Gnetophyta
Temporal range:
Welwitschia mirabilis female plant with cones
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Gymnospermae
Division: Gnetophyta
Bessey 1907
Class: Gnetopsida
Thom 1886
Families and genera

Gnetaceae
  Gnetum
Welwitschiaceae
  Welwitschia
Ephedraceae
  Ephedra

A distribution map of Gnetophyta colour-coded by genus
Distribution, separated by genus:
Green – Welwitschia
Blue – Gnetum
Red – Ephedra
Purple – Gnetum and Ephedra

Gnetophyta (/nɛˈtɒfɪtə, ˈnɛtoʊfaɪtə/) is a division of plants (alternatively considered the subclass Gnetidae or order Gnetales), grouped within the gymnosperms (which also includes conifers, cycads, and ginkgos), that consists of some 70 species across the three relict genera: Gnetum (family Gnetaceae), Welwitschia (family Welwitschiaceae), and Ephedra (family Ephedraceae). The earliest unambiguous records of the group date to the Jurassic, and they achieved their highest diversity during the Early Cretaceous. The primary difference between gnetophytes and other gymnosperms is the presence of vessel elements, a system of small tubes (xylem) that transport water within the plant, similar to those found in flowering plants. Because of this, gnetophytes were once thought to be the closest gymnosperm relatives to flowering plants, but more recent molecular studies have brought this hypothesis into question, with many recent phylogenies finding them to be nested within the conifers.

Though it is clear they are all related, the exact evolutionary inter-relationships between gnetophytes are unclear. Some classifications hold that all three genera should be placed in a single order (Gnetales), while other classifications say they should be distributed among three separate orders, each containing a single family and genus. Most morphological and molecular studies confirm that the genera Gnetum and Welwitschia diverged from each other more recently than they did from Ephedra.[1][2][3][4][5]

Welwitschia mirabilis bearing male cones
Ephedra distachya (male cones)
Ephedra distachya (female plant in bloom)
Gnetum gnemon male strobili
Gnetum gnemon female strobilus
Female Ephedra californica cone

Ecology and morphology

Unlike most biological groupings, it is difficult to find many common characteristics between all of the members of the gnetophytes.[6] The two common characteristics most commonly used are the presence of enveloping bracts around both the ovules and microsporangia as well as a micropylar projection of the outer membrane of the ovule that produces a pollination droplet,[7] though these are highly specific compared to the similarities between most other plant divisions. L. M. Bowe refers to the gnetophyte genera as a "bizarre and enigmatic" trio[2] because the gnetophytes' specialization to their respective environments is so complete that they hardly resemble each other at all. Gnetum species are mostly woody vines in tropical forests, though the best-known member of this group, Gnetum gnemon,[8] is a tree native to western Malesia. The one remaining species of Welwitschia, Welwitschia mirabilis, native only to the dry deserts of Namibia and Angola, is a ground-hugging species with only two large strap-like leaves that grow continuously from the base throughout the plant's life. Ephedra species, known as "jointfirs" in the United States, have long slender branches which bear tiny scale-like leaves at their nodes. Infusions from these plants have been traditionally used as a stimulant, but ephedrine is a controlled substance today in many places because of the risk of harmful or even fatal overdosing.

Classification

With just three well-defined genera within an entire division, there still is understandable difficulty in establishing an unambiguous interrelationship among them; in earlier times matters were even more difficult and we find for example Pearson in the early 20th century speaking of the class Gnetales, rather than the order.[9] G.H.M. Lawrence referred to them as an order, but remarked that the three families were distinct enough to deserve recognition as separate orders.[10] Foster & Gifford accepted this principle, and placed the three orders together in a common class for convenience, which they called Gnetopsida.[11] In general the evolutionary relationships among the seed plants still are unresolved, and the Gnetophyta have played an important role in the formation of phylogenetic hypotheses. Molecular phylogenies of extant gymnosperms have conflicted with morphological characters with regard to whether the gymnosperms as a whole (including gnetophytes) comprise a monophyletic group or a paraphyletic one that gave rise to angiosperms. At issue is whether the Gnetophyta are the sister group of angiosperms, or whether they are sister to, or nested within, other extant gymnosperms. Numerous fossil gymnosperm clades once existed that are morphologically at least as distinctive as the four living gymnosperm groups, such as Bennettitales, Caytonia and the glossopterids. When these gymnosperm fossils are considered, the question of gnetophyte relationships to other seed plants becomes even more complicated. Several hypotheses, illustrated below, have been presented to explain seed plant evolution. Some morphological studies have supported a close relationship between Gnetophyta, Bennettitales and the Erdtmanithecales.[12]

