Friday, June 02, 2023

Research project analyzes medical, nutritional and environmental applications of new Antarctic bacteria


Discovered by Uruguayan scientists in 2013, two psychrophilic (cold-adapted) species have been experimented with since 2018 by a partnership between IIBCE in Montevideo and the University of São Paulo in Brazil.

Peer-Reviewed Publication

FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO

New Antarctic bacteria 

IMAGE: RESEARCH PROJECT ANALYZES MEDICAL, NUTRITIONAL AND ENVIRONMENTAL APPLICATIONS view more 

CREDIT: INSTITUTO DE INVESTIGACIONES BIOLÓGICAS CLEMENTE ESTABLE



A scientific collaboration between the University of São Paulo (USP) in Ribeirão Preto, Brazil, and Clemente Estable Institute of Biological Research (IIBCE) in Montevideo, Uruguay, is experimenting with two new bacteria discovered in the Antarctic ten years ago, in order to verify the possibility of applications in healthcare, food processing and environmental rehabilitation.

An article describing part of the results appeared in the March issue of the journal ACS Synthetic Biology, a publication of the American Chemical Society. 

The use of bacteria in biotechnology offers many potential benefits for human beings and the planet, including the absence of toxic waste and lack of dependence on fossil energy sources. Bacteria are microscopic organisms that have the ability to adapt to various environments and perform a range of important functions. Bacteria retrieved from terrestrial extremes have even more interesting physiological characteristics. Antarctica is the coldest continent, with temperatures ranging from -10 °C to -60 °C in winter and from -5 °C to -20 °C in summer.

Bacteria with cold-adapted enzymes are known as psychrophiles. Enzymes are proteins that catalyze specific chemical reactions. The enzymes produced by psychrophiles are very important to biotechnological processes because they remain highly active even at low temperatures. As a result, they are less expensive and more sustainable than enzymes produced by bacteria in temperate environments.

“Bacteria isolated from the environment are often very hard to ‘domesticate’ with a view to using their enzymes. We studied two bacteria belonging to the genus Pseudomonas isolated from sediment in the Antarctic. They’re both new species that have never been described before. We set out to see if we could take advantage of their metabolism with our gene editing tools and succeeded in establishing the correct functioning of several plasmids in these two bacteria, facilitating their use for expression of psychrophilic enzymes in biotech applications,” said María Eugenia Guazzaroni, last author of the article and a professor in the Biology Department of the Ribeirão Preto School of Philosophy, Sciences and Letters (FFCLRP-USP). Her research is supported by FAPESP.

Applications 

Bacterial plasmids are small DNA molecules commonly used in bacterial cloning. Expression plasmids are used to produce specific proteins. The plasmid is introduced into a cell, where it replicates, and the protein is expressed by its DNA.

Expression plasmids are widely used in scientific research and by pharmaceutical and biotech firms to produce large quantities of specific recombinant proteins for the development of medical therapies with hormones or antibodies. 

Psychrophilic enzymes can also be used to produce refrigerated foods such as ice cream and yogurt with enhanced quality and texture. Yet another application involves additives in detergent and washing powder to improve the efficacy of stain and dirt removal. These enzymes function at comparatively low temperatures and can therefore be used for washing laundry in cold water, economizing energy. They also improve the quality of detergent and washing powder, so that clothes and other items made of fabric are less damaged and last longer.

Psychrophilic enzymes can also be used in bioremediation to remove pollutants from cold environments such as the Antarctic.

Cross-border collaboration

The study was conducted in collaboration with Uruguayan scientists who discovered the new bacteria in 2012 in the Antarctic and have been working with the Ribeirão Preto group since 2018. “Vanesa Amarelle, a co-author of the article, visited us as a postdoctoral fellow with a scholarship for training mobility at research institutes abroad in priority areas awarded by Uruguay’s National Research and Innovation Agency [ANII] in 2018,” said Guazzaroni, who has a PhD in biochemistry and molecular biology from Zaidín Experiment Station (EEZ) in Granada, run by Spain’s National Research Council (CSIC), with postdoctoral qualifications in environmental metagenomics and functional metagenomics of extreme environments, also earned in Spain, as well as postdoctoral studies at FFCLRP-USP.

