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At least 937 records · Page 52Linked to original sources

Wave-current interaction in Willapa Bay

This paper describes the importance of wave-current interaction in an inlet-estuary system. The three-dimensional, fully coupled, Coupled Ocean-Atmosphere-Wave-Sediment Transport (COAWST) modeling system was applied in Willapa Bay (Washington State) from 22 to 29 October 1998 that included a large storm event. To represent the interaction between waves and currents, the vortex-force method was used. Model results were compared with water elevations, currents, and wave measurements obtained by the U.S. Army Corp of Engineers. In general, a good agreement between field data and computed results was achieved, although some discrepancies were also observed in regard to wave peak directions in the most upstream station. Several numerical experiments that considered different forcing terms were run in order to identify the effects of each wind, tide, and wave-current interaction process. Comparison of the horizontal momentum balances results identified that wave-breaking-induced acceleration is one of the leading terms in the inlet area. The enhancement of the apparent bed roughness caused by waves also affected the values and distribution of the bottom shear stress. The pressure gradient showed significant changes with respect to the pure tidal case. During storm conditions the momentum balance in the inlet shares the characteristics of tidal-dominated and wave-dominated surf zone environments. The changes in the momentum balance caused by waves were manifested both in water level and current variations. The most relevant effect on hydrodynamics was a wave-induced setup in the inner part of the estuary.

Washington↗

Testing megathrust rupture models using tsunami deposits

The 26 January 1700 CE Cascadia subduction zone earthquake ruptured much of the plate boundary and generated a tsunami that deposited sand in coastal marshes from northern California to Vancouver Island. Although the depositional record of tsunami inundation is extensive in some of these marshes, few sites have been investigated in enough detail to map the inland extent of sand deposition and depict variability in tsunami deposit thickness and grain size. We collected 129 cores in marshes of the Salmon River estuary in Oregon and reanalyzed 114 core logs from a 1987–88 study that mapped the inland extent of circa 1700 CE sandy tsunami deposits. The ca. 1700 CE tsunami deposit in the Salmon River estuary is easily recognized in cores ≤1 m deep in which a buried marsh peat is overlain by a well sorted sand bed with a sharp lower contact that thins and fines inland. We use tsunami deposit data and models of sandy tsunami sediment transport (using Delft3D-FLOW) to test 15 rupture models that could represent a ca. 1700 CE earthquake. At least 12–16 m of slip offshore of the Salmon River, which results in 0.8–1.0 m of coastal coseismic subsidence, is required to match the ca. 1700 CE sand deposit's inland extent, which is consistent with models of heterogeneous megathrust slip in ca. 1700 CE. Our methods of detailed tsunami deposit mapping, combined with sediment transport modeling, can be used to test models of megathrust ruptures and their tsunamis to potentially improve earthquake and tsunami hazard assessments.

JGR Earth Surface↗

Biophysical drivers of coastal treeline elevation

Sea level rise is leading to the rapid migration of marshes into coastal forests and other terrestrial ecosystems. Although complex biophysical interactions likely govern these ecosystem transitions, projections of sea level driven land conversion commonly rely on a simplified “threshold elevation” that represents the elevation of the marsh-upland boundary based on tidal datums alone. To determine the influence of biophysical drivers on threshold elevations, and their implication for land conversion, we examined almost 100,000 high-resolution marsh-forest boundary elevation points, determined independently from tidal datums, alongside hydrologic, ecologic, and geomorphic data in the Chesapeake Bay, the largest estuary in the U.S. located along the mid-Atlantic coast. We find five-fold variations in threshold elevation across the entire estuary, driven not only by tidal range, but also salinity and slope. However, more than half of the variability is unexplained by these variables, which we attribute largely to uncaptured local factors including groundwater discharge, microtopography, and anthropogenic impacts. In the Chesapeake Bay, observed threshold elevations deviate from predicted elevations used to determine sea level driven land conversion by as much as the amount of projected regional sea level rise by 2050. These results suggest that local drivers strongly mediate coastal ecosystem transitions, and that predictions based on elevation and tidal datums alone may misrepresent future land conversion.

