanted species, and exotic species were similar to those recorded in 2010. Cover of the noxious weed Cirsium arvense had also declined by an average of 49% without herbicide from a peak in 2007 to low stable levels from 2010 to 2015. Richness of planted forbs, on the other hand, were still increasing in high-richness broadcast treatments (e.g. 17–59% increase 2010–1015 in Minnesota). Two results in 2015 are reasons for concern: cover of planted species is only slightly over 50% in both Minnesota and Iowa, though with forbs still increasing, this may improve; and the cool-season exotic grasses Poa pratensis and Bromus inermis are increasing at both Minnesota and Iowa sites. Control of these invasive grasses will be necessary, but care will be needed to avoid negative impacts of control methods on natives.

Restoration Ecology↗

Response of Everglades tree islands to environmental change

Tree islands are centers of biodiversity within the Florida Everglades, USA, but the factors controlling their distribution, formation, and development are poorly understood. We use pollen assemblages from tree islands throughout the greater Everglades ecosystem to reconstruct the timing of tree island formation, patterns of development, and response to specific climatic and environmental stressors. These data indicate that fixed (teardrop-shaped) and strand tree islands developed well before substantial human alteration of the system, with initial tree island vegetation in place between 3500 and 500 calibrated years before present (cal yr BP), depending on the location in the Everglades wetland. Tree island development appears to have been triggered by regional- to global-scale climatic events at 2800 cal yr BP, 1600–1500 cal yr BP, 1200–1000 cal yr BP (early Medieval Warm Period), and 500–200 cal yr BP (Little Ice Age). These periods correspond to drought intervals documented in Central and South America and periods of southward displacement of the Intertropical Convergence Zone. The records indicate a coherence of climate patterns in both subtropical North America and the Northern Hemisphere Neotropics. Water management practices of the 20th century altered plant communities and size of tree islands throughout the Everglades. Responses range from loss of tree islands due to artificially long hydroperiods and deep water to expansion of tree islands after flow reductions. These data provide evidence for the rapidity of tree island response to specific hydrologic change and facilitate prediction of the response to future changes associated with Everglades restoration plans.

Florida↗

Bay Miwok evening primrose: A new subspecies of Oenothera deltoides (Onagraceae) endemic to California

California contains exceptional biodiversity in geography and plant life, including numerous endemic species, some of which are cryptic. The Oenothera deltoides Torr. & Frém. species complex represents a prime example of cryptic diversity. Here, we recognize a new subspecies of Oenothera deltoides , O. deltoides subsp. julpunensis S.F.Jones, subsp. nov., that is a local endemic of windblown sand deposits on the eastern Antioch Dunes sand sheet in the San Francisco Bay-Delta region of California, USA. With the goal of providing clarity to managers of listed species and better understanding of California's diverse flora, we addressed the puzzle of O. deltoides in the region by combining range-wide field surveys with modern genomic tools. We describe the proposed subspecies, its ecology and distribution, and discuss its conservation. As a somewhat cryptic local endemic with small population size and disappearing habitat, the proposed subspecies would benefit from conservation and management to persist as a member of the California flora.

California↗

A review of natural and managed revegetation responses in two de-watered reservoirs after large dam removals on the Elwha River, Washington, USA

Large dam removals are increasing in frequency and the response of natural and managed revegetation is a critical consideration for managed restoration of dewatered reservoir landscapes post dam removal. The removal of two large dams on the Elwha River in 2011-2014 provides insight into reservoir revegetation. We review literature and datasets from 2012 through 2018, 1-6 years since reservoir dewatering, to compare pre-dam removal predictions on the Elwha to post-dam removal of natural revegetation, managed revegetation effects and invasive non-native vegetation response. Pre-dam removal hypotheses about natural revegetation did not predict species performance on reservoir sediments, seed rain patterns, or seed bank response. Sediment texture and landform affected multiple aspects of revegetation, including vegetation cover, species richness, woody stem densities and species composition. Reservoir drawdown timing influenced species composition and seedling densities. Predictions about managed revegetation effects were mixed. Planting trees and shrubs did not accelerate woody cover but did increase species richness. Seeding reduced non-native vegetation frequency and species richness, had no effect on vegetation cover on fine sediments, but increased vegetation cover on coarse sediments. Planting trees and shrubs during drawdown appeared to result in higher survival rates compared to plantings installed 1+ years post drawdown. Seeding Lupinus rivularis (riverbank lupine) on coarse sediments was successful and increased foliar nitrogen in planted conifers. Invasive non-native vegetation was correctly predicted to be more abundant in the Aldwell reservoir but did not preclude native species establishment in either reservoir, likely due to rapid establishment of native species and robust management that occurred before, during and after dam removal.

