黑海和亚速海沿岸(克拉斯诺达尔地区)沙生植物群落的分类学

Q4 Agricultural and Biological Sciences Rastitel''nost'' Rossii Pub Date : 2022-01-01 DOI:10.31111/vegrus/2022.43.23
N. Grechushkina, A. V. Chuvashov, V. B. Golub
{"title":"黑海和亚速海沿岸(克拉斯诺达尔地区)沙生植物群落的分类学","authors":"N. Grechushkina, A. V. Chuvashov, V. B. Golub","doi":"10.31111/vegrus/2022.43.23","DOIUrl":null,"url":null,"abstract":"The psammophytic communities on sandy accumulative coasts of the Black and Azov Seas were studied in the Krasnodar Territory (Russia) in 2004, 2006 and 2009, when 1610 relevés were made. Of these, 203 relevés were previously classified and published. In this paper based on 23 relevés two new associations and two new subassociations of the class Ammophiletea Br.-Bl. et Tx. ex Westhoff et al. 1946 and one rankless transitional community (Fig. 1) are described according to Braun-Blanquet approach. The abundance of plants estimated in the field as a percentage of the projective cover was converted to scale points: 5 — > 50 %, 4 — 26–50 %, 3 — 16–25 %, 2 — 6–15 %, 1 — 1–5 %, + — < 1 %. Clustering of the relevés (phytocenon isolation) was carried out by flexible beta linkage (β = –0.25) based on the Sørensen coefficient in PC-ORD 5.0, available through the JUICE 7.1 software package (Tichý, Jason, 2006). As a result four phytocenons were established. Their species composition was compared with the species lists of the lower 676 coastal syntaxa of the Azov-Black Sea region, taken from literature and stored in authors’ syntaxon database (GIVD ID EU-RU-005) based on the TURBOVEG program (Hennekens, Schaminée, 2001). An initial assessment of the similarity of littoral syntaxa and phytocenons was performed using several methods available in the JUICE 7.1 software package. In all cases bryophytes and lichens as well as vascular plant species with frequency less than 20 % in any community were excluded from the analysis. All these excluded species are present in Tables 1 and 2. To classify the established phytocenons, their species composition was compared with similar protologues of the lower syntaxa (Table 1). The vascular plant taxa names are by Tutin et al., (2001). In naming the taxa below, a broad understanding of species (s. l.), their aggregation (agg.), or the combination of several species (with “+”) are used: Artemisia campestris+A. tschernieviana, Cakile maritima s. l. (C. maritima, C. maritima subsp. euxina), Centaurea arenaria s. l.(C. arenaria, C. arenaria subsp. odessana), Leymus racemosus s. l. (L. racemosus, L. racemosus subsp. sabulosus); S. kali aggr. (Salsola kali, S. kali subsp. ruthenica or S. kali subsp. tragus) based on P. Uotila (2011) and S. L. Mosyakin (2017); Xanthium strumarium s. l. (X. strumarium, X. strumarium subsp. italicum, X. strumarium subsp. strumarium × subsp. italicum). Few bryophyte and lichen taxa are given with their authors. The names of the new syntaxa are formed according to the ICPN rules (Theurillat et al., 2021). The terrain in the study area is flat. The natural banks are represented by abrasion and accumulative types. The latter is often in