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1. A117 VALIDITY EVIDENCE FOR ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY COMPETENCY ASSESSMENT TOOLS: A SYSTEMATIC REVIEW

Author

Khan, R, primary, Homsi, H, additional, Gimpaya, N, additional, Sabrie, N, additional, Gholami, R, additional, Bansal, R, additional, Scaffidi, M, additional, Lightfoot, D, additional, James, P, additional, Siau, K, additional, Forbes, N, additional, Wani, S, additional, Keswani, R, additional, Walsh, C, additional, and Grover, S, additional

Published
2023
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4. Gender differences in mortality and quality of life after septic shock: A post-hoc analysis of the ARISE study

Author

Luethi, N, Bailey, M, Higgins, A, Howe, B, Peake, S, Delaney, A, Bellomo, R, Bennett, V, Board, J, McCracken, P, McGloughlin, S, Nanjayya, V, Teo, A, Hill, E, O'Brien, PJE, Sawtell, F, Schimanski, K, Wilson, D, Bolch, S, Eastwood, G, Kerr, F, Peak, L, Young, H, Edington, J, Fletcher, J, Smith, J, Ghelani, D, Nand, K, Sara, T, Cross, A, Flemming, D, Grummisch, M, Purdue, A, Fulton, E, Grove, K, Harney, A, Milburn, K, Millar, R, Mitchell, I, Rodgers, H, Scanlon, S, Coles, T, Connor, H, Dennett, J, Van Berkel, A, Barrington-Onslow, S, Henderson, S, Mehrtens, J, Dryburgh, J, Tankel, A, Braitberg, G, O'Bree, B, Shepherd, K, Vij, S, Allsop, S, Haji, D, Haji, K, Vuat, J, Bone, A, Elderkin, T, Orford, N, Ragg, M, Kelly, S, Stewart, D, Woodward, N, Harjola, V-P, Pettila, MO, Sutinen, S, Wilkman, E, Fratzia, J, Halkhoree, J, Treloar, S, Ryan, K, Sandford, T, Walsham, J, Jenkins, C, Williamson, D, Burrows, J, Hawkins, D, Tang, C, Dimakis, A, Holdgate, A, Micallef, S, Parr, M, White, H, Morrison, L, Sosnowski, K, Ramadoss, R, Soar, N, Wood, J, Franks, M, Williams, A, Hogan, C, Song, R, Tilsley, A, Rainsford, D, Wells, R, Dowling, J, Galt, P, Lamac, T, Lightfoot, D, Walker, C, Braid, K, DeVillecourt, T, Tan, HS, Seppelt, I, Chang, LF, Cheung, WS, Fok, SK, Lam, PK, Lam, SM, So, HM, Yan, W, Altea, A, Lancashire, B, Gomersall, CD, Graham, CA, Leung, P, Arora, S, Bass, F, Shehabi, Y, Isoardi, J, Isoardi, K, Powrie, D, Lawrence, S, Ankor, A, Chester, L, Davies, M, O'Connor, S, Poole, A, Soulsby, T, Sundararajan, K, Williams, J, Greenslade, JH, MacIsaac, C, Gorman, K, Jordan, A, Moore, L, Ankers, S, Bird, S, Fogg, T, Hickson, E, Jewell, T, Kyneur, K, O'Connor, A, Townsend, J, Yarad, E, Brown, S, Chamberlain, J, Cooper, J, Jenkinson, E, McDonald, E, Webb, S, Buhr, H, Coakley, J, Cowell, J, Hutch, D, Gattas, D, Keir, M, Rajbhandari, D, Rees, C, Baker, S, Roberts, B, Farone, E, Holmes, J, Santamaria, J, Winter, C, Finckh, A, Knowles, S, McCabe, J, Nair, P, Reynolds, C, Ahmed, B, Barton, D, Meaney, E, Nichol, A, Harris, R, Shields, L, Thomas, K, Karlsson, S, Kuitunen, A, Kukkurainen, A, Tenhunen, J, Varila, S, Ryan, N, Trethewy, C, Crosdale, J, Smith, JC, Vellaichamy, M, Furyk, J, Gordon, G, Jones, L, Senthuran, S, Bates, S, Butler, J, French, C, Tippett, A, Kelly, J, Kwans, J, Murphy, M, O'Flynn, D, Kurenda, C, Otto, T, Raniga, V, Williams, P, Ho, HF, Leung, A, Wu, H, Luethi, N, Bailey, M, Higgins, A, Howe, B, Peake, S, Delaney, A, Bellomo, R, Bennett, V, Board, J, McCracken, P, McGloughlin, S, Nanjayya, V, Teo, A, Hill, E, O'Brien, PJE, Sawtell, F, Schimanski, K, Wilson, D, Bolch, S, Eastwood, G, Kerr, F, Peak, L, Young, H, Edington, J, Fletcher, J, Smith, J, Ghelani, D, Nand, K, Sara, T, Cross, A, Flemming, D, Grummisch, M, Purdue, A, Fulton, E, Grove, K, Harney, A, Milburn, K, Millar, R, Mitchell, I, Rodgers, H, Scanlon, S, Coles, T, Connor, H, Dennett, J, Van Berkel, A, Barrington-Onslow, S, Henderson, S, Mehrtens, J, Dryburgh, J, Tankel, A, Braitberg, G, O'Bree, B, Shepherd, K, Vij, S, Allsop, S, Haji, D, Haji, K, Vuat, J, Bone, A, Elderkin, T, Orford, N, Ragg, M, Kelly, S, Stewart, D, Woodward, N, Harjola, V-P, Pettila, MO, Sutinen, S, Wilkman, E, Fratzia, J, Halkhoree, J, Treloar, S, Ryan, K, Sandford, T, Walsham, J, Jenkins, C, Williamson, D, Burrows, J, Hawkins, D, Tang, C, Dimakis, A, Holdgate, A, Micallef, S, Parr, M, White, H, Morrison, L, Sosnowski, K, Ramadoss, R, Soar, N, Wood, J, Franks, M, Williams, A, Hogan, C, Song, R, Tilsley, A, Rainsford, D, Wells, R, Dowling, J, Galt, P, Lamac, T, Lightfoot, D, Walker, C, Braid, K, DeVillecourt, T, Tan, HS, Seppelt, I, Chang, LF, Cheung, WS, Fok, SK, Lam, PK, Lam, SM, So, HM, Yan, W, Altea, A, Lancashire, B, Gomersall, CD, Graham, CA, Leung, P, Arora, S, Bass, F, Shehabi, Y, Isoardi, J, Isoardi, K, Powrie, D, Lawrence, S, Ankor, A, Chester, L, Davies, M, O'Connor, S, Poole, A, Soulsby, T, Sundararajan, K, Williams, J, Greenslade, JH, MacIsaac, C, Gorman, K, Jordan, A, Moore, L, Ankers, S, Bird, S, Fogg, T, Hickson, E, Jewell, T, Kyneur, K, O'Connor, A, Townsend, J, Yarad, E, Brown, S, Chamberlain, J, Cooper, J, Jenkinson, E, McDonald, E, Webb, S, Buhr, H, Coakley, J, Cowell, J, Hutch, D, Gattas, D, Keir, M, Rajbhandari, D, Rees, C, Baker, S, Roberts, B, Farone, E, Holmes, J, Santamaria, J, Winter, C, Finckh, A, Knowles, S, McCabe, J, Nair, P, Reynolds, C, Ahmed, B, Barton, D, Meaney, E, Nichol, A, Harris, R, Shields, L, Thomas, K, Karlsson, S, Kuitunen, A, Kukkurainen, A, Tenhunen, J, Varila, S, Ryan, N, Trethewy, C, Crosdale, J, Smith, JC, Vellaichamy, M, Furyk, J, Gordon, G, Jones, L, Senthuran, S, Bates, S, Butler, J, French, C, Tippett, A, Kelly, J, Kwans, J, Murphy, M, O'Flynn, D, Kurenda, C, Otto, T, Raniga, V, Williams, P, Ho, HF, Leung, A, and Wu, H

Abstract

PURPOSE: To assess the impact of gender and pre-menopausal state on short- and long-term outcomes in patients with septic shock. MATERIAL AND METHODS: Cohort study of the Australasian Resuscitation in Sepsis Evaluation (ARISE) trial, an international randomized controlled trial comparing early goal-directed therapy (EGDT) to usual care in patients with early septic shock, conducted between October 2008 and April 2014. The primary exposure in this analysis was legal gender and the secondary exposure was pre-menopausal state defined by chronological age (≤ 50 years). RESULTS: 641 (40.3%) of all 1591 ARISE trial participants in the intention-to-treat population were females and overall, 337 (21.2%) (146 females) patients were 50 years of age or younger. After risk-adjustment, we could not identify any survival benefit for female patients at day 90 in the younger (≤50 years) (adjusted Odds Ratio (aOR): 0.91 (0.46-1.89), p = .85) nor in the older (>50 years) age-group (aOR: 1.10 (0.81-1.49), p = .56). Similarly, there was no gender-difference in ICU, hospital, 1-year mortality nor quality of life measures. CONCLUSIONS: This post-hoc analysis of a large multi-center trial in early septic shock has shown no short- or long-term survival effect for women overall as well as in the pre-menopausal age-group.

Published
2020

5. Variation between pathogenic serovars within Salmonella pathogenicity islands

Author

Amavisit, P., Lightfoot, D., Browning, G.F., and Markham, P.F.

Subjects
Variation (Biology) -- Genetic aspects, Genetic transformation -- Analysis, Salmonella -- Identification and classification, Bacteria, Pathogenic -- Genetic aspects, Biological sciences
Abstract

Although four of the five Salmonella pathogenicity islands (SPIs) have been characterized in detail for Salmonella enterica serovar Typhimurium, and the fifth has been characterized for Salmonella enterica serovar Dublin, there have been limited studies to examine them in detail in a range of pathogenic serovars of S. enterica. The aim of this study was to examine these regions, shown to be crucial in virulence, in pathogenic serovars to identify any major deletions or insertions that may explain variation in virulence and provide further understanding of the elements involved in the evolution of these regions. Multiple strains of each of the 13 serovars were compared by Southern blot hybridization using a series of probes that together encompassed the full length of all five SPIs. With the exception of serovar Typhimurium, all strains of the same serovar were identical in all five SPIs. Those serovars that differed from serovar Typhimurium in SPI-1 to SPI-4 and from serovar Dublin in SPI-5 were examined in more detail in the variant regions by PCR, and restriction endonuclease digestion and/or DNA sequencing. While most variation in hybridization patterns was attributable to loss or gain of single restriction endonuclease cleavage sites, three regions, in SPI-1, SPI-3, and SPI-5, had differences due to major insertions or deletions. In SPI-1 the avrA gene was replaced by a 200-base fragment in three serovars, as reported previously. In SPI-5, two serovars had acquired an insertion with similarity to the pagJ and pagK genes between pipC and pipD. In SPI-3 the genes sugR and rhuM were deleted in most serovars and in some were replaced by sequences that were very similar to either the Escherichia coli fimbrial operon, flanked by two distinct insertion sequence elements, or to the E. coli retron phage [PHI]R73. The distribution of these differences suggests that there have been a number of relatively recent horizontal transfers of genes into S. enterica and that in some cases the same event has occurred in multiple lineages of S. enterica. Thus, it seems that insertion sequences and retron phages are likely to be involved in continuing evolution of the pathogenicity islands of pathogenic Salmonella serovars.

