Gnetophyta, commonly known as gnetophytes, is a division of gymnosperm plants characterized by their production of naked seeds and inclusion of three highly distinct extant genera—Ephedra, Gnetum, and Welwitschia—encompassing approximately 115 species in total.[1] These plants are distinguished by several angiosperm-like features, including vessel elements in the xylem for efficient water transport, compound strobili (cone-like structures) for reproduction, and non-motile sperm cells, setting them apart from other gymnosperms.[2] With a fossil record dating back to the Early Cretaceous (around 125 million years ago), gnetophytes represent a relict group adapted to diverse habitats, from arid deserts to humid tropics, and include economically important species such as Ephedra for its medicinal alkaloids like ephedrine.[3][4]Taxonomically, Gnetophyta is classified under the subclass Gnetidae within the coniferophytes (Pinopsida), comprising three orders: Ephedrales (family Ephedraceae, genus Ephedra with about 70 species), Gnetales (family Gnetaceae, genus Gnetum with about 45 species), and Welwitschiales (family Welwitschiaceae, monotypic genus Welwitschia with one species, W. mirabilis).[3])[5] The genera exhibit striking morphological diversity: Ephedra consists of jointed-stemmed shrubs or vines prevalent in dry and cold regions, often lacking true leaves; Gnetum features woody climbers or trees with broad, net-veined leaves resembling those of dicotyledonous angiosperms in tropical and subtropical forests; and Welwitschia is a bizarre, long-lived desertperennial from southwestern Africa, characterized by a massive woody base and two persistent, strap-like leaves that can grow indefinitely.[6] This diversity underscores their adaptation to extreme environments, with Welwitschia capable of surviving over 2,000 years in the Namib Desert through deep taproots and minimal foliage.[2]Key reproductive and structural characteristics of gnetophytes include bisporangiate strobili (containing both microsporangia and megasporangia in some cases), double integuments around ovules forming a seed envelope, and verified double fertilization in species like Ephedra, a process long thought unique to angiosperms.[3] Their vascular system features both tracheids and vessels with porose perforation plates, enhancing hydraulic efficiency, while pollen grains are striate and boat-shaped, aiding wind or insect dispersal in nectar-producing species.[1] Ecologically, gnetophytes play roles in arid ecosystems as pioneer species and provide pharmacological resources, such as pseudoephedrine from Ephedra for respiratory treatments.[6]Phylogenetically, molecular and phylogenomic studies have resolved Gnetophyta as a monophyletic clade nested within the conifers (Pinophyta), specifically as the sister group to the pine family (Pinaceae), challenging earlier views that positioned them as the closest relatives to flowering plants (angiosperms).[3] This placement suggests convergent evolution of angiosperm-like traits, such as vessels and double fertilization, possibly driven by similar selective pressures for efficient reproduction and water conduction. Genome analyses reveal smaller sizes in gnetophytes compared to other gymnosperms, attributed to higher rates of transposable element elimination, providing insights into early seed plant diversification around 300 million years ago. Ongoing research highlights their evolutionary significance in understanding gymnosperm diversification and the origins of key innovations in seed plants.[3]
Overview
Definition and Characteristics
Gnetophyta, also known as gnetophytes, is a small but distinctive division within the gymnosperms, comprising vascular seed plants that produce naked seeds not enclosed in an ovary and lack true flowers. These plants represent one of four major groups of gymnosperms, alongside conifers, cycads, and ginkgo, and are characterized by their unique combination of primitive and derived traits that set them apart from other seed plants.[7]Key defining characteristics of Gnetophyta include the presence of vessel elements in their xylem, a feature rare among gymnosperms but common in angiosperms, which enhances water conduction efficiency. Some species exhibit a double fertilization-like process, where two sperm cells fuse with female gametophyte nuclei, producing two embryos rather than the single embryo typical of most gymnosperms; this has been documented in genera like Gnetum and Ephedra. Additionally, gnetophytes produce compound strobili, complex cone-like structures that house their reproductive organs, further distinguishing them from the simpler cones of other gymnosperms. These angiosperm-like traits contribute to their evolutionary significance, with recent studies placing Gnetophyta as the sister group to Pinaceae within conifers.