35 results
VERTICO V: The environmentally driven evolution of the inner cold gas discs of Virgo cluster galaxies
- Adam B. Watts, Luca Cortese, Barbara Catinella, Toby Brown, Christine D. Wilson, Nikki Zabel, Ian D. Roberts, Timothy A. Davis, Mallory Thorp, Aeree Chung, Adam R.H. Stevens, Sara L. Ellison, Kristine Spekkens, Laura C. Parker, Yannick M. Bahé, Vicente Villanueva, María Jiménez-Donaire, Dhruv Bisaria, Alessandro Boselli, Alberto D. Bolatto, Bumhyun Lee
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- Journal:
- Publications of the Astronomical Society of Australia / Volume 40 / 2023
- Published online by Cambridge University Press:
- 27 April 2023, e017
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The quenching of cluster satellite galaxies is inextricably linked to the suppression of their cold interstellar medium (ISM) by environmental mechanisms. While the removal of neutral atomic hydrogen (H i) at large radii is well studied, how the environment impacts the remaining gas in the centres of galaxies, which are dominated by molecular gas, is less clear. Using new observations from the Virgo Environment traced in CO survey (VERTICO) and archival H i data, we study the H i and molecular gas within the optical discs of Virgo cluster galaxies on 1.2-kpc scales with spatially resolved scaling relations between stellar ($\Sigma_{\star}$), H i ($\Sigma_{\text{H}\,{\small\text{I}}}$), and molecular gas ($\Sigma_{\text{mol}}$) surface densities. Adopting H i deficiency as a measure of environmental impact, we find evidence that, in addition to removing the H i at large radii, the cluster processes also lower the average $\Sigma_{\text{H}\,{\small\text{I}}}$ of the remaining gas even in the central $1.2\,$kpc. The impact on molecular gas is comparatively weaker than on the H i, and we show that the lower $\Sigma_{\text{mol}}$ gas is removed first. In the most H i-deficient galaxies, however, we find evidence that environmental processes reduce the typical $\Sigma_{\text{mol}}$ of the remaining gas by nearly a factor of 3. We find no evidence for environment-driven elevation of $\Sigma_{\text{H}\,{\small\text{I}}}$ or $\Sigma_{\text{mol}}$ in H i-deficient galaxies. Using the ratio of $\Sigma_{\text{mol}}$-to-$\Sigma_{\text{H}\,{\small\text{I}}}$ in individual regions, we show that changes in the ISM physical conditions, estimated using the total gas surface density and midplane hydrostatic pressure, cannot explain the observed reduction in molecular gas content. Instead, we suggest that direct stripping of the molecular gas is required to explain our results.
5 - Female Intersexual Selection
- from Part I - Precopulatory Adaptations
- Edited by Todd K. Shackelford, Oakland University, Michigan
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- Book:
- The Cambridge Handbook of Evolutionary Perspectives on Sexual Psychology
- Published online:
- 30 June 2022
- Print publication:
- 21 July 2022, pp 118-150
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Summary
Relative to other species, human females invest considerable effort in attracting and retaining mates. Stroll the aisles of any bookstore and you may come across titles such as “Get the guy: Learn secrets of the male mind to find the man you want and the love you deserve” (Hussey, 2014), and “Texts so good he can't ignore: Sassy texting secrets for attracting high-quality men” (Bryans, 2018). A desire to attract and retain mates underlies diverse facets of women’s psychology and behavior, including displaying or enhancing aspects of one’s personality and physical appearance. Not surprisingly, these efforts correspond with men’s mate preferences. Human males are unique in their relative choosiness surrounding their mates, especially within the context of long-term pair-bonding. Look further in that bookstore aisle and you might come across a title such as “The man's handbook for choosing the right woman” (Daniels, 2009). In this chapter, we examine the theoretical rationale underlying female intersexual selection. We begin with a discussion of the theory underlying human mate choice, highlighting why men’s choosiness has been selected for, and why this compels women to exert effort toward attracting men. We then discuss specific characteristics of men’s short-term and long-term mate choice, and the multitude of tactics women utilize to better embody those traits. We describe preliminary evidence surrounding how intersexual selection may have shaped some phenotypic traits in women as costly signals of underlying fertility or immunocompetence. Finally, we discuss both individual and contextual differences among women in their mating effort and provide suggestions for future research directions aimed at further understanding how intersexual selection has shaped women’s mating psychology.
2 - Men’s Extra-Pair Sexual Interest
- from Part I - Precopulatory Adaptations
- Edited by Todd K. Shackelford, Oakland University, Michigan
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- Book:
- The Cambridge Handbook of Evolutionary Perspectives on Sexual Psychology
- Published online:
- 30 June 2022
- Print publication:
- 21 July 2022, pp 24-56
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Summary
Despite a tendency to form socially monogamous pair-bonds that carry expectations of sexual exclusivity, infidelity has been a recurrent feature of human mating across societies. The attitudes, social cognition, affect, and behavior associated with infidelity vary in patterned ways between women and men. In the current chapter, we use an evolutionary perspective to make sense of the historical and cross-cultural ubiquity of extradyadic behavior, as well the adaptative costs and benefits of men’s infidelity. Specifically, we review theory and research pertaining to men’s extra-pair mating and consider salient individual differences, romantic relationship dynamics, and social–ecological factors that influence mating strategies and extradyadic involvement. Following other scholars, we argue that men have evolved adaptations for short-term mating that facilitate opportunistic extra-pair behavior in a “quantity-over-quality” reproductive strategy. Consequently, on average, men are predicted to express a stronger desire to engage in sexual infidelity and to have more permissive attitudes toward extradyadic involvement than women. However, only particular men appear to execute a mixed mating strategy involving a long-term mate and an extra-pair partner, such as those with greater mate value. Satisfaction with and commitment to the relationship appear to be crucial in preventing men’s infidelity, and socio-ecological factors, including cultural dynamics (e.g., norms surrounding infidelity) and sex ratios that create conditions of mate scarcity, are inextricably tied to men’s extra-pair mating.
Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 3: Drivers of seed shatter
- Lauren M. Schwartz-Lazaro, Lovreet S. Shergill, Jeffrey A. Evans, Muthukumar V. Bagavathiannan, Shawn C. Beam, Mandy D. Bish, Jason A. Bond, Kevin W. Bradley, William S. Curran, Adam S. Davis, Wesley J. Everman, Michael L. Flessner, Steven C. Haring, Nicholas R. Jordan, Nicholas E. Korres, John L. Lindquist, Jason K. Norsworthy, Tameka L. Sanders, Larry E. Steckel, Mark J. VanGessel, Blake Young, Steven B. Mirsky
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- Journal:
- Weed Science / Volume 70 / Issue 1 / January 2022
- Published online by Cambridge University Press:
- 15 November 2021, pp. 79-86
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Seed retention, and ultimately seed shatter, are extremely important for the efficacy of harvest weed seed control (HWSC) and are likely influenced by various agroecological and environmental factors. Field studies investigated seed-shattering phenology of 22 weed species across three soybean [Glycine max (L.) Merr.]-producing regions in the United States. We further evaluated the potential drivers of seed shatter in terms of weather conditions, growing degree days, and plant biomass. Based on the results, weather conditions had no consistent impact on weed seed shatter. However, there was a positive correlation between individual weed plant biomass and delayed weed seed–shattering rates during harvest. This work demonstrates that HWSC can potentially reduce weed seedbank inputs of plants that have escaped early-season management practices and retained seed through harvest. However, smaller individuals of plants within the same population that shatter seed before harvest pose a risk of escaping early-season management and HWSC.
Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 1: Broadleaf species
- Lauren M. Schwartz-Lazaro, Lovreet S. Shergill, Jeffrey A. Evans, Muthukumar V. Bagavathiannan, Shawn C. Beam, Mandy D. Bish, Jason A. Bond, Kevin W. Bradley, William S. Curran, Adam S. Davis, Wesley J. Everman, Michael L. Flessner, Steven C. Haring, Nicholas R. Jordan, Nicholas E. Korres, John L. Lindquist, Jason K. Norsworthy, Tameka L. Sanders, Larry E. Steckel, Mark J. VanGessel, Blake Young, Steven B. Mirsky
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- Journal:
- Weed Science / Volume 69 / Issue 1 / January 2021
- Published online by Cambridge University Press:
- 04 November 2020, pp. 95-103
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Potential effectiveness of harvest weed seed control (HWSC) systems depends upon seed shatter of the target weed species at crop maturity, enabling its collection and processing at crop harvest. However, seed retention likely is influenced by agroecological and environmental factors. In 2016 and 2017, we assessed seed-shatter phenology in 13 economically important broadleaf weed species in soybean [Glycine max (L.) Merr.] from crop physiological maturity to 4 wk after physiological maturity at multiple sites spread across 14 states in the southern, northern, and mid-Atlantic United States. Greater proportions of seeds were retained by weeds in southern latitudes and shatter rate increased at northern latitudes. Amaranthus spp. seed shatter was low (0% to 2%), whereas shatter varied widely in common ragweed (Ambrosia artemisiifolia L.) (2% to 90%) over the weeks following soybean physiological maturity. Overall, the broadleaf species studied shattered less than 10% of their seeds by soybean harvest. Our results suggest that some of the broadleaf species with greater seed retention rates in the weeks following soybean physiological maturity may be good candidates for HWSC.
Seed-shattering phenology at soybean harvest of economically important weeds in multiple regions of the United States. Part 2: Grass species
- Lauren M. Schwartz-Lazaro, Lovreet S. Shergill, Jeffrey A. Evans, Muthukumar V. Bagavathiannan, Shawn C. Beam, Mandy D. Bish, Jason A. Bond, Kevin W. Bradley, William S. Curran, Adam S. Davis, Wesley J. Everman, Michael L. Flessner, Steven C. Haring, Nicholas R. Jordan, Nicholas E. Korres, John L. Lindquist, Jason K. Norsworthy, Tameka L. Sanders, Larry E. Steckel, Mark J. VanGessel, Blake Young, Steven B. Mirsky
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- Journal:
- Weed Science / Volume 69 / Issue 1 / January 2021
- Published online by Cambridge University Press:
- 26 October 2020, pp. 104-110
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Seed shatter is an important weediness trait on which the efficacy of harvest weed seed control (HWSC) depends. The level of seed shatter in a species is likely influenced by agroecological and environmental factors. In 2016 and 2017, we assessed seed shatter of eight economically important grass weed species in soybean [Glycine max (L.) Merr.] from crop physiological maturity to 4 wk after maturity at multiple sites spread across 11 states in the southern, northern, and mid-Atlantic United States. From soybean maturity to 4 wk after maturity, cumulative percent seed shatter was lowest in the southern U.S. regions and increased moving north through the states. At soybean maturity, the percent of seed shatter ranged from 1% to 70%. That range had shifted to 5% to 100% (mean: 42%) by 25 d after soybean maturity. There were considerable differences in seed-shatter onset and rate of progression between sites and years in some species that could impact their susceptibility to HWSC. Our results suggest that many summer annual grass species are likely not ideal candidates for HWSC, although HWSC could substantially reduce their seed output during certain years.
18 - Evolutionary Roots of Women’s Aggression
- from Section 3 - Cognitive and Social Factors
- Edited by Fanny M. Cheung, The Chinese University of Hong Kong, Diane F. Halpern, Claremont McKenna College, California
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- The Cambridge Handbook of the International Psychology of Women
- Published online:
- 20 July 2020
- Print publication:
- 06 August 2020, pp 258-272
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From an evolutionary perspective, aggression is viewed as a flexible context-specific adaption that was selected for because it enhanced the survival and reproductive success of ancestral humans. Evolutionary pressures have impinged differentially on the sexes, leading to the hypothesis that sex differences should be manifest in aggressive behavior. Evidence to date supports key predictions made from sexual selection theory that women direct their aggression primarily toward same-sex competitors, which peaks as mate competition intensifies. Women demonstrate a notable preference across cultures for more indirect, as opposed to direct, forms of intrasexual rivalry as a likely consequence of heightened obligatory parental investment, lower lifetime reproductive potential, and the greater importance of maternal survival for the health and longevity of offspring. An evolutionary approach can yield unique insights into the sex-differentiated functions, development, and outcomes of aggressive behavior.