Besides Guazzaroni and Amarelle, the other co-authors of the article are Diego M. Roldán and Elena Fabiano, both of whom are affiliated with IIBCE’s Department of Microbial Biochemistry and Genomics. 

About São Paulo Research Foundation (FAPESP)

The São Paulo Research Foundation (FAPESP) is a public institution with the mission of supporting scientific research in all fields of knowledge by awarding scholarships, fellowships and grants to investigators linked with higher education and research institutions in the State of São Paulo, Brazil. FAPESP is aware that the very best research can only be done by working with the best researchers internationally. Therefore, it has established partnerships with funding agencies, higher education, private companies, and research organizations in other countries known for the quality of their research and has been encouraging scientists funded by its grants to further develop their international collaboration. You can learn more about FAPESP at www.fapesp.br/en and visit FAPESP news agency at www.agencia.fapesp.br/en to keep updated with the latest scientific breakthroughs FAPESP helps achieve through its many programs, awards and research centers. You may also subscribe to FAPESP news agency at http://agencia.fapesp.br/subscribe.

Little-known microbes could help predict climate tipping points

Rising temperatures could push ocean plankton and other single-celled creatures toward a carbon tipping point that fuels more warming. But new research shows it’s also possible to detect early distress signals before they get there.

Peer-Reviewed Publication

DUKE UNIVERSITY

Tipping-point detection 

IMAGE: FOUND IN LAKES AND RIVERS WORLDWIDE, SINGLE-CELLED CREATURES LIKE THESE PARAMECIUM BURSARIA CAN BOTH EAT AND PHOTOSYNTHESIZE. MICROBES LIKE THIS PLAY A DOUBLE ROLE IN CLIMATE CHANGE, RELEASING OR ABSORBING CARBON DIOXIDE -- THE HEAT-TRAPPING GREENHOUSE GAS THAT IS THE PRIMARY DRIVER OF WARMING -- DEPENDING ON WHETHER THEY RELY ON AN ANIMAL-LIKE LIFESTYLE OR A PLANT-LIKE LIFESTYLE. view more 

CREDIT: DANIEL J. WIECZYNSKI, DUKE UNIVERSITY



DURHAM, N.C. -- Researchers studying a group of widespread but often overlooked microbes have identified a climate feedback loop that could accelerate climate change. But it’s not all bad news: this one comes with an early warning signal.

Using a computer simulation, a team of scientists from Duke University and the University of California, Santa Barbara, showed that most of the world’s ocean plankton and many other single-celled creatures in lakes, peatlands and other ecosystems could cross a threshold where instead of soaking up carbon dioxide, they start doing the opposite. That’s because of how warming affects their metabolism.

Because carbon dioxide is a greenhouse gas, that in turn could drive up temperatures further -- a positive feedback loop that could lead to runaway change, where small amounts of warming have an outsized impact.

But by carefully monitoring the abundances of these organisms, we might be able to anticipate the tipping point before it gets here, the researchers report in a study published June 1 in the journal Functional Ecology.

In the new study, researchers focused on a group of tiny organisms called mixotrophs, so named because they mix up two modes of metabolism: they can photosynthesize like a plant or hunt food like an animal, depending on conditions.

“They're like the Venus fly traps of the microbial world,” said first author Daniel Wieczynski, a postdoctoral associate at Duke.

During photosynthesis, they soak up carbon dioxide, a heat-trapping greenhouse gas. And when they eat, they release carbon dioxide. These versatile organisms aren’t considered in most models of global warming, yet they play an important role in regulating climate, said senior author Jean P. Gibert of Duke.

Most of the plankton in the ocean -- things like diatoms, dinoflagellates -- are mixotrophs. They’re also common in lakes, peatlands, in damp soils and beneath fallen leaves.

“If you were to go to the nearest pond or lake and scoop a cup of water and put it under a microscope, you’d likely find thousands or even millions of mixotrophic microbes swimming around,” Wieczynski said.