Washington↗

Feeding preferences of West Indian manatees in Florida, Belize, and Puerto Rico as indicated by stable isotope analysis

The endangered West Indian manatee Trichechus manatus has 2 recognized subspecies: the Florida T. m. latirostris and Antillean T. m. manatus manatee, both of which are found in freshwater, estuarine, and marine habitats. A better understanding of manatee feeding preferences and habitat use is essential to establish criteria on which conservation plans can be based. Skin from manatees in Florida, Belize, and Puerto Rico, as well as aquatic vegetation from their presumed diet, were analyzed for stable carbon and nitrogen isotope ratios. This is the first application of stable isotope analysis to Antillean manatees. Stable isotope ratios for aquatic vegetation differed by plant type (freshwater, estuarine, and marine), collection location, and in one instance, season. Carbon and nitrogen isotope ratios for manatee skin differed between collection location and in one instance, season, but did not differ between sex or age class. Signatures in the skin of manatees sampled in Belize and Puerto Rico indicated a diet composed primarily of seagrasses, whereas those of Florida manatees exhibited greater regional variation. Mixing model results indicated that manatees sampled from Crystal River and Homosassa Springs (Florida, USA) ate primarily freshwater vegetation, whereas manatees sampled from Big Bend Power Plant, Ten Thousand Islands, and Warm Mineral Springs (Florida) fed primarily on seagrasses. Possible diet–tissue discrimination values for 15 N were estimated to range from 1.0 to 1.5‰. Stable isotope analysis can be used to interpret manatee feeding behavior over a long period of time, specifically the use of freshwater vegetation versus seagrasses, and can aid in identifying critical habitats and improving conservation efforts.

Florida↗

Effects of climate and water balance across grasslands of varying C 3 and C 4 grass cover

Climate change in grassland ecosystems may lead to divergent shifts in the abundance and distribution of C 3 and C 4 grasses. Many studies relate mean climate conditions over relatively long time periods to plant cover, but there is still much uncertainty about how the balance of C 3 and C 4 species will be affected by climate at a finer temporal scale than season (individual events to months). We monitored cover at five grassland sites with co-dominant C 3 and C 4 grass species or only dominant C 3 grass species for 6 yr in national parks across the Colorado Plateau region to assess the influence of specific months of climate and water balance on changes in grass cover. C 4 grass cover increased and decreased to a larger degree than C 3 grass cover with extremely dry and wet consecutive years, but this response varied by ecological site. Climate and water balance explained 10–49% of the inter-annual variability of cover of C 3 and C 4 grasses at all sites. High precipitation in the spring and in previous year monsoon storms influenced changes in cover of C 4 grasses, with measures of water balance in the same months explaining additional variability. C 3 grasses in grasslands where they were dominant were influenced primarily by longer periods of climate, while C 3 grasses in grasslands where they were co-dominant with C 4 grasses were influenced little by climate anomalies at either short or long periods of time. Our results suggest that future changes in spring and summer climate and water balance are likely to affect cover of both C 3 and C 4 grasses, but cover of C 4 grasses may be affected more strongly, and the degree of change will depend on soils and topography where they are growing and the timing of the growing season.

