Levi Storks

Aquatic ecosystems are routinely exposed to natural and anthropogenic stressors, and when multiple pollutants co-occur, their synergistic effects may exceed those of individual contaminants. This study evaluated the individual and combined effects of the widely used agrochemical Roundup^®, whose active ingredient is glyphosate (GLY) and the cyanobacterial toxin microcystin-LR (MC-LR) on the hepatopancreas of crayfish. Following a seven-day exposure to MC-LR (15 ppb), GLY (75 ppb), or their combination (MC-LR + GLY), cellular and morphological alterations were assessed using flow cytometry and histological analyses. MC-LR exposure increased hepatopancreatic vacuole number 3.7-fold and vacuole proportion 6.8-fold relative to controls, whereas GLY increased vacuole proportion 5.2-fold. Combined exposure increased tubule lumen proportion by approximately 65%, while epithelial height remained unchanged. GLY reduced viable (fluorescein diacetate-positive) hepatopancreatic cells by approximately 86%, and both GLY and MC-LR + GLY increased non-viable (propidium iodide-positive) cells by 4.8-fold and 4.3-fold, respectively. MC-LR alone did not significantly affect cell viability. These findings indicate that MC-LR primarily induces structural alterations, whereas GLY causes pronounced cellular cytotoxicity. Although co-exposure did not consistently produce synergistic toxicity, it enhanced tissue remodeling, emphasizing the importance of evaluating environmentally relevant contaminant mixtures and their implications for freshwater ecosystem health.

Industrialization has caused extensive environmental change, including a global surge in plastic production and pollution. This has resulted in the accumulation of microplastics (MPs; <5 mm) and nanoplastics (NPs; <1 μm) in ecosystems worldwide. MPs originate from both primary sources, such as cosmetics and industrial applications, and secondary sources, through the degradation of larger plastic debris. As a result, MPs and NPs have become ubiquitous contaminants, posing significant toxicological risks to living organisms. These persistent pollutants are diverse polymers that vary in size, shape, and chemical composition, making their impacts on organism physiology complex and difficult to disentangle. Plastic pollution is particularly severe in aquatic environments, where particles accumulate from terrestrial sources such as urban dust, agricultural runoff, industrial discharges, and wastewater effluents. Although most research has centered on marine ecosystems, emerging evidence indicates that freshwater environments may contain comparable or even higher concentrations of MPs. Once inside the body, MPs can translocate into tissues and exert toxic effects on multiple organ systems. Collectively, plastic pollution poses not only physiological but also neurological and behavioral risks to aquatic life, with potential consequences for ecosystem stability and trophic interactions. Both MPs and NPs are sufficiently small to cross the blood–brain barrier, raising concerns about their potential impacts on the nervous system by interfering with neuronal function and brain development. Plastic particles can accumulate in neural tissues, inducing oxidative stress, neuroinflammation, and disruption of neurotransmitter signaling. Such neurotoxic effects are linked to altered locomotion, feeding, predator avoidance, and social behaviors across multiple species. This review examines current evidence on the neurotoxic effects of plastic pollution in aquatic organisms and underscores the urgent need for further research and action to mitigate its impact. In light of escalating plastic production and inadequate waste management, the growing evidence that MPs and NPs disrupt aquatic nervous systems, behavior, and ecosystem stability underscores an urgent need for intensified research, improved mitigation strategies, particularly for nanoplastics, and the accelerated development of truly safe and sustainable alternatives.

Elucidating the selective forces shaping the diversity of vertebrate brains continues to be a major area of inquiry, particularly as it relates to cognition. Historically brain evolution was interpreted through the lens of relative brain size; however, recent evidence has challenged this approach. Investigating neuroanatomy at a finer scale, such as neuron number, can provide new insights into the forces shaping brain evolution in the context of information processing capacity. Ecological factors, such as the complexity of a species' habitat, place demands on cognition that could shape neuroanatomy. In this study, we investigate the relationship between neuron number and habitat complexity in three brain regions across six closely related anole species from Puerto Rico. After controlling for brain mass, we found that the number of neurons increased with habitat complexity across species in the telencephalon and ‘rest of the brain,’ but not in the cerebellum. Our results demonstrate that habitat complexity has shaped neuroanatomy in the Puerto Rican anole radiation and provide further evidence of the role of habitat complexity in vertebrate brain evolution.

Animals differ in their ability to learn. One potential factor contributing to learning differences is personality types. We investigated the relationship between learning and the bold-shy continuum by comparing performance of bold and shy zebrafish in conditioned place preference (CPP) and 2 choice tasks. Bold fish learned significantly faster than the shy fish but there were no differences in their final performance. When tested in the 2 choice task, we found no clear evidence of learning, however bold fish made more initial choices than shy fish. Overall,our study suggests that bold fish tend to be faster learners when compared to shy fish. The lack of differences in the final change in behavior suggests that the learning difference is due to neophobic tendencies and resulting initial interactions with the learning stimulus.

Integrative and Comparative Biology, icaa129, https://doi.org/10.1093/icb/icaa129

Studies of vertebrate brain evolution have mainly focused on measures of brain size, particularly relative mass and its allometric scaling across lineages, commonly with the goal of identifying the substrates that underly differences in cognition. However, recent studies on birds and mammals have demonstrated that brain size is an imperfect proxy for neuronal parameters that underly function, such as the number of neurons that make up a given brain region. Here we present estimates of neuron numbers and density in two species of lizard, Anolis cristatellus and A. evermanni, representing the first such data from squamate species, and explore its implications for differences in cognitive performance and vertebrate brain evolution. The isotropic fractionator protocol outlined in this article is optimized for the unique challenges that arise when using this technique with lineages having nucleated erythrocytes and relatively small brains. The number and density of neurons and other cells we find in Anolis for the telencephalon, cerebellum, and the rest of the brain (ROB) follow similar patterns as published data from other vertebrate species. Anolis cristatellus and A. evermanni exhibited differences in their performance in a motor task frequently used to evaluate behavioral flexibility, which was not mirrored by differences in the number, density, or proportion of neurons in either the cerebellum, telencephalon, or ROB. However, the brain of A. evermanni had a significantly higher number of nonneurons across the whole brain, which could contribute to the observed differences in problem solving between A. cristatellus and A. evermanni. Although limited to two species, our findings suggest that neuron number and density in lizard brains scale similarly to endothermic vertebrates in contrast to the differences observed in brain to body mass relationships. Data from a wider range of species are necessary before we can fully understand vertebrate brain evolution at the neuronal level.