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Effect of height and orientation (microclimate) on geomorphic degradation rates and processes, late-glacial terrace scarps in central Idaho

Skip Nav Destination RESEARCH ARTICLE | JULY 01, 1986 Effect of height and orientation (microclimate) on geomorphic degradation rates and processes, late-glacial terrace scarps in central Idaho KENNETH L. PIERCE ; STEVEN M. COLMAN Author and Article Information GSA Bulletin (1986) 97 (7): 869–885. https://doi.org/10.1130/0016-7606(1986)97<869:EOHAOM>2.0.CO;2 Article history Standard View 2.0.CO;2" data-doctype="contentPdf" data-article-id="188507" data-mce-href="https://pubs.geoscienceworld.org/gsa/gsabulletin/article-pdf/97/7/869/3434736/i0016-7606-97-7-869.pdf"> Open the PDF for in another window Cite Share Icon Share Permissions Abstract Terrace scarps can serve as a nearly ideal natural laboratory for the study of the evolution of slopes. This paper examines the effects of scarp size (height) and orientation (microclimate) by keeping constant variables such as age, lithology, and regional climate. If a scarp degrades as a closed system, and downslope movement is directly proportional to surface gradient , the evolution of the scarp is modeled by the diffusion equation. For a group of scarps of same age and known starting angle, the diffusion-equation model predicts the relation between maximum scarp angle (𝛉) and scarp height ( h ). Late Pleistocene terrace scarps now as steep as 33.25°, as well as measured angles of repose for sand and gravel, require a starting angle as steep as 33.5°. For latest Pleistocene Idaho and Utah scarps, as h increases, 𝛉 is gentler (more degraded) than modeled by the diffusion equation with a constant rate coefficient. The degradation-rate coefficient ( c ) increases tenfold with scarp height; it should not change with scarp height if downslope movement is solely determined by surface gradient (to the first power). Soil wash appears to be responsible for this departure from the diffusion-equation model, for transport rate by soil wash is a function of scarp size (height). South-facing scarps are less vegetated and more degraded than north-facing scarps. For scarps 2 m high, the degradation rate ( c *) on S-facing scarps is 2 times that on N-facing scarps; for 10-m scarps, it is 5 times. The observed dependence of the rate coefficient c * on scarp height can be removed by normalizing c * to values for west-facing scarps of the same height. The residual c * values calculated by this method correlate well with differences in incident solar radiation resulting from the different scarp orientations and maximum gradients. This correlation demonstrates the importance of orientation on slope processes and their rates through the differences in freeze-thaw cycles, soil moisture, and vegetative cover. Scarp morphology may be used to estimate age, if one accounts for the effects of climate and for scarp height, orientation, and lithology. For example, using the dated Bonneville shoreline scarps for calibration and comparing only scarps of equal height, we estimate the Drum Mountains fault scarps to be 9,000 yr old. This age is about twice that produced by previous diffusion-equation calculations that have not accounted for the height as we have here, but it is the same as independent geologic estimates of their age.