Chapter 2 - The Intertidal Zone of the North-East Atlantic Region
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- By Stephen J. Hawkins, Kathryn E. Pack, Louise B. Firth, Nova Mieszkowska, Ally J. Evans, Gustavo M. Martins, Per Åberg, Leoni C. Adams, Francisco Arenas, Diana M. Boaventura, Katrin Bohn, C. Debora G. Borges, João J. Castro, Ross A. Coleman, Tasman P. Crowe, Teresa Cruz, Mark S. Davies, Graham Epstein, João Faria, João G. Ferreira, Natalie J. Frost, John N. Griffin, ME Hanley, Roger J. H. Herbert, Kieran Hyder, Mark P. Johnson, Fernando P. Lima, Patricia Masterson-Algar, Pippa J. Moore, Paula S. Moschella, Gillian M. Notman, Federica G. Pannacciulli, Pedro A. Ribeiro, Antonio M. Santos, Ana C. F. Silva, Martin W. Skov, Heather Sugden, Maria Vale, Kringpaka Wangkulangkul, Edward J. G. Wort, Richard C. Thompson, Richard G. Hartnoll, Michael T. Burrows, Stuart R. Jenkins
- Edited by Stephen J. Hawkins, Marine Biological Association of the United Kingdom, Plymouth, Katrin Bohn, Louise B. Firth, University of Plymouth, Gray A. Williams, The University of Hong Kong
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- Book:
- Interactions in the Marine Benthos
- Published online:
- 07 September 2019
- Print publication:
- 29 August 2019, pp 7-46
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Summary
The rocky shores of the north-east Atlantic have been long studied. Our focus is from Gibraltar to Norway plus the Azores and Iceland. Phylogeographic processes shape biogeographic patterns of biodiversity. Long-term and broadscale studies have shown the responses of biota to past climate fluctuations and more recent anthropogenic climate change. Inter- and intra-specific species interactions along sharp local environmental gradients shape distributions and community structure and hence ecosystem functioning. Shifts in domination by fucoids in shelter to barnacles/mussels in exposure are mediated by grazing by patellid limpets. Further south fucoids become increasingly rare, with species disappearing or restricted to estuarine refuges, caused by greater desiccation and grazing pressure. Mesoscale processes influence bottom-up nutrient forcing and larval supply, hence affecting species abundance and distribution, and can be proximate factors setting range edges (e.g., the English Channel, the Iberian Peninsula). Impacts of invasive non-native species are reviewed. Knowledge gaps such as the work on rockpools and host–parasite dynamics are also outlined.
Characterization of multiple herbicide–resistant waterhemp (Amaranthus tuberculatus) populations from Illinois to VLCFA-inhibiting herbicides
- Seth A. Strom, Lisa C. Gonzini, Charlie Mitsdarfer, Adam S. Davis, Dean E. Riechers, Aaron G. Hager
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- Journal:
- Weed Science / Volume 67 / Issue 4 / July 2019
- Published online by Cambridge University Press:
- 27 May 2019, pp. 369-379
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Field experiments were conducted in 2016 and 2017 in Champaign County, IL, to study a waterhemp [Amaranthus tuberculatus (Moq.) J. D. Sauer] population (CHR) resistant to 2,4-D and 4-hydroxyphenylpyruvate dioxygenase (HPPD)-, photosystem II–, acetolactate synthase (ALS)-, and protoporphyrinogen oxidase–inhibiting herbicides. Two field experiments were designed to investigate the efficacy of very-long-chain fatty-acid (VLCFA)-inhibiting herbicides, including a comparison of active ingredients at labeled use rates and a rate titration experiment. Amaranthus tuberculatus density and control were evaluated at 28 and 42 d after treatment (DAT). Nonencapsulated acetochlor, alachlor, and pyroxasulfone provided the greatest PRE control of CHR (56% to 75%) at 28 DAT, while metolachlor, S-metolachlor, dimethenamid-P, and encapsulated acetochlor provided less than 27% control. In the rate titration study, nonencapsulated acetochlor controlled CHR more than equivalent field use rates of S-metolachlor. Subsequent dose–response experiments with acetochlor, S-metolachlor, dimethenamid-P, and pyroxasulfone in the greenhouse included three multiple herbicide–resistant (MHR) A. tuberculatus populations: CHR-M6 (progeny generated from CHR), MCR-NH40 (progeny generated from Mclean County, IL), and ACR (Adams County, IL), in comparison with a sensitive population (WUS). Both CHR-M6 and MCR-NH40 are MHR to atrazine and HPPD, and ALS inhibitors and demonstrated higher survival rates (LD50) to S-metolachlor, acetochlor, dimethenamid-P, or pyroxasulfone than ACR (atrazine resistant but HPPD-inhibitor sensitive) and WUS. Based on biomass reduction (GR50), resistant to sensitive (R:S) ratios between CHR-M6 and WUS were 7.5, 6.1, 5.5, and 2.9 for S-metolachlor, acetochlor, dimethenamid-P, and pyroxasulfone, respectively. Values were greater for MCR-NH40 than CHR-M6, and ACR was the most sensitive to all VLCFA inhibitors tested. Complete control of all populations was achieved at or below a field use rate of acetochlor. In summary, field studies demonstrated CHR is not controlled by several VLCFA-inhibiting herbicides. Greenhouse dose–response experiments corroborated field results and generated R:S ratios (LD50) ranging from 4.5 to 64 for CHR-M6 and MCR-NH40 among the four VLCFA-inhibiting herbicides evaluated.
Treatment exposures stratify need for echocardiographic screening in asymptomatic long-term survivors of hematopoietic stem cell transplantation
- Seth J. Rotz, Adam Powell, Kasiani C. Myers, Michael D. Taylor, John L. Jefferies, Adam Lane, Javier A. El-Bietar, Stella M. Davies, Christopher E. Dandoy, Thomas D. Ryan
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- Journal:
- Cardiology in the Young / Volume 29 / Issue 3 / March 2019
- Published online by Cambridge University Press:
- 12 February 2019, pp. 338-343
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We sought to define the prevalence of echocardiographic abnormalities in long-term survivors of paediatric hematopoietic stem cell transplantation and determine the utility of screening in asymptomatic patients. We analysed echocardiograms performed on survivors who underwent hematopoietic stem cell transplantation from 1982 to 2006. A total of 389 patients were alive in 2017, with 114 having an echocardiogram obtained ⩾5 years post-infusion. A total of 95 patients had echocardiogram performed for routine surveillance. The mean time post-hematopoietic stem cell transplantation was 13 years. Of 95 patients, 77 (82.1%) had ejection fraction measured, and 10/77 (13.0%) had ejection fraction z-scores ⩽−2.0, which is abnormally low. Those patients with abnormal ejection fraction were significantly more likely to have been exposed to anthracyclines or total body irradiation. Among individuals who received neither anthracyclines nor total body irradiation, only 1/31 (3.2%) was found to have an abnormal ejection fraction of 51.4%, z-score −2.73. In the cohort of 77 patients, the negative predictive value of having a normal ejection fraction given no exposure to total body irradiation or anthracyclines was 96.7% at 95% confidence interval (83.3–99.8%). Systolic dysfunction is relatively common in long-term survivors of paediatric hematopoietic stem cell transplantation who have received anthracyclines or total body irradiation. Survivors who are asymptomatic and did not receive radiation or anthracyclines likely do not require surveillance echocardiograms, unless otherwise indicated.