Delaware, Maryland, Virginia↗

Extreme Potomac floods at Washington D.C. during the past 500 years

Washington D.C. faces one of the highest 100-year flood risks of any major city along the U.S. East Coast. In addition to storm-surge inundation during hurricanes and nor'easters, water-level observations for Washington are strongly skewed by major floods on the Potomac River. Using geologic and historic records we find new evidence for ice-jam flooding at Georgetown during the Little Ice Age, as recently as 1784, that was up to ∼2x the magnitude of the largest events of the past hundred years (1936, 1942). Over the 19th century (a) human modifications to the Potomac estuary as well as (b) increasingly heavy rainfall and (c) land-clearance in the watershed may have contributed to increasingly frequent large floods at Washington. Early surveys of the U.S. Capitol Building and other local landmarks also suggest sea level on the Potomac estuary at Washington has risen by upwards of 0.7 m (2.2 ft) since the 1790s.

Maryland, Virginia↗

Spatial heterogeneity of salt marsh vulnerability to sea-level rise: Dual controls of hydrological setting and salinity regime

Salt marsh vulnerability to sea-level rise (SLR) is typically assessed using point measurements of vertical accretion, neglecting three-dimensionality of geomorphic evolution and spatial variability. Recent studies suggest links between vertical and horizontal vulnerability, with differences between oligohaline and polyhaline marshes, yet these relationships remain untested in estuary-marsh systems. Here we combine geospatial analysis with hydrodynamic modeling to evaluate how unvegetated/vegetated marsh ratio (UVVR), a metric of marsh degradation, relates to elevation across hydrological regions and salinity regimes in the Albemarle-Pamlico Estuarine System, the largest lagoonal estuary in U.S. We show that at given normalized elevation, UVVR decreases across hydrological regions and salinity regimes from offshore to inland. UVVR-elevation relationship varies systematically with both hydrological setting and salinity regime, with hydrology exerting stronger influence. These findings challenge the assumption of a universal marsh deterioration trajectory and underscore the need to account for spatial heterogeneity when predicting responses to SLR.

North Carolina↗

Nitrogen and phosphorus speciation and flux in a large Florida river wetland System

Hydrologic measurements and analyses of various nitrogen and phosphorus species were made on the Apalachicola River system in northern Florida in 1979 and 1980. Annual outflows of total nitrogen (TN) and total phosphorus (TP) were not substantially different from annual inflows. However, there was significant net import of ammonia and soluble reactive phosphorus and net export of some particulate and organic species. The TN: TP ratio ranged from 12 to 15, but the specific ratio of dissolved inorganic nitrogen: soluble reactive phosphorus was much higher (up to 40) and increased in a downstream direction; this contributed to a phosphorus-limiting situation in Apalachicola estuary. Processes within the flood plain ecosystem accounted for much of the release of organic and particulate species and retention of inorganic species. This flood plain function is probably critical for maintaining a nutrient pool in the estuary which supports secondary productivity and a detrital-based food web.

Florida↗

On tide-induced Lagrangian residual current and residual transport: 1. Lagrangian residual current

Residual currents in tidal estuaries and coastal embayments have been recognized as fundamental factors which affect the long-term transport processes. It has been pointed out by previous studies that it is more relevant to use a Lagrangian mean velocity than an Eulerian mean velocity to determine the movements of water masses. Under weakly nonlinear approximation, the parameter k , which is the ratio of the net displacement of a labeled water mass in one tidal cycle to the tidal excursion, is assumed to be small. Solutions for tides, tidal current, and residual current have been considered for two-dimensional, barotropic estuaries and coastal seas. Particular attention has been paid to the distinction between the Lagrangian and Eulerian residual currents. When k is small, the first-order Lagrangian residual is shown to be the sum of the Eulerian residual current and the Stokes drift. The Lagrangian residual drift velocity or the second-order Lagrangian residual current has been shown to be dependent on the phase of tidal current. The Lagrangian drift velocity is induced by nonlinear interactions between tides, tidal currents, and the first-order residual currents, and it takes the form of an ellipse on a hodograph plane. Several examples are given to further demonstrate the unique properties of the Lagrangian residual current.

Water Resources Research↗

On tide-induced Lagrangian residual current and residual transport: 2. Residual transport with application in south San Francisco Bay, California

