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Australian Journal of Botany Australian Journal of Botany Society
Southern hemisphere botanical ecosystems
RESEARCH ARTICLE

Structure, function and secretory products of the peltate glands of Centrolobium tomentosum (Fabaceae, Faboideae)

Esmeire Cruz Matos A and Élder Antônio Sousa Paiva B C
+ Author Affiliations
- Author Affiliations

A Fundação Ezequiel Dias – FUNED, Laboratório de Microscopia de Produtos, 30510-010, Belo Horizonte, MG, Brazil.

B Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, 31270-901, Belo Horizonte, MG, Brazil.

C Corresponding author. Email: epaiva@icb.ufmg.br

Australian Journal of Botany 60(4) 301-309 https://doi.org/10.1071/BT12009
Submitted: 16 January 2012  Accepted: 13 April 2012   Published: 19 June 2012

Abstract

The glandular structures of Centrolobium tomentosum Guill. ex Benth. have been little studied despite the economic importance of this species. We describe here the distribution, development, structure and ultrastructure of the secretory cells of the peltate glands found on the vegetative organs of this species. Stem apices and leaves in various stages of development were collected and prepared for examination by light, scanning and transmission electron microscopy. Chemical analyses and conventional histochemical tests to determine the chemical nature of the secretory products were also carried out. Peltate glands occur on aerial vegetative organs during their primary growth stage. These trichomes are structurally stable, persisting throughout the development of the organ. During the initial stages of the gland development, cell separation creates a central space that expands as secretions accumulate. Maximum secretion rates occur during this phase and the secreting cells characteristically have well developed smooth and rough endoplasmic reticulum, and high numbers of plastids and mitochondria. During the later stages of the secretory phase, the central cells show symptoms of cell death and are incorporated in to the secretions. At trichome maturity, the central space is delimited by a uniseriate epithelium. In addition to the resin, which is the main secretory product, an extensive three-dimensional carbohydrate matrix was observed that extended throughout the central space, apparently giving support to the resin droplets. The terpenic nature of the secretion was confirmed by thin-layer chromatography. Given the terpenic nature of the secretion and the permanence of trichomes throughout all phases of leaf development, it is postulated that the resin-secreting trichomes act to protect the plant against herbivores.


References

Argyropoulou C, Akoumianaki-Ioannidou A, Christodoulakis NS, Fasseas C (2010) Leaf anatomy and histochemistry of Lippia citriodora (Verbenaceae). Australian Journal of Botany 58, 398–409.
Leaf anatomy and histochemistry of Lippia citriodora (Verbenaceae).Crossref | GoogleScholarGoogle Scholar |

Bell JM, Curtis J (1985) Development and ultrastructure of foliar glands of Comptonia peregrina (Myricaceae). Botanical Gazette 146, 288–292.
Development and ultrastructure of foliar glands of Comptonia peregrina (Myricaceae).Crossref | GoogleScholarGoogle Scholar |

Bennici A, Tani C (2004) Anatomical and ultrastructural study of the secretory cavity development of Citrus sinensis and Citrus limon: evaluation of schizolysigenous ontogeny. Flora 199, 464–475.
Anatomical and ultrastructural study of the secretory cavity development of Citrus sinensis and Citrus limon: evaluation of schizolysigenous ontogeny.Crossref | GoogleScholarGoogle Scholar |

Bisio A, Corallo A, Gastaldo P, Romussi G, Ciarallo G, Fontana N, De Tommasi N, Profumo P (1999) Glandular hairs and secreted material in Salvia blepharophylla Brandegee ex Epling grown in Italy. Annals of Botany 83, 441–452.
Glandular hairs and secreted material in Salvia blepharophylla Brandegee ex Epling grown in Italy.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXitVClu7Y%3D&md5=7bc8a417e355e1b19c0dd228c07e826cCAS |

Bosabalidis AM (1990) Glandular trichomes in Satureja thymbra leaves. Annals of Botany 65, 71–78.

