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526 results for “compensation”
Compensating for climate change-induced cue-environment mismatches: evidence for contemporary evolution of a photoperiodic reaction norm in Colias butterflies
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Data from: Natural Zeitgebers under temperate conditions cannot compensate for the loss of a functional circadian clock in timing of a vital behavior in Drosophila
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Data from: An immune challenge induces a decline in parental effort and compensation by the mate
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Wildlife density estimation by distance sampling: A novel technique with movement compensation
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Functional impact of subunit composition and compensation on Drosophila melanogaster nicotinic receptors: Targets of neonicotinoids
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Raw data for: Over-eruption in marsupial carnivore teeth: compensation for a constraint
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Carryover effects in a sea star: Juvenile resource availability does not compensate for a poor larval environment
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Dataset for Neural Network 3D Body Pose Tracking and Prediction for Motion-to-Photon Latency Compensation in Distributed Virtual Reality
<p>Distributed Virtual Reality (DVR) systems enable geographically dispersed users to interact in a shared virtual environment. The realism of the interaction is crucial to increase the feeling of co-presence. Latency, produced either by hard- or software components of DVR applications, impedes reaching high realism levels of the DVR experience. For example, the time delay between the user's motion and the corresponding display rendering of the DVR system might lead to adverse effects such as a reduced sense of presence or motion sickness. One way of minimizing the latency is to predict user's motion and thus compensate for the inherent latency in the system. In order to address this problem, we propose a neural network 3D pose tracking and prediction system with latency guarantees for end-to-end avatar reconstruction. We evaluate and compare our system against multiple traditional methods and provide a thorough analysis on real-world human motion data. Datasets used in the paper experiments. Datasets used in paper experiments.</p>
Data from: Earlier plant growth helps compensate for reduced carbon fixation after 13 years of warming
1.Drylands play a dominant role in global carbon cycling and are particularly vulnerable to increasing temperatures, but our understanding of how dryland ecosystems will respond to climatic change remains notably poor. Considering that the area of drylands is projected to increase 11–23% by 2100, understanding the impacts of warming on the functions and services furnished by these arid and semiarid ecosystems has numerous implications. 2.In a unique 13‐year ecosystem warming experiment in a southwestern U.S. dryland, we investigated the consequences of rising temperature on Achnatherum hymenoides, a widespread, keystone grass species on the Colorado Plateau. We tracked individual‐ and population‐level responses to identify optimal strategies that may have been masked if considering only one level of plant response. 3.We found several factors combined to affect the timing and magnitude of plant responses during the 13th year of warming. These included large warming‐induced biomass increases for individual plants, an 8.5‐day advancement in the growing season, and strong reductions in photosynthetic rates and population cover. 4.Importantly, we observed a lack of photosynthetic acclimation and, thus, a warming‐induced downregulation of photosynthetic rates. However, these physiological responses were concurrent with warmed‐plant increases in growing season length and investment in photosynthetic surfaces, demonstrating the species' ability to balance carbon fixation limitations with warming. 5.These results, which bring together ecophysiological, phenological, reproductive, and morphological assessments of plant responses to warming, suggest that the extent of change in A. hymenoides populations will be based upon numerous adaptive responses that vary in their direction and magnitude. Plant population responses to climatic warming remain poorly resolved, particularly for Earth's drylands, and our in situ experiment assessing multiple strategies offers a novel look into a warmer world.
Data from: Diversity matters: effects of density compensation in pollination service during rainfall shift
1. Extreme weather events are increasing in frequency due to the warming climate. Such extremities can jeopardise ecosystem services and create economic imbalances. Tropical developing countries are predicted to suffer the maximum consequences of such events. 2. We examined the impact of such an event – extreme rainfall fluctuation - on a critical ecosystem service – pollination, which can be intricately linked to a country's economy. We performed this study in a dominant peri-urban vegetable hub of an agriculture-dependent developing country. 3. We found that the yield of all pollinator-dependent crops grown across a large spatial scale (district) over multiple years (six) drastically declined with the decrease in rainfall. 4. At the local scale, we found that the dominant crop (representative horticultural crop) had a significant drop in yield during drought, likely due to the production of fewer female flowers and a significant shift in the pollinator community. 5. We found that Trigona sp. (one of the four pollinators) was the critical pollinator positively influencing fruit to flower ratio (FFR) (an indicator of pollination service) in the normal rainfall year. However, despite its sharp decline during drought, the FFR remained unaffected. We found that during drought, Apis dorsata was crucial in maintaining FFR and compensated for the decline of the critical pollinator across 67% farmlands. 6. Our study demonstrates the role of ecosystem stabilising mechanism rescuing the crucial ecosystem service during climatic variability over the temporal scale.