Published
2003

11. Can pre-hospital administration reduce time to initial antibiotic therapy in septic patients?.

Author

Lightfoot D., Santamaria J., Winter C., Bates S., Butler J., French C., Tippett A., Shepherd K., Vij S., Cudini D., Smith K., Bernard S., Stephenson M., Andrew E., Cameron P., Lum M., Udy A., Bennett V., Board J., McCracken P., McGloughlin S., Nanjayya V., Teo A., Bellomo R., Bolch S., Eastwood G., Kerr F., Peak L., Young H., Edington J., Fletcher J., Smith J., Cross A., Flemming D., Grummisch M., Purdue A., Coles T., Connor H., Dennett J., Van Berkel A., Braitberg G., O'Bree B., Allsop S., Haji D., Haji K., Vuat J., Bone A., Elderkin T., Orford N., Ragg M., Dowling J., Galt P., Lamac T., Walker C., MacIsaac C., Gorman K., Jordan A., Moore L., Farone E., Holmes J., Lightfoot D., Santamaria J., Winter C., Bates S., Butler J., French C., Tippett A., Shepherd K., Vij S., Cudini D., Smith K., Bernard S., Stephenson M., Andrew E., Cameron P., Lum M., Udy A., Bennett V., Board J., McCracken P., McGloughlin S., Nanjayya V., Teo A., Bellomo R., Bolch S., Eastwood G., Kerr F., Peak L., Young H., Edington J., Fletcher J., Smith J., Cross A., Flemming D., Grummisch M., Purdue A., Coles T., Connor H., Dennett J., Van Berkel A., Braitberg G., O'Bree B., Allsop S., Haji D., Haji K., Vuat J., Bone A., Elderkin T., Orford N., Ragg M., Dowling J., Galt P., Lamac T., Walker C., MacIsaac C., Gorman K., Jordan A., Moore L., Farone E., and Holmes J.

Abstract

Objective: To quantify the potential time saved with pre-hospital antibiotic therapy in sepsis. Method(s): Study data for adult patients transported by Ambulance Victoria (AV), and enrolled into the Australasian Resuscitation In Sepsis Evaluation (ARISE), were linked with pre-hospital electronic records. Result(s): An AV record was identified for 240 of 341 ARISE patients. The pre-hospital case notes referred to potential infection in 165 patients. The median time to first antibiotic administration from loading the patient into the ambulance was 107 (74-160) min. Conclusion(s): ARISE patients in Victoria were frequently identified pre-hospital. An opportunity exists to study the feasibility of pre-hospital antibiotic therapy.Copyright © 2019 Australasian College for Emergency Medicine

Published
2019

17. BioTIME : a database of biodiversity time series for the Anthropocene [data paper]

Author

Dornelas, M., Antao, L. H., Moyes, F., Bates, A. E., Magurran, A. E., Adam, D., Akhmetzhanova, A. A., Appeltans, W., Arcos, J. M., Arnold, H., Ayyappan, N., Badihi, G., Baird, A. H., Barbosa, M., Barreto, T. E., Baessler, C., Bellgrove, A., Belmaker, J., Benedetti-Cecchi, L., Bett, B. J., Bjorkman, A. D., Blazewicz, M., Blowes, S. A., Bloch, C. P., Bonebrake, T. C., Boyd, S., Bradford, M., Brooks, A. J., Brown, J. H., Bruelheide, H., Budy, P., Carvalho, F., Castaneda-Moya, E., Chen, C. A., Chamblee, J. F., Chase, T. J., Collier, L., Collinge, S. K., Condit, R., Cooper, E. J., Cornelissen, J. H. C., Cotano, U., Crow, S. K., Damasceno, G., Davies, C. H., Davis, R. A., Day, F. P., Degraer, S., Doherty, T. S., Dunn, T. E., Durigan, G., Duffy, J. E., Edelist, D., Edgar, G. J., Elahi, R., Elmendorf, S. C., Enemar, A., Ernest, S. K. M., Escribano, R., Estiarte, M., Evans, B. S., Fan, T. Y., Farah, F. T., Fernandes, L. L., Farneda, F. Z., Fidelis, A., Fitt, R., Fosaa, A. M., Franco, G. A. C., Frank, G. E., Fraser, W. R., Garcia, H., Gatti, R. C., Givan, O., Gorgone-Barbosa, E., Gould, W. A., Gries, C., Grossman, G. D., Gutierrez, J. R., Hale, S., Harmon, M. E., Harte, J., Haskins, G., Henshaw, D. L., Hermanutz, L., Hidalgo, P., Higuchi, P., Hoey, A., Hoey, G., Hofgaard, A., Holeck, K., Hollister, R. D., Holmes, R., Hoogenboom, M., Hsieh, C. H., Hubbell, S. P., Huettmann, F., Huffard, C. L., Hurlbert, A. H., Ivanauskas, N. M., Janik, D., Jandt, U., Jazdzewska, A., Johannessen, T., Johnstone, J., Jones, J., Jones, F. A. M., Kang, J., Kartawijaya, T., Keeley, C., Kelt, D. A., Kinnear, R., Klanderud, K., Knutsen, H., Koenig, C. C., Kortz, A. R., Kral, K., Kuhnz, L. A., Kuo, C. Y., Kushner, D. J., Laguionie-Marchais, C., Lancaster, L. T., Lee, C., Lefcheck, J. S., Levesque, E., Lightfoot, D., Lloret, F., Lloyd, J. D., Lopez-Baucells, A., Louzao, M., Madin, J. S., Magnusson, B., Malamud, S., Matthews, I., McFarland, K. P., McGill, B., McKnight, D., McLarney, W. O., Meador, J., Meserve, P. L., Metcalfe, D. J., Meyer, C. F. J., Michelsen, A., Milchakova, N., Moens, T., Moland, E., Moore, J., Moreira, C. M., Mueller, J., Murphy, G., Myers-Smith, I. H., Myster, R. W., Naumov, A., Neat, F., Nelson, J. A., Nelson, M., Newton, S. F., Norden, N., Oliver, J. C., Olsen, E. M., Onipchenko, V. G., Pabis, K., Pabst, R. J., Paquette, A., Pardede, S., Paterson, D. M., and Pélissier, Raphaël

Subjects
spatial, temporal, turnover, species richness, global, biodiversity
Abstract

Motivation: The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community-led open-source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene. Main types of variables included: The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record. Spatial location and grain: BioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km(2) (158 cm(2)) to 100 km(2) (1,000,000,000,000 cm(2)). Time period and grainBio: TIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year. Major taxa and level of measurement: BioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates.

Published
2018

18. First draft genome assembly of the Argane tree (Argania spinosa) [version 1; peer review: 1 approved, 1 approved with reservations]

Author

Khayi, S., Elhouda Azza, N., Gaboun, F., Pirro, S., Badad, O., Gonzalo Claros, M., Lightfoot, D. A., Unver, T., Chaouni, B., Merrouch, R., Rahim, B., Essayeh, S., Ganoudi, M., Abdelwahd, R., Diria, G., Alaoui Mdarhi, M., Labhilili, M., Iraqi, D., Mouhaddab, J., Sedrati, H., Memari, M., Hamamouch, N., Alché Ramírez, Juan de Dios, Boukhatem, N., Mrabet, R., Dahan, R., Legssyer, A., Khalfaoui, M., Badraoui, M., Vande Peer, Y., Tatusova, T., El Mousadik, A., Mentag, R., Ghazal, Hassan, Fulbright Commission, and Iridian Genome Foundation

Subjects
Endemic, Morocco, Argane, Argania spinosa, Genome, Assembly, International Argane Genome Consortium
Abstract

Background: The Argane tree (Argania spinosa L. Skeels) is an endemic tree of southwestern Morocco that plays an important socioeconomic and ecologic role for a dense human population in an arid zone. Several studies confirmed the importance of this species as a food and feed source and as a resource for both pharmaceutical and cosmetic compounds. Unfortunately, the argane tree ecosystem is facing significant threats from environmental changes (global warming, over-population) and over-exploitation. Limited research has been conducted, however, on argane tree genetics and genomics, which hinders its conservation and genetic improvement. Methods: Here, we present a draft genome assembly of A. spinosa. A reliable reference genome of A. spinosa was created using a hybrid de novo assembly approach combining short and long sequencing reads. Results: In total, 144 Gb Illumina HiSeq reads and 7.2 Gb PacBio reads were produced and assembled. The final draft genome comprises 75 327 scaffolds totaling 671 Mb with an N50 of 49 916 kb. The draft assembly is close to the genome size estimated by k-mers distribution and covers 89% of complete and 4.3% of partial Arabidopsis orthologous groups in BUSCO. Conclusion: The A. spinosa genome will be useful for assessing biodiversity leading to efficient conservation of this endangered endemic tree. Furthermore, the genome may enable genome-assisted cultivar breeding, and provide a better understanding of important metabolic pathways and their underlying genes for both cosmetic and pharmacological purposes., This work was supported by the Iridian Genome Foundation (MD, USA). H.G. is supported by a Grant from the NIH (MD, USA) for H3ABioNet/H3Africa (grant numbers U41HG006941 and U24 HG006941). O.B. and B.C. are Fulbright JSD (USA) grant recipients. This work also benefited from support of Midterm Research Program of INRA-Morocco through the use of its bioinformatics platform.

