Print version ISSN 0716-078X
Rev. chil. hist. nat. vol.77 no.3 Santiago Sept. 2004
| Revista Chilena de Historia Natural 77: 411-437, 2004 |
Disruption of ecosystem processes in western North America by invasive species
Alteración de procesos en ecosistemas en el oeste de Norteamérica producidos por especies invasoras
Jeffrey S. Dukes1 & Harold A. Mooney
Department of Biological Sciences, Stanford University, Stanford, California 94305-5020 USA Current address1: Biology Department, University of Massachusetts, Boston, Massachusetts 02125 USA; e-mail: firstname.lastname@example.org
Many ecosystems of western North America have been dramatically changed by non-native species. Here, we review ecological impacts of 56 plant, animal, fungus, and protist species that were brought to this region by humans. We discuss characteristics of invasive species that can lead to major ecosystem impacts, and explore how invasive species alter many different attributes of ecosystems. Specifically, we include examples of invasive species that affect geomorphology, fire regimes, hydrology, microclimate, atmospheric composition, nutrient cycling, and productivity. Finally, we review the direct consequences of biological invasions for some native species. We summarize examples from this paper in Appendix 1. Our examples illustrate how, as invasive species have become dominant across large areas of western North America's grassland, shrubland, dune, riparian, and estuarine ecosystems, the properties and functioning of these systems have changed. To date, some systems in this region, such as its forests, remain relatively unaffected by invasive species. However, recent attacks of forest pathogens highlight the potential vulnerability of these ecosystems.
Key words: biological invasions, ecosystem functioning, community structure, exotic species, impact.
Muchos ecosistemas de Norteamérica occidental han cambiado dramáticamente a causa del efecto producido por especies no autóctonas. Aquí se muestra una revisión del impacto ecológico producido por 56 especies diferentes de plantas, animales y hongos, y especies de protistas que fueron traídos a esta región por humanos. Discutimos las características de las especies invasoras que pueden producir un gran impacto en el ecosistema, y exploramos cómo las especies invasoras pueden alterar de forma muy diferente los atributos de un ecosistema. Específicamente, incluimos ejemplos de especies invasoras que afectan a la geomorfología, a los regímenes del fuego, a la hidrología, al microclima, a la composición atmosférica, al ciclo de nutrientes, y a la productividad. Finalmente, revisamos las consecuencias directas de invasiones biológicas de algunas especies autóctonas. Resumimos los ejemplos de este artículo en el Anexo 1. Nuestros ejemplos ilustran cómo, a medida que la especie invasora llega a ser dominante a lo largo de áreas extensas de ecosistemas como los prados del oeste de Norteamérica occidental, en zonas arbustivas, dunas, cauces de ríos y estuarios, las propiedades y el funcionamiento de estos ecosistemas han cambiado. Hasta ahora, algunos ecosistemas en esta región, como los bosques, permanecen relativamente intactos por efecto de la especies invasoras. Sin embargo, ataques recientes de patógenos a los bosques ponen de manifiesto la vulnerabilidad potencial de estos ecosistemas.
Palabras clave: invasiones biológicas, funcionamiento ecosistémico, estructura de comunidades, especies exóticas, impacto.
As global transport becomes faster and cheaper, the distant corners of our planet become increasingly connected. People and their products, traveling from continent to continent, provide opportunities for thousands of plant and animal species to be transported, or even to hitchhike along. Most of the hitchhiking species do not survive in their new environment. However, some thrive, and some of those that thrive cause great ecological or economic harm. Many alien species attack or outcompete native species, and a small percentage cause major changes in the appearance and operation of ecosystems (Vitousek et al. 1997, Sala et al. 1999). Invasive species (those aliens that thrive and increase their ranges) have already done great economic harm in countries around the world, either by depressing growth or populations of more valuable species, or by directly impeding human activity (e.g., Pimentel et al. 2000). The acceleration of international trade is likely to increase the number of propagules that are transported out of their home ranges each day. Thus, unless measures are taken to prevent propagules from hitching rides, the ongoing expansion of global commerce is likely to exacerbate the problem of biological invasions.
Here, we examine some of the ecological impacts of a variety of alien species, including several invasives. First, we examine characteristics of species that can lead to large ecosystem impacts after their introduction. Then, we explore how alien species are altering many different attributes of ecosystems, such as geomorphology, fire regime, hydrology, microclimate, atmospheric composition, nutrient cycling, and productivity. Finally, we review the direct consequences of biological invasions for some native species. Where possible we use examples of invasive species in western North American ecosystems. These examples are summarized in Appendix 1.
Invasive species that affect ecosystem processes may indirectly impact populations of native species. A simplified conceptual model of direct and indirect interactions among native and alien species is shown in Fig. 1.
We must emphasize that the ecological impacts of many of western North America's invasive species have not been studied, and so this review should not be viewed as comprehensive. We have simply attempted to compile a survey of some invaders' impacts (and potential impacts) in this region.
WHICH BIOLOGICAL INVADERS ARE MOST LIKELY TO ALTER ECOSYSTEM?
Much of western North America's current biota is non-native. For instance, the latest surveys show that 1,109 of California's 8,274 catalogued species (13.4 %) were introduced from elsewhere (Hobbs & Mooney 1998). Which of the invaders have the potential to disrupt ecosystems? Invasive species that differ from natives in some trait, behavior, or function increasingly alter ecosystem properties and processes as their populations expand. Such species can be grouped into two categories: discrete trait invaders and continuous trait invaders. Discrete trait invaders add a new function to the invaded ecosystem, such as nitrogen fixation, hydraulic lift, or predation on a particular trophic level. Continuous trait invaders differ from natives only in traits that are continuously distributed among species such as litter quality or relative growth rate. Chapin et al. (1996) argue that discrete trait invaders are more likely than continuous trait invaders to have large ecosystem effects, and a recent meta-analysis of invaders' effects on disturbance regimes supports this argument (D'Antonio et al. 1999). However, continuous trait invaders can also alter ecosystem structure and functioning, especially if they constitute a large proportion of the ecosystem's biomass at one trophic level.
The conceptual model in Fig. 2 illustrates how an invader that replaces other species in its trophic level can alter properties of an ecosystem such as water use, flammability, or isoprene emission. In this example, the invading species has a higher inherent value for the hypothetical ecosystem function than the native species (although this value could just as easily be lower than that of the native). In an uninvaded ecosystem, the value of the ecosystem function may vary over time due to shifts in species dominance. As an invasion progresses, the invader makes up an increasing proportion of biomass at its trophic level. This forces the value of the function toward the inherent value of the invader. If the function crosses some threshold (increased water use draws down water tables below a certain level, increased flammability accelerates the fire cycle, increased predation on an herbivore reduces vegetation disturbance, among others), the species composition of the region may change, either as a result of the local elimination of a native species that required the pre-invasion conditions for survival or due to an increase in the susceptibility of the system to invasion by other species. Species composition change could further displace the ecosystem function or trait from its initial value. However, competition with native species may prevent the invader from achieving a great enough dominance to force the value of the ecosystem function across a threshold.
IMPACTS OF NON-NATIVE SPECIES
Geomorphology and soil disturbance regimes
Introduced animals and plants have altered geomorphic processes in many of western North America's ecosystems. Beaver (Castor canadensis) are native to some parts of the west, but have been introduced in areas beyond their original range (Johnson & Harris 1990). By building dams, beaver directly modify the morphology and hydrology of streams. Dams create ponds, slow the stream current, increase sediment retention, alter seasonal stream discharge regimes, and expand the influence of the water table (Naiman et al. 1988). Decomposition, nutrient cycling, and water quality are also altered by beaver ponds (Naiman et al. 1986). These effects can influence the composition of downstream plant and animal communities (Pollock et al. 1995).
Although the introduction of beaver can substantially alter stream geomorphology, the extent of these changes is limited by the number of suitable sites for beaver ponds (Johnston & Naiman 1990).
Just as beaver dams trap substrate and increase sedimentation in an area, other introduced animals cause soil to be lost. Many species contribute to erosion by disturbing the soil or overgrazing vegetation. Studies of these phenomena on California's Channel Islands led to the implementation of new land management practices. For instance, feral goats (Capra hircus) and sheep (Ovis aries) were removed or exterminated on some islands once their impacts on geomorphology and vegetation were understood (Schuyler 1987, Keegan et al. 1994, Laughrin et al. 1994). Before their eradication in 1987, sheep compacted the soils of Santa Cruz Island and overgrazed the plants. These activities suppressed woody species regeneration (Wehtje 1994), reduced the amount of herbaceous cover (Klinger et al. 1994), and contributed to the development of deep hillslope gullies (Brumbaugh 1980). Feral goats on Santa Catalina Island (Coblentz 1980) and European rabbits (Oryctolagus cuniculus) on Santa Barbara Island (Halvorson personal communication) accelerated erosion by similar means. Herbaceous cover rebounded on these islands after the animals were removed (Klinger et al. 1994, Laughrin et al. 1994). Disturbance by feral pigs (Sus scrofa) may still contribute to erosion on the Channel Islands. Feral pig activity hampers regeneration of woody species such as the native oak Quercus agrifolia (coast live oak) on Santa Cruz Island (Peart et al. 1994).
On the California mainland, the range and population size of pigs has expanded since the 1950s (Waithman et al. 1999). Feral pigs are now the primary agents of soil disturbance in some California grasslands. Kotanen (1995) found that pigs overturned 7.4 % of the surface of five Californian coastal meadows annually, changing the species composition and richness of the grubbed areas. Pigs may increase siltation of streams by turning up soil along streambanks and wallowing in the channel (Ray 1988, Peart et al. 1994).
Mountain goats (Oreamnos americanus), which are native to some parts of Washington, were transported outside of their range to that state's Olympic Mountains in the 1920s. The goats caused serious damage to native vegetation and increased erosion in alpine areas of Olympic National Park, leading to the development of a goat population management plan (Carlquist 1990).
We found no research on the effects of alien invertebrates on the geomorphology of western ecosystems. It seems likely that some burrowing invertebrate invaders have affected the movement of the substrate in which they live. For instance, since at least 1893, San Francisco Bay's terraces and margins have been under attack from the isopod Sphaeroma quoyanum. This native of Australia and New Zealand riddles sediments and structures with half-centimeter-wide burrows. Such burrows may increase erosion at the Bay's edge (Cohen & Carlton 1995).
Plant invaders can affect geomorphology by altering the stability of the substrate in which they live. For instance, two species of introduced beachgrass have slowed dune movement on the west coast of United States. The most widespread of these, Ammophila arenaria (European beachgrass), was imported from northern Europe around 1869 to stabilize dunes in San Francisco's Golden Gate Park (Lamb 1898). Three factors may have contributed to A. arenaria's subsequent colonization of the majority of dunes on the United States' Pacific coast. First, widespread planting of A. arenaria continued for a period of 100 years (Wiedemann & Pickart 1996). Second, lateral growth of rhizomes allowed the grass to spread rapidly. Finally, living rhizome fragments may have washed down the shore to colonize new sites (Wallén 1980).
Ammophila arenaria collects sand more effectively than the previously dominant native grass Leymus mollis (native dune grass; Barbour et al. 1985, Barbour & Johnson 1988), and its invasion has caused the rapid development of steep, continuous foredunes along the coast. In some locations, foredunes have grown to a height of 10 m (Wiedemann & Pickart 1996). These large foredunes, which border the upper beach above the mean high tide line, may starve active inland dune systems of sand, causing them to become more static and allowing vegetation to become established (Wiedemann & Pickart 1996). This phenomenon, in combination with the rapid spread of A. arenaria on the dunes themselves, has reduced the area of open dunes on the coast (Wiedemann 1984). In addition, the changes in foredune characteristics have led to a new alignment of some inland dunes. The dunes and swales inland of Leymus foredunes were oriented roughly perpendicular to the shore, but those inland of A. arenaria foredunes tend to run parallel to the coast (Barbour & Johnson 1988).
Wiedemann & Pickart (1996) argue that the Pacific northwest coast has experienced periods of slow foredune stabilization followed by strong erosion events for thousands of years, and suggest that although A. arenaria has accelerated sand stabilization, native plants would also eventually cause the formation of an unbroken foredune. However, a native-dominated foredune might not attain the height or strength of A. arenaria foredunes, and might be more rapidly eroded by waves during storms.
