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StellarPath: Hierarchical-vertical multi-omics classifier synergizes stable markers and interpretable similarity networks for patient profiling StellarPath:层次-垂直多组学分类器协同稳定标记物和可解释的相似性网络,用于患者特征分析
IF 4.3 2区 生物学 Pub Date : 2024-04-01 DOI: 10.1371/journal.pcbi.1012022
Luca Giudice, Ahmed Mohamed, T. Malm
The Patient Similarity Network paradigm implies modeling the similarity between patients based on specific data. The similarity can summarize patients’ relationships from high-dimensional data, such as biological omics. The end PSN can undergo un/supervised learning tasks while being strongly interpretable, tailored for precision medicine, and ready to be analyzed with graph-theory methods. However, these benefits are not guaranteed and depend on the granularity of the summarized data, the clarity of the similarity measure, the complexity of the network’s topology, and the implemented methods for analysis. To date, no patient classifier fully leverages the paradigm’s inherent benefits. PSNs remain complex, unexploited, and meaningless. We present StellarPath, a hierarchical-vertical patient classifier that leverages pathway analysis and patient similarity concepts to find meaningful features for both classes and individuals. StellarPath processes omics data, hierarchically integrates them into pathways, and uses a novel similarity to measure how patients’ pathway activity is alike. It selects biologically relevant molecules, pathways, and networks, considering molecule stability and topology. A graph convolutional neural network then predicts unknown patients based on known cases. StellarPath excels in classification performances and computational resources across sixteen datasets. It demonstrates proficiency in inferring the class of new patients described in external independent studies, following its initial training and testing phases on a local dataset. It advances the PSN paradigm and provides new markers, insights, and tools for in-depth patient profiling.
患者相似性网络范式意味着根据特定数据对患者之间的相似性进行建模。这种相似性可以从生物组学等高维数据中总结出患者之间的关系。最终的患者相似性网络可以完成非监督/监督学习任务,同时具有很强的可解释性,适合精准医疗,并可随时使用图论方法进行分析。然而,这些优势并不能保证,它们取决于汇总数据的粒度、相似性度量的清晰度、网络拓扑结构的复杂性以及实施的分析方法。迄今为止,还没有一种病人分类器能充分利用这种模式的固有优势。PSN仍然是复杂的、未开发的和无意义的。我们介绍的 StellarPath 是一种分层垂直患者分类器,它利用路径分析和患者相似性概念,为类别和个体寻找有意义的特征。StellarPath 处理全息数据,将其分层整合到通路中,并使用新颖的相似性来衡量患者通路活动的相似性。它在考虑分子稳定性和拓扑结构的基础上,选择与生物相关的分子、通路和网络。然后,图卷积神经网络会根据已知病例预测未知患者。StellarPath 在 16 个数据集的分类性能和计算资源方面表现出色。在本地数据集的初始训练和测试阶段之后,它能熟练推断外部独立研究中描述的新患者类别。它推动了 PSN 模式的发展,并为深入的患者特征分析提供了新的标记、见解和工具。
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引用次数: 0
Optimizing strategies for slowing the spread of invasive species 优化减缓入侵物种扩散的战略
IF 4.3 2区 生物学 Pub Date : 2024-04-01 DOI: 10.1371/journal.pcbi.1011996
Adam Lampert
Invasive species are spreading worldwide, causing damage to ecosystems, biodiversity, agriculture, and human health. A major question is, therefore, how to distribute treatment efforts cost-effectively across space and time to prevent or slow the spread of invasive species. However, finding optimal control strategies for the complex spatial-temporal dynamics of populations is complicated and requires novel methodologies. Here, we develop a novel algorithm that can be applied to various population models. The algorithm finds the optimal spatial distribution of treatment efforts and the optimal propagation speed of the target species. We apply the algorithm to examine how the results depend on the species’ demography and response to the treatment method. In particular, we analyze (1) a generic model and (2) a detailed model for the management of the spongy moth in North America to slow its spread via mating disruption. We show that, when utilizing optimization approaches to contain invasive species, significant improvements can be made in terms of cost-efficiency. The methodology developed here offers a much-needed tool for further examination of optimal strategies for additional cases of interest.
