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USGS2025

Quantifying sea otter abundance, distribution, habitat use, and foraging intake in Cook Inlet, Alaska

Following near extirpation from the fur trade, sea otters ( Enhydra lutris ) have returned to occupy lower Cook Inlet since the 1950s, or earlier, with numbers increasing to ~11,000 and ~9,000 on the west and east side, respectively, by 2017. Northward range expansion on the west side has been negligible for decades with few animals found north of Kamishak Bay, while northward expansion on the east side has been more pronounced in recent decades. The reasons for these contrasting distribution patterns are not certain. Possible explanations for lack of expansion on the west side included 1) poor sea otter habitat north of Kamishak Bay; 2) adequate habitat north of Kamishak Bay but no incentive for sea otters to move north because of abundant food in Kamishak Bay, and/or sea otters discouraged from moving north of Kamishak Bay; 3) seasonal ice formation; or 4) seasonal presence of killer whales. This project was designed to document current sea otter abundance and distribution in lower Cook Inlet, including seasonal variation, and evaluate drivers of habitat use and foraging conditions, including how these overlap with Bureau of Ocean Energy Management (BOEM) Lease Sale blocks. We found that the probability of sea otter presence in lower Cook Inlet was significantly related to depth and distance from shore with the highest probabilities of sea otter presence in areas ~7–8 kilometers (km) from shore in water ~20–30 meters (m) deep. Historical survey data suggest sea otter distribution has not changed dramatically since 2002, and while we detected significant seasonal changes including due to presence of heavy sea ice, the seasonal changes were modest and primarily related to locations with consistent winter ice formation on the west side of lower Cook Inlet. Overall, throughout the year, sea otters appeared to be utilizing most of the habitat within the 40-m depth contour on the east side of lower Cook Inlet, including Kachemak Bay. Sea otters on the west side reside largely within Kamishak Bay. Because of the shallow bathymetry of lower Cook Inlet, sea otters consistently occurred farther offshore than in many other areas of Alaska. The presence of sea otters, including females with pups, in these offshore waters indicates that sea otters can forage productively in these open water areas. Importantly, we documented that sea otters, including females with pups, occurred in most of the eastern BOEM lease blocks including the original Lease Sale 244 blocks 7064, 7114, 6162, 6310, 6360, 6410, 6458 and 6457. The relinquishments for these 7 leases were effective September 17, 2024: OCS-Y-02434 (block # 7064), OCS-Y-02435 (7114), OCS-Y-02436 (6162), OCS-Y-02438 (6357), OCS-Y-02442 (6407), OCS-Y02446 (6457), OCS-Y-02447 (6458) https://www.boem.gov/sites/default/files/documents/environment/Map%20of%20Active%20Leases%20 Cook%20Inlet%20OCS_0.pdf Regarding differential northward expansion on the east and west side of lower Cook Inlet, we found that wind and water circulation patterns make winter sea ice more prominent on the west side, but this had minimal effects on sea otter distribution. In addition, although there have been observations of killer whale ( Orcinus orca ) predation on sea otters in Cook Inlet, we did not see behavioral or distributional evidence that it was prevalent enough to have strong effects on sea otter habitat use. Benthic surveys using a remotely operated vehicle (ROV) indicated that epibenthic substrate and biological community heterogeneity differed between areas with and without otters, suggesting that these factors may explain the current distribution of otters within lower Cook Inlet. However, ROV surveys cannot assess infaunal prey abundance, making assessments of the role of prey availability difficult. The existence of a healthy Pacific razor clam ( Siliqua patula ) fishery along western lower Cook Inlet along the Lake Clark coast north of Kamishak Bay suggests there may still be a resource base for eventual expansion of sea otters into this area. Our shore-based forage observations indicated that sea otters exist near carrying capacity densities relative to nearshore prey resources. However, our distribution model suggests the bulk of the population lives offshore beyond our ability to observe their feeding activity. The fact that sea otters are a consistent presence in offshore areas suggests that prey resources in these areas were relatively abundant in comparison to nearshore prey resources, making foraging in offshore areas, with water depths of 0–40 m, energetically profitable. Prey types in these offshore areas of lower Cook Inlet likely included epifauna such as crabs and large urchins, in addition to infaunal clams based on the soft substrate habitat types that characterize lower Cook Inlet. Collectively, our results suggest that sea otters occupy most areas of lower Cook Inlet with appropriate benthic habitat types and prey resources, which includes areas within BOEM Lease Sale blocks. With the exception of the Lake Clark coast, sea otters may be approaching a food- and habitat-limited distribution and carrying capacity, suggesting that the current status of sea otters in lower Cook Inlet is likely to remain similar in the absence of significant changes to prey, habitat, predation, or anthropogenic disturbance.

Alaska↗

USGS2020

Evaluation of a roughness length parametrization accounting for wind–wave alignment in a coupled atmosphere–wave model

