• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

寻找未来的生物防治剂:跗线螨类中后胸沟的比较功能。

Looking for future biological control agents: the comparative function of the deutosternal groove in mesostigmatid mites.

机构信息

Mathematical Institute, University of Oxford, Oxford, OX2 6GG, UK.

出版信息

Exp Appl Acarol. 2023 Oct;91(2):139-235. doi: 10.1007/s10493-023-00832-0. Epub 2023 Sep 7.

DOI:10.1007/s10493-023-00832-0
PMID:37676375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10562343/
Abstract

The physics of fluid laminar flow through an idealised deutosternum assembly is used for the first time to review predatory feeding designs over 72 different-sized example species from 16 mesostigmatid families in order to inform the finding of new biological control agents. Gnathosomal data are digitised from published sources. Relevant gnathosomal macro- and micro-features are compared and contrasted in detail which may subtly impact the control of channel- or 'pipe'-based transport of prey liquids around various gnathosomal locations. Relative deutosternal groove width on the mesostigmatid subcapitulum is important but appears unrelated to the closing velocity ratio of the moveable digit. Big mites are adapted for handling large and watery prey. The repeated regular distance between deutosternal transverse ridges ('Querleisten') supports the idea of them enabling a regular fluctuating bulging or pulsing droplet-based fluid wave 'sticking' and 'slipping' along the groove. Phytoseiids are an outlier functional group with a low deutosternal pipe flow per body size designed for slot-like microchannel transport in low volume fluid threads arising from daintily nibbling nearby prey klinorhynchidly. Deutosternal groove denticles are orientated topographically in order to synergise flow and possible mixing of coxal gland-derived droplets and circumcapitular reservoir fluids across the venter of the gnathosomal base back via the hypostome to the prey being masticated by the chelicerae. As well as working with the tritosternum to mechanically clean the deutosternum, denticles may suppress fluid drag. Shallow grooves may support edge-crawling viscous flow. Lateral features may facilitate handling unusual amounts of fluid arising from opportunistic feeding on atypical prey. Various conjectures for confirmatory follow-up are highlighted. Suggestions as to how to triage non-uropodoid species as candidate plant pest control agents are included.

摘要

首次利用理想的二盾胸节组件中的层流流体物理学来回顾 72 种不同大小的 16 个中气门目科的捕食性进食设计,以寻找新的生物防治剂。从已发表的资料中数字化了关节的数据。详细比较和对比了相关的关节宏观和微观特征,这些特征可能会微妙地影响到围绕各种关节位置的通道或“管道”式猎物液体输送的控制。在中气门亚头壳上相对的二盾胸节槽的宽度很重要,但与可动指的关闭速度比无关。大螨类适应处理大而多汁的猎物。二盾胸节横脊(“ Querleisten ”)之间重复的规则距离支持了它们能够使规则波动的凸起或脉冲液滴基流体波“粘住”和“滑动”沿着槽的想法。植绥螨是一个功能异常的功能群,其低二盾胸节管流设计用于低体积流体线中的狭缝状微通道输送,这些流体线源自小心翼翼地小口啃食附近猎物 klinorhynchidly。二盾胸节槽小齿在地形上定向,以便协同流动和可能的混合coxal 腺衍生的液滴和围绕头壳基部腹面的环头腔储液器流体,通过口后板返回正在被螯肢咀嚼的猎物。小齿除了与三盾胸节一起机械清洁二盾胸节外,还可能抑制流体阻力。浅槽可能支持边缘爬行粘性流。侧向特征可能有助于处理由于机会性捕食非典型猎物而产生的异常量的流体。突出强调了各种可供证实的后续研究的推测。还包括如何将非跗节类物种作为候选植物害虫防治剂进行分类的建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/1c561aa10db2/10493_2023_832_Fig30_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/31b14b721864/10493_2023_832_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/ffdf6b60ba28/10493_2023_832_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/647dba365783/10493_2023_832_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/dba4f44a1dc7/10493_2023_832_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/8a3f960a9aa6/10493_2023_832_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/997d2228ae28/10493_2023_832_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/cd52e51b2dfe/10493_2023_832_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c683a30f27f9/10493_2023_832_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/38fe9ab289b6/10493_2023_832_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/40dc7f3b1247/10493_2023_832_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c9c92c80ce33/10493_2023_832_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c21fc69f5770/10493_2023_832_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/1a32c09c8808/10493_2023_832_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/967b4f1e2748/10493_2023_832_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/1ae153a7ff19/10493_2023_832_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/4129ac48b4be/10493_2023_832_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/e75d8233b994/10493_2023_832_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/2856088216be/10493_2023_832_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/df4c6a80d00b/10493_2023_832_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/95263aa054a9/10493_2023_832_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/176a5788f8a8/10493_2023_832_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/e537766b9061/10493_2023_832_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/9af885a41ad1/10493_2023_832_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/584bd7c32f29/10493_2023_832_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/2376a6fd0514/10493_2023_832_Fig25_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c53a784c0126/10493_2023_832_Fig26_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/35f0408098bb/10493_2023_832_Fig27_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/8d7879219480/10493_2023_832_Fig28_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/971ab004ddc7/10493_2023_832_Fig29_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/1c561aa10db2/10493_2023_832_Fig30_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/31b14b721864/10493_2023_832_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/ffdf6b60ba28/10493_2023_832_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/647dba365783/10493_2023_832_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/dba4f44a1dc7/10493_2023_832_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/8a3f960a9aa6/10493_2023_832_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/997d2228ae28/10493_2023_832_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/cd52e51b2dfe/10493_2023_832_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c683a30f27f9/10493_2023_832_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/38fe9ab289b6/10493_2023_832_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/40dc7f3b1247/10493_2023_832_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c9c92c80ce33/10493_2023_832_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c21fc69f5770/10493_2023_832_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/1a32c09c8808/10493_2023_832_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/967b4f1e2748/10493_2023_832_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/1ae153a7ff19/10493_2023_832_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/4129ac48b4be/10493_2023_832_Fig16_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/e75d8233b994/10493_2023_832_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/2856088216be/10493_2023_832_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/df4c6a80d00b/10493_2023_832_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/95263aa054a9/10493_2023_832_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/176a5788f8a8/10493_2023_832_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/e537766b9061/10493_2023_832_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/9af885a41ad1/10493_2023_832_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/584bd7c32f29/10493_2023_832_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/2376a6fd0514/10493_2023_832_Fig25_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/c53a784c0126/10493_2023_832_Fig26_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/35f0408098bb/10493_2023_832_Fig27_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/8d7879219480/10493_2023_832_Fig28_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/971ab004ddc7/10493_2023_832_Fig29_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fda/10562343/1c561aa10db2/10493_2023_832_Fig30_HTML.jpg