入侵物种正在全球蔓延,对生态系统、生物多样性、农业和人类健康造成破坏。因此,一个主要问题是如何在空间和时间上经济有效地分配处理工作,以防止或减缓入侵物种的扩散。然而,为复杂的种群时空动态寻找最佳控制策略非常复杂,需要新颖的方法。在此,我们开发了一种可应用于各种种群模型的新型算法。该算法能找到治疗工作的最佳空间分布和目标物种的最佳传播速度。我们应用该算法来研究结果如何取决于物种的种群结构和对处理方法的反应。特别是,我们分析了(1)一个通用模型和(2)一个管理北美海绵蛾的详细模型,以通过破坏交配来减缓其传播速度。我们的研究表明,在利用优化方法控制入侵物种时,可以显著提高成本效益。本文所开发的方法为进一步研究其他相关案例的优化策略提供了亟需的工具。
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引用次数: 0
Indirect reciprocity with Bayesian reasoning and biases 间接互惠与贝叶斯推理和偏见
IF 4.3 2区 生物学 Pub Date : 2024-04-01 DOI: 10.1371/journal.pcbi.1011979
Bryce Morsky, Joshua B Plotkin, Erol Akçay
Reputations can foster cooperation by indirect reciprocity: if I am good to you then others will be good to me. But this mechanism for cooperation in one-shot interactions only works when people agree on who is good and who is bad. Errors in actions or assessments can produce disagreements about reputations, which can unravel the positive feedback loop between social standing and pro-social behaviour. Cooperators can end up punished and defectors rewarded. Public reputation systems and empathy are two possible mechanisms to promote agreement about reputations. Here we suggest an alternative: Bayesian reasoning by observers. By taking into account the probabilities of errors in action and observation and their prior beliefs about the prevalence of good people in the population, observers can use Bayesian reasoning to determine whether or not someone is good. To study this scenario, we develop an evolutionary game theoretical model in which players use Bayesian reasoning to assess reputations, either publicly or privately. We explore this model analytically and numerically for five social norms (Scoring, Shunning, Simple Standing, Staying, and Stern Judging). We systematically compare results to the case when agents do not use reasoning in determining reputations. We find that Bayesian reasoning reduces cooperation relative to non-reasoning, except in the case of the Scoring norm. Under Scoring, Bayesian reasoning can promote coexistence of three strategic types. Additionally, we study the effects of optimistic or pessimistic biases in individual beliefs about the degree of cooperation in the population. We find that optimism generally undermines cooperation whereas pessimism can, in some cases, promote cooperation.
声誉可以通过间接互惠促进合作:如果我对你好,那么其他人也会对我好。但是,只有当人们对谁好谁坏达成一致时,这种一次性互动中的合作机制才会起作用。行动或评估中的错误会导致对声誉的分歧,从而破坏社会地位和亲社会行为之间的正反馈循环。合作者最终会受到惩罚,而叛逃者则会得到奖励。公共声誉系统和同理心是促进就声誉达成一致的两种可能机制。在此,我们提出了一种替代方案:观察者的贝叶斯推理。通过考虑行动和观察中的错误概率,以及他们对人群中好人比例的先验信念,观察者可以使用贝叶斯推理来判断某人是否是好人。为了研究这种情况,我们建立了一个进化博弈理论模型,在这个模型中,参与者可以公开或私下使用贝叶斯推理来评估声誉。我们针对五种社会规范(打分、回避、简单站队、逗留和严厉评判)对这一模型进行了分析和数值探索。我们将结果与代理人在确定声誉时不使用推理的情况进行了系统比较。我们发现,相对于不推理的情况,贝叶斯推理减少了合作,但 "打分 "规范除外。在评分规范下,贝叶斯推理可以促进三种战略类型的共存。此外,我们还研究了个人对群体合作程度的乐观或悲观偏差的影响。我们发现,乐观主义通常会破坏合作,而悲观主义在某些情况下会促进合作。
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引用次数: 0
DBDNMF: A Dual Branch Deep Neural Matrix Factorization method for drug response prediction DBDNMF:用于药物反应预测的双分支深度神经矩阵因式分解方法
IF 4.3 2区 生物学 Pub Date : 2024-04-01 DOI: 10.1371/journal.pcbi.1012012
Hui Liu, Feng Wang, Jian Yu, Yong Pan, Chaoju Gong, Liang Zhang, Lin Zhang
