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In general, saline and arid environments are poor in species. A total of 728 taxa of halophytes are recorded for SW Asia belonging to 68 families (compared to 117 plant families worldwide). The majority of halophytes belong to the families Chenopodiaceae, Poaceae, Leguminosae (Papiliondeae), Asteraceae and Cyperaceae. Chenopodiaceae has the largest number of species and genera of all families only exceeded by Poaceae which has more genera but fewer species. These numbers are in accordance with those found for halophytes of the world. From the data available, Turkey has the most halophytes (±600 taxa), followed by Pakistan (±361 taxa), Iran ± 350 taxa), Afghanistan, Saudi Arabia, Oman and Yemen (±120 taxa). Halophytes in SW Asia constitute about half the number of halophyte taxa (and families) recorded for the world. Information on halophytes is collated from published sources, and names of accepted taxa (and synonyms) are compiled in the database BRAHMS. A preliminary checklist (of names only) produced from this database is provided in this chapter.
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105
M.A. Khan et al. (eds.), Sabkha Ecosystems: Volume IV: Cash Crop Halophyte and Biodiversity
Conservation, Tasks for Vegetation Science 47, DOI 10.1007/978-94-007-7411-7_8,
© Springer Science+Business Media Dordrecht 2014
Abstract
In general, saline and arid environments are poor in species. A total
of 728 taxa of halophytes are recorded for SW Asia belonging to 68
families (compared to 117 plant families worldwide). The majority of
halophytes belong to the families Chenopodiaceae, Poaceae, Leguminosae
(Papiliondeae), Asteraceae and Cyperaceae. Chenopodiaceae has the
largest number of species and genera of all families only exceeded by
Poaceae which has more genera but fewer species. These numbers are in
accordance with those found for halophytes of the world. From the data
available, Turkey has the most halophytes (±600 taxa), followed by
Pakistan (±361 taxa), Iran ± 350 taxa), Afghanistan, Saudi Arabia, Oman
and Yemen (±120 taxa). Halophytes in SW Asia constitute about half the
number of halophyte taxa (and families) recorded for the world.
Information on halophytes is collated from published sources, and
names of accepted taxa (and synonyms) are compiled in the database
BRAHMS. A preliminary checklist (of names only) produced from this
database is provided in this chapter.
S. A. Ghazanfar (*) J. Osborne
Royal Botanic Gardens Kew , Richmond, Surrey ,
London TW9 3AB , UK
E. Altundag
Department of Biology, Faculty of Arts and Sciences ,
Duzce University , 81620 Duzce , Turkey
A. E. Yaprak G. N. Tug
Department of Biology, Faculty of Sciences ,
Ankara University , 06100 Ankara , Turkey
M. Vural
Department of Biology, Faculty of Sciences ,
Gazi University , 06500 Ankara , Turkey
Halophytes of Southwest Asia
Shahina A. Ghazanfar , Ernaz Altundag ,
Ahmet Emre Yaprak , Joanna Osborne ,
Gull Nilhan Tug , and Mecit Vural
1 Introduction
Halophytes are plants that are specially adapted
to live in saline environments. Salt affected areas
amount to about 955 million ha worldwide, with
the tropical African and SW Asian deserts con-
stituting a major part of this area. In semi arid
areas about 30 % of all irrigated land suffers
from salinization, and with the present trend in
global warming and climate change towards
aridity, more and more land will eventually fall
to salinity.
106
Information on saline ecosystems, correct
identifi cation of halophytes and their potential
uses is scattered or lacking, especially in parts of
SW Asia. This chapter is aimed towards under-
standing and identifying the plants that tolerate
saline conditions in SW Asia; it collates the
information that is available at present, and aims
towards updating the nomenclature of this group
of salt tolerant plants. This information is neces-
sary for any research on biosaline agriculture,
rangeland and coastal management and restora-
tion of degraded arid and saline habitats.
1.1 Geographical Scope
For the purpose of this chapter, Southwest Asia is
taken to include Turkey, Lebanon, Israel,
Palestine, Jordan, all countries of the Arabian
Peninsula (Bahrain, Kuwait, Oman, Qatar, Saudi
Arabia, Yemen, and the United Arab Emirates),
Iraq, Iran, Afghanistan and Pakistan (Fig. 1 ).
Southwest Asia is mostly arid with large
gravel and sandy desert areas. The region lies at
the edge of a large tectonic plate such that the
Arabian Peninsula is pulling away from Africa,
F i g . 1 Countries of SW Asia included in the study. Turkey, Lebanon, Israel, Palestine, Jordan, all countries of the
Arabian Peninsula, Iraq, Iran, Afghanistan and Pakistan (From Google maps)
S.A. Ghazanfar et al.
107
and parts of the Anatolian Peninsula (Turkey)
are sliding past parts of Asia. Continental rift-
ing has caused some areas to be below sea level,
such as the Dead Sea located between Israel
and Jordan.
The Arabian Peninsula lies between the Red
Sea and Persian Gulf and the Anatolian Peninsula
lies between the Black Sea and Mediterranean
Sea. In the north, the Zagros, Elbruz and Taurus
mountains are present. The Arabian Peninsula is
mostly covered by sandy and gravelly plains with
escarpment mountains in the southwest, and Rub'
al Khali, one of the world’s largest sand deserts,
spanning the southern third. In Yemen, the moun-
tains reach up to 3,700 m and the highlands extend
north along the Red Sea coast and north into
Lebanon. The Zagros Mountains located in Iran
also border with parts of northern Iraq. The central
plateau of Iran, a hyper arid area, is divided into
two drainage basins, Dasht-e-Kavir (Great Salt
Desert) in the north and Dasht-e-Lut in the south.
Though surrounded by water, the region of
Southwest Asia is arid and lacks water resources.
The few rivers, such as the Tigris and Euphrates
which fl ow through Turkey, Syria and Iraq and
the Jordan River (which fl ows from Mt. Hermon
in Lebanon through Jordan into the Dead Sea) are
critical for agriculture.
Climatically most areas in the plains receive
less than 400 mm of precipitation a year (Fig. 2 ).
Large areas of deserts are saline with inland
sabkhas (salt fl ats). Some of the largest salt areas
lie in the central plateau of Iran, and Umm as
Samim, a big inland salt plain (a former lake) lies
in western Oman.
1.2 What Are Halophytes
Halphytes can be defi ned in various ways, but for
our purpose, we have taken halophytes as those
plants that are able to complete their life cycle
under saline conditions, where salt concentration
is at least 200 mM NaCl [ 1 ]. Plants that are classi-
ed as “true” or “obligate” halophytes such as
mangroves, seagrasses or some species of
Amaranthaceae (in the former Chenopodiaceae)
are not able to exist in non saline habitats, while
“facultative” halophytes can live in non saline
habitats. The majority of halophytes depend on
rain for seed to germinate, but can fl ower and fruit
in saline environments, and seeds of halophytes
can survive long periods in saline conditions.
Many eudicot halophytes do not show opti-
mum growth in salinity concentrations of
50–250 mM NaCl, while monocot halophytes
generally grow optimally in the absence of salt,
or if growth is stimulated, it is by a low concen-
tration of NaCl (50 mM or less) [ 2 ]. All halo-
phytes need to regulate their cellular Na
+ , Cl - and
K
+ concentrations as they adjust to the external
water potential. However species differ in the
succulence ( water content per unit area of leaf);
[ 1 ] and in the solutes accumulated. Detailed
account of salinity tolerance in fl owering plants
is given in [ 3 ].
Nearly all salt-tolerant plants belong to the
angiosperms, although a few are ferns (in families
Pteridaceae and Ophioglossaceae). Halophytes
are widely distributed among the families of
owering plants, and are found in about a third
of the total plant families [ 4 ]. There are about
500 genera of halophytes worldwide, of which
about half belong to only 20 families (Table 1 ).
Amongst monocotyledons, the Poaceae contain
more halophytic genera than any other family
(7 % of the family), in Cyperaceae 14 % of the
genera are halophytic. Amongst the eudicots,
Chenopodiaceae has the highest proportion of
halophytic genera followed by Asteraceae,
Aizoaceae, Leguminosae, Apiaceae, Euphor-
biaceae, Brassicaceae, Plantaginaceae and
Caryophyllaceae [ 1 ]. [In the APG III (2009)
classifi cation Chenopodiaceae is included in the
Amaranthaceae. In this chapter, for the sake of
convenience, we have kept the name Chenopo-
diaceae as used earlier.]
2 Distribution and
Biogeography of the SW
Asia Halophytic Flora
A fair amount of literature exists on halophytes of
the countries of SW Asia and a number of papers
are present on the physiology and germination
Halophytes of Southwest Asia
108
studies of halophytes [ 1 , 3 ]. More recently, several
studies have concentrated on the phylogeny of
halophytes mainly in the Family Chenopodiaceae
leading to revised classifi cations and changes in
the nomenclature of species [ 5 ].
A total of 728 taxa of halophytes are recorded
for SW Asia. This information has been collated
from Published sources of which the main ones
are: Pakistan: [ 6 ]; Turkey: [ 714 ]; Iran: [ 15 ];
Arabian Peninsula: [ 1618 ]; Jordan: [ 17 ] (Fig. 3 ).
Nomenclature of taxa (especially those in the
Chenopodiaceae) are updated to the accepted
names as provided in various publications [
5 ,
2025 ].
Names of taxa are databased in [ 26 ] used at
the Royal Botanic Gardens Kew. This data base
will be updated as and when new information
becomes available. A preliminary checklist (of
Fig. 2 Climate diagrams of nine countries of SW Asia
S.A. Ghazanfar et al.
109
names only) is produced from this database
which is given in the Appendix .
From the data available, Turkey has the
most halophytes (±600 taxa), followed by Pakistan
361 taxa), ( Iran ± 350 taxa), Afghanistan,
Saudi Arabia, Oman and Yemen (±120 taxa).
Halophytes in SW Asia constitute about half the
number of halophyte taxa (and families) recorded
for the world by [ 27 ].
In general, saline and arid environments are
poor in species. Of the total 415 plant families
[ 28 ] halophytes of SW Asia are recorded in 68
families (117 families worldwide as recorded
[ 27 ]). The majority of halophytes belong to the
families Chenopodiaceae, Poaceae, Leguminosae:
Papiliondeae, Asteraceae and Cyperaceae.
Chenopodiaceae has the largest number of spe-
cies and genera of all families only exceeded by
Poaceae which has more genera (but fewer spe-
cies) than Chenopodiaceae (Table 1 ). These data
are in accordance with that found for halophytes
of the world [ 1 ] (Table 2 ).
The SW Asian ora mainly falls within the
Saharo-Sindian and Irano-Turanian fl oristic
Table 1 Families, genera and species in the halophytic
families of SW Asia
Family Genera Species
Chenopodiaceae s.str. 49 183
Poaceae 55 112
Asteraceae 26 55
Leguminosae: Papilionoideae 27 48
Cyperaceae 10 44
Zygophyllaceae 8 17
Caryophyllaceae 8 16
Tamaricaceae 2 16
Juncaceae 1 15
Boraginaceae 9 14
Apiaceae 7 13
Brassicaceae 9 12
Polygonaceae 4 10
Liliaceae 3 10
Apocynaceae 8 9
Euphorbiaceae 2 9
Aizoaceae 5 8
Lamiaceae 5 8
Leguminosae: Mimosoideae 2 8
Plantaginaceae 2 7
Gentianaceae 3 7
Plumbaginaceae 3 6
Solanaceae 3 6
Ranunculaceae 4 5
Primulaceae 4 4
Arecaceae 2 4
Cymodoceaceae 2 4
Iridaceae 2 4
Rosaceae 1 4
Typhaceae 1 4
Malvaceae 3 3
Rhizophoraceae 3 3
Verbenaceae 3 3
Convolvulaceae 2 3
Hydrocharitaceae 2 3
Frankeniaceae 1 3
Juncaginaceae 1 3
Amaranthaceae s.str. 2 2
Orchidaceae 2 2
Rubiaceae 2 2
Valerianaceae 2 2
Elatinaceae 1 2
Goodeniaceae 1 2
Linaceae 1 2
Myrsinaceae 1 2
Najadaceae 1 2
(continued)
Table 1 (continued)
Family Genera Species
Orobanchaceae 1 2
Portulacaceae 1 2
Thymelaeaceae 1 2
Leguminosae: Caesalpinioideae 2 2
Scrophulariaceae 2 1
Avicenniaceae 1 1
Cistaceae 1 1
Combretaceae 1 1
Cynomoriaceae 1 1
Molluginaceae 1 1
Moraceae 1 1
Nyctaginaceae 1 1
Pandanaceae 1 1
Pedaliaceae 1 1
Resedaceae 1 1
Rhamnaceae 1 1
Ruppiaceae 1 1
Salicaceae 1 1
Sonneratiaceae 1 1
Sterculiaceae 1 1
Tiliaceae 1 1
Halophytes of Southwest Asia
110
regions [ 29 , 30 ], to which the majority of the
halophytic communities belong.
Biogeographically, the Irano-Turanian region,
including the area around Persian Gulf and west-
ern Pakistan (Makran and Baluchistan) can be
considered as a centre of diversity of many halo-
phytic genera of Chenopodiaceae such as
Bienertia , Caroxylon , Climacoptera , Gamanthus ,
Halanthium , Halimocnemis , Halostachys ,
Kalidium , Piptoptera , Petrosimonia , Salsola and
Suaeda . Except the cosmopolitan genus Suaeda
s.lat. and Eurasian and African genus Salsola
s.lat., all other genera are exclusively Irano-
Turanian endemics [ 15 , 31 ]. The largest diver-
sity both in quantity and sections in the Salsola
can be seen in SW and Central Asia. The genus
Tamarix , as a second important halophytic genus
in SW Asia is similar in its diversity to Salsola
such that most are found in the Irano-Turanian
region and a few species in the Mediterranean
area, North and South Africa [ 32 ]. Halocnemum
strobilaceum is the most salt tolerant and com-
mon halophyte in northern Iran, Afghanistan and
Central Asia, but less common in southern Iran
and the Arabian Peninsula.
2.1 Turkey
In Turkey there are about 300 species that are true
halophytes with Chenopodiaceae, Asteraceae and
Fabaceae at the top of the list [
7 ]. There are
coastal and inland halophytic habitats in Turkey,
coastal halophytic habitats are mainly distributed
in Mediterranean and Aegean Sea coasts, and
there are also a few in Black Sea and Marmara
Sea coasts. The most common coastal halophytic
species in Turkey are Cakile maritima, Salicornia
emerici, Sarcocornia perennis, Sarcocornia
obclavata, Arthrocnemum macrostachyum and
Atriplex portulacoides . Inland halophytic habi-
tats are mainly distributed in Central and Eastern
Anatolia. Species composition of Eastern
Anatolian salt marshes and salt stepes is quite
similar to North western Iranian salt marshes and
F i g . 3 Number of halophytic species in countries of SW
Asia. TUR Turkey, PA K Pakistan, IRN Iran, SAU Saudi
Arabia, OMA Oman, AFG Afghanistan, YEM Yemen,
GST-UA United Arab Emirates, IRQ Iraq, GST-QA Qatar,
GST-BA Bahrain (Data from published sources – see
references)
Table 2 Families of owering plants in which halophytic
genera worldwide occur most frequently
Family Percentage of halophytic genera
Chenopodiaceae 44
Aizoaceae 15
Cyperaceae 14
Caryophyllaceae 11
Poaceae 7
Arecaceae 6
Asteraceae 3
Fabaceae 3
Adapted from [ 1 ]
S.A. Ghazanfar et al.
