Academic literature on the topic 'Plant genetics; Pollen; Seed development'

Lycopersicon esculentum Mill. `Laura' plants were grown in the North Carolina State Univ. phytotron at 26C day temperature and 18, 22, 24, or 26C night temperatures to determine the effects of night temperature on pollen characteristics, growth, fruit set, and early fruit growth. Total and percentage normal pollen grains were higher in plants grown at night temperatures of 18 and 22C than at 24 and 26C, but germination was highest in pollen produced at 26C. Seed content was rated higher on the plants grown at 18C night temperatures than in any of the other treatments. Numbers of flowers and fruit on the first cluster were lower in the 26C night treatment than in the other night temperature treatments. Plant height was greatest but total shoot dry mass was lowest in the 22C night temperature treatments. Fruit fresh mass increased with night temperature, reflecting more rapid development, but the experiment was not continued to fruit maturity, so the effect of night temperature on final fruit size and total plant production could not be determined. Night temperatures of 26C reduced fruit number and percentage fruit set only slightly at a day temperature of 26C, even though these temperatures were above optimal for pollen production and seed formation. To separate temperature effects on pollen from direct or developmental effects on female reproductive structures, pollen was collected from plants in the four night temperature treatments and applied to stigmas of a male-sterile cultivar kept at 24-18C minimum temperatures in adjacent greenhouses. In the greenhouse-grown male sterile plants, no consistent effects of night temperature treatment given the pollen could be seen in fruit set, fruit mass, seed content (either on a rating or seed count basis), seedling germination, or seedling dry mass.

The genus Coreopsis L. is Florida’s state wildflower; there is a strong interest in commercial production and large-scale planting of Coreopsis seed in Florida, especially the seed of Coreopsis leavenworthi Torr. & A. Gray (COLE) and Coreopsis tinctoria Nutt. (COTI). Both species belong to the same section [Calliopsis (Reichenb.) Nutt.] within Coreopsis and were known to be cross-compatible and produce interspecific hybrids when hand-pollinated or grown in close proximity. Little was known about the effects of such hybridization on progeny growth, development, and reproduction, which are very important to seed production and planting. F1 and F2 interspecific populations between COLE and COTI were created in the greenhouse and then evaluated in replicated field studies in two growing seasons. Results showed that interspecific hybridization between COLE (as the maternal parent) and COTI (as the paternal parent) significantly increased the plant height (by 11.4% to 18.7%), plant dry weight (by 38.6% to 63.9%), and time to flower (by 3.7 to 9.8 days) of the F1 and F2 progeny of COLE × COTI crosses. By contrast, interspecific hybridization between COTI (as the maternal parent) and COLE (as the paternal parent) did not cause significant changes in these characteristics of the F1 and F2 progeny of COTI × COLE crosses. The differences between the two species in responding to interspecific hybridization suggest that COTI played a more dominant role in controlling plant height, dry weight, and time to flower in its hybrids with COLE. Results pooled from all F1 or F2 progeny of reciprocal interspecific crosses showed that interspecific hybridization did not seem to affect the plant height and seedling emergence of F1 and F2 progeny but affected the dry weight, time to flower, pollen stainability, and seed production (per seed head) of these progeny. Heterosis was observed in the time to flower of F1 progeny in 2009. Heterosis was also evident in F1 progeny’s dry weight but followed with slight hybrid breakdown in F2 progeny. Pollen stainability and seed production both showed significant breakdown in F1 and F2 progeny: 53.3% to 81.1% reduction in pollen stainability and 12.6% to 38.2% reduction in seed production, respectively. Chromosome mispairing resulting from reported reciprocal translocations between the chromosomes of COLE and COTI might be the primary cause of low pollen stainability and seed production in F1 and F2 progeny. Maternal effects were detected in plant height and dry weight of F1 and F2 progeny. These results showed that interspecific hybridization between COLE and COTI would result in deleterious effects to both species; thus, it is very important to prevent cross-pollination and hybridization between them in commercial seed production and native plantings.

