France

Male northern quolls (Dasyurus hallucatus) die after a single synchronous breeding season, while females live and breed for 2-3 years. This provides a unique life history strategy in which to explore sex differences in performance trade-offs. Here, we assessed whether sprinting and biting performance trade-off for male or female northern quolls before, during, or after breeding (2012-2014). The activities that define survival and reproductive success for all animals depend on movement. However, movement is a complex trait, affected by multiple underlying factors, and organisms must balance the competing demands of these factors whenever they move. The morphology that increases bite force in northern quolls (i.e., increased head size)—which can improve fighting ability—should constrain sprinting performance by adding mass to the body. Trade-offs between fighting and escape performance might therefore be sex-specific or manifest only during particular times, such as during breeding. We studied northern quolls in the wild, and found that bite force and sprint speed do not trade-off functionally — bigger, heavier quolls with greater bite forces are not slower sprinters. We also found that males sprint slower in the post-breeding season. Because we have high recapture rates, we also assessed the repeatability of performance traits across several temporal scales. Performance was highly repeatable within seasons, but less repeatable across seasons, likely associated with the costs of the species’ extreme breeding. These findings suggest that ecologically relevant tasks important for survival and reproduction—fighting capacity and locomotor performance—may evolve independently in male and female northern quolls.

SEB Annual Conference 2022

Performance trade-offs in the world’s largest semelparous mammal, the Australian northern quoll (Dasyurus hallucatus)

Welcome Seabirders!  

Welcome to Virtual World Seabird Conference 3 - vWSC3! Whether you are in your office or lab, at home, in a coffee shop or bar poaching some wifi, or at a remote field site or research vessel – we are very excited to welcome you to the third ever World Seabird Conference. 

We would like to thank ALL of you for being so patient as WSC3 was scheduled, postponed, rescheduled, revised to virtual, and scheduled again. Throughout all those iterations there was one message that remained perfectly clear – seabirders were eager to meet and share their science. If we could not meet in person then virtual it would have to be, but a 3rd WSC was something everyone wanted. That support and commitment helped the WSU Board of Directors and Member Societies sort through all of the challenges they faced to plan and hold this conference. 

The list of those that need to be thanked is long and, while we plan on recognizing many during the live closing plenary, it is important to do so here in writing as well. 

The Australasian Seabird Group was our Local Host for our plan to meet in Hobart, Tasmania. They invested substantial time and effort to find venues and plan events that we unfortunately were not able to visit. Nonetheless we appreciate their work on behalf of WSC3 and encourage all of you to thank them when you see their members in Gathertown or elsewhere during our virtual meeting. Their willingness to host created the initial excitement for WSC3 and without that our vWSC would not have been possible.

We also wish to thank the Science Program Committee, the Virtual Committee, and the Early Career Scientist Committee for their hard work planning the logistics, events, and schedule for vWSC3. These committees also had to deal with changing parameters and short timelines that made what is always a challenging task even more challenging. The Travel Awards Committee also invested time and effort in developing procedures for awarding travel funds that ultimately would not be implemented. 

Our ability to shift from an in-person to a virtual meeting, and to do so in a way that would be financially feasible, was due to the effective efforts of The International Fundraising Committee and to our financial sponsors. The IFC raised funds to support WSC3 and then, through the good relationships they built with sponsors, ensured we could re-envision how those funds could be used to support a virtual conference that would be affordable and high-quality.

We all owe the WSU Board of Directors and the Representatives of the Member Societies a great deal of thanks. They are the ones who manage the WSU and, for the past 18 months, have had to have a series of challenging meetings and conversations, have had to make a series of difficult choices, have had to do all of that while considering the short- and long-term health of WSU and the World Seabird Conferences, and did this while also managing their own challenges at their day jobs. We are grateful for their diligence, patience, foresight, and throughout all of the meetings, their collegiality. Also – a 6-year term is quite a commitment!

