Tamaricetea arceuthoidis: una nueva clase para la vegetacion arbustiva riparia continental de Oriente medio, Asia central y regiones subaridas del valle del bajo Volga.
DISTRIBUTION AND ECOLOGY OF TAMARIX THICKETS
Tamarix thickets are a typical vegetation feature of semi-arid (seasonally arid) and arid (desert-like) environments of Macaronesia, Southern Europe, North Africa, Middle East, Arabian Peninsula and Central Asia. They also occur in the semi-deserts of southern Africa (MUCINA & al., 2006) and as introduced plants they currently occupy large areas of riparian vegetation in the S and SW of N. America (SHER & QUIGLEY, 2013).
In the Mediterranean Basin, the Tamarix species (typically together with Nerium oleander and Vitex agnus-castus) form riparian thickets on alluvia of intermittent rivers fed by winter and spring rains. These riparian thickets have been classified in the Nerio-Tamaricetea (BRAUN-BLANQUET & DE BOLOS, 1958) and become a subject of several syntaxonomic studies (e.g. IZCO & al., 1984, FERNANDEZ-GONZALEZ & al., 1990, ASENSI & DIEZ-GARRETAS, 2011) just to mention the most important ones. This class reaches as far east (and southeast) as Anatolia (KAMAOMERIOBLU, 2007) and the Levante (EIG, 1946; ZOHARY, 1973). It also occurs in North Africa (e.g. BARBAGALLO & al., 1990, BRULLO & FURNARI, 1994). The diagnostic species of this class include: Tamarix africana, T. arborea, T. boveana, T. canariensis, T. dalmatica, T. gallica, T. hampeana, T. tetrandra, T. tetragyna, Nerium oleander and Vitex-agnus-castus.
Further eastwards, towards the semi-arid regions of European Lower Volga and Ural River valleys, Central Asia, Middle East and the Arabian Peninsula, the Tamarix vegetation is quite common. Here the thickets dominated by Tamarix occupy different habitats from those known from the Mediterranean, the Balkans or the regions of the Ukrainian-Russian steppe zone. The Tamarix communities here fringe the intermittent and permanent river margins, estuaries and depressions in inundated plains, water runnels, wetlands margin and even on desert sand dunes with high underground water table; all these habitats show a notable levels of ambient salinity. They also may form phytogenic mounds (locally called 'nebka' both is sand dunes or around playas (inland saline intermittent lakes) (MAGHSOUDI & al., 2012). The Tamarix communities occur in habitats with considerable water supply where the amount of water and its salinity change during the year (AKHANI, 2004). Thanks to the unique salt excreting mechanism (BOSABALIDIS & THOMSON, 1984) in Tamarix that allow them to adapt in such extreme and unstable environments. The excreting of salts by salt glands increases the ground salinity as a result of shedding of leaves and falling of excreted salt. The accumulation of which leads to an increase in surface salinity, eventually preventing germination of new plants in the absence of enough washing. Therefore the Tamarix communities are well adapted along rivers or depressions where there is fresh water flow at least in part of the annual life cycle. The salt glands do not only serve as machinery to remove extra salt from twigs, they also function as a hygroscopic solute to reduce duration of transpiration and finally proving an enriched environment for CO2 (WAISEL, 1991). These advantages help Tamarix shrubs with [C.sub.3] photosynthetic type to have fast growth under high temperature in desert environment.
There are ca. 65 species of Tamarix (cf. BAUM, 1978; QAISER, 1981) and many of them hybridize and/or form new hybrid swarms (SAMADI & al., 2013; MAYONDE & al., 2015; H. AKHANI & T. BORSCH, unpublished data). The genetic flow between the different species of Tamarix increases adaptability and genetic diversity of Tamarix species for successful occupation of new niches (GASKIN & SCHAAL, 2002). Vegetative reproduction and production of many seeds are additional advantages for Tamarix scrub to dominate suitable habitats. Diversity and species combination strongly depends on water supply, stability of habitat and salinity. In fresh and brackish water, Tamarix species associate with many non-halophilous and ruderal species. By increasing salinity, irregular interruption of water availability, decreasing altitude and higher temperature the associated species restricts to a number of highly tolerant halophytes which eventually may form poor scrub communities of only couple of Tamarix species. Other shrubby and small tree species may associate with Tamarix depending on surrounding vegetation types and geography. Elaeagnus turcomanica and Halimodendron halodendron co-occur with Tamarix communities in the European part of the class, Trans-Caucasus and sometimes even in northwestern edge of iran. in the western iran Tamarix associate with Salix, however as a consequence of drying of rivers, Tamarix would as a rule dominate.