Abstract Plant mitochondrial genomes sometimes carry cytoplasmic male sterility (CMS)-associated genes. These genes have been harnessed in various crops to produce high-yielding F1 hybrid seeds. The gene open reading frame 352 (orf352) was reported to be an RT102-type CMS gene in rice (Oryza sativa), although the mechanism underlying its role in CMS is unknown. Here, we employed mitochondrion-targeted transcription activator-like effector nucleases (mitoTALENs) to knockout orf352 from the mitochondrial genome in the CMS rice RT102A. We isolated 18 independent transformation events in RT102A that resulted in genome editing of orf352, including its complete removal from the mitochondrial genome in several plants. Sequence analysis around the mitoTALEN target sites revealed their induced double-strand breaks were repaired via homologous recombination. Near the 5ʹ-target site, repair involved sequences identical to orf284, while repair of the 3ʹ-target site yielded various new sequences that generated chimeric genes consisting of orf352 fragments. Plants with a chimeric mitochondrial gene encoding amino acids 179–352 of ORF352 exhibited the same shrunken pollen grain phenotype as RT102A, whereas plants either lacking orf352 or harboring a chimeric gene encoding amino acids 211–352 of ORF352 exhibited partial rescue of pollen viability and germination, although these plants failed to set seed. These results demonstrated that disruption of orf352 partially restored pollen development, indicating that amino acids 179–210 from ORF352 may contribute to pollen abortion.

Grape (Vitis vinifera) is among the world’s most important fruit crops and is a commonly used woody plant for genomics and post-genomics research. NAC transcription factors play central roles in plant growth and development, floral organ morphogenesis, and responses to biological stress. It is therefore important to identify key transcription factors from grape and clarify their mechanisms of action to generate genetic resources for grape molecular improvement. Our research group previously cloned a NAC transcription factor from V. vinifera ‘Yatomi Rosa’ [drought and leaf roll gene 1 (DRL1)] and demonstrated that it caused dwarfing of tobacco (Nicotiana benthamiana) plants when overexpressed. In the present work, we demonstrate that overexpression of DRL1 in transgenic tobacco delays flowering time and markedly reduces pollen viability. Furthermore, crosses between male DRL1 transgenic tobacco and female wild-type tobacco exhibit substantially lower fruit set, fruit and seed weights, fruit and seed shape indices, and seed germination rates than selfed wild-type plants or crosses with a transgenic female parent. DLR1 overexpression strongly influences flowering time and reproduction in transgenic tobacco, primarily through its effects on pollen development. These results provide a foundation for further functional characterization of DLR1 in grape.

Sorghum (Sorghum bicolor (L.) Moench) is grown as a dryland crop in semiarid subtropical and tropical environments where it is often exposed to high temperatures around flowering. Projected climate change is likely to increase the incidence of exposure to high temperature, with potential adverse effects on growth, development and grain yield. The objectives of this study were to explore genetic variability for the effects of high temperature on crop growth and development, in vitro pollen germination and seed-set. Eighteen diverse sorghum genotypes were grown at day : night temperatures of 32 : 21°C (optimum temperature, OT) and 38 : 21°C (high temperature, HT during the middle of the day) in controlled environment chambers. HT significantly accelerated development, and reduced plant height and individual leaf size. However, there was no consistent effect on leaf area per plant. HT significantly reduced pollen germination and seed-set percentage of all genotypes; under HT, genotypes differed significantly in pollen viability percentage (17–63%) and seed-set percentage (7–65%). The two traits were strongly and positively associated (R2 = 0.93, n = 36, P < 0.001), suggesting a causal association. The observed genetic variation in pollen and seed-set traits should be able to be exploited through breeding to develop heat-tolerant varieties for future climates.

Genetic modification (GM) of plants has great potential in the production of food and industrial compounds, and in molecular pharming. One of the greatest public concerns regarding this technology is effective pollen flow, in which wind- or insect-borne transgenic pollen is able to fertilise either non-GM crops of the same species, or closely related weed species, and lead to viable seed formation. In this paper we describe a novel concept, based on epigenetic inheritance (imprinting) and post-transcriptional gene silencing (PTGS)/RNA interference (RNAi), designed to prevent transgene escape via pollen flow from transgenic plants. A key advantage of this strategy is that it would allow all seeds from self-pollinated transgenic plants to be harvested and re-sown, without the need for specific treatments, while retaining all of the transgenes present in the parent. Thus, this strategy is not a Genetic Use Restriction Technology (GURT) and if implemented would not prevent seed saving by end-users.

