Showing 1151 - 1200 of 5831 Items

Bowdoin Orient, v. 91, no. 4

Date: 1961-05-12

Access: Open access



Bowdoin Orient, v. 91, no. 17

Date: 1962-03-08

Access: Open access



Bowdoin Orient, v. 108, no. 7

Date: 1978-11-03

Access: Open access



Bowdoin Orient, v. 108, no. 6

Date: 1978-10-27

Access: Open access



Bowdoin Orient, v. 108, no. 11

Date: 1978-12-08

Access: Open access



Bowdoin Orient, v. 110, no. 10

Date: 1980-11-21

Access: Open access



Bowdoin Orient, v. 92, no. 6

Date: 1962-05-18

Access: Open access



Bowdoin Orient, v. 94, no. 18

Date: 1964-10-30

Access: Open access



Bowdoin Orient, v. 95, no. [13]

Date: 1965-10-08

Access: Open access



Bowdoin Orient, v. 96, no. 7

Date: 1966-11-11

Access: Open access



Bowdoin Orient, v. 95, no. 27

Date: 1966-03-11

Access: Open access



Bowdoin Orient, v. 95, no. 1

Date: 1965-02-19

Access: Open access



Bowdoin Orient, v. 94, no. 6

Date: 1964-03-20

Access: Open access



Bowdoin Orient, v. 95, no. 24

Date: 1966-02-18

Access: Open access



Bowdoin Orient, v. 95, no. 14

Date: 1965-10-15

Access: Open access



Bowdoin Orient, v. 95, no. 18

Date: 1965-11-12

Access: Open access



Bowdoin Orient, v. 96, no. 13

Date: 1967-02-17

Access: Open access



Bowdoin Orient, v. 96, no. 19

Date: 1967-04-14

Access: Open access



Bowdoin Orient, v. 95, no. 16

Date: 1965-10-29

Access: Open access



Bowdoin Orient, v. 109, no. 5

Date: 1979-10-05

Access: Open access



Bowdoin Orient, v. 109, no. 1

Date: 1979-09-07

Access: Open access



Bowdoin Orient, v. 94, no. 9

Date: 1964-05-01

Access: Open access



Bowdoin Orient, v. 94, no. 19

Date: 1964-11-06

Access: Open access



Bowdoin Orient, v. 109, no. 21

Date: 1980-04-11

Access: Open access



Bowdoin Orient, v. 110, no. 1

Date: 1980-09-12

Access: Open access



Bowdoin Orient, v. 93, no. 5

Date: 1963-05-10

Access: Open access



Bowdoin Orient, v. 93, no. 10

Date: 1963-10-25

Access: Open access



Bowdoin Orient, v. 117, no. 6

Date: 1987-10-23

Access: Open access



Bowdoin Orient, v. 118, no. 13

Date: 1989-01-27

Access: Open access



Bowdoin Orient, v. 118, no. 10

Date: 1988-11-18

Access: Open access



Bowdoin Orient, v. 118, no. 14

Date: 1989-02-03

Access: Open access



Bowdoin Orient, v. 116, no. 22

Date: 1987-03-12

Access: Open access



Bowdoin Orient, v. 117, no. 18

Date: 1988-03-04

Access: Open access



Bowdoin Orient, v. 116, no. [9]