Recent research by Lee, Cibrian-Jaramillo, et al. (2011) suggests that the Gnetophyta are a sister group to the rest of the gymnosperms,[13] contradicting the anthophyte hypothesis, which held that gnetophytes were sister to the flowering plants.

Gnetifer hypothesis

In the gnetifer hypothesis, the gnetophytes are sister to the conifers, and the gymnosperms are a monophyletic group, sister to the angiosperms.The gnetifer hypothesis first emerged formally in the mid-twentieth century, when vessel elements in the gnetophytes were interpreted as being derived from tracheids with circular bordered pits, as in conifers.[7] It however only gained strong support with the emergence of molecular data in the late 1990s.[14][15][16][17] Although the most salient morphological evidence still largely supports the anthophyte hypothesis, some more obscure morphological commonalities between the gnetophytes and conifers lend support to the gnetifer hypothesis.These shared traits include: tracheids with scalariform pits with tori interspersed with annular thickenings, absence of scalariform pitting in primary xylem, scale-like and strap-shaped leaves of Ephedra and Welwitschia; and reduced sporophylls.[18][19][20]

  angiosperms (flowering plants)

  gymnosperms  

  cycads

  Ginkgo

  “Gnetifers”  

  conifers

  gnetophytes

Anthophyte hypothesis

From the early twentieth century, the anthophyte hypothesis was the prevailing explanation for seed plant evolution, based on shared morphological characters between the gnetophytes and angiosperms. In this hypothesis, the gnetophytes, along with the extinct order Bennettitales, are sister to the angiosperms, forming the "anthophytes".[7] Some morphological characters that were suggested to unite the anthophytes include vessels in wood, net-veined leaves (in Gnetum only), lignin chemistry, the layering of cells in the apical meristem, pollen and megaspore features (including thin megaspore wall), short cambial initials, and lignin syringal groups.[7][21][22][23] However, most genetic studies, as well as more recent morphological analyses,[24] have rejected the anthophyte hypothesis.[2][14][15][18][19][25][26][27][28][29]

Several of these studies have suggested that the gnetophytes and angiosperms have independently derived characters, including flower-like reproductive structures and tracheid vessel elements, that appear shared but are actually the result of parallel evolution.[2][7][25]

  Ginkgo

  cycads

  conifers

  anthophytes  

  angiosperms (flowering plants)

  gnetophytes

Gnepine hypothesis

The gnepine hypothesis is a modification of the gnetifer hypothesis, and suggests that the gnetophytes belong within the conifers as a sister group to the Pinaceae.[7] According to this hypothesis, the conifers as currently defined are not a monophyletic group, in contrast with molecular findings that support its monophyly.[16] All existing evidence for this hypothesis comes from molecular studies since 1999.[2][3][25][27][18][15][19][20][30][31] A 2018 phylogenomic study estimated the divergence between Gnetales and Pinaceae at around 241 millions of years ago, in the early Triassic[30] while a 2021 study placed it earlier, in the Carboniferous.[31]

However, the morphological evidence remains difficult to reconcile with the gnepine hypothesis. If the gnetophytes are nested within conifers, they must have lost several shared derived characters of the conifers (or these characters must have evolved in parallel in the other two conifer lineages): narrowly triangular leaves (gnetophytes have diverse leaf shapes), resin canals, a tiered proembryo, and flat woody ovuliferous cone scales.[18] These kinds of major morphological changes are not without precedent in the Pinales, however: the Taxaceae, for example, have lost the classical cone of the conifers in favor of a single-terminal ovule, surrounded by a fleshy aril.[25]

  angiosperms (flowering plants)

  gymnosperms

  cycads

  Ginkgo

  conifers  
  “Gnepines”   

