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Branch

A branch is a secondary stem or limb of a plant, such as a tree or shrub, that arises from the main trunk or a larger stem and typically supports leaves, flowers, fruits, or smaller branches.^[1] In botany, branches develop from buds on the main axis and can vary in size from small twigs to large boughs, contributing to the plant's structural framework, photosynthesis, and reproduction.^[2] They often exhibit patterns of growth influenced by factors like light, gravity, and hormones, leading to forms such as horizontal, upright, or weeping branches in different species.^[1] The term "branch" extends metaphorically to various fields beyond botany, denoting a division, offshoot, or subdivision of a larger whole. In geography, a branch refers to a tributary or secondary channel of a river that diverges from the main stream, as seen in river deltas where multiple branches distribute water and sediment.^[3] In business and organizations, a branch is a local office or operational unit of a larger company, sharing the parent entity's legal and financial structure without forming a separate entity.^[4] For instance, banks commonly establish branches in different cities to extend services while remaining integrated with the central headquarters.^[5] In governance, particularly within democratic systems like the United States, "branch" describes one of the three independent divisions of government—legislative, executive, and judicial—designed to prevent concentration of power through checks and balances. The legislative branch enacts laws, the executive implements them, and the judicial interprets them, a framework rooted in the U.S. Constitution's separation of powers.^[6] Additionally, in computer science and version control systems like Git, a branch represents a parallel line of development in code, allowing teams to work on features independently before merging changes.^[7] These diverse applications highlight the term's versatility in describing hierarchical or divergent structures across natural, social, and technical domains.

Definition and Etymology

Botanical Definition

In botany, a branch is defined as a lateral extension of the main stem, typically developing above ground from an axillary bud located in the axil where a leaf meets the stem.^[8] This structure arises when the axillary bud elongates, forming a secondary axis that can further subdivide into additional shoots.^[1] Branches are distinguished from the primary stem, which serves as the main vertical axis of the plant, by their subordinate position and origin from lateral buds rather than the apical meristem.^[9] Unlike twigs, which are the youngest and smallest extensions of woody stems—usually representing the current or previous year's growth—branches are generally more mature structures, often exceeding one year in age and capable of supporting lateral offshoots.^[1] For instance, in trees, branches manifest as robust limbs that extend outward from the trunk, while in vines, they appear as elongated shoots that facilitate climbing or trailing.^[8] This distinction highlights the developmental stage and scale, with twigs serving as precursors that may mature into branches over time. Classification of a branch relies on key morphological criteria, including the presence of nodes—points along the axis where leaves or buds attach—and internodes, the segments between nodes that represent periods of elongation.^[8] Branches also possess the potential to bear leaves, flowers, or fruits, underscoring their role in reproductive and photosynthetic functions, though this capacity varies by plant species and environmental conditions.^[1] These features ensure branches contribute to the overall architecture and adaptability of vascular plants.

Etymology and Historical Usage

The English word "branch," referring to a division of a plant stem, entered the language around 1300 as "braunch" or "branche," borrowed from Old French branche (12th century), which denoted a bough, twig, or limb-like extension. This Old French term derives from Late Latin branca, originally meaning "paw" or "claw," an association likely stemming from the grasping, appendage-like form of tree limbs. The Late Latin word may trace to Gaulish branka, a Celtic term for a forked or clawed structure, reflecting pre-Roman influences in the Indo-European linguistic family. By the 14th century, "branch" had supplanted the native Old English bōh (bough), becoming the standard term for plant subdivisions in Middle English texts.^[10] In ancient Roman agricultural writings, the equivalent Latin term ramus—meaning a branch or bough—was frequently employed to describe woody extensions of trees, particularly in horticultural practices. Lucius Junius Moderatus Columella, in his comprehensive treatise De Re Rustica (ca. 60–65 AD), extensively references rami in discussions of orchard management, advising farmers to prune unproductive branches to enhance fruit yield and tree vigor. For instance, Columella recommends selecting healthy rami for grafting and propagation, underscoring their essential role in sustaining agricultural productivity across the Roman Empire. This usage highlights the practical, economic significance of branches in classical farming, influencing subsequent medieval and Renaissance agronomy. The concept of "branch" gained precision in 16th-century botanical literature amid the European Renaissance, as scholars revived and expanded classical terminology to catalog the expanding New World flora. Herbalists such as Leonhart Fuchs in his De Historia Stirpium (1542) described plant architectures using terms akin to "branch" for stems and offshoots, often illustrated to distinguish morphological variations.^[11] Carl Linnaeus, in the 18th century, integrated branching metaphors into his binomial nomenclature system, conceptualizing taxonomic hierarchies as a "natural system" where genera formed "branches" diverging from familial trunks, as outlined in Systema Naturae (1758).^[12] This Linnaean framework standardized "branch" as both a literal descriptor and a classificatory tool, shaping modern botany's structural vocabulary. Beyond botany, the imagery of plant branches permeated cultural expressions, inspiring metaphors like "branches of knowledge," which evoke a tree's divergent limbs to represent subdivided disciplines. This analogy, rooted in ancient arborial symbolism, appeared in encyclopedic diagrams by the 12th century and was popularized by Francis Bacon's Advancement of Learning (1605), portraying philosophy as a tree with memory, reason, and imagination as its branches. In heraldry, branches such as the laurel or olive symbolize triumph and peace, as seen in Roman-inspired emblems where a palm branch signifies martyrdom or victory. Folklore similarly draws on branch motifs for lineage and renewal, with tales across Indo-European traditions likening family descent to sprouting boughs, as in Celtic myths of sacred groves where severed branches foretell prosperity or peril.^[13]^[14]^[15]