Anti-cancer response of cell lines to drugs is in urgent need for individualized precision medical decision-making in the era of precision medicine. Measurements with wet-experiments is time-consuming and expensive and it is almost impossible for wide ranges of application. The design of computational models that can precisely predict the responses between drugs and cell lines could provide a credible reference for further research. Existing methods of response prediction based on matrix factorization or neural networks have revealed that both linear or nonlinear latent characteristics are applicable and effective for the precise prediction of drug responses. However, the majority of them consider only linear or nonlinear relationships for drug response prediction. Herein, we propose a Dual Branch Deep Neural Matrix Factorization (DBDNMF) method to address the above-mentioned issues. DBDNMF learns the latent representation of drugs and cell lines through flexible inputs and reconstructs the partially observed matrix through a series of hidden neural network layers. Experimental results on the datasets of Cancer Cell Line Encyclopedia (CCLE) and Genomics of Drug Sensitivity in Cancer (GDSC) show that the accuracy of drug prediction exceeds state-of-the-art drug response prediction algorithms, demonstrating its reliability and stability. The hierarchical clustering results show that drugs with similar response levels tend to target similar signaling pathway, and cell lines coming from the same tissue subtype tend to share the same pattern of response, which are consistent with previously published studies.
在精准医疗时代,细胞系对药物的抗癌反应迫切需要个性化的精准医疗决策。湿法实验测量耗时长、成本高,而且几乎不可能广泛应用。设计能精确预测药物与细胞系之间反应的计算模型,可为进一步的研究提供可靠的参考。现有的基于矩阵因式分解或神经网络的反应预测方法表明,线性或非线性潜特征都适用于药物反应的精确预测,且效果显著。然而,大多数方法仅考虑药物反应预测中的线性或非线性关系。在此,我们提出一种双分支深度神经矩阵因式分解(DBDNMF)方法来解决上述问题。DBDNMF 通过灵活的输入学习药物和细胞系的潜在表征,并通过一系列隐藏的神经网络层重建部分观察到的矩阵。在癌症细胞系百科全书(CCLE)和癌症药物敏感性基因组学(GDSC)数据集上的实验结果表明,药物预测的准确性超过了最先进的药物反应预测算法,证明了其可靠性和稳定性。分层聚类结果表明,具有相似反应水平的药物往往针对相似的信号通路,来自相同组织亚型的细胞系往往具有相同的反应模式,这与之前发表的研究结果一致。
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引用次数: 0
Mathematical model for the role of multiple pericentromeric repeats on heterochromatin assembly 多中心染色体周围重复序列对异染色质组装作用的数学模型
IF 4.3 2区 生物学 Pub Date : 2024-04-01 DOI: 10.1371/journal.pcbi.1012027
P. Ghimire, Mo Motamedi, Richard Joh
Although the length and constituting sequences for pericentromeric repeats are highly variable across eukaryotes, the presence of multiple pericentromeric repeats is one of the conserved features of the eukaryotic chromosomes. Pericentromeric heterochromatin is often misregulated in human diseases, with the expansion of pericentromeric repeats in human solid cancers. In this article, we have developed a mathematical model of the RNAi-dependent methylation of H3K9 in the pericentromeric region of fission yeast. Our model, which takes copy number as an explicit parameter, predicts that the pericentromere is silenced only if there are many copies of repeats. It becomes bistable or desilenced if the copy number of repeats is reduced. This suggests that the copy number of pericentromeric repeats alone can determine the fate of heterochromatin silencing in fission yeast. Through sensitivity analysis, we identified parameters that favor bistability and desilencing. Stochastic simulation shows that faster cell division and noise favor the desilenced state. These results show the unexpected role of pericentromeric repeat copy number in gene silencing and provide a quantitative basis for how the copy number allows or protects repetitive and unique parts of the genome from heterochromatin silencing, respectively.