the form of sandy or sandy-shelly spits. There are low-lying near-mouth and delta accumulative banks at the mouths of large rivers. Widespread are solonchaks both not vegetated or with halophytic communities. The climate is temperate with continental features. The month mean temperatures and sums of precipitation amounts for the ten-year period (2001–2010) are reflected in the climate diagrams (Fig. 2). The closest in species composition to the established phytocenons were the lower syntaxa (among the protologues) described in Russia, Romania and Ukraine (Table 1), attributed by their authors to the alliance Elymion gigantei Morariu 1957 (class Ammophiletea Br.-Bl. et Tx. ex Westhoff et al. 1946). However, the identified species differences did not allow us to assign the phytocenons (Table 1) to these syntaxonomical units. All phytocenons are classified as new syntaxa (Table 2). The geographical location of the lower syntaxa presented in Table 1 see on Fig. 3. Ass. Eryngio maritimi–Leymetum sabulosi ass. nov: Table 2, rel. 1–13, Fig. 4; holotypus: Table 2, rel. 6, Krasnodar Territory, Anapa sandbar opposite the settlement Blagoveshchenskaya (coast of the Black Sea), fixed dunes in the distance from the sea, 25.08.2004. Diagnostic taxa (d. t.): Artemisia campestris+A. tschernieviana, Eryngium maritimum, Leymus racemosus s. l. The association includes psammophytic herb–dwarf-semishrub communities on fixed and mobile sandy substrates. Subass. Eryngio maritimi–Leymetum sabulositypicum subass. nov.: Table 2, rel. 1–7; holotypus: Table 2, rel. 6, Fig. 5. The diagnostic attributes of the typical subassociation communities are the same as of the association. Plant communities of the subassociation inhabit both mobile and weakly fixed sandy sediments of the accumulative coasts of the Black and Azov Seas. Subass. Eryngio maritimi–Leymetum sabulosi crambetosum maritimae subass. nov.: Table 2, rel. 8–13, Fig. 6; holotypus: Table 2, rel. 10, Krasnodar Territory, 4 km ENE from the settlement Golubitskaya, coast of the Temryuk Bay (Azov Sea), low dune (1.5–2 m high), 04.09.2004, D. t. of the subassociation: Crambe maritima, Lactuca tatarica. Communities occur on fixed sands on accumulative banks. Community Conium maculatum–Centaurea arenaria: Table 2, rel. 14–18. D. t.: Astragalus onobrychis, Centaurea arenaria s. l., Conium maculatum, Galium humifusum, Torilis arvensis. The communities of this rankless transitional unit occur on flat or depressed terrain areas on the Temryuk Bay coast. Ass. Cakilo euxinae–Glycyrrhizetum glabrae ass. nov.: Table 2, rel. 19–23, Fig. 7; holotypus: Table 2, rel. 19, Krasnodar Territory, Bugazsk Spit, opposite Veselovka village, the coast between the Black Sea and Bugaz Liman, slope of sandy sediment (north-east exposure, 1–2° slope) toward the estuary, 19.08.2004. D. t.: Cakile maritima s. l., Glycyrrhiza glabra, Carex ligerica, Salsola kali aggr. Communities are distributed on the southern part of the Taman Peninsula. They are found on tops of the avandunes, as well as away from them on the elevated parts of the marine spits.","PeriodicalId":37606,"journal":{"name":"Rastitel''nost'' Rossii","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Syntaxonomy of psammophytic communities of the Black and Azov Sea coasts (Krasnodar Territory)\",\"authors\":\"N. Grechushkina, A. 