Open Access
How to translate text using browser tools
6 April 2016 Contribution to the vascular flora of Chalki Island (East Aegean, Greece) and biomonitoring of a local endemic taxon
Maria Tsakiri, Konstantinos Kougioumoutzis, Gregoris Iatrou
Author Affiliations +

The island of Chalki, located W of Rhodos, belongs to the East Aegean Islands and is situated at the E part of the South Aegean Island Arc. The flora of Chalki consists of 519 vascular plant taxa, 29 of which are under statutory protection, 22 are Greek endemics and 109 are reported here for the first time. We show that Chalki has the second highest percentage of Greek endemics in the phytogeographical region of the East Aegean Islands. The known distribution of Limonium ocymifolium, L. sitiacum and Phoenix theophrasti is expanded, being reported for the first time for the phytogeographical region of the East Aegean Islands. Finally, we assess for the first time the conservation status of Allium chalkii, a single-island endemic, by biomonitoring its populations.

Version of record first published online on 6 April 2016 ahead of inclusion in April 2016 issue.


With more than 7000 islands and islets (Triantis & Mylonas 2009), the Aegean archipelago is one of the largest archipelagos in the world, after the Caribbean, Indonesia and the South Pacific (Blondel & al. 2010). The Aegean has long served as a meeting ground for species of varying origin, since it lies at the crossroads of three continents, namely Europe, Asia and Africa (Poulakakis & al. 2014). Its high environmental and topographical heterogeneity (Blondel & al. 2010), complex geological and palaeogeographical history, as well as its high diversity and endemism (Strid 1996) render it as an ideal stage for biodiversity studies. Intensive field work has taken place in the Aegean phytogeographical regions of Greece, and numerous biodiversity and biogeographical studies have been carried out in recent years (e.g. Livaniou-Tiniakou & al. 2003; Kallimanis & al. 2010; Kagiampaki & al. 2011; Raus 2012; Trigas & al. 2013; Kougioumoutzis & al. 2014a) and more specifically in the phytogeographical region of the East Aegean Islands (e.g. Panitsa & al. 2006, 2010; Constantinidis 2013), which has been characterized as one of the most floristically explored phytogeographical regions of Greece (Dimopoulos & al. 2013; Bergmeier & Strid 2014). However, certain islands have not yet been the main focal areas of floristic research, leaving our knowledge of the flora of the East Aegean islands still incomplete.

Eighteen large islands and numerous islets comprise the phytogeographical region of the East Aegean Islands, which is the floristically richest insular phytogeographical region of Greece (Dimopoulos & al. 2013). The East Aegean Islands host 2541 taxa (Dimopoulos & al. 2013), 160 of which are Greek endemics (6.3 %) and demonstrate lower than normal endemism, as expected by their size (Georghiou & Delipetrou 2010). Even though the flora of the large East Aegean islands (e.g. Papatsou 1971; Carlström 1987; Christodoulakis 1996a; Brofas & al. 2001; Panitsa & Tzanoudakis 2001, 2010; Biel 2002; Panitsa & al. 2003, 2006; Bazos 2005; Zervou & al. 2009) and islets (Panitsa 1997; Panitsa & al. 2008) is well known, the flora of the smaller East Aegean islands is rather underexplored. As a contribution to fill this gap we thoroughly investigated the flora of Chalki Island.

Chalki Island (Fig. 1) is located in the E part of the South Aegean Island Arc, an island chain connecting the coasts of SE continental Greece (Peloponnisos) with SW Asia Minor and forming the S closure of the Aegean archipelago. Chalki belongs to the archipelago of Rhodos, lying c. 9 km W of Cape Armenistis. The islands comprising the Rhodos archipelago have been isolated from the adjacent island complex of Karpathos since the late Pliocene (Böger & Dermitzakis 1987) and from the Marmaris (Datça) peninsula of Asia Minor since 800 000 b.p. (Perissoratis & Conispoliatis 2003), while Chalki has been isolated from Rhodos since the offset of the last glacial maximum (Lykousis 2009). Chalki acquired its present configuration c. 8000 b.p., when the last of Chalki's surrounding islets detached from the study area (Maroukian & al. 2004).

Chalki is part of the outer island arc of the Hellenides and belongs to the geotectonic zone of Tripoli. Despite its small size (27 km2), it is characterized by a variety of geological substrates, viz. dolines with terra rossa bodies, flysch, limestone, conglomerates, scree, alluvial deposits and secondary pumice deposits (Maroukian & al. 2004).

The study area is mainly hilly with a very intense relief (especially in the SW part of Chalki), the highest peak being Maistros hill (601 m). The coastline is c. 34 km long, hosting several precipitous, coastal cliffs and many inaccessible gravelly beaches. The hydrographical network of Chalki is rather limited, with only one seasonally active stream.

The nearest meteorological station to Chalki lies in Rhodos; according to Gouvas & Sakellariou (2011), this station and hence the study area belongs to the subhumid bioclimatic zone with a warm winter and also to the Thermo-mediterranean zone.

Fig. 1.

Location of Chalki Island in relation to nearby islands and in the SE Aegean (inset).


Rechinger (1944) was the first botanist to report on plants from Chalki. Most records, however, were reported thereafter in the frame of the project Flora of Turkey and the East Aegean Islands (Davis 1965–1985; Davis & al. 1988; Güner & al. 2001), as well as by Carlström (1987). Information on some endemic and/or rare taxa occurring in the area is given by Strid & Tan (1997, 2002). From a phytogeographical point of view, however, the interesting flora of the island of Chalki has not yet received the attention it deserves in spite of these earlier records.

Finally, Allium chalkii Tzanoud. & Kollmann is confined to Chalki, and thus Chalki is the smallest island in the phytogeographical region of the East Aegean Islands that hosts at least one single-island endemic. Even though A. chalkii is a very rare taxon, it has never before been monitored or evaluated under IUCN criteria.

Therefore, the scope of the present study aims at thoroughly investigating (1) the flora of Chalki; (2) whether its flora is impoverished or not, compared to that of the other East Aegean islands; and (3) the conservation status of Allium chalkii with a preliminary assessment of its population size, area of occupancy and extent of occurrence.

Material and methods

Several collection and field observation trips to the study area were carried out from April 2012 to May 2014 in order to acquire an integrated knowledge of the flora of Chalki. Herbarium specimens are deposited at the Botanical Museum of the University of Patras (UPA; herbarium code according to Thiers [continuously updated]). Species identification and nomenclature are according to Davis (1965–1985), Tutin & al. (1968–1980, 1993), Greuter & al. (1984–1989), Davis & al. (1988), Strid & Tan (1997, 2003), Güner & al. (2001), Tan & al. (2001), Greuter & Raab-Straube (2008) and Dimopoulos & al. (2013). For family delimitations we follow Dimopoulos & al. (2013). The status of the alien taxa occurring in the study area is according to Arianoutsou & al. (2010) and Dimopoulos & al. (2013). The nomenclature and status of the endemic taxa recorded from Chalki are based on Dimopoulos & al. (2013). The life-form and chorological categories follow Dimopoulos & al. (2013 — see Appendix for abbreviations used). Data regarding the endemism levels in the phytogeographical region of the East Aegean Islands are based on Panitsa & al. (2010) and Dimopoulos & al. (2013).

In order to compare the floristic diversity between islands of different size, we investigated the island speciesarea relationships (ISARs) for the native and endemic species occurring in the East Aegean islands (as in Panitsa & al. 2010), by fitting the logarithmic transformation of the Arrhenius (1921) power model: Log(S) = c + z*Log(A), where S is the value of each of the richness metrics used, A is the area of the respective island in km2 and c, z the fitted parameters. A value of 1 was added to certain cases before log10 transformation, because zero values were reported for some islands. Then, we used the values of the residuals from ISAR log10-transfomed models of the native and endemic species occurring in the East Aegean islands, as these values are interpreted as a measure of island species diversity and do not reflect the influence of island area (Hobohm's α-index; Hobohm 2000, 2003). Positive and negative values of Hobohm's α-index refer to areas with species diversity above and below average, respectively (Hobohm 2000, 2003). All the diversity analyses were carried out in the R computing environment (R Core Team 2015) using core functions and functions from the ggplot2 package (Wickham 2009).

