Heteroblasty (botany)

Last updated
Heteroblasty in a Mauritian species of plant, Tarenna borbonica Bois de Rat 1 Juvenile and subadult foliage - Terenna borbonica.jpg
Heteroblasty in a Mauritian species of plant, Tarenna borbonica
Heterophylly in Coriandrum sativum. Heterophylly.jpg
Heterophylly in Coriandrum sativum.

Heteroblasty is the significant and abrupt change in form and function, that occurs over the lifespan of certain plants. Characteristics affected include internode length and stem structure as well as leaf form, size and arrangement. [1] It should not be confused with seasonal heterophylly, where early and late growth in a season are visibly different. [2] This change is different from a homoblastic change which is a gradual change or little change at all, so that there is little difference between the juvenile and adult stages. [3] Some characteristics affected by heteroblastic change include the distance between successive leaves (internode length) and stem structure as well as leaf form, size and arrangement. [1] Heteroblasty is found in many plant families as well as only some species within a genus. This random spread of heteroblastic plants across species is believed to be caused by convergent evolution. [4]

Contents

The earlier and later stages of development are commonly labeled as juvenile and adult respectively, particularly in relation to leaves. [5] Heteroblastic change is thus often referred to as ‘vegetative phase change’ (distinct from reproductive phase change) in the plant molecular biology literature. [6]

The term heteroblasty was coined by the German botanist Karl Ritter von Goebel, along with homoblasty for plants with leaf characteristics that do not change significantly. Leonard Cockayne observed that heteroblasty occurred in an unusually high proportion of tree species native to New Zealand. [7]

Origins

There are two ways to look at how heteroblasty developed. The first is to look at the evolution of heteroblasty, and the second is to consider the ecological interactions of heteroblastic plants.

Evolution

Many hypothesize that heteroblasty is a result of natural selection for species, that can best survive in both low and high light environments. As a plant grows in the forest it experiences predictable changes in light intensity. With this in mind a plant that changes its leaf morphology and phyllotaxy to best suit these changes in light intensity could be more competitive than one that has only on leaf form and phyllotaxy. [3] It is also hypothesized that the development of heteroblastic trees preceded the development of divaricating shrub forms, which are now very common in New Zealand. It is thought that these shrubs are a mutation from the heteroblastic trees and have lost the ability to develop into the adult stage and so are very similar to heteroblastic trees in their juvenile form. It has also been observed that heteroblastic species do not stem from a single point of origin they are found in many different and unrelated species, because of this it is believed that large-scale convergent evolution has to have occurred for so many unrelated plants to exhibit similar behavior. [4]

Ecology

Heteroblasty can affect all parts of the plant but the leaves are the most common examples and by far the most studied. It has been hypothesized that the heteroblastic changes are due to changes in the plant's exposure to sun, because many species spend their juvenile years in the understory then grow to maturity where they are a part of the top canopy and so have full exposure to the sun. This has not been well studied, because the common heteroblastic plants are woody and take so long to grow such as Eucalyptus grandis . [1] The juvenile plants tend to face more competition and must make special adaptations to succeed that are then unnecessary as a mature plant. For example, a sampling in a dense forest must grow quickly to succeed at first but once it has established itself most woody plants no longer compete severely with their neighbor and so the adaptations needed as a juvenile plant are no longer necessary. This can lead to a change in growth in maturity as the tree faces new environmental factors. [7] Such as a need to resist new pathogens or parasites. [8]

Mechanism

At the cellular level, there are different ways that a plant controls its growth and development. There are internal and external signals that result in a change in the plant's response. The plants also have genetic predetermined growth patterns.

Signaling

Hormones are known to regulate heteroblastic change in plants. One hormone that has been identified is gibberellin. In a study, it was used to spontaneously revert the mature form of Hedera helix (a common English ivy) to its juvenile form. After being sprayed with gibberellin acid some of the ivies began to produce aerial roots which are a characteristic of the juvenile form as well as three lobed leaves another characteristic. [9] It is also hypothesized that auxin and cytokinin when working together can cause the sudden change in phyllotaxy of heterogenetic plants. [1] The gene ABPH1 has been found to code for cytokinin and when changed in a mutant affected the plant's ability to regulate the phyllotaxy of the stem. [10] The hypothesis is based mostly on studies done on non-heteroblastic plants and so it is not certain that these are the cause of the sudden changes in a heteroblastic plant. A dramatic change in leaf size is another example of a heteroblastic change in plants and researchers have looked to studies done on non-heteroblastic plants for answers about what hormones and genes could regulate these changes. Aintegumenta has been found to be one of these regulatory genes that regulated cell growth. [11] It is believed that many genes are involved in the regulation of leaf size and these genes do not closely interact meaning they are not caused by a master regulator but instead are a part of many different pathways. [1]

