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Nodal anatomical study of certain members of the Rutaceae
Keywords:
Rutaceae, Node, Nodal evolution.
ABSTRACT:
The vascular organization of the node in 12 genera has been investigated.
The leaves are unifoliate in Atalantia, Citrus and Paramignya, 3-5 foliate in Aegle,
Luvunga, Toddalia and Glycosmis, decompounds in Ruta and imparipinnately
compound in other taxa. These are alternate or opposite and exstipulate. The foliar
nodes are trilacunar, three-trace in the majority of the plants. It is unilacunar in
Atalantia racemosa, Citrus jambhiri, C. maxima and Glycosmis pentaphylla. The
results are discussed with respect to the evolutionary conception of node.
177-181 | JRPS | 2013 | Vol 2 | No 1
This article is governed by the Creative Commons Attribution License (http://creativecommons.org/
licenses/by/2.0), which gives permission for unrestricted use, non-commercial, distribution and
reproduction in all medium, provided the original work is properly cited.
www.plantsciences.info
Journal of Research in
Plant Sciences
An International Scientific
Research Journal
Authors:
Snehal P. Salunke,
Sarala C. Tadavi and
Vijay V. Bhadane.
Institution:
Centre for Post-Graduate
Studies and Research in
Botany, Pratap College,
Amalner - 425 401 [M.S.],
India.
Corresponding author:
Snehal P. Salunke.
Email:
snehal2106@ymail.com
Fax No.:
+91 (02587) 223103
Web Address:
http://www.plantsciences.info
documents/PS0053.pdf.
Dates:
Received: 04 Feb 2013 Accepted: 09 Feb 2013 Published: 05 Mar 2013
Article Citation:
Snehal P. Salunke, Sarala C. Tadavi and Vijay V. Bhadane
Nodal anatomical study of certain members of the Rutaceae.
Journal of Research in Plant Sciences (2013) 2(1): 177-181
An International Scientific Research Journal
Original Research
Journal of Research in Plant Sciences
JournalofResearchinPlantSciences
INTRODUCTION
The Rutaceae family includes about 160 genera
and 1,900 species that are widely distributed in tropical
and temperate regions around the world, but they are
especially abundant in Australia and South Africa
(Groppo et al., 2008; Cronquist, 1988). While studying
the nodal organization in the angiosperms, Sinnott
(1914) have reported the trilacunar and unilacunar nodal
structure in Rutaceae. Hayward and Long (1942) have
also made observations on variations in the cotyledonary
nodes in Valencia orange. Since the nodal vasculature in
the family has received little attention, it warrants a
detailed study. Consequently the present study were
undertaken to study the nodal organization of
16 species distributed in 12 genera.
MATERIAL AND METHODS
The plant materials of Atalantia monophylla DC,
Toddalia asiatica Lamk. and Glycosmis mauritiana
(Lam.) Tanaka were collected from Lalbagh Botanical
Garden, Bangalore, Citrus jambhiri Lush and
Citrus maxima Merr. were obtained from Parbhani where
as Luvunga eleutherandra Dalz., Clausena dentata
(Willd) Roem and Fagara budrunga Roxb. were
collected from Ratnagiri. Glycosmis pentaphylla (Retz)
DC. was collected from Kalakadu, Tamilnadu.
Paramignya monophylla Wight was collected from
Kegadi forest Nandore while Atalantia racemosa Wight.
Ex. Hook was collected from Gandhinagar, Matheran.
Ruta graveolens L. and Aegle marmelos (L.) Corr. were
obtained from the Pal forest. The young twigs of
Murraya koenigii (L.) Spreng., Murraya paniculata Jack.
and Limonia acidissima L. were locally collected from
the botanical garden of Pratap College, Amalner. The
plant materials fixed in F.A.A. were preserved in 70%
alcohol. Free hand serial sections of the young nodal
regions as well as microtome sections were prepared
following usual method of dehydration, clearing and
embedding in paraffin wax. These were stained either in
safranin-light green combination or crystal violet and
erythrosine.
Observations
The leaves are alternate or opposite, simple or
palmately or pinnately compound, or sometimes heath
like or reduced to spines; stipules are absent. In all the
species examined, the internodal region shows a
complete vascular cylinder. In the nodal region, variable
numbers of leaf traces diverge from the main vascular
cylinder leaving behind prominent gaps.