The importance of wind energy as an alternative energy source has increased over the latest years with more focus on offshore winds. A good estimation of the offshore winds is thus of major importance for this industry. Up to now the effect of the wind–wave (mis)alignment has not yet been taken into account in coupled atmosphere–wave models to study the vertical wind profile and power production estimations of offshore wind farms. In this study the roughness length parametrization of Drennan et al . in 2003, and its extension addressing the wind–wave (mis)alignment proposed by Porchetta et al . in 2019, are investigated in the Coupled Ocean–Atmosphere–Wave–Sediment Transport (COAWST) model. This study shows that the yearly mean wind estimation at hub height (100 m) is improved by the roughness length parametrization of Porchetta et al . compared to Drennan. This is mainly due to the increased roughness of the former parametrization compare to the latter, even in aligned wind–wave conditions. This difference in roughness is caused by the dataset used to obtain the constants, deep‐water conditions versus mixed offshore conditions. Moreover, the roughness length parametrization of Porchetta et al . performs better in two of three alignment categories. Furthermore, similar model performances are obtained if we exclude the wind directions from the wind shadow zone of the measurement mast or the wind directions from the recently built Alpha Ventus wind farm, which is in close vicinity of the measurement mast. Investigating different wind conditions shows that the new roughness length parametrization of Porchetta et al . performs best for both offshore and onshore winds. Additionally, we show that the coupled model estimations of the vertical wind are only slightly affected by significant wave height estimations. Similar model performances for different accuracies of significant wave height estimations are presented. One exception is the perpendicular alignment category where the new roughness length of Porchetta et al . outperforms the roughness length of Drennan when investigating the wind estimations related to significant wave heights with a higher accuracy. The roughness length parametrization of Porchetta et al . reduced the power production overestimation of the coupled model from 5.7 to 2.8%. We also show that the standalone atmospheric model including the roughness length of Charnock in 1955 has a degraded performance compared to the coupled model including the roughness length parametrization of Porchetta et al . for yearly average wind profiles.

Quarterly Journal of the Royal Meteorological Soci↗

USGS2000

Recolonization and possible recovery of burrowing mayflies (Ephemeroptera: Ephemeridae: Hexagenia spp.) in Lake Erie of the Laurentian Great Lakes

Burrowing mayflies of the genus Hexagenia spp. were widely distributed (ca. 80% of sites) and abundant (ca. 160 nymphs/m 2 ) in the western basin of Lake Erie of the Laurentian Great Lakes in 1929–1930, prior to a period of anoxia in the mid 1950s. Nymphs were absent or rare in the basin between 1961 and 1973–1975. In 1979–1991, nymphs were infrequently found (13–46% of sites) in low abundance (3–40 nymphs/m 2 ) near shore (<7.5 km from shore), but were absent or rare offshore (0–7% of sites at 0–1 nymphs/m 2 ). Increased abundance occurred offshore between 1991 (0% of sites) and 1993 (52% of sites at 7/m 2 ). Annual sampling, beginning in 1995, indicates that nymphs increased in both nearshore and offshore waters. By 1997, nymphs were found throughout the lake (88% of sites) at a mean density 40-fold greater (392/m 2 ) than that observed in 1993 (11/m 2 ). In 1998, the distribution of nymphs remained the same as 1997 (88% of sites) but density declined 3-fold (392 to 134/m 2 ). These data indicate that mayflies have recolonized sediments of western Lake Erie and that their abundance may be similar to levels observed before their disappearance in the mid 1950s. However, prior to the mid 1950s, densities were greater in offshore than nearshore waters, but between 1979 and 1998 greater densities occurred near shore than offshore. In addition, there were two areas in the 1990s where low densities consistently occurred. Therefore, recovery of nymphs in western Lake Erie may not have been complete in 1998. At present we do not know the cause for the sudden recolonization of nymphs in large portions of western Lake Erie. Undoubtedly, pollution-abatement programs contributed to improved conditions that would have ultimately led to mayfly recovery in the future. However, the explosive growth of the exotic zebra mussel, Dreissena polymorpha , undoubtedly diverted plankton foods to bottom substrates which could have increased the speed at which Hexagenia spp. nymphs recolonized sediments in western Lake Erie in the 1990s.

Journal of Aquatic Ecosystem Stress and Recovery↗

USGS2005

Net dextral slip, Neogene San Gregorio–Hosgri fault zone, coastal California: Geologic evidence and tectonic implications

Reinterpretation of onshore and offshore geologic mapping, examination of a key offshore well core, and revision of cross-fault ties indicate Neogene dextral strike slip of 156 ± 4 km along the San Gregorio–Hosgri fault zone, a major strand of the San Andreas transform system in coastal California. Delineating the full course of the fault, defining net slip across it, and showing its relationship to other major tectonic features of central California helps clarify the evolution of the San Andreas system. San Gregorio–Hosgri slip rates over time are not well constrained, but were greater than at present during early phases of strike slip following fault initiation in late Miocene time. Strike slip took place southward along the California coast from the western fl ank of the San Francisco Peninsula to the Hosgri fault in the offshore Santa Maria basin without significant reduction by transfer of strike slip into the central California Coast Ranges. Onshore coastal segments of the San Gregorio–Hosgri fault include the Seal Cove and San Gregorio faults on the San Francisco Peninsula, and the Sur and San Simeon fault zones along the flank of the Santa Lucia Range. Key cross-fault ties include porphyritic granodiorite and overlying Eocene strata exposed at Point Reyes and at Point Lobos, the Nacimiento fault contact between Salinian basement rocks and the Franciscan Complex offshore within the outer Santa Cruz basin and near Esalen on the flank of the Santa Lucia Range, Upper Cretaceous (Campanian) turbidites of the Pigeon Point Formation on the San Francisco Peninsula and the Atascadero Formation in the southern Santa Lucia Range, assemblages of Franciscan rocks exposed at Point Sur and at Point San Luis, and a lithic assemblage of Mesozoic rocks and their Tertiary cover exposed near Point San Simeon and at Point Sal, as restored for intrabasinal deformation within the onshore Santa Maria basin. Slivering of the Salinian block by San Gregorio–Hosgri displacements elongated its northern end and offset its western margin delineated by the older Nacimiento fault, a sinistral strike-slip fault of latest Cretaceous to Paleocene age. North of its juncture with the San Andreas fault, dextral slip along the San Gregorio–Hosgri fault augments net San Andreas displacement. Alternate restorations of the Gualala block imply that nearly half the net San Gregorio–Hosgri slip was accommodated along the offshore Gualala fault strand lying west of the Gualala block, which is bounded on the east by the current master trace of the San Andreas fault. With San Andreas and San Gregorio–Hosgri slip restored, there remains an unresolved proto–San Andreas mismatch of ∼100 km between the offset northern end of the Salinian block and the southern end of the Sierran-Tehachapi block. On the south, San Gregorio–Hosgri strike slip is transposed into crustal shortening associated with vertical-axis tectonic rotation of fault-bounded crustal panels that form the western Transverse Ranges, and with kinematically linked deformation within the adjacent Santa Maria basin. The San Gregorio–Hosgri fault serves as the principal link between transrotation in the western Transverse Ranges and strike slip within the San Andreas transform system of central California.