Bosabalidis AM (2010) Ultrastructure, development and histochemistry of the polysaccharide-containing subcuticular compartments in Origanum dictamus L. peltate glandular hairs. Flavour and Fragrance Journal 25, 202–205.
Ultrastructure, development and histochemistry of the polysaccharide-containing subcuticular compartments in Origanum dictamus L. peltate glandular hairs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXpslymt7g%3D&md5=816f3131a3a4ff45b04ba7d5ed91c2faCAS |

Brundrett MC, Kendrick B, Peterson CA (1991) Efficient lipid staining in plant material with Sudan Red 7B or fluoral yellow 088 in polyethylene glycol–glycerol. Biotechnic & Histochemistry 66, 111–116.
Efficient lipid staining in plant material with Sudan Red 7B or fluoral yellow 088 in polyethylene glycol–glycerol.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3MzmtlCktg%3D%3D&md5=e7a073185a5f27b01a06d7106ac224bdCAS |

Choi JS, Lee NY, Oh SE, Son KC, Kim ES (2011) Developmental ultrastructure of glandular trichomes of Rosmarinus officinalis: secretory cavity and secretory vesicle formation. Journal of Plant Biology 54, 135–142.
Developmental ultrastructure of glandular trichomes of Rosmarinus officinalis: secretory cavity and secretory vesicle formation.Crossref | GoogleScholarGoogle Scholar |

David R, Carde JP (1964) Colaration différentielle des inclusions lipidique et terpeniques des pseudophylles du pine maritime au moyen du reactif Nadi. Comptés Rendus de L’Academie des Sciences Paris, Série D 258, 1338–1340.

Dell B, McComb AJ (1979) Plant resins: their formation, secretion and possible functions. Advances in Botanical Research 6, 277–316.
Plant resins: their formation, secretion and possible functions.Crossref | GoogleScholarGoogle Scholar |

Durkee LT, Baird CW, Cohen PF (1984) Light and electron microscopy of resin glands of Passiflora foetida (Passifloraceae). American Journal of Botany 71, 596–602.
Light and electron microscopy of resin glands of Passiflora foetida (Passifloraceae).Crossref | GoogleScholarGoogle Scholar |

Fahn A (2002) Functions and location of secretory tissues in plants and their possible evolutionary trends. Israel Journal of Plant Sciences 50, S59–S64.
Functions and location of secretory tissues in plants and their possible evolutionary trends.Crossref | GoogleScholarGoogle Scholar |

Feucht W, Schmid PPS, Christ E (1986) Distribution of flavonols in meristematic tissues of Prunus avium shoots. Journal of Plant Physiology 125, 1–8.
Distribution of flavonols in meristematic tissues of Prunus avium shoots.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL28XmtVKgsr8%3D&md5=43fb35a25cc817bc7ea00f4733561d03CAS |

Gaffal KP, Friedrichis GJ, El-Gammal S (2007) Ultrastructural evidence for a dual function of the phloem and programmed cell death in the floral nectary of Digitalis purpurea. Annals of Botany 99, 593–607.
Ultrastructural evidence for a dual function of the phloem and programmed cell death in the floral nectary of Digitalis purpurea.Crossref | GoogleScholarGoogle Scholar |

Giuliani C, Bini LM (2008) Insight into the structure and chemistry of glandular trichomes of Labiatae, with emphasis on subfamily Lamioideae. Plant Systematics and Evolution 276, 199–208.
Insight into the structure and chemistry of glandular trichomes of Labiatae, with emphasis on subfamily Lamioideae.Crossref | GoogleScholarGoogle Scholar |

Heil M, McKey D (2003) Protective ant–plant interactions as model systems in ecological and evolutionary research. Annual Review of Ecology Evolution and Systematics 34, 425–453.
Protective ant–plant interactions as model systems in ecological and evolutionary research.Crossref | GoogleScholarGoogle Scholar |

Jensen WA (1962) ‘Botanical histochemistry: principles and practice.’ (W.H. Freeman: San Francisco)

Johansen DA (1940) ‘Plant microtechnique.’ (McGraw Book: New York)

Karnovsky MJ (1965) A formaldehyde–glutaraldehyde fixative of light osmolality for use in eletron microscopy. The Journal of Cell Biology 27, 137A–138A.

