Applying SNP marker technology in the cacao breeding programme in Ghana

In this investigation 45 parental cacao plants and five progeny derived from the parental stock studied were genotyped using six SNP markers to determine off-types or mislabeled clones and to authenticate crosses made in the Cocoa Research Institute of Ghana (CRIG) breeding programme. Investigation was based on the 5\u2019 nuclease SNPassay using Illustra Hot Start mix Ready-To-Go PCR strips and BioTek FLx800TBP Fluorescence Microplate Reader. In a group of six cacao plants labeled as PA150 clones and another five labeled as Pound7, one clone in each group was unambiguously determined as off-type or mislabeled. Similarly, in a cohort of 23 PA7 "clones", four genotypes were differentiated. Cross-checking the fidelity of five progeny from the parental stock under study, it was established that no errors were made in the crossing. The most significant outcome of this study, however, was that out of the four categories of 23 PA7 candidate parental trees only one category can be comparable to the reference clone in the International Cacao Germplasm collection, Trinidad (ICG,T); thus informing the need for further work to find the correct clone among these for the breeding programme. It was thus concluded that thissimple yet cutting-edge genotyping procedure can be used in applied cocoa breeding programmes in a cocoa producing country. This work represents a first step in the genotypic characterisation of the CRIG germplasm collection and Seed Gardens.Au cours de cette recherche, 45 plants de cacao parentaux et 5 descendants d\ue9rivant du stock parental ont \ue9t\ue9 g\ue9notyp\ue9 en utilisant 6 marqueurs SNP, afin de d\ue9terminer les clones mal \ue9tiquet\ue9s et d\u2019authentifier les croisements effectu\ue9s dans le programme d\u2019am\ue9lioration de l\u2019Institut de Recherche sur le Cacao au Ghana (CRIG). Cette \ue9tude a \ue9t\ue9 bas\ue9e sur les 5' nucl\ue9ases SNP en utilisant des bandes PCR "Hot Start mix Ready-To-Go PCR strips" et un Lecteur Microplat \ue0 Fluorescence "BioTek FLx800TBP". Au sein d\u2019un groupe de six plants de cacao \ue9tiquet\ue9 PA150 et d\u2019un autre groupe de cinq \ue9tiquet\ue9 Pound 7, il a \ue9t\ue9 d\ue9termin\ue9 sans ambigu\ueft\ue9 qu\u2019un clone par groupe \ue9tait mal \ue9tiquet\ue9. De fa\ue7on similaire, quatre g\ue9notypes diff\ue9rents ont \ue9t\ue9 identifi\ue9s dans une m\ueame cohorte de clones 23PA7. En v\ue9rifiant la fid\ue9lit\ue9 de cinq descendants issus du stock parental \ue9tudi\ue9, il a \ue9t\ue9 \ue9tabli qu\u2019aucune erreur n\u2019avait \ue9t\ue9 faite lors du croisement. Le r\ue9sultat le plus significatif de cette \ue9tude a \ue9t\ue9 que, sur quatre cat\ue9gories de 23 candidats PA7 de souches parentales, une seule pouvait \ueatre comparable au clone de r\ue9f\ue9rence dans la collection Internationale du Germoplasme de Cacao, Trinidad (ICG,T), d\ue9montrant ainsi la n\ue9cessit\ue9 de travaux suppl\ue9mentaires pour d\ue9terminer le clone exact parmi ceux \ue9voqu\ue9s pr\ue9c\ue9demment. Il a ainsi \ue9t\ue9 conclu que cette m\ue9thode avant-gardiste de g\ue9notypage, pourtantsimple, peut \ueatre utilis\ue9e dans les programmes appliqu\ue9s d\u2019am\ue9lioration du cacao dans un pays producteur. Ce travail repr\ue9sente une premi\ue8re \ue9tape dans la caract\ue9risation g\ue9n\ue9tique de la collection du germoplasme CRIG et jardins semenciers

