Vincetoxicum tmoleum, Boissier (1844: 38)

Güven, Seher, Makbul, Serdar, Coskuncelebi, Kamil & Pinar, Nur Münevver, 2015, Pollinarium morphology of Vincetoxicum (Apocynaceae: Asclepiadoideae) in Turkey, Phytotaxa 230 (1), pp. 22-38 : 30-32

publication ID

https://doi.org/ 10.11646/phytotaxa.230.1.2

persistent identifier

https://treatment.plazi.org/id/2D7D87DD-FF8D-FFF5-FF54-FB44FC3136A4

treatment provided by

Felipe

scientific name

Vincetoxicum tmoleum
status

 

V. tmoleum Boissier (1844: 38) View in CoL :

Pollinium ovate, 259.1 (±7.28) × 149.8 (±5.02) μm; pollen cells 40.5 (±2.76) × 27.8 (±3.07) μm, inaperturate; ornamentation tectate-perforate, rugulate. Corpusculum ovate, 223.7 (±6.73) × 108.6 (±5.21) μm. Caudicle attached to the corpusculum sub-apically and to the pollinium sub-basally, 113.4 (±4.63) × 19.4 (±1.30) μm ( Fig. 11 View FIGURE 11 ).

Numerical analysis

The dendrogram resulting from the cluster analysis (based on 11 palynological characters of 20 samples representing ten taxa) is given in Fig. 12 View FIGURE 12 . As seen in the dendrogram, all investigated taxa fall into two major clusters at 98.75% dissimilarity level. The first cluster, labeled “a”, comprises nine samples belonging to V. canescens subsp. canescens , V. canescens subsp. pedunculata , V. parviflorum , and V. tmoleum . The second cluster, labeled “b”, includes the remaining eleven samples (representing six taxa) of Turkish Vincetoxicum . The cophenetic correlation coefficient of the dendogram is 0.86. Cluster “a” is characterized by ovate or elliptical pollinia with width/length ratios ranging from 0.58 to 0.65. Cluster “b” is represented by clavate or obovate pollinia with width/length ratios ranging from 0.30 to 0.47.

Cluster “a” is divided into two subclusters, linked to each other at a 83.75% dissimilarity level. The first subcluster contains seven different populations in total, representing two subspecies of V. canescens , as well as V. tmoleum . V. canescens subsp. canescens and V. canescens subsp. pedunculata were noted as phenetically similar taxa by Browicz (1978). These two taxa, previously distinguished from one another based on peduncle length, are also similar in palynological traits, but can be distinguished by pollinium length (see key below). V. canescens and V. tmoleum share similar yellow or greenish flowers ( Browicz 1978), but can be distinguished by stems decumbent and indumentum grey-tomentose in the former ( Browicz 1978). Our results demonstrate that the two can also be distinguished by palynological characters, including the length of the corpusculum.

Vincetoxicum parviflorum View in CoL , a member of the second subcluster of cluster “a”, is easily distinguished from the rest of the three taxa in the cluster by the pollinaria smaller, the pollinia elliptical, the corpuscula oblong, and the pollen gemmate. Browicz (1978) suggested that V. parviflorum View in CoL could be a variety of V. fuscatum View in CoL with small-flowers, but our palynological results are not in accordance with this view, supporting instead Boissier (1875), who considered the taxa distinct at the species level. In fact, Boissier (1875) noted that these two taxa differ from each other in a number of morphological characters related to the stem and flower ( Boissier 1875). For example, V. fuscatum View in CoL is characterized by a cup-shaped, 5-parted corona, the scales of which exhibit intermediate short teeth and are nearly equal with the gynostegium length. In contrast, in the smaller flowers of V. parviflorum View in CoL , the corona is deeply 5-parted and the corona scales are triangular-ovate and quite shorter than gynostegium. Additionally, while V. parviflorum View in CoL exhibits densely branched stems, V. fuscatum View in CoL exhibits simple or few-branched stems ( Boissier 1875).

The second major cluster is also divided into two subclusters. Subcluster “d” consists of four populations belonging to V. fuscatum subsp. boissieri View in CoL and V. scandens View in CoL , while subcluster “c” includes V. funebre View in CoL , V. fuscatum subsp. fuscatum View in CoL , V. hirundunaria subsp. hirundinaria View in CoL , and V. speciosum View in CoL . Browicz (1978) recognized two phenetically similar subspecies of V. fuscatum View in CoL subsp. boissieri View in CoL and subsp. fuscatum View in CoL —distinguished only by corolla indumentum. In contrast to Browicz (1978), these two subspecies were recognized as separate species by Pobedimova (1952) (as Antitoxicum boissieri (Kusnezov) Pobedimova (1952: 680) View in CoL [= V. fuscatum subsp. boissieri View in CoL ] and Antitoxicum minus (C.Koch) Pobedimova (1952: 687) View in CoL [= V. fuscatum subsp. fuscatum View in CoL ]). Although the general appearance and corona structure of V. fuscatum subsp. boissieri View in CoL and V. fuscatum subsp. fuscatum View in CoL are very similar ( Pobedimova 1952), Pobedimova (1952) suggested that these two taxa be classified under different series based on the pubescence of the inner surface of corolla. As seen in the dendrogram resulting from our cluster analysis, the two subspecies emerged in different subclusters based on palynological features, including the size of pollinia, corpuscula, and caudicles. Thus, our results support Pobedimova’s (1952) view, but further morphological and molecular studies are required to better understand the evolutionary relationship of these phenetically similar taxa.

In subcluster “c”, samples of V. speciosum differed from the other three taxa on the basis of the long pollinia (341.6 ±11.42 μm) and the low pollinium width/length ratio (0.30). Interestingly, the phenetically rather different species V. funebre (corollas dark purple and stems erect, to 70 cm) and V. hirundinaria subsp. hirundinaria (corollas white or pale yellow and stems twining, ca. 120 cm) ( Browicz 1978) emerged in the same subcluster. This is likely the result of similarities in the size, shape, and surface ornamentation of their pollinia.

An ordination derived from PCA based on 11 palynological traits is given in Fig. 13 View FIGURE 13 . The eigenvalues of the first, second, and third component in percentages are 66.17%, 19.97%, 6.58%, respectively ( Table 3). The first three components explain 92.72% of the total variation among the investigated taxa, suggesting that the shape of the pollinium and corpusculum, the size and surface ornamentation of pollen cells, and the size of the corpusculum and caudicle are valuable palynological characters for grouping the investigated taxa.

Kingdom

Plantae

Phylum

Tracheophyta

Class

Magnoliopsida

Order

Gentianales

Family

Apocynaceae

Genus

Vincetoxicum

Loc

Vincetoxicum tmoleum

Güven, Seher, Makbul, Serdar, Coskuncelebi, Kamil & Pinar, Nur Münevver 2015
2015
Loc

V. tmoleum

Boissier, P. E. 1844: )
1844
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