BALWOIS 2010 - Ohrid, Republic of Macedonia - 25, 29 May 2010 1 Salt Marshes Plant Diversity of Coastal Zone in Albania Julian Shehu, Alfred Mullaj, Alban Ibraliu Department of Crop Production, Faculty of Agronomy and Environment, Agricultural University of Tirana, Albania Abstract The salt marshes of Albania comprise a narrow belt along the Adriatic and Ionian Seas, with a total length of 476 km from the north to south. They have long been the subject of a range of human activities causing habitat loss. Enclosure for agricultural use, ports and other infrastructure has reduced many salt marshes to a narrow fringe along estuary shores. Salt marshes are important for a range of interests. In particular they support a range of specialist plant communities and associated animals (especially breeding and wintering birds) and often have a high nature conservation interest. They rarely exist in isolation and form an integral part of many estuaries, other tidal inlets and bays. The objectives of this study are flora and vegetation of salt marshes. In this study, on the basis of field surveys, is given a phytosociological classification of the Albanian salt marshes vegetation by the European standard methods of phytosociology (Zurich-Montpellier). The salt marsh communities of Albania are poor in endemism and generally similar to relevant vegetation types elsewhere in the Mediterranean. The flora of coastal salt marshes is differentiated into levels according to the plants' individual tolerance of salinity and water table levels. Coastal salt marshes of Albania are offered a number of 62 taxa, extended in 16 diverse families. The most presented families are Chenopodiaceae 24 %, followed by Poaceae and Asteraceae with 11%, with dominating genera like: Arthrocnemum, Limonium, Puccinellia, Chenopodium, Plantago, Tamarix and Juncus. The representative species recorded were Arthrocnemum fruticosum, Halimione portulacoides, Halocnemum strobilaceum, Juncus acutus, J. maritimus, Limonium vulgare, Polypogon monspeliensis, Salicornia europaea, Suaeda maritima, and Tamarix dalmatica. The most common salt marsh plant communities in coastal area of Albania are salt meadows dominated by glasswort (Salicornia europaea), pioneer marsh communities, perennial vegetation of marine saline mud’s mainly composed of scrub such as Sarcocornia fruticosa, Sarcocornia perennis and belonging to the Sarcocornetea fruticosi class, tall rush salt marshes dominated by Juncus maritimus or J. acutus (Juncetalia maritime). Phytosociological analysis evidenced 16 associations, which belong to 4 classes, 5 orders and 6 alliances. Key words: plant salt marshes, flora and vegetation, Zosteretea Marinae, Arthrocnemetea; Juncetea maritimi; coastal vegetation; halophytes; phytosociological analysis. Introduction On the coastal area of Albania, salt marshes are one of the most prevalent habitats, mainly around the coastline of Lagoons, in both sides near the deltas of many rivers and also in depressions behinds sand dunes and low-being alluvial plains. The most important areas in Albania are those around Viluni, KuneVain, Patok, Bishtaraka, Karavasta, Narta, Orikumi, Butrinti Lagoons and Buna, Drini, Mati, Ishmi, Erzeni, Shkumbini, Semani, Vjosa delta’s rivers. Salt marshes area is considered as one of the most important areas in Albania based on the high biodiversity values and the number of habitat found there. The biodiversity found in salt marshes is unique and highly adapted. Salt marshes are populated by halophytes, plants that can live under saline conditions. Plant species diversity is low, since the flora must be tolerant of salt and anoxic mud substrate. The plant communities’ composition of salt marshes area is rather variable depending on the nature of the