“Because mixotrophs can both capture and emit carbon dioxide, they're like ‘switches’ that could either help reduce climate change or make it worse,” said co-author Holly Moeller, an assistant professor at the University of California, Santa Barbara.

To understand how these impacts might scale up, the researchers developed a mathematical model to predict how mixotrophs might shift between different modes of metabolism as the climate continues to warm.

The researchers ran their models using a 4-degree span of temperatures, from 19 to 23 degrees Celsius (66-73 degrees Fahrenheit). Global temperatures are likely to surge 1.5 degrees Celsius above pre-industrial levels within the next five years, and are on pace to breach 2 to 4 degrees before the end of this century.

The analysis showed that the warmer it gets, the more mixotrophs rely on eating food rather than making their own via photosynthesis. As they do, they shift the balance between carbon in and carbon out.

The models suggest that, eventually, we could see these microbes reach a tipping point -- a threshold beyond which they suddenly flip from carbon sink to carbon source, having a net warming effect instead of a cooling one.

This tipping point is hard to undo. Once they cross that threshold, it would take significant cooling -- more than one degree Celsius -- to restore their cooling effects, the findings suggest.

But it’s not all bad news, the researchers said. Their results also suggest that it may be possible to spot these shifts in advance, if we watch out for changes in mixotroph abundance over time.

“Right before a tipping point, their abundances suddenly start to fluctuate wildly,” Wieczynski said. “If you went out in nature and you saw a sudden change from relatively steady abundances to rapid fluctuations, you would know it’s coming.”

Whether the early warning signal is detectable, however, may depend on another key factor revealed by the study: nutrient pollution.

Discharges from wastewater treatment facilities and runoff from farms and lawns laced with chemical fertilizers and animal waste can send nutrients like nitrate and phosphate into lakes and streams and coastal waters.

When Wieczynski and his colleagues included higher amounts of such nutrients in their models, they found that the range of temperatures over which the telltale fluctuations occur starts to shrink until eventually the signal disappears and the tipping point arrives with no apparent warning.

The predictions of the model still need to be verified with real-world observations, but they “highlight the value of investing in early detection,” Moeller said.

“Tipping points can be short-lived, and thus hard to catch,” Gibert said. “This paper provides us with a search image, something to look out for, and makes those tipping points -- as fleeting as they may be -- more likely to be found.”

This research was supported by grants from the Simons Foundation (689265), the National Science Foundation (1851194), and the U.S. Department of Energy (DE-SC0020362).

CITATION: "Mixotrophic Microbes Create Carbon Tipping Points Under Warming," Daniel J. Wieczynski, Holly V. Moeller and Jean P. Gibert. Functional Ecology, May 23, 2023. DOI:  10.1111/1365-2435.14350

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Q&A: Virginia Tech researchers discover new, more effective candidates for treatment of syphilis

Researchers found two antimicrobial agents that were more effective in treating the disease-causing agent Treponema pallidum in a laboratory setting

Peer-Reviewed Publication

VIRGINIA TECH

Researchers 

IMAGE: BRANDON JUTRAS AND KATHRYN HAYES FOUND NEW CANDIDATES FOR THE TREATMENT OF SYPHILIS WITH SEVERAL BEING MORE EFFECTIVE THAN THE CURRENT TREATMENT OPTIONS. PHOTO BY MAX ESTERHUIZEN FOR VIRGINIA TECH. view more 

CREDIT: VIRGINIA TECH


Since 2000, sexually transmitted infection rates have been on the rise. Syphilis, a disease that was nearly eradicated in the United States at that time, now affects more than 18 million people worldwide each year with few options for effective treatment.

One challenge that has plagued syphilis researchers for decades was the inability to culture and study the disease-causing agent in a laboratory setting.

“The incredible efforts of our colleagues and collaborators produced a faithful system to propagate the disease-causing agent in vitro, or in a laboratory setting. Being able to culture the bacterium opens new doors in terms of understanding it in terms of how it causes disease, ways we can prevent infection, and in efforts in which we may be able to intervene,” said Brandon Jutras, the principal investigator of the project, an assistant professor of biochemistry in the College of Agriculture and Life Sciences, and affiliated faculty of the Fralin Life Sciences Institute and the Center for Emerging, Zoonotic, and Arthropod-borne Pathogens.

