Intrinsic temporal structure and lagged environmental effects shape the dynamics of airborne microscopic eukaryotes.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
So-Yeon Jeong, Chi Won Lee, Tae Gwan Kim
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引用次数: 0

Abstract

Airborne microscopic eukaryotes play important ecological roles, yet their temporal dynamics often appear stochastic and difficult to predict using concurrent meteorological variables. We conducted a high-resolution, 3-year survey of airborne fungi, protists, and metazoa in a temperate urban environment using quantitative PCR and amplicon sequencing. Seasonality varied markedly among groups: fungi and metazoa exhibited distinct annual cycles (peaking in late summer and winter, respectively), while protists displayed stochastic fluctuations. Taxonomically, fungi were dominated by soil- and plant-associated taxa (e.g., Cladosporium), protists by aquatic and terrestrial taxa (e.g., Phytophthora), and metazoa by DNA from mammals and insects. Static (i.e., contemporaneous, non-time lagged) analyses based on correlation and multiple linear regression identified concurrent environmental associations but explained only a limited proportion of the variance (28%, 6%, and 14% for fungi, protists, and metazoa, respectively). In contrast, incorporating time-lagged effects using Granger causality and autoregressive integrated moving average with exogenous variables (ARIMAX) substantially improved explanatory power, accounting for up to 47% of the variance for fungi and ~29% for protists and metazoa. These improvements primarily reflected intrinsic temporal dependence, indicating that antecedent biological states and prior environmental conditions contributed to eukaryotic abundances. Our results suggest that relying solely on concurrent meteorology is insufficient, whereas integrating temporal dependence and lagged environmental effects provides a robust framework for predicting airborne eukaryotic dynamics.IMPORTANCEAirborne microscopic eukaryotes influence ecosystems, agriculture, and human health, yet their temporal behavior in the atmosphere remains poorly understood and difficult to predict. Using a 3-year, high-resolution survey, this study shows that different airborne eukaryotic groups follow fundamentally different temporal rules. Airborne fungi, dominated by plant- and soil-associated taxa such as Cladosporium, and animal-derived metazoan material exhibit clear and contrasting seasonal cycles, whereas protists, including the plant pathogen Phytophthora, fluctuate irregularly. Importantly, models based only on current weather conditions explain little of this variability. By incorporating biological memory and delayed environmental effects, time-series models substantially improve predictability across all groups. These findings demonstrate that airborne eukaryotes respond not only to present conditions but also to prior environmental states, providing a more realistic framework for forecasting bioaerosols relevant to ecosystem connectivity, plant disease spread, and air-quality risk assessment.

内在的时间结构和滞后的环境效应塑造了空气中微观真核生物的动力学。
空气中微小的真核生物发挥着重要的生态作用,但它们的时间动态往往是随机的,难以用同步的气象变量来预测。我们利用定量PCR和扩增子测序技术对温带城市环境中空气传播的真菌、原生生物和后生动物进行了为期3年的高分辨率调查。不同类群之间的季节性差异显著:真菌和后生动物表现出明显的年周期(分别在夏末和冬季达到峰值),而原生动物表现出随机波动。在分类学上,真菌以土壤和植物相关的分类群(如枝孢菌)为主,原生生物以水生和陆生分类群(如疫霉)为主,后生动物以哺乳动物和昆虫的DNA为主。基于相关性和多元线性回归的静态(即同期,非时间滞后)分析确定了并发环境关联,但只能解释有限比例的方差(真菌,原生生物和后生动物分别为28%,6%和14%)。相比之下,使用格兰杰因果关系和自回归外生变量综合移动平均(ARIMAX)纳入时间滞后效应大大提高了解释力,对真菌的解释高达47%,对原生生物和后生动物的解释约为29%。这些改进主要反映了内在的时间依赖性,表明先前的生物状态和先前的环境条件有助于真核生物丰度。我们的研究结果表明,仅仅依靠同步气象学是不够的,而整合时间依赖性和滞后环境效应为预测空气真核生物动力学提供了一个强大的框架。空气中的微观真核生物影响着生态系统、农业和人类健康,但它们在大气中的时间行为仍然知之甚少,难以预测。通过一项为期3年的高分辨率调查,这项研究表明,不同的空气真核生物群体遵循着根本不同的时间规则。空气传播的真菌,主要是植物和土壤相关的类群,如枝孢菌,以及动物衍生的后生动物材料,表现出清晰而鲜明的季节周期,而原生生物,包括植物病原体疫霉,波动不规则。重要的是,仅基于当前天气条件的模型几乎不能解释这种变化。通过结合生物记忆和延迟的环境影响,时间序列模型大大提高了所有群体的可预测性。这些发现表明,空气中的真核生物不仅对当前条件有反应,而且对先前的环境状态也有反应,为预测与生态系统连通性、植物疾病传播和空气质量风险评估相关的生物气溶胶提供了一个更现实的框架。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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