[7][8][9]The division encompasses three extant genera, each with highly specialized forms adapted to diverse environments. Ephedra consists of shrubby plants, often resembling broom-like shrubs, with green, photosynthetic stems that perform the primary role of photosynthesis while scale-like leaves are reduced and non-photosynthetic. Gnetum includes tropical lianas, shrubs, or small trees bearing broad, net-veined leaves reminiscent of those in angiosperms, enabling efficient light capture in forested habitats. Welwitschia, represented by a single species, forms a basal rosette with two strap-like, persistent leaves that grow continuously from the base, splitting longitudinally over time and adapted to extreme aridity in desert conditions. Collectively, these genera account for approximately 119 living species worldwide as of 2025.[10][7][11]
Diversity and Distribution
Gnetophyta is a relatively small division within the gymnosperms, consisting of three extant families—Ephedraceae, Gnetaceae, and Welwitschiaceae—each represented by a single genus.[12] The genus Ephedra (Ephedraceae) includes approximately 74 species, Gnetum (Gnetaceae) comprises 44 species, and Welwitschia (Welwitschiaceae) has 1 species, yielding a total of 119 species as of 2025.[13][5][14] Highest diversity occurs in Ephedra, which accounts for the majority of species in the division.[15]The genera exhibit strikingly disjunct global distributions, reflecting their adaptation to specific environmental conditions across continents. Ephedra species are primarily found in arid and semi-arid regions of both the New and Old Worlds, including North America (e.g., southwestern United States), Eurasia (e.g., central Asia and the Mediterranean basin), and North Africa (e.g., Morocco and the Canary Islands).[16] In contrast, Gnetum is confined to humid tropical forests, with species distributed in central Africa (e.g., West Africa), Southeast Asia (e.g., Indomalaysia), and northern South America (e.g., Amazon basin), as well as isolated occurrences in Fiji and China.[17]Welwitschia is highly restricted, being endemic to the coastal Namib Desert in southwestern Africa, spanning parts of Angola and Namibia.[18]These disjunct patterns suggest historical biogeographic connections, particularly for Gnetum and Welwitschia, which show affinities to ancient Gondwanan landmasses through their presence in southern continents. For instance, the separation between African and South American Gnetum lineages is hypothesized to stem from vicariance events associated with the breakup of Gondwana during the Cretaceous. In comparison to other gymnosperm groups like conifers, which boast thousands of species, Gnetophyta's limited diversity underscores its relictual status.[12]
Morphology and Anatomy
Vegetative Structures
Gnetophyta display remarkable diversity in vegetative structures among their three extant genera—Ephedra, Gnetum, and Welwitschia—reflecting adaptations to varied environments while sharing certain anatomical innovations. Growth forms range from shrubs and herbs in Ephedra, which often appear as branching, upright or prostrate structures in arid regions, to woody climbers, shrubs, or trees in Gnetum, typically found in tropical forests as lianas with robust support tissues, and basal rosettes in Welwitschia, characterized by a low, disk-like woody crown that anchors the plant in hyper-arid deserts.[2][19][20]Stems in Ephedra are prominently photosynthetic and jointed, with green, ridged internodes that facilitate upright growth and resemble those of horsetails, while the leaves are reduced to small, whorled, scale-like sheaths at the nodes that provide minimal shading. In contrast, Gnetum features solid, woody stems capable of secondary thickening, supporting climbing habits through twining or attachment, paired with opposite, broad leaves exhibiting net venation akin to many dicotyledons. Welwitschia possesses a short, unbranched, woody stem emerging from the ground as a swollen base, from which only two (occasionally four) persistent, strap-like leaves emerge and grow indeterminately from basal meristems, often fraying into ribbons over time due to environmental wear.