California↗

USGS2005

Temporal and spatial variation in relative abundance and length structure of salmonids in reservoirs: Implications for monitoring

Spatial and temporal variations in salmonid catch per unit effort (C/f) may affect monitoring efforts in lakes and reservoirs. This study evaluated the spatial and temporal variation in gill-net C/f and length structure of captured salmonids in nearshore (???7.6-m bottom depth) and offshore (>7.6-m bottom depth) areas of two Wyoming reservoirs. Floating experimental gill nets were set as nearshore and offshore pairs at 24 locations in both reservoirs during each of four sampling periods (spring, early summer, late summer, and fall). Salmonid C/f was significantly higher in nearshore areas than in offshore areas during all periods in one reservoir and during all periods except spring in the other reservoir. Mean C/f of rainbow trout Oncorhynchus mykiss was not significantly different between nearshore and offshore areas when water temperatures were 10-13??C in both reservoirs. Length structure of salmonids differed significantly between nearshore and offshore locations and among periods in both reservoirs. These patterns should be considered in both the design and analysis phases of monitoring efforts that use floating experimental gill nets and other sampling gears. ?? Copyright by the American Fisheries Society 2005.

North American Journal of Fisheries Management↗

USGS2001

Petroleum geology and resources of the middle Caspian Basin, Former Soviet Union

The Middle Caspian basin occupies a large area between the Great Caucasus foldbelt and the southern edge of the Precambrian Russian craton. The basin also includes the central part of the Caspian Sea and the South Mangyshlak subbasin east of the sea. The basin was formed on the Hercynian accreted terrane during Late Permian?Triassic through Quaternary time. Structurally, the basin consists of the fold-and-thrust zone of the northern Caucasus foothills, the foredeep and foreland slope, the Stavropol-Prikumsk uplift and East Manych trough to the north of the slope, and the South Mangyshlak subbasin and slope of the Karabogaz arch east of the Caspian Sea. All these major structures extend offshore. Four total petroleum systems (TPS) have been identified in the basin. The South Mangyshlak TPS contains more than 40 discovered fields. The principal reserves are in Lower?Middle Jurassic sandstone reservoirs in structural traps. Source rocks are poorly known, but geologic data indicate that they are in the Triassic taphrogenic sequence. Migration of oil and gas significantly postdated maturation of source rocks and was related to faulting and fracturing during middle Miocene to present time. A single assessment unit covers the entire TPS. Largest undiscovered resources of this assessment unit are expected in the largely undrilled offshore portion of the TPS, especially on the western plunge of the Mangyshlak meganticline. The Terek-Caspian TPS occupies the fold-and-thrust belt, foredeep, and adjoining foreland slope. About 50 hydrocarbon fields, primarily oil, have been discovered in the TPS. Almost all hydrocarbon reserves are in faulted structural traps related to thrusting of the foldbelt, and most traps are in frontal edges of the thrust sheets. The traps are further complicated by plastic deformation of Upper Jurassic salt and Maykop series (Oligocene? lower Miocene) shale. Principal reservoirs are fractured Upper Cretaceous carbonates and middle Miocene sandstones. Principal source rocks are organic-rich shales in the lower part of the Maykop series. Source rocks may also be present in the Eocene, Upper Jurassic, and Middle Jurassic sections, but their contribution to discovered reserves is probably small. Three assessment units are delineated in the TPS. One of them encompasses the thrust-and-fold belt of northern Caucasus foothills. This assessment unit contains most of the undiscovered oil resources. The second assessment unit occupies the foredeep and largely undeformed foreland slope. Undiscovered resources of this unit are relatively small and primarily related to stratigraphic traps. The third unit is identified in almost untested subsalt Jurassic rocks occurring at great depths and is speculative. The unit may contain significant amounts of gas under the Upper Jurassic salt seal. The Stavropol-Prikumsk TPS lies north of the Terek-Caspian TPS and extends offshore into the central Caspian Sea where geologic data are scarce. More than one hundred oil and gas fields have been found onshore. Offshore, only one well was recently drilled, and this well discovered a large oil and gas field. Almost the entire sedimentary section of the TPS is productive; however, the principal oil reserves are in Lower Cretaceous clastic reservoirs in structural traps of the Prikumsk uplift. Most original gas reserves are in Paleogene reservoirs of the Stavropol arch and these reservoirs are largely depleted. At least three source rock formations, in the Lower Triassic, Middle Jurassic, and Oligocene?lower Miocene (Maykop series), are present in the TPS. Geochemical data are inadequate to correlate oils and gases in most reservoirs with particular source rocks, and widespread mixing of hydrocarbons apparently took place. Three assessment units encompassing the onshore area of the TPS, the offshore continuation of the Prikumsk uplift, and the central Caspian area, are identified. The