Idaho↗

Geology of the Southern Guadalupe Mountains, Texas

This report deals with an area of 425 square miles in the western part of Texas, immediately south of the New Mexico line. The area comprises the south end of the Guadalupe Mountains and the adjacent part of the Delaware Mountains; it includes the highest peaks in the State of Texas. The area is a segment of a large mountain mass that extends 50 miles or more northward and southward. The report describes the geology of the area, that is, the nature of its rocks, tectonics, and surface features, and the evidence that they give as to the evolution of the area through geologic time. Incidental reference is made to the geology of surrounding regions in order to place the area in its environment. The Permian system of the southwestern United States has been until recently one of the intriguing but little known subjects of American stratigraphy. In the latter half of the nineteenth century after the western. United States was settled, the "red bed" sections of the Permian were studied and reported on by many geologists, but up to 1920 the existence of a contemporaneous marine sequence in western Texas and southeastern New Mexico was little appreciated. Since that year the discovery of extensive oil fields and potash beds in this region gave an impetus to the study of the Permian rocks, and furnished the geologist with records of hundreds of drill holes from which to deduce the nature of the strata not exposed at the surface. At the same time geologists have studied the rocks in the outcropping areas, and have compared them with the strata encountered by drilling. Much remains to be done in order to understand the history of Permian time in the region. The physical and chemical conditions that caused. the deposition of .the various and often complexly related deposits need to be better understood. More of the fossils of the rich and interesting marine faunas should be described, and the relations of the fossils to their environments should be determined. Further, a satisfactory scheme of correlation is needed, and also a subdivision into series that will express the contemporaneity of strata in different areas. One useful contribution to the solution of these problems is the detailed study of sequences of rocks exposed at the surface in the different mountain ranges of Texas and New Mexico. This report deals with one such sequence of rocks in western Texas, the one exposed in the southern Guadalupe Mountains (fig. 1). Here, the Permian rocks are magnificently exposed, to a thickness of about 4,000 feet (pl. 1). They are all of marine origin, and belong to the middle part of the system, with the base concealed and the top absent. Overlying and underlying beds, however, are found in nearby areas.

Texas↗

The history of mammal eradications in Hawai`i and the United States associated islands of the Central Pacific

Many eradications of mammal taxa have been accomplished on United States associated islands of the Central Pacific, beginning in 1910. Commonly eradicated species are rabbits ( Oryctolagus cuniculus ), rats ( Rattus spp.), feral cats ( Felis catus ), and several feral ungulates from smaller islands and fenced natural areas on larger Hawaiian Islands. Vegetation and avifauna have demonstrated dramatic recovery as a direct result of eradications. Techniques of worldwide significance, including the Judas goat method, were refined during these actions. The land area from which ungulates have been eradicated on large Hawaiian Islands is now greater than the total land area of some smaller Hawaiian Islands. Large multi-tenure islands present the greatest challenge to eradication because of conflicting societal interests regarding introduced mammals, mainly sustained-yield hunting. The difficulty of preventing reinvasion poses a persistent threat after eradication, particularly for feral pigs ( Sus scrofa ) on multi-tenure islands. Larger areas and more challenging species are now under consideration for eradication. The recovery of endangered Hawaiian birds may depend on the creation of large predator-proof exclosures on some of the larger islands. Large scale eradications of small Indian mongooses ( Herpestes auropunctatus ) would be beneficial to ground-nesting birds such as nēnē ( Branta sandvicensis ), but this has been achieved only in small exclosures.

Hawaii↗

Ecosystem history of southern and central Biscayne Bay: Summary report on sediment core analyses