Published
2018

19. BioTIME: a database of biodiversity time series for the Anthropocene

Author

Dornelas, M, Antão, LH, Moyes, F, Bates, AE, Magurran, AE, Adam, D, Akhmetzhanova, AA, Appeltans, W, Arcos, JM, Arnold, H, Ayyappan, N, Badihi, G, Baird, AH, Barbosa, M, Barreto, TE, Bässler, C, Bellgrove, Alecia, Belmaker, J, Benedetti-Cecchi, L, Bett, BJ, Bjorkman, AD, Błażewicz, M, Blowes, SA, Bloch, CP, Bonebrake, TC, Boyd, S, Bradford, M, Brooks, AJ, Brown, JH, Bruelheide, H, Budy, P, Carvalho, F, Castañeda-Moya, E, Chen, CA, Chamblee, JF, Chase, TJ, Siegwart Collier, L, Collinge, SK, Condit, R, Cooper, EJ, Cornelissen, JHC, Cotano, U, Kyle Crow, S, Damasceno, G, Davies, CH, Davis, RA, Day, FP, Degraer, S, Doherty, Timothy, Dunn, TE, Durigan, G, Duffy, JE, Edelist, D, Edgar, GJ, Elahi, R, Elmendorf, SC, Enemar, A, Ernest, SKM, Escribano, R, Estiarte, M, Evans, BS, Fan, T-Y, Turini Farah, F, Loureiro Fernandes, L, Farneda, FZ, Fidelis, A, Fitt, R, Fosaa, AM, Daher Correa Franco, GA, Frank, GE, Fraser, WR, García, H, Cazzolla Gatti, R, Givan, O, Gorgone-Barbosa, E, Gould, WA, Gries, C, Grossman, GD, Gutierréz, JR, Hale, S, Harmon, ME, Harte, J, Haskins, G, Henshaw, DL, Hermanutz, L, Hidalgo, P, Higuchi, P, Hoey, A, Van Hoey, G, Hofgaard, A, Holeck, K, Hollister, RD, Holmes, R, Hoogenboom, M, Hsieh, C-H, Hubbell, SP, Huettmann, F, Huffard, CL, Hurlbert, AH, Macedo Ivanauskas, N, Janík, D, Jandt, U, Jażdżewska, A, Johannessen, T, Johnstone, J, Jones, J, Jones, FAM, Kang, J, Kartawijaya, T, Keeley, EC, Kelt, DA, Kinnear, R, Klanderud, K, Knutsen, H, Koenig, CC, Kortz, AR, Král, K, Kuhnz, LA, Kuo, C-Y, Kushner, DJ, Laguionie-Marchais, C, Lancaster, LT, Min Lee, C, Lefcheck, JS, Lévesque, E, Lightfoot, D, Lloret, F, Lloyd, JD, López-Baucells, A, Louzao, M, Madin, JS, Magnússon, B, Malamud, S, Matthews, I, McFarland, KP, McGill, B, McKnight, D, McLarney, WO, Meador, J, Meserve, PL, Metcalfe, DJ, Meyer, CFJ, Michelsen, A, Milchakova, N, Moens, T, Moland, E, Moore, J, Mathias Moreira, C, Müller, J, Murphy, G, Myers-Smith, IH, Myster, RW, Naumov, A, Neat, F, Nelson, JA, Paul Nelson, M, Newton, SF, Norden, N, Oliver, JC, Olsen, EM, Onipchenko, VG, Pabis, K, Pabst, RJ, Paquette, A, Pardede, S, Paterson, DM, Pélissier, R, Peñuelas, J, Pérez-Matus, A, Pizarro, O, Pomati, F, Post, E, Prins, HHT, Priscu, JC, Provoost, P, Prudic, KL, Pulliainen, E, Ramesh, BR, Mendivil Ramos, O, Rassweiler, A, Rebelo, JE, Reed, DC, Reich, PB, Remillard, SM, Richardson, AJ, Richardson, JP, van Rijn, I, Rocha, R, Rivera-Monroy, VH, Rixen, C, Robinson, KP, Ribeiro Rodrigues, R, de Cerqueira Rossa-Feres, D, Rudstam, L, Ruhl, H, Ruz, CS, Sampaio, EM, Rybicki, N, Rypel, A, Sal, S, Salgado, B, Santos, FAM, Savassi-Coutinho, AP, Scanga, S, Schmidt, J, Schooley, R, Setiawan, F, Shao, K-T, Shaver, GR, Sherman, S, Sherry, TW, Siciński, J, Sievers, C, da Silva, AC, Rodrigues da Silva, F, Silveira, FL, Slingsby, J, Smart, T, Snell, SJ, Soudzilovskaia, NA, Souza, GBG, Maluf Souza, F, Castro Souza, V, Stallings, CD, Stanforth, R, Stanley, EH, Mauro Sterza, J, Stevens, M, Stuart-Smith, R, Rondon Suarez, Y, Supp, S, Yoshio Tamashiro, J, Tarigan, S, Thiede, GP, Thorn, S, Tolvanen, A, Teresa Zugliani Toniato, M, Totland, Ø, Twilley, RR, Vaitkus, G, Valdivia, N, Vallejo, MI, Valone, TJ, Van Colen, C, Vanaverbeke, J, Venturoli, F, Verheye, HM, Vianna, M, Vieira, RP, Vrška, T, Quang Vu, C, Van Vu, L, Waide, RB, Waldock, C, Watts, D, Webb, S, Wesołowski, T, White, EP, Widdicombe, CE, Wilgers, D, Williams, R, Williams, SB, Williamson, M, Willig, MR, Willis, TJ, Wipf, S, Woods, KD, Woehler, EJ, Zawada, K, Zettler, ML, Hickler, T, Dornelas, M, Antão, LH, Moyes, F, Bates, AE, Magurran, AE, Adam, D, Akhmetzhanova, AA, Appeltans, W, Arcos, JM, Arnold, H, Ayyappan, N, Badihi, G, Baird, AH, Barbosa, M, Barreto, TE, Bässler, C, Bellgrove, Alecia, Belmaker, J, Benedetti-Cecchi, L, Bett, BJ, Bjorkman, AD, Błażewicz, M, Blowes, SA, Bloch, CP, Bonebrake, TC, Boyd, S, Bradford, M, Brooks, AJ, Brown, JH, Bruelheide, H, Budy, P, Carvalho, F, Castañeda-Moya, E, Chen, CA, Chamblee, JF, Chase, TJ, Siegwart Collier, L, Collinge, SK, Condit, R, Cooper, EJ, Cornelissen, JHC, Cotano, U, Kyle Crow, S, Damasceno, G, Davies, CH, Davis, RA, Day, FP, Degraer, S, Doherty, Timothy, Dunn, TE, Durigan, G, Duffy, JE, Edelist, D, Edgar, GJ, Elahi, R, Elmendorf, SC, Enemar, A, Ernest, SKM, Escribano, R, Estiarte, M, Evans, BS, Fan, T-Y, Turini Farah, F, Loureiro Fernandes, L, Farneda, FZ, Fidelis, A, Fitt, R, Fosaa, AM, Daher Correa Franco, GA, Frank, GE, Fraser, WR, García, H, Cazzolla Gatti, R, Givan, O, Gorgone-Barbosa, E, Gould, WA, Gries, C, Grossman, GD, Gutierréz, JR, Hale, S, Harmon, ME, Harte, J, Haskins, G, Henshaw, DL, Hermanutz, L, Hidalgo, P, Higuchi, P, Hoey, A, Van Hoey, G, Hofgaard, A, Holeck, K, Hollister, RD, Holmes, R, Hoogenboom, M, Hsieh, C-H, Hubbell, SP, Huettmann, F, Huffard, CL, Hurlbert, AH, Macedo Ivanauskas, N, Janík, D, Jandt, U, Jażdżewska, A, Johannessen, T, Johnstone, J, Jones, J, Jones, FAM, Kang, J, Kartawijaya, T, Keeley, EC, Kelt, DA, Kinnear, R, Klanderud, K, Knutsen, H, Koenig, CC, Kortz, AR, Král, K, Kuhnz, LA, Kuo, C-Y, Kushner, DJ, Laguionie-Marchais, C, Lancaster, LT, Min Lee, C, Lefcheck, JS, Lévesque, E, Lightfoot, D, Lloret, F, Lloyd, JD, López-Baucells, A, Louzao, M, Madin, JS, Magnússon, B, Malamud, S, Matthews, I, McFarland, KP, McGill, B, McKnight, D, McLarney, WO, Meador, J, Meserve, PL, Metcalfe, DJ, Meyer, CFJ, Michelsen, A, Milchakova, N, Moens, T, Moland, E, Moore, J, Mathias Moreira, C, Müller, J, Murphy, G, Myers-Smith, IH, Myster, RW, Naumov, A, Neat, F, Nelson, JA, Paul Nelson, M, Newton, SF, Norden, N, Oliver, JC, Olsen, EM, Onipchenko, VG, Pabis, K, Pabst, RJ, Paquette, A, Pardede, S, Paterson, DM, Pélissier, R, Peñuelas, J, Pérez-Matus, A, Pizarro, O, Pomati, F, Post, E, Prins, HHT, Priscu, JC, Provoost, P, Prudic, KL, Pulliainen, E, Ramesh, BR, Mendivil Ramos, O, Rassweiler, A, Rebelo, JE, Reed, DC, Reich, PB, Remillard, SM, Richardson, AJ, Richardson, JP, van Rijn, I, Rocha, R, Rivera-Monroy, VH, Rixen, C, Robinson, KP, Ribeiro Rodrigues, R, de Cerqueira Rossa-Feres, D, Rudstam, L, Ruhl, H, Ruz, CS, Sampaio, EM, Rybicki, N, Rypel, A, Sal, S, Salgado, B, Santos, FAM, Savassi-Coutinho, AP, Scanga, S, Schmidt, J, Schooley, R, Setiawan, F, Shao, K-T, Shaver, GR, Sherman, S, Sherry, TW, Siciński, J, Sievers, C, da Silva, AC, Rodrigues da Silva, F, Silveira, FL, Slingsby, J, Smart, T, Snell, SJ, Soudzilovskaia, NA, Souza, GBG, Maluf Souza, F, Castro Souza, V, Stallings, CD, Stanforth, R, Stanley, EH, Mauro Sterza, J, Stevens, M, Stuart-Smith, R, Rondon Suarez, Y, Supp, S, Yoshio Tamashiro, J, Tarigan, S, Thiede, GP, Thorn, S, Tolvanen, A, Teresa Zugliani Toniato, M, Totland, Ø, Twilley, RR, Vaitkus, G, Valdivia, N, Vallejo, MI, Valone, TJ, Van Colen, C, Vanaverbeke, J, Venturoli, F, Verheye, HM, Vianna, M, Vieira, RP, Vrška, T, Quang Vu, C, Van Vu, L, Waide, RB, Waldock, C, Watts, D, Webb, S, Wesołowski, T, White, EP, Widdicombe, CE, Wilgers, D, Williams, R, Williams, SB, Williamson, M, Willig, MR, Willis, TJ, Wipf, S, Woods, KD, Woehler, EJ, Zawada, K, Zettler, ML, and Hickler, T