Furthermore, extensive field research has taken place in order to locate the exact locus classicus of Allium chalkii, and to discover possible new localities and subpopulations of this taxon in the study area. We used the Technical Guide for Mapping (Dafis & al. 2001) for the determination of the habitat types where A. chalkii occurs. The terms population size, subpopulation, location, area of occupancy (AOO) and extent of occurrence (EOO) are used according to the definitions established by IUCN (IUCN Standards and Petitions Subcommittee 2010). The RAMAS Red List 3.0 software package was used for the conservation status assessment of A. chalkii according to the IUCN criteria (Akcakaya & Ferson 2007). All known localities of A. chalkii were surveyed for two consecutive years (2013–2014). Detailed mapping was performed using a GPS device and occasionally a tape measure. Polygons of the local extent of occurrence of each subpopulation were constructed. The QGIS (QGIS Development Team 2015) software package was used for data digitization and area estimations. Population size was measured by counting every individual that was at anthesis. Finally, the direct threats in the environment where A. chalkii occurs and the stresses they cause to its individuals were recorded and classified according to the IUCN categories (IUCN & CMP 2006).



The vascular flora of Chalki comprises 519 taxa, belonging to 296 genera and 79 families (Table 1). Nine alien taxa are included in the plant list, but have not been considered in the floristic analysis.

The literature survey revealed 408 bibliographical reports for the study area (Rechinger 1944; Davis 1965–1986; Carlström 1987; Tzanoudakis & Kollmann 1991; Strid & Tan 1997, 2002; Cattaneo 2015). We report 109 taxa as new to Chalki (see Appendix). Twenty-two taxa are Greek endemics, four of which are new records for the study area. Eleven of the new records and 29 taxa overall are under statutory protection.

The most species-rich families in the flora of Chalki are Asteraceae (73 taxa), followed by Fabaceae (63 taxa) and Poaceae (47 taxa). These three families account for more than one third of the total flora (35.88 %). Caryophyllaceae (27 taxa), Brassicaceae (23 taxa), Apiaceae (20 taxa) and Lamiaceae (20 taxa) are also well represented.

Among the life forms, therophytes (55.69 %) dominate, followed by hemicryptophytes (18.23 %), geophytes (11.18 %), chamaephytes (9.21 %) and phanerophytes (5.69 %).

According to their general distribution, the vascular plants of Chalki can be classified into 16 main chorological categories (Table 2). The endemic group represents 4.31 % of the total flora with 22 taxa. Phytogeographically, the endemic element is the most important group and is discussed separately. The Mediterranean chorological group predominates, highlighting the geographical position and climatic characteristics of Chalki. Within this group, the circum-Mediterranean elements are dominant, followed by the East Mediterranean taxa. The other elements are represented in lower percentages, with a relatively high portion of SW Asian elements due to the phytogeographical position of the study area.

Table 1.

Number of vascular plant taxa in the flora of Chalki Island.


The alien flora of Chalki comprises nine taxa (1.73 %), belonging to nine genera and nine families, all reported for the first time from Chalki. Eight of them are neophytes, and the most prominent among the invasive species are Nicotiana glauca Graham, Opuntia ficus-indica (L.) Mill. and Oxalis pes-caprae L., which occupy large areas.

Table 2.

Chorological groups in the native flora of Chalki Island.



The level of endemism in Chalki (4.31 %) is rather low compared to that in the whole of Greece (22.2 % - Dimopoulos & al. 2013) but, taking into consideration the small size of the study area, the short distance from the mainland, as well as the intense human pressure present on the island (i.e. high-intensity grazing, track and road construction, discarded waste materials), this percentage is rather significant. Furthermore, compared to endemism levels of those East Aegean Islands with a larger size than that of the study area (Table 3), that of Chalki is rather high, even appearing to be the second highest in the phytogeographical region of the East Aegean Islands.

The endemic species belong to 15 families and 20 genera. Families rich in endemic species in absolute numbers are Asteraceae and Plumbaginaceae, their degree of endemism (5.48 % and 75.00 %, respectively) being higher than that of the general flora (4.31 %). These results agree with the trend observed in the whole Greek endemic flora (Georghiou & Delipetrou 2010).

Among the 22 Greek endemic taxa (Table 4), there are two that obviously reflect the unique position of the study area, as it is found on the borderline of three phytogeographical regions, namely the Kiklades (Kik), the East Aegean Islands (EAe) and Kriti and Karpathos (KK): Limonium ocymifolium (Poir.) Kuntze and L. sitiacum Rech. f. These two taxa are found for the first time not only on Chalki, but in the entire phytogeographical region of the East Aegean Islands. Previously, L. ocymifolium was thought to be confined to Kik, while L. sitiacum was considered as a KK endemic.

Table 3.

Endemism in Chalki and the phytogeographical region of the East Aegean Islands, as well as in the other East Aegean islands. Data extracted from Panitsa & al. (2010) and Dimopoulos & al. (2013). The endemism percentage refers to species.


Table 4.

Greek endemic taxa in Chalki, their geographical distribution and their protection/conservation status.


Range-restricted and other interesting taxa

Greece hosts 1956 range-restricted taxa (Dimopoulos & al. 2013), amounting to 29.6 % of its total flora. Among the phytogeographical regions of Greece, Peloponnisos (Pe) is the richest in absolute numbers (514 taxa, 16 %), while Kriti and Karpathos (KK) has the highest percentage (17.5 %) of range-restricted taxa. In comparison, the phytogeographical region of the East Aegean Islands (EAe) hosts 263 (10.3 %) range-restricted taxa.

All except one (Odontites linkii Heldr. & Sartori ex Boiss.) of the Greek endemic taxa occurring on Chalki, and 34 taxa overall (6.67 %), are characterized as range restricted sensu Dimopoulos & al. (2013).

The flora of Chalki hosts 103 East Mediterranean elements, 13 of which are considered as range-restricted taxa. Chalki constitutes the southwesternmost distributional border for at least five Anatolian taxa [Gladiolus anatolicus (Boiss.) Stapf, Ophrys speculum subsp. regisferdinandii (Acht. & Kellerer ex Renz) Soó, Quercus aucheri Jaub. & Spach, Symphytum circinale Runemark and Verbascum propontideum Murb.] and the westernmost distributional border for Campanula hagielia Boiss., Scorzonera elata Boiss. and Silene echinospermoides Hub.-Mor.

A very interesting record is Phoenix theophrasti Greuter, a taxon known to occur in the Aegean region, mainly in Kriti, as well as in three areas of SW Turkey (Boydak & Barrow 1995). We believe its occurrence on Chalki to be of native origin, as its individuals were found to occupy similar ecological niches as in the Cretan locus classicus (stream banks near sea level), in two different localities. Thus, P. theophrasti is recorded as an indigenous member of the flora of the East Aegean Islands, whereas previous reports from Kalymnos, Kos, Nisyros and Symi have not yet been confirmed (Turland & al. 1993: 194; Thymakis 2009; Dimopoulos & al. 2013). Phoenix theophrasti has also been recorded from a single locality in Peloponnisos (Thymakis 2009) and in the phytogeographical region of the Kiklades on Milos (Kalheber in Raus 2012), Anafi (Kougioumoutzis & al. 2012) and Amorgos (Biel & Tan 2015). The presence of P. theophrasti on Chalki and probably other East Aegean Islands bridges the range gap between Kriti and SW Turkey.

Fig. 2.

Residuals scatterplot of Hobohm's α-index for Greek endemic species (y-axis) versus Greek native species (x-axis), as estimated from the ISAR power function model.


Table 5.

Hobohm's α-index values for the total Greek native and Greek endemic species present in 20 East Aegean islands.


Fig. 3.

Allium chalkii — a tuft of plants growing on a rocky, calcareous escarpment, its usual habitat. — Chalki, Lendaki, 6 May 2013, photographed by M. Tsakiri.


