107 research outputs found

    James Pinckney Kinard Papers - Accession 8

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    The James Pinckney Kinard Papers consist of family history charts of the Kinard family and related Kuhn and Summer families, and a Kinard family history, personal correspondence including letters to and from his wife Lee Wicker Kinard (1873-1963), their daughter Nelle Kinard, and other family members, business correspondence, financial papers, literary manuscripts, scrapbooks, and photographs pertaining to Kinard’s student days at the Citadel, his personal and family affairs, his teaching career, his presidency of Winthrop, and his efforts to get his literary manuscripts published. This collection consists primarily of correspondence and offers an informative insight into the personal lives and family affairs of Dr. Kinard and his wife, Mrs. Lee Wicker Kinard. The correspondence generally deals with Dr. Kinard’s struggle against the South Carolina legislature’s cuts in educational appropriations for Winthrop during the Depression; and his varied activities on behalf of Winthrop as President Emeritus. The collection also includes several unpublished manuscripts ranging from his student days at the Citadel to his later life. Areas of research would perhaps include, among others, biographical information on Dr. Kinard and social history during the Depression.https://digitalcommons.winthrop.edu/manuscriptcollection_findingaids/1018/thumbnail.jp

    Effects of Tidal Stage and Sun Angles on Intertidal Benthic Microalgal Productivity

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    Motile benthic diatoms exhibit rhythmic vertical migrations that are influenced by tidal and light cycles. As a consequence of these periodic migrations, corresponding periodicities in benthic microalgal production should occur. Using oxygen microelectrodes, hourly measurements of microalgal production were obtained from subaerially exposed cores collected from low-intertidal muddy sediments in North Inlet estuary, South Carolina, USA Microalgal productivity at low tide was twice that at high tide (mean difference 52 %) and was significantly correlated with diurnal and tidal periodicities (r2 = 0.41; p \u3c 0.0001). Production values ranged from 28.0 to 460.5 µmol O2 mg chl a-1 h-1 and maximum rates were achieved during mid-afternoon low tides. A curvilinear regression equation was constructed to simulate daily and monthly benthic microalgal production based on tidal and light cycles. Comparisons between predictions of the curvilinear equation and published data sets showed a reasonable agreement (r2 = 0.77), suggesting similar phenomena in other estuaries. Current benthic microalgal production models do not account for hourly variability in productivity, leading to potentially large errors when measurements are extrapolated over monthly and annual time scales. Although other physiological and abiotic factors also influence benthic microalgal productivity, much of the short-term variability in production rates may be simply attributed to migratory rhythms within estuarine sediments

    W403-002B-01 - Office of the President: James Pinckney Kinard: Various Records

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    Impacts of Seasonality and Nutrients on Microbial Mat Community Structure and Function

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    To understand the mechanisms responsible for seasonal fluctuations in growth and N2 fixation in intertidal microbial mat communities, we quantified seasonal changes in mat community composition, related these changes to diel and seasonal N2 fixation rates, and evaluated community responses (growth, N2fixation, composition) to long-term (22 d) nutrient addition bioassays. A temperate intertidal cyanobacterial mat community, located in coastal North Carolina, USA, was sampled at monthly intervals for 1 yr (1993-94) to determine changes in community composition. The abundances of major phototrophic groups were quantified based on the relative concentrations of taxaspecific photopigments (chlorophylls and carotenoids). The most abundant phototrophs were cyanobacteria, diatoms, and photosynthetic bacteria. Mat blomass and community composition underwent marked changes on both monthly and seasonal scales and corresponded with seasonal shifts in the diel patterns of N2 fixation. Diatom biomass increased during periods of low N2 fixation. Nutrient (nitrate and phosphate) addition bioassays indicated that both cyanobacterial and diatom growth were N limited. Cyanobacteria were able to circumvent N limitation by N2 fixation. The addition of high concentrations of N (100µM NaNO3) in combination with P (100 µM NaH2P04) resulted in an increase (163%) in the relative abundance of diatoms The addition of P alone more than doubled N2 fixation rates and cyanobacterial abundance increased (+34%) relative to diatoms. However, N and NP additions significantly lowered (by more than 75%) N2 fixation rates. Here we show that manipulative experiments, together with quantitative assessments of community composition based on chemotaxonomic pigments, can provide useful insights into the mechanisms that relate mat community structure and function to environmental constraints, including nutrient limitation and seasonal climatic changes

    Fish Kills and Bottom-Water Hypoxia in the Neuse River and Estuary: Reply to Burkholder et al.