相似文献

1
Looking for future biological control agents: the comparative function of the deutosternal groove in mesostigmatid mites.寻找未来的生物防治剂:跗线螨类中后胸沟的比较功能。
Exp Appl Acarol. 2023 Oct;91(2):139-235. doi: 10.1007/s10493-023-00832-0. Epub 2023 Sep 7.
2
Feeding design in free-living mesostigmatid chelicerae (Acari: Anactinotrichida).自由生活的中气门目(蜱螨亚纲:Actinotrichida)螯肢的取食设计。
Exp Appl Acarol. 2021 May;84(1):1-119. doi: 10.1007/s10493-021-00612-8. Epub 2021 Apr 30.
3
Cheliceral chelal design in free-living astigmatid mites.自由生活的粗脚盲蝽中螯肢的螯肢器设计。
Exp Appl Acarol. 2021 Jun;84(2):271-363. doi: 10.1007/s10493-021-00625-3. Epub 2021 May 14.
4
Evidence of Amblyseius largoensis and Euseius alatus as biological control agent of Aceria guerreronis.拉哥钝绥螨和翼钝绥螨作为咖啡刺皮瘿螨生物防治剂的证据。
Exp Appl Acarol. 2015 Nov;67(3):411-21. doi: 10.1007/s10493-015-9963-7. Epub 2015 Aug 9.
5
Potential of astigmatid mites (Acari: Astigmatina) as prey for rearing edaphic predatory mites of the families Laelapidae and Rhodacaridae (Acari: Mesostigmata).粉螨(蜱螨亚纲:粉螨目)作为饲养厉螨科和罗德螨科(蜱螨亚纲:中气门目)土壤捕食性螨类猎物的潜力。
Exp Appl Acarol. 2016 Jul;69(3):289-96. doi: 10.1007/s10493-016-0043-4. Epub 2016 Apr 26.
6
Does Long-Term Feeding on Alternative Prey Affect the Biological Performance of Neoseiulus barkeri (Acari: Phytoseiidae) on the Target Spider Mites?长期以替代猎物为食会影响巴氏新小绥螨(蜱螨亚纲:植绥螨科)对目标叶螨的生物学性能吗?
J Econ Entomol. 2017 Jun 1;110(3):915-923. doi: 10.1093/jee/tox055.
7
Tracking mite trophic interactions by multiplex PCR.通过多重 PCR 追踪螨类的营养相互作用。
Pest Manag Sci. 2020 Feb;76(2):597-608. doi: 10.1002/ps.5555. Epub 2019 Oct 3.
8
Thus far but no further: predatory mites do not migrate effectively into strawberry plantations.到此为止,不会再有进一步的情况:捕食螨无法有效地迁移到草莓种植园中。
Exp Appl Acarol. 2019 Mar;77(3):359-373. doi: 10.1007/s10493-019-00357-5. Epub 2019 Mar 27.
9
Both host and diet shape bacterial communities of predatory mites.宿主和饮食都会影响捕食性螨虫的细菌群落。
Insect Sci. 2024 Apr;31(2):551-561. doi: 10.1111/1744-7917.13253. Epub 2023 Jul 19.
10
Impact of a tarsonemid prey mite and its fungal diet on the reproductive performance of a predatory mite.捕食螨及其真菌性食物对捕食螨生殖性能的影响。
Exp Appl Acarol. 2021 Mar;83(3):313-323. doi: 10.1007/s10493-021-00594-7. Epub 2021 Feb 15.

