Natasha S Lawrie, Nekane Medrano Cuetos, Francesca Sini, Ghifary A Salam, Hangyu Ding, Arthur Vancolen, Jessica M Nelson, Roy H J Erkens, Giuditta Perversi
Calcium oxalate (CaOx) crystals are biominerals present in a wide variety of plants. Formation of these crystals is a biomineralization process occurring in vacuoles within specialized cells called crystal idioblasts. This process is dependent on two key components: deprotonated oxalic acid, and calcium ions (Ca2+), and can result in multiple crystal morphologies. Raphides are needle-like CaOx crystals found in various plant organs and tissues. Though their function is highly debated, they can potentially store calcium, sequester heavy metals, protect against herbivory and possibly programmed cell death. The last review of the taxonomic and anatomical distribution of raphides across the plant kingdom dates back to 1980, in a review by Franceschi and Horner, prompting an updated systematic review of raphides in plants. We conduct a broad literature search to record plant taxa and tissue locations containing raphides. We provide an overview of raphide-forming plant taxa, discussing phylogenetic distribution of raphides at the order level, and report on the specific locations of raphides within plants. Our review reveals raphide occurrence has been studied in 33 orders, 76 families and 1305 species, with raphides presence confirmed in 24 orders, 46 families and 797 species. These taxa represented less than 1 % of known species per family. Leaves are the most prominent raphide-containing primary location in all three major angiosperm clades investigated: Eudicots, Magnoliids, and Monocots. Roots are least reported to contain raphides. The collation of such information lays the groundwork to unveil the genetic origin and evolution of raphides in plants, and highlights targets for future studies of the presence and role of plant raphides.
{"title":"Systematic review on raphide morphotype calcium oxalate crystals in angiosperms.","authors":"Natasha S Lawrie, Nekane Medrano Cuetos, Francesca Sini, Ghifary A Salam, Hangyu Ding, Arthur Vancolen, Jessica M Nelson, Roy H J Erkens, Giuditta Perversi","doi":"10.1093/aobpla/plad031","DOIUrl":"https://doi.org/10.1093/aobpla/plad031","url":null,"abstract":"<p><p>Calcium oxalate (CaOx) crystals are biominerals present in a wide variety of plants. Formation of these crystals is a biomineralization process occurring in vacuoles within specialized cells called crystal idioblasts. This process is dependent on two key components: deprotonated oxalic acid, and calcium ions (Ca<sup>2+</sup>), and can result in multiple crystal morphologies. Raphides are needle-like CaOx crystals found in various plant organs and tissues. Though their function is highly debated, they can potentially store calcium, sequester heavy metals, protect against herbivory and possibly programmed cell death. The last review of the taxonomic and anatomical distribution of raphides across the plant kingdom dates back to 1980, in a review by Franceschi and Horner, prompting an updated systematic review of raphides in plants. We conduct a broad literature search to record plant taxa and tissue locations containing raphides. We provide an overview of raphide-forming plant taxa, discussing phylogenetic distribution of raphides at the order level, and report on the specific locations of raphides within plants. Our review reveals raphide occurrence has been studied in 33 orders, 76 families and 1305 species, with raphides presence confirmed in 24 orders, 46 families and 797 species. These taxa represented less than 1 % of known species per family. Leaves are the most prominent raphide-containing primary location in all three major angiosperm clades investigated: Eudicots, Magnoliids, and Monocots. Roots are least reported to contain raphides. The collation of such information lays the groundwork to unveil the genetic origin and evolution of raphides in plants, and highlights targets for future studies of the presence and role of plant raphides.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad031"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406436/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10337537","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Over centuries of plant morphological research, biologists have enthusiastically explored how distinct vascular arrangements have diversified. These investigations have focused on the evolution of steles and secondary growth and examined the diversity of vascular tissues (xylem and phloem), including atypical developmental pathways generated through modifications to the typical development of ancestral ontogenies. A shared vernacular has evolved for communicating on the diversity of alternative ontogenies in seed plants. Botanists have traditionally used the term 'anomalous secondary growth' which was later renamed to 'cambial variants' by late Dr. Sherwin Carlquist (1988). However, the term 'cambial variants' can be vague in meaning since it is applied for developmental pathways that do not necessarily originate from cambial activity. Here, we review the 'cambial variants' concept and propose the term 'vascular variants' as a more inclusive overarching framework to interpret alternative vascular ontogenies in plants. In this framework, vascular variants are defined by their developmental origin (instead of anatomical patterns), allowing the classification of alternative vascular ontogenies into three categories: (i) procambial variants, (ii) cambial variants and (iii) ectopic cambia. Each category includes several anatomical patterns. Vascular variants, which represent broader developmental based groups, can be applied to both extant and fossil plants, and thereby offer a more adequate term from an evolutionary perspective. An overview of the developmental diversity and phylogenetic distribution of vascular variants across selected seed plants is provided. Finally, this viewpoint discusses the evolutionary implications of vascular variants.
