{"title":"Damages of aged-PVC microplastics exceed the enhanced resistance of chlorella pyrenoidosa induced by phosphorus limitation","authors":"Xiao Tan , Lv Wang , Chao Xing , Zhipeng Duan , Jia Liang , Rui Zhu , Jiang Huang , Shichao Chen , Yijia Wei","doi":"10.1016/j.aquatox.2026.107715","DOIUrl":null,"url":null,"abstract":"<div><div>Phytoplankton could adapt to multiple natural stresses. However, few have explicitly explored their complex adaptation patterns to emerging chemical contaminants (ECCs), such as microplastics (MPs), under nutrient-limited conditions. Here, we experimentally investigated the patterns of <em>Chlorella pyrenoidosa</em> responding to aged polyvinyl chloride (aged-PVC) and their leachate with a series of concentrations (0–20 mg/L) under phosphorus (P) repletion conditions (7.14 mg P/L) and P limitation conditions (0.1 mg P/L). Results revealed that <em>C. pyrenoidosa</em> displayed comparable patterns in response to aged-PVC treatments, regardless of P availability, showing significant decreases in growth rate but increases in photosynthetic efficiency (1.7%-39.6%), and the early-stage growth stimulation (day 2–14) may be attributed to the leachate. Moreover, cells of <em>C. pyrenoidosa</em> under both P availability elevated their cellular P quotas at the stationary phase under the low aged-PVC concentration (0.1 mg/L). These are significantly inconsistent with the responses of phytoplankton to multiple natural stresses, where phytoplankton typically enhance their resistance to environmental stresses under nutrient-limited conditions. This can be attributed to the stronger chemical toxicity of aged-PVC on enzymes and physical damage to the cell membrane. These findings suggest that cellular adaptive mechanisms of phytoplankton to natural stresses may fail against chemical contaminants, therefore providing crucial insights into the threshold dynamics of ecosystem resilience.</div></div>","PeriodicalId":248,"journal":{"name":"Aquatic Toxicology","volume":"292 ","pages":"Article 107715"},"PeriodicalIF":4.6000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquatic Toxicology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166445X26000111","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/15 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MARINE & FRESHWATER BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Phytoplankton could adapt to multiple natural stresses. However, few have explicitly explored their complex adaptation patterns to emerging chemical contaminants (ECCs), such as microplastics (MPs), under nutrient-limited conditions. Here, we experimentally investigated the patterns of Chlorella pyrenoidosa responding to aged polyvinyl chloride (aged-PVC) and their leachate with a series of concentrations (0–20 mg/L) under phosphorus (P) repletion conditions (7.14 mg P/L) and P limitation conditions (0.1 mg P/L). Results revealed that C. pyrenoidosa displayed comparable patterns in response to aged-PVC treatments, regardless of P availability, showing significant decreases in growth rate but increases in photosynthetic efficiency (1.7%-39.6%), and the early-stage growth stimulation (day 2–14) may be attributed to the leachate. Moreover, cells of C. pyrenoidosa under both P availability elevated their cellular P quotas at the stationary phase under the low aged-PVC concentration (0.1 mg/L). These are significantly inconsistent with the responses of phytoplankton to multiple natural stresses, where phytoplankton typically enhance their resistance to environmental stresses under nutrient-limited conditions. This can be attributed to the stronger chemical toxicity of aged-PVC on enzymes and physical damage to the cell membrane. These findings suggest that cellular adaptive mechanisms of phytoplankton to natural stresses may fail against chemical contaminants, therefore providing crucial insights into the threshold dynamics of ecosystem resilience.
期刊介绍:
Aquatic Toxicology publishes significant contributions that increase the understanding of the impact of harmful substances (including natural and synthetic chemicals) on aquatic organisms and ecosystems.
Aquatic Toxicology considers both laboratory and field studies with a focus on marine/ freshwater environments. We strive to attract high quality original scientific papers, critical reviews and expert opinion papers in the following areas: Effects of harmful substances on molecular, cellular, sub-organismal, organismal, population, community, and ecosystem level; Toxic Mechanisms; Genetic disturbances, transgenerational effects, behavioral and adaptive responses; Impacts of harmful substances on structure, function of and services provided by aquatic ecosystems; Mixture toxicity assessment; Statistical approaches to predict exposure to and hazards of contaminants
The journal also considers manuscripts in other areas, such as the development of innovative concepts, approaches, and methodologies, which promote the wider application of toxicological datasets to the protection of aquatic environments and inform ecological risk assessments and decision making by relevant authorities.