200 research outputs found

    The Kara Sea: geologic structure and water characteristics

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    Movement of Atlantic Water into the Kara Sea is controlled by the bathymetry which funnels the inflow up three canyons along the eastern margin of the Svyataya Anna Trough. Mixing of the warm, saline Atlantic Water in these canyons with the considerable summer outflow of the Ob-Yenisey rivers results in the formation of Arctic Bottom Water and due to the presence and cooling by ice, in the formation of Arctic Surface Water. Both of these water masses then exit the Kara Sea as deep and shallow countercurrents to the incoming Atlantic Water. The northernmost canyon allows some Atlantic Water to exit the Kara Sea almost upon entrance, reducing the amount of heat and salt entering the Kara Sea. The presence and extent of the bottom sediments reflect the path of the rivers across the Kara. Inflow of deep Atlantic Water tends to reduce this effect and results in scoured areas at the heads of the canyons, which are sites of turbulent mixing. Ice is a major factor in the Kara Sea. It cools and dilutes the surrounding water. In the form of icebergs, it gouges paths through the soft, shallow, deltaic sediments and in the deeper areas, deposits ice rafted material

    Within-Litter Birth Weight Variation in the Domestic Pig and its Relation to Pre-Weaning Survival, Weight Gain, and Variation in Weaning Weights

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    To determine the relationship between within-litter birth weight variation and pre-weaning survival and weight gain, and to provide practical guidance on fostering low-birth-weight piglets, we analyzed piglet survival and weight gain in litters of piglets from 52 sows followed through eight consecutive parities. Litters with high variation in birth weight had more deaths, especially if the litterā€™s mean birth weight was low. High variation in birth weight was also associated with high variation in weaning weight, but was not significantly related to mean weaning weight. Piglets with birth weights well below the range of most of the litter (ā€˜low-birth-weight pigletsā€™) were more likely to die than their litter-mates, but their weight gains were normal for their birth weight if they survived. These piglets experienced particularly low survival in larger litters and litters from sows of sixth parity or older. Litters containing low-birth-weight piglets started, on average, with more piglets born alive and had a lower pre-weaning survival (with the majority of deaths being low-birth-weight piglets), but did not wean significantly more piglets than litters without low-birth-weight piglets. The majority of litters had a negatively skewed distribution of birth weights, with more piglets well below the mean than well above it. Our data are consistent with the hypothesis that high variation in birth weight contributes to reduced survival, at least for litters of low mean birth weight, and to variable weaning weights. Our data also support the hypothesis that in terms of survival, small piglets have a competitive disadvantage compared to their heavier litter-mates, a disadvantage that is exacerbated in large litters and litters from older sows. Our data suggest that selection for increased litter size that results in more low-birth-weight piglets per litter may not be beneficial unless measures are undertaken to improve the survival of low-birth-weight piglets

    The Effect of Littermate Weight on Survival, Weight Gain, and Suckling Behavior of Low-Birth-Weight Piglets in Cross-Fostered Litters

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    Objective: To determine whether low-birth-weight piglets show better survival, weight gain, and suckling behavior when grouped with other small piglets by cross-fostering. Methods: We manipulated the number and size of foster littermates for low-birth-weight piglets in 31 small (eight or nine piglets) and 22 large (11 or 12 piglets) litters. Experimental litters were composed of four to six piglets of lowest birth weight and either four to six slightly heavier or four to six much heavier piglets from two combined litters. Results: Low-birth-weight piglets raised with much heavier littermates had somewhat lower survival rates, but showed no tendency towards lower weight gains or less successful suckling behavior than low-birth-weight piglets raised with slightly heavier littermates. The somewhat higher survival rate of low-birth-weight piglets raised with slightly heavier littermates was largely offset by more deaths in the foster littermates, so there was no overall reduction in total losses. Low-birth-weight piglets fought more when raised with slightly heavier piglets than with much heavier piglets, and they missed more nursing episodes and had smaller weight gains than littermates, regardless of littermate weight. Implications: Cross-fostering low-birth-weight pigs into litters with other small pigs, compared to fostering into litters with high-birth-weight pigs, slightly improved their survival, but did not affect their weight gain or ability to suckle successfully, nor overall litter survival, even in litters as large as 11 or 12 piglets. Cross-fostering low-birth-weight pigs to litters of similar birth weight increased the level of fighting

    Within-Litter Birth Weight Variation in the Domestic Pig and its Relation to Pre-Weaning Survival, Weight Gain, and Variation in Weaning Weights

