31 research outputs found

    Multiple Complications from a Finger Fracture in a Basketball Player

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    Minor finger and hand problems resulting from NCAA Division-1 Basketball competition are fairly common. True injuries— those requiring removal from participation— are rare, as suggested by injury surveillance and epidemiological data. The objective of this study is to present the case of multiple complications resulting from an original finger dislocation and fracture. Improper fracture healing led to tendon imbalances, causing finger angulation. The extended period of time the finger was deformed further resulted in osteoarthritis (progressive wearing down of the cartilage and bones that comprise a joint). Severe complications stemming from the original injury occur infrequently in the general population and are virtually unheard of in the athletic population. Seemingly routine or inconsequential finger injuries may produce serious, permanent, and uncorrectable damage. Sports medicine practitioners should be familiar with the effects of injury on surrounding small and large tissue structures to provide optimal intervention and patient understanding. This knowledge will increase treatment compliance, preventing severe complications or permanent dysfunction

    Anomalous radiocarbon ages for foraminifera shells

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    The causes for discordant radiocarbon results on multiple species of planktonic foraminifera from high-sedimentation-rate marine sediments are investigated. We have documented two causes for these anomalous results. One is the addition of secondary radiocarbon for which we have, to date, only one firm example. It involves an opal-rich sediment. The other is the incorporation of reworked material. Again, we have, to date, only one firm example. It involves a rapidly deposited ocean margin sediment. However, we have three other examples where reworking is the most likely explanation. On the basis of this study it is our conclusion that, where precise radiocarbon dating of high-deposition-rate marine sediment is required, a prerequisite is to demonstrate that concordant ages can be obtained on pairs of fragile and robust planktic shells. For sediment rich in opal, it is advisable to check for secondary calcite by comparing ages obtained on acid-leached samples with those on unleached samples

    Radiocarbon age offsets of foraminifera resulting from differential dissolution and fragmentation within the sedimentary bioturbated zone

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    Shells of coexisting species of planktonic foraminifera from the Ontong Java Plateau reveal radiocarbon age offsets of up to 2200 years. Similar offsets are found between fragments and whole shells of single species. Steady state modelling of dissolution and bioturbation within the sedimentary mixed layer predicts age differences of up to several kiloyears due to the interplay between differential dissolution and fragmentation of foraminifer shells and bioturbation. The observation that fragile foraminiferal shells are systematically older than those of more robust species is more difficult to explain. Mechanisms of chemical erosion, interface dissolution, and sediment redistribution are all apparently unable to explain this phenomenon. A possible solution is presented in which a particular species may be represented by two distinct classes of shells which are more or less robust. In this case, differential dissolution and fragmentation causes an increase in the mean age as the fragile class contributes less to the remaining intact shells. This study highlights the vulnerability of low sedimentation rate cores to the effects of dissolution and bioturbation

    (Table 1) Age determination on various planktonic foraminifera from Ontong Java Plateau core top sediments

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    Shells of coexisting species of planktonic foraminifera from the Ontong Java Plateau reveal radiocarbon age offsets of up to 2200 years. Similar offsets are found between fragments and whole shells of single species. Steady state modelling of dissolution and bioturbation within the sedimentary mixed layer predicts age differences of up to several kiloyears due to the interplay between differential dissolution and fragmentation of foraminifer shells and bioturbation. The observation that fragile foraminiferal shells are systematically older than those of more robust species is more difficult to explain. Mechanisms of chemical erosion, interface dissolution, and sediment redistribution are all apparently unable to explain this phenomenon. A possible solution is presented in which a particular species may be represented by two distinct classes of shells which are more or less robust. In this case, differential dissolution and fragmentation causes an increase in the mean age as the fragile class contributes less to the remaining intact shells. This study highlights the vulnerability of low sedimentation rate cores to the effects of dissolution and bioturbation

    Age determination of foraminifera shells

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    The causes for discordant radiocarbon results on multiple species of planktonic foraminifera from high-sedimentation-rate marine sediments are investigated. We have documented two causes for these anomalous results. One is the addition of secondary radiocarbon for which we have, to date, only one firm example. It involves an opal-rich sediment. The other is the incorporation of reworked material. Again, we have, to date, only one firm example. It involves a rapidly deposited ocean margin sediment. However, we have three other examples where reworking is the most likely explanation. On the basis of this study it is our conclusion that, where precise radiocarbon dating of high-deposition-rate marine sediment is required, a prerequisite is to demonstrate that concordant ages can be obtained on pairs of fragile and robust planktic shells. For sediment rich in opal, it is advisable to check for secondary calcite by comparing ages obtained on acid-leached samples with those on unleached samples

    Radiocarbon age of late glacial deep water from the equatorial Pacific

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    Radiocarbon age differences for pairs of coexisting late glacial age benthic and planktic foraminifera shells handpicked from 10 sediment samples from a core from a depth of 2.8 km in the western equatorial Pacific are not significantly different from that of 1600 years calculated from measurements on prenuclear seawater. This places a lower limit on the depth of the interface for the hypothetical radiocarbon-depleted glacial age seawater reservoir required to explain the 190% drop in the (14)C/C for atmospheric CO(2), which occurred during the mystery interval (17.5 to 14.5 calendar years ago). These measurements restrict the volume of this reservoir to be no more than 35% that of the ocean. Further, (14)C measurements on a single Last Glacial Maximum age sample from a central equatorial Pacific core from a depth of 4.4 km water fail to reveal evidence for the required 5- to 7-kyr age difference between benthic and planktic foraminifera shells if the isolated reservoir occupied only one third of the ocean. Nor does the (13)C record for benthic forams from this abyssal core yield any evidence for the excess respiration CO(2) expected to be produced during thousands of years of isolation. Nor, as indicated by the presence of benthic foraminifera, was the dissolved oxygen used up in this abyssal water
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