During the last century, the environs of Biscayne Bay have been greatly affected by anthropogenic alteration through urbanization of the Miami/Dade County area. The sources, timing, delivery, and quality of freshwater flow into the Bay have been changed by construction of a complex canal system that controls movement of water throughout south Florida. Changes in shoreline and sub-aquatic vegetation and marine organisms have been observed and changes in water delivery are believed to be the cause. Current restoration goals are attempting to restore natural flow of fresh water into Biscayne and Florida Bays and to restore the natural fauna and flora, but first we need to determine pre-alteration baseline conditions in order to establish targets and performance measures for restoration. This research is part of an ongoing study designed to address the needs of the Biscayne Bay Coastal Wetlands Project (BBCW) of the Comprehensive Everglades Restoration Plan (CERP). By establishing the natural patterns of temporal change in salinity, water quality, vegetation, and benthic fauna in Biscayne Bay and the nearby wetlands over the last 100- 500 years the USGS, in collaboration with our partners, will provide the data necessary to set realistic targets to achieve the BBCW Project goals. Six cores from three sites in Biscayne Bay were collected in April 2002 for multidisciplinary multi-proxy analyses. This report details the results of these analyses and compares the 2002 cores to cores collected in 1997. The following are our significant findings to date: The salinity of central Biscayne Bay has become increasingly marine and increasingly stable over the last 100 years. At No Name Bank, prior to approximately 1915, the inter-decadal and decadal salinity fluctuations appear to have been greater than after 1915 when salinities stabilized at that site. Continental shelf/open marine influence on the sites has increased during the 20th century. There is no indication of inter-decadal salinity extremes or periods of hypersalinity. Freshwater and mesohaline salinities have had a minor influence on No Name bank throughout the time of deposition. At Featherbed Bank, the influence is reduced to mesohaline salinities. Card Bank has experienced relatively large swings in salinity over multi-decadal and centennial timescales, compared to central Biscayne Bay, but marine influence at the site has increased over the last century. Indications of regional scale patterns have been found, especially in the shell chemistry data and the pollen assemblages. These regional patterns indicate that the changes are not site specific and may not be limited to Biscayne Bay. Sub-aquatic vegetation has undergone bay-wide patterns of change over the last 200-500 years, which includes expansion prior to 1900 and declines during the last century in central Biscayne Bay. Thalassia appears to have increased at all three core sites sometime between 1550 and 1750 AD. A decline in Thalassia appears to have occurred after 1950 at No Name Bank and slightly earlier in the 20th century at Featherbed Bank. Card Bank does not appear to have experienced any declines in vegetation on an inter-decadal scale during the 20th century. Molluscan faunal abundance and diversity have undergone significant changes in central Biscayne Bay. Indicators of increased organic-rich sediments at No Name occur between 1869 to 1888 and between the 1930’s to 1975. These changes may correlate to human activities (settlement, population growth). These findings represent a first step towards the project’s goal to reconstruct the history of Biscayne Bay and they provide us with a working model to be tested at other sites. It is clear from our findings that Biscayne Bay has been a dynamic environment over the last 500 years, with natural changes occurring in salinity and benthic habitats. However, several significant changes have occurred in the 20th century: 1) increased stabilization of marine salinities; 2) declines in seagrass in central Biscayne Bay; 3) dramatic changes in molluscan abundance and diversity in central Biscayne Bay. The question remains - how do we better differentiate natural cycles of change from anthropogenic change within these observed trends? The preliminary implications from our research are that changes in salinity and benthic habitats have occurred naturally in Biscayne Bay on inter-decadal to centennial scales, perhaps due to climatic changes, changes in sea level, bank migrations, or a combination of factors. However, further work needs to be done to determine which components of change in the 20th century are human-induced and which are natural. By examining the historical records preserved in the sediments of Biscayne Bay, we can provide restoration trust agencies with the information necessary to set realistic targets and performance measures for Biscayne Bay.

Florida↗

Inter-laboratory comparison of X-ray fluorescence analyses of eruptive products of El Chichón Volcano, Chiapas, Mexico

An inter-laboratory comparison has been made of X-ray fluorescence analyses of 10 samples of lava and pumices from El Chich&oacute;n Volcano, Chiapas, Mexico. Some determinations of major-element constituents agree within analytical uncertainty, whereas others exchibit significant bias. Analyses carried out at the Michigan Technological University (MTU) laboratory are systematically lower in MgO (26&ndash;48%), Fe total (5&ndash;18%), CaO (4&ndash;15%) and higher in K 2 O (0&ndash;15%) than analyses made at the U.S. Geological Survey (USGS) Denver laboratory. These differences are ascribed in part to a complex combination of calibration assumptionsand mineralogical and particle-size effects inherent in the use of pressed rock-powder pellets in the analytical procedure of the MTU laboratory. Other, but as yet unknown, differences in sample preparation and/or analytical technique may also be important; effects related to natural sample inhomogeneityare believed to be insignificant. The inter-laboratory differences in the analytical data complicated accurate assessment of whether El Chich&oacute;n magmas have changed composition during the past 300 000 a. Knowledge of such change is needed for understanding petrogenetic history and for such related studies as evaluation of volcanic hazards.