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    Burkholder et al. (1999) authored a comment in Manne Ecology Progress Series (MEPS) that selectively criticizes elements of our findings that appeared earlier in the same journal (Paerl et al. 1998). For the benefit of the readership of MEPS, it would have been useful to have had both their comment and our reply in the same volume. Unfortunately, we were not informed of their comment pnor to its publication

    Age and Growth of King Mackerel, \u3cem\u3eScomberomorus cavalla\u3c/em\u3e, from the Atlantic Coast of the United States

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    Whole sagittae from 683 and sectioned sagittae from 773 adult (age\u3e 0 ; 437-1.310 mm FL), and lapilli from 29 larval (2-7 mm SL) and 69 young-of-the-year (79-320 mm FL) king mackerel, were examined. All fish were from waters off the Atlantic coast of the southeastern United States (Cape Canaveral, Florida to Cape Fear. North Carolina). Back-calculated lengths at ages and von Bertalanffy growth equations were calculated from both whole and sectioned sagittae. Ages determined from sectioned sagittae were significantly greater than ages determined from whole sagittae, and the magnitude of the difference increased with age (from sections). Rings on sectioned sagittae are considered to be true annual increments, forming during June-September. There was no clear pattern to ring formation on whole otoliths. The oldest fish examined was age 21. The daily nature of rings on lapilli of age 0 king mackerel was not validated, but if the marks are formed daily they suggest growth rates of approximately 0.47 mm/d for early larvae and 2.9 mm/d for fish 1-3 months of age

    Ecosystem Responses to Internal and Watershed Organic Matter Loading: Consequences for Hypoxia in the Eutrophying Neuse River Estuary, North Carolina, USA

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    The contrasting impacts of externally supplied (runoff) and internally generated (nutrient stimulated phytoplankton blooms) organic matter on oxygen (02) depletion were examined and evaluated in the eutrophic, salinity-stratified Neuse River Estuary, North Carolina, USA. This nitrogen (N)- limited estuary is experiencing increasing anthropogenic N loading from expanding urban, agricultural and industrial development in its watershed. Resultant algal blooms, which provided organic matter loads capable of causing extensive low 02 (hypoxic) and depleted 02 (anoxic) conditions, have induced widespread mortality of resident fin- and shellfish. Phytoplankton blooms followed periods of elevated N loading, except during extremely high runoff periods (e.g. hurricanes), when high rates of flushing and reduced water residence times did not allow sufficient time for bloom development. During these periods, hypoxia and anoxia were dominated by watershed-derived organic matter loading. Externally vs internally generated organic matter loading scenarios were examined in sequential years (1994 to 1996) to compare the differential impacts of an average discharge year (l0 yr mean hydrological conditions) (1994), N-stimulated summer algal blooms [1995), and a major hurricane (Fran; September 1996). The responses of primary production, hypoxia, and anoxia to these hydrologically contrasting years and resultant organic matter loadings help distinguish watershed from internal forcing of 02 dynamics and fish kills

    Effects of Microzooplankton Growth and Trophic Interactions on Herbivory in Coastal and Offshore Environments

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    We performed serial dilution experiments to estimate rates of gross phytoplankton growth (L) and grazing mortality (m) in both eutrophic (Corpus Christi Bay, Texas, USA) and oligotrophic (offshore Gulf of Mexico) waters. Two parallel experiments were performed in both environments, with seawater pre-screened through 153 or 25 Inn mesh to observe the responses of microzooplankton (MZP) to dilution treatments. MZP biomass changed over the duration of the experimental incubations; in several treatments, MZP net growth rates were \u3e1 d(-1). Patterns of growth varied between dilutions and initial screening size. In the eutrophic system, the ratio of phytoplankton grazing mortality rate to gross phytoplankton growth rate (m/mu) was 1.10 +/- 0.54 (mean +/- SD) versus 0.41 +/- 0.65 when screened through 153 and 25 pm mesh, respectively. This difference was attributed to cascading trophic interactions among MZP size groups leading to suppression of the primary herbivores in the 25 pm fraction and, in turn, a lower value of m. A food web model consisting of multiple trophic levels was constructed to examine the role of MZP growth and trophic interactions on measurements of p and m. The model, using 3 interacting groups of MZP, was able to reproduce experimental results. Model simulations demonstrated that MZP growth during incubation leads to an overestimation of m. Non-linearity in the phytoplankton growth response curves was due to MZP growth and trophic interactions in these model simulations, as variable feeding responses were not incorporated into the models. Trophic interactions among MZP can provide context to measurements of P. and m and insight into microbial food web efficiency
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