Published
2018

20. BioTIME:a database of biodiversity time series for the Anthropocene

Author

Dornelas, M. (Maria), Antao, L. H. (Laura H.), Moyes, F. (Faye), Bates, A. E. (Amanda E.), Magurran, A. E. (Anne E.), Adam, D. (Dusan), Akhmetzhanova, A. A. (Asem A.), Appeltans, W. (Ward), Arcos, J. M. (Jose Manuel), Arnold, H. (Haley), Ayyappan, N. (Narayanan), Badihi, G. (Gal), Baird, A. H. (Andrew H.), Barbosa, M. (Miguel), Barreto, T. E. (Tiago Egydio), Baessler, C. (Claus), Bellgrove, A. (Alecia), Belmaker, J. (Jonathan), Benedetti-Cecchi, L. (Lisandro), Bett, B. J. (Brian J.), Bjorkman, A. D. (Anne D.), Blazewicz, M. (Magdalena), Blowes, S. A. (Shane A.), Bloch, C. P. (Christopher P.), Bonebrake, T. C. (Timothy C.), Boyd, S. (Susan), Bradford, M. (Matt), Brooks, A. J. (Andrew J.), Brown, J. H. (James H.), Bruelheide, H. (Helge), Budy, P. (Phaedra), Carvalho, F. (Fernando), Castaneda-Moya, E. (Edward), Chen, C. A. (Chaolun Allen), Chamblee, J. F. (John F.), Chase, T. J. (Tory J.), Siegwart Collier, L. (Laura), Collinge, S. K. (Sharon K.), Condit, R. (Richard), Cooper, E. J. (Elisabeth J.), Cornelissen, J. H. (J. Hans C.), Cotano, U. (Unai), Crow, S. K. (Shannan Kyle), Damasceno, G. (Gabriella), Davies, C. H. (Claire H.), Davis, R. A. (Robert A.), Day, F. P. (Frank P.), Degraer, S. (Steven), Doherty, T. S. (Tim S.), Dunn, T. E. (Timothy E.), Durigan, G. (Giselda), Duffy, J. E. (J. Emmett), Edelist, D. (Dor), Edgar, G. J. (Graham J.), Elahi, R. (Robin), Elmendorf, S. C. (Sarah C.), Enemar, A. (Anders), Ernest, S. K. (S. K. Morgan), Escribano, R. (Ruben), Estiarte, M. (Marc), Evans, B. S. (Brian S.), Fan, T.-Y. (Tung-Yung), Farah, F. T. (Fabiano Turini), Fernandes, L. L. (Luiz Loureiro), Farneda, F. Z. (Fabio Z.), Fidelis, A. (Alessandra), Fitt, R. (Robert), Fosaa, A. M. (Anna Maria), Daher Correa Franco, G. A. (Geraldo Antonio), Frank, G. E. (Grace E.), Fraser, W. R. (William R.), Garcia, H. (Hernando), Gatti, R. C. (Roberto Cazzolla), Givan, O. (Or), Gorgone-Barbosa, E. (Elizabeth), Gould, W. A. (William A.), Gries, C. (Corinna), Grossman, G. D. (Gary D.), Gutierrez, J. R. (Julio R.), Hale, S. (Stephen), Harmon, M. E. (Mark E.), Harte, J. (John), Haskins, G. (Gary), Henshaw, D. L. (Donald L.), Hermanutz, L. (Luise), Hidalgo, P. (Pamela), Higuchi, P. (Pedro), Hoey, A. (Andrew), Van Hoey, G. (Gert), Hofgaard, A. (Annika), Holeck, K. (Kristen), Hollister, R. D. (Robert D.), Holmes, R. (Richard), Hoogenboom, M. (Mia), Hsieh, C.-h. (Chih-hao), Hubbell, S. P. (Stephen P.), Huettmann, F. (Falk), Huffard, C. L. (Christine L.), Hurlbert, A. H. (Allen H.), Ivanauskas, N. M. (Natalia Macedo), Janik, D. (David), Jandt, U. (Ute), Jazdzewska, A. (Anna), Johannessen, T. (Tore), Johnstone, J. (Jill), Jones, J. (Julia), Jones, F. A. (Faith A. M.), Kang, J. (Jungwon), Kartawijaya, T. (Tasrif), Keeley, E. C. (Erin C.), Kelt, D. A. (Douglas A.), Kinnear, R. (Rebecca), Klanderud, K. (Kari), Knutsen, H. (Halvor), Koenig, C. C. (Christopher C.), Kortz, A. R. (Alessandra R.), Kral, K. (Kamil), Kuhnz, L. A. (Linda A.), Kuo, C.-Y. (Chao-Yang), Kushner, D. J. (David J.), Laguionie-Marchais, C. (Claire), Lancaster, L. T. (Lesley T.), Min Lee, C. (Cheol), Lefcheck, J. S. (Jonathan S.), Levesque, E. (Esther), Lightfoot, D. (David), Lloret, F. (Francisco), Lloyd, J. D. (John D.), Lopez-Baucells, A. (Adria), Louzao, M. (Maite), Madin, J. S. (Joshua S.), Magnusson, B. (Borgpor), Malamud, S. (Shahar), Matthews, I. (Iain), McFarland, K. P. (Kent P.), McGill, B. (Brian), McKnight, D. (Diane), McLarney, W. O. (William O.), Meador, J. (Jason), Meserve, P. L. (Peter L.), Metcalfe, D. J. (Daniel J.), Meyer, C. F. (Christoph F. J.), Michelsen, A. (Anders), Milchakova, N. (Nataliya), Moens, T. (Tom), Moland, E. (Even), Moore, J. (Jon), Moreira, C. M. (Carolina Mathias), Mueller, J. (Joerg), Murphy, G. (Grace), Myers-Smith, I. H. (Isla H.), Myster, R. W. (Randall W.), Naumov, A. (Andrew), Neat, F. (Francis), Nelson, J. A. (James A.), Paul Nelson, M. (Michael), Newton, S. F. (Stephen F.), Norden, N. (Natalia), Oliver, J. C. (Jeffrey C.), Olsen, E. M. (Esben M.), Onipchenko, V. G. (Vladimir G.), Pabis, K. (Krzysztof), Pabst, R. J. (Robert J.), Paquette, A. (Alain), Pardede, S. (Sinta), Paterson, D. M. (David M.), Pelissier, R. (Raphael), Penuelas, J. (Josep), Perez-Matus, A. (Alejandro), Pizarro, O. (Oscar), Pomati, F. (Francesco), Post, E. (Eric), Prins, H. H. (Herbert H. T.), Priscu, J. C. (John C.), Provoost, P. (Pieter), Prudic, K. L. (Kathleen L.), Erkki, P. (Pulliainen), Ramesh, B. R. (B. R.), Mendivil Ramos, O. (Olivia), Rassweiler, A. (Andrew), Rebelo, J. E. (Jose Eduardo), Reed, D. C. (Daniel C.), Reich, P. B. (Peter B.), Remillard, S. M. (Suzanne M.), Richardson, A. J. (Anthony J.), Richardson, J. P. (J. Paul), van Rijn, I. (Itai), Rocha, R. (Ricardo), Rivera-Monroy, V. H. (Victor H.), Rixen, C. (Christian), Robinson, K. P. (Kevin P.), Rodrigues, R. R. (Ricardo Ribeiro), Rossa-Feres, D. d. (Denise de Cerqueira), Rudstam, L. (Lars), Ruhl, H. (Henry), Ruz, C. S. (Catalina S.), Sampaio, E. M. (Erica M.), Rybicki, N. (Nancy), Rypel, A. (Andrew), Sal, S. (Sofia), Salgado, B. (Beatriz), Santos, F. A. (Flavio A. M.), Savassi-Coutinho, A. P. (Ana Paula), Scanga, S. (Sara), Schmidt, J. (Jochen), Schooley, R. (Robert), Setiawan, F. (Fakhrizal), Shao, K.-T. (Kwang-Tsao), Shaver, G. R. (Gaius R.), Sherman, S. (Sally), Sherry, T. W. (Thomas W.), Sicinski, J. (Jacek), Sievers, C. (Caya), da Silva, A. C. (Ana Carolina), da Silva, F. R. (Fernando Rodrigues), Silveira, F. L. (Fabio L.), Slingsby, J. (Jasper), Smart, T. (Tracey), Snell, S. J. (Sara J.), Soudzilovskaia, N. A. (Nadejda A.), Souza, G. B. (Gabriel B. G.), Souza, F. M. (Flaviana Maluf), Souza, V. C. (Vinicius Castro), Stallings, C. D. (Christopher D.), Stanforth, R. (Rowan), Stanley, E. H. (Emily H.), Sterza, J. M. (Jose Mauro), Stevens, M. (Maarten), Stuart-Smith, R. (Rick), Rondon Suarez, Y. (Yzel), Supp, S. (Sarah), Yoshio Tamashiro, J. (Jorge), Tarigan, S. (Sukmaraharja), Thiede, G. P. (Gary P.), Thorn, S. (Simon), Tolvanen, A. (Anne), Zugliani Toniato, M. T. (Maria Teresa), Totland, O. (Orjan), Twilley, R. R. (Robert R.), Vaitkus, G. (Gediminas), Valdivia, N. (Nelson), Vallejo, M. I. (Martha Isabel), Valone, T. J. (Thomas J.), Van Colen, C. (Carl), Vanaverbeke, J. (Jan), Venturoli, F. (Fabio), Verheye, H. M. (Hans M.), Vianna, M. (Marcelo), Vieira, R. P. (Rui P.), Vrska, T. (Tomas), Vu, C. Q. (Con Quang), Vu, L. V. (Lien Van), Waide, R. B. (Robert B.), Waldock, C. (Conor), Watts, D. (Dave), Webb, S. (Sara), Wesolowski, T. (Tomasz), White, E. P. (Ethan P.), Widdicombe, C. E. (Claire E.), Wilgers, D. (Dustin), Williams, R. (Richard), Williams, S. B. (Stefan B.), Williamson, M. (Mark), Willig, M. R. (Michael R.), Willis, T. J. (Trevor J.), Wipf, S. (Sonja), Woods, K. D. (Kerry D.), Woehler, E. J. (Eric J.), Zawada, K. (Kyle), Zettler, M. L. (Michael L.), Dornelas, M. (Maria), Antao, L. H. (Laura H.), Moyes, F. (Faye), Bates, A. E. (Amanda E.), Magurran, A. E. (Anne E.), Adam, D. (Dusan), Akhmetzhanova, A. A. (Asem A.), Appeltans, W. (Ward), Arcos, J. M. (Jose Manuel), Arnold, H. (Haley), Ayyappan, N. (Narayanan), Badihi, G. (Gal), Baird, A. H. (Andrew H.), Barbosa, M. (Miguel), Barreto, T. E. (Tiago Egydio), Baessler, C. (Claus), Bellgrove, A. (Alecia), Belmaker, J. (Jonathan), Benedetti-Cecchi, L. (Lisandro), Bett, B. J. (Brian J.), Bjorkman, A. D. (Anne D.), Blazewicz, M. (Magdalena), Blowes, S. A. (Shane A.), Bloch, C. P. (Christopher P.), Bonebrake, T. C. (Timothy C.), Boyd, S. (Susan), Bradford, M. (Matt), Brooks, A. J. (Andrew J.), Brown, J. H. (James H.), Bruelheide, H. (Helge), Budy, P. (Phaedra), Carvalho, F. (Fernando), Castaneda-Moya, E. (Edward), Chen, C. A. (Chaolun Allen), Chamblee, J. F. (John F.), Chase, T. J. (Tory J.), Siegwart Collier, L. (Laura), Collinge, S. K. (Sharon K.), Condit, R. (Richard), Cooper, E. J. (Elisabeth J.), Cornelissen, J. H. (J. Hans C.), Cotano, U. (Unai), Crow, S. K. (Shannan Kyle), Damasceno, G. (Gabriella), Davies, C. H. (Claire H.), Davis, R. A. (Robert A.), Day, F. P. (Frank P.), Degraer, S. (Steven), Doherty, T. S. (Tim S.), Dunn, T. E. (Timothy E.), Durigan, G. (Giselda), Duffy, J. E. (J. Emmett), Edelist, D. (Dor), Edgar, G. J. (Graham J.), Elahi, R. (Robin), Elmendorf, S. C. (Sarah C.), Enemar, A. (Anders), Ernest, S. K. (S. K. Morgan), Escribano, R. (Ruben), Estiarte, M. (Marc), Evans, B. S. (Brian S.), Fan, T.-Y. (Tung-Yung), Farah, F. T. (Fabiano Turini), Fernandes, L. L. (Luiz Loureiro), Farneda, F. Z. (Fabio Z.), Fidelis, A. (Alessandra), Fitt, R. (Robert), Fosaa, A. M. (Anna Maria), Daher Correa Franco, G. A. (Geraldo Antonio), Frank, G. E. (Grace E.), Fraser, W. R. (William R.), Garcia, H. (Hernando), Gatti, R. C. (Roberto Cazzolla), Givan, O. (Or), Gorgone-Barbosa, E. (Elizabeth), Gould, W. A. (William A.), Gries, C. (Corinna), Grossman, G. D. (Gary D.), Gutierrez, J. R. (Julio R.), Hale, S. (Stephen), Harmon, M. E. (Mark E.), Harte, J. (John), Haskins, G. (Gary), Henshaw, D. L. (Donald L.), Hermanutz, L. (Luise), Hidalgo, P. (Pamela), Higuchi, P. (Pedro), Hoey, A. (Andrew), Van Hoey, G. (Gert), Hofgaard, A. (Annika), Holeck, K. (Kristen), Hollister, R. D. (Robert D.), Holmes, R. (Richard), Hoogenboom, M. (Mia), Hsieh, C.-h. (Chih-hao), Hubbell, S. P. (Stephen P.), Huettmann, F. (Falk), Huffard, C. L. (Christine L.), Hurlbert, A. H. (Allen H.), Ivanauskas, N. M. (Natalia Macedo), Janik, D. (David), Jandt, U. (Ute), Jazdzewska, A. (Anna), Johannessen, T. (Tore), Johnstone, J. (Jill), Jones, J. (Julia), Jones, F. A. (Faith A. M.), Kang, J. (Jungwon), Kartawijaya, T. (Tasrif), Keeley, E. C. (Erin C.), Kelt, D. A. (Douglas A.), Kinnear, R. (Rebecca), Klanderud, K. (Kari), Knutsen, H. (Halvor), Koenig, C. C. (Christopher C.), Kortz, A. R. (Alessandra R.), Kral, K. (Kamil), Kuhnz, L. A. (Linda A.), Kuo, C.-Y. (Chao-Yang), Kushner, D. J. (David J.), Laguionie-Marchais, C. (Claire), Lancaster, L. T. (Lesley T.), Min Lee, C. (Cheol), Lefcheck, J. S. (Jonathan S.), Levesque, E. (Esther), Lightfoot, D. (David), Lloret, F. (Francisco), Lloyd, J. D. (John D.), Lopez-Baucells, A. (Adria), Louzao, M. (Maite), Madin, J. S. (Joshua S.), Magnusson, B. (Borgpor), Malamud, S. (Shahar), Matthews, I. (Iain), McFarland, K. P. (Kent P.), McGill, B. (Brian), McKnight, D. (Diane), McLarney, W. O. (William O.), Meador, J. (Jason), Meserve, P. L. (Peter L.), Metcalfe, D. J. (Daniel J.), Meyer, C. F. (Christoph F. J.), Michelsen, A. (Anders), Milchakova, N. (Nataliya), Moens, T. (Tom), Moland, E. (Even), Moore, J. (Jon), Moreira, C. M. (Carolina Mathias), Mueller, J. (Joerg), Murphy, G. (Grace), Myers-Smith, I. H. (Isla H.), Myster, R. W. (Randall W.), Naumov, A. (Andrew), Neat, F. (Francis), Nelson, J. A. (James A.), Paul Nelson, M. (Michael), Newton, S. F. (Stephen F.), Norden, N. (Natalia), Oliver, J. C. (Jeffrey C.), Olsen, E. M. (Esben M.), Onipchenko, V. G. (Vladimir G.), Pabis, K. (Krzysztof), Pabst, R. J. (Robert J.), Paquette, A. (Alain), Pardede, S. (Sinta), Paterson, D. M. (David M.), Pelissier, R. (Raphael), Penuelas, J. (Josep), Perez-Matus, A. (Alejandro), Pizarro, O. (Oscar), Pomati, F. (Francesco), Post, E. (Eric), Prins, H. H. (Herbert H. T.), Priscu, J. C. (John C.), Provoost, P. (Pieter), Prudic, K. L. (Kathleen L.), Erkki, P. (Pulliainen), Ramesh, B. R. (B. R.), Mendivil Ramos, O. (Olivia), Rassweiler, A. (Andrew), Rebelo, J. E. (Jose Eduardo), Reed, D. C. (Daniel C.), Reich, P. B. (Peter B.), Remillard, S. M. (Suzanne M.), Richardson, A. J. (Anthony J.), Richardson, J. P. (J. Paul), van Rijn, I. (Itai), Rocha, R. (Ricardo), Rivera-Monroy, V. H. (Victor H.), Rixen, C. (Christian), Robinson, K. P. (Kevin P.), Rodrigues, R. R. (Ricardo Ribeiro), Rossa-Feres, D. d. (Denise de Cerqueira), Rudstam, L. (Lars), Ruhl, H. (Henry), Ruz, C. S. (Catalina S.), Sampaio, E. M. (Erica M.), Rybicki, N. (Nancy), Rypel, A. (Andrew), Sal, S. (Sofia), Salgado, B. (Beatriz), Santos, F. A. (Flavio A. M.), Savassi-Coutinho, A. P. (Ana Paula), Scanga, S. (Sara), Schmidt, J. (Jochen), Schooley, R. (Robert), Setiawan, F. (Fakhrizal), Shao, K.-T. (Kwang-Tsao), Shaver, G. R. (Gaius R.), Sherman, S. (Sally), Sherry, T. W. (Thomas W.), Sicinski, J. (Jacek), Sievers, C. (Caya), da Silva, A. C. (Ana Carolina), da Silva, F. R. (Fernando Rodrigues), Silveira, F. L. (Fabio L.), Slingsby, J. (Jasper), Smart, T. (Tracey), Snell, S. J. (Sara J.), Soudzilovskaia, N. A. (Nadejda A.), Souza, G. B. (Gabriel B. G.), Souza, F. M. (Flaviana Maluf), Souza, V. C. (Vinicius Castro), Stallings, C. D. (Christopher D.), Stanforth, R. (Rowan), Stanley, E. H. (Emily H.), Sterza, J. M. (Jose Mauro), Stevens, M. (Maarten), Stuart-Smith, R. (Rick), Rondon Suarez, Y. (Yzel), Supp, S. (Sarah), Yoshio Tamashiro, J. (Jorge), Tarigan, S. (Sukmaraharja), Thiede, G. P. (Gary P.), Thorn, S. (Simon), Tolvanen, A. (Anne), Zugliani Toniato, M. T. (Maria Teresa), Totland, O. (Orjan), Twilley, R. R. (Robert R.), Vaitkus, G. (Gediminas), Valdivia, N. (Nelson), Vallejo, M. I. (Martha Isabel), Valone, T. J. (Thomas J.), Van Colen, C. (Carl), Vanaverbeke, J. (Jan), Venturoli, F. (Fabio), Verheye, H. M. (Hans M.), Vianna, M. (Marcelo), Vieira, R. P. (Rui P.), Vrska, T. (Tomas), Vu, C. Q. (Con Quang), Vu, L. V. (Lien Van), Waide, R. B. (Robert B.), Waldock, C. (Conor), Watts, D. (Dave), Webb, S. (Sara), Wesolowski, T. (Tomasz), White, E. P. (Ethan P.), Widdicombe, C. E. (Claire E.), Wilgers, D. (Dustin), Williams, R. (Richard), Williams, S. B. (Stefan B.), Williamson, M. (Mark), Willig, M. R. (Michael R.), Willis, T. J. (Trevor J.), Wipf, S. (Sonja), Woods, K. D. (Kerry D.), Woehler, E. J. (Eric J.), Zawada, K. (Kyle), and Zettler, M. L. (Michael L.)