Meta-Analysis of Crop and Weed Growth Responses to Arbuscular Mycorrhizal Fungi: Implications for Integrated Weed Management
- Meng Li, Nicholas R. Jordan, Roger T. Koide, Anthony C. Yannarell, Adam S. Davis
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- Journal:
- Weed Science / Volume 64 / Issue 4 / December 2016
- Published online by Cambridge University Press:
- 20 January 2017, pp. 642-652
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Integrated weed management (IWM) relies upon multiple chemical, physical, or biological weed management techniques to achieve an acceptable level of weed control. Agents that selectively suppress weeds but not crops and that can be manipulated in agriculture will be promising components for inclusion in IWM. We used a meta-analytic approach to investigate the potential of arbuscular mycorrhizal fungi (AMF) to contribute to IWM. We quantified the effect of crop and weed host status (strong and weak AMF hosts are divided in this study by a 10% root length colonization threshold), AMF diversity (single vs. mixed), and soil N and P fertility management on plant mycorrhizal growth responses (MGRs). Our results indicated that weak host weeds had consistently lower MGRs than strong host crops in both controlled and field conditions. Moreover, these differences in MGRs between weak host weeds and strong host crops were more pronounced under mixed AMF inoculum and low N and P nutrient availability. In contrast, MGR of strong host weeds was not different from strong host crops in general. However, we observed a wide range of MGRs among strong host weeds, some of which had much lower MGRs than strong host crops. In addition, in the presence of N and P fertilizers, strong host crops had a stronger positive response to AMF than strong host weeds. Thus, our meta-analysis indicates that AMF have potential to contribute to weed control by direct and indirect pathways: directly suppress weak host weeds, and indirectly suppress some strong host weeds mediating by competitive effects exerted by strong host crops. We suggest that management practices affecting AMF diversity and crop and weed mycorrhizal responses could be chosen to improve the contribution of AMF to IWM. Better understanding is needed of crop–weed–AMF interactions and management practices that enhance this form of weed management.
Environmental factors affecting seed persistence of annual weeds across the U.S. corn belt
- Adam S. Davis, John Cardina, Frank Forcella, Gregg A. Johnson, George Kegode, John L. Lindquist, Edward C. Luschei, Karen A. Renner, Christy L. Sprague, Martin M. Williams II
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- Journal:
- Weed Science / Volume 53 / Issue 6 / December 2005
- Published online by Cambridge University Press:
- 20 January 2017, pp. 860-868
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Weed seedbanks have been studied intensively at local scales, but to date, there have been no regional-scale studies of weed seedbank persistence. Empirical and modeling studies indicate that reducing weed seedbank persistence can play an important role in integrated weed management. Annual seedbank persistence of 13 summer annual weed species was studied from 2001 through 2003 at eight locations in the north central United States and one location in the northwestern United States. Effects of seed depth placement, tillage, and abiotic environmental factors on seedbank persistence were examined through regression and multivariate ordinations. All species examined showed a negative relationship between hydrothermal time and seedbank persistence. Seedbank persistence was very similar between the two years of the study for common lambsquarters, giant foxtail, and velvetleaf when data were pooled over location, depth, and tillage. Seedbank persistence of common lambsquarters, giant foxtail, and velvetleaf from October 2001 through 2002 and October 2002 through 2003 was, respectively, 52.3% and 60.0%, 21.3% and 21.8%, and 57.5% and 57.2%. These results demonstrate that robust estimates of seedbank persistence are possible when many observations are averaged over numerous locations. Future studies are needed to develop methods of reducing seedbank persistence, especially for weed species with particularly long-lived seeds.
Annual Postdispersal Weed Seed Predation in Contrasting Field Environments
- Adam S. Davis, Erin C. Taylor, Erin R. Haramoto, Karen A. Renner
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- Journal:
- Weed Science / Volume 61 / Issue 2 / June 2013
- Published online by Cambridge University Press:
- 20 January 2017, pp. 296-302
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Interest in weed seed predation as an ecological weed management tactic has led to a growing number of investigations of agronomic and environmental effects on predation rates. Whereas the measurements in most of these studies have taken place at very short timescales, from days to weeks, measurements at longer timescales (from several months to a year) have greater relevance to the demographic impact of weed seed predation and potential contributions from this process to ecological weed management. Our aim was to quantify the impact of crop phase, within a corn–soybean–wheat crop sequence, on quarterly and annual seed predation rates of giant foxtail, giant ragweed, and velvetleaf. The study took place in areas of the northern U.S. Corn Belt contrasting in dominant land use: Savoy, IL (2005–2007), where corn and soybean production predominates, and East Lansing, MI (2005–2008), where crop production occurs within an old field/forest landscape matrix. Mean annual rates of weed seed predation by the combined action of invertebrate and vertebrate predators were 31 ± 1.6% for giant ragweed, 37 ± 1.4% for velvetleaf, and 53 ± 1.4% for giant foxtail. Crop phase had negligible effects upon long-term seed predation rates, accounting for less than 2% of observed variation. Weed species and site-year, in contrast, contributed 35% and 40%, respectively, of the variation in cumulative annual seed predation. These results are consistent with the spatial variability in best management practices seen at spatial scales greater than the county level: weed seed predation appears to be an inherently site-specific phenomenon. New developments in managing weed seed predation as an ecosystem service are therefore likely to have local recommendation domains or to be driven by stochastic annual variation related to weather or granivore demography.