Data from: Fecundity compensation is dependent on the generalised stress response in a nematode host
Background: Fecundity compensation, increased offspring output following parasite exposure, is widely reported, but the underlying mechanisms remain unclear. General stress responses are linked to other indirect defences against parasites, and therefore may be responsible. We challenged strains of Caenorhabditis elegans (wild-type and mutants with compromised or strengthened stress responses) with Staphylococcus aureus. Results: In all strains except the compromised stress response mutant, we saw elevated offspring production if hosts survived initial parasite exposure. Conclusion: We infer that general stress responses are linked with fecundity compensation. These results may explain why trade-offs are not observed among parasite defence mechanisms.
Breaking Free from Thermodynamic Constraints: Thermal Acclimation and Metabolic Compensation in a freshwater zooplankton species
<p>Ectothermic organisms' respiration rates are largely controlled by environment temperatures and the ability to meet metabolic demands at high temperatures sometimes sets their upper thermal limit. Organisms are hypothesized to exhibit acclimatory effects, adjusting their metabolism and physiology by deceleration of metabolic processes including respiration below Arrhenius expectations based in temperature alone. Such deceleration is termed metabolic compensation. We test the hypothesis that either heritable (among genotypes) or plastic (between acclimation regimes) heat tolerance differences can be explained by metabolic compensation in the eurythermal freshwater zooplankton crustacean Daphnia magna. We measured oxygen consumption rates over a range of assay temperatures (5°C - 37°C) in 8 genotypes of Daphnia representing a range of previously reported genotype-specific acute heat tolerance values and, in a narrower range of temperatures (10°C - 35°C) in Daphnia with different acclimation history (either 10°C or 25°C). In a ramp-up experiment we discovered no difference in temperature-specific respiration rates between heat tolerant and heat-sensitive genotypes. In contrast, we observed compensatory differences in respiration rates at both extremes of the temperature range studied. Notably, there was a deceleration of oxygen consumption at higher temperature in the 25°C-acclimated Daphnia relative to their 10°C-acclimated counterparts, observed in active, but not anaesthetized animals, a pattern corroborated by similar changes in filtering rate and, partly, by changes in mitochondrial membrane potential. Daphnia exposed to a sublethal temperature (35°C) with a 24-hour recovery period at a 25°C-acclimation temperature showed no difference in respiration compared to unexposed 25°C-acclimated Daphnia, indicating that the reduction of respiration is not caused by irreversible damage. Response time necessary to acquire the respiratory adjustment to high temperature was much lower than to low temperature, indicating that metabolic compensation at the lower temperatures require slower structural changes.</p>
Data from: Temperature compensation in a small rhythmic circuit
<p>Temperature affects the conductances and kinetics of the ionic channels that underlie neuronal activity. Each membrane conductance has a different characteristic temperature sensitivity, which raises the question of how neurons and neuronal circuits can operate robustly over wide temperature ranges. To address this, we employed computational models of the pyloric network of crabs and lobsters. We employed a landscape optimization scheme introduced previously (Alonso and Marder, 2019) to produce multiple different models that exhibit a triphasic pyloric rhythm over a range of temperatures. We use the currentscapes introduced in (Alonso and Marder, 2019) to explore the dynamics of model currents and how they change with temperature. We found that temperature changes the relative contributions of the currents to neuronal activity so that rhythmic activity smoothly slides through changes in mechanisms. Moreover, the responses of the models to extreme perturbations—such as gradually decreasing a current type—are often qualitatively different at different temperatures.</p>
Helpers compensate for age-related declines in parental care and offspring survival in a cooperatively breeding bird
<p>Offspring from elderly parents often have lower survival due to parental senescence. In cooperatively breeding species, where offspring care is shared between breeders and helpers, the alloparental care provided by helpers is predicted to mitigate the impact of parental senescence on offspring provisioning and, subsequently, offspring survival. We test this prediction using data from a long-term study on cooperatively breeding Seychelles warblers (<i>Acrocephalus sechellensis</i>). We find that the nestling-provisioning rate of female breeders declines with their age. Further, the total brood provisioning rate and the first-year survival probability of offspring decline progressively with age of the female breeder, but these declines are mitigated when helpers are present. This effect does not arise because individual helpers provide more care in response to the lower provisioning of older dominant females, but because older female breeders have recruited more helpers, thereby receiving more overall care for their brood. We do not find such effects for male breeders. These results indicate that alloparental care can alleviate the fitness costs of senescence for breeders, which suggests an interplay between age and cooperative breeding.</p>
Data from: The role of predation and food limitation on claims for compensation, reindeer demography and population dynamics