  Pinaceae (the pine family)

  gnetophytes

  (other conifers)

Gnetophyte-sister hypothesis

Some partitions of the genetic data suggest that the gnetophytes are sister to all of the other extant seed plant groups.[4][7][18][19][16][32][33] However, there is no morphological evidence nor examples from the fossil record to support the gnetophyte-sister hypotheses.[20]

  gnetophytes  

  angiosperms (flowering plants)  

  cycads

  Ginkgo

  conifers

Fossil Gnetophytes

Knowledge of gnetophyte history through fossil discovery has increased greatly since the 1980s.[1] Although some fossils that have been proposed to be gnetophytes have been found as far back as the Permian,[34] their affinites to the group are equivocal. The oldest fossils that are definitely assignable to the group date to the Late Jurassic.[35] Overall, the fossil record of the group is richest during the Early Cretaceous, exhibiting a substantial decline during the Late Cretaceous.[35]

Ephedraceae

  • Leongathia V.A. Krassilov, D.L. Dilcher & J.G. Douglas 1998[36] Koonwarra fossil bed, Australia, Early Cretaceous (Aptian)
  • Jianchangia Yang, Wang and Ferguson, 2020[37] Jiufotang Formation, China, Early Cretaceous (Aptian)
  • Eamesia Yang, Lin and Ferguson, 2018[38] Yixian Formation, China, Early Cretaceous (Aptian)
  • Prognetella Krassilov et Bugdaeva, 1999 Yixian Formation, China, Early Cretaceous (Aptian) (initially interpreted as an angiosperm)[39]
  • Chengia Yang, Lin & Wang, 2013,[40] Yixian Formation, China, Early Cretaceous (Aptian)
  • Chaoyangia Duan, 1998 Yixian Formation, China, Early Cretaceous (Aptian)
  • Eragrosites Yixian Formation, China, Early Cretaceous (Aptian)
  • Gurvanella China, Mongolia, Early Cretaceous
  • Alloephedra China, Early Cretaceous
  • Amphiephedra China, Early Cretaceous
  • Beipiaoa China, Early Cretaceous
  • Ephedrispermum Portugal, Early Cretaceous (Aptian-Albian)
  • Ephedrites China, Early Cretaceous
  • Erenia China, Mongolia, Early Cretaceous
  • Liaoxia China, Early Cretaceous
  • Dichoephedra China, Early Cretaceous

Gnetaceae

  • Khitania Guo et al. 2009[41] Yixian Formation, China, Early Cretaceous (Aptian)

Welwitschiaceae

  • Priscowelwitschia Dilcher et al., 2005 Crato Formation, Brazil, Early Cretaceous (Aptian)
  • Cratonia Rydin et al., 2003 Crato Formation, Brazil, Early Cretaceous (Aptian)
  • Welwitschiostrobus Dilcher et al., 2005 Crato Formation, Brazil, Early Cretaceous (Aptian)

Incertae sedis:

  • Archangelskyoxylon Brea, Gnaedinger & Martínez, 2023 Roca Blanca Formation, Argentina, Sinemurian–Toarcian (closely related to Weltwitschia and Gnetum).[42]
  • Drewria Crane & Upchurch, 1987 Potomac Group, USA, Albian (possible affinities to Welwitschiaceae)[43]
  • Bicatia Friis, Pedersen and Crane, 2014[43] Figueira da Foz Formation, Portugal, Early Cretaceous (late Aptian early Albian), Potomac Group, USA, Albian (possible affinities to Welwitschiaceae)
  • Liaoningia Yang et al, 2017[44] Yixian Formation, China, Early Cretaceous (Aptian)
  • Protognetum Y. Yang, L. Xie et D.K. Ferguson, 2017[45] Daohugou Bed, China, Middle Jurassic (Callovian)
  • Itajuba Ricardi-Branco et al, 2013,[46] Crato Formation, Brazil, Early Cretaceous (Aptian)
  • Protoephedrites Rothwell et Stockey, 2013[47] Canada, Valanginian (possible ephedroid affinities)
  • Siphonospermum Rydin et Friis, 2010[48] Yixian Formation, China, Early Cretaceous (Aptian)
  • Welwitschiophyllum Dilcher et al., 2005 Crato Formation, Brazil, Early Cretaceous (Aptian), Akrabou Formation, Morocco, Late Cretaceous (Cenomanian-Turonian) (Initially interpreted as a member of Welwitschiaceae, later considered uncertain).[49][50]
  • Dayvaultia Manchester et al. 2021[51] Morrison Formation, USA, Late Jurassic (Tithonian)
  • Daohugoucladus Yang et al. 2023[52] Daohugou Bed, China, Middle Jurassic (Callovian)

