26 research outputs found

    FieldSimR: an R package for simulating plot data in multi-environment field trials

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    This paper presents a general framework for simulating plot data in multi-environment field trials with one or more traits. The framework is embedded within the R package FieldSimR, whose core function generates plot errors that capture global field trend, local plot variation, and extraneous variation at a user-defined ratio. FieldSimR's capacity to simulate realistic plot data makes it a flexible and powerful tool for a wide range of improvement processes in plant breeding, such as the optimisation of experimental designs and statistical analyses of multi-environment field trials. FieldSimR provides crucial functionality that is currently missing in other software for simulating plant breeding programmes and is available on CRAN. The paper includes an example simulation of field trials that evaluate 100 maize hybrids for two traits in three environments. To demonstrate FieldSimR's value as an optimisation tool, the simulated data set is then used to compare several popular spatial models for their ability to accurately predict the hybrids' genetic values and reliably estimate the variance parameters of interest. FieldSimR has broader applications to simulating data in other agricultural trials, such as glasshouse experiments.</p

    Genomic selection using random regressions on known and latent environmental covariates

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    KEY MESSAGE: The integration of known and latent environmental covariates within a single-stage genomic selection approach provides breeders with an informative and practical framework to utilise genotype by environment interaction for prediction into current and future environments. ABSTRACT: This paper develops a single-stage genomic selection approach which integrates known and latent environmental covariates within a special factor analytic framework. The factor analytic linear mixed model of Smith et al. (2001) is an effective method for analysing multi-environment trial (MET) datasets, but has limited practicality since the underlying factors are latent so the modelled genotype by environment interaction (GEI) is observable, rather than predictable. The advantage of using random regressions on known environmental covariates, such as soil moisture and daily temperature, is that the modelled GEI becomes predictable. The integrated factor analytic linear mixed model (IFA-LMM) developed in this paper includes a model for predictable and observable GEI in terms of a joint set of known and latent environmental covariates. The IFA-LMM is demonstrated on a late-stage cotton breeding MET dataset from Bayer CropScience. The results show that the known covariates predominately capture crossover GEI and explain 34.4% of the overall genetic variance. The most notable covariates are maximum downward solar radiation (10.1%), average cloud cover (4.5%) and maximum temperature (4.0%). The latent covariates predominately capture non-crossover GEI and explain 40.5% of the overall genetic variance. The results also show that the average prediction accuracy of the IFA-LMM is [Formula: see text] higher than conventional random regression models for current environments and [Formula: see text] higher for future environments. The IFA-LMM is therefore an effective method for analysing MET datasets which also utilises crossover and non-crossover GEI for genomic prediction into current and future environments. This is becoming increasingly important with the emergence of rapidly changing environments and climate change. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-022-04186-w

    Additive and non-additive genetic variance in juvenile Sitka spruce (Picea sitchensis Bong. Carr)

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    Many quantitative genetic models assume that all genetic variation is additive because of a lack of data with sufficient structure and quality to determine the relative contribution of additive and non-additive variation. Here the fractions of additive (fa) and non-additive (fd) genetic variation were estimated in Sitka spruce for height, bud burst and pilodyn penetration depth. Approximately 1500 offspring were produced in each of three sib families and clonally replicated across three geographically diverse sites. Genotypes from 1525 offspring from all three families were obtained by RADseq, followed by imputation using 1630 loci segregating in all families and mapped using the newly developed linkage map of Sitka spruce. The analyses employed a new approach for estimating fa and fd, which combined all available genotypic and phenotypic data with spatial modelling for each trait and site. The consensus estimate for fa increased with age for height from 0.58 at 2 years to 0.75 at 11 years, with only small overlap in 95% support intervals (I95). The estimated fa for bud burst was 0.83 (I95=[0.78, 0.90]) and 0.84 (I95=[0.77, 0.92]) for pilodyn depth. Overall, there was no evidence of family heterogeneity for height or bud burst, or site heterogeneity for pilodyn depth, and no evidence of inbreeding depression associated with genomic homozygosity, expected if dominance variance was the major component of non-additive variance. The results offer no support for the development of sublines for crossing within the species. The models give new opportunities to assess more accurately the scale of non-additive variation

    Bedform migration in a mixed sand and cohesive clay intertidal environment and implications for bed material transport predictions