Weed Science Research and Funding: A Call to Action
- Adam S. Davis, J. Christopher Hall, Marie Jasieniuk, Martin A. Locke, Edward C. Luschei, David A. Mortensen, Dean E. Riechers, Richard G. Smith, Tracy M. Sterling, James H. Westwood
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- Journal:
- Weed Science / Volume 57 / Issue 4 / August 2009
- Published online by Cambridge University Press:
- 20 January 2017, pp. 442-448
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Weed science has contributed much to agriculture, forestry and natural resource management during its history. However, if it is to remain relevant as a scientific discipline, it is long past time for weed scientists to move beyond a dominating focus on herbicide efficacy testing and address the basic science underlying complex issues in vegetation management at many levels of biological organization currently being solved by others, such as invasion ecologists and molecular biologists. Weed science must not be circumscribed by a narrowly-defined set of tools but rather be seen as an integrating discipline. As a means of assessing current and future research interests and funding trends among weed scientists, the Weed Science Society of America conducted an online survey of its members in summer of 2007. There were 304 respondents out of a membership of 1330 at the time of the survey, a response rate of 23%. The largest group of respondents (41%) reported working on research problems primarily focused on herbicide efficacy and maintenance, funded mainly by private industry sources. Another smaller group of respondents (22%) reported focusing on research topics with a complex systems focus (such as invasion biology, ecosystem restoration, ecological weed management, and the genetics, molecular biology, and physiology of weedy traits), funded primarily by public sources. Increased cooperation between these complementary groups of scientists will be an essential step in making weed science increasingly relevant to the complex vegetation management issues of the 21st century.
Do microorganisms influence seed-bank dynamics?
- Joanne C. Chee-Sanford, Martin M. Williams II, Adam S. Davis, Gerald K. Sims
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- Journal:
- Weed Science / Volume 54 / Issue 3 / June 2006
- Published online by Cambridge University Press:
- 20 January 2017, pp. 575-587
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Reduction of seed-bank persistence is an important goal for weed management systems. Recent interest in more biological-based weed management strategies has led to closer examination of the role of soil microorganisms. Incidences of seed decay with certain weed species occur in the laboratory; however, their persistence in soil indicates the presence of yet-unknown factors in natural systems that regulate biological mechanisms of seed antagonism by soil microorganisms. A fundamental understanding of interactions between seeds and microorganisms will have important implications for future weed management systems targeting seed banks. Laboratory studies demonstrate susceptibility to seed decay among weed species, ranging from high (velvetleaf) to very low (giant ragweed). Microscopic examinations revealed dense microbial assemblages formed whenever seeds were exposed to soil microorganisms, regardless of whether the outcome was decay. Microbial communities associated with seeds of four weed species (woolly cupgrass, jimsonweed, Pennsylvania smartweed, and velvetleaf) were distinct from one another. The influence of seeds on microbial growth is hypothesized to be due to nutritional and surface-attachment opportunities. Data from velvetleaf seeds suggests that diverse assemblages of bacteria can mediate decay, whereas fungal associations may be more limited and specific to weed species. Though microbial decay of seeds presents clear opportunities for weed biocontrol, limited success is met when introducing exogenous microorganisms to natural systems. Alternatively, a conservation approach that promotes the function of indigenous natural enemies through habitat or cultural management may be more promising. A comprehensive ecological understanding of the system is needed to identify methods that enhance the activities of microorganisms. Herein, we provide a synthesis of the relevant literature available on seed microbiology; we describe some of the major challenges and opportunities encountered when studying the in situ relationships between seeds and microorganisms, and present examples from studies by the ARS Invasive Weed Management Unit.
Introduction to the Invasive Plant Species and the New Bioeconomy Symposium
- Adam S. Davis, Daniel C. Brainard, Eric R. Gallandt
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- Journal:
- Weed Science / Volume 56 / Issue 6 / December 2008
- Published online by Cambridge University Press:
- 20 January 2017, p. 866
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The rapid expansion of the plant bioeconomy is creating strong economic incentives to distribute novel plant material, including transgenic cultivars, exotic species, and species that were formerly constrained to small geographical areas, at large geographical scales. Such introductions carry with them the risk of invasive spread of the introduced species (Simberloff and Alexander 1998). Deployment of plant species for biofuel production offers a clear example of the benefits and risks associated with the new bioeconomy (Raghu et al. 2006).
In a measure aimed at reducing U.S. dependence upon foreign petroleum reserves for energy production, President Bush announced the Advanced Energy Initiative (AEI) in his 2006 State of the Union address. This initiative provides federal funding and guidelines for the development of renewable energy sources, including plant biofuels. The objectives of the AEI, though admirable, have the potential to create a conflict with Executive Order 13112, which states that “[Federal agencies shall] not authorize, fund, or carry out actions that it believes are likely to cause or promote the introduction or spread of invasive species in the United States or elsewhere unless, pursuant to guidelines that it has prescribed, the agency has determined and made public its determination that the benefits of such actions clearly outweigh the potential harm caused by invasive species; and that all feasible and prudent measures to minimize risk of harm will be taken in conjunction with the actions.”
Cover Crop Impact on Weed Dynamics in an Organic Dry Bean System
- Erin C. Hill, Karen A. Renner, Christy L. Sprague, Adam S. Davis
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- Journal:
- Weed Science / Volume 64 / Issue 2 / June 2016
- Published online by Cambridge University Press:
- 20 January 2017, pp. 261-275
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Weed suppression is one possible benefit of including cover crops in crop rotations. The late spring planting date of dry beans allows for more growth of cover crops in the spring. We assessed the influence of cover crops on weed dynamics in organic dry beans and weed seed persistence. Medium red clover, oilseed radish, and cereal rye were planted the year before dry beans; a no-cover-crop control was also included. After cover-crop incorporation, common lambsquarters, giant foxtail, and velvetleaf seeds were buried in the red clover, cereal rye, and no-cover control treatments and then retrieved 0, 1, 2, 4, 6, and 12 mo after cover-crop incorporation. Dry beans were planted in June and weed emergence and biomass measured. Eleven or more site-years of data were collected for each cover-crop treatment between 2011 and 2013, allowing for structural equation modeling (SEM), in addition to traditional analyses. Cereal rye residue increased giant foxtail and velvetleaf seed persistence by up to 12%; red clover decreased common lambsquarters seed persistence by 22% in 1 of 2 yr relative to the no-cover-crop control. Oilseed radish and incorporated cereal rye rarely reduced weed densities. When red clover biomass exceeded 5 Mg ha−1, soil inorganic N was often higher (5 of 6 site-years), as were weed density and biomass (5 and 4 of 12 main site sample times, respectively). Using SEM, we identified one causal relationship between cover-crop N content and weed biomass at the first flower stage (R1), as mediated through soil N at the time of dry bean planting and at the stage with two fully expanded trifoliates. Increasing cover-crop C : N ratios directly reduced weed biomass at R1, not mediated through changes in soil N. Cover crops that make a significant contribution to soil N may also stimulate weed emergence and growth.