Plant diversity of Chalki Island

Using Hobohm's α-index (Table 5) for the Greek native and endemic species occurring in 20 East Aegean islands, Chalki presents values well above average for both of these categories (0.74 for native, 1.61 for endemic). Lesvos could be regarded as floristically impoverished, as it presents very low α-values for both the native and endemic species. Chalki, Ikaria and Samos have high α-values for both native and endemic species (Fig. 2), while more than half of the East Aegean islands display low α-values for both species-richness metrics. Our results indicate that Chalki, Ikaria and Samos in fact constitute plant diversity hotspots, whereas islands with a large total number of native and Greek endemic species, such as Chios and Lesvos, are not characterized as such. Rhodos seems to be an endemic plant diversity hotspot in the phytogeographical region of the East Aegean Islands.

Preliminary assessment and conservation status of Allium chalkii

Allium chalkii is an erect, bulbous geophyte up to 8 cm tall, with membranous outer bulb tunics, bearing 2 or 3 glabrous leaves, a persistent, erect, sometimes divaricate spathe and a fastigiate, few-flowered inflorescence. The ovary is ellipsoid to oblong-ellipsoid and the capsule is globose, 3-valved, c. 3.5 mm in diam., containing black, 2–2.5 mm-long seeds. Allium chalkii grows in calcareous, rocky and stony crevices at 100–350 m a.s.l. and flowers from April to June (Fig. 3). Historical knowledge about this single-island endemic is scarce: A. chalkii was described in 1991 (Tzanoudakis & Kollmann 1991) from specimens collected in the frame of the project Flora Hellenica from several localities between Chorio and Kastro settlements (locus classicus) in 1986 by G. Iatrou and Th. Georgiadis and in rocky, calcareous escarpments on Chalki in 1988 by E. Karavokyrou.

Allium chalkii has not been evaluated before and its EOO, AOO and population size are reported here for the first time.

The current and past distribution of Allium chalkii is shown in Fig. 4 and Table 6. The entire population of the species consists of three subpopulations (AC1, AC2 and AC3), corresponding to the localities Lendaki, Mesovounia and Petrolakki for AC1, Agia Varvara and Kakoskali for AC2, and finally Ais Giorgis tou Riakiou for AC3.

The area of the locus classicus was searched repeatedly (2012–2014) and exhaustively, but no plants were found. The fact that A. chalkii has not been reported from its locus classicus since 1988, suggests that this subpopulation may be extinct.

All subpopulations are scattered in seven different locations (Fig. 4, Table 6). During the two years of monitoring (2013–2014), both the EOO and the AOO — based on a 1 × 1 km grid — were estimated at 5 km2. The whole population local extent was 225 m2 in 2013 and 250 m2 in 2014.

Population size, expressed as the total number of mature individuals in all subpopulations, as well as the size of each subpopulation, exhibited a slight annual increase in 2014 compared to 2013 (Table 6). Total population size, local extent and the number of plants per m2 (a rough estimation of plant density) were highest in 2014 in subpopulation AC1.

Allium chalkii occurs in stony or rocky meadows with typical Mediterranean phrygana, dominated by Sarcopoterium spinosum (L.) Spach and other spiny and aromatic shrubs, as well as in steep, calcareous cliffs near the sea, at 100–270 m a.s.l. Allium chalkii does not seem to face any imminent and direct threats, as its occurrence inside spiny phrygana and on precipitous cliffs protects it from grazing and trampling. However, habitat degradation and/or loss due to excessive grazing (stress codes 1.3 & 2.2) and road construction works (stress code 4.1), may constitute a potential threat for this species in the near future.

Allium chalkii is suggested to be classified as Endangered (EN), according to the IUCN (2012) criterion D, since its total population consists of fewer than 250 mature individuals.


The high percentages of therophytes (55.69 %) and of leguminous taxa (12.35 %) in Chalki indicates characteristic disturbance in Mediterranean ecosystems (Naveh 1974; Arianoutsou & Margaris 1981; Barbero & al. 1990; Panitsa & al. 1994, 2003; Panitsa & Tzanoudakis 1998). Intense grazing and other agricultural activities have not yet ceased on Chalki and have clearly altered the island's floristic character.

Fig. 4.

Geographical distribution and area of occupancy (AOO ) of Allium chalkii.


According to Arianoutsou & al. (2010), the total number of alien taxa accounts for c. 5 % of the native flora of Greece, and this percentage is significantly higher than that of Chalki (1.54 %). Nevertheless, on Chalki, where grazing grounds and abandoned farm lands occupy large areas, Nicotiana glauca, Opuntia ficus-indica and Oxalis pes-caprae have heavily contaminated and altered these habitats, which would otherwise be colonized by native pioneer herbs and shrubs. This phenomenon is also observed in other Aegean islands (Arianoutsou & al. 2010; Kougioumoutzis & al. 2012, 2014b, 2015).

The high percentages of chamaephytes and hemicryptophytes depend on the frequency of limestone cliffs, which very often harbour endemic taxa (Kypriotakis 1998; Kypriotakis & Tzanoudakis 2001; Tzanoudakis & al. 2006). In Chalki, the majority (63.6 %) of the endemic plants are chamaephytes or hemicryptophytes, which are scattered in the numerous steep calcareous cliffs and crevices present on the island.

Table 6.

Locations, subpopulations and numbers of individuals per subpopulation per year of Allium chalkii. — Abbreviations: SP = subpopulation; MI = mature individuals; ImI = immature individuals.


Chalki is floristically more diverse than the other parts of the phytogeographical region of the East Aegean Islands, probably because of the increased habitat diversity due to its great local topographic and geological heterogeneity (intense hilly relief with many different inclinations and exposures, and numerous geological substrates of different age), factors known to promote species richness (Whittaker & Fernández-Palacios 2007; Sfenthourakis & Triantis 2009; Panitsa & al. 2010). Its rather high level of endemism is due to its palaeogeographical history, as Chalki, contrary to the majority of the East Aegean islands (Parmakelis & al. 2006; Triantis & al. 2008), has been isolated from the adjacent mainland (Asia Minor) for the last 0.8 My (Perissoratis & Conispoliatis 2003). Our results are in accordance with Sfenthourakis & Panitsa (2011), who stated that in small Aegean islands diversity at the whole-island scale is shaped mainly by heterogeneity among local communities. According to Hobohm's index, Chalki seems to be a plantdiversity hotspot in the phytogeographical region of the East Aegean Islands, since it has a higher Hobohm's α-index value than Ikaria and Rhodos, two islands considered highly important in terms of phytogeography and endemism (Carlström 1986; Christodoulakis 1996b).

The palaeogeographical events that shaped the presentday South Aegean region are reflected in the occurrence of several taxonomically isolated and relict species in the flora of Chalki. Among these, Allium chalkii is the most prominent representative, since it constitutes a very rare, ancient, geographically isolated, single-island endemic confined to refuge habitats and considered as a member of the Tertiary Aegean flora because it bears some primitive morphological features (i.e. erect-divaricate-spathe, fewflowered inflorescence; Tzanoudakis & Kollmann 1991; Brullo & al. 2001). Arenaria aegaea Rech. f., Asyneuma giganteum (Boiss.) Bornm., Centaurea lactucifolia Boiss. and Umbilicus albido-opacus Carlström are probably Pliocene relicts (Carlström 1986), while the occurrence of Lomelosia variifolia (Boiss.) Greuter & Burdet on Karpathos, Chalki and Rhodos seems to reflect the South Aegean palaeogeography during the early Pliocene, since Karpathos was joined with Chalki, Rhodos and Anatolia at that time (Daams & van der Weerd 1980). The distributions of Colchicum macrophyllum B. L. Burtt and Valeriana asarifolia Dufr. reflect the land-bridge connection that existed in the South Aegean during the Messinian salinity crisis (Carlström 1986; Schüle 1993; Cattaneo 2015): the former can be found on Kriti, Karpathos, Chalki and Rhodos, extending to SW Anatolia, while the latter is a South Aegean Island Arc endemic, occurring on Antikythira, Kriti, Karpathos and Chalki. On the other hand, Campanula rhodensis A. DC., Dianthus fruticosus subsp. rhodius (Rech. f.) Runemark, Nigella arvensis subsp. brevifolia Strid and Symphytum circinale may have resulted from random genetic drift during the climatic fluctuations and sea-level oscillations of the Pleistocene (Carlström 1986; Comes & al. 2008).

