Search USGS⌕ Search

Geology topics

Research about Chesapeake Bay

Source-linked reports with geographic coverage including Chesapeake Bay.

At least 127 records · Page 7Linked to original sources
USGS2005

Crystalline-rock ejecta and shocked minerals of the Chesapeake Bay impact structure, USGS-NASA Langley core, Hampton, Virginia, with supplemental constraints on the age of impact

The USGS-NASA Langley corehole at Hampton , Va., was drilled 2000 as the first in a series of new coreholes drilled in the late Eocene Chesapeake Bay impact structure to gain a comprehensive understanding of its three-dimensional character. This understanding is important for assessing ground-water resources in the region, as well as for learning about marine impacts on Earth. We studied crystalline-rock ejecta and shock-metamorphosed minerals from the Langley core to determine what they reveal about the geology of crystalline rocks beneath the Atlantic Coastal Plain and how those rocks were affected by the impact . An unusual polymict diamicton, informally called the Exmore beds (upper Eocene), is 33.8 meters (m; 110.9 feet (ft)) thick and lies at a depth of 269.4 to 235.65 m (884.0 to 773.12 ft) in the core . This matrix-supported sedimentary deposit contains clasts of Tertiary and Cretaceous sediment (ranging up to boulder size) and sparse pebbles of crystalline rock . The matrix consists of muddy sand that contains abundant quartz grains and minor glauconite and potassium feldspar. Significantly, the sandy matrix of the Exmore beds contains sparse quartz grains (0.1 to 0.3 millimeter (0.004 to 0.012 inch) in diameter) that contain multiple sets of intersecting planar deformation features formerly referred to as shock lamellae. As many as five different sets have been observed in some quartz grains. Planar deformation features also occur in quartz grains in reworked crystalline-rock clasts in the Exmore beds. Such grains are clearly of shock-metamorphic origin. The presence of these features indicates that the quartz grains have experienced pressures greater than 6 gigapascals (GPa) and strain rates greater than 10 6 /second. Thus, the shock-metamorphosed quartz grains, although rare, provide clear and convincing evidence that the Exmore beds are of hybrid impact origin. Identification of shocked quartz grains in the Langley core adds to the number of sites in the structure where their presence is confirmed. Most of the clasts of crystalline rock that are in and just below the Exmore beds are rounded, detrital, and typical of coastal plain sediments. However, a few have angular shapes and consist of cataclastically deformed felsite having aphanitic-porphyritic to aphanitic texture and peraluminous rhyolite composition. Three of these clasts contain quartz grains that display two sets of planar deformation features of shock-metamorphic origin. Shock-metamorphosed quartz is an integral part of the cataclastic fabric in these three clasts, indicating that both the fabric and the shocked quartz were produced by the same high-energy impact event. Some felsite clasts have spherulitic textures that may be features either of an impact melt or of preimpact volcanic rocks. A weighted-mean total-fusion 40 Ar/ 39 Ar age of 35.3±0.1 Ma (±lσ) for 19 analyses of 4 North American tektites records the age of the late Eocene Chesapeake Bay impact event.

Chesapeake Bay↗
USGS2004

Isolation and characterization of mycobacteria from striped bass Morone saxatilis from the Chesapeake Bay

