G. Ladizinsky

Founder effect in crop-plant evolution

Seed-crop plants apparently originated from a limited number of mutants in which seed dispersal was changed from that found in nondomesticated populations. Seed nonshattering in cultivated plants may be controlled by a single gene or a small number of genes. Allopolyploid crop plants were derived from a limited number of interspecific hybridizations followed by chromosome doubling. The consequence of this founder effect is a narrow genetic variability in the crop population compared to its wild progenitor. Natural hybridization between the two is prevented by various isolating mechanisms, and gene flow, if it exists, is apparently more effective in the direction from the cultivated to the wild populations. Founder effect in crop-plant evolution indicates the value and the breeding potential of the genetic variability remaining in its wild relatives.

Plant evolution under domestication

Preface. 1. Origin of agriculture. 2. Increasing diversity under domestication. 3. The course of reducing and maintaining genetic diversity under domestication. 4. Speciation under domestication. 5. Weeds and their evolution. 6. Evolution of selected crop plants. 7. Genetic resources for future crop evolution. References. Index.

The origin of lentil and its wild genepool

SummaryFollowing hybridization experiments and cytogenetic analysis of interspecific hybrids three chromosome interchanges were found between the cultivated lentil L. culinaris and L. nigricans, and only one between the cultivated species and L. orientalis. This indicates that the latter species is more likely to be wild progenitor of lentil. The partial fertility of the interspecific hybrids indicate further that both L. nigricans and L. orientalis should be included in the wild genepool of lentil, and their variation can be exploited by relatively simple hybridization techniques. The wild lentils L. orientalis and L. nigricans are morphologically very similar but reproductively strongly isolated from one another by the albino seedling of their hybrids. It has been suggested that the populations of L. orientalis that gave rise to the cultivated lentil still possess a similar chromosome arrangement as in L. culinaris and are also capable of forming normal hybrids with L. nigricans. According to these considerations it is unlikely that lentil originated from populations at the south western corner of the distribution area of L. orientalis.

Inheritance and linkage relationships of morphological and isozyme loci in chickpea (Cicer arietinum L.)

Inheritance and linkage relationships of several morphological and isozyme loci are described in chickpea (Cicer arietinum L.). Segregation data obtained from several F2 families confirmed the previously observed mode of inheritance for most of the morphological loci. Additional morphological markers in chickpea are also described. Most of the isozyme loci studied showed codominant expression and fit expected Mendelian segregation ratios. However, distorted ratios were also observed for some loci. Linkage was found betweenPgd-c, the locus encoding the cytosolic form of 6-phosphogluconate dehydrogenase, andHg, the locus controlling plant growth habit. These 2 loci were separated by approximately 18 recombinational map units. A similar linkage between comparable loci was previously reported in pea (Pisum sativum L.) (Weeden and Wolko 1990). Linkage was also detected among 3 isozyme loci; the cytosolic form of phosphoglucomutase (Pgm-c), glucose-1-phosphate transferase (Gpt1), and the plastid specific form of 6-phosphogluconate dehydrogenase (Pgd-p). The linkage of 2 loci (Pgm-c andPgd-p) in this cluster is also conserved in pea and lentil (Lens Miller). The linkage between an acid phosphatase locus (Acp3) and the locus specifying the cytosolic form of glucosephosphate isomerase (Gpi-c) in chickpea suggested another linkage group in common with pea. Additionally, other linkages that were not previously observed in chickpea or related genera included the linkage of the cytosolic form of aconitase (Aco-c) with adenylate kinase (Adk1) and fructokinase (Fk3), and the linkage of a locus encoding the mitochondrial specific aconitase (Aco-m) with a seed protein locus (Spr1). The loci determining flower color (P), epicotyl color (Gst), seed coat color (T3), and seed surface (Rs) were associated with the locus encoding glucose-1-phosphate transferase (Gpt2). These results, along with previous studies, suggest that pea, lentil and chickpea have several common linkage groups consisting of homologous genes. This also indicates that linkages found in one genus can be used to predict similar linkages in related genera in the development of linkage maps.

Pulse domestication before cultivation

Comparative studies of the pulses of the Middle East and of their wild progenitors indicate that the pattern of pulse domestication is completely different from that of cereals in the same region. Wild legumes are not suitable for cultivation because of their conspicuous seed dormancy. Pre-adaptation of wild pulses for cultivation through loss of the seed dormancy mechanism apparently occurred in wild populations and may have been influenced by the gathering practices of man in pre-agricultural times. Pod indehiscence was of low value in pulse domestication and had evolved after the crop was well established and widespread.

Genetic mapping of an ancient translocation in the genus Lens.