soil. The development from constantly submerged areas and ending in areas that are always above water level is marked by the increasing diversity which follows the arrival of a range of new species. The salt marsh vegetation has been the object of scientific investigation of several recent phytosociological studies (Géhu & Biondi 1996; Géhu 1999; Poldini et al. 1999). BALWOIS 2010 - Ohrid, Republic of Macedonia - 25, 29 May 2010 2 Coastal salt marshes rank among the systems with the highest productivity of any in the world. High productivity of salt marshes is just one reason we are protecting and restoring these valuable "liquid assets." Materials and methods A total of 33 phytosociological releve’s were made in the period between 2004 and 2009. The vegetation releve’s were made and elaborated according to the standard procedures of the Braun-Blanquet methods of phytosociology (Zurich-Montpellier). (Braun-Blanquet 1964). The standard keys for determination of plants and nomenclature of plant species were used (Tutin et al. 1964-1980, 1993; Paparisto et al. 1984- 2000). All releve´s available were collected and classified using numerical methods (TWINSPAN). A database was built of these releve´s using TURBOVEG (Hennekens 1996a). For syntaxonomic nomenclature of the higher levels of classification (class, order and alliance) we followed Rivas-Martinez et al. (1999). Species cover-abundance values we followed the Braun Blanquet scale. A structured table was produced by running TWINSPAN (Hill 1979). Some clearly heterogeneous releve´s were removed. For each syntaxon the location where the releve´s have been made is listed. Attention is paid to ecological requirements and geographical distribution. The characteristic and differential species for each syntaxon are also described. Human impact and conservation of coastal communities is discussed. Results and Discussion 1. Flora. Along the Albanian coast, some salt-marshes, sometimes very extended, are frequent. These are submerged in winter and dry (partly or totally) in summer. Around these salt-marshes there is developed and extended halophilous vegetation. Generally, this vegetation, mainly shrubby, presents a remarkable analogy with formations known in other marshy coastal areas of Europe Salt-marshes are presented from a number of 62 species (Annex 1), extended in 16 different families. The most presented families are Chenopodiaceae 24 %, followed by Graminae and Compositae with 11% (Graph. 1). The dominant forms in this type of habitat are succulent plants. . 24% 11% 11% 8% 6% 6% 6% 4% 4% 4% 4% 4% 4% 4% Chenopodiaceae Gramineae Compositae Juncaceae Plantaginaceae Leguminosae Cyperales Cyperaceae Liliaceae Caryophyllaceae Gentianaceae Plumbaginaceae Tamaricaceae Juncaginaceae Graph. 1 Family’s richness (percentage) of flowering plant species of the Salt marshes In these habitats, frequent floristical elements are: Mediterranean and Mediterranean-Atlantic (Inula crithmoides, Parapholis filiformis, Centarium spicatum, Centarium tenuiflorum, Lotus preslii, Plantago coronopus, Limonium oleifolium, Parapholis incurve, Juncus subulatus, Triglochin bulbosum); BorealoTropical and Circum Boreal (Halimione portulacoides, Suaeda maritima, Salicornia europaea, Carex extensa, Juncus acutus, Juncus maritimus: Paleo-Temperate (Spergularia marina, Carex divisa); Mediterranean-Irano-Turanian (Arthrocnemum glaucum, Halocnemum strobilaceum, Frankenia pulverulenta, Hordeum marinum; Cosmopolitan (Polypogon monspeliensis, Ruppia cirrhosa. BALWOIS 2010 - Ohrid, Republic of Macedonia - 25, 29 May 2010 3 2. Habitat types and Syntaxonomic scheme of the studied vegetation: Habitats pertaining to salt marsh vegetation of the studied area are recorded at a total of 10 localities Fig.1. Map of lagoons of Albania With regard to its floristic composition the studied vegetation can be classified within classes: Zosteretea Marinae, Ruppietea Maritimae, Thero-Salicornietea , Sarcocornietea Fruticosae and Juncetea maritimi. The performed numerical analysis supports such syntaxonomic division. 