Date: 1986-10-31

Access: Open access



Bowdoin Orient, v. 116, no. 6

Date: 1986-10-03

Access: Open access



Reference Points, Prospect Theory, and Momentum on the PGA Tour

Date: 2016-06-01

Creator: Daniel F. Stone, Jeremy Arkes

Access: Open access

Pope and Schweitzer (2011) study predictions of prospect theory for the reference point of par on the current hole in professional golf. We study prospect-theory predictions of three other plausible reference points: par for recent holes, for the round, and for the tournament. A potentially competing force is momentum in quality of play, that is, the hot or cold hand. While prospect theory predicts negative serial correlation in better (worse)-than-average performance across holes, the hot (cold) hand implies the opposite. We find evidence that, for each of the reference points we study, when scores are better than par, hot-hand effects are dominated by prospect-theory effects. These effects can occur via two mechanisms: greater conservatism or less effort. We find evidence that the former (latter) dominates for scores closer to (further from) the reference point. We also find evidence of prospect theory effects (greater risk seeking) when scores are worse than par for the round in Round 1 and of cold-hand effects for scores worse than par for the tournament in Round 3. The magnitudes of some of the joint effects are comparable to those found by Pope and Schweitzer and other related papers. We conclude by discussing how, rather than compete, prospect-theory and cold-hand forces might also cause one another.


Quantification and Characterization of AST-C Peptides in Homarus americanus Using Mass Spectrometry

Date: 2014-08-01

Creator: Amanda Howard

Access: Open access

Neuropeptides are small signaling molecules found throughout the nervous system that are responsible for influencing animal behavior. They consist of short amino acid chains and interact with cell-membrane receptors in order to regulate behavioral responses (Fig. 1a). The American lobster, Homarus americanus, has proven to be a strong model organism in which to study such activity due to the simplicity of the system and the wealth of existing knowledge about the animal. One neuropeptide found in H. americanus is a C-type allatostatin (AST-C). Allatostatins are a family of neuropeptides originally identified in insects that inhibits juvenile hormone production. The H. americanus AST-C has a pyroglutamate blocked N-terminus and an unmodified C-terminus (Fig. 1b). In addition to AST-C, a different, yet structurally similar neuropeptide has been found in H. americanus. This peptide has an unmodified N-terminus and an amidated C-terminus (Fig. 1c). Both forms of AST-C (referred to as ASTC-real and ASTC-like) also have a disulfide bond between their two cysteine residues. In the lobster, both peptides influence cardiac muscle contraction patterns and have been found in various tissues throughout the nervous system [1, 2]. In order to establish the purpose of the observed post-translational modifications, this study aims to find whether these peptides exist in other forms in the lobster and to determine their relative and absolute concentrations.Liquid chromatography-mass spectrometry (LC-MS) and tandem mass spectrometry (MS/MS) are often used in analytical chemistry to characterize complex samples and identify neuropeptides. First, sample components are separated by chromatography based on properties such as size and hydrophobicity. Using mass spectrometry (MS), peptides are protonated (positively charged) and their mass is determined from their measured mass-to-charge ratios. These peptides are lastly fragmented into many ions using MS/MS, which ultimately allows them to be sequenced in order to determine their identity. This summer, standards of the two AST-C peptides have been characterized by LC-MS/MS. The reduced forms of both peptides have been synthesized by chemically reducing the disulfide bond and were also analyzed by MS/MS. As expected, the structural stability provided by the disulfide bond prevented fragmentation during MS/MS analysis; that is, there was evidence of more fragmentation in the reduced forms than in the fully processed forms (Fig. 2). When looking for other forms of ASTC, these findings will facilitate the identification of the reduced forms in crustacean tissue.To assess the accuracy of the detection method used, detection limits were assessed by analyzing sample matrices augmented with known amounts of peptide standards. The smallest amount of peptide detected from a single injection was 25 fmol (2.5Ā·10-14 mol) peptide. There appeared to be a strongly linear relationship between the amount of ASTC-real injected and the instrument response (chromatographic peak area) (R2=0.996, n=6). However, the relationship between the amount of ASTC-like injected and the instrument response was less linear (R2=0.802, n=5), and the calibration slope was more shallow, indicating that this peptide is more difficult to detect. This is possibly because ASTC-real, unlike ASTC-like, contains an arginine (R) and a histidine (H) residue, two basic amino acids susceptible to protonation. Therefore, it seems that ASTC-real is more easily protonated during the ionization process in MS analysis, causing it to be more readily detected.Lastly, ASTC-real has been identified in the pericardial organ (PO), a tissue responsible for delivering neuropeptides manufactured in the thoracic ganglion to the heart in order to control muscle contraction. ASTC-like is also believed to be present in the PO based on previous work in the Dickinson lab (E. Dickinson, unpublished data), but it is likely that it has not yet been detected in this study due to the detection limitations described above. To address these issues, more tissues will be pooled to increase the amount of peptide in each sample analyzed.Currently, tissue extraction methods are being optimized to eliminate phospholipid contamination and to maximize detection sensitivity. Specifically, two separate extraction solvents as well as a chloroform delipidation procedure are being tested. Future goals include quantifying peptide levels by adding a known amount of internal standard to the samples and comparing instrument responses for ASTC and for internal standard. Additionally, known amounts of peptide standard will be brought through the extraction process to determine the amount of peptide loss throughout this procedure. During the upcoming academic year, this study will be continued as an Honor’s project. Further research in these areas will ultimately help explain how neuropeptides interact to regulate behavior within the lobster and in more complex systems. Final Report of research funded by the Henry L. and Grace Doherty Charitable Foundation Coastal Studies Research Fellowship.