Genetics

Some most common model plants include Arabidopsis thaliana (common name: mouse-ear cress), Antirrhinum majus (common name: snapdragon), and Zea mays (common name: corn). Some authors have argued that these species are not useful models for the study of gene expression in heteroblastic plants because none of them express obvious heteroblastic traits. [1] Researchers in this area of study can use Arabidopsis to some degree for study as it does undergo some change from the juvenile phase to the mature phase but it is not clearly heteroblastic. If we assume the process of change is similar and uses similar regulations we can use Arabidopsis to analyze the causes of change in plant growth that may be occurring in the same way but more dramatically in heteroblastic plants and so can only be used to analyze heteroblastic changes. This involves many assumptions though and so researchers are seeking other plants to use as model subjects. The problem with this is that most plants that display heteroblastic growth are woody plants. Their life spans are much longer in general and unlike Arabidopsis very little of their genomes are known or mapped. A species that shows promise is Eucalyptus grandis . This tree is grown commonly because of its many uses for teas, oils, and wood. [12] The tree overall is fast growing and widely grown due to its many uses and so is one of the best candidates for genome sequencing, which is being done now so that the tree can be better studied in the future. There is already a complete quantitative trait loci map for the juvenile traits. [13]

Examples

These plants are a few of the common examples of heteroblastic plants often found in studies and is far from an all-encompassing list. All listed are plants, because they are the only organisms that have been found to undergo this growth change it is absent in animals, fungi, and microbes as far as is known to this point.

  1. Lightwood ( Acacia implexa ) is a fast wood tree found in Australia [14]
  2. Spiral ginger ( Costus pulverulentus C.Presl) is an herb found in South America [15] found primarily in Nicaragua [16] and is used as a traditional medicine in teas for pain and inflammation. It is also used to treat cancer. [17]
  3. Lance wood ( Pseudopanax crassifolius) is a native of New Zealand [18]
  4. Pōkākā ( Elaeocarpus hookerianus ) native to New Zealand [18]
  5. Bucket-of-water tree or Maple leaf ( Carpodetus serratus ) native to New Zealand [18]

Geographic distribution

This is a list of places heteroblastic plants have been commonly found and documented but not a complete list of all places as heteroblastic plants can be hard to identify and do not appear in families predictably.

Similar processes

Processes often confused with heteroblasty include:

  1. Homoblasty is the first example of this. To understand Heteroblasty you must first understand that homoblasty is different. Homoblastic change is the slight change a plant experiences over a long period of time as it grows to maturity. Examples of this are a plants leaves growing slightly larger over time as it matures or a trees trunk growing in girth. [1]
  2. Heterophylly is another term that is often used interchangeably with Heteroblasty. The process of heterophylly refers to specific changes in leaf morphology that lead to variation in leaf shape or size on a single plant. This type of change is seen when you study the individual leaves and compare them, this is different than homoblasty in which the entire foliage changes dramatically but for the most part uniformly. A heteroblastic plant can have heterophyllic changes but they are not the same. [19]
  3. Phenotypic Plasticity changes the structure of plants as well but should not be confused with Heteroblasty. Phenotypic plasticity is when an individual can use the same genes to create a different phenotype based on environmental signals. [20] Such as when a plant is adapting its immune system to a new pathogen or when a reptile changes its sex based on environmental queues. [21] The difference here is that Heteroblasty is not entirely dependent on the environment, though it can be affected by it, and happens throughout the plant's maturity instead of at random points because of an environmental change. [1]

See also

Related Research Articles

<i>Arabidopsis thaliana</i> Model plant species in the family Brassicaceae

Arabidopsis thaliana, the thale cress, mouse-ear cress or arabidopsis, is a small flowering plant native to Eurasia and Africa. A. thaliana is considered a weed; it is found along the shoulders of roads and in disturbed land.