Fertilization and seed formation are fundamental events in the life cycle of flowering plants. The seed is a functional unit whose main purpose is to propagate the plant. The first step in seed development is the formation of male and female gametophytes and subsequent steps culminate in successful fertilization. The detailed study of this process is highly relevant because it directly impacts human needs, such as protecting biodiversity and ensuring sustainable agriculture to feed the increasing world population. Cytokinins comprise a class of phytohormones that play many important roles during plant growth and development and in recent years, the role of this class of phytohormones during reproduction has become clear. Here, we review the role of cytokinins during ovule, pollen and seed formation at the genetic and molecular levels. The expansion of knowledge concerning the molecular mechanisms that control plant reproduction is extremely important to optimise seed production.

Abstract Seed setting rate is one of the critical factors that determine rice yield. Grain formation is a complex biological process, whose molecular mechanism is yet to be improved. Here we investigated the function of an OVATE family protein, Embryo Sac Development 1 (ESD1), in the regulation of seed setting rate in rice (Oryza sativa) by examining its loss-of-function mutants generated via clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated9 (Cas9) technology. ESD1 was predominantly expressed at Stage 6 of panicle development, especially in the ovules. esd1 mutants displayed reduced seed setting rates with normal stamen development and pollen tube growth but abnormal pistil group. Investigation of embryo sacs revealed that during the mitosis of functional megaspores, some egg cells degraded during differentiation in esd1 mutants, thereby hindering subsequent fertilization process and reducing seed setting rate. In addition, the transcriptional level of O. sativa anaphase-promoting complex 6, a reported embryo sac developing gene, was significantly reduced in esd1 mutants. These results support that ESD1 is an important modulator of ESD and seed setting rate in rice. Together, this finding demonstrates that ESD1 positively regulates the seed setting rate by controlling ESD in rice and has implications for the improvement of rice yield.

There is concern that high temperatures resulting from global warming could reduce fruit set of tomato (Solanum lycopersicum). However, fruit set of parthenocarpic tomato genotypes, which often bears seedless fruit, is not reduced when grown under a high temperature. The cause of seedless fruit development was studied with the aim of increasing the seed number in parthenocarpic tomato. Ovule number at anthesis in parthenocarpic and non-parthenocarpic fruit did not differ, but the proportion of undeveloped ovules increased with time after anthesis in parthenocarpic tomato, whereas most ovules in non-parthenocarpic tomato developed normally. Pollen grains germinated on the stigma and extruded pollen tubes in parthenocarpic and non-parthenocarpic tomatoes, but in parthenocarpic tomato, pollen tube elongation was markedly inhibited in the style base. Elongation of pollen tubes on agar containing indoleacetic acid (IAA) was depressed in parthenocarpic and non-parthenocarpic tomato plants. p-Chlorophenoxyisobutyric acid (PCIB), which inhibits auxin action, did not affect the fruit set and fresh weight in either type of tomato, although seed number per fruit in parthenocarpic tomato was significantly increased from 13 ± 2 to 74 ± 6 seeds by PCIB treatment. These results indicated that a high IAA concentration in the ovary of parthenocarpic tomato inhibited pollen tube elongation, and that poor fertilization resulted in failure of ovule development. Moreover, floral organs in parthenocarpic tomato were normally developed as in non-parthenocarpic tomato, and seed development could be induced in parthenocarpic tomato by PCIB treatment.

Abstract The female gametophyte of higher plants gives rise, by double fertilization, to the diploid embryo and triploid endosperm, which develop in concert to produce the mature seed. What roles gametophytic maternal factors play in this process is not clear. The female-gametophytic effects on embryo and endosperm development in the Arabidopsis mea, fis, and fie mutants appear to be due to gametic imprinting that can be suppressed by METHYL TRANSFERASE1 antisense (MET1 a/s) transgene expression or by mutation of the DECREASE IN DNA METHYLATION1 (DDM1) gene. Here we describe two novel gametophytic maternal-effect mutants, capulet1 (cap1) and capulet2 (cap2). In the cap1 mutant, both embryo and endosperm development are arrested at early stages. In the cap2 mutant, endosperm development is blocked at very early stages, whereas embryos can develop to the early heart stage. The cap mutant phenotypes were not rescued by wild-type pollen nor by pollen from tetraploid plants. Furthermore, removal of silencing barriers from the paternal genome by MET1 a/s transgene expression or by the ddm1 mutation also failed to restore seed development in the cap mutants. Neither cap1 nor cap2 displayed autonomous seed development, in contrast to mea, fis, and fie mutants. In addition, cap2 was epistatic to fis1 in both autonomous endosperm and sexual development. Finally, both cap1 and cap2 mutant endosperms, like wild-type endosperms, expressed the paternally inactive endosperm-specific FIS2 promoter GUS fusion transgene only when the transgene was introduced via the embryo sac, indicating that imprinting was not affected. Our results suggest that the CAP genes represent novel maternal functions supplied by the female gametophyte that are required for embryo and endosperm development.

