Showing 1621 - 1630 of 5709 Items
Winslow Homer's Work in Black and White: Selected Works from the Bowdoin College Museum of Art
Date: 1975-01-01
Access: Open access
- Exhibition catalogue Bowdoin College, Museum of Art.
Chloroplasts of Arabidopsis thaliana homozygous for the ch-1 locus lack chlorophyll b, lack stable LHCPII and have stacked thylakoids
Date: 1991-07-01
Creator: David L. Murray, Bruce D. Kohorn
Access: Open access
The Effects of Host Plant Species and Plant Quality on Growth and Development in the Meadow Spittlebug (Philaenus spumarius) on Kent Island in the Bay of Fundy
Date: 2020-03-01
Creator: Zoe M. Wood, Patricia L. Jones
Access: Open access
- Philaenus spumarius (Meadow Spittlebug, Homoptera: Cercopoidea) is a cosmopolitan generalist insect that feeds on a wide repertoire of host plants in the field. We studied density and growth of Meadow Spittlebugs on a range of host plants on Kent Island, a boreal island in the Bay of Fundy, NB, Canada. The highest spittlebug densities were on Cirsium arvense (Canadian Thistle), although spittlebugs had larger body sizes on Solidago rugosa (Rough-stemmed Goldenrod) and Anaphalis margaritacea (Pearly Everlasting). We fertilized plots of Rough-stemmed Goldenrod in the field over 3 weeks to examine the effects of plant quality on development of Meadow Spittlebugs. Following fertilization, there were fewer nymphs present in fertilized plots than in unfertilized plots, indicating faster nymph maturation to adulthood on fertilized plants. This study offers an initial report of the host plants used by Meadow Spittlebugs in northeastern boreal habitat, variation in density and performance of the species on a range of host plants, and the effects of plant fertilization on spittlebug life history.
A mutation in Tac1p, a transcription factor regulating CDR1 and CDR2, is coupled with loss of heterozygosity at chromosome 5 to mediate antifungal resistance in Candida albicans
Date: 2006-04-01
Creator: Alix Coste, Vincent Turner, Françoise Ischer, Joachim Morschhäuser, Anja, Forche, Anna Selmecki, Judith Berman, Jacques Bille, Dominique Sanglard
Access: Open access
- TAC1, a Candida albicans transcription factor situated near the mating-type locus on chromosome 5, is necessary for the upregulation of the ABC-transporter genes CDR1 and CDR2, which mediate azole resistance. We showed previously the existence of both wild-type and hyperactive TAC1 alleles. Wild-type alleles mediate upregulation of CDR1 and CDR2 upon exposure to inducers such as fluphenazine, while hyperactive alleles result in constitutive high expression of CDR1 and CDR2. Here we recovered TAC1 alleles from two pairs of matched azole-susceptible (DSY294; FH1: heterozygous at mating-type locus) and azole-resistant isolates (DSY296; FH3: homozygous at mating-type locus). Two different TAC1 wild-type alleles were recovered from DSY294 (TAC1-3 and TAC1-4) while a single hyperactive allele (TAC1-5) was isolated from DSY296. A single amino acid (aa) difference between TAC1-4 and TAC1-5 (Asn977 to Asp or N977D) was observed in a region corresponding to the predicted activation domain of Tac1p. Two TAC1 alleles were recovered from FH1 (TAC1-6 and TAC1-7) and a single hyperactive allele (TAC1-7) was recovered from FH3. The N977D change was seen in TAC1-7 in addition to several other aa differences. The importance of N977D in conferring hyperactivity to TAC1 was confirmed by site-directed mutagenesis. Both hyperactive alleles TAC1-5 and TAC1-7 were codominant with wild-type alleles and conferred hyperactive phenotypes only when homozygous. The mechanisms by which hyperactive alleles become homozygous was addressed by comparative genome hybridization and single nucleotide polymorphism arrays and indicated that loss of TAC1 heterozygosity can occur by recombination between portions of chromosome 5 or by chromosome 5 duplication. Copyright © 2006 by the Genetics Society of America.
Development of Rare Bacterial Monosaccharide Analogs for Metabolic Glycan Labeling in Pathogenic Bacteria
Date: 2016-12-16
Creator: Emily L. Clark, Madhu Emmadi, Katharine L. Krupp, Ananda R. Podilapu, Jennifer D., Helble, Suvarn S. Kulkarni, Danielle H. Dube
Access: Open access
- Bacterial glycans contain rare, exclusively bacterial monosaccharides that are frequently linked to pathogenesis and essentially absent from human cells. Therefore, bacterial glycans are intriguing molecular targets. However, systematic discovery of bacterial glycoproteins is hampered by the presence of rare deoxy amino sugars, which are refractory to traditional glycan-binding reagents. Thus, the development of chemical tools that label bacterial glycans is a crucial step toward discovering and targeting these biomolecules. Here, we explore the extent to which metabolic glycan labeling facilitates the studying and targeting of glycoproteins in a range of pathogenic and symbiotic bacterial strains. We began with an azide-containing analog of the naturally abundant monosaccharide N-acetylglucosamine and discovered that it is not broadly incorporated into bacterial glycans, thus revealing a need for additional azidosugar substrates to broaden the utility of metabolic glycan labeling in bacteria. Therefore, we designed and synthesized analogs of the rare deoxy amino d-sugars N-acetylfucosamine, bacillosamine, and 2,4-diacetamido-2,4,6-trideoxygalactose and established that these analogs are differentially incorporated into glycan-containing structures in a range of pathogenic and symbiotic bacterial species. Further application of these analogs will refine our knowledge of the glycan repertoire in diverse bacteria and may find utility in treating a variety of infectious diseases with selectivity.
