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Variation in offspring sex ratio, particularly in birds, has been frequently studied over the last century, although seldom using long-term monitoring data. In raptors, the cost of raising males and females is not equal, and several variables have been found to have significant effects on sex ratio, including food availability, parental age, and hatching order. Sex ratio differences between island populations and their mainland counterparts have been poorly documented, despite broad scientific literature on the island syndrome reporting substantial differences in population demography and ecology. Here, we assessed individual and environmental factors potentially affecting the secondary sex ratio of the long-lived Egyptian vulture Neophron percnopterus. We used data collected from Spanish mainland and island populations over a ca. 30-year period (1995-2021) to assess the effects of insularity, parental age, breeding phenology, brood size, hatching order, type of breeding unit (pairs vs. trios), and spatial and temporal variability on offspring sex ratio. No sex bias was found at the population level, but two opposite trends were observed between mainland and island populations consistent with the island syndrome. Offspring sex ratio was nonsignificantly female-biased in mainland Spain (0.47, n = 1112) but significantly male-biased in the Canary Islands (0.55, n = 499), where a male-biased mortality among immatures could be compensating for offspring biases and maintaining a paired adult sex ratio. Temporal and spatial variation in food availability might also have some influence on sex ratio, although the difficulties in quantifying them preclude us from determining the magnitude of such influence. This study shows that insularity influences the offspring sex ratio of the Egyptian vulture through several processes that can affect island and mainland populations differentially. Our research contributes to improving our understanding of sex allocation theory by invest

Autophagy is a catabolic process by which eukaryotic cells degrade and recycle unnecessary or damaged intracellular components to maintain cellular homeostasis and to cope with stress. The development of specific tools to monitor autophagy in microalgae and plants has been fundamental to investigate this catabolic pathway in photosynthetic organisms. The protein ATG8 is a widely used molecular marker of autophagy in all eukaryotes, including the model microalga Chlamydomonas reinhardtii. The drug concanamycin A, a specific inhibitor of vacuolar ATPase, has also been extensively used to block autophagic flux in the green lineage. In Chlamydomonas, inhibition of autophagic flux by concanamycin A has been shown to prevent the degradation of ribosomal proteins and the formation of lipid bodies under nitrogen or phosphorous starvation. Here, we detail how the abundance and lipidation state of ATG8 can be used to monitor autophagic flux in Chlamydomonas by western blot analysis.

Extremophilic microalgae have the ability to grow and adapt their metabolism to extreme conditions including acidic pH, high or very low temperature, or the presence of high concentrations of heavy metals. In addition to their ecological importance as primary producers in extreme environments, these organisms also have biotechnological potential since they produce several beneficial compounds as metabolism side-products including lipids or carbohydrates. Autophagy is a degradative process by which eukaryotic cells eliminate toxic or superfluous cellular components in order to cope with stress or unfavorable conditions and maintain cellular homeostasis. We have demonstrated that autophagy is a pro-survival mechanism that is upregulated by a wide range of stress conditions such as nutrient starvation or metal toxicity in the model microalga Chlamydomonas reinhardtii. However, autophagy has never been investigated in extremophiles and it is currently unknown whether this catabolic process play a role in the adaptation of these organisms to adverse environments. To address this question, we have isolated a new microalga, Chlamydomonas urium, from the Tinto River (Nerva, Spain), a well-characterized extremely acidic river with a high content of heavy metals. Genome sequencing and annotation revealed that core ATG genes are conserved in C. urium, indicating that autophagy must be conserved in extremophilic organisms. Our studies by western blot analysis, ultrastructural microscopy and metabolomics showed that autophagy is a highly dynamic process in C. urium. Interestingly, the inhibition of autophagic flux results in a large increase of triacylglycerols and starch, the two main carbon storage molecules. Thus, our results pinpoint autophagy as a central process regulating carbon storage in the new extremophilic microalga C. urium.

The target of rapamycin (TOR) kinase is a master regulator that integrates nutrient signals to promote cell growth in all eukaryotes. It is well established that amino acids and glucose are major regulators of TOR signaling in yeast and metazoan, but whether and how TOR responds to carbon availability in photosynthetic organisms is less understood. In this study, we showed that photosynthetic assimilation of CO2 by the Calvin–Benson–Bassham (CBB) cycle regulates TOR activity in the model single-celled microalga Chlamydomonas reinhardtii. Stimulation of CO2 fixation boosted TOR activity, whereas inhibition of the CBB cycle and photosynthesis down-regulated TOR. We uncovered a tight link between TOR activity and the endogenous level of a set of amino acids including Ala, Glu, Gln, Leu, and Val through the modulation of CO2 fixation and the use of amino acid synthesis inhibitors. Moreover, the finding that the Chlamydomonas starch-deficient mutant sta6 displayed disproportionate TOR activity and high levels of most amino acids, particularly Gln, further connected carbon assimilation and amino acids to TOR signaling. Thus, our results showed that CO2 fixation regulates TOR signaling, likely through the synthesis of key amino acids.