Bulletin↗

USGS2022

Aerial counts for surface-nesting seabirds at Lehua Island and Moku Manu Islet and Ulupaʻu Crater, Oʻahu, in 2019

Among important seabird breeding sites in the main Hawaiian Islands, Lehua Island offshore Niʻihau and Moku Manu Islets offshore Oʻahu support diverse and abundant seabird breeding populations. Both offshore islands provide excellent nesting habitat for surface-nesting boobies ( Sula spp .) and terns but, of the two, only Moku Manu supports relatively large breeding populations of Sooty Tern ( Onychoprion fuscatus ) and Brown Noddy ( Anous stolidus ). Additionally, Ulupaʻu Crater, near Moku Manu on Oʻahu, is one of only a few sites within the eight main Hawaiian islands and the only site on the main island of Oʻahu that supports a nesting population of Red-footed Boobies ( Sula sula ). Despite their importance for informing renewable offshore energy planning off Hawaiʻi, robust and accurate seabird population survey data exist and are available for some locations (Lehua; Raine and others, 2021), but at Moku Manu and Ulupa‘u Crater, recent information are not yet available (E. VanderWerf, written commun. 2021). In this study, we completed comprehensive aerial photographic counts at these three sites for six surface-nesting seabird species present during the 2019 breeding season: Brown Booby ( Sula leucogaster ), Red-footed Booby, Masked Booby ( S. dactylatra ), Great Frigatebird ( Fregata minor ), Sooty Tern, and Brown Noddy. We estimated 5,782, 102, and 1,446 nesting pairs of Red-footed Boobies at Lehua, Ulupaʻu Crater, and Moku Manu, respectively. At Lehua and Moku Manu, we estimated 692 and 65 nesting pairs of Brown Boobies, respectively. At Moku Manu, we estimated 95 nesting pairs of Masked Boobies, one of only three nesting locales for this species in the main Hawaiian Islands. Based on digital photograph counts of sampled areas and area-based extrapolation, we estimated 17,938 terns (mostly Sooty Tern with fewer Brown Noddy) on Moku Manu. We observed Great Frigatebirds roosting at the two island sites, but we did not detect any sign of nesting for this species. We found that inter-observer counts for behavioral classifications (nesting, roosting, unknown) ranged in precision (D=0.13–0.31), but generally, counts among photographs accounting for all seabird targets (D=0.10–0.22) and for boobies classified as nesting (D=0.13–0.18) were more precise than for roosting and unknown categories (D=0.13–0.31), indicating that at least some of the variation in count precision relates to differences in how independent counters identified behavioral classifications. The nesting population sizes (and number of terns present on Moku Manu) present during aerial counts likely are minimum estimates because individuals among these species can exhibit asynchronous nesting phenologies, and not all members of the nesting populations would be expected to be attending the sites when we surveyed. The results of these counts provide current and accurate abundance estimates for these species that can serve as benchmarks for future management and monitoring and as important components of population-level assessments aimed at quantifying seabird vulnerability to potential offshore wind energy development in the main Hawaiian Islands.

Hawaii↗

USGS1972

Mercury distribution in ancient and modern sediment of northeastern Bering Sea

A reconnaissance of surface and subsurface sediments to a maximum depth of 244 feet below the sea floor shows that natural mercury anomalies from 0.2 to 1.3 ppm have been present in northeastern Bering Sea since early Pliocene. The anomalies and mean values are highest in modern beach (maximum 1.3 and mean 0.22 ppm Hg) and nearshore subsurface gravels (maximum 0.6 and mean .06 ppm Hg) along the highly mineralized Seward Peninsula and in organic rich silt (maximum 0.16 and mean 0.10 ppm Hg) throughout the region; the mean values are lowest in offshore sands (0.03 ppm Hg). Although gold mining may be partially responsible for high mercury levels in the beaches near Nome, Alaska, equally high or greater concentrations of mercury occur in ancient glacial sediments immediately offshore (0.6 ppm) and in modern unpolluted beach sediments at Bluff (0.45 - 1.3 ppm); this indicates that the contamination effects of mining may be no greater than natural concentration processes in the Seward Peninsula region. The background content of mercury (0.03) throughout the central area of northeastern Bering Sea is similar to that elsewhere in the world. The low mean values (0.04 ppm) even immediately offshore from mercury-rich beaches, suggests that in the surface sediments of northeastern Bering Sea, the highest concentrations are limited to the beaches near mercury sources; occasionally, however, low mercury anomalies occur offshore in glacial drift derived from mercury source regions of Chukotka and Seward Peninsula and reworked by Pleistocene shoreline processes. The minimal values offshore may be attributable to beach entrapment of heavy minerals containing mercury and/or dilution effects of modern sedimentation.