Another introduced species of beachgrass now dominates the foredunes of southern Washington, and alternates with A. arenaria as the dominant foredune species in the northern part of the state (Seabloom & Wiedemann 1994). This species is Ammophila brevigulata (American beachgrass), a native of the east coast and Great Lakes regions of North America. Both Ammophila species cause the formation of long, unbroken foredunes, but those formed by A. brevigulata are lower than those formed by A. arenaria (Seabloom & Wiedemann 1994).
As introduced beachgrasses reshape the west coast's dunes, introduced cordgrass species (Spartina spp.) stabilize sediments in its estuaries. The most widespread alien cordgrass is Spartina alterniflora (smooth cordgrass). This native of North America's east coast now grows in San Francisco Bay, Suislaw Estuary in Oregon, and in two locations in Washington (Daehler & Strong 1996). Spartina alterniflora outcompetes the native cordgrass Spartina foliosa in parts of San Francisco Bay where the two species co-occur (Callaway & Josselyn 1992). The upper boundaries of these two perennials are roughly the same, but S. alterniflora can colonize areas 9 to 20 cm below the lower limit of the native (Callaway & Josselyn 1992). This encroachment into lower tidal areas extends the marshlands and reduces mudflat area. The denser growth and thicker stems of S. alterniflora slow the tidal flow more effectively, causing suspended sediment to precipitate and become trapped in the alien's thick network of roots and rhizomes (Daehler & Strong 1996). In a study of a New Zealand estuary, Bascand (1970) found that areas colonized by S. alterniflora accumulated up to 5 cm of sediment per year, while open mud flats trapped little or no sediment. Sayce (1991)1, who has studied S. alterniflora in Washington, asserts that the invader can trap as much as 15 cm of material annually. As sediment accumulates in formerly open areas, these areas may rise above the intertidal zone. In some estuaries, sediment accretion and growth of S. alterniflora has restricted tidal channels and waterways (Asher 1991). For example, the invader colonized and threatened the flow capacity of a major flood control channel in San Francisco Bay, leading to the initiation of an eradication program (Daehler 1996).
Three other introduced cordgrass species, S. anglica, S. densiflora, and S. patens, now grow in estuarine ecosystems of the Pacific coast (Daehler & Strong 1996), and may cause similar changes to those driven by S. alterniflora. Spartina anglica, which has invaded Puget Sound in Washington, is particularly well known for its ability to rapidly colonize mudflats and accrete sediment in European marshlands (Thompson 1991, Daehler & Strong 1996).
Exotic invaders also affect riparian geomorphology. Shrubs of the genus Tamarix have caused the most widespread changes. Recent estimates suggest that Tamarix spp. (tamarisk, salt cedar) has invaded approximately 4,700 km2 of western United States floodplain (Zavaleta 2000). Blackburn et al. (1982) studied the impact of Tamarix spp. invasion on sedimentation processes in the Brazos River in Texas. As the phreatophytic shrub encroached onto formerly unoccupied sandbanks along the river, it stabilized sediments and slowed water velocity. As water slowed, sediment deposition increased and the river channel narrowed. When channel sizes are reduced, flooding frequencies and flood levels increase. Tamarix has caused similar changes to the geomorphology of the Green River in Canyonlands National Park, Utah (Graf 1978).
Other exotic plant species may also increase sediment deposition, although the evidence is less solid. Arundo donax (arundo, giant reed) has invaded many waterways of southern and central coastal California (Hickman 1993, Dudley & Collins 1995). This tall perennial reed purportedly traps and stabilizes more sediment than native vegetation, thus decreasing channel sizes (Frandsen & Jackson 1993). Arundo is also said to grow densely enough to substantially reduce the carrying capacity of small waterways (Robbins et al. 1951). However, no data have been published to support these observations. In larger streams and rivers, rafts of the reed can lodge against natural obstructions, bridges, or culverts, forming debris dams (Frandsen & Jackson 1993). Arundo clogging is suspected to have played a role in the bursting of a levee on the Santa Margarita river, which caused $12.5 million dollars in damage to the Camp Pendleton military base (La Rue 1996). Mats of Senecio mikanoides (German ivy) may also form debris dams in some California waterways, redirecting water out of its channel (Chippin personal communication).
Another exotic plant species stabilizes sediment in some Arizona streams. During floods, mats of Cynodon dactylon (bermudagrass) protect streambanks from erosion and shelter the basal fragments of native aquatic macrophytes. Recovery of the aquatic macrophyte communities proceeds more rapidly in these stabilized sites than in areas without C. dactylon (Dudley & Grimm 1994).
Since its introduction for landscaping purposes, Cortaderia jubata (pampas grass) has colonized disturbed areas such as eroding banks, dry washes, cliffs, and logged redwood forests throughout coastal California (Kerbavaz 1985). Dense stands of the perennial must alter erosion rates from invaded areas, but no studies have quantified these changes.
Invading plants can also increase rates of erosion. The biennial forb Centaurea maculosa (spotted knapweed) is replacing native bunchgrasses throughout many rangelands of western North America (Roché & Roché 1988, Tyser & Key 1988, Lindquist et al. 1996). Lacey et al. (1989) found greater losses of sediment and greater runoff from areas dominated by C. maculosa than from bunchgrass communities. The C. maculosa community's larger fraction of bare ground may explain these differences.
From the above examples it is clear that in the case of both plants and animals, some invaders accelerate the process of erosion, and others stabilize substrates or trap sediments. Of the invasive plants that affect geomorphology, most slow erosion. Of the nonindigenous animals, most accelerate erosion, especially on islands. In addition to the types of species mentioned above, some biological invaders influence geomorphic processes through their effects on disturbance regimes. For instance, alien plants that alter the fire frequency or intensity in an area also affect erosion because fire reduces plant and litter cover (Swanson 1981). We discuss invaders that alter fire regimes in the next section.
Exotic grasses have replaced or currently threaten vast regions of western deserts and shrublands through their influence on fire regimes (D'Antonio & Vitousek 1992). The invading grasses occupy gaps between native plants in these sparsely vegetated systems, creating a continuous path of fine fuel that promotes the spread of fire. The grass populations tend to rebound quickly after fires, but many of the native perennials recover slowly. Short fire-return intervals decimate populations of many shrubs and desert perennials. Thus, by accelerating fire frequencies, grass invaders can reduce the density of widely spaced perennials, turning shrublands to annual grasslands.
The most dramatic conversion of this kind is occurring in the mixed-shrub steppe of Nevada, western Utah, southern Idaho, eastern Oregon, and eastern Washington. Many areas formerly dominated by Artemisia tridentata (big sagebrush) and other shrubs are today covered with exotic annual grasses, primarily Bromus tectorum (cheatgrass; Young & Evans 1978, Whisenant 1990, Billings 1994, Pellant & Hall 1994) and Taeniatherum caput-medusae (medusahead, Young 1992). Mack (1981) chronicled the invasion of B. tectorum into the region, and Whisenant (1990) documented the accompanying change in fire-return intervals. Pinyon-juniper woodland ecosystems of the Great Basin region have undergone a similar metamorphosis due to anthropogenic disturbance of native vegetation and the spread of B. tectorum (Billings 1994).
Introduced grasses and forbs also threaten to accelerate fire cycles in portions of the Mojave and Sonora deserts. The most prevalent exotic annuals in these deserts are Bromus madritensis ssp. rubens (red brome, syn. Bromus rubens) and B. tectorum, but B. trinii (Chilean chess), Schismus barbatus (Mediterranean grass), and Erodium cicutarium (redstem filaree) are also common in some areas (Brown & Minnich 1986, Hunter 1991, Rundel & Gibson 1996, Brooks 1999). Hunter (1991) studied populations of brome grasses in the transition zone between the Mojave and Great Basin deserts, and found that a series of wet years allowed B. madritensis to become quite dense. At its peak in 1988, B. madritensis produced 34 g m-2, which was 97 % of that year's total biomass production. Although exotic annuals are the most prolific invaders of North America's deserts, perennial species also pose a threat to the Sonoran desert. Cenchrus ciliaris (Buffel grass, syn. Pennisetum ciliare) has been widely planted in northern Mexico as a forage species for cattle, and was planted in the southwestern United States by the Soil Conservation Service and the Arizona Department of Transportation (Pater personal communication). This southern African perennial can survive in a wide variety of Sonora desert microenvironments, and has spread into many undisturbed areas (Burgess et al. 1991, Búrquez & Quintana 1994). Lehmann lovegrass (Eragrostis lehmanniana), another African perennial that was once recommended by the Soil Conservation Service, has also spread from planted areas and become dominant in some areas of Arizona's Sonora desert (Anable et al. 1992). Grass litter decomposes slowly in dry desert climates, maintaining a continuous fuel load through years of low biomass production. Fires carried by grass litter threaten populations of native annuals (Hunter 1991) or long-lived perennials (Brown & Minnich 1986, Búrquez & Quintana 1994) in at least three types of North American deserts.
Deliberate post-fire seeding and accidental invasion of non-native annuals into chaparral and coastal sage scrub may facilitate an increase in fire frequencies in some areas of southern California. Planted annuals such as the grasses Lolium multiflorum (Italian ryegrass) and Vulpia myuros (rattail fescue) and the mustard Hirschfeldia incana, and invaders such as Bromus madritensis and B. diandrus (ripgut brome) have recently increased in dominance in these ecosystems (Keeley 1995, Minnich & Dezzani 1998). These exotics persist through frequent fires more successfully than native shrubs such as Adenostoma fasciculatum (chamise), Ceanothus oliganthus, and Salvia mellifera (black sage; Zedler et al. 1983, Keeley 1995). A combination of increased fire frequencies, competition from introduced annuals, and other anthropogenic factors may drive the replacement of chaparral and coastal sage scrub ecosystems by grassland in many areas of southern California (Keeley 1995, Minnich & Dezzani 1998).
Fire-promoting exotic grasses also threaten riparian ecosystems. Arundo donax (arundo, giant reed) has invaded many waterways of southern and central coastal California. The tall perennial reed quickly colonizes areas left bare from flooding, achieving dominance along riverbanks and even in some estuaries (Dudley & Collins 1995). Arundo increases the fuel load in riparian zones and provides an unbroken fuel corridor along which fire can spread (Jackson 1993, Scott 1993). Increased fire frequencies may prevent recovery of native plant species and purportedly changes the successional cycle of the cottonwood-willow riparian system, converting the vegetation to an Arundo monoculture (Bell 1993).
In western North America, most of the invasive species that affect fire regimes are grasses, and most of these species decrease fire-return intervals. Many native species, especially longer-lived plants in arid regions, cannot tolerate these frequent fires. Of all the ways that invasive species modify ecosystems in western North America, this impact on fire regime may have the most widespread repercussions for native species.
The invasion of exotic plants into North American ecosystems has altered the hydrology of vast areas of western North America. Invasions of Tamarix spp. have lowered water tables in many riparian zones of the southwestern United States (e.g., Neill 1983, Weeks et al. 1987). On a per-unit-leaf-area basis, water loss of Tamarix is comparable to that of native phreatophytes (Sala et al. 1996, Cleverly et al. 1997), so what characteristics of Tamarix lead to such great water loss? Two mechanisms have been proposed. First, monospecific stands of the invasive shrub may develop a higher leaf area index (LAI) than would be found in native stands. Second, Tamarix stands tend to occupy a wider cross-section of the riparian zone than native stands (Sala et al. 1996).
Spanish colonists began altering the composition and hydrology of California grasslands around 1769 when they introduced plants from Mediterranean Europe (Frenkel 1970). Until that time, perennial grasses such as Nassella pulchra (purple needlegrass) probably dominated most California grasslands (Heady 1988; but see Mooney et al. 1986). Under conditions of heavy grazing and possibly drought, introduced annuals outcompeted most of the original species (Hendry 1931, Mack 1989, Rejmánek et al. 1991). The annual grasses such as Avena spp. and Bromus spp. that now dominate extensive areas use less of the available deep water over the course of a growing season than do native perennial grasses, probably because they senesce earlier and have shallower roots (Holmes & Rice 1996, Gerlach 2000). The excess water left by annual grasses may have created favorable conditions for Centaurea solstitialis (yellow starthistle, Dyer & Rice 1999), a more recent invader of these grasslands (Maddox & Mayfield 1985). Centaurea is a late-season annual that now draws deep soil moisture down to levels found under native perennial grasses (Gerlach 2000). Borman et al. (1992) observed similar soil moisture dynamics among introduced annual and native perennial grasses and C. solstitialis in southwestern Oregon. Hydrologic changes caused by grassland invaders may affect the establishment of native woody perennials (Da Silva & Bartolome 1984, Gordon & Rice 1993).