1. A major challenge in biodiversity conservation is to facilitate viable populations of large apex predators in ecosystems where they were recently driven to ecological extinction due to resource conflict with humans. 2. Monetary compensation for losses of livestock due to predation is currently a key instrument to encourage human–carnivore coexistence. However, a lack of quantitative estimates of livestock losses due to predation leads to disagreement over the practise of compensation payments. This disagreement sustains the human–carnivore conflict. 3. The level of depredation on year-round, free-ranging, semi-domestic reindeer by large carnivores in Fennoscandia has been widely debated over several decades. In Norway, the reindeer herders claim that lynx and wolverine cause losses of tens of thousands of animals annually and cause negative population growth in herds. Conversely, previous research has suggested that monetary predator compensation can result in positive population growth in the husbandry, with cascading negative effects of high grazer densities on the biodiversity in tundra ecosystems. 4. We utilized a long-term, large-scale dataset to estimate the relative importance of lynx and wolverine predation and density-dependent and climatic food limitation on claims for losses, recruitment and population growth rates in Norwegian reindeer husbandry. 5. Claims of losses increased with increasing predator densities, but with no detectable effect on population growth rates. Density-dependent and climatic effects on claims of losses, recruitment and population growth rates, were much stronger than the effects of variation in lynx and wolverine densities. 6. Synthesis and applications. Our analysis provides a quantitative basis for predator compensation and estimation of the costs of reintroducing lynx and wolverine in areas with free-ranging semi-domestic reindeer. We outline a potential path for conflict management which involves adaptive monitoring programs, open access to data, herder involvement, and development of management strategy evaluation (MSE) models to disentangle complex responses including multiple stakeholders and individual harvester decisions.
Data from: Defoliation of a grass by reindeer is compensated by the positive effects of its soil legacy, dung deposition, and moss removal
Herbivory is one of the key drivers shaping plant community dynamics. Herbivores can strongly influence plant productivity directly through defoliation and the return of nutrients in the form of dung and urine, but also indirectly by reducing the abundance of neighbouring plants and inducing changes in soil processes. However, the relative importance of these processes is poorly understood. We, therefore, established a common garden experiment to study plant responses to defoliation, dung addition, moss cover, and the soil legacy of reindeer grazing. We used an arctic tundra grazed by reindeer as our study system, and Festuca ovina, a common grazing-tolerant grass species as the model species. The soil legacy of reindeer grazing had the strongest effect on plants, and resulted in higher growth in soils originating from previously heavily-grazed sites. Defoliation also had a strong effect and reduced shoot and root growth and nutrient uptake. Plants did not fully compensate for the tissue lost due to defoliation, even when nutrient availability was high. In contrast, defoliation enhanced plant nitrogen concentrations. Dung addition increased plant production, nitrogen concentrations and nutrient uptake, although the effect was fairly small. Mosses also had a positive effect on aboveground plant production as long as the plants were not defoliated. The presence of a thick moss layer reduced plant growth following defoliation. This study demonstrates that grasses, even though they suffer from defoliation, can tolerate high densities of herbivores when all aspects of herbivores on ecosystems are taken into account. Our results further show that the positive effect of herbivores on plant growth via changes in soil properties is essential for plants to cope with a high grazing pressure. The strong effect of the soil legacy of reindeer grazing reveals that herbivores can have long-lasting effects on plant productivity and ecosystem functioning after grazing has ceased.
Data from: Field crickets compensate for unattractive static long-distance call components by increasing dynamic signalling effort
The evolution of multiple sexual signals presents a dilemma since individuals selecting a mate should pay attention to the most honest signal and ignore the rest; however, multiple signals may evolve if, together, they provide more information to the receiver than either one would alone. Static and dynamic signals, for instance, can act as multiple messages, providing information on different aspects of signaller quality that reflect condition at different time scales. While the nature of static signals makes them difficult or impossible for individuals to augment, dynamic signals are much more susceptible to temporary fluctuations in effort. We investigated whether male Texas field crickets, Gryllus texensis, that produce unattractive static signals compensate by dynamically increasing their calling effort. Our findings lend partial support to the compensation hypothesis, as males that called at unattractive carrier frequencies (a static trait) spent more time calling each night (a dynamic trait). Interestingly, this finding was most pronounced in males that called with attractive pulse characteristics (static traits) but did not occur in males that called with unattractive pulse characteristics. Males that signalled with unattractive pulse characteristics (duration and pause) spent less time calling through the night. Our correlative findings on wild caught males suggest that only males that signal with attractive pulse characteristics may be able to afford to pay the costs of both trait exaggeration and increased calling effort to compensate for poor carrier frequencies.