Mycobacteriosis in striped bass Morone saxatilis of Chesapeake Bay, USA, was first diagnosed in 1997 based on the presence of granulomatous inflammation and acid-fast bacteria in skin and spleen. To confirm histopathology, bacteriological detection and identification of mycobacteria were begun using splenic tissue from fish with and without skin ulcerations. On the basis of initial studies using a variety of selective and nonselective media, decontamination, homogenization and incubation conditions, a simple and quantitative recovery method using aseptic necropsy of splenic tissue was developed. Optimal recovery was obtained by spread-plating homogenates on Middlebrook 7H10 agar with incubation for 3 mo at 23°C. Mycobacteria were recovered from 76% (n = 149/196) of fish examined. Mycobacterial densities exceeded 10 4 colony forming units · g tissue -1 in 38% of samples (n = 63/168) that were examined using a quantitative approach. The most frequently recovered mycobacterium, present in 57% (n = 109/192) of characterized samples, was the recently named new species Mycobacterium shottsii. Polyinfections of M. shottsii and other mycobacteria were observed in 25% of samples (n = 47/192) with densities of M. shottsii usually 1 or more orders of magnitude higher than co-isolate(s). Other mycobacteria recovered included isolates that, based on phenotypic traits, resembled M. interjectum, M. marinum, M. scrofulaceum, M. szulgai and M. triplex . M. marinum , commonly associated with fish mycobacteriosis and human disease, was recovered infrequently (3%, n = 6/192). The presence of multiple mycobacterial types occurring at high densities suggests that a variety of mycobacteria could be causative agents of mycobacteriosis in striped bass from the Chesapeake Bay. Striped bass is the major recreational fish species in the Chesapeake Bay, and the significance of the current epizootic to human health and the potential adverse effects on fish stocks are not known.

Maryland, Virginia↗
USGS2004

Ultrastructure of Mycobacterium marinum granuloma in striped bass Morone saxatilis

An emerging epizootic of mycobacteriosis currently threatens striped bass Morone saxatilis populations in Chesapeake Bay, USA. Several species of mycobacteria, including Mycobacterium marinum , species resembling M. avium , M. gordonae , M. peregrinum , M. scrofulaceum and M. terrae , and the new species M. shottsii have been isolated from diseased and healthy bass. In this study, we describe the ultrastructure of developing M. marinum granulomas in experimentally infected bass over a period of 45 wk. The primary host response to injected mycobacteria was formation of large macrophage aggregations containing phagocytosed bacilli. M. marinum were always contained within phagosomes. Close association of lysosomes with mycobacterial phagosomes, as well as the presence of electron-opaque material within phagosomes, suggested phagolysosomal fusion. Development of granulomas involved epithelioid transformation of macrophages, followed by appearance of central necrosis. Desmosomes were present between mature epithelioid cells. The necrotic core region of M. marinum granulomas was separated from overlying epithelioid cells by several layers of flattened, electron-opaque spindle-shaped cells. These cells appeared to be formed by compression of epithelioid cells and, aside from a flattened nucleus, did not possess recognizable organelles. Following the development of well-defined, paucibacillary granulomas, secondary disease was observed. Recrudescence was marked by bacterial replication followed by disruption of granuloma architecture, including loss of epithelioid and spindle cell layers. In advanced recrudescent lesions, normal tissue was replaced by macrophages, fibroblasts, and other inflammatory leukocytes. Large numbers of mycobacteria were observed, both intracellular and suspended in cellular debris.

Maryland, Virginia↗
USGS2004

Mute swans and their Chesapeake Bay habitats: proceedings of a symposium

The symposium 'Mute Swans and their Chesapeake Bay Habitats,' held on June 7, 2001, provided a forum for biologists and managers to share research findings and management ideas concerning the exotic and invasive mute swan (Cygnus olar). This species has been increasing in population size and is considered by many to be a problem in regard to natural food resources in the Bay that are used by native waterfowl during the winter months. Other persons, however, feel that resource managers are attempting to create a problem to justify more killing of waterfowl by hunters. Some persons also believe that managers should focus on the larger issues causing the decline of native food resources, such as the unabated human population increase in the Bay watershed and in the immediate coastal areas of the Bay. The symposium, sponsored by the Wildfowl Trust of North America and the U.S. Geological Survey, provided the atmosphere for presentation of mute swan data and opinions in a collegial setting where discussion was welcomed and was often informative and enthusiastic. An interesting historic review of the swan in regard to the history of mankind was presented, followed by a discussion on the positive and negative effects of invasive species. Biologists from different parts of the continent discussed the population status of the species in several states in the east and in the Great Lakes area. Data on the food habits of this species were presented in regard to submerged aquatic vegetation, and an interesting discussion on the role that the food habits of Canada geese in regard to native vegetation was presented. Findings and recommendations of the Mute Swan Task Force were presented. Finally, a representative of the Friends of Animals gave a thought-provoking presentation in defense of the mute swan. The presentations, in general, provided the necessary information and recommendations to allow managers to proceed with management of this controversial species with new and valuable perspectives.

