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MORPHO-ANATOMIC FEATURES AND CHEMICAL COMPOUNDS IN
SOME AQUATIC PLANT SPECIES – PRELIMINARY DATA
Emilia Brîndu a S NDULESCU, Mala-Maria STAVRESCU-BEDIVAN, Gina VASILE SC E EANU, Tudor CHIOPU
University of Agronomic Sciences and Veterinary Medicine of Bucharest, Faculty of Agriculture
59 Marasti Blvd, District 1, 011464, Bucharest, Romania
Corresponding author email: [email protected] Abstract Plants live everywhere, populating all major habitats (air, land, water). Their life cycle takes place under the influence of environmental factors and is therefore subject to large variations in abiotic factors. In this context, plants have changed over time their structures, organ shape and appearance, resulting from their adaptation to living environment. Some changes in the structure and function of the vegetative organs, arising as a result of their adaptation to the plant were followed by one of the greatest figures in literature and the founder of morphology as a science – J.W. von Goethe, who in 1790 formulated a theory of plant metamorphosis (adaptive change). This paper highlights such adaptive changes but seeks and identifies chemical elements in plant composition under study (Hydrocharis morsus-ranae, Anubias barteri, Hygrophila odora, Bacopa caroliniana) – the first step in trying as thorough knowledge of aquatic plants to establish their possible uses. Key words: aquatic plants, metamorphosis, chemical elements. INTRODUCTION The aquatic plants can live underwater (submerged) or can float on water surface (natant). Some of them have adapted their morphology to aquatic environment: large intercellular spaces in lamina are connected with aeriferous canals from petiole that extend as aerenchyma in the rhizome and roots, ensuring their oxygenation. Other plant species compensate the underdeveloped aerenchyma by highlighting the mechanical and conducting tissues. The aim of thus study was to investigate the morpho-anatomic features and chemical compounds in the following aquatic plant species: Hydrocharis morsus-ranae, Anubias barteri, Hygrophila odora, Bacopa caroliniana. Hydrocharis morsus-ranae (Alismatales, Hydrocharitaceae) or frogbit, native to Europe and parts of Asia, is a free-floating annual herbaceous aquatic plant, but its leaves can become emergent when the vegetation is dense enough (O’Neil, 2007). Anubias barteri (Alismatales, Araceae), a West African species, survives either totally or
partially submersed (http://www.liveaquaria.com/). The Hygrophila species usually are growing emersed along natural bodies of water (http://naturalaquariums.com/). Hygrophila odora (Lamiales, Acanthaceae) is a plant species distributed in Western Africa; its emersed form has a strong, ascending to upright stems that lignify at the basis, and lanceolate leaves (http://www.flowgrow.de/db/aquaticplants/). Bacopa caroliniana (Lamiales, Scrophulariaceae) comes from South America, where it is found growing in swampy areas, emerged and submerged. One of the basic characteristics of this plant is lemon smell of the leaves when they are broken (www.aquascaping.ro). MATERIALS AND METHODS For identification and description purposes, we used preserved material belonging to four aquatic plant species: Hydrocharis morsus-ranae, Anubias barteri, Hygrophila odora, Bacopa caroliniana. Macroscopic observations were performed on plants with the help of identification handbooks. Microscopic
441
Scientific Papers. Series A. Agronomy, Vol. LVII, 2014ISSN 2285-5785; ISSN CD-ROM 2285-5793; ISSN Online 2285-5807; ISSN-L 2285-5785
observationwere madestudied plaObservatioIOR microBiology, Utaken withDMC - LSSodium anby flame (extractant RESULTS Results regof aquatic(frogbit) Hydrocharnatant hydstolons andleaves. It flowing wa
Figure Hydrocharepidermis covered wi
Figure 2. H
Fundamenthaving manThe mechais limited vessel. Tissue dimranae leaf’
ns and mie on numerants (Andreions were caoscope belonUASVM Buh the digital
60 (6MPX,nd potassium
photometryt ratio 1:20)
S AND DIS
garding moc plant Hy
ris morsus-drophyte pld long-petiois commo
aters.
1. Hydrochari
ris morsus-rformed fro
ith a thin cu
Hydrocharis msection
tal parenchny aerifer canical elemand the wo
mensions fr’s petiole ar
icrometric rous cross-si, 2003). arried out wnging to th
ucharest. Thcamera Pan
, 3X opticalm levels wey, using 2.
