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Three Florida high schools used the computer-based PLATO Basic Skills Mathematics program for remedial mathematics lessons. Students showed a median gain of 1.5 grade equivalents and improved attitudes toward mathematics and school. A model of the project's cost effectiveness indicates the need to manage the program carefully. (Author/RW)

Radiometric age dating of reef cores acquired at the Dry Tortugas coral reef ecosystem (DTCRE) was merged with lidar topographic mapping to examine Holocene reef development linked to spatial variation in growth and erosion under the control of sea level. Analysis of variance of lidar topography confirmed the presence of three distinct terraces on all three major DTCRE banks (Loggerhead Bank, Garden Bank, and Pulaski Bank). Reef building on the middle terrace (T2) began atop Pleistocene edifices on Loggerhead Bank by 8.0 ka (thousands of years ago) and on Garden Bank by 7.2 ka at elevations of about −16.0 m and −11.9 m, respectively, relative to present mean sea level. Following this initiation at different elevations, T2 aggraded vertically on both banks at different rates during the early Holocene under foundering conditions until a highstand at 5.2 ka, resulting in a 2.21 m offset in present mean T2 elevation between these banks. Initiation of an upper terrace (T1) occurred on both Loggerhead Bank and Garden Bank in association with sea-level fall to a lowstand at near 4.8 ka. This upper terrace initiated on Garden Bank at about 5.0 ka and then grew upward at rate of 2.5 mm year until approximately 3.8 ka On Loggerhead Bank, the upper T1 terrace formed after 4.5 ka at a higher vertical aggradation rate of 4.1 mm year, but at a lower elevation than on Garden Bank. Terrace T1 aggraded on Loggerhead Bank below the elevation of lowstands during late Holocene sea-level oscillation, and consequently erosion on Loggerhead Bank was minimal and likely limited to the crest of the upper terrace. In contrast, after 3.8 ka terrace T1 on Garden Bank likely tracked sea level and consequently underwent erosion when sea level fell to second, third and fourth lowstands at 3.3, 1.1, and 0.3 ka. [ABSTRACT FROM AUTHOR]

Pleistocene carbonates of south Florida and islands of the Florida Keys are currently divided into five marine sequences designated, from oldest to youngest, the Q1-Q5 units. The units include a mosaic of freshwater and shallow marine deposits that accumulated on the Florida platform during high sea-level stands. The units are separated by regionalscale subaerial-exposure surfaces that formed during glacioeustatic lowstands. Analyses of cores recovered at Grossman Ridge Rock Reef and Joe Ree Rock Reef in the Florida Everglades reveal additional subaerial-exposure surfaces that are used to delineate subdivisions within units Q1 (Q1a-Q1b), Q2 (Q2a-Q2d), and Q4 (Q4a-Q4b). Units Q1-Q5 preserve evidence of at least 10 separate sea-level highstands, rather than 5 as indicated by previous studies. Compilation of available uranium-series dates on corals recovered from the Florida Keys indicates that the Q4 unit accreted during sea-level maxima associated with marine oxygen-isotope Stage 9 (Q4a) and isotope Stage 7 (Q4b). The Q5 unit formed during isotope Stage 5. No reliable dates are available for units Q1-Q3. We infer that unit Q3 was formed during the extended sea-level highstand of isotope Stage 11 and that units Q2 and Q1 predate isotope Stage 11. [ABSTRACT FROM AUTHOR]

A program of geophysical mapping and vibracoring was conducted to better understand the geologic evolution of Apalachicola Bay. Analyses of the geophysical data and sediment cores along with age control provided by 34 AMS 14C dates on marine shells and wood reveal the following history. As sea level rose in the early Holocene, fluvial deposits filled the Apalachicola River paleochannel, which extended southward under the central part of the bay and seaward across the continental shelf. Sediments to either side of the paleochannel contain abundant wood fragments, with dates documenting that those areas were forested at 8,000 14C years b.p. As sea level continued to rise, spits formed of headland prodelta deposits. Between ∼6,400 and ∼2,500 14C years b.p., an Apalachicola prodelta prograded and receded several times across the inner shelf that underlies the western part of the bay. An eastern deltaic lobe was active for a shorter time, between ∼5,800 and 5,100 14C years b.p. Estuarine benthic foraminiferal assemblages occurred in the western bay as early as 6,400 14C years b.p., and indicate that there was some physical barrier to open-ocean circulation and shelf species established by that time. It is considered that shoals formed in the region of the present barrier islands as the rising sea flooded an interstream divide. Estuarine conditions were established very early in the post-glacial flooding of the bay. [ABSTRACT FROM AUTHOR]

Abstract: Apalachicola Bay and St. George Sound contain the largest oyster fishery in Florida, and the growth and distribution of the numerous oyster reefs here are the combined product of modern estuarine conditions in the bay and its late Holocene evolution. Sidescan-sonar imagery, bathymetry, high-resolution seismic profiles, and sediment cores show that oyster beds occupy the crests of a series of shoals that range from 1 to 7 km in length, trend roughly north-south perpendicular to the long axes of the bay and sound, and are asymmetrical with steeper sides facing to the west. Surface sediment samples show that the oyster beds consist of shelly sand, while much of the remainder of the bay floor is covered by mud delivered by the Apalachicola River. The present oyster reefs rest on sandy delta systems that advanced southward across the region between 6400 and 4400yr BP when sea level was 4–6m lower than present. Oysters started to colonize the region around 5100yr BP and became extensive by 1200 and 2400yr BP. Since 1200yr BP, their aerial extent has decreased due to burial of the edges of the reefs by the prodelta mud that continues to be supplied by the Apalachicola River. Oyster reefs that are still active are narrower than the original beds, have grown vertically, and become asymmetrical in cross-section. Their internal bedding indicates they have migrated westward, suggesting a net westerly transport of sediment in the bay. [Copyright &y& Elsevier]