Applied Geochemistry↗

Introduction to the special issue on ‘Frontiers in gas geochemistry’

The study of the geochemistry of gases pervades the Earth and Environmental Sciences. This is due in no small measure to the well-established thermodynamic properties of gases which allow their application to a variety of processes occurring over a wide spectrum of natural conditions. In this respect, both major and associated minor gases have been proven useful: indeed, the trace gases have been particularly important given their role as sensitive geochemical tracers. Examples where gas geochemistry places key constraints on geochemical processes include the degassing history of the solid Earth to form the atmosphere and oceans, the origin and migration characteristics of hydrocarbon deposits, the scale of climate variability, the P–T characteristics of geothermal reservoirs, and the dynamics of the earthquake cycle and volcanic activity, to name but a few. This volume continues this rich tradition with an eclectic selection of papers aimed at exploring and exploiting gas geochemistry over a myriad set of research themes.

Chemical Geology↗

Causes and implications of the correlation between forest productivity and tree mortality rates

At global and regional scales, tree mortality rates are positively correlated with forest net primary productivity (NPP). Yet causes of the correlation are unknown, in spite of potentially profound implications for our understanding of environmental controls of forest structure and dynamics and, more generally, our understanding of broad-scale environmental controls of population dynamics and ecosystem processes. Here we seek to shed light on the causes of geographic patterns in tree mortality rates, and we consider some implications of the positive correlation between mortality rates and NPP. To reach these ends, we present seven hypotheses potentially explaining the correlation, develop an approach to help distinguish among the hypotheses, and apply the approach in a case study comparing a tropical and temperate forest. Based on our case study and literature synthesis, we conclude that no single mechanism controls geographic patterns of tree mortality rates. At least four different mechanisms may be at play, with the dominant mechanisms depending on whether the underlying productivity gradients are caused by climate or soil fertility. Two of the mechanisms are consequences of environmental selection for certain combinations of life-history traits, reflecting trade-offs between growth and defense (along edaphic productivity gradients) and between reproduction and persistence (as manifested in the adult tree stature continuum along climatic and edaphic gradients). The remaining two mechanisms are consequences of environmental influences on the nature and strength of ecological interactions: competition (along edaphic gradients) and pressure from plant enemies (along climatic gradients). For only one of these four mechanisms, competition, can high mortality rates be considered to be a relatively direct consequence of high NPP. The remaining mechanisms force us to adopt a different view of causality, in which tree growth rates and probability of mortality can vary with at least a degree of independence along productivity gradients. In many cases, rather than being a direct cause of high mortality rates, NPP may remain high in spite of high mortality rates. The independent influence of plant enemies and other factors helps explain why forest biomass can show little correlation, or even negative correlation, with forest NPP.

Ecological Monographs↗

The geochemistry of pesticides

The mid-1970s marked a major turning point in human history, for it was at that moment that the ability of the Earth&rsquo;s ecosystems to absorb most of the biological impacts of human activities appears to have been exceeded by the magnitude of those impacts. This conclusion is based partly upon estimates of the rate of carbon dioxide emission during the combustion of fossil fuels, relative to the rate of its uptake by terrestrial ecosystems ( Loh, 2002 ). A very different threshold, however, had already been crossed several decades earlier with the birth of the modern chemical industry, which produced novel substances for which no such natural assimilative capacity existed. Among these new chemical compounds, none has posed a greater challenge to the planet&rsquo;s ecosystems than synthetic pesticides, compounds that have been intentionally released into the hydrologic system in vast quantities&mdash;several hundred million pounds of active ingredient (a.i.) per year in the United States alone ( Donaldson et al. , 2002 )&mdash;for many decades. To gauge the extent to which we are currently able to assess the environmental implications of this new development in the Earth&rsquo;s history, this chapter presents an overview of current understanding regarding the sources, transport, fate, and biological effects of pesticides, their transformation products, and selected adjuvants in the hydrologic system. (Adjuvants are the so-called inert ingredients included in commercial pesticide formulations to enhance the effectiveness of the active ingredients.)

