Premise: Volatile emissions from flowers and fruits play a key role in signalling to animals responsible for pollination and seed dispersal. Here, we investigated the pollination biology and chemical ecology of reproduction in Apodolirion buchananii, an African amaryllid that flowers in a leafless state soon after grassland vegetation is burnt in the dry late-winter season.
Methods: Pollinators were identified through field collection and pollen loads were quantified. Floral traits including spectral reflectance and scent chemistry were documented. Bioassays using cup traps were used to test the function of floral volatiles. Fruiting biology was investigated using controlled hand-pollination experiments and chemical analysis of fruit scent. Seed germination was scored in greenhouse trials. Seed dispersal was monitored using observations and camera trapping.
Results: The sweetly scented white flowers of A. buchananii are pollen-rewarding and pollinated mainly by a diverse assemblage of bees. Cup-trap experiments demonstrated that pollinators are attracted to phenylacetaldehyde, the dominant volatile in the floral scent. Plants are shown to be self-incompatible, and the fleshy fruits were found to emerge from the soil six months after pollination during the peak of the summer rains. Fruits emit a diverse blend of aliphatic and aromatic esters and contain large fleshy recalcitrant seeds which germinate within days of fruits splitting open. Seed dispersal by ants was recorded.
Conclusions: This first account of the reproductive biology of a species in the genus Apodolirion highlights an outcrossing mating system involving bees attracted to color and scent as well as the unusual fruiting biology and ant-mediated system of seed dispersal.
{"title":"Scent-mediated bee pollination and myrmecochory in an enigmatic geophyte with pyrogenic flowering and subterranean development of fleshy fruits.","authors":"Ian Kiepiel, Steven D Johnson","doi":"10.1002/ajb2.16421","DOIUrl":"https://doi.org/10.1002/ajb2.16421","url":null,"abstract":"<p><strong>Premise: </strong>Volatile emissions from flowers and fruits play a key role in signalling to animals responsible for pollination and seed dispersal. Here, we investigated the pollination biology and chemical ecology of reproduction in Apodolirion buchananii, an African amaryllid that flowers in a leafless state soon after grassland vegetation is burnt in the dry late-winter season.</p><p><strong>Methods: </strong>Pollinators were identified through field collection and pollen loads were quantified. Floral traits including spectral reflectance and scent chemistry were documented. Bioassays using cup traps were used to test the function of floral volatiles. Fruiting biology was investigated using controlled hand-pollination experiments and chemical analysis of fruit scent. Seed germination was scored in greenhouse trials. Seed dispersal was monitored using observations and camera trapping.</p><p><strong>Results: </strong>The sweetly scented white flowers of A. buchananii are pollen-rewarding and pollinated mainly by a diverse assemblage of bees. Cup-trap experiments demonstrated that pollinators are attracted to phenylacetaldehyde, the dominant volatile in the floral scent. Plants are shown to be self-incompatible, and the fleshy fruits were found to emerge from the soil six months after pollination during the peak of the summer rains. Fruits emit a diverse blend of aliphatic and aromatic esters and contain large fleshy recalcitrant seeds which germinate within days of fruits splitting open. Seed dispersal by ants was recorded.</p><p><strong>Conclusions: </strong>This first account of the reproductive biology of a species in the genus Apodolirion highlights an outcrossing mating system involving bees attracted to color and scent as well as the unusual fruiting biology and ant-mediated system of seed dispersal.</p>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Reduced snow cover and increasing temperature variability can increase freezing stress for herbaceous plants in northern temperate regions. Legumes have emerged as a plant functional group that is highly sensitive to these changes relative to other herbaceous species in these regions. We explored root-nodulating bacterial associations and cyanogenesis as potential mechanisms explaining this relatively low freezing tolerance of legumes.
Methods
To examine the influence of bacterial associations, we grew four legume species with or without crushed-nodule inoculum at three severities of freezing, and three concentrations of nitrogen to disambiguate the direct benefits of increased nitrogen from the total bacterial effect. We quantified cyanogenesis via hydrogen cyanide production in both true leaves and cotyledons for nine legume species.