SCUSSION
orpho-anatoydrocharis
-ranae (Filant. It hasolate, ovate on in stagn
is morsus-ran
ranae leaf’som a singleuticle (Figur
morsus-ranaen (original)
hyma is highchannels of vents are red
ood is reduc
rom Hydrocre shown in
measuremesections of
with a ML-e laboratoryhe photos wnasonic Lum zoom). ere determi% acetic a
NS
omic structmorsus-ra
igure 1) is long, slenkidney-sha
nant or slo
nae (original)
s petiole hase row of cere 2).
e: petiole cross
hly developvarying sizeduced. Phloced to a sin
charis morsTable 1.
ents the
-4M y of
were mix
ined acid
ture anae
s a nder aped wly
s an ells,
s-
ped, es. oem ngle
sus-
Tab
NR123
Hywitpreand
F
Thelonidiointr(FiTheBetcollamTismo
NR123
Resof a AnufouIn exoaer
ble 1. Tisues mto H
R. Cortex Con
drocharis mth a dorsesenting a md lower epid
Figure 3. Hydr
e mesophylng cells, roblasts. Tracelular gure 3). e ribs presetween ribs lenchyma mina’s resistssue’s leaforsus-ranae
Table 2. Tisumo
R. Up Lo
sults regardaquatic plan
ubias barteund in aquarcross sectio
odermis, corenchyma ti
measurement fHydrocharis m
TISSUE Epidermis
x, Central cylinducting fasci
morsus-ranaiventral he
mesophyll tisdermis (Figu
rocharis mors(origin
ll presents arich in ch
The lacunaspaces (a
ent a very wand lower is differe
tance. f dimensioplant are in
ues measuremorsus-ranae le
TISSUE pper epidermiMesophyll
ower epidermi
ding morphnt Anubias b
ri (Figure 4riums. on, the adveortex and vssues are di
from leaf petimorsus-ranae
M
inder icle
ae has a beterofacial, ssue lie betwure 3).
sus-ranae : leanal)
a palisadic hloroplasts ar tissue aeriferi pa
weak develoepidermis,
entiated, t
ons in Hndicated in T
ments from Hydeaf structures
Mis
is
ho-anatomibarteri
4) is a plant
entitious rovascular cyifferentiated
ole belonging
MEAN (μ) 72
2448 216
bifacial leafstructure,
ween upper
af structure
tissue withincludinghas big,
arenchyma)
oped xylem.an angular
that gives
HydrocharisTable 2.
drocharis
MEAN (μ) 28.8 360 57.6
ic structure
t commonly
oot presentsylinder. Nod.
g
f , r
h g , )
. r s
s
e
y
s o
442
Fi
In the vasphloem velignificatedpith contai
Figure 5. C
Dimensiontissues are
Table 3. T
NR. 1 2 3 4 5
Table 4. Tisu
NR. 1 2 3 4
igure 4. Anubi
scular cylinessels alterd cells betwns lignifica
Cross section (o
ns recorded shown in T
Tisues measure
TISSUExoderm
CorteEndoder
Vascular cyPith
ues measuremto Anu
TISSUECuticle
EpidermConducting fa
Sclerenchy
ias barteri (or
nder (Figurernates with
ween those tated cells.
through Anubriginal)
for Anubias
Table 3.
ements from Aroots
UE mis
ex rmis ylinder
h
ment from leaf ubias barteri E e
mis fascicle yma
riginal)
e 5) numerh xylem, wtwo layers. T
bias barteri ro
s barteri ro
Anubias barte
MEAN (28.857614.4
662.4360
petiole belong
MEAN (μ14.4 28.8 57.6 72
rous with The
oot
ot’s
eri
(μ)
ging
μ)
In unicutdevsclpetmicare
Fig
Thewita vlowsiz
Thesevsparichbun7). meTab
cross-sectioistratified eticle. The coveloped; pherencyma ctiole being crometric m
e indicated i
gure 6. Cross-
e leaves arth pinnate v
very thin cutwer epiderme) (Figure 7
Figure 7. Cr
e mesophylveral rows aces. Rows h in chlorondles surro
Dimensioeasured inble 5.
on (Figure 6epidermis, ortical parenhloem and caps) are di
polistelic. measuremenn Table 4.
-section througbarte
re large, grvenation. In ticle, upper
mis (formed7).
oss section thr
ll is homogof cells below the
oplasts. Thunded by ns recordeAnubias b
6), leaf’s pecovered wnchyma is v
xylem veisorderly ar
The tissunts in Anub
ugh petiole beleri
reen, ovatecross sectioepidermis,
d by cells o
hrough a A. ba
geneous, cowithout i
e upper epihe ribs havsclerenchym
ed for leabarteri are
etiole has awith a thinvery poorlyssels (with
rranged, theue’s petiolebias barteri
longing to A.