Abstract

Motivation: The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community‐led open‐source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene. Main types of variables included: The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record. Spatial location and grain: BioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km² (158 cm²) to 100 km² (1,000,000,000,000 cm²). Time period and grain: BioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year. Major taxa and level of measurement: BioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates. Software format: .csv and .SQL.

Published
2018

21. First draft genome assembly of the Argane tree (Argania spinosa) [version 1; peer review: 1 approved, 1 approved with reservations]

Author

Fulbright Commission, Iridian Genome Foundation, Khayi, S., Elhouda Azza, N., Gaboun, F., Pirro, S., Badad, O., Gonzalo Claros, M., Lightfoot, D. A., Unver, T., Chaouni, B., Merrouch, R., Rahim, B., Essayeh, S., Ganoudi, M., Abdelwahd, R., Diria, G., Alaoui Mdarhi, M., Labhilili, M., Iraqi, D., Mouhaddab, J., Sedrati, H., Memari, M., Hamamouch, N., Alché Ramírez, Juan de Dios, Boukhatem, N., Mrabet, R., Dahan, R., Legssyer, A., Khalfaoui, M., Badraoui, M., Vande Peer, Y., Tatusova, T., El Mousadik, A., Mentag, R., Ghazal, Hassan, Fulbright Commission, Iridian Genome Foundation, Khayi, S., Elhouda Azza, N., Gaboun, F., Pirro, S., Badad, O., Gonzalo Claros, M., Lightfoot, D. A., Unver, T., Chaouni, B., Merrouch, R., Rahim, B., Essayeh, S., Ganoudi, M., Abdelwahd, R., Diria, G., Alaoui Mdarhi, M., Labhilili, M., Iraqi, D., Mouhaddab, J., Sedrati, H., Memari, M., Hamamouch, N., Alché Ramírez, Juan de Dios, Boukhatem, N., Mrabet, R., Dahan, R., Legssyer, A., Khalfaoui, M., Badraoui, M., Vande Peer, Y., Tatusova, T., El Mousadik, A., Mentag, R., and Ghazal, Hassan

Abstract

Background: The Argane tree (Argania spinosa L. Skeels) is an endemic tree of southwestern Morocco that plays an important socioeconomic and ecologic role for a dense human population in an arid zone. Several studies confirmed the importance of this species as a food and feed source and as a resource for both pharmaceutical and cosmetic compounds. Unfortunately, the argane tree ecosystem is facing significant threats from environmental changes (global warming, over-population) and over-exploitation. Limited research has been conducted, however, on argane tree genetics and genomics, which hinders its conservation and genetic improvement. Methods: Here, we present a draft genome assembly of A. spinosa. A reliable reference genome of A. spinosa was created using a hybrid de novo assembly approach combining short and long sequencing reads. Results: In total, 144 Gb Illumina HiSeq reads and 7.2 Gb PacBio reads were produced and assembled. The final draft genome comprises 75 327 scaffolds totaling 671 Mb with an N50 of 49 916 kb. The draft assembly is close to the genome size estimated by k-mers distribution and covers 89% of complete and 4.3% of partial Arabidopsis orthologous groups in BUSCO. Conclusion: The A. spinosa genome will be useful for assessing biodiversity leading to efficient conservation of this endangered endemic tree. Furthermore, the genome may enable genome-assisted cultivar breeding, and provide a better understanding of important metabolic pathways and their underlying genes for both cosmetic and pharmacological purposes.