The replacement of native and naturalized systems by Eucalyptus spp. forests (Boyd 1985, Bulman 1988, Westman 1990) may have altered the hydrology of large tracts of California, although no studies have quantitatively documented these changes. Eucalyptus (primarily Eucalyptus globulus, blue gum) forests have replaced many different ecosystem types in California. These forests probably altered hydrology most drastically where they replaced grassland. Eucalyptus roots grow much deeper than those of grassland species (Canadell et al. 1996), and extract water from lower in the soil profile. Eucalyptus globulus is the only widespread woody alien known to transport deep soil moisture to shallower layers through hydraulic lift (Dawson personal communication). It is not known whether this process eases drought stress for nearby shallow-rooted plants, as occurs around other hydraulic lifters (Dawson 1993). Evergreen eucalypts transpire year-round, but California's grasslands are mostly dormant in the summer. Although Eucalyptus forests probably transpire more water than grasslands on an annual, per-area basis, the forests have greater surface roughness and deeper litter layers than grasslands (Poore & Fries 1985, Robles & Chapin 1995), and may lose less water to surface evaporation. On balance, eucalypt forests probably extract more water from the ground than California grasslands. Such a difference has been observed in South Africa, where Van Lill et al. (1980) documented a dramatic reduction in runoff from a grassland after its conversion to an E. grandis plantation. In areas where Eucalyptus forests have replaced native forests or woodlands, alterations to local hydrology were probably less drastic.
Replacement of native perennial vegetation by Bromus tectorum in western shrublands (see above) reduced rooting depths and shortened the period when plants in these systems are photosynthetically active. As a consequence, annual evapotranspiration has declined in some of these systems (Cline et al. 1977, Kremer & Running 1996).
Although relatively few studies have compared the hydrology of invaded and pristine plant communities in western North America, these few studies have examined changes caused by some of the most widespread species that are likely to have effects. Two alien genera, Tamarix and Eucalyptus, probably increase water use rates beyond what the invaded ecosystems experienced previously. The invasion of California's alien-dominated annual grasslands by Centaurea solstitialis may move the hydrological cycle closer to a pre-European settlement dynamic. In some parts of western North America, the invasion of annual grasses has reduced plant water use, primarily by reducing the abundance of deeply rooted species.
Climate and microclimate
Biological invasions have altered moisture transport and land surface characteristics of a large portion of western North America (see above). However, the extent and implications of these changes are poorly understood. Recent studies have indicated that changes in vegetation types can alter local or regional climatic patterns (Lean & Warrilow 1989, Shukla et al. 1990, Chase et al. 1999, Hoffman & Jackson 2000). While it seems possible that some invaders of western North America, particularly the annual grasses, have altered the land surface characteristics and hydrology of sufficient area to affect the regional climate, this hypothesis has not yet been tested.
Plant invaders can also alter the microclimate of invaded areas. For instance, dense stands of Ammophila arenaria sharply reduce temperatures and available light at the underlying surface of the Pacific coast's dunes relative to stands of the native grass Leymus mollis (Barbour et al. 1985). Spartina alterniflora may similarly reduce light levels under the plant canopy of marshes, which could depress estuarine algal production (Callaway & Josselyn 1992). Soil temperature, soil moisture, and light conditions under the plant canopy affect the germination and establishment success of plants (Evans & Young 1970, Evans & Young 1972), and the suitability of habitat for animals.
Invasive species have undoubtedly altered microclimates in many other ecosystems, but we did not find studies that documented these changes.
Composition of the atmosphere
Biological invaders can alter the flux of gases between the land surface and the atmosphere. In the United States, annual emissions of volatile organic compounds (VOCs) from vegetation equal or exceed anthropogenic emissions (Guenther 1997), although the biogenic output is more evenly distributed across the landscape. Because vegetation contributes such a great proportion of atmospheric VOCs, and because plant species vary widely in their rate of VOC emission (Evans et al. 1982, Winer et al. 1992, Arey et al. 1995), regional atmospheric VOC pools depend largely on the species composition of local plants. Invasive species that overrun large areas can alter regional VOC emissions and atmospheric composition (Monson et al. 1995), with important consequences for atmospheric chemistry and air quality (Mooney et al. 1987). Air quality of the west coast may have been adversely affected by the introduction of Eucalyptus globulus and Arundo donax, which emit high levels of isoprene relative to many native species (Evans et al. 1982, Hewitt et al. 1990, Arey et al. 1995).
The invasion of plants of one growth form into a region dominated by another may alter the local rate of CO2 uptake and storage. For instance, the replacement of shrublands and pinyon-juniper woodlands by annual grasslands probably reduces long-term carbon storage in biotic pools. Conversely, replacement of grassland with Eucalyptus globulus or other woody species may increase both biotic carbon storage and net primary productivity (NPP, Robles & Chapin 1995).
Invaders may also alter the emission of NOx, N2O, NH3, and CH4 from the landscape. Chatigny et al. (1996) found evidence that the species composition of a plant community affects local rates of nitrification and denitrification, which in turn moderate the emission of nitrogenous gases by the microbial community (Schlesinger 1991). By creating ponds, beaver (Castor canadensis) can substantially increase methane emissions from an area (Yavitt et al. 1992). Naiman et al. (1991) estimated that North America's expanding beaver population has contributed 1 % of the recent rise in atmospheric methane. Methane release rates from wetlands also depend on the biomass and structural properties of the inhabitant vascular plants (Sebacher et al. 1985, Schimel 1995, Verville et al. 1998). Invaders such as Lepidium latifolium (perennial pepperweed) and Lythrum salicaria (purple loosestrife) change the amount and composition of wetland vegetation in western North America, and may alter regional methane emission, although this remains unstudied.
Plant invaders can also affect atmospheric composition by altering fire frequencies. During fires, carbon, nitrogen and other elements enter the atmosphere through gasification, volatilization, and convection (Christensen 1994). However, the contribution of exotic grass-fueled fires to changes in atmospheric composition is estimated to be small (D'Antonio & Vitousek 1992).
The effects of biological invaders on the composition of the atmosphere remain largely unstudied. Although these effects are probably small at the global and regional scales, they may in some cases (such as near large eucalypt forests, in the case of VOCs) be locally important.
Nutrient cycling and soil chemistry
Non-native plants and animals can alter ecosystem nutrient cycling and soil chemistry through a number of mechanisms. Nitrogen-fixing invaders increase the rate of N input to a system when they replace non- or less-efficiently fixing plants, and when they colonize open areas. Vitousek & Walker (1989) and Vitousek et al. (1987) found that the invasion of an N-fixing plant into a young ecosystem in Hawaii increased the rate of ecosystem N accumulation more than fourfold.
Horticulturists have introduced many species of leguminous European shrubs to the western United States, including gorse Ulex europaea, and the brooms Cytisus scoparius, Genista monspessulana and Spartium junceum. The nitrogen-fixing capacity of brooms has stimulated research into their potential as yield enhancing understory shrubs in commercial Pseudotsuga menziesii (Douglas-fir) plantations. Studies have focused on C. scoparius, which fixes nitrogen year-round under mild conditions, albeit at relatively low levels (Wheeler et al. 1979, Wheeler et al. 1987). Helgerson et al. (1979) integrated a year's worth of nitrogenase activity measurements on a young stand of broom in Oregon, and estimated an annual fixation rate of 35 kg N ha-1 year-1. This value itself represents a substantial input, but because this method of estimation is imprecise, the actual fixation rate could be twice as high (Wheeler et al. 1987). In addition to the brooms and gorse, several leguminous annual and perennial herbs such as Medicago polymorpha (burr medic), Melilotus alba (white sweetclover), and Trifolium hirtum (rose clover) have invaded Western ecosystems (Hickman 1993). It is not known whether all of the invasive legumes actively fix N.
Nitrogen inputs to a system from N-fixing alien plants may be constrained by the compatibility of the plants with local symbionts. Absence of a compatible Rhizobium strain could explain the low nodulation on C. scoparius roots observed by Wheeler et al. (1987) in Oregon and Scotland, although acidic soil conditions or other factors could also have limited nodulation.
Some plant invaders may decrease nitrogen inputs in their vicinity by leaching chemicals that reduce the ability of other species to fix N (Rice 1992). In glasshouse and pasture studies in New Zealand, Wardle et al. (1994) found evidence that decomposing leaves of the invasive thistle Carduus nutans inhibit nitrogen fixation by Trifolium repens. Carduus nutans has invaded many areas of western North America, but no published studies have examined whether this thistle adversely affects growth and nitrogen fixation of native legumes.
Both N-fixing and non-fixing plants directly affect the nutrient retention of ecosystems by moderating erosion of nutrient-rich topsoil, and by sequestering available soil nutrients, thus reducing leaching losses. Gholz et al. (1985) found that the invasive annual Senecio sylvaticus took up a large fraction of the nutrients released from unburned clear-cut stands of old-growth Douglas-fir in Oregon. Invaders can also indirectly modulate N losses by influencing soil moisture and nitrate levels, which can constrain denitrification rates. We found no studies of invasive plants that examined indirect effects on nutrient retention.
Although fires increase short-term N-availability in a system, frequent fires generally cause long-term loss of N (Ojima et al. 1994), depending on grazing practices (Hobbs et al. 1991). Alien species that accelerate fire cycles (such as those mentioned above) could eventually increase N losses from ecosystems.
Plant species strongly influence the rate at which nutrients cycle within an ecosystem through litter-quality feedbacks (Wedin & Tilman 1996, Evans et al. 2001; for review see Hobbie 1992). The invasion of a species with rapidly decomposing litter into an ecosystem dominated by plants with slow-decomposing litter will accelerate net nutrient mineralization in the system (Van Vuuren et al. 1992, Van Vuuren & Berendse 1993, Van Vuuren et al. 1993). For instance, leaves of the notorious wetland invader Lythrum salicaria (purple loosestrife) have higher phosphorus (P) concentrations and decompose more quickly than shoots of native Typha spp. (Emery & Perry 1996). These characteristics will force changes in the nutrient dynamics of invaded wetlands that may accelerate eutrophication of downstream water bodies.
Introduced detritivores also alter ecosystems' internal nitrogen cycling. In Kansas' tallgrass prairie, James (1991) observed that the invasion of European earthworms has decreased nutrient mineralization and soil turnover rates. At least 45 species of exotic earthworms have been introduced to North America north of Mexico (Reynolds 1995). These species have been particularly successful in disturbed habitats, and also dominate some wildland habitats including southern California chaparral and riparian zones (Kalisz & Wood 1995). It is unclear how detritivore invasions have affected these ecosystems.
A few of western North America's most invasive plants release compounds that alter the soil's nutrient availability or suitability for other species of plants. For instance, the ubiquitous tumbleweed Salsola tragus (syn. S. iberica) releases oxalate in leachate from its canopy and litter (Cannon et al. 1995). The leached oxalic acid increases phosphorus (P) availability in the soil by solubilizing it from the pool of inorganic-bound soil P. Other western invaders such as Halogeton glomeratus and some plants in the Oxalidaceae probably affect P availability similarly, as they also produce high concentrations of oxalic acid (Kingsbury 1964, Whitson et al. 1996).
The iceplant Mesembryanthemum crystallinum exploits its high salt tolerance to outcompete native species in coastal areas of California. This South African annual stockpiles salts in living tissue. Once the tissue has senesced, rainfall and fog drip leach the salts out and deposit them on the soil surface. The high concentrations of salt that accumulate around populations of this grassland invader exclude competitors through osmotic interference (Vivrette & Muller 1977).
Another iceplant that plagues California's coastal plant communities, Carpobrotus edulis, modifies soil in a different way. This rapidly spreading succulent acidifies the soil around its roots (D'Antonio 1990), through an as yet unstudied mechanism. Investigations in England suggest that the common west coast invader Ulex europaea may affect soils similarly (Grubb et al. 1969, Grubb & Suter 1971). Changes in soil pH can influence the dominance of different plant species in old fields (Tilman & Olff 1991) and montane forests (Goldberg 1985).
Other introduced species release compounds that can inhibit their own growth, as well as that of competitors. Phytotoxic chemicals that leach from the leaves and litter of eucalypts during rainfall and fog drip events can directly inhibit germination and retard seedling growth of grasses, as well as of the eucalypts themselves (del Moral & Muller 1969, del Moral & Muller 1970).
Nutrient cycles and soil properties are subject to change by many of western North America's invasive species. The most widespread change may be an increase in N inputs from nonindigenous legumes. However, few researchers have studied the amount of atmospheric N fixed by these species. Exotic earthworms may also have caused important and widespread changes in nutrient cycles, but these changes remain unstudied.