Results
Root nodulation generally only affected legume survival under low nitrogen, when freezing severity was moderate or low. However, for the frost-surviving plants, the growth advantage provided by nodulation decreased (it was often no longer significant with increasing freezing severity), and greater freezing severity reduced total nodule mass. In contrast, cyanogenesis was only detected in two of the nine species.
Conclusions
The diminished performance of nodulated plants in response to freezing could place legumes at a competitive disadvantage and potentially explain their high sensitivity to freezing relative to other herbaceous species in northern temperate regions. Overall, this result has important implications for changes in soil fertility, community composition, and plant productivity in these ecosystems in the context of a changing winter climate.
{"title":"The roles of root-nodulating bacterial associations and cyanogenesis in the freezing sensitivities of herbaceous legumes","authors":"Samuel L. Rycroft, Hugh A. L. Henry","doi":"10.1002/ajb2.16424","DOIUrl":"10.1002/ajb2.16424","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Premise</h3>\u0000 \u0000 <p>Reduced snow cover and increasing temperature variability can increase freezing stress for herbaceous plants in northern temperate regions. Legumes have emerged as a plant functional group that is highly sensitive to these changes relative to other herbaceous species in these regions. We explored root-nodulating bacterial associations and cyanogenesis as potential mechanisms explaining this relatively low freezing tolerance of legumes.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>To examine the influence of bacterial associations, we grew four legume species with or without crushed-nodule inoculum at three severities of freezing, and three concentrations of nitrogen to disambiguate the direct benefits of increased nitrogen from the total bacterial effect. We quantified cyanogenesis via hydrogen cyanide production in both true leaves and cotyledons for nine legume species.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Root nodulation generally only affected legume survival under low nitrogen, when freezing severity was moderate or low. However, for the frost-surviving plants, the growth advantage provided by nodulation decreased (it was often no longer significant with increasing freezing severity), and greater freezing severity reduced total nodule mass. In contrast, cyanogenesis was only detected in two of the nine species.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>The diminished performance of nodulated plants in response to freezing could place legumes at a competitive disadvantage and potentially explain their high sensitivity to freezing relative to other herbaceous species in northern temperate regions. Overall, this result has important implications for changes in soil fertility, community composition, and plant productivity in these ecosystems in the context of a changing winter climate.</p>\u0000 </section>\u0000 </div>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456043","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Premise: There are advantages to flowering early in the spring, including greater pollinator fidelity and longer fruit maturation time. But plant phenology has advanced in recent years, making many plants vulnerable to freezing damage from late frosts.
Methods: To determine the costs and benefits of flowering early in the growing season, we exposed Prunus pumila plants to two freezing treatments and a delayed flowering treatment in subsequent years. Data were collected on ovary swelling, fruit production, and pollinator visitation on hand- and open-pollinated plants in all treatments. We also measured tissue damage after freeze events.
Results: Our results suggest that flowering time and temperature affect reproductive success, with fewer fruits produced after hard freezes. The same was not true for light freezes, which had minimal impact on reproduction. Freezing damage to plants after a hard freeze did affect the number of dipteran pollinators but not the overall pollinator visitation rate. Despite the clear impact of freezing temperatures on plant reproduction, flowering early provided an advantage in that reproductive output decreased with delayed flowering.
Conclusions: Our findings suggest that Prunus pumila will retain the ability to attract pollinators and produce viable seeds if exposed to false spring conditions that involve a light freeze, but hard freezes may reduce yield by an order of magnitude. Although the advantages to flowering early may outweigh the risk of freezing damage under current conditions, it is possible that flower viability may be constrained under continued climate warming.