Types of Branches

Woody Branches

Woody branches develop in perennial plants such as trees and shrubs through secondary growth, a process driven by the vascular cambium—a thin layer of meristematic tissue that forms between the primary xylem and phloem. This cambium divides to produce secondary xylem inward, which lignifies to create rigid wood, and secondary phloem outward, contributing to the inner bark; lignification involves the deposition of lignin in cell walls during secondary wall formation, enhancing mechanical strength and water impermeability.^[16]^[17]^[18] The structure of woody branches includes distinct layers adapted for support, transport, and protection. The core consists of wood, or secondary xylem, which provides structural integrity and conducts water and minerals upward; surrounding this is the phloem layer for distributing sugars and nutrients, while the outermost bark—comprising dead phloem, cork cambium, and cork cells—shields against pathogens, desiccation, and physical damage. These features enable branches to thicken over time, with annual growth rings visible in cross-sections, distinguishing them from softer tissues.^[18]^[8]^[19] Prominent examples include the stout limbs of oak trees (Quercus spp.), which extend horizontally to support broad leaves, and the flexible boughs of pines (Pinus spp.), often arranged in whorls to maximize light capture. These branches collectively form the canopy layer in forest ecosystems, creating a dense overhead structure that intercepts sunlight, reduces wind exposure, and influences understory microclimates.^[20]^[21] Unlike branches in herbaceous plants, which lack extensive secondary growth and remain flexible and short-lived, woody branches exhibit greater durability due to lignification, allowing them to withstand mechanical stresses like wind and snow loads while resisting environmental challenges such as drought and frost through compartmentalized water storage and protective bark. This perennial nature enables long-term structural expansion and resource allocation.^[22]^[23]

Herbaceous and Specialized Branches

Herbaceous branches are soft, flexible stems that exhibit annual growth and lack secondary thickening, distinguishing them from the rigid, lignified structures of woody plants. These branches occur in non-woody species such as grasses and herbaceous perennials, where above-ground parts die back to the soil surface at the end of the growing season, relying on primary growth from apical and lateral meristems for elongation.^[24]^[25] In contrast to woody branches, herbaceous ones remain green and succulent, supporting rapid seasonal regeneration without persistent vascular reinforcement.^[26] Specialized branches represent morphological modifications that enhance survival in specific niches, often diverging from typical herbaceous forms. Cladodes, for instance, are flattened, photosynthetic stems that mimic leaves while functioning as primary branches in arid-adapted plants like cacti, where they expand surface area for light capture and carbon fixation.^[27]^[28] These structures also facilitate water storage through thickened parenchyma tissues, allowing species such as Opuntia to endure prolonged droughts by retaining moisture in their succulent pads.^[29]^[30] Other specialized forms include thorns, which are sharply pointed branches modified for defense against herbivores, as observed in hawthorns (Crataegus spp.), where they arise from axillary buds and deter browsing without compromising the plant's vascular integrity.^[31]^[32] Tendrils serve as coiling, prehensile branches in climbing vines, enabling attachment to supports; in grapevines (Vitis spp.), these leafless stems twist around structures via thigmotropism, facilitating upward growth in forested or open habitats.^[33]^[34] Notable examples illustrate these adaptations' diversity. In strawberries (Fragaria spp.), stolons function as elongated, horizontal branches that root at nodes to produce clonal offspring, promoting vegetative spread across soil surfaces in temperate meadows.^[35]^[8] Similarly, phylloclades in asparagus (Asparagus spp.) appear as needle-like or flattened branches that supplement photosynthesis, reducing reliance on true leaves in nutrient-poor or shaded environments.^[27]^[36]

