Environmental sex determination in plants

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Environmental sex determination is present in several animal and plant lineages, in which gender depends on diverse factors such as. Environmental Factors Responsible for Determination of Sex in Plants and Animals! In some organisms, the environment determines the sexual phenotype of. By contrast, many animal and plant species exhibit environmental sex determination, wherein an individual's sex is instead determined by some aspect of the.

Environmental sex determination is the establishment of sex by a non-genetic cue, such as nutrient availability, experienced within a discrete period after. Request PDF on ResearchGate | Plant Sex Determination | Sex This phenomenon is known as environmental sex determination (ESD), and. The practical and theoretical aspects of the problem of sex regulation by Influence of Environmental Factors and Nutrition on Sex Determination in Plants (​A.

By contrast, many animal and plant species exhibit environmental sex determination, wherein an individual's sex is instead determined by some aspect of the. Summary 1 In environmental sex determination (ESD) gender is decided after conception, ESD in plants has been mainly studied in an. Most theorising about sex determination in plants has focused on dioecious and that involving responses to environmental or hormonal cues.

The practical and theoretical aspects of the problem of sex regulation by external factors have been of environmental interest to many botanists. The answers to these questions will increase our ability determination understand and direct the growth plants development of plants. Dtermination determination of sex and the retermination of sex organs during growth and development are determined not only by the genetic apparatus, but also sxe environmental factors.

There is a considerable body of evidence indicating that external forces cause changes of sex characteristics in animals and environmental, under both natural and experimental conditions Pezard ; Zavadovskyi ; Morgan ; Grishko ; Astaurov, ; Minina ; Heslop-Harrison ; Enviromnental ; Djaparidze; Lvova ; Vince-Prue determination Frankel and Galun Sex yet, all the extensive environmental material and theoretical plants have failed to give a definite answer to the question of exactly sex environmental conditions act to change the sex in different plant groups.

The extent to which these sex transformations involve solely plants control Corrensor solely metabolic changes Schaffneror both Sabinin remains an open question.

Unable to display preview. Download preview PDF. Environmental to main content. Advertisement Hide. Sex Authors and affiliations M. Chailakhyan V. This process is experimental plants the keywords determination be updated as the learning algorithm sex. This is a preview of subscription content, log in to check detrrmination. Chailakhyan 1 V. Determination 1 1. Moscow USSR. Personalised recommendations. Cite chapter How to cite? ENW EndNote. Buy options.

Many studies e. Testo et al. These controls can be useful to verify that a study species actually does not produce antheridiogens and does not respond to it, respectively. However, our three study species produced antheridiogens that in turn induced maleness in the three study species and thus these controls are not necessary. Dependence solely upon environmental factors can expose species to biased sex ratios, with potentially harmful effects for populations Stelkens and Wedekind For example, sexual reproduction would not be possible if all individuals were male under harsh conditions.

However, as seen above, water scarcity does not favour maleness in the study species. In ESD, sex is determined by the interaction between environmental, genetic and hormonal factors Valenzuela et al. This may be what we actually see in homosporous ferns: they have the tendency to follow a default development programme, but it can vary depending on environmental signals Masuyama ; Rubin and Paolillo ; Korpelainen The lower percentage of bisexuals we found at lower levels of water availability may be related to the reduction of vegetative growth.

Moisture deficit produced smaller gametophytes Fig. Because a multicellular meristem and a multilayered cushion is necessary for the production of bisexual gametophytes, the low proportion of bisexuals at lower moisture levels is probably due to not reaching the size and morphology thresholds required due to the delayed vegetative development under those conditions. Our results are not in concordance with the rise in reproductive effort i.

The allotetraploid C. Both species had higher percentages of females and bisexuals than C. Regarding mortality, it was equally low in all the three moisture regimes for each species. Low mortality is not surprising as fern gametophytes exhibit desiccation tolerance that is greater in species from xeric habitats Watkins et al. However, there were significant differences in mortality among species, with C.

This result suggests hybrid vigour but see below. Polyploids of flowering plants tend to have higher selfing rates than their diploid relatives Stebbins ; Mable ; Barringer , and this trend has been observed in homosporous ferns too Soltis and Soltis ; Masuyama and Watano Against this expectation, C.

This contrasts with the expectation for polyploid ferns to exhibit less inbreeding depression than their diploid parents and, therefore, being able to tolerate higher selfing rates Soltis and Soltis In addition, it is generally assumed that polyploids are more successful than their diploid parents, at least in novel and disturbed habitats Levin ; Otto and Whitton This is not valid for the study species as, in the Iberian Peninsula Anthos , the diploid C.

This could mean that the supposedly superior colonizing ability of the tetraploid is surpassed by that of one of the diploid parents. In other terms, that there is not hybrid vigour that gives advantage to the tetraploid relative to its parents, and the allotetraploid exhibits an intermediate colonizing ability between both diploids.

Evidence of very limited advantage of allopolyploids has been found in North American allotetraploid species of Dryopteris Sessa and Givnish An intermediate behaviour in other traits of an allotetraploid relative to its diploid parents was observed in some Asplenium Prada et al.

The response to the antheridiogen showed a similar model, high effect in one diploid, C. The ability of gametophytes to generate young sporophytes through automixis was positively correlated with moisture, as expected from their need for water for fertilization.

The three species under study can self-fertilize and raise completely homozygous sporophytes, which represents an advantage for long distance dispersal, but a disadvantage for genetic variation over the long-term. It may also be an adaptation to xeric habitats, where microsites for spore germination are scarce and sperm movement between gametophytes may be hindered by the absence of water.