Effects of octopamine and tyramine on the cardiac system of the lobster, Homarus americanus

Date: 2019-05-01

Creator: Casey Breslow

Access: Open access

Modulation in neural systems is important for regulating physiology and behavior (Wright et al., 2010). Peptides, hormones, and amines are common neural modulators, acting on many neural systems across species. One group of neural networks that can be regulated are central pattern generators (CPGs), which generate rhythmic neural patterns, which drive behaviors (Marder and Bucher, 2001). Octopamine, and its precursor tyramine, are two amines that have been found to regulate (CPGs) across species (Cooke, 2002; Fussnecker et al., 2006). One role of octopamine in the decapod neurogenic heart is regulating the frequency and the duration of heart beats. However, the precise site of octopamine modulation within the cardiac system is not yet known (Kurumoto and Ebara, 1991). One possible site of action is the cardiac ganglion (CG), the CPG in decapod hearts. The transcripts for the enzymes required to synthesize octopamine from tyramine have been identified and localized in the CG (Christie et al., 2018). This would suggest that octopamine is produced in the CG, where it could have a direct action on those neurons, or it could be released peripherally. We have found individual variation in the response to octopamine and its precursor tyramine, and significant effects of frequency and contraction amplitude in the whole heart.


Holocene peatland carbon dynamics in the circum-Arctic region: An introduction

Date: 2014-01-01

Creator: Zicheng Yu, Julie Loisel, Daniel J. Charman, David W. Beilman, Philip, Camill

Access: Open access

Peatlands represent the largest and most concentrated carbon pool in the terrestrial biosphere, and their dynamics during the Holocene have had significant impacts on the global carbon cycle. In this Introduction paper, we provide an overview of the contributions presented in this Special Issue on Holocene peatland carbon dynamics. We also provide a brief history and current status of peat-core-based research on peatland carbon dynamics. Finally, we identify and discuss some challenges and opportunities that would guide peatland carbon research in the near future. These challenges and opportunities include the need to fill data gaps and increase geographic representations of peat carbon accumulation records, a better understanding of peatland lateral expansion process and improved estimate of peatland area change over time, developing regional carbon accumulation histories and carbon pool estimates, and projecting and quantifying overall peatland net carbon balance in a changing world.


Midterm Decline in Comparative Perspective

Date: 2019-05-01

Creator: Duncan Gans

Access: Open access



Aneuploidy and isochromosome formation in drug-resistant Candida albicans

Date: 2006-07-21

Creator: Anna Selmecki, Anja Forche, Judith Berman

Access: Open access

Resistance to the limited number of available antifungal drugs is a serious problem in the treatment of Candida albicans. We found that aneuploidy in general and a specific segmental aneuploidy, consisting of an isochromosome composed of the two left arms of chromosome 5, were associated with azole resistance. The isochromosome forms around a single centromere flanked by an inverted repeat and was found as an independent chromosome or fused at the telomere to a full-length homolog of chromosome 5. Increases and decreases in drug resistance were strongly associated with gain and loss of this isochromosome, which bears genes expressing the enzyme in the ergosterol pathway targeted by azole drugs, efflux pumps, and a transcription factor that positively regulates a subset of efflux pump genes.