Virginia Tech researchers set out to determine if there were possible treatment options that could serve as an alternative for the millions of people impacted by the disease each year.

What the College of Agriculture and Life Sciences researchers discovered exceeded all expectations. Not only did they find another treatment option to benzathine penicillin G, but they found two antimicrobial agents that were more effective in treating the disease-causing agent Treponema pallidum in a laboratory setting.

The research was published today in “Antimicrobial and Resistance,” a newcomer to the Nature Portfolio Journals, and was funded by the National Institutes of Health and the U.S. Department of Agriculture with additional internal funding from the Center of Emerging, Zoonotic, and Arthropod-borne Diseases.

A fluorescent image of Treponema pallidum in a laboratory setting.

These drugs are already approved by the Food and Drug Administration, so they are safe for humans, which could accelerate the rollout.

“It’s a disease for which we have very few therapeutic options,” said Kathryn Hayes, the lead author and Ph.D. candidate in Virginia Tech’s Translational Biology, Medicine, and Health program. “We were able to do the first large-scale drug screen for syphilis treatment alternatives, efforts that would not have been possible without an in vitro culture system.”

Now, hear directly from the researchers on their project:

What inspired you to carry out this research?

Hayes: I have a huge passion for sexual health and a nerdy interest in infectious diseases. This research allowed me to combine these two interests as syphilis is a disease that has been around for centuries but little is known about it due to the difficulty of growing the bacteria in a lab setting. Having more data and research on the disease is a pressing clinical need.

What spurred your interest in sexual health?

Hayes: My own queer identity and how disproportionally impacted the queer community is by sexually transmitted diseases motivated me. The other is the stigma around sexually transmitted infections [STIs]. People will talk about how they have the flu, or even COVID-19, but no one will say they have syphilis. Education, or lack thereof, around sexual health, particularly STIs, has impacted how people talk about it and has continued to reinforce the importance of this research.

The research team of Kathryn Hayes and Brandon Jutras found two antimicrobial agents that were more effective in treating the syphilis disease-causing agent Treponema pallidum in a laboratory setting. Photo by Max Esterhuizen for Virginia Tech.

A year and 100 days: Can you describe the process you used to culture syphilis?

Hayes: The reason it is so hard is that the bacteria require very strict microaerophilic conditions – a low oxygen environment – which, in this case, means exactly 1.5 percent oxygen. We have an incubator that uses nitrogen to force out the excess oxygen so it keeps that exact percentage. The day before I culture, I take a supportive mammalian cell line and put it onto traditional plates, because they still need a co-culture to support growth. I have to make fresh media for the culture myself.

We have a few components that I make quarterly, and then every week I have to combine 12 ingredients to make the media, which then have to equilibrate overnight in our special incubator.

On average it was a two-hour prep the day before at minimum and then anywhere from like three to seven hours the day of depending on the number of bacteria I'm working with in that culture. As of last week, it has been a year and 100 days of culturing.

How did you conduct the drug screening?

Jutras: We started with nearly 100 antibiotics of a particular class, and two tetracyclines, which are in a different class of antibiotic, used as a cross-comparison. We incubated the bacteria with the antibiotics at an extraordinarily low concentration (five nanomolar) to get an initial reading of how effective they were at preventing growth.

From there, we took our top 25 percent of compounds and retested them to ensure that our analytical methods were accurate.

The top 10 percent were further investigated using sophisticated microscopy techniques in conjunction with antibiotic treatment. In essence, we could watch these compounds in action

In addition, we determined their minimum inhibitory concentrations, and that's where we further confirmed that new candidates Azlocillin and Mezlocillin were more effective than our current standard of care, in vitro.

This research could have major implications. What’s next in the process for you?

Jutras: This project was a big risk. Addie could spend all this time and perform all this incredible research just to have discovered that nothing worked better than benzathine penicillin G. The surprising thing is that she found multiple options that work better.

