蜜蜂群中昼夜节律钟信息的集体流动

Julia Mellert, Weronika Kłos, David Michael Dormagen, Benjamin Wild, Adrian Zachariae, Michael L. Smith, C. Giovanni Galizia, Tim Landgraf
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摘要

蜜蜂群表现出集体的昼夜节律,反映了环境的周期性动态。成千上万的工蜂,包括在蜂巢内工作的工蜂,必须在各种过程中同步,这些过程可能是节律性的,如花蜜流入,也可能是非节律性的,如育雏,但这些不同的节律如何整合成蜂群水平的昼夜节律仍是未知数。利用人工智能驱动的自动跟踪系统,我们对两个蜜蜂蜂群中的所有个体进行了不间断的长期跟踪。我们的研究表明,昼夜节律存在于所有年龄组,而且这种节律已融入所有个体,但是,离入口最远的工蜂的活动峰值最多会偏移 2 个小时。广泛的数据分析和基于代理的模型表明,个体之间的机械互动促进了运动速度的传递,从而促进了 "昼夜节律 "信息的传递。最后,我们证明,这种速度传递会导致从巢穴入口处开始的集体慢波活动,并扩散到整个巢穴。这种简单的机制--工蜂相互碰撞--使蜂群能够根据外部环境的日周期调整自己的节奏,而且由于巢穴的空间组织,不同的工蜂群会依次活动。速度传递互动展示了一种紧密调整的机制,凸显了超级有机体优雅的自组织能力。
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Collective flow of circadian clock information in honeybee colonies
Honeybee colonies exhibit a collective circadian rhythm reflecting the periodic dynamics of the environment. Thousands of workers, including those engaged in in-hive tasks, must synchronize in various processes that may be rhythmic, such as nectar inflows, or non-rhythmic, such as brood care but it remains unknown how those different rhythms are integrated into a colony-level circadian rhythm. Using an AI-driven automated tracking system, we obtained uninterrupted long-term tracking of all individuals in two honeybee colonies. We demonstrate that circadian rhythmicity is present across all age groups and that this rhythm is entrained into all individuals, however, with peak activity shifting by up to 2 hours in workers furthest from the entrance. Extensive data analysis and an agent-based model suggest that mechanical interactions between individuals facilitate the transfer of movement speed, and hence Zeitgeber information. Finally, we show that this speed transfer leads to a collective slow wave of activity that initiates at the nest entrance, spreading throughout the nest. This simple mechanism, workers bumping into each other, enables colonies to entrain their rhythm to the daily cycle of the external environment and, because of the spatial organization of the nest, activates different groups of workers sequentially. The speed transfer interactions demonstrate a tightly-tuned mechanism that underlines the elegant self-organization of the superorganism.
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