SummarySegregation of 18 marker genes was monitored in selfed progeny of a Lens culinaris × L. ervoides hybrid; five linkage groups were mapped, one of which contained a reciprocal translocation break-point that differentiates between the parents. Four markers were found to be linked to the translocation break-point: Aco-1 and Pgm-2 on one side and Gs and Got-2 on the other. The gene pairs on both sides of the translocation are not linked in L. culinaris or in L. orientalis. The L. ervoides gene order was also found in L. odemensis but with significantly reduced map distances. Analysis of monogenic segregations in a number of Lens inter-specific crosses revealed some consistent patterns of deviations from the expected Mendelian ratios. The factors responsible for these unequal segregations, genotypic effects on recombination frequencies, negative interference, and the possible ancient origin of the translocation are discussed.

Notes on species delimination, species relationships and polyploidy in Avena L.

SummaryOn the combined evidence from morphology, ecology, and cytogenetics, seven species are recognized in the genus Avena L. 1. A. claudaDur., 2. A. ventricosaBal. 3. A. longiglumisDur, 4. A. strigosaSchreb., 5. A. magnaMurphy et Terr., 6. A. murphyiLadiz. and 7. A. sativa L. The first three species are wild diploids. The fourth is a diploid-tetraploid complex of wild forms, weeds and cultivars. The fifth and sixth are wild tetraploids and the seventh constitutes a hexaploid aggregate of wild forms, weeds and cultivated forms. A short morphological and ecological characterization is given to each species.The cytogenetic, ecological and morphological evidence available on the evolutionary divergence and on the genetic affinities between the seven species is reviewed and discussed. The conclusion in drawn that in Avena there are two independent developments of polyploidy: 1. strigosa tetraploids, where the diploid background is well known; 2. the tetraploid-hexaploid of A. magna, A. murphyi and A. sativa (series Denticulatae). Here the first two species apparently represent the general tetraploid background from which hexaploid A. sativa evolved. It is also argued that it is impossible to explain the morphology, ecology and cytology of series Denticulatae in terms of the known diploid species of Avena, and a yet missing hypothetical diploid ancestor was extrapolated.

On the Origin of Almond

Almond, Amygdalus communis L., is an ancient crop of south west Asia. Selection of the sweet type marks the beginning of almond domestication. Wild almonds are bitter and eating even a relatively small number of nuts can be fatal. How man selected the sweet type remains a riddle. Also, the wild ancestor of almond has not been properly identified among the many wild almond species. Breeding experiment, which is the most critical test for identifying the wild progenitors of other crops, is ineffective in almond, because it is interfertile with many wild taxa. The so-called wild A. communis of central Asia cannot be regarded as a genuine wild form, but as a feral form, or remains of old afforestation. The wild taxa morphologically akin to almond, A. korshinskyi (H.-M.) Bomm. and A. webbii Spach, are also feral types occurring in the Middle East and southern Europe, respectively. The taxon A. fenzliana (Fritsch) Lipsky is the most likely wild ancestor of almond for three reasons: 1. It is a genuine wild type forming extensive thickets of large trees young seedlings and all the intergradations between them in nature; 2. Its morphology, and particularly the partially pitted grooved nut-shell are within the range of variation of almond, and 3. A. fenzliana is native of Armenia and western Azerbaijan in the Middle East where almond was apparently domesticated.

Chloroplast DNA variation and evolution in the genus Lens Mill

Abstract Chloroplast DNA (cpDNA) restriction site diversity was assessed by 21 enzyme/probe combinations in 30 accessions of six Lens species, including the recently recognized L. lamottei and L. tomentosus. A total of 118 fragments were scored and 26 restriction site mutations were identified. The cpDNA restriction pattern supports circumscribing L. lamottei and L. tomentosus as independent species. The value of the data for reconstructing phylogeny in the genus is discussed. The cpDNA of all 13 accessions of the lentil’s wild progenitor, L. culinaris subsp. orientalis, differed from that of the single lentil cultivars used in this study. This diversity indicates that other populations of this subspecies from Turkey and Syria examined by Mayer and Soltis (1994) are potentially the founder members of lentil. Examination of L. lamottei×L. nigricans hybrids between accessions having different restriction patterns showed paternal plastid inheritance in L. nigricans.

Genetics of allozyme variants and linkage groups in lentil

SummaryThe genetics of 8 electrophoretically detectable enzymes in lentil was examined. The enzyme systems glutamic-oxaloacetic transaminase, malic enzyme, phosphoglucomutase, alcohol dehydrogenase, 6-phosphogluconate dehydrogenase, shikimic dehydrogenase and isocitrate dehydrogenase were assayed. The allozymes at each of the studied loci behaved in a codominant manner and segregated in the expected Mendelian fashion. Linkage tests between these loci and an additional morphological trait revealed two linkage groups that involved 5 loci, the rest were independent of each other.