Hayes: I want to look at modeling how these antibiotics are affecting bacteria. So, looking at protein drug interaction and how those interactions affect overall drug efficacy. I think that's a very interesting mechanistic step because once you understand what's happening to the bacteria on a molecular level, you can synthesize compounds that are very similar, but slightly different, to create more effective treatments.

KEEPING ELDERS DRUGGED IN STUPOR

Antipsychotic drugs use increased in Canadian long-term care homes in first year of pandemic

Peer-Reviewed Publication

UNIVERSITY OF WATERLOO



While most aspects of care quality in long-term care homes did not differ in the first year of the pandemic from pre-pandemic levels, a new study shows that the use of antipsychotic drugs increased in all provinces.

The study analyzed health system performance reports provided by the Canadian Institute for Health Information (CIHI) over three years: two before the pandemic and the first year of COVID-19. The reports are based on more than half a million resident assessments completed in Ontario, Manitoba, Alberta and British Columbia. 

Researchers focused on these four provinces because they had the highest incidence of COVID-19 in long-term care homes during the initial waves of the pandemic.

"The COVID-19 pandemic brought immense challenges to long-term care homes, resulting in higher mortality rates," said Dr. John Hirdes, a researcher in the School of Public Health Sciences. "Our study focused on other aspects of care quality during the pandemic, revealing only modest changes overall with the exception of increases in problematic antipsychotic use."

The percentage of residents who received antipsychotic medications without a diagnosis of psychosis increased in all provinces, not just the four that were studied. The highest increase was in Alberta, and the lowest in Ontario. "We did not observe a significant increase in behavioural symptoms, which raises the question of whether these medications were used preemptively in anticipation of challenges during outbreaks and staffing shortages," said Hirdes. 

The research team found no significant changes in other areas, such as falls, pressure ulcers and physical restraints. 

"These data emphasize the importance of the effort put forth by long-term care teams – nurses, personal support workers and others – to maintain care quality during unprecedented times," said co-author Dr. George Heckman, also in the School of Public Health Sciences, and Schlegel Research Chair in Geriatric Medicine.

While this study focused on provincial-level results, CIHI's publicly available evidence could also be used by individual long-term care homes to assess whether they can improve their record on resident care, said lead author Dr. Luke Turcotte, a Waterloo PhD graduate, now an assistant professor at Brock University. "For example, homes with a high rate of antipsychotic drug use could employ previous interventions in Canada that successfully reduced their unnecessary use."

The study, "Long-Term Care Resident Health and Quality of Care During the COVID-19 Pandemic: A Synthesis Analysis of Canadian Institute for Health Information Data Tables," was published in the scientific journal Health Services Insights. The Government of Canada's New Frontiers in Research and the Canadian Institutes of Health Research partly funded the study.

Evolution driving improvements in racehorse speed, study shows

Peer-Reviewed Publication

UNIVERSITY OF EXETER

A new study by experts from the University of Exeter has found that genetic improvement is underlying the increasing speed of Britain’s thoroughbreds. This contrasts with earlier studies that suggested racehorses were showing no genetic improvement in response to selection by breeders. 

However, the new study has also revealed that rates of genetic progress are relatively low, particularly over long-distance races. Further research is required to determine what is preventing more rapid improvement. 

Researchers analysed a data set of 692,534 race times run by more than 76,000 horses born between 1995-2012. Over sprint, middle-distance and long-distance races, genetic improvement for thoroughbred speed was found to be ongoing and statistically significant.  

The study found that genetic improvement accounts for 60%, 55% and 17% of the total increase in speed observed over short, middle and long distances respectively. 

The research also showed that thoroughbred speed is only weakly heritable across all distances - in part explaining the slow rates of genetic improvement. 

The researchers suggest the low rates of genetic improvement also raises the possibility that selection of racehorses for breeding may be weaker than previously assumed, particularly over long distances, or some other constraint may be at play. 

Dr Patrick Sharman from the Centre for Ecology and Conservation at the University of Exeter’s Penryn Campus in Cornwall said: “There has been plenty of debate over the recent decades whether racehorses have reached a genetic limit to how fast they can run.  

“Our analysis suggests that is not the case, and on the contrary, provides strong statistical evidence that racehorses continue to evolve to run faster in Great Britain. The question now is why are rates relatively low, particularly over long-distances?  