Anatomy and Structure

Internal Anatomy

The internal anatomy of plant branches is characterized by specialized tissues that facilitate transport, provide structural support, and enable growth. These tissues are organized in a cylindrical fashion, with vascular elements running longitudinally through the branch to connect roots, stems, and leaves. Ground tissues fill the spaces between vascular bundles, while meristematic regions drive elongation and radial expansion. This organization varies between herbaceous and woody branches but shares fundamental components across vascular plants. Vascular tissues form the primary conduit system within branches. Xylem, located toward the interior of vascular bundles, transports water and dissolved minerals upward from roots to aerial parts via dead, hollow vessel elements and tracheids that form continuous pipelines.^[37] Phloem, positioned exterior to the xylem, distributes sugars, amino acids, and other organic nutrients produced in leaves to non-photosynthetic tissues through living sieve tube elements connected by sieve plates.^[38] In branches, these tissues are bundled together, often surrounded by protective layers, ensuring efficient resource allocation throughout the plant body.^[39] Support structures in branches include collenchyma and sclerenchyma tissues, which provide mechanical reinforcement without compromising flexibility. Collenchyma, composed of living cells with unevenly thickened primary walls rich in cellulose and pectin, offers elastic support in young, growing branches, particularly beneath the epidermis where it resists bending stresses.^[40] Sclerenchyma, featuring dead cells with lignified secondary walls, delivers rigid, long-term strength in mature branches; fibers elongate alongside vascular tissues, while sclereids add localized reinforcement.^[9] These tissues collectively maintain branch integrity against environmental forces like wind and gravity. Meristematic regions within branches consist of undifferentiated cells capable of division, driving primary and secondary growth. Apical meristems, located at branch tips, produce new cells for elongation, organizing into zones that differentiate into protoderm, ground meristem, and procambium.^[41] Lateral meristems, such as the vascular cambium in woody branches, form a thin cylindrical sheath that adds secondary xylem inward and phloem outward, contributing to girth increase.^[18] These regions ensure continuous development, with activity modulated by hormonal and environmental cues. In woody branches, cross-sections display annual rings as concentric layers of secondary xylem, reflecting seasonal growth patterns. Each ring comprises earlywood—large, thin-walled vessels formed in spring for rapid water conduction—and latewood—denser, thicker-walled cells produced in summer for added strength—delimiting one year's increment.^[18] These rings, visible under magnification, originate from the vascular cambium's annual cycle and provide a record of environmental history.^[42]

External Morphology

The external morphology of branches encompasses the visible structural features that define their form and arrangement on the plant stem. Nodes represent the discrete points along the branch where leaves, flowers, or lateral branches attach, serving as key morphological markers that distinguish stems from roots.^[43] Internodes, the elongated segments between consecutive nodes, vary in length and girth depending on species and environmental conditions, contributing to the overall shape and spacing of external appendages.^[44] Buds and scars further characterize the external surface of branches. Axillary buds, located in the axil formed by the leaf and stem at each node, are embryonic shoots capable of developing into new branches or flowers.^[45] Leaf scars, the remnants left after leaves detach, appear as raised or depressed marks on the branch surface, often accompanied by bundle scars indicating vascular connections.^[45] Surface variations on branches include textural and porous features, particularly in woody types. Bark on mature woody branches exhibits diverse textures, from smooth and thin on young twigs to deeply furrowed, ridged, or scaly on older ones, reflecting developmental stages and species-specific traits.^[46] Lenticels, small lens-shaped openings scattered across the bark surface, appear as slightly raised or roughened areas that facilitate gas diffusion through the otherwise impermeable outer layer.^[47] Branching angles and orientations influence the architectural layout of the plant. Orthotropic branches grow vertically upward, maintaining a straight or upright posture from the main axis.^[48] In contrast, plagiotropic branches exhibit horizontal or oblique orientations, often diverging from the main stem at acute angles to form lateral extensions.^[48]

