Spatial analysis methods for forest genetic trials

2002 ◽  
Vol 32 (12) ◽  
pp. 2201-2214 ◽  
Author(s):  
Gregory W Dutkowski ◽  
João Costa e Silva ◽  
Arthur R Gilmour ◽  
Gustavo A Lopez

Spatial analysis, using separable autoregressive processes of residuals, is increasingly used in agricultural variety yield trial analysis. Interpretation of the sample variogram has become a tool for the detection of global trend and "extraneous" variation aligned with trial rows and columns. We applied this methodology to five selected forest genetic trials using an individual tree additive genetic model. We compared the base design model with post-blocking, a first-order autoregressive model of residuals (AR1), that model with an independent error term (AR1η), a combined base and autoregressive model, an autoregressive model only within replicates and an autoregressive model applied at the plot level. Post-blocking gave substantial improvements in log-likelihood over the base model, but the AR1η model was even better. The independent error term was necessary with the individual tree additive genetic model to avoid substantial positive bias in estimates of additive genetic variance in the AR1 model and blurred patterns of variation. With the combined model, the design effects were eliminated, or their significance was greatly reduced. Applying the AR1η model to individual trees was better than applying it at the plot level or applying it on a replicate-by-replicate basis. The relative improvements achieved in genetic response to selection did not exceed 6%. Examination of the spatial distribution of the residuals and the variogram of the residuals allowed the identification of the spatial patterns present. While additional significant terms could be fitted to model some of the spatial patterns and stationary variograms were attained in some instances, this resulted in only marginal increases in genetic gain. Use of a combined model is recommended to enable improved analysis of experimental data.

2011 ◽  
Vol 60 (1-6) ◽  
pp. 25-35 ◽  
Author(s):  
E. P. Cappa ◽  
M. Lstiburek ◽  
A. D. Yanchuk ◽  
Y. A. El-Kassaby

AbstractSpatial environmental heterogeneity are well known characteristics of field forest genetic trials, even in small experiments (<1ha) established under seemingly uniform conditions and intensive site management. In such trials, it is commonly assumed that any simple type of experimental field design based on randomization theory, as a completely randomized design (CRD), should account for any of the minor site variability. However, most published results indicate that in these types of trials harbor a large component of the spatial variation which commonly resides in the error term. Here we applied a two-dimensional smoothed surface in an individual-tree mixed model, using tensor product of linear, quadratic and cubic B-spline bases with different and equal number of knots for rows and columns, to account for the environmental spatial variability in two relatively small (i.e., 576 m2and 5,705 m2) forest genetic trials, with large multiple-tree contiguous plot configurations. In general, models accounting for site variability with a two-dimensional surface displayed a lower value of the deviance information criterion than the classical RCD. Linear B-spline bases may yield a reasonable description of the environmental variability, when a relatively small amount of information available. The mixed models fitting a smoothed surface resulted in a reduction in the posterior means of the error variance (σ2e), an increase in the posterior means of the additive genetic variance (σ2a) and heritability (h2HT), and an increase of 16.05% and 46.03% (for parents) or 11.86% and 44.68% (for offspring) in the accuracy of breeding values, respectively in the two experiments.


Genetics ◽  
2001 ◽  
Vol 157 (4) ◽  
pp. 1773-1787 ◽  
Author(s):  
Bruno Bost ◽  
Dominique de Vienne ◽  
Frédéric Hospital ◽  
Laurence Moreau ◽  
Christine Dillmann

Abstract The L-Shaped distribution of estimated QTL effects (R2) has long been reported. We recently showed that a metabolic mechanism could account for this phenomenon. But other nonexclusive genetic or nongenetic causes may contribute to generate such a distribution. Using analysis and simulations of an additive genetic model, we show that linkage disequilibrium between QTL, low heritability, and small population size may also be involved, regardless of the gene effect distribution. In addition, a comparison of the additive and metabolic genetic models revealed that estimates of the QTL effects for traits proportional to metabolic flux are far less robust than for additive traits. However, in both models the highest R2's repeatedly correspond to the same set of QTL.


2020 ◽  
Vol 135 (4) ◽  
pp. 472-482
Author(s):  
Elisabeth Dowling Root ◽  
Emelie D. Bailey ◽  
Tyler Gorham ◽  
Christopher Browning ◽  
Chi Song ◽  
...  

Objectives Geovisualization and spatial analysis are valuable tools for exploring and evaluating the complex social, economic, and environmental interactions that lead to spatial inequalities in health. The objective of this study was to describe spatial patterns of infant mortality and preterm birth in Ohio by using interactive mapping and spatial analysis. Methods We conducted a retrospective cohort study using Ohio vital statistics records from 2008-2015. We geocoded live births and infant deaths by using residential address at birth. We used multivariable logistic regression to adjust spatial and space–time cluster analyses that examined the geographic clustering of infant mortality and preterm birth and changes in spatial distribution over time. Results The overall infant mortality rate in Ohio during the study period was 6.55 per 1000 births; of 1 097 507 births, 10.3% (n = 112 552) were preterm. We found significant geographic clustering of both infant mortality and preterm birth centered on large urban areas. However, when known demographic risk factors were taken into account, urban clusters disappeared and, for preterm birth, new rural clusters appeared. Conclusions Although many public health agencies have the capacity to create maps of health outcomes, complex spatial analysis and geovisualization techniques are still challenging for public health practitioners to use and understand. We found that actively engaging policymakers in reviewing results of the cluster analysis improved understanding of the processes driving spatial patterns of birth outcomes in the state.