虽然真核生物中中心周重复序列的长度和构成序列差异很大,但多个中心周重复序列的存在是真核染色体的保守特征之一。围中心染色质异染色质在人类疾病中经常被误调,人类实体癌中的围中心染色质重复序列会扩大。在这篇文章中,我们建立了一个裂殖酵母围中心染色质区 H3K9 的 RNAi- 依赖性甲基化数学模型。我们的模型将拷贝数作为一个明确的参数,预测只有当重复拷贝数很多时,周室才会沉默。如果重复序列的拷贝数减少,它就会变得双稳态或沉默。这表明,仅中心染色体周围重复序列的拷贝数就能决定裂殖酵母中异染色质沉默的命运。通过敏感性分析,我们确定了有利于双稳态和去沉默的参数。随机模拟显示,更快的细胞分裂和噪声有利于去沉默状态。这些结果表明了近中心染色体重复拷贝数在基因沉默中所起的意想不到的作用,并为拷贝数如何分别允许或保护基因组的重复部分和独特部分免受异染色质沉默提供了定量依据。
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引用次数: 0
Ten simple rules for leading a successful undergraduate-intensive research lab 成功领导本科生密集型研究实验室的十条简单规则
IF 4.3 2区 生物学 Pub Date : 2024-04-01 DOI: 10.1371/journal.pcbi.1011994
Kje Hickman, Geoffrey L. Zahn
Participating in mentored research is an enormous benefit to undergraduate students. These immersive experiences can dramatically improve retention and completion rates, especially for students from traditionally underserved populations in STEM disciplines. Scientists typically do not receive any formal training in management or group dynamics before taking on the role of a lab head. Thus, peer forums and shared wisdom are crucial for developing the vision and skills involved with mentorship and leading a successful research lab. Faculty at any institution can help improve student outcomes and the success of their labs by thoughtfully including undergraduates in their research programs. Moreover, faculty at primarily undergraduate institutions have special challenges that are not often acknowledged or addressed in public discussions about best practices for running a lab. Here, we present 10 simple rules for fostering a successful undergraduate research lab. While much of the advice herein is applicable to mentoring undergraduates in any setting, it is especially tailored to the special circumstances found at primarily undergraduate institutions.
参与指导研究对本科生大有裨益。这些身临其境的经历可以极大地提高学生的保留率和毕业率,尤其是对于来自传统上得不到充分服务的 STEM 学科人群的学生而言。科学家在担任实验室负责人之前,通常不会接受任何有关管理或团体动力的正规培训。因此,同行论坛和分享智慧对于培养导师的远见和技能以及领导一个成功的研究实验室至关重要。任何院校的教师都可以通过深思熟虑地将本科生纳入研究计划,帮助提高学生的学习成绩和实验室的成功率。此外,以本科生为主的院校的教师还面临着一些特殊的挑战,而这些挑战在有关实验室管理最佳实践的公开讨论中并不常见。在此,我们提出了培养一个成功的本科生研究实验室的 10 条简单规则。虽然这里的大部分建议都适用于指导任何环境下的本科生,但特别适合以本科生为主的院校的特殊情况。
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引用次数: 0
A probabilistic knowledge graph for target identification 用于目标识别的概率知识图谱
IF 4.3 2区 生物学 Pub Date : 2024-04-01 DOI: 10.1371/journal.pcbi.1011945
Chang Liu, Kaimin Xiao, Cuinan Yu, Yipin Lei, Kangbo Lyu, Tingzhong Tian, Dan Zhao, Fengfeng Zhou, Haidong Tang, Jianyang Zeng
Early identification of safe and efficacious disease targets is crucial to alleviating the tremendous cost of drug discovery projects. However, existing experimental methods for identifying new targets are generally labor-intensive and failure-prone. On the other hand, computational approaches, especially machine learning-based frameworks, have shown remarkable application potential in drug discovery. In this work, we propose Progeni, a novel machine learning-based framework for target identification. In addition to fully exploiting the known heterogeneous biological networks from various sources, Progeni integrates literature evidence about the relations between biological entities to construct a probabilistic knowledge graph. Graph neural networks are then employed in Progeni to learn the feature embeddings of biological entities to facilitate the identification of biologically relevant target candidates. A comprehensive evaluation of Progeni demonstrated its superior predictive power over the baseline methods on the target identification task. In addition, our extensive tests showed that Progeni exhibited high robustness to the negative effect of exposure bias, a common phenomenon in recommendation systems, and effectively identified new targets that can be strongly supported by the literature. Moreover, our wet lab experiments successfully validated the biological significance of the top target candidates predicted by Progeni for melanoma and colorectal cancer. All these results suggested that Progeni can identify biologically effective targets and thus provide a powerful and useful tool for advancing the drug discovery process.