The transports of solutes and other tracers are fundamental to estuarine processes. The apparent transport mechanisms are convection by tidal current and current-induced shear effect dispersion for processes which take place in a time period of the order of a tidal cycle. However, as emphasis is shifted toward the effects of intertidal processes, the net transport is mainly determined by tide-induced residual circulation and by residual circulation due to other processes. The commonly used intertidal conservation equation takes the form of a convection-dispersion equation in which the convective velocity is the Eulerian residual current, and the dispersion terms are often referred to as the phase effect dispersion or, sometimes, as the “tidal dispersion.” The presence of these dispersion terms is merely the result of a Fickian type hypothesis. Since the actual processes are not Fickian, thus a Fickian hypothesis obscures the physical significance of this equation. Recent research results on residual circulation have suggested that long-term transport phenomena are closely related to the Lagrangian residual current or the Lagrangian residual transport. In this paper a new formulation of an intertidal conservation equation is presented and examined in detail. In a weakly nonlinear tidal estuary the resultant intertidal transport equation also takes the form of a convection-dispersion equation without the ad hoc introduction of phase effect dispersion in a form of dispersion tensor. The convective velocity in the resultant equation is the first-order Lagrangian residual current (the sum of the Eulerian residual current and the Stokes drift). The remaining dispersion terms are important only in higher-order solutions; they are due to shear effect dispersion and turbulent mixing. There exists a dispersion boundary layer adjacent to shoreline boundaries. An order of magnitude estimate of the properties in the dispersion boundary layer is given. The present treatment of intertidal transport processes is illustrated by an analytical solution for an amphidromic system and by a numerical application in South San Francisco Bay, California. The present formulation reveals that the mechanism for long-term transport of solutes is mainly convection due to the Lagrangian residual current in the interior of a tidal estuary. This result also points out the weakness in the tidal dispersion formulation, and explains the large variability of the observed values for tidal dispersion coefficients. Further research on properties of the dispersion boundary layer is needed.

California↗

Top-predator recovery abates geomorphic decline of a coastal ecosystem

The recovery of top predators is thought to have cascading effects on vegetated ecosystems and their geomorphology 1,2 , but the evidence for this remains correlational and intensely debated 3,4 . Here we combine observational and experimental data to reveal that recolonization of sea otters in a US estuary generates a trophic cascade that facilitates coastal wetland plant biomass and suppresses the erosion of marsh edges—a process that otherwise leads to the severe loss of habitats and ecosystem services 5,6 . Monitoring of the Elkhorn Slough estuary over several decades suggested top-down control in the system, because the erosion of salt marsh edges has generally slowed with increasing sea otter abundance, despite the consistently increasing physical stress in the system (that is, nutrient loading, sea-level rise and tidal scour 7,8,9 ). Predator-exclusion experiments in five marsh creeks revealed that sea otters suppress the abundance of burrowing crabs, a top-down effect that cascades to both increase marsh edge strength and reduce marsh erosion. Multi-creek surveys comparing marsh creeks pre- and post-sea otter colonization confirmed the presence of an interaction between the keystone sea otter, burrowing crabs and marsh creeks, demonstrating the spatial generality of predator control of ecosystem edge processes: densities of burrowing crabs and edge erosion have declined markedly in creeks that have high levels of sea otter recolonization. These results show that trophic downgrading could be a strong but underappreciated contributor to the loss of coastal wetlands, and suggest that restoring top predators can help to re-establish geomorphic stability.

California↗

Water quality measurements in San Francisco Bay by the U.S. Geological Survey, 1969–2015

The U.S. Geological Survey (USGS) maintains a place-based research program in San Francisco Bay (USA) that began in 1969 and continues, providing one of the longest records of water-quality measurements in a North American estuary. Constituents include salinity, temperature, light extinction coefficient, and concentrations of chlorophyll- a , dissolved oxygen, suspended particulate matter, nitrate, nitrite, ammonium, silicate, and phosphate. We describe the sampling program, analytical methods, structure of the data record, and how to access all measurements made from 1969 through 2015. We provide a summary of how these data have been used by USGS and other researchers to deepen understanding of how estuaries are structured and function differently from the river and ocean ecosystems they bridge.

California↗

Physiological characteristics of wild Atlantic salmon post-smolts during estuarine and coastal migration

Changes were measured in some of the major physiological variables associated with seawater adaptability, growth and energetics in wild Atlantic salmon Salmo salar smolts and post-smolts migrating from the river and through the estuary, fjord and coastal areas in the River Orkla and the Trondheimsfjord, Norway during late May to early June. Gill Na+,K+-ATPase activity increased to levels of 12-16 ??mol ADP mg protein-1 h -1 in post-smolts caught in higher salinity zones, probably representing long-term levels of Atlantic salmon post-smolts in oceanic conditions. Muscle moisture was regulated within narrow limits (77.7-78.7%) in fish from all zones during both years, suggesting that post-smolts adapt to marine conditions without any long-term disturbance of hydro-mineral balance. Lipid and glycogen content showed a general trend towards depletion from the river, through the fjord and into the ocean. There was, however, no significant change in protein content. The present results confirm that smolts are naturally 'energy deficient' during downstream migration, and suggest that post-smolts also mobilize energy reserves during their early marine phase, while protein is allocated for somatic growth. Plasma growth hormone (GH) levels increased transiently during passage through the estuary and fjord, with lower levels observed in post-smolts caught off-shore, i.e. in fish which were feeding on marine prey and had adapted to the marine environment. These physiological changes may confer substantial selective advantages during the critical early marine phase of anadromous salmonids, and hence are adaptive for long-term survival in sea water. ?? 2003 The Fisheries Society of the British Isles.