Alaska↗

USGS1977

Geology of the Monterey Bay region

Geophysical data and sea floor samples collected from the continental shelf and slope between Ano Nuevo Point and Point Sur, California indicate that the Monterey Bay region has had a complex late Cenozoic tectonic history. Uplift and depression have produced a succession of regressive and transgressive sedimentary units, while contemporaneous right-slip along faults of the San Andreas system have offset major structural and lithologic elements. This deformation produced three regional and several local unconformities within upper Tertiary rocks and initiated development of a canyon system that today includes the Monterey, Ascension, Carmel, and other large submarine canyons. The Tertiary stratigraphy of the offshore Monterey Bay area is divided into two provinces by a major structural boundary, the north-trending Palo Colorado-San Gregorio fault zone. East of this zone in the offshore are four seismically distinct sequences that can be correlated with major sequences onshore. These sequences comprise (1) pre-Tertiary basement, and (2) middle Miocene, (3) upper Miocene to Pliocene, and (4) upper Pliocene to Holocene sedimentary intervals. Each of the latter three sequences is bounded by unconformities, as is its counterpart on land. Only Neogene sedimentary rocks are present offshore; Paleogene units, if originally present, have been removed completely by pre-middle Miocene erosion. An extensive erosional surface was cut during Zemorrian time into the late Mesozoic granitic basement rocks. Incised into this surface are the ancestral Monterey Canyon and an unnamed canyon. Marine sedimentary rocks of upper Miocene and Pliocene age overlie this unconformably and fill the unnamed canyon. Similar rocks also may have once filled Monterey Canyon. Near shore these strata are covered by terrestrial alluvial and eolian deposits, deltaic deposits, marine canyon fill, landslide and slump deposits, and unconsolidated sediments that range in age from upper Pliocene to Holocene. Monterey Canyon appears to have been filled and exhumed at least twice since its inception in Oligocene time, once in late Miocene and once in Pleistocene time. Three major seismic stratigraphic units are apparent in continuous seismic reflection profiles from the offshore area west of the Palo Colorado-San Gregorio fault zone. These are (1) acoustical basement, and (2) middle Tertiary and (3) late Tertiary to Quaternary sedimentary intervals. Acoustical basement comprises Cretaceous to early Tertiary sedimentary rocks, Mesozoic or older metamorphic rocks, and Cretaceous or Jurassic rocks of the Franciscan assemblage. The middle Tertiary sequence consists of sedimentary rocks of questionable Miocene age. The late Tertiary to Quaternary sequence is composed of Pliocene sedimentary rocks and unconsolidated marine sediments, and submarine landslide and slump deposits. Seismic reflection surveys indicate two major, intersecting, northwest-trending fault zones to be present in the offshore Monterey Bay area. The Palo Colorado-San Gregorio fault zone may be more than 200 km long; it is narrow (approximately 3 km wide) and is represented in most places by one or two faults. This zone appears to connect with faults mapped on land near Ano Nuevo Point and Point Sur. The Monterey Bay fault zone, located in the area between Santa Cruz and Monterey, is a diffuse zone, approximately 10 to 15 km wide, of en echelon faults. Faults within this zone appear to connect with faults on land near Monterey, and the zone appears to be truncated by the Palo Colorado-San Gregorio fault zone west of Santa Cruz. Locations of more than 110 earthquakes (1968-1976) show that the newly mapped fault zones in Monterey Bay are seismically active. Epicenters in the bay form two clusters, one at the intersection of the Monterey Bay and Palo Colorado-San Gregorio fault zones, and the other in a linear belt that trends northwest along the Palo Colorado-San Gregorio fault zone. Faults within th

California↗

USGS2009

Simulation of Variable-Density Ground-Water Flow and Saltwater Intrusion beneath Manhasset Neck, Nassau County, New York, 1905-2005

The coastal-aquifer system of Manhasset Neck, Nassau County, New York, has been stressed by pumping, which has led to saltwater intrusion and the abandonment of one public-supply well in 1944. Measurements of chloride concentrations and water levels in 2004 from the deep, confined aquifers indicate active saltwater intrusion in response to public-supply pumping. A numerical model capable of simulating three-dimensional variable-density ground-water flow and solute transport in heterogeneous, anisotropic aquifers was developed using the U.S. Geological Survey finite-element, variable-density, solute-transport simulator SUTRA, to investigate the extent of saltwater intrusion beneath Manhasset Neck. The model is composed of eight layers representing the hydrogeologic system beneath Manhasset Neck. Four modifications to the area?s previously described hydrogeologic framework were made in the model (1) the bedrock-surface altitude at well N12191 was corrected from a previously reported value, (2) part of the extent of the Raritan confining unit was shifted, (3) part of the extent of the North Shore confining unit was shifted, and (4) a clay layer in the upper glacial aquifer was added in the central and southern parts of the Manhasset Neck peninsula. Ground-water flow and the location of the freshwater-saltwater interface were simulated for three conditions (time periods) (1) a steady-state (predevelopment) simulation of no pumping prior to about 1905, (2) a 40-year transient simulation based on 1939 pumpage representing the 1905-1944 period of gradual saltwater intrusion, and (3) a 60-year transient simulation based on 1995 pumpage representing the 1945-2005 period of stabilized withdrawals. The 1939 pumpage rate (12.1 million gallons per day (Mgal/d)) applied to the 1905-1944 transient simulation caused modeled average water-level declines of 2 and 4 feet (ft) in the shallow and deep aquifer systems from predevelopment conditions, respectively, a net decrease of 5.2 Mgal/d in freshwater discharge to offshore areas and a net increase of 6.9 Mgal/d of freshwater entering the model from the eastern, western, and southern lateral boundaries. The 1995 pumpage rate (43.3 Mgal/d) applied to the 1945-2005 transient simulation caused modeled average water-level declines of 5 and 8 ft in the shallow and deep aquifer systems from predevelopment conditions, respectively, a net decrease of 13.2 Mgal/d in freshwater discharge to offshore areas and a net increase of 30.1 Mgal/d of freshwater entering the model from the eastern, western, and southern lateral boundaries. The simulated decrease in freshwater discharge to the offshore areas caused saltwater intrusion in two parts of the deep aquifer system under Manhasset Neck. Saline ground water simulated in a third part of the deep aquifer system under Manhasset Neck was due to the absence of the North Shore confining unit near Sands Point. Simulated chloride concentrations greater than 250 milligrams per liter (mg/L) were used to represent the freshwater-saltwater interface, and the movement of this concentration was evaluated for transient simulations. The decrease in the 1905-1944 simulated freshwater discharge to the offshore areas caused the freshwater-saltwater interface in the deep aquifer system to advance landward more than 1,700 ft from its steady-state position in the vicinity of Baxter Estates Village, Long Island, New York. The decrease in the 1945-2005 simulated freshwater discharge to the offshore areas caused a different area of the freshwater-saltwater interface in the deep aquifer system to advance more than 600 ft from its steady-state position approximately 1 mile south of the Baxter Estates Village. However, the 1945-2005 transient simulation underestimates the concentration and extent of saltwater intrusion determined from water-quality samples collected from wells N12508 and N12793, where measured chloride concentrations increased from 625 and 18 mg/L in 1997 t

