Sex- and Male-Morph-Specific Variation in Brain Mass and Cell Number Scaling in Solitary Centris pallida (Hymenoptera: Apidae) Bees.

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Meghan Barrett, R Keating Godfrey
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引用次数: 0

Abstract

Intraspecific variation in behavior is associated with variable brain resource allocation patterns: There is frequently increased tissue investment in discrete regions that support fitness-relevant cognitive abilities. However, the relationships between tissue volume and actual cell numbers have rarely been explored for insects due to methodological hurdles recently addressed via the application of isotropic fractionation. In solitary desert Centris pallida (Hymenoptera: Apidae) bees, there are two major levels of intraspecific variation: sex (males vs. females) and male morph (as a result of alternative reproductive tactics, large morph and small morph males rely on scent or sight, respectively, for mate location). Using isotropic fractionation, we separately analyzed optic lobe (OL) and central brain (CB) cell numbers of males and females to determine the impacts of sex and morph on brain cell allometry. Female bees' brains were bigger and had higher cell numbers and cell densities than males of the same size. In both sexes, total brain cell number increased with brain size, driven by increases in OL cell numbers. Between male morphs, we found that OL masses were relatively larger in small-morph males, consistent with the relationship between body size and OL volumes reported in prior studies. However, small-morph C. pallida males had fewer total cells (as represented by cell nuclei) and reduced cell density, in their OLs. Together, these data suggest that there is intraspecific and brain-region-specific variation in brain cell numbers and that variation in brain tissue volume may not match other levels of neural organization like brain cell numbers/densities.

孤斑中蜂(膜翅目:蜂科)脑质量和细胞数目的性别和雄性形态特异性变异。
行为的种内变异与大脑资源分配模式的变化有关:在支持健康相关认知能力的离散区域,组织投资经常增加。然而,由于最近通过应用各向同性分馏法解决了方法上的障碍,很少探索昆虫组织体积和实际细胞数量之间的关系。在孤独的沙漠白斑蜜蜂(膜翅目:蜜蜂科)中,有两个主要的种内变异水平:性别(雄性与雌性)和雄性形态(由于不同的繁殖策略,大形态和小形态的雄性分别依靠气味或视觉来寻找配偶)。采用各向同性分选法,分别分析了雄性和雌性的视叶(OL)和中央脑(CB)细胞数量,以确定性别和形态对脑细胞异速生长的影响。雌性蜜蜂的大脑比同等大小的雄性蜜蜂更大,细胞数量和细胞密度也更高。在两性中,由于OL细胞数量的增加,总脑细胞数量随着大脑大小的增加而增加。在雄性形态之间,我们发现小形态雄性的OL质量相对较大,这与先前研究中报道的体型和OL体积之间的关系一致。然而,小形态白桦尺蠖雄性的细胞总数较少(以细胞核为代表),细胞密度降低。总之,这些数据表明,脑细胞数量存在种内和脑区域特异性的变化,脑组织体积的变化可能与脑细胞数量/密度等神经组织的其他水平不匹配。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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