Journal of Fish Biology↗

Nitrous oxide emission from denitrification in stream and river networks

Nitrous oxide (N 2 O) is a potent greenhouse gas that contributes to climate change and stratospheric ozone destruction. Anthropogenic nitrogen (N) loading to river networks is a potentially important source of N 2 O via microbial denitrification that converts N to N 2 O and dinitrogen (N 2 ). The fraction of denitrified N that escapes as N 2 O rather than N 2 (i.e., the N 2 O yield) is an important determinant of how much N 2 O is produced by river networks, but little is known about the N 2 O yield in flowing waters. Here, we present the results of whole-stream 15 N-tracer additions conducted in 72 headwater streams draining multiple land-use types across the United States. We found that stream denitrification produces N 2 O at rates that increase with stream water nitrate (NO 3 − ) concentrations, but that <1% of denitrified N is converted to N 2 O. Unlike some previous studies, we found no relationship between the N 2 O yield and stream water NO 3 − . We suggest that increased stream NO 3 − loading stimulates denitrification and concomitant N 2 O production, but does not increase the N 2 O yield. In our study, most streams were sources of N 2 O to the atmosphere and the highest emission rates were observed in streams draining urban basins. Using a global river network model, we estimate that microbial N transformations (e.g., denitrification and nitrification) convert at least 0.68 Tg·y −1 of anthropogenic N inputs to N 2 O in river networks, equivalent to 10% of the global anthropogenic N 2 O emission rate. This estimate of stream and river N 2 O emissions is three times greater than estimated by the Intergovernmental Panel on Climate Change. Humans have more than doubled the availability of fixed nitrogen (N) in the biosphere, particularly through the production of N fertilizers and the cultivation of N-fixing crops ( 1 ). Increasing N availability is producing unintended environmental consequences including enhanced emissions of nitrous oxide (N 2 O), a potent greenhouse gas ( 2 ) and an important cause of stratospheric ozone destruction ( 3 ). The Intergovernmental Panel on Climate Change (IPCC) estimates that the microbial conversion of agriculturally derived N to N 2 O in soils and aquatic ecosystems is the largest source of anthropogenic N 2 O to the atmosphere ( 2 ). The production of N 2 O in agricultural soils has been the focus of intense investigation (i.e., >1,000 published studies) and is a relatively well constrained component of the N 2 O budget ( 4 ). However, emissions of anthropogenic N 2 O from streams, rivers, and estuaries have received much less attention and remain a major source of uncertainty in the global anthropogenic N 2 O budget. Microbial denitrification is a large source of N 2 O emissions in terrestrial and aquatic ecosystems. Most microbial denitrification is a form of anaerobic respiration in which nitrate (NO 3 − , the dominant form of inorganic N) is converted to dinitrogen (N 2 ) and N 2 O gases ( 5 ). The proportion of denitrified NO 3 − that is converted to N 2 O rather than N 2 (hereafter referred to as the N 2 O yield and expressed as the mole ratio) partially controls how much N 2 O is produced via denitrification ( 6 ), but few studies provide information on the N 2 O yield in streams and rivers because of the difficulty of measuring N 2 and N 2 O production in these systems. Here we report rates of N 2 and N 2 O production via denitrification measured using whole-stream 15 NO 3 − -tracer experiments in 72 headwater streams draining different land-use types across the United States. This project, known as the second Lotic Intersite Nitrogen eXperiment (LINX II), provides unique whole-system measurements of the N 2 O yield in streams. Although N 2 O emission rates have been reported for streams and rivers ( 7 , 8 ), the N 2 O yield has been studied mostly in lentic freshwater and marine ecosystems, where it generally ranges between 0.1 and 1.0%, although yields as high as 6% have been observed ( 9 ). These N 2 O yields are low compared with observations in soils (0–100%) ( 10 ), which may be a result of the relatively lower oxygen (O 2 ) availability in the sediments of lakes and estuaries. However, dissolved O 2 in headwater streams is commonly near atmospheric equilibrium and benthic algal biofilms can produce O 2 at the sediment–water interface, resulting in strong redox gradients more akin to those in partially wetted soils. Thus, streams may have variable and often high N 2 O yields, similar to those in soils ( 11 ). The N 2 O yield in headwater streams is of particular interest because much of the NO 3 − input to rivers is derived from groundwater upwelling into headwater streams. Furthermore, headwater streams compose the majority of stream length within a drainage network and have high ratios of bioreactive benthic surface area to water volume ( 12 ).