Trilacunar three-trace node
In Atalantia monophylla, Clausena,
Glycosmis mauritiana, Limonia, Luvunga, Paramignya,
Toddalia and Ruta (Figures 1-4), the median trace
emerges out first and the two lateral traces diverge out at
the higher level, whereas all the three traces are given out
simultaneously from the main stele in Aegle, Fagara and
Murraya (Figures 5-8).
The median bundle is broad in Limonia, Luvunga
and Ruta and more prominent arc-like in Aegle, Atalantia
monophylla, Clausena, Fagara, Glycosmis mauritiana,
Murraya, Paramignya and Toddalia wherein it breaks up
into 6, 12 or more traces. The lateral bundles divide, may
not divide during their upward course and extend along
with the daughter strands of median, into the rachis. The
three leaf traces - a median and two laterals enter into the
petiole without a division in Limonia acidissima.
Unilacunar one-trace node
This type of node has been observed in
Atalantia racemosa, Citrus jambhiri, C. maxima and
Glycosmis pentaphylla. A prominent arc shaped solitary
vascular trace diverges out leaving a gap in axial
vascular cylinder. It divides in their upward course with
6-9 daughter strands before entering in to the leaf
(Figures 9-15). The node is unilacunar one-trace.
DISCUSSION
A study of the nodal organisation of 16 species
distributed in 12 genera of this family revealed two nodal
Salunke et al.,2013
178 Journal of Research in Plant Sciences (2013) 2(1): 177-181
types: I. Trilacunar three-traced and II. Unilacunar
one-traced. The most common nodal condition is
trilacunar three-traced, it has been observed in 12 out of
16 species investigated. The unilacunar one-traced
condition is exhibited by Atalantia racemosa,
Citrus jambhiri, C. maxima and Glycosmis pentaphylla.
Generally, the median trace emerges prior to the laterals.
It is interesting to note that the median trace and lateral
Salunke et al.,2013
Journal of Research in Plant Sciences (2013) 2(1): 177-181 179
Explanation of Figures:
Figures 1-15 Transections showing structure of foliar node
Figures 1-4. Clausena dentata; Figures 5-8. Aegle marmelos; Figures 9-12. Atalantia racemosa;
Figures 13-15. Glycosmis pentaphylla.
Abbreviations used: MT- Median trace; LT- Lateral trace
traces emerge simultaneously in Murraya, Fagara and
Aegle. The median bundle is broad or more prominent,
arc-like in the majority of the plants and shows a number
of divisions in its upward course. These variations in the
division of the medians and laterals may be looked upon
from the points of view of mechanical strength and size
of leaf.
However, in Limonia acidissima the three leaf
traces-one median and two laterals-extend into the
petiole without a division (cf. Metcalfe and Chalk, 1950).
While reviewing the nodal structure in
angiosperms, Sinnott (1914) writes that the Rutaceae
possess a trilacunar and unilacunar structure. Unilacunar
condition was recorded by Hayward and Long (1942),
while investigating cotyledonary nodes in Citrus
[Valencia orange]. The present study indicates that the
trilacunar-three trace node occurs in majority of the taxa
studied, while the unilacunar structure is noted only in
three genera.
Sinnott (1914) has emphasized the significance
of the leaf trace and leaf gap in the systematics.
Conflicting views have been expressed by various
workers regarding the evolutionary conception of
vegetative node in angiosperms, suggesting both
reduction and/or amplification of vascular traces during
the course of specialization (see Sinnott, 1914; Ozenda,
1949; Marsden and Bailey, 1955; Meeuse, 1966;
Dickson, 1969; Stebbins, 1974). Later, Takhtajan (1969,
1980) postulated tri-or multilacunar type of nodal
structure with double trace in median gap as the most
primitive one, which has given rise to all the nodal types
known presently.
The present study demonstrates that the
trilacunar three-trace node occur in all the taxa except
Atalantia racemosa, Citrus jambhiri, C. maxima and
Glycosmis pentaphylla. Obviously, trilacunar three-
traced condition is considered to be basic for this group
and it is believed that the unilacunar one traced condition
is derived by approximation and coalescence of laterals
with the median, followed by the obliteration of their
gaps. Such a tendency has been observed in some
members of group and a reduction series has been traced.
Thus the present observations lend support to the view of
Sinnott (1914) and Dickson (1969).
ACKNOWLEDGEMENT
The authors are thankful to the Principal, Pratap
College, Amalner for encouragement and providing the
laboratory facilities during the course of investigation.