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Clustering of the relevés (phytocenon isolation) was carried out by flexible beta linkage (β = –0.25) based on the Sørensen coefficient in PC-ORD 5.0, available through the JUICE 7.1 software package (Tichý, Jason, 2006). As a result four phytocenons were established. Their species composition was compared with the species lists of the lower 676 coastal syntaxa of the Azov-Black Sea region, taken from literature and stored in authors’ syntaxon database (GIVD ID EU-RU-005) based on the TURBOVEG program (Hennekens, Schaminée, 2001). An initial assessment of the similarity of littoral syntaxa and phytocenons was performed using several methods available in the JUICE 7.1 software package. In all cases bryophytes and lichens as well as vascular plant species with frequency less than 20 % in any community were excluded from the analysis. All these excluded species are present in Tables 1 and 2. To classify the established phytocenons, their species composition was compared with similar protologues of the lower syntaxa (Table 1). The vascular plant taxa names are by Tutin et al., (2001). In naming the taxa below, a broad understanding of species (s. l.), their aggregation (agg.), or the combination of several species (with “+”) are used: Artemisia campestris+A. tschernieviana, Cakile maritima s. l. (C. maritima, C. maritima subsp. euxina), Centaurea arenaria s. l.(C. arenaria, C. arenaria subsp. odessana), Leymus racemosus s. l. (L. racemosus, L. racemosus subsp. sabulosus); S. kali aggr. (Salsola kali, S. kali subsp. ruthenica or S. kali subsp. tragus) based on P. Uotila (2011) and S. L. Mosyakin (2017); Xanthium strumarium s. l. (X. strumarium, X. strumarium subsp. italicum, X. strumarium subsp. strumarium × subsp. italicum). Few bryophyte and lichen taxa are given with their authors. The names of the new syntaxa are formed according to the ICPN rules (Theurillat et al., 2021). The terrain in the study area is flat. The natural banks are represented by abrasion and accumulative types. The latter is often in the form of sandy or sandy-shelly spits. There are low-lying near-mouth and delta accumulative banks at the mouths of large rivers. Widespread are solonchaks both not vegetated or with halophytic communities. The climate is temperate with continental features. The month mean temperatures and sums of precipitation amounts for the ten-year period (2001–2010) are reflected in the climate diagrams (Fig. 2). The closest in species composition to the established phytocenons were the lower syntaxa (among the protologues) described in Russia, Romania and Ukraine (Table 1), attributed by their authors to the alliance Elymion gigantei Morariu 1957 (class Ammophiletea Br.-Bl. et Tx. ex Westhoff et al. 1946). 