Possible gnetophytes (not confirmed as members of the group)

  • Archaestrobilus Trujillo Formation, Texas, United States, Upper Triassic
  • Dechellyia-Masculostrobus Mongolia, Early Cretaceous (Aptian-Albian)
  • Dinophyton Chinle Formation, United States, Upper Triassic
  • Nataligma Molteno Formation, South Africa, Upper Triassic (Carnian)
  • Palaeognetaleana Wang, 2004,[34] China, Upper Permian
  • Sanmiguelia United States, Late Triassic-Early Jurassic
  • Eoantha Russia, Early Cretaceous
  • Bassitheca Morrison Formation, USA, Late Jurassic (Tithonian)

References

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  36. ↑ Krassilov, V.A.; Dilcher, D.L.; Douglas, J.G. (January 1998). "New ephedroid plant from the Lower Cretaceous Koonwarra Fossil Bed, Victoria, Australia". Alcheringa: An Australasian Journal of Palaeontology. 22 (2): 123–133. doi:10.1080/03115519808619195. ISSN 0311-5518.
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  38. ↑ Yang, Yong; Lin, Longbiao; Ferguson, David K.; Wang, Yingwei (December 2018). "Macrofossil evidence unveiling evolution of male cones in Ephedraceae (Gnetidae)". BMC Evolutionary Biology. 18 (1): 125. doi:10.1186/s12862-018-1243-9. ISSN 1471-2148. PMC 6116489. PMID 30157769.
  39. ↑ Yang, Yong; Ferguson, David K. (October 2015). "Macrofossil evidence unveiling evolution and ecology of early Ephedraceae". Perspectives in Plant Ecology, Evolution and Systematics. 17 (5): 331–346. doi:10.1016/j.ppees.2015.06.006.
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  42. ↑ Brea, Mariana; Silvia, Gnaedinger; Martínez, Leandro C.A. (2023). "Archangelskyoxylon carlquistii gen. et sp. nov. Taxonomy and phylogeny of an unequivocal gnetoid Jurassic fossil wood". Review of Palaeobotany and Palynology (105035). Retrieved 29 November 2023.
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  45. ↑ Yang, Yong; Xie, Lei; Ferguson, David K. (October 2017). "Protognetaceae: A new gnetoid macrofossil family from the Jurassic of northeastern China". Perspectives in Plant Ecology, Evolution and Systematics. 28: 67–77. doi:10.1016/j.ppees.2017.08.001.
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  47. ↑ Rothwell, Gar W.; Stockey, Ruth A. (March 2013). "Evolution and Phylogeny of Gnetophytes: Evidence from the Anatomically Preserved Seed Cone Protoephedrites eamesii gen. et sp. nov. and the Seeds of Several Bennettitalean Species". International Journal of Plant Sciences. 174 (3): 511–529. doi:10.1086/668688. ISSN 1058-5893. S2CID 84063572.
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  51. ↑ Manchester, Steven R.; Zhang, Xiaoqing; Hotton, Carol L.; Wing, Scott L.; Crane, Peter R. (2021-05-19). "Distinctive quadrangular seed-bearing structures of gnetalean affinity from the Late Jurassic Morrison Formation of Utah, USA". Journal of Systematic Palaeontology. 19 (10): 743–760. doi:10.1080/14772019.2021.1968522. ISSN 1477-2019. S2CID 239021014.
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