Scientific Investigations Report↗

USGS2017

Determining fine-scale use and movement patterns of diving bird species in federal waters of the Mid-Atlantic United States using satellite telemetry

Offshore wind energy development in the United States is projected to expand in the upcoming decades to meet growing energy demands and reduce fossil fuel emissions. There is particular interest in commercial offshore wind development within Federal waters (i.e., > 3 nautical miles from shore) of the mid-Atlantic. In order to understand the potential for adverse effects on marine birds in this area, information on distribution and behavior (e.g., flight pathways, timing, etc.) is required for a broad suite of species. In areas where offshore wind development is likely to occur, such information can be used to identify high use areas during critical life stages, which can inform the siting of offshore facilities. It can also be used to provide baseline data for understanding broad changes in distributions that occur after offshore wind developments are constructed in a specific area.

Report↗

USGS2017

Nutrients, phytoplankton, zooplankton, and macrobenthos

Lower trophic levels support the prey fish on which most sport fish depend. Therefore, understanding the production potential of lower trophic levels is integral to the management of Lake Ontario’s fishery resources. Lower trophic-level productivity differs among offshore and nearshore waters. In the offshore, there is concern about the ability of the lake to support Alewife (Table 1) production due to a perceived decline in productivity of phytoplankton and zooplankton whereas, in the nearshore, there is a concern about excessive attached algal production (e.g., Cladophora) associated with higher nutrient concentrations—the oligotrophication of the offshore and the eutrophication of the nearshore (Mills et al. 2003; Holeck et al. 2008; Dove 2009; Koops et al. 2015; Stewart et al. 2016). Even though the collapse of the Alewife population in Lake Huron in 2003 (and the associated decline in the Chinook Salmon fishery) may have been precipitated by a cold winter (Dunlop and Riley 2013), Alewife had not returned to high abundances in Lake Huron as of 2014 (Roseman et al. 2015). Failure of the Alewife population to recover from collapse has been attributed to declines in lower trophic-level production (Barbiero et al. 2011; Bunnell et al. 2014; but see He et al. 2015). In Lake Michigan, concerns of a similar Alewife collapse led to a decrease in the number of Chinook Salmon stocked. If lower trophic-level production declines in Lake Ontario, a similar management action could be considered. On the other hand, in Lake Erie, which supplies most of the water in Lake Ontario, eutrophication is increasing and so are harmful algal blooms. Thus, there is also a concern that nutrient levels and algal blooms could increase in Lake Ontario, especially in the nearshore. Solutions to the two processes of concern—eutrophication in the nearshore and oligotrophication in the offshore—may be mutually exclusive. In either circumstance, fisheries management needs information on the productivity of lower trophic levels in Lake Ontario. In this chapter, we review the status of lower trophic levels in Lake Ontario with special attention to the current (2008-2013) and previous (2003-2007) reporting periods. During the two reporting periods, three whole-lake surveys of lower trophic levels were conducted: the Lower Trophic Level Assessment (LOLA) in 2003 and 2008 (Makarewicz and Howell 2012; Munawar et al. 2015b) and the Cooperative Science and Management Initiative (CSMI) in 2013. Analyses of the CSMI data are ongoing. In addition to the three one-year sources of information on lower trophic levels, several multi-year sources of information are available, including data from the surveillance program conducted since 1965 by Environment Canada (EC) (Dove 2009), monitoring conducted since 1980 by the U.S. Environmental Protection Agency’s (EPA) Great Lakes National Program Office (GLNPO) (Barbiero et al. 2014; Reavie et al. 2014), sampling for a Bioindex Program at two stations, one offshore and one in the Eastern Basin, assessments of Mysis diluviana (formerly Mysis relicta) conducted since 1980 by Fisheries and Oceans Canada (Johannsson et al. 1998, 2011) and the Ontario Ministry of Natural Resources and Forestry (OMNRF), and monitoring conducted since 1995 by the Biomonitoring Program (BMP) on the New York side of the lake (Holeck et al. 2015b). The BMP is a collaboration of the New York State Department of Environmental Conservation (DEC), U.S. Fish and Wildlife Service, U.S. Geological Survey (USGS), and Cornell University.