Ecosphere↗

Riparian ecosystem creation and restoration: a literature summary

Riparian ecosystems generally compose a minor proportion of surrounding areas, but typically are more structurally diverse and more productive in plant and animal biomass than adjacent upland areas. Riparian areas supply food, cover, and water (especially important in the arid West) for a large diversity of animals, and serve as migration routes and forest connectors between habitats for a variety of wildlife, particularly ungulates and birds. Because riparian ecosystems often are relatively small areas and occur in conjunction with waterways, they are vulnerable to severe alteration. Riparian ecosystems throughout the U.S. have been heavily impacted by man's activities. Riparian ecosystem creation and restoration have been used as mitigation for project impacts from highway, bridge, and pipeline construction; water development; flood control channel modifications; industrial and residential development; agriculture; irrigation; livestock grazing; mining; and accidental habitat loss. Creation of a riparian ecosystem in| a more mesic upland area (e.g., ‘grassland or cropland) adjacent to a river requires appropriate water supply and grading the topography to suitable elevations to support plantings of riparian vegetation. Restoration involves returning the ecosystem to pre disturbance conditions and typically implies revegetation. Removing exotic vegetation or restoring water supplies to pre disturbance level also may be involved. Enhancement of riparian ecosystems commonly refers to improving existing conditions to increase habitat value, usually by increasing plant or community diversity to increase value for wildlife. Managing a riparian ecosystem typically involves enhancement techniques. However, creation and restoration projects often involve use of techniques considered more management-oriented (e.g., fencing to prevent cattle grazing until planted vegetation of a created or restored wetland is established). Protection of an existing riparian ecosystem from impact should be of utmost importance during planning and construction phases of development projects. If loss or damage is unavoidable, wetland creation or restoration can be used as mitigation. Compared to other wetland types (e.g., coastal wetlands), projects and techniques involving creation or restoration of riparian ecosystems are not well documented. For example, only 8% of the records in the WCR Data Base contained information on riparian ecosystems, whereas 31% of the records contained information on coastal emergent or forested ecosystems. To provide a source of currently available literature, riparian information from 92 records (primarily published papers or reports) in the U.S. Fish and Wildlife Service's (FWS) Wetland Creation-Restoration (WCR) Data Base (Schneller-McDonald et al. 1988) was used to develop a literature summary of creation and restoration of riparian ecosystems. The summary provides an overview of the status of riparian ecosystems in the U.S., a discussion of several riparian functions, and a review of some techniques used for planning, implementing, monitoring, and measuring project success of creation-restoration efforts. Case studies of various creation or restoration projects are used to demonstrate these techniques and to report some results of their use. Several well-documented case studies are discussed in detail to illustrate more extensive efforts to plan, implement, or monitor riparian ecosystem creation-restoration projects. For the purpose of this report, riparian ecosystems are defined as landscapes adjacent to drainageways of floodplains that exhibit vegetation, soil, and hydrologic mosaics along topographic and moisture gradients that are distinct from the predominant landscape surface types. Major plant communities are described under palustrine system in Cowardin et al. (1979). Literature from the WCR Data Base was used to provide a summary of riparian ecosystem creation-restoration literature. Thus, information concerning natural systems is not included unless discussed in these articles. This focus allows the reader to compare relative information available on riparian ecosystem creation-restoration efforts. However, this focus also results in limited information in some sections of the report (e.g., Status of Riparian Ecosystems in the U.S.). Individuals involved in riparian ecosystem creation-restoration efforts are encouraged to thoroughly examine available literature on natural and altered systems. Brinson et al. (1981) provide a comprehensive review and synthesis of the ecology and status of riparian ecosystems. Over 500 articles are cited in their 124-page report. Chapters include the following topics: status of riparian ecosystems in the U.S., ecological functions and properties of riparian ecosystems (e.g., geomorphology, primary productivity, nutrient cycling, hydrology), importance of riparian ecosystems to fish and wildlife, and considerations in valuation (ecologic and economic) of riparian ecosystems. Brinson et al. (1981) also discuss management of riparian ecosystems. Riparian ecosystem management literature was not included in the WCR Data Base, unless the article also discussed creation or restoration.

Report↗

Effects of a changing climate on the hydrological cycle in cold desert ecosystems of the Great Basin and Columbia Plateau