{"title":"Weighing the risks and benefits of flowering early in the spring for the woody perennial Prunus pumila.","authors":"Danielle A Lake Diver, Jessica A Savage","doi":"10.1002/ajb2.16417","DOIUrl":"https://doi.org/10.1002/ajb2.16417","url":null,"abstract":"<p><strong>Premise: </strong>There are advantages to flowering early in the spring, including greater pollinator fidelity and longer fruit maturation time. But plant phenology has advanced in recent years, making many plants vulnerable to freezing damage from late frosts.</p><p><strong>Methods: </strong>To determine the costs and benefits of flowering early in the growing season, we exposed Prunus pumila plants to two freezing treatments and a delayed flowering treatment in subsequent years. Data were collected on ovary swelling, fruit production, and pollinator visitation on hand- and open-pollinated plants in all treatments. We also measured tissue damage after freeze events.</p><p><strong>Results: </strong>Our results suggest that flowering time and temperature affect reproductive success, with fewer fruits produced after hard freezes. The same was not true for light freezes, which had minimal impact on reproduction. Freezing damage to plants after a hard freeze did affect the number of dipteran pollinators but not the overall pollinator visitation rate. Despite the clear impact of freezing temperatures on plant reproduction, flowering early provided an advantage in that reproductive output decreased with delayed flowering.</p><p><strong>Conclusions: </strong>Our findings suggest that Prunus pumila will retain the ability to attract pollinators and produce viable seeds if exposed to false spring conditions that involve a light freeze, but hard freezes may reduce yield by an order of magnitude. Although the advantages to flowering early may outweigh the risk of freezing damage under current conditions, it is possible that flower viability may be constrained under continued climate warming.</p>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456044","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Diego P. Vélez-Mora, Karla Trigueros-Alatorre, David H. Duncan, Pedro F. Quintana-Ascencio
Premise
Agriculture expansion, livestock, and global change have transformed biological communities and altered, through aerosols and direct deposition, N:P balance in soils of inter-Andean valleys, potentially affecting flowering phenology of many species and thereby flowering synchrony and plant reproduction.
Methods
We evaluated the influence of variation in temperature and moisture along the local elevational gradient and treatments with the addition of N and P and grazing on flowering synchrony and reproduction of Croton, a dominant shrub of the inter-Andean dry scrub. Along the elevational gradient (300 m difference between the lowest and highest site), we set up plots with and without grazing nested with four nutrient treatments: control and addition of N or P alone or combined N + P. We recorded the number of female and male flowers in bloom monthly from September 2017 to August 2019 to calculate flowering synchrony. We assessed fruiting, seed mass, and pre-dispersal seed predation.
Results
Higher growing-season soil temperatures, which were negatively associated with local elevation and higher nitrogen availability promoted flowering synchrony of Croton, particularly among larger plants. Greater flowering synchrony, high soil temperatures, and addition of N + P resulted in production of more fruits of Croton, but also intensified pre-dispersal seed predation.
Conclusions
Temperature, availability of moisture throughout the elevational gradient, and nutrient manipulation affected flowering synchrony, which subsequently affected production of fruits in Croton. These results emphasize the critical role of current anthropogenic changes in climate and nutrient availability on flowering synchrony and reproduction of Croton, a dominant plant of the inter-Andean scrub.
{"title":"Natural and anthropogenic factors influence flowering synchrony and reproduction of a dominant plant in an inter-Andean scrub","authors":"Diego P. Vélez-Mora, Karla Trigueros-Alatorre, David H. Duncan, Pedro F. Quintana-Ascencio","doi":"10.1002/ajb2.16416","DOIUrl":"10.1002/ajb2.16416","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Premise</h3>\u0000 \u0000 <p>Agriculture expansion, livestock, and global change have transformed biological communities and altered, through aerosols and direct deposition, N:P balance in soils of inter-Andean valleys, potentially affecting flowering phenology of many species and thereby flowering synchrony and plant reproduction.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We evaluated the influence of variation in temperature and moisture along the local elevational gradient and treatments with the addition of N and P and grazing on flowering synchrony and reproduction of <i>Croton</i>, a dominant shrub of the inter-Andean dry scrub. Along the elevational gradient (300 m difference between the lowest and highest site), we set up plots with and without grazing nested with four nutrient treatments: control and addition of N or P alone or combined N + P. We recorded the number of female and male flowers in bloom monthly from September 2017 to August 2019 to calculate flowering synchrony. We assessed fruiting, seed mass, and pre-dispersal seed predation.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Higher growing-season soil temperatures, which were negatively associated with local elevation and higher nitrogen availability promoted flowering synchrony of <i>Croton</i>, particularly among larger plants. Greater flowering synchrony, high soil temperatures, and addition of N + P resulted in production of more fruits of <i>Croton</i>, but also intensified pre-dispersal seed predation.