[2][19][20]Root systems in desert-adapted species emphasize deep penetration for water access; Ephedra develops extensive taproots and lateral roots that extend deeply in sandy soils to tap groundwater, enhancing survival in arid habitats. Similarly, Welwitschia mirabilis has a taproot reaching up to 1.5 meters in depth, supplemented by extensive shallow lateral roots that capture moisture from fog and form the bulk of the plant's underground biomass, with some roots accessing depths up to 1.25 meters horizontally.[21] Gnetum roots, while less documented in detail, support the climbing or arboreal habits with typical woody root architectures in humid tropics.[22][20]Vascular anatomy in Gnetophyta is distinguished by the presence of true vessels in the xylem—porous, efficient water-conducting elements with perforation plates—alongside tracheids, a feature unique among gymnosperms and resembling angiosperm wood for enhanced hydraulic efficiency. The phloem consists of sieve cells with simple sieve areas, accompanied by parenchyma, lacking the companion cells and sieve tubes typical of flowering plants. These vascular traits occur across all genera, supporting diverse habits from herbaceous to woody.[2][22][23]
Reproductive Structures
Gnetophytes possess unisexual reproductive structures organized as compound strobili, which are cone-like aggregations of bracts bearing fertile appendages. Male strobili contain microsporangia that produce pollen grains, typically bisaccate or boat-shaped in Ephedra to facilitate wind dispersal, while female strobili feature ovules enveloped by bracts serving as protective structures. These strobili are dioecious in most species, with Ephedra and Welwitschia strictly dioecious and Gnetum functionally so, as female strobili may include abortive microsporangia.[2][24][2]Pollination in Gnetophyta involves pollen capture via a pollination droplet secreted by the ovule, followed by pollen tube growth toward the ovule. Ephedra and Welwitschia are primarily wind-pollinated, with pollen adapted for aerial transport, whereas Gnetum employs insect pollination, where thrips and other small insects transfer pollen between strobili. Upon germination, the pollen tube delivers non-motile sperm cells directly to the female gametophyte.[2][25][2]The life cycle of Gnetophyta follows an alternation of generations typical of seed plants, but with highly reduced gametophytes confined within sporophyte tissues. Male gametophytes develop within pollen grains as prothallial cells and sperm cells, while female gametophytes are monosporic and lack archegonia in Gnetum and Welwitschia, consisting instead of free-nuclei stages or simplified egg cells. Fertilization involves double fertilization in Ephedra and Gnetum, where one sperm fuses with the egg to form the zygote and the second sperm fuses with a ventral canal nucleus or similar cell, producing a diploid product that develops as a supernumerary embryo rather than endosperm; this process is considered analogous to angiosperm double fertilization but its functional role remains debated. In Welwitschia, fertilization typically involves the fusion of one sperm with the egg, though rare double fertilization events have been observed, with the zygote migrating within the reduced female gametophyte.[2][9][26][2]Following fertilization, seeds develop as naked gymnosperm seeds with two integument layers: an inner layer forming a micropylar tube and an outer layer derived from fused bracts. In Gnetum, seeds are enclosed by a fleshy aril attractive to dispersers, while in Ephedra, they feature papery wings from bracts enabling wind dispersal; Welwitschia seeds are also winged but larger and adapted for occasional animal dispersal. Seed maturation involves maternal provisioning, with the embryo embedded in nutritive tissue from the female gametophyte.[2][27][28]
Ecology and Uses
Habitats and Adaptations
