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Endophytic bacteria in grass crop growth promotion and biostimulation

Plants naturally carry microbes on seeds and within seeds that may facilitate development and early survival of seedlings. Some crops have lost seed-vectored microbes in the process of domestication or during seed storage and seed treatment. Biostimulant microbes from wild plants were used by pre-modern cultures to re-acquire beneficial seed microbes. Today some companies have developed or are developing the use of microbes obtained from soils or plant sources to stimulate plant development and growth. Many of these biostimulant microbes are endophytic in plants. Biostimulant products also include humic substances, which appear to function as signal molecules in plants, triggering increased internalization of soil microbes into root cells and tissues. In addition, protein coatings on seeds fuel the growth of seed surface-vectored microbes, increasing microbial activity around and within roots. In this article, we provide evidence of the endophytic nature of many biostimulant microbes, and suggest that many of the beneficial effects of microbial biostimulants stem from their action as endophytes or as participants or stimulants of rhizophagy cycle activity.

Grass Research

The history of stream gaging in Ohio

Introduction Streams are a natural resource that can influence economic growth and the development of communities. They supply water for many uses, provide habitat for aquatic plants and animals, and sup-port recreational activities such as boat-ing and fishing. The amount of water (flow) in a stream — either too little or too much — can seriously affect these uses and human life. By using a method called stream gaging , information about the flow in a stream and the fluctuations in that flow can be obtained. n its simplest form, stream gaging may consist of measuring any number of the following stream characteristics: stage (or depth), cross-sectional area, velocity, and (or) flow (or discharge). When the depth and velocity are measured at several points across the stream channel so that the flow (or discharge ) is calculated, a streamflow measurement (or discharge measurement ) is made. By making streamflow measurements at the same site on a stream over a wide range of stages, a relation between stage and discharge can be developed. This relation can be used to provide information on the magnitude and fluctuations of flow on a stream. If long-term or continuous information is needed on a specific site, a stream-gaging station can be established. A stream-gaging station is a site where stage is monitored and recorded and streamflow measurements are made to provide a stage-discharge relation. Ever since the first documented streamflow measurement was made in Ohio — on the Sandusky River — stream-gaging information has been used to minimize the effects of floods and droughts, determine locations for water intakes and wastewater-treatment plants, and provide data for many other uses. Today, stream gaging is a routine activity in managing the State’s water resources.

Ohio

Molecular analysis of a 11 700-year-old rodent midden from the Atacama Desert, Chile

DNA was extracted from an 11 700-year-old rodent midden from the Atacama Desert, Chile and the chloroplast and animal mitochondrial DNA (mtDNA) gene sequences were analysed to investigate the floral environment surrounding the midden, and the identity of the midden agent. The plant sequences, together with the macroscopic identifications, suggest the presence of 13 plant families and three orders that no longer exist today at the midden locality, and thus point to a much more diverse and humid climate 11 700 years ago. The mtDNA sequences suggest the presence of at least four different vertebrates, which have been putatively identified as a camelid (vicuna), two rodents (Phyllotis and Abrocoma), and a cardinal bird (Passeriformes). To identify the midden agent, DNA was extracted from pooled faecal pellets, three small overlapping fragments of the mitochondrial cytochrome b gene were amplified and multiple clones were sequenced. These results were analysed along with complete cytochrome b sequences for several modern Phyllotis species to place the midden sequence phylogenetically. The results identified the midden agent as belonging to an ancestral P. limatus. Today, P. limatus is not found at the midden locality but it can be found 100 km to the north, indicating at least a small range shift. The more extensive sampling of modern Phyllotis reinforces the suggestion that P. limatus is recently derived from a peripheral isolate.