In the center of the species diversity and the highest incidence of the occurrence of hybrids is found in Iranian playas and along rivers. T. ramosissima occurs mostly in higher altitudes or milder climates along fresh and brackish water river and wetlands. In NW of Iran T. octandra, T. meyeri and T. ramosissima are common. But in the central part T. arceuthoides s.l., T. meyeri, T. kotschyi and T. androsowii and in the southern part T. mascatensis, T. kermanensis, T. kotschyi, T. meyeri and T. stricta are common, the latter is a tree species and occurs in dry or moist valleys in SE Iran and adjacent Pakistan.
T. pycnocarpa (=T. aucheriana) is very common in the central and southern part of Iran and adjacent area in hypersaline moist habitats. Shrubby species include Halostachys belangeriana, Caroxylon imbricatum, Salsola drummondii, S. rosmarinus, Suaeda fruticosa, S. physophora and some Lycium species (L. depressum, L. kopetdaghi, L. shawii). In the warmer zone with high water table or permanent fresh water supply in most rivers running from Zagros Mountains and in the Mesopotamia Populus euphratica and Nerium oleander co-occur with Tamarix communities. The occurrence of Nerium oleander in SW Iran is in consensus with extension of the distribution of Mediterranean elements into western and southern Iran (AKHANI & DEIL, 2012).
The Tamarix thickets of the arid regions of the Central Asia and the Middle East (biogeographically falling within the Irano-Turanian Region, as defined by ZOHARY, 1973) have so far been largely syntaxonomically misunderstood and classified within the Nerio-Tamaricetea (typical for the Mediterranean Region). The works of M. Zohary and H. Akhani are notable exceptions as they have coined the terms 'Retamo-Tamaricetea fluviatila', 'Tamaricetea salina' (ZOHARY, 1973) and 'Tamaricetea ramosissimae' (AKHANI, 2004).
Probably the first data-rich account of this vegetation from Central Asia is from the book by BAKHIEV (1985) that used the Russian formation-approach to describe the vegetation unit. BAKHIEV & al. (1994) later embraced the Braun-Blanquet approach and adopted the concepts of the Mediterranean order Tamaricetalia and Nerio-Tamaricetea (BRAUN-BLANQUET & DE BOLOS, 1958) and suggested 5 new alliances for the Amu Darya River valley (Central Asia). In the same year, BARMIN & GOLUB (1995) published these alliances effectively. Crucial for the recognition of the Tamaricetea arceuthoidis as presented in our paper was the paper by BARMIN (2001) who attempted to show (his synoptic Table 1) that the Eastern European and Central Asiatic Tamarix-dominated communities belong to the Nerio-Tamaricetea. In fact this synoptic table shows clearly that they have floristically hardly anything in common with the Nerio-Tamaricetea. Therefore we decided to rectify this situation and recognise those communities as a class in its own right.
DESCRIPTION OF NEW SYNTAXA
Tamaricetea arceuthoidis class. nov. hoc loco
Type: Holotypus hoc loco: Tamaricetalia arceuthoidis Akhani et Mucina 2015 (see below) Synonyms: 'Retamo-Tamaricetea fluviatila' Zohary 1973 (ICPN Arts. 2b, 8 & 34a); Tamaricetea salina Zohary 1973 (ICPN Arts. 2b, 8, 34a); Tamaricetea ramosissimae Akhani 2004 (ICPN Arts. 2b, 3b, 5 & 8) CHARACTER TAXA OF THE CLASS: Caroxylon imbricatum, Desmostachys bipinnata, Elaeagnos turcomanica, Nerium oleander (in the Saharo-Sindian/Irano-Turanian Floristic Region), Ochradenus aucheri subsp. rechingeri, Phragmites australis, P. karka, Prosopis koeltziana, Suaeda fruticosa, S. physophora, Tamarix aphylla, T. arceuthoides, T. aucheriana, T. dubia, T. hispida, T. kermanensis, T. kotschyi, T. mascatensis, T. ramosissima, T. rosea, T. stricta, Vitex pseudonegundo, Ziziphus spina-christi.
The following grass and herb species can be considered as differential of the Tamaricetea arceuthoidis against the Nerio-Tamaricetea: Aeluropus lagopoides, A. littoralis, Alhagi pseudalhagi, Calamagrostis dubia, Cynanchum acutum, Karelinia caspia, Suaeda arcuata.
The new class (Tamaricetea arceuthoidis) comprises riparian scrub communities of saline and sub-saline alluvial habitats along mainly intermittent rivers of the Irano-Turanian Floristic Region (sensu Zohary, 1973) of the continental Central Asia and Middle East. Here it is confined to the semi-desert and desert vegetation zones. This vegetation type reaches eastwards as far as the deserts of Gobi (e.g. KURSCHNER, 2004; LIU BING & al., 2008) and Taklamakan (THEVS, 2005). Except for the significant exceptions of ZOHARY (1973) and AKHANI (2004), these communities has been treated as part of the Nerio-Tamaricetea Br.-Bl. et O. de Bolos 1958, described for the Mediterranean Floristic Region and Macaronesia (e.g. BAKHIEV & al., 1994; GOLUB & al., 1998; BARMIN, 2001). However, as a reanalysis of these latter sources is showing, the Nerio-Tamaricetea and the new class--the Tamaricetea arceuthoidis floristically have hardly any significant group of species in common.