111
salt steppes. Central Anatolia is the richest region
in terms of halophytic species as several salt and
brackish water lakes are present there with Tuz
Lake (Konya-Ankara- Aksaray), Seyfe Lake
(Kırşehir) and Sultansazlığı (Kayseri) as some of
the largest ones surrounded by salt marshes [ 9 ].
Tuz Lake is a special case as it also has the high-
est endemism of halophytes in Turkey. Detailed
studies on the vegetation are given by [ 3337 ].
Halophytic vegetation usually forms zones
depending on the salinity of the soils. Aksoy and
Hamzaoğlu [ 37 ] give the zonation of the halo-
phytic vegetation of Central Anatolia. In the fi rst
zone where salt density is maximum (Tuz Lake,
Seyfe Lake and Sultansazlığı), Salicornia freita-
gii, S. perennas and Halocnemum strobilaceum
are dominant. The general cover in this zone
ranges between 10 and 80 % and depends on the
concentration of salt. The width of this zone also
differs and depends on the topography of the
area. It is narrower in areas where the slopes are
steeper, but can continue for kilometers where
the slopes are low. Because of its high and fl uctu-
ating salinity, this zone is poor in terms of species
richness, with one to ten species occurring and no
endemics. Halocnemum strobilaceum , one of the
dominant species in this zone can also be found
in the second zone where the salt concentration is
less. Depending on the gradually decreasing
salinity a second zone can be recognised with an
increase in the number of species. Where a water
source is not present, succulents and hemicrypto-
phyts are dominant and the species richness
ranges between 65 and 80 species, and endemism
between 16 and 21 %. The most common species
in this zone are Limonium iconicum , Frankenia
hirsuta , Lepidium cartilagineum , Atriplex verru-
cifera , Caroxylon stenopterum ( Salsola stenop-
tera ), Puccinellia convoluta and Halocnemum
strobilaceum. Limonium iconicum , Lepidium
cartilagineum and Caroxylon stenopterum are
endemic to the salt marshes of Central Anatolia.
Where a water source feeding the marsh is
present, tall herbaceous hemicryptophyts are
dominant. Amongst these, Elymus elongatus ,
Puccinellia koeieana subsp. anatolica , Inula
aucherana , Juncus maritimus , Juncus heldreichi-
anus subsp. orientalis and Puccinellia convoluta
are dominant. The number of species ranges
between 45 and 60 and endemism between 26
and 32 %. Generally speaking families
Chenopodiaceae and Plumbaginaceae are domi-
nant where the salt marshes are not fed by a
water source, while Poaceae and Juncaceae are
dominant where water is available and feeds the
salt marshes [ 35 , 38 , 39 ].
The outermost zone of the salt marshes of
Central Anatolia is characterized by Artemisia
santonicum . This zone, called the “salty steppe”,
borders with the non-halophytic communities.
Succulent species are mostly absent; Artemisia
santonicum is dominant sometimes with a cover
of 70 %. Other common species of this zone
are Peganum harmala , Alhagi pseudalhagi ,
Achillea santolinoides subsp. wilhelmsii ,
Noaea mucronata subsp. mucronata and Apera
intermedia . The number of species ranges
between 70 and 95 and endemism is between
17 and 23 %.
2.2 The Arabian Peninsula
About 140 taxa are recorded as halophytes in the
Arabian Peninsula. This constitutes about 4 % of
the total fl ora of the Arabian Peninsula (± 3500
taxa). Not surprisingly the majority of halophytes
belong to the families Chenopodiaceae, Poaceae,
Zygophyllaceae, Fabaceae and Plumbaginaceae.
Table 3 shows the distribution of halophytic taxa
and their families in the Arabian Peninsula [ 16 ,
17 , 19 , 4050 ].
Key species in saline habitats of Arabia are
nearly always perennial. The predominant life-
forms are succulent, semi-woody dwarf shrubs
belonging to the families Chenopodiaceae,
Zygophyllaceae and Plumbaginaceae, and
hemicryptophytes with runners and spiny
leaves belonging to the families Poaceae and
Juncaceae. Annual succulents such as Bienertia
cycloptera and Tetraena simplex are excep-
tions. Coastal species are either obligate
halophytes like the representatives of the
families Chenopodiaceae, Frankeniaceae and
Plumbaginaceae, or salt tolerant genera from
unspecialized families, such as Sporobolus and
Halophytes of Southwest Asia
112
Aeluropus (Poaceae), or salt secreting species
such as Avicennia (Acanthaceae) and Limonium
(Plumbaginaceae). The most common coastal
and salt tolerant species are Arthrocnemum
macrostachyum, Halocnemum strobilaceum,
Halopeplis perfoliata, Salsola spp., Suaeda
spp., (Chenopodiaceae); Aeluropus lagopoides,
Odyssea mucronata, Sporobolus spicatus, S.
consimilis (Poaceae); Juncus rigidus (Juncaceae),
Tetraena spp. (Zygophyllaceae); Limonium
spp. (Plumbaginaceae) and Avicennia marina
(Acanthaceae) [
18 , 50 ].
The submerged coastal vegetation of the
Arabian Peninsula especially that of the Gulf, has
been particularly well studied owing to the rapid
coastal development. The submerged seagrass
beds are one of the most important vegetation
types and highly productive ecosystems of great
importance to the marine fauna especially the
marine turtles, shrimps and numerous species of
sh. Sheppard et al. [
51 ] report four species of
seagrasses from the Gulf, Halodule uninervis ,
H. wrightii , Halophila stipulacea , H. ovalis and
Syringodium isoetifolium. Ruppia maritima is also
reported in several coastal lagoons [
52 ]. Halodule
uninervis , Halophila stipulacea , H. ovalis are
most widespread and the most common.
2.3 Iran
The halophytic and salt tolerant fl ora of Iran is
very diverse compared to other countries of
SW Asia. About 365 species in 51 genera and
44 families of vascular plants are recorded as
true halophytes [ 15 ]. Akhani [ 15 ] lists 12 halophytic
plant communities for Iran: (1) Mangrove
communities (Avicennio Sonneratietea); (2)
Submerged aquatic plant communities
(Ruppietea maritimae); (3) Annual obligatory
hygro-halophytic communities on sea, lake and
river marshes dominated by stem or leaf succu-
lent C3 chenopods (Thero-Salicornietea); (4)
Semi-woody or perennial halophytic communi-
ties on muddy or coastal salt fl ats dominated by
stem succulent C3 chenopods (Salicornietea
fruticosae); (5) Hydrophilous euryhalophytic
rush communities, Phragmitetea australis; (6)
Halophytic grassland and herbaceous perennial
sedge communities belonging to genera
Puccinellia and Juncus (Juncetea maritimi); (7)
Salt marsh and riverine brushwood communi-
ties dominated by salt-excreting halophytes
(Tamaricetea ramosissimae, prov.); (8): Annual
halophytic communities dominated by C4 che-
nopods in temporary moist and inundated, or
Table 3 Number of halophytic taxa in plant families in the Arabian Peninsula [ 18 ]
Family No. halophytic species Family No. halophytic species
Acanthaceae 1 Juncaceae 2
Aizoaceae 4 Liliaceae 1
Apocynaceae 2 Mimosaceae 2
Arecaceae 1 Najadaceae 1
Asteraceae 2 Orobanchaceae 1
Boraginaceae 2 Plumbaginaceae 6
Chenopodiaceae 41 Poaceae 17
Caryophyllacae 8 Portulacaceae 1
Ceratophyllaceae 1 Potamogetonaceae 1
Convolvulaceae 2 Rhizophoraceae 2
Cymodoceaceae 3 Ruppiaceae 1
Cynomoriaceae 1 Salvadoraceae 1
Cyperaceae 4 Tamaricaceae 3
Fabaceae 5 Typhaceae 1
Frankeniaceae 1 Zygophyllaceae 11
Hydrocharitaceae 2
S.A. Ghazanfar et al.
113
disturbed salty soils (Climacopteretea crassae,
prov.); (9) Halophytic shrubby, semi-woody or
hemicrytophytic communities on salty and dry
soils dominated by leaf or stem succulent C4
chenopods (Haloxylo-Salsoletea tomentosae,
prov.); (10) Halophytic shrub communities on
salty and sandy coastal or margin of sabkhas
with high water table dominated by Nitraria
schoberi and Reaumuria fruticosa ; (11)
Psamohalophytic shrub communities along
sandy coasts of Persian Gulf and Oman sea
(Sphaerocomion aucheri and communities of
Tetraena qatarense and Heliotropium bac-
ciferum s.lat.; (12) Unclassifi ed halophytic
communities of herbaceous perennial and
hemicryptophyte halophytic communities of
secondary origin.
Four distribution patterns are distinguished
amongst the halophytes in the Irano-Turanian
oristic region of Iran [ 15 ]: (1) The Aralo-
Caspian/Central Iranian species which contains
the highest number of taxa. Examples of this
group are Suaeda arcuata, Suaeda linifolia,
Nitraria schoberi, Climacoptera turcomanica,
Halimocnemis pilifera, H. mollissima, H. longi-
folia, Bassia eriantha, Gamanthus gamocarpus,
Bienertia cycloptera, Petrosimonia glaucescens,
Halothamnus subaphyllus, Haloxylon ammoden-
dron, Xylosalsola arbuscula, S. arbusculiformis,
Caroxylon incanescens ; (2) The Central Iranian
endemics such as Caroxylon abarghuensis,
Anabasis haussknechtii, A. calcarea, Hypocylix
kerneri ( Salsola kerneri ) , Salicornia persica,
Hypericopsis persica, Limonium perfoliatum
and Halimocnemis occulta (3) Endemic species
in Azerbaijan or linking species between Iran,
Turkey, Armenia and Azerbaijan. Examples
are Gamanthus pilosus, Kali tamamschjanae
( Salsola tamamschjanae ) , Salsola ericoides,
Salsola dendroides, Caroxylon persicum ( Salsola
persica ) , Suaeda dendroides and Suaeda graci-
lis. The discovery of two extremely endangered
disjunct species Asparagus lycaonicus and
Microcnemum corralloides in West Iran and
Central Anatolia are interesting phytogeographi-
cal links between these areas [ 53 , 54 ]; (4) The
fourth group are those species distributed around
and along the Persian Gulf area and further East
into Balochistan of Pakistan. Examples are
Bienertia sinuspersici , Salsola drummondii [ 26 ],
Kali griffi thii ( Salsola griffi thii ) , Suaeda fruticosa,
Halothamnus iranicus, Halanthium purpureum,
Salicornia sp., Suaeda sp., Tamarix kermanen-
sis , Limonium stocksii, lndigofera stricta and
Tetraena qatarense . In southern Iran there are
some Saharo-Arabian, Somalia-Masai and tropi-
cal species such as Avicennia marina, Suaeda
monoica, Juncus socotranus or Saharan- Arabian/
Mediterranean species such as Arthrocnemum
macrostachyum.
2.4 Afghanistan
The saline vegetation of Afghanistan is compa-
rable to that of Iran. The large arid and saline
regions of Afghanistan (Seistan, Dasht-e-Margo
and Registan) lie in the southwest and southeast
of the country and the vegetation falls under the
infl uence of the Irano-Turanian fl oristic ele-
ments that overlaps with that of Iran and to some
extent that of northern Pakistan. Amongst the
halophytic communities, Halocnemum strobila-
ceum with Salsola rosmarinus ( Seidlitzia ros-
marinus ) is dominant in most of the saline areas.
Halocnemum strobilaceum is the most abundant
halophyte in northern Iran, Afghanistan and
Central Asia. Other species include those of
Haloxylon , Anabasis , Aeluropus lagopoides ,
Atriplex , Limonium , Lycium , Fortuynia ,
Alhagi , Salsola and Tetraena spp. ( Zygophyllum )
[ 55 , 56 ].
2.5 Iraq
The halophytic vegetation in Iraq is present in
the large desert areas of southwest Iraq. As for
most arid regions, the fl ora of Iraq is poor in
species, with the majority of the perennial
plants in saline areas belonging to the family
Chenopodiaceae [ 57 ].
The following account is adapted from [ 57 ] and
[ 58 ]. The most characteristic plant communities
Halophytes of Southwest Asia
114
with halophytic fl ora are: (1) Haloxyletum ammo-
dendri. The main component of this association
is Haloxylon ammodendron (= H. aphylla ), which
is found only in the sandy desert with unstabilized
sand dunes, also prevalent in southern Palestine
and northern Arabia. In Iraq this community
stretches along the Euphrates sand-belt. It is evi-
dent that this community was once much more
widespread and closed than it is perhaps in recent
times due to degradation from fuel gatherers who
use it for making charcoal. The dominant species
is Haloxylon ammodendron , common associates
are Panicum turgidum and Calligonum comosum ;
other members of this community include species
such as Haloxylon salicornicum , Salsola spp.,
Aristida plumosa , Salsola rosmarinus , Moltkiopsis
ciliata , Neurada procumbens , Plantago spp.,
Cyperus conglomeratus , Silene villosa ,
Anisosciadium lanatum , Eremobium aegyptiacum ,
Cutandia memphitica , Bassia muricata and
Astragalus gyzensis. Cistanche is parasitic on the
saline shrubs especially Haloxylon ; (2)
Haloxyletum salicornici . This is the most charac-
teristic and important community of the desert
region of Iraq and is widespread throughout the
deserts of the Arabian Peninsula [ 44 , 59 ]. This
community is found on calcareous substrate with a
gypsophilous underlying substrate. The dominant
species of this community is Haloxylon salicorni-
cum which usually grows in small mounds made
from aeolian sand. Major associates of Haloxylon
salicornicum are Salsola setifera ( Anabasis set-
ifera ), Caroxylon jordanicola ( Salsola jordanic-
ola ), Salsola rosmarinus , Cornulaca aucheri ,
Cymbopogon olivieri , Aristida plumosa , and
Annothamnus gibbous. Salsola rosmarinus is
found on higher ground at the edges of saline mud
ats as opposed to the halophyte Halopeplis perfo-
liata found in the sabkhas of the Sultanate of
Oman [ 60 ]. Other associates are Heliotropium
ramosissimum s.lat., Farsetia aegytiaca , Plantago
ciliata , Teucrium oliverianum and Neurada
procumbens ; (3) Zygophylletum coccinei . This
community is usually found on sandy soil overly-
ing saline fl ats. The shrub, Tetraena coccinea
( Zygophyllum coccineum ) grows on small hum-
mocks made from wind-blown sand. In Iraq often
found in the southern desert, this species often
occurs near the sea in Kuwait and southern Arabia;
(4) Seidlitzietum rosmarini . This is another halo-
phytic or semi-halophytic community often found
on fringes of saline or brackish water pools. Other
Salsola species are often associated with Salsola
rosmarinus in this community; (5) Halocnemum
strobilacei . This is the most characteristic commu-
nity of sabkha areas and is prevalent on the saline
mud-fl ats in south western Iraq. Halocnemum
strobilaceum is the dominant species, with occa-
sional associates of Aeluropus lagopoides and
Cressa cretica ; (6) Bienertietum cyclopterae . This
community consisting of a single species,
Bienertia cycloptera , is found on margins of small
saline depressions in sandy areas. Associated with
it in some areas, such as at the margins of Bahr al
Milh in the western desert, are Frankenia pulveru-
lenta and Aleuropus lagopoides . In addition to
these communities, scattered plants of Tamarix
passerinoides , and Peganum harmala are often
found in saline habitats. In particular Peganum
harmala is present often on disturbed and waste
ground where there is a high level of soil nitrates.