We did not find aborted embryos and selfed sporophytes showed normal growth. However, it must be noted that we only studied early development of sporophytes a 23 weeks culture whereas inbreeding depression might act later in the life cycle e. Morgante et al. Moreover, we found that the three study species are sensitive to the action of antheridiogen. This fact allows us to advance the following scenario. Adequate water availability would allow germination of several spores present in a safe site.

The fastest gametophytes to develop would become female and secrete antheridiogen, thus inducing maleness in the surrounding ones and promoting outcrossing.

In harsh conditions, however, only a few isolated spores would germinate, and their final development as bisexuals would facilitate self-fertilization assuring reproduction as observed in some flowering plants Evans et al. This mixed mating system, known in fern species with high colonization potential Wubs et al. These strategies would confer, respectively, two advantages: promotion of outcrossing and reproductive assurance Goodwillie et al.

It could be predicted that, as the response to antheridiogens is weaker in C. In the allopolyploid complex examined here, the effect of water availability on gender expression is small. Isolated gametophytes show an asexual to female to bisexual sequence that does not depend upon the degree of soil moisture. Both gender expression and growth reduction in response to water scarcity of the allotetraploid resemble one of the diploid parents.

In all moisture regimes, mortality is lower in the allotetraploid, suggesting hybrid vigour, whereas automixis rate is similar in the three species.

Sex is environmentally determined by antheridiogens. The allotetraploid shows an intermediate response to antheridiogens relative to its parents. The production of bisexual gametophytes allows for self-fertilization, while the presence of male gametophytes when antheridiogen is present promotes outcrossing.

Thus, it can be speculated that this mixed mating system could be advantageous in the xeric habitat of these species. The study of population's genetic structure and of ecological niche differences among the three species would help to clarify their reproductive behaviour and the reasons behind their geographical distribution. We thank very much Dr James E. Watkins for his comments and suggestions on an earlier draft of the manuscript that greatly improved this final version, and also for his help with English editing.

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Sign In. Advanced Search. Article Navigation. Close mobile search navigation Article Navigation. Volume 7. Article Contents. Sources of Funding. Contributions by the Authors. Conflict of Interest Statement. Literature Cited. Oxford Academic. Google Scholar. Emilia Pangua. Luis G.

Associate Editor: Dennis F. Cite Citation. Permissions Icon Permissions. Abstract Environmental sex determination ESD is present in several animal and plant lineages. Allopolyploid , antheridiogen , Cheilanthes , environmental sex determination , gametophyte gender , mixed mating , water availability , xerophytic ferns. Open in new tab. Open in new tab Download slide. Google Preview. Search ADS. The birds and the bees and the flowers and the trees: lessons from genetic mapping of sex determination in plants and animals.

Environmental sex determination in ferns: effects of nutrient availability and individual density in Woodwardia radicans. Growth regulation by ethylene in fern gametophytes. Inhibition of spore germination. Extreme environments select for reproductive assurance: evidence from evening primroses Oenothera.

Flora Iberica. I: Lycopodiaceae-Papaveraceae. The evolutionary enigma of mixed mating systems in plants: occurrence, theoretical explanations, and empirical evidence. Gametophytic plasticity among four species of ferns with contrasting ecological distributions.

Environmental sex determination in response to light and biased sex ratios in Equisetum gametophytes. Environmental sex determination in the genus Equisetum : sugars induce male sex expression in cultured gametophytes. Generalized linear and generalized additive models in studies of species distributions: setting the scene. Skip to main content. Advertisement Hide. Authors Authors and affiliations M. Chailakhyan V. This process is experimental and the keywords may be updated as the learning algorithm improves.

This is a preview of subscription content, log in to check access. Chailakhyan 1 V. Other recessive genes affecting the development of male and female gametes are known in maize, e.

Sex-linked X-linked genes which are not concerned with sex determination are present in two doses in the mammalian and Drosophila females XX , while their males XY contain a single dose. However, the intensity of phenotypes, the amounts of the concerned enzymes, and even the amount of RNA produced by the X-linked genes in the females are equal to those in the males.

This phenomenon is known as dosage compensation Muller, , and regulates the function of X-linked genes in such a manner that their expression is comparable in both females and males even though they have different dosage number of copies of these genes. It has been demonstrated that in homogametic XX female individuals, one X-chromosome gets characteristically condensed and inactivated.

The phenomenon of inactivation of X-chromosome was confirmed by the observation of a. Barr body Barr body. Ban body was first observed by Barr and Bertram in in female cat and later identified as X-chromosome by Ohno et-al, Later Lyon confirmed the existence of Barr body in normal females, superfemales and in Klinefelter males. Such Barr body has also been observed in most of the body cells e.

Human females have the Barr body in the nuclei of their body cells in higher proportion than males and are, therefore, referred to as sex chromatin positive. Since it was found that whenever the number of X-chromosomes was two or more than two, the number of Barr bodies was one less than the number of X-chromosomes e. Which of the two X-chromosomes remains active in female individuals is determined at the early stages of development. It was observed by Lyon that each of the paternal P and maternal M X-chromosomes has a chance to become inactive i.

Barr body. In other words, the inactivation of X-chromosomes is a random phenomenon in most species. In some species, however the X-chromosome inactivation may not be random, e. In mammals, the inactivation usually takes place in early embryogenesis.