Gnetophyta species exhibit diverse habitat preferences shaped by their three extant genera: Ephedra, Welwitschia, and Gnetum. Ephedra species, comprising the majority of gnetophytes, predominantly occupy arid deserts and steppes across both hemispheres, thriving in cool, dry environments with sandy or rocky soils. In contrast, Welwitschia mirabilis is restricted to hyper-arid coastal deserts, notably the Namib Desert in southwestern Africa, where it endures extreme fog-dependent moisture regimes.[29] Gnetum species favor humid tropical understories in lowland rainforests of Central and South America, Africa, and Southeast Asia, often as vines in shaded, moist conditions.[1]These plants have evolved specialized physiological adaptations to their respective niches. In Welwitschia, crassulacean acid metabolism (CAM) photosynthesis enables nocturnal CO₂ uptake, minimizing daytime transpiration and conserving water in desiccating conditions; this facultative CAM mode supplements standard C₃ photosynthesis during stress.[29] Ephedra species feature drought-tolerant, photosynthetic stems with reduced, scale-like leaves that limit transpirational water loss, coupled with anisohydric water regulation to maintain hydraulic function under prolonged aridity.[30] Gnetum's climbing lianescent habit allows seedlings to ascend from shaded understories toward canopy gaps, optimizing light capture through acclimation of leaf anatomy and gas exchange to varying irradiance levels.[31]Ecological interactions further enhance Gnetophyta resilience. Many Gnetum species form ectomycorrhizal symbioses with diverse fungal partners, facilitating nutrient acquisition in nutrient-poor tropical soils and promoting seedling establishment.[32] In Ephedra, ephedrine-type alkaloids serve as chemical defenses, exhibiting neurotoxic effects that deter vertebrate and insect herbivores, thereby reducing browsing pressure in open arid landscapes.[33]Habitat loss from desertification, urbanization, and deforestation poses significant threats, rendering several Gnetophyta species, particularly range-restricted Gnetum and Ephedra taxa, vulnerable according to 2025 IUCN assessments. For example, in the 2025 IUCN update, Gnetum arboreum was uplisted from Data Deficient to Vulnerable due to habitat degradation.[34][35] Recent analyses link Quaternary aridity cycles to Ephedra diversification, with intensified dry periods driving speciation and adaptation in arid biomes across continents.[36]
Human Uses
Gnetophyta species, particularly those in the genus Ephedra, have been utilized for medicinal purposes for millennia, primarily due to their alkaloid content. Ephedra plants are the primary natural source of ephedrine and pseudoephedrine, compounds extracted for use in over-the-counter decongestants, cold remedies, and asthma treatments, where they act as bronchodilators to alleviate respiratory symptoms.[37][38] In traditional Chinese medicine, Ephedra sinica, known as ma huang, has been employed for over 2,000 years to treat conditions such as asthma, coughs, and nasal congestion by promoting sweating and lung qi circulation.[39][40]Several Gnetophyta species contribute to food and beverage traditions. The seeds of Gnetum species, such as G. gnemon, are nutritious and commonly boiled or roasted as a snack similar to peanuts, providing protein and antioxidants, while the leaves are consumed as a vegetable in various African and Asian cuisines.[41][42] In North American indigenous cultures, stems of Ephedra species like E. viridis are brewed into caffeine-free Mormon tea, valued as a tonic and blood purifier; this practice extends to Mexican communities where it serves as a traditional beverage for medicinal and ceremonial purposes.[43][44]Beyond medicine and nutrition, Gnetophyta offer practical and aesthetic applications. In Namibia, the broad, leathery leaves of Welwitschia mirabilis lie flat on the ground, effectively preventing wind-induced soil erosion in arid environments.[45][46] This species also holds ornamental value, cultivated in botanical gardens and by enthusiasts worldwide for its unique, long-lived form resembling a living fossil.[47] Fibers extracted from the bark and stems of Gnetum species, such as G. montanum and G. buchholzianum, are strong and durable, used locally to produce ropes, fishing nets, and carrying straps in tropical regions.[48][49]The economic significance of Gnetophyta is driven largely by the pharmaceutical demand for ephedrine-derived products, with the global ephedrine market valued at approximately $2.5 billion in 2025 and projected to grow at a CAGR of 4.8%.[50] However, this demand has led to conservation challenges, including overharvesting of wild Ephedra populations, which contributes to habitat degradation and population declines in regions like the Himalayas and arid grasslands, prompting calls for sustainable cultivation to mitigate ecological conflicts.[51][52]Despite these benefits, human uses of Gnetophyta carry risks, particularly with Ephedra. In the United States, the FDA banned ephedra-containing dietary supplements in 2004 following reports of severe adverse effects, including cardiovascular events such as heart attacks, strokes, and arrhythmias linked to its sympathomimetic properties.[53][54] Similar restrictions exist in other countries due to these side effects, which can include elevated blood pressure and irregular heartbeats even at low doses.[55][56]