The control of pollen viability and release is of major commercial importance in the development of crops for hybrid seed production and selective breeding. It has been shown that key transcription factors in Arabidopsis particularly MALE STERILITY1 (MS1), are functionally conserved in rice (Li et al., 2011), therefore extending this comparative analysis and controlling fertility in temperate cereals, such as barley, is the long term goal of this project. Although anther and pollen development of barley seems morphologically similar to Arabidopsis, the genes involved and how they are regulated are currently unknown. Arabidopsis MS1 is a tapetum specific transcription factor which is expressed exclusively from the tetrad stage to early microspores release. Identification and accurate staging of barley anther development is essential for expression analysis and functional characterisation of genes involved in pollen development. Therefore, a complete morphological study of barley development was conducted. External characteristics have been described in parallel to anther development in order to predict anther stages by the observation of external stages phenotypic traits. Characterization of the barley orthologue of MS1 (HvMS1) has been conducted. Recently a new grass genome has been released, Brachypodium distachyion. This new resource has been used to aid primers design alongside the rice OsPTC1 sequence, the orthologue of MS1 (Li et al., 2011). Genome sequencing has indicated that the Brachypodium genus is more closely related to wheat and barley than it is to rice, Due to the close relationship between Brachypodium and barley, this new grass has been used as intermediary to identify the OsPTC1 orthologue in barley as well as downstream MS1 targets. A highly similar sequence to OsPTC1 was found in Brachypodium, Bradi4g31760. This new gene, as a result of its similarities to OsPTC1, was considered as its putative orthologue gene in Brachypodium. Therefore, the most conserved areas between OsPTC1-Bradi4g31760 were used for primers design to successfully amplify equivalent gene in barley (HvMS1). The characterization of this barley gene showed a similar expression pattern to the MS1 putative orthologue in Arabidopsis of tapetum specific expression. In addition, RNAi silencing of this gene has revealed that it is essential for the normal development of pollen, with a lack of viable pollen produced in the putative HvMS1 silenced transgenic lines.

An essential component of development is the accumulation of specific metabolites in a temporal and tissue-specific manner. The growth regulator abscisic acid (ABA), which accumulates at a specific time during seed development, is required for seed maturation and prevents the premature developmental switch from dormancy to germination ABA accumulates differently in two tissues of the seed; levels in the embryo are several-fold higher than in the endosperm and the temporal accumulation of ABA is also different between these tissues. To begin to understand how ABA accumulation is regulated during seed development, the regulation of ABA biosynthesis was investigated. The approach taken was to examine the expression of the biosynthetic enzyme, phytoene desaturase (PDS), which catalyzes a regulated step in ABA synthesis in several other organisms (Bramley, 1985, Sandmann et al., 1989, Hugueney et al., 1992 and Giuliano et al., 1993). Unlike ABA accumulation, PDS transcript and protein levels were higher in the endosperm than in the embryo. The spatial difference in PDS levels did correlate with levels of the pathway intermediate, beta-carotene, suggesting that PDS may control the synthesis of ABA precursors while subsequent enzymes may regulate ABA accumulation. The temporal expression of Pds was also unrelated to ABA accumulation. In the endosperm, transcript levels were initially high and declined during desiccation while protein levels remained high throughout development. In the embryo, transcript levels were low and constant while protein levels declined. There are several maize mutants (viviparous mutants) disrupted in ABA biosynthesis, resulting in decreased levels of ABA and premature germination. Analysis of the Pds allele and transcript in the viviparous-5 mutant showed that the gene contains multiple insertions and deletions, giving rise to a larger transcript. In addition, the 55 kDa PDS protein was not detected in the vp5 mutant by immunoblot analysis, indicating that the vp5 phenotype results from a mutation at the PDS locus. To determine whether the wild type protein encoded by the ABA mutant, vp2, or the pathway intermediate, lycopene, regulate PDS, transcript and protein levels were compared in wild type and mutant (vp2 and vp7, respectively) seeds. The levels of PDS were not significantly different in vp2 or vp7 wild type and mutant seeds, suggesting that neither the VP2 protein nor lycopene regulate PDS at the steady-state transcript or protein level.