<span class="mw-page-title-main">Shoot</span> Young stem or branch

In botany, a plant shoot consists of any plant stem together with its appendages, leaves and lateral buds, flowering stems, and flower buds. The new growth from seed germination that grows upward is a shoot where leaves will develop. In the spring, perennial plant shoots are the new growth that grows from the ground in herbaceous plants or the new stem or flower growth that grows on woody plants.

<span class="mw-page-title-main">Root</span> Basal organ of a vascular plant

In vascular plants, the roots are the organs of a plant that are modified to provide anchorage for the plant and take in water and nutrients into the plant body, which allows plants to grow taller and faster. They are most often below the surface of the soil, but roots can also be aerial or aerating, that is, growing up above the ground or especially above water.

<span class="mw-page-title-main">Vine</span> Plant with a growth habit of trailing or scandent stems or runners

A vine is any plant with a growth habit of trailing or scandent stems, lianas or runners. The word vine can also refer to such stems or runners themselves, for instance, when used in wicker work.

<span class="mw-page-title-main">Meristem</span> Type of plant tissue involved in cell proliferation

The meristem is a type of tissue found in plants. It consists of undifferentiated cells capable of cell division. Cells in the meristem can develop into all the other tissues and organs that occur in plants. These cells continue to divide until a time when they get differentiated and then lose the ability to divide.

<span class="mw-page-title-main">Plant hormone</span> Chemical compounds that regulate plant growth and development

Plant hormone are signal molecules, produced within plants, that occur in extremely low concentrations. Plant hormones control all aspects of plant growth and development, from embryogenesis, the regulation of organ size, pathogen defense, stress tolerance and through to reproductive development. Unlike in animals each plant cell is capable of producing hormones. Went and Thimann coined the term "phytohormone" and used it in the title of their 1937 book.

<span class="mw-page-title-main">Vegetative reproduction</span> Asexual method of reproduction in plants

Vegetative reproduction is any form of asexual reproduction occurring in plants in which a new plant grows from a fragment or cutting of the parent plant or specialized reproductive structures, which are sometimes called vegetative propagules.

A maternal effect is a situation where the phenotype of an organism is determined not only by the environment it experiences and its genotype, but also by the environment and genotype of its mother. In genetics, maternal effects occur when an organism shows the phenotype expected from the genotype of the mother, irrespective of its own genotype, often due to the mother supplying messenger RNA or proteins to the egg. Maternal effects can also be caused by the maternal environment independent of genotype, sometimes controlling the size, sex, or behaviour of the offspring. These adaptive maternal effects lead to phenotypes of offspring that increase their fitness. Further, it introduces the concept of phenotypic plasticity, an important evolutionary concept. It has been proposed that maternal effects are important for the evolution of adaptive responses to environmental heterogeneity.

<span class="mw-page-title-main">Trichome</span> Fine hair-like growth on plants

Trichomes ; from Ancient Greek τρίχωμα (tríkhōma) 'hair') are fine outgrowths or appendages on plants, algae, lichens, and certain protists. They are of diverse structure and function. Examples are hairs, glandular hairs, scales, and papillae. A covering of any kind of hair on a plant is an indumentum, and the surface bearing them is said to be pubescent.

<span class="mw-page-title-main">Auxin</span> Plant hormone

Auxins are a class of plant hormones with some morphogen-like characteristics. Auxins play a cardinal role in coordination of many growth and behavioral processes in plant life cycles and are essential for plant body development. The Dutch biologist Frits Warmolt Went first described auxins and their role in plant growth in the 1920s. Kenneth V. Thimann became the first to isolate one of these phytohormones and to determine its chemical structure as indole-3-acetic acid (IAA). Went and Thimann co-authored a book on plant hormones, Phytohormones, in 1937.

<span class="mw-page-title-main">Cytokinin</span> Class of plant hormones promoting cell division

Cytokinins (CK) are a class of plant hormones that promote cell division, or cytokinesis, in plant roots and shoots. They are involved primarily in cell growth and differentiation, but also affect apical dominance, axillary bud growth, and leaf senescence.

<span class="mw-page-title-main">Callus (cell biology)</span> Growing mass of unorganized plant parenchyma cells

Plant callus is a growing mass of unorganized plant parenchyma cells. In living plants, callus cells are those cells that cover a plant wound. In biological research and biotechnology callus formation is induced from plant tissue samples (explants) after surface sterilization and plating onto tissue culture medium in vitro. The culture medium is supplemented with plant growth regulators, such as auxin, cytokinin, and gibberellin, to initiate callus formation or somatic embryogenesis. Callus initiation has been described for all major groups of land plants.