2.1 Sea grass beds of coastal lagoons ZOSTERETEA MARINAE Pignatti 1953 Zosteretalia marinae Beguinot 1941 em. R.Tx. et Oberdorfer 1958 Zosterion marinae Christiansen 1934 Zosteretum noltii Harmsen 1936 RUPPIETEA MARITIMAE J.Tüxen 1960 RUPPIETALIA MARITIMAE J. Tüxen 1960 Ruppion maritimae Br.-Bl. 1931 Ruppietum cirrhosae Hocquette 1927 The seagrass beds are a common feature of shallower waters on firm sands, sandy muds and gravelly flats of the Albanian lagoons. Where seagrass beds occur, eelgrass (Zostera noltii) is the most dominant species. Eelgrass (Zostera noltii) communities are prominent, usually with very few other vascular species but often with abundant algae. Zostera noltii forms stands with a cover of delicate trailing narrow leaves up to about 20 cm long. It often occurs in pure stands on mud/sand mixtures of a variety of consistencies from very soft to quite firm. Z. BALWOIS 2010 - Ohrid, Republic of Macedonia - 25, 29 May 2010 4 noltii experiences considerable leaf loss in autumn and early winter through natural shedding, storm damage and wildfowl grazing, but plants towards the lower limit may remain winter-green. In Europe the Zosteretum noltii is widespread in similar situations to those in Albania (Beeftink 1962, Géhu 1975). In shallow areas whole prairies settle, dominated by the spiral tasselweed (Ruppia cirrhosa). Fluctuating algae populations of Ulva rigida (a variety of green seaweed) settle on soft, muddy substrata while the gut weed (Enteromorpha sp.) lives on harder (sandy) substrata. The seagrass beds have few species, but reach enormous quantities of biomass and in these communities live a large number of planktonic and benthonic animals. These plant communities cover important surfaces in the bottoms of the Albanian Lagoons. Such beds play an important role in influencing the shape and stability of the shoreline, regulating dissolved oxygen and filtering suspended matter. They can enhance the biodiversity of a lagoon by providing a physical refuge from predation and also serve as nursery and feeding habitats for a variety of organisms. 2.2 Salt-marshes plant communities THERO-SALICORNIETEA (Pignatti 1953) R.Tx. in R.Tx. et Oberdorfer 1958 Thero-Salicornietalia Pignatti 1953 em. R.Tx. 1954 ex R.Tx. et Oberdorfer 1958 Thero-Salicornion strictae Br.-Bl. 1933 em. R.Tx. 1950 in Tx et Oberdorfer 1958 Salicornietum europaeae Warming 1906 Suaedetum maritimae (Conard 1935) Pignatti 1953 SARCOCORNIETEA FRUTICOSAE R.Tx. et Oberd. 1958 Sarcocornietalia fruticosae (Br.-Bl. 1931) R.Tx. et Oberd. 1958 Sarcocornion fruticosae Br.-Bl. 1931 Puccinellio festuciformis - Sarcocornietum fruticosae (Br.-Bl. 1928) Géhu 1976 Halimionetum portulacoidis (Kuhnholtz-Lordat 1927) Des Abbayes et Corillion 1949 Halocnemenion strobilacei Géhu et Costa in Géhu et al. 1984 Halocnemetum strobilacei Oberd. 1952 em. Géhu 1994 Limonion angustifolii Br.-Bl. (1933) 1934 Limonio-Artemisietum coerulescentis Horvatic (1933) 1934 JUNCETEA MARITIMI Br.-Bl. 1952 em. Beeft. 1965 Juncetalia maritimi Br.-Bl. 1931 Juncion maritimi Br.