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Annual Review of Plant Biology - Current Issue
Volume 74, 2023
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Mycorrhizal Symbiosis in Plant Growth and Stress Adaptation: From Genes to Ecosystems
Jincai Shi, Xiaolin Wang, and Ertao WangVol. 74 (2023), pp. 569–607More LessPlant roots associate with diverse microbes (including bacteria, fungi, archaea, protists, and viruses) collectively called the root-associated microbiome. Among them, mycorrhizal fungi colonize host roots and improve their access to nutrients, usually phosphorus and nitrogen. In exchange, plants deliver photosynthetic carbon to the colonizing fungi. This nutrient exchange affects key soil processes, the carbon cycle, and plant health and therefore has a strong influence on the plant and microbe ecosystems. The framework of nutrient exchange and regulation between host plant and arbuscular mycorrhizal fungi has recently been established. The local and systemic regulation of mycorrhizal symbiosis by plant nutrient status and the autoregulation of mycorrhizae are strategies by which plants maintain a stabilizing free-market symbiosis. A better understanding of the synergistic effects between mycorrhizal fungi and mycorrhizosphere microorganisms is an essential precondition for their use as biofertilizers and bioprotectors for sustainable agriculture and forestry management.
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Where, When, and Why Do Plant Volatiles Mediate Ecological Signaling? The Answer Is Blowing in the Wind
Vol. 74 (2023), pp. 609–633More LessPlant volatiles comprise thousands of molecules from multiple metabolic pathways, distinguished by sufficient vapor pressure to evaporate into the headspace under normal environmental conditions. Many are implicated as ecological signals, but what is the evidence—and how do they work? Volatiles diffuse, are carried by wind, and may be taken up by other organisms or degrade with exposure to atmospheric ozone, radicals, and UV light; visual signals such as color are not subject to these complications (but require a line of sight). Distantly related plants—and nonplants—produce many of the same volatiles, yet specific compounds and blends may be distinct. Here, I present a quantitative review of the literature on plant volatiles as ecological signals, illustrating a field that has focused on developing ideas as much as reporting primary data. I discuss advantages and constraints, review recent advances, and propose considerations for primary studies to elucidate particular functions of plant volatiles.
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Why Are Invasive Plants Successful?
Vol. 74 (2023), pp. 635–670More LessPlant invasions, a byproduct of globalization, are increasing worldwide. Because of their ecological and economic impacts, considerable efforts have been made to understand and predict the success of non-native plants. Numerous frameworks, hypotheses, and theories have been advanced to conceptualize the interactions of multiple drivers and context dependence of invasion success with the aim of achieving robust explanations with predictive power. We review these efforts from a community-level perspective rather than a biogeographical one, focusing on terrestrial systems, and explore the roles of intrinsic plant properties in determining species invasiveness, as well as the effects of biotic and abiotic conditions in mediating ecosystem invasibility (or resistance) and ecological and evolutionary processes. We also consider the fundamental influences of human-induced changes at scales ranging from local to global in triggering, promoting, and sustaining plant invasions and discuss how these changes could alter future invasion trajectories.
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Salt-Tolerant Crops: Time to Deliver
Vol. 74 (2023), pp. 671–696More LessDespite the numerous advances made in our understanding of the physiology and molecular genetics of salinity tolerance, there have been relatively few applications of these to improve the salt tolerance of crops. The most significant advances have historically utilized intraspecific variation, introgression of traits from close crop wild relatives, or, less frequently, introgression from more distant relatives. Advanced lines often fail due to difficulties in the introgression or tracking of traits or due to yield penalties associated with the alleles in nonsaline environments. However, the greatest limitation is that salinity is not a primary trait for breeders. We must close the gap between research and delivery, especially for farmers who have precious few alternatives. These efforts should include a reassessment of old techniques such as grafting current crops with salt-tolerant hybrid rootstocks. Alternatively, future crops can be produced via domestication of salt-tolerant wild species—an approach that is now feasible in our lifetime.
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Replicated Evolution in Plants
Vol. 74 (2023), pp. 697–725More LessSimilar traits and functions commonly evolve in nature. Here, we explore patterns of replicated evolution across the plant kingdom and discuss the processes responsible for such patterns. We begin this review by defining replicated evolution and the theoretical, genetic, and ecological concepts that help explain it. We then focus our attention on empirical cases of replicated evolution at the phenotypic and genotypic levels. We find that replication at the ecotype level is common, but evidence for repeated ecological speciation is surprisingly sparse. On the other hand, the replicated evolution of ecological strategies and physiological mechanisms across similar biomes appears to be pervasive. We conclude by highlighting where future efforts can help us bridge the understanding of replicated evolution across different levels of biological organization. Earth's landscape is diverse but also repeats itself. Organisms seem to have followed suit.