Special Publication↗

USGS2018

Status and Trends in the Lake Superior Fish Community, 2017

In 2017, the Lake Superior fish community was sampled with daytime bottom trawls at 76 nearshore and 36 offshore stations. Spring nearshore and summer offshore water temperatures in 2017 were similar to slightly cooler than the 1991-2017 average. In the nearshore zone, a total of 28,902 individual fish from 27 species or morphotypes were collected. The number of species collected at each station ranged from 0 to 13, with a mean of 5.5 and median of 5. Lakewide nearshore mean biomass was 3.8 kg/ha which was below the long-term average of 8.7 kg/ha and the median lakewide biomass was 1.8 kg/ha. which was similar to the long-term average median value of 1.9 kg/ha. Lake Whitefish, Rainbow Smelt, Bloater, Longnose Sucker, and lean Lake Trout were the species with the highest lakewide average biomass. In the offshore zone, a total of 16,674 individuals from 13 species were collected lakewide. The average and median observed species richness at each station was 3.8 and 4 species, respectively, and ranged from 2 to 6 species. Deepwater Sculpin, Kiyi, and siscowet Lake Trout made up 99% of the total number of individuals and biomass collected in offshore waters. Mean and median lakewide biomass for all species in 2017 was 6.8 kg/ha and 6.6 kg/ha, respectively. This was similar to the long-term mean of 6.9 kg/ha and greater than that observed in 2014-2016. Nearshore average larval Coregonus densities in 2017 were greater than observed in any previous year; whereas offshore larval Coregonus densities were much less than observed in previous years.

Lake Superior↗

USGS2019

Impacts to wildlife of wind energy siting and operation in the United States

Electricity from wind energy is a major contributor to the strategy to reduce greenhouse gas emissions from fossil fuel use and thus reduce the negative impacts of climate change. Wind energy, like all power sources, can have adverse impacts on wildlife. After nearly 25 years of focused research, these impacts are much better understood, although uncertainty remains. In this report, we summarize positive impacts of replacing fossil fuels with wind energy, while describing what we have learned and what remains uncertain about negative ecological impacts of the construction and operation of land-based and offshore wind energy on wildlife and wildlife habitat in the U.S. Finally, we propose research on ways to minimize these impacts. TO SUMMARIZE: 1 Environmental and other benefits of wind energy include near-zero greenhouse gas emissions, reductions of other common air pollutants, and little or no water use associated with producing electricity from wind energy. Various scenarios for meeting U.S. carbon emission reduction goals indicate that a four- to five-fold expansion of land-based wind energy from the current 97 gigawatts (GW) by the year 2050 is needed to minimize temperature increases and reduce the risk of climate change to people and wildlife. 2 Collision fatalities of birds and bats are the most visible and measurable impacts of wind energy production. Current estimates suggest most bird species, especially songbirds, are at low risk of population-level impacts. Raptors as a group appear more vulnerable to collisions. Population-level impacts on migratory tree bats are a concern, and better information on population sizes is needed to evaluate potential impacts to these species. Although recorded fatalities of cave-dwelling bat species are typically low at most wind energy facilities, additional mortality from collisions is a concern given major declines in these species due to white-nose syndrome (WNS). Assessments of regional and cumulative fatality impacts for birds and bats have been hampered by the lack of data from areas with a high proportion of the nation’s installed wind energy capacity. Efforts to expand data accessibility from all regions are underway, and this greater access to data along with improvements in statistical estimators should lead to improved impact assessments. 3 Habitat impacts of wind energy development are difficult to assess. An individual wind energy facility may encompass thousands of acres, but only a small percentage of the landscape within the project area is directly transformed. If a project is sited in previously undisturbed habitat, there is concern for indirect impacts, such as displacement of sensitive species. Studies to date indicate displacement of some species, but the long-term population impacts are unknown. 4 Offshore wind energy development in the U.S. is just beginning. Studies at offshore wind facilities in Europe indicate some bird and marine mammal species are displaced from project areas, but substantial uncertainty exists regarding the individual or population-level impacts of this displacement. Bird and bat collisions with offshore turbines are thought to be less common than at terrestrial facilities, but currently the tools to measure fatalities at offshore wind energy facilities are not available. The wind energy industry, state and federal agencies, conservation groups, academia, and scientific organizations have collaborated for nearly 25 years to conduct the research needed to improve our understanding of risk to wildlife and to avoid and minimize that risk. Efforts to reduce the uncertainty about wildlife risk must keep up withthe pace and scale of the need to reduce carbon emissions. This will require focusing our research priorities and increasing the rate at which we incorporate research results into the development and validation of best practices for siting and operating wind energy facilities.

Issues in Ecology↗

USGS2019

Status and trends in the Lake Superior fish community, 2019

The Lake Superior fish community was sampled in 2019 with daytime bottom trawls at 76 nearshore and 35 offshore stations distributed throughout the lake. In the nearshore zone, 25,131 fish from 24 species or morphotypes were collected. The number of species collected at nearshore stations ranged from 0 to 15, with a mean of 5.6 and median of five. Nearshore mean biomass was 5.7 kg/ha which was similar to the past twenty-year average of 5.2 kg/ha and less than the 42-year period-of-record mean of 8.5 kg/ha. Lake Whitefish, Rainbow Smelt, Longnose Sucker, Bloater, lean Lake Trout, Cisco, Burbot, and siscowet Lake Trout had the highest total collected biomass. In the offshore zone, 13,145 fish from 11 species or morphotypes were collected. The number of species collected at offshore stations ranged from two to six, with a mean 3.6 and median of four. Deepwater Sculpin, Kiyi, and siscowet Lake Trout made up 99% of the total number of individuals and biomass collected in offshore waters. Mean and median offshore biomass for all species in 2019 was 7.0 kg/ha which was greater than the past eight-year average of 6.6 kg/ha. Recruitment, as measured by age-1 densities, was near the period-of-record lakewide average for Lake Whitefish (7 fish/ha) and Rainbow Smelt (137 fish/ha) and was lower than the period-of-record lakewide average for Bloater (4 fish/ha), Kiyi (1 fish/ha), and Cisco (<1 fish/ha). Lakewide average age-1 Cisco densities have been estimated at <1 fish/ha in twelve of the last twenty years. Survival of Coregonus species to age-1 continues to be a major concern of fishery managers.