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    To determine the relationship between within-litter birth weight variation and pre-weaning survival and weight gain, and to provide practical guidance on fostering low-birth-weight piglets, we analyzed piglet survival and weight gain in litters of piglets from 52 sows followed through eight consecutive parities. Litters with high variation in birth weight had more deaths, especially if the litterā€™s mean birth weight was low. High variation in birth weight was also associated with high variation in weaning weight, but was not significantly related to mean weaning weight. Piglets with birth weights well below the range of most of the litter (ā€˜low-birth-weight pigletsā€™) were more likely to die than their litter-mates, but their weight gains were normal for their birth weight if they survived. These piglets experienced particularly low survival in larger litters and litters from sows of sixth parity or older. Litters containing low-birth-weight piglets started, on average, with more piglets born alive and had a lower pre-weaning survival (with the majority of deaths being low-birth-weight piglets), but did not wean significantly more piglets than litters without low-birth-weight piglets. The majority of litters had a negatively skewed distribution of birth weights, with more piglets well below the mean than well above it. Our data are consistent with the hypothesis that high variation in birth weight contributes to reduced survival, at least for litters of low mean birth weight, and to variable weaning weights. Our data also support the hypothesis that in terms of survival, small piglets have a competitive disadvantage compared to their heavier litter-mates, a disadvantage that is exacerbated in large litters and litters from older sows. Our data suggest that selection for increased litter size that results in more low-birth-weight piglets per litter may not be beneficial unless measures are undertaken to improve the survival of low-birth-weight piglets

    Diversity of Lecidea (Lecideaceae, Ascomycota) species revealed by molecular data and morphological characters

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    The diversity of lichens, especially crustose species, in continental Antarctica is still poorly known. To overcome difficulties with the morphology based species delimitations in these groups, we employed molecular data (nuclear ITS and mitochondrial SSU rDNA sequences) to test species boundaries within the genus Lecidea. Sampling was done along a northā€“south transect at five different areas in the Ross Sea region (Cape Hallett, Botany Bay to Mount Suess, Taylor Valley, Darwin Area and Mount Kyffin). A total of 153 specimens were collected from 13 localities. Phylogenetic analyses also include specimens from other regions in Antarctica and non-Antarctic areas. Maximum parsimony, maximum likelihood and Bayesian analyses agreed in placing the samples from continental Antarctica into four major groups. Based on this phylogenetic estimate, we restudied the micromorphology and secondary chemistry of these four clades to evaluate the use of these characters as phylogenetic discriminators. These clades are identified as the following species Lecidea cancriformis, L. andersonii as well as the new species L. polypycnidophora Ruprecht & TĆ¼rk sp. nov. and another previously unnamed clade of uncertain status, referred to as Lecidea sp. (L. UCR1)

    PSP toxin levels and plankton community composition and abundance in size-fractionated vertical profiles during spring/summer blooms of the toxic dinoflagellate Alexandrium fundyense in the Gulf of Maine and on Georges Bank, 2007, 2008, and 2010 : 1. Toxin levels

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    This paper is not subject to U.S. copyright. The definitive version was published in Deep Sea Research Part II: Topical Studies in Oceanography 103 (2014): 329ā€“349, doi:10.1016/j.dsr2.2013.04.013.As part of the NOAA ECOHAB funded Gulf of Maine Toxicity (GOMTOX)1 project, we determined Alexandrium fundyense abundance, paralytic shellfish poisoning (PSP) toxin composition, and concentration in quantitatively-sampled size-fractionated (20ā€“64, 64ā€“100, 100ā€“200, 200ā€“500, and >500 Ī¼m) particulate water samples, and the community composition of potential grazers of A. fundyense in these size fractions, at multiple depths (typically 1, 10, 20 m, and near-bottom) during 10 large-scale sampling cruises during the A. fundyense bloom season (Mayā€“August) in the coastal Gulf of Maine and on Georges Bank in 2007, 2008, and 2010. Our findings were as follows: (1) when all sampling stations and all depths were summed by year, the majority (94%Ā±4%) of total PSP toxicity was contained in the 20ā€“64 Ī¼m size fraction; (2) when further analyzed by depth, the 20ā€“64 Ī¼m size fraction was the primary source of toxin for 97% of the stations and depths samples over three years; (3) overall PSP toxin profiles were fairly consistent during the three seasons of sampling with gonyautoxins (1, 2, 3, and 4) dominating (90.7%Ā±5.5%), followed by the carbamate toxins saxitoxin (STX) and neosaxitoxin (NEO) (7.7%Ā±4.5%), followed by n-sulfocarbamoyl toxins (C1 and 2, GTX5) (1.3%Ā±0.6%), followed by all decarbamoyl toxins (dcSTX, dcNEO, dcGTX2&3) (<1%), although differences were noted between PSP toxin compositions for nearshore coastal Gulf of Maine sampling stations compared to offshore Georges Bank sampling stations for 2 out of 3 years; (4) surface cell counts of A. fundyense were a fairly reliable predictor of the presence of toxins throughout the water column; and (5) nearshore surface cell counts of A. fundyense in the coastal Gulf of Maine were not a reliable predictor of A. fundyense populations offshore on Georges Bank for 2 out of the 3 years sampled.Vangie Shue was supported through the FDA and also through the Thomas Jefferson High School for Science and Technology Mentorship Program. Research support was provided by National Oceanic and Atmospheric Administration Grant NA06NOS4780245 for the Gulf of Maine Toxicity (GOMTOX) program. BAK, DJM, and DMA were partially supported by the Woods Hole Center for Oceans and Human Health through National Science Foundation Grants OCE-0430724 and OCE-0911031 and National Institute of Environmental Health Sciences Grant 1P50-ES01274201

