INSIGHTS OF CASTE DETERMINATIONS IN SOCIAL INSECTS

Md. Mamunur Rahman, Shazzad Hossain, G. M. Riaz, H. Rahman
{"title":"INSIGHTS OF CASTE DETERMINATIONS IN SOCIAL INSECTS","authors":"Md. Mamunur Rahman, Shazzad Hossain, G. M. Riaz, H. Rahman","doi":"10.26480/asm.02.2022.48.54","DOIUrl":null,"url":null,"abstract":"Eusocial insects display caste structures in which reproductive ability is possessed by a single or a few queens while all other colony members act as workers. In social insects like ants, bees, and termites, vital physiological processes are regulated at the colony scale. Females in social insects have at least one reproductive caste and one nonreproductive caste; many termites have at least two male castes. The castes have considerable anatomical, physiological, and behavioural differences in higher social insects. Organismal systems, such as pheromone sensing, hormone signaling, and brain signaling pathways, are deployed in novel circumstances to impact nestmate and colony behaviours due to physiological decentralization over evolutionary time. Significant morphogenesis with region-specific cellular proliferation and degradation occurs during soldier development through two moulting via a presoldier stage in termite. JH action has been developed, in which a high JH titer causes soldier differentiation and a low JH titer causes alate differentiation. A monogamous pair of primary reproductives (one king and one queen) generated from alates normally establishes termite colonies (winged adults). The nymph-alate pathway (sexual pathway) or the worker pathway differentiates larvae in Reticulitermes termites (neuter pathway). Haplo-diploid sex determination controls the first developmental transition, in which unfertilized (haploid) embryos become males and fertilized (diploid) embryos become females in the case of Cataglyphis ant genus. The queen’s mandibular gland secretion, a mix of fatty acids and aromatic chemicals, is critical for maintaining the reproductive division of labour in honeybees (Apis mellifera), suppressing ovary growth in workers. Besides this, the brood produced by the queen also inhibits ovary development in workers by emitting two pheromones: the brood pheromone (BP), mainly composed of esters, and the highly volatile E-b-ocimene.","PeriodicalId":53069,"journal":{"name":"Acta Scientifica Malaysia","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Scientifica Malaysia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26480/asm.02.2022.48.54","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Eusocial insects display caste structures in which reproductive ability is possessed by a single or a few queens while all other colony members act as workers. In social insects like ants, bees, and termites, vital physiological processes are regulated at the colony scale. Females in social insects have at least one reproductive caste and one nonreproductive caste; many termites have at least two male castes. The castes have considerable anatomical, physiological, and behavioural differences in higher social insects. Organismal systems, such as pheromone sensing, hormone signaling, and brain signaling pathways, are deployed in novel circumstances to impact nestmate and colony behaviours due to physiological decentralization over evolutionary time. Significant morphogenesis with region-specific cellular proliferation and degradation occurs during soldier development through two moulting via a presoldier stage in termite. JH action has been developed, in which a high JH titer causes soldier differentiation and a low JH titer causes alate differentiation. A monogamous pair of primary reproductives (one king and one queen) generated from alates normally establishes termite colonies (winged adults). The nymph-alate pathway (sexual pathway) or the worker pathway differentiates larvae in Reticulitermes termites (neuter pathway). Haplo-diploid sex determination controls the first developmental transition, in which unfertilized (haploid) embryos become males and fertilized (diploid) embryos become females in the case of Cataglyphis ant genus. The queen’s mandibular gland secretion, a mix of fatty acids and aromatic chemicals, is critical for maintaining the reproductive division of labour in honeybees (Apis mellifera), suppressing ovary growth in workers. Besides this, the brood produced by the queen also inhibits ovary development in workers by emitting two pheromones: the brood pheromone (BP), mainly composed of esters, and the highly volatile E-b-ocimene.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
群居昆虫种姓决定的洞见
群居昆虫表现出种姓结构,在这种结构中,繁殖能力由一个或几个蜂王拥有,而所有其他群体成员都是工蜂。在蚂蚁、蜜蜂和白蚁等群居昆虫中,重要的生理过程是在群体规模上进行调节的。群居昆虫中的雌性至少有一个生殖阶层和一个非生殖阶层;许多白蚁至少有两个雄性种姓。在高等社会昆虫中,种姓有相当大的解剖、生理和行为差异。生物系统,如信息素传感、激素信号和大脑信号通路,在新的环境中被部署,以影响由于进化时间的生理分散的巢和群体行为。白蚁士兵发育过程中发生了显著的形态发生,具有区域特异性的细胞增殖和降解。JH作用已经发展,其中高JH滴度导致士兵分化,低JH滴度导致盐分化。由白蚁产生的一对一夫一妻制初级繁殖体(一个国王和一个王后)通常建立白蚁群落(有翅膀的成年白蚁)。白蚁幼虫的分化有雌雄途径(性途径)和工蜂途径(中性途径)。单倍体-二倍体性别决定控制着第一次发育转变,在此过程中,未受精的(单倍体)胚胎变成雄性,而受精的(二倍体)胚胎变成雌性。蜂王的下颌腺分泌一种脂肪酸和芳香化学物质的混合物,对维持蜜蜂(Apis mellifera)的生殖分工至关重要,抑制工蜂卵巢的生长。除此之外,蜂王所产的幼虫还通过释放两种信息素来抑制工蜂卵巢的发育:一种是主要由酯类组成的幼虫信息素(BP),另一种是挥发性很强的E-b-ocimene。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
12 weeks
期刊最新文献
INFLUENCE OF CANOPY TYPES ON NUTRIENT AVAILABILITY IN SOIL AND LITTER POOLS OF A FOREST ECOSYSTEM ALLELOPATHIC RESPONSE OF ROOT EXUDATES OF FIVE COMMON WEEDS IN YARD LONG BEAN (VIGNA UNGUICULATA SUBSP. SESQUIPEDALIS L. VERD] AND MAIZE (ZEA MAYS L.) GREEN SYNTHESIS APPROACH, CHARACTERIZATION, AND APPLICATIONS OF MgO NANO PARTICLES USING CURRY LEAF (MURRAYA KOENIGII) MAGNETORECEPTION IN FRUIT FLIES, BEES AND ANTS A REVIEW OF GROUP B STREPTOCOCCUS (GBS) VAGINAL COLONIZATION AND ASCENDING INTRAUTERINE INFECTION: INTERACTION BETWEEN HOST IMMUNE RESPONSES AND GBS VIRULENCE FACTORS
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1