Summary
The gross form of the nuclear genome varies greatly among plant species in both anatomy and genetic organization. Chromosome number (ft) ranges from 2 to over 600, and ploidy from 1 to over 20. The amount of DNA in the unreplicated haplophase genome (the 1C value) differs by more than 2500-fold among angiosperms. Although it has been questioned since the 1930s whether such variation is of adaptive significance and whether it is related, perhaps causally, with environmental factors, no direct or causal links have yet been found. However, variation in DNA C-value has far-reaching biological consequences and can be of considerable adaptive and hence ecological significance. Strikingly precise interspecific relationships exist between DNA C-value and many diverse phenotypic characters at the cellular level, and DNA can affect the phenotype in two ways, firstly by expression of its genie content and, secondly, by the biophysical effects of its mass and volume, the latter defined as nucleotypic effects. Nucleotypic variation in DNA C-value sets absolute limits to both the minimum size and mass of the basic unit of plant anatomy (i.e. the cell) and the minumum time needed to produce a similar cell with newly synthesized organic molecules. Moreover, in complex multicellular vascular plants, such effects at successive cell cycles are additive, so that DNA C-value influences many characters, including growth rate, seed weight, minimum generation time and type of life-cycle. Thus, the nucleotype profoundly affects where, when and how plants grow. Selection for a particular genomic form acting on its spatial or temporal consequences may occur at various levels ranging from the cell to the whole organism and may operate throughout the life-cycle or at just one stage. DNA C-value is often indirectly related to environmental factors which determine time-limited environments via selection acting on the temporal phenotypic consequences of nucleotypic variation. However, in the case of radio-sensitivity, selection for a low DNA C-value may act directly on the nucleotype itself, as the size of the nuclear DNA target directly affects the ability of the plant to survive.

Variation in genomic form in plants and its ecological implications

Publisher Summary This chapter discusses the B-chromosome systems in flowering plants and animal species. The term B chromosome is introduced to describe extra chromosome which have little if any effect on visible characters of the plant, which are not homologous with the A chromosomes of the normal complement, and which are extremely irregular in their meiotic distribution. B Chromosomes are now known under a variety of different names, including supernumerary and accessory, which are the most common alternatives. B chromosomes are dispensable and nonhomologous with A chromosomes. These two characteristics above all others most sharply differentiate them from members of the basic A-chromosome complement. The distribution of B chromosome in plant and animal species is discussed. In many plants and animals the B chromosomes are completely stable during the cell cycle and are inherited in a constant and unchanging form along with the A chromosomes. Some plant species have an apparent order in their instability, which results in exclusion and/or accumulation of B chromosomes in specific tissues and organs. The significance of B-chromosome effects in flowering plants and animals is discussed.

B-Chromosome Systems in Flowering Plants and Animal Species

It is timely to re-examine the phenomenon of polyploidy in plants. Indeed, the power of modern molecular technology to provide new insights, and the impetus of genomics, make polyploidy a fit, fashionable and futuristic topic for review. Some historical perspective is essential to understand the meaning of the terms, to recognize what is already known and what is dogma, and to frame incisive questions for future research. Polyploidy is important because life on earth is predominantly a polyploid phenomenon. Moreover, civilization is mainly powered by polyploid food – notably cereal endosperm. Ongoing uncertainty about the origin of triploid endosperm epitomizes our ignorance about somatic polyploidy. New molecular information makes it timely to reconsider how to identity polyploids and what is a polyploid state. A functional definition in terms of a minimal genome may be helpful. Genes are known that can raise or lower ploidy level. Molecular studies can test if, contrary to dogma, the relationship between diploids and polyploids is a dynamic two-way system. We still need to understand the mechanisms and roles of key genes controlling ploidy level and disomic inheritance. New evidence for genome duplications should be compared with old ideas about cryptopolyploidy, and new views of meiosis should not ignore premeiotic genome separation. In practice, new knowledge about polyploidy will be most useful only when it reliably predicts which crops can be usefully improved as stable autopolyploids and which genomes combined to create successful new allopolyloids. © 2004 The Linnean Society of London, Biological Journal of the Linnean Society, 2004, 82, 411–423.

Perspectives on polyploidy in plants – ancient and neo

Robertsonian fusion and centric fission are uniquely detectable in comparative studies of karyotype patterns. They are the most important types of karyotype change in animals but seem to be relatively uncommon in higher plants. Both modify intra- and interchromosomal recombination and linkage relationships and consequently patterns of genetic variation. When differentiating populations or species they can produce postulating barriers to gene flow. The number of reported cases of fusion or fission in higher plants has increased over the years but remains low, and most of these are casual comparisons of karyotypes without any follow-up investigation. This review focuses on more adequate studies made in a few groups. Studies in the Tradescantieae produce the strongest evidence for fusion as a type of orthoselection in the subfamily. Some species ofLycoris are also considered to have evolved their karyotypes in that way. Some genera of slipper orchids and the cycad genusZamia have populations where atypical chromosome number increase can be attributed to fission probably as a result of stressful influences. It is suggested that fusion may have been involved in the evolution of many stable karyotypes and that fission is generally a secondary destabilizing mechanism which may lead to refusion in the long term. Their proven incidence remains making it unwise to suggest that they have been major influences in karyotype evolution in higher plants.

Robertsonian Fusion and Centric Fission in Karyotype Evolution of Higher Plants

Chromosome changes in plant evolution.

SUMMARYThe somatic chromosomes of 28 accessions of Crinum have been studies. Ten of these were polyploid (3x, 4x, 6x, 8x) and the remainder diploid. B chromosomes were present in seven plants. Aneusomatic variation does not occur to any significant extent.The common basic number is x = 11 but accessions, based on x = 12 derive from the Accra Plains of Ghana. Comparative chromosome morphology shows that a uniform pattern prevails throughout the x = 11 species but that of the x = 12 plants is quite distinct and includes three pairs of telocentrics. There is every indication that this unique karyotype is closely correlated with the distribution of the species in an area of particular ecological interest.

https://www.tandfonline.com/doi/pdf/10.1080/00087114.1967.10796255

Keith Jones

Papers

Chromosome Evolution in the Genus Crinum