Maryland, Virginia↗
USGS2003

Eutrophication and carbon sources in Chesapeake Bay over the last 2700 yr: Human impacts in context

To compare natural variability and trends in a developed estuary with human-influenced patterns, stable isotope ratios (δ 13 C and δ 15 N) were measured in sediments from five piston cores collected in Chesapeake Bay. Mixing of terrestrial and algal carbon sources primarily controls patterns of δ 13 C org profiles, so this proxy shows changes in estuary productivity and in delivery of terrestrial carbon to the bay. Analyses of δ 15 N show periods when oxygen depletion allowed intense denitrification and nutrient recycling to develop in the seasonally stratified water column, in addition to recycling taking place in surficial sediments. These conditions produced 15 N-enriched (heavy) nitrogen in algal biomass, and ultimately in sediment. A pronounced increasing trend in δ 15 N of +4‰ started in about A.D. 1750 to 1800 at all core sites, indicating greater eutrophication in the bay and summer oxygen depletion since that time. The timing of the change correlates with the advent of widespread land clearing and tillage in the watershed, and associated increases in erosion and sedimentation. Isotope data show that the region has experienced up to 13 wet-dry cycles in the last 2700 yr. Relative sea-level rise and basin infilling have produced a net freshening trend overprinted with cyclic climatic variability. Isotope data also constrain the relative position of the spring productivity maximum in Chesapeake Bay and distinguish local anomalies from sustained changes impacting large regions of the bay. This approach to reconstructing environmental history should be generally applicable to studies of other estuaries and coastal embayments impacted by watershed development.

Chesapeake Bay↗
USGS2003

Medieval Warm Period, Little Ice Age and 20th century temperature variability from Chesapeake Bay

We present paleoclimate evidence for rapid (< 100 years) shifts of ~2-4 o C in Chesapeake Bay (CB) temperature ~2100, 1600, 950, 650, 400 and 150 years before present (years BP) reconstructed from magnesium/calcium (Mg/Ca) paleothermometry. These include large temperature excursions during the Little Ice Age (~1400-1900 AD) and the Medieval Warm Period (~800-1300 AD) possibly related to changes in the strength of North Atlantic thermohaline circulation (THC). Evidence is presented for a long period of sustained regional and North Atlantic-wide warmth with low-amplitude temperature variability between ~450 and 1000 AD. In addition to centennial-scale temperature shifts, the existence of numerous temperature maxima between 2200 and 250 years BP (average ~70 years) suggests that multi-decadal processes typical of the North Atlantic Oscillation (NAO) are an inherent feature of late Holocene climate. However, late 19th and 20th century temperature extremes in Chesapeake Bay associated with NAO climate variability exceeded those of the prior 2000 years, including the interval 450-1000 AD, by 2-3 o C, suggesting anomalous recent behavior of the climate system.

Maryland↗
USGS2003

Anthropogenically induced changes in sediment and biogenic silica fluxes in Chesapeake Bay

Sediment cores as long as 20 m, dated by 14C, 210Pb, and 137Cs methods and pollen stratigraphy, provide a history of diatom productivity and sediment-accumulation rates in Chesapeake Bay. We calculated the flux of biogenic silica and total sediment for the past 1500 yr for two high-sedimentation-rate sites in the mesohaline section of the bay. The data show that biogenic silica flux to sediments, an index of diatom productivity in the bay, as well as its variability, were relatively low before European settlement of the Chesapeake Bay watershed. In the succeeding 300-400 yr, the flux of biogenic silica has increased by a factor of 4 to 5. Biogenic silica fluxes still appear to be increasing, despite recent nutrient-reduction efforts. The increase in diatom-produced biogenic silica has been partly masked (in concentration terms) by a similar increase in total sediment flux. This history suggests the magnitude of anthropogenic disturbance of the estuary and indicates that significant changes had occurred long before the twentieth century.

