Permanent Genetic Resources added to Molecular Ecology Resources database 1 January 2009-30 April 2009.

This article documents the addition of 283 microsatellite marker loci to the Molecular Ecology Resources Database. Loci were developed for the following species: Agalinis acuta; Ambrosia artemisiifolia; Berula erecta; Casuarius casuarius; Cercospora zeae-maydis; Chorthippus parallelus; Conyza canadensis; Cotesia sesamiae; Epinephelus acanthistius; Ficedula hypoleuca; Grindelia hirsutula; Guadua angustifolia; Leucadendron rubrum; Maritrema novaezealandensis; Meretrix meretrix; Nilaparvata lugens; Oxyeleotris marmoratus; Phoxinus neogaeus; Pristomyrmex punctatus; Pseudobagrus brevicorpus; Seiridium cardinale; Stenopsyche marmorata; Tetranychus evansi and Xerus inauris. These loci were cross-tested on the following species: Agalinis decemloba; Agalinis tenella; Agalinis obtusifolia; Agalinis setacea; Agalinis skinneriana; Cercospora zeina; Cercospora kikuchii; Cercospora sorghi; Mycosphaerella graminicola; Setosphaeria turcica; Magnaporthe oryzae; Cotesia flavipes; Cotesia marginiventris; Grindelia Xpaludosa; Grindelia chiloensis; Grindelia fastigiata; Grindelia lanceolata; Grindelia squarrosa; Leucadendron coniferum; Leucadendron salicifolium; Leucadendron tinctum; Leucadendron meridianum; Laodelphax striatellus; Sogatella furcifera; Phoxinus eos; Phoxinus rigidus; Phoxinus brevispinosus; Phoxinus bicolor; Tetranychus urticae; Tetranychus turkestani; Tetranychus ludeni; Tetranychus neocaledonicus; Tetranychus amicus; Amphitetranychus viennensis; Eotetranychus rubiphilus; Eotetranychus tiliarium; Oligonychus perseae; Panonychus citri; Bryobia rubrioculus; Schizonobia bundi; Petrobia harti; Xerus princeps; Spermophilus tridecemlineatus and Sciurus carolinensis.

Which role can arbuscular mycorrhizal fungi play in the facilitation of Ambrosia artemisiifolia L. invasion in France?

Ambrosia artemisiifolia L. (common ragweed), an annual invasive plant, was introduced more than 100 years ago from North America to Europe. Like the majority of other invasive plants in Europe, it develops in open, disturbed areas such as fields, wastelands, roadsides, and riverbanks. Recently, arbuscular mycorrhizal fungi (AMF) have been suspected to play a role in some plant invasion processes. As the common ragweed is known to be colonized by AMF in its native range, the intensity of mycorrhizal root colonization was studied in 35 natural populations in eastern France. About 94% of the A. artemisiifolia populations sampled were mycorrhizal. Root colonization levels varied from 1 to 40% depending on the ecological sites, with lower levels for agricultural habitats and higher levels in disturbed sites, such as wastelands or roadsides. A subsequent greenhouse experiment showed positive impacts of AMF on the growth and development of A. artemisiifolia. It is proposed that the spread of this invasive plant species could be facilitated by AMF, underlining the need to integrate symbiotic interactions in future work on invasive plant processes.

Evolutionary consequences of diploid-polyploid hybrid zones in wild species.

Hybrid zones between cytotypes with different ploidy levels are particularly interesting for studying the ecology and the evolution of reproductive interactions between closely related taxa. Diploid-polyploid hybrid zones differ fundamentally from those between diploids in that they reflect certain conditions that are characteristic of the early stage of polyploid establishment, and allow tests of hypotheses relating to the dynamics and evolution of polyploid complexes. Recent theoretical and empirical studies have provided important data on the evolution of isolating mechanisms in diploid-polyploid contact zones, but have also shown that introgression might counteract the evolution of isolating mechanisms.

Gametes with the somatic chromosome number: mechanisms of their formation and role in the evolution of autopolyploid plants.

The production of 2n gametes in plants, i.e. gametes with a somatic chromosome number, is considered to be the dominant process involved in the origin of polyploid plants. In this review, we provide a synthesis of current knowledge concerning the production of 2n gametes. Firstly, we describe the different methods used to detect and quantify the production of 2n gametes in plants, which include morphological and flow cytometry screening of the occurrence of 2n pollen, the analysis of crosses among diploid and tetraploid parents and the instigation of micro-and mega-sporogenesis. Secondly, the high level of inter- and infra-specific variation in 2n gametes production is described. Thirdly, the various cytological anomalies responsible for the production of 2n gametes are reviewed, with particular reference to the relative genetic consequences of the first and second restitution divisions that give rise to 2n gametes. Fourthly, the significance of 2n gametes in crop plant improvement is discussed, in relation to somatic chromosome doubling to obtain new polyploid varieties. In particular, we compare the genetic and yield consequences of methods based on unilateral and bilateral sexual polyploidization. Finally, we outline how knowledge of the variety of mechanisms involved in 2n gamete production have increased our understanding of the evolutionary significance of polyploidy and the population biology of polyploid plants. Contents Summary 1 I. Introduction 2 II. Methods used to detect the presence and frequency of 2n gametes 3 III. Frequency of 2n gamete production 5 IV. Mechanisms of formation and the influence of external factors 6 V. The genetic consequences of First Division Restitution (FDR) and Second Division Restitution (SDR) 12 VI. 2n gametes and the unilateral and bilateral sexual polyploidization of crop plants 13 VII. The evolutionary significance of 2n gamete production 15 Acknowledgements 18 References 18.