The Tamarix ramosissima communities described from the marginal steppe zone of the Eurosiberian Region (southern Russia, Ukraine and Moldova: POPESCU & al., 1984; GOLUB & al., 1998; CHIFU & al., 2006) neither belong to the Tamaricetea arcenthoidis, nor to the Nerio-Tamaricetea, but are rather classified as part of the Salicetea purpureae Moor 1958 as an order in its own right--the Tamaricetalia ramosissimae Borza et Boscaiu ex Dolju et al. 1980). The Table 22 in CHIFU & al. (2006: 403-413) supports this view very well.
Sometimes the vegetation classified here as the Tamaricetea arceuthoidis is considered as part of the Populetea euphraticae Zohary 1962 nom. inval. (e.g. KURSCHNER, 2004). The species typical of the Tamaricetea arceuthoidis are salttolerant and can survive changing of salinity over the year but Populus euphratica rarely occur in brackish water habitat or in places with high fresh water table or in riparian habitat.
The new class contains, at this stage, two orders--the Tamaricetalia arceuthoidis and the Elaeagno turcomanicae-Tamaricetalia.
Tamaricetalia arceuthoidis ordo nov. hoc loco
TYPE: Holotypus hoc loco: Tamaricion arceuthoidis Akhani et Mucina 2015 (see below)
DIAGNOSTIC SPECIES: identical with those of the Tamaricion arceuthoidis Akhani et Mucina 2015 (see below)
Tamaricion arceuthoidis all. nov. hoc loco
PYPE: Holotypus hoc loco: Tamaricetum arceuthoidis Leonard 1992
DIAGNOSTIC TAXA: Desmostachys bipinnata, Nerium oleander (in Turcomanian Region), Ochradenus aucheri subsp. rechingeri, Phragmites australis, P. karka, Prosopis koeltziana, Tamarix androssowii, T. aphylla, T. arceuthoides, T. dubia, T. kermanensis, T. kotschyi, T. mascatensis, T. meyeri, T. pycnocarpa, T. serotina, T. stricta, Vitex pseudonegundo, Ziziphus spina-christi.
This alliance encompasses communities of the core distribution area of the class where salinity and strong continental climate are major environmental stresses for many other plant groups. These communities are composed of two main functional groups, typical for environments experiencing combined effect of prolonged drought and high salinity; (1) the [C.sub.4] halophytes occupying flat-terrain alluvia belonging mostly to chenopodiaceae, and (2) the Tamarix shrubs occurring on the seasonally river margins, playa margins and the water runnels. Tamarix arceuthoides s.l. (including microspecies such as T. mascatensis, T. karakalensis, T. aralensis) and T. androssowii s.l. (including T. litvinovii) are very common. Tamarix aucheriana dominates on the hypersaline river and playa margins (see ALAEI, 2001, AKHANI, 2015 for more details).
We classify within the Tamaricion arceuthoidis the following validly described associations:
Tamaricetum arceuthoidis Leonard 1992 Tamaricetum aucherianae Leonard 1992
Elaeagno turcomanicae-Tamaricetalia ramosissimae ordo. nov. hoc loco
TYPE: Agropyro fragilis-Tamaricion ramosissimae Golub in Barmin 2001, holotypus hoc loco (see Barmin, 2011: 143)
SYNONYMS: Tamaricetalia ramosissimae Golub et Kuzmina in Kuzmina 1996 (ICPN Art. 1); Tamaricetalia ramosissimae Golub in Barmin 2001 (ICPN Arts. 2b, 5, 8 & 31)
This order has only one, validly described alliance--the Agropyro fragilis-Tamaricion ramosissimae Golub in Barmin 2001.
Received: 23 September 2015 Accepted: 12 October 2015
Paul Macintyre kindly corrected our English and Tatiana Lysenko assisted in locating poorly-accessible literature sources.
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Hossein Akhani (1) & Ladislav Mucina (2)
(1) Department of Plant Sciences, School of Biology, College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.
(2) School of Plant Biology, The University of Western Australia, 35 Stirling Highway, Crawley, WA 6009, Perth, Australia; Department of Geography & Environmental Studies, Stellenbosch University, Private Bag X1, Matieland 7602, Stellenbosch, South Africa. Email: firstname.lastname@example.org
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|Author:||Akhani, Hossein; Mucina, Ladislav|
|Date:||Jan 1, 2015|
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