Droseridites Temporal range: | |
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Photomicrographs of D. echinosporus pollen taken at 1000× magnification | |
Scientific classification | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Clade: | Angiosperms |
Clade: | Eudicots |
Order: | Caryophyllales |
Family: | Droseraceae (?) |
Genus: | † Droseridites Cookson (1947) ex R.Potonié (1960) |
Type species | |
Droseridites spinosus (Cookson) R.Potonié (1960) | |
Species | |
Droseridites is a genus of extinct plants of possible droseracean or nepenthacean affinity. It is a form taxon known only from fossil pollen. Species assigned to this genus originate from numerous regions of the world, including Europe (from France to the Caucasus), [1] India, [2] Egypt, [3] the Arabian Peninsula, [4] and the Kerguelen Islands. [5]
This genus is characterised by inaperturate and spinose pollen grains that are united in loose tetrahedral tetrads (groups of four). The grains are prolate, striate, and tricolpate. The colpi are slender and long, whereas the striae are very fine, densely packed, and situated parallel to the polar axis. [6]
Droseridites spinosus, the type species, has been recorded from the Tertiary of the Kerguelen Islands [4] and the Miocene of India, including the Warkalli Formation (Bharathi and Kundra Clay Mines, Kerala) and the Sindhudurg Formation (Mavli Mine at Redi, Sindhudurg District, Maharashtra). [2] It is of possible nepenthacean affinity. [5] Specimens identified in the literature as D. cf. spinosus have also been reported from Hungarian Miocene deposits. [4]
Droseridites baculatus was described from the Ghazalat-1 Well, Qattara Depression, Egypt. [3]
Droseridites echinosporus has been recorded from European Tertiary strata and is a member of a group of similar species that have been interpreted as belonging to the genus Nepenthes . [1]
Sites for D. major, a possible nepenthacean species, [1] include the Tertiary of Europe [1] and the Palaeocene-early Eocene Rekmangiri Coalfield of Garo Hills, Meghalaya, India. [2]
Droseridites parvus was originally described from the lower Eocene Cherry Formation of Assam, India. [4] It has also been recorded from the Palaeocene Tura Formation of the " Retialetes emendatus zone" in Assam [4] and the Oligocene-Neogene Dharmsala and Siwalik (Dharmsala and Nurpur areas, Kangra District, Himachal Pradesh). [2] The species is characterised by wart-like sculpturing and is "presently impossible to interpret". [4]
Pollen matching the description of D. senonicus has been found in formations of the Arabian Peninsula dating to as early as the Middle Cretaceous to late Upper Cretaceous, and it has been suggested that this species may represent an early palm taxon. [4]
Unidentified Droseridites palynomorphs have been recorded from numerous sites in India, including the Miocene Cuddalore Formation (Neyveli Lignitefield, Tamil Nadu), the Palaeocene Tura Formation (Langrin Coalfield, Khasi Hills, Meghalaya), the Palaeocene Seam No. 1 (Rekmangiri Coalfield, Garo Hills, Meghalaya), and the Oligocene-Neogene Dharmsala and Siwalik. [2]
Pollen of a number of species originally described under the genus Droseridites has been tentatively assigned to Nepenthes . In 1985, Wilfried Krutzsch transferred three species of the "D. echinosporus group", creating the new combinations Nepenthes echinatus, N. echinosporus, and N. major. [1] [7] [8] However, at more than 40 μm in diameter, the tetrads of D. major are larger than those of any known extant Nepenthes, and within the lower range of extant Drosera tetrads. [8] Pollen from the Kerguelen Islands originally described as D. spinosus has also been interpreted as belonging to Nepenthes. [5] [9]
Some authors consider D. major and D. parvus as synonyms of Nepenthidites laitryngewensis of the Palaeocene Lakadong Sandstone in Laitryngew, Khasi Hills, Meghalaya, India. [10] [2]
Nepenthes veitchii, or Veitch's pitcher-plant, is a Nepenthes species from the island of Borneo. The plant is widespread in north-western Borneo and can also be found in parts of Kalimantan. Nepenthes veitchii usually grows as an epiphyte, though the form from Bario seems to be strictly terrestrial and has not been observed to climb trees.