Proceedings of the National Academy of Sciences of↗

Movements and demography of spawning American Shad in the Penobscot River, Maine, prior to dam removal

We conducted a baseline study to better understand the migratory movements and age and spawning histories of American Shad Alosa sapidissima in the Penobscot River, Maine. The Penobscot River is currently undergoing a major dam removal project that is focused on restoring migratory connectivity and recovering diadromous fish populations including American Shad. This study addresses key data gaps for a previously unstudied native population of shad prior to restoration. A combination of radio- ( n = 70) and acoustic telemetry ( n = 14) was used to investigate the movements of migratory adult fish in 2010 and 2011. Scale-based analyses were used to assess spawner age and iteroparity. Radiotelemetry results indicated that few tagged fish (5–8%) approached the head-of-tide dam. Tagged fish exhibited three general patterns of movement in the accessible freshwater river habitat: use of the upper river reach, the lower river reach, or both. Mean freshwater residence time ranged from 9.1 to 14.0 d. Congregating fish were observed at two sites in the upper river reach and spawning activity was observed. Freshwater survival and survival to the estuary were at least 71%. This observed high survival was consistent with the estimated age and spawning histories of tracked fish, which indicated that 75–95% of the sampled fish were repeat spawners. Estimated age of adult migrants ranged from age 4 to age 9. Postspawning acoustic-tagged American Shad exhibited a series of prolonged upstream and downstream reversals upon entering the lower estuary. These movements have been previously unreported, and suggest that estuarine residency after spawning is important to osmoregulatory acclimatization for re-entry into salt water and the resumption of postspawning feeding activity.

Transactions of the American Fisheries Society↗

Shortnose sturgeon in the Gulf of Maine: Use of spawning habitat in the Kennebec System and response to dam removal

Evidence has become available in this century indicating that populations of the endangered Shortnose Sturgeon Acipenser brevirostrum migrate outside their natal river systems, but the full extent and functional basis of these migrations are not well understood. Between 2007 and 2013, 40 Shortnose Sturgeon captured and tagged in four Gulf of Maine river systems migrated long distances in coastal waters to reach the Kennebec System where their movements were logged by an acoustic receiver array. Twenty-one (20%) of 104 Shortnose Sturgeon tagged in the Penobscot River, two (50%) of four tagged in the Kennebec System, one (50%) of two tagged in the Saco River, and 16 (37%) of 43 tagged in the Merrimack River moved to a previously identified spawning site or historical spawning habitat in the Kennebec System in spring. Most (65%) moved in early spring from the tagging location directly to a spawning site in the Kennebec System, whereas the rest moved primarily in the fall from the tagging location to a wintering site in that system and moved to a spawning site the following spring. Spawning was inferred from the location, behavior, and sexual status of the fish and from season, water temperature, and discharge, and was confirmed by the capture of larvae in some years. Tagged fish went to a known spawning area in the upper Kennebec Estuary (16 events) or the Androscoggin Estuary (14 events), an historical spawning habitat in the restored Kennebec River (8 events), or two spawning areas in a single year (7 events). We have provided the first evidence indicating that Shortnose Sturgeon spawn in the restored Kennebec River in an historical habitat that became accessible in 1999 when Edwards Dam was removed, 162 years after it was constructed. These results highlight the importance of the Kennebec System to Shortnose Sturgeon throughout the Gulf of Maine.

Maine↗

Effects of salinity on freshwater fishes in coastal plain drainages in the southeastern U.S.