Maryland, Virginia↗
USGS2003

Motorized migrations: The future or mere fantasy?

In 15 experiments from 1993-2002, we led cranes, geese, or swans on their first southward migration with either ultralight aircraft or vehicles on the ground. These experiments reveal that large birds can be readily trained to follow and most will return north (and south) in subsequent migrations unassisted. These techniques can now be used to teach birds new (or forgotten) migration paths. Although we are constantly improving our training techniques, we now have an operational program that can be broadly applied to those species where juveniles learn migration routes from their parents.

Arizona, Florida, Idaho, Indiana, Maryland, New Me↗
USGS2003

Impact damage to dinocysts from the Late Eocene Chesapeake Bay event

The Chesapeake Bay impact structure, formed by a comet or meteorite that struck the Virginia continental shelf about 35.5 million years ago, is the focus of an extensive coring project by the U.S. Geological Survey and its cooperators. Organic-walled dinocysts recovered from impact-generated deposits in a deep core inside the 85-90 km-wide crater include welded organic clumps and fused, partially melted and bubbled dinocysts unlike any previously observed. Other observed damage to dinocysts consists of breakage, pitting, and folding in various combinations. The entire marine Cretaceous, Paleocene, and Eocene section that was once present at the site has been excavated and redeposited under extreme conditions that include shock, heat, collapse, tsunamis, and airfall. The preserved dinocysts reflect these conditions and, as products of a known impact, may serve as guides for recognizing impact-related deposits elsewhere. Features that are not unique to impacts, such as breakage and folding, may offer new insights into crater-history studies in general, and to the history of the Chesapeake Bay impact structure in particular. Impact-damaged dinocysts also are found sporadically in post-impact deposits and add to the story of continuing erosion and faulting of crater material.

Chesapeake Bay↗
USGS2003

Benthic sulfate reduction along the Chesapeake Bay central channel. II. Temporal controls

Seasonal and interannual controls of benthic sulfate reduction (SR) were examined at 3 sites (upper [UB], mid- [MB] and lower [LB] bay) along the Chesapeake Bay central channel, from early spring through fall, for 6 yr (1989 to 1994). The combined influences of temperature, sulfate, organic loading and bioturbation affected seasonal SR rates differently in the 3 regions. Consistently low SR rates at UB resulted from low overlying-water sulfate concentrations and the dominance of refractory organic terrestrial material. Combined seasonal variation in temperature and sulfate accounted for 50% of the annual variability in 0 to 2 cm depth interval SR rates, while sediment organic content had no significant seasonal influence. In contrast, MB and LB sites had high rates of SR fostered by high levels of overlying water SO42- and organic input dominated by labile phytoplankton detritus. New organic loading (measured as chl a) stimulated 0 to 2 cm SR during spring at both sites. Combined organic quantity (as particulate C and/or N) and temperature accounted for > 75% of the variability in 0 to 2 cm SR at MB during spring and fall. Molecular diffusion supplied 25 to 45% of the SO 42- needed to fuel 0 to 12 cm depth interval SR at MB, with the balance presumably supplied by S-recycling. Interannual differences in summertime SR rates were linked to the extent of freshwater flow during spring, with high-flow years associated with high SR rates at UB and MB, and low rates at LB. The negative trend between benthic SR and river flow at LB may result from the up-estuary transport of senescing organic matter in bottom water, which increases in the lower reach of the estuary with increasing freshwater inflow.