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    Many coastal and estuarine environments are dominated by mixtures of non-cohesive sand and cohesive mud. The migration rate of bedforms, such as ripples and dunes, in these environments is important in determining bed material transport rates to inform and assess numerical models of sediment transport and geomorphology. However, these models tend to ignore parameters describing the physical and biological cohesion (resulting from clay and extracellular polymeric substances, EPS) in natural mixed sediment, largely because of a scarcity of relevant laboratory and field data. To address this gap in knowledge, data were collected on intertidal flats over a spring-neap cycle to determine the bed material transport rates of bedforms in biologically-active mixed sand-mud. Bed cohesive composition changed from below 2 vol% up to 5.4 vol% cohesive clay, as the tide progressed from spring towards neap. The amount of EPS in the bed sediment was found to vary linearly with the clay content. Using multiple linear regression, the transport rate was found to depend on the Shields stress parameter and the bed cohesive clay content. The transport rates decreased with increasing cohesive clay and EPS content, when these contents were below 2.8 vol% and 0.05 wt%, respectively. Above these limits, bedform migration and bed material transport was not detectable by the instruments in the study area. These limits are consistent with recently conducted sand-clay and sand-EPS laboratory experiments on bedform development. This work has important implications for the circumstances under which existing sand-only bedform migration transport formulae may be applied in a mixed sand-clay environment, particularly as 2.8 vol% cohesive clay is well within the commonly adopted definition of “clean sand”

    Incretin Receptor Null Mice Reveal Key Role of GLP-1 but Not GIP in Pancreatic Beta Cell Adaptation to Pregnancy

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    Islet adaptations to pregnancy were explored in C57BL6/J mice lacking functional receptors for glucagon-like peptide 1 (GLP-1) and gastric inhibitory polypeptide (GIP). Pregnant wild type mice and GIPRKO mice exhibited marked increases in islet and beta cell area, numbers of medium/large sized islets, with positive effects on Ki67/Tunel ratio favouring beta cell growth and enhanced pancreatic insulin content. Alpha cell area and glucagon content were unchanged but prohormone convertases PC2 and PC1/3 together with significant amounts of GLP-1 and GIP were detected in alpha cells. Knockout of GLP-1R abolished these islet adaptations and paradoxically decreased pancreatic insulin, GLP-1 and GIP. This was associated with abolition of normal pregnancy-induced increases in plasma GIP, L-cell numbers, and intestinal GIP and GLP-1 stores. These data indicate that GLP-1 but not GIP is a key mediator of beta cell mass expansion and related adaptations in pregnancy, triggered in part by generation of intra-islet GLP-1

    Genomic epidemiology of SARS-CoV-2 in a UK university identifies dynamics of transmission

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    AbstractUnderstanding SARS-CoV-2 transmission in higher education settings is important to limit spread between students, and into at-risk populations. In this study, we sequenced 482 SARS-CoV-2 isolates from the University of Cambridge from 5 October to 6 December 2020. We perform a detailed phylogenetic comparison with 972 isolates from the surrounding community, complemented with epidemiological and contact tracing data, to determine transmission dynamics. We observe limited viral introductions into the university; the majority of student cases were linked to a single genetic cluster, likely following social gatherings at a venue outside the university. We identify considerable onward transmission associated with student accommodation and courses; this was effectively contained using local infection control measures and following a national lockdown. Transmission clusters were largely segregated within the university or the community. Our study highlights key determinants of SARS-CoV-2 transmission and effective interventions in a higher education setting that will inform public health policy during pandemics.</jats:p

    Sex-specific vulnerability of Portunus armatus to capture in round traps with traditional and novel fish baits

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    In response to few data describing the effects of bait on trap efficiencies for blue swimmer crabs, Portunus armatus in an Australian fishery and an impetus to reduce costs, traditional baits (sea mullet, Mugil cephalus and luderick, Girella tricuspidata) were compared against a novel, less-expensive bait (European carp, Cyprinus carpio). Eight replicate traps with each bait type were fished over four days at one location in the fishery for a total of 96 trap lifts. Traps baited with sea mullet caught significantly more (by >1.5×) total blue swimmer crabs and at a greater net-profit trap deployment (>3.7×) than traps with the other two baits, which produced similar catches and profits. But, the superior performance of sea mullet as bait was due to greater catches of female blue swimmer crabs (which were larger and are more valuable owing to ovarian development), with no significant difference in catches of males among bait types. Such sex specificity was attributed to possible divergent, temporal nutritional requirements including a dietary bias among mature females preparing to migrate to oceanic areas prior to reproduction. Additional data are required across larger spatio-temporal scales to further elucidate patterns; however there are clear implications for fishers that seek to maximise catches of females in the studied fishery or potentially minimise female catches which are prohibited in other Australian fisheries. Further, it is also clear that sex-specific catch data acquired during surveys should be considered for possible confounding effects of bait (and other technical factors) prior to extrapolating relative abundances