Nearly half (nine) of the endemic taxa found on Chalki correspond to one or two phytogeographical areas (Table 4), thus providing valuable information regarding the phytogeographical position of the study area, as the existence of biregional endemics is a good indication of phytogeographical connections between regions (Georghiou & Delipetrou 2010). It would be expected that Chalki shows higher affinities with the phytogeographical area of the Kiklades (Kik) since, according to Georghiou & Delipetrou (2010), the phytogeographical area of the East Aegean Islands (EAe) is chorologically closer connected to Kik than to that of Kriti and Karpathos (KK). While this may be true for the majority of the East Aegean Islands, our results demonstrate that Chalki is phytogeographically closer to KK, as we recorded three endemic taxa (Asyneuma giganteum, Limonium sitiacum and Lomelosia variifolia) occurring exclusively in KK and EAe and only one taxon (Limonium ocymifolium) occurring exclusively in Kik and EAe. More specifically, A. giganteum and L. variifolia are found only on Karpathos, Chalki and Rhodos, while L. sitiacum occurs only in E Kriti, an islet N of Kasos (Raus 1990) and Chalki. Thus, Chalki and its adjacent islands (Rhodos and Symi) seem to have higher phytogeographical affinities with Kriti and Karpathos than with the Kiklades, concurring with previous studies in the area (Carlström 1986). This phenomenon could possibly be attributed to (1) the close palaeogeographical distance between these islands and Kriti and Karpathos during the Messinian salinity crisis (Hsü 1972), as well as during the Pliocene (Creutzburg 1963; Greuter 1970; Daams & van der Weerd 1980; Wiedenbein 1991c; Lymberakis & Poulakakis 2010) and the Pleistocene (Dermitzakis & de Vos 1987); and (2) the South Aegean Island Arc (of which Chalki is a part) being isolated from the rest of the Aegean region by extensive saline deserts or even saline/hypersaline lakes during the Messinian salinity crisis, even though dispersal through land was feasible at that time (Poulakakis & al. 2014).

Five very narrowly distributed taxa are present on Chalki (Allium chalkii, Campanula rhodensis, Centaurea lactucifolia, Dianthus fruticosus subsp. rhodius and Umbilicus albido-opacus), with C. lactucifolia being the most variable taxon, especially in terms of leaf and involucral appendage shape; it was once divided by Wagenitz (1975) into two varieties, var. lactucifolia and var. halkensis (Fors.-Major & Barbey) Wagenitz. Chalki is floristically more closely connected with Rhodos, since all of these taxa — except for A. chalkii — also occur on Rhodos. This phenomenon can be attributed to the two islands having been connected until the offset of the last glacial maximum (Lykousis 2009).

Chalki also seems to have close phytogeographical affinities with the Muğa province of Turkey, and more specifically, with the Marmaris (Datça) peninsula, since virtually all (apart from Ophrys speculum subsp. regisferdinandii) of its range-restricted East Mediterranean taxa occur also there. This phenomenon can be attributed to the cliff flora of the outer Marmaris (Datça) peninsula mainly resembling a slightly impoverished Aegean flora, since it hosts several typical Aegean species, such as Campanula hagielia, Symphytum circinale and Verbascum propontideum (Carlström 1986).

Finally, regarding the conservation status of Allium chalkii, its known population size and density and its area of occupancy were increased during the two years of monitoring, although the population at the type locality was apparently lost. Habitat loss due to human-induced activities constitutes the main threat faced by this taxon. Ex situ conservation seems to be an appropriate measure for A. chalkii, while an effort should be made to minimize the direct threats it is facing by informing the local residents about its rarity and importance.


The authors would like to thank Prof. Dimitris Tzanoudakis for his useful comments, determination and confirmation of species of the genus Allium; Ass. Prof. Rea Artelari for her invaluable help in the identification of species of the genus Limonium; Dr Ioannis Kokkoris for his help in constructing the geographical map of Chalki Island; and Dr Thomas Raus (B) and an anonymous reviewer for their comments on an earlier draft of this paper.



Akcakaya H. R. & Ferson S. 2007: RAMAS Red List 3.0. Threatened species classification under uncertainty. — Setauket: Applied Biomathematics, Inc. — Published at  Google Scholar


Arianoutsou M. , Bazos I. , Delipetrou P. & Kokkoris Y. 2010: The alien flora of Greece: taxonomy, life traits and habitat preferences. —  Biol. Invas. 12: 3525–3549. Google Scholar


Arianoutsou M. & Margaris N. S. 1981: Producers and the fire cycle in a phryganic ecosystem. — Pp. 181–190 in: Margaris N. S. & Mooney H. A. (ed.), Components of productivity of Mediterranean climate regions. Basic and applied aspects. —  The Hague, Boston, London : W. Junk Publishers. Google Scholar


Arrhenius O. 1921: Species and area. —  J. Ecol. 9: 95–99. Google Scholar


Barbero M. , Bonin G. , Loisel R. & Quézel P. 1990: Changes and disturbances of forest ecosystems caused by human activities in the western part of the Mediterranean basin. —  Vegetatio 87: 151–173. Google Scholar


Bazos I. 2005: Meleti tis chloridas kai tis vlastisis tis Lesvou [Study of the flora and vegetation of Lesvos (East Aegean Islands, Greece)]. — Athens: Ph.D. thesis, University of Athens. Google Scholar


Bergmeier E. & Strid A. 2014: Regional diversity, population trends and threat assessment of the weeds of traditional agriculture in Greece. —  Bot. J. Linn. Soc. 175: 607–623. Google Scholar


Biel B. 2002: Contributions to the flora of the Aegean islands of Lesvos and Limnos, Greece. —  Willdenowia 32: 209–219. Google Scholar


Biel B. & Tan. K. 2015: Reports 17–69. — Pp. 56–61 in: Vladimirov V. , Dane F. & Tan K. (ed.), New floristic records in the Balkans 26. — Phytol. Balcan. 21: 53–91. Google Scholar


Blondel J. , Aronson J. , Bodiou J. Y. & Boeuf G. 2010: The Mediterranean region. Biological diversity in space and time. — Oxford: Oxford University Press. Google Scholar


Böger H. & Dermitzakis D. M. 1987: Neogene palaeogeography in the central Aegean region. — Ann. Hung. Geol. Inst. 70: 217–220. Google Scholar


Boydak, M. & Barrow S. 1995: A new locality for Phoenix in Turkey: Gölköy-Bödrum. — Principes 39(3): 117–122. Google Scholar


Brofas G. , Karetsos G. , Panitsa M. & Theocharopoulos M. 2001: The flora and vegetation of Gyali island, SE Aegean, Greece. —  Willdenowia 31: 51–70. Google Scholar


Brullo S. , Pavone P. Salmeri C. 2001: Allium brachyspathum (Alliaceae), a new species from the island of Karpathos (S Aegean area, Greece). — Bocconea 13: 413–417. Google Scholar


Carlström A. 1986: The phytogeographical position of Rodhos. — Proc. Roy. Soc. Edinburgh, B, Biol. Sci. 89B: 79–88. Google Scholar


Carlström A. 1987: A survey of the flora and phytogeography of Rodhos, Simi, Tilos and the Marmaris peninsula (SE Greece, SW Turkey). — Lund: Ph.D. thesis, University of Lund. Google Scholar


Cattaneo C. 2015: Valeriana asarifolia Dufr. — P. 459 in: Raab-Straube E. & Raus Th. (ed.), Euro+Med-Checklist Notulae, 5 — Willdenowia 45: 449–464. Google Scholar


Christodoulakis D. 1996a: The flora of Ikaria (Greece, E. Aegean islands). — Phyton (Horn) 36: 63–91. Google Scholar


Christodoulakis D. 1996b: The phytogeographical distribution patterns of the flora of Ikaria (E Aegean, Greece) within the E Mediterranean. — Flora 191: 393–399. Google Scholar