Chesapeake Bay↗
USGS2002

Birth of the modern Chesapeake Bay estuary between 7.4 and 8.2 ka and implications for global sea-level rise

Two major pulses of sea-level rise are thought to have taken place since the last glacial maximum — meltwater pulses (mwp) 1A (12 cal ka) and 1B (9.5 cal ka). Between mwp 1B and about 6 cal ka, many of the complex coastal ecosystems which ring the world’s oceans began to form. Here we report data for rhenium, carbon isotopes, total organic carbon, and fossil oysters from Chesapeake Bay which span the transition from fresh to brackish water conditions in the bay in the mid-Holocene. These data constrain sea-level change and resulting environmental change in the bay. They indicate that the transition was rapid, and that it was produced by (1) a third pulse of rapid eustatic sea-level rise, or (2) a geometry of the prehistoric Chesapeake Bay basin which predisposed it to a nonlinear response to a steadily rising sea level. Similar nonlinear changes in vulnerable coastal environments are likely to take place in the future due to polar warming, regardless of the timing or rate of sea-level rise.

Chesapeake Bay↗
USGS2002

Distribution and movement of shortnose sturgeon (Acipenser brevirostrum) in the Chesapeake Bay

During a reward program for Atlantic sturgeon ( Acipenser oxyrinchus ), 40 federally endangered shortnose sturgeon ( Acipenser brevirostrum ) were captured and reported by commercial fishers between January 1996 and January 2000 from the Chesapeake Bay. Since this is more than double the number of published records of shortnose sturgeon in the Chesapeake Bay between 1876 and 1995, little information has been available on distributions and movement. We used fishery dependent data collected during the reward program to determine the distribution of shortnose sturgeon in the Chesapeake Bay. Sonically-tagged shortnose sturgeon in the Chesapeake Bay and Delaware River were tracked to determine if individuals swim through the Chesapeake and Delaware Canal. Shortnose sturgeon were primarily distributed within the upper Chesapeake Bay. The movements of one individual, tagged within the Chesapeake Bay and later relocated in the canal and Delaware River, indicated that individuals traverse the Chesapeake and Delaware Canal.

Maryland, Virginia↗
USGS2002

Synimpact-postimpact transition inside Chesapeake Bay crater

The transition from synimpact to postimpact sedimentation inside Chesapeake Bay impact crater began with accumulation of fallout debris, the final synimpact deposit. Evi dence of a synimpact fallout layer at this site comes from the presence of unusual, millimeter- scale, pyrite microstructures at the top of the Exmore crater-fill breccia. The porous geometry of the pyrite microstructures indicates that they originally were part of a more extensive pyrite lattice that encompassed a layer of millimeter-scale glass microspherules—fallout melt particles produced by the bolide impact. Above this microspherule layer is the initial postimpact deposit, a laminated clay-silt-sand unit, 19 cm thick. This laminated unit is a dead zone, which contains abundant stratigraphically mixed and diagenetically altered or impact-altered microfossils (foraminifera, calcareous nannofossils, dinoflagellates, ostracodes), but no evidence of indigenous biota. By extrapolation of sediment- accumulation rates, I estimate that conditions unfavorable to microbiota persisted for as little as <1 k.y. to 10 k.y. after the bolide impact. Subsequently, an abrupt improvement of the late Eocene paleoenvironment allowed species-rich assemblages of foraminifera, ostracodes, dinoflagellates, radiolarians, and calcareous nannoplankton to quickly reoccupy the crater basin, as documented in the first sample of the Chickahominy Formation above the dead zone.

Chesapeake Bay↗
USGS2002

Black ducks and their Chesapeake Bay habitats: Proceedings of a symposium

The symposium 'Black Ducks and Their Chesapeake Bay Habitats,' held October 4, 2000, provided a forum for scientists to share research about the American black duck (Anas rubripes), an important breeding and wintering waterfowl species dependent upon the Chesapeake Bay habitats. American black ducks have declined significantly in the last 50 years and continue to be a species of management concern. The symposium, sponsored by the Wildfowl Trust of North America and the U.S. Geological Survey, highlighted papers and posters on a range of topics, from the traditional concerns of hunting, habitat, and hybridization to the more recent concerns of human disturbance and neophobia. Other presentations provided a historical perspective of black duck management. The direction that black duck conservation initiatives could and/or should take in the future was also discussed. As populations of humans in the Chesapeake Bay region continue to increase, we can expect that these subjects will receive increased discussion in the future.

