HACQUETIA 3/2 • 2004, 95–105 SCIRPUS GEORGIANUS HARPER – A NEW SPECIES IN SLOVENIAN FLORA AND CHARACTER SPECIES OF THE ASSOCIATION DACTYLORHIZO MAJALISSCIRPETUM GEORGIANI ASS. NOVA Igor ZELNIK* Abstract Scirpus georgianus Harper, a species, native of North America and new to Slovenia, was found in the Krakovo forest (near Kostanjevica, Malence and Virgin forest reserve); moreover, a new community Dactylorhizo majalis-Scirpetum georgiani ass. nova was described after close examination of stands. The characteristic inflorescence clearly distinguishes the mentioned species from the other two of the genus Scirpus L., section Scirpus (S. sylvaticus L. and S. radicans Schkuhr); new key for genus Scirpus L. was also made. The studied species thrives in wet meadows, where it sometimes builds larger stands, as well as in gaps in swamps where there is still enough light. On the basis of specific ecological conditions of sites and multivariate analyses, the mentioned stands were classified into a new community, which was given the name Dactylorhizo majalis-Scirpetum georgiani. The mentioned community thrives on drier sites than the community Scirpetum sylvatici Rałski 1931, which is similar to it. Izvleček Na območju Krakovskega gozda (v bližini Kostanjevice, Malenc, krakovskega pragozda) smo našli za Slovenijo novo vrsto Scirpus georgianus Harper, ki izhaja iz Severne Amerike; po preučitvi sestojev pa smo opisali tudi novo združbo Dactylorhizo majalis-Scirpetum georgiani ass. nova. Od ostalih dveh vrst iz rodu Scirpus L., sekcije Scirpus (S. sylvaticus L. in S. radicans Schkuhr), se vrsta na prvi pogled loči po značilnem socvetju; izdelan je bil tudi nov ključ za rod Scirpus L. Vrsta uspeva na mokrotnih travnikih, kjer ponekod gradi večje sestoje in na presvetlitvah v močvirnih gozdovih. Na podlagi specifičnosti ekoloških razmer rastišč in multivariatnih analiz smo te sestoje uvrstili v svojo združbo, ki smo jo poimenovali Dactylorhizo majalis-Scirpetum georgiani. Ta združba uspeva na bolj suhih rastiščih kot podobna združba Scirpetum sylvatici Rałski 1931. Key words: Dactylorhizo majalis-Scirpetum georgiani, Scirpus, phytosociology, flora, ecology, wet meadows, Slovenia Ključne besede: Dactylorhizo majalis-Scirpetum georgiani, Scirpus, fitocenologija, flora, ekologija, mokrotni travniki, Slovenija 1. INTRODUCTION The investigation of wet meadows was also stim ulated by a demarcation-line between the alliances On the basis of intensive investigation of vegetation Molinion and Deschampsion, which was established in south-eastern Slovenia in the last decade, several by Horvatić (1939). Later on, these topics, namely works have been published so far. Forest vegetation, distribution and ecology of communities in wet especially distribution and characteristics of forest meadows, became the scope of our further detailed communities (Marinček & al. 2003a, b), virgin for-investigation (Zelnik 2003). ests (Marinček & Marinšek 2003), individual forest During the research work in glades of the south- communities (Košir & Marinček 1999), willow western part of the Krakovo forest the species Scirstands (Šilc 2003), riparian and tall forb vegetation pus georgianus Harper – new to Slovenian flora – was (Čarni 1995), weed vegetation (Šilc 2003) and wet found. In Slovenia two species of the genus Scirpus grasslands (Seliškar 1993; Zelnik 2003) have all L. s. str. have been known so far (Martinčič & al. been studied in the mentioned region. 1999), the widespread species S. sylvaticus L. and * Institute of Biology, Scientific Research Centre of the Slovenian Academy of Sciences and Arts, Novi trg 2, p. b. 306, SI-1001 Ljubljana, izelnik@zrc-sazu.si 95 HACQUETIA 3/2 • 2004 also S. radicans Schkuhr. Our attention was drawn by inflorescences, different from the ones of wood club rush; moreover proliferating spikelets were found later on as well; therefore the fact of having to deal with the species Scirpus sylvaticus L. started to be seriously dubious. After the specimens had been analysed, consulting several determination keys enabled us to discover that it was actually Scirpus georgianus (Zelnik 2002). Consequently the relevés were classified into its own community, namely Dactylorhizo majalis-Scirpetum georgiani ass. nova on the basis of characteristics concerning ecological site-conditions, multivariate analyses and its unique physiognomy. 