Comes H. P. , Tribsch A. & Bittkau C. 2008: Plant speciation in continental island floras as exemplified by Nigella in the Aegean archipelago. — Philos. Trans., Ser. B 363: 3083–3096. Google Scholar


Constantinidis Th. 2013: The flora of the Kastellorizo island group (East Aegean Islands, Greece): new records and comments. — Fl. Medit. 23: 69–86. Google Scholar


Creutzburg N. 1963: Palaeogeographic evolution of Crete from Miocene till our days. — Cret. Ann. 15/16: 336–342. Google Scholar


Daams R. & van der Weerd A. V. 1980: Early Pliocene small mammals from the Aegean island of Karpathos (Greece) and their palaeogeographic significance. — Geol. Mijnbouw 59: 327–331. Google Scholar


Dafis S. , Papastergiadou E. , Lazaridou E. & Tsiafouli M. 2001: Technical guide for the identification description and mapping of habitat types in Greece. — Thessaloniki: Greek Biotope/Wetland Centre. Google Scholar


Davis P. H. (ed.) 1965–1985: Flora of Turkey and the East Aegean Islands 1 (1965), 2 (1967), 3 (1970), 4 (1972), 5 (1975), 6 (1978), 7 (1982), 8 (1984), 9 (1985). — Edinburgh: Edinburgh University Press. Google Scholar


Davis P. H. , Mill R. R. & Tan K. (ed.) 1988: Flora of Turkey and the East Aegean Islands 10 (Supplement). — Edinburgh: Edinburgh University Press. Google Scholar


Dermitzakis M. D. & de Vos J. 1987: Faunal succession and the evolution of mammals in Crete during the Pleistocene. — N. Jahrb. Geol. Palaeont. Abh. 173: 377–408. Google Scholar


Dimopoulos P. , Raus Th. , Bergmeier E. , Constantinidis Th. , Iatrou G. , Kokkini S. , Strid A. & Tzanoudakis D. 2013: Vascular plants of Greece: an annotated checklist. — Berlin: Botanic Garden and Botanical Museum Berlin-Dahlem; Athens: Hellenic Botanical Society. — Englera 31. Google Scholar


Georghiou K. & Delipetrou P. 2010: Patterns and traits of the endemic plants of Greece. —  Bot. J. Linn. Soc. 162: 130–422. Google Scholar


Gouvas M. & Sakellariou N. 2011: Climate and forest vegetation of Greece. — Athens: Institute of Environmental Research and Sustainable Development, National Observatory of Athens. Google Scholar


Greuter W. 1970: Zur Paläogeographie und Florengeschichte der südlichen Ägäis. — Feddes Repert.  81 : 233–242. Google Scholar


Greuter W. , Burdet H. M. & Long G. 1984–1989: Med-Checklist. A critical inventory of vascular plants of the circum-mediterranean countries 1 (1984), 3 (1986), 4 (1989). — Genève: Conservatoire et Jardin botaniques de la Ville de Genève; Berlin: Secrétariat Med-Checklist, Botanischer Garten und Botanisches Museum Berlin-Dahlem. Google Scholar


Greuter W. & Raab-Straube E. von (ed.) 2008: Med-Checklist. A critical inventory of vascular plants of the circum-mediterranean countries 2. — Palermo, Genève & Berlin: OPTIMA. Google Scholar


Güner A. , Özhatay N. , Ekim T. & Başer K. H. C. (ed.) 2001 [“2000”]: Flora of Turkey and the East Aegean Islands 11 (Supplement 2). — Edinburgh: Edinburgh University Press. Google Scholar


Hobohm C. 2000: Plant species diversity and endemism on islands and archipelagos, with special reference to the Macaronesian Islands. — Flora 195: 9–24. Google Scholar


Hobohm C. 2003: Characterization and ranking of biodiversity hotspots: centres of species richness and endemism. —  Biodivers. & Conservation 12: 279–287. Google Scholar


Hsü K. J. 1972: Origin of saline giants: a critical review after the discovery of the Mediterranean evaporite. — Earth.-Sci. Rev. 8: 371–396. Google Scholar


IUCN 2012: IUCN Red List categories and criteria. Version 3.1, ed. 2. — Gland & Cambridge: IUCN. — Published at  Google Scholar


IUCN Standards and Petitions Subcommittee 2010: Guidelines for using the IUCN Red List categories and criteria. Version 8. Prepared by the Standards and Petitions Working Subcommittee in March 2010. — Version 11 (February 2014) published at  Google Scholar


IUCN—CMP 2006: Unified Classification of Conservation Actions. Version 1.0. — Published at  Google Scholar


Kagiampaki A. , Triantis K. , Vardinoyannis K. & Mylonas M. 2011: Factors affecting species richness and endemism in the South Aegean (Greece). — J. Biol. Res. 16: 282–295. Google Scholar


Kallimanis A. S. , Bergmeier E. , Panitsa M. , Georghiou K. , Delipetrou P. & Dimopoulos P. 2010: Determinants for total and endemic species richness in a continental archipelago. —  Biodivers. & Conservation 19: 1225–1235. Google Scholar


Kougioumoutzis K. , Simaiakis S. M. & Tiniakou A. 2014a: Network biogeographical analysis of the central Aegean archipelago. —  J. Biogeogr. 41: 1848–1858. Google Scholar


Kougioumoutzis K. , Tiniakou A. , Georgiou O. & Georgiadis Th. 2012: Contribution to the flora of the South Aegean Volcanic Arc: Anafi Island (Kiklades, Greece). —  Willdenowia 42: 127–141. Google Scholar


Kougioumoutzis K. , Tiniakou A. , Georgiou O. & Georgiadis Th. 2014b: Contribution to the flora and biogeography of the Kiklades: Folegandros Island (Kiklades, Greece). —  Edinburgh J. Bot. 71: 135–160. Google Scholar


Kougioumoutzis K. , Tiniakou A. , Georgiou O. & Georgiadis Th. 2015: Contribution to the flora of the South Aegean Volcanic Arc: Kimolos Island (Kiklades, Greece). —  Edinburgh J. Bot. 72: 391–412. Google Scholar


Kypriotakis Z. 1998: Contribution to the study of the chasmophytic flora of Crete. — Patras: Ph.D. thesis, University of Patras. Google Scholar


Kypriotakis Z. & Tzanoudakis, D. 2001: Contribution to the study of the Greek insular flora: The chasmophytic flora of Crete. — Bocconea 13: 495–503. Google Scholar


Livianiou-Tiniakou A. , Christodoulakis D. , Georgiou O. & Artelari R. 2003: Floristic dynamics in correlation with the type of substrate and human activities: the example of Serifos (Kiklades Islands, Greece). — Fresenius Environm. Bull 12: 1520–1529. Google Scholar


Lykousis V. 2009: Sea-level changes and shelf break prograding sequences during the last 400 ka in the Aegean margins: Subsidence rates and palaeogeographic implications. —  Continental Shelf Res. 29: 2037–2044. Google Scholar


Lymberakis P. & Poulakakis N. 2010: Three continents claiming an archipelago: the evolution of Aegean's herpetofaunal diversity. —  Diversity 2: 233–255. Google Scholar


Maroukian H. , Pavlopoulos K. & Fokas E. 2004: Geomorphological observations in Halki Island, Dodecanese — Proc. 7th Panhellenic Geogr. Congr. 1: 271–277. Google Scholar


Naveh Z. 1974: Effects of fire in the Mediterranean region. — In: Kozlowski T. T. & Ahlgren C. E. (ed.), Fire and ecosystems. —  New York : Elsevier Inc. Google Scholar


Panitsa M. 1997: Contribution to the knowledge of the East Aegean islands' flora and Vegetation. — Patras: Ph.D. thesis, University of Patras. Google Scholar


Panitsa M. , Dimopoulos P. , Iatrou G. & Tzanoudakis D. 1994: Contribution to the study of the Greek flora: flora and vegetation of the Enousses (Oinousses) islands (E Aegean area). — Flora 189: 367–374. Google Scholar


