Gnetophyta

Unlike most biological groupings, it is difficult to find many common characteristics among all of the members of the gnetophytes. 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, 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 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, 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 has been difficulty in establishing an unambiguous interrelationship among them; in earlier times matters were even more difficult, with Pearson in the early 20th century discussing about the class Gnetales, rather than the order. 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. Foster & Gifford accepted this principle, and placed the three orders together in a common class for convenience, which they called Gnetopsida. 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. Other authors have suggested that the Gnetophyta are a sister group to the rest of the gymnosperms, 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. 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. 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". However, most genetic studies, as well as more recent morphological analyses, have rejected the anthophyte hypothesis. 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. One of the traits shared by both groups, is the absence of biflavonoids. A 2018 phylogenomic study estimated the divergence between Gnetales and Pinaceae at around 241 millions of years ago, in the early Triassic However, there is no morphological evidence nor examples from the fossil record to support the gnetophyte-sister hypotheses. == Fossil history ==

Knowledge of gnetophyte history through fossil discovery has increased greatly since the 1980s. their affinities to the group are equivocal. The oldest fossils that are definitely assignable to the group date to the Late Jurassic. Overall, the fossil record of the group is richest during the Early Cretaceous, exhibiting a substantial decline during the Late Cretaceous. Koonwarra fossil bed, Australia, Early Cretaceous (Aptian) • Jianchangia Yang, Wang and Ferguson, 2020 Jiufotang Formation, China, Early Cretaceous (Aptian) • Eamesia Yang, Lin and Ferguson, 2018 Yixian Formation, China, Early Cretaceous (Aptian) • Prognetella Krassilov et Bugdaeva, 1999 Yixian Formation, China, Early Cretaceous (Aptian) (initially interpreted as an angiosperm) • Chengia Yang, Lin & Wang, 2013, 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 • Laiyangia P.H. Jin, 2024 China, Early Cretaceous Gnetaceae • Khitania Guo et al. 2009 Yixian Formation, China, Early Cretaceous (Aptian) • Gnetaceaepollenites (Wodehouse) R. Potonié, 1958 Green River Formation, USA, Early Eocene 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). • Drewria Crane & Upchurch, 1987 Potomac Group, USA, Albian (possible affinities to Welwitschiaceae) • Bicatia Friis, Pedersen and Crane, 2014 Yixian Formation, China, Early Cretaceous (Aptian) • Protognetum Y. Yang, L. Xie et D.K. Ferguson, 2017 Daohugou Bed, China, Middle Jurassic (Callovian) • Itajuba Ricardi-Branco et al., 2013, Crato Formation, Brazil, Early Cretaceous (Aptian) • Protoephedrites Rothwell et Stockey, 2013 Canada, Valanginian (possible ephedroid affinities) • Siphonospermum Rydin et Friis, 2010 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). • Dayvaultia Manchester et al. 2021 Morrison Formation, USA, Late Jurassic (Tithonian) • Daohugoucladus Yang et al. 2023 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 et al, 2004, China, Upper Permian • Sanmiguelia United States, Late Triassic-Early Jurassic • Eoantha Russia, Early Cretaceous • Bassitheca Morrison Formation, USA, Late Jurassic (Tithonian) == References ==