{"title":"Vascular variants in seed plants-a developmental perspective.","authors":"Israel L Cunha Neto","doi":"10.1093/aobpla/plad036","DOIUrl":"https://doi.org/10.1093/aobpla/plad036","url":null,"abstract":"<p><p>Over centuries of plant morphological research, biologists have enthusiastically explored how distinct vascular arrangements have diversified. These investigations have focused on the evolution of steles and secondary growth and examined the diversity of vascular tissues (xylem and phloem), including atypical developmental pathways generated through modifications to the typical development of ancestral ontogenies. A shared vernacular has evolved for communicating on the diversity of alternative ontogenies in seed plants. Botanists have traditionally used the term 'anomalous secondary growth' which was later renamed to 'cambial variants' by late Dr. Sherwin Carlquist (1988). However, the term 'cambial variants' can be vague in meaning since it is applied for developmental pathways that do not necessarily originate from cambial activity. Here, we review the 'cambial variants' concept and propose the term 'vascular variants' as a more inclusive overarching framework to interpret alternative vascular ontogenies in plants. In this framework, vascular variants are defined by their developmental origin (instead of anatomical patterns), allowing the classification of alternative vascular ontogenies into three categories: (i) <i>procambial variants</i>, (ii) <i>cambial variants</i> and (iii) <i>ectopic cambia</i>. Each category includes several anatomical patterns. Vascular variants, which represent broader developmental based groups, can be applied to both extant and fossil plants, and thereby offer a more adequate term from an evolutionary perspective. An overview of the developmental diversity and phylogenetic distribution of vascular variants across selected seed plants is provided. Finally, this viewpoint discusses the evolutionary implications of vascular variants.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad036"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355320/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9935735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Shitephen Wang, Daniel Epron, Keito Kobayashi, Satoru Takanashi, Masako Dannoura
Phyllostachys edulis is a spectacularly fast-growing species that completes its height growth within 2 months after the shoot emerges without producing leaves (fast-growing period, FGP). This phase was considered heterotrophic, with the carbon necessary for the growth being transferred from the mature culms via the rhizomes, although previous studies observed key enzymes and anatomical features related to C4-carbon fixation in developing culms. We tested whether C4-photosynthesis or dark-CO2 fixation through anaplerotic reactions significantly contributes to the FGP, resulting in differences in the natural abundance of δ13C in bulk organic matter and organic compounds. Further, pulse-13CO2-labelling was performed on developing culms, either from the surface or from the internal hollow, to ascertain whether significant CO2 fixation occurs in developing culms. δ13C of young shoots and developing culms were higher (-26.3 to -26.9 ‰) compared to all organs of mature bamboos (-28.4 to -30.1 ‰). Developing culms contained chlorophylls, most observed in the skin tissues. After pulse-13CO2-labelling, the polar fraction extracted from the skin tissues was slightly enriched in 13C, and only a weak 13C enrichment was observed in inner tissues. Main carbon source sustaining the FGP was not assimilated by the developing culm, while a limited anaplerotic fixation of respired CO2 cannot be excluded and is more likely than C4-photosynthetic carbon fixation.