There would not be a WSC3 without a successful WSC1 and WSC2. Thanks go to the Pacific Seabird Group for their support of WSC1 in Victoria, Canada, and to the African Seabird Group for their support of WSC2 in Cape Town, South Africa. In each of these endeavors and for our current conference we were fortunate to work with a dependable and trustworthy partner in Podium Conferences. Michelle Smith and Marischal de Armond have become valued members of our team and have not only helped us plan conferences but have assisted and advised the WSU Chairs and Board on issues above and beyond conference planning. 

As we embark on our vWSC3 week we extend to all of you our thanks for showing up, for being patient, and most importantly for the work you do with seabirds. We are all part of a unique, global community that shares an interest, a fascination, and a passion for birds that make a living in our world’s oceans. We have advanced the science, conservation, and management of seabirds as well the ecosystems they inhabit. We are consistently impressed and motivated by the work you do. 

The WSU formed in 2010 because we saw the need for a global organization to address challenges at a global level. Over the past 11 years WSU has grown, adapted, and evolved to become the community that this week is making vWSC3 a reality. Enjoy the week, appreciate and support the friends and colleagues you have made in the community, and if you see us in a virtual hallway please stop and say hello! 

Thank you for the opportunity to serve all of you and the WSU over the past few years,

Nicholas Carlile, Interim Chair, WSU<br>
Patrick Jodice, 2nd Chair of the WSU<br><br>

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3rd World Seabird Conference

Join us for four days of science, networking and virtual engagement with delegates from around the world!

technical paper

Discover the art of creating extraordinary science at SEB’s Annual Conference at Le Corum Conference Center     in Montpellier, France from 5 to  8 July 2022.

SEB’s Annual Conference is celebrated for creating the perfect composition of research, new discoveries and collaborative connections. Be creative and innovative by exchanging ideas and knowledge with masters of biology from all over the world.

2022 will find over 1500 experimental biologists from across the globe converging on the third-largest French city near the Mediterranean coast and the fastest-growing city in the country over the past 25 years.
	<br><br><br>


Please register for the conference by clicking on this link:

https://www.sebiology.org/events/seb-annual-conference-2022/registration.html

The site will be open for registered participants closer to the event.

2022 will find over 1500 experimental biologists from across the globe converging on the third-largest French city near the Mediterranean coast and the fastest-growing city in the country over the past 25 years - Montpellier, France

Locomotion is essential for fitness as it facilitates predation, escape, and reproductive behaviours. The energy expended for a given distance travelled (cost of transport; COT) varies significantly between individuals of the same species. Lower COT allows animals to allocate more of their energy budget to growth and reproduction. High COT may cause animals to adjust their movements to reduce energy allocated to movement, and potentially reduce energy allocation trade-offs. Our aim was to determine whether COT is a repeatable trait within individuals, and to determine its physiological causes and ecological consequences. We found that COT is a repeatable trait in zebrafish (Danio rerio). We rejected the hypothesis that mitochondrial efficiency (P/O ratio) predicted COT. We also rejected the hypothesis that COT is sensitive to temperature acclimation, exercise training, or their interaction, although COT increased with increasing acute test temperature. There was a weak but significant negative correlation between COT and dispersal, measured as the number of exploration decisions made by fish, and the distance travelled against the current in an artificial stream. However, COT did not correlate with the realised speed of fish swimming against the current. The implications of these results are that COT is an inherent characteristic of an individual which reflects a fixed physiological phenotype. Consequently, different energy budgets may be associated with individual movement patterns across environments. Warming environments may increase COT and exacerbate the magnitude of difference between individuals.