1.1 Distribution and taxonomic problems The species is native of North America, where 15 other species, including the closely related S. atrovirens Willd, of the genus Scirpus L., section Scirpus thrive as well. It is spread over natural and human- disturbed wetlands (wet meadows, marshes, edges of lakes and ponds, draining-ditches) from Texas to Georgia in the south to the Great Lakes and Newfoundland in the north. (Whittemore & Schuyler 2002) This species is similar to wood club-rush (Scirpus sylvaticus) (Fig. 4), nevertheless it has a typical inflorescence (Fig. 2 & 3) which differentiates it at a glance from the other two species S. sylvaticus L. and S. radicans Schkuhr, because 4-35 spikelets (largest at least 16) (Whittemore & Schuyler 2002) form head-shaped fascicles, which are at the apices of ultimate rays of different length, jutting out in all directions, or else fascicles of spikelets are aggregated, in mostly head-shaped clusters. Mature spikelets are brownish red, brown, greenish brown or blackish brown (Kiffe 1998), while those of wood club-rush are blackish green; they often proliferate in bulblets (Fig. 3). In order to be distinguished from the most similar, closely-related and sometimes misidentified and/or mixed up with species S. atrovirens Willd.; Kiffe (1998) states that there are not only differences in leaf-structure, but also major differences in the number of perianth-bristles and size of spikelets and nuts. S. georgianus is mostly completely lacking in perianth-bristles, in some cases 1-3 bristles, shorter than the nut are found, which can rarely reach 3 of length of a nut; nut (0.6–)0.8–1.1 mm long (Kiffe 1998, Whittemore & Schuyler 2002). When examining S. atrovirens six perianth–bristles are found as a rule, which are shorter or slightly longer than nuts, the length of which is (0.8–)1–1.3 mm (Kiffe 1998, Whittemore & Schuyler 2002). Spikelets and glumes (scales) of this species are a bit longer. About the distribution of the studied species, some troubles occur due to taxonomic problems and equalling the species S. georgianus with S. atrovirens. The naturalized taxon with the name S. atrovirens pallidus Britton was mentioned as early as 1903 in northern France (Fournier 1990). The species, named S. atrovirens Willd. is frequently mentioned as being occasional in Central Europe as well as in northern France and possibly naturalized (DeFilipps 1980, Lambinon & al. 1992), where it thrives in tractions of damp forests (swamps). The species with the mentioned name is stated as being rare in Germany (Oberdorfer 1994) as well as in north-western Italy (Pignatti 1982). However, this taxon has not been recorded yet in Croatia, Austria and Switzerland. For Germany, Kiffe (1998) mentioned the species Scirpus georgianus Harper, but not S. atrovirens; or other synonyms (e.g. S. atrovirens var. georgianus (Harper) Fernald, Scirpus atrovirens auct. non Willd. s. str.). On the basis of taxonomic revision of the genus Scirpus s. str. in North America, Schuyler (1967) had already stated that there are two distinctly separated species: S. atrovirens and S. georgianus. At the same time Kiffe (1998) states that it is not yet clear whether S. atrovirens has ever been found in Germany, that is to say in Central Europe; it might have been S. georgianus in all cases. The thriving of S. atrovirens has not yet been recorded in Slovenia, so this problem has not appeared here. The studied species was probably introduced by members of the North American Mycological Association, who visited the Krakovo virgin forest reserve in the 1980‘s. 2. MATERIALS AND METHODS 2.1 Area of research The swampy area of the Krakovo forest is covered with grey and light brown clays. At Kostanjevica, the thickness of clay is 