Book chapter↗

The role of giant impacts in planet formation

Planets are expected to conclude their growth through a series of giant impacts: energetic, global events that significantly alter planetary composition and evolution. Computer models and theory have elucidated the diverse outcomes of giant impacts in detail, improving our ability to interpret collision conditions from observations of their remnants. However, many open questions remain, as even the formation of the Moon—a widely suspected giant-impact product for which we have the most information—is still debated. We review giant-impact theory, the diverse nature of giant-impact outcomes, and the governing physical processes. We discuss the importance of computer simulations, informed by experiments, for accurately modeling the impact process. Finally, we outline how the application of probability theory and computational advancements can assist in inferring collision histories from observations, and we identify promising opportunities for advancing giant-impact theory in the future. Giant impacts exhibit diverse possible outcomes leading to changes in planetary mass, composition, and thermal history depending on the conditions. Improvements to computer simulation methodologies and new laboratory experiments provide critical insights into the detailed outcomes of giant impacts. When colliding planets are similar in size, they can merge or escape one another with roughly equal probability, but with different effects on their resulting masses, densities, and orbits. Different sequences of giant impacts can produce similar planets, encouraging the use of probability theory to evaluate distinct formation hypothesis.

Annual Reviews of Earth and Planetary Science↗

Optimization of a suite of flathead catfish (Pylodictis olivaris) microsatellite markers for understanding the population genetics of introduced populations in the northeast United States

Flathead catfish are rapidly expanding into nonnative waterways throughout the United States. Once established, flathead catfish may cause disruptions to the local ecosystem through consumption and competition with native fishes, including species of conservation concern. Flathead catfish often become a popular sport fish in their introduced range, and so management strategies must frequently balance the need to protect native and naturalized fauna while meeting the desire to maintain or enhance fisheries. However, there are currently few tools available to inform management of invasive flathead catfish ( Pylodictis olivaris ). We describe a suite of microsatellite loci that can be used to characterize population structure, predict invasion history, and assess potential mitigation strategies for flathead catfish.

Pennsylvania↗

Biological pathways of exposure and ecotoxicity values for uranium and associated radionuclides: Chapter D in Hydrological, geological, and biological site characterization of breccia pipe uranium deposits in Northern Arizona

This chapter compiles available chemical and radiation toxicity information for plants and animals from the scientific literature on naturally occurring uranium and associated radionuclides. Specifically, chemical and radiation hazards associated with radionuclides in the uranium decay series including uranium, thallium, thorium, bismuth, radium, radon, protactinium, polonium, actinium, and francium were the focus of the literature compilation. In addition, exposure pathways and a food web specific to the segregation areas were developed. Major biological exposure pathways considered were ingestion, inhalation, absorption, and bioaccumulation, and biota categories included microbes, invertebrates, plants, fishes, amphibians, reptiles, birds, and mammals. These data were developed for incorporation into a risk assessment to be conducted as part of an environmental impact statement for the Bureau of Land Management, which would identify representative plants and animals and their relative sensitivities to exposure of uranium and associated radionuclides. This chapter provides pertinent information to aid in the development of such an ecological risk assessment but does not estimate or derive guidance thresholds for radionuclides associated with uranium. Previous studies have not attempted to quantify the risks to biota caused directly by the chemical or radiation releases at uranium mining sites, although some information is available for uranium mill tailings and uranium mine closure activities. Research into the biological impacts of uranium exposure is strongly biased towards human health and exposure related to enriched or depleted uranium associated with the nuclear energy industry rather than naturally occurring uranium associated with uranium mining. Nevertheless, studies have reported that uranium and other radionuclides can affect the survival, growth, and reproduction of plants and animals. Exposure to chemical and radiation hazards is influenced by a plant’s or an animal’s life history and surrounding environment. Various species of plants, invertebrates, fishes, amphibians, reptiles, birds, and mammals found in the segregation areas that are considered species of concern by State and Federal agencies were included in the development of the site-specific food web. The utilization of subterranean habitats (burrows in uranium-rich areas, burrows in waste rock piles or reclaimed mining areas, mine tunnels) in the seasonally variable but consistently hot, arid environment is of particular concern in the segregation areas. Certain species of reptiles, amphibians, birds, and mammals in the segregation areas spend significant amounts of time in burrows where they can inhale or ingest uranium and other radionuclides through digging, eating, preening, and hibernating. Herbivores may also be exposed though the ingestion of radionuclides that have been aerially deposited on vegetation. Measured tissues concentrations of uranium and other radionuclides are not available for any species of concern in the segregation areas. The sensitivity of these animals to uranium exposure is unknown based on the existing scientific literature, and species-specific uranium presumptive effects levels were only available for two endangered fish species known to inhabit the segregation areas. Overall, the chemical toxicity data available for biological receptors of concern were limited, although chemical and radiation toxicity guidance values are available from several sources. However, caution should be used when directly applying these values to northern Arizona given the unique habitat and life history strategies of biological receptors in the segregation areas and the fact that some guidance values are based on models rather than empirical (laboratory or field) data. No chemical toxicity information based on empirical data is available for reptiles, birds, or wild mammals; therefore, the risks associated with uranium and other radionuclides are unknown for these biota.