Classification and Phylogeny
Taxonomic Classification
Gnetophyta, also known as Gnetales in some classification systems, is recognized as a distinct division within the gymnosperms, encompassing three extant families, each monotypic at the genus level. This division was formally established by Charles E. Bessey in 1907 to group the vessel-bearing gymnosperms separately from other seed plant lineages. The class Gnetopsida contains three orders: Ephedrales, Gnetales, and Welwitschiales, reflecting the morphological and reproductive distinctions among the genera while maintaining their unity as a clade./08:_Gymnosperms/8.05:_Gnetophytes)The order Ephedrales includes the family Ephedraceae and the genus Ephedra, which comprises approximately 71 species of shrubs or small trees characterized by jointed, green stems that function photosynthetically in place of reduced leaves.[28] Notable species include Ephedra sinica, a medicinal plant native to Asia and the source of the alkaloid ephedrine used in traditional Chinese medicine.[2] The order Gnetales consists of the family Gnetaceae and the genus Gnetum, with about 40 species of tropical trees, shrubs, or lianas featuring opposite, broad, net-veined leaves that resemble those of angiosperms. An example is Gnetum gnemon, a tree from Southeast Asia and the Pacific whose edible aril and seeds are consumed in local cuisines.The order Welwitschiales is represented by the family Welwitschiaceae and the monotypic genus Welwitschia, containing only Welwitschia mirabilis, a unique perennial gymnosperm endemic to the Namib Desert with a basal rosette of two persistent, strap-like leaves that grow continuously from meristematic tips. Collectively, these three genera account for around 112 species worldwide, as estimated in recent global plant inventories.The taxonomic nomenclature of Gnetophyta has evolved significantly; in the 19th century, George Bentham in Genera Plantarum (1862) treated the three genera as separate classes within gymnosperms—Chlamydospermae for Ephedra, etc.—reflecting their perceived distinctiveness, but 20th-century botanists unified them into a single division based on shared anatomical features like vessels in xylem. This consolidation was further supported by subsequent revisions, such as those by Mark W. Chase and others, emphasizing their monophyly despite ongoing phylogenetic debates.
Phylogenetic Hypotheses
In the early 20th century, botanists viewed Gnetophyta as a distinct class of seed plants that bridged gymnosperms and angiosperms, based on their unique combination of gymnospermous and angiosperm-like features such as vessel elements in the xylem and compound reproductive structures.[57] This perspective, advanced by researchers like Agnes Arber and John Parkin in 1907–1908, emphasized Gnetales (now Gnetophyta) as evolutionary intermediates, with Ephedra serving as a model for ancestral angiosperm forms due to similarities in strobilar organization and pollen tube development.[58] Similarly, Richard Wettstein's 1907 phylogenetic system proposed a close affinity between Gnetales and angiosperms, placing them adjacent in seed plant evolution and highlighting shared traits like opposite-decussate phyllotaxis.[59] These ideas positioned Gnetophyta outside traditional gymnosperm classes like Cycadopsida and Coniferopsida, often as Gnetopsida, to underscore their transitional role.[60]The Gnetifer hypothesis, emerging in the 1920s from morphological comparisons, posited Gnetophyta as sister to conifers, rendering gymnosperms monophyletic and sister to angiosperms overall.[61] This view, supported by shared features such as linear leaves, reduced sporophylls, and the interpretation of gnetophyte vessels as homologous to conifer tracheids, gained traction through studies like those of William Thompson in 1918, who noted anatomical parallels in wood structure and reproductive scales.[58] Charles Joseph Chamberlain's 1935 classification further integrated Gnetophyta into Coniferophyta, citing common traits like resin canals and tiered proembryos as evidence of close kinship.