Kennedy GG (2003) Tomato, pest, parasitoids, and predators: tritrophic interactions involving the genus Lycopersicon. Annual Review of Entomology 48, 51–72.
Tomato, pest, parasitoids, and predators: tritrophic interactions involving the genus Lycopersicon.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXnvVymtg%3D%3D&md5=ac5590e079396a45abd55f76ca5f89bdCAS |

Langenheim JH (2003) ‘Plant resins: chemistry, evolution, ecology and ethnobotany.’ (Timber Press: Cambridge, UK)

Lapinjoki SP, Elo HA, Taipali HT (1991) Development and structure of resin glands on tissues of Betula pendula Roth, during growth. New Phytologist 117, 219–223.
Development and structure of resin glands on tissues of Betula pendula Roth, during growth.Crossref | GoogleScholarGoogle Scholar |

Lersten NR, Curtis JD (1996) Survey of leaf anatomy, especially secretory structures, of tribe Caesalpinieae (Leguminosae, Caesalpinioideae). Plant Systematics and Evolution 200, 21–39.
Survey of leaf anatomy, especially secretory structures, of tribe Caesalpinieae (Leguminosae, Caesalpinioideae).Crossref | GoogleScholarGoogle Scholar |

Lima HC (1985) Centrolobium Martius ex Bentham (Leguminosae-Papilionoideae) estudo taxonômico das espécies brasileiras extra-amazônicas. Arquivos do Jardim Botânico do Rio de Janeiro XXVII, 177–191.

Machado SR, Gregório EA, Guimarães E (2006) Ovary peltate trichomes of Zeyheria montana (Bignoniaceae): developmental ultrastructure and secretion in relation to function. Annals of Botany 97, 357–369.
Ovary peltate trichomes of Zeyheria montana (Bignoniaceae): developmental ultrastructure and secretion in relation to function.Crossref | GoogleScholarGoogle Scholar |

O’Brien TP, Feder N, McCully ME (1964) Polychromatic staining of plant cell walls by toluidine blue. Protoplasma 59, 368–373.
Polychromatic staining of plant cell walls by toluidine blue.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF2MXmtVOmsw%3D%3D&md5=28fe26e8aaabb3e67b4de87e0932d5bcCAS |

O’Brien SP, Loveys BR, Grant WJR (1996) Ultrastructure and function of floral nectaries of Chamelaucium uncinatum (Myrtaceae). Annals of Botany 78, 189–196.
Ultrastructure and function of floral nectaries of Chamelaucium uncinatum (Myrtaceae).Crossref | GoogleScholarGoogle Scholar |

Onelli E, Rivetta A, Giorgi A, Bignami M, Cocucci M, Patrignani G (2002) Ultrastructural studies on the developing secretory nodules of Hypericum perforatum. Flora 197, 92–102.
Ultrastructural studies on the developing secretory nodules of Hypericum perforatum.Crossref | GoogleScholarGoogle Scholar |

Paiva EAS (2009) Ultrastructure and post-floral secretion of the pericarpial nectaries of Erythrina speciosa (Fabaceae). Annals of Botany 104, 937–944.
Ultrastructure and post-floral secretion of the pericarpial nectaries of Erythrina speciosa (Fabaceae).Crossref | GoogleScholarGoogle Scholar |

Paiva EAS, Machado SR (2006) Structural and ultrastructural aspects of ontogenesis and differentiation of resin secretory cavities in Hymenaea stigonocarpa (Fabaceae–Caesalpinioideae) leaves. Nordic Journal of Botany 24, 423–431.
Structural and ultrastructural aspects of ontogenesis and differentiation of resin secretory cavities in Hymenaea stigonocarpa (Fabaceae–Caesalpinioideae) leaves.Crossref | GoogleScholarGoogle Scholar |

Paiva EAS, Martins LC (2011) Calycinal trichomes in Ipomoea cairica (Convolvulaceae): ontogenesis, structure and functional aspects. Australian Journal of Botany 59, 91–98.
Calycinal trichomes in Ipomoea cairica (Convolvulaceae): ontogenesis, structure and functional aspects.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhslGis7c%3D&md5=7d5135b50bada97a45202641fb635dd4CAS |