Arizona↗

Geologic sources of energy

This chapter describes the exploration, development, and geologic setting of petroleum resources (including tar sands), coal resources (including coalbed methane), and geothermal energy resources of the Northern Cordillera.For petroleum resources, the chapter describes: (1) the history of petroleum development and production, first for Alaska and then for the Canadian Cordillera; and (2) generalized basin analysis geologic settings for the six major petroleum basins that are illustrated in summary maps and cross sections. Subsequent sections of the chapter describe the nature and geologic setting of tar sand resources, geothermal energy resources, and coal resources. The area distribution of the energy resources of the region are depicted in the Energy Resources Map that has multiple layers that can be displayed in various arrangements. Employing this map in a separate window while reading the text will be greatly beneficial. Many geographic names are employed in the descriptions throughout this chapter. While reading this chapter, viewing the Geographic Regions Layer of the Energy Resources Map, as needed, will be valuable.

Book chapter↗

Foreward: The paleoclimatic and paleobiogeographic significance of the Tjörnes Basin, Northern Iceland

Since the mid-19th century, geologists and paleontologists have recognized the scientific importance and unique nature of the richly fossiliferous sediments exposed along the Tjörnes Peninsula in Northern Iceland. In the following century and a half, Tjörnes has attracted the attention of an international “who’s who” in Cenozoic paleontology, as well as many paleoclimatologists unraveling the complex climatic history of the North Atlantic and Arctic Oceans. In a seminal meeting, sponsored by the Royal Society of London in 1984, and published in Philosophical Transactions of the Royal Society of London, Series B, volume 318 (“The past three million years: evolution of climatic variability in the North Atlantic region”), an international group of experts addressed climatic history of the last 3 million years. Notably, one of the main invited participants was Iceland’s Dr. Thorleifur Einarsson, who literally wrote the book “Geology of Iceland” (1994, 1999), and was also known for his expertise in Tjörnes paleoclimatology. Einarsson’s key contribution was linking the marine history of Tjörnes to the rapidly growiing paleoclimate records from deep-sea marine sediment cores and improving chronology of climate evolution. This work was closely linked to the dating of Pliocene-Pleistocene glacial sediments and volcanics in Iceland and on Tjörnes in particular, based on paleomagnetic data and biostratigraphic work which was presented jointly with a group from the U.S. Geological Survey at the 1965 INQUA meeting in Boulder, Colorado.