Published
2018

22. BioTIME: A database of biodiversity time series for the Anthropocene

Author

Dornelas, M., Antão, L. H., Moyes, F., Bates, A. E., Magurran, A. E., Adam, D., Akhmetzhanova, A. A., Appeltans, W., Arcos, J. M., Arnold, H., Ayyappan, N., Badihi, G., Baird, A. H., Barbosa, M., Barreto, T. E., Bässler, C., Bellgrove, A., Belmaker, J., Benedetti-Cecchi, L., Bett, B. J., Bjorkman, A. D., Błażewicz, M., Blowes, S. A., Bloch, C. P., Bonebrake, T. C., Boyd, S., Bradford, M., Brooks, A. J., Brown, J. H., Bruelheide, H., Budy, P., Carvalho, F., Castañeda-Moya, E., Chen, C. A., Chamblee, J. F., Chase, T. J., Siegwart Collier, L., Collinge, S. K., Condit, R., Cooper, E. J., Cornelissen, J. H. C., Cotano, U., Kyle Crow, S., Damasceno, G., Davies, C. H., Davis, R. A., Day, F. P., Degraer, S., Doherty, T. S., Dunn, T. E., Durigan, G., Duffy, J. E., Edelist, D., Edgar, G. J., Elahi, R., Elmendorf, S. C., Enemar, A., Ernest, S. K. M., Escribano, R., Estiarte, M., Evans, B. S., Fan, T. Y., Turini Farah, F., Loureiro Fernandes, L., Farneda, F. Z., Fidelis, A., Fitt, R., Fosaa, A. M., Daher Correa Franco, G. A., Frank, G. E., Fraser, W. R., García, H., Cazzolla Gatti, R., Givan, O., Gorgone-Barbosa, E., Gould, W. A., Gries, C., Grossman, G. D., Gutierréz, J. R., Hale, S., Harmon, M. E., Harte, J., Haskins, G., Henshaw, D. L., Hermanutz, L., Hidalgo, P., Higuchi, P., Hoey, A., Van Hoey, G., Hofgaard, A., Holeck, K., Hollister, R. D., Holmes, R., Hoogenboom, M., Hsieh, C. H., Hubbell, S. P., Huettmann, F., Huffard, C. L., Hurlbert, A. H., Macedo Ivanauskas, N., Janík, D., Jandt, U., Jażdżewska, A., Johannessen, T., Johnstone, J., Jones, J., Jones, F. A. M., Kang, J., Kartawijaya, T., Keeley, E. C., Kelt, D. A., Kinnear, R., Klanderud, K., Knutsen, H., Koenig, C. C., Kortz, A. R., Král, K., Kuhnz, L. A., Kuo, C. Y., Kushner, D. J., Laguionie-Marchais, C., Lancaster, L. T., Min Lee, C., Lefcheck, J. S., Lévesque, E., Lightfoot, D., Lloret, F., Lloyd, J. D., López-Baucells, A., Louzao, M., Madin, J. S., Magnússon, B., Malamud, S., Matthews, I., McFarland, K. P., McGill, B., McKnight, D., McLarney, W. O., Meador, J., Meserve, P. L., Metcalfe, D. J., Meyer, C. F. J., Michelsen, A., Milchakova, N., Moens, T., Moland, E., Moore, J., Mathias Moreira, C., Müller, J., Murphy, G., Myers-Smith, I. H., Myster, R. W., Naumov, A., Neat, F., Nelson, J. A., Paul Nelson, M., Newton, S. F., Norden, N., Oliver, J. C., Olsen, E. M., Onipchenko, V. G., Pabis, K., Pabst, R. J., Paquette, A., Pardede, S., Paterson, D. M., Pélissier, R., Peñuelas, J., Pérez-Matus, A., Pizarro, O., Pomati, F., Post, E., Prins, H. H. T., Priscu, J. C., Provoost, P., Prudic, K. L., Pulliainen, E., Ramesh, B. R., Mendivil Ramos, O., Rassweiler, A., Rebelo, J. E., Reed, D. C., Reich, P. B., Remillard, S. M., Richardson, A. J., Richardson, J. P., van Rijn, I., Rocha, R., Rivera-Monroy, V. H., Rixen, C., Robinson, K. P., Ribeiro Rodrigues, R., de Cerqueira Rossa-Feres, D., Rudstam, L., Ruhl, H., Ruz, C. S., Sampaio, E. M., Rybicki, N., Rypel, A., Sal, S., Salgado, B., Santos, F. A. M., Savassi-Coutinho, A. P., Scanga, S., Schmidt, J., Schooley, R., Setiawan, F., Shao, K. T., Shaver, G. R., Sherman, S., Sherry, T. W., Siciński, J., Sievers, C., da Silva, A. C., Rodrigues da Silva, F., Silveira, F. L., Slingsby, J., Smart, T., Snell, S. J., Soudzilovskaia, N. A., Souza, G. B. G., Maluf Souza, F., Castro Souza, V., Stallings, C. D., Stanforth, R., Stanley, E. H., Mauro Sterza, J., Stevens, M., Stuart-Smith, R., Rondon Suarez, Y., Supp, S., Yoshio Tamashiro, J., Tarigan, S., Thiede, G. P., Thorn, S., Tolvanen, A., Teresa Zugliani Toniato, M., Totland, Ø, Twilley, R. R., Vaitkus, G., Valdivia, N., Vallejo, M. I., Valone, T. J., Van Colen, C., Vanaverbeke, J., Venturoli, F., Verheye, H. M., Vianna, M., Vieira, R. P., Vrška, T., Quang Vu, C., Van Vu, L., Waide, R. B., Waldock, C., Watts, D., Webb, S., Wesołowski, T., White, E. P., Widdicombe, C. E., Wilgers, D., Williams, R., Williams, S. B., Williamson, M., Willig, M. R., Willis, T. J., Wipf, S., Woods, K. D., Woehler, E. J., Zawada, K., Zettler, M. L., Dornelas, M., Antão, L. H., Moyes, F., Bates, A. E., Magurran, A. E., Adam, D., Akhmetzhanova, A. A., Appeltans, W., Arcos, J. M., Arnold, H., Ayyappan, N., Badihi, G., Baird, A. H., Barbosa, M., Barreto, T. E., Bässler, C., Bellgrove, A., Belmaker, J., Benedetti-Cecchi, L., Bett, B. J., Bjorkman, A. D., Błażewicz, M., Blowes, S. A., Bloch, C. P., Bonebrake, T. C., Boyd, S., Bradford, M., Brooks, A. J., Brown, J. H., Bruelheide, H., Budy, P., Carvalho, F., Castañeda-Moya, E., Chen, C. A., Chamblee, J. F., Chase, T. J., Siegwart Collier, L., Collinge, S. K., Condit, R., Cooper, E. J., Cornelissen, J. H. C., Cotano, U., Kyle Crow, S., Damasceno, G., Davies, C. H., Davis, R. A., Day, F. P., Degraer, S., Doherty, T. S., Dunn, T. E., Durigan, G., Duffy, J. E., Edelist, D., Edgar, G. J., Elahi, R., Elmendorf, S. C., Enemar, A., Ernest, S. K. M., Escribano, R., Estiarte, M., Evans, B. S., Fan, T. Y., Turini Farah, F., Loureiro Fernandes, L., Farneda, F. Z., Fidelis, A., Fitt, R., Fosaa, A. M., Daher Correa Franco, G. A., Frank, G. E., Fraser, W. R., García, H., Cazzolla Gatti, R., Givan, O., Gorgone-Barbosa, E., Gould, W. A., Gries, C., Grossman, G. D., Gutierréz, J. R., Hale, S., Harmon, M. E., Harte, J., Haskins, G., Henshaw, D. L., Hermanutz, L., Hidalgo, P., Higuchi, P., Hoey, A., Van Hoey, G., Hofgaard, A., Holeck, K., Hollister, R. D., Holmes, R., Hoogenboom, M., Hsieh, C. H., Hubbell, S. P., Huettmann, F., Huffard, C. L., Hurlbert, A. H., Macedo Ivanauskas, N., Janík, D., Jandt, U., Jażdżewska, A., Johannessen, T., Johnstone, J., Jones, J., Jones, F. A. M., Kang, J., Kartawijaya, T., Keeley, E. C., Kelt, D. A., Kinnear, R., Klanderud, K., Knutsen, H., Koenig, C. C., Kortz, A. R., Král, K., Kuhnz, L. A., Kuo, C. Y., Kushner, D. J., Laguionie-Marchais, C., Lancaster, L. T., Min Lee, C., Lefcheck, J. S., Lévesque, E., Lightfoot, D., Lloret, F., Lloyd, J. D., López-Baucells, A., Louzao, M., Madin, J. S., Magnússon, B., Malamud, S., Matthews, I., McFarland, K. P., McGill, B., McKnight, D., McLarney, W. O., Meador, J., Meserve, P. L., Metcalfe, D. J., Meyer, C. F. J., Michelsen, A., Milchakova, N., Moens, T., Moland, E., Moore, J., Mathias Moreira, C., Müller, J., Murphy, G., Myers-Smith, I. H., Myster, R. W., Naumov, A., Neat, F., Nelson, J. A., Paul Nelson, M., Newton, S. F., Norden, N., Oliver, J. C., Olsen, E. M., Onipchenko, V. G., Pabis, K., Pabst, R. J., Paquette, A., Pardede, S., Paterson, D. M., Pélissier, R., Peñuelas, J., Pérez-Matus, A., Pizarro, O., Pomati, F., Post, E., Prins, H. H. T., Priscu, J. C., Provoost, P., Prudic, K. L., Pulliainen, E., Ramesh, B. R., Mendivil Ramos, O., Rassweiler, A., Rebelo, J. E., Reed, D. C., Reich, P. B., Remillard, S. M., Richardson, A. J., Richardson, J. P., van Rijn, I., Rocha, R., Rivera-Monroy, V. H., Rixen, C., Robinson, K. P., Ribeiro Rodrigues, R., de Cerqueira Rossa-Feres, D., Rudstam, L., Ruhl, H., Ruz, C. S., Sampaio, E. M., Rybicki, N., Rypel, A., Sal, S., Salgado, B., Santos, F. A. M., Savassi-Coutinho, A. P., Scanga, S., Schmidt, J., Schooley, R., Setiawan, F., Shao, K. T., Shaver, G. R., Sherman, S., Sherry, T. W., Siciński, J., Sievers, C., da Silva, A. C., Rodrigues da Silva, F., Silveira, F. L., Slingsby, J., Smart, T., Snell, S. J., Soudzilovskaia, N. A., Souza, G. B. G., Maluf Souza, F., Castro Souza, V., Stallings, C. D., Stanforth, R., Stanley, E. H., Mauro Sterza, J., Stevens, M., Stuart-Smith, R., Rondon Suarez, Y., Supp, S., Yoshio Tamashiro, J., Tarigan, S., Thiede, G. P., Thorn, S., Tolvanen, A., Teresa Zugliani Toniato, M., Totland, Ø, Twilley, R. R., Vaitkus, G., Valdivia, N., Vallejo, M. I., Valone, T. J., Van Colen, C., Vanaverbeke, J., Venturoli, F., Verheye, H. M., Vianna, M., Vieira, R. P., Vrška, T., Quang Vu, C., Van Vu, L., Waide, R. B., Waldock, C., Watts, D., Webb, S., Wesołowski, T., White, E. P., Widdicombe, C. E., Wilgers, D., Williams, R., Williams, S. B., Williamson, M., Willig, M. R., Willis, T. J., Wipf, S., Woods, K. D., Woehler, E. J., Zawada, K., and Zettler, M. L.