Pirie MD, Klitgaard BB, Pennington RT (2009) Revision and Biogeography of Centrolobium (Leguminosae–Papilionoideae). Systematic Botany 34, 345–359.
Revision and Biogeography of Centrolobium (Leguminosae–Papilionoideae).Crossref | GoogleScholarGoogle Scholar |

Ranger CM, Winter REK, Rottinghaus GE, Backus EA, Johnson DW (2005) Mass spectral characterization of fatty acid amides from alfalfa trichomes and their deterrence against the potato leafhopper. Phytochemistry 66, 529–541.
Mass spectral characterization of fatty acid amides from alfalfa trichomes and their deterrence against the potato leafhopper.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhsVyksL8%3D&md5=3cfea7e568094cc376f2ee244c133b92CAS |

Robards AW (1978) An introduction to techniques for scanning electron microscopy of plant cells. In ‘Electron microscopy and cytochemistry of plant cells’. (Ed. JL Hall) pp. 343–403. (Elsevier: New York)

Rodrigues TM, Teixeira SP, Machado SR (2011) The oleoresin secretory system in seedlings and adult plants of copaíba (Copaifera langsdorffii Desf., Leguminosae–Caesalpinioideae). Flora 206, 585–594.
The oleoresin secretory system in seedlings and adult plants of copaíba (Copaifera langsdorffii Desf., Leguminosae–Caesalpinioideae).Crossref | GoogleScholarGoogle Scholar |

Roland AM (1978) General preparations and staining of thin sections. In ‘Electron microscopy and cytochemistry of plant cells’. (Ed. JL Hall) pp. 1–62. (Elsevier: New York)

Russell GB (1977) Plant chemicals affecting insect development. New Zealand Entomologist 6, 229–234.

Shorey HH, Gaston LK, Gerber RG, Sisk CB, Phillips PA (1996) Formulating farnesol and other ant-repellent semiochemicals for exclusion of Argentine ants (Hymenoptera: Formicidae) from citrus trees. Environmental Entomology 25, 114–119.

Solereder H (1908) ‘Systematic anatomy of the dicotyledons. Vol. I.’ (Clarendon Press: Oxford, UK)

Tang XR, Chen SL, Wang L (2011) Isolation and Insecticidal activity of farnesol from Stellera chamaejasme. Asian Journal of Chemistry 23, 1233–1235.

Turner GW (1986) Comparative development of secretory cavities in the tribes Amorpheae and Psoraleeae (Leguminosae: Papilionoideae). American Journal of Botany 73, 1178–1192.
Comparative development of secretory cavities in the tribes Amorpheae and Psoraleeae (Leguminosae: Papilionoideae).Crossref | GoogleScholarGoogle Scholar |

Turner GW, Croteau R (2004) Organization of monoterpene biosynthesis in Mentha. Immunocytochemical localizations of geranyl diphosphate synthase, limonene-6-hydroxylase, isopiperitenol dehydrogenase, and pulegone reductase. Plant Physiology 136, 4215–4227.
Organization of monoterpene biosynthesis in Mentha. Immunocytochemical localizations of geranyl diphosphate synthase, limonene-6-hydroxylase, isopiperitenol dehydrogenase, and pulegone reductase.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXjtVarsQ%3D%3D&md5=64a6214b54ec4c93c3e0130fdd0755d9CAS |

Wagner H, Bladt S (2001) ‘Plant drug analysis: a thin layer chromatography atlas.’ (Springer-Verlag: Berlin)

Wagner GJ, Wang E, Shepherd RW (2004) New approaches for studying and exploiting an old protuberance, the plant trichome. Annals of Botany 93, 3–11.
New approaches for studying and exploiting an old protuberance, the plant trichome.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3srps1KjsA%3D%3D&md5=1b49e8280506a8a0a38481c02962d922CAS |

Werker E (2000) Trichome diversity and development. Advances in Botanical Research 31, 1–35.
Trichome diversity and development.Crossref | GoogleScholarGoogle Scholar |