    Using clay to control harmful algal blooms : deposition and resuspension of clay/algal flocs

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    Author Posting. Ā© Elsevier B.V, 2005. This is the author's version of the work. It is posted here by permission of Elsevier B.V for personal use, not for redistribution. The definitive version was published in Harmful Algae 4 (2005): 123-138, doi:10.1016/j.hal.2003.12.008.Harmful algal blooms (HABs) may be legitimate targets for direct control or mitigation, due to their impacts on commercial fisheries and public health. One promising control strategy is the rapid sedimentation of HABs through flocculation with clay. The objective of this study was to evaluate flow environments in which such a control strategy might be effective in removing harmful algae from the water column and depositing a layer of clay/algal flocs on the sea floor. We simulated the natural environment in two laboratory flumes: a straight-channel ā€œ17-m flumeā€ in which flocs settled in a still water column and a ā€œracetrack flumeā€ in which flocs settled in flow. The 17-m flume experiments were designed to estimate the critical bed shear stress for resuspension of flocs that had settled for different time periods. The racetrack flume experiments were designed to examine the deposition and repeated resuspension of flocs in a system with tidal increases in flow speed. All flume runs were conducted with the non-toxic dinoflagellate Heterocapsa triquetra and phosphatic clay (IMC-P4). We repeated the experiments with a coagulant, polyaluminum hydroxychloride (PAC), expected to enhance the removal efficiency of the clay. Our experiments indicated that at low flow speeds (ā‰¤ 10 cm s-1), phosphatic clay was effective at removing algal cells from the water column, even after repeated resuspension. Once a layer of flocs accumulated on the bed, the consolidation, or dewatering, of the layer over time increased the critical shear stress for resuspension (i.e. decreased erodibility). Resuspension of a 2-mm thick layer that settled for 3 hours in relatively low flow speeds (ā‰¤ 3 cm s-1) would be expected at bed shear stress of ~0.06-0.07 Pa, as compared to up to 0.09 Pa for a layer that was undisturbed for 9 or 24 hours. For the same experimental conditions, the addition of PAC decreased the removal efficiency of algal cells in flow and increased the erodibility of flocs from the bottom. By increasing the likelihood that flocs remain in suspension, the addition of PAC in field trials of clay dispersal might have greater impact on sensitive, filter-feeding organisms. Overall, our experiments suggest that the flow environment should be considered before using clay as a control strategy for HABs in coastal waters.This project was funded by the Florida Institute of Phosphate Research (Grant # 99-03-138), with facilities provided by the Rinehart Coastal Research Center at WHOI

    Outcomes after alemtuzumab-containing reduced-intensity allogeneic transplantation regimen for relapsed and refractory non-Hodgkin lymphoma

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    18-60 months) , the actuarial overall survival (OS) rates at 3 years were 34% for HG-NHL, 60% for MCL, and 73% for LG-NHL (P &lt; .001). The 100-day and 3-year transplant-related mortality (TRM) rates for patients with LG-NHL were 2% and 11%, respectively, and were better (P ā€«Ųā€¬ .01) than they were for patients with HG-NHL (27% and 38%, respectively). The actuarial current progression-free survival (PFS) rate at 3 years, including the rate for patients who achieved remission after donor lymphocyte infusion (DLI) for progression, was 65% for LG-NHL, 50% for MCL, and 34% for HG-NHL (P ā€«Ųā€¬ .002)
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