Living Boundaries: Tracking Weed Seed Movement With Nondormant Seed
- Adam S. Davis, Edward C. Luschei
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- Journal:
- Weed Science / Volume 57 / Issue 2 / April 2009
- Published online by Cambridge University Press:
- 20 January 2017, pp. 163-168
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Synthetic seed banks are a useful tool for tracking how weed populations change over time. By sowing a known number of seeds of a given species within a quadrat with defined boundaries, an investigator can measure the number remaining and thereby calculate demographic rates (e.g., mortality). The alternative is to use in situ seeds and estimate their initial population density via sampling. To make a synthetic seed bank approach useful within an agricultural system subjected to soil disturbances such as tillage, one would need a way to account for seeds leaving the initial quadrat (i.e., a way to follow how the area encompassing the sown seeds changes over time). Without accounting for the change in location/extent of the synthetic seed bank, any field operation moving soil will create additional uncertainty in population size. Depending on the “aggressiveness” of specific field operations and the initial size of the quadrat, this effect might be negligible or so large as to be intractable. Here, we describe a method for following a synthetic seed bank over time using a “living boundary” of nondormant seeds, which effectively play the role of tracers used in the study of dynamics in other scientific disciplines. Study quadrats in East Lansing, MI, and Arlington, WI, were sown with giant foxtail and velvetleaf at a rate of 2,000 seeds m−2. The study quadrats were marked on the perimeter and diagonals using nondormant seeds of three marker species: kale, radish, and rye. The areas were then subjected to tillage and planting operations. Spatial coordinates of seedling locations for the marker and weed species were obtained through digital image processing. A nonparametric comparison of the spatial displacement of marker and weed species indicated that their empirical spatial distributions did not differ. The marker species quadrats described by the 50th, 90th, and 99th quantiles of movement contained all velvetleaf seedlings in Wisconsin, all velvetleaf seedlings in Michigan, and all giant foxtail seedlings in Michigan, respectively. The results suggest a simple rule for applying the method to field demography studies: after the original quadrat is deformed and seedlings have emerged, flag the polygon containing all marker seedlings to obtain the expanded quadrat containing the study weed population.
Provision of NHS generalist and specialist services to care homes in England: review of surveys
- Steve Iliffe, Susan L. Davies, Adam L. Gordon, Justine Schneider, Tom Dening, Clive Bowman, Heather Gage, Finbarr C. Martin, John R.F. Gladman, Christina Victor, Julienne Meyer, Claire Goodman
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- Journal:
- Primary Health Care Research & Development / Volume 17 / Issue 2 / March 2016
- Published online by Cambridge University Press:
- 05 May 2015, pp. 122-137
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Background
The number of beds in care homes (with and without nurses) in the United Kingdom is three times greater than the number of beds in National Health Service (NHS) hospitals. Care homes are predominantly owned by a range of commercial, not-for-profit or charitable providers and their residents have high levels of disability, frailty and co-morbidity. NHS support for care home residents is very variable, and it is unclear what models of clinical support work and are cost-effective.
ObjectivesTo critically evaluate how the NHS works with care homes.
MethodsA review of surveys of NHS services provided to care homes that had been completed since 2008. It included published national surveys, local surveys commissioned by Primary Care organisations, studies from charities and academic centres, grey literature identified across the nine government regions, and information from care home, primary care and other research networks. Data extraction captured forms of NHS service provision for care homes in England in terms of frequency, location, focus and purpose.
ResultsFive surveys focused primarily on general practitioner services, and 10 on specialist services to care home. Working relationships between the NHS and care homes lack structure and purpose and have generally evolved locally. There are wide variations in provision of both generalist and specialist healthcare services to care homes. Larger care home chains may take a systematic approach to both organising access to NHS generalist and specialist services, and to supplementing gaps with in-house provision. Access to dental care for care home residents appears to be particularly deficient.
ConclusionsHistorical differences in innovation and provision of NHS services, the complexities of collaborating across different sectors (private and public, health and social care, general and mental health), and variable levels of organisation of care homes, all lead to persistent and embedded inequity in the distribution of NHS resources to this population. Clinical commissioners seeking to improve the quality of care of care home residents need to consider how best to provide fair access to health care for older people living in a care home, and to establish a specification for service delivery to this vulnerable population.