Cost of transport is a repeatable trait but is not determined by mitochondrial efficiency in zebrafish (Danio rerio)

Rose chafer beetles (Protetia cuprea) are pollinators as well as agricultural pests, flying between flowers and trees while foraging for pollen and fruits. Calculating the energy they expend on flying during foraging activity faces the challenge of measuring the metabolic rate (MR) of free-flying insects in an open space. We overcame this challenge by using the bolus injection of 13C Na-bicarbonate technique to measure their metabolic energy expenditure while flying in a large flight arena. Concurrently, we tracked the insects with high-speed cameras to extract their flight trajectory, from which we calculated the mechanical power invested in flying for each flight bout. We found that the chemical (metabolic) energy input converted to mechanical flight energy output at a mean efficiency of 10.4 ± 5.2 %, with a trend of increased efficiency in larger conspecifics (efficiency scaled with body mass to the power of 1.4). The transition during summer from a diet of pollen to that of fruits may affect the energy budget available for foraging. Starved P. cuprea, feeding on apples ad libitum, increased their body mass by an average of 6% in two hours. According to our calculations such a meal can power a 630-meter flight (assuming a carbohydrate assimilation efficiency of 90%). The high cost of aerial locomotion is inherent to the foraging behaviour of rose chafers, explaining their short flight bouts followed by prolonged feeding activity. The ability to measure both flight and its energetic cost is crucial for obtaining realistic estimates for the cost of locomotion.

The metabolic cost of flight and aerobic efficiency in the rose chafer, Protaetia cuprea (Cetoniinae)

Wing morphing during flight expands the performance envelope of flying animals and likely facilitates their ability to adapt to a broad range of habitats and atmospheric conditions. In birds, wing morphing is achieved by coupling a series of flexible and passive individual feathers to active musculoskeletal components. Although the aerodynamic effects of wing shape are relatively well characterised, the changes to the mechanical properties due to the structural rearrangement of feathers and the effects these changes have on flight performance are unknown. We first used dynamic mechanical testing at the base of in situ feathers of pigeons (Columba livia) to characterise the local mechanical properties. Wing folding decreased feather-anchoring tissue stiffness, an effect overcome in the proximal wing by an increase in stiffness via feather-feather interaction. We next applied computational fluid-structural interaction methods to quantify the effect of increasing or decreasing wing stiffness in the context of wing shape. These data revealed that the trends in wing stiffness due to wing folding can enhance lift production. Specifically, folding prevented destructive interference by the aerostructural deformations on flow vortices during high speed gliding flight. In conclusion, this study proposes that the natural coupling in the avian wing structural system between passive flight feathers and active musculoskeletal actuators allows for aerostructural flow control for enhanced flight performance over a variety of flight speeds.

Mechanisms for aerostructural flow control during avian wing morphing

When flying in near ground environments, birds encounter obstacles that force deviations from their flight paths. This raises the question of how they achieve the necessary guidance and control to perform these manoeuvres safely. In a flight arena equipped with a motion capture system, we challenged four Harris' hawks to negotiate a horizontal bar along their flight path between two perches (14 m apart). The unobstructed trajectory of the birds consists of a powered dive followed by glide up to the landing perch. The horizontal bar was positioned halfway between the perches, and was actuated to go through a vertical composite sinusoidal motion. While the minimum height of the bar was such that the typical unobstructed trajectory would not lead to a collision, the perceived risk of collision caused approximately half of the 880 flights to divert over the bar. The likelihood of diverting was primarily affected by the height of the bar and variation in individual preference. In cases where they would pass over the bar, three individuals directed their flight paths towards the bar shortly after take-off. This tracking mechanism, which arises as a risk averse behaviour, guides the birds nearer to the obstacle and thus increases the risk of collision. Obstacles acting as attractors would explain how many birds collide with overhead lines, despite the marginal probability for a random trajectory to encounter them.