Ziziphus nummularia is a constant species of
sandy depressions.
2.6 Pakistan
The halophytic fl ora of Pakistan has been sum-
marised by [ 6 ]. They list the distribution, life
form and potential economic uses of about 410
taxa. As with most halophytes, the family
Chenopodiaceae has the highest number of spe-
cies (90 spp.) followed by Poaceae (68 spp.),
Cyperaceae (30 spp.), Fabaceae (29 spp.),
Asteraceae (24 spp.) and Tamaricaceae (23 spp.).
Most of the halophytes are found in the
Balochistan plains and Sind (especially coastal);
fewer halophytes are found in the mountains,
Potwar plateau and the deserts of Punjab [ 6 ].
Balochistan is the most species rich in halo-
phytic diversity. There are several brackish
lakes in the Salt Range in the Punjab (Kalar
Kahar in Chakwal District, Khabikki Lake in
Soan Sakesar valley) and Hadero Lake in Sind
S.A. Ghazanfar et al.
115
(which is also a wildlife bird sanctuary) that
show a range of halophytes.
The most distinctive halophytic fl ora is found
in the mangroves of the coastal tidal zone in Sind
and Balochistan with Avicennia , Sonneratia ,
Rhizophora , Ceriops , Aegicerus and Scaveola .
The inland, saline desert areas and plains of
Balochistan are poor in species and are domi-
nated by Tamarix , with Haloxylon , Atriplex ,
Salsola , and other halophytes as associates.
3 Economic Uses
Halophytes have their greatest potential in
their utilization in restoration of degraded
saline locations, coastal stabilization, produc-
tion of cheap biomass for renewable energy,
cash crops for fodder, medicine, building mate-
rials and other utilitarian objects and for
sequestering CO
2 .
The use of halophytes as fodder, food plants,
medicinals and fuel wood has been documented
extensively for most regions of SW Asia [ 6 , 61
63 ]. Ghazanfar in her works on the medicinal
plants of the Arabian Peninsula [ 64 ] and The
Middle East [ 60 ] lists uses of several halo-
phytes. Species such as Portulaca oleracea ,
Aerva javanica , Vernonia cinerea and
Heliotropium have been used traditionally in the
treatment of skin disorders, burns, stings and
insect bites; Apium graveolens and Centella asi-
atica have been used as diuretics; Artemesia as
an antihelmintic, Teucrium spp. for abdominal
pain and colic, and Salvadora persica as tooth
cleaner. The multiple uses of Cocos nucifera
and Phoenix dactylifera have been known since
ancient times, as have the uses of species of
Typha and Phragmites for making thatching,
mats and boats.
The use of halophytes is also studied as
potential biomass crops to directly sequester up
to 0.7 Gt C, similar to tree plantations [ 66 ].
Halophytes can play a role in absorbing C from
the atmosphere while providing food, fodder
and energy crops on previously unused saline
land. Thus, through halophyte plantations,
unused saline land can be restored and become
productive.
Appendix: A Preliminary List
of the Halophytes of SW Asia
Several names in the Che nopodiaceae are still
unresolved. Only critical synonyms are provided.
AIZOACEAE
Aizoon canariense L.
Mesembryanthemum crystillinum L.
Mesembryanthemum nodifl orum L.
Sesuvium verrucosum Raf.
Sesuvium sesuvioides (Fenzl) Verdc.
Sesuviumportulacastrum (L.) L.
Trianthema portulacastrum L.
Trianthema triquetra Rott. ex Willd.
Zaleya pentandara (L.) Jeffrey
ACANTHACEAE
Avicennia marina (Forssk.) Vierh.
Syn.: Sceura marina Forssk . (formerly in
Avicenniaceae)
AMARANTHACEAE s.str.
Aerva javanica (Brum.f.) Juss. ex J.A. Schultes
Amaranthus retrofl exus L.
APIACEAE
Ammi visnaga (L.) Lam.
Apium graveolens L.
Apium nodifl orum (L.) Lag.
Bupleurum euboeum Beauverd
Syn.: Bupleurum gracile auct. mult. non
(M.Bieb.) DC. non Odontites gracilis Bie;
Bupleurum heldreichii Boiss. & Bal.
Bupleurum semicompotisum L.
Syn.: Bupleurum glaucum Ledeb.
Bupleurum tenuissimum L.
Bupleurum turcicum Snogerup
Centella asiatica (L.) Urban
Echinophora orientalis Hedge & Lamond
Syn.: Echinophora trichophylla J.E. Smith
Falcaria falcarioides (Bornm. & Wolff) Wolff
Syn.: Pimpinella falcarioides Bornm. & Wolff
Ferula caspica M. Bieb.
Syn.: Ferula aciphylla M. Bieb. ex Ledeb.; Ferula
orientalis Eichw.; Peucedanum caspicum
(M. Bieb.) Link
Ferula halophila Pesmen
Halophytes of Southwest Asia
116
APOCYNACEAE (incl. Asclepiadaceae)
Calotropis procera (Ait.) Ait.
Cionura erecta (L.) Griseb.
Syn .: Cionura erectum (L.) Griseb.
Cynanchum acutum L. subsp. acutum
Syn .: Cynanchum monspeliacum L.
Glossonema varians (Stocks.) Hook. f.
Leptadenia pyrotechnica (Forssk.) Decne.
Oxystelma esculentum (Linn. f.) R. Brown
Pentatropis nivalis (J.F. Gmel.) D.V. Field &
J.R.I. Wood
Pergularia daemia (Forssk.) Chiov.
Pergularia tomentosa L.
ARECACEAE
Cocos nucifera L.
Phoenix caespitosa Chiov.
Syn.: Phoenix comorensis Becc.
Phoenix dactylifera L.
Phoenix reclinata Jacq.
ASTERACEAE
Achillea millefolium L. subsp. millefolium
Achillea santolinoides subsp. wilhelmsii (K. Koch )
Greuter
Syn.: Achillea wilhelmsii K. Koch
Achillea schischkinii Sosn.
Syn.: Achillea muschensis Bornm.
Achillea sieheana Stapf
Syn.: Achillea salsuginea Bornm.
Anthemis halophila Boiss. & Bal.
Syn.: Anthemis alexandrettae Eig
Artemisia campestris L.
Artemisia herba-alba Asso
Syn.: Artemisia arragonensis Lam.; Artemisia
herba-alba Asso var. tenuifolia Boiss.
Artemisia santonicum L.
Syn.: Artemisia maritima (Waldst. & Kit)
Gams subsp. monogyna ; Artemisia monogyna
Waldst. & Kit.
Artemisia scoparia Waldst. & Kit.
Aster tripolium L.
Syn.: Tripolium vulgare Nees
Bellis annua L.
Bellis perennis L.
Syn.: Bellis armena Boiss.
Bellis sylvestris Cyr.
Bidens cernua L.
Centaurea balsamita Lam.
Centaurea halophila Hub.-Mor.
Centaurea tuzgoluensis Aytaç & Duman
Centaurea virgata Lam.
Cirsium alatum (Gmelin) Bobrov subsp.
alatum
Syn.: Serratula alata Gmelin
Cousinia birandiana Hub.-Mor.
Cousinia humilis Boiss.
Syn.: Arctium humile (Boiss.) O. Kuntze
Crepis foetida L. subsp. rhoeadifoli (M. Bieb.)
Celak.
Syn.: Crepis foetida L. var. rhoeadifoli Boiss.;
Crepis nemetzii Rech.f.; Crepis nestmeiri
Herro. & Degen; Crepis rhoeadifoli M. Bieb.
Crepis sancta (L.) Babcock
Syn.: Crepinia marschalliana Reichb.; Crepis
kochiana Boiss.; Crepis sancta subsp. bifi da
(Vis.) Babcock; Crepis sancta subsp. nemau-
sensis (Gouan) Babcock; Crepis sancta subsp.
obovata (Boiss. & Noe) Babcock; Hieracium
sanctum L.; Lagoseris orientalis Boiss.
Cymbolaena griffi thii (A. Gray) Wagenitz
Handelia tricophylla (Schrenk.) Heimerl
Inula aucherana DC.
Syn.: Inula armena Bordz.; Inula seidlitzii Boiss.
Inula britannica L.
Inula crithmoides L.
Inula graveolens (L.) Desf.
Syn.: Dittrichia graveolens (L.) Greuter; Erigeron
graveolens L.
Iphiona aucherii (Boiss.) Anderb.
Launaea procumbens (Roxb.) Ramayya &
Rajagopal
Microcephala lamellate (Bunge) Pobed.
Mulgedium tataricum (L.) DC.
Pluchea arguta Boiss.
Pluchea dioscoridis (L.) DC.
Syn.: Conyza dioscoridis Desf.
Pseudognaphalium luteoalbum (L.) O.M.
Hilliard & B.L. Burtt
Pulicaria boissieri Hook. f.
Pulicaria carnosa (Boiss.) Burkill.
Pulicaria dysenterica (L.) Bernh.
Syn.: Inula dysenterica L.; Pulicaria dysenterica
var. microcephala Boiss.; Pulicaria uliginosa
Stev.
Pulicaria gnaphalodes (Vent.) Boiss.
S.A. Ghazanfar et al.
117
Pulicaria hadramautica E. Gmal-Eldin &
Boulos
Pulicaria undulata (L.) C.A. Meyer
Senecio doriiformis DC. subsp. orientalis
(Fenzl) Matthews
Syn.: Senecio doriaeformis DC. var. megaloph-
ron ; Senecio doriaeformis DC. var. orientais ;
Senecio nemorensis L. var. orientalis
Senecio salsuginea H. Duman & Vural
Seriphidium quettense (Podlech) Ling
Sonchus asper (L.) Hill subsp. asper
Sonchus erzincanicus Matthews
Sonchus maritimus L.
Sonchus tenerrimus L.
Taraxacum bessarabicum (Hornem.) Hand.-
Mazz. var. bessarabicum
Syn.: Leontodon besarabicus Hornem.;
Taraxacum fulvipile Harv.; Taraxacum lepto-
cephalum Rchb.; Taraxacum stenocephalum
Boiss. & Kotschy ex Boiss.
Taraxacum farinosum Hausskn. & Bomm.
Taraxacum mirabile Wagenitz
Taraxacum tuzgoluensis Yildirimli & A.
Dogrukoca var. tuzgoluensis
Taraxacum tuzgoluensis Yildirimli & A.
Dogrukoca var. eskilensis Yildirimli & A.
Dogrukoca
Tripleurospermum callosum (Fisch. & Mey.)
Bornm.
Tripleurospermum decipiens (Boiss. & Heldr.)
E. Hossain
Syn.: Chamaemelum decipiens (Fisch. & Mey.)
Boiss.; Pyrethrum decipiens Fisch. & Mey.
Xanthium sibiricum Patrin. ex Widder
BORAGINACEAE
Caccinia macranthera (Banks & Sol.) Brafi d
var. macranthera
Syn.: Borago macranthera Banks & Sol.
Conringia persica Boiss.
Coronopus didymus (L.) Smith
Cynoglossum creticum Miller
Heliotropium aucheri DC.
Heliotropium bacciferum Forssk. s.lat.
Syn.: Heliotropium undulatum Vahl; H. ramosis-
simum (Lehm.) DC.; H. kotschyi Bunge nom.
nud.; H. Persicum auct., Boiss.; H. lignosum
Bornm.; H. fartakense O. Schwartz
Heliotropium curassavicum L.
Heliotropium dolosum De Not.
Syn.: Heliotropium eichwaldii Steud.; Heliotropium
macrocarpum Guss.
Heliotropium lasiocarpum Fisch. & Mey.
Syn.: Heliotropium eichwaldii Steud. var. lasio-
carpum (Fisch & Mey.) C. B. Clarke;
Heliotropium ellipticum Ledeb. var. lasiocar-
pum (Fisch. & Mey.) M. Popov; Heliotropium
europaeum L. var. tenuifl orum Boiss.;
Heliotropium tenuifolium Bunge non Guss.
Heliotropium remotifl orum Rech.f. & Riedl
Moltkia coerulea (Willd.) Lehm.
Syn.: Moltkia anatolica Boiss.; Moltkia punctata
Lehm.; Onosma coeruleum Willd.
Moltkiopsis ciliata (Forssk.) I.M. Johnst.
Onosma halophilum Boiss. & Heldr.
Tournefortia sibirica L. var. sibirica
Syn.: Tournefortia sibirica L.
BRASSICACEAE
Cakile maritima Scop.
Syn.: Cakile euxina Pobed. ex Grossheim
Dilophia salsa Thompson
Erysimum crassipes Fisch. & Mey.
Eutrema parvulum (Schrenk) Al-Shehbaz &
Warwick
Iberis halophila Vural & H. Duman
Isatis kotschyana Boiss. & Hohen.
Lepidium latifolium L.
Lepidium cartilagineum (J. May) Thell.
Syn.: Lepidium caespitosum Desv.; Lepidium
cartilagineum (J. May.) Thell. subsp. caespi-
tosum ; Lepidium cartilagineum (J. May.)
Thell. subsp. crassifolium (Waldst. & Kit.)
Thell.; Lepidium crassifolium Waldst. & Kit.;
Lepidium crenatifolium Boiss. & Bal.; Thlaspi
cartilagineum J. May.
Lobularia maritima (L.) Desv.
Raphanus raphanistrum L.
Sinapis arvensis L.
Sisymbrium loeselii L.
Syn.: Sisymbrium glabratum Schulz
CARYOPHYLLACEAE
Cerastium dubium (Bastard) Guepin
Syn.: Cerastium anomalum Waldst. & Kit.
Cerastium glomeratum Thuill.
Halophytes of Southwest Asia
118
Gypsophila oblanceolata Bark.
Gypsophila perfoliata L.
Syn.: Gypsophila anatolica Boiss. & Heldr.;
Gypsophila hygrophila Post; Gypsophila
pauli Klokov; Gypsophila tekirae Stef.;
Gypsophila trichotoma Wenderoth
Minuartia urumiensis (Bornm.) Bornm.
Syn.: Alsine urumiensis Bornm.
Polycarpaea spicata Wight ex Arn. var. spicata
Polycarpaea spicata Wight ex Arn. var. capil-
laris Balf. f.
