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L. J. Moore

Publications and source records attributed to L. J. Moore.

3 recordsLinked to original sources

The influence of sea level rise and changes in fringing reef morphology on gradients in alongshore sediment transport

Climate‐change‐induced alterations to coral reef ecosystems, in combination with sea level rise, have the potential to significantly alter wave dissipation across reefs, leading to shifts in alongshore sediment transport gradients and alterations to tropical coastlines. We used Delft3D to model schematized profiles of two reef flat widths based on the south Molokai, Hawaii coast. Simulated anthropogenic modifications include incremental degradation of the reef structure as well as sea level rise. Our findings indicate that sea level rise has a greater relative effect on wave energy flux and alongshore sediment transport over a wide flat, whereas both reef degradation and sea level rise exert similar influence over a narrow flat. These results suggest reefs that vary in width alongshore are more likely to experience changes in alongshore sediment transport gradients, and therefore shifts in shoreline erosion and accretion patterns, than more uniform reef systems.

Hawai'i

Comparing mean high water and high water line shorelines: Should prosy-datum offsets be incorporated into shoreline change analysis?

More than one type of shoreline indicator can be used in shoreline change analyses, and quantifying the effects of this practice on the resulting shoreline change rates is important. Comparison of three high water line (proxy-based) shorelines and a mean high water intercept (datum-based) shoreline collected from simultaneous aerial photographic and lidar surveys of a relatively steep reflective beach (tan ?? = 0.07), which experiences a moderately energetic wave climate (annual average Hs = 1.2 m), reveals an average horizontal offset of 18.8 m between the two types of shoreline indicators. Vertical offsets are also substantial and are correlated with foreshore beach slope and corresponding variations in wave runup. Incorporating the average horizontal offset into both a short-term, endpoint shoreline change analysis and a long-term, linear regression analysis causes rates to be shifted an average of -0.5 m/y and -0.1 m/y, respectively. The rate shift increases with increasing horizontal offset and decreasing measurement intervals and, depending on the rapidity of shoreline change rates, is responsible for varying degrees of analysis error. Our results demonstrate that under many circumstances, the error attributable to proxy-datum offsets is small relative to shoreline change rates and thus not important. Furthermore, we find that when the error associated with proxy-datum offsets is large enough to be important, the shoreline change rates themselves are not likely to be significant. A total water level model reveals that the high water line digitized by three independent coastal labs for this study was generated by a combination of large waves and a high tide several days before the collection of aerial photography. This illustrates the complexity of the high water line as a shoreline indicator and calls into question traditional definitions, which consider the high water line a wetted bound or "marks left by the previous high tide.".

Journal of Coastal Research

Determination of lead, uranium, thorium, and thallium in silicate glass standard materials by isotope dilution mass spectrometry

A set of four standard glasses has been prepared which have been doped with 61 different elements at the 500-, 50-, 1-, and 0.02-ppm level. The concentrations of lead, uranium, thorium, and thallium have been determined by isotope dilution mass spectrometry at a number of points in each of the glasses. The results obtained from independent determinations in two laboratories demonstrate the homogeneity of the samples and that precision of the order of 0.5% (95% L.E.) may be obtained by the method even at the 20-ppb level for these elements. The chemical and mass spectrometric procedures necessary are presented.

Analytical Chemistry