Climate change is already resulting in changes in cold desert ecosystems, lending urgency to the need to understand climate change effects and develop effective adaptation strategies. In this review, we synthesize information on changes in climate and hydrologic processes during the last century for the Great Basin and Columbia Plateau, and discuss future projections for the 21st century. We develop mid-century projections of temperature and climate for the Great Basin and Columbia Plateau at timescales relevant to managers (2020 -2050), and discuss concepts and strategies for adapting to the projected changes. For the instrumented record in the Great Basin and Columbia Plateau (1985-2011), a temperature increase of 0.7°C to 1.4°C has been documented, but changes in precipitation have been relatively minor with no clear trends. Climate projections for 2020 to 2050 indicate that temperatures will continue to increase, especially in winter and during the night. Precipitation is more difficult to project and estimates range from an 11% decrease to 25% increase depending on location. Recent records indicate that the Great Basin and Columbia Plateau are becoming more arid, a trend that is projected to continue. Droughts are likely to become more frequent and last longer, invasive annual grasses are likely to continue to expand, and the duration and severity of wildfire seasons are likely to increase. Climate projections can help in developing adaptive management strategies for actual or expected changes in climate. Strategies include reducing the risks of nonnative invasive plant spread and wildfires that result in undesirable transitions, planning for drought, and where necessary, facilitating the transition of populations, communities and ecosystems to new climatic conditions. A proactive approach to planning for and adapting to climate change is needed and publicly available internet based resources on climate data and planning strategies are available to help meet that need.

California, Idaho, Nevada, Oregon, Utah, Washingto↗

Interaction of beaver and elk herbivory reduces standing crop of willow

Populations of beaver and willow have not thrived in riparian environments that are heavily browsed by livestock or ungulates, such as elk. The interaction of beaver and elk herbivory may be an important mechanism underlying beaver and willow declines in this competitive environment. We conducted a field experiment that compared the standing crop of willow three years after simulated beaver cutting on paired plants with and without intense elk browsing (∼85% utilization rate). Simulated beaver cutting with intense elk browsing produced willow that was small (biomass and diameter) and short, with far fewer, but longer, shoots and a higher percentage of dead biomass. In contrast, simulated beaver cutting without elk browsing produced willow that was large, tall, and leafy, with many more, but shorter, shoots (highly branched) and a lower percentage of dead biomass. Total stem biomass after three years was 10 times greater on unbrowsed plants than on browsed plants. Unbrowsed plants recovered 84% of their pre-cut biomass after only two growing seasons, whereas browsed plants recovered only 6%. Thus, the interaction of beaver cutting and elk browsing strongly suppressed the standing crop of willow. We predict that a lack of willow suitable as winter food for beaver can cause beaver populations to decline, creating a feedback mechanism that reduces beaver and willow populations. Thus, intense herbivory by ungulates or livestock can disrupt beaver–willow mutualisms that naturally occur in less competitive environments.

Ecological Applications↗

An emerging crisis across northern prairie refuges: Prevalence of invasive plants and a plan for adaptive management

In the northern Great Plains, native prairies managed by the U.S. Fish and Wildlife Service (Service) can be pivotal in conservation of North America's biological diversity. From 2002 to 2006, we surveyed 7,338 belt transects to assess the general composition of mixed-grass and tallgrass prairie vegetation across five "complexes" (i.e., administrative groupings) of national wildlife refuges managed by the Service in North Dakota and South Dakota. Native grasses and forbs were common (mean frequency of occurrence 47%-54%) on two complexes but uncommon (4%-13%) on two others. Conversely, an introduced species of grass, smooth brome (Bromus inermis), accounted for 45% to 49% of vegetation on two complexes and another species, Kentucky bluegrass (Poa pratensis) accounted for 27% to 36% of the vegetation on three of the complexes. Our data confirm prior suspicions of widespread invasion by introduced species of plants on Service-owned tracts of native prairie, changes that likely stem in part from a common management history of little or no disturbance (e.g., defoliation by grazing or fire). However, variability in the degree and type of invasion among prairie tracts suggests that knowledge of underlying causes (e.g., edaphic or climatic factors, management histories) could help managers more effectively restore prairies. We describe an adaptive management approach to acquire such knowledge while progressing with restoration. More specifically, we propose to use data from inventories of plant communities on Service-owned prairies to design and implement, as experiments, optimal restoration strategies. We will then monitor these experiments and use the results to refine future strategies. This comprehensive, process-oriented approach should yield reliable and robust recommendations for restoration and maintenance of native prairies in the northern Great Plains. 2009 by the Board of Regents of the University of Wisconsin System.