Saponaria halophila Hedge & Hub.-Mor
Saponaria karapinarensis Vural & N. Adygüzel
Silene nocturna L.
Silene salsuginea Hub.-Mor.
Spergularia diandra (Guss.) Heldr.
Syn.: Arenaria diandra L.; Spergulariasalsuginea
Fenzl
Spergularia marina (L.) Gris.
Syn.: Arenaria rubra var. campestris L.; Arenaria
rubra L. var. marina ; Spergula marina (L.)
Bartl. & H. L. Wendl.; Spergularia campestris
(L.) Aschers.; Spergularia salina J.& C. Presl
Spergularia media (L.) C. Presl
Syn.: Arenaria media L.; Spergularia marginata
(DC.) Kitt.
Spergularia rubra (L.) J. & C. Presl
Sphaerocoma aucheri Boiss.
CHENOPODIACEAE
Anabasis aphylla L.
Syn.: Anabasis aphylla Iljin subsp. australis ;
Anabasis aphylla Iljin subsp. rubra ; Anabasis
tatarica Pall.
Anabasis calcarea (Charif & Aellen) Bokhari &
Wendelbo
Anabasis ehrenbergii Schwinf. ex Boiss.
Anabasis eugeniae Iljin
Anabasis haussknechtii Bunge ex Boiss.
Anabasis iranica Iljin
Anabasis lachnantha Allen & Rech.f.
Anabasis salsa (C.A. Mey.) Benth.
Arthrocnemum macrostachyum (Moric.)
K. Koch
Syn.: Arthrocnemum fruticosum (L.) var. macro-
stachyum (Moric.) Moq.;
Salicornia macrostachya Moric.; Arthrocnemem
glaucum (Delile) Ung.-Sternb.
Atriplex aucheri Moq.
Syn.: Atriplex amblyostegia Turcz.; Atriplex hor-
tensis L. subsp. desertorum (Sosn.) Aellen;
Atriplex nitens Schkuhr subsp. aucheri (Moq.)
Takht. & A.A. Fedor.; Atriplex nitens Schkuhr
subsp. desertorum Iljin
Atriplex davisii Aellen
Atriplex dimorphostegia Kar. & Kir.
Atriplex farinosa Forssk. subsp. farinosa
Atriplex fl abellum Bunge ex Boiss
Atriplex halimus L.
Atriplex hortensis L.
Atriplex laevis Ledeb.
Syn.: Atriplex littorale Boiss.
Atriplex lasiantha Boiss.
Atriplex lehmanniana Bunge
Atriplex leucoclada Boiss. var. inamoena
(Allen) Zohary
Syn.: Atriplex inamoena Allen
Atriplex micrantha Ledeb.
Syn.: Atriplex heterosperma Bunge
Atriplex nogalensis Friis & M.G. Gilbert
Atriplex portulacoides L.
Syn.: Halimione portulacoides (L.) Aellen
Atriplex prostrata Boucher ex DC.
subsp. calotheca (Raf.) M.A. Gust.
Syn.: Atriplex hastata Forssk.
Atriplex sagitata Borkh.
Syn.: Atriplex nitens Schkuhr, nom illegit.
Atriplex schugnanica Iljin
Atriplex stocksii Boiss.
Syn.: Atriplex griffi thii Moq. var. stocksii (Boiss.)
Boiss.
Atriplex tatarica L
Atriplex tatarica L. var. pamirica (Iljin)
G.L. Chu
Syn.: Atriplex pamirica Iljin
Atriplex verrucifera M. Bieb.
Syn.: Halimione verrucifera (M. Bieb.) Aellen
Bassia crassifolia (Pall.) Soldano
Syn.: Salsola stenoptera Wagenitz; Suaeda
crassifolia Pall.
Bassia dasyphylla (Fisch. & C.A. Mey.) Kuntze
Bassia eriophora (Schrad.) Asch.
Syn.: Kochia eriophora Schrader; Kochia latifo-
lia Fresen.; Londesia eriantha Fisch. & C.A.
Mey.
Bassia hyssopifolia (Pall.) Kuntze
S.A. Ghazanfar et al.
119
Bassia odontoptera (Schrenk) Freitag & G.
Kadereit
Syn.: Kochia odontoptera Schrenck; Kochia stel-
laris Moq.; Kochia iranica Litv. ex Bornm.
Bassia muricata (L.) Asch.
Syn.: Salsola muricata L.; Echinopsilon murica-
tus (L.) Moq.; Kochia muricata (L.) Schrad.
Bassia pilosa (Fisch. & C.A. Mey.) Freitag & G.
Kadereit
Syn.: Panderia pilosa Fisch. & C.A. Mey.
Bassia prostrata (L.) Beck
Syn.: Kochia prostrata (L.) Schrad.; Salsola
prostrata L.
Bassia scoparia (L.) A.J. Scott
Syn.: Kochia scoparia (L.) Schrad.
Bassia sedifolia (Pall.) ined.
Syn.: Bassia sedoides Asch. nom. illegit.
Bassia tomentosa (Lowe) Maire & Weiller
Syn.: Chenoleoides tomentosa (Lowe) Botsch
Beta vulgaris L.
Syn.: Beta maritima L.
Bienertia cycloptera Bunge ex Boiss.
Bienertia sinuspersici Akhani
Camphorosma monspeliaca L.
Syn.: Camphorosma ruthenica M. Bieb.
Camphorosma monspeliaca L. subsp. lessingii
(Litv.) Aellen
Syn.: Camphorosma lessingii Litw.
Caroxylon abarghuense (Assadi) Akhani &
Roalson
Syn.: Salsola abarghuense Assadi
Caroxylon canescens (Moq.) Akhani
Syn .: Noaea canescens Moq.; Salsola canescens
(Moq.) Boiss.
Caroxylon carpatha (P.H. Davis) Akhani
Syn.: Salsola carpatha P.H. Davis
Caroxylon chorassanicum (Botsch.) Akhani
Syn.: Salsola chorassanica Botsch.
Caroxylon cyclophyllum (Baker) Akhani
Syn.: Salsola cyclophylla Baker
Caroxylon dzhungaricum (Iljin) Akhani
Syn.: Salsola dzhungarica Iljin
Caroxylon imbricatum (Forsskal) Akhani
Syn.: Salsola imbricata Forssk. ; Salsola foetida
Del. ex Sprengel
Caroxylon incanescens (C.A. Mey.) Akhani
Syn.: Salsola incanescens C.A. Mey.; Salsola
ruthenica lljin
Caroxylon jordanicola (Eig) Akhani & Roalson
Syn.: Salsola jordanicola Eig
Caroxylon nitrarium (Pall.) Akhani & Roalson
Syn.: Salsola nitraria Pall.; Salsola macera Litv.
Caroxylon persicum (Bunge ex Boiss.) Akhani
& Roalson
Syn.: Salsola persica Bunge ex Boiss.
Caroxylon stenopterum (Wagenitz) Akhani &
Roalson
Syn.: Salsola stenoptera Wagenitz
Caroxylon tomentosum (Moq.) Tzvelev
Syn.: Salsola tomentosa (Moq.) Spach
Ceratocarpus arenarius L.
Syn.: Ceratocarpus turkestanicus Sav.-Rycz.
Chenopodium album L. subsp. album var.
album
Syn.: Chenopodium album var. microphyllum Boenn.
Chenopodium album L. subsp. iranicum Aellen
Chenopodium album L. subsp. album
v a r . microphyllum (Boenn.) Aellen
Chenopodium chenopodioides (L.) Aellen
Syn.: Blitum chenopodoides L.; Chenopodium
botryoides Sm.
Chenopodium fi cifolium Sm.
Chenopodium foliosum Asch.
Syn.: Blitum virgatum L.; Morocarpus foliosus
Moench
Chenopodium glaucum L.
Chenopodium murale L.
Chenopodium sosnowskyi Kapeller
Choriptera semhahensis (Vierh.) Botsch.
Syn.: Salsola semhahensis Vierh.
Climacoptera brachiata (Pall.) Botsch.
Climacoptera crassa (M. Bieb.) Botsch.
Climacoptera glaberrima Botsch.
Climacoptera iranica U.P. Pratov
Climacoptera iraqensis Botsch.
Climacoptera lanata (Pall.) Botsch.
Climacoptera longipistillata Botsch.
Climacoptera turcomanica (Litv.) Botsch.
Corispermum korovinii Iljin
Cornulaca aucheri Moq.
Syn.: Cornulaca leucacantha Charif & Aellen
Cornulaca ehrenbergii Asch.
Cornulaca monacantha Delile
Syn.: Cornulaca arabica Botsch.
Cyathobasis fruticulosa (Bunge) Aellen
Syn.: Girgensohnia fruticulosa Bunge
Halophytes of Southwest Asia
120
Dysphania ambrosioides (L.) Mosyakin &
Clemants
Syn.: Chenopodium ambrosioides L.
Dysphania botrys (L.) Mosyakin & Clemants
Syn.: Chenopodium botrys L.
Girgensohnia imbricata Bunge
Girgensohnia minima Korovin
Girgensohnia oppositifl ora (Pall.) Fenzl
Halimocnemis commixtus (Bunge) Akhani
Syn: Gamanthus commixtus Bunge
Halimocnemis gamocarpa Moq.
Syn.: Gamanthus gamocarpus (Moq.) Bunge
Halimocnemis longifolia Bunge
Halimocnemis occulta (Bunge) Hedge
Syn.: Halotis occulta Bunge
Halimocnemis pilifera Moq.
Syn.: Halotis pilifera Botsch
Halimocnemis pilosa Moq.
Syn.: Gamanthus pilosus (Pall.) Bunge;
Halimocnemis pilosa (Pall.) Akhani (later
homonym)
Halimocnemis purpurea Moq.
Syn.: Halanthium purpureum Bunge
Halimocnemis pycnantha K. Koch
Syn.: Halocharis kulpianum K. Koch;
Halanthium kulpianum (K. Koch) Bunge
Halimocnemis rarifolia (K. Koch.) Akhani
Syn.: Halanthium rarifolium K. Koch; Halanthium
roseum Iljin
Halocharis hispida (Schrenk ex C.A. Mey.)
Bunge
Halocharis sulphurea (Moq.) Moq.
Halocnemum strobilaceum (Pallas) M. Bieb
Syn.: Salicornia strobilacea Pallas
Halocnemum yurdakulolii Yaprak
Halogeton alopecuroides (Del.) Moq.
Syn.: Agathophora alopecuroides (Del.) Fenzl ex
Bunge var. alopecuroides ; Agathophora
algeriensis Botsch.; Agathophora alopecuroi-
des (Eig) Botsch.; Agathophora galalensis
Botsch.; Agathophora iraqensis Botsch.
Halogeton glomeratus (M. Bieb.) Ledeb.
Syn.: Anabasis glomerata M. Bieb.
Halogeton glomeratus (M. Bieb.) Ledeb. var.
tibeticus (Bunge) Grubov
Halopeplis nodulosa (Del.) Bunge ex
Ung.-Sternb.
Syn.: Halopeplis amplexicaulis (Vahl.) Bunge ex
Ung.-Sternb.; Salicornia amplexicaulis Vahl.
Halopeplis perfoliata (Forssk.) Bunge ex
Schweinf.
Syn.: Salicornia perfoliata Forssk.
Halopeplis pygmaea (Pall.) Bunge ex
Ung.-Sternb.
Halosarcia indica (Willd.) Paul G. Wilson
Halostachys caspica (M. Bieb.) C.A. Mey. ex
Schrenk.
Syn.: Arthrocnemum belangerianum Moq.;
Halostachys belangeriana (Moq.) Botsch
Halostachys caspica (Moq.) Moq. var. belan-
geriana ; S alicornia caspica Pall.
Halothamnus auriculus (C.A. Mey.) Botch.
subsp. acutifolius (Moq.) Kothe-Heinr.
Halothamnus glaucus (M. Bieb.) Botsch.
Syn.: Caroxylon glaucum (M. Bieb.) Moq.;
Salsola brachyphylla Boiss. & Hausskn.;
Salsola glauca M. Bieb.
Halothamnus iranicus Botsch.
Halothamnus subaphyllus (C.A. Mey.) Botsch.
Haloxylon ammodendron (C.A. Mey.) Bunge
ex Fenzl
Syn.: Haloxylon aphyllum (Minkw.) IIjin
Haloxylon griffi thii (Moq.) Boiss. subsp.
griffi thii
Syn.: Hammada griffi thii (Moq.) Iljin
Haloxylon griffi thii (Moq.) Boiss. subsp.
wakhanicum (Paulsen) Hedge
Haloxylon persicum Bunge ex Boiss. & Buhse
Haloxylon salicornicum (Moq.) Bunge ex
Boiss.
Syn.: Caroxylon salicornicum Moq.; Hammada
salicornica (Moq.) Iljin;
Haloxylon stocksii (Boiss.) Benth. & Hook. f.
Syn.: Haloxylon recurvum (Wall.) Bunge ex
Boiss.
Hammada scoparia (Pomel) Iljin.
Horaninovia ulicina Fisch. & C.A. Mey.
Kali australis (R.Br.) Akhani & Roalson
Syn .: Salsola kali L.; Salsola australis R.Br.
Kali griffi thi (Bunge) Akhani & Roalson
Syn.: Noaea griffi thii Bunge; Salsola griffi thii
(Bunge) Freitag & Akhani
Kali paulsenii (Litv.) Akhani
Syn.: Salsola paulsenii Litv.
Kali tamamschjanae (Iljin) Akhani & Roalson
Syn: Salsola tamamschjanae Iljin
Kali tragus (L.) Scop.
Syn: Salsola tragus L.
S.A. Ghazanfar et al.
121
Kalidium caspicum (L.) Ung.-Sternb.
Syn.: Salicornia caspia L.
Kalidium wagenitzii (Aellen) Freitag & G.
Kadereit
Syn.: Kalidiopsis wagenitzii Aellen
Kaviria rubescens (Franch.) Akhani
Syn.: Salsola rubescens Franch.; Salsola hadra-
mautica Baker; Salsola leucophylla Baker.
Kirilowia eriantha Bunge
Krascheninnikovia ceratoides (L.) Guldenst.
Lagenantha cycloptera (Stapf) M.G. Gilbert &
Friis
Syn.: Salsola cycloptera Stapf; Gyroptera cyclop-
tera (Stapf) Botsch .
Maireana coronata (J.M. Black) Paul G.
Wilson
Micronemum fastigiatum Ung.-Sternb.
Microcnemum coralloides (Loscos & Pardo)
Font-Quer subsp. anatolicum Wagenitz
Syn.: Micronemum fastigiatum Ung.-Sternb.;
Arthrocnemum corraloides (Loscos & Pardo)
Font-Quer
Nanophyton erinaceum (Pall.) Bunge
Noaea minuta Boiss. & Balansa
Noaea mucronata (Forssk.) Asch. & Schweinf.
Syn.: Noaea spinosissima (L. F.) Moq.; Salsola
mucronata Forssk.
Petrosimonia brachiata (Pall.) Bunge
Syn.: Polycnemum brachiatum Pall
Petrosimonia glaucescens (Bunge) Iljin
Syn.: Polycnemum glaucum Pall.