[60]A contrasting proposal, the anthophyte hypothesis, arose in the 1980s through cladistic analyses and placed Gnetophyta as sister to angiosperms within a broader clade including extinct groups like Bennettitales.[62] Formulated by Peter R. Crane in 1985, it drew on morphological synapomorphies such as vessel elements, double fertilization, and flower-like strobili, interpreting these as evolutionary precursors to angiosperm innovations.[63] This hypothesis, refined by James A. Doyle and Michael J. Donoghue in 1986 and 1992, dominated discussions through the 1990s, as it resolved ambiguities in seed plant phylogeny by emphasizing reproductive similarities over vegetative ones.[58]The gnepine hypothesis refined the gnetifer idea by positioning Gnetophyta specifically as sister to Pinaceae within conifers, implying conifer paraphyly.[61] Initially implicit in Chamberlain's 1935 work linking gnetophytes to pines via needle-like leaves and ovulate cone scales, it was explicitly articulated in molecular contexts but rooted in morphological evidence like shared metaxylem lacking scalariform pitting.[60] Meanwhile, the gnetophyte-sister hypothesis suggested Gnetophyta as basal to all other gymnosperms, based on early cladistic treatments of vegetative and reproductive traits like the micropylar tube.[64] These pre-molecular theories faced challenges from emerging molecular data in the late 1990s, which often conflicted with morphological signals due to rapid evolutionary rates in Gnetophyta lineages.[58]
Modern Molecular Evidence
Modern molecular studies have firmly established the monophyly of Gnetophyta through analyses of DNA sequences from nuclear, chloroplast, and mitochondrial genomes, resolving earlier uncertainties about the relationships among its three genera: Ephedra, Gnetum, and Welwitschia.[65][66] These datasets, encompassing thousands of genes, consistently recover Gnetales as a cohesive clade within gymnosperms, distinct from other seed plant lineages.[67]The prevailing consensus from phylogenomic research positions Gnetales as sister to Pinaceae, supporting the Gnepine hypothesis and embedding Gnetophyta within the broader Coniferales clade of gymnosperms.[65][58] This arrangement contrasts with earlier hypotheses that allied Gnetales more closely to angiosperms, as multi-genome comparisons highlight shared genomic features with conifers, such as conserved gene arrangements and synteny patterns.[66]Seminal studies have bolstered this view, including the 2018 genome sequencing of Welwitschia mirabilis published in Nature Plants, which demonstrated strong conifer affinities through nuclear and organellar data, including evidence of ancient whole-genome duplications aligning with conifer evolutionary patterns.[66] Complementing this, a 2022 phylogenomic analysis in Frontiers in Ecology and Evolution utilized extensive transcriptomic and genomic sampling to mitigate long-branch attraction artifacts, confirming the Gnepine topology with high bootstrap support across diverse gene sets.[58]As of 2025, integrated multi-omics approaches, building on these foundations, continue to affirm Gnetophyta's position sister to Pinaceae, with molecular clock estimates indicating a divergence approximately 300 million years ago during the late Carboniferous.[66][65] However, challenges persist, including long-branch attraction due to elevated substitution rates in Gnetales lineages, which can distort tree topologies in single-gene analyses, and potential incomplete lineage sorting that contributes to gene-tree discordance in deep gymnosperm phylogenies.[58][67] Advanced models and increased sampling have largely overcome these issues in recent reconstructions.[65]
Evolutionary History
Fossil Record