Ecological Restoration↗

Dispersal limitation does not control high elevational distribution of alien plant species in the southern Sierra Nevada, California

Patterns of elevational distribution of alien plant species in the southern Sierra Nevada of California were used to test the hypothesis that alien plant species invading high elevations around the world are typically climate generalists capable of growing across a wide elevational range. The Sierra Nevada has been heavily impacted for more than a century and a half, first by heavy grazing up into high elevation meadows, followed by major logging, and finally, by impacts associated with recreational use. The comparative elevational patterns of distribution and growth form were compared for native and alien plant species in the four families (Asteraceae, Brassicaceae, Fabaceae, and Poaceae) that contribute the majority of naturalized aliens in the study area. The distribution of realized climatic niche breadth, as measured by elevational range of occurrence, was virtually identical for alien and native species, with both groups showing a roughly Gaussian distribution peaking with species whose range covers a span of 1500–1999 m. In contrast to alien species, which only rarely occurred at higher elevations, native species showed a distribution of upper elevation limits peaking at 3000–3499 m, an elevation that corresponds to the zone of upper montane and subalpine forests. Consistent with a hypothesis of abiotic limitations, only a few alien species have been ecologically successful invaders at subalpine and alpine elevations above 2500 m. The low diversity of aliens able to become established in these habitats is unlikely due to dispersal limitations, given the long history of heavy grazing pressure at high elevations across this region. Instead, this low diversity is hypothesized to be a function of life history traits and multiple abiotic stresses that include extremes of cold air and soil temperature, heavy snowfall, short growing seasons, and low resource availability. These findings have significant implications for resource managers.

California↗

Survey of invasive ants at Hakalau Forest National Wildlife Refuge

We conducted a survey for invasive ants at Hakalau Forest National Wildlife Refuge, Hawai‘i Island, during 2009–2010 to evaluate potential threats to native arthropod communities and food webs. The focal area of the survey was the upper portion of the Hakalau Unit of the refuge, where native forest was being restored in abandoned cattle pastures. This area, between 1575 and 1940 m elevations, contained much alien kikuyu grass (Pennisetum clandestinum), but koa (Acacia koa) trees and other native species that were planted in the past 20 years were rapidly filling in the pasture. We surveyed for ants at predetermined points along roads, fences, and corridors of planted koa. Sampling methods primarily consisted of hand searching and pitfall traps, but bait cards were used additionally in some instances. Our results indicated that a single species, Cardiocondyla kagutsuchi, was widespread across the upper portion of the refuge. Cardiocondyla kagutsuchi seemed absent, or at least rare, in areas of tall, dense grass. Due to the undulating topography of the area, however, the dense grass cover was interspersed with outcroppings of exposed, gravelly soil. Presumably due to warming by the sun, many of the outcropped habitats supported colonies of C. kagutsuchi. We did not detect ants in the old-growth forest below the abandoned pastures, presumably because microhabitat conditions under the forest canopy were unsuitable. Although ecological impacts of C. kagutsuchi have not been reported, they may be limited by the small size of the ant, the relatively small size of colonies, and the apparent preference of the ant for disturbed areas that are dominated by alien species. Notably, our survey of Keanakolu-Mana Road between the Observatory Road (John A. Burns Way) and the town of Waimea detected a population of Argentine ants (Linepithema humile) approximately 5.1 km north of the Maulua Section of the refuge. We also surveyed for ants on the Kona Forest Unit of the refuge. This small survey focused on approximately 14 km of roads located below about 1600 m elevation. We found two species, Solenopsis papuana and Nylanderia bourbonica. Solenopsis papuana was more widespread, being found along the southern, northern, and western boundaries, while N. bourbonica was detected only at 790 m elevation on the southern boundary. Of the two species, S. papuana seemed more likely to affect native arthropod communities due to its tendency to form relatively large, aggressive colonies and its ability to inhabit intact mesic and wet forests below 1100 m elevation. In contrast, the restriction of N. bourbonica to disturbed habitats indicated a reduced threat to native arthropod communities. Our results on the Kona Forest Unit corroborated those of a study conducted during 1999–2000, although the earlier study was more intensive over time and yielded small numbers of two additional species, Cardiocondyla wroughtonii and Tetramorium bicarinatum, both of which were detected below 792 m elevation along the southern boundary.