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Plant communities of the subassociation inhabit both mobile and weakly fixed sandy sediments of the accumulative coasts of the Black and Azov Seas. Subass. Eryngio maritimi–Leymetum sabulosi crambetosum maritimae subass. nov.: Table 2, rel. 8–13, Fig. 6; holotypus: Table 2, rel. 10, Krasnodar Territory, 4 km ENE from the settlement Golubitskaya, coast of the Temryuk Bay (Azov Sea), low dune (1.5–2 m high), 04.09.2004, D. t. of the subassociation: Crambe maritima, Lactuca tatarica. Communities occur on fixed sands on accumulative banks. Community Conium maculatum–Centaurea arenaria: Table 2, rel. 14–18. D. t.: Astragalus onobrychis, Centaurea arenaria s. l., Conium maculatum, Galium humifusum, Torilis arvensis. The communities of this rankless transitional unit occur on flat or depressed terrain areas on the Temryuk Bay coast. Ass. Cakilo euxinae–Glycyrrhizetum glabrae ass. nov.: Table 2, rel. 19–23, Fig. 7; holotypus: Table 2, rel. 19, Krasnodar Territory, Bugazsk Spit, opposite Veselovka village, the coast between the Black Sea and Bugaz Liman, slope of sandy sediment (north-east exposure, 1–2° slope) toward the estuary, 19.08.2004. D. t.: Cakile maritima s. l., Glycyrrhiza glabra, Carex ligerica, Salsola kali aggr. Communities are distributed on the southern part of the Taman Peninsula. 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摘要

2004年、2006年和2009年在俄罗斯克拉斯诺达尔地区对黑海和亚速海沙质堆积海岸的沙生植物群落进行了研究,共进行了1610次相关采样。其中,203份相关文件先前已分类并公布。本文在23篇文献的基础上,对嗜Ammophiletea Br.-Bl纲的2个新属和2个新亚属进行了综述。et txex Westhoff et al. 1946和一个无秩过渡群落(图1)是根据布朗-布兰凯方法描述的。将估算的植物丰度与投影覆盖的百分比转换为以下尺度点:5 - 50 %、4 - 26-50 %、3 - 16-25 %、2 - 6-15 %、1 - 1 - 5 %、+ - < 1 %。通过JUICE 7.1软件包(Tichý, Jason, 2006),基于PC-ORD 5.0中的Sørensen系数,通过灵活的β链接(β = -0.25)对相关的<s:1> <s:1> <s:1> <s:1> <s:1>化学物质(phytocenon分离)进行聚类。结果建立了四个植物群落。将它们的物种组成与基于TURBOVEG程序(Hennekens, schamin<s:1>, 2001)的作者语法数据库(GIVD ID EU-RU-005)中文献中676个亚速海-黑海沿岸低级句法类群的物种表进行比较。使用JUICE 7.1软件包中提供的几种方法对沿海句法群和植物群落的相似性进行了初步评估。在所有情况下,在任何群落中,苔藓植物、地衣和维管植物物种的频率低于20%,均被排除在分析之外。所有这些被排除的物种都出现在表1和表2中。为了对已建立的植物类群进行分类,将它们的物种组成与低等植物类群的相似原生生物进行了比较(表1)。维管植物类群的名称由Tutin et al.,(2001)提供。在命名下面的分类群时,使用了对物种(s. l.),它们的聚集(agg.)或几个物种的组合(带“+”)的广泛理解:Artemisia campestris+ a。(1)海棠花,海棠花子;半人马花(Centaurea arenaria);砂藻,砂藻亚种。总状羊草(l.总状羊草,l.总状羊草亚种);sabulosus);锦葵。酸菜,酸菜亚种;真丝孢菌或菌类。P. Uotila(2011)和S. L. Mosyakin (2017);苍耳菌(X. strumarium, X. strumarium)柱头属,柱头属。瘤x亚种italicum)。苔藓植物和地衣植物的分类很少,作者也很少。新句法的名称是根据ICPN规则形成的(Theurillat et al., 2021)。研究区的地形是平坦的。天然河岸以磨蚀型和堆积型为代表。后者通常以沙状或雪状唾液的形式出现。大河入海口处有低洼的近河口滩和三角洲堆积滩。广泛分布的是无植被或有盐生植物群落的独刺林。气候属温带大陆性气候。在物种组成上,与已建立的植物群落最接近的是在俄罗斯、罗马尼亚和乌克兰描述的较低的合成类(在原生类群中)(表1),它们的作者将其归因于Elymion gigantei Morariu 1957(类Ammophiletea Br.-Bl)。et Tx. ex Westhoff et al. 1946)。然而,已鉴定的物种差异不允许我们将植物分类学单位(表1)分配给这些单位。所有植物群落都被归类为新句法(表2)。表1中较低句法的地理位置见图3。海绵草-沙绵草:表2,rel. 1-13,图4;holotypus:表2,第6卷,克拉斯诺达尔地区,布拉戈维申斯卡亚定居点对面的阿纳帕沙洲(黑海海岸),远离大海的固定沙丘,2004年8月25日。诊断分类群(d.t .):黄花蒿+黄花蒿。该协会包括固定和流动沙质基质上的沙生草本-矮-半灌木群落。Subass。海燕草-海燕草。11月:表2,rel. 1-7;holotypus:表2,rel. 6,图5。典型子关联团体的诊断属性与关联相同。亚群落的植物群落栖息在黑海和亚速海积聚海岸的流动和弱固定的沙质沉积物中。Subass。海鲈-海鲈。