2.5 m; those layers are supposed to belong to the last glacial period (Würm). Within paludal sediments, there are thinner layers of light soil, which alternate with clayey and organogenic marshy sediments (Pleničar & Premru 1977). Various soil types have developed on this ground and all of them are more or less hydromorphic, 96 IGOR ZELNIK: SCIRPUS GEORGIANUS HARPER – A NEW SPECIES IN SLOVENIAN FLORA … variously manifested amphigleys, hypogley and riverine soil (Zupan 1996). Here, soil moisture is increased not only by a high level of ground water, but also by rain water which is perched in upper horizons because of the almost impermeable layers. During the periods of abundant precipitations special conditions are therefore created, namely waterlogged or even inundated soil. Dystric and gleyic soil, which is acid, nutrient-poor and waterlogged during the period of abundant precipitations especially in spring, is predominant in this area. The climate of the Krško basin is classified into a type of temperate continental climate of eastern Slovenia, namely a Pannonian climate (Ogrin 1996). Average April temperatures are higher than October ones or the same, average annual rainfall being from 800 to 1000 mm, as is characteristic of this climate type. The Krško basin belongs to the area of transit to the Pannonian climate, the influence of which is diminishing westwards (Gams 1962). The average annual rainfall in Kostanjevica, which is situated on the southern edge of the Krakovo forest, is 1169 mm and 1083 mm in Smednik (Zupančič 1996), situated on its northern edge. The Krško basin is classified into the Subpannonian phytogeographical area (Wraber 1969). According to phytogeographical classification by Zupančič & al. (1987), this area is classified into the Krško-Bizeljsko district of Pannonian subsector, west Dinaric sector and into the Illyrian flora province. The studied species Scirpus georgianus thrives on forest edges and in gaps in swamps and damp woods of the following communities: Pseudostellario europaeae-Carpinetum betuli, Pseudostellario europaeae- Quercetum roboris, Carici elongatae-Alnetum glutinosae, Carici brizoides-Alnetum glutinosae. Distribution of the above listed forest communities is presented in Marinček & al. (2003a). 2.2 Methods Vegetation was sampled and elaborated according to the standard central European method (Braun- Blanquet 1964; Westhoff & van der Maarel 1973). Vegetation relevés were made in 2001 and 2002, in June, when vegetation was optimally developed. The size of plots varies from 8 to 32 m2 and adjusts to the microrelief. The criterion for the choice of a plot was homogeneity of vegetation. Only combined cover and abundance values are indicated in the table. Cover-abundance values were transformed according to van der Maarel (1979). Numerical analyses of relevés were carried out using the computer program SYN-TAX (Podani 2001); the hierarchic classification method (Complete Linkage Clustering) was performed. The dissimilarity of relevés was measured by the Similarity ratio complement. Nomenclature of ferns and flowering plants follows Martinčič & al. (1999), with the exception of Scirpus georgianus Harper, which is in accordance with Schuyler (1967), Kiffe (1998), Whittemore & Schuyler (2002). Plant taxa were classified into syntaxa, taking into consideration the synthesis works of Mucina & al.(1993) and Oberdorfer (1994). The classification of individual syntaxa by the principle ofincreasingcomplexityfollowsOberdorfer(1994). During the process of defining character species, principles suggested by Dierschke (1994) were taken into consideration. Nomenclature of the newly described association is in accordance with the code of Weber & al. (2000). Apart from flora and vegetation, abiotic factors were examined as well. Representative soil samples were taken from chosen plots and analysed at the Centre for Soil and Environmental Sciences of the Biotechnical Faculty. In accordance with standard methods the following soil factors were measured: pH, content of plant-accessible potassium and phosphorus, content of organic matter and total nitrogen, C/N ratio, soil texture, content of exchangeable basic cations (Ca, Mg, K, Na), electric conductivity of soil. After analysis and comparisons of several keys for genus Scirpus L., through the compilation of these a new one was made, which now enables the determination of all known species from this genus in Central Europe. 