Obstacle negotiation in the vertical plane

To produce the aerodynamic forces required for flight, two-winged insects (Diptera) move their wings back and forth at high wingbeat frequencies. Because the angular accelerations of this oscillating wing system scales quadratically with the wing-beat frequency, acceleration-based forces as a result of wing stroke-accelerations are expected to be particularly high for these flying insects. These acceleration-based forces consist of added-mass forces and Wagner-effect-based forces. Added-mass forces are resulting from the acceleration of fluid around the wing, and the Wagner-effect describes the delay in bound circulation build-up in accelerating wings. Here, we used computational fluid dynamics (CFD) simulations to systematically study how both added-mass forces and the Wagner-effect affect aerodynamic force production and airflow dynamics in accelerating insect wings. Based on the simulation results, we developed an aerodynamic model that captures the stroke-acceleration forces based on the wing-beat kinematics and wing morphology. This shows that current added-mass models fail to accurately predict added-mass forces on insect wings, primarily because these semi-empirical models ignore the Wagner-effect. Our novel Wagner-effect model is based on the interaction between stroke-rate and stroke-acceleration, and accurately predicts the delay in Leading-Edge Vortex build-up in accelerating wings as well as the delay in Leading-Edge Vortex reduction in decelerating wings. Finally, we applied our newly-developed aerodynamic model in a quasi-steady approach to the wingbeats of a fruit fly and malaria mosquito. This shows that particularly for high-frequency flapping flyers such as the mosquito, acceleration-based forces contribute substantially to aerodynamic lift and drag production.

Added-mass and Wagner-effect-based forces in high-frequency flapping insect wings

Humans are efficient bipedal walker and runner. Extant non-human primates (NHP) are not habitual bipeds, yet, they occasionally walk bipedally. According to 2D kinematics, they use a typical &quot;bent-hip, bent-knee&quot; posture coupled with a forward-leaning trunk, a limited stride length, a high stride frequency, and knees that remain flexed during the stance phase. No structural specialization is required for them to occasionally walk bipedally and compared to humans, extant NHPs do not exhibit any adaptations for bipedalism. Hence, it is suggested that the origin of a more habitual form of bipedal locomotion emerged from the common pattern observed in NHPs. However, one wonders whether the general lens through which the bipedal gait in NHPs has been described is discriminating enough to identify subtle differences that might exist between species. We conducted a study on the bipedal walking of olive baboons, at the Primatology Station of the CNRS (UAR 846). We provide detailed information on the 3D kinematics of bipedal walking. Our results show that the common pattern of the joint and segment angles can be easily described in the sagittal plan, but specificities related to the baboon model can be described in the frontal plan, such as the adduction of the thigh at touch-down. We compare these results with the 3D kinematics available for chimpanzees, capuchins, macaques and gibbons and identify subtle differences between species. Fundings: IRN-GDRI0870 & HoBiS-ANR-18-CE27-0010-01

3D kinematics of bipedal walking in the olive baboon, Papio anubis: evolutionary implications

It is well established that conditions experienced during prenatal development affect postnatal telomere length and dynamics in humans and laboratory animal models. However, we still know little about how prenatal environmental and social conditions shape telomere dynamics in wild animal populations. In the last years, we have performed several experimental studies to elucidate the role played by maternal glucocorticoids and the exposure to prenatal social stressors (e.g. exposure to predator cues) on postnatal telomere length and dynamics in a long-lived seabird species, the Yellow-legged gull (Larus michahellis). The results of these studies show that in contrast to previously thought, mothers may promote longer telomeres in their offspring by mildly increasing the allocation of glucocorticoids into their eggs (i.e. corticosterone). However, the effect of glucocorticoids hormones seems to differ depending on their intensity, origin and duration. Indeed, when late-stage embryos are repeatedly exposed to predator cues, they show increased secretion of glucocorticoids soon after hatching, an effect that was accompanied by a loss of telomere length during the early postnatal development. Together, our results show that embryos are not passive agents against their developmental environment, as their telomere dynamics are influenced by the maternal phenotype and the social cues they are able to integrate during their development.

Telomeres in the ocean: how pre- and postnatal factors shape telomere dynamics in a colonial long-lived seabird