Petrosimonia nigdeensis Aellen
Petrosimonia squarrosa (Schrenk) Bunge
Syn.: Halocnemis squarrosa Schrenk
Pyankovia brachiata (Pall.) Akhani & Roalson
Syn.: Salsola brachiata Pall.
Salicornia bigelovii Torr.
Salicornia dolichostachya Moss
Syn.: Salicornia stricta D. König
Salicornia emerici Duval-Jouve
Salicornia iranica Akhani
Salicornia persica Akhani
Salicornia persica subsp.
rudshurensis Akhani
Salicornia perspolitana Akhani
Salicornia perennas Wild.
Syn.: Salicornia prostrata Pall.
Salicornia sinus-persica Akhani
Salicornia ramosissima J. Woods
Salicornia × tashkensis Akhani
Salsola arbusculiformis Drobov.
Salsola anatolica Aellen
Salsola baryosma (Schult.) Dandy
Syn.: Chenopodium baryosmon Roemer &
Schultes
Salsola crassa M. Bieb.
Salsola cyrenaica (Maire & Weiller) Brullo
subsp. antalyensis Freitag & H. Duman
Salsola dendroides Pall.
Syn.: Salsola verrucosa M. Bieb.
Salsola drummondii Ulbr.
Syn.: Salsola obpyrifolia Botsch & Akhani
Salsola ericoides M. Bieb
Salsola grandis Freitag, Vural & N. Adigüzel
Salsola foliosa (L.) Schrad. ex Schult.
Salsola kerneri (Wol.) Botsch.
Syn.: Hypocylix kerneri Wol.
Salsola laricina Pall.
Salsola leptoclada Gand.
Salsola makranica Freitag
Salsola montana Litv.
Syn.: Salsola masenderanica Botsch.
Salsola nodulosa (Moq.) Iljin
Syn.: Caroxylon nodulosum Moq.
Salsola orientalis S.G. Gmel.
Salsola praecox (Litv.) Iljin
Salsola rosmarinus (Ehrenb. ex Boiss.) Akhani
Syn: Seidlitzia rosmarinus Ehrenb. ex Boiss.
Salsola richteri (Moq.) Karel. ex Litv.
Salsola schweinfurthii Solms-Laub.
Syn.: Darniella schweinfurthii (Solms-Laub.)
Brullo;
Salsola sclerantha C.A. Mey
Salsola setifera (Moq.) Akhani
Syn.: Anabasis setifera Moq.
Salsola soda L.
Salsola turcica Yild.
Salsola turcomanica Litv.
Syn.: Salsola crassa subsp. turcomanica (Litv.)
Freitag
Salsola vermiculata L.
Salsola zygophylla Batt. & Trab.
Salsola zygophylloides (Aellen & Townsend)
Akhani
Syn.: Fadenia zygophylloides Aellen & Townsend
Sarcocornia fruticosa (L.) A.J. Scott
Syn.: Arthrocnemum fruticosum (L.) Moq.;
Salicornia europaea L. var. fruticosa ;
Halophytes of Southwest Asia
122
Salicornia fruticosa (L.) L.; Salicornia patula
Duval-Jouve
Sarcocornia perennis (Mill.) A.J. Scott
Syn.: Arthrocnemum perenne (Mill.) Moss ex
Fourcade; Salicornia perennis Mill.;
Salicornia radicans Sm.
Sarcocornia obclavata Yaprak
Seidlitzia fl orida (M. Bieb.) Bunge
Syn.: Anabasis fl orida M. Bieb.
Sevada schimperi Moq.
Syn.: Suaeda schimperi (Moq.) Martelli
Suaeda aegyptiaca (Hasselq.) Zohary
Syn.: Chenopodium aegyptiacum Hasselq.;
Schanginia aegyptiaca (Hasselq.) Aellen;
Suaeda maris-mortui Post; Schanginia bac-
cata (Forsskal ex Gmelin) Moq.; Suaeda
hortensis Forsskal ex Gmelin
Suaeda acuminata (C.A. Mey) Moq.
(incl. S. baccifera Pall., S. confusa Iljin &
S. pterantha (Kar. & Kir.) Bunge
Suaeda altissima (L.) Pall. ex J.F. Gmel.
Syn.: Chenopodium altissimum L.
Suaeda arcuata Bunge
Suaeda carnosissima Post
Suaeda corniculata (C.A. Mey.) Bunge var.
olufsenii (Paulsen) G.L. Chu
Syn.: Suaeda olufensii Paulsen
Suaeda cucullata Aellen
Suaeda dendroides (C.A. May.) Moq.
Suaeda eltonica Iljin
Suaeda fruticosa Forssk. ex J.F. Gmel.
Syn: Suaeda baluchestanica Akhani & Podlech
Suaeda gracilis Moq.
Suaeda heterophylla Bunge ex Boiss.
Suaeda linifolia Pall. Ex J.F. Gmel.
Suaeda maritima (L.) Dumort
Syn.: Chenopodium maritimum L.; Suaeda
prostrata Pall; Suaeda indica Willd.; Kochia
indica Wight
Suaeda microphylla Pall.
Suaeda monoica Forssk. ex J.F. Gmel.
Suaeda moschata A.J. Scott
Suaeda physophora Pall.
Suaeda prostrata Pall. subsp. anatolica Aellen
Suaeda splendens (Pourr.) Gren. & Godr.
Syn.: Chenopodium setigerum DC.; Salsola
splendens Pourr.; Suaeda setigera (DC.)
Moq.
Suaeda vermiculata Forssk. ex J. F. Gmel.
Syn.: Suaeda pruinosa Willk. & Lange
Suaeda vermiculata Forssk. ex J. F. Gmel. var.
puberula C.B. Clarke
Traganum nudatum Delile
Xylosalsola arbuscula (Pall.) Tzvelev.
Syn.: Salsola arbuscula Pall.
CISTACEAE
Helianthemum ledifolium (L.) Miller var.
mucrocarpum Willk.
COMBRETACEAE
Conocarpus lancifolius Engl. & Diels
CONVOLVULACEAE
Cressa cretica L.
Evolvulus alsinoides (L.) L.
Ipomoea alba L.
Ipomoea fi stulosa Mart. ex Choisy
Ipomoea pes-caprae Roth
CYMODOCEACEAE
Halodule uninervis (Forssk.) Boiss.
Halodule wrightii Asch.
Syringodium isoetifolium (Asch.) Dandy
Thalassodendron ciliatum (Forssk.) Hartog
CYNOMORIACEAE
Cynomorium coccineum L.
CYPERACEAE
Blysmus rufus (Huds.) Link.
Bolboschoenus glaucus (Lam.) S.G. Sm.
Bolboschoenus maritimus (L.) Palla var.
maritimus
Syn.: Scirpus maritimus L.
Bolboschoenus maritimus (L.) Palla var. affi nis
(Roth) T. Koyama
Carex capitellata Boiss. & Bal.
Carex diluta M. Bieb.
Carex distans L.
Carex divisa Huds.
Carex extensa Good.
Carex heterostachya Bunge
Carex medwedewii Leskov
Syn.: Carex atrata Boiss.; Carex kukkonenii
O. Nilsson
S.A. Ghazanfar et al.
123
Carex stenophylla Wahlenb. subsp. stenophyl-
loides (V.I. Krecz.) T.V. Egorova
Carex vesicaria L.
Cladium mariscus (L.) Pohl
Syn.: Schoenus mariscus L.; Mariscus cladium
Kuntze;
Cyperus noeanus Boiss.
Cyperus alopecuroides Rottb.
Cyperus arenarius Retz.
Cyperus atkinsonii C.B. Clarke
Cyperus aucheri Jaub. & Spach
Cyperus bulbosus Vahl
Cyperus capitatus Vandelli
Syn.: Cyperus schoenoides Griseb.; Galilaea
mucronata (L.) Parl.
Cyperus conglomeratus Rottb. subsp.
conglomeratus
Cyperus conglomeratus Rottb. subsp. curvulus
(Boeckeler) Kukkonen
Cyperus conglomeratus Rottb. subsp. pachyr-
rhizus (Nees) T. Koyama
Cyperus laevigatus L.
Cyperus longus L.
Syn.: Cyperus longus subsp. badius (Desf.)
Murb; Pycreus longus (L.) Hayek
Cyperus malaccensis Lam.
Cyperus niveus Retz.
Cyperus pangorei Rottb.
Cyperus rotundus L.
Cyperus stoloniferus Retz.
Eleocharis mitracarpa Steudel
Syn.: Eleocharis argyrolepidoides Zinserl.
Eleocharis palustris (L.) Roemer & Schultes
Syn.: Eleocharis crassa Fisch. & Mey. ex A.
Becker; Eleocharis crassa Fisch. & Mey. ex
A. Becker var. glaucescens Zinserl.;
Eleocharis gracilis Hayek non R. Br.(1810);
Eleocharis intersita Zinserl.; Eleocharis
palustris (L.) Roemer & Schultes subsp.
microcarpa Walters; Eleocharis palustris (L.)
Roemer & Schultes var. communis Schmalh.
f. eupalustris (Lindb. fi l.) Krylov; Eleocharis
palustris (L.) Roemer & Schultes var. eupalus-
tris (Lindb. fi l.) Syreish.; Eleocharis palustris
(L.) Roemer & Schultes var. gracilis
Suesseng . ; Heleocharis eupaluster Lindb.f.;
Scirpus palustris L .
Eleocharis quinquefl ora (Hartmann) O. Schwarz
Eleocharis uniglumis (Link.) Schult.
Fimbristylis complanata (Retz.) Link
Fimbristylis cymosa R.Br.
Cyperus pannonicus Jacq .
Syn.: Acorellus pannonicus (Jacq.) Palla;
Juncellus pannonicus (Jacq.) C.B. Clarke
Schoenoplectus lacustris (Schrad.) Palla subsp.
hippolyti (V.I. Krecz.) Kukkonen
Syn.: Schoenoplectus tabernaemontani (C.C.
Gmel.) Palla; Scirpus glaucus Sm. Non Lam.
(179I); Scirpus lacustris L. subsp. glaucus
(Sm.) Hartman; Scirpus lacustris L. subsp.
tabernamontanae (C.C. Gmelin) Syme;
Scirpus lacustris L. var. digynus Godron;
Scirpus lacustris L. var. tabernaemontani
(C.C. Gmelin) Doll
Schoenoplectus litoralis (Schrad.) Palla
Syn.: Heleogiton litorale (Schrad.) Rchb.;
Scirpus aegyptiacus Decne.; Scirpus litoralis
Schrad.
Schoenoplectus triqueter (L.) Palla
Schoenus nigricans L.
Syn.: Chaetospora nigricans (L.) Kunth
Scirpoides holoschoenus (L.) Sojak
Syn.: Holoschoenus australis (Murray) Reichb.;
Holoschoenus romanus (L.) Fritsch;
Holoschoenus vulgaris Link; Holoschoenus
vulgaris Link subsp. australis (Murray)
Hayek; Holoschoenus vulgaris Link subsp.
eu-vulgaris Hayek; Isolepis holoschoenus (L.)
Roemer & Schultes; Scirpus australis Murray;
Scirpus holoschoenus L.; Scirpus holoschoe-
nus L. var. australis (Murray) W.D.J. Koch;
Scirpus holoschoenus L. var. genuinus Boiss.;
Scirpus holoschoenus L. var. romanus (L.)
W.D.J. Koch; Scirpus romanus L.; Scirpus
tabernaemontani C.C. Gmelin; Scirpus uligi-
nosus Kar. & Kir.
ELATINACEAE
Bergia aestivosa (Wight) Steud.
Bergia ammannioides Roxb. ex Roth.
EUPHORBIACEAE
Andrachne telephioides L.
Euphorbia boissieriana (Woronow) Prokh.
Euphorbia falcata L. subsp. falcata var.
falcata
Halophytes of Southwest Asia
124
Syn.: Euphorbia falcata L. var. falciformis Griseb.;
Euphorbia falcata L. var. rubra (Cav.) Boiss.
Euphorbia granulata Forssk.
Euphorbia hirsuta L.
Syn.: Euphorbia pubescens Vahl
Euphorbia indica Lam.
Euphorbia macroclada Boiss.
Syn.: Euphorbia macroclada Boiss. var. aceras
Hand.-Mazz.; Euphorbia schizoceras Boiss.
& Hohen.; Euphorbia syspirensis C. Koch;
Euphorbia tinctoria Boiss. & Huet ex Boiss.
Euphorbia paralias L.
Euphorbia repens K. Koch
Euphorbia thymifolia L.
Euphorbia verrucosa L.
FRANKENIACEAE
Frankenia hirsuta L.
Syn.: Frankenia hispida DC.; Frankenia interme-
dia DC.; Frankenia revoluta Forssk.
Frankenia pulverulenta L .
Frankenia salsuginea Adilguzel & Aytac
Hypericopsis persica Boiss.
GENTIANACEAE
Blackstonia perfoliata (L.) Hudson subsp.
serotina (W. Koch ex Reichb.) Vollmann
Syn.: Chlora acuminata W. Koch & Ziz.; Chlora
serotina W. Koch ex Reichb.
Blackstonia perfoliata (L.) Hudson subsp.
perfoliata
Syn.: Chlora perfoliata (L.)L.; Gentiana per-
foliata L.
Centaurium erythraea Rafn subsp. erythraea
Syn.: Erythraea centaurium Boiss.
Centaurium pulchellum (Swartz) Druce
Syn.: Erythraea anatolica C. Koch; Erythraea
caspica Fischer; Erythraea pulchella (Swartz)
Fries; Erythraea ramosissima (Viii.) Pers.;
Gentiana pulchella Swartz
Centaurium spicatum (L.) Fritsch
Centaurium tenuifl orum (Hotfmanns. & Link)
Fritsch subsp. tenuifl orum
Enicostema axillare (Poir. ex Lam.) A. Raynal
GOODENIACEAE
Scaevola plumieri (L.) Vahl.
Scaevola taccada (Gaertn.) Roxb.
GUTTIFERAE
Hypericum salsugineum Rabson & Hub.-Mor.
HYDROCHARITACEAE
Halophila ovalis (R.Br.) Hook f.
Halophila stipulacea (Forssk.) Asch.
Thalassia hemprechii (Ehrenb. ex Solms.) Asch.
IRIDACEAE
Gladiolus halophilus Boiss. & Heldr.
Gladiolus italicus Mill.
Iris orientalis Miller
Syn.: Iris longipedicellata Czecz.
Iris paradoxa Steven
Iris spuria L. subsp. musulmanica (Fomin)
Takht.
JUNCACEAE
Juncus acutus L.
Juncus articulatus L.
Juncus bufonius L.
Juncus fontanesii J. Gay apud Laharpe subsp.
pyramidatus (Laharpe) Snog.
Syn.: Juncus camptotropus V. Krecz.; Juncus
pyramidatus Laharpe
Juncus persicus Boiss. subsp. libanoticus
(Thieb.) Snog.
Syn.: Juncus gerardii Loisel. subsp. libanoticus
(Thieb.) Snog.
Juncus gerardii Loisel.