2020 ◽  
pp. 239965442094152
Author(s):  
Kawtar Najib

This paper draws upon quantitative data collected from one of the principal associations fighting Islamophobia in France along with the population census, and provides a step forward in understanding the operation and distribution of Islamophobia. It presents a geography of Islamophobia in Paris based on statistical data, and aims to observe whether or not this geography corresponds or contrasts with geographies of inequality (such as those associated with gentrification, deprivation and marginalisation), by analysing the various spatial patterns stemming from the maps. This socio-spatial analysis of anti-Muslim discrimination is important in Paris because since the terrorist attacks in 2015, anti-Muslim sentiment has increased sharply. The mapping of Islamophobia and its association with the spatial distribution of different socioeconomic and demographic variables synthetized in a typological map display significant forms, relations and diversities within Paris. This cartographic analysis demonstrates that the geography of Islamophobia does not necessarily refer to spaces where ‘Muslims’ and the victims of Islamophobia live in great majority, and rather refers to more privileged and central areas such as Paris intra-muros. Victims mostly experience anti-Muslim incidents outside their everyday spaces away from their homes, such as public institutions and workplaces. Indeed, the findings raise the significance of the exact place where incidents occur as well as societal attitudes to these ‘hierarchical’ places where the perpetrator probably feels more comfortable in behaving in an antisocial and sometimes violent way.


2014 ◽  
Vol 2 (3) ◽  
pp. 226-235
Author(s):  
Yuanqing Zhang

Abstract In this paper, we study estimation of a partially specified spatial autoregressive model with heteroskedasticity error term. Under the assumption of exogenous regressors and exogenous spatial weighting matrix, we propose an instrumental variable estimation. Under some sufficient conditions, we show that the proposed estimator for the finite dimensional parameter is root-n consistent and asymptotically normally distributed and the proposed estimator for the unknown function is consistent and also asymptotically distributed though at a rate slower than root-n. Monte Carlo simulations verify our theory and the results suggest that the proposed method has some practical value.


2020 ◽  
Author(s):  
Ruifang Li-Gao ◽  
Dorret I. Boomsma ◽  
Eco J. C. de Geus ◽  
Johan Denollet ◽  
Nina Kupper

Abstract Type D (Distressed) personality combines negative affectivity (NA) and social inhibition (SI) and is associated with an increased risk of cardiovascular disease. We aimed to (1) validate a new proxy based on the Achenbach System of Empirically Based Assessment (ASEBA) for Type D personality and its NA and SI subcomponents and (2) estimate the heritability of the Type D proxy in an extended twin-pedigree design in the Netherlands Twin Register (NTR). Proxies for the dichotomous Type D classification, and continuous NA, SI, and NAxSI (the continuous measure of Type D) scales were created based on 12 ASEBA items for 30,433 NTR participants (16,449 twins and 13,984 relatives from 11,106 pedigrees) and sources of variation were analyzed in the ‘Mendel’ software package. We estimated additive and non-additive genetic variance components, shared household and unique environmental variance components and ran bivariate models to estimate the genetic and non-genetic covariance between NA and SI. The Type D proxy showed good reliability and construct validity. The best fitting genetic model included additive and non-additive genetic effects with broad-sense heritabilities for NA, SI and NAxSI estimated at 49%, 50% and 49%, respectively. Household effects showed small contributions (4–9%) to the total phenotypic variation. The genetic correlation between NA and SI was .66 (reflecting both additive and non-additive genetic components). Thus, Type D personality and its NA and SI subcomponents are heritable, with a shared genetic basis for the two subcomponents.


Author(s):  
Imelda Escamilla ◽  
Miguel Torres-Ruiz ◽  
Marco Moreno-Ibarra ◽  
Rolando Quintero ◽  
Giovanni Guzmán ◽  
...  

In this paper, an approach to geocode tweets published in Spanish is proposed. The tweets are related to traffic events within an urban context of the Mexico City. They are generated by a particular phenomenon for knowing the behavior of the involved geographic entities. In order to disambiguate and verify the consistency of information, an application ontology was defined. Thus, the core goal is to identify location as well as spatial relationships between entities presented in the events, using semantic and spatial analysis of the collected dataset. In consequence, a visualization method for presenting the results was also proposed. The paper describes the methodology for enabling the discovery of spatial patterns within traffic tweets and provides useful information to make timely decisions and contribute in the context of Knowledge Society.


Sign in / Sign up

Export Citation Format

Share Document