REFERENCES
Cronquist A. 1988. The evolution and classification of
flowering plants, 2nd
edn. The new York Botanical
Garden. New York.
Dickson WC. 1969. Comparative morphological studies
in Dilleniaceae IV Anatomy of node and vascularization
of leaf. J. Arnold Arbor Havri. Univ., 50: 384 - 410.
Groppo M, Pirani JR, Salatino MLF and Blanco SR.
2008. Phylogeny of Rutaceae based on two noncoding
regions from cpDNA. Am. J. Bot., 95: 985 - 1005.
Hayward HE and Long EM. 1942. The Anatomy of
the Seedling and Roots of the Valencia Orange’
Technical Bulletin 786: 1 - 31.
Marsden MPF and Bailey IW. 1955. A fourth type of
nodal anatomy in dicots Illustrated by Clerodendron
trichotomum Thunb. J. Arnold Arbor. Havr. Univ., 36:
36 - 150.
Meeuse ADJ. 1966. Fundamentals of Phytomorphology.
The Ronald Press Co New York.
Metcalfe CR and Chalk L. 1950. Anatomy of the
Dicotyledons: Vol. I, Clarendon Press, Oxford.
Ozenda P. 1949. Recherches sur les dicotyledones
apocarpiques. Publ Lab l’ Ecole Normal Supesieura Ser
Biol Fase II Paris.
Salunke et al.,2013
180 Journal of Research in Plant Sciences (2013) 2(1): 177-181
Sinnott EW. 1914. Investigations on the phylogeny of
the angiosperms I The anatomy of the node as an aid in
the classification of the angiosperms. Amer. J. Bot., 1:
303 - 322.
Sinnott EW and Bailey IW. 1914. Investigations on the
phylogeny of the angiosperms 3: Nodal anatomy and the
morphology of the stipules. Amer. J. Bot., 1: 144 - 459.
Stebbins GL. 1974. Flowering Plants Evolution above
the species level. Edward Arnold Ltd. London.
Takhtajan AL. 1969. Flowering Plants Origin and
Dispersal. (Translated from Russian by C Jeffrey) Oliver
and Boyd Edinburgh.
Takhtajan AL. 1980. Outline of the classification of
flowering plants (Magnoliophyta). Bot. Rev., 46: 225-
359.
Salunke et al.,2013
Journal of Research in Plant Sciences (2013) 2(1): 177-181 181
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Nodal anatomical study of certain members of the Rutaceae

  • 1. Nodal anatomical study of certain members of the Rutaceae Keywords: Rutaceae, Node, Nodal evolution. ABSTRACT: The vascular organization of the node in 12 genera has been investigated. The leaves are unifoliate in Atalantia, Citrus and Paramignya, 3-5 foliate in Aegle, Luvunga, Toddalia and Glycosmis, decompounds in Ruta and imparipinnately compound in other taxa. These are alternate or opposite and exstipulate. The foliar nodes are trilacunar, three-trace in the majority of the plants. It is unilacunar in Atalantia racemosa, Citrus jambhiri, C. maxima and Glycosmis pentaphylla. The results are discussed with respect to the evolutionary conception of node. 177-181 | JRPS | 2013 | Vol 2 | No 1 This article is governed by the Creative Commons Attribution License (http://creativecommons.org/ licenses/by/2.0), which gives permission for unrestricted use, non-commercial, distribution and reproduction in all medium, provided the original work is properly cited. www.plantsciences.info Journal of Research in Plant Sciences An International Scientific Research Journal Authors: Snehal P. Salunke, Sarala C. Tadavi and Vijay V. Bhadane. Institution: Centre for Post-Graduate Studies and Research in Botany, Pratap College, Amalner - 425 401 [M.S.], India. Corresponding author: Snehal P. Salunke. Email: snehal2106@ymail.com Fax No.: +91 (02587) 223103 Web Address: http://www.plantsciences.info documents/PS0053.pdf. Dates: Received: 04 Feb 2013 Accepted: 09 Feb 2013 Published: 05 Mar 2013 Article Citation: Snehal P. Salunke, Sarala C. Tadavi and Vijay V. Bhadane Nodal anatomical study of certain members of the Rutaceae. Journal of Research in Plant Sciences (2013) 2(1): 177-181 An International Scientific Research Journal Original Research Journal of Research in Plant Sciences JournalofResearchinPlantSciences