Molecular Ecology

Middle Pliocene vegetation: Reconstructions, paleoclimatic inferences, and boundary conditions for climate modeling

The general characteristics of global vegetation during the middle Pliocene warm period can be reconstructed from fossil pollen and plant megafossil data. The largest differences between Pliocene vegetation and that of today occurred at high latitudes in both hemispheres, where warming was pronounced relative to today. In the Northern Hemisphere coniferous forests lived in the modern tundra and polar desert regions, whereas in the Southern Hemisphere southern beech apparently grew in coastal areas of Antarctica. Pliocene middle latitude vegetation differed less, although moister-than-modern conditions supported forest and woodland growth in some regions now covered by steppe or grassland. Pliocene tropical vegetation reflects essentially modem conditions in some regions and slightly cooler-than-or warmer-than- modern climates in other areas. Changes in topography induced by tectonics may be responsible for many of the climatic changes since the Pliocene in both middle and lower latitudes. However, the overall latitudinal progression of climatic conditions on land parallels that seen in the reconstruction of middle Pliocene sea-surface temperatures. Pliocene paleovegetational data was employed to construct a 2 ° × 2 ° global grid of estimated mid-Pliocene vegetational cover for use as boundary conditions for numerical General Circulation Model simulations of middle Pliocene climates. Continental outlines and topography were first modified to represent the Pliocene landscape on the 2 ° × 2 ° grid. A modern 1 ° × 1 ° vegetation grid was simplified and mapped on this Pliocene grid, and then modified following general geographic trends evident in the Pliocene paleovegetation data set.

Marine Micropaleontology

Oblique map showing maximum extent of 20,000-year-old (Tioga) glaciers, Yosemite National Park, central Sierra Nevada, California

This map shows the alpine ice field and associated valley glaciers at their maximum extent during the Tioga glaciation. The Tioga glaciation, which peaked about 15,000-20,OOO years ago, was the last major glaciation in the Sierra Nevada. The Tuolumne ice field fed not only the trunk glacier that moved down the Tuolumne River canyon through the present-day Hetch Hetchy Reservoir, but it also overflowed major ridge crests into many adjoining drainage systems. Some of the ice flowed over low passes to augment the flows moving from the Merced basin down through little Yosemite Valley. Tuolumne ice flowed southwest down the Tuolumne River into the Tenaya Lake basin and then down Tenaya Canyon to join the Merced glacier in Yosemite Valley. During the Tioga glaciation, the glacier in Yosemite Valley reached only as far as Bridalveil Meadow, although during a much earlier glaciation, a glacier extended about 10 miles farther down the Merced River to the vicinity of El Portal. Ice of the Tioga glaciation also flowed eastward from the summit region to cascade down the canyons that cut into the eastern escarpment of the Sierra Nevada [see errata, below]. Southeast of the present-day Yosemite Park, glaciers formed in the Mount Lyell region flowed east onto the Mono lowland and southeast and south down the Middle and North Forks of the San Joaquin River. In the southern part of the park, glaciers nearly reached to the present-day site of Wawona along the South Fork of the Merced River. At the time of the maximum extent of the Tioga glaciation, Lake Russell (Pleistocene Mono Lake) had a surface elevation of 6,800 feet, 425 feet higher than the 1980 elevation and 400 feet lower than its maximum level at the end of the Tioga glaciation. Only a few volcanic domes of the Mono Craters existed at the time of the Tioga glaciation. <.p> The distribution of vegetation, as suggested by the green overprint, is based on our interpretation. Forests were restricted to lower elevations than present day, but alpine plant species probably thrived where snow was seasonal, much as they occur today. Erratum The branching arrow on the map showing ice flowing from the basin east of Kuna Crest both northeastward around Mount Dana into the Mono Lake drainage and westward to the Tuolumne River is in error. No ice flowed northeastward from this basin through the site of Tioga Pass into the Mono Lake drainage. Although such an interpretation might be possible on the basis oJ the estimated elevation of the ice surface, the field evidence does not support it. A large and persistent boulder train of metamorphic rocks derived from Mount Dana and the mountain (Mount Gibbs) immediately to the south of Mount Dana has been mapped from near the base of Mount Dana westward toward the ice-filled gorge between Pettit Peak and Double Rock (the present Grand Canyon of the Tuolumne), indicating that ice from the west flank of Mount Dana flowed westward down the Tuolumne. In addition, glacial erratics of Cathedral Peak Granodiorite were observed near Tioga Pass (near the head of the erroneous arrow between Mount Dana and Mount Conness). These boulders must have come from the east face of Mount Conness or the mountain south of Mount Conness (White Mountain) and been transported by ice' flowing toward the Tioga Pass area, although the main mass of that ice turned eastward and flowed into the Mono Lake drainage. Tioga Pass was then the site of more-or-less stagnant ice between the Tuolumne drainage and that east of Mount Conness. Both the metamorphic boulder train and the glacial erratics of Cathedral Peak Granodiorite are incompatible with any flow of ice northeastward from the basin east of Kuna Crest into the Mono Lake drainage north of Mount Dana.