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Temperature, availability of moisture throughout the elevational gradient, and nutrient manipulation affected flowering synchrony, which subsequently affected production of fruits in <i>Croton</i>. These results emphasize the critical role of current anthropogenic changes in climate and nutrient availability on flowering synchrony and reproduction of <i>Croton</i>, a dominant plant of the inter-Andean scrub.</p>\u0000 </section>\u0000 </div>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456041","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<p>Darwinian evolution relies on mutation as a constant source of variation, yet in evolutionary biology, mutation is often taken for granted, pushed to the background and treated as if it was random and uniform across all genes and all species. Mutation is an essential parameter in many evolutionary models, although often regarded as a “nuisance parameter” rather than the focus of interest—but mutation is a fundamental driver of evolution. Studying how rates and patterns of mutation are shaped by chance and selection is critical for understanding evolution of biodiversity, and has practical consequences for the way we use DNA to understand evolutionary history. Many evolutionary analyses—including genomics, population genetics, and phylogenetics—make simplifying assumptions about mutation rate, and the nature of these assumptions can influence the answers we get (e.g., Ritchie et al., <span>2022</span>).</p><p>Mutation rate is a balancing act, playing out at many different evolutionary levels simultaneously. At the biochemical level, single-base changes to DNA sequences result from replication errors or imperfectly repaired damage. Cells have an impressive arsenal of equipment for repairing damage and correcting errors, but repair must be “paid for” in energy and time, which could otherwise be invested in growth and reproduction (Avila and Lehmann, <span>2023</span>). Individuals can vary in repair efficiency, or in the amount of energy available to invest in repair, and therefore in their patterns and rates of mutation. On longer timescales, lineage persistence depends on finding a balance between risk of mutation and costs of error correction and repair. Undirected changes to functional sequences are typically more likely to ruin than improve, so mutation is expected to exact a cost in terms of chances of success. If mutation rate is too high, offspring might not reliably inherit their parents’ advantageous traits, yet mutation provides the chance of generating variations that might allow individuals to better survive in a changing environment or have an increased chance of avoiding parasites and predators. If there is too little mutation, evolution grinds to a halt. If there is too much mutation, it runs into the ground, scrambling the hereditary message passed to subsequent generations and overwriting adaptations. The relative risks and benefits of mutation may vary between lineages and depend upon the environment, shifting when a lineage must adapt to changing conditions (Weng et al., <span>2021</span>). Mutation rates are a balance between the chance of beneficial variation and the risk of destroying key genome functions. This balancing act plays out in individual lives and over evolutionary time.</p><p>Mutation rate is governed by the rate at which changes happen to the genome and the rate at which they are repaired, both of which vary among organisms. Considering one universal mutagen—ultraviolet (UV) light—provides a useful illustration
{"title":"Mutation rate is central to understanding evolution","authors":"Lindell Bromham","doi":"10.1002/ajb2.16422","DOIUrl":"10.1002/ajb2.16422","url":null,"abstract":"<p>Darwinian evolution relies on mutation as a constant source of variation, yet in evolutionary biology, mutation is often taken for granted, pushed to the background and treated as if it was random and uniform across all genes and all species. Mutation is an essential parameter in many evolutionary models, although often regarded as a “nuisance parameter” rather than the focus of interest—but mutation is a fundamental driver of evolution. Studying how rates and patterns of mutation are shaped by chance and selection is critical for understanding evolution of biodiversity, and has practical consequences for the way we use DNA to understand evolutionary history. Many evolutionary analyses—including genomics, population genetics, and phylogenetics—make simplifying assumptions about mutation rate, and the nature of these assumptions can influence the answers we get (e.g., Ritchie et al., <span>2022</span>).</p><p>Mutation rate is a balancing act, playing out at many different evolutionary levels simultaneously. At the biochemical level, single-base changes to DNA sequences result from replication errors or imperfectly repaired damage. Cells have an impressive arsenal of equipment for repairing damage and correcting errors, but repair must be “paid for” in energy and time, which could otherwise be invested in growth and reproduction (Avila and Lehmann, <span>2023</span>). Individuals can vary in repair efficiency, or in the amount of energy available to invest in repair, and therefore in their patterns and rates of mutation. On longer timescales, lineage persistence depends on finding a balance between risk of mutation and costs of error correction and repair. Undirected changes to functional sequences are typically more likely to ruin than improve, so mutation is expected to exact a cost in terms of chances of success. If mutation rate is too high, offspring might not reliably inherit their parents’ advantageous traits, yet mutation provides the chance of generating variations that might allow individuals to better survive in a changing environment or have an increased chance of avoiding parasites and predators. If there is too little mutation, evolution grinds to a halt. If there is too much mutation, it runs into the ground, scrambling the hereditary message passed to subsequent generations and overwriting adaptations. The relative risks and benefits of mutation may vary between lineages and depend upon the environment, shifting when a lineage must adapt to changing conditions (Weng et al., <span>2021</span>). Mutation rates are a balance between the chance of beneficial variation and the risk of destroying key genome functions. This balancing act plays out in individual lives and over evolutionary time.