及早发现安全有效的疾病靶点对于降低药物研发项目的巨大成本至关重要。然而,现有的鉴定新靶点的实验方法一般都是劳动密集型的,而且容易失败。另一方面,计算方法,尤其是基于机器学习的框架,已在药物发现中显示出显著的应用潜力。在这项工作中,我们提出了基于机器学习的新型靶点识别框架 Progeni。除了充分利用各种来源的已知异构生物网络外,Progeni 还整合了有关生物实体之间关系的文献证据,构建了一个概率知识图谱。然后,Progeni 利用图神经网络来学习生物实体的特征嵌入,从而促进生物相关候选目标的识别。对 Progeni 的全面评估表明,它在目标识别任务上的预测能力优于基线方法。此外,我们进行的大量测试表明,Progeni 对推荐系统中常见的暴露偏差的负面影响表现出很高的鲁棒性,并能有效识别出得到文献有力支持的新靶点。此外,我们的湿实验室实验成功验证了 Progeni 预测的黑色素瘤和结直肠癌顶级候选靶点的生物学意义。所有这些结果表明,Progeni 可以识别生物学上有效的靶点,从而为推进药物发现过程提供了一个强大而有用的工具。
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引用次数: 0
Recombulator-X: A fast and user-friendly tool for estimating X chromosome recombination rates in forensic genetics. Recombulator-X:一种快速且用户友好的工具,用于估计法医遗传学中X染色体重组率。
IF 4.3 2区 生物学 Pub Date : 2023-09-18 eCollection Date: 2023-09-01 DOI: 10.1371/journal.pcbi.1011474
Serena Aneli, Piero Fariselli, Elena Chierto, Carla Bini, Carlo Robino, Giovanni Birolo

Genetic markers (especially short tandem repeats or STRs) located on the X chromosome are a valuable resource to solve complex kinship cases in forensic genetics in addition or alternatively to autosomal STRs. Groups of tightly linked markers are combined into haplotypes, thus increasing the discriminating power of tests. However, this approach requires precise knowledge of the recombination rates between adjacent markers. The International Society of Forensic Genetics recommends that recombination rate estimation on the X chromosome is performed from pedigree genetic data while taking into account the confounding effect of mutations. However, implementations that satisfy these requirements have several drawbacks: they were never publicly released, they are very slow and/or need cluster-level hardware and strong computational expertise to use. In order to address these key concerns we developed Recombulator-X, a new open-source Python tool. The most challenging issue, namely the running time, was addressed with dynamic programming techniques to greatly reduce the computational complexity of the algorithm. Compared to the previous methods, Recombulator-X reduces the estimation times from weeks or months to less than one hour for typical datasets. Moreover, the estimation process, including preprocessing, has been streamlined and packaged into a simple command-line tool that can be run on a normal PC. Where previous approaches were limited to small panels of STR markers (up to 15), our tool can handle greater numbers (up to 100) of mixed STR and non-STR markers. In conclusion, Recombulator-X makes the estimation process much simpler, faster and accessible to researchers without a computational background, hopefully spurring increased adoption of best practices.