IMAP

Mediterranean biomes: Evolution of their vegetation, floras and climate

Mediterranean-type ecosystems (MTEs) possess the highest levels of plant species richness in the world outside of the wet tropics. Sclerophyll vegetation similar to today’s mediterranean-type shrublands was already present on oligotrophic soils in the wet and humid climate of the Cretaceous, with fire-adapted Paleogene lineages in southwestern Australia and the Cape Region. The novel MTC seasonality present since the mid-Miocene has allowed colonization of MTEs from a regional species pool with associated diversification. Fire persistence has been a primary driving factor for speciation in four of the five regions. Understanding the regional patterns of plant species diversity among the MTEs involves complex interactions of geologic and climatic histories for each region as well as ecological factors that have promoted diversification in the Neogene and Quaternary. A critical element of species richness for many MTE lineages has been their ability to speciate and persist at fine spatial scales, with low rates of extinction.

Annual Review of Ecology, Evolution, and Systemati

Transport and degradation of water-soluble creosote-derived compounds

Creosote is the most extensively used insecticide and industrial wood preservative today. It is estimated that there are more than 600 wood-preserving plants in the United States, and their collective use of creosote exceeds 4.5xl0 6 kg/yr (von Rumker et al ., 1975). Creosote is a complex mixture of more than 200 major individual organic compounds with differing molecular weights, polarities, and functionalities, along with dispersed solids and products of polymerization (Novotny et al ., 1981). The major classes of compounds previously identified in creosote show that it consists of ∼85% (w/w) polynuclear aromatic compounds (PAH), ∼12% phenolic compounds, and ∼3% heterocyclic nitrogen, sulfur, and oxygen containing compounds (NSO).

Book chapter

Eco-evolutionary responses of Bromus tectorum to climate change: implications for biological invasions

How plant populations, communities, and ecosystems respond to climate change is a critical focus in ecology today. The responses of introduced species may be especially rapid. Current models that incorporate temperature and precipitation suggest that future Bromus tectorum invasion risk is low for the Colorado Plateau. With a field warming experiment at two sites in southeastern Utah, we tested this prediction over 4 years, measuring B. tectorum phenology, biomass, and reproduction. In a complimentary greenhouse study, we assessed whether changes in field B. tectorum biomass and reproductive output influence offspring performance. We found that following a wet winter and early spring, the timing of spring growth initiation, flowering, and summer senescence all advanced in warmed plots at both field sites and the shift in phenology was progressively larger with greater warming. Earlier green-up and development was associated with increases in B. tectorum biomass and reproductive output, likely due early spring growth, when soil moisture was not limiting, and a lengthened growing season. Seeds collected from plants grown in warmed plots had higher biomass and germination rates and lower mortality than seeds from ambient plots. However, in the following two dry years, we observed no differences in phenology between warmed and ambient plots. In addition, warming had a generally negative effect on B. tectorum biomass and reproduction in dry years and this negative effect was significant in the plots that received the highest warming treatment. In contrast to models that predict negative responses of B. tectorum to warmer climate on the Colorado Plateau, the effects of warming were more nuanced, relied on background climate, and differed between the two field sites. Our results highlight the importance of considering the interacting effects of temperature, precipitation, and site-specific characteristics such as soil texture, on plant demography and have direct implications for B. tectorum invasion dynamics on the Colorado Plateau.