Attention training toward and away from threat in social phobia: Effects on subjective, behavioral, and physiological measures of anxiety

Date: 2012-01-01

Creator: Alexandre Heeren, Hannah E. Reese, Richard J. McNally, Pierre Philippot

Access: Open access

Social phobics exhibit an attentional bias for threat in probe detection and probe discrimination paradigms. Attention training programs, in which probes always replace nonthreatening cues, reduce attentional bias for threat and self-reported social anxiety. However, researchers have seldom included behavioral measures of anxiety reduction, and have never taken physiological measures of anxiety reduction. In the present study, we trained individuals with generalized social phobia (n = 57) to attend to threat cues (attend to threat), to attend to positive cues (attend to positive), or to alternately attend to both (control condition). We assessed not only self-reported social anxiety, but also behavioral and physiological measures of social anxiety. Participants trained to attend to nonthreatening cues demonstrated significantly greater reductions in self-reported, behavioral, and physiological measures of anxiety than did participants from the attend to threat and control conditions. Ā© 2011 Elsevier Ltd.


Report of the President, Bowdoin College 1907-1908

Date: 1908-01-01

Access: Open access



Estimated stocks of circumpolar permafrost carbon with quantified uncertainty ranges and identified data gaps

Date: 2014-12-01

Creator: G. Hugelius, J. Strauss, S. Zubrzycki, J. W. Harden, E. A.G., Schuur, C. L. Ping, L. Schirrmeister, G. Grosse, G. J. Michaelson, C. D. Koven, J. A. O'Donnell, B. Elberling, U. Mishra, P. Camill, Z. Yu, J. Palmtag

Access: Open access

Soils and other unconsolidated deposits in the northern circumpolar permafrost region store large amounts of soil organic carbon (SOC). This SOC is potentially vulnerable to remobilization following soil warming and permafrost thaw, but SOC stock estimates were poorly constrained and quantitative error estimates were lacking. This study presents revised estimates of permafrost SOC stocks, including quantitative uncertainty estimates, in the 0-3 m depth range in soils as well as for sediments deeper than 3 m in deltaic deposits of major rivers and in the Yedoma region of Siberia and Alaska. Revised estimates are based on significantly larger databases compared to previous studies. Despite this there is evidence of significant remaining regional data gaps. Estimates remain particularly poorly constrained for soils in the High Arctic region and physiographic regions with thin sedimentary overburden (mountains, highlands and plateaus) as well as for deposits below 3 m depth in deltas and the Yedoma region. While some components of the revised SOC stocks are similar in magnitude to those previously reported for this region, there are substantial differences in other components, including the fraction of perennially frozen SOC. Upscaled based on regional soil maps, estimated permafrost region SOC stocks are 217 ± 12 and 472 ± 27 Pg for the 0-0.3 and 0-1 m soil depths, respectively (±95% confidence intervals). Storage of SOC in 0-3 m of soils is estimated to 1035 ± 150 Pg. Of this, 34 ± 16 Pg C is stored in poorly developed soils of the High Arctic. Based on generalized calculations, storage of SOC below 3 m of surface soils in deltaic alluvium of major Arctic rivers is estimated as 91 ± 52 Pg. In the Yedoma region, estimated SOC stocks below 3 m depth are 181 ± 54 Pg, of which 74 ± 20 Pg is stored in intact Yedoma (late Pleistocene ice- and organic-rich silty sediments) with the remainder in refrozen thermokarst deposits. Total estimated SOC storage for the permafrost region is ∼1300 Pg with an uncertainty range of ∼1100 to 1500 Pg. Of this, ∼500 Pg is in non-permafrost soils, seasonally thawed in the active layer or in deeper taliks, while ∼800 Pg is perennially frozen. This represents a substantial ∼300 Pg lowering of the estimated perennially frozen SOC stock compared to previous estimates.