-Bl. 1931 Puccinellio festuciformis - Juncetum maritimi (Pign. 1966) Géhu et al.1984 Juncetum maritimo - acuti Horvatic 1934 Salt marshes are one of the most prevalent habitats around the coastline of Albanian Lagoons, near the deltas of the rivers and also in depressions behinds sand dunes and low-being alluvial plain. The biodiversity found in salt marshes is unique and highly adapted, able to survive high salt concentrations, periodical submersion, and low-nutrient conditions. Salt marshes are populated by halophytes, plants that can live under saline conditions. The flora of a salt marsh is differentiated into levels according to the plants' individual tolerance of salinity and water table levels. Under regular conditions it is possible to encounter the whole range of typical species by traveling from constantly submerged areas or lower marsh communities, moving on to areas subject to tidal movements, and ending in areas that are always above water level. The most common salt marsh plant community in Coastal area of Albania is Salicornietum europaeae, dominated by glasswort (Salicornia europaea. Glasswort is often the first plants to take hold in a mudflat and begin its ecological succession into a salt marsh. Their shoots lift the main flow of the tide above the mud surface while their roots spread into the substrate and stabilize the sticky mud and carry oxygen into it so that other plants can establish themselves as well. Plants such as sea lavender (Limonium vulgare), BALWOIS 2010 - Ohrid, Republic of Macedonia - 25, 29 May 2010 5 Spiny rush (Juncus acutus) and Sea rush (Juncus maritimus) grow once the mud has been vegetated by the pioneer species. The Salicornia europaea (pioneer marsh communities) takes place in the space of just a few months between summer and early autumn. Salicornia europaea stands may form a distinct zone in the lower marsh. At some sites, particularly those on sandy substrates (Patok and Narta areas), patches of Salicornia europaea may be separated from the main marsh front by several hundred metres of bare flat. At a number of sites, Salicornietum europaeae forms an open mosaic with Suaedetum maritimae, which is a species-poor community, generally open, though always dominated by Suaeda maritima the density of which is high, sometimes associated by Salicornia europaea, Halimione portulacoides and Aster tripolium. Suaeda maritima is an annual and it is tolerant of a wide range of soil types subject to various submersion regimes. Like the Salicornietum europaeae, its growth appears heavily dependent upon sediment nutrients, especially nitrogen, and it is particularly characteristic of open situations free of competition from established perennials. Following this layer is a plant community of Puccinellia festuciformis and Sarcocornia fruticosa or association Puccinellio festuciformis - Sarcocornietum fruticosae. Stands of this association occur on the lower parts of salt-marshes covered by water for the greater part of a year, whose surface becomes driedup and parched only at extremely hot temperatures. They develop on clayish and marshy soils, periodically or permanently flooded, showing a high rate of salinity. The association Puccinellio festuciformis - Sarcocornietum fruticosae is poor in species. This association is easily recognized and differs from a related ass. Halocnemetum strobilacei by the abundant presence of Sarcocornia fruticosa, which is a characteristic and dominant species of the association. The community reaches its optimum development during the summer. The associations Limonio-Artemisietum coerulescentis, Halimionetum portulacoidis develops outside of the tidal zone, on less saline and moist soils, such as embankments and meadows. They represent perennial communities of the middle parts of salt-marshes, rarely inundated by spring tides, with more species compared to other communities within the class Sarcocornietea Fruticosae. The community reaches its optimum development by the end of the summer and at the beginning of autumn, As the saltmarsh develops, the accumulation of new material raises the surface level of the new marsh in relation to the sea and this reduces the frequency and duration of