Lake Superior↗

USGS2021

A study of marine temperature variations in the northern Gulf of Alaska across years of marine heatwaves and cold spells

We use over 100 in situ and remotely sensed temperature datasets to investigate thermal variability within and across the intertidal nearshore, coastal and offshore waters of the northern Gulf of Alaska. For the years 1970 through 2019 we document a warming trend of 0.24±0.10 °C per decade for the coastal northern shelf (0-250 m depth average) and a Gulf-wide sea surface temperature (SST) trend of 0.25±0.11 °C per decade. The Gulf-wide SST trend in the last halfcentury is more than twice that of the 0.11±0.003 °C warming rate computed for 1900-2019. Decorrelation length scales vary regionally and correlation of synoptic scale fluctuations (less than one month) between two stations rapidly degrades with increasing station distance, accounting for less than 10% of the covariance for separations exceeding 100 km. In contrast, stations separated by as much as 500 km retain 50% of their covariance in common for seasonal and sub-seasonal fluctuations. While satellite-based measures often capture most of the daily SST anomaly in coastal and offshore waters, a significant portion of the variance (30-40%) can remain unresolved, even exceeding 75% in the nearshore realm. Similarly, the North Pacific and Gulf of Alaska leading modes of SST variability leave large fractions (25-50%) of the subseasonal thermal variance unresolved. These evaluations show the importance of in situ temperature records for studies that seek to understand mechanistic responses of marine organisms to habitat variability at biologically important time and space scales. We find that near-bottom temperature anomalies on the outer shelf vary inversely with surface temperatures and with near-bottom salinity, suggesting that thermal anomalies are also linked with nutrient flux anomalies. A case study of the recent Pacific marine heatwave and transition out of preceding cool years shows that the northern Gulf of Alaska surface temperatures (0-50 m) were elevated from 2014 to 2019 relative to the long-term record. Coastal temperatures warmed contemporaneously with offshore waters through the 2013 calendar year. In contrast, deep inner shelf waters (200-250 m) exhibited delayed warming relative to the surface and relative to deep waters offshore at the same depth. While offshore surface waters cooled from early 2014 into 1-2 Science Synthesis Final Report Gulf Watch Alaska, 2021 early 2016, the shelf continued to warm over this time as the effects of local air-sea and advective heat fluxes continued to permeate across the northern Gulf. These results highlight the importance of different heating mechanisms for surface and near-bottom waters across the northern Gulf of Alaska.

Alaska↗

USGS2002

Late Miocene and early Pliocene biosiliceous sedimentation along the California margin

Biogenic opal sedimentation is compared between offshore and onshore areas of the California margin during the late middle Miocene, the late Miocene, and the early Pliocene. The records from offshore ODP Sites 1010 and 1021 have declining opal abundance, with a dramatic three-fold decline at about 11.5 Ma and a second, less pronounced drop occurring at about 7.6 Ma. Thick stratigraphic sections of diatomaceous sediments dated between 11.5 and 10.0 Ma and between 7.6 and 6.5 Ma are found onshore in California, whereas coeval intervals in offshore deep sea sites display relatively low opal percentages. This suggests that during periods of reduced strength in the California Current, diatom production declined in offshore areas while it increased in more coastal regions. The early Pliocene and early part of the late Pliocene (4.6 to ca. 2.7 Ma) are marked by the near absence of diatoms in offshore sites, while diatoms are masked by clastic components in onshore sections. Diatom production was greatly reduced along the California margin during this climatically warm period of the Pliocene at the same time that production dramatically increased in the subarctic northwest Pacific, suggesting fractionation of opal to higher latitudes.

Baja California, California↗

USGS2014

The vertical structure of the circulation and dynamics in Hudson Shelf Valley

Hudson Shelf Valley is a 20–30 m deep, 5–10 km wide v-shaped submarine valley that extends across the Middle Atlantic Bight continental shelf. The valley provides a conduit for cross-shelf exchange via along-valley currents of 0.5 m s −1 or more. Current profile, pressure, and density observations collected during the winter of 1999–2000 are used to examine the vertical structure and dynamics of the flow. Near-bottom along-valley currents having times scales of a few days are driven by cross-shelf pressure gradients setup by wind stresses, with eastward (westward) winds driving onshore (offshore) flow within the valley. The along-valley momentum balance in the bottom boundary layer is predominantly between the pressure gradient and bottom stress because the valley bathymetry limits current veering. Above the bottom boundary layer, the flow veers toward an along-shelf (cross-valley) orientation and a geostrophic balance with some contribution from the wind stress (surface Ekman layer). The vertical structure and strength of the along-valley current depends on the magnitude and direction of the wind stress. During offshore flows driven by westward winds, the near-bottom stratification within the valley increases resulting in a thinner bottom boundary layer and weaker offshore currents. Conversely, during onshore flows driven by eastward winds the near-bottom stratification decreases resulting in a thicker bottom boundary layer and stronger onshore currents. Consequently, for wind stress magnitudes exceeding 0.1 N m −2 , onshore along-valley transport associated with eastward wind stress exceeds the offshore transport associated with westward wind stress of the same magnitude.

Hudson Shelf Valley↗