Utah

The geologic story of Isle Royale National Park

Isle Royale is an outstanding example of relatively undisturbed northwoods lake wilderness. But more than simple preservation of such an environment is involved in its inclusion in our National Park System. Its isolation from the mainland provides an almost untouched laboratory for research in the natural sciences, especially those studies whose very nature depends upon such isolation. One excellent example of such research is the intensive study of the predator-prey relationship of the timber wolf and moose, long sponsored by the National Park Service and Purdue University. In probably no other place in North America are the necessary ecological conditions for such a study so admirably fulfilled as on Isle Royale. The development of a natural laboratory with such conditions is ultimately dependent upon geologic processes and events that although not unique in themselves, produced in their interplay a unique result, the island archipelago as we know it today, with its hills and valleys, swamps and bogs the ecological framework of the plant and animal world. Even the most casual visitor can hardly fail to be struck by the fiordlike nature of many of the bays, the chains of fringing islands, the ridge-and-valley topography, and the linear nature of all these features. The distinctive topography of the archipelago is, of course, only the latest manifestation of geologic processes in operation since time immemorial. Fragments of geologic history going back over a billion years can be read from the rocks of the island, and with additional data from other parts of the Lake Superior region, we can fill in some of the story of Isle Royale. After more than a hundred years of study by man, the story is still incomplete. But then, geologic stories are seldom complete, and what we do know allows a deeper appreciation of one of our most naturally preserved parks and whets our curiosity about the missing fragments.

Michigan

Paraquat Hazards to Fish, Wildlife, and Invertebrates: A Synoptic Review

Paraquat (1,1`dimethyl4,4`bipyridinium) are broad-spectrum contact plant killers and herbage desiccants that were introduced commercially during the past 25 years. Today, they rank among the most widely used herbicides globally and are frequently used in combination with other herbicides. The recommended paraquat field application rates for terrestrial weed control usually range between 0.28 and 1.12 kg/ha (0.25 and 1.0 lb/acre), and for aquatic weed control the range is 0.12.0 mg/l. Paraquat in surface soils generally photodecomposes in several weeks, but paraquat in subsurface soils and sediments may remain bound and biologically unavailablefor many years without significant degradation. Paraquat is not significantly accumulated by earthworms and other species of soil invertebrates and is usually excreted rapidly by higher animals; however, delayed toxic effects including death of birds and mammals are common. At concentrations below the recommended application rate, paraquat is embryotoxic to developing eggs of migratory waterfowl and adversely affects sensitive species of freshwater algae and macrophytes, larvae of crustaceans and frog tadpoles and carp. Sensitive species of birds are negatively affected at daily dose rates of 10 mg/kg body weight or when fed diets containing 20 mg/kg ration or drinking water containing 40 mg/l.

Contaminant Hazard Reviews

50,000 years of vegetation and climate history on the Colorado Plateau, Utah and Arizona, USA

Sixty packrat middens were collected in Canyonlands and Grand Canyon National Parks, and these series include sites north of areas that produced previous detailed series from the Colorado Plateau. The exceptionally long time series obtained from each of three sites (> 48,000 14 C yr BP to present) include some of the oldest middens yet discovered. Most middens contain a typical late-Wisconsinan glaciation mixture of mesic and xeric taxa, evidence that plant species responded to climate change by range adjustments of elevational distribution based on individual criteria. Differences in elevational range from today for trees and shrubs ranged from no apparent change to as much as 1200 m difference. The oldest middens from Canyonlands NP, however, differ in containing strictly xeric assemblages, including middens incorporating needles of Arizona single-leaf pinyon, far north of its current distribution. Similar-aged middens from the eastern end of Grand Canyon NP contain plants more typical of glacial climates, but also contain fossils of one-seed juniper near its current northern limit in Arizona. Holocene middens reveal the development of modern vegetation assemblages on the Colorado Plateau, recording departures of mesic taxa from low elevation sites, and the arrival of modern dominant components much later.