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The Power and Perils of De Novo Domestication Using Genome Editing
Vol. 74 (2023), pp. 727–750More LessThere is intense interest in using genome editing technologies to domesticate wild plants, or accelerate the improvement of weakly domesticated crops, in de novo domestication. Here, we discuss promising genetic strategies, with a focus on plant development. Importantly, genome editing releases us from dependence on random mutagenesis or intraspecific diversity, allowing us to draw solutions more broadly from diversity. However, sparse understanding of the complex genetics of diversity limits innovation. Beyond genetics, we urge the ethical use of indigenous knowledge, indigenous plants, and ethnobotany. De novo domestication still requires conventional breeding by phenotypic selection, especially in the development of crops for diverse environments and cultures. Indeed, uniting genome editing with selective breeding could facilitate faster and better outcomes than either technology alone. Domestication is complex and incompletely understood, involving changes to many aspects of plant biology and human culture. Success in de novo domestication requires careful attention to history and collaboration across traditional boundaries.
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Causes of Mutation Rate Variability in Plant Genomes
Vol. 74 (2023), pp. 751–775More LessMutation is the source of all heritable diversity, the essential material of evolution and breeding. While mutation rates are often regarded as constant, variability in mutation rates has been observed at nearly every level—varying across mutation types, genome locations, gene functions, epigenomic contexts, environmental conditions, genotypes, and species. This mutation rate variation arises from differential rates of DNA damage, repair, and transposable element activation and insertion that together produce what is measured by DNA mutation rates. We review historical and recent investigations into the causes and consequences of mutation rate variability in plants by focusing on the mechanisms shaping this variation. Emerging mechanistic models point to the evolvability of mutation rate variation across genomes via mechanisms that target DNA repair, shaping the diversification of plants at phenotypic and genomic scales.
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Engineering Themes in Plant Forms and Functions
Vol. 74 (2023), pp. 777–801More LessLiving structures constantly interact with the biotic and abiotic environment by sensing and responding via specialized functional parts. In other words, biological bodies embody highly functional machines and actuators. What are the signatures of engineering mechanisms in biology? In this review, we connect the dots in the literature to seek engineering principles in plant structures. We identify three thematic motifs—bilayer actuator, slender-bodied functional surface, and self-similarity—and provide an overview of their structure–function relationships. Unlike human-engineered machines and actuators, biological counterparts may appear suboptimal in design, loosely complying with physical theories or engineering principles. We postulate what factors may influence the evolution of functional morphology and anatomy to dissect and comprehend better the why behind the biological forms.
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Previous Volumes
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Volume 74 (2023)
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Volume 73 (2022)
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Volume 72 (2021)
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Volume 71 (2020)
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Volume 70 (2019)
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Volume 69 (2018)
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Volume 68 (2017)
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Volume 67 (2016)
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Volume 66 (2015)
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Volume 65 (2014)
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Volume 64 (2013)
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Volume 63 (2012)
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Volume 62 (2011)
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Volume 61 (2010)
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Volume 60 (2009)
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Volume 59 (2008)
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Volume 58 (2007)
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Volume 57 (2006)
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Volume 56 (2005)
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Volume 55 (2004)
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Volume 54 (2003)
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Volume 53 (2002)
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Volume 52 (2001)
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Volume 51 (2000)
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Volume 50 (1999)
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Volume 49 (1998)
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Volume 48 (1997)
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Volume 47 (1996)
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Volume 46 (1995)
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Volume 45 (1994)
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Volume 44 (1993)
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Volume 43 (1992)
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Volume 42 (1991)
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Volume 41 (1990)
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Volume 40 (1989)
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Volume 39 (1988)
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Volume 38 (1987)
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Volume 37 (1986)
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Volume 36 (1985)
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Volume 35 (1984)
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Volume 34 (1983)
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Volume 33 (1982)
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Volume 32 (1981)
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Volume 31 (1980)
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Volume 30 (1979)
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Volume 29 (1978)
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Volume 28 (1977)
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Volume 27 (1976)
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Volume 26 (1975)
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Volume 25 (1974)
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Volume 24 (1973)
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Volume 23 (1972)
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Volume 22 (1971)
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Volume 21 (1970)
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Volume 20 (1969)
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Volume 19 (1968)
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Volume 18 (1967)
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Volume 17 (1966)
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Volume 16 (1965)
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Volume 15 (1964)
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Volume 14 (1963)
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Volume 13 (1962)
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Volume 12 (1961)
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Volume 11 (1960)
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Volume 10 (1959)
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Volume 9 (1958)
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Volume 8 (1957)
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Volume 7 (1956)
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Volume 6 (1955)
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Volume 5 (1954)
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Volume 4 (1953)
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Volume 3 (1952)
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Volume 2 (1951)
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Volume 1 (1950)
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Volume 0 (1932)