3. RESULTS AND DISCUSSION 3.1 Dactylorhizo majalis-Scirpetum georgiani ass. nova hoc loco (Tab. 1, holotypus Tab. 1/ 3) Syntaxonomic scheme: Molinio-Arrhenatheretea R.Tx. 1937 em. R.Tx. 1970 Molinietalia Koch 1926 Calthion R.Tx 1937 em. Bal.-Tul. 1978 Calthenion R.Tx 1937 em. Bal.-Tul. 1978 Dactylorhizo majalis-Scirpetum georgiani ass. nova 97 HACQUETIA 3/2 • 2004 Table 1: Analytical table of association Dactylorhizo majalis-Scirpetum georgiani ass. nova hoc loco Tabela 1: Analitična tabela asociacije Dactylorhizo majalis-Scirpetum georgiani ass. nova hoc loco Relevé number 12345 Day 13171313 6 Month 66666 Year (+ 2000) 01 02 01 01 01 Altitude (m) 153 153 153 153 151 Plot size (m2) 24 12 12 8 32 coverage (%) 98 98 98 96 100 Character species of the association Scirpus georgianus 5 5 5 5 4 5 100 V Ca Calthion Lysimachia vulgaris 1 1 + + 2 5 100 V Dactylorhiza majalis + . + + . 3 60 III Senecio aquaticus agg. 1 . + . + 3 60 III Valeriana dioica + . + . . 2 40 II Myosotis scorpioides + . . . . 1 20 I Caltha palustris . . + . . 1 20 I Cirsium oleraceum . . . 1 . 1 20 I MO Molinietalia Gratiola officinalis 1 2 2 3 + 5 100 V Betonica officinalis + + + 1 3 5 100 V Lythrum salicaria + 1 + + + 5 100 V Juncus conglomeratus + 1 + + 1 5 100 V Juncus acutiflorus + 2 1 + . 4 80 IV Juncus effusus 2 + . + + 4 80 IV Centaurea carniolica . . + + + 3 60 III Succisella inflexa . . + + . 2 40 II Stachys palustris . . + . . 1 20 I Ophioglossum vulgatum . . . + . 1 20 I Carex distans . . . + . 120 I Selinum carvifolia . . . . 1 1 20 I Succisa pratensis . . . . + 1 20 I MA Molinio-Arrhenatheretea Plantago lanceolata + + + + . 4 80 IV Holcus lanatus 1 1 + . 3 4 80 IV Anthoxanthum odoratum + 1 . + 1 4 80 IV Ajuga reptans + + . . 1 3 60 III Ranunculus acris + . + + . 3 60 III Centaurea macroptilon . . . + 1 2 40 II Leucanthemum ircutianum . . . + 2 2 40 II Lotus corniculatus . . . + + 2 40 II Festuca pratensis . . . + + 2 40 II Trifolium pratense . . . + + 2 40 II Festuca rubra agg. . . . . + 1 20 I Centaurea jacea . . . . + 1 20 I PP Potentillo-Polygonetalia Ranunculus repens + 1 + + + 5 100 V Carex hirta + . + + + 4 80IV Lysimachia nummularia + . . . . 1 20 I Mentha x verticillata . . 1 . . 1 20 I Potentilla reptans . . . 1 . 1 20 I AR Arrhenatheretalia Cynosurus cristatus + + + + + 5 100 V presencefrequency % frequency class 98 IGOR ZELNIK: SCIRPUS GEORGIANUS HARPER – A NEW SPECIES IN SLOVENIAN FLORA … Relevé number 12345 Prunella vulgaris + . + + 1 4 80 IV Trifolium patens . . . . + 1 20 I Hypochaeris radicata . . . . + 1 20 I Rumex acetosa . . . . + 120 I SC Scheuchzerio-Caricetea fuscae Agrostis canina 3 3 3 + 1 5 100 V Carex flava agg. + + + + + 5 100 V Juncus articulatus + + + + + 5 100 V Carex panicea + 1 + + + 5 100 V Ranunculus flammula + 1 1 . . 3 60 III Taraxacum palustre + + + . . 3 60 III Orchis palustris . . + + . 2 40 II Veronica scutellata + . . . . 1 20 I Viola uliginosa . . + . . 1 20 I PM Phragmiti-Magnocaricetea Lycopus europaeus + . + + + 4 80 IV Galium palustre . + + . + 3 60 III Iris pseudacorus . . + . . 1 20 I CU Calluno-Ulicetea Potentilla erecta + + . + + 4 80 IV Carex pallescens . + + . + 3 60 III Carex leporina . + . . . 1 20 I Danthonia decumbens . . . + . 1 20 I Luzula campestris agg. . . . . + 1 20 I Nardus stricta . . . . + 1 20 I Briza media . . . . + 120I O Other (ostale) Anemone nemorosa . . + . + 2 40 II Leucojum vernum . . + . . 