离开孵育室:智利南部quempillsamuen河口,Anthopleura hermaphroditica (Carlgren, 1899)海葵幼体阶段的细胞和生理挑战,以应对波动的环境压力。

IF 3 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
Marine environmental research Pub Date : 2025-02-01 Epub Date: 2025-01-11 DOI:10.1016/j.marenvres.2025.106962
V M Cubillos, J A Montory, O R Chaparro, E Cruces, C J Segura, E F Ramírez-Kuschel, D A Mardones, N Valdivia, F J Paredes-Molina, I Echeverría-Pérez, L P Salas-Yanquin, J A Büchner-Miranda
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引用次数: 0

摘要

生命早期阶段的环境压力对个体表现和种群动态有严重影响。共生潮间带海葵(Anthopleura hermaphroditica)的内部孵化过程在幼鱼离开成虫胃血管腔时结束,此时它们暴露在quempillemac河口潮汐变化和环境辐射的高度应激环境中。为了确定海葵幼鱼对放弃胃血管腔引起的盐度和环境辐射变化的细胞和生理耐受能力,采用正交设计对暴露于4种盐度水平(30.0、22.5、15.0和7.5 psu)和两种太阳辐射水平(P/50)的个体进行了实验。总体而言,盐度、辐射和光合条件(及其相互作用)影响雌雄同体幼鱼的脂质过氧化水平和总抗氧化能力。因此,氧化损伤和抗氧化反应水平随着盐度的降低而增加,并且在盐度为7.5 psu并结合UV-R辐射(PAB处理)时加剧。共生复合体虫黄藻的光合作用不仅增加了细胞损伤和抗氧化反应,而且通过耗氧速率产生比海葵所利用的更高的氧水平。在这种情况下,盐度≤15 psu和≤22.5 psu分别降低了P和PAB条件下共生复体的产氧/耗氧。因此,与单独暴露于P辐射处理的非光合生物(EC50 = 18 psu)相比,在PAB存在下进行光合作用的幼体对低盐条件的生理耐受范围(EC50 = 23 psu)更窄。辐射对雌雄同体幼鱼从成体海葵胃血管腔中释放的影响有待进一步研究。因此,共生光合作用介导了盐度和辐射对幼鱼细胞反应和生理能力的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leaving the incubation chamber: Cellular and physiological challenges of the juvenile stage of the sea anemone Anthopleura hermaphroditica (Carlgren, 1899) to cope with fluctuating environmental stressors in the Quempillén estuary, southern Chile.

Environmental stress on early life stages has severe consequences for individual performance and population dynamics. The internal incubation process of the symbiotic intertidal anemone Anthopleura hermaphroditica ends when the juveniles leave the gastrovascular cavity of the adult, at which moment they are exposed to a highly stressful environment due to tidal changes and environmental radiation in the Quempillén estuary. To determine the cellular and physiological tolerance capabilities of juvenile anemones to changes in salinity and environmental radiation resulting from the abandonment of the gastrovascular cavity, an experiment with an orthogonal design was performed on individuals exposed to four levels of salinity (30.0, 22.5, 15.0 and 7.5 psu) and two of solar radiation (P/<400-700 nm; PAB/<280-700 nm). The cellular response was evaluated by estimation of peroxidative damage and total antioxidant capacity. In addition, the effects of salinity and radiation on the photosynthetic process (with and without inhibition of the photosynthetic process by the addition of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU)) and on the oxygen consumption rate were determined. Finally, the mean maximum effective concentration (EC50) was determined for each of the experimental conditions. Overall, salinity, radiation and photosynthetic condition (and their interaction) influence the level of lipid peroxidation and total antioxidant capacity of juvenile A. hermaphroditica. Thus, levels of oxidative damage and antioxidant response increase with decreasing salinity and are exacerbated at salinities of 7.5 psu combined with UV-R radiation (PAB treatment). Photosynthesis by the zooxanthellae of the symbiont complex not only increases cell damage and antioxidant response, but also generates elevated oxygen levels higher than those utilized by the anemone through oxygen consumption rate. In this context, salinities ≤15 and ≤ 22.5 psu reduce oxygen production/consumption by the symbiont complex under P and PAB conditions, respectively. Consequently, juveniles photosynthesizing in the presence of PAB generate narrower physiological tolerance ranges to hyposaline conditions (EC50 = 23 psu) than non-photosynthetic organisms exposed to P radiation treatment alone (EC50 = 18 psu). Future studies are needed to determine the effect of radiation on the release of juvenile A. hermaphroditica from the gastrovascular cavity of adult anemones. Therefore, symbiotic photosynthetic activity mediates the interdependent effects of salinity and radiation on juveniles' cellular responses and physiological capabilities.

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来源期刊
Marine environmental research
Marine environmental research 环境科学-毒理学
CiteScore
5.90
自引率
3.00%
发文量
217
审稿时长
46 days
期刊介绍: Marine Environmental Research publishes original research papers on chemical, physical, and biological interactions in the oceans and coastal waters. The journal serves as a forum for new information on biology, chemistry, and toxicology and syntheses that advance understanding of marine environmental processes. Submission of multidisciplinary studies is encouraged. Studies that utilize experimental approaches to clarify the roles of anthropogenic and natural causes of changes in marine ecosystems are especially welcome, as are those studies that represent new developments of a theoretical or conceptual aspect of marine science. All papers published in this journal are reviewed by qualified peers prior to acceptance and publication. Examples of topics considered to be appropriate for the journal include, but are not limited to, the following: – The extent, persistence, and consequences of change and the recovery from such change in natural marine systems – The biochemical, physiological, and ecological consequences of contaminants to marine organisms and ecosystems – The biogeochemistry of naturally occurring and anthropogenic substances – Models that describe and predict the above processes – Monitoring studies, to the extent that their results provide new information on functional processes – Methodological papers describing improved quantitative techniques for the marine sciences.
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