引用本文的文献

1
Transecting and contrasting the feeding designs of the astigmatan community from bird nests.剖析并对比鸟巢中散光类群落的觅食设计。
Exp Appl Acarol. 2025 Apr 15;94(3):52. doi: 10.1007/s10493-025-01014-w.
2
Do astigmatid teeth matter: a tribological review of cheliceral chelae in co-occuring mites from UK beehives.散光齿重要吗:对来自英国蜂箱中共存螨虫螯肢的摩擦学综述。
Exp Appl Acarol. 2024 May;92(4):567-686. doi: 10.1007/s10493-023-00876-2. Epub 2024 Apr 19.

本文引用的文献

1
Mouthpart adaptations of antlion larvae facilitate prey handling and fluid feeding in sandy habitats.沙坑捕食者幼虫的口器适应性促进了猎物处理和液体摄取在沙质生境中的进行。
J Exp Biol. 2022 Oct 1;225(19). doi: 10.1242/jeb.244220. Epub 2022 Oct 12.
2
Review: predatory soil mites as biocontrol agents of above- and below-ground plant pests.综述:捕食性土壤螨作为地上和地下植物害虫的生物防治剂。
Exp Appl Acarol. 2022 Jul;87(2-3):143-162. doi: 10.1007/s10493-022-00723-w. Epub 2022 Aug 8.
3
A new species of the genus Proctogastrolaelaps McGraw amp; Farrier (Acari: Melicharidae) from the Far East of Russia, and contributions to knowledge of this genus.
一种来自俄罗斯远东地区的新种 Proctogastrolaelaps McGraw amp; Farrier(蜱螨目:Melicharidae),以及对该属的认识贡献。
Zootaxa. 2021 Dec 1;5072(4):380-388. doi: 10.11646/zootaxa.5072.4.5.
4
Morphology and Surface Properties of Roach Water Transport Arrays.蟑螂水运输阵列的形态学与表面特性
ACS Appl Bio Mater. 2019 Jun 17;2(6):2650-2660. doi: 10.1021/acsabm.9b00318. Epub 2019 May 23.
5
In vitro evaluation of a cysteine protease from poultry red mites, Demanyssus gallinae, as a vaccine antigen for chickens.鸡血红螨(Demanyssus gallinae)半胱氨酸蛋白酶的体外评估作为鸡用疫苗抗原。
Poult Sci. 2022 Mar;101(3):101638. doi: 10.1016/j.psj.2021.101638. Epub 2021 Dec 1.
6
Capillary flow of liquids in open microchannels: overview and recent advances.开放微通道中液体的毛细流动:综述与最新进展
NPJ Microgravity. 2021 Dec 9;7(1):51. doi: 10.1038/s41526-021-00180-6.
7
An energy-efficient pathway to turbulent drag reduction.一种实现湍流减阻的节能途径。
Nat Commun. 2021 Oct 4;12(1):5805. doi: 10.1038/s41467-021-26128-8.
8
Unsaturated hemiwicking dynamics on surfaces with irregular roughness.具有不规则粗糙度表面上的不饱和半芯吸动力学。
J Colloid Interface Sci. 2021 Dec 15;604:104-112. doi: 10.1016/j.jcis.2021.06.175. Epub 2021 Jul 5.
9
Cheliceral chelal design in free-living astigmatid mites.自由生活的粗脚盲蝽中螯肢的螯肢器设计。
Exp Appl Acarol. 2021 Jun;84(2):271-363. doi: 10.1007/s10493-021-00625-3. Epub 2021 May 14.
10
Characterisation of a cysteine protease from poultry red mites and its potential use as a vaccine for chickens.从家禽红螨中鉴定一种半胱氨酸蛋白酶及其作为鸡疫苗的潜在用途。
Parasite. 2021;28:9. doi: 10.1051/parasite/2021005. Epub 2021 Feb 3.