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Nutrient composition varies greatly across landscapes, influencing the spatiotemporal dynamics of populations. However, few studies have explored this pattern across multiple scales. We tested how nutrient limitation affects herbivore populations, from individual behavior to landscape‐level dynamics, using the Australian plague locustChortoicetes terminifera. Our study combined field populations and long‐term survey data across their range. At the individual level, juvenile locusts selected a carbohydrate‐biased intake target of 1 protein (p) to 2 carbohydrate (c) and exhibited the highest growth rates and shortest development times when fed artificial diets matching this 1p:2c ratio during their final juvenile instar. In the field, locusts exposed to protein‐biased plants corrected their nutritional imbalance by initially selecting carbohydrate‐heavy diets (up to a 1p:20c ratio). Over a week after removal from the protein‐rich environment, they returned to the 1p:2c intake target once the deficiency was balanced. At the landscape level, locust outbreaks were negatively correlated with soil nitrogen and exhibited a non‐linear relationship with soil phosphorus, peaking at approximately 4% phosphorus content. By disentangling the interaction between mean annual precipitation and soil nitrogen, using comprehensive locust surveys and remotely sensed soil and weather data spanning decades, we show how environmental factors drive population dynamics. This study integrates lab, field and remote sensing approaches, highlighting the importance of nutrient balancing across scales for herbivores. Specifically, we demonstrate that low‐nitrogen environments promote locust outbreaks, likely by reducing plant protein‐to‐carbohydrate ratios. Incorporating soil quality data into locust plague forecasting models could significantly improve prediction accuracy. 

Swarming locusts present a quintessential example of animal collective motion. Juvenile locusts march and hop across the ground in coordinated groups called hopper bands. Composed of up to millions of insects, hopper bands exhibit aligned motion and various collective structures. These groups are well-documented in the field, but the individual insects themselves are typically studied in much smaller groups in laboratory experiments. We present, to our knowledge, the first trajectory data that detail the movement of individual locusts within a hopper band in a natural setting. Using automated video tracking, we derive our data from footage of four distinct hopper bands of the Australian plague locust,Chortoicetes terminifera. We reconstruct nearly 200 000 individual trajectories composed of over 3.3 million locust positions. We classify these data into three motion states: stationary, walking and hopping. Distributions of relative neighbour positions reveal anisotropies that depend on motion state. Stationary locusts have high-density areas distributed around them apparently at random. Walking locusts have a low-density area in front of them. Hopping locusts have low-density areas in front and behind them. Our results suggest novel insect interactions, namely that locusts change their motion to avoid colliding with neighbours in front of them. 

Adaptive plasticity requires an integrated suite of functional responses to environmental variation, which can include social communication across life stages. Desert locusts ( Schistocerca gregaria ) exhibit an extreme example of phenotypic plasticity called phase polyphenism, in which a suite of behavioral and morphological traits differ according to local population density. Male and female juveniles developing at low population densities exhibit green- or sand-colored background-matching camouflage, while at high densities they show contrasting yellow and black aposematic patterning that deters predators. The predominant background colors of these phenotypes (green/sand/yellow) all depend on expression of the carotenoid-binding “Yellow Protein” ( YP ). Gregarious (high-density) adults of both sexes are initially pinkish, before a YP -mediated yellowing reoccurs upon sexual maturation. Yellow color is especially prominent in gregarious males, but the reason for this difference has been unknown since phase polyphenism was first described in 1921. Here, we use RNA interference to show that gregarious male yellowing acts as an intrasexual warning signal, which forms a multimodal signal with the antiaphrodisiac pheromone phenylacetonitrile (PAN) to prevent mistaken sexual harassment from other males during scramble mating in a swarm. Socially mediated reexpression of YP thus adaptively repurposes a juvenile signal that deters predators into an adult signal that deters undesirable mates. These findings reveal a previously underappreciated sexual dimension to locust phase polyphenism, and promote locusts as a model for investigating the relative contributions of natural versus sexual selection in the evolution of phenotypic plasticity.