  • 2. INTRODUCTION The Rutaceae family includes about 160 genera and 1,900 species that are widely distributed in tropical and temperate regions around the world, but they are especially abundant in Australia and South Africa (Groppo et al., 2008; Cronquist, 1988). While studying the nodal organization in the angiosperms, Sinnott (1914) have reported the trilacunar and unilacunar nodal structure in Rutaceae. Hayward and Long (1942) have also made observations on variations in the cotyledonary nodes in Valencia orange. Since the nodal vasculature in the family has received little attention, it warrants a detailed study. Consequently the present study were undertaken to study the nodal organization of 16 species distributed in 12 genera. MATERIAL AND METHODS The plant materials of Atalantia monophylla DC, Toddalia asiatica Lamk. and Glycosmis mauritiana (Lam.) Tanaka were collected from Lalbagh Botanical Garden, Bangalore, Citrus jambhiri Lush and Citrus maxima Merr. were obtained from Parbhani where as Luvunga eleutherandra Dalz., Clausena dentata (Willd) Roem and Fagara budrunga Roxb. were collected from Ratnagiri. Glycosmis pentaphylla (Retz) DC. was collected from Kalakadu, Tamilnadu. Paramignya monophylla Wight was collected from Kegadi forest Nandore while Atalantia racemosa Wight. Ex. Hook was collected from Gandhinagar, Matheran. Ruta graveolens L. and Aegle marmelos (L.) Corr. were obtained from the Pal forest. The young twigs of Murraya koenigii (L.) Spreng., Murraya paniculata Jack. and Limonia acidissima L. were locally collected from the botanical garden of Pratap College, Amalner. The plant materials fixed in F.A.A. were preserved in 70% alcohol. Free hand serial sections of the young nodal regions as well as microtome sections were prepared following usual method of dehydration, clearing and embedding in paraffin wax. These were stained either in safranin-light green combination or crystal violet and erythrosine. Observations The leaves are alternate or opposite, simple or palmately or pinnately compound, or sometimes heath like or reduced to spines; stipules are absent. In all the species examined, the internodal region shows a complete vascular cylinder. In the nodal region, variable numbers of leaf traces diverge from the main vascular cylinder leaving behind prominent gaps. Trilacunar three-trace node In Atalantia monophylla, Clausena, Glycosmis mauritiana, Limonia, Luvunga, Paramignya, Toddalia and Ruta (Figures 1-4), the median trace emerges out first and the two lateral traces diverge out at the higher level, whereas all the three traces are given out simultaneously from the main stele in Aegle, Fagara and Murraya (Figures 5-8). The median bundle is broad in Limonia, Luvunga and Ruta and more prominent arc-like in Aegle, Atalantia monophylla, Clausena, Fagara, Glycosmis mauritiana, Murraya, Paramignya and Toddalia wherein it breaks up into 6, 12 or more traces. The lateral bundles divide, may not divide during their upward course and extend along with the daughter strands of median, into the rachis. The three leaf traces - a median and two laterals enter into the petiole without a division in Limonia acidissima. Unilacunar one-trace node This type of node has been observed in Atalantia racemosa, Citrus jambhiri, C. maxima and Glycosmis pentaphylla. A prominent arc shaped solitary vascular trace diverges out leaving a gap in axial vascular cylinder. It divides in their upward course with 6-9 daughter strands before entering in to the leaf (Figures 9-15). The node is unilacunar one-trace. DISCUSSION A study of the nodal organisation of 16 species distributed in 12 genera of this family revealed two nodal Salunke et al.,2013 178 Journal of Research in Plant Sciences (2013) 2(1): 177-181
  • 3. types: I. Trilacunar three-traced and II. Unilacunar one-traced. The most common nodal condition is trilacunar three-traced, it has been observed in 12 out of 16 species investigated. The unilacunar one-traced condition is exhibited by Atalantia racemosa, Citrus jambhiri, C. maxima and Glycosmis pentaphylla. Generally, the median trace emerges prior to the laterals. It is interesting to note that the median trace and lateral Salunke et al.,2013 Journal of Research in Plant Sciences (2013) 2(1): 177-181 179 Explanation of Figures: Figures 1-15 Transections showing structure of foliar node Figures 1-4. Clausena dentata; Figures 5-8. Aegle marmelos; Figures 9-12. Atalantia racemosa; Figures 13-15. Glycosmis pentaphylla. Abbreviations used: MT- Median trace; LT- Lateral trace