Tjornes Basin↗

The Holocene history of the North American Monsoon: 'known knowns' and 'known unknowns' in understanding its spatial and temporal complexity

Evidence for climatic change across the North American Monsoon (NAM) and adjacent areas is reviewed, drawing on continental and marine records and the application of climate models. Patterns of change at 12,000, 9000, 6000 and 4000 cal yr BP are presented to capture the nature of change from the Younger Dryas (YD) and through the mid-Holocene. At the YD, conditions were cooler overall, wetter in the north and drier in the south, while moving into the Holocene wetter conditions became established in the south and then spread north as the NAM strengthened. Until c. 8000 cal yr BP, the Laurentide Ice Sheet influenced precipitation in the north by pushing the Bermuda High further south. The peak extent of the NAM seems to have occurred around 6000 cal yr BP. 4000 cal yr BP marks the start of important changes across the NAM region, with drying in the north and the establishment of the clear differences between the summer-rain dominated south and central areas and the north, where winter rain is more important. This differentiation between south and north is crucial to understanding many climate responses across the NAM. This increasing variability is coincident with the declining influence of orbital forcing. 4000 cal yr BP also marks the onset of significant anthropogenic activity in many areas. For the last 2000 years, the focus is on higher temporal resolution change, with strong variations across the region. The Medieval Climate Anomaly (MCA) is characterised by centennial scale &lsquo;megadrought&rsquo; across the southwest USA, associated with cooler tropical Pacific SSTs and persistent La Ni&ntilde;a type conditions. Proxy data from southern Mexico, Central America and the Caribbean reveal generally wetter conditions, whereas records from the highlands of central Mexico and much of the Yucatan are typified by long -term drought. The Little Ice Age (LIA), in the north, was characterised by cooler, wetter winter conditions that have been linked with increased frequency of El Ni&ntilde;o's. Proxy records in the central and southern regions reveal generally dry LIA conditions, consistent with cooler SSTs in the Caribbean and Gulf of Mexico. This synthesis demonstrates that in some periods, one major forcing can dominate across the whole area (e.g. insolation in the early-mid Holocene), but at other times there is strong variability in patterns of change due to the differential impact of forcings such as the Pacific Decadal Oscillation (PDO) and the Atlantic Multidecadal Oscillation (AMO) on precipitation seasonality.

Quaternary Science Reviews↗

Slope evolution at the Calvert Cliffs, Maryland — Measuring the change from eroding bluffs to stable slopes

Despite a long history of geomorphic studies, it is difficult to ascertain the time required for slopes to change from near vertical exposures to relatively stable slopes due to inadequate age control. Actively eroding coastal bluffs along the western shore of the Chesapeake Bay provide a key for understanding the centennial-scale development of stable slopes from eroding bluff faces. The Calvert Cliffs are composed of sandy silts, silty sands, and clayey silts of Miocene-age. Active wave erosion at the bluff toes encourages rapid sloughing from bluff faces and maintains slope angles of 70-80 degrees and relatively constant bluff-retreat rates. Naturally stabilized slopes are preserved as a fossil bluff line inland from a prograding cuspate foreland at Cove Point. The foreland is migrating southward at a rate of ca. 1.5 m/yr. As it moves south, it progressively protects bluffs from wave action as new beaches are deposited at their toes. Wave erosion is reinitiated at the northern end of the complex as the landform passes. An incremental record of slope change is preserved along the fossil bluff line. 14C dating of swales between beach ridges shows the complex to span 1700 years of progressive migration history. We hypothesized that slopes would change from steep, eroding faces to low-angle slopes covered with vegetation and sought to document the rate of change. Our team measured slope angles at intervals along the fossil bluff line and dated profiles by interpolating 14C ages of adjacent beach ridges. There was no progressive decrease in slope with age. All slopes along the fossil bluff line were 30-40 degrees with a mean of 35 degrees. Constancy in slope angle suggests that steep, actively eroding bluffs were quickly changed to stable slopes by landslides and slumping once they were protected. Given the accuracy of our age control, we conclude that the time required to attain a stable slope under natural processes is less than one century. This indicates that once toe erosion is ended (naturally or through engineering) slopes are reduced to 35-degrees over a period of decades and not centuries.