Functions and Development

Growth and Branching Mechanisms

Branch growth in plants is primarily governed by apical dominance, a process in which the shoot apical meristem inhibits the development of axillary buds located along the stem. This inhibition is mediated by the plant hormone auxin (indole-3-acetic acid, IAA), which is synthesized in the growing tip and transported basipetally through the polar auxin transport stream to suppress lateral bud outgrowth. The mechanism involves auxin signaling that downregulates genes promoting cell division in buds, such as those encoding cytokinin biosynthesis enzymes, thereby maintaining a dominant main axis while limiting excessive branching until the apex is removed or damaged. Hormonal interactions further refine branching patterns, with cytokinins playing a key role in counteracting apical dominance to promote lateral bud activation. Cytokinins, such as zeatin and kinetin, are synthesized in root tips and transported to shoots, where they stimulate cell division and axillary meristem activity, often in opposition to auxin gradients.^[49] Meanwhile, gibberellins contribute to branch elongation by enhancing internode expansion through the loosening of cell walls and promotion of expansive growth in existing tissues, without directly initiating new branches.^[50] These hormones interact dynamically; for instance, reduced auxin levels post-decapitation allow cytokinin accumulation to release buds from dormancy.^[51] Environmental stimuli also trigger branching responses to optimize resource acquisition. Phototropism directs branch tips toward light sources via asymmetric auxin redistribution, causing differential cell elongation on shaded sides, while gravitropism orients branches upward against gravity through sedimenting amyloplasts that initiate auxin signaling cascades.^[52]^[53] Wounding, such as from pruning or herbivory, induces epicormic shoots from dormant adventitious buds beneath the bark, driven by jasmonic acid signaling and increased cytokinin levels that override suppression and promote rapid regrowth for tissue repair.^[54] Branching patterns exhibit mathematical regularity, often modeled as self-organizing systems where primordia spacing minimizes overlap for efficient packing. A prominent example is phyllotaxis, the arrangement of leaves or scales on branches, which frequently follows the Fibonacci sequence (e.g., ratios approximating the golden angle of approximately 137.5° between successive organs) to maximize light exposure and space utilization.^[55] These models, based on reaction-diffusion dynamics or inhibitory fields around meristems, predict stable spiral patterns observed in species like sunflowers and pines, with deviations arising from genetic or environmental perturbations.^[56]

Physiological Roles

Branches serve as primary structural supports for leaves, positioning them to maximize exposure to sunlight and facilitate the capture of light energy for photosynthesis, while also enabling the diffusion of carbon dioxide into leaf tissues for fixation into organic compounds.^[9] In woody plants, branches elevate foliage above the canopy understory, reducing self-shading and optimizing photosynthetic efficiency across the plant's crown.^[57] In reproduction, branches act as key sites for the development and display of flowers, which attract pollinators, and subsequently support the maturation of fruits and seed dispersal structures, ensuring the propagation of the species. For instance, axillary buds on branches often give rise to inflorescences or directly bear reproductive organs, integrating structural support with reproductive functionality.^[9] This positioning enhances pollination success and protects developing fruits from ground-based threats.^[58] Branches function as vital conduits for the transport of water, minerals, and nutrients upward from roots via xylem tissue, and for the downward movement of carbohydrates produced during photosynthesis through phloem, maintaining overall plant hydration and energy distribution. Additionally, in many species, branch sapwood and ray tissues store nonstructural carbohydrates, such as starch, serving as reserves for regrowth, stress recovery, and seasonal demands.^[59]^[9] These storage pools can fluctuate seasonally, supporting bud break and new leaf expansion. For defense, branches produce secondary metabolites, particularly in their bark and vascular tissues, including phenolics and terpenoids that deter herbivores and inhibit pathogen invasion by disrupting microbial enzymes or acting as toxins. These compounds, such as tannins in oak branches, create chemical barriers that reduce palatability and infection risk, contributing to long-term plant survival.^[60]^[61]