Die vorliegende Arbeit prüft bei der gärtnerischen Modell-Kultur Cyclamen den Einfluss des Genotyps (interspezifische Hybriden) auf generative Merkmale sowie bei C. persicum `Melody´ den Einfluss von Kultivierungsmaßnahmen wie die Besiedelung der Wurzeln durch einen symbiontischen Pilz (Piriformospora indica) in Kombination mit einem differenzierten Phosphor-Angebot auf vegetative und generative Merkmale: (1) Pflanzendurchmesser, (2) Blühzeitpunkt und Blütenanzahl, (3) Anzahl Samenanlagen pro Fruchtknoten, (4) Vitalität von Pollen und Samenanlagen, (5) Mikrosporogenese, (6) Befruchtungsvorgang (Pollenschlauchwachstum, Anteil Fruchtknoten mit Pollenschläuchen, Anzahl Pollenschläuche im Griffel und Penetration der Pollenschläuche in die Micropyle), (7) abortierte Blüten nach der Bestäubung (8) Samenbildung und (9) Samenanzahl.
The present paper investigates Cyclamen as an horticultural model-culture. A main Focus is on the characteristics of the Cyclamen genotype, notably with interspecific hybrids. Further, Cyclamen persicum cv. served as a model to analyse effects on parameters of pollination, seed development and number of ovules per ovary, which are caused by a root colonization of the seed bearer with the symbiotic fungus Piriformospora indica (Piri) in combination with a differentiated phosphorus supply. In this regard, plant diameter, flowering time and flower number, the viability of pollen and ovules, the microsporogenesis, the growth of pollen tubes, the seed formation and the seed count were considered among important parameters of pollination and seed development.

Cuphea is an herbaceous genus having species whose seed storage lipids are predominantly medium-chain triglycerides (MCTs). Cuphea lanceolate Ait, and Cuphea viscosissima Jacq. are central to the breeding of Cuphea as a new commercial source of MCTs. The objectives of this thesis were to develop a reliable method to extract DNA from Cuphea, to construct a molecular-marker linkage map of C. lanceolate, and to evaluate quantitative-trait loci (QTL) affecting seed capric acid content, seed oil content, and embryo development in C. lanceolate. We used allozyme and restriction-fragment- length-polymorphism (RFLP) markers to study Cuphea because molecular markers are the best method available to investigate the Mendelian genetics underlying quantitative traits, and are useful in breeding. Adequate yield of clean DNA is essential for RFLP mapping. We tried numerous DNA extraction methods that failed to remove contaminants that interfere with restriction digests of Cuphea DNA. The method described here was developed to remove those contaminants and maintain relatively high DNA yields. In this method, the critical step in purification consists of washing the DNA with phenol while it is complexed with CTAB and dissolved in 1 M NaCl. An RFLP and allozyme linkage map of C. lanceolate was constructed having 37 markers in six linkage groups with a total distance of 288 cM. Levels of polymorphism were estimated for three lines of C. lanceolate and one line of C. viscosissima using 84 random genomic clones and two restriction enzymes, EcoRI and HindIII. Twenty-nine percent of the probes detected RFLPs between C. lanceolate lines, whereas 63% of the probes detected RFLPs between C. lanceolate and C. viscosissima lines. Thirty RFLP and four allozyme markers were used to locate on the C. lanceolata linkage map QTL affecting seed capric acid content, seed oil content, and embryo development. Three unlinked QTL explained 19.4% of the phenotypic variation in capric acid content in F₂ seed. Seed oil content and seed weight were measured on seed from field-grown F₂ plants. Seed weight was indicative of embryo size (development). Four unlinked QTL explained 33.9% of the phenotypic variation in embryo size. One of these QTL, which explained 20.3% of the variation, may have been a chromosomal deletion detected by a marker having a null allele. Three QTL pleiotropically affected seed oil by affecting embryo size. The one QTL that only affected seed oil accounted for 2.8% of the phenotypic variation.
Graduation date: 1991

Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2009.
Source: Dissertation Abstracts International, Volume: 70-06, Section: B, page: 3290. Adviser: Lila O. Vodkin. Includes bibliographical references (leaves 159-165) Available on microfilm from Pro Quest Information and Learning.