{"title":"Sources of carbon supporting the fast growth of developing immature moso bamboo (<i>Phyllostachys edulis</i>) culms: inference from carbon isotopes and anatomy.","authors":"Shitephen Wang, Daniel Epron, Keito Kobayashi, Satoru Takanashi, Masako Dannoura","doi":"10.1093/aobpla/plad046","DOIUrl":"https://doi.org/10.1093/aobpla/plad046","url":null,"abstract":"<p><p><i>Phyllostachys edulis</i> is a spectacularly fast-growing species that completes its height growth within 2 months after the shoot emerges without producing leaves (fast-growing period, FGP). This phase was considered heterotrophic, with the carbon necessary for the growth being transferred from the mature culms via the rhizomes, although previous studies observed key enzymes and anatomical features related to C<sub>4</sub>-carbon fixation in developing culms. We tested whether C<sub>4</sub>-photosynthesis or dark-CO<sub>2</sub> fixation through anaplerotic reactions significantly contributes to the FGP, resulting in differences in the natural abundance of <i>δ</i><sup>13</sup>C in bulk organic matter and organic compounds. Further, pulse-<sup>13</sup>CO<sub>2</sub>-labelling was performed on developing culms, either from the surface or from the internal hollow, to ascertain whether significant CO<sub>2</sub> fixation occurs in developing culms. <i>δ</i><sup>13</sup>C of young shoots and developing culms were higher (-26.3 to -26.9 ‰) compared to all organs of mature bamboos (-28.4 to -30.1 ‰). Developing culms contained chlorophylls, most observed in the skin tissues. After pulse-<sup>13</sup>CO<sub>2</sub>-labelling, the polar fraction extracted from the skin tissues was slightly enriched in <sup>13</sup>C, and only a weak <sup>13</sup>C enrichment was observed in inner tissues. Main carbon source sustaining the FGP was not assimilated by the developing culm, while a limited anaplerotic fixation of respired CO<sub>2</sub> cannot be excluded and is more likely than C<sub>4</sub>-photosynthetic carbon fixation.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad046"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368343/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10258892","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mayumi Vega-Polanco, Lislie Solís-Montero, Julio C Rojas, Leopoldo Cruz-López, David Alavez-Rosas, Mario Vallejo-Marín
Floral scents shape plant-pollinator interactions. Although populations of the same species can vary in their floral scent, little is known about how this variation affects pollinator visitation. In this study, we compare the scents emitted by buzz-pollinated Solanum rostratum (Solanaceae) in two areas of its distribution (Mexico and USA) and investigate how these differences in scent affect pollinator preferences and attraction. We determined the variation of floral volatile compounds using hexane extraction followed by gas chromatography coupled with spectrometry. We also performed a field cage multiple-choice bioassay and a Y-tube behavioural bioassay using Bombus impatiens. We recorded 13 volatile compounds in floral extracts for plants from both ranges that varied qualitative and semi-quantitatively among populations. We found that in the field cage experiment, bumble bees visited plants from the US populations more frequently than plants from Mexican populations. However, bees showed no difference in preference between extracts from Mexican or US flowers. We conclude that although bees show differential visitation to whole plants of different regions, variation in floral extract alone does not translate into differences in preference by B. impatiens. The potential effects of variation in floral scent on the other native bee pollinators remain to be assessed.
{"title":"Intraspecific variation of scent and its impact on pollinators' preferences.","authors":"Mayumi Vega-Polanco, Lislie Solís-Montero, Julio C Rojas, Leopoldo Cruz-López, David Alavez-Rosas, Mario Vallejo-Marín","doi":"10.1093/aobpla/plad049","DOIUrl":"https://doi.org/10.1093/aobpla/plad049","url":null,"abstract":"<p><p>Floral scents shape plant-pollinator interactions. Although populations of the same species can vary in their floral scent, little is known about how this variation affects pollinator visitation. In this study, we compare the scents emitted by buzz-pollinated <i>Solanum rostratum</i> (Solanaceae) in two areas of its distribution (Mexico and USA) and investigate how these differences in scent affect pollinator preferences and attraction. We determined the variation of floral volatile compounds using hexane extraction followed by gas chromatography coupled with spectrometry. We also performed a field cage multiple-choice bioassay and a Y-tube behavioural bioassay using <i>Bombus impatiens</i>. We recorded 13 volatile compounds in floral extracts for plants from both ranges that varied qualitative and semi-quantitatively among populations. We found that in the field cage experiment, bumble bees visited plants from the US populations more frequently than plants from Mexican populations. However, bees showed no difference in preference between extracts from Mexican or US flowers. We conclude that although bees show differential visitation to whole plants of different regions, variation in floral extract alone does not translate into differences in preference by <i>B. impatiens</i>. The potential effects of variation in floral scent on the other native bee pollinators remain to be assessed.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad049"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407983/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10292003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plant hydraulic conductivity and its decline under water stress are the focal point of current plant hydraulic research. The common methods of measuring hydraulic conductivity control a pressure gradient to push water through plant samples, submitting them to conditions far away from those that are experienced in nature where flow is suction driven and determined by the leaf water demand. In this paper, we present two methods for measuring hydraulic conductivity under closer to natural conditions, an artificial plant setup and a horizontal syringe pump setup. Both approaches use suction to pull water through a plant sample while dynamically monitoring the flow rate and pressure gradients. The syringe setup presented here allows for controlling and rapidly changing flow and pressure conditions, enabling experimental assessment of rapid plant hydraulic responses to water stress. The setup also allows quantification of dynamic changes in water storage of plant samples. Our tests demonstrate that the syringe pump setup can reproduce hydraulic conductivity values measured using the current standard method based on pushing water under above-atmospheric pressure. Surprisingly, using both the traditional and our new syringe pump setup, we found a positive correlation between changes in flow rate and hydraulic conductivity. Moreover, when flow or pressure conditions were changed rapidly, we found substantial contributions to flow by dynamic and largely reversible changes in the water storage of plant samples. Although the measurements can be performed under sub-atmospheric pressures, it is not possible to subject the samples to negative pressures due to the presence of gas bubbles near the valves and pressure sensors. Regardless, this setup allows for unprecedented insights into the interplay between pressure, flow rate, hydraulic conductivity and water storage in plant segments. This work was performed using an Open Science approach with the original data and analysis to be found at https://doi.org/10.5281/zenodo.7322605.
{"title":"A new experimental setup to measure hydraulic conductivity of plant segments.","authors":"Louis Krieger, Stanislaus J Schymanski","doi":"10.1093/aobpla/plad024","DOIUrl":"https://doi.org/10.1093/aobpla/plad024","url":null,"abstract":"<p><p>Plant hydraulic conductivity and its decline under water stress are the focal point of current plant hydraulic research. The common methods of measuring hydraulic conductivity control a pressure gradient to push water through plant samples, submitting them to conditions far away from those that are experienced in nature where flow is suction driven and determined by the leaf water demand. In this paper, we present two methods for measuring hydraulic conductivity under closer to natural conditions, an artificial plant setup and a horizontal syringe pump setup. Both approaches use suction to pull water through a plant sample while dynamically monitoring the flow rate and pressure gradients. The syringe setup presented here allows for controlling and rapidly changing flow and pressure conditions, enabling experimental assessment of rapid plant hydraulic responses to water stress. The setup also allows quantification of dynamic changes in water storage of plant samples. Our tests demonstrate that the syringe pump setup can reproduce hydraulic conductivity values measured using the current standard method based on pushing water under above-atmospheric pressure. Surprisingly, using both the traditional and our new syringe pump setup, we found a positive correlation between changes in flow rate and hydraulic conductivity. Moreover, when flow or pressure conditions were changed rapidly, we found substantial contributions to flow by dynamic and largely reversible changes in the water storage of plant samples. Although the measurements can be performed under sub-atmospheric pressures, it is not possible to subject the samples to negative pressures due to the presence of gas bubbles near the valves and pressure sensors. Regardless, this setup allows for unprecedented insights into the interplay between pressure, flow rate, hydraulic conductivity and water storage in plant segments. This work was performed using an Open Science approach with the original data and analysis to be found at https://doi.org/10.5281/zenodo.7322605.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad024"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10418303/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10352552","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mark Davidson Jewell, Sofia J van Moorsel, Graham Bell
Plants live in close association with microbial organisms that inhabit the environment in which they grow. Much recent work has aimed to characterize these plant-microbiome interactions, identifying those associations that increase growth. Although most work has focused on terrestrial plants, Lemna minor, a floating aquatic angiosperm, is increasingly used as a model in host-microbe interactions and many bacterial associations have been shown to play an important role in supporting plant fitness. However, the ubiquity and stability of these interactions as well as their dependence on specific abiotic environmental conditions remain unclear. Here, we assess the impact of a full L. minor microbiome on plant fitness and phenotype by assaying plants from eight natural sites, with and without their microbiomes, over a range of abiotic environmental conditions. We find that the microbiome systematically suppressed plant fitness, although the magnitude of this effect varied among plant genotypes and depended on the abiotic environment. Presence of the microbiome also resulted in phenotypic changes, with plants forming smaller colonies and producing smaller fronds and shorter roots. Differences in phenotype among plant genotypes were reduced when the microbiome was removed, as were genotype by environment interactions, suggesting that the microbiome plays a role in mediating the plant phenotypic response to the environment.
{"title":"Presence of microbiome decreases fitness and modifies phenotype in the aquatic plant <i>Lemna minor</i>.","authors":"Mark Davidson Jewell, Sofia J van Moorsel, Graham Bell","doi":"10.1093/aobpla/plad026","DOIUrl":"https://doi.org/10.1093/aobpla/plad026","url":null,"abstract":"<p><p>Plants live in close association with microbial organisms that inhabit the environment in which they grow. Much recent work has aimed to characterize these plant-microbiome interactions, identifying those associations that increase growth. Although most work has focused on terrestrial plants, <i>Lemna minor</i>, a floating aquatic angiosperm, is increasingly used as a model in host-microbe interactions and many bacterial associations have been shown to play an important role in supporting plant fitness. However, the ubiquity and stability of these interactions as well as their dependence on specific abiotic environmental conditions remain unclear. Here, we assess the impact of a full <i>L. minor</i> microbiome on plant fitness and phenotype by assaying plants from eight natural sites, with and without their microbiomes, over a range of abiotic environmental conditions. We find that the microbiome systematically suppressed plant fitness, although the magnitude of this effect varied among plant genotypes and depended on the abiotic environment. Presence of the microbiome also resulted in phenotypic changes, with plants forming smaller colonies and producing smaller fronds and shorter roots. Differences in phenotype among plant genotypes were reduced when the microbiome was removed, as were genotype by environment interactions, suggesting that the microbiome plays a role in mediating the plant phenotypic response to the environment.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad026"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327544/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10168265","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Peter Petrík, Anja Petek-Petrik, Mohammad Mukarram, Bernhard Schuldt, Laurent J Lamarque
The increasing evaporative demand due to climate change will significantly affect the balance of carbon assimilation and water losses of plants worldwide. The development of crop varieties with improved water-use efficiency (WUE) will be critical for adapting agricultural strategies under predicted future climates. This review aims to summarize the most important leaf morpho-physiological constraints of WUE in C3 plants and identify gaps in knowledge. From the carbon gain side of the WUE, the discussed parameters are mesophyll conductance, carboxylation efficiency and respiratory losses. The traits and parameters affecting the waterside of WUE balance discussed in this review are stomatal size and density, stomatal control and residual water losses (cuticular and bark conductance), nocturnal conductance and leaf hydraulic conductance. In addition, we discussed the impact of leaf anatomy and crown architecture on both the carbon gain and water loss components of WUE. There are multiple possible targets for future development in understanding sources of WUE variability in plants. We identified residual water losses and respiratory carbon losses as the greatest knowledge gaps of whole-plant WUE assessments. Moreover, the impact of trichomes, leaf hydraulic conductance and canopy structure on plants' WUE is still not well understood. The development of a multi-trait approach is urgently needed for a better understanding of WUE dynamics and optimization.
{"title":"Leaf physiological and morphological constraints of water-use efficiency in C<sub>3</sub> plants.","authors":"Peter Petrík, Anja Petek-Petrik, Mohammad Mukarram, Bernhard Schuldt, Laurent J Lamarque","doi":"10.1093/aobpla/plad047","DOIUrl":"https://doi.org/10.1093/aobpla/plad047","url":null,"abstract":"<p><p>The increasing evaporative demand due to climate change will significantly affect the balance of carbon assimilation and water losses of plants worldwide. The development of crop varieties with improved water-use efficiency (WUE) will be critical for adapting agricultural strategies under predicted future climates. This review aims to summarize the most important leaf morpho-physiological constraints of WUE in C<sub>3</sub> plants and identify gaps in knowledge. From the carbon gain side of the WUE, the discussed parameters are mesophyll conductance, carboxylation efficiency and respiratory losses. The traits and parameters affecting the waterside of WUE balance discussed in this review are stomatal size and density, stomatal control and residual water losses (cuticular and bark conductance), nocturnal conductance and leaf hydraulic conductance. In addition, we discussed the impact of leaf anatomy and crown architecture on both the carbon gain and water loss components of WUE. There are multiple possible targets for future development in understanding sources of WUE variability in plants. We identified residual water losses and respiratory carbon losses as the greatest knowledge gaps of whole-plant WUE assessments. Moreover, the impact of trichomes, leaf hydraulic conductance and canopy structure on plants' WUE is still not well understood. The development of a multi-trait approach is urgently needed for a better understanding of WUE dynamics and optimization.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad047"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407996/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10345261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Under the changing climate, the persistence of Afrotemperate taxa may be threatened as suitable habitat availability decreases. The unique disjunct ranges of podocarps in southern Africa raise questions about the persistence of these species under climate change. Here, we identified likely environmental drivers of these distributions, characterized the current and future (2070) environmental niches, and projected distributions of four podocarp species in South Africa. Species distribution models were conducted using species locality data for Afrocarpus falcatus, Podocarpus latifolius, Pseudotropheus elongatus and Podocarpus henkelii and both historical climate data (1970-2000) and future climate scenarios (Representative Concentration Pathway [RCP] 4.5 and 8.5, 2061-2080) to estimate the current and future distributions. We also used this opportunity to identify the most important climatic variables that likely govern each species' distribution. Using niche overlap estimates, a similarity test, and indices of niche expansion, stability and unfilling, we explored how niches change under different climate scenarios. The distribution of the study species was governed by the maximum temperature of the warmest month, temperature annual range, mean temperature of the wettest quarter, and precipitation of the wettest, driest and warmest quarters. The current distribution of A. falcatus was predicted to expand to higher elevations under RCP 4.5 and RCP 8.5. Podocarpus henkelii was predicted to lose most of its suitable habitat under RCP 4.5 and expand under RCP 8.5; however, this was the opposite for P. elongatus and P. latifolius. Interestingly, P. elongatus, which had the smallest geographic distribution, showed the most vulnerability to climate change in comparison to the other podocarps. Mapping the distribution of podocarps and understanding the differences in their current and future climate niches provide insight into potential climate drivers of podocarp persistence and the potential for adaptation of these species. Overall, these results suggest that P. elongatus and P. henkelii may expand to novel environmental niches.
{"title":"Projecting Podocarpaceae response to climate change: we are not out of the woods yet.","authors":"Thando C Twala, Jolene T Fisher, Kelsey L Glennon","doi":"10.1093/aobpla/plad034","DOIUrl":"https://doi.org/10.1093/aobpla/plad034","url":null,"abstract":"<p><p>Under the changing climate, the persistence of Afrotemperate taxa may be threatened as suitable habitat availability decreases. The unique disjunct ranges of podocarps in southern Africa raise questions about the persistence of these species under climate change. Here, we identified likely environmental drivers of these distributions, characterized the current and future (2070) environmental niches, and projected distributions of four podocarp species in South Africa. Species distribution models were conducted using species locality data for <i>Afrocarpus falcatus</i>, <i>Podocarpus latifolius</i>, <i>Pseudotropheus elongatus</i> and <i>Podocarpus henkelii</i> and both historical climate data (1970-2000) and future climate scenarios (Representative Concentration Pathway [RCP] 4.5 and 8.5, 2061-2080) to estimate the current and future distributions. We also used this opportunity to identify the most important climatic variables that likely govern each species' distribution. Using niche overlap estimates, a similarity test, and indices of niche expansion, stability and unfilling, we explored how niches change under different climate scenarios. The distribution of the study species was governed by the maximum temperature of the warmest month, temperature annual range, mean temperature of the wettest quarter, and precipitation of the wettest, driest and warmest quarters. The current distribution of <i>A. falcatus</i> was predicted to expand to higher elevations under RCP 4.5 and RCP 8.5. <i>Podocarpus henkelii</i> was predicted to lose most of its suitable habitat under RCP 4.5 and expand under RCP 8.5; however, this was the opposite for <i>P. elongatus</i> and <i>P. latifolius</i>. Interestingly, <i>P. elongatus,</i> which had the smallest geographic distribution, showed the most vulnerability to climate change in comparison to the other podocarps. Mapping the distribution of podocarps and understanding the differences in their current and future climate niches provide insight into potential climate drivers of podocarp persistence and the potential for adaptation of these species. Overall, these results suggest that <i>P. elongatus</i> and <i>P. henkelii</i> may expand to novel environmental niches.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad034"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321399/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10182389","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Gabriela Auge, Valentin Hankofer, Martin Groth, Rea Antoniou-Kourounioti, Irja Ratikainen, Christian Lampei
Plants are extremely plastic organisms. They continuously receive and integrate environmental information and adjust their growth and development to favour fitness and survival. When this integration of information affects subsequent life stages or the development of subsequent generations, it can be considered an environmental memory. Thus, plant memory is a relevant mechanism by which plants respond adaptively to different environments. If the cost of maintaining the response is offset by its benefits, it may influence evolutionary trajectories. As such, plant memory has a sophisticated underlying molecular mechanism with multiple components and layers. Nonetheless, when mathematical modelling is combined with knowledge of ecological, physiological, and developmental effects as well as molecular mechanisms as a tool for understanding plant memory, the combined potential becomes unfathomable for the management of plant communities in natural and agricultural ecosystems. In this review, we summarize recent advances in the understanding of plant memory, discuss the ecological requirements for its evolution, outline the multilayered molecular network and mechanisms required for accurate and fail-proof plant responses to variable environments, point out the direct involvement of the plant metabolism and discuss the tremendous potential of various types of models to further our understanding of the plant's environmental memory. Throughout, we emphasize the use of plant memory as a tool to unlock the secrets of the natural world.
{"title":"Plant environmental memory: implications, mechanisms and opportunities for plant scientists and beyond.","authors":"Gabriela Auge, Valentin Hankofer, Martin Groth, Rea Antoniou-Kourounioti, Irja Ratikainen, Christian Lampei","doi":"10.1093/aobpla/plad032","DOIUrl":"https://doi.org/10.1093/aobpla/plad032","url":null,"abstract":"<p><p>Plants are extremely plastic organisms. They continuously receive and integrate environmental information and adjust their growth and development to favour fitness and survival. When this integration of information affects subsequent life stages or the development of subsequent generations, it can be considered an environmental memory. Thus, plant memory is a relevant mechanism by which plants respond adaptively to different environments. If the cost of maintaining the response is offset by its benefits, it may influence evolutionary trajectories. As such, plant memory has a sophisticated underlying molecular mechanism with multiple components and layers. Nonetheless, when mathematical modelling is combined with knowledge of ecological, physiological, and developmental effects as well as molecular mechanisms as a tool for understanding plant memory, the combined potential becomes unfathomable for the management of plant communities in natural and agricultural ecosystems. In this review, we summarize recent advances in the understanding of plant memory, discuss the ecological requirements for its evolution, outline the multilayered molecular network and mechanisms required for accurate and fail-proof plant responses to variable environments, point out the direct involvement of the plant metabolism and discuss the tremendous potential of various types of models to further our understanding of the plant's environmental memory. Throughout, we emphasize the use of plant memory as a tool to unlock the secrets of the natural world.