Contributors
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- By Mitchell Aboulafia, Frederick Adams, Marilyn McCord Adams, Robert M. Adams, Laird Addis, James W. Allard, David Allison, William P. Alston, Karl Ameriks, C. Anthony Anderson, David Leech Anderson, Lanier Anderson, Roger Ariew, David Armstrong, Denis G. Arnold, E. J. Ashworth, Margaret Atherton, Robin Attfield, Bruce Aune, Edward Wilson Averill, Jody Azzouni, Kent Bach, Andrew Bailey, Lynne Rudder Baker, Thomas R. Baldwin, Jon Barwise, George Bealer, William Bechtel, Lawrence C. Becker, Mark A. Bedau, Ernst Behler, José A. Benardete, Ermanno Bencivenga, Jan Berg, Michael Bergmann, Robert L. Bernasconi, Sven Bernecker, Bernard Berofsky, Rod Bertolet, Charles J. Beyer, Christian Beyer, Joseph Bien, Joseph Bien, Peg Birmingham, Ivan Boh, James Bohman, Daniel Bonevac, Laurence BonJour, William J. Bouwsma, Raymond D. Bradley, Myles Brand, Richard B. Brandt, Michael E. Bratman, Stephen E. Braude, Daniel Breazeale, Angela Breitenbach, Jason Bridges, David O. Brink, Gordon G. Brittan, Justin Broackes, Dan W. Brock, Aaron Bronfman, Jeffrey E. Brower, Bartosz Brozek, Anthony Brueckner, Jeffrey Bub, Lara Buchak, Otavio Bueno, Ann E. Bumpus, Robert W. Burch, John Burgess, Arthur W. Burks, Panayot Butchvarov, Robert E. Butts, Marina Bykova, Patrick Byrne, David Carr, Noël Carroll, Edward S. Casey, Victor Caston, Victor Caston, Albert Casullo, Robert L. Causey, Alan K. L. Chan, Ruth Chang, Deen K. Chatterjee, Andrew Chignell, Roderick M. Chisholm, Kelly J. Clark, E. J. Coffman, Robin Collins, Brian P. Copenhaver, John Corcoran, John Cottingham, Roger Crisp, Frederick J. Crosson, Antonio S. Cua, Phillip D. Cummins, Martin Curd, Adam Cureton, Andrew Cutrofello, Stephen Darwall, Paul Sheldon Davies, Wayne A. Davis, Timothy Joseph Day, Claudio de Almeida, Mario De Caro, Mario De Caro, John Deigh, C. F. Delaney, Daniel C. Dennett, Michael R. DePaul, Michael Detlefsen, Daniel Trent Devereux, Philip E. Devine, John M. Dillon, Martin C. Dillon, Robert DiSalle, Mary Domski, Alan Donagan, Paul Draper, Fred Dretske, Mircea Dumitru, Wilhelm Dupré, Gerald Dworkin, John Earman, Ellery Eells, Catherine Z. Elgin, Berent Enç, Ronald P. Endicott, Edward Erwin, John Etchemendy, C. Stephen Evans, Susan L. Feagin, Solomon Feferman, Richard Feldman, Arthur Fine, Maurice A. Finocchiaro, William FitzPatrick, Richard E. Flathman, Gvozden Flego, Richard Foley, Graeme Forbes, Rainer Forst, Malcolm R. Forster, Daniel Fouke, Patrick Francken, Samuel Freeman, Elizabeth Fricker, Miranda Fricker, Michael Friedman, Michael Fuerstein, Richard A. Fumerton, Alan Gabbey, Pieranna Garavaso, Daniel Garber, Jorge L. A. Garcia, Robert K. Garcia, Don Garrett, Philip Gasper, Gerald Gaus, Berys Gaut, Bernard Gert, Roger F. Gibson, Cody Gilmore, Carl Ginet, Alan H. Goldman, Alvin I. Goldman, Alfonso Gömez-Lobo, Lenn E. Goodman, Robert M. Gordon, Stefan Gosepath, Jorge J. E. Gracia, Daniel W. Graham, George A. Graham, Peter J. Graham, Richard E. Grandy, I. Grattan-Guinness, John Greco, Philip T. Grier, Nicholas Griffin, Nicholas Griffin, David A. Griffiths, Paul J. Griffiths, Stephen R. Grimm, Charles L. Griswold, Charles B. Guignon, Pete A. Y. Gunter, Dimitri Gutas, Gary Gutting, Paul Guyer, Kwame Gyekye, Oscar A. Haac, Raul Hakli, Raul Hakli, Michael Hallett, Edward C. Halper, Jean Hampton, R. James Hankinson, K. R. Hanley, Russell Hardin, Robert M. Harnish, William Harper, David Harrah, Kevin Hart, Ali Hasan, William Hasker, John Haugeland, Roger Hausheer, William Heald, Peter Heath, Richard Heck, John F. Heil, Vincent F. Hendricks, Stephen Hetherington, Francis Heylighen, Kathleen Marie Higgins, Risto Hilpinen, Harold T. Hodes, Joshua Hoffman, Alan Holland, Robert L. Holmes, Richard Holton, Brad W. Hooker, Terence E. Horgan, Tamara Horowitz, Paul Horwich, Vittorio Hösle, Paul Hoβfeld, Daniel Howard-Snyder, Frances Howard-Snyder, Anne Hudson, Deal W. Hudson, Carl A. Huffman, David L. Hull, Patricia Huntington, Thomas Hurka, Paul Hurley, Rosalind Hursthouse, Guillermo Hurtado, Ronald E. Hustwit, Sarah Hutton, Jonathan Jenkins Ichikawa, Harry A. Ide, David Ingram, Philip J. Ivanhoe, Alfred L. Ivry, Frank Jackson, Dale Jacquette, Joseph Jedwab, Richard Jeffrey, David Alan Johnson, Edward Johnson, Mark D. Jordan, Richard Joyce, Hwa Yol Jung, Robert Hillary Kane, Tomis Kapitan, Jacquelyn Ann K. Kegley, James A. Keller, Ralph Kennedy, Sergei Khoruzhii, Jaegwon Kim, Yersu Kim, Nathan L. King, Patricia Kitcher, Peter D. Klein, E. D. Klemke, Virginia Klenk, George L. Kline, Christian Klotz, Simo Knuuttila, Joseph J. Kockelmans, Konstantin Kolenda, Sebastian Tomasz Kołodziejczyk, Isaac Kramnick, Richard Kraut, Fred Kroon, Manfred Kuehn, Steven T. Kuhn, Henry E. Kyburg, John Lachs, Jennifer Lackey, Stephen E. Lahey, Andrea Lavazza, Thomas H. Leahey, Joo Heung Lee, Keith Lehrer, Dorothy Leland, Noah M. Lemos, Ernest LePore, Sarah-Jane Leslie, Isaac Levi, Andrew Levine, Alan E. Lewis, Daniel E. Little, Shu-hsien Liu, Shu-hsien Liu, Alan K. L. Chan, Brian Loar, Lawrence B. Lombard, John Longeway, Dominic McIver Lopes, Michael J. Loux, E. J. Lowe, Steven Luper, Eugene