Panitsa M. , Snogerup B. , Snogerup S. & Tzanoudakis D. 2003: Floristic investigation of Lemnos island (NE Aegean area, Greece). —  Willdenowia 33: 79–105. Google Scholar


Panitsa M. , Trigas P. , Iatrou G. & Sfenthourakis S. 2010: Factors affecting plant species richness and endemism on land-bridge islands — An example from the East Aegean archipelago. —  Acta Oecol. 36: 431–437. Google Scholar


Panitsa M. & Tzanoudakis D. 1998: Contribution to the study of the Greek flora: flora and vegetation of the islands Agathonisi and Pharmakonisi (East Aegean area, Greece). —  Willdenowia 28: 95–116. Google Scholar


Panitsa M. & Tzanoudakis D. 2001: A floristic investigation of the islet groups Arki and Lipsi (East Aegean area, Greece). —  Folia Geobot. 36: 265–279. Google Scholar


Panitsa M. & Tzanoudakis D. 2010: Floristic diversity on small islands and islets: Leros islets' group (East Aegean area, Greece). — Phytol. Balcan. 16: 271–284. Google Scholar


Panitsa M. , Tzanoudakis D. & Sfenthourakis S. 2008: Turnover of plants on small islets of the eastern Aegean Sea within two decades. —  J. Biogeogr. 35: 1049–1061. Google Scholar


Panitsa M. , Tzanoudakis D. , Triantis K. A. & Sfenthourakis S. 2006: Patterns of species richness on very small islands: the plants of the Aegean archipelago. —  J. Biogeogr. 33: 1223–1234. Google Scholar


Papatsou S. 1974: Flora and vegetation of Nisiros island and the surrounding islets. — Patras: Ph.D. thesis, University of Patras. Google Scholar


Parmakelis A. , Stathi I. , Spanos L. , Louis C. & Mylonas M. 2006: Phylogeography of Iurus dufoureius (Brullé, 1832) (Scorpiones, Iuridae). —  J. Biogeogr. 33: 251–260. Google Scholar


Perissoratis C. & Conispoliatis N. 2003: The impacts of sea-level changes during latest Pleistocene and Holocene times on the morphology of the Ionian and Aegean seas (SE Alpine Europe). —  Marine Geol. 196: 145–156. Google Scholar


Poulakakis N. , Kapli P. , Lymberakis P. , Trichas A. , Vardinoyannis K. , Sfenthourakis S. & Mylonas M. 2014: A review of phylogeographic analyses of animal taxa from the Aegean and surrounding regions. —  J. Zool. Syst. Evol. Res. 53: 18–32. Google Scholar


QGIS Development Team. 2015: QGIS Geographic Information System. Open Source Geospatial Foundation Project. — Published at  Google Scholar


R Core Team 2015: R: A language and environment for statistical computing. — Vienna: R Foundation for Statistical Computing. — Published at  Google Scholar


Raus Th. 1990 [“1989”]: Die Flora von Armathia und der Kleininseln um Kasos (Dodekanes, Griechenland). — Bot. Chron. (Patras) 9: 19–39. Google Scholar


Raus Th. 2012: Gefäßpflanzen von Milos (Kykladen, Griechenland) — eine floristische Handreichung. — Verh. Zool.-Bot. Ges. Österreich 148/149: 197–235. Google Scholar


Rechinger K. H 1944 [“1943”]: Flora aegaea. Flora der Inseln und Halbinseln des ägäischen Meeres. — Denkschr. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 105(1). Google Scholar


Schüle W. 1993: Mammals, vegetation and the initial human settlement of the Mediterranean islands: a palaeoecological approach.—  J. Biogeogr. 20:399–412. Google Scholar


Sfenthourakis S. & Panitsa M. 2011: From plots to islands: species diversity at different scales. —  J. Biogeogr. 39: 750–759. Google Scholar


Sfenthourakis S. & Triantis K. A. 2009: Habitat diversity, ecological requirements of species and the small island effect. —  Diversity & Distrib. 15: 131–140. Google Scholar


Strid A. 1996: Phytogeographia aegaea and the Flora Hellenica project. — Ann. Naturhist. Mus. Wien 98B: 279–289. Google Scholar


Strid A. & Tan K. (ed.) 1997: Flora hellenica 1. — Königstein: Koeltz Scientific Books. Google Scholar


Strid A. & Tan K. (ed.) 2003 [“2002”]: Flora hellenica 2. — Ruggell: A. R. G. Gantner. Google Scholar


Tan K. , Iatrou G. & Johnsen B. 2001: Endemic plants of Greece. The Peloponnese. — Copenhagen: Gad Publishers. Google Scholar


Thiers B. [continuously updated]. Index Herbariorum: A global directory of public herbaria and associated staff. New York Botanical Garden's Virtual Herbarium. — Published at [last accessed 21 Mar 2016]. Google Scholar


Thymakis N. 2009: Phoenix theophrasti Greuter. — Pp. 256–258 in: Phitos D. , Constantinidis Th. & Kamari G. (ed.) 2009: The Red Data Book of rare and threatened plants of Greece 2 E-Z. — Patras: Hellenic Botanical Society. Google Scholar


Triantis K. A. & Mylonas M. 2009: Greek islands, biology. — Pp. 388–392 in: Gillespie R. & Glague D. A. (ed.), Encyclopaedia of islands. — Berkeley: University of California Press. Google Scholar


Triantis K. A. , Vardinoyannis K. & Mylonas M. 2008: Biogeography, land snails and incomplete datasets: the case of three island groups in the Aegean Sea. —  J. Nat. Hist. 42: 467–490. Google Scholar


Trigas P. , Panitsa M. & Tsiftsis S. 2013: Elevational gradient of vascular plant species richness and endemism in Crete — The effect of post-isolation mountain uplift on a continental island system. —  PLoS ONE 8: e59425. Google Scholar


Turland N. J. , Chilton L. & Press J. R. 1993: Flora of the Cretan area: annotated checklist & atlas. — London: The Natural History Museum & HMSO. Google Scholar


Tutin T. G. , Burges N. A. , Chater A. O. , Edmondson J. R. , Heywood V. H. , Moore D. M. , Valentine D. H. , Walters S. M. & Webb D. A. (ed.) 1993: Flora europaea 1 Psilotaceae to Platanaceae , ed. 2. — Cambridge: Cambridge University Press. Google Scholar


Tutin T. G. , Heywood V. H. , Burges N. A. , Moore D. M. , Valentine D. H. , Walters S. M. & Webb D. A. (ed.) 1964–1980: Flora europaea 1 (1964), 2 (1968), 3 (1972), 4 (1976), 5 (1980). — Cambridge: Cambridge University Press. Google Scholar


Tzanoudakis D. & Kollmann F. 1991: Allium chalkii (Liliaceae), a new species from the Eastern Aegean island of Chalki (Greece). — Israel J. Bot. 40: 61–64. Google Scholar


Tzanoudakis D. , Panitsa M. , Trigas P. & Iatrou G. 2006: Floristic and phytosociological investigation of the island Antikythera and nearby islets (SW Aegean, Greece). —  Willdenowia 36: 285–301. Google Scholar


Wagenitz, G. 1975: Centaurea. — Pp. 465–585. — In: Davis P. H. (ed.), Flora of Turkey and the East Aegean Islands 5. — Edinburgh: Edinburgh University Press. Google Scholar


Whittaker R. J. & Fernández-Palacios J. M. (ed.) 2007: Island biogeography. Ecology, evolution and conservation. — Oxford: Oxford University Press. Google Scholar


Wickham H. 2009: ggplot2: elegant graphics for data analysis. — New York: Springer. Google Scholar


Wiedenbein F. W. 1991: Biogeographic patterns of the Aegean region and their geological origin. — Bull. Geol. Soc. Greece 25: 423–435. Google Scholar


Zervou S. , Raus Th. & Yannitsaros A. 2009: Additions to the flora of the island of Kalimnos (SE Aegean, Greece). —  Willdenowia 39: 165–177. Google Scholar



Only taxa new to Chalki Island are listed.