位于X染色体上的遗传标记(特别是短串联重复序列或STR)是解决法医遗传学中复杂亲属关系案件的宝贵资源,除了常染色体STR之外,或作为常染色体STR的替代。紧密连接的标记组合成单倍型,从而增加了测试的辨别能力。然而,这种方法需要精确了解相邻标记之间的重组率。国际法医遗传学学会建议,根据谱系遗传数据对X染色体的重组率进行估计,同时考虑突变的混杂效应。然而,满足这些要求的实现有几个缺点:它们从未公开发布,速度非常慢,和/或需要集群级硬件和强大的计算专业知识才能使用。为了解决这些关键问题,我们开发了Recombulator-X,这是一个新的开源Python工具。最具挑战性的问题,即运行时间,用动态编程技术来解决,以大大降低算法的计算复杂度。与以前的方法相比,Recombulator-X将典型数据集的估计时间从几周或几个月缩短到不到一小时。此外,包括预处理在内的估计过程已经简化,并打包成一个简单的命令行工具,可以在普通PC上运行。以前的方法仅限于STR标记的小面板(最多15个),我们的工具可以处理更多数量(最多100个)的混合STR和非STR标记。总之,Recombulator-X使估计过程变得更简单、更快,并且研究人员可以在没有计算背景的情况下访问,有望推动更多地采用最佳实践。
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引用次数: 0
Marginal effects of public health measures and COVID-19 disease burden in China: A large-scale modelling study. 公共卫生措施的边际效应与中国新冠肺炎疾病负担:一项大型模型研究。
IF 4.3 2区 生物学 Pub Date : 2023-09-18 eCollection Date: 2023-09-01 DOI: 10.1371/journal.pcbi.1011492
Zengmiao Wang, Peiyi Wu, Lin Wang, Bingying Li, Yonghong Liu, Yuxi Ge, Ruixue Wang, Ligui Wang, Hua Tan, Chieh-Hsi Wu, Marko Laine, Henrik Salje, Hongbin Song

China had conducted some of the most stringent public health measures to control the spread of successive SARS-CoV-2 variants. However, the effectiveness of these measures and their impacts on the associated disease burden have rarely been quantitatively assessed at the national level. To address this gap, we developed a stochastic age-stratified metapopulation model that incorporates testing, contact tracing and isolation, based on 419 million travel movements among 366 Chinese cities. The study period for this model began from September 2022. The COVID-19 disease burden was evaluated, considering 8 types of underlying health conditions in the Chinese population. We identified the marginal effects between the testing speed and reduction in the epidemic duration. The findings suggest that assuming a vaccine coverage of 89%, the Omicron-like wave could be suppressed by 3-day interval population-level testing (PLT), while it would become endemic with 4-day interval PLT, and without testing, it would result in an epidemic. PLT conducted every 3 days would not only eliminate infections but also keep hospital bed occupancy at less than 29.46% (95% CI, 22.73-38.68%) of capacity for respiratory illness and ICU bed occupancy at less than 58.94% (95% CI, 45.70-76.90%) during an outbreak. Furthermore, the underlying health conditions would lead to an extra 2.35 (95% CI, 1.89-2.92) million hospital admissions and 0.16 (95% CI, 0.13-0.2) million ICU admissions. Our study provides insights into health preparedness to balance the disease burden and sustainability for a country with a population of billions.