Ecological and Evolutionary Aspects

Ecological Significance

Branches serve as critical microhabitats within forest ecosystems, supporting a diverse array of epiphytes, insects, and vertebrates. Large branches, particularly dead or decaying ones, provide substrates for epiphytes such as lichens, bryophytes, and ivy, which in turn attract insects and serve as foraging sites for birds. Tree hollows formed in branches and trunks host nesting and roosting for species like woodpeckers, owls, and bats, with older trees (over 200 years) containing multiple cavities that support secondary cavity-nesters and endangered invertebrates like the beetle Osmoderma eremita. In unmanaged European forests, habitat trees with such features number 10–20 per hectare, sustaining over 25% of forest biodiversity, including threatened species reliant on these structures.^[62] Leaf fall from branches plays a pivotal role in nutrient cycling, as fallen leaves form litter layers that decompose and return essential nutrients to the soil, enhancing fertility and supporting plant regrowth. Decomposition rates vary by tree species; for instance, slower-decomposing litter from sycamores delays nutrient release but protects soil from erosion and temperature fluctuations, while faster breakdown in other species accelerates fertilization. This process maintains ecosystem productivity, with leaf litter acting as a natural reservoir that recycles nitrogen, phosphorus, and other elements, preventing soil depletion in temperate and tropical forests.^[63] The structural complexity of branching patterns significantly boosts canopy diversity and overall forest biodiversity by creating varied niches and microclimates. In tropical broadleaf forests, intricate branching contributes to high vertical layering and space-filling in the canopy, fostering greater species richness among plants, insects, and vertebrates through enhanced light penetration and habitat partitioning. Global assessments using lidar data reveal that forests with elevated canopy structural complexity, driven by branching heterogeneity, exhibit higher biodiversity compared to simpler stands, underscoring their role in ecosystem resilience.^[64] Human activities, particularly deforestation, severely disrupt branch-dependent wildlife by fragmenting canopies and eliminating critical habitats in tropical rainforests. In the Lacandona rainforest of Mexico, forest loss increases canopy openness, reducing arboreal mammal richness by up to 52% through indirect effects on habitat availability, with rare species like margays and tayras suffering most while common ones such as kinkajous persist in disturbed areas. Such impacts threaten biodiversity hotspots, where forests support over 80% of terrestrial species, leading to cascading effects on ecosystem services like pollination and seed dispersal.^[65]^[66]

Evolutionary Adaptations

The evolution of branches in vascular plants originated during the Devonian period, approximately 400 million years ago, marking a pivotal adaptation for terrestrial colonization. Early tracheophytes, such as rhyniophytes and cooksonioids, displayed simple dichotomous branching, where stems forked equally to support upright growth and sporangia positioning without lateral buds.^[67] This primitive architecture, seen in plants like Cooksonia from the Early Devonian, prioritized structural simplicity over complexity, enabling efficient resource transport in nutrient-poor soils.^[68] In fern-like plants that emerged later in the Devonian, branching remained relatively simple, often dichotomous or pseudomonopodial, facilitating planar arrangements for spore release and basic photosynthesis.^[69] These patterns contrasted with later innovations but laid the groundwork for more elaborate systems. By the Late Devonian, zygopterid ferns and related euphyllophytes began showing webbed branchlets, hinting at evolutionary pressures toward foliar integration.^[70] Gymnosperms, evolving from progymnosperm ancestors in the Middle Devonian, adapted increased branching density to compete for sunlight in dense vegetation, with fronds and lateral shoots optimizing canopy expansion.^[71] Angiosperms further refined this through monopodial dominance, where a primary axis produced subordinate laterals, enhancing light interception in understories and promoting diverse crown architectures.^[72] Key innovations included the transition from dichotomous to monopodial branching, which allowed asymmetrical growth for better environmental responsiveness, and the development of spiny branches in some lineages as a defense against arthropod herbivory, reducing tissue loss in early ecosystems.^[72]^[73] Fossil evidence from Archaeopteris, a widespread Middle-to-Late Devonian tree-like progymnosperm, illustrates primitive woody branches with reinforced joints and fern-like foliage, bridging non-woody ancestors to seed plant forms through secondary xylem and iterative dichotomous patterns up to 10 meters in height.^[71] These structures, preserved in sites like New York and China, demonstrate how branching evolved to support height and stability, foreshadowing modern arborescence.^[74]