Maize grain contains high levels of phytic acid which chelates iron, zinc and other micronutrients as it passes through the digestive systems of monogastric consumers reducing their bioavailability. Breeding for low phytic acid (LPA) content to improve micronutrient bioavailability is hampered by a tedious and destructive colorimetric method on the grain, low yields compared to the wild-types and reduced seed germination and vigour of LPA mutants. Breeding for LPA therefore should also incorporate breeding for improved germination and vigour in the mutants. Molecular markers to speed up the selection process and studies on gene action and combining ability for germination, vigour and yield parameters of the LPA mutants in combinations with other different maize germplasm will speed up breeding for this trait. The objectives of this study were: to develop a molecular marker linked to the lpa1-1 gene and apply this marker for foreground selection in a backcross breeding programme and to use amplified fragment length polymorphism (AFLP) markers for background selection to recover the recurrent parent genome to speed up the backcrossing process; to study gene action and combining ability for seed germination, vigour and yield from diallel crosses involving LPA mutants, QPM and normal endosperm maize inbred lines by replicated laboratory seed tests ( standard germination test and accelerated aging test) and field evaluations in South Africa and Zimbabwe. A co-dominant single nucleotide polymorphism (SNP) marker which detects the transition base change of C/T nucleotides was developed from the gene sequence to identify the lpa1-1 trait. The 150 bp lpa1-1 SNP marker was validated by forward and reverse DNA sequencing of the parental amplification products which confirmed the C to T base change resulting in the LPA phenotype. The lpa1-1 SNP marker was used for foreground selection in 250 BC(2)F(1) progenies of CM 32 (LPA) x P 16 as the recurrent parent. This SNP marker was used to genotype the lines into homozygous dominant (wild type) and homozygous recessive (LPA) genotypes by their melting profiles and heterozygous genotypes by the normalised difference plots using high resolution melt (HRM) analysis. Seventeen heterozygous and 11 homozygous recessive lines were identified for background selection by fingerprinting with AFLP markers to determine the amount of recurrent parent (P 16) genome present. There were six EcoRI/MseI primer combinations tested with 277 data points scored (84% polymorphism rate). The amount of recurrent parent (P 16) genome recovered ranged from 62% to 92% with 13 lines showing greater than 83% of the recurrent parent genome. The effects of diallel crosses generated between four LPA, three QPM and three normal endosperm maize lines were determined for seed germination and vigour using the standard germination and accelerated aging seed tests under laboratory conditions in accordance with the procedures of the International Seed Testing Association. The specific combining ability (SCA) effects and general combining ability (GCA) effects were significant for the seed germination and vigour traits, indicating that genes with non-additive and additive effects were important in controlling these traits. However, the SCA effects were greater than GCA effects suggesting that genes with non-additive effects were predominant. The LPA parents showed reduced vigour compared to the normal and QPM inbred lines under both conditions, with LPA lines CM 31 and CM 32 showing stress tolerance. There were some combinations involving LPA lines, such as LPA x normal, LPA x QPM and LPA x LPA that retained high vigour and high germination rates under accelerated aging conditions, suggesting that they could be stress-tolerant.. A 10 x 10 diallel involving four LPA, three QPM and three Nm inbred lines was evaluated in replicated trials across six environments. Results show that both additive and non-additive gene effects were significant for resistance to northern corn leaf blight (NCLB), grey leaf spot (GLS) and Phaeosphaeria leaf spot (PLS) diseases. The additive gene effects were predominant for the yield and associated secondary traits such as days to mid-pollen shed (DMP), days to mid-silking (DMS), ear per plant (EPP) and grain moisture content (GMC) and grain yield. The LPA lines were early flowering and had quick grain dry down rate but all showed undesirable negative and significant GCA effects for yield. The yield of the LPA x LPA, LPA x Nm and LPA x QPM group of crosses was lower than the check hybrids by about 32 to 67% showing the need for yield improvement of the LPA combinations. An eight x eight diallel involving two LPA and six normal endosperm lines was evaluated over two seasons in five locations with two replications for grain yield components and foliar diseases. There was significant additive and non-additive gene action for both seed germination and vigour traits with predominance of non-additive gene effects. Both additive and non-additive gene effects were significant for yield and associated traits such as anthesis dates and number of ears per plant. However, the additive gene action was predominant for yield and associated traits. Generally the LPA lines and their combinations showed lower germination and vigour. The LPA line, CM 32 showed stress tolerance under accelerated aging conditions. There were three LPA x Nm crosses that showed improvements to the means of seed germination and vigour and yield traits. Results indicated that there was not any significant correlation between yield and seed germination and between yield and vigour. Yield was, however, significantly and positively correlated with anthesis dates and GMC, indicating that higher yield was associated with longer growing cycles. This study was able to successfully develop and apply the lpa1-1 SNP marker for foreground selection and AFLP markers for background selection in a backcross breeding programme. Problems of low seed germination, seedling vigour and grain yield of LPA lines and their combinations were confirmed. However results also indicated some potential of combining the LPA and QPM traits in a single cultivar. In general, procedures such as reciprocal recurrent selection, that emphasise both GCA and SCA effects would be recommended to improve seed germination, seedling vigour and yield in developing varieties with LPA trait.
Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2010.