Syn.: Juncus libanoticus Thieb.
Juncus heldreichianus Marsson ex Parl. subsp.
heldreichianus
Juncus heldreichianus Marsson ex Parl. subsp.
orientalis Snog.
Juncus littoralis C.A. Meyer
Syn.: Juncus acutus L. subsp. tyraicus Paczoski;
Juncus tommasinii Parl.; Juncus tyraicus
(Paczoski) V. Krecz. & Gontsch.
Juncus maritimus Lam.
Juncus punctorius L.f.
Juncus rigidus Desf.
Juncus subnodulosus Schrank
Syn.: Juncus nodosus Weber non L.(1762);
Juncus obtusifl orus Ehrh. ex Hoffm.; Juncus
sylvaticus Reichard non Hudson(1762)
Juncus subulatus Forssk.
Syn.: Juncus multifl orus Desf.
S.A. Ghazanfar et al.
125
JUNCAGINACEAE
Triglochin bulbosa L. subsp. barrelieri (Loisel.)
Rouy
Syn.: Triglochin barrelieri Loisel.
Triglochin maritima L.
Syn.: Triglochin ani C. Koch
Triglochin palustris L.
LAMIACEAE
Mentha aquatica L.
Syn.: Mentha hirsuta Hudson; Mentha stricta L.
var. stricta C. Koch in
Phlomis armeniaca Willd.
Syn.: Phlomis linearis Boiss. & Bal. subsp. anti-
cragi P.H. Davis; Phlomis nympharum O.
Schwarz
Salvia syriaca L.
Salvia halophila Hedge
Salvia staminea Montbret & Aucher ex
Bentham
Syn.: Salvia armeniaca (Bordz.) Grossh.; Salvia
staminea Montbret & Aucher ex Bentham
subsp. armeniaca Bordz.; Salvia staminea
Montbret & Aucher ex Bentham var. latifolia
Bornm.; Salvia staminea Montbret & Aucher
ex Bentham var. persica Bornm.; Salvia trans-
caucasica Pobed.
Scutellaria orientalis L. subsp. orientalis
Syn.: Scutellaria caucasica A. Ham.; Scutellaria
taurica Juz.
Teucrium polium L.
Teucrium scordium L. subsp. scordioides
(Schreber) Maire & Petitmengin
Syn.: Teucrium lanuginosum Hoffmanns. &
Link; Teucrium petkovii Urumov; Teucrium
scordioides Schreber
LEGUMINOSAE: CAESALPINIOIDEA
Caesalpinia bonduc (L.) Roxb.
Senna italica Mill.
LEGUMINOSAE: MIMOSIOIDEAE
Acacia leucophloea (Roxb.) Willd.
Acacia nilotica (L.) Delile subsp. nilotica
Acacia sphaerocephala Schltdl. & Cham.
Acacia tortilis (Forssk.) Hayne
Syn.: Acacia raddiana Savi
Prosopis cineraria (L.) Druce
Prosopis farcta (Banks & Sol.) J.F. Macbr.
Prosopis julifl ora (Sw.) DC.
Prosopis koelziana Burk.
LEGUMINOSAE: PAPILIONOIDEAE
Aeschynomene indica L.
Alhagi graecorum Boiss.
Syn.: Alhagi maurorum Medik.
Alhagi pseudalhagi (M. Bieb.) Desv.
Astragalus ovalis Boiss. & Ball.
Astragalus shelkovnikovii Grossh.
Astragalus tribuloides Delile
Syn.: Astragalus kirghisicus Schtschegleev;
Oxyglottis tribuloides (Delile) Nevski
Astragalus vogelii (Webb) Bornm.
Crotalaria persica (Burm. f.) Merr.
Crotalaria saltiana T. Anders
Dalbergia sissoo DC.
Dorycnium strictum (Fisch. & Mey.) Lassen
Syn.: Lotus albus Janka; Lotus strictus Fisch. &
Mey.; Lotus strictus Fisch. & Mey. var. rotun-
difolius Boiss.; Lotus thermalis Boiss.
Erythrina herbacea L.
Indigofera argentea Burm. f.
Indigofera cordifolia Roth
Indigofera intricata Boiss.
Indigofera linifolia (L.f.) Retz.
Indigofera oblongifolia Forsk.
Lespedeza juncea (Linn.f.) Pers. var. sericea
(Thunb.) Lace & Hauech
Lotus corniculatus L. var. tenuifolius L.
Lotus garcinii DC.
Syn.: Lotus stocksii Boiss.
Lotus halophilus Boiss. & Spruner
Syn.: Lotus villosus Forssk.
Macroptilium lathyroides (L.) Urb.
Medicago lupulina L.
Medicago minima (L.) Bart. var. minima
Medicago falcata L.
Melilotus indicus (L.) All.
Syn.: Melilotus indica (L.)
Melilotus messanensis (L.) All.
Syn.: Trifolium messanense L.
Melilotus offi cinalis (L.) Desr.
Syn.: Trifolium offi cinalis L.
Pongamia pinnata (L.) Merrill
Prosopis farcta (Banks & Sol.)
Sesbania grandifl ora (L.) Pers.
Halophytes of Southwest Asia
126
Sesbania sesban (L.) Merr.
Sophora alopecuroides L. var. alopecuroides
Syn.: Goebelia alopecuroides (L.) Bunge
Sphaerophysa kotschyana Boiss.
Taverniera cuneifolia (Roth) Arn.
Taverniera spartea (Burm. f.) DC.
Tephrosia apollinea (Delile) DC.
Tephrosia purpurea (L.) Pers.
Lotus maritimus L.
Syn.: Lotus siliquosus L.;
Trifolium fragiferum L.
Trifolium repens L
Trifolium resupinatum L.
Trifolium tomentosum L.
Medicago orthoceras (Kar. & Kir.) Trautv.
Syn.: Trigonella orthoceras Kar. & Kir.;
Trigonella orthoceras Kar. & Kir. var. anatol-
ica (Boiss. & Bal.) Boiss.; Trigonella poly-
cerata M. Bieb. non L.
Vicia sativa L.
Vigna trilobata (L.) Verdc.
LILIACEAE
Allium cupani Rafi n. subsp. hirtovaginatum
(Kunth) Stearn
Syn.: Allium hirtovaginatum Kunth; Allium
moschatum d'Urv. non L.(1753)
Allium macrochaetum Boiss. & Hausskn.
subsp. macrochaetum
Syn.: Allium laeve Wendelbo & von Bothmer
Allium nevsehirense Koyuncu & Kollmann
Allium sieheanum (Hausskn. ex) Kollmann
Allium scabrifl orum Boiss.
Syn.: Allium vuralii Kit Tan
Asparagus gharoensis Blatt.
Asparagus lycaonicus P. H. Davis
Asparagus persicus Baker
Syn.: Asparagus leptophyllus Schischkin;
Asparagus oligophyllus Baker
Dipcadi bifl orum Ghaz.
Drimia indica (Roxb.) Jessop
LINACEAE
Linum bienne Miller
Syn.: Linum angustifolium Hud.
Linum seljukorum Davis
LYTHRACEAE
Lythrum salicaria L.
Syn.: Lythrum cinereum Gris.; Lythrum tomento-
sum DC.
MALVACEAE
Alcea calvertii (Boiss.) Boiss.
Syn.: Althaea calvertii Boiss.
Gossypium stocksii Mast.
Thespesia populneoides (Roxb.) Kostel.
MOLLUGINACEAE
Glinus lotoides L.
MORACEAE
Ficus microcarpa L.f.
MYRSINACEAE
Aegiceras corniculatum (L.) Blanco
Ardisia solanacea (Poir.) Roxb.
NAJADACEAE
Najas graminea Delile
Najas marina L.
Najas minor All.
NYCTAGINACEAE
Pisonia grandis R.Br.
ORCHIDACEAE
Epipactis palustris (L.) Crantz
Orchis palustris Jacq.
Syn.: Orchis elegans Heuffel; Orchis laxifl ora
Lam. subsp. dielsianus Soo; Orchis laxifl ora
Lam. subsp. paluster (Jacq.) Aschers. &
Graebn; Orchis laxifl ora Lam. subsp. palus-
tris (Jacq.) Bonnier & Layens; Orchis pseu-
dolaxifl ora Czernjak.
OROBANCHACEAE
Cistanche salsa (C. A. Mey.) Beck
Cistanche tubulosa (Schenk) Wight
The generic name Phelypaea is unresolved.
PANDANACEAE
Pandanus odorifer (Forssk.) Kuntze
S.A. Ghazanfar et al.
127
PEDALIACEAE
Pedalium murex L.
PLANTAGINACEAE
Bacopa monnieri (L.) Wettst. (formerly in
Scrophulariaceae)
Plantago coronopus L. subsp. coronopus
Plantago coronopus L. subsp. commutata
(Guss.) Pilger
Syn.: Plantago commutata Guss.;
Plantago lanceolata L.
Plantago major L. subsp. intermedia (Gilib.)
Lange
Syn.: Plantago intermedia Glib.; Plantago major
L. subsp. pleiosperma Pilger
Plantago maritima L.
Plantago scabra Moench
Syn.: Plantago arenaria Waldst. & Kit.; Plantago
indica L.; Plantago psyllium L. non L.(1759)
nee L.(1762) nom. ambig; Plantago ramosa
Ascherson
PLUMBAGINACEAE
Acantholimon halophilum Bokhari
Limonium axillare (Forssk.) Kuntze
Syn.: Statice axillaris Forssk.
Limonium carnosum (Boiss.) O. Kuntze
Limonium cylindrifolium Verdc.
Limonium gmelinii (Willd.) Kuntze
Syn.: Limonium hirsuticalyx Pignatti; Limonium
pycnanthum (C. Koch) Kuntze; Statice gmelini
Willd.; Statice
pychnantha C. Koch
Limonium graceum (Poiret) Rech.f.
Syn.: Statice graeca Poiret; Statice prolifera
d'Urv.; Statice rorida Sibth. & Sm.
Limonium iconicum Kuntze
Limonium milleri Ghaz. & J.R. Edm.
Limonium sarcophyllum Ghaz. & J.R. Edm.
Limonium sinuatum (L.) Miller
Syn.: Statice sinuata L.
Limonium stocksii Kuntze
Limonium suffruticosum (L.) Kuntze
Limonium perfoliatum (Kar. ex Boiss.)
Kuntze
Psylliostachys spicata (Willd.) Nevski
POACEAE
Aeluropus lagopoides (L.) Thwaites
Syn.: Aeluropus littoralis (Gouan) Parl. var.
repens (Desf.) Casson & Dur.; Aeluropus
massauensis (Fresen.) Mattei;
Aeluropus littoralis (Gouan) Parl.
Syn.: Aeluropus intermedius Regel; Aeluropus
laevis Trin. var. dasyphyllum Trautv.;
Aeluropus littoralis (Gouan) Parl. subsp.
intermedius (Regel) Tzvelev; Aeluropus litto-
ralis (Gouan) Parl. subsp. kuschkensis
Tzvelev; Aeluropus littoralis (Gouan) Parl.
subsp. pungens (M. Bieb.) Tzvelev; Aeluropus
pungens (M. Bieb.) C. Koch; Calotheca litto-
ralis (Gouan) Sprengel; Dactylis littoralis
(Gouan) Willd.; Poa littoralis Gouan
Aeluropus macrostachyus Hack.
Agrostis stolonifera L.
Aira elegantissima Schur var. elegantissima
Syn.: Aira capillaris Host; Fussia capillaris
(Host) Schur var. elegantissima (Schur) Schur
Alopecurus myosuroides Hudson var.
myosuroides
Syn.: Aira agrestis L.
Alopecurus myosuroides Hudson var. latialatus
M. Dogan
Ammophila arenaria (L.) Link subsp. arundi-
naea H. Lindb.fi l.
Syn.: Arundo arenaria L.; Psamma arenaria (L.)
Roemer & Schultes
Apera intermedia Hackel
Syn.: Apera spica-venti (L.) P. Beauv. subsp.
intermedia (Hackel) Hackel ex Bornm.
Aristida abnormis Chiov.
Aristida adscensionis L.
Aristida mutabilis Trin. & Rupr.
Arundo donax L.
Bromus arvensis L.
Bromus inermis Leyss.
Syn.: Zerna inermis (Leyss.) Lindm.
Bromus rubens L.
Bromus tectorum L.
Calamagrostis pseudophragmites (Haller fi l.)
Koeler
Syn.: Arundo glauca M. Bieb.; Arundo pseudo-
phragmites Haller fi l.; Calamagrostis littorea
Halophytes of Southwest Asia
128
(Schrader) P. Beauv. var . persica (Boiss.)
Boiss.; Calamagrostis persica Boiss.
Catabrosa aquatica (L.) P. Beauv.
Cenchrus bifl orus Roxb.
Cenchrus ciliaris L.
Cenchrus pennisetiformis Steud.
Chloris gayana Kunth
Chloris quinquesetica Bhide
Chloris virgata Sw.
Coelachyrum piercei (Benth.) Bor
Crypsis aculeata (L.) Aiton
Crypsis faktorovskyi Eig
Syn.: Heleochloa faktorovskyi (Eig) Pilger
Cynodon dactylon (L.) Pers. var. dactylon
Syn.: Panicum dactylon L.
Cynodon dactylon (L.) Pers. var. villosus Regel
Syn.: Cynodon dactylon (L.) Pers. var. villosum
Roshev. ex Grossh.
Dactyloctenium aegyptium (L.) Willd.
Dactyloctenium aristatum Link
Dactyloctenium scindicum Boiss.
Desmostachya bipinnata (L.) Stapf
Dichanthium annulatum (Forssk.) Stapf
Digitaria longifl ora (Retz.) Pers.
Echinochloa colona (L.) Link
Eleusine indica (L.) Gaertn.
Elymus elongatus (Host) Runemark
Syn.: Triticum obtusifl orum DC.; Triticum ponti-
cum Podp.
Elymus farctus Viv.Runemark ex Melderis
Syn.: Agropyron junceum (L.) P. Beauv.; Elytrigia
juncea (L.) Nevski subsp. juncea ; Triticum
farctum Viv.; Triticum junceum L.
Elymus hispidus (Opiz) Melderis subsp.
hispidus
Syn.: Agropyron glaucum (Desf. ex DC.) Roemer
& Schultes; Agropyron hispidum Opiz;
Agropyron laevifolium Opiz; Agropyron latro-
num (Godron) Cand.; Agropyron validum
Opiz; Elytrigia intermedia (Host) Nevski;
Triticum glaucum Desf.; Triticum interme-
dium Host; Triticum latronum Godron;
Triticum truncatum Wallr.
Eragrostis collina Trin.
Syn.: Eragrostis arundinacea (L.) Roshev.;
Eragrostis tatarica (Fischer ex Griseb.)
Nevski; Poa tatarica Fischer ex Bess.
Eragrostis curvula (Schrad.) Nees
Eragrostis japonica (Thunb.) Trin.
Eragrostis superba Peyr.
Syn.: Aira aquatica L.
Festuca arundinacea Schreber subsp.
arundinacea
Syn.: Festuca elatior L. subsp. arundinacea
(Schreber) Hackel
Festuca rubra L.