tidal inundation. This enables species less tolerant of inundation to colonize, and more complex plant communities gradually develop. The next stage is the development of the plant communities dominated by Spiny rush (Juncus acutus) and Sea rush (Juncus maritimus) that cover a large surface in this area. Ass. Juncetum maritimo-acuti, Puccinellio festuciformis - Juncetum maritime extends across the entire area of the Albanian coasts, usually closed swards on the silt and sand of coastal salt-marshes in the area of highly moist and marshy soils with sea and brackish water. Floristic composition of the both associations is very similar, mostly elements of halophilous vegetation of the class Sarcocornietea Fruticosae. The association reaches its optimum development in the summer. The development of the saltmarshes in terms of plant species and communities is also accompanied by developments in the soil structure and microflora. These developments involve the establishment of populations of bacteria and fungi which are involved in biogeochemical processes controlling the breakdown of organic matter and the cycling of plant nutrients. Conclusions Salt marshes area is considered as one of the most important areas in Albania based on the high biodiversity values and the number of habitat found there. The biodiversity found in salt marshes is unique and highly adapted. The flora of coastal salt marshes is differentiated into levels according to the plants' individual tolerance of salinity and water table levels. Coastal salt marshes of Albania are offered a number of 62 taxa, extended BALWOIS 2010 - Ohrid, Republic of Macedonia - 25, 29 May 2010 6 in 16 diverse families. The most presented families are Chenopodiaceae 24 %, followed by Poaceae and Asteraceae with 11%. Phytosociological analysis evidenced 11 associations, which belong to 5 classes, 5 orders and 7 alliances. The most common salt marsh plant communities in coastal area of Albania are salt meadows dominated by glasswort (Salicornia europaea), pioneer marsh communities, perennial vegetation of marine saline mud’s mainly composed of scrub such as Sarcocornia fruticosa, Sarcocornia perennis and belonging to the Sarcocornetea fruticosi class, tall rush salt marshes dominated by Juncus maritimus or J. acutus (Juncetalia maritimi). The plant communities’ composition of salt marshes area is rather variable depending on the nature of the soil. The development from constantly submerged areas and ending in areas that are always above water level is marked by the increasing diversity which follows the arrival of a range of new species. Coastal salt marshes rank among the systems with the highest productivity of any in the world. High productivity of salt marshes is just one reason we are protecting and restoring these valuable "liquid assets." References: 1. Dring J., Hoda P., Mersinllari M., Pignatti S., Mullaj A., Rodwell J. 2001-2002- Vegetation of Albania - Preliminary overview, . Annali di Botanica.. II: p. 7-30. 2. Hennekens S. 1995 – 2004 – Turbo(Veg) Software package for input, processing and presentation of phytosociological data. Wageningen. 3. Hill M. O., 1979 - TWINSPAN- A FORTRAN program for arranging multivariate data in an ordered two-way table by classification of the individuals and attributes. Cornell University, Ithaca. 4. Horvat I., GlavacV., Ellemberg H., 1974 - Die Vegetation Sudosteuropas. Geobotanica Selecta. Vol. IV., Stuttgart. 5. Mucina L. 1997. Conspectus of classes of European vegetation. Folia Geobot. Phytotax. 32: 117– 172. 6. Paparisto K., Demiri M., Mitrushi I., Qosja Xh., Vangjeli J., Ruci B., Mullaj A. 1988-2000 – Flora e Shqipërisë. Instituti i Kërkimeve Biologjike. Vol.1-4, Tiranë 7. Pignatti S. 1982. Flora d’Italia 2. Edagricole, Bologna. 