</p><p>Mutation rate is governed by the rate at which changes happen to the genome and the rate at which they are repaired, both of which vary among organisms. Considering one universal mutagen—ultraviolet (UV) light—provides a useful illustration","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajb2.16422","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jessica Chu, Thibault Durieux, Alexandru M. F. Tomescu
Premise
Cladoxylopsids, one of the first lineages with complex organization to rise from the plexus of structurally simple plants that comprised the earliest euphyllophyte floras, are moniliformopsid euphyllophytes. They formed Earth's earliest forests by the Middle Devonian and are thought to have given rise to the equisetopsids and probably some fern lineages. The Lower Devonian (Emsian) Battery Point Formation (Quebec, Canada) contains previously unrecognized cladoxylopsids preserved anatomically. One of these provides new data on structural evolution among euphyllophytes and is described here.
Methods
The anatomy and morphology of permineralized axes of the new plant were studied with light and electron microscopy on sections produced using the cellulose acetate peel technique. Morphological comparisons and phylogenetic analysis were used for taxonomic placement of the plant.
Results
The plant represents a new species, Paracladoxylon kespekianum Chu et Tomescu, gen. et sp. nov., that has tracheids with modern-looking bordered pits and the complex cauline vascular architecture characteristic of the genus Cladoxylon. Its dissected ultimate appendages have complex regular taxis and a pattern of vascularization that suggests bilateral symmetry.
Conclusions
Paracladoxylon kespekianum is one of the largest Early Devonian euphyllophytes, among the oldest representatives of the cladoxylopsid group, and older than any species of the closely related Cladoxylon by at least 35 million years. It is also one of the oldest anatomically preserved representatives of the cladoxylopsid group. Its anatomical organization pushes the rise of complex vascular architecture among moniliformopsid euphyllophytes deeper in time than previously recognized.
{"title":"An early cladoxylopsid with complex vascular architecture: Paracladoxylon kespekianum gen. et sp. nov. from the Lower Devonian (Emsian) of Quebec, Canada","authors":"Jessica Chu, Thibault Durieux, Alexandru M. F. Tomescu","doi":"10.1002/ajb2.16418","DOIUrl":"10.1002/ajb2.16418","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Premise</h3>\u0000 \u0000 <p>Cladoxylopsids, one of the first lineages with complex organization to rise from the plexus of structurally simple plants that comprised the earliest euphyllophyte floras, are moniliformopsid euphyllophytes. They formed Earth's earliest forests by the Middle Devonian and are thought to have given rise to the equisetopsids and probably some fern lineages. The Lower Devonian (Emsian) Battery Point Formation (Quebec, Canada) contains previously unrecognized cladoxylopsids preserved anatomically. One of these provides new data on structural evolution among euphyllophytes and is described here.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>The anatomy and morphology of permineralized axes of the new plant were studied with light and electron microscopy on sections produced using the cellulose acetate peel technique. Morphological comparisons and phylogenetic analysis were used for taxonomic placement of the plant.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The plant represents a new species, <i>Paracladoxylon kespekianum</i> Chu et Tomescu, gen. et sp. nov., that has tracheids with modern-looking bordered pits and the complex cauline vascular architecture characteristic of the genus <i>Cladoxylon</i>. Its dissected ultimate appendages have complex regular taxis and a pattern of vascularization that suggests bilateral symmetry.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p><i>Paracladoxylon kespekianum</i> is one of the largest Early Devonian euphyllophytes, among the oldest representatives of the cladoxylopsid group, and older than any species of the closely related <i>Cladoxylon</i> by at least 35 million years. It is also one of the oldest anatomically preserved representatives of the cladoxylopsid group. Its anatomical organization pushes the rise of complex vascular architecture among moniliformopsid euphyllophytes deeper in time than previously recognized.</p>\u0000 </section>\u0000 </div>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456036","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Matthew J. Butrim, Alexander J. Lowe, Ellen D. Currano
Premise
Leaf mass per area (LMA) is a widely used functional trait in both neobotanical and paleobotanical research that provides a window into how plants interact with their environment. Paleobotanists have used site-level measures of LMA as a proxy for climate, biome, deciduousness, and community-scale plant strategy, yet many of these relationships have not been grounded in modern data. In this study, we evaluated LMA from the paleobotanical perspective, seeking to add modern context to paleobotanical interpretations and discover what a combined modern and fossil data set can tell us about how LMA can be best applied toward interpreting plant communities.