Productivity and decomposition
An ecosystem's live biomass (LB) and NPP may respond to the addition of a species with novel traits. For instance, invaders that access or use existing resources more completely or efficiently than native plant species, or that produce more readily mineralizable litter than native species, may cause increases in LB and NPP. Examples of exotic species that access previously untapped water and nutrient stores can be found in previous sections (see sections on hydrology and nutrient cycling). Invaders that represent a new life form or that eliminate a prominent life form may also alter an area's LB and NPP. Unfortunately, relatively few studies of invaders in western North America have included data on these basic ecosystem properties.
Along the edges of San Francisco Bay, invading Spartina alterniflora produces six to seven times as much aboveground biomass per unit area as the native cordgrass Spartina foliosa, and 1.6 to 3.2 times as much belowground biomass (Callaway & Josselyn 1992). The great aboveground production of S. densiflora, deposited as wrack on the upper marsh in Humbolt Bay, California, smothers native marsh species, opening space for further S. densiflora invasion (Daehler & Strong 1996).
Along the California coast, Ammophila arenaria-dominated beach communities have up to three times as much standing biomass as native-dominated communities (Barbour & Robichaux 1976, Pavlik 1983a). The difference in aboveground biomass of stands of A. arenaria and the native perennial grass Leymus mollis stems from A. arenaria's higher nitrogen use efficiency, greater allocation of nitrogen and photosynthetic assimilate to leaf blades, different architecture, and slower leaf senescence (Pavlik 1983a, 1983b, 1983c).
Robles & Chapin (1995) compared adjacent exotic-dominated annual grassland and eucalypt-covered sites in the San Francisco Bay area. Annual aboveground production of Eucalyptus globulus forests was more than twice that of grassland, and the layer of slow-decomposing E. globulus litter had grown nine times thicker than the litter layer of the grassland.
Growth and decomposition rates of primary producers can be affected by organisms on other trophic levels. Plant pathogens that attack one of the dominant species in an ecosystem can, at least temporarily, lower the system's productivity and live biomass. At least three exotic fungi are causing widespread damage to western trees, and must have temporarily lowered the productivity of some forests. The fungal pathogen Fusarium subglutinans f. sp. pini, endemic to the southeastern United States, causes pitch canker disease in a number of coniferous tree species (Storer et al. 1994). The disease appeared in California in 1986 (McCain et al. 1987), and spread rapidly, killing off Pinus radiata stands along much of the coast. The disease has now reached all three of California's relictual P. radiata stands (Gordon et al. 1997), and may eventually infect as many as 85 % of the trees in these stands (Wood personal communication). Pitch canker has also been found in a native Pinus attenuata stand near Mendocino (Storer et al. 1994).
The fungus Cronartium ribicola, which causes white pine blister rust, has infected pines in the Cascades, Rocky Mountains, and the Sierra Nevada (Kinloch & Dulitz 1990). Growth of the pathogen can rapidly girdle and kill shoots of pines in the subgenus Strobus (white pines), or lead to their attack by Dioryctria spp. larvae. White pine blister rust epidemics generally lead to the loss of all infected seedlings and saplings, and the death of many adult trees (Kinloch & Dulitz 1990, Tomback et al. 1995)
A third imported fungus has attacked the roots of Port-Orford-cedar (Chamaecyparis lawsoniana) throughout its native range in southwestern Oregon and northwestern California. This fungus, Phytophthora lateralis, probably arrived from Asia on ornamental plants sometime in the 1920s. A field survey of three infested drainages found 46 % mortality of Port-Orford-cedar and 10 % mortality of another native, Pacific yew (Taxus brevifolia, Murray & Hansen 1997).
The recent invasion of Asian clams (Potamocorbula amurensis) has probably increased consumption rates of bacterioplankton and phytoplankton in San Francisco Bay. These clams, which can reach densities as high as 10,000 individuals m-2 (Carlton et al. 1990), filter the water column more than once per day in deep waters, and as much as 13 times per day in shallow waters (Werner & Hollibaugh 1993). This rapid filtration equals or exceeds planktonic growth rates, and may affect the standing crop of plankton and intensity of the annual spring algal blooms in San Francisco Bay.
Although relatively few studies have compared the productivity of invaded and uninvaded communities in western North America, it seems likely that most invasive plants have increased resource use of invaded communities, and also increased ecosystem-level productivity. Invasive species that alter disturbance regimes or otherwise eliminate other life forms from the community may be the most common exceptions to this trend. The effects of invasive animals on primary productivity are rarely examined, and we can only speculate that these species have had relatively little effect on the productivity of most ecosystems, excepting the case of Asian clams in San Francisco Bay.
Although biological invaders add to the species richness of an area upon their arrival, some can eventually cause the decline or even extinction of native species through predation, competition, disease, or replacement of resource species. In fact, the spread of biological invaders is generally regarded to be the second greatest agent of species endangerment and extinction after habitat destruction (Wilcove et al. 1998). As a general rule, native populations are more likely to be impacted by invaders if they are in isolated systems such as on islands, in lakes or in streams than if they are on the mainland (D'Antonio & Dudley 1995).
Introduced fish and amphibians have suppressed native fish and amphibian populations in the majority of lakes and rivers in western North America. Non-native bullfrogs (Rana catesbeiana) prey on and compete with yellow-legged frogs (Rana boylii) (Moyle 1973, Kupferberg 1997), and introduced predatory fish appear to be a factor in the decline of mountain yellow-legged frogs (Rana pipiens) in Yosemite National Park (Drost & Fellers 1996). Bullfrogs and exotic fish both may have contributed to the decline in red-legged frog (Rana aurora) populations (Kiesecker & Blaustein 1998, Adams 2000).
Nonindigenous fish species are dominant through most of the San Joaquin river drainage, and the entire Colorado river drainage, where most of the native fish species are listed as threatened or endangered (Moyle 1986). The exotic protozoan Myxobolus cerebralis, the causative agent of whirling disease, is likely responsible for recent declines in populations of the rainbow trout (Oncorhynchus mykiss) (Nehring & Walker 1996, Bergersen & Anderson 1997). However, in many other cases, the decline of native fish can be directly attributed to competition with or predation by fish species that were introduced for sportfishing. Such is the case with the endangered razorback sucker (Xyrauchen texanus) in the Colorado river basin (Minckley et al. 1991). There, heavy predation by introduced fish on larval razorback suckers prevents the regrowth of native populations. Some suspect that the thicktail chub (Gila crassicauda), a native fish species that once populated the Sacramento-San Joaquin delta, was extirpated by the predation of introduced largemouth bass (Micropterus salmoides) and striped bass (Morone saxatilis, Cohen & Carlton 1995). Although non-native fish species have depressed populations of native fauna in many western rivers, global extinctions such as that of the thicktail chub are rare (Moyle & Light 1996).
Just downstream from the thicktail chub's former habitat lies one of the world's most biologically polluted ecosystems, the San Francisco Bay estuary (Cohen & Carlton 1998). Invaders have relegated native species to obscurity in much of this isolated system. The most abundant invader is probably the Asian clam (Potamocorbula amurensis). This small bivalve blankets sediments in many regions of the bay (see above), precluding the establishment of other benthic organisms (Carlton et al. 1990, Cohen & Carlton 1995). Another invader, the mudsnail Ilyanassa obseleta, has usurped much of the former habitat of Cerithidea californica, relegating the native mudsnail to the estuary's highly saline margins (Race 1982). Advancing across the mudflats, Spartina alterniflora has reduced feeding habitat for many species of shorebirds (Callaway & Josselyn 1992). In creeks that feed into San Francisco Bay, two species of introduced crayfish (Orconectes virilis and Pacifastacus leniusculus) may have contributed to the extinction of the native sooty crayfish (Pacifastacus nigrescens). These invaders may now be factors in the decline of the Shasta crayfish (Pacifasctacus fortis) in other regions of California (Light et al. 1995).
At one time, 17 of 19 threatened or endangered plant species on California's Channel Islands were imperiled by exotic species, primarily feral animals (D'Antonio & Dudley 1995). Feral animal disturbance also lowered soil mite diversity (Bennett 1987). Removal of livestock and feral fauna may have allowed regrowth of threatened populations on some of these islands, but Foeniculum vulgare (fennel) and other invasive plants have also benefited from the reduction in herbivory (Beatty & Licari 1992, Brenton & Klinger 1994). Persistent alien plants may now pose the greatest risk to some of the Channel Islands' beleaguered native plant populations.
Although native populations in isolated systems are at the greatest risk from biological invaders, native species in mainland terrestrial ecosystems can also be affected. Some dramatic instances have been mentioned in the above sections (e.g., displacement of western shrublands and California's native grassland community by introduced annual grasses, attack of California's relictual Pinus radiata stands by the pitch canker fungus Fusarium subglutinans, among others); we add and expand on a few examples here.
Argentine ants (Linepithema humile) have been introduced to every continent except Antarctica (Hölldobler & Wilson 1990), and have spread to much of western North America, including California, Arizona, southern Nevada, and Mexico (Wheeler & Wheeler 1986). The invaders displace native ant colonies in California (e.g., Ward 1987, Human & Gordon 1996, Human & Gordon 1997), and possibly throughout the zone of invasion. The displacement of native seed-burying ants by Argentine ants has reduced the establishment of some native shrubs in South Africa (Bond & Slingsby 1984, Slingsby & Bond 1985), and may affect plant species distributions in California grasslands as well (Human 1996).
Argentine ants are known to tend aphids and scale insects; the ecological consequences of this behavior have yet to be investigated (Human 1996).
Non-native eastern gray (Sciurus carolinensis) and fox (S. niger) squirrels have developed large populations in and around California's suburban environments, particularly in the San Francisco Bay area. Native western gray squirrels (S. griseus) have been displaced from some areas where they overlapped with the introduced species, but they maintain dominance in xeric sites (Byrne 1979).
Physical disturbance by feral burros (Equus asinus) once caused contamination of water sources and local elimination of native plant species in Death Valley, California. These burros may have once contributed to the decline of native bighorn sheep (Ovis Canadensis, McMichael 1964 as cited by Woodward 1976), but the population of burros has now been effectively controlled (Loope et al. 1988).
According to Vuilleumier (1991), most of Mediterranean California's non-native bird species have only small populations or are restricted to urban environments, and are unlikely to adversely impact native species. However, some of the state's most abundant bird species were introduced from elsewhere, including the European starling (Sturnus vulgaris), house sparrow (Passer domesticus), and rock dove (Columbia livia). Starlings are thought to have the most negative impact on native bird species, as they occupy the nest sites of other cavity-nesting birds. This behavior may be contributing to the decline of the purple martin (Progne subis) in California (Small 1994).
Exotic plant invasions can also reduce the amount of habitat available for native birds. An invasion of Tamarix spp. at Eagle Borax Spring in Death Valley, California, caused a large marsh to dry up, reducing habitat for migratory birds (Neill 1983). Subsequent removal of the invader led to the return of surface water and wildlife. Along western North American rivers, stands of Tamarix spp. (Cohan et al. 1978, Hunter et al. 1988) and Elaeagnus angustifolia (Russian-olive, Knopf & Olson 1984) support a more depauperate avian fauna than do native stands. Government-subsidized replacement of cottonwood-dominated riparian vegetation with invasive Russian-olive may have reduced habitat for cavity-nesting birds (Olson & Knopf 1986). Invasions of Lythrum salicaria (purple loosestrife) are thought to have degraded wetland habitat for waterfowl and other
In addition to providing poor foraging for quail, Eragrostis-dominated desert supports a more depauperate faunal community than native-dominated areas (Bock et al. 1986). Similarly, Pacific coast dunes dominated by the introduced beachgrass Ammophila arenaria support fewer species of arthropods (Slobodchikoff & Doyen 1977) and plants (Barbour et al. 1976, Boyd 1992) than native-dominated dunes. The Eurasian perennial herb Euphorbia esula (leafy spurge), which as of 1997 infested more than 110 km2 in the United States and Canada (including parts of Idaho, Montana, Wyoming, and Colorado, Lajeunesse et al. 1999), decreases habitat quality for bison (Bos bison) and deer (Odocoileus spp.) in Theodore Roosevelt National Park, North Dakota (Trammell & Butler 1995).