“We estimated relatively low heritability for racehorse speed which goes some way to explaining it, but it would appear there is more to it. The selection of racehorses for breeding may be less accurate and weaker than generally assumed, particularly over long-distance races, but other factors could be constraining genetic improvement”. 

Genetic improvement of speed across distance categories in thoroughbred racehorses in Great Britain by Patrick Sharman and Alastair J. Wilson is published in HeredityGenetic improvement of speed across distance categories in thoroughbred racehorses in Great Britain | Heredity (nature.com) 

The making of a Mona Lisa hologram


A deep learning algorithm and metasurface combine to recreate a high-resolution image of the famous portrait


Peer-Reviewed Publication

AMERICAN INSTITUTE OF PHYSICS

Holographic reconstruction of the Mona Lisa by a megapixel acoustic metasurface 

IMAGE: HOLOGRAPHIC RECONSTRUCTION OF THE MONA LISA BY A MEGAPIXEL ACOUSTIC METASURFACE. view more 

CREDIT: MIAO ET AL.



WASHINGTON, May 30, 2023 – Holograms are often displayed in science fiction as colorful, life-sized projections. But what seems like the technology of the future is actually the technology of the present, and now it has been used to recreate the Mona Lisa.

In Applied Physics Reviews, by AIP Publishing, researchers from Tianjin University, the Beijing Institute of Technology, Rowan University, the University of Missouri, Qingdao University, Shijiazhuang Tiedao University, and Beijing Jiaotong University developed an acoustic metasurface-based holography technique that uses a deep learning algorithm to generate and iteratively improve a hologram of the Mona Lisa.

Holograms are images created by recording and reconstructing the interference pattern of light or sound waves. They provide realistic and immersive visual or auditory experiences and can be applied in entertainment, medical imaging, and communication, among other fields.

Metasurfaces, or two-dimensional materials made of an array of tiny antenna-like components, can help a lot with the holography process.

“A metasurface-based hologram works by precisely controlling the phase and amplitude of the waves interacting with the metasurface,” said author Yue-Sheng Wang. “As a result, the outgoing waves at each pixel exhibit a certain amplitude and phase, which results in the desired holographic image based on their interference.”

The team wanted to develop a metasurface holography optimization method to enhance efficiency and precision. They used a deep neural network-based algorithm to customize the antenna-like structures within their metasurface. By iteratively reducing inconsistencies between the original and holographic image, they tweaked the metasurface and created a high-quality hologram.

“We chose to recreate the Mona Lisa as a proof of concept,” said Wang. “It is so famous that almost everyone knows about it. It is filled with countless delicate and subtle transitions of layers, which enhances the softness, haziness, and mystery of the painting. So it is a great way to demonstrate the effectiveness of our method.”

The holographic method successfully reconstructed the Mona Lisa, and, in even more detail, her left eye. While the Mona Lisa hologram is two-dimensional, the technique can be extended to create three-dimensional images as well.

“The precise control of sound waves offered by our holography method is crucial for advancing non-invasive medical therapies, effective noise control, and optimizing acoustic environments like concert halls,” said Wang. “These improvements have the potential to enhance quality of life and various technological applications.”

The authors believe their technique could revolutionize the field of holography. They plan to explore ways to generalize it, make it compatible with 3D printing, and reduce training time.

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The article, "Deep-Learning-Aided Metasurface Design for Megapixel Acoustic Hologram," is authored by Xuan-Bo Miao, Hao-Wen Dong, Sheng-Dong Zhao, Shi-Wang Fan, Guoliang Huang, Chen Shen, and Yue-Sheng Wang. It will appear in Applied Physics Reviews on May 30, 2023 (DOI: 10.1063/5.0136802). After that date, it can be accessed at https://doi.org/10.1063/5.0136802.

ABOUT THE JOURNAL

Applied Physics Reviews features articles on significant and current topics in experimental or theoretical research in applied physics, or in applications of physics to other branches of science and engineering. The journal publishes both original research on pioneering studies of broad interest to the applied physics community, and reviews on established or emerging areas of applied physics. See https://aip.scitation.org/journal/are.