Methods
We built a modern data set by pulling plant trait data from the TRY database, and a fossil data set by compiling data from studies that have used the petiole-width proxy for LMA. We then investigated the relationships of species-mean, site-mean, and site-distribution LMA with different climatic, phylogenetic, and physiognomic variables.
Results
We found that LMA distributions are correlated with climate, site taxonomic composition, and deciduousness. However, the relative contributions of these factors are not distinctive, and ultimately, LMA distributions cannot accurately reconstruct the biome or climate of an individual site.
Conclusions
The correlations that make up the leaf economics spectrum are stronger than the correlations between LMA and climate, phylogeny, morphospace, or depositional environment. Fossil LMA should be understood as the culmination of the influences of these variables rather than as a predictor.
{"title":"Leaf mass per area: An investigation into the application of the ubiquitous functional trait from a paleobotanical perspective","authors":"Matthew J. Butrim, Alexander J. Lowe, Ellen D. Currano","doi":"10.1002/ajb2.16419","DOIUrl":"10.1002/ajb2.16419","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Premise</h3>\u0000 \u0000 <p>Leaf mass per area (LMA) is a widely used functional trait in both neobotanical and paleobotanical research that provides a window into how plants interact with their environment. Paleobotanists have used site-level measures of LMA as a proxy for climate, biome, deciduousness, and community-scale plant strategy, yet many of these relationships have not been grounded in modern data. In this study, we evaluated LMA from the paleobotanical perspective, seeking to add modern context to paleobotanical interpretations and discover what a combined modern and fossil data set can tell us about how LMA can be best applied toward interpreting plant communities.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We built a modern data set by pulling plant trait data from the TRY database, and a fossil data set by compiling data from studies that have used the petiole-width proxy for LMA. We then investigated the relationships of species-mean, site-mean, and site-distribution LMA with different climatic, phylogenetic, and physiognomic variables.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>We found that LMA distributions are correlated with climate, site taxonomic composition, and deciduousness. However, the relative contributions of these factors are not distinctive, and ultimately, LMA distributions cannot accurately reconstruct the biome or climate of an individual site.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>The correlations that make up the leaf economics spectrum are stronger than the correlations between LMA and climate, phylogeny, morphospace, or depositional environment. Fossil LMA should be understood as the culmination of the influences of these variables rather than as a predictor.</p>\u0000 </section>\u0000 </div>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456039","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Damon Vaughan, Cameron B. Williams, Nalini Nadkarni, Todd E. Dawson, Danel Draguljic, Rikke Reese Næsborg, Sybil G. Gotsch
Premise
Vascular epiphytes of tropical montane cloud forests are vulnerable to climate change, particularly as cloud bases elevate and reduce atmospheric inputs to the system. However, studies have generally focused on epiphytes in contiguous forests, with little research being done on epiphytes on isolated pasture trees. We investigated water relations of pasture-tree epiphytes at three sites located below and above the elevation of the average cloud base in Monteverde, Costa Rica.
Methods
We measured sap velocity and four microclimate variables in both the dry and wet season of 2018. We also measured functional traits, including pressure volume (PV) curves, predawn/midday water potential, and various lab-based water relations traits. We used linear mixed models to assess the correlation between microclimate and sap velocity in both seasons and ANOVA to assess the variation in PV curve and water potential variables.