This review focuses on the influence of salinity on freshwater fishes in coastal rivers and estuaries of the southeastern U.S. Influences of salinity on freshwater fish species can be explained partly through responses evidenced by behavior, physiology, growth, reproduction, and food habits during all aspects of life history. Factors influencing the rate of salinity change affect the community structure and dynamics of freshwater fishes in brackish environments. Our understanding of the relation between salinity and the life history of freshwater fishes is limited because little ecological research has been conducted in low-salinity habitats that we consider an “interface” between freshwater streams and the estuary proper. Much of the available data are descriptive in nature and describe best general patterns, but more specific studies are required to better determine the influence of salinity on freshwater fishes. Improved understanding of the influence of human-induced changes on the productivity and viability of these important systems will require a new research focus.

Reviews in Fisheries Science↗

Atlantic sturgeon status and movement ecology in an extremely small spawning habitat: The Nanticoke River-Marshyhope Creek, Chesapeake Bay

Biotelemetry of Atlantic sturgeon Acipenser oxyrinchus oxyrinchus has exposed spawning behaviors in ever-smaller estuaries, surprising for the NW Atlantic’s largest anadromous species. Small estuary — the Nanticoke River and Marshyhope Creek (Chesapeake Bay) — spawning-run adults and their habitat affinities are described based upon direct sampling and biotelemetry for the period 2014–2018. High rates of recapture over this period indicate a very small adult population size. Genetics revealed a very small effective population size ( N e = 12.2, 95% CI = 6.7–21.9). Most returns occurred during September at 20–27 °C. All fish departed as fall temperatures declined below 20 °C. Multi-beam sonar identified small-dispersed areas of sand-cobble and cobble, which could support adhesive embryo attachment. Movements of adults were higher during nighttime than daytime, with habitat preference for hard bottom habitats. Genetic evidence indicates that the sudden discovery of this population was unrelated to a hatchery release of several thousand juvenile sturgeon (Hudson River progeny) in 1997. The newly discovered population in the Nanticoke River exhibits a degree of resilience including multiple spawning regions and suitable spawning habitat. Still, critical vulnerabilities persist including curtailed habitat, continued agricultural and maritime development, invasive blue catfish, and a very small apparent population size.

Delaware, Maryland↗

Cycle of earthquake-induced aggradation and related tidal channel shifting, upper Turnagain Arm, Alaska, USA.

Aggradation of intertidal sediment in upper Turnagain Arm, a macrotidal estuary located in southern Alaska near Anchorage, began because of subsidence caused by sediment consolidation and tectonic lowering of the land during the earthquake of March 27, 1964. At the head of the Arm, decrease in percent sand of surface sediments with time and return of rodents, pulmonate gastropods, trees, bushes, and grasses to the intertidal region, indicate that the rate of sediment deposition has slowed and the Upper Turnagain Arm area has returned to a state of preearthquake equilibrium only 17 years after the event. Comparison of channel locations before and after the earthquake indicates the possibility of regional postseismic tilting of the estuary.

Alaska↗

Apogean-perigean signals encoded in tidal flats at the fluvio-estuarine transition of Glacier Creek, Turnagain Arm, Alaska; implications for ancient tidal rhythmites

Turnagain Arm is a macrotidal fjord‐style estuary. Glacier Creek is a small, glacially fed stream which enters the estuary tangentially near Girdwood, Alaska. Trenches and daily sedimentation measurements were made in a mudflat along the fluvio–estuarine transition of Glacier Creek during several summers since 2003. Each year, the flats appear to erode during the winter and then accrete vertically in the spring and summer. In each of the years studied, tidal laminae in vertically thickening and thinning laminae bundles were deposited by twice daily tides in neap–spring tidal cycles. In 2004, bundles of thickening and thinning laminae couplets were noted in trenches cut into the flats. Five laminae bundles alternated between thicker and thinner bundles, corresponding to the perigean (high spring) and apogean (low spring) tides. Well‐preserved apogean–perigean cycles have rarely been documented in modern tidal flat sediments. At this location, vertical accretion of tidal rhythmites with well‐developed neap–spring cyclicity is possible because of the near‐complete removal of the flat from the previous year, which creates accommodation space for vertical accretion without significant reworking. Macrotidal conditions, no reworking by infaunal invertebrates, protection from the main tidal channel by a gravel bar and protection from storm waves and fluvial erosion by a recess in the sedge marsh that surrounds the flats all aid in preservation of rhythmites during aggradation. The position of the flats relative to tidal range allows for accumulation of complete spring cycles and incomplete neap cycles. In the summer of 2004, apogee and perigee were closely aligned with the new and full moons, resulting in successive strong perigee and apogee tides which probably aided in the accumulation of successive thick–thin spring cycles encoding the apogean and perigean tidal cycle. The apogean–perigean signal was not observed in subsequent years.

Alaska↗