11月:表2,rel. 8-13,图6;holotypus:表2,第10期,Krasnodar领土,距Golubitskaya定居点东北4公里,Temryuk湾(亚速海)海岸,低沙丘(1.5-2米高),2004年9月4日,亚群博士:Crambe maritima, Lactuca tatarica。群落出现在累积河岸的固定沙上。 2004年、2006年和2009年在俄罗斯克拉斯诺达尔地区对黑海和亚速海沙质堆积海岸的沙生植物群落进行了研究,共进行了1610次相关采样。其中,203份相关文件先前已分类并公布。本文在23篇文献的基础上,对嗜Ammophiletea Br.-Bl纲的2个新属和2个新亚属进行了综述。et txex Westhoff et al. 1946和一个无秩过渡群落(图1)是根据布朗-布兰凯方法描述的。将估算的植物丰度与投影覆盖的百分比转换为以下尺度点:5 - 50 %、4 - 26-50 %、3 - 16-25 %、2 - 6-15 %、1 - 1 - 5 %、+ - < 1 %。通过JUICE 7.1软件包(Tichý, Jason, 2006),基于PC-ORD 5.0中的Sørensen系数,通过灵活的β链接(β = -0.25)对相关的<s:1> <s:1> <s:1> <s:1> <s:1>化学物质(phytocenon分离)进行聚类。结果建立了四个植物群落。将它们的物种组成与基于TURBOVEG程序(Hennekens, schamin<s:1>, 2001)的作者语法数据库(GIVD ID EU-RU-005)中文献中676个亚速海-黑海沿岸低级句法类群的物种表进行比较。使用JUICE 7.1软件包中提供的几种方法对沿海句法群和植物群落的相似性进行了初步评估。在所有情况下,在任何群落中,苔藓植物、地衣和维管植物物种的频率低于20%,均被排除在分析之外。所有这些被排除的物种都出现在表1和表2中。为了对已建立的植物类群进行分类,将它们的物种组成与低等植物类群的相似原生生物进行了比较(表1)。维管植物类群的名称由Tutin et al.,(2001)提供。在命名下面的分类群时,使用了对物种(s. l.),它们的聚集(agg.)或几个物种的组合(带“+”)的广泛理解:Artemisia campestris+ a。(1)海棠花,海棠花子;半人马花(Centaurea arenaria);砂藻,砂藻亚种。总状羊草(l.总状羊草,l.总状羊草亚种);sabulosus);锦葵。酸菜,酸菜亚种;真丝孢菌或菌类。P. Uotila(2011)和S. L. Mosyakin (2017);苍耳菌(X. strumarium, X. strumarium)柱头属,柱头属。瘤x亚种italicum)。苔藓植物和地衣植物的分类很少,作者也很少。新句法的名称是根据ICPN规则形成的(Theurillat et al., 2021)。研究区的地形是平坦的。天然河岸以磨蚀型和堆积型为代表。后者通常以沙状或雪状唾液的形式出现。大河入海口处有低洼的近河口滩和三角洲堆积滩。广泛分布的是无植被或有盐生植物群落的独刺林。气候属温带大陆性气候。在物种组成上,与已建立的植物群落最接近的是在俄罗斯、罗马尼亚和乌克兰描述的较低的合成类(在原生类群中)(表1),它们的作者将其归因于Elymion gigantei Morariu 1957(类Ammophiletea Br.-Bl)。et Tx. ex Westhoff et al. 1946)。然而,已鉴定的物种差异不允许我们将植物分类学单位(表1)分配给这些单位。所有植物群落都被归类为新句法(表2)。表1中较低句法的地理位置见图3。海绵草-沙绵草:表2,rel. 1-13,图4;holotypus:表2,第6卷,克拉斯诺达尔地区,布拉戈维申斯卡亚定居点对面的阿纳帕沙洲(黑海海岸),远离大海的固定沙丘,2004年8月25日。诊断分类群(d.t .):黄花蒿+黄花蒿。该协会包括固定和流动沙质基质上的沙生草本-矮-半灌木群落。Subass。海燕草-海燕草。11月:表2,rel. 1-7;holotypus:表2,rel. 6,图5。典型子关联团体的诊断属性与关联相同。亚群落的植物群落栖息在黑海和亚速海积聚海岸的流动和弱固定的沙质沉积物中。Subass。海鲈-海鲈。11月:表2,rel. 8-13,图6;holotypus:表2,第10期,Krasnodar领土,距Golubitskaya定居点东北4公里,Temryuk湾(亚速海)海岸,低沙丘(1.5-2米高),2004年9月4日,亚群博士:Crambe maritima, Lactuca tatarica。群落出现在累积河岸的固定沙上。 群落黄斑锥体-半人马:表2,rel. 14-18。主要品种:黄芪、半人马花、金盏花、金盏花、金盏花。这种无等级的过渡单位的群落出现在天育克湾海岸的平坦或洼地地区。11月:表2,rel. 19-23,图7;holotypus:表2,第19 rel. 19, Krasnodar Territory, Bugazsk Spit, Veselovka村对面,黑海和Bugaz Liman之间的海岸,沙质沉积物斜坡(东北暴露,1-2°斜坡)朝向河口,2004年8月19日。博士论文:海苔草、甘草、毛苔草、水蛭。社区分布在塔曼半岛的南部。它们在avandunes的顶部被发现,也在远离它们的海洋喷口的高处被发现。
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Syntaxonomy of psammophytic communities of the Black and Azov Sea coasts (Krasnodar Territory)
The psammophytic communities on sandy accumulative coasts of the Black and Azov Seas were studied in the Krasnodar Territory (Russia) in 2004, 2006 and 2009, when 1610 relevés were made. Of these, 203 relevés were previously classified and published. In this paper based on 23 relevés two new associations and two new subassociations of the class Ammophiletea Br.