<span class="mw-page-title-main">Phenotypic plasticity</span> Trait change of an organism in response to environmental variation

Phenotypic plasticity refers to some of the changes in an organism's behavior, morphology and physiology in response to a unique environment. Fundamental to the way in which organisms cope with environmental variation, phenotypic plasticity encompasses all types of environmentally induced changes that may or may not be permanent throughout an individual's lifespan.

<span class="mw-page-title-main">Primordium</span> Organ in the earliest recognizable stage of embryonic development

A primordium in embryology, is an organ or tissue in its earliest recognizable stage of development. Cells of the primordium are called primordial cells. A primordium is the simplest set of cells capable of triggering growth of the would-be organ and the initial foundation from which an organ is able to grow. In flowering plants, a floral primordium gives rise to a flower.

<span class="mw-page-title-main">Plant morphology</span> Study of the structure of plants

Phytomorphology is the study of the physical form and external structure of plants. This is usually considered distinct from plant anatomy, which is the study of the internal structure of plants, especially at the microscopic level. Plant morphology is useful in the visual identification of plants. Recent studies in molecular biology started to investigate the molecular processes involved in determining the conservation and diversification of plant morphologies. In these studies transcriptome conservation patterns were found to mark crucial ontogenetic transitions during the plant life cycle which may result in evolutionary constraints limiting diversification.

<i>Rhodococcus fascians</i> Species of bacterium

Rhodococcus fascians is a Gram positive bacterial phytopathogen that causes leafy gall disease. R. fascians is the only phytopathogenic member of the genus Rhodococcus; its host range includes both dicotyledonous and monocotyledonous hosts. Because it commonly afflicts tobacco (Nicotiana) plants, it is an agriculturally significant pathogen.

<span class="mw-page-title-main">Evolutionary history of plants</span> Origin and diversification of plants through geologic time

The evolution of plants has resulted in a wide range of complexity, from the earliest algal mats, through multicellular marine and freshwater green algae, terrestrial bryophytes, lycopods and ferns, to the complex gymnosperms and angiosperms of today. While many of the earliest groups continue to thrive, as exemplified by red and green algae in marine environments, more recently derived groups have displaced previously ecologically dominant ones; for example, the ascendance of flowering plants over gymnosperms in terrestrial environments.

Evolutionary developmental biology (evo-devo) is the study of developmental programs and patterns from an evolutionary perspective. It seeks to understand the various influences shaping the form and nature of life on the planet. Evo-devo arose as a separate branch of science rather recently. An early sign of this occurred in 1999.

Important structures in plant development are buds, shoots, roots, leaves, and flowers; plants produce these tissues and structures throughout their life from meristems located at the tips of organs, or between mature tissues. Thus, a living plant always has embryonic tissues. By contrast, an animal embryo will very early produce all of the body parts that it will ever have in its life. When the animal is born, it has all its body parts and from that point will only grow larger and more mature. However, both plants and animals pass through a phylotypic stage that evolved independently and that causes a developmental constraint limiting morphological diversification.

Cryptic mimicry is observed in animals as well as plants. In animals, this may involve nocturnality, camouflage, subterranean lifestyle, and mimicry. Generally, plant herbivores are visually oriented. So a mimicking plant should strongly resemble its host; this can be done through visual and/or textural change. Previous criteria for mimicry include similarity of leaf dimensions, leaf presentation, and intermodal distances between the host and mimicking plant.