1 20 I Erigeron annuus . . . . + 1 20 I Salix cinerea . . . . + 120 I Calystegia sepium . . . . + 1 20 I Populus tremula . . . . + 1 20 I Cirsium sp. . . . . + 120I Localities of the relevés from Table 1: 1: 0158/1 Krakovo virgin forest reserve; 2: 0158/1 Krakovo virgin forest reserve; 3: 0158/1 Krakovo virgin forest reserve; 4: 0158/1 Krakovo virgin forest reserve; 5: 0158/1 Malence, Robič. Lokalitete popisov iz tabele 1: 1: 0158/1 Pragozdni rezervat Krakovski g.; 2: 0158/1 Pragozdni rezervat Krakovski g.; 3: 0158/1 Pragozdni rezervat Krakovski g.; 4: 0158/1 Pragozdni rezervat Krakovski g.; 5: 0158/1 Malence, Robič. As for Scirpetum sylvatici Rałski 1931, so too this may think that – like Scirpetum sylvatici – this assoassociation is defined by its character species Scir-ciation is not very well defined. pus georgianus (Tab. 1). This species is exclusively Despite different contact communities these characteristic for the association if it appears as a stands are similar enough (Fig. 1) to be defined as dominant species and edificator of the association, specific association. They are distinguished from the physiognomy of which makes it explicitly dif-the contact communities by dominance of a charferent from contact communities, besides the dif-acter species as well as by absence of several species ferent soil conditions. Apart from the dominant of the class Molinio-Arrhenatheretea, especially of the species Scirpus georgianus, there are no other char-order Arrhenatheretalia, as those sites are too wet acter species and, hence, some phytosociologists and thus too infertile for these species to thrive. 99 HACQUETIA 3/2 • 2004 .... ... .... ... .... ... .... ... .... ... .... ............. ..... Figure 1: Dendrogram of the association Dactylorhizo majalis-Scirpetum georgiani ass. nova (Tab. 1; Complete linkage, complement of Similarity ratio). Slika 1: Dendrogram asociacije Dactylorhizo majalis-Scirpetum georgiani ass. nova (tab. 1; metoda največjih razdalj, komplement indeksa podobnosti) No data concerning the studied community have been found in the literature, due to the fact that this Northern American species rarely occurs in Europe and is still in the phase of spreading. These stands were only found in two meadows (glades) of the Krakovo forest, because the dominant and/or character species has not yet spread elsewhere so far. 3.1.1 Floristic composition The majority of the species in relevés (Tab. 1) are characters of the class Molinio-Arrhenatheretea and order Molinietalia, respectively. Within the mentioned order, the character species of the alliance Calthion are the most common, so the association was classified into this alliance. Further classification into suballiance Calthenion is evident from the management-type of the wet meadow, as the classification on the base of character species of suballiances is sometimes not possible. Species from the class Scheuchzerio-Caricetea fuscae are also frequent, what indicates the fen characteristics of the studied meadows, namely Agrostis canina, Juncus articulatus, Carex flava agg., C. panicea, Ranunculus flammula, Taraxacum palustre, Orchis palustris, Viola uliginosa, Veronica scutellata. There are also many character species of the class Calluno- Ulicetea such as Potentilla erecta, Carex pallescens, C. leporina, Luzula campestris agg., Danthonia decumbens, Nardus stricta, which give evidence that the sites are oligotrophic. Species which often occur in the contact community Angelico-Cirsietum oleracei, such as Cirsium oleraceum, Carex distans and many other species from the class Molinio-Arrhenatheretea, do not occur here. 3.1.2 Synecology The community is similar in appearance to Scirpetum sylvatici Rałski 1931, there are some similarities regarding ecology as well; however, like the dominant species itself, it thrives in a slightly less wet soil, which is poorer in bases. The soil is acid and base-poor (dystric), pH value is among the lowest, measured in this area (4.6 on average), like in other communities belonging to the acidophilous group of suballiance Calthenion (e.g. Agrostio-Juncetum conglomerati Šegulja 1974). (Zelnik 2003) The content of total nitrogen in the soil is relatively high in comparison with other communities of wet meadows in the research area. The content of exchangeable Ca in the soil is low, while the content of Mg