Invasive exotic plants can threaten populations of rare native plant species, but few cases have been documented. Some findings: on Montana rangeland, introduced Centaurea maculosa can reduce recruitment and population growth of the rare native Arabis fecunda (Lesica & Shelly 1996). Phalaris arundinacea (reed canarygrass), which has genotypes native to both northern North America and northern Europe, appears to have displaced the endangered aquatic annual Howellia aquatilis (Lesica 1997) from parts of two Montana marshes. In central New Mexico, habitat for the endemic thistle Cirsium vinaceum, a federally listed threatened species, is being taken over by the Eurasian biennial Dipsacus fullonum (teasel). Studies by Huenneke & Thompson (1995) suggest that the native thistle could decline if the Dipsacus invasion continues unchecked.
Plant invaders can also depress fungal communities. Allen et al. (1995) report lower fungal diversity and colony numbers under introduced annual grasses and forbs compared with neighboring coastal sage habitat. In the intermountain west, most native plant species are mycorrhizal, whereas some invaders are not. When nonmycorrhizal species such as Salsola tragus invade rangeland in this region, populations of vesicular-arbuscular mycorrhizae decline (Goodwin 1992).
Although we found many reports of declines of native biodiversity following invasions, we also found some cases where native species preferentially made use of habitat created by introduced species. In these cases the introduced species were generally replacing habitat that had formerly been provided by native species. For instance, monarch butterflies (Danaus plexippus) that overwinter on the west coast of United States most commonly roost in groves of Eucalyptus globulus. For the monarchs, this introduced species probably replaces habitat that was lost when groves of native trees were logged in the late 1800s (Lane 1993). However, the eucalypts may not provide suitable replacement habitat for all the species that had used the native groves.
It is clear from the above examples that invasive species pose significant threats to native populations. A handful of the most successful invasive species has contributed to declines in populations of several native species through competition, predation, and habitat alteration. Native populations on islands or in isolated systems such as creeks and estuaries seem much more likely to be impacted by invasive species than mainland populations. Considering the number of alien species that have become established in mainland systems, it seems that a minority of these invaders has widespread and adverse impacts on native species. However, effects of the vast majority of mainland invaders remain unstudied.
A small number of biological invaders have drastically changed the structure and functioning of ecosystems in western North America, and thousands of other invaders have wrought more subtle changes. The ecological disruption caused by invasive species, in combination with other factors (including land development and elements of global change such as N deposition, climate change, among others), threatens to drive species extinctions and to reduce the dominance of natives in many ecosystems, altering the character of much of western North America (Fig. 1).
Many of western North America's grassland, shrubland, dune, riparian, and estuarine ecosystems are already dominated, probably irreversibly, by non-native species. Some of California's remaining coastal scrub is undergoing annual grass invasion, and some of the state's chaparral faces threats from management practices that encourage annual grass dominance. The forests of the west coast have escaped threats from biological invaders more successfully than other systems. However, the current declines of Port-Orford-cedar, relictual stands of Pinus radiata, and five-needled pines in the Sierra Nevada, all due to introduced fungi, highlight the potential vulnerability of these ecosystems.
We know very little about the impacts of most biological invaders on native species and on ecosystem functioning (Levine et al. 2003). Even some potentially dramatic impacts of the most widespread invasions have yet to be studied. For example, the large-scale replacement of mixed-shrub steppe with annual grasslands must have affected the energy and water balance of the intermountain west, and thus may have affected regional weather patterns. Transformations such as this would have important ecological and economic consequences, and should be examined. We do know that some invaders are causing important ecological changes. If we observe and quantify these changes, and we identify viable ecosystem restoration strategies, then our society (and its land managers) will be better able to make informed decisions about which of these invaders are noxious enough to merit large-scale eradication campaigns.
We thank J. Canadell, C. D'Antonio, G. Joel, J. Polsenberg, J. Randerson, C. Still, J. Verville and an anonymous reviewer for helpful criticism of drafts of this manuscript. We are grateful to Marta Berrocal-Lobo for help with Spanish translations. J.S.D. received support from a NASA Earth System Science Fellowship.
1 Sayce K (1991) Species displaced by Spartina in the Pacific Northwest. In: Mumford TF Jr, P Peyton, JR Sayce & S Harbell (eds) Spartina workshop record: 26-27. Washington Sea Grant Program, Seattle, Washington, USA.
Adams MJ (2000) Pond permanence and the effects of exotic vertebrates on anurans. Ecological Applications 10: 559-568. [ Links ]
Allen MF, SJ Morris, F Edwards & EB Allen (1995) Microbe-plant interactions in Mediterranean-type habitats: Shifts in fungal symbiotic and saprophytic functioning in response to global change. In: Moreno JM & WC Oechel (eds) Global change and Mediterranean-type ecosystems: 287-305. Springer-Verlag, New York, New York, USA. [ Links ]
Anable ME, MP McClaran & GB Ruyle (1992) Spread of introduced Lehmann lovegrass Eragrostis lehmanniana Nees. in southern Arizona. Biological Conservation 61: 181-188. [ Links ]
Anderson MG (1995) Interactions between Lythrum salicaria and native organisms: a critical review. Environmental Management 19: 225-231. [ Links ]
Arey J, DE Crowley, M Crowley, M Resketo & J Lester (1995) Hydrocarbon emissions from natural vegetation in California's south coast air basin. Atmospheric Environment 29: 2977-2988. [ Links ]
Asher R (1991) Spartina introduction in New Zealand. In: Mumford Jr. TF, P Peyton, JR Sayce & S Harbell (eds) Spartina workshop record: 23-24. Washington Sea Grant Program, Seattle, Washington, USA. [ Links ]
Barbour MG, TM De Jong & AF Johnson (1976) Synecology of beach vegetation along the Pacific Coast of the United States of America: a first approximation. Journal of Biogeography 3: 55-69. [ Links ]
Barbour MG, TM DeJong & BM Pavlik (1985) Marine beach and dune plant communities. In: Chabot BF & HA Mooney (eds) Physiological ecology of North American plant communities: 296-322. Chapman and Hall, New York, New York, USA. [ Links ]
Barbour MG & AF Johnson (1988) Beach and dune. In: Barbour MG & J Major (eds) Terrestrial vegetation of California: 223-261. California Native Plant Society, Sacramento, California, USA. [ Links ]
Barbour MG & RH Robichaux (1976) Beach phytomass along the California coast. Bulletin of the Torrey Botanical Club 103: 16-20. [ Links ]
Bascand LD (1970) The roles of Spartina species in New Zealand. Proceedings of the New Zealand Ecological Society 17: 33-40. [ Links ]
Beatty SW & DL Licari (1992) Invasion of fennel (Foeniculum vulgare) into shrub communities on Santa Cruz Island, California. Madroño (United States) 39: 54-66. [ Links ]
Bell GP (1993) Biology and growth habits of giant reed (Arundo donax). In: Jackson NE, P Frandsen & S Duthoit (eds) Proceedings of the Arundo donax workshop, Ontario, California: 1-6. California Exotic Pest Plant Council, Berkeley, California, USA. [ Links ]
Bennett SG (1987) The effects of feral animals on soil mites recovered from Catalina ironwood groves (Lyonothamnus floribundus) on Santa Catalina Island, California. In: Hochberg FG (ed) Third California islands symposium: recent advances in research in the California islands: 155-170. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Bergersen EP & DE Anderson (1997) The distribution and spread of Myxobolus cerebralis in the United States. Fisheries 22: 6-7. [ Links ]
Billings WD (1994) Ecological impacts of cheatgrass and resultant fire on ecosystems in the western Great Basin. In: Monsen SB & SG Kitchen (eds) Proceedings in ecology and management of annual rangelands: 22-30. United States Department of Agriculture, Forest Service Intermountain Research Station, Ogden, Utah, USA. [ Links ]
Blackburn WH, RW Knight & JL Schuster (1982) Saltcedar influence on sedimentation in the Brazos River. Journal of Soil and Water Conservation 37: 298-301. [ Links ]
Bock CE, JH Bock, KL Jepson & JC Ortega (1986) Ecological effects of planting African lovegrasses in Arizona. National Geographic Research 2: 456-463. [ Links ]
Bond W & P Slingsby (1984) Collapse of an ant-plant mutualism: the Argentine ant (Iridomyrmex humilis) and myrmecochorous Proteaceae. Ecology 65: 1031-1037. [ Links ]
Borman MM, DE Johnson & WC Krueger (1992) Soil moisture extraction by vegetation in a Mediterranean/maritime climatic regime. Agronomy Journal 84: 897-904. [ Links ]
Boyd D (1985) Status report on invasive weeds: Eucalyptus. Fremontia (United States) 12: 19-20. [ Links ]
Boyd RS (1992) Influence of Ammophila arenaria on foredune plant microdistributions at Point Reyes National Seashore, California. Madroño (United States) 39: 67-76. [ Links ]
Brenton B & R Klinger (1994) Modeling the expansion and control of fennel (Foeniculum vulgare) on the Channel Islands. In: Halvorson WL & GJ Maender (eds) The fourth California islands symposium: update on the status of resources: 497-504. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Brooks ML (1999) Alien annual grasses and fire in the Mojave desert. Madroño 46: 13-19. [ Links ]
Brown DE & RA Minnich (1986) Fire and changes in creosote bush scrub of the western Sonora Desert, California. American Midland Naturalist 116: 411-422. [ Links ]
Brumbaugh RW (1980) Recent geomorphic and vegetal dynamics on Santa Cruz Island, California. In: Power DM (ed) The California islands: proceedings of a multidisciplinary symposium: 139-158. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Bulman TL (1988) The eucalyptus in California. Fremontia (United States) 16: 9-12. [ Links ]
Burgess TL, JE Bowers & RM Turner (1991) Exotic plants at the desert laboratory, Tucson, Arizona. Madroño (United States) 38: 96-114. [ Links ]
Búrquez A & M Quintana (1994) Islands of diversity: Ironwood ecology and the richness of perennials in a Sonora desert biological reserve. In: Nabhan GP & JL Carr (eds) Ironwood: an ecological and cultural keystone of the Sonora desert: 9-27. Conservation International, Washington, District of Columbia, USA. [ Links ]
Byers JE (2000) Competition between two estuarine snails: implications for invasions of exotic Species. Ecology 81: 1225-1239. [ Links ]
Byrne S (1979) The distribution and ecology of the non-native tree squirrels Sciurus carolinensis and Sciurus niger in northern California. Ph.D. Thesis, University of California, Berkeley, California. 190 pp. [ Links ]
Callaway JC & MN Josselyn (1992) The introduction and spread of smooth cordgrass (Spartina alterniflora) in south San Francisco Bay. Estuaries 15: 218-226. [ Links ]
Canadell J, RB Jackson, JR Ehleringer, HA Mooney, OE Sala & ED Schulze (1996) Maximum rooting depth of vegetation types at the global scale. Oecologia 108: 583-594. [ Links ]
Cannon JP, EB Allen, MF Allen, LM Dudley & JJ Jurinak (1995) The effects of oxalates produced by Salsola tragus on the phosphorus nutrition of Stipa pulchra. Oecologia 102: 265-272. [ Links ]
Carlquist B (1990) An effective management plan for the exotic mountain goats in Olympic National Park, Washington USA. Natural Areas Journal 10: 12-18. [ Links ]
