186 research outputs found

    Simulating the onset and spread of anoxic conditions during Cretaceous OAE2

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    A new model of the global atmosphere-ocean-continent-mantle system was set-up to investigate the triggering of the Oceanic Anoxic Event OAE2 through volcanic degassing processes at large igneous provinces (LIPs). The model simulates the changes in oceanic dissolved oxygen, phosphate, and carbon and the evolution of atmospheric pCO2 values under mid-Cretaceous boundary conditions. It considers the effects of pCO2 on element ratios in marine plankton (C : P) and includes new parameterizations for phosphorus and carbon burial at the seafloor based on modern observations. Independent isotopic and chemical time-series of ocean and atmosphere change over OAE2 are applied to evaluate the model results. The model results support the hypothesis that OAE2 was triggered by massive CO2 emissions at LIPs. According to the model, the phosphorus weathering flux into the ocean and the C : P ratio in marine plankton were enhanced by the rise in surface temperature and atmosphere pCO2 caused by mantle degassing. Marine export production and oxygen consumption in intermediate and deep water masses increased in response to the expansion of the dissolved phosphate inventory of the ocean and the change in plankton element ratios. The spread of anoxic conditions in bottom waters -induced by enhanced carbon export and respiration- was further amplified by the oxygen-dependent burial of phosphorus in marine sediments in a positive feedback loop. The modeling implies that enhanced CO2 emissions favor the spread of low-oxygen conditions also in modern oceans

    Terrestrial locomotion imposes high metabolic requirements on bats

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    The evolution of powered flight involved major morphological changes in Chiroptera. Nevertheless, all bats are also capable of crawling on the ground and some are even skilled sprinters. We asked if a highly derived morphology adapted for flapping flight imposes high metabolic requirements on bats when moving on the ground. We measured the metabolic rate during terrestrial locomotion in mastiff bats, Molossus currentium, a species that is both a fast-flying aerial-hawking bat and an agile crawler on the ground. Metabolic rates of bats averaged 8.0±4.0 ml CO2 min–1 during a 1-min period of sprinting at 1.3±0.6 km h–1. With rising average speed, mean metabolic rates increased, reaching peak values that were similar to those of flying conspecifics. Metabolic rates of M. currentium were higher than those of similar-sized rodents that sprinted at similar velocities under steady-state conditions. When M. currentium sprinted at peak velocities, its aerobic metabolic rate was 3–5 times higher than those of rodent species running continuously in steady-state conditions. Costs of transport (J kg–1 m–1) were more than 10 times higher for running than for flying bats. We conclude that at the same speed bats experience higher metabolic rates during short sprints than quadruped mammals during steady-state terrestrial locomotion, yet running bats achieve higher maximal mass-specific aerobic metabolic rates than non-volant mammals such as rodents

    Rain increases the energy cost of bat flight

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    Similar to insects, birds and pterosaurs, bats have evolved powered flight. But in contrast to other flying taxa, only bats are furry. Here, we asked whether flight is impaired when bat pelage and wing membranes get wet. We studied the metabolism of short flights in Carollia sowelli, a bat that is exposed to heavy and frequent rainfall in neotropical rainforests. We expected bats to encounter higher thermoregulatory costs, or to suffer from lowered aerodynamic properties when pelage and wing membranes catch moisture. Therefore, we predicted that wet bats face higher flight costs than dry ones. We quantified the flight metabolism in three treatments: dry bats, wet bats and no rain, wet bats and rain. Dry bats showed metabolic rates predicted by allometry. However, flight metabolism increased twofold when bats were wet, or when they were additionally exposed to rain. We conclude that bats may not avoid rain only because of sensory constraints imposed by raindrops on echolocation, but also because of energetic constraints

    Biogeochemical effects of volcanic degassing on the oxygen-state of the oceans during the Cenomanian/Turonian Anoxic Event 2

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    ABSTRACT FINAL ID: PP11A-1769 Cretaceous anoxic events may have been triggered by massive volcanic CO2 degassing as large igneous provinces (LIPs) were emplaced on the seafloor. Here, we present a comprehensive modeling study to decipher the marine biogeochemical consequences of enhanced volcanic CO2 emissions. A biogeochemical box model has been developed for transient model runs with time-dependent volcanic CO2 forcing. The box model considers continental weathering processes, marine export production, degradation processes in the water column, the rain of particles to the seafloor, benthic fluxes of dissolved species across the seabed, and burial of particulates in marine sediments. The ocean is represented by twenty-seven boxes. To estimate horizontal and vertical fluxes between boxes, a coupled ocean–atmosphere general circulation model (AOGCM) is run to derive the circulation patterns of the global ocean under Late Cretaceous boundary conditions. The AOGCM modeling predicts a strong thermohaline circulation and intense ventilation in the Late Cretaceous oceans under high pCO2 values. With an appropriate choice of parameter values such as the continental input of phosphorus, the model produces ocean anoxia at low to mid latitudes and changes in marine ή13C that are consistent with geological data such as the well established ή13C curve. The spread of anoxia is supported by an increase in riverine phosphorus fluxes under high pCO2 and a decrease in phosphorus burial efficiency in marine sediments under low oxygen conditions in ambient bottom waters. Here, we suggest that an additional mechanism might contribute to anoxia, an increase in the C:P ratio of marine plankton which is induced by high pCO2 values. According to our AOGCM model results, an intensively ventilated Cretaceous ocean turns anoxic only if the C:P ratio of marine organic particles exported into the deep ocean is allowed to increase under high pCO2 conditions. Being aware of the uncertainties such as diagenesis, this modeling study implies that potential changes in Redfield ratios might be a strong feedback mechanism to attain ocean anoxia via enhanced CO2 emissions. The formation of C-enriched marine organic matter may also explain the frequent occurrence of global anoxia during other geological periods characterized by high pCO2 values