8. Poldini L., Vidali M. & Fabiani M.L. 1999. La vegetazione del litorale sedimentario del Friuli Venezia Giulia (NE Italia) con riferimenti ala regione Alto-Adriatica. Studia Geobotanica 17: 3–68. 9. Rodwell J.S., Schaminee J.H.J., Mucina L., Pignatii S., Dring J., Moss D., 2002 - The diversity of european vegetation-An overview of phytosocioligical and their relationships to EUNIS habitats. 10. Rogel J.A., Ariza F.A. & Silla R.O. 2000. Soil salinity and moisture gradients and plant zonation in Mediterranean salt marshes of Southeast Spain. Wetlands 20: 357–372. 11. Tichy L., 2001 - Juice-Program for vegetation analysis and classification. Ann. Bot. (Roma) Annex 1: Salt marshes floristic richness of the Albanian Coastal area Nr. Latin name Family name Flowering time 1 Anthrocnemum fruticosum (L.)Maq Chenopodiaceae VII-IX 2 Aeluropus littoralis (Gouan) Parl Gramineae VI-VIII 3 Artemisia coerulescens L. Compositae VII-IX 4 Arthrocemum glaucum (Delile) Ung Chenopodiaceae VIII-X 5 Arthrocemum perenne (Miller) Moss Chenopodiaceae VII-VIII 6 Asparagus maritimus (L.)Miller-Gard Liliaceae V-VI 7 Asphodelus aestivus Brot Liliaceae III-V 8 Aster squamatus Sprengel Compositae VIII-XI 9 Aster tripolium L. Compositae VIII-IX 10 Asteriscus aquaticus (L.) Less Compositae IV-VIII 11 Atriplex hastata L. Chenopodiaceae VII-IX 12 Carex extensa Good Cyperaceae V-VI BALWOIS 2010 - Ohrid, Republic of Macedonia - 25, 29 May 2010 7 13 Centaurium erythraea Rafn. Gentianaceae V-VIII 14 Centaurium spicatum (L.)Fritsch Gentianaceae V-IX 15 Chenopodium glaucum L. Chenopodiaceae VI-IX 16 Chrypsis aculeata (L.)Aiton Gramineae VII-IX 17 Cynanchum acutum (L.)Plian Asclepidaceae V-VII 18 Elymus pycnanthus Godron Gramineae V-VI 19 Equisetum ramosissimum Desf. Equisetaceae V-VI 20 Frankenia pulverulenta L. Frankeniaceae IV-VI 21 Halimione portulacoides (L.)Aellen Chenopodiaceae VII-X 22 Halocnemum strobilaceum (Pallas) Chenopodiaceae IX-X 23 Inula crithmoides L. Compositae VII-XI 24 Juncus acutus L. Juncaceae V-VII 25 Juncus compressus Jacq. Juncaceae VI-VII 26 Juncus littoralis C.A.Meyer Juncaceae V-VII 27 Juncus maritimus Lam. Juncaceae VI-VIII 28 Lepidium ruderale L. Cruciferae V-VIII 29 Limonium oleifolium Miller Plumbaginaceae VI-VIII 30 Limonium vulgare Miller Plumbaginaceae VI-IX 31 Linum maritimum L. Linaceae V-IX 32 Lotus tenuis Ëaldst. & Kit. Leguminosae IV-VI 33 Lythrum salicaria L. Lythraceae VI-IX 34 Melilotus alba Medicus Vorl.Churpf Leguminosae VII-IX 35 Mentha pulegium L. Labiateae V-IX 36 Parapholis incurva L.C.E.Hubbort Gramineae IV-VI 37 Petrosimonia oppositifolia Pallas Chenopodiaceae VI-VIII 38 Phragmites australis (Cav)Trin.ex Gramineae VI-X 39 Plantago coronopus L. Plantaginaceae V-VIII 40 Plantago crassifolia Forskal Plantaginaceae IV-IX 41 Plantago maritima L. Plantaginaceae IV-VIII 42 Polypogon monspeliensis (L.)Desf. Gramineae III-V 43 Potentilla reptans L. Rosaceae VI-VIII 44 Rumex conglomeratus Murray Polygonaceae VI-IX 45 Saccharum ravennae (L.)Murray Gramineae VII-X 46 Sagina procumbens L. Carophyllaceae III-VIII 47 Salicornia europaea L. Chenopodiaceae VII-X 48 Salsola soda L. Chenopodiaceae VIIVIII 49 Samolus valerandi L. Primulaceae VI-VIII 50 Schoenus nigricans L. Cyperaceae IV-VIII 51 Scirpus holoschoenus L Cyperaceae IV-VI 52 Scirpus maritimus L Cyperaceae VI-IX 53 Sonchus maritimus L. Compositae VI-IX 54 Spergularia marina L. Carophyllaceae III-IX 55 Suaeda maritima (L.)Dumort Chenopodiaceae VII-X 56 Suaeda splendens Pourret.Gren Chenopodiaceae VII-IX 57 Suaeda vera J.F.Gmelin Chenopodiaceae V-X 58 Tamarix dalmatica Baum. Tamaricaceae V-VI 59 Tamarix hampeana Boiss. & Heldr. Tamaricaceae IV-V 60 Trifolium fragiferum L. Leguminosae IV-VIII 61 Triglochin bulbosa L. Juncaginaceae IV-XI 62 Triglochin maritima L. Juncaginaceae IV-V