    Appropriate morphometrics for the first assessment of juvenile green turtle (Chelonia mydas) age and growth in the south-western Atlantic

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    In response to an absence of size-at-age information for juvenile Chelonia mydas in the South Atlantic Ocean, but the need for such regional data to support global ecological monitoring and conservation actions, skeletochronological analyses (using humeri) were undertaken for 63 stranded dead specimens (30.0-58.0 cm curved carapace length-CCL) collected between 2008 and 2013 from 40 km of beaches off southern Brazil. Specimens were defined as being 2-8 years old and from various nesting sites (based on mitochondrial haplotypes). Parametric mixed-effect models were used to examine variation among CCL, maximum humeral length (MHL) and medial humeral width (MHW) due to age (fitted with a natural cubic smoothing spline), genetic haplotype and various random factors. Genetic haplotype was not significant and subsequently removed from analyses. All three size-at-age parameters had random variability, but changes in somatic C. mydas growth described by MHW were less representative than the others, remaining constant through a linear relationship with age. By contrast, both CCL and the preferred MHL similarly displayed positive exponential-shaped splines, with age-specific growth rates (3- to 7-year-olds) predicted at 1.4-3.4 cm year-1 CCL or 0.2-0.7 cm year-1 MHL. The observed CCL growth was comparable to recent estimates for other global populations, but with southern Brazilian C. mydas generally having larger sizes-at-age. Such intra-population differences can be attributed not only to regional prerecruitment environmental parameters and associated ecological implications (e.g. foraging ecology), but also divergent analytical methods. The choice of the latter to accurately model variable growth rates has implications for comparing size-at-age among other sea-turtle populations

    Appropriate morphometrics for the first assessment of juvenile green turtle (Chelonia mydas) age and growth in the south-western Atlantic

    No full text
    In response to an absence of size-at-age information for juvenile Chelonia mydas in the South Atlantic Ocean, but the need for such regional data to support global ecological monitoring and conservation actions, skeletochronological analyses (using humeri) were undertaken for 63 stranded dead specimens (30.0–58.0\ua0cm curved carapace length—CCL) collected between 2008 and 2013 from 40\ua0km of beaches off southern Brazil. Specimens were defined as being 2–8\ua0years old and from various nesting sites (based on mitochondrial haplotypes). Parametric mixed-effect models were used to examine variation among CCL, maximum humeral length (MHL) and medial humeral width (MHW) due to age (fitted with a natural cubic smoothing spline), genetic haplotype and various random factors. Genetic haplotype was not significant and subsequently removed from analyses. All three size-at-age parameters had random variability, but changes in somatic C. mydas growth described by MHW were less representative than the others, remaining constant through a linear relationship with age. By contrast, both CCL and the preferred MHL similarly displayed positive exponential-shaped splines, with age-specific growth rates (3- to 7-year-olds) predicted at 1.4–3.4\ua0cm\ua0year CCL or 0.2–0.7\ua0cm\ua0year MHL. The observed CCL growth was comparable to recent estimates for other global populations, but with southern Brazilian C. mydas generally having larger sizes-at-age. Such intra-population differences can be attributed not only to regional prerecruitment environmental parameters and associated ecological implications (e.g. foraging ecology), but also divergent analytical methods. The choice of the latter to accurately model variable growth rates has implications for comparing size-at-age among other sea-turtle populations

    Optimising mesh size with escape gaps in a dual-species portunid-trap fishery

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    In south-eastern Australia, the same baited, round traps (comprising 50–57-mm mesh netting) are used to target giant mud, Scylla serrata and blue swimmer crabs, Portunus armatus in spatially separated fisheries. Both fisheries are characterised by the common, problematic discarding of undersized portunids
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