Pseudamussium alicei

Sponges are ancient filter-feeding animals that rely on maintaining a flow of water through their bodies to obtain suspended food and dissolved <a href="https://www.earth.com/news/oxygen-may-have-come-from-ancient-rocks-of-early-earth/">oxygen</a>. They do not have a nervous, digestive or circulatory system, and remove waste products by releasing them into this same flow of water. However, a new study that analyzed videos of sponges over extended time periods has identified a special technique that they use to get rid of unwanted material from inside their bodies.&nbsp;



As one of the oldest multicellular organisms in existence, a sponge spends most of its life stuck to the substratum and cannot move away when conditions become unpleasant. Under these circumstances it may take in unwanted particles of sediment with its constant inflow of water. These waste particles would soon clog up a sponge’s filtration system and so they need to be removed. And the sponge does this by undergoing an extended contraction, referred to as a “sneeze.”



"Our data suggest that sneezing is an adaptation that sponges evolved to keep themselves clean,” said study senior author Jasper de Goeij, a marine biologist at the <a href="https://www.uva.nl/en">University of Amsterdam</a>.



While biologists have known about the contraction behavior, the authors of this paper show that these sneezes get rid of materials the sponges cannot use. “Let’s be clear: sponges don’t sneeze like humans do. A sponge sneeze takes about half an hour to complete. But both sponge and human sneezes exist as a waste disposal mechanism,” says de Goeij.



The researchers used time-lapse videos of sponges to show that these organisms do not simply dispose of waste and unwanted particles with water that flows away through the outlet pores. They actively secrete mucus, often against the direction of water flow, onto their outer surfaces. They then expel unwanted particles through their pores and these become aggregated in the stringy clumps of mucus. Every now and then, the sponge goes through a contraction (sneeze) that loosens the strings of mucus and accumulated particulate matter, dispatching them into the water column.



What is a sponge’s waste is a fish’s windfall. Fish hang around the sponges waiting for these strings of mucus to be shed so that they may eat them.



“We also observed fish and other animals feeding off of the sponge mucus as food,” explained study first author Niklas Kornder. “Some organic matter exists in the water surrounding the coral reef, but most of it is not concentrated enough for other animals to eat. Sponges transform this material into eatable mucus."



The researchers noted this “sneezing” behavior in two species of sponges, the Caribbean tube sponge&nbsp;Aplysina archeri&nbsp;and another Indo-Pacific species of the genus&nbsp;Chelonaplysilla.&nbsp;



“We actually think that most, if not all, sponges sneeze. I’ve seen mucus accumulate on different sponges while diving and in pictures taken by other scientists for other purposes,” said Kornder. 



“Our findings highlight opportunities to better understand material cycling in some of the most ancient Metazoans,” wrote the study authors.



There are still many aspects about sponge “sneezes” that remain to be investigated. “In the videos, you can see that the mucus moves along defined paths on the surface of the sponge before accumulating. I have some hypotheses, but more analysis is needed to find out what is happening,” said Kornder.



“There are a lot of scientists that think sponges are very simple organisms, but more often than not we are amazed by the flexibility that they show to adapt to their environment,” said de Goeij.



The study is, published in the journal <a href="http://dx.doi.org/10.1016/j.cub.2022.07.017">Current Biology</a>.



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Sponges “sneeze” to get rid of unwanted waste

Sponges are ancient filter-feeding animals that rely on maintaining a...

How did enormous dinosaurs like Brontosaurus carry so much weight on land? A new study led by the <a href="https://www.uq.edu.au/">University of Queensland</a> has finally solved this mystery. Using 3D modeling, the experts digitally reconstructed the foot bones of various <a href="https://www.earth.com/news/giant-sauropods-walked-more-like-hippos-than-elephants/">sauropods</a> to test their function. 



Dr. Andréas Jannel conducted the research during his PhD studies at UQ’s Dinosaur Lab. He said the team discovered that the hind feet of sauropods had a soft tissue pad beneath the "heel" that added cushioning to absorb their immense weight.



“We’ve finally confirmed a long-suspected idea and we provide, for the first time, biomechanical evidence that a soft tissue pad – particularly in their back feet – would have played a crucial role in reducing locomotor pressures and bone stresses,” said Dr. Jannel. “It is mind-blowing to imagine that these giant creatures could have been able to support their own weight on land.”



It was once assumed that sauropods were semi-aquatic and that water buoyancy took literal tons of weight off their relatively small legs. This theory was contradicted in the mid-twentieth century when scientists analyzed sauropod tracks that were found in deposits on land.



Sauropods were also once believed to have feet similar to a modern-day elephant, noted study co-author Dr. Olga Panagiotopoulou of Monash University.



“Popular culture - think Jurassic Park or Walking with Dinosaurs - often depicts these behemoths with almost-cylindrical, thick, elephant-like feet,” said Dr. Panagiotopoulou. “But when it comes to their skeletal structure, elephants are actually ‘tip-toed’ on all four feet, whereas sauropods have different foot configurations in their front and back feet."



“Sauropod’s front feet are more columnar-like, while they present more ‘wedge high heels’ at the back supported by a large soft tissue pad.”



This was because sauropods and elephants had different evolutionary origins, explained study co-author Professor Steve Salisbury.&nbsp;



“Elephants belong to an ancient order of mammals called proboscideans, which first appeared in Africa roughly 60 million years ago as small, nondescript herbivores. In contrast, sauropods – whose ancestors first appeared 230 million years ago – are more closely related to birds," said Professor Salisbury.



“They were agile, two-legged herbivores and it was only later in their evolution that they walked on all fours. Crucially, the transition to becoming the largest land animals to walk the earth seems to have involved the adaptation of a heel pad.”



The study is published in the journal <a href="https://www.science.org/journal/sciadv">Science Advances</a>.



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By <a href="http://csexton@earth.com">Chrissy Sexton</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Mystery solved: how massive dinosaurs carried their weight

How did enormous dinosaurