Chu Alexandra, Li Danhong Ally, Bell-Tilcock Miranda, Lowe-Webb Miranda, Jeffres Carson, Johnson Rachel C
Center for Watershed Sciences, University of California, Davis, California, United States of America.
Delta Stewardship Council, Sacramento, California, United States of America.
PLoS One. 2025 Jun 26;20(6):e0326345. doi: 10.1371/journal.pone.0326345. eCollection 2025.
Analyzing stable isotopes in archival tissues, such as fish eye lenses, is used to document shifts in feeding ecology, diet, habitat use, and to reconstruct life history. Fish eye lenses grow throughout their ontogeny, forming multiple sequential layers, or laminae. These laminae represent the chronology of the fish's life, much like tree rings, which record environmental conditions over time. Lenses are protein-rich, which makes them an ideal structure for analyzing light isotopes such as δ¹³C, δ¹⁵N, and δ34S. These light isotopes are primarily integrated into the lens tissue through the fish's diet, where they are bound to amino acid structures during protein synthesis. As research begins to emerge using eye lenses to reconstruct the life histories of fishes, the need for a reproducible method of delamination grows. For this study, each researcher independently delaminated one lens from each of the 10 adult Chinook Salmon (Oncorhynchus tshawytscha). Lens lamina number, diameter (mm), and mass (mg) of each lamina were recorded. Laminae were then submitted for stable isotope analysis of both δ¹³C and δ¹⁵N. Isotope values were used as a validation to compare delamination patterns between researchers. δ¹³C and δ¹⁵N values from the lenses were then plotted using both the assigned lamina number and lens diameter to compare the difference between researchers. Analysis based on lamina number showed significant shifts in isotope values and variability in lamina counts between researchers. However, when lens diameter was used instead of lamina number, isotope patterns throughout the lenses of the same fish were nearly identical. Using lens diameter removes subjectivity between researchers, thereby increasing the reproducibility of the technique and providing a more robust interpretation of the data.
分析存档组织(如鱼眼晶状体)中的稳定同位素,可用于记录摄食生态、饮食、栖息地利用的变化,并重建生活史。鱼眼晶状体在其个体发育过程中不断生长,形成多个连续的层,即薄片。这些薄片代表了鱼的生活年表,很像树木的年轮,记录着随时间变化的环境条件。晶状体富含蛋白质,这使其成为分析诸如δ¹³C、δ¹⁵N和δ34S等轻同位素的理想结构。这些轻同位素主要通过鱼的饮食整合到晶状体组织中,在蛋白质合成过程中它们与氨基酸结构结合。随着利用眼晶状体重建鱼类生活史的研究开始出现,对一种可重复的分层方法的需求也在增加。在本研究中,每位研究人员独立地从10条成年奇努克鲑(Oncorhynchus tshawytscha)的每条鱼身上分层取出一个晶状体。记录每个薄片的薄片层数、直径(毫米)和质量(毫克)。然后将薄片送去进行δ¹³C和δ¹⁵N的稳定同位素分析。同位素值用作验证,以比较研究人员之间的分层模式。然后使用指定的薄片层数和晶状体直径绘制晶状体的δ¹³C和δ¹⁵N值,以比较研究人员之间的差异。基于薄片层数的分析显示,研究人员之间同位素值有显著变化,薄片计数也存在差异。然而,当使用晶状体直径而非薄片层数时,同一条鱼的整个晶状体中的同位素模式几乎相同。使用晶状体直径消除了研究人员之间的主观性,从而提高了该技术的可重复性,并为数据提供了更可靠的解释。