Results
The turgor loss point generally increased from the wettest to driest site. However, this trend was driven primarily by the increasing prevalence of leaf succulence at drier sites. Microclimatic variables correlated strongly with sap velocity in the wet season, but low soil moisture availability caused this correlation to break down during the dry season.
Conclusions
Our results emphasize the vulnerability of cloud forest epiphytes to rising cloud bases. This vulnerability may be more severe in pasture trees that lack the potential buffer of surrounding forest, but additional research that directly compares the canopy microclimate conditions between forest and pasture trees is needed to confirm this possibility.
{"title":"Drought response strategies of vascular epiphytes in isolated pasture trees in a Costa Rican tropical montane landscape","authors":"Damon Vaughan, Cameron B. Williams, Nalini Nadkarni, Todd E. Dawson, Danel Draguljic, Rikke Reese Næsborg, Sybil G. Gotsch","doi":"10.1002/ajb2.16423","DOIUrl":"10.1002/ajb2.16423","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Premise</h3>\u0000 \u0000 <p>Vascular epiphytes of tropical montane cloud forests are vulnerable to climate change, particularly as cloud bases elevate and reduce atmospheric inputs to the system. However, studies have generally focused on epiphytes in contiguous forests, with little research being done on epiphytes on isolated pasture trees. We investigated water relations of pasture-tree epiphytes at three sites located below and above the elevation of the average cloud base in Monteverde, Costa Rica.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We measured sap velocity and four microclimate variables in both the dry and wet season of 2018. We also measured functional traits, including pressure volume (PV) curves, predawn/midday water potential, and various lab-based water relations traits. We used linear mixed models to assess the correlation between microclimate and sap velocity in both seasons and ANOVA to assess the variation in PV curve and water potential variables.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The turgor loss point generally increased from the wettest to driest site. However, this trend was driven primarily by the increasing prevalence of leaf succulence at drier sites. Microclimatic variables correlated strongly with sap velocity in the wet season, but low soil moisture availability caused this correlation to break down during the dry season.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Our results emphasize the vulnerability of cloud forest epiphytes to rising cloud bases. This vulnerability may be more severe in pasture trees that lack the potential buffer of surrounding forest, but additional research that directly compares the canopy microclimate conditions between forest and pasture trees is needed to confirm this possibility.</p>\u0000 </section>\u0000 </div>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456038","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jacob E. Herschberger, Lukasz Ciesla, Christopher R. Stieha, Mônica F. Kersch-Becker
Premise
Plants produce an array of floral olfactory and visual cues to attract pollinators, including volatile organic compounds (VOC), which mediate plant–pollinator interactions and may be influenced by herbivory and neighboring plants. Consequently, these factors may affect plant fitness by disrupting pollination. However, most evidence comes from controlled experiments, limiting our understanding of how VOCs function in natural populations. This study investigated how herbivory and conspecific ramet density influence floral VOC profile, pollination, and seed production in a naturally occurring population of Solidago altissima.
Methods
We recorded leaf herbivory and ramet density surrounding one focal ramet in 1-m2 plots. We collected VOCs from the floral headspace and measured ovary fertilization as a proxy for pollination success and the number of seeds produced by the focal ramet.
Results
Our findings revealed interactive effects between ramet density and herbivory on floral VOC emission, richness, and diversity. Specifically, at lower ramet densities, herbivory did not affect floral volatile emissions. However, in highly dense stands, herbivory suppressed floral volatile emissions. Despite these changes, floral volatiles did not affect pollination and the number of seeds in S. altissima.
Conclusions
Our field-based findings underscore the importance of understanding the complex responses of floral VOCs to environmental stressors and their contributions to plant reproduction within natural communities. Our results suggest that while herbivory and ramet density influence floral scent, these changes do not affect reproduction in our study. Ultimately, generalist-pollinated plants like S. altissima might not rely heavily on chemical signaling during pollination.