Abstract

Motivation: The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community-led open-source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene. Main types of variables included: The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record. Spatial location and grain: BioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km2 (158 cm2) to 100 km2 (1,000,000,000,000 cm2). Time period and grain: BioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year. Major taxa and level of measurement: BioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates. Software format:.csv and.SQL.

Published
2018

23. Human salmonellosis and peanut butter

Author

Scheil, W, Cameron, S, Heaton, S, Kirk, M, Vulcanis, M, Holland, R, Dedman, R, Eckert, P, Feldheim, J, Rose, N, Rouch, G, Lightfoot, D, McLennan, L, Tan, A, Harries, B, Murray, C, Ng, S, Boyden, A, Hogg, G, and Beaton, S

Published
1996

24. Research data management in academic institutions: A scoping review

Author

Perrier, L. (Laure), Blondal, E. (Erik), Ayala, A.P. (A. Patricia), Dearborn, D. (Dylanne), Kenny, T. (Tim), Lightfoot, D. (David), Reka, R. (Roger), Thuna, M. (Mindy), Trimble, L. (Leanne), MacDonald, H. (Heather), Perrier, L. (Laure), Blondal, E. (Erik), Ayala, A.P. (A. Patricia), Dearborn, D. (Dylanne), Kenny, T. (Tim), Lightfoot, D. (David), Reka, R. (Roger), Thuna, M. (Mindy), Trimble, L. (Leanne), and MacDonald, H. (Heather)

Abstract

Objective: The purpose of this study is to describe the volume, topics, and methodological nature of the existing research literature on research data management in academic institutions. Materials and methods: We conducted a scoping review by searching forty literature databases encompassing a broad range of disciplines from inception to April 2016. We included all study types and data extracted on study design, discipline, data collection tools, and phase of the research data lifecycle. Results: We included 301 articles plus 10 companion reports after screening 13,002 titles and abstracts and 654 full-text articles. Most articles (85%) were published from 2010 onwards and conducted within the sciences (86%). More than three-quarters of the articles (78%) reported methods that included interviews, cross-sectional, or case studies. Most articles (68%) included the Giving Access to Data phase of the UK Data Archive Research Data Lifecycle that examines activities such as sharing data. When studies were grouped into five dominant groupings (Stakeholder, Data, Library, Tool/Device, and Publication), data quality emerged as an integral element. Co

Published
2017
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26. Global agricultural intensification during climate change: A role for genomics

Author

Abberton, M., Batley, J., Bentley, A., Bryant, J., Cai, H., Cockram, J., Costa de Oliveira, A., Cseke, L.J., Dempewolf, H., De Pace, C., Edwards, D., Gepts, P., Greenland, A., Hall, A.E., Henry, R., Hori, K., Howe, G.T., Hughes, S., Humphreys, M., Lightfoot, D., Marshall, A., Mayes, S., Nguyen, H.T., Ogbonnaya, F.C., Ortiz, R., Paterson, A.H., Tuberosa, R., Valliyodan, B., Varshney, R.K., Yano, M., Abberton, M., Batley, J., Bentley, A., Bryant, J., Cai, H., Cockram, J., Costa de Oliveira, A., Cseke, L.J., Dempewolf, H., De Pace, C., Edwards, D., Gepts, P., Greenland, A., Hall, A.E., Henry, R., Hori, K., Howe, G.T., Hughes, S., Humphreys, M., Lightfoot, D., Marshall, A., Mayes, S., Nguyen, H.T., Ogbonnaya, F.C., Ortiz, R., Paterson, A.H., Tuberosa, R., Valliyodan, B., Varshney, R.K., and Yano, M.

Abstract

Agriculture is now facing the ‘perfect storm’ of climate change, increasing costs of fertilizer and rising food demands from a larger and wealthier human population. These factors point to a global food deficit unless the efficiency and resilience of crop production is increased. The intensification of agriculture has focused on improving production under optimized conditions, with significant agronomic inputs. Furthermore, the intensive cultivation of a limited number of crops has drastically narrowed the number of plant species humans rely on. A new agricultural paradigm is required, reducing dependence on high inputs and increasing crop diversity, yield stability and environmental resilience. Genomics offers unprecedented opportunities to increase crop yield, quality and stability of production through advanced breeding strategies, enhancing the resilience of major crops to climate variability, and increasing the productivity and range of minor crops to diversify the food supply. Here we review the state of the art of genomic-assisted breeding for the most important staples that feed the world, and how to use and adapt such genomic tools to accelerate development of both major and minor crops with desired traits that enhance adaptation to, or mitigate the effects of climate change.

Published
2016

27. CIDE: An Integrated Development Environment for Microservices

Author

Liu, D, Zhu, H, Xu, C, Bayley, I, Lightfoot, D, Green, M, Marshall, P, Liu, D, Zhu, H, Xu, C, Bayley, I, Lightfoot, D, Green, M, and Marshall, P

Abstract

Microservices is a flexible architectural style that has many advantages over the alternative monolithic style. These include better performance and scalability. It is particularly suitable, and widely adopted, for cloud-based applications, because in this architecture a software system consisting of a large suite of services of fine granularity, each running its own process and communicating with the others. However, programming such systems is more complex. In this paper we report on CIDE, an integrated software development environment that helps with this. CIDE supports programming in a novel agent-oriented language called CAOPLE and tests their execution in a cluster environment. We present the architecture of CIDE, discuss its design based on the principles of the DevOps software development methodology, and describe facilities that support continuous testing and seamless integration, two other advantages of Microservices.

Published
2016

28. CAOPLE: A Programming Language for Microservices SaaS

Author

Xu, C, Zhu, H, Bayley, I, Lightfoot, D, Green, M, Marshall, P, Xu, C, Zhu, H, Bayley, I, Lightfoot, D, Green, M, and Marshall, P

Abstract

The microservices architecture is widely regarded as a promising approach to service-oriented systems. However, developing applications in the microservices architecture presents three main challenges: (a) how to program systems that consists of a large number of services running in paral- lel and distributed over a cluster of computers; (b) how to reduce the communication overhead caused by executing a large number of small services; (c) how to support the flexi- ble deployment of services to a network to achieve system load balance. This paper presents a programming language called CAOPLE and reports the implementation of the lan- guage on a virtual machine called CAVM-2. The paper demonstrates how this approach meets these challenges.

Published
2016

29. Diversity of Arthropod Responses to Host-plant Water Stress in a Desert Ecosystem in Southern New Mexico

Author

Schowalter, T. D., Lightfoot, D. C., and Whitford, W. G.

Subjects
Biotic communities -- Demographic aspects -- Environmental aspects, Phytophagous insects -- Environmental aspects, Plant spacing -- Evaluation -- Environmental aspects, Biological sciences, Earth sciences, Evaluation, Demographic aspects, Environmental aspects
Abstract

Previous studies of insect-plant interactions have produced the contradictory Plant Stress Hypothesis (that stressed plants are more suitable hosts for phytophages) and Plant Vigor Hypothesis (that vigorous plants are more suitable hosts for phytophages). However, experimental studies of phytophage responses to host stress have involved only one, or a few, related phytophagous species, not whole communities of organisms associated with a particular plant species. We evaluated responses of various arthropods associated with creosotebush Larrea tridentata to manipulated water availability and plant stress in southern New Mexico during 1990-1991. Of 44 arthropod groups (taxa or functional groups) evaluated in our study only two taxa (including a lepidopteran folivore) showed significant negative response to water availability, thereby supporting the Plant Stress Hypothesis. Ten taxa (including eight phytophages) responded positively to water availability, supporting the Plant Vigor Hypothesis. One phytophage showed a nonlinear response, supporting neither hypothesis. Detrended Correspondence Analysis significantly distinguished the arthropod community on water-deprived shrubs from the communities on watered shrubs. The variation in responses among phytophagous insects on creosotebush indicated that the effect of plant water stress likely reflects the choice of phytophage, and perhaps the host plant, being studied. Therefore, neither the Plant Stress Hypothesis nor the Plant Vigor Hypothesis can explain responses of all phytophages on a particular plant species., INTRODUCTION Field observations that outbreaks of phytophagous arthropods are frequently associated with stressed plants generated the Plant Stress Hypothesis, i.e., that stressed plants are more susceptible hosts for phytophages (White, [...]

Published
1999

31. Emergence and evolution of multiply antibiotic-resistant Salmonella enterica serovar paratyphi B D-tartrate-utilizing strains containing SGI1

Author

Djordjevic, SP, Cain, AK, Evershed, NJ, Falconer, L, Levings, RS, Lightfoot, D, and Hall, RM

Subjects
Genomic Islands, Salmonella paratyphi B, Drug Resistance, Multiple, Bacterial, DNA Transposable Elements, Microbiology, Tartrates, Electrophoresis, Gel, Pulsed-Field
Abstract

The first Australian isolate of Salmonella enterica serovar Paratyphi B D-tartrate-utilizing (dT+) that is resistant to ampicillin, chloramphenicol, florfenicol, streptomycin, spectinomycin, sulfonamides, and tetracycline (ApCmFlSmSpSuTc) and contains SGI1 was isolated from a patient with gastroenteritis in early 1995. This is the earliest reported isolation globally. The incidence of infections caused by these SGI1-containing multiply antibiotic-resistant S. enterica serovar Paratyphi B dT+ strains increased during the next few years and occurred sporadically in all states of Australia. Several molecular criteria were used to show that the early isolates are very closely related to one another and to strains isolated during the following few years and in 2000 and 2003 from home aquariums and their owners. Early isolates from travelers returning from Indonesia shared the same features. Thus, they appear to represent a true clone arising from a single cell that acquired SGI1. Some minor differences in the resistance profiles and molecular profiles also were observed, indicating the ongoing evolution of the clone, and phage type differences were common, indicating that this is not a useful epidemiological marker over time. Three isolates from 1995, 1998, and 1999 contained a complete sul1 gene but were susceptible to sulfamethoxazole due to a point mutation that creates a premature termination codon. This SGI1 type was designated SGI1-R. The loss of resistance genes also was examined. When strains were grown for many generations in the absence of antibiotic selection, the loss of SGI1 was not detected. However, variants SGI1-C (resistance profile SmSpSu) and SGI1-B (resistant to ApSu), which had lost part of the integron, arose spontaneously, presumably via homologous recombination between duplications in the In104 complex integron. Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Published
2009

32. Multigeneic QTL: The Laccase Encoded within the Soybean Rfs2/rhg1 Locus Inferred to Underlie Part of the Dual Resistance to Cyst Nematode and Sudden Death Syndrome

Author

Iqbal, M. J., Ahsan, R., Afzal, A. J., Jamai, A., Khalid Meksem, El-Shemy, H. A., and Lightfoot, D. A.