中国采取了一些最严格的公共卫生措施来控制连续出现的严重急性呼吸系统综合征冠状病毒2型变种的传播。然而,这些措施的有效性及其对相关疾病负担的影响很少在国家一级得到定量评估。为了解决这一差距,我们基于366个中国城市的4.19亿次旅行,开发了一个包含检测、接触者追踪和隔离的随机年龄分层集合人口模型。该模型的研究期从2022年9月开始。考虑到中国人口的8种潜在健康状况,对新冠肺炎疾病负担进行了评估。我们确定了检测速度和疫情持续时间缩短之间的边际效应。研究结果表明,假设疫苗覆盖率为89%,奥密克戎样波可以通过3天间隔的人群水平检测(PLT)来抑制,而它将在4天间隔的PLT中成为地方病,如果不进行检测,它将导致流行病。每3天进行一次PLT不仅可以消除感染,还可以使医院的床位占用率保持在呼吸道疾病容量的29.46%(95%CI,22.73-38.68%)以下,在疫情爆发期间,ICU床位占用率低于58.94%(95%CI,45.70-76.90%)。此外,潜在的健康状况将导致额外235万(95%置信区间,189-292)人入院,0.16万(95%可信区间,1-30.2)人入住重症监护室。我们的研究为一个拥有数十亿人口的国家平衡疾病负担和可持续性的卫生准备提供了见解。
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引用次数: 0
Human-environment feedback and the consistency of proenvironmental behavior. 人类环境反馈和环保行为的一致性。
IF 4.3 2区 生物学 Pub Date : 2023-09-18 eCollection Date: 2023-09-01 DOI: 10.1371/journal.pcbi.1011429
Claire Ecotière, Sylvain Billiard, Jean-Baptiste André, Pierre Collet, Régis Ferrière, Sylvie Méléard

Addressing global environmental crises such as anthropogenic climate change requires the consistent adoption of proenvironmental behavior by a large part of a population. Here, we develop a mathematical model of a simple behavior-environment feedback loop to ask how the individual assessment of the environmental state combines with social interactions to influence the consistent adoption of proenvironmental behavior, and how this feeds back to the perceived environmental state. In this stochastic individual-based model, individuals can switch between two behaviors, 'active' (or actively proenvironmental) and 'baseline', differing in their perceived cost (higher for the active behavior) and environmental impact (lower for the active behavior). We show that the deterministic dynamics and the stochastic fluctuations of the system can be approximated by ordinary differential equations and a Ornstein-Uhlenbeck type process. By definition, the proenvironmental behavior is adopted consistently when, at population stationary state, its frequency is high and random fluctuations in frequency are small. We find that the combination of social and environmental feedbacks can promote the spread of costly proenvironmental behavior when neither, operating in isolation, would. To be adopted consistently, strong social pressure for proenvironmental action is necessary but not sufficient-social interactions must occur on a faster timescale compared to individual assessment, and the difference in environmental impact must be small. This simple model suggests a scenario to achieve large reductions in environmental impact, which involves incrementally more active and potentially more costly behavior being consistently adopted under increasing social pressure for proenvironmentalism.

应对人为气候变化等全球环境危机需要大部分人口持续采取有利于环境的行为。在这里,我们开发了一个简单行为-环境反馈回路的数学模型,以询问环境状态的个人评估如何与社会互动相结合,从而影响对环保行为的一致采用,以及这如何反馈到感知的环境状态。在这个基于随机个体的模型中,个体可以在两种行为之间切换,“主动”(或主动亲环境)和“基线”,这两种行为的感知成本(主动行为较高)和环境影响(主动行为较低)不同。我们证明了系统的确定动力学和随机波动可以用常微分方程和Ornstein-Uhlenbeck型过程来近似。根据定义,当在种群静止状态下,其频率较高且频率的随机波动较小时,亲环境行为被一致采用。我们发现,社会和环境反馈的结合可以促进代价高昂的亲环境行为的传播,而在孤立的情况下,两者都不会。为了始终如一地被采纳,有必要对环保行动施加强大的社会压力,但与个人评估相比,没有足够的社会互动必须在更快的时间内发生,并且环境影响的差异必须很小。这个简单的模型提出了一种大幅减少环境影响的方案,即在日益增加的环保主义社会压力下,不断采取更积极、潜在成本更高的行为。
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引用次数: 0
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PLoS Computational Biology
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