Carlton JT, JK Thompson, LE Schemel & FH Nichols (1990) Remarkable invasion of San Francisco Bay (California, USA) by the Asian clam Potamocorbula amurensis: introduction and dispersal. Marine Ecology Progress Series 66: 81-94. [ Links ]
Chapin FS III, HL Reynolds, CM D'Antonio & VM Eckhart (1996) The functional role of Invasive species disrupt ecosystem processes species in terrestrial ecosystems. In: Walker B & W Steffen (eds) Global change and terrestrial ecosystems: 403-428. Cambridge University Press, Cambridge, United Kingdom. [ Links ]
Chase TN, RA Pielke, TGF Kittel, JS Baron & TJ Stohlgren (1999) Potential impacts on Colorado Rocky Mountain weather due to land use changes on the adjacent Great Plains. Journal of Geophysical Research Atmospheres 104: 16673-16690. [ Links ]
Chatigny MH, D Prevost, DA Angers, LP Vezina & FP Chalifour (1996) Microbial biomass and N transformations in two soils cropped with annual and perennial species. Biology and Fertility of Soils 21: 239-244. [ Links ]
Cheater M (1992) Alien invasion. Nature Conservancy (United States) 42: 24-29. [ Links ]
Christensen NL (1994) The effects of fire on physical and chemical properties of soils in Mediterranean-climate shrublands. In: Moreno JM & WC Oechel (eds) The role of fire in Mediterranean-type ecosystems: 79-95. Springer-Verlag, New York, New York, USA. [ Links ]
Cleverly JR, SD Smith, A Sala & DA Devitt (1997) Invasive capacity of Tamarix ramosissima in a Mojave desert floodplain: the role of drought. Oecologia 111: 12-18. [ Links ]
Cline JF, DW Uresk & WH Rickard (1977) Comparison of water used by a sagebrush-bunchgrass community and a cheatgrass community. Journal of Range Management 30: 199-201. [ Links ]
Coblentz BE (1980) Effects of feral goats on the Santa Catalina Island ecosystem. In: Power DM (ed) The California islands: proceedings of a multidisciplinary symposium: 167-170. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Cohan DR, BW Anderson & RD Ohmart (1978) Avian population responses to saltcedar along the lower Colorado River. Forest Service General Technical Report WO-12: 371-381, United States Forest Service, Washington, USA. [ Links ]
Cohen AN & JT Carlton (1995) Non-indigenous aquatic species in a United States estuary: a case study of the biological invasions of the San Francisco Bay and Delta. United States Fish and Wildlife Service, Washington, District of Columbia, USA. 272 pp. [ Links ]
Cohen AN & JT Carlton (1998) Accelerating invasion rate in a highly invaded estuary. Science 279: 555-558. [ Links ]
Correll JC, TR Gordon, AH McCain, JW Fox, CS Koehler, DL Wood & ME Schultz (1991) Pitch canker disease in California: pathogenicity, distribution, and canker development on Monterey pine (Pinus radiata). Plant Disease 75: 676-682. [ Links ]
D'Antonio CM (1990) Invasion of coastal plant communities by the introduced succulent, Carpobrotus edulis (Aizoaceae). Ph.D. Thesis, University of California, Santa Barbara, California, USA. 212 pp. [ Links ]
D'Antonio CM & TL Dudley (1995) Biological invasions as agents of change on islands versus mainlands. In: Vitousek PM, LL Loope & H Adsersen (eds) Islands: biological diversity and ecosystem function: 103-121. Springer-Verlag, New York, New York, USA. [ Links ]
D'Antonio CM, TL Dudley & M Mack (1999) Disturbance and biological invasions: direct effects and feedbacks. In: Walker LR (ed) Ecosystems of disturbed ground: 413-452. Elsevier, Amsterdam, The Netherlands. [ Links ]
D'Antonio CM & PM Vitousek (1992) Biological invasions by exotic grasses, the grass/fire cycle, and global change. Annual Review of Ecology and Systematics 23: 63-87. [ Links ]
da Silva PG & JW Bartolome (1984) Interaction between a shrub, Baccharis pilularis consanguinea (Asteraceae), and an annual grass, Bromis mollis (Poaceae), in coastal California. Madroño (United States) 31: 93-101. [ Links ]
Daehler CC (1996) Spartina invasions in Pacific estuaries: biology, impact, and management. In: Sytsma MD (ed) Proceedings of the symposium on non-indigenous species in western aquatic ecosystems. Portland State University Lakes and Reservoirs Program, Publication (USA) 96-98: 1-6. [ Links ]
Daehler CC & DR Strong (1996) Status, prediction and prevention of introduced cordgrass Spartina spp. invasions in Pacific estuaries, USA. Biological Conservation 78: 51-58. [ Links ]
Dawson TE (1993) Hydraulic lift and water use by plants: implications for water balance, performance and plant-plant interactions. Oecologia 95: 565-574. [ Links ]
del Moral R & CH Muller (1969) Fog drip: a mechanism of toxin transport from Eucalyptus globulus. Bulletin of the Torrey Botanical Club 96: 467-475. [ Links ]
del Moral R & CH Muller (1970) The allelopathic effects of Eucalyptus camaldulensis. The American Midland Naturalist 83: 254-282. [ Links ]
Drost CA & GM Fellers (1996) Collapse of a regional frog fauna in the Yosemite area of the California Sierra Nevada, USA. Conservation Biology 10: 414-425. [ Links ]
Dudley T & B Collins (1995) Biological invasions in California Wetlands. Pacific Institute for Studies in Development, Environment, and Security, Oakland, California, USA. 62 pp. [ Links ]
Dudley TL & NB Grimm (1994) Modification of macrophyte resistance to disturbance by an exotic grass, and implications for desert stream succession. Verhandlungen der Internationalen Vereinigung für Theoretische und Angewandte Limnologie 25: 1456-1460. [ Links ]
Dukes JS & HA Mooney (1999) Does global change increase the success of biological invaders? Trends in Ecology and Evolution 14: 135-139. [ Links ]
Dyer AR & KJ Rice (1999) Effects of competition on resource availability and growth of a California bunchgrass. Ecology 80: 2697-2710. [ Links ]
Egunjobi JK (1969) Dry matter and nitrogen accumulation in secondary successions involving gorse (Ulex europaeus L.) and associated shrubs and trees. New Zealand Journal of Science 12: 175-193. [ Links ]
Egunjobi JK (1971) Ecosystem processes in a stand of Ulex europaeus L. I. Dry matter production, litter fall and efficiency of solar utilization. Journal of Ecology 59: 31-38. [ Links ]
El-Ghareeb RM (1991) Suppression of annuals by Tribulus terrestris in an abandoned field in the sandy desert of Kuwait. Journal of Vegetation Science 2: 147-154. [ Links ]
Emery SL & JA Perry (1996) Decomposition rates and phosphorus concentrations of purple loosestrife (Lythrum salicaria) and cattail (Typha spp.) in fourteen Minnesota wetlands. Hydrobiologia 323: 129-138. [ Links ]
Evans RA & JA Young (1970) Plant litter and establishment of alien annual weed species in rangeland communities. Weed Science 18: 697-703. [ Links ]
Evans RA & JA Young (1972) Microsite requirements for establishment of annual weeds. Weed Science 20: 350-356. [ Links ]
Evans RC, DT Tingey, ML Gumpertz & WF Burns (1982) Estimates of isoprene and monoterpene emission rates in plants. Botanical Gazette 143: 304-310. [ Links ]
Evans RD, R Rimer, L Sperry & J Belnap (2001) Exotic plant invasion alters nitrogen dynamics in an arid grassland. Ecological Applications 11: 1301-1310. [ Links ]
Frandsen P & N Jackson (1993) Impact of Arundo donax on flood control and endangered species. In: Jackson NE, P Frandsen & S Duthoit (eds) Proceedings of the Arundo donax workshop, Ontario, California: 13-16. California Exotic Pest Plant Council, Berkeley, California, USA. [ Links ]
Frenkel RE (1970) Ruderal vegetation along some California roadsides. University of California Press, Berkeley, California, USA. 163 pp. [ Links ]
Gerlach JD, Jr (2000) A model experimental system for predicting the invasion success and ecosystem impacts of non-indigenous summer-flowering annual plants in California's central valley grasslands and oak woodlands. Ph.D. Thesis, University of California, Davis, California, USA. v + 102 pp. [ Links ]
Gholz HL, GM Hawk, A Campbell & K Cromack, Jr (1985) Early vegetation recovery and element cycles on a clear-cut watershed in western Oregon. Canadian Journal of Forest Research 15: 400-409. [ Links ]
Goldberg DE (1985) Effects of soil pH, competition, and seed predation on the distributions of two tree species. Ecology 66: 503-511. [ Links ]
Goodwin J (1992) The role of mycorrhizal fungi in competetive interactions among native bunchgrasses and alien weeds: a review and synthesis. Northwest Science 66: 251-260. [ Links ]
Gordon DR & KJ Rice (1993) Competitive effects of grassland annuals on soil water and blue oak (Quercus douglasii) seedlings. Ecology 74: 68-82. [ Links ]
Gordon TR, KR Wikler, AJ Storer & DL Wood (1997) Pitch canker and its potential impacts on Monterey pine forests in California. Fremontia (United States) 25: 5-9. [ Links ]
Graf WL (1978) Fluvial adjustments to the spread of tamarisk in the Colorado plateau region. Geological Society of America Bulletin 89: 1491-1501. [ Links ]
Grozholz ED, GM Ruiz, CA Dean, KA Shirley, JL Maron & PG Connors (2000) The impacts of a nonindigenous marine predator in a California bay. Ecology 81: 1206-1224. [ Links ]
Grubb PJ, HE Green & RCJ Merrifield (1969) The ecology of chalk heath: its relevance to the calcicole-calcifuge and soil acidification problems. Journal of Ecology 57: 175-212. [ Links ]
Grubb PJ & MB Suter (1971) The mechanism of acidification of soil by Calluna and Ulex and the significance for conservation. In: Duffey E & AS Watt (eds) The scientific management of animal and plant communities for conservation: 115-133. Blackwell Scientific Publications, Oxford, United Kingdom. [ Links ]
Guenther A (1997) Seasonal and spatial variations in natural volatile organic compound emissions. Ecological Applications 7: 34-45. [ Links ]
Hager HA & KD McCoy (1998) The implications of accepting untested hypotheses: a review of the effects of purple loosestrife (Lythrum salicaria) in North America. Biodiversity and Conservation 7: 1069-1079. [ Links ]
Heady HF (1988) Valley grassland. In: Barbour MG & J Major (eds) Terrestrial vegetation of California: 491-514. California Native Plant Society, Sacramento, California, USA. [ Links ]
Helgerson OT, CT Wheeler, DA Perry & JC Gordon (1979) Annual nitrogen fixation in Scotchbroom. In: Gordon JC, CT Wheeler & DA Perry (eds) Symbiotic nitrogen fixation in the management of temperate forests. Oregon State University, Corvallis, Oregon, USA. [ Links ]
Hendry GW (1931) The adobe brick as a historical source. Agricultural History 5: 110-127. [ Links ]
Hewitt CN, RK Monson & R Fall (1990) Isoprene emissions from the grass Arundo donax L. are not linked to photorespiration. Plant Science 66: 139-144. [ Links ]
Hickman JC (ed) (1993) The Jepson manual: higher plants of California. University of California Press, Berkeley, California, USA. xvii + 1,400 pp. [ Links ]
Hobbie SE (1992) Effects of plant species on nutrient cycling. Trends in Ecology and Evolution 7: 336-339. [ Links ]
Hobbs NT, DS Schimel, CE Owensby & DS Ojima (1991) Fire and grazing in the tallgrass prairie: contingent effects on nitrogen budgets. Ecology 72: 1374-1382. [ Links ]
Hobbs RJ & HA Mooney (1998) Broadening the extinction debate: Population deletions and additions in California and western Australia. Conservation Biology 12: 1-14. [ Links ]
Hoffman WA & RB Jackson (2000) Vegetation-climate feedbacks in the conversion of tropical savanna to grassland. Journal of Climate 13: 1593-1602. [ Links ]
Hölldobler B & EO Wilson (1990) The ants. Harvard University Press, Cambridge, Massachusetts, USA. 732 pp. [ Links ]
Holmes TH & KJ Rice (1996) Patterns of growth and soil-water utilization in some exotic annuals and native perennial bunchgrasses of California. Annals of Botany 78: 233-243. [ Links ]
Holway DA (1999) Competitive mechanisms underlying the displacement of native ants by the invasive Argentine ant. Ecology 80: 238-251. [ Links ]
Huenneke LF & JK Thomson (1995) Potential interference between a threatened endemic thistle and an invasive non-native plant. Conservation Biology 9: 416-425. [ Links ]