Hawaii↗

Northern tamarisk beetle (Diorhabda carinulata) and tamarisk (Tamarix spp.) interactions in the Colorado River basin

Northern tamarisk beetles (Diorhabda carinulata) were released in the Upper Colorado River Basin in the United States in 2004–2007 to defoliate introduced tamarisk shrubs (Tamarix spp.) in the region’s riparian zones. The primary purpose was to control the invasive shrub and reduce evapotranspiration (ET) by tamarisk in an attempt to increase stream flows. We evaluated beetle–tamarisk interactions with MODIS and Landsat imagery on 13 river systems, with vegetation indices used as indicators of the extent of defoliation and ET. Beetles are widespread and exhibit a pattern of colonize–defoliate–emigrate, so that riparian zones contain a mosaic of completely defoliated, partially defoliated, and refoliated tamarisk stands. Based on satellite data and ET algorithms, mean ET before beetle release (2000–2006) was 416 mm/year compared to postrelease (2007–2015) ET of 355 mm/year (p<0.05) for a net reduction of 61 mm/year. This is lower than initial literature projections that ET would be reduced by 300–460 mm/year. Reasons for the lower-than-expected ET reductions are because baseline ET rates are lower than initially projected, and percentage ET reduction is low because tamarisk stands tend to regrow new leaves after defoliation and other plants help maintain canopy cover. Overall reductions in tamarisk green foliage during the study are 21%. However, ET in the Upper Basin has shown a steady decline since 2007 and equilibrium has not yet been reached. Defoliation is now proceeding from the Upper Basin into the Lower Basin at a rate of 40 km/year, much faster than initially projected.

Colorado River↗

The Yellowstone hotspot, Greater Yellowstone ecosystem, and human geography

Active geologic processes associated with the Yellowstone hotspot are fundamental in shaping the landscapes of the greater Yellowstone ecosystem (GYE), a high volcanic plateau flanked by a crescent of still higher mountainous terrain. The processes associated with the Yellowstone hotspot are volcanism, faulting, and uplift and are observed in the geology at the surface. We attribute the driving forces responsible for the northeastward progression of these processes to a thermal plume rising through the Earth&rsquo;s mantle into the base of the southwest-moving North American plate. This progression began 16 million years ago (Ma) near the Nevada-Oregon border and arrived at Yellowstone about 2 Ma. Before arrival of the hotspot, an older landscape existed, particularly mountains created during the Laramide orogeny about 70&ndash;50 Ma and volcanic terrain formed by Absaroka andesitic volcanism mostly between 50&ndash;45 Ma. These landscapes were more muted than the present, hotspot-modified landscape because the Laramide-age mountains had worn down and an erosion surface of low relief had developed on the Absaroka volcanic terrain. The Yellowstone Plateau was built by hotspot volcanism of rhyolitic lavas and caldera-forming rhyolite tuffs (ignimbrites). Streams eroding back into the edges of this plateau have created scenic waterfalls and canyons such as the Grand Canyon of the Yellowstone and Lewis Canyon. Rhyolite is poor in plant nutrients and forms sandy, well-drained soils that support the monotonous, fire-adapted lodgepole pine forests of the Yellowstone Plateau. Non-rhyolitic rocks surround this plateau and sustain more varied vegetation, including spruce, fir, and whitebark pine forests broken by grassy meadows. Heat from the hotspot rises upward and drives Yellowstone&rsquo;s famed geysers, hot springs, and mudpots. These thermal waters are home to specialized, primitive ecosystems, rich in algae and bacteria. The rock alteration associated with hydrothermal systems creates the bright colors of Yellowstone&rsquo;s Grand Canyon. Basin-and-range-style faulting has accompanied migration of the hotspot to Yellowstone and formed the linear mountains and valleys that occur north and south of the hotspot track, which is the present-day eastern Snake River Plain. High rates of basin-and-range faulting occurred adjacent to the migrating Yellowstone hotspot, creating distinctive landscapes within the GYE such as the Teton Range/Jackson Hole, with characteristic rugged, forested ranges and adjacent flat-floored grassy valleys. The difference in altitude between the mountains and valleys provides a topographic gradient in which vegetation maturation advances with altitude; animal-migration patterns also follow this trend. The valleys provide natural meadows, agricultural land, town sites, and corridors for roads. Uplift of the GYE by as much as 1 km (3,000 ft) during the last 5 million years has resulted in ongoing erosion of deep, steep-walled valleys. Many prominent ecological characteristics of Yellowstone derive from this hotspot-induced uplift, including the moderate- to high- altitude terrain and associated cool temperatures and deep snowfall. Modern and Pleistocene climate and associated vegetation patterns strongly relate to the topography created by the hotspot and its track along the eastern Snake River Plain. Winter air masses from the moist northern Pacific Ocean traverse the topographic low of the Snake River Plain to where orographic rise onto the Yellowstone Plateau and adjacent mountains produces deep snow. A winter precipitation shadow forms on the lee (eastern) sides of the GYE. During Pleistocene glacial times, this moisture conduit provided by the hotspot-track-produced ice-age glaciers that covered the core of the present GYE. These glaciers sculpted bedrock and produced glacial moraines that are both forested and unforested, sand and gravel of ice-marginal streams and outwash gravels that are commonly covered with sagebrush-grassland, and silty lake sediments that are commonly covered by lush grassland such as Hayden Valley. The effects of the Yellowstone hotspot also profoundly shaped the human history in the GYE. Uplift associated with the hotspot elevates the GYE to form the Continental Divide, and streams drain radially outward like spokes from a hub. Inhabitants of the GYE 12,000&ndash;10,000 years ago, as well as more recent inhabitants, followed the seasonal green-up of plants and migrating animals up into the mountain areas. During European immigration, people settled around Yellowstone in the lower parts of the drainages and established roads, irrigation systems, and cultural associations. The core Yellowstone highland is too harsh for agriculture and inhospitable to people in the winter. Beyond this core, urban and rural communities exist in valleys and are separated by upland areas. The partitioning inhibits any physical connection of communities, which in turn complicates pursuit of common interests across the whole GYE. Settlements thus geographically isolated evolved as diverse, independent communities