Nepenthes khasiana is an endangered tropical pitcher plant of the genus Nepenthes. It is the only Nepenthes species native to India. It is thought to attract prey by means of blue fluorescence.
Nepenthes pervillei is the only pitcher plant found in the Seychelles, where it is endemic to the islands of Mahé and Silhouette. It grows in rocky areas near granitic mountain summits, its roots reaching deep into rock fissures. The species has an altitudinal range of 350–750 m above sea level. Like all members of the genus, N. pervillei is dioecious, having separate male and female plants.
Nepenthes clipeata, or the shield-leaved pitcher-plant, is a tropical pitcher plant known only from the near-vertical granite cliff faces of Mount Kelam in west kalimantan, Indonesia. It has an altitudinal distribution between approximately 600 and 800 m.
Nepenthes boschiana, or Bosch's pitcher-plant, is a tropical pitcher plant endemic to Borneo. It is most closely allied to N. faizaliana. Nepenthes borneensis is considered a synonym of this species. Nepenthes boschiana has no known natural hybrids. No valid forms or varieties have been described. Nepenthes boschiana belongs to the loosely defined "N. maxima complex", which also includes, among other species, N. chaniana, N. epiphytica, N. eymae, N. faizaliana, N. fusca, N. klossii, N. maxima, N. platychila, N. stenophylla, and N. vogelii.
Nepenthes faizaliana is a tropical pitcher plant endemic to the limestone cliffs of Gunung Mulu National Park in Sarawak, Borneo. It is thought to be most closely related to N. boschiana.
Nepenthes mapuluensis, the Mapulu pitcher-plant, is a species of tropical pitcher plant native to East Kalimantan, Borneo. It is known only from a restricted geographical range and is listed as Endangered on the IUCN Red List.
Nepenthes lamii is a tropical pitcher plant endemic to New Guinea, where it grows at an altitude of up to 3520 m above sea level, higher than any other Nepenthes species. Although once confused with N. vieillardii and previously regarded as conspecific with the closely related N. monticola, it is now recognised as a distinct species.
Nepenthes mira is a highland pitcher plant endemic to Palawan in the Philippines. It grows at elevations of 1550–1605 m above sea level.
Nepenthes mikei is a tropical pitcher plant endemic to Sumatra. It is characterised by its black mottled lower and upper pitchers. The species is closely related to N. angasanensis and N. tobaica.
Nepenthes tobaica is a tropical pitcher plant endemic to Sumatra. It is particularly abundant around Lake Toba, after which it is named.
Nepenthes lavicola is a tropical pitcher plant species endemic to the Geureudong Massif of Aceh, northern Sumatra, where it grows at 2000–2600 m above sea level. It is thought to be most closely related to N. singalana and N. spectabilis.
Nepenthes masoalensis is one of two tropical pitcher plant species from Madagascar, the other being N. madagascariensis.
Archaeamphora longicervia is a fossil plant species, the only member of the genus Archaeamphora. Fossil material assigned to this taxon originates from the Yixian Formation of northeastern China, dated to the Early Cretaceous.
Droserapollis is a genus of extinct plants in the family Droseraceae. It is a form taxon known only from fossil pollen.
This article contains papers in paleobotany that were published in 2016.
This article records new taxa of plants that are scheduled to be described during the year 2018, as well as other significant discoveries and events related to paleobotany that occurred in the year 2018.
This article records new taxa of plants that were described during the year 2014, as well as other significant discoveries and events related to paleobotany that occurred in the year 2014.
Rajendra Nath Lakhanpal was an Indian paleobotanist. He was a specialist on palaeo-ecology and the identification of plants from pollen microfossils.