Life forms:


= Chamaephyte


= Geophyte


= Hemicryptophyte


= Phanerophyte


= Therophyte

Chorological groups:
Widely distributed taxa:


= European


= European-SW Asian


= Euro-Siberian


= Paleotemperate


= Circumtemperate


= Subtropical-Tropical


= Cosmopolitan

Mediterranean taxa:


= Eastern Mediterranean


= Mediterranean


= Mediterranean-Atlantic


= Mediterranean-European


= Mediterranean-SW Asian

Balkan taxa:


= Balkan


= Balkan-Italian


= Balkan-Anatolian


= Endemic taxa

Alien taxa; name and origin given in [square brackets], as follows:


= Neotropical


= Paleotropical


= North American


= South American


= South African


= Australian


= West Australian

Collection sites:

  • 1: 36°13′43.7″N, 27°35′22.9″E, 370 m

  • 2: 36°13′13.3″N, 27°34′34.4″E, 80 m

  • 3: 36°13′43.9″N, 27°31′34.7″E, 180 m

  • 4: 36°14′42.0″N, 27°36′00.8″E, 60 m

  • 5: 36°14′07.5″N, 27°34′14.4″E, 460 m

  • 6: 36°13′26.8″N, 27°37′14.1″E, 18 m

  • 7: 36°13′19.0″N, 27°31′53.6″E, 283 m

  • 8: 36°13′36.0″N, 27°32′20.0″E, 402 m

  • 9: 36°13′02.4″N, 27°34′19.3″E, 17 m

  • 10: 36°13′26.9″N, 27°36′38.8″E, 47 m

  • 11: 36°13′59.4″N, 27°32′23.2″E, 293 m

  • 12: 36°14′03.9″N, 27°37′02.9″E, 40 m

  • 13: 36°14′13.1″N, 27°34′54.8″E, 302 m

  • 14: 36°13′49.6″N, 27°33′02.4″E, 316 m

  • 15: 36°12″58.2″N, 27°36′47.3″E, 43 m

  • 16: 36°13′31.1″N, 27°34′50.3″E, 308 m

  • 17: 36°13′38.9″N, 27°36′33.5″E, 103 m

  • 18: 36°13′11.9″N, 27°35′45.3″E, 130 m

  • 19: 36°14′09.9″N, 27°36′11.9″E, 318 m

  • 20: 36°13′20.2″N, 27°36′06.4″E, 24 m

  • 21: 36°13′29.1″N, 27°34′04.0″E, 495 m

  • 22: 36°13′36.9″N, 27°33′16.1″E, 403 m

  • 23: 36°13′54.1″N, 27°36′27.9″E, 159 m

  • 24: 36°13′18.4″N, 27°35′19.8″E, 156 m

Collection dates:

  • a: 17 – 22 Apr 2012

  • b: 14 – 22 Nov 2012

  • c: 1 – 10 Mar 2013

  • d: 1 – 9 May 2013

  • e: 14 – 22 Apr 2014

Recorder information:

  • TS = M. Tsakiri [with collection number]

  • obs. = field observation

  • phot. = photograph


  • Pteridaceae

    Anogramma leptophylla (L.) Link — T, Co; 24, d, TS 294.


  • Acanthaceae

    Acanthus spinosus L. — H, Me; 24, d, TS 748.

  • Agavaceae

    [Agave americana L.] — P, [N-Am.]; 20, a, TS phot.

  • Aizoaceae

    [Carpobrotus edulis (L.) N. E. Br.] — C, [S-Afr.]; 20, a, TS obs.

  • Amaryllidaceae

    Allium amethystinum Tausch — G, EM; 17, d, TS 664.

    Allium subhirsutum L. subsp. subhirsutum — G, Me; 11, d, TS 666; 13, d, TS 749; 5, d, TS 750.

    Pancratium maritimum L. — G, Me; 20, b, TS 754.

  • Anacardiaceae

    Pistacia terebinthus subsp. palaestina (Boiss.) Engl. — P, EM; 24, a, TS 409.

  • Apiaceae

    Crithmum maritimum L. — C, ME; 20, b, TS 169; 12, b, TS 170.

    Smyrnium creticum Mill. — H, EM; 11, e, TS obs.; 13, e, TS obs.

    Smyrnium olusatrum L. — H, MA; 10, c, TS 186.

    Torilis arvensis subsp. neglecta (Spreng.) Thell. — T, ME; 20, a, TS 186.

  • Araceae

    Arum creticum Boiss. & Heldr. — G, EM; 6, d, TS phot.; 7, d, TS phot.; 13, d, TS obs.; 14, d, TS obs.

  • Arecaceae

    Phoenix theophrasti Greuter — P, EM; 10, a, TS obs.; 20, c, TS obs.

  • Asparagaceae

    Asparagus acutifolius L. — C, Me; 6, b, TS 681; 15, b, TS 744.

  • Asteraceae

    Anthemis macrotis (Rech. f.) Oberpr. & Vogt — T, EM; 9, a, TS 286; 12, a, TS 287; 20, a, TS 289; 8, d, TS 290.

    Cichorium intybus L. — H, EA; 8, d, TS 269; 24, d, TS 271.

    Dittrichia graveolens (L.) Greuter — T, Me; 9, b, TS 768.

    Dittrichia viscosa (L.) Greuter — C, Me; 15, b, TS 769.

    Filago pygmaea L. — T, Me; 20, d, TS 226; 15, d, TS obs.

    Lactuca acanthifolia (Willd.) Boiss. — C, EM; 11, e, TS 766; 13, e, TS phot.; 18, e, TS obs.; 7, e, TS obs.; 21, e, TS obs.; 22, e, TS obs.; 23, e, TS obs.

    Picnomon acarna (L.) Cass. — T, Pt; 6, b, TS 248.

    Reichardia intermedia (Sch. Bip.) Samp. — T, Me; 23, c, TS 278.

    Reichardia picroides (L.) Roth — H, Me; 15, d, TS 277.

    Scorzonera mollis M. Bieb. subsp. mollis — H, EA: 20, d, TS 246; 8, d, TS 247.

    Senecio leucanthemifolius Poir. — T, Me; 24, c, TS phot.

    Senecio vulgaris L. — T, Pt; 21, c, TS 284; 20, c, TS 285.

    Taraxacum hellenicum Dahlst. — H, Me; 24, c, TS 224.

    Taraxacum scolopendrinum Dahlst. — H, Me; 3, b, TS 207; 15, b, TS 209; 12, b, TS 210.

  • Boraginaceae

    Buglossoides arvensis subsp. sibthorpiana (Griseb.) R. Fern. — T, EA; 17, c, TS 742; 8, c, TS phot.; 3, c, TS phot.

    Echium angustifolium Mill. subsp. angustifolium — H, EM; 20, d, TS 741; 15, d, TS phot.

    Myosotis incrassata Guss. — T, Me; 21, c, TS 743; 8, c, TS phot.

  • Brassicaceae

    Arabis verna (L.) W. T. Aiton; 8, c, TS 507; 24, c, TS 508; 12, c, TS 509.

    Malcolmia chia (L.) DC. — T, EM; 20, a, TS 526; 22, d, TS 525.

    Matthiola tricuspidata (L.) R. Br. — T, Me; 20, d, TS 528; 20, d, 529; 12, d, TS obs.; 15, d, TS obs.

    Raphanus raphanistrum L. subsp. raphanistrum — T, EA; 12, d, TS 534.

    Sinapis alba L. subsp. alba — T, ME; 10, c, TS 511.

  • Cactaceae

    [Opuntia ficus-indica (L.) Mill.] — P, [Neotrop.]; 20, a, TS phot.

  • Campanulaceae

    Campanula erinus L. — T, ME; 8, d, TS 628; 8, d, TS 629; 8, d, TS 630.

  • Caryophyllaceae

    Silene behen L. — T, ME; 17, c, TS 364; 12, c, TS 366.

  • Cistaceae

    Cistus creticus L. — C, Me; 17, c, TS 403.

  • Colchicaceae

    Colchicum pusillum Sieber — G, EM; 8, b, TS 686; 3, b, TS 740.