Females compensate for moult-associated male nest desertion in the Hooded Warbler
<p>Uniparental offspring desertion occurs in a wide variety of avian taxa and usually reflects sexual conflict over parental care. In many species desertion yields immediate reproductive benefits for deserters if they can remate and breed again during the same nesting season; in such cases desertion may be selectively advantageous even if it significantly reduces fitness of the current brood. However, in many other species parents desert late-season offspring when opportunities to renest are absent. In these cases, any reproductive benefits of desertion are delayed, and desertion is unlikely to be advantageous unless the deserted parent can compensate for the loss of its partner and minimize costs to the current brood. We tested this parental compensation hypothesis in Hooded Warblers <i>Setophaga citrina</i>, a species in which males regularly desert late-season nestlings and fledglings during moult. Females from deserted nests effectively doubled their provisioning efforts, and nestlings from deserted nests received just as much food, gained mass at the same rate, and were no more likely to die from either complete nest predation or brood reduction as young from biparental nests. The female provisioning response, however, was significantly related to nestling age; females undercompensated for male desertion when the nestlings were young, but overcompensated as nestlings approached fledging age, probably because of time constraints that brooding imposed on females with young nestlings. Overall, our results indicate that female Hooded Warblers completely compensate for male moult-associated nest desertion, and that deserting males pay no reproductive cost for desertion, at least through the point of fledging. Along with other studies, our findings support the general conclusion that late-season offspring desertion is likely to evolve only when parental compensation by the deserted partner can minimize costs to the current brood.</p>
Data from: Evolving from static to dynamic signals: evolutionary compensation between two communicative signals
Signals that convey related information may impose selection on each other, creating evolutionary links between different components of the communicative repertoire. Here, we ask about the consequences of the evolutionary loss of one signal (a colour patch) on another (a motion display) in Sceloporus lizards. We present data on male lizards of four species: two pairs of sister taxa representing two independent evolutionary losses of the static colour patch (S. cozumelae and S. parvus; S. siniferus and S. merriami). Males of the two species that have undergone an evolutionary loss of blue-belly patches (S. cozumelae, S. siniferus) were less active than their blue-bellied sister taxa (S. parvus, S. merriami), consistent with the suggestion that the belly patches were lost to reduce conspicuousness of species with high predation pressure. In contrast, the headbob display appears to have become more, rather than less, conspicuous over evolutionary time. The colour patch is exhibited primarily during aggressive encounters, whereas headbob displays are multifunction signals used in several different contexts, including aggressive encounters. Males of species that have lost the colour patch produced more motion displays, and the structure of those motion displays were more similar to those produced during combat. In both evolutionary episodes, a static colour signal appears to have been replaced by dynamic motion displays that can be turned off in the presence of predators and other unwanted receivers. The predominant pattern is one of evolutionary compensation and interactions between multiple signals that convey related information.
Data from: The design of a beautiful weapon: compensation for opposing sexual selection on a trait with two functions
Male fiddler crabs, genus Uca, have one greatly enlarged claw with which they court females and threaten and fight other males. Longer claws are more effective signals but are thought to be less effective weapons because the relative closing force at the tip of the claw decreases with claw length. We studied claw morphology and fighting in Uca terpsichores and Uca beebei and found a mechanism that may resolve opposing selection for signaling and fighting ability. When males fought they delivered gripping forces not at the tips but at the tubercles on the inner margins of their claws' fingers. As claws grow, these tubercles remain relatively close to the apex of the gape. Consequently, the mechanical advantage that governs the forces that can be delivered at these tubercles decreases only slightly with increasing claw length allowing the claw to be an effective signal and a powerful weapon. Animal weapons are exceptionally diverse in form and detail of armature and the causes of this diversity are poorly understood. We suggest that the designs of weapons may often reflect compensatory patterns of growth and placement of armature that enhances the weapon's overall utility for multiple uses in competition for mates.
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