How insects track odors by navigating microscale winds

An optimal range of wind speed and environmental surface complexity may help flying insects locate an odor source

Peer-Reviewed Publication

AMERICAN INSTITUTE OF PHYSICS

The standard deviation in wind direction generally increases for larger time windows and is a function of wind speed and environment, so the researchers computed the standard deviation in wind direction over varying time windows for all points throughout 

IMAGE: THE STANDARD DEVIATION IN WIND DIRECTION GENERALLY INCREASES FOR LARGER TIME WINDOWS AND IS A FUNCTION OF WIND SPEED AND ENVIRONMENT, SO THE RESEARCHERS COMPUTED THE STANDARD DEVIATION IN WIND DIRECTION OVER VARYING TIME WINDOWS FOR ALL POINTS THROUGHOUT EACH DATA COLLECTION. EACH SUBPLOT (A-P) REPRESENTS THE PROBABILITY DISTRIBUTION OF WIND DIRECTION CORRESPONDING TO A TIME SERIES. view more 

CREDIT: CREDIT: JALEESA HOULE AND FLORIS VAN BREUGEL



WASHINGTON, May 30, 2023 -- How do flying insects like important pollinators locate odor sources in the great outdoors, despite encountering highly variable wind conditions? They use odor plumes — which travel like smoke and form when the wind blows odor molecules from their source — to track down sources such as flowers or pheromones.

But wind tunnels are typically unable to replicate realistic outdoor wind conditions. In Physics of Fluids, by AIP Publishing, University of Nevada at Reno researchers decided to explore microscale wind conditions in various outdoor environments to better understand what flying insects might experience while tracking odor plumes.

Authors Jaleesa Houle and Floris Van Breugel assessed the mechanical turbulence produced by ambient wind flowing over surface roughness elements such as buildings, trees, and fences and its role in odor plume tracking.

“Since we’re studying wind dynamics within the surface roughness sublayer, most known atmospheric similarity theories that describe properties of the wind profile are not applicable,” said Houle. “So, we use statistical analysis to find both spatial and temporally significant correlations between wind measurements for various sites where we collected data.”

They collected near-surface wind data from several sage steppe (shrub-filled grassland), forest, and urban areas in Northern Nevada and discovered near-surface wind direction is often highly variable over timescales of less than 10 minutes. They also found wind direction variability to be consistently higher in environments with greater surface complexity (urban areas) and lower at higher wind speeds.

“This is important because insects are typically tracking odor plumes in lower wind speeds, which indicates they are somehow making sense of the high directional variability they encounter,” said Houle. “Turbulence intensity is strongly correlated with standard deviations in wind direction, which might be useful for future wind tunnel experimental designs aimed at recreating more ‘natural’ winds.”

Based on their findings, Houle and van Breugel hypothesize an optimal range of wind speed and environmental surface complexity may exist to help insects locate an odor source.

“Further experiments will be needed to test our hypothesis and may help us better understand the implications of land fragmentation on the success of ecologically significant plume tracking insects, such as pollinators,” said Houle. “Beyond this, our results give a compelling reason for researchers to focus on increasing directional variability in wind tunnel studies if they want to uncover plume tracking behaviors that more closely resemble what we might see in nature.”

Next, the researchers will apply their findings to plume tracking wind tunnel experiments and a series of outdoor studies.

“During the summer, we plan to test our hypothesis regarding the types of wind conditions insects might prefer while tracking odor plumes,” said Houle. “In the lab, we’re actively looking for ways to create greater directional variability to better mimic natural wind.”

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The article, "Near-surface wind variability over spatiotemporal scales relevant to plume tracking insects," is authored by Jaleesa Houle and Floris Van Breugel. It will appear in Physics of Fluids on May 30, 2023 (DOI: 10.1063/5.0147945). After that date, it can be accessed at https://doi.org/10.1063/5.0147945.

ABOUT THE JOURNAL

Physics of Fluids is devoted to the publication of original theoretical, computational, and experimental contributions to the dynamics of gases, liquids, and complex fluids. See https://aip.scitation.org/journal/phf.