Recent cross-sectional comparisons of telomere lengths, a hallmark of ageing, suggest that high temperatures may increase the rate of senescence in ectotherms. Telomeres shorten as a result of exposure to ROS produced by the mitochondria. Given that the rate of ROS production varies with mitochondrial efficiency, there may be a link between an individual’s mitochondrial efficiency and its telomere dynamics, which may be more acute at high temperatures. We tested this hypothesis by examining the relationship between telomere length and mitochondrial function from white muscle and liver of brown trout Salmo trutta of similar age and size, fed ad libitum, and acclimated to high-constant (19.5°C), high-variable (19.5 ± 2.5°C, daily cycle), or ideal (12°C) temperature regimes. Fish under high-constant and high-variable temperature regimes had greater higher average rates of telomere attrition, mitochondrial oxygen consumption rates, and ROS release rates along with lower mitochondrial phosphorylation efficiencies when compared to 12°C acclimated fish. However, telomere changes were positively correlated with mitochondrial phosphorylation efficiency in muscle, but not liver, in fish from the high-constant and high-variable temperature regimes: telomeres shortened in the least efficient individuals but increased in length in the most efficient fish. No relationship was observed in fish acclimated to 12°C. Therefore, individual diversity in muscle mitochondrial efficiency seems to cause variation in cellular senescence, where less efficient individuals have a more rapid shortening of telomeres. This may ultimately suggest that less efficient individuals will have shorter lifespans in warming and fluctuating environments.

Lower muscle mitochondrial efficiency results in more rapid shortening of telomeres in ectotherms at high and fluctuating temperatures

Climate change is increasing both the average ambient temperature and the frequency and severity of heat waves. While direct mortality induced by heat waves is increasingly reported, sub-lethal effects are also likely to impact population dynamics and persistence. We hypothesized that accelerated cellular ageing could be a cost of being exposed to higher ambient temperature. We tested this hypothesis in two common European passerine species by experimentally increasing nest box temperature by ca. 2°C during postnatal growth and measuring telomere length as a biomarker of ageing. In great tits, we also estimated the impact on medium-term survival and measured a large set of physiological markers including thyroid hormones, glucocorticoid signaling, oxidative stress, mitochondrial density and telomere maintenance mechanisms. We show that in both species, increasing early-life temperature does not affect growth or survival to fledging, but leads to an acceleration in the shortening of telomeres. In great tits, such shortening of telomeres was not explained by increased oxidative stress levels, but more likely by an increase in energy demand (i.e. higher thyroid hormones levels, increased expression of glucocorticoid receptor, increased mitochondrial density) leading to a reduction in telomere maintenance mechanisms (i.e. decrease in the gene expression of telomerase and protective shelterin). Additionally, medium-term survival was reduced from 34% in control nests to 19% in heated nests. Our results thus suggest that climate warming might affect cellular ageing in wild passerine populations, with potential impact on population dynamics and persistence.

From climate warming to accelerated cellular ageing: insights from two experimental studies in wild passerine birds

Individual variation in telomere length has been linked with health, survival and senescence. Individual variation in telomere length is due to environmental and genetic effects, which can be partitioned into their relative variance components. Estimating the ratio of additive genetic variance to the total phenotypic variance of telomere length, known as the heritability of telomere length, then facilitates understanding of the evolutionary potential of telomere length. However, telomere length heritability estimates vary greatly, and there is a limited understanding of why this is. To fill this knowledge gap, we conducted a systematic review and meta-analysis. We extracted 104 estimates from 43 studies and 18 species to test whether variation in telomere length heritability estimates is due to: phylogeny, species, environmental setting, age at sampling, laboratory methods, statistical methods, and individual repeated measurements. Overall, we found a moderate heritability of 45% (95% CI: 25% – 65%), and significant phylogenetic and species-specific effects, suggesting differential selection pressures on telomere length across taxa. Twin-based and SNP-based estimates were lower than correlation-based or pedigree-based estimates. Furthermore, we detected a publication bias, where small studies with low or non-significant heritability were under-represented. Our results demonstrate an overall heritable basis of telomere length, and the need for careful selection of statistical methods. Specifically, we recommend variance-partitioning methods with relatedness or SNP data over correlation methods to minimize bias. We also recommend future research to expand into a wider range of taxa, and to explore and validate the use of genome-wide correlation data in calculating quantitative genetic metrics.

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Performance trade-offs in the world’s largest semelparous mammal, the Australian northern quoll (Dasyurus hallucatus)

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Cost of transport is a repeatable trait but is not determined by mitochondrial efficiency in zebrafish (Danio rerio)

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