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad032"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321398/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10182390","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Agustina Yañez, Ignacio H Escapa, Thereis Y S Choo
Goeppertella has been postulated as a monophyletic group, whose precise position within the Gleichenoid families Dipteriaceae and Matoniaceae, remains poorly understood. Previously described Goeppertella specimens are based on frond fragments and its fertile morphology is represented by a few, poorly preserved specimens. We describe a new species based on the largest collection of fertile specimens known to date and discuss the evolutionary history of the genus based on the additional reproductive characters provided by the fossils described. Plant impressions were collected in Early Jurassic sediments of Patagonia, Argentina. The specimens were described, and silicone rubber casts were developed to examine in detail vegetative and reproductive features. The new species was compared with other Goeppertella species. Finally, a backbone analysis was performed in the context of a previously published combined matrix of Dipteridaceae, using the maximum parsimony criterion. The new species is described based on a combination of features that have not been previously reported. The vegetative morphology shows affinities with most fossil and extant Dipteriaceae, contrasting with the reproductive morphology which is more comparable with the scarce number of fossil dipteridaceous forms and it is more spread in the sister family, Matoniaceae. The backbone analysis indicates that the position of the new species vary among different positions among Dipteridaceae and Matoniaceae. Additional analyses, discriminating the signal of reproductive and vegetative character, are provided to discuss the base of this uncertainty. We consider Goeppertella as a member of the family Dipteridaceae since we interpret most shared features with Matoniaceae as plesiomorphic conditions for the family. In contrast, most shared features with Dipteridaceae represent apomorphies for the group. Thus, Goeppertella would represent an early diverging genus in Dipteridaceae, considering the venation characters as the most important in order to define the family.
{"title":"Fertile <i>Goeppertella</i> from the Jurassic of Patagonia: mosaic evolution in the Dipteridaceae-Matoniaceae lineage.","authors":"Agustina Yañez, Ignacio H Escapa, Thereis Y S Choo","doi":"10.1093/aobpla/plad007","DOIUrl":"https://doi.org/10.1093/aobpla/plad007","url":null,"abstract":"<p><p><i>Goeppertella</i> has been postulated as a monophyletic group, whose precise position within the Gleichenoid families Dipteriaceae and Matoniaceae, remains poorly understood. Previously described <i>Goeppertella</i> specimens are based on frond fragments and its fertile morphology is represented by a few, poorly preserved specimens. We describe a new species based on the largest collection of fertile specimens known to date and discuss the evolutionary history of the genus based on the additional reproductive characters provided by the fossils described. Plant impressions were collected in Early Jurassic sediments of Patagonia, Argentina. The specimens were described, and silicone rubber casts were developed to examine in detail vegetative and reproductive features. The new species was compared with other <i>Goeppertella</i> species. Finally, a backbone analysis was performed in the context of a previously published combined matrix of Dipteridaceae, using the maximum parsimony criterion. The new species is described based on a combination of features that have not been previously reported. The vegetative morphology shows affinities with most fossil and extant Dipteriaceae, contrasting with the reproductive morphology which is more comparable with the scarce number of fossil dipteridaceous forms and it is more spread in the sister family, Matoniaceae. The backbone analysis indicates that the position of the new species vary among different positions among Dipteridaceae and Matoniaceae. Additional analyses, discriminating the signal of reproductive and vegetative character, are provided to discuss the base of this uncertainty. We consider <i>Goeppertella</i> as a member of the family Dipteridaceae since we interpret most shared features with Matoniaceae as plesiomorphic conditions for the family. In contrast, most shared features with Dipteridaceae represent apomorphies for the group. Thus, <i>Goeppertella</i> would represent an early diverging genus in Dipteridaceae, considering the venation characters as the most important in order to define the family.</p>","PeriodicalId":48955,"journal":{"name":"AoB Plants","volume":"15 4","pages":"plad007"},"PeriodicalIF":2.9,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324646/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10187000","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}