Idaho, Montana, Utah, Wyoming↗

Non-native fishes in Florida freshwaters: a literature review and synthesis

Non-native fishes have been known from freshwater ecosystems of Florida since the 1950s, and dozens of species have established self-sustaining populations. Nonetheless, no synthesis of data collected on those species in Florida has been published until now. We searched the literature for peer-reviewed publications reporting original data for 42 species of non-native fishes in Florida that are currently established, were established in the past, or are sustained by human intervention. Since the 1950s, the number of non-native fish species increased steadily at a rate of roughly six new species per decade. Studies documented (in decreasing abundance): geographic location/range expansion, life- and natural-history characteristics (e.g., diet, habitat use), ecophysiology, community composition, population structure, behaviour, aquatic-plant management, and fisheries/aquaculture. Although there is a great deal of taxonomic uncertainty and confusion associated with many taxa, very few studies focused on clarifying taxonomic ambiguities of non-native fishes in the State. Most studies were descriptive; only 15 % were manipulative. Risk assessments, population-control studies and evaluations of effects of non-native fishes were rare topics for research, although they are highly valued by natural-resource managers. Though some authors equated lack of data with lack of effects, research is needed to confirm or deny conclusions. Much more is known regarding the effects of lionfish ( Pterois spp.) on native fauna, despite its much shorter establishment time. Natural-resource managers need biological and ecological information to make policy decisions regarding non-native fishes. Given the near-absence of empirical data on effects of Florida non-native fishes, and the lengthy time-frames usually needed to collect such information, we provide suggestions for data collection in a manner that may be useful in the evaluation and prediction of non-native fish effects.

Florida↗

Klamath-Siskiyou herpetofauna: Biogeographic patterns and conservation strategies

The Klamath-Siskiyou region of southwest Oregon and northwest California (USA) has some of the most complex landscape mosaics and plant communities in western North America, reflecting its marked diversity of precipitation and topography. With 38 native species of amphibians and reptiles, the Klamath-Siskiyou region has the most species-rich herpetofauna of any similarly sized mountain range in the Pacific Northwest. Although it is a biodiversity 'hot spot,' there are only two endemic species, both salamanders, in the Klamath-Siskiyou region. High diversity is due to the overlap of two major biogeographic groups: the Arcto- (= northern) and Madro- (= southern) Tertiary herpetofaunas. Many of the amphibians in the Klamath-Siskiyou region are restricted to specialized habitats. Much of our knowledge about the biology of the regional fauna is based on studies elsewhere. Distributional surveys and ecological research are needed to address how the herpetofauna responds to timber harvest and other human activities that may reduce populations and increase fragmentation of suitable habitats. Conservation of the region's diverse herpetofauna should emphasize strategies directed at habitat specialists and species at the latitudinal limits of their ranges.