C. Luschei, William G. Lycan, David Lyons, David Macarthur, Danielle Macbeth, Scott MacDonald, Jacob L. Mackey, Louis H. Mackey, Penelope Mackie, Edward H. Madden, Penelope Maddy, G. B. Madison, Bernd Magnus, Pekka Mäkelä, Rudolf A. Makkreel, David Manley, William E. Mann (W.E.M.), Vladimir Marchenkov, Peter Markie, Jean-Pierre Marquis, Ausonio Marras, Mike W. Martin, A. P. Martinich, William L. McBride, David McCabe, Storrs McCall, Hugh J. McCann, Robert N. McCauley, John J. McDermott, Sarah McGrath, Ralph McInerny, Daniel J. McKaughan, Thomas McKay, Michael McKinsey, Brian P. McLaughlin, Ernan McMullin, Anthonie Meijers, Jack W. Meiland, William Jason Melanson, Alfred R. Mele, Joseph R. Mendola, Christopher Menzel, Michael J. Meyer, Christian B. Miller, David W. Miller, Peter Millican, Robert N. Minor, Phillip Mitsis, James A. Montmarquet, Michael S. Moore, Tim Moore, Benjamin Morison, Donald R. Morrison, Stephen J. Morse, Paul K. Moser, Alexander P. D. Mourelatos, Ian Mueller, James Bernard Murphy, Mark C. Murphy, Steven Nadler, Jan Narveson, Alan Nelson, Jerome Neu, Samuel Newlands, Kai Nielsen, Ilkka Niiniluoto, Carlos G. Noreña, Calvin G. Normore, David Fate Norton, Nikolaj Nottelmann, Donald Nute, David S. Oderberg, Steve Odin, Michael O’Rourke, Willard G. Oxtoby, Heinz Paetzold, George S. Pappas, Anthony J. Parel, Lydia Patton, R. P. Peerenboom, Francis Jeffry Pelletier, Adriaan T. Peperzak, Derk Pereboom, Jaroslav Peregrin, Glen Pettigrove, Philip Pettit, Edmund L. Pincoffs, Andrew Pinsent, Robert B. Pippin, Alvin Plantinga, Louis P. Pojman, Richard H. Popkin, John F. Post, Carl J. Posy, William J. Prior, Richard Purtill, Michael Quante, Philip L. Quinn, Philip L. Quinn, Elizabeth S. Radcliffe, Diana Raffman, Gerard Raulet, Stephen L. Read, Andrews Reath, Andrew Reisner, Nicholas Rescher, Henry S. Richardson, Robert C. Richardson, Thomas Ricketts, Wayne D. Riggs, Mark Roberts, Robert C. Roberts, Luke Robinson, Alexander Rosenberg, Gary Rosenkranz, Bernice Glatzer Rosenthal, Adina L. Roskies, William L. Rowe, T. M. Rudavsky, Michael Ruse, Bruce Russell, Lilly-Marlene Russow, Dan Ryder, R. M. Sainsbury, Joseph Salerno, Nathan Salmon, Wesley C. Salmon, Constantine Sandis, David H. Sanford, Marco Santambrogio, David Sapire, Ruth A. Saunders, Geoffrey Sayre-McCord, Charles Sayward, James P. Scanlan, Richard Schacht, Tamar Schapiro, Frederick F. Schmitt, Jerome B. Schneewind, Calvin O. Schrag, Alan D. Schrift, George F. Schumm, Jean-Loup Seban, David N. Sedley, Kenneth Seeskin, Krister Segerberg, Charlene Haddock Seigfried, Dennis M. Senchuk, James F. Sennett, William Lad Sessions, Stewart Shapiro, Tommie Shelby, Donald W. Sherburne, Christopher Shields, Roger A. Shiner, Sydney Shoemaker, Robert K. Shope, Kwong-loi Shun, Wilfried Sieg, A. John Simmons, Robert L. Simon, Marcus G. Singer, Georgette Sinkler, Walter Sinnott-Armstrong, Matti T. Sintonen, Lawrence Sklar, Brian Skyrms, Robert C. Sleigh, Michael Anthony Slote, Hans Sluga, Barry Smith, Michael Smith, Robin Smith, Robert Sokolowski, Robert C. Solomon, Marta Soniewicka, Philip Soper, Ernest Sosa, Nicholas Southwood, Paul Vincent Spade, T. L. S. Sprigge, Eric O. Springsted, George J. Stack, Rebecca Stangl, Jason Stanley, Florian Steinberger, Sören Stenlund, Christopher Stephens, James P. Sterba, Josef Stern, Matthias Steup, M. A. Stewart, Leopold Stubenberg, Edith Dudley Sulla, Frederick Suppe, Jere Paul Surber, David George Sussman, Sigrún Svavarsdóttir, Zeno G. Swijtink, Richard Swinburne, Charles C. Taliaferro, Robert B. Talisse, John Tasioulas, Paul Teller, Larry S. Temkin, Mark Textor, H. S. Thayer, Peter Thielke, Alan Thomas, Amie L. Thomasson, Katherine Thomson-Jones, Joshua C. Thurow, Vzalerie Tiberius, Terrence N. Tice, Paul Tidman, Mark C. Timmons, William Tolhurst, James E. Tomberlin, Rosemarie Tong, Lawrence Torcello, Kelly Trogdon, J. D. Trout, Robert E. Tully, Raimo Tuomela, John Turri, Martin M. Tweedale, Thomas Uebel, Jennifer Uleman, James Van Cleve, Harry van der Linden, Peter van Inwagen, Bryan W. Van Norden, René van Woudenberg, Donald Phillip Verene, Samantha Vice, Thomas Vinci, Donald Wayne Viney, Barbara Von Eckardt, Peter B. M. Vranas, Steven J. Wagner, William J. Wainwright, Paul E. Walker, Robert E. Wall, Craig Walton, Douglas Walton, Eric Watkins, Richard A. Watson, Michael V. Wedin, Rudolph H. Weingartner, Paul Weirich, Paul J. Weithman, Carl Wellman, Howard Wettstein, Samuel C. Wheeler, Stephen A. White, Jennifer Whiting, Edward R. Wierenga, Michael Williams, Fred Wilson, W. Kent Wilson, Kenneth P. Winkler, John F. Wippel, Jan Woleński, Allan B. Wolter, Nicholas P. Wolterstorff, Rega Wood, W. Jay Wood, Paul Woodruff, Alison Wylie, Gideon Yaffe, Takashi Yagisawa, Yutaka Yamamoto, Keith E. Yandell, Xiaomei Yang, Dean Zimmerman, Günter Zoller, Catherine Zuckert, Michael Zuckert, Jack A. Zupko (J.A.Z.)
- Edited by Robert Audi, University of Notre Dame, Indiana
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- The Cambridge Dictionary of Philosophy
- Published online:
- 05 August 2015
- Print publication:
- 27 April 2015, pp ix-xxx
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