    Nathusius’ bats, Pipistrellus nathusii, bypass mating opportunities of their own species, but respond to foraging heterospecifics on migratory transit flights

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    In late summer, migratory bats of the temperate zone face the challenge of accomplishing two energy-demanding tasks almost at the same time: migration and mating. Both require information and involve search efforts, such as localizing prey or finding potential mates. In non-migrating bat species, playback studies showed that listening to vocalizations of other bats, both con-and heterospecifics, may help a recipient bat to find foraging patches and mating sites. However, we are still unaware of the degree to which migrating bats depend on con-or heterospecific vocalizations for identifying potential feeding or mating opportunities during nightly transit flights. Here, we investigated the vocal responses of Nathusius’ pipistrelle bats, Pipistrellus nathusii, to simulated feeding and courtship aggregations at a coastal migration corridor. We presented migrating bats either feeding buzzes or courtship calls of their own or a heterospecific migratory species, the common noctule, Nyctalus noctula. We expected that during migratory transit flights, simulated feeding opportunities would be particularly attractive to bats, as well as simulated mating opportunities which may indicate suitable roosts for a stopover. However, we found that when compared to the natural silence of both pre-and post-playback phases, bats called indifferently during the playback of conspecific feeding sounds, whereas P. nathusii echolocation call activity increased during simulated feeding of N. noctula. In contrast, the call activity of P. nathusii decreased during the playback of conspecific courtship calls, while no response could be detected when heterospecific call types were broadcasted. Our results suggest that while on migratory transits, P. nathusii circumnavigate conspecific mating aggregations, possibly to save time or to reduce the risks associated with social interactions where aggression due to territoriality might be expected. This avoidance behavior could be a result of optimization strategies by P. nathusii when performing long-distance migratory flights, and it could also explain the lack of a response to simulated conspecific feeding. However, the observed increase of activity in response to simulated feeding of N. noctula, suggests that P. nathusii individuals may be eavesdropping on other aerial hawking insectivorous species during migration, especially if these occupy a slightly different foraging niche

    Metabolic costs of bat echolocation in a non-foraging context support a role in communication

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    The exploitation of information is a key adaptive behavior of social animals, and many animals produce costly signals to communicate with conspecifics. In contrast, bats produce ultrasound for auto-communication, i.e., they emit ultrasound calls and behave in response to the received echo. However, ultrasound echolocation calls produced by non-flying bats looking for food are energetically costly. Thus, if they are produced in a non-foraging or navigational context this indicates an energetic investment, which must be motivated by something. We quantified the costs of the production of such calls, in stationary, non-foraging lesser bulldog bats (Noctilio albiventris) and found metabolic rates to increase by 0.021 ± 0.001 J/pulse (mean ± standard error). From this, we estimated the metabolic rates of N. albiventris when responding with ultrasound echolocation calls to playbacks of echolocation calls from familiar and unfamiliar conspecific as well as heterospecific bats. Lesser bulldog bats adjusted their energetic investment to the social information contained in the presented playback. Our results are consistent with the hypothesis that in addition to orientation and foraging, ultrasound calls in bats may also have function for active communication

    Food Deprivation, Body Weight Loss and Anxiety-Related Behavior in Rats

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    In behavioral studies, food deprivation protocols are routinely used to initiate or maintain motivational states that are required in a particular test situation. However, there is limited evidence as to when food deprivation compromises animal welfare. This study investigated the effects of different lengths of food deprivation periods and restricted (fixed-time) feeding on body weight loss as well as anxiety-related and motivated behavior in 5–6 month old male and female Wistar rats. The observed body weight loss was not influenced by sex and ranged between 4% (16 h deprivation) to approximately 9% (fixed-time feeding). Despite significant body weight loss in all groups, the motivation to eat under the aversive test conditions of the modified open field test increased only after 48 h of food deprivation. Long-lasting effects on anxiety as measured in the elevated plus maze test 24 h after refeeding have not been observed, although fixed-time feeding could possibly lead to a lasting anxiogenic effect in female rats. Overall, female rats showed a more anxiolytic profile in both tests when compared to male rats. Despite these sex differences, results suggest that food deprivation is not always paralleled by an increased motivation to feed in a conflict situation. This is an important finding as it highlights the need for tailored pilot experiments to evaluate the impact of food deprivation protocols on animals in regard to the principles of the 3Rs introduced by Russell and Burch. View Full-Tex
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