is relatively high, namely 6.5 meq /100 g of soil. 3.2 Scirpus georgianus Harper – character and edificator species of the association During the period from 1997 to 2002, S. georgianus Harper (Fig. 2), the third species from genus Scirpus (L.) for Slovenia, was found in the area of the southern part of the Krakovo forest. The localities belong to quadrants 0158/1 and 0158/2 according to Central European mapping (Fig. 5). This species thrives in a wet meadow, on the forest edge as well as at a draining ditch. Smaller stands and individual specimens were also found in swamp, along the Ressel path. The studied species was probably introduced by members of the North American Mycological Association, who visited the area of the Krakovo virgin forest reserve in the 1980’s. The German name for S. georgianus Harper is ‘Schwarzgrüne Simse’ (Kiffe 1998), in translation »blackish green bulrush«, which is more suitable for the species S. atrovirens. In English-speaking countries, the name ‘Georgia bulrush’ (translation of a Latin name) is used for the mentioned taxa, therefore the Slovene name ‘georgijski sitec’ is more appropriate. 100 IGOR ZELNIK: SCIRPUS GEORGIANUS HARPER – A NEW SPECIES IN SLOVENIAN FLORA … Figure 2: Herbarium specimen of the species Scirpus geor- gianus Harper (Herbarium of the Academy of Natural Sci ences of Philadelphia nr. PH 1023385) Slika 2: Herbarijski primerek vrste Scirpus georgianus Harper (Herbarium of the Academy of Natural Sciences of Philadelphia nr. PH 1023385) 3.2.1 Key After examination of several determination keys for genus Scirpus we have found out that none of them contained all four known species (S. sylvaticus, S. radicans, S. georgianus, S. atrovirens). In order to enable easy and exact determination of the mentioned species in Slovenia and Central Europe respectively, a new key was compiled on the basis of keys in Martinčič & al. (1999), Oberdorfer (1994), Kiffe (1998), Whittemore & Schuyler (2002). Key for the genus Scirpus L., Sect. Scirpus in Central Europe: Spikelets mostly in fascicles at the apices of ultimate rays of inflorescence or aggregated in heads. 2 Inflorescence mostly lax, spikelets in fascicles of 2–5(–8) at apices of ultimate rays. Scales (glumes) blackish-green. Perianth-bristles retrorsely barbed on the whole. Leaves light green...........S. sylvaticus 2* Inflorescence always compact, spikelets in dense fascicles of 4–35(–110), mostly head-shaped, at the apices of the ultimate rays. Scales brownish. Perianth-bristles smooth below. Leaves dark green......... .......................................................(S. atrovirens agg.) 3 Perianth-bristles mostly absent, sometimes 1–3 bristles, shorter than nut (rarely equaling). Nut (0.6–)0.8–1.1 mm long. Spikelets 2–4 mm long; scales (1–)1.2–1.8 mm long............S. georgianus 3* Perianth-bristles usually 6, shorter than or slightly longer than nut. Nut (0.8–)1–1.3 mm long. Spikelets 2–5(–8) mm long; scales (1.2–)1.4–2.1 mm long....................................................S. atrovirens * Spikelets solitary, mostly with long pedicels, but plants often sterile with prolonged and reclining non-flow- Figure 3: Bulblets burst into leaf, species Scirpus georgianus Harper Slika 3: Vzbrsteli brstiči, vrsta Scirpus georgianus Harper 101 HACQUETIA 3/2 • 2004 Figure 4: Inflorescence of the species Scirpus sylvaticus L. Slika 4: Socvetje vrste Scirpus sylvaticus L. 3.2.2 Localities in Slovenia • 0158/1 Slo.: Dolenjska – Posavje, the Krakovo forest, wet meadow and traction near virgin forest reserve. Leg.: I. Zelnik, June 13th 2002 (herbarium of ZRC SAZU, nr.: 8391; Herbarium of the Academy of Natural Sciences of Philadelphia nr.: PH 1023385). • 0158/1 Slo.: Dolenjska – Posavje, the Krakovo forest, Malence, meadow and ditch at a forest lane on the south-western edge of the Krakovo forest, direction north from the Robič farm. Leg.: I. Zelnik, Sept. 20th 2001 (author’s herbarium). • 0158/2 Slo.: Dolenjska – Posavje, the Krakovo forest, Kostanjevica, at the (Ressel) forest lane on the edge of a marshy area. Leg.: I. Zelnik, Sept. 5th 2002 (author’s herbarium). Figure 5: Localities of the species Scirpus georgianus Harper in Slovenia Slika 5: Lokalitete vrste Scirpus georgianus Harper v Sloveniji 102 IGOR ZELNIK: SCIRPUS GEORGIANUS HARPER – A NEW SPECIES IN SLOVENIAN FLORA … 3.2.3 Species ecology The largest stands of species Scirpus georgianus Harper thrive in an extensively cultivated wet meadow on a glade beside the Krakovo virgin forest reserve, where its population visibly increases every year. On the northern and southern edge of the meadow, which is mown once a year, it builds extensive and dense stands, covering an area of 40– 100 m2, whereas in the middle of the meadow it occurs more or less individually, mostly in depressions. The sites of the studied species are less wet than sites of the species S. sylvaticus L. as it was stated also by DeFilipps (1980). The species has probably spread elsewhere from this meadow. The species thrives in a stand (measuring cca. 80 m2) on the slightly shaded edge of an extensively cultivated wet meadow near the village of Malence, and individually in hollows in the middle of the meadow as well; moreover, in the year 2003 it was also found on the forest edge around that meadow and at a draining-ditch by the road. Smaller stands and individual specimens were found along the Ressel path, especially in gaps, where there is still enough light, on forest ground, in tractions and at draining-ditches along the forest lane, about a kilometre towards the interior of the forest. The Ressel path connects all the sites, therefore the conclusion was drawn that the species spreads in an antropochorous way, as is also confirmed by the fact that its fruits are likely to fasten on clothes; on the other hand, the fact that its fruits are eaten by birds indicates its endozoochorous propagation. On the basis of the distribution of the species Scirpus georgianus Harper and its preferences for the specific sites, we have defined it as a character species of the order Molinietalia and, more specifically, of the alliance Calthion. 4. ACKNOWLEDGMENTS I would like to thank Prof. Dr. Andrej Martinčič and Dr. Andraž Čarni for help and revision of the text. For the revision of the herbarium specimens of S. georgianus and the key, I owe special thanks to Dr. Alfred E. Schuyler, curator emeritus of Botany (Academy of Natural Sciences, Philadelphia). For revision of specimens I also thank Dr. Branko Vreš. Thanks are also extended to Prof. Dr. Franc Lobnik et al. (Centre for Soil and Environmental Sciences of Biotechnical Faculty) for the soil analyses performed. For designing the distribution map, I thank Marjan Jarnjak. 5. POVZETEK Scirpus georgianus Harper – nova vrsta v slovenski flori in značilna vrsta asociacije Dactylorhizo majalis- Scirpetum georgiani ass.nova V sklopu raziskav vegetacije jugovzhodne Slovenije v zadnjem desetletju smo še posebej intenzivno proučevali mokrotne travnike. Tako smo v letih 1997–2002 na jasah v jugozahodnem delu Krakovskega gozda našli za Slovenijo novo vrsto – Scirpus georgianus Harper. Domovina vrste je Severna Amerika, kjer je razširjena po mokriščih od Teksasa in Georgie na jugu do Velikih jezer in Nove Fundlandije na severu. Od ostalih dveh vrst iz rodu Scirpus L. (S. sylvaticus L. in S. radicans Schkuhr), ki jih sicer najdemo v Sloveniji, se vrsta loči po značilnem socvetju, kjer so klaski v šopih na koncu togih vejic, periantove ščetine pa večinoma manjkajo. Taksonomska problematika in enačenje vrst S. georgianus in S. atrovirens onemogočata natančen pregled razširjenosti obravnavane vrste v Evropi. Na osnovi taksonomske revizije rodu Scirpus v Severni Ameriki pa Schuyler (1967) trdi, da gre za dve jasno ločeni vrsti: S. atrovirens in S. georgianus. Kiffe (1998) celo navaja, da še ni jasno, ali je bil S. atrovirens s. str. sploh kdaj najden v srednji Evropi ali gre v vseh primerih za S. georgianus. Na podlagi specifičnosti ekoloških razmer rastišč, multivariatnih analiz in značilne fiziognomije sestojev smo te uvrstili v posebno združbo in opisali novo asociacijo z imenom