  • Crassulaceae

    Umbilicus rupestris (Salisb.) Dandy — G, MA; 24, d, TS 738; 24, d, TS 739.

  • Cucurbitaceae

    Ecballium elaterium (L.) A. Rich. — G, MS; 10, d, TS 333; 10, e, TS 334.

  • Euphorbiaceae

    Euphorbia helioscopia L. — T, Co; 9, c, TS 751.

    [Ricinus communis L.] — P, [Paleotrop.]; 20, a, TS obs.

  • Fabaceae

    Hymenocarpos circinnatus (L.) Savi — T, Me; 20, a, TS 478; 12, c, TS 479.

    Lathyrus amphicarpos L. — T, Me; 16, c, TS 467.

    Lathyrus annuus L. — T, MS; 24, d, TS 447.

    Ononis pubescens L. — T, Me; 20, a TS 453.

    Spartium junceum L. — P, Me; 10, a TS 486.

    Trifolium boissieri Guss. — T, EM; 20, a TS 441; 20, d TS 482.

  • Fagaceae

    Quercus aucheri Jaub. & Spach — P, EM; 18, e, TS 777.

  • Gentianaceae

    Blackstonia perfoliata (L.) Huds. subsp. perfoliata — T, ME; 17, d, TS 752.

  • Geraniaceae

    Geranium molle L. — T, Pt; 17, c, TS obs.

  • Hyacinthaceae

    Bellevalia dubia subsp. boissieri (Freyn) Feinbrun — G, Me; 12, c, TS 680.

    Bellevalia trifoliata (Ten.) Kunth — G, Me; 17, a, TS 679; 20, c, TS 734; 1, c, TS 735.

    Muscari comosum (L.) Mill. — G, ME; 3, d, TS 671; 20, a, TS 733.

    Muscari neglectum Ten. — G, EA; 21, a, TS 676; 5, a, TS 723.

    Prospero autumnale (L.) Speta — G, Me; 6, b, TS 687, 15, b, TS 688, 24, b, TS 689; 12, b, TS 736.

  • Iridaceae

    Crocus tournefortii J. Gay — G, Endemic; 3, b, TS 643; 8, b TS 644.

    Romulea tempskyana Freyn — G, EM; 6, c, TS 746; 17, c, TS 747.

  • Lamiaceae

    Lamium amplexicaule L. — T, Pt; 24, c, TS 731; 12, c, TS 129.

    Sideritis purpurea Benth. — T, Bk; 20, a, TS 110; 20, a, TS 117.

    Teucrium divaricatum Heldr. subsp. divaricatum — C, EM; 11, d, TS 121; 13, d, TS 753; 5, d, TS phot.

  • Liliaceae

    Gagea peduncularis (J. Presl & C. Presl) Pascher — G, Me; 12, c, TS 728; 14, c,TS 729; 21, c, TS obs.; 22, c, TS phot.

  • Malvaceae

    Malva nicaeensis All. — T, Me; 20, a, TS 725; 20, a TS 726.

    Malva punctata (All.) Alef. — T, Me; 20, d, TS 727.

  • Mimosaceae

    [Acacia saligna (Labill.) H. Wendl.] — P, [W-Austr.]; 20, a TS 444.

  • Myrtaceae

    [Eucalyptus camaldulensis Dehnh.] — P, [Austr.]; 20, a TS 416.

  • Orchidaceae

    Anacamptis papilionacea (L.) R. M. Bateman & al. — G, MS; 7, d, TS 609; 7, d, TS phot.

    Ophrys ferrum-equinum Desf. — G, BA; 20, c, TS phot.

    Ophrys fusca Link — G, Me; 12, c, TS 610; 12, c, TS phot.

    Ophrys lutea Cav. — G, Me; 12, c,TS 612; 19, c, TS phot.

    Ophrys speculum subsp. regis-ferdinandii (Acht. & Kellerer ex Renz) Soó. — G, EM; 12, c, TS 608; 12, c, TS phot.

    Ophrys tenthredinifera Willd. — G, Me; 3, c, TS phot.

    Orchis anatolica Boiss. — G, EM; 20, a, TS 605.

    Spiranthes spiralis (L.) Chevall. — G, EA; 15, b, TS 724.

  • Orobanchaceae

    Phelipanche ramosa (L.) Pomel — T, Pt; 20, c, TS 133.

  • Oxalidaceae

    [Oxalis pes-caprae L.] — G, [S-Afr.]; 21, c, TS 412.

  • Papaveraceae

    Papaver apulum Ten. — T, BI; 20, a, TS 146.

  • Plantaginaceae

    Plantago indica L. — T, MS; 10, a, TS 150; 17, a, TS 152; 15, a, TS 154.

  • Plumbaginaceae

    Limonium ocymifolium (Poir.) Kuntze — C, Endemic; 15, b, TS 132.

    Limonium proliferum (d'Urv.) Erben & Brullo — C, Endemic; 4, d, TS 130.

    Limonium sitiacum Rech. f. — C, Endemic; 12, c, TS 131.

  • Poaceae

    Aegilops comosa Sm. — T, EM; 5, d, TS 5.

    Avenula pubescens (Huds.) Dumort. subsp. pubescens — H, EA; 6, d, TS 31.

    Bromus hordeaceus L. — T, Co; 10, a, TS 33.

    Bromus lanceolatus Roth — T, Pt; 15, a, TS 32.

    Bromus rigidus Roth — T, ST; 20, d, TS 17; 20, c, TS 29; 10, c TS 61; 10, a, TS 68.

    Hordeum vulgare L. — T, Me; 10, c, TS 23; 20, a, TS 24.

    Piptatherum miliaceum (L.) Coss. subsp. miliaceum — C, Me;16, d, TS 65.

    Poa bulbosa L. — H, Pt; 3, d, TS 30.

    Setaria adhaerens (Forssk.) Chiov. — T, Ct;10, b, TS 69.

  • Polygalaceae

    Polygala venulosa Sm. — H, EM; 17, c, TS 721.

  • Primulaceae

    Anagallis foemina Mill. — T, EA; 20, a, TS 719; 12, a, TS 720.

    Cyclamen graecum subsp. anatolicum Grey-Wilson — G, EM; 10, c, TS 698.

  • Ranunculaceae

    Anemone coronaria L. — G, Me; 6, c, TS 415.

    Ficaria verna subsp. ficariiformis (Rouy & Foucaud) Soó — G, Me; 21, c, TS 424.

    Ranunculus creticus L. — H, EM; 8, c, TS 417; 24, c, TS 419.

  • Rosaceae

    [Prunus dulcis (Mill.) D. A. Webb] — P, [SW & C-As.]; 12, b, TS 317; 20, b, TS obs.

  • Rubiaceae

    Galium aparine L. — T, EA; 20, c, TS 571.

  • Scrophulariaceae

    Verbascum sinuatum L. — H, MS; 10, d, TS 715, 12, d, TS 716.

  • Solanaceae

    [Nicotiana glauca R. C. Graham] — P, [S-Am.]; 15, c, TS 635; 2, c, TS phot.; 10, c, TS phot.

  • Tamaricaceae

    Tamarix smyrnensis Bunge — P, EA; 20, a, TS 655; 10, a, TS 656.

  • Valerianaceae

    Centranthus ruber (L.) DC. — H, Me; 10, e, TS 413.

    Valerianella discoidea (L.) Loisel. — T, Me; 20, c, TS 415.

    Valerianella obtusiloba Boiss. — T, EM; 20, c, TS 414; 12, c, TS 694, 17, c, TS 709.

  • Veronicaceae

    Kickxia elatine subsp. crinita (Mabille) Greuter — T, Me; 20, a, TS 754, 12, a, TS 755.

© 2016 The Authors · This open-access article is distributed under the CC BY 4.0 licence
Maria Tsakiri, Konstantinos Kougioumoutzis, and Gregoris Iatrou "Contribution to the vascular flora of Chalki Island (East Aegean, Greece) and biomonitoring of a local endemic taxon," Willdenowia 46(1), 175-190, (6 April 2016).
Published: 6 April 2016
Allium chalkii
island plant diversity
land-bridge islands
Back to Top