  • 4. traces emerge simultaneously in Murraya, Fagara and Aegle. The median bundle is broad or more prominent, arc-like in the majority of the plants and shows a number of divisions in its upward course. These variations in the division of the medians and laterals may be looked upon from the points of view of mechanical strength and size of leaf. However, in Limonia acidissima the three leaf traces-one median and two laterals-extend into the petiole without a division (cf. Metcalfe and Chalk, 1950). While reviewing the nodal structure in angiosperms, Sinnott (1914) writes that the Rutaceae possess a trilacunar and unilacunar structure. Unilacunar condition was recorded by Hayward and Long (1942), while investigating cotyledonary nodes in Citrus [Valencia orange]. The present study indicates that the trilacunar-three trace node occurs in majority of the taxa studied, while the unilacunar structure is noted only in three genera. Sinnott (1914) has emphasized the significance of the leaf trace and leaf gap in the systematics. Conflicting views have been expressed by various workers regarding the evolutionary conception of vegetative node in angiosperms, suggesting both reduction and/or amplification of vascular traces during the course of specialization (see Sinnott, 1914; Ozenda, 1949; Marsden and Bailey, 1955; Meeuse, 1966; Dickson, 1969; Stebbins, 1974). Later, Takhtajan (1969, 1980) postulated tri-or multilacunar type of nodal structure with double trace in median gap as the most primitive one, which has given rise to all the nodal types known presently. The present study demonstrates that the trilacunar three-trace node occur in all the taxa except Atalantia racemosa, Citrus jambhiri, C. maxima and Glycosmis pentaphylla. Obviously, trilacunar three- traced condition is considered to be basic for this group and it is believed that the unilacunar one traced condition is derived by approximation and coalescence of laterals with the median, followed by the obliteration of their gaps. Such a tendency has been observed in some members of group and a reduction series has been traced. Thus the present observations lend support to the view of Sinnott (1914) and Dickson (1969). ACKNOWLEDGEMENT The authors are thankful to the Principal, Pratap College, Amalner for encouragement and providing the laboratory facilities during the course of investigation. REFERENCES Cronquist A. 1988. The evolution and classification of flowering plants, 2nd edn. The new York Botanical Garden. New York. Dickson WC. 1969. Comparative morphological studies in Dilleniaceae IV Anatomy of node and vascularization of leaf. J. Arnold Arbor Havri. Univ., 50: 384 - 410. Groppo M, Pirani JR, Salatino MLF and Blanco SR. 2008. Phylogeny of Rutaceae based on two noncoding regions from cpDNA. Am. J. Bot., 95: 985 - 1005. Hayward HE and Long EM. 1942. The Anatomy of the Seedling and Roots of the Valencia Orange’ Technical Bulletin 786: 1 - 31. Marsden MPF and Bailey IW. 1955. A fourth type of nodal anatomy in dicots Illustrated by Clerodendron trichotomum Thunb. J. Arnold Arbor. Havr. Univ., 36: 36 - 150. Meeuse ADJ. 1966. Fundamentals of Phytomorphology. The Ronald Press Co New York. Metcalfe CR and Chalk L. 1950. Anatomy of the Dicotyledons: Vol. I, Clarendon Press, Oxford. Ozenda P. 1949. Recherches sur les dicotyledones apocarpiques. Publ Lab l’ Ecole Normal Supesieura Ser Biol Fase II Paris. Salunke et al.,2013 180 Journal of Research in Plant Sciences (2013) 2(1): 177-181
  • 5. Sinnott EW. 1914. Investigations on the phylogeny of the angiosperms I The anatomy of the node as an aid in the classification of the angiosperms. Amer. J. Bot., 1: 303 - 322. Sinnott EW and Bailey IW. 1914. Investigations on the phylogeny of the angiosperms 3: Nodal anatomy and the morphology of the stipules. Amer. J. Bot., 1: 144 - 459. Stebbins GL. 1974. Flowering Plants Evolution above the species level. Edward Arnold Ltd. London. Takhtajan AL. 1969. Flowering Plants Origin and Dispersal. (Translated from Russian by C Jeffrey) Oliver and Boyd Edinburgh. Takhtajan AL. 1980. Outline of the classification of flowering plants (Magnoliophyta). Bot. Rev., 46: 225- 359. Salunke et al.,2013 Journal of Research in Plant Sciences (2013) 2(1): 177-181 181 Submit your articles online at www.plantsciences.info Advantages Easy online submission Complete Peer review Affordable Charges Quick processing Extensive indexing You retain your copyright submit@plantsciences.info www.plantsciences.info/Submit.php.