Chesapeake Bay↗
USGS2000

Climatic variability in the eastern United States over the past millennium from Chesapeake Bay sediments

Salinity oscillations caused by multidecadal climatic variability had major impacts on the Chesapeake Bay estuarine ecosystem during the past 1000 yr. Microfossils from sediments dated by radiometry (14C, 137Cs, 210Pb) and pollen stratigraphy indicate that salinity in mesohaline regions oscillated 10-15 ppt during periods of extreme drought (low fresh-water discharge) and wet climate (high discharge). During the past 500 yr, 14 wet-dry cycles occurred, including sixteenth and early seventeenth century megadroughts that exceeded twentieth century droughts in their severity. These droughts correspond to extremely dry climate also recorded in North American tree-ring records and by early colonists. Wet periods occurred every ~60-70 yr, began abruptly, lasted <20 yr, and had mean annual rainfall ~25%-30% and fresh-water discharge ~40%-50% greater than during droughts. A shift toward wetter regional climate occurred in the early nineteenth century, lowering salinity and compounding the effects of agricultural land clearance on bay ecosystems.

Chesapeake Bay↗
USGS2000

Historical trends in Chesapeake Bay dissolved oxygen based on benthic foraminifera from sediment cores

Environmentally sensitive benthic foraminifera (protists) from Chesapeake Bay were used as bioindicators to estimate the timing and degree of changes in dissolved oxygen (DO) over the past five centuries. Living foraminifers from 19 surface samples and fossil assemblages from 11 sediment cores dated by 210 Pb, 137 Cs, 14 C, and pollen stratigraphy were analyzed from the tidal portions of the Patuxent, Potomac, and Choptank Rivers and the main channel of the Chesapeake Bay. Ammonia parkinsoniana , a facultative anaerobe tolerant of periodic anoxic conditions, comprises an average of 74% of modern Chesapeake foraminiferal assemblages (DO-0.47 and 1.72 ml l −1 ) compared to 0% to 15% of assemblages collected in the 1960s. Paleoecological analyses show that A. parkinsoniana was absent prior to the late 17th century, increased to 10–25% relative frequency between approximately 1670–1720 and 1810–1900, and became the dominant (60–90%) benthic formaniferal species in channel environments beginning in the early 1970s. Since the 1970s, deformed tests of A. parkinsoniana occur in all cores (10–20% of Ammonia ), suggesting unprecedented stressful benthic conditions. These cores indicate that prior to the late 17th century, there was limited oxygen depletion. During the past 200 years, decadal scale variability in oxygen depletion has occurred, as dysoxic (DO=0.1–1.0 ml l −1 ), perhaps short-term anoxic (DO<0.1 ml l −1 ) conditions developed. The most extensive (spatially and temporally) anoxic conditions were reached during the 1970s. Over decadal timescales, DO variability seems to be linked closely to climatological factors influencing river discharge; the unprecedented anoxia since the early 1970s is attributed mainly to high freshwater flow and to an increase in nutrient concentrations from the watershed.

Maryland, Virginia↗
USGS2000

Hydrogeomorphic Regions of the Chesapeake Bay Watershed: HGMR

Generalized lithology (rock type) and physiography based on geologic formations were used to characterize hydrgeomorphic regions (HGMR) within the Chesapeake Bay watershed. These HGMRs were used in conjunction with existing data to assess the significance of ground-water discharge as a source of nitrate load to nontidal streams in the Chesapeake Bay watershed (Bachman and others, 1998). This work is part of the U.S. Geological Survey's (USGS) Chesapeake Bay initative to develop an understanding and provide scientific information for the restoration of the Chesapeake Bay and its watershed (Phillips and Caughron, 1997).

Maryl↗