Pub Date : 2024-11-14DOI: 10.1016/j.cois.2024.101299
Abin Thomas, Madhurima Roy, Nitin Gupta
Odors serve as important cues for many behaviors in mosquitoes, including host-seeking, foraging, and oviposition. They are detected by olfactory receptor neurons present on the sensory organs, whose axons take this signal to the antennal lobe, the first olfactory processing center in the insect brain. We review the organization and the functioning of the antennal lobe in mosquitoes, focusing on two populations of interneurons present there: the local neurons (LNs) and the projection neurons (PNs). LNs enable information processing in the antennal lobe by providing lateral inhibition and excitation. PNs carry the processed output to downstream neurons in the lateral horn and the mushroom body. We compare the ideas of labeled lines and combinatorial codes, and argue that the PN population encodes odors combinatorially. Throughout this review, we discuss the observations from Aedes, Anopheles, and Culex mosquitoes in the context of previous findings from Drosophila and other insects.
{"title":"Olfactory coding in the mosquito antennal lobe: labeled lines or combinatorial code?","authors":"Abin Thomas, Madhurima Roy, Nitin Gupta","doi":"10.1016/j.cois.2024.101299","DOIUrl":"https://doi.org/10.1016/j.cois.2024.101299","url":null,"abstract":"<p><p>Odors serve as important cues for many behaviors in mosquitoes, including host-seeking, foraging, and oviposition. They are detected by olfactory receptor neurons present on the sensory organs, whose axons take this signal to the antennal lobe, the first olfactory processing center in the insect brain. We review the organization and the functioning of the antennal lobe in mosquitoes, focusing on two populations of interneurons present there: the local neurons (LNs) and the projection neurons (PNs). LNs enable information processing in the antennal lobe by providing lateral inhibition and excitation. PNs carry the processed output to downstream neurons in the lateral horn and the mushroom body. We compare the ideas of labeled lines and combinatorial codes, and argue that the PN population encodes odors combinatorially. Throughout this review, we discuss the observations from Aedes, Anopheles, and Culex mosquitoes in the context of previous findings from Drosophila and other insects.</p>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":" ","pages":"101299"},"PeriodicalIF":5.8,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142643741","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-13DOI: 10.1016/j.cois.2024.101298
Xinhai Ye, Yi Yang, Qi Fang, Gongyin Ye
Currently, a wealth of genomic data is now accessible for numerous insect natural enemies, serving as valuable resources that deepen our understanding of the genetic basis of biocontrol traits in these organisms. We summarize the current state of genome sequencing and highlight candidate genes related to biocontrol traits that hold promise for genetic improvement. We also review the recent population genomic studies in biological control and the discovery of potential insecticidal genes in parasitoid wasps. Collectively, current genomic works have shown the powerful ability to identify candidate genes responsible for desirable traits or promising effectors. However, further functional study is necessary to gain a mechanistic understanding of these genes, and future efforts are also needed to develop suitable approaches to translate genomic insights into field applications.
{"title":"Genomics of insect natural enemies in agroecosystems.","authors":"Xinhai Ye, Yi Yang, Qi Fang, Gongyin Ye","doi":"10.1016/j.cois.2024.101298","DOIUrl":"https://doi.org/10.1016/j.cois.2024.101298","url":null,"abstract":"<p><p>Currently, a wealth of genomic data is now accessible for numerous insect natural enemies, serving as valuable resources that deepen our understanding of the genetic basis of biocontrol traits in these organisms. We summarize the current state of genome sequencing and highlight candidate genes related to biocontrol traits that hold promise for genetic improvement. We also review the recent population genomic studies in biological control and the discovery of potential insecticidal genes in parasitoid wasps. Collectively, current genomic works have shown the powerful ability to identify candidate genes responsible for desirable traits or promising effectors. However, further functional study is necessary to gain a mechanistic understanding of these genes, and future efforts are also needed to develop suitable approaches to translate genomic insights into field applications.</p>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":" ","pages":"101298"},"PeriodicalIF":5.8,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142638663","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-08DOI: 10.1016/j.cois.2024.101296
Ryosuke Hayashi, Ryusuke Niwa
Female germline stem cells (fGSCs) are essential for generating mature oocytes. In general, self-renewal and differentiation of fGSCs into germ cells are regulated by niche signals from neighboring niche cells. In addition, fGSCs and their niche cells are greatly influenced by physiological and environmental factors, especially nutritional status. To clarify molecular mechanisms involved in regulating fGSC proliferation and maintenance, the fruit fly Drosophila melanogaster has served as an excellent genetic model organism. In recent years, along with sophisticated genetic tools for D. melanogaster, large-scale transcriptome, proteome, and metabolome analyses have provided new insights into D. melanogaster fGSC biology. These large-scale analyses have identified new markers and regulators for D. melanogaster fGSCs, including Netrin-A, Helical factor, eggplant, Gr43a, and genes controlling the polyol pathway, some of which are involved in nutrient-responsive control of fGSC behavior.
{"title":"Large-scale omics analyses of nutrition-responsive mechanisms of female germline stem cell proliferation and maintenance in Drosophila melanogaster.","authors":"Ryosuke Hayashi, Ryusuke Niwa","doi":"10.1016/j.cois.2024.101296","DOIUrl":"https://doi.org/10.1016/j.cois.2024.101296","url":null,"abstract":"<p><p>Female germline stem cells (fGSCs) are essential for generating mature oocytes. In general, self-renewal and differentiation of fGSCs into germ cells are regulated by niche signals from neighboring niche cells. In addition, fGSCs and their niche cells are greatly influenced by physiological and environmental factors, especially nutritional status. To clarify molecular mechanisms involved in regulating fGSC proliferation and maintenance, the fruit fly Drosophila melanogaster has served as an excellent genetic model organism. In recent years, along with sophisticated genetic tools for D. melanogaster, large-scale transcriptome, proteome, and metabolome analyses have provided new insights into D. melanogaster fGSC biology. These large-scale analyses have identified new markers and regulators for D. melanogaster fGSCs, including Netrin-A, Helical factor, eggplant, Gr43a, and genes controlling the polyol pathway, some of which are involved in nutrient-responsive control of fGSC behavior.</p>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":" ","pages":"101296"},"PeriodicalIF":5.8,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-07DOI: 10.1016/j.cois.2024.101294
Ayushi Gupta, Suresh Nair
Insects exhibit remarkable adaptability to a wide range of environmental stressors, including temperature fluctuations, pathogens, and changes in diet. This adaptability is often driven by epigenetic processes, which regulate gene expression without altering the underlying DNA sequence. This review provides a comprehensive overview of these epigenetic processes in insect adaptation, highlighting their impact on development, behaviour, and stress resilience. Understanding these mechanisms is essential for pest management and conservation efforts, offering insights into the rapid adaptive capacity of insects. By examining recent studies on epigenetics in insects, we aim to elucidate the molecular underpinnings of their adaptation and suggest future research directions in this evolving field.
昆虫对包括温度波动、病原体和饮食变化在内的各种环境压力因素表现出惊人的适应能力。这种适应性通常是由表观遗传过程驱动的,这种过程在不改变基本 DNA 序列的情况下调节基因表达。这篇综述全面概述了昆虫适应性中的这些表观遗传过程,强调了它们对发育、行为和抗逆性的影响。了解这些机制对害虫管理和保护工作至关重要,可深入了解昆虫的快速适应能力。通过考察最近对昆虫表观遗传学的研究,我们旨在阐明昆虫适应性的分子基础,并为这一不断发展的领域提出未来的研究方向。
{"title":"Epigenetic processes in insect adaptation to environmental stress.","authors":"Ayushi Gupta, Suresh Nair","doi":"10.1016/j.cois.2024.101294","DOIUrl":"https://doi.org/10.1016/j.cois.2024.101294","url":null,"abstract":"<p><p>Insects exhibit remarkable adaptability to a wide range of environmental stressors, including temperature fluctuations, pathogens, and changes in diet. This adaptability is often driven by epigenetic processes, which regulate gene expression without altering the underlying DNA sequence. This review provides a comprehensive overview of these epigenetic processes in insect adaptation, highlighting their impact on development, behaviour, and stress resilience. Understanding these mechanisms is essential for pest management and conservation efforts, offering insights into the rapid adaptive capacity of insects. By examining recent studies on epigenetics in insects, we aim to elucidate the molecular underpinnings of their adaptation and suggest future research directions in this evolving field.</p>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":" ","pages":"101294"},"PeriodicalIF":5.8,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-07DOI: 10.1016/j.cois.2024.101295
Diogo C Cabral-de-Mello, Octavio M Palacios-Gimenez
Like other eukaryotes, insect genomes contain a large portion of repetitive sequences, particularly transposable elements (TEs) and satellite DNAs (satDNAs). This review highlights key studies on repetitive DNAs and examines their structural, functional, and evolutionary impact in insect genomes. Repetitive sequences promote genetic diversification through mutations and large-scale rearrangements, playing a crucial role in shaping genomic architecture, aiding organismal adaptation and driving speciation. We also explore the influence of repeats in genome size variation and species incompatibilities, along with their contribution to adaptive phenotypes and gene regulation. Studying repetitive DNA in insects not only provides insights into basic genomic features but also offers valuable information for conservation strategies, pest control, and advancements in genetics, ecology, and evolutionary biology.
与其他真核生物一样,昆虫基因组也含有大量重复序列,尤其是转座元件(TE)和卫星 DNA(satDNA)。这篇综述重点介绍了有关重复 DNA 的主要研究,并探讨了它们在昆虫基因组中的结构、功能和进化影响。重复序列通过突变和大规模重排促进基因多样化,在塑造基因组结构、帮助生物适应和推动物种分化方面发挥着至关重要的作用。我们还探索了重复序列对基因组大小变异和物种不相容性的影响,以及它们对适应性表型和基因调控的贡献。研究昆虫的重复 DNA 不仅能深入了解基本的基因组特征,还能为保护策略、害虫控制以及遗传学、生态学和进化生物学的发展提供有价值的信息。
{"title":"Repetitive DNAs: The \"invisible\" regulators of insect adaptation and speciation.","authors":"Diogo C Cabral-de-Mello, Octavio M Palacios-Gimenez","doi":"10.1016/j.cois.2024.101295","DOIUrl":"https://doi.org/10.1016/j.cois.2024.101295","url":null,"abstract":"<p><p>Like other eukaryotes, insect genomes contain a large portion of repetitive sequences, particularly transposable elements (TEs) and satellite DNAs (satDNAs). This review highlights key studies on repetitive DNAs and examines their structural, functional, and evolutionary impact in insect genomes. Repetitive sequences promote genetic diversification through mutations and large-scale rearrangements, playing a crucial role in shaping genomic architecture, aiding organismal adaptation and driving speciation. We also explore the influence of repeats in genome size variation and species incompatibilities, along with their contribution to adaptive phenotypes and gene regulation. Studying repetitive DNA in insects not only provides insights into basic genomic features but also offers valuable information for conservation strategies, pest control, and advancements in genetics, ecology, and evolutionary biology.</p>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":" ","pages":"101295"},"PeriodicalIF":5.8,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616353","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-28DOI: 10.1016/j.cois.2024.101291
Florencia Fernández-Chiappe , Gabriel K Ocker , Meg A Younger
The Aedes aegypti mosquito utilizes olfaction during the search for humans to bite. The attraction to human body odor is an innate behavior for this disease-vector mosquito. Many well-studied model species have olfactory systems that conform to a particular organization that is sometimes referred to as the ‘one-receptor-to-one-neuron’ organization because each sensory neuron expresses only a single type of olfactory receptor that imparts the neuron’s chemical selectivity. This sensory architecture has become the canon in the field. This review will focus on the recent finding that the olfactory system of Ae. aegypti has a different organization, with multiple olfactory receptors co-expressed in many of its olfactory sensory neurons. We will discuss the canonical organization and how this differs from the non-canonical organization, examine examples of non-canonical olfactory systems in other species, and discuss the possible roles of receptor co-expression in odor coding in the mosquito and other organisms.
{"title":"Prospects on non-canonical olfaction in the mosquito and other organisms: why co-express?","authors":"Florencia Fernández-Chiappe , Gabriel K Ocker , Meg A Younger","doi":"10.1016/j.cois.2024.101291","DOIUrl":"10.1016/j.cois.2024.101291","url":null,"abstract":"<div><div>The <em>Aedes aegypti</em> mosquito utilizes olfaction during the search for humans to bite. The attraction to human body odor is an innate behavior for this disease-vector mosquito. Many well-studied model species have olfactory systems that conform to a particular organization that is sometimes referred to as the ‘one-receptor-to-one-neuron’ organization because each sensory neuron expresses only a single type of olfactory receptor that imparts the neuron’s chemical selectivity. This sensory architecture has become the canon in the field. This review will focus on the recent finding that the olfactory system of <em>Ae. aegypti</em> has a different organization, with multiple olfactory receptors co-expressed in many of its olfactory sensory neurons. We will discuss the canonical organization and how this differs from the non-canonical organization, examine examples of non-canonical olfactory systems in other species, and discuss the possible roles of receptor co-expression in odor coding in the mosquito and other organisms.</div></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"67 ","pages":"Article 101291"},"PeriodicalIF":5.8,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142544296","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-28DOI: 10.1016/j.cois.2024.101290
Delia M Pinto-Zevallos, James D Blande
Herbivore-induced plant volatiles (HIPVs) are reliable cues that parasitoids can use to locate host patches. Interactions mediated by plant volatile organic compounds (VOCs) are vulnerable to disturbance by predicted climate change and air pollution scenarios. Abiotic stress–induced VOCs may act as false signals to parasitoids. Air pollutants can disrupt signalling by degrading HIPVs at different rates and preventing the perception of olfactory signals by reducing the sensitivity of olfactory receptors or by occluding insect sensillae. As essential components of biological control programmes, efforts should be made to assess how different parasitoid species respond and adapt to HIPVs in predicted scenarios. Since providing parasitoid food sources is a promising practice for boosting biological control, parasitoid–flower interactions deserve attention.
{"title":"Challenges of climate change and air pollution for volatile-mediated plant–parasitoid signalling","authors":"Delia M Pinto-Zevallos, James D Blande","doi":"10.1016/j.cois.2024.101290","DOIUrl":"10.1016/j.cois.2024.101290","url":null,"abstract":"<div><div>Herbivore-induced plant volatiles (HIPVs) are reliable cues that parasitoids can use to locate host patches. Interactions mediated by plant volatile organic compounds (VOCs) are vulnerable to disturbance by predicted climate change and air pollution scenarios. Abiotic stress–induced VOCs may act as false signals to parasitoids. Air pollutants can disrupt signalling by degrading HIPVs at different rates and preventing the perception of olfactory signals by reducing the sensitivity of olfactory receptors or by occluding insect sensillae. As essential components of biological control programmes, efforts should be made to assess how different parasitoid species respond and adapt to HIPVs in predicted scenarios. Since providing parasitoid food sources is a promising practice for boosting biological control, parasitoid–flower interactions deserve attention.</div></div>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"66 ","pages":"Article 101290"},"PeriodicalIF":5.8,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142544294","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-28DOI: 10.1016/j.cois.2024.101292
Susan E Fahrbach
{"title":"Editorial overview: Diverse actions of GABA in insect nervous systems","authors":"Susan E Fahrbach","doi":"10.1016/j.cois.2024.101292","DOIUrl":"10.1016/j.cois.2024.101292","url":null,"abstract":"","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":"67 ","pages":"Article 101292"},"PeriodicalIF":5.8,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142567658","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-27DOI: 10.1016/j.cois.2024.101293
Saheli Sengupta, Kravitz A Edward
Sexually dimorphic behaviors are fundamental to the biology of many species, including fruit flies and humans. These behaviors are regulated primarily by sex-specific neural circuits or the sex-specific modulation of shared neuronal substrates. In fruit flies, GABAergic neurotransmission plays a critical role in governing sexually dimorphic behaviors such as courtship, copulation, and aggression. This review explores the intricate roles of GABAergic neurons in these behaviors, and focuses on how sex-specific differences in GABAergic circuits contribute to their modulation and execution. By examining these mechanisms in Drosophila, we reveal broader implications for understanding sexual dimorphism in more complex organisms.
{"title":"Decoding Sex Differences: How GABA Shapes Drosophila Behavior.","authors":"Saheli Sengupta, Kravitz A Edward","doi":"10.1016/j.cois.2024.101293","DOIUrl":"https://doi.org/10.1016/j.cois.2024.101293","url":null,"abstract":"<p><p>Sexually dimorphic behaviors are fundamental to the biology of many species, including fruit flies and humans. These behaviors are regulated primarily by sex-specific neural circuits or the sex-specific modulation of shared neuronal substrates. In fruit flies, GABAergic neurotransmission plays a critical role in governing sexually dimorphic behaviors such as courtship, copulation, and aggression. This review explores the intricate roles of GABAergic neurons in these behaviors, and focuses on how sex-specific differences in GABAergic circuits contribute to their modulation and execution. By examining these mechanisms in Drosophila, we reveal broader implications for understanding sexual dimorphism in more complex organisms.</p>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":" ","pages":"101293"},"PeriodicalIF":5.8,"publicationDate":"2024-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142544295","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-25DOI: 10.1016/j.cois.2024.101288
Hua Yan
Insects represent the most diverse group of animals in the world. While the olfactory systems of different species share general principles of organization, they also exhibit a wide range of structural and functional diversity. Scientists have gained tremendous insight into olfactory neural development and function, notably in Drosophila, but also in other insect species (see reviews in [1-3]). In the last few years, new evidence has steadily mounted, e.g. the stoichiometry of odorant receptor and co-receptor (OR-Orco) complex. This review aims to highlight the recent progress on four aspects: (1) the structure and function of the OR-Orco complex, (2) chemosensory gene co-expression, (3) diverse neural developmental processes, and (4) the role of genes and neurons in olfactory development and olfactory-mediated behavior.
{"title":"Insect olfactory neurons: receptors, development and function.","authors":"Hua Yan","doi":"10.1016/j.cois.2024.101288","DOIUrl":"https://doi.org/10.1016/j.cois.2024.101288","url":null,"abstract":"<p><p>Insects represent the most diverse group of animals in the world. While the olfactory systems of different species share general principles of organization, they also exhibit a wide range of structural and functional diversity. Scientists have gained tremendous insight into olfactory neural development and function, notably in Drosophila, but also in other insect species (see reviews in [1-3]). In the last few years, new evidence has steadily mounted, e.g. the stoichiometry of odorant receptor and co-receptor (OR-Orco) complex. This review aims to highlight the recent progress on four aspects: (1) the structure and function of the OR-Orco complex, (2) chemosensory gene co-expression, (3) diverse neural developmental processes, and (4) the role of genes and neurons in olfactory development and olfactory-mediated behavior.</p>","PeriodicalId":11038,"journal":{"name":"Current opinion in insect science","volume":" ","pages":"101288"},"PeriodicalIF":5.8,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142567705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}