The fossil record of Gnetophyta begins in the Late Permian, approximately 260 million years ago, with the discovery of isolated gnetalean cones from the Cathaysian flora in northern China. These cones, described as Gnetum-like structures with compound strobili featuring bract-scale complexes and winged seeds, represent the earliest unequivocal evidence of the group and extend its stratigraphic range far beyond previous estimates.[68]Mesozoic deposits reveal a marked increase in gnetophyte diversity, with Jurassic fossils including members of the Protognetaceae family from northeastern China, such as Protognetum jurassicum, characterized by decussate branching, scalelike leaves, and bisporangiate reproductive units dated to around 165 million years ago. In the Early Cretaceous, macrofossils like the ephedroid Jianchangia verticillata from the Jiufotang Formation (approximately 120 million years ago) exhibit whorled bracts and tubular reproductive axes, marking the first such records from this stratigraphic unit and highlighting transitional morphologies. A 2023 discovery from the Mid-Jurassic Daohugou Formation further enriches this record, with Daohugoucladus sinensis preserving opposite phyllotaxy, linear-lanceolate leaves with midveins, and pedicellate fertile shoots, suggesting broader morphological experimentation in Jurassic gnetophytes.Gnetophyte diversity peaked in the mid-Cretaceous, around 100 million years ago, with numerous species across several genera documented from global localities, reflecting cosmopolitan distribution and varied habits from herbaceous to scandent forms.[69] This era includes debated Bennettitales-like fossils, such as those with flower-like strobili and bisporangiate microsporangia, whose gnetophyte affinities stem from shared traits like bract-enclosed ovules, though anatomical differences persist in ongoing discussions.[70]Post-Eocene Cenozoic records are sparse, indicating a sharp decline in gnetophyte abundance and diversity, with most evidence limited to dispersed pollen. Ephedra-type pollen grains from Miocene sediments (approximately 15-20 million years ago) across Eurasia and North America link directly to extant lineages, often associated with arid paleoenvironments and preserved in lacustrine deposits.[71][58] These fossils, including polyplicate grains with gemmate surfaces, underscore the relictual nature of modern gnetophytes like Ephedra.
Evolutionary Insights
The origins of Gnetophyta trace back to stem-group representatives in the Permian period, approximately 299–252 million years ago, when they diverged from the conifer lineage around 310 million years ago based on molecular clock estimates integrated with fossil calibrations.[58][72] This divergence is supported by Permian fossils, such as gnetalean cones from China. The early radiation of Gnetophyta appears linked to the contemporaneous rise of angiosperms in the Early Cretaceous, as gnetophytes occupied overlapping ecological niches in warmer, more humid environments, potentially facilitating shared adaptations like efficient pollination syndromes.[1]A key phase of diversification occurred during the Jurassic (201–145 million years ago), driven by adaptations to increasingly arid conditions, including reduced leaf surfaces and prostrate growth forms in ephedroid lineages that allowed persistence in dry, open habitats.[73] This was followed by a peak in the Early Cretaceous (145–100 million years ago), marked by widespread fossil occurrences and the evolution of insect pollination in groups like Ephedra, where ancestral pollen structures attracted beetles and other vectors, contributing to higher diversification rates amid global warmth and biotic interactions.[58] However, post-Cretaceous declines, particularly after the Early Cretaceous, are attributed to global climate cooling and the Eocene-Oligocene Transition around 34 million years ago, which intensified aridity and favored competitors like wind-pollinated grasses over specialized gnetophyte lineages.[74]Fossil insights further illuminate these patterns, with Permian evidence indicating early hydraulic innovations in gymnosperms that may have enabled survival in variable climates, while 2025 analyses of Ephedra fossils reveal aridity-driven biodiversity crises in the Cenozoic, where dust storms and cooling events triggered shifts from insect to wind pollination, decimating diverse Cretaceous forms.[75][74] Overall, Gnetophyta transitioned from a diverse Mesozoicclade, abundant in low-latitude floras, to a relictual group of extant species confined to extreme niches like deserts and coastal dunes, underscoring their resilience amid mass extinctions but vulnerability to long-term climatic shifts.[76]Ongoing debates center on whether pre-Cretaceous fossils represent true crown-group Gnetophyta or stem relatives, as ambiguous Permian and Triassic records complicate phylogenetic placement, and molecular clocks often yield older divergence estimates (e.g., 310 million years ago) than the Jurassic onset of unambiguous fossils, necessitating refined calibrations to reconcile these discrepancies.[58][72]