Human KG (1996) Interactions between the invasive Argentine ant, Linepithema humile, and native ant species. Ph.D. Thesis, Stanford University, Stanford, California, USA. 121 pp. [ Links ]
Human KG & DM Gordon (1996) Exploitation and interference competition between the invasive Argentine ant, Linepithema humile, and native ant species. Oecologia 105: 405-412. [ Links ]
Human KG & DM Gordon (1997) Effects of Argentine ants on invertebrate biodiversity in northern California. Conservation Biology 11: 1242-1248. [ Links ]
Hunter R (1991) Bromus invasions on the Nevada test site: present status of B. rubens and B. tectorum with notes on their relationship to disturbance and altitude. Great Basin Naturalist 51: 176-182. [ Links ]
Hunter WC, RD Ohmart & BW Anderson (1988) Use of exotic saltcedar (Tamarix chinensis) by birds in arid riparian systems. Condor 90: 113-123. [ Links ]
Jackson N (1993) The story of team arundo. California EPPC News (United States) 1: 6-7. [ Links ]
James SW (1991) Soil, nitrogen, phosphorus, and organic matter processing by earthworms in tallgrass prairie. Ecology 72: 2101-2109. [ Links ]
Johnson V & J Harris (1990) Beaver. In: Zeiner DC, WF Laudenslayer, Jr, KE Mayer & M White (eds) California's wildlife: mammals: 60-61. Department of Fish and Game, Sacramento, California, USA. [ Links ]
Johnston CA & RJ Naiman (1990) The use of a geographic information system to analyze long-term landscape alteration by beaver. Landscape Ecology 4: 5-20. [ Links ]
Kalisz PJ & HB Wood (1995) Native and exotic earthworms in wildland ecosystems. In: Hendrix PF (ed) Earthworm ecology and biogeography in North America: 117-126. Lewis Publishers, Boca Raton, Florida, USA. [ Links ]
Keegan DR, BE Coblentz & CS Winchell (1994) Ecology of feral goats eradicated on San Clemente island, California. In: Halvorson WL & GJ Maender (eds) The fourth annual California islands symposium: update on the status of resources: 323-330. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Keeley JE (1995) Future of California floristics and systematics: wildfire threats to the California flora. Madroño (United States) 42: 175-179. [ Links ]
Kerbavaz JH (1985) Status reports on invasive weeds: pampas grass. Fremontia (United States) 12: 18-19. [ Links ]
Kiesecker JM & AR Blaustein (1998) Effects of introduced bullfrogs and smallmouth bass on microhabitat use, growth, and survival of native red-legged frogs (Rana aurora). Conservation Biology 12: 776-787. [ Links ]
Kingsbury JM (1964) Poisonous plants of the United States and Canada. Prentice-Hall, Englewood Cliffs, New Jersey, USA. 626 pp. [ Links ]
Kinloch BB, Jr & D Dulitz (1990) White pine blister rust at Mountain Home Demonstration State Forest: a case study of the epidemic and prospects for genetic control. Research Paper PSW-204. United States Department of Agriculture, Forest Service, Pacific Southwest Research Station, Berkeley, California, USA. [ Links ]
Klinger RC, PT Schuyler & JD Sterner (1994) Vegetation response to the removal of feral sheep from Santa Cruz island. In: Halvorson WL & GJ Maender (eds) The fourth annual California islands symposium: update on the status of resources: 341-350. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Knopf FL & TE Olson (1984) Naturalization of Russian-olive: implications to Rocky Mountain wildlife. Wildlife Society Bulletin 12: 289-298. [ Links ]
Kotanen PM (1995) Responses of vegetation to a changing regime of disturbance: effects of feral pigs in a Californian coastal prairie. Ecography 18: 190-198. [ Links ]
Kremer RG & SW Running (1996) Simulating seasonal soil water balance in contrasting semi-arid vegetation communities. Ecological Modelling 84: 151-162. [ Links ]
Kupferberg SJ (1997) Bullfrog (Rana catesbeiana) invasion of a California river: the role of larval competition. Ecology 78: 1736-1751. [ Links ]
La Rue S (1996). Seeds of destruction: exotic invaders crowd out native plant species. The San Diego Union-Tribune, San Diego, California, USA, October 16, pp E1, E4. [ Links ]
Lacey JR, CB Marlow & JR Lane (1989) Influence of spotted knapweed (Centaurea maculosa) on surface runoff and sediment yield. Weed Technology 3: 627-631. [ Links ]
Lajeunesse S, R Sheley, C Duncan & R Lym (1999) Leafy Spurge. In: Sheley RL & JK Petroff (eds) Biology and management of noxious rangeland weeds: 249-260. Oregon State University Press, Corvallis, Oregon, USA. [ Links ]
Lamb FH (1898) Sand dune reclamation on the Pacific coast. The Forester 4: 141-142. [ Links ]
Lane J (1993) Overwintering monarch butterflies in California: past and present. In: Malcolm SB & MP Zalucki (eds) Biology and conservation of the monarch butterfly: 335-344. Natural History Museum of Los Angeles County, Los Angeles, California, USA. [ Links ]
Laughrin L, M Carroll, A Bromfield & J Carroll (1994) Trends in vegetation changes with removal of feral animal grazing pressures on Santa Catalina island. In: Halvorson WL & GJ Maender (eds) The fourth annual California islands symposium: update on the status of resources: 523-530. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Laycock WA (1991) Stable states and thresholds of range condition on North American rangelands: a viewpoint. Journal of Range Management 44: 427-433. [ Links ]
Lean J & DA Warrilow (1989) Simulation of the regional climatic impact of Amazon deforestation. Nature 342: 411-413. [ Links ]
Lesica P (1997) Spread of Phalaris arundinacea adversely impacts the endangered plant Howellia aquatilis. Great Basin Naturalist 57: 366-368. [ Links ]
Lesica P & JS Shelly (1996) Competitive effects of Centaurea maculosa on the population dynamics of Arabis fecunda. Bulletin of the Torrey Botanical Club 123: 111-121. [ Links ]
Levine JM, M Vilá, CM D'Antonio, JS Dukes, K Grigulis & S Lavorel (2003) Mechanisms underlying the impacts of exotic plant invasions. Proceedings of the Royal Society of London B 270: 775-781. [ Links ]
Light T, DC Erman, C Myrick & J Clarke (1995) Decline of the Shasta crayfish (Pacifastacus fortis Faxon) of northeastern California. Conservation Biology 9: 1567-1577. [ Links ]
Lindquist JL, BD Maxwell & T Weaver (1996) Potential for controlling the spread of Centaurea maculosa with grass competition. Great Basin Naturalist 56: 267-271. [ Links ]
Loope LL, PG Sánchez, PW Tarr, WL Loope & RL Anderson (1988) Biological invasions of arid land nature reserves. Biological Conservation 44: 95-118. [ Links ]
Mack RN (1981) Invasion of Bromus tectorum L. into western North America: an ecological chronicle. Agro-Ecosystems 7: 145-165. [ Links ]
Mack RN (1989) Temperate grasslands vulnerable to plant invasions: characteristics and consequences. In: Drake JA, HA Mooney, F di Castri, RH Groves, FJ Kruger, M Rejmánek & M Williamson (eds) Biological invasions: a global perspective: 155-179. John Wiley & Sons, Chichester, New York, USA. [ Links ]
Maddox DM & A Mayfield (1985) Yellow starthistle infestations are on the increase. California Agriculture 39: 10-12. [ Links ]
McCain AH, CS Koehler & SA Tjosvold (1987) Pitch canker threatens California pines. California Agriculture 41: 22-23. [ Links ]
Medina AL (1988) Diets of scaled quail in southern Arizona. Journal of Wildlife Management 52: 753-757. [ Links ]
Minckley WL, PC Marsh, JE Brooks, JE Johnson & BL Jensen (1991) Management toward recovery of the razorback sucker. In: Minckley WL & JE Deacon (eds) Battle against extinction: native fish management in the American west: 303-357. The University of Arizona Press, Tucson, Arizona, USA. [ Links ]
Minnich RA & RJ Dezzani (1998) Historical decline of coastal sage scrub in the Riverside-Perris Plain, California. Western Birds (United States) 29: 366-391. [ Links ]
Monson RK, MT Lerdau, TD Sharkey, DS Schimel & R Fall (1995) Biological aspects of constructing volatile organic compound emission inventories. Atmospheric Environment 29: 2989-3002. [ Links ]
Mooney HA, SP Hamburg & JA Drake (1986) The invasions of plants and animals into California. In: Mooney HA & JA Drake (eds) Ecology of biological invasions of North America and Hawaii: 250-272. Springer-Verlag, New York, New York, USA. [ Links ]
Mooney HA, PM Vitousek & PA Matson (1987) Exchange of materials between terrestrial ecosystems and the atmosphere. Science 238: 926-932. [ Links ]
Moyle PB (1973) Effects of introduced bullfrogs, Rana catesbeiana, on the native frogs of the San Joaquin valley, California. Copeia 1973: 18-22. [ Links ]
Moyle PB (1986) Fish introductions into North America: Patterns and ecological impact. In: Mooney HA & JA Drake (eds) Ecology of biological invasions of North America and Hawaii: 27-43. Springer-Verlag, New York, New York, USA. [ Links ]
Moyle PB & T Light (1996) Fish invasions in California: do abiotic factors determine success? Ecology 77: 1666-1670. [ Links ]
Murray MS & EM Hansen (1997) Susceptibility of Pacific Yew to Phytophthora lateralis. Plant Disease 81: 1400-1404. [ Links ]
Naiman RJ, CA Johnston & JC Kelley (1988) Alteration of North American streams by beaver. Bioscience 38: 753-762. [ Links ]
Naiman RJ, T Manning & CA Johnston (1991) Beaver population fluctuations and tropospheric methane emissions in boreal wetlands. Biogeochemistry 12: 1-16. [ Links ]
Naiman RJ, JM Mellilo & JE Hobbie (1986) Ecosystem alteration of boreal forest streams by beaver (Castor canadensis). Ecology 67: 1254-1269. [ Links ]
Nehring RB & PG Walker (1996) Whirling disease in the wild: the new reality in the intermountain west. Fisheries 21: 28-30. [ Links ]
Neill WM (1983) The tamarisk invasion of desert riparian areas. Educational Bulletin 83-84, Desert Protective Council, Spring Valley, California, USA. 4 pp. [ Links ]
Ojima DS, DS Schimel, WJ Parton & CE Owensby (1994) Long- and short-term effects of fire on nitrogen cycling in tallgrass prairie. Biogeochemistry 24: 67-84. [ Links ]
Olson TE & FL Knopf (1986) Agency subsidation of a rapidly spreading exotic. Wildlife Society Bulletin 14: 492-493. [ Links ]
Pavlik BM (1983a) Nutrient and productivity relations of the dune grasses Ammophila arenaria and Elymus mollis. I. Blade photosynthesis and nitrogen use efficiency in the laboratory and field. Oecologia 57: 227-232. [ Links ]
Pavlik BM (1983b) Nutrient and productivity relations of the dune grasses Ammophila arenaria and Elymus mollis. II. Growth and patterns of dry matter and nitrogen allocation as influenced by nitrogen supply. Oecologia 57: 233-238. [ Links ]
Pavlik BM (1983c) Nutrient and productivity relations of the dune grasses Ammophila arenaria and Elymus mollis. III. Spatial aspects of clonal expansion with reference to rhizome growth and dispersal of buds. Bulletin of the Torrey Botanical Club 110: 271-279. [ Links ]
Peart D, DT Patten & SL Lohr (1994) Feral pig disturbance and woody species seedling regeneration and abundance beneath coast live oaks (Quercus agrifolia) on Santa Cruz island, California. In: Halvorson WL & GJ Maender (eds) The fourth annual California islands symposium: update on the status of resources: 313-322. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Pellant M & C Hall (1994) Distribution of two exotic grasses on intermountain rangelands: status in 1992. In: Monsen SB & SG Kitchen (eds) Proceedings in ecology and management of annual rangelands: 109-112. United States Department of Agriculture, Forest Service Intermountain Research Station, Ogden, Utah, USA. [ Links ]
Pimentel D, L Lach, R Zúñiga & D Morrison (2000) Environmental and economic costs of nonindigenous species in the United States. Bioscience 50: 53-65. [ Links ]
Pollock MM, RJ Naiman, HE Erickson, CA Johnston, J Pastor & G Pinay (1995) Beaver as engineers: influences on biotic and abiotic characteristics of drainage basins. In: Jones CG & JH Lawton (eds) Linking species and ecosystems: 117-126. Chapman and Hall, New York, New York, USA. [ Links ]
Race MS (1982) Competitive displacement and predation between introduced and native mud snails. Oecologia 54: 337-347. [ Links ]
Ray JC (1988) Wild pigs in California: a major threat in California. Fremontia (United States) 16: 3-8. [ Links ]