Arizona, Utah

Evolution of CAM and C 4 carbon-concentrating mechanisms

Mechanisms for concentrating carbon around the Rubisco enzyme, which drives the carbon-reducing steps in photosynthesis, are widespread in plants; in vascular plants they are known as crassulacean acid metabolism (CAM) and C 4 photosynthesis. CAM is common in desert succulents, tropical epiphytes, and aquatic plants and is characterized by nighttime fixation of CO2. The proximal selective factor driving the evolution of this CO2-concentrating pathway is low daytime CO2, which results from the unusual reverse stomatal behavior of terrestrial CAM species or from patterns of ambient CO2 availability for aquatic CAM species. In terrestrials the ultimate selective factor is water stress that has selected for increased water use efficiency. In aquatics the ultimate selective factor is diel fluctuations in CO2 availability for palustrine species and extreme oligotrophic conditions for lacustrine species. C4 photosynthesis is based on similar biochemistry but carboxylation steps are spatially separated in the leaf rather than temporally as in CAM. This biochemical pathway is most commonly associated with a specialized leaf anatomy known as Kranz anatomy; however, there are exceptions. The ultimate selective factor driving the evolution of this pathway is excessively high photorespiration that inhibits normal C3 photosynthesis under high light and high temperature in both terrestrial and aquatic habitats. CAM is an ancient pathway that likely has been present since the Paleozoic era in aquatic species from shallow-water palustrine habitats. While atmospheric CO2 levels have undoubtedly affected the evolution of terrestrial plant carbon-concentrating mechanisms, there is reason to believe that past atmospheric changes have not played as important a selective role in the aquatic milieu since palustrine habitats today are not generally carbon sinks, and the selective factors driving aquatic CAM are autogenic. Terrestrial CAM, in contrast, is of increasing selective value under extreme water deficits, and undoubtedly, high Mesozoic CO2 levels reduced the amount of landscape perceived by plants as water limited. Late Tertiary and Quaternary reductions in atmospheric CO2, coupled with increasing seasonality, were probably times of substantial species radiation and ecological expansion for CAM plants. C4 photosynthesis occurs in only about half as many families as CAM, and three-fourths of C4 species are either grasses or sedges. Molecular phylogenies indicate C4 is a more recent innovation than CAM and that it originated in the mid-Tertiary, 20–30 Ma, although some data support an earlier origin. While the timing of the origin of C4 remains controversial, the nearly explosive increase in C4 species is clearly documented in the late Miocene, 4–7 Ma. Increasing seasonality has been widely suggested as an important climatic stimulus for this C4 expansion. Alternatively, based on models of photosynthetic quantum yield at different temperatures and CO2 concentration, it has been hypothesized that the late Miocene C4 expansion resulted from declining atmospheric CO2 levels. This model is most appropriate for explaining the transition from C3 grasslands to C4 grasslands but by itself may not be sufficient to explain the more likely scenario of a late Miocene transition from C3 woodland/ savanna to C4 grasslands. A largely unexplored hypothesis is that climatic changes in late Miocene altered disturbance regimes, in particular the incidence of fires, which today are often associated with maintenance of C4 grasslands. Oceanic charcoal sediments that appear to represent Aeolian deposits from continental wildfires follow a strikingly similar pattern of explosive increase in late Miocene. Climate, CO2, and disturbance are not mutually exclusive explanations and probably all acted in concert to promote the expansion of C4 grasslands. More recently, late Quaternary changes in CO2 may have been responsible for driving major changes in the landscape distribution of C4 species. The theory is sound; however, many of the studies cited in support of this model are open to alternative interpretations, and none has eliminated climatic factors as important selective agents. CAM and C4 evolution required coupling of biochemical pathways with structural changes in photosynthetic tissues, succulence in CAM and Kranz in C4. This was apparently accomplished by piecemeal evolution beginning with mechanisms for recapturing respiratory CO2, although this need not have been so in aquatic CAM species. It has been proposed that the extreme rarity of both pathways in the same plant results from biochemical and structural incompatibilities (Sage 2002). Equally important is the fact that the selective environments are quite different, with CAM evolution thriving on stressful sites inhospitable to C3 species whereas C4 evolution has selected for rapid growth capable of outcompeting associated C3 plants.