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Phototropism, or the differential cell elongation exhibited by a plant organ in response to directional blue light, provides the plant with a means to optimize ...Missing: epicormic | Show results with:epicormic
[52]
Interactions between gravitropism and phototropism in plants
To receive adequate light and nutrients for survival, plants orient stems and stem-like organs toward light and away from the gravity vector and, ...
[53]
Production and role of epicormic shoots in pruned hybrid poplar
Dec 19, 2014 · Epicormic shoot formation is generally thought to be a response to a sudden light increase (Gordon et al. 2006; Wignall and Browning 1988) or ...
[54]
Phyllotaxis and the Fibonacci Series - Science
The principal conclusion is that Fibonacci phyllotaxis follows as a mathematical necessity from the combination of an expanding apex and a suitable spacing ...Missing: seminal | Show results with:seminal
[55]
[PDF] Polygonal planforms and phyllotaxis on plants - Arizona Math
The occurrences of Fibonacci sequences in plants has intrigued natural scientists since the time of Kepler. As the plant grows, the pattern will change. Indeed,.Missing: branching | Show results with:branching
[56]
Tree Structure & Light Capture | Fruit & Nut Research & Information ...
Embedded within the woody support tissue are points of living tissue, called meristem, which produce new branches, leaves, and flowers. Apical and lateral ...
[57]
What is a Tree? How Does it Work? - Colorado State Forest Service
Tree Physiology. A tree is a tall plant with woody tissue. Trees gather light ... Twigs and Branches – support structures for leaves, flowers and fruits ...
[58]
Water Transport in Plants: Xylem | Organismal Biology
The phloem is the tissue primarily responsible for movement of nutrients and photosynthetic produces, and xylem is the tissue primarily responsible for movement ...
[59]
Plant Secondary Metabolites as Defense Tools against Herbivores ...
Plant secondary metabolites (PSMs) are synthesized to provide defensive functions and regulate defense signaling pathways to safeguard plants against herbivores ...Missing: branches | Show results with:branches
[60]
[PDF] Overview of Plant Defenses
Secondary metabolites are not directly involved in growth or reproduction but they are often involved with plant defense. These compounds usually belong to one ...
[61]
[PDF] 2.1 Habitat trees: key elements for forest biodiversity
Today, the importance of habitat trees for forest biodiversity is widely accepted and their ecological services are becoming increasingly valued by society.
[62]
Exploring the Role of Leaf Litter In Our Forests
May 4, 2022 · Through decomposition, nutrients stored in the dead material re-enter the system and act as a natural fertilizer for plants throughout the year.
[63]
Characterizing the structural complexity of the Earth's forests with ...
Sep 16, 2024 · Forest structural complexity is a key element of ecosystem functioning, impacting light environments, nutrient cycling, biodiversity, ...
[64]
Tropical forest loss impoverishes arboreal mammal assemblages by ...
Nov 27, 2022 · We found that forest loss had negative indirect effects on mammal richness through the increase of tree canopy openness.
[65]
The origin and early evolution of vascular plant shoots and leaves
Dec 18, 2017 · This review discusses fossil, developmental and genetic evidence relating to the evolution of vascular plant shoots and leaves in a phylogenetic framework.
[66]
Branching - Digital Atlas of Ancient Life
Aug 24, 2021 · Branching occurs when one axis (root or stem) divides, or when a smaller axis develops on a larger, more dominant axis.
[67]
insights from a new fern-like plant from the Late Devonian of China
This study presents a novel fern-like taxon with pinnules, which provides new insights into the early evolution of laminate leaves in early-diverging ferns.
[68]
The ecology of Paleozoic ferns - ScienceDirect.com
The early ferns. The earliest fern or fern-like plant is Ellesmeris sphenopteroides (Hill et al., 1997) from the Late Devonian (Frasnian) of the high Arctic.
[69]
Great moments in plant evolution - PNAS
Middle Devonian progymnosperms such as Archaeopteris (Fig. 1) are among the oldest known trees. Along with cladoxyl tree ferns such as Wattieza, increased ...
[70]
Evolution and ecology of plant architecture: integrating insights from ...
Nov 28, 2017 · Dichotomously branching Paleozoic plants already encompassed a considerable diversity of growth forms, here captured in 12 new architectural ...
[71]
Spiny plants, mammal browsers, and the origin of African savannas
Using a dated phylogeny for the same tree species, we found that spinescence evolved at least 55 times. The diversification of spiny plants occurred long after ...
[72]
Mid-Devonian Archaeopteris Roots Signal Revolutionary Change in ...
Feb 3, 2020 · Here we show that Archaeopteris had a highly advanced root system essentially comparable to modern seed plants.