Dactylorhizo majalis-Scirpetum georgiani ass. nova. Močvirno območje Krakovskega gozda prekrivajo gline iz mlajšega würma, na katerih so nastala bolj ali manj hidromorfna tla (amfiglej, hipoglej, obrečna tla). Tla so distrična in v času obilnejših padavin razmočena. Ploskve v sklopu ekstenzivno gojenih mokrotnih travnikov kosijo enkrat letno. Vegetacijo smo popisovali po standardni srednjeevropski metodi (Braun-Blanquet 1964). Numerične analize smo izvedli s programskim paketom SYN-TAX (Podani 2001), z metodo hierarhične klasifikacije (Complete Linkage Clustering, komplement koeficienta podobnosti). Poimenovanje novo opisane združbe je v skladu s kodeksom Weber & al. (2000). Na izbranih popisnih ploskvah smo nabrali vzorce tal, pri katerih smo izmerili: pH, vsebnosti 103 HACQUETIA 3/2 • 2004 dostopnega kalija in fosforja, organske snovi in skupnega dušika, C/N razmerje, teksturo tal, vsebnost izmenljivih bazičnih kationov (Ca, Mg, K, Na), električno prevodnost tal. Združba ima podoben videz kot Scirpetum sylvatici Rałski 1931, definirana je namreč predvsem z dominanco vrste Scirpus georgianus. Poleg značilnic razreda Molinio-Arrhenatheretea in reda Molinietalia, ki so v sestojih najštevilčnejše, tu najdemo tudi značilnice razreda Scheuchzerio-Caricetea fuscae ter razreda Calluno-Ulicetea, ki nakazujejo oligotrofnost rastišč. Sintaksonomski položaj združbe: Molinio-Arrhenatheretea R.Tx. 1937 em. R.Tx. 1970 Molinietalia Koch 1926 Calthion R.Tx 1937 em. Bal.-Tul. 1978 Calthenion R.Tx 1937 em. Bal.-Tul. 1978 Dactylorhizo majalis-Scirpetum georgiani ass. nova Združba, tako kot tudi sama dominantna vrsta, uspeva na nekoliko manj vlažnih in z bazami revnejših tleh kot Scirpetum sylvatici Rałski 1931. Tla so kisla, revna s hranili, predvsem z bazami, oziroma kalcijem. Tu so pH vrednosti med najnižjimi od izmerjenih na tem območju, vsebnosti skupnega dušika pa so, v primerjavi z drugimi združbami mokrotnih travnikov, relativno visoke (Zelnik 2003). Vrsta Scirpus georgianus uspeva na travniku pri rezervatu Krakovski pragozd, na mokrotnem travniku, gozdnem robu ter ob odvodnem jarku ob cesti pri Malencah, SV od Kostanjevice in drugod ob Resslovi poti. Sklepamo, da se vrsta razširja antropohorno (plodovi se pritrjajo na oblačila) in endozoohorno – s plodovi se namreč hranijo ptice. Za slovensko ime vrste S. georgianus Harper predlagamo ime »georgijski sitec« – prevod latinskega imena, ki je bolj utemeljeno kot »črno zeleni sitec« (nem. Schwarzgrüne Simse), ki ga za to vrsto uporablja Kiffe (1998), saj je to preveč podobno prevodu imena S. atrovirens – »temno zeleni sitec«. Po pregledu številnih ključev za rod Scirpus smo ugotovili, da noben ne vsebuje vseh štirih vrst, ki uspevajo na območju srednje Evrope (S. sylvaticus, S. radicans, S. georgianus, S. atrovirens). Za enostavno in zanesljivo določanje omenjenih vrst v Sloveniji oziroma srednji Evropi smo s kombinacijo obstoječih ključev v Martinčič & al. (1999), Oberdorfer (1994), Kiffe (1998), Whittemore & Schuyler (2002) izdelali novega: Ključ za rod Scirpus L., Sect. Scirpus v srednji Evropi: 1 Klaski večinoma glavičasto združeni na koncu vejic ali pa vsi klaski združeni v šope. 2 Socvetje večinoma rahlo, po 2–5(–8) klaskov v šopih na koncu vejic socvetja. Pleve črnikasto-zelene. Perigonove ščetine v celoti hrapave, z izrastki, ki so obrnjeni proti bazi. Listi svetlo zeleni....................... .................................................................S. sylvaticus 2* Socvetje vedno glavičasto zgoščeno, po (4–)8–35 (–110) klaskov v šopih na koncu vejic socvetja. Pleve rjavkaste. Perigonove ščetine hrapave le v zgornjem delu. Listi temno zeleni.....(S. atrovirens agg.) 3 Perigonove ščetine večinoma manjkajo, včasih najdemo 1–3 ščetine, ki so krajše od ahene (redko enako dolge). Ahene dolge (0,6–)0,8– 1,1 mm. Klaski 2–4 mm dolgi; pleve 1,2–1,8 mm dolge................................................ S. georgianus 3* Perigonovih ščetin ponavadi 6, krajše ali rahlo daljše kot ahena. Ahene (0,8–)1–1,3 mm dolge. 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