California, Oregon↗

Ecological influence and pathways of land use in sagebrush

Land use in sagebrush (Artemisia spp.) landscapes influences all sage-grouse (Centrocer-cus spp.) populations in western North America. Croplands and the network of irrigation canals cover 230,000 km2 and indirectly influence up to 77% of the Sage-Grouse Conservation Area and 73% of sagebrush land cover by subsidizing synanthropic predators on sage-grouse. Urbanization and the demands of human population growth have created an extensive network of con-necting infrastructure that is expanding its influence on sagebrush landscapes. Over 2,500 km 2 are now covered by interstate highways and paved roads; when secondary roads are included, 15% of the Sage-Grouse Conservation Area and 5% of existing sagebrush habitats are 2.5 km from roads. Density of secondary roads often exceeds 5 km/km 2 , resulting in widespread motorized access for recreation, creating extensive travel corridors for management actions and resource development, subsidizing predators adapted to human presence, and facilitating spread of exotic or invasive plants. Sagebrush lands also are being used for their wilderness and recreation values, including off highway vehicle use. Approximately 12,000,000 animal use months (AUM amount of forage to support one livestock unit per month) are permitted for grazing livestock on public lands in the western states. Direct effects of grazing on sage-grouse populations or sagebrush landscapes are not possible to assess from current data. However, management of lands grazed by livestock has influenced sagebrush ecosystems by vegetation treatments to increase forage and reduce sagebrush and other plant species unpalatable to livestock. Fences (2 km/km 2 in some regions), roads, and water developments to manage livestock movements further modify the landscape. Oil and gas development influences 8% of the sagebrush habitats with the highest intensities occurring in the eastern range of sage-grouse; 20% of the sagebrush distribution is indirectly influenced in the Great Plains, Wyoming Basin, and Colorado Plateau SMZs. Energy development physically removes habitat to construct well pads, roads, power lines, and pipelines; indirect effects include habitat fragmentation, soil disturbance, and facilitation of exotic plant and animal spread. More recent development of alternative energy, such as wind and geothermal, creates infrastructure in new regions of the sage-grouse distribution. Land use will continue to be a dominant stressor on sage-brush systems; its individual and cumulative effects will challenge long-term conservation of sage-grouse populations.

Book chapter↗

Sea otter predation and community organization in the western Aleutian Island, Alaska

Predation by the sea otter (Enhydra lutris) limits epibenthic invertebrates, especially sea urchins (Strongylocentrotus polyacanthus), in turn allowing a luxuriant development of the macroalgal canopy. Where sea otters are abundant, sea urchins are small and scarce in shallow water, and the association of fleshy macroalgae apparently is regulated by competition. Sea urchins are larger and more abundant in deeper water, where they are less accessible to sea otters. Macroalgae are most abundant, and competition in the plant association is severest, near the sublittoral fringe where sea otters can remove sea urchins most efficiently. In deep water, competition among maccroalgae is reduced because the light intensity is lower and grazing by sea urchins increases. On islands where sea otters are absent, sea urchins are abundant, large, and are probably limited by intraspecific competition; and they have eliminated fleshly macroalgae. Available data suggest that the association of Laminaria spp. and Agarum cribrosum contributes most to primary production in nearshore areas of the western Aleutian Islands. Where sea otters are absent and sea urchins have eliminated this plant association, some higher trophic forms also are absent or less abundant than where sea otters are common and the plant association is well developed. Earlier studies of sea otter food suggested that low—density populations of sea otters consume primarily sea urchins and mollusks in the western Aleutian Islands. Later studies of high—density populations showed a wider variety of foods consumed, with fish an important component of the diet. These studies support our observations on the differences in availability of these foods between islands with and without sea otters.

Ecology↗