Subjects
soybean laccase gene-family, food and beverages, SDS resistance
Abstract

Multigeneic QTL present significant problems to analysis. Resistance to soybean (Glycine max (L) Merr.) sudden death syndrome (SDS) caused by Fusarium virguliforme was partly underlain by QRfs2 that was clustered with, or pleiotropic to, the multigeneic rhg1 locus providing resistance to soybean cyst nematode (SCN, Heterodera glycines ). A group of five genes were found between the two markers that delimited the Rfs2/rhg1 locus. One of the five genes was predicted to encode an unusual diphenol oxidase (laccase, EC 1.10.3.2). The aim of this study was to characterize this member of the soybean laccase gene-family and explore its involvement in SDS resistance. A genomic clone and a full length cDNA was isolated from resistant cultivar 'Forrest' that were different among susceptible cultivars 'Asgrow 3244' and 'Williams 82' at four residues R/H168, I/M271, R/H330, E/K470. Additional differences were found in six of the seven introns and the promoter region. Transcript abundance (TA) among genotypes that varied for resistance to SDS or SCN did not differ significantly. Therefore the protein activity was inferred to underlie resistance. Protein expressed in yeast pYES2/NTB had weak enzyme activity with common substrates but good activity with root phenolics. The Forrest isoform may underlie both QRfs 2 and rhg1

Published
2009

34. New integron-associated gene cassette encoding a 3-N-aminoglycoside acetyltransferase

Author

Levings, RS, Partridge, SR, Lightfoot, D, Hall, RM, and Djordjevic, SP

Subjects
Aminoglycosides, Base Sequence, Acetyltransferases, Drug Resistance, Bacterial, Molecular Sequence Data, bacteria, Salmonella enterica, Amino Acid Sequence, biochemical phenomena, metabolism, and nutrition, bacterial infections and mycoses, Microbiology, Integrons
Abstract

A fifth gene cassette containing an aacC gene, aacCA5, was found in an aacCA5-aadA7 cassette array in a class 1 integron isolated from a multiply drug resistant Salmonella enterica serovar Kentucky strain. The AacC-A5 or AAC(3)-Ie acetyltransferase encoded by aacCA5 is related to other AAC(3)-I enzymes and confers resistance to gentamicin. Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Published
2005

35. An outbreak of Salmonella Typhimurium 9 at a school camp linked to contamination of rainwater tanks

Author

Franklin, Lucinda, Fielding, James E, Gregory, Joy, Gullan, L, Lightfoot, D, Poznanski, SY, Vally, Hassan, Franklin, Lucinda, Fielding, James E, Gregory, Joy, Gullan, L, Lightfoot, D, Poznanski, SY, and Vally, Hassan

Abstract

In March 2007, an outbreak of gastroenteritis was identified at a school camp in rural Victoria, Australia, affecting about half of a group of 55 students. A comprehensive investigation was initiated to identify the source. Twenty-seven attendees were found to have abdominal pain, diarrhoea and nausea (attack rate 49%). Of 11 faecal specimens tested all were positive for Salmonella Typhimurium definitive phage type 9 (DT9). Of four samples taken from the untreated private water supply, two were positive for DT9. Drinking water from containers filled from rainwater tanks [relative risk (RR) 3·2, P = 0·039] and participation in two recreational activities - flying fox (RR 5·3, P = 0·011), and beam-balance (RR 3·9, P = 0·050) - were indicative of a link with illness. Environmental and epidemiological investigations suggested rainwater collection tanks contaminated with DT9 as being the cause of the outbreak. Increased use of rainwater tanks may heighten the risk of waterborne disease outbreaks unless appropriate preventative measures are undertaken.

Published
2009

36. Aquariums as reservoirs for multidrug-resistant Salmonella paratyphi B

Author

Levings, Renee, Lightfoot, D., Hall, R. M., Djordjevic, Steven P., Levings, Renee, Lightfoot, D., Hall, R. M., and Djordjevic, Steven P.

Abstract

Multidrug-resistant Salmonella enterica serovar Paratyphi B dT+ isolates from patients with gastroenteritis were identical with isolates from their home aquariums. Matched isolates had identical phage types, XbaI and IS200 profiles, and Salmonella genomic island 1 (SGI1). Ornamental fish tanks are reservoirs for SGI1-containing S. Paratyphi B dT+.

Published
2006

37. New integron-associated gene cassette encoding a trimethoprim-resistant DfrB-type dihydrofolate reductase

Author

Levings, Renee, Lightfoot, D., Elbourne, Liam, Hall, R. M., Djordjevic, Steven P., Levings, Renee, Lightfoot, D., Elbourne, Liam, Hall, R. M., and Djordjevic, Steven P.

Abstract

A sixth gene cassette containing a dfrB-type gene, dfrB6, was found in a dfrB6-aadA1 cassette array in class 1 integrons. This array was isolated from several multiply antibiotic-resistant Salmonella enterica serovar Infantis strains that appear to be clonally related. The DfrB6 dihydrofolate reductase conferred resistance to trimethoprim.

Published
2006

38. Aquariums as reservoirs for multidrug-resistant Salmonella Paratyphi B

Author

Levings, RS, Lightfoot, D, Hall, RM, Djordjevic, SP, Levings, RS, Lightfoot, D, Hall, RM, and Djordjevic, SP

Abstract

Multidrug-resistant Salmonella enterica serovar Paratyphi B dT+ isolates from patients with gastroenteritis were identical with isolates from their home aquariums. Matched isolates had identical phage types, XbaI and IS200 profiles, and Salmonella genomic island 1 (SGI1). Ornamental fish tanks are reservoirs for SGI1-containing S. Paratyphi B dT+.

Published
2006

39. New integron-associated gene cassette encoding a trimethoprim-resistant DfrB-type dihydrofolate reductase

Author

Levings, RS, Lightfoot, D, Elbourne, LDH, Djordjevic, SP, Hall, RM, Levings, RS, Lightfoot, D, Elbourne, LDH, Djordjevic, SP, and Hall, RM

Abstract

A sixth gene cassette containing a dfrB-type gene, dfrB6, was found in a dfrB6-aadA1 cassette array in class 1 integrons. This array was isolated from several multiply antibiotic-resistant Salmonella enterica serovar Infantis strains that appear to be clonally related. The DfrB6 dihydrofolate reductase conferred resistance to trimethoprim. Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Published
2006

40. The genomic island SGI1, containing the multiple antibiotic resistance region of Salmonella enterica serovar typhimurium DT104 or variants of it, is widely distributed in other S. enterica serovars

Author

Levings, RS, Lightfoot, D, Partridge, SR, Hall, RM, Djordjevic, SP, Levings, RS, Lightfoot, D, Partridge, SR, Hall, RM, and Djordjevic, SP

Abstract

The global dissemination of the multiply-antibiotic-resistant Salmonella enterica serovar Typhimurium DT104 clone with the resistance genes located in a class 1 integron, here designated In104, within genomic island SGI1 is a significant public health issue. Here, we have shown that SGI1 and variants of it carrying different combinations of resistance genes are found in several Salmonella enterica serovars. These are serovars Cerro, Derby, Dusseldorf, Infantis, Kiambu, and Paratyphi B dT+ isolated from human infections and serovar Emek from sewage effluent. Two new variants, SGI1-I and SGI1-J, both of which include the dfrA1-orfC cassette array, were identified. Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Published
2005

41. Variation between pathogenic serovars within Salmonella pathogenicity islands

Author

Amavisit, P, Lightfoot, D, Browning, GF, Markham, PF, Amavisit, P, Lightfoot, D, Browning, GF, and Markham, PF

Abstract

Although four of the five Salmonella pathogenicity islands (SPIs) have been characterized in detail for Salmonella enterica serovar Typhimurium, and the fifth has been characterized for Salmonella enterica serovar Dublin, there have been limited studies to examine them in detail in a range of pathogenic serovars of S. enterica. The aim of this study was to examine these regions, shown to be crucial in virulence, in pathogenic serovars to identify any major deletions or insertions that may explain variation in virulence and provide further understanding of the elements involved in the evolution of these regions. Multiple strains of each of the 13 serovars were compared by Southern blot hybridization using a series of probes that together encompassed the full length of all five SPIs. With the exception of serovar Typhimurium, all strains of the same serovar were identical in all five SPIs. Those serovars that differed from serovar Typhimurium in SPI-1 to SPI-4 and from serovar Dublin in SPI-5 were examined in more detail in the variant regions by PCR, and restriction endonuclease digestion and/or DNA sequencing. While most variation in hybridization patterns was attributable to loss or gain of single restriction endonuclease cleavage sites, three regions, in SPI-1, SPI-3, and SPI-5, had differences due to major insertions or deletions. In SPI-1 the avrA gene was replaced by a 200-base fragment in three serovars, as reported previously. In SPI-5, two serovars had acquired an insertion with similarity to the pagJ and pagK genes between pipC and pipD. In SPI-3 the genes sugR and rhuM were deleted in most serovars and in some were replaced by sequences that were very similar to either the Escherichia coli fimbrial operon, flanked by two distinct insertion sequence elements, or to the E. coli retron phage PhiR73. The distribution of these differences suggests that there have been a number of relatively recent horizontal transfers of genes into S. enterica and that in some

Published
2003

43. A nitrate reduetase gene of the cyanobacterium Synechococcus PCC6301 inferred by heterologous hybridization, cloning and targeted mutagenesis

Author

Lightfoot, D, Baron, A J, Cock, J. Mark, Wootton, J, Végétaux marins et biomolécules, Station biologique de Roscoff [Roscoff] (SBR), and Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-GOEMAR-Centre National de la Recherche Scientifique (CNRS)

Subjects
[SDV]Life Sciences [q-bio], bacteria
Abstract

International audience; DNA probes from the narG gene of Escherichia coil, which encodes the large polypeptide of respiratory nitrate reductase, show cross-hybridization at low stringency to a single region of the genome of the cyanobacterium Synechococcus PCC6301. This segment of cyanobacterial DNA was cloned as the insert of plasmid pDN 1 and characterized. RNA complementary to pDN 1 was shown to be substantially more abundant in nitrate grown cells of Synechococcus PCC6301 than in ammonium grown cells, thus parallelling the nitrate induction and ammonium repression of nitrate reductase activity in cultures of this cyanobacterium. A mutant of Synechococcus PCC6301 deficient in nitrate reductase activity was obtained after a potentially mutagenic transformation treatment using pDN 1 as a donor. This mutant was restored to the wild type phenotype following stable integrative transformation with pDN1 DNA. Taken together these data suggest that pDN1 might encode a polypeptide of nitrate reductase. pDN 1 is distinct from three clones of genes involved in nitrate assimilation that were isolated previously from the related cyanobacterium Synechococcus PCC7942 (Kuhlemeier et al., 1984a, J.Bact. 159, 36-41, and 1984b, Gene 31, 109-116).

Published
1991

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