-lanceolate,on, presentsmesophyll,
of different
arteri leaf
onsisting ofntercellularidermis areve vascularma (Figureaf’s tissues
shown in
a n y h e e i
, s , t
f r e r e s n
443
Table 5. Tissue dimensions in Anubias barteri leaves
NR. TISSUE MEAN (μ) 1 Cuticle 14.4 2 Upper epidermis 72 3 Mesophyll 316 5 Lower epidermis 28.8 6 Midrib 144
Results regarding morpho-anatomy of Hygrophila odora aquatic plant Hygrophila odora (Figure 8) is an aquatic plant species.
Figure 8. Hygrophila odora (original)
The cylindrical stem has nodes and internodes, with dorso-ventral flattened, pinnate leaves in nodes. It forms adventive roots. In cross-section, the root appears to be formed by rhizodermis lacking absorbing hairs (one layer of cells); cortex is very well developed, with large intercellular spaces found in aerenchyma (Figure 9).
Figure 9. Hygrophila odora: root cross section (original) The mechanical elements and central cylinder are very reduced (Figure 9). The dimensions for measured tissues in Hygrophila odora root are indicated in Table 6. The stem has a unistratified epidermis, covered by a thin cuticle (Figure 10).
Table 6. Tissue dimensions from Hygrophila odora roots
NR. TISSUE MEAN (μ) 1 Rizhodermis 28.8 2 Cortex 244.8 3 Central cylinder 115.2
Figure 10. Hygrophila odora: cross section of a cortex
(original) In the highly developed cortex, there are three or four layers of colechyma but the major part is occupied by aerenchyma with intercellular spaces by different sizes (Figure 10), forming air chambers. The last layer of the cortex, endodermis, is formed by one single row of different size cells.
Figure 11. Hygrophila odora: cross section of a central
cylinder (original) The conducting tissue is formed by poor developed collateral fascicles, orderly arranged (Figure 11). The dimensions for measured tissues in Hygrophila odora stem are shown in Table 7. In cross section, the leaf of Hygrophila odora presents the upper epidermis with smaller cells on one single row, covered by a thin cuticle and the lower epidermis formed by bigger cells (Figure 12).
444
Table 7. M
NR . 1 2 3 4 5 6 7 8
Figure 12
Below thepresenting (Figure 12)air chambeThe ribs arfor measuleaves are p
Table 8. T
NR. 1 2 3 4
Results regof aquatichyssop) Bacopa c(Figure 13)years. In stem’s leaves (oblIn cross-serhizodemisand centrhizodermicortex hasintercellulalayer of differentiat
easurements fo
TISSCutic
EpiderCort
EndodeCollenc
PithCentral c
Conducting
2. Hygrophila (o
e upper epcells
), and it is ers. re poorly deured tissuepresented in
Tissue dimensl
TISSUpper epLower ep
MesopRib
garding moc plant Ba
caroliniana), ubiquitou
nodes therelong, succulection, the s, exodermtral cylindis is lackins cells withar spaces the cortex
ted, present
for stem tissueodora
UE cule rmis tex ermis chyma h
cylinder g fascicle
odora: cross riginal)
pidermis, thrich in crossed by
eveloped. Tes in Hygrn Table 8.
ions from Hygleaves SUE pidermis pidermis phyll b
orpho-anato
acopa carol
is an us in aquari
e are advenlents, oppos
adventive mis, corticader (Figurng in absorh thin cell
(aerenchymx, endoderting Caspari
es in Hygroph
MEAN (μ)14.4 43.2 1584 28,8 144 1008 1224 259.2
section of lea
he mesophchloropl
y different s
The dimensirophila od
grophila odor
MEAN(28.857.6
115.2100.8
omic structliniana (wa
aquatic piums for m
ntive roots site arrange
root preseal parenchyre 14). Trbent hair; walls and
ma). The rmis, is wian strips.
hila
af
hyll, lasts size
ions dora
ra
(μ)
ture ater
lant many
and d). ents yma The the
few last
well
In fassepwitThelignTheBac9.In epi(FiThecutcan
Figure 13
Figure 14. Ba
central cycicles, resp
parated by th cellulosice pith is nificated wae dimensiocopa coroli
cross-sectidermis, cgure 15). e unistratiticle. The cnals by diffe
3. Bacopa car
acopa carolini(origin
ylinder, thepectively fomedullary
c, thin wallsformed by
alls. ons for miniana roots
tion, the cortex an
fied epiderortex is occerent size (a
roliniana (orig
iana: root cronal)
ere are foour woodenrays forme
s. y cells wi
measured s, are show
stem prend central
ermis is ccupied withaerenchyma
ginal)
oss section
ur liberiann fascicles,ed by cells
ith slightly
tissues, inwn in Table
esents thel cylinder
covered byh aeriferousa) separated
n , s
y
n e
e r
y s d
445
through a cellulosic, developed.by many xon two con
Tabl
NR. 1 2 3
Figur
The pith isThe dimeBacopa ca
Table 10
NR. 1 2 3 4
In cross-seof B. carocuticle; thethin wallepidermis
single layethin walls.