David Batchelder: Photographs

Date: 1969-01-01

Creator: Richard V. West

Access: Open access

Catalog of an exhibition held at the Bowdoin College Museum of Art.


Lesley Vance

Date: 2011-01-01

Creator: Diana K. Tuite

Access: Open access

Catalog of an exhibition held April 12-July 1, 2012, at the Bowdoin College Museum of Art, Brunswick, Maine. Includes essay "Conspiring forms" by Diana Tuite (p. 2-3)


Report of the President, Bowdoin College 1994-1995

Date: 1995-01-01

Access: Open access



Kernel functions on domains with hyperelliptic double

Date: 1977-01-01

Creator: William H. Barker

Access: Open access

Iii this paper we show that the structure of the Bergman and Szegö kernel functions is especially simple on domains with hyperelliptic double. Each such domain is conformally equivalent to the exterior of a system of slits taken from the real axis, and on such domains the Bergman kernel function and its adjoint are essentially the same, while the Szegö kernel function and its adjoint are elementary and can be written in a closed form involving nothing worse than fourth roots of polynomials. Additionally, a number of applications of these results are obtained. © 1977 American Mathematical Society.


The premonitory urge to tic: Measurement, characteristics, and correlates in older adolescents and adults

Date: 2014-01-01

Creator: Hannah E. Reese, Lawrence Scahill, Alan L. Peterson, Katherine Crowe, Douglas W., Woods, John Piacentini, John T. Walkup, Sabine Wilhelm

Access: Open access

In addition to motor and/or vocal tics, many individuals with Tourette syndrome (TS) or chronic tic disorder (CTD) report frequent, uncomfortable sensory phenomena that immediately precede the tics. To date, examination of these premonitory sensations or urges has been limited by inconsistent assessment tools. In this paper, we examine the psychometric properties of a nine-item self-report measure, the Premonitory Urge to Tic Scale (PUTS) and examine the characteristics and correlates of the premonitory urge to tic in a clinical sample of 122 older adolescents and adults with TS or CTD. The PUTS demonstrated adequate internal consistency, temporal stability, and concurrent validity. Premonitory urges were endorsed by the majority of individuals. Most individuals reported some relief from the urges after completing a tic and being able to stop their tics even if only temporarily. Degree of premonitory urges was not significantly correlated with age, and we did not observe any gender differences. Degree of premonitory urges was significantly correlated with estimated IQ and tic severity, but not severity of comorbid obsessive-compulsive disorder or attention-deficit hyperactivity disorder. Also, it was not related to concomitant medication status. These findings represent another step forward in our understanding of the premonitory sensations associated with TS and CTD. Ā© 2013.


The capacity to act in trans varies among drosophila enhancers

Date: 2016-05-01

Creator: Amanda J. Blick, Ilana Mayer-Hirshfeld, Beatriz R. Malibiran, Matthew A. Cooper, Pieter A., Martino, Justine E. Johnson, Jack R. Bateman

Access: Open access

The interphase nucleus is organized such that genomic segments interact in cis, on the same chromosome, and in trans, between different chromosomes. In Drosophila and other Dipterans, extensive interactions are observed between homologous chromosomes, which can permit enhancers and promoters to communicate in trans. Enhancer action in trans has been observed for a handful of genes in Drosophila, but it is as yet unclear whether this is a general property of all enhancers or specific to a few. Here, we test a collection of well-characterized enhancers for the capacity to act in trans. Specifically, we tested 18 enhancers that are active in either the eye or wing disc of third instar Drosophila larvae and, using two different assays, found evidence that each enhancer can act in trans. However, the degree to which trans-action was supported varied greatly between enhancers. Quantitative analysis of enhancer activity supports a model wherein an enhancer’s strength of transcriptional activation is a major determinant of its ability to act in trans, but that additional factors may also contribute to an enhancer’s trans-activity. In sum, our data suggest that a capacity to activate a promoter on a paired chromosome is common among Drosophila enhancers.