Applying SNP marker technology in the cacao breeding programme in Ghana

In this investigation 45 parental cacao plants and five progeny derived from the parental stock studied were genotyped using six SNP markers to determine off-types or mislabeled clones and to authenticate crosses made in the Cocoa Research Institute of Ghana (CRIG) breeding programme. Investigation was based on the 5’ nuclease SNPassay using Illustra Hot Start mix Ready-To-Go PCR strips and BioTek FLx800TBP Fluorescence Microplate Reader. In a group of six cacao plants labeled as PA150 clones and another five labeled as Pound7, one clone in each group was unambiguously determined as off-type or mislabeled. Similarly, in a cohort of 23 PA7 "clones", four genotypes were differentiated. Cross-checking the fidelity of five progeny from the parental stock under study, it was established that no errors were made in the crossing. The most significant outcome of this study, however, was that out of the four categories of 23 PA7 candidate parental trees only one category can be comparable to the reference clone in the International Cacao Germplasm collection, Trinidad (ICG,T); thus informing the need for further work to find the correct clone among these for the breeding programme. It was thus concluded that thissimple yet cutting-edge genotyping procedure can be used in applied cocoa breeding programmes in a cocoa producing country. This work represents a first step in the genotypic characterisation of the CRIG germplasm collection and Seed Gardens.Au cours de cette recherche, 45 plants de cacao parentaux et 5 descendants dérivant du stock parental ont été génotypé en utilisant 6 marqueurs SNP, afin de déterminer les clones mal étiquetés et d’authentifier les croisements effectués dans le programme d’amélioration de l’Institut de Recherche sur le Cacao au Ghana (CRIG). Cette étude a été basée sur les 5' nucléases SNP en utilisant des bandes PCR "Hot Start mix Ready-To-Go PCR strips" et un Lecteur Microplat à Fluorescence "BioTek FLx800TBP". Au sein d’un groupe de six plants de cacao étiqueté PA150 et d’un autre groupe de cinq étiqueté Pound 7, il a été déterminé sans ambiguïté qu’un clone par groupe était mal étiqueté. De façon similaire, quatre génotypes différents ont été identifiés dans une même cohorte de clones 23PA7. En vérifiant la fidélité de cinq descendants issus du stock parental étudié, il a été établi qu’aucune erreur n’avait été faite lors du croisement. Le résultat le plus significatif de cette étude a été que, sur quatre catégories de 23 candidats PA7 de souches parentales, une seule pouvait être comparable au clone de référence dans la collection Internationale du Germoplasme de Cacao, Trinidad (ICG,T), démontrant ainsi la nécessité de travaux supplémentaires pour déterminer le clone exact parmi ceux évoqués précédemment. Il a ainsi été conclu que cette méthode avant-gardiste de génotypage, pourtantsimple, peut être utilisée dans les programmes appliqués d’amélioration du cacao dans un pays producteur. Ce travail représente une première étape dans la caractérisation génétique de la collection du germoplasme CRIG et jardins semenciers

Rethinking maps

In this paper we argue that cartography is profitably conceived as a processual, rather than representational, science. Building on recent analysis concerning the philosophical underpinnings of cartography we question the ontological security of maps, contending that it is productive to rethink cartography as ontogenetic in nature; that is maps emerge through practices and have no secure ontological status. Drawing on the concepts of transduction and technicity we contend that maps are of-themoment, brought into being through practices (embodied, social, technical); that mapping is a process of constant re-territorialization. Maps are never fully formed and their work is never complete. Maps are transitory and fleeting, being contingent, relational and context-dependent; they are always mappings; spatial practices enacted to solve relational problems (e.g., how best to create a spatial representation, how to understand a spatial distribution, how to get between A and B, and so on). Such a rethinking, we contend, provides a fresh perspective on cartographic epistemology, and could work to provide a common framework for those who undertake mapping as applied knowledge (asking technical questions) and those that seek to critique such mapping as a form of power/knowledge (asking ideological questions). We illustrate our argument through an analysis of mapping practices

Explorations in player motivations: Virtual agents

10.1007/978-3-642-15399-0_26Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)6243 LNCS262-26