-Bl. et Tx. ex Westhoff et al. 1946 and one rankless transitional community (Fig. 1) are described according to Braun-Blanquet approach. The abundance of plants estimated in the field as a percentage of the projective cover was converted to scale points: 5 — > 50 %, 4 — 26–50 %, 3 — 16–25 %, 2 — 6–15 %, 1 — 1–5 %, + — < 1 %. Clustering of the relevés (phytocenon isolation) was carried out by flexible beta linkage (β = –0.25) based on the Sørensen coefficient in PC-ORD 5.0, available through the JUICE 7.1 software package (Tichý, Jason, 2006). As a result four phytocenons were established. Their species composition was compared with the species lists of the lower 676 coastal syntaxa of the Azov-Black Sea region, taken from literature and stored in authors’ syntaxon database (GIVD ID EU-RU-005) based on the TURBOVEG program (Hennekens, Schaminée, 2001). An initial assessment of the similarity of littoral syntaxa and phytocenons was performed using several methods available in the JUICE 7.1 software package. In all cases bryophytes and lichens as well as vascular plant species with frequency less than 20 % in any community were excluded from the analysis. All these excluded species are present in Tables 1 and 2. To classify the established phytocenons, their species composition was compared with similar protologues of the lower syntaxa (Table 1). The vascular plant taxa names are by Tutin et al., (2001). In naming the taxa below, a broad understanding of species (s. l.), their aggregation (agg.), or the combination of several species (with “+”) are used: Artemisia campestris+A. tschernieviana, Cakile maritima s. l. (C. maritima, C. maritima subsp. euxina), Centaurea arenaria s. l.(C. arenaria, C. arenaria subsp. odessana), Leymus racemosus s. l. (L. racemosus, L. racemosus subsp. sabulosus); S. kali aggr. (Salsola kali, S. kali subsp. ruthenica or S. kali subsp. tragus) based on P. Uotila (2011) and S. L. Mosyakin (2017); Xanthium strumarium s. l. (X. strumarium, X. strumarium subsp. italicum, X. strumarium subsp. strumarium × subsp. italicum). Few bryophyte and lichen taxa are given with their authors. The names of the new syntaxa are formed according to the ICPN rules (Theurillat et al., 2021). The terrain in the study area is flat. The natural banks are represented by abrasion and accumulative types. The latter is often in the form of sandy or sandy-shelly spits. There are low-lying near-mouth and delta accumulative banks at the mouths of large rivers. Widespread are solonchaks both not vegetated or with halophytic communities. The climate is temperate with continental features. The month mean temperatures and sums of precipitation amounts for the ten-year period (2001–2010) are reflected in the climate diagrams (Fig. 2). The closest in species composition to the established phytocenons were the lower syntaxa (among the protologues) described in Russia, Romania and Ukraine (Table 1), attributed by their authors to the alliance Elymion gigantei Morariu 1957 (class Ammophiletea Br.