International Journal of Plant Sciences

Tectonic uplift of a middle Wisconsin marine platform near the Mendocino triple junction California

An uplifted wave-cut marine platform eroded across bedrock of the Franciscan Complex at Point Delgada, northern California, is overlain by 0.5 to 5 m of wave-worked pea gravel, which is in turn directly overlain by fluvial gravel and silt deposited as alluvial fans. Woody plant debris at the base of the fluvial deposits includes cones of Brewer spruce ( Picea breweriana ), which today are found only at higher elevations and latitudes. Fossil wood debris from this horizon yields a 14 C date of 44,800 ± 1,300 yr. The 44,800 yr radiocarbon age for the base of the fluvial deposits establishes an approximate age for the immediately underlying marine gravels and wave-cut platform. We tentatively correlate this terrace with the middle Wisconsin high sea-level stand at −37 m, dated at about 45,000 yr B.P. If this age is correct, the tectonic uplift since middle Wisconsin time has been 44 m, and the average rate of uplift has been at least 1.0 m/1,000 yr. This relatively high rate is probably related to interaction among the Pacific, Gorda, and North American plates at the Mendocino triple junction.

Geology

Ecological response to global climatic change

Climate change and ecological change go hand in hand. Because we value our ecological environment, any change has the potential to be a problem. Geographers have been drawn to this challenge, and have been successful in addressing it, because the primary ecological response to climate changes in the past &mdash; the waxing and waning of the great ice sheets over the past 2 million years &ndash; was the changing geographic range of the biota. Plants and animals changed their location. Geographers have been deeply involved in documenting the changing biota of the past, and today we are called upon to help assess the possible responses to ongoing and future climatic change and, thus, their impacts. Assessing the potential responses is important for policy makers to judge the outcomes of action or inaction and also sets the stage for preparation for and mitigation of change.

Book chapter

Small anthropogenic landforms from past charcoal production control moisture dynamics and chemistry in northcentral Appalachian soils

Throughout the northeastern United States (U.S.) and Europe, relict charcoal hearths (RCHs) are regularly being discovered in proximity to furnaces once used for the extraction of metal from ore or quick-lime production; charcoal produced in hearths was used as a furnace fuel. Given previous research has shown that topographic and subsurface disturbance can be great when a hearth is constructed, we hypothesize that hearth construction alters surface hydrology and soil chemistry in environments in and near hearths. We used a landscape classification process to identify 6,758 hearths near furnaces at Greenwood and Pine Grove Furnace State Park, central and southcentral Pennsylvania, U.S. Two types of digital elevation model wetness indexes were used to quantify surface hydrology effects in and around hearths. Modeled wetness conditions were compared to field soil volumetric water content in RCHs near Greenwood Furnace State Park. Modeled wetness indexes indicate that RCH interiors are significantly wetter than RCH rim areas; RCHs are acting as a landscape moisture sink. Results also indicate that RCHs on slopes result in downslope drier conditions below RCHs. Field measured volumetric water content indicates that as distance from the center of the hearth increases, soil moisture significantly decreases. Geomorphic position was found to not be related to RCH wetness. Soil from RCHs, compared to nearby native soils, has significantly higher total C, a lower Mehlich 3 extractable acidity, higher Ca and P. No trend was evident with RCH soil chemistry and geomorphic position. The high frequency of RCH occurrence, in proximity to the furnace’s RCHs supported, suggests that RCHs today could locally be an important niche for understory flora and fauna. Further research could explore how RCHs might be affecting surrounding plant populations and how within RCH patterns, especially on hillslopes, might represent a distinctly different scale of physical and chemical variability.