. The centrxylem and ncentric circ
le 9. Tissue diBacopa ca
TISSRizhod
CortCentral c
re 15. Bacopa section
s formed by nsions for roliniana st
. Tissue dimecaroli
TISSUE Cuticle
EpidermisCortex
Central cylin
ection, the moliniana leae upper epled cells;
containin
er of cells. T. The endoral cylinder
phloem vecles.
imensions mearoliniana roo
UE ermis tex cylinder
caroliniana: n (original)
parenchimameasured
tem are sho
nsions measuiniana stalk
s
nder
morpho-anataves presentidermis for
mesophylng differen
The cells hdermis is wis represen
essels arran
easured in ots
MEAN72
288144
stem cross
atous cells. tissues fr
wn Table 1
red in Bacopa
MEAN (μ)14.4 57.6 1728 864
tomic structts: a very t
rmed by larl; the lownt size c
have well nted nged
(μ)
from 0.
a
)
ture thin rger wer
cells
(sm(Fi
Fi
TheundcelspaepichlThefasThecor
NR
1234
ResandmoodoReschecom
T
B
maller than gure 16).
igure 16. Baco
e mesodifferentiatels lacking
aces are idermis theloroplasts. e ribs hacicles (wooe measuremroliniana ar
Table 11. Tis
R.
UppLow
M
sults regardd sodium
orsus-ranae,ora, Bacopasults regaemical idemposition ar
Table 12. Potas
SamplesHydrocharmorsus-ran
Anubias barHygrophila oBacopa caroli
those of
opa carolinian(origin
ophyll ed, formed
intercellureduced.
ere are lay
ave poor ody-adaxial ments for lere indicated
ssue dimensioncaroliniana
TISSUE
per epidermis wer epidermis Mesophyll
Midrib
ding determin aquatic Anubias
a carolinianrding sodntifying inre shown in
ssium and sod
studied aqua
s K+
ris nae
11
rteri 8odora 9iniana
4
the upper
na: cross sectnal)
is homby severa
ular spacesBeneath
yer of cel
developed and liberian
eaf’s tissuesin Table 11
ns measured ia leaves
M
mination ofc plant: H
barteri, Hna dium and n the stun Table 12.
dium determinatic plants
+, ppm N112.97
839.08 919.17
461.18
epidermis)
ion of a leaf
mogeneous,al layers ofs or thesethe upperlls rich in
collateraln-abaxial).s in Bacopa1.
in Bacopa
MEAN (μ)
28.8 28.8 288
187.2
f potassiumHydrocharisHygrophila
potassiumdied plant
nation in the
Na+, ppm 639.40
747.17 779.52
638.82
)
, f e r n
l
a
m s a
m t
446
CONCLUSIONS Although the specialist literature presents aquatic plants having a well developed aerenchyma and reduced mechanical and conducting elements, the submerged plant species Anubias barteri, Hygrophila odora and Bacopa caroliniana show important differences regarding these morpho-anatomic structures. Aerenchyma’s absence both in root, petiole and leaves (Anubias barteri) is correlated with developed conducting elements and sclerenchyma’s presence. The aeriferous tissues recorded in Bacopa caroliniana are reduced, correlated with numerous conducting elements. Hygrophila odora presents a well developed aerenchyma in organ’s structures; the mechanical and conducting elements are reduced, although the xylem vessels are numerous in stem’s structure.
Potassium and sodium identification in the studied plant species (Hydrocharis morsus-ranae, Anubias barteri, Hygrophila odora, Bacopa caroliniana) represent a first step in trying as thorough knowledge of aquatic plants to establish their possible uses. REFERENCES Andrei M., 2003. Microtehnic botanic . Editura
Niculescu SRL, Bucure ti. O’Neil C.R., 2007. European Frog-Bit (Hydrocharis
morsus-ranae) – Floating Invader of Great Lakes Basin Waters. Available online: http://www.seagrant.sunysb.edu/ais/pdfs/Frog-bitFactsheet.pdf
NYSG Invasive Species Factsheet Series: 07-1 ***http://www.liveaquaria.com ***http://naturalaquariums.com/ ***http://www.aquascaping.ro/ ***http://www.flowgrow.de/db/aquaticplants
447