-Bl. et Tx. ex Westhoff et al. 1946). However, the identified species differences did not allow us to assign the phytocenons (Table 1) to these syntaxonomical units. All phytocenons are classified as new syntaxa (Table 2). The geographical location of the lower syntaxa presented in Table 1 see on Fig. 3. Ass. Eryngio maritimi–Leymetum sabulosi ass. nov: Table 2, rel. 1–13, Fig. 4; holotypus: Table 2, rel. 6, Krasnodar Territory, Anapa sandbar opposite the settlement Blagoveshchenskaya (coast of the Black Sea), fixed dunes in the distance from the sea, 25.08.2004. Diagnostic taxa (d. t.): Artemisia campestris+A. tschernieviana, Eryngium maritimum, Leymus racemosus s. l. The association includes psammophytic herb–dwarf-semishrub communities on fixed and mobile sandy substrates. Subass. Eryngio maritimi–Leymetum sabulositypicum subass. nov.: Table 2, rel. 1–7; holotypus: Table 2, rel. 6, Fig. 5. The diagnostic attributes of the typical subassociation communities are the same as of the association. Plant communities of the subassociation inhabit both mobile and weakly fixed sandy sediments of the accumulative coasts of the Black and Azov Seas. Subass. Eryngio maritimi–Leymetum sabulosi crambetosum maritimae subass. nov.: Table 2, rel. 8–13, Fig. 6; holotypus: Table 2, rel. 10, Krasnodar Territory, 4 km ENE from the settlement Golubitskaya, coast of the Temryuk Bay (Azov Sea), low dune (1.5–2 m high), 04.09.2004, D. t. of the subassociation: Crambe maritima, Lactuca tatarica. Communities occur on fixed sands on accumulative banks. Community Conium maculatum–Centaurea arenaria: Table 2, rel. 14–18. D. t.: Astragalus onobrychis, Centaurea arenaria s. l., Conium maculatum, Galium humifusum, Torilis arvensis. The communities of this rankless transitional unit occur on flat or depressed terrain areas on the Temryuk Bay coast. Ass. Cakilo euxinae–Glycyrrhizetum glabrae ass. nov.: Table 2, rel. 19–23, Fig. 7; holotypus: Table 2, rel. 19, Krasnodar Territory, Bugazsk Spit, opposite Veselovka village, the coast between the Black Sea and Bugaz Liman, slope of sandy sediment (north-east exposure, 1–2° slope) toward the estuary, 19.08.2004. D. t.: Cakile maritima s. l., Glycyrrhiza glabra, Carex ligerica, Salsola kali aggr. Communities are distributed on the southern part of the Taman Peninsula. They are found on tops of the avandunes, as well as away from them on the elevated parts of the marine spits.
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来源期刊
Rastitel''nost'' Rossii
Rastitel''nost'' Rossii Agricultural and Biological Sciences-Plant Science
CiteScore
1.20
自引率
0.00%
发文量
5
期刊介绍: The scientific journal Rastitel''nost'' Rossii is included in the Scopus database. Publisher country is Russia. The main subject areas of published articles are Ecology, Evolution, Behavior and Systematics, Plant Science, Общая биология.
期刊最新文献
Ranunculetum mongolicin — a new association of aquatic vegetation from the Republic of Altai Class Festuco-Brometea Br.-Bl. et Tx. ex Soó 1947 in the Southern Trans-Urals (the steppe zone of Chelyabinsk Region) Vegetation of segde-hypnum and wooded rich fens and swamps on the north border of their distribution in Western Siberia Plant communities of the Sarykum sand massif (Republic of Dagestan) Field mire seminar with international participation in Polistovsky state nature reserve (Pskov Region, Bezhanitsy settlement, September 8–9, 2022)
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