Rejmánek M, CD Thomsen & ID Peters (1991) Invasive vascular plants of California. In: Groves RH & F di Castri (eds) Biogeography of Mediterranean invasions: 81-101. Cambridge University Press, Cambridge, United Kingdom. [ Links ]
Reynolds JW (1995) Status of exotic earthworm systematics and biogeography in North America. In: Hendrix PF (ed) Earthworm ecology and biogeography in North America: 1-27. Lewis Publishers, Boca Raton, Florida, USA. [ Links ]
Rice EL (1992) Allelopathic effects on nitrogen cycling. In: Rizvi SJH & V Rizvi (eds) Allelopathy: basic and applied aspects: 31-58. Chapman and Hall, London, United Kingdom. [ Links ]
Robbins WW, MK Bellue & WS Ball (1951) Weeds of California. Printing Division, Sacramento, California, USA. 547 pp. [ Links ]
Robles M & FS Chapin, III (1995) Comparison of the influence of two exotic communities on ecosystem processes in the Berkeley hills. Madroño (United States) 42: 349-357. [ Links ]
Roché CT & BF Roché, Jr (1988) Distribution and amount of four knapweed (Centaurea L.) species in eastern Washington. Northwest Science 62: 242-253. [ Links ]
Rundel PW & AC Gibson (1996) Ecological communities and processes in a Mojave desert ecosystem: Rock Valley, Nevada. Cambridge University Press, Cambridge, United Kingdom. 369 pp. [ Links ]
Sala A, SD Smith & DA Devitt (1996) Water use by Tamarix ramosissima and associated phreatophytes in a Mojave Desert floodplain. Ecological Applications 6: 888-898. [ Links ]
Sala OE, FS Chapin, III, RH Gardner, WK Lauenroth, HA Mooney & PS Ramakrishnan (1999) Global change, biodiversity and ecological complexity. In: Walker B, W Steffen, J Canadell & J Ingram (eds) The terrestrial biosphere and global change: implications for natural and managed ecosystems: 304-328. Cambridge University Press, Cambridge, United Kingdom. [ Links ]
Sanders NJ, NJ Gotelli, NE Heller & DM Gordon (2003) Community disassembly by an invasive species. Proceedings of the National Academy of Sciences of the United States 100: 2474-2477. [ Links ]
Schimel JP (1995) Plant transport and methane production as controls on methane flux from arctic wet meadow tundra. Biogeochemistry 28: 183-200. [ Links ]
Schlesinger WH (1991) Biogeochemistry: an analysis of global change. Academic Press, San Diego, California, USA. 443 pp. [ Links ]
Schuyler P (1987) Control of feral sheep (Ovis aries) on Santa Cruz island, California. In: Hochberg FG (ed) Third California islands symposium: recent advances in research in the California islands: 443-452. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Scott GD (1993) Fire threat from Arundo donax. In: Jackson NE, P Frandsen & S Duthoit (eds) Proceedings of the Arundo donax workshop, Ontario, California: 17-18. California Exotic Pest Plant Council, Berkeley, California, USA. [ Links ]
Seabloom EW & AM Wiedemann (1994) Distribution and effects of Ammophila breviligulata Fern (American beachgrass) on the foredunes of the Washington coast. Journal of Coastal Research 10: 178-188. [ Links ]
Sebacher DI, RC Harriss & KB Bartlett (1985) Methane emissions to the atmosphere through aquatic plants. Journal of Environmental Quality 14: 40-46. [ Links ]
Shukla J, C Nobre & P Sellers (1990) Amazon deforestation and climate change. Science 247: 1322-1325. [ Links ]
Slingsby P & WJ Bond (1985) The influence of ants on the dispersal distance and seedling recruitment of Leucospermum conocarpodendron (L.) Buek (Proteaceae). South African Journal of Botany 51: 30-34. [ Links ]
Slobodchikoff CN & JT Doyen (1977) Effects of Ammophila arenaria on sand dune arthropod communities. Ecology 58: 1171-1175. [ Links ]
Small A (1994) California birds: their status and distribution. Ibis Publishing Company, Vista, California, USA. 342 pp. [ Links ]
Storer AJ, TR Gordon & PL Dallara (1994) Pitch canker kills pines, spreads to new species and regions. California Agriculture 48: 9-13. [ Links ]
Suarez AV & TJ Case (2002) Bottom-up effects on persistence of a specialist predator: ant invasions and horned lizards. Ecological Applications 12: 291-298. [ Links ]
Swanson FJ (1981) Fire and geomorphic processes. In: Mooney HA, NL Bonnicksen, NL Christensen, JE Lotan & WA Reiners (eds) Fire regimes and ecosystem properties: 401-420. United States Department of Agriculture, Forest Service, Washington, District of Columbia, USA. [ Links ]
Thompson DQ (1987) Spread, impact, and control of purple loosestrife (Lythrum salicaria) in North American wetlands. United States Department of the Interior, Fish and Wildlife Service, Washington, District of Columbia, USA. 55 pp. [ Links ]
Thompson JD (1991) The biology of an invasive plant. Bioscience 41: 393-401. [ Links ]
Tilman D & H Olff (1991) An experimental study of the effects of pH and nitrogen on grassland vegetation. Acta Oecologia 12: 427-442. [ Links ]
Tomback DF, JK Clary, J Koehler, RJ Hoff & SF Arno (1995) The effects of blister rust on post-fire regeneration of whitebark pine: the sundance burn of northern Idaho (USA). Conservation Biology 9: 654-664. [ Links ]
Trammell MA &+ JL Butler (1995) Effects of exotic plants on native ungulate use of habitat. Journal of Wildlife Management 59: 808-816. [ Links ]
Tyser RW & CH Key (1988) Spotted knapweed in natural area fescue grasslands: an ecological assessment. Northwest Science 62: 151-160. [ Links ]
Van Lill WS, FJ Kruger & DB Van Wyk (1980) The effect of afforestation with Eucalyptis grandis Hill ex Maiden and Pinus patula Schlecht et Cham on streamflow from experimental catchments at Mokobulaan, Transvaal. Journal of Hydrology 48: 107-118. [ Links ]
Van Vuuren MMI, R Aerts, F Berendse & W De Visser (1992) Nitrogen mineralization in heathland ecosystems dominated by different plant species. Biogeochemistry 16: 151-166. [ Links ]
Van Vuuren MMI & F Berendse (1993) Changes in soil organic matter and net nitrogen mineralization in heathland soils, after removal, addition or replacement of litter from Erica tetralix or Molinia caerulea. Biology and Fertility of Soils 15: 268-274. [ Links ]
Van Vuuren MMI, F Berendse & W De Visser (1993) Species and site differences in the decomposition of litters and roots from wet heathlands. Canadian Journal of Botany 71: 167-173. [ Links ]
Verville JH, FS Chapin, III, SE Hobbie & DU Hooper (1998) Response of tundra CH4 and CO2 flux to manipulation of temperature and vegetation. Biogeochemistry 41: 215-235. [ Links ]
Vitousek PM & LR Walker (1989) Biological invasion by Myrica faya in Hawaii: Plant demography, nitrogen fixation, ecosystem effects. Ecological Monographs 59: 247-266. [ Links ]
Vitousek PM, CM D'Antonio, LL Loope, M Rejmánek & R Westbrooks (1997) Introduced species: a significant component of human-caused global change. New Zealand Journal of Ecology 21: 1-16. [ Links ]
Vitousek PM, LR Walker, LD Whiteaker, D Mueller-Dombois & PA Matson (1987) Biological invasion by Myrica faya alters ecosystem development in Hawaii. Science 238: 802-804. [ Links ]
Vivrette NJ & CH Muller (1977) Mechanism of invasion and dominance of coastal grassland by Mesembryanthemum crystallinum. Ecological Monographs 47: 301-318. [ Links ]
Waithman JD, RA Sweitzer, D vanVuren, JD Drew, AJ Brinkhaus & IA Gardner (1999) Range expansion, population sizes, and management of wild pigs in California. Journal of Wildlife Management 63: 298-308. [ Links ]
Wallén B (1980) Changes in structure and function of Ammophila during primary succession. Oikos 34: 227-238. [ Links ]
Ward PS (1987) Distribution of the introduced Argentine ant (Iridomyrmex humilis) in natural habitats of the lower Sacramento River Valley and its effects on the indigenous ant fauna. Hilgardia 55: 1-16. [ Links ]
Wardle DA, KS Nicholson, M Ahmed & A Rahman (1994) Interference effects of the invasive plant Carduus nutans L. against the nitrogen fixation ability of Trifolium repens L. Plant and Soil 163: 287-297. [ Links ]
Wedin DA & D Tilman (1996) Influence of nitrogen loading and species composition on the carbon balance of grasslands. Science 274: 1720-1723. [ Links ]
Weeks EP, HL Weaver, GS Campbell & BD Tanner (1987) Water use by saltcedar and by replacement vegetation in the Pecos River floodplain between Acme and Artesia, New Mexico. United States Geological Survey Professional Paper 491-G. 33 pp. [ Links ]
Wehtje W (1994) Response of a bishop pine (Pinus muricata) population to removal of feral sheep on Santa Cruz Island, California. In: Halvorson WL & GJ Maender (eds) The fourth annual California islands symposium: update on the status of resources: 331-340. Santa Barbara Museum of Natural History, Santa Barbara, California, USA. [ Links ]
Werner I & JT Hollibaugh (1993) Potamocorbula amurensis: comparison of clearance rates and assimilation efficiencies for phytoplankton and bacterioplankton. Limnology and Oceanography 38: 949-964. [ Links ]
Westman WE (1990) Park management of exotic plant species problems and issues. Conservation Biology 4: 251-260. [ Links ]
Wetterer JK, AL Wetterer & E Hebard (2001) Impact of the Argentine ant, Linepithema humile on the native ants of Santa Cruz island, California. Sociobiology 38: 709-721. [ Links ]
Wheeler CT, OT Helgerson, DA Perry & JC Gordon (1987) Nitrogen fixation and biomass accumulation in plant communities dominated by Cytisus scoparius L. in Oregon and Scotland. Journal of Applied Ecology 24: 231-237. [ Links ]
Wheeler CT, DA Perry, O Helgerson & JC Gordon (1979) Winter fixation of nitrogen in Scotch broom (Cytisus scoparius L.). New Phytologist 82: 697-701. [ Links ]
Wheeler GC & JN Wheeler (1986) The ants of Nevada. Natural History Museum of Los Angeles County and Allen Press, Inc., Lawrence, Kansas, USA. 138 pp. [ Links ]
Whisenant SG (1990) Changing fire frequencies on Idaho's snake river plains: ecological and management implications. In: McArthur ED, EM Romney, SD Smith & PT Tueller (eds) Proceedings of the symposium on cheat grass invasion, shrub die-off, and other aspects of shrub biology and management: 4-10. Intermountain Research Station, United States, Forest Service, Ogden, Utah, USA [ Links ]
Whitson TD, LC Burrill, SA Dewey, DW Cudney, BE Nelson, RD Lee & R Parker (1996) Weeds of the west. Pioneer of Jackson Hole, Jackson, Wyoming, USA. 630 pp. [ Links ]
Wiedemann AM (1984) The ecology of Pacific northwest coastal sand dunes: a community profile. FWS/OBS-84/04. United States Fish and Wildlife Service, Washington, District of Columbia, USA. [ Links ]
Wiedemann AM & A Pickart (1996) The Ammophila problem on the northwest coast of North America. Landscape and Urban Planning 34: 287-299. [ Links ]
Wilcove DS, D Rothstein, J Dubow, A Phillips & E Losos (1998) Quantifying threats to imperiled species in the United States. BioScience 48: 607-615. [ Links ]
Winer AM, J Arey, R Atkinson, SM Aschmann, WD Long, CL Morrison & DM Olszyk (1992) Emission rates of organics from vegetation in California's central valley. Atmospheric Environment 26: 2647-2659. [ Links ]
Woodward SL (1976) Feral burros of the Chemehuevi Mountains, California: the biogeography of a feral exotic. Ph.D. Thesis, University of California, Los Angeles, California, USA. 178 pp. [ Links ]
Yavitt JB, LL Angell, TJ Fahey, CP Cirmo & CT Driscoll (1992) Methane fluxes, concentrations, and production in two Adirondack beaver impoundments. Limnology and Oceanography 37: 1057-1066. [ Links ]
Young JA (1992) Ecology and management of medusahead (Taeniatherum caput medusae ssp. asperum [Simk.] Melderis). Great Basin Naturalist 52: 245-252. [ Links ]
Young JA & RA Evans (1978) Population dynamics after wildfires in sagebrush grasslands. Journal of Range Management 31: 283-289. [ Links ]
Zavaleta E (2000) Valuing ecosystem services lost to Tamarix invasion in the United States. In: Mooney HA & RJ Hobbs (eds) Invasive species in a changing world: 261-300. Island Press, Washington, District of Columbia, USA. [ Links ]
Zedler PH, CR Gautier & GS McMaster (1983) Vegetation change in response to extreme events: the effect of a short interval between fires in California chaparral and coastal scrub. Ecology 64: 809-818. [ Links ]
Associate Editor: Pablo Marquet