Maryland↗

A global ecological signal of extinction risk in marine ray-finned fishes (class Actinopterygii)

Many marine fish species are experiencing population declines, but their extinction risk profiles are largely understudied in comparison to their terrestrial vertebrate counterparts. Selective extinction of marine fish species may result in rapid alteration of the structure and function of ocean ecosystems. In this study, we compiled an ecological trait dataset for 8,185 species of marine ray-finned fishes (class Actinopterygii) from FishBase and used phylogenetic generalized linear models to examine which ecological traits are associated with increased extinction risk, based on the International Union for the Conservation of Nature Red List. We also assessed which threat types may be driving these species toward greater extinction risk and whether threatened species face a greater average number of threat types than non-threatened species. We found that larger body size and/or fishes with life histories involving movement between marine, brackish, and freshwater environments are associated with elevated extinction risk. Commercial harvesting threatens the greatest number of species, followed by pollution, development, and then climate change. We also found that threatened species, on average, face a significantly greater number of threat types than non-threatened species. These results can be used by resource managers to help address the heightened extinction risk patterns we found.

Cambridge Prisms: Extinction↗

A space‐for‐time substitution reveals the long‐term decline in genotypic diversity of a widespread salt marsh plant, Spartina alterniflora, over a span of 1500 years

Clonal populations face a trade‐off between sexual recruitment and vegetative growth and, once established, may undergo continuous declines in genotypic diversity if their sexual recruits make poor competitors. The geological history of delta formation in the Lower Mississippi River Valley was used to age eight S. alterniflora marshes for use in a space‐for‐time substitution ranging over 1500 years, in order to determine the long‐term effects of clonal growth on genotypic diversity in natural populations. 2 We also predicted that highly heterozygous clones are competitively superior, leading to an increase in the overall level of genetic diversity as a marsh ages and/or to an increasingly positive relationship between clone size and individual heterozygosity, and that the clumping of ramets within clones will occur over increasingly large distances as populations age, while the clumping of genetically related clones will become less pronounced as intraclonal competition begins to obscure the initial effects of localized seedling recruitment. Using molecular markers to differentiate clones, we documented a decline in clonal richness at the rate of approximately 1% 100 years −1 that was accompanied for the first 300–500 years by an increase in the distance over which clumping of ramets within genets occurred. Older populations, in the 500–1500‐year range, showed evidence of clone fragmentation. The spatial clustering of kin was observed for only two marshes, and exhibited no clear relationship with marsh age. Whereas the overall level of genetic diversity was consistent among marshes and showed no clear relationship with marsh age, the relationship between heterozygosity and individual clone size became increasingly pronounced within older marshes. Our results suggest that under natural conditions S. alterniflora marshes will rarely reach ages sufficient for the loss of all clonal diversity, or for the effects of inbreeding and drift to pose a significant threat to population viability.

Journal of Ecology↗

The population genetics of the causative agent of snake fungal disease indicate recent introductions to the USA

Snake fungal disease (SFD; ophidiomycosis), caused by the pathogen Ophidiomyces ophiodiicola ( Oo ), has been documented in wild snakes in North America and Eurasia, and is considered an emerging disease in the eastern United States of America. However, a lack of historical disease data has made it challenging to determine whether Oo is a recent arrival to the USA or whether SFD emergence is due to other factors. Here, we examined the genomes of 82 Oo strains to determine the pathogen’s history in the eastern USA. Oo strains from the USA formed a clade (Clade II) distinct from European strains (Clade I), and molecular dating indicated that these clades diverged too recently (approximately 2,000 years ago) for transcontinental dispersal of Oo to have occurred via natural snake movements across Beringia. A lack of nonrecombinant intermediates between clonal lineages in Clade II indicates that Oo has actually been introduced multiple times to North America from an unsampled source population, and molecular dating indicates that several of these introductions occurred within the last few hundred years. Molecular dating also indicated that the most common Clade II clonal lineages have expanded recently in the USA, with time of most recent common ancestor mean estimates ranging from 1985 to 2007 CE. The presence of Clade II in captive snakes worldwide demonstrates a potential mechanism of introduction and highlights that additional incursions are likely unless action is taken to reduce the risk of pathogen translocation and spillover into wild snake populations.

PLoS Biology↗