Pennsylvania

Biomes of western North America at 18,000, 6000 and 0 14C yr BP reconstructed from pollen and packrat midden data

A new compilation of pollen and packrat midden data from western North America provides a refined reconstruction of the composition and distribution of biomes in western North America for today and for 6000 and 18,000 radiocarbon years before present (14C yr BP). Modern biomes in western North America are adequately portrayed by pollen assemblages from lakes and bogs. Forest biomes in western North America share many taxa in their pollen spectra and it can be difficult to discriminate among these biomes. Plant macrofossils from packrat middens provide reliable identification of modern biomes from arid and semiarid regions, and this may also be true in similar environments in other parts of the world. However, a weighting factor for trees and shrubs must be used to reliably reconstruct modern biomes from plant macrofossils. A new biome, open conifer woodland, which includes eurythermic conifers and steppe plants, was defined to categorize much of the current and past vegetation of the semiarid interior of western North America. At 6000 14C yr BP, the forest biomes of the coastal Pacific North-west and the desert biomes of the South-west were in near-modern positions. Biomes in the interior Pacific North-west differed from those of today in that taiga prevailed in modern cool/cold mixed forests. Steppe was present in areas occupied today by open conifer woodland in the northern Great Basin, while in the central and southern Rocky Mountains forests grew where steppe grows today. During the mid-Holocene, cool conifer forests were expanded in the Rocky Mountains (relative to today) but contracted in the Sierra Nevada. These differences from the forests of today imply different climatic histories in these two regions between 6000 14C yr BP and today. At 18,000 14C yr BP, deserts were absent from the South-west and the coverage of open conifer woodland was greatly expanded relative to today. Steppe and tundra were present in much of the region now covered by forests in the Pacific North-west.

Journal of Biogeography

Elk response to the La Mesa fire and current status in the Jemez Mountains

Faunal remains in local archeological sites and historic information suggest that elk populations in the Jemez Mountains were low from ca. 1200 A.D. through ca. 1900 A.D., when they were extirpated from this region. Elk were reintroduced to the Jemez country in 1948 and 1964- 1965, and their population apparently grew exponentially, reaching 1000 animals in the 1970's and about 7000 by 1991. Elk populations in Bandelier National Monument and adjoining areas increased rapidly after the 1977 La Mesa Fire. Winter use by elk in the La Mesa Fire area, centered on Bandelier, grew from about 100 animals in .1978 to around 1500 elk by 1992. The dramatic increase in the Bandelier elk herd (an annual growth rate of 21.3% and a 3.6 year population doubling time) was due in part to the creation of about 6000 hectares of grassy winter range in and around the park by the La Mesa Fire. Some of this local population increase reflects concentration of elk into this favorable wintering habitat from surrounding portions of the Jemez Mountains. Existing data are inadequate to determine whether elk populations are still growing rapidly in the Jemez Mountains. While annual aerial surveys since 1990 in Bandelier reveal no clear population trend, a variety of observations demonstrate increasing elk use of lower elevation areas. Negative resource impacts from today's high elk populations are beginning to be widely noted across the Jemez Mountains, especially in high-use portions of the Bandelier National Monument area. Affected resources range from plant communities to soils and even archeological sites. Given the large uncertainties associated with the current data on elk populations, care should be taken to avoid further population increases until the resource impacts of this new phenomenon (large numbers of elk) can be identified, desirable population levels identified (based to a significant degree upon ecological information and resource carrying capacities, as well as social considerations), and appropriate cooperative management strategies implemented.

General Technical Report