Increased awareness on the effects of food on human health and the environment has compelled the need to look for alternative food sources. This resulted in the steady increase in demand for plant-based protein foods as opposed to animal food sources on the premises of significant health benefits, environment-friendly sustainable production systems and moral ethics. This trend has also been reflected in recently reviewed national food guides. Research on plant-based food systems primarily aims to understand the nutritional and functional roles of dietary proteins sourced from crop seeds. Recent scientific advances in this field explore the use innovative technologies in the research and commercial applications of seed proteins. The objective of this paper is to review and summarize key research efforts and recent advances on the utility of seed-sourced proteins in the food product development applications. Important topics covered in the review are: exploration of sources of dietary protein seeds, the status of seed dietary protein research for nutrition and health, and the deployment of new and innovative technologies for developing dietary seed proteins. The topics draw on research and publications on the availability, functionality, quality, genetics, and innovative technologies to develop value-added products from dietary plant-based proteins. The review will fill knowledge gaps in the utilization of emerging plant-based protein food systems in relation to nutritional and health benefits, process technologies and promoting food system sustainability.

Methods of paleovegetation analysis can be grouped into two broad categories. Those that use plant microfossils for reconstructing terrestrial vegetation, past environments, migrations, and evolutionary histories constitute a part of paleopalynology that includes the study of pollen, spores, other acid-resistant microscopic structures, and phytoliths (distinctive, microscopic silicate particles produced by vascular plants). Those that use plant megafossils such as leaves, cuticles, cones, flowers, fruits, and seeds constitute paleobotany. Two important subdisciplines of paleobotany are dendrochronology (fossil woods) and analysis of packrat middens. The latter are sequences of nesting materials, constructed by packrats of the genus Neotoma, preserved in arid environments of the American southwest. The study of fossil fruits and seeds is a specialized field within paleobotany, and it is also used in studies on Quaternary vegetational history in the preparation of seed diagrams accompanying pollen and spore profiles from bog and lake sequences. In 1916 Swedish geologist Lennart von Post demonstrated that pollen grains and spores were abundantly preserved in Quaternary peat deposits and could be used to trace recent forest history and climatic change (Davis and Faegri, 1967). The term palynology was subsequently introduced by Hyde and Williams in 1944 to include all studies concerned with pollen and spores. Paleopalynology has come to denote the study of acid-resistant microfossils generally, while pollen analysis designates those investigations dealing specifically with the Quaternary. In the early 1950s researchers in the petroleum industry began to routinely apply paleopalynology to problems of stratigraphic correlation and the reconstruction of depositional environments in Tertiary and older strata (Hoffmeister, 1959). This added a practical dimension to a mostly academic pursuit and fostered interest in applied palynology and its use as a paleoecological research tool. This important development is reflected in the increased number of publications after about 1955. As the history of other innovations might predict, there was a period of exuberant claims, isolated specialization, and exaggerated charges of deficiency in the method; but for palynology this seemingly inevitable period was mercifully brief. The different terminology, principles, and techniques involved in megafossil paleobotany and paleopalynology still result in specialization, but this limitation is frequently overcome by coordinated or collaborative projects, and an increasing number of practitioners work in both disciplines.