{"title":"Impacts of ramet density and herbivory on floral volatile emissions and seed production in Solidago altissima","authors":"Jacob E. Herschberger, Lukasz Ciesla, Christopher R. Stieha, Mônica F. Kersch-Becker","doi":"10.1002/ajb2.16414","DOIUrl":"10.1002/ajb2.16414","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Premise</h3>\u0000 \u0000 <p>Plants produce an array of floral olfactory and visual cues to attract pollinators, including volatile organic compounds (VOC), which mediate plant–pollinator interactions and may be influenced by herbivory and neighboring plants. Consequently, these factors may affect plant fitness by disrupting pollination. However, most evidence comes from controlled experiments, limiting our understanding of how VOCs function in natural populations. This study investigated how herbivory and conspecific ramet density influence floral VOC profile, pollination, and seed production in a naturally occurring population of <i>Solidago altissima</i>.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We recorded leaf herbivory and ramet density surrounding one focal ramet in 1-m<sup>2</sup> plots. We collected VOCs from the floral headspace and measured ovary fertilization as a proxy for pollination success and the number of seeds produced by the focal ramet.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Our findings revealed interactive effects between ramet density and herbivory on floral VOC emission, richness, and diversity. Specifically, at lower ramet densities, herbivory did not affect floral volatile emissions. However, in highly dense stands, herbivory suppressed floral volatile emissions. Despite these changes, floral volatiles did not affect pollination and the number of seeds in <i>S. altissima</i>.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Our field-based findings underscore the importance of understanding the complex responses of floral VOCs to environmental stressors and their contributions to plant reproduction within natural communities. Our results suggest that while herbivory and ramet density influence floral scent, these changes do not affect reproduction in our study. Ultimately, generalist-pollinated plants like <i>S. altissima</i> might not rely heavily on chemical signaling during pollination.</p>\u0000 </section>\u0000 </div>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajb2.16414","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142387327","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This essay discusses how the ultrastructural changes in chloroplasts, particularly the mechanisms of thylakoid membrane unstacking, help maintain the photosynthetic performance of photosystem II (PSII) under stress conditions. This phenomenon may facilitate the repair of damaged PSII by providing access to the repair machinery. It is argued that this PSII repair mechanism accelerates PSII recovery, optimizing photosynthetic processes in stressed plants. Although some studies demonstrate the relationship between thylakoid membrane unstacking in stress conditions, these studies were developed with model species under controlled conditions. Thus, this essay serves as a validation tool for these previous studies, because it demonstrates that the relationships between ultrastructural changes in chloroplasts and the functioning of PSII are essential acclimative strategies for nonmodel plants to survive the constant edaphoclimatic changes of natural environments. Understanding these subcellular dynamics can significantly inform biologists about the plastic potential of plants, especially in heterogeneous environments. An integrated approach in future studies is necessary, highlighting the importance of exploring plant functional traits at multiple scales, because subcellular characteristics have great potential to understand plant acclimatization.
{"title":"Unraveling subcellular functional traits: Adaptive insights into chloroplast ultrastructure in nonmodel species","authors":"Saulo Pireda, Maura Da Cunha","doi":"10.1002/ajb2.16415","DOIUrl":"10.1002/ajb2.16415","url":null,"abstract":"<p>This essay discusses how the ultrastructural changes in chloroplasts, particularly the mechanisms of thylakoid membrane unstacking, help maintain the photosynthetic performance of photosystem II (PSII) under stress conditions. This phenomenon may facilitate the repair of damaged PSII by providing access to the repair machinery. It is argued that this PSII repair mechanism accelerates PSII recovery, optimizing photosynthetic processes in stressed plants. Although some studies demonstrate the relationship between thylakoid membrane unstacking in stress conditions, these studies were developed with model species under controlled conditions. Thus, this essay serves as a validation tool for these previous studies, because it demonstrates that the relationships between ultrastructural changes in chloroplasts and the functioning of PSII are essential acclimative strategies for nonmodel plants to survive the constant edaphoclimatic changes of natural environments. Understanding these subcellular dynamics can significantly inform biologists about the plastic potential of plants, especially in heterogeneous environments. An integrated approach in future studies is necessary, highlighting the importance of exploring plant functional traits at multiple scales, because subcellular characteristics have great potential to understand plant acclimatization.</p>","PeriodicalId":7691,"journal":{"name":"American Journal of Botany","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2024-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajb2.16415","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142387328","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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