References

  1. 1 2 3 4 5 6 7 8 Zotz G, Wilhelm K, Becker A (June 2011). "Heteroblasty—A Review". The Botanical Review. 77 (2): 109–151. doi:10.1007/s12229-010-9062-8. S2CID   39829971.
  2. Eckenwalder JE (1980). "Foliar Heteromorphism in Populus (Salicaceae), a Source of Confusion in the Taxonomy of Tertiary Leaf Remains". Systematic Botany. 5 (4): 366–383. doi:10.2307/2418518. JSTOR   2418518.
  3. 1 2 Gamage HK, Jesson L (2007). "Leaf heteroblasty is not an adaptation to shade: seedling anatomical and physiological responses to light". New Zealand Journal of Ecology. 31 (2): 245–254. JSTOR   24058149.
  4. 1 2 3 Day JS (1998). "Light Conditions and the Evolution of Heterblasty (and the Divaricate Form) In New Zealand". New Zealand Journal of Ecology. 22 (1): 43–54. JSTOR   24054547.
  5. McCusker A. "Flora of Australia Glossary". Department of the Environment, Water, Heritage, and the Arts. Retrieved 23 December 2014.
  6. Poethig, R. S. (2010). "The past, present, and future of vegetative phase change". Plant Physiology. 154 (2): 541–544. doi:10.1104/pp.110.161620. PMC   2949024 . PMID   20921181.
  7. 1 2 Cockayne L (1912). "Observations concerning evolution, derived from ecological studies in New Zealand". Transactions and Proceedings of the New Zealand Institute. 44: 1–50.
  8. Karban R, Thaler JS (1999-03-01). "Plant Phase Change and Resistance to Herbivory". Ecology. 80 (2): 510–517. doi:10.1890/0012-9658(1999)080[0510:ppcart]2.0.co;2.
  9. Robbins WJ (1957). "Gibberellic Acid and the Reversal of Adult Hedera to a Juvenile State". American Journal of Botany. 44 (9): 743–746. doi:10.1002/j.1537-2197.1957.tb08259.x. JSTOR   2438395.
  10. Lee BH, Johnston R, Yang Y, Gallavotti A, Kojima M, Travençolo BA, Costa L, Sakakibara H, Jackson D (May 2009). "Studies of aberrant phyllotaxy1 mutants of maize indicate complex interactions between auxin and cytokinin signaling in the shoot apical meristem". Plant Physiology. 150 (1): 205–16. doi:10.1104/pp.109.137034. PMC   2675719 . PMID   19321707.
  11. Mizukami Y, Fischer RL (January 2000). "Plant organ size control: AINTEGUMENTA regulates growth and cell numbers during organogenesis". Proceedings of the National Academy of Sciences of the United States of America. 97 (2): 942–7. Bibcode:2000PNAS...97..942M. doi: 10.1073/pnas.97.2.942 . PMC   15435 . PMID   10639184.
  12. Santos R (1997). "The Eucalyptus of California" (PDF). California State University Library. Archived from the original (PDF) on September 27, 2019. Retrieved April 21, 2018.
  13. Grattapaglia D, Kirst M (2008-09-01). "Eucalyptus applied genomics: from gene sequences to breeding tools". The New Phytologist. 179 (4): 911–29. doi: 10.1111/j.1469-8137.2008.02503.x . PMID   18537893.
  14. Forster MA, Bonser SP (January 2009). "Heteroblastic development and the optimal partitioning of traits among contrasting environments in Acacia implexa". Annals of Botany. 103 (1): 95–105. doi:10.1093/aob/mcn210. PMC   2707286 . PMID   18978364.
  15. 1 2 Guzmán JA (2015). "Ecological advantage of leaf heteroblasty in Costus pulverulentus (Costaceae)". Botany. 93 (3): 151–158. doi:10.1139/cjb-2014-0157.
  16. "Name - Costus pulverulentus C. Presl". Tropicos. Retrieved 2018-04-01.
  17. Alonso-Castro AJ, Zapata-Morales JR, González-Chávez MM, Carranza-Álvarez C, Hernández-Benavides DM, Hernández-Morales A (March 2016). "Pharmacological effects and toxicity of Costus pulverulentus C. Presl (Costaceae)". Journal of Ethnopharmacology. 180: 124–30. doi:10.1016/j.jep.2016.01.011. PMID   26778604.
  18. 1 2 3 Gamage HK (2011). "Phenotypic variation in heteroblastic woody species does not contribute to shade survival". AoB Plants. 2011: plr013. doi:10.1093/aobpla/plr013. PMC   3129537 . PMID   22476483.
  19. Winn A (1999). "The functional significance and fitness consequences of heterophylly". International Journal of Plant Sciences. 160 (S6): 113–121. doi:10.1086/314222. PMID   10572026. S2CID   24787793.
  20. Pigliucci M, Murren CJ, Schlichting CD (June 2006). "Phenotypic plasticity and evolution by genetic assimilation". The Journal of Experimental Biology. 209 (Pt 12): 2362–7. doi: 10.1242/jeb.02070 . PMID   16731812.
  21. Fusco G, Minelli A (February 2010). "Phenotypic plasticity in development and evolution: facts and concepts. Introduction". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 365 (1540): 547–56. doi:10.1098/rstb.2009.0267. PMC   2817147 . PMID   20083631.