Long-term trends in tropical fish larvae of the Hawaiian Islands revealed by DNA barcoding
Date: 2014-08-01
Creator: Jack Mitchell
Access: Open access
- DNA Barcoding is the identification of organisms through the use of a standardized portion of the genome, a concept first suggested by Hebert, et al (2003) and since developed to include standard databases and many campaigns internationally to identify and barcode all species in the world. Because DNA barcoding uses molecular data, rather than morphology, to identify organisms, it allows for the identification of organisms that are morphologically similar or have been processed to the point of unrecognizability. Barcoding has the potential to streamline and enhance conservation efforts drastically. Its "quick and easy" identification process allows better fisheries management, market regulation to ensure vendors are selling what they say they're selling (no more horsemeat burgers or dolphin sushi), and greater enforcement of regulations against the killing and selling of endangered animal products (Minhos et al., 2013). In my work this summer, I've been using DNA barcoding to examine the dynamics of a community of larval fish off the coast of Oahu through a seven-year longitudinal barcoding study. Fish larvae are very hard to identify morphologically because they lack obvious identifying characteristics. For this reason, barcoding is essential for accurately understanding the community structure of such fish. In my work, I analyze a set of sequences from the 5-prime region of the mitochondrial gene cytochrome oxidase subunit 1, widely used as a barcode in the animal kingdom, gathered from fish larvae collected off the coast of Oahu by the University of Hawaii Manoa Biology 301L class. The sampling consisted of a series of oblique plankton tows taken at three depths (5m, 25m, and 50m) between January and April every year from 2007 to 2013. During this period, a total of 833 fish larvae were sampled and sequenced. Using the Barcode of Life Data Systems (BOLD Systems) Identification Engine, I was able to identify 78% of all specimens to family-level or better, representing about 25% of the 202 families of shore fishes known to occur in Hawaiian coastal waters. The data stratification consisted of 7 years, each with three depths and 56 family groups, a 21 by 56 data matrix. In order to see the patterns of the matrix, I used Principal Components Analysis, a form of ordination, which distills multidimensional data to a form that is more easily visualized. This ordination revealed that 2009 and 2011 had highly anomalous community structure in which there were large increases in abundance (greater than three (3) Standard Deviations from the mean) of 12 family groups in each year, indicating concerted change in the structure of ichythoplankton in those years, though the families may be represented by a low number of specimens in the sample. Because these families had little to no representation in other years, we are able to rule out the possibility of results being skewed by a couple of families that showed up in our nets by chance that don't reflect the actual community structure. In these years, the highly anomalous families did not overlap, indicating that the factors causing the anomalies were non-identical. In 2009 there were eight families that deviated from the mean by over four (4) Standard Deviations, and in 2011 there were ten. Though the biggest groups of deviant families in both years were reef fish and mesopelagic fish, tropical habitat ranged from shallow water benthic (sea-bed) fish such as Ophichthidae, to bathypelagic (deep sea) fish such as the anglerfish family Ceratiidae. In my last few weeks working on this project I am exploring what environmental factors may have had a hand in such anomalies. El Niño cycles may have had a hand, as there was a weak La Niña (slightly cooler waters) anomaly leading into 2009, and a very strong La Niña (drastically cooler waters) anomaly leading into 2011 ("Cold and Warm Episodes by Season," 2014). The differences in community structure I detected had different signs, that is the co-variance of fish families was different for each of these years. This suggests that water temperature itself may not be causing these ecological patterns. A more likely hypothesis links the effects of El Niño/La Niña on oceanographic circulation throughout the Pacific and even near-shore in the Hawaiian Islands. These changes can drive differences in the delivery of larvae to the islands, as well as advection away from the islands. Further research in the remainder of the summer will attempt to gather more information on what may have caused the community structure anomalies. Final Report of research funded by Mary Lou Zeeman’s NSF grant - Computational Sustainability (NSF-CCF-0832788).
Multi-colony calibrations of coral Ba/Ca with a contemporaneous in situ seawater barium record
Date: 2016-04-15
Creator: Michèle LaVigne, Andréa G. Grottoli, James E. Palardy, Robert M. Sherrell
Access: Open access
- The coral skeleton barium to calcium ratio (Ba/Ca ), a proxy for seawater barium concentrations (Ba ), has been interpreted as a tracer of upwelling based on the characteristic "nutrient like" depth profile of Ba . However, in some tropical regions, such as the Gulf of Panamá, substantial influence of terrestrial runoff inputs and differences between the vertical distribution of Ba and that of the major nutrients (nitrate and phosphate) in the upper water column can complicate the interpretation of Ba/Ca as an upwelled nutrient proxy. In the Gulf of Panamá, contemporaneous Ba/Ca records from multiple colonies of Porites lobata, Pavona gigantea, and Pavona clavus corals record a nearly twofold change in surface water Ba as a 20-70% increase in skeletal Ba/Ca with excellent correlation among Ba/Ca records from co-located colonies (r = 0.86-0.99). These results provide, for the first time, an absolute calibration of the coral Ba proxy with a contemporaneous Ba record. Compiling the Ba/Ca records from three co-located colonies of each species into taxon-specific composite regressions reveals strong statistically significant correlations with the Ba time-series record (p < 0.001). Differences among taxa in regression slope, y-intercept, and average distribution coefficient, as well as a demonstration of the application of the P. clavus calibration to a previously published Ba/Ca record, emphasize the necessity of using taxon-specific calibrations to reconstruct changes in Ba with accuracy. These results support the application of Ba/Ca to reconstruct past changes in absolute Ba concentrations, adding an important tool to the collection of geochemical proxies for reconstructing surface ocean biogeochemical processes in the past. coral SW SW SW coral coral SW SW coral SW coral SW coral SW