Halopyrum mucronatum (L.) Stapf
Holcus lanatus L.
Hordeum bogdanii Wilensky
Hordeum brevisubulatum (Trin.) Link
Hordeum marinum Huds.
Imperata cylindrica (L.) Raeusch.
Lagurus ovatus L.
Lasiurus scindicus Henrard
Leptochloa fusca (L.) Kunth
Leymus cappadocicus (Boiss. et Bal.) Melderis
Syn.: Elymus cappadocicus Boiss. & Bal.
Leymus secalinus (Georgi) Tzvelev
Lolium rigidum Gaudin
Syn.: Lolium subulatum Vis.
Lolium multifl orum Lam.
Molinia caerulea (L.) Moench
Syn.: Aira caerulea L.
Ochthochloa compressa (Forssk.) Hilu
Panicum antidotale Retz.
Panicum turgidum Forssk.
Parapholis fi liformis (Roth) C.E. Hubbard
Syn.: Lepturus fi liformis (Roth) Trin.; Ophiurus
liformis (Roth) Roemer & Schultes;
Pholiurus fi liformis (Roth) Schinz & Thell.;
Rottboellia erecta Savi; Rottboellia fi liformis
Roth; Rottboellia incurvata (L.) L. fi l.
Parapholis incurva (L.) C.E. Hubbard
Syn.: Aegilops incurva L.; Aegilops incurvata L.;
Lepturus incurvatus (L.) Trin.; Lepturus
incurvatus (L.) Trin. subsp. curvatissimus
(Aschers. & Graebn.) Rouy; Pholiurus incur-
vatus (L.) Hitchc.
Paspalidium desertorum (A. Rich.) Staph
Paspalum distichum L.
Paspalum vaginatum Sw.
Phalaris arundinacea L.
Syn.: Digraphis arundinaceae (L.) Trin.;
Phalaroides arundinaceae (L.) Rauschaert;
Typhoides arundinaceae (L.) Moench
Phalaris canariensis L.
S.A. Ghazanfar et al.
129
Phalaris minor Retz.
Phleum exaratum Hochst. ex Griseb. subsp.
exaratum
Syn.: Phleum arenarium L. var. breviglume
Bornm.; Phleum cornutum Mez; Phleum
graecum Boiss. & Heldr. ex Boiss.
Phragmites australis (Cav.) Trin. ex Steud.
Phragmites karka (Retz.) Trin. ex Steud.
Poa annua L.
Poa bulbosa L.
Poa pratensis L.
Poa trivialis L.
Polypogon maritimus Willd. subsp. maritimus
Syn.: Polypogon monspeliensis (L.) Desf. var.
maritimus (Willd.) Casson & Durieu
Polypogon monspeliensis (L.) Desf.
Syn.: Alopecurus monspeliensis L.
Porteresia coarctata (Roxb.) Tateoka
Puccinellia bulbosa (Grossh.) Grossh. subsp.
caesarea Kit Tan
Puccinellia bulbosa (Grossh.) Grossh. subsp.
bulbosa (Grossh.) Grossh.
Syn.: Atropis bulbosa Grossh.; Puccinellia
gigantea (Grossh.) Tzvelev subsp. bulbosa
Puccinellia convoluta (Hornem.) Fourr.
Syn.: Atropis convoluta (Hornem.) Griseb.;
Festuca convoluta (Hornem.) Kunth; Glyceria
convoluta (Hornem.) Fries; Glyceria distans
(L.) Wahlenb. var. convulata (Hornem.) Regel
non Boiss. ex Hooker fi l.(1896); Poa con-
voluta Hornem. non Hartm. ex Reichb.(1830);
Puccinellia anisoclada V. Krecz.; Puccinellia
festuciformis (Host) Parl. subsp. convoluta
(Hornem.) W.E. Hughes; Puccunellia con-
voluta (Hornem.) Hayek
Puccinellia distans (Jacq.) Parl. subsp. distans
(Jacq.) Parl.
Syn.: Atropis distans (Jacq.) Griseb.; Glyceria
distans (Jacq.) Wahlenb.; Poa distans Jacq.;
Puccinellia pseudoconvoluta Klokov
Puccinellia festuciformis (Host) Parl.
Syn.: Atropis festucaeformis (Host) K. Richter;
Festuca hostii Kunth non Schott. ex Roemer
& Schultes(1817); Festuca palustris Seenus;
Glyceria convulata (Hornem.) Fries subsp.
festucaeformis (Host) Douin; Glyceria festu-
caeformis (Host) Heynh. ex Reichb.; Poa fes-
tuciformis Host; Puccinellia palustris
(Seenus) Podp. non(Seenus) Grossh.(1928);
Puccinellia palustris (Seenus) Podp. subsp.
festucaeformis (Host) Maire
Puccinellia gigantea (Grossh.) Grossh.
Syn.: Puccinellia anisoclada (V.I. Krecz.) V.I.
Krecz. subsp. melderisiana Kit Tan
Puccinellia intermedia (Schur) Janch.
Syn.: Atropis festucaeformis (Schur) Hack. var.
intermedia (Schur) Hackel; Atropis interme-
dia Schur; Puccinellia festuciformis (Host)
Parl. subsp. intermedia (Schur) W.E. Hughes
Puccinellia koeieana Melderis subsp. anatolica
Kit Tan
Rostraria cristata (L.) Tzvelev var. cristata
Syn.: Festuca cristata L.
Sacchraum bengalense Retz.
Sacchraum spontaneum L.
Setaria viridis (L.) P. Beauv.
Sphenopus divaricatus (Gouan) Rchb.
Sporobolus coromandelianus (Retz.) Kunth
Sporobolus helvolus (Trin.) Durand & Schinz
Sporobolus ioclados (Nees ex Trin.) Nees
Syn.: Sporobolus arabicus Boiss.; Sporobolus
jemenicus Pilg. ex Schwartz; Sporobolus ken-
trophyllus (K. Schum.) Clayton; Sporobolus
marginatus Hochst. ex A. Rich.
Sporobolus robustus Kunth.
Sporobolus tourneuxii Coss.
Sporobolus virginicus (L.) Kunth
Syn.: Agrostis arenaria Gouan; Agrostis conge-
ner Schumach.; Agrostis virginica Forssk.;
Sporobolus arenarius (Gouan) Duval-Jouve;
Sporobolus confertus J. A. Schmidt;
Sporobolus pungens (Shreb.) Kunth
Sporobolus spicatus (Vahl) Kunth
Stipa himalaica Roshev.
Stipa splendens Trin.
Urochondra setulosa (Trin.) C.E. Hubb.
POLYGONACEAE
Atraphaxis spinosa L.
Persicaria vivipara (L.) Ronse Decr.
Polygonum arenastrum Bor.
Syn.: Polygonum aequale Lindm.; Polygonum
aviculare subsp. aequale (Lindm.) Asch. &
Graebn.
Polygonum aviculare L.
Syn.: Polygonum heterophyllum Lindman
Halophytes of Southwest Asia
130
Polygonum bellardii All.
Polygonum effusum Meisn.
Polygonum maritimum L.
Polygonum plebeium R.Br.
Polygonum sibiricum Laxm. var. thomsonii
Meisn.
Rumex vesicarius L.
PORTULACACEAE
Portulaca oleracea L.
Portulaca quadrifi da L.
PRIMULACEAE
Anagallis arvensis L. var. arvensis
Glaux maritima L.
Lysimachia maritima (L.) Galasso, Banfi &
Soldano
Primula algida Weber & Mohr
Syn.: Primula hookeri Freyn & Sint.
Samolus valerandi L.
RANUNCULACEAE
Consolida anthoroidea (Boiss.) Schrod.
Nigella turcica Dönmez & Mutlu
Pseudodelphinium turcicum H. Duman, Vural,
Aytaç & Adıgüzel
Ranunculus marginatus d'Urv. var. marginatus
Thalictrum lucidum L.
Thalictrum simplex L.
RESEDACEAE
Oligomeris linifolia (Vahl) J.F. Macbr.
RHAMNACEAE
Zizyphus nummularia (Burm. f.) Wight & Arn.
RHIZOPHORACEAE
Bruguiera gymnorrhiza (L.) Lam.
Ceriops tagal (Perr.) C.B. Rob.
Rhizophora mucronata Lam.
ROSACEAE
Potentilla anserina L.
Potentilla bifurca L. subsp. orientalis (Juz.)
Sojak
Potentilla reptans Laicharding
Syn.: Potentilla nemoralis Nestler; Potentilla
procumbens Sibth.
Potentilla supina L.
RUBIACEAE
Cruciata taurica (Pallas ex Willd.) Ehrend.
Syn.: Valantia taurica Pallas ex Willd.
Galium verum L.
RUPPIACEAE
Ruppia maritima L.
SALICACEAE
Populus euphratica Olivier
SANTALACEAE
Thesium compressum Boiss. & Heldr.
SCROPHULARIACEAE
Scrophularia bicolor Sibht. & Sm.
Verbascum helianthemoides Hub.-Mor.
Verbascum pyroliforme Kuntze
Verbascum sinuatum L.
SOLANACEAE
Lycium depressum Stocks
Lycium ruthenicum Murray
Lycium shawii Roem. & Schult.
Solanum incanum L.
Solanum virginianum L.
Withania somnifera (L.) Dunal
SONNERATIACEAE
Sonneratia caseolaris (L.) Engl.
STERCULACEAE
Melhania denhamii R.Br.
TAMARICACEAE
Reaumuria alternifolia Britten
Syn.: Hypericum alternifolium Labill.; Reumuria
cistoides Adam; Reumuria hypericoides
Willd.
Reaumuria fruticosa Boiss.
Tamarix androssowii Litv. subsp. androssowii
Tamarix aphylla (L.) H. Karst.
Tamarix aralensis Bunge
Tamarix arceuthoides Bunge
Tamarix gallica L. var. indica (Willd.) Ehrenb.
Tamarix hampeana Boiss. & Heldr.
Tamarix hispida Willd.
Tamarix kermanensis Baum.
Tamarix karelinii Bunge
S.A. Ghazanfar et al.
131
Tamarix kotschyi Bunge
Tamarix leptostachya Bunge
Tamarix parvifl ora DC.
Syn.: Tamarix cretica Bunge
Tamarix passerinoides Delile
Tamarix rosea Bunge
Tamarix smyrnensis Bunge
Syn.: Tamarix pallasii Desv. var. smyrnensis
(Bunge) Boiss.; Tamarix ramosissima Ledeb.
Tamarix tetragyna (Boiss.) Boiss. var. meyeri
THYMELAEACEAE
Thymelaea hirsuta (L.) Endl.
Thymelaea passerina (L.) Casson & Germ.
TILIACEAE
Corchorus depressus (L.) Stocks
TYPHACEAE
Typha australis K. Schum. & Thonner
Typha domingensis Pers.
Typha latifolia L.
Typha laxmannii Lepechin
Syn.: Typha stenophylla Fisch. & Mey.
Typha minima Funck var. gracilis Ducomm.
Syn.: Typha gracilis Jordan non Rafi n.(1836);
Typha lugdunensis Chabert; Typha martini
Jordan
VALERIANACEAE
Centranthus longiflorus Stev. subsp.
longifl orus
Valerianella vesicaria (L.) Moench
VERBENACEAE
Clerodendrum inerme (L.) Gaertn.
Phyla nodifl ora (L.) Greene
Verbena offi cinalis L.
Globularia trichosantha Fisch. & Mey.
(Formerly in Globulariaceae)
ZYGOPHYLLACEAE
Fagonia bruguieri DC.
Fagonia indica Burm. f.
Fagonia ovalifolia Hadidi
Malacocarpus crithmifolius (Retz.) C.A. Mey.
Nitraria retusa (Forssk.) Asch.
Nitraria schoberi L.
Syn.: Nitraria olivieri Jaub. & Spach
Seetzenia lanata (Willd.) Bullock
Tetradiclis tenella (Ehrenb.) Litv.
Syn.: Anatropa tenella Ehrenb.; Tetradiclis
caspia Lindl. in Chesney; Tetradiclis salsa
C.A. Mey.
Tetraena alba (L.f.) Beier & Thulin
Syn.: Zygophyllum album L.f.
Tetraena simplex (L.) Beier & Thulin
Syn . Zygophyllum simplex L
Tetraena coccinea (L.) Beier & Thulin
Syn.: Zygophyllum coccineum L.
Tetraena qatarensis (Hadidi) Beier & Thulin
Syn.: Zygophyllum qatarense Hadidi
Tribulus arabicus Hosni
Syn.: Tribulus omanensis Hosni
Tribulus terrestris L .
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Halophytes of Southwest Asia
... In nature, there are species -halophytes -that have adapted to the salinity of the habitat even salinity above 200 nM NaCl [FLOWERS, COLMER 2008], which supports their growth [KHAN et al. 2015]. Halophytes include Najas marina L., species of invasive traits [GHAZANFAR et al. 2014]. ...
... On the other hand, the study of the efficiency of the photosynthetic apparatus of halophytes [GHAZANFAR et al. 2014;KRAWCZYK et al. 2016] in reservoirs with different salinity will answer the following questions: 1) does different salinity of the habitat affect the changes in photosynthetic activity of facultative halophytes?; 2) what salinity of water reservoirs will be conducive to the spread of halophytes in the era of climate change? ...
... Globally, more than 500 halophytes genera exist under different angiosperm families, of which Poaceae and Chenopodiaceae (now Amaranthaceae) have highest share of halophytic genera amongst monocot and dicots, respectively (Flowers et al. 1986). A total of 728 taxa of halophytes are recorded for South West Asia belonging to 68 families (Ghazanfar et al. 2014). However, India has huge diversity of salt-tolerant plant communities on both the coastal and an inland region, a detailed literature of its biodiversity is not available yet. ...
... At the generic level, Suaeda with four, Sporobolus, Tamarix, and Avicennia, each with three are the most species rich genera, followed by Haloxylon, Sesuvium, Salicornia, Trianthema, and Salsola, each with two species, Aeluropus, Atriplex, and Rhizophora, each with only single species. These results show resemblance to the halophytic communities that are commonly occur in saline habitats of the Southwest Asia (Ghazanfar et al. 2014). In our laboratory we have collection of certain halophytes such as Cressia critica, Suaeda monoica, S. nudiflora, S. fruticosa, and Tamarix indica (Fig. 4) to study the ...
Chapter
Halophytes constitute a fascinating group of higher plants which exhibits unique morphological, anatomical, and physiological adaption in order to perpetuate and survive in highly saline conditions. India has significantly large extend of saline land under coastal and inland regions where both the natural and anthropogenic practices resulted in extensive salt flats. The coastal salt flats are distributed irregularly over the East and West coast. Salinity is due to abundance of NaCl and Na2SO4 salts and reaches up to 70 dS m−1 EC values during the summer. The dominant vegetation cover includes true halophytes (Sesuvium spp., Suaeda spp.), seagrasses (Ruppia spp.), and mangroves (Avicennia spp., Rhizophora spp.). Such halophytic life forms are imperative for the estuarine food web and typically used by the local inhabitant for food, fodder, fuel and fiber production. Inland salt flats are frequently found in the arid and semiarid areas of the Rajasthan and Gujarat. Low annual rainfall, existence of inherent salt sources, and high rate of evaporation collectively promote salinity and can reach up to 4–50 dS m−1 EC values during the summer. There is a distinct pattern of halophytic vegetation including grasses, shrubs, and trees that are native to tropical regions of the South Asia. The dominant halophytic families are Chenopodiaceae with Salicornia brachiata, Suaeda fruticosa, and Poaceae with Aeluropus lagopoides and Sporobolus coromandelianus species. This review containing biodiversity, biology, and economic utility of halophytes on Indian salt flats would be a first and valuable scientific document for active researchers in this field and helpful at improving and conserving these sustainable plants.
... Over In the world, around 550 genera belonging to about 117 families and around 1560 halophyte species have been identified [3] and these species constitute 1% of the total number of plant species [14] [20]. In Turkey, it is known that there are over 300 halophytic species [21] and in Irano-Turanian Phytogeographic Region of Turkey, there are 34 families belonging to 88 genera and 137 halophytic species [4]. Asteraceae, Chenopodiaceae, Fabaceae and Liliaceae are the most common species in terms of the species they contain and the dominant genera belong to Salsola, Chenopodium, Limonium, Alhagi and Allium respectively [4]. ...
... Although there are many definitions of cotyledons show optimal development in the absence of salt. If stimulated, Monocotyledon may also develop at 50 mM or less than halophytes[14] [21]. ...
Article
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As a result of the global warming caused by increasing industrialization, changes in vegetation have occurred on the earth. Halophyte species have been observed in many areas including native vegetation and agricultural land due to increased drought and warming and also over irrigation during formation of secondary vegetation. Soil samples were taken seasonally from selected three areas (Timurlenk, Karapinar and Fakili) in Araban (Gaziantep Turkey) and the pH, electrical conductivity (EC), lime (CaCO3), nitrogen (N), phosphorus (P), potassium (K), sodium (Na) and calcium (Ca) analyzes were performed in this samples. In addition, the presence of taxa known to be halophytes in these areas has been investigated. As a result of the analysis, it was found that there was no seasonal difference (p > 0.05), but there were significant differences between lime (CaCO3), phosphorus (P), potassium (K) and calcium (Ca) among the localities (p < 0.05). Alhagi pseudoalhagi M. Bieb. was found in Timurlenk and Karapinar, Salsola kali spp. ruthenica Iljin was found in Timurlenk and Juncus inflexus L. was found in Timurlenk, Karapinar, Fakili. Although the soil is not salty, the presence of three different taxa that can tolerate the salt in three localities shows that the amount of salt in the soil may increase in time. The information presented in this study contributes to the salinization of soils and their effects on agriculture in the region.
... In field and glasshouse trials, several halophytic species absorbed the equivalent of 2 to 6 tonnes salt ha −1 yr −1 (Panta et al., 2014). Approximately 140 halophytic taxa from 31 plant families have been recorded on the Arabian Peninsula, which constitutes about 4% of the total flora (Ghazanfar et al., 2014). Halophytes are used for medicine, fodder, phytoremediation, biofuel and ornamentals (El Shaer, 2010;Qasim et al., 2010;Rabhi et al., 2010;Abideen et al., 2011;Manousaki and Kalogerakis, 2011;Ali et al., 2012;Gairola et al., 2015;Bañuelos et al., 2018). ...
Article
Coastal desert vegetation of the Arabian Peninsula is almost entirely dominated by halophytes. Natural populations provide a genetic resource for ecological remediation and may also have direct economic value. High intrapopulation variation of seed traits is presumed to increase population persistence in the unpredictable climatic conditions of this hyper-arid desert. We investigated whether intrapopulation variation of seed mass, dormancy and germinability of four species was attributable to maternal individuals. Arthrocnemum macrostachyum, Halothamnus iraquensis, Haloxylon salicornicum and Seidlitzia rosmarinus are commonly distributed Arabian halophytes with differing seed weight variation. All species exhibited a higher germination when exposed daily to 12 hours light, compared to seeds in darkness. A higher germination was correlated with a shorter germination time. For H. iraquensis and S. rosmarinus a shorter germination time was negatively correlated with germination synchrony. H. salicornicum showed the highest intrapopulation variation of seed traits, followed by A. macrostachyum, S. rosmarinus and H. iraqensis. We found that individuals within populations of all the studied species showed variability in germination but the extent of variation was species specific. The variation in seed mass and germination among the individuals of the studied species may facilitate a temporal distribution of germination, which may reduce the risk of seed bank exhaustion. The results of this study could assist conservation and management by improving the efficiency of seed collection from wild populations of these species.
... Chenopodiaceae was the most prominent family in this study with the greatest number of genera and species, followed by Poaceae, and Asteraceae (Compositae). Similar results of the most abundant salt marsh families and species were found by (Ghazanfar et al., 2014(Ghazanfar et al., , Öztürk et al., 2019. Many species of Chenopodiaceae are adapted to arid environments and are considered very important as animal forage in the desert, semi-desert, and prairie regions, and used as good windbreaks and soil binders, in addition to their medical uses, e.g., the species Anabasis aphylla can be used as an insecticide (Wu et al., 2003). ...
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Salt marshes form along coastlines and are very interesting ecosystems due to their function and services. In the future, salt marsh plants might provide food and medicine as crops irrigated via seawater in hyper-arid regions. In the Arabian Gulf, little is known about salt marsh vegetation. Therefore, a targeted search on scientific literature was performed to provide a comprehensive assessment. Hence, current knowledge of the extent and status of salt marsh in the Arabian Gulf region was reviewed, based on literature-based analysis. Then, historic trends of salt marsh publications were carefully inspected. This study provides a list of salt marsh families and their genera and species, with a total of 51 family 179 genera 316 species in the Arabian Gulf. The largest family was Chenopodiaceae followed by Poaceae, Asteraceae. Moreover, this study identified some of the gaps that could help future directions for scientific research, and help making decisions of conservation, management policies and procedures
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C₄ is one of three known photosynthetic processes of carbon fixation in flowering plants. It evolved independently more than 61 times in multiple angiosperm lineages and consists of a series of anatomical and biochemical modifications to the ancestral C3 pathway increasing plant productivity under warm and light‐rich conditions. The C4 lineages of eudicots belong to seven orders and 15 families, are phylogenetically less constrained than those of monocots and entail an enormous structural and ecological diversity. Eudicot C4 lineages likely evolved the C4 syndrome along different evolutionary paths. Therefore, a better understanding of this diversity is key to understanding the evolution of this complex trait as a whole. By compiling 1207 recognised C4 eudicots species described in the literature and presenting trait data among these species, we identify global centres of species richness and of high phylogenetic diversity. Furthermore, we discuss climatic preferences in the context of plant functional traits. We identify two hotspots of C4 eudicot diversity: arid regions of Mexico/Southern United States and Australia, which show a similarly high number of different C4 eudicot genera but differ in the number of C4 lineages that evolved in situ. Further eudicot C4 hotspots with many different families and genera are in South Africa, West Africa, Patagonia, Central Asia and the Mediterranean. In general, C4 eudicots are diverse in deserts and xeric shrublands, tropical and subtropical grasslands, savannas and shrublands. We found C4 eudicots to occur in areas with less annual precipitation than C4 grasses which can be explained by frequently associated adaptations to drought stress such as among others succulence and salt tolerance. The data indicate that C4 eudicot lineages utilising the NAD‐ME decarboxylating enzyme grow in drier areas than those using the NADP‐ME decarboxylating enzyme indicating biochemical restrictions of the later system in higher temperatures. We conclude that in most eudicot lineages, C4 evolved in ancestrally already drought‐adapted clades and enabled these to further spread in these habitats and colonise even drier areas.
Chapter
Halophytic plants are a fascinating group of plants that also serve as dietary feed for livestock. Their utilization is essential for sustainable agriculture and maintaining ecological balance. This book explains the nature of halophytic plants through an in-depth presentation of their botanical and nutritional characteristics. Chapters of the book highlight different aspects of halophytes on a botanical, histological, ecological and nutritional basis when utilized as animal feed components. The issues of the histo-chemical aspects of halophytes are addressed with regard to their impact on nutrient compositions and availability to animals, while the important nutrient contents of halophytes are considered in relation to their value to animals. Key Features: - 10 organized chapters on halophytic plants - Explains the relationship between botanical and nutritional characteristics of halophytes when utilized as animal feed components - Covers information about important nutrient contents and secondary metabolites in halophytes - Includes information on nutritional and feeding values for animals - Includes informative diagram and tables - Includes references for further reading This book fills a notable gap in available literature on the subject, and will stimulate researchers to pursue the many unanswered questions in the field of biosaline agriculture. This text serves as reading material for undergraduate and graduate level courses and specializations in agriculture, animal nutrition, animal physiology, botany and plant physiology. It also serves as supplementary reading for students of taxonomy, ecology, and environmental science courses. Professional and apprentice livestock farmers will also benefit from the information presented by the book.
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Halophytes.tn (http://halophytes.rnrt.tn/) is a web-based database of Tunisian halophyte species. Halophytes are salt-tolerant plants able to grow above 85 mM of salt, even up to 2 M as for Tecticornia spp. Tunisia, a North African country located on the Mediterranean border, covering ∼165 000 km2, harbors several types of saline habitats and biotopes where halophytes preferably vegetate. With ∼6000 worldwide and over 420 Tunisian species, halophytes represent a huge potential in several fields, including desalination, phytoremediation, agrofarming, medicinal use, industrial applications, pharmacology and even nanotechnology. We describe the practical and technical steps followed and bioinformatics tools used to conceive and design the first Tunisian halophytes database, enabling species identification and characterization. As a first version, information about botany, morphology, ecophysiology and biochemistry were provided for the identified species with their sites of growing in Tunisia, first step of biodiversity conservation, management and valorization. The database will be regularly maintained, updated and enriched to achieve the goal of whole Tunisian halophyte species and fit the needs of scientists and all category of users.Database URL: http://halophytes.rnrt.tn/
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Agriculture has played an essential role in the provision of food and has been a major factor in overall economic development for societies around the world for millennia. In the past, agriculture in hot, arid countries like Qatar faced many challenges, the primary one being a dearth of water for irrigation. Historically this severely limited Qatar’s economic development, which was based largely on resource exploitation, pearl fishing, and only more recently, on the exploitation of its oil and gas reserves which subsequently has led to Qatar’s great wealth. This paper gives an overview of the recent evolution of Qatar’s agricultural sector and investigates future trends that tackle the challenges of its hot arid climate and the limited availability of agricultural resources. Specifically, the review analyses Qatar’s potential to develop a national food security strategy based on a significant expansion of food production in the country. We review recent policy actions implemented to address challenges in the food supply chain caused by a 3.5-year blockade imposed by the adjacent Arab Gulf States, discussing the renewed interest in the potential that an enhanced agricultural sector must provide some aspects of food security and the implications for policymakers that would logically ensue.
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Iran with its diverse climatic conditions and geologic and land use history support large areas of saline habitats and diverse halophytic flora. The halophytic diversity in not only enriched by the evolving of a large number of autochthonous Irano-Turanian elements, but also many of the halophytes of other phytochoria like Saharo-Arabian, Mediterranean and even Euro-Siberian elements are represented in Iran. Therefore most of the higher syntaxa of Euro-Mediterranean and Afro-Asian-at least partly-occur in Iran. Prior to a consolidated syntaxonomical system for the halophytic vegetation of Iran, major halophytic vegetation units of Iran are summarized and shown along salinity and moisture gradients. These include: (1): Mangrove communities (Avicennio-Sonneratietea). (2): Submerged aquatic plant communities (Ruppietea maritimae). (3): Annual obligatory hygro-halophytic communities on sea, lake and river marshes dominated by stem or leaf succulent C3 chenopods (Thero-Salicornietea). (4) Semi-woody or perennial halophytic communities on muddy or coastal salt flats dominated by stem succulent C3 chenopods (Salicornietea fruticosae). (5): Hydrophilous euryhalophytic rush communities: Phragmitetea australis. (6): Halophytic grassland and herbaceous perennial sedge communities belonging to genera Puccinellia and Juncus (Juncetea maritimi). (7): Salt marsh and riverine bruchwood communities dominated by salt-excreting halophytes (Tamaricetea ramosissimae, prov.). (8): Annual halophytic communities dominated by C4 chenopods in temporary moist and inundated, or disturbed salty soils (Climacopteretea crassae, prov.). (9): Halophytic shrubby, semi-woody or hemicrytophytic communities on salty and dry soils dominated by leaf or stem succulent C4 chenopods (Haloxylo-Salsoletea tomentosae, prov.). (10): Halophytic shrub communities on salty and sandy coastal or margin of sabkhas with high water table dominated by Nitraria schoberi and Reaumuria fruticosa. (11). Psamo-halophytic shrub communities along sandy coasts of Persian Gulf and Oman sea (Sphaerocomion aucheri and communities of Zygophyllum qatarense and Heliotropium bacciferum and (12): Unclassified halophytic communities: Herbaceous perennial and hemicryptophyte halophytic communities of secondary origin. © 2004, Universita degli Studi di Roma 'La Sapienza'. All rights reserved.
Article
The main purposes are to collate information of the region, to review marine systems and processes in the intertidal and shallow sublittoral parts of the Arabian seas, and to highlight human utilisation and environmental consequences. The first section presents the geological, geographical, climatic and oceanographic background to the area. The second section examines what is known of the region's marine communities, interpreting the relationships between the marine systems and physical conditions for: reefs and coral communities; coral reef fish assemblages; other reef components and processes; seaweeds and seasonality; seagrasses and other dynamic substrates; intertidal areas - mangal associated ecosystems, marshes, sabkha and beaches; and the pelagic system. The next section synthesizes and concludes the biogeographical material and interprets the effects of natural stress on the biota. The final section describes and discusses the human use and management of the region, including fisheries. -after Authors
Article
Although we have a superficial overview of the main plant communities of coastal areas of the western and southern Gulf, in-depth studies are generally lacking, with a few notable exceptions. Coastal vegetation in the region is often equated solely to halophytic communities growing under the direct influence of salt-water, in extreme cases only to mangroves, the latter which in fact account for only a very small percentage of the total coastal vegetation. This narrow perspective has important conservation repercussions, especially given the current mass destruction of many parts of the Gulf coastline. Important speciesrich communities (flora and fauna) are being destroyed at an alarming rate without any mitigation measures, and even high-profile ecosystems, such as mangroves, are by no means immune from the on-going development frenzy. An important step towards the protection and sustainable use of environmental resources is their detailed characterisation and inventory, as well as elucidating their spatial distribution. The aims of this contribution are therefore three-fold: 1) to give an overview of the coastal vegetation of the area (Gulf coastline of the GCC countries), examining both halophytic and non-halophytic communities; 2) to highlight the most critical issues affecting coastal vegetation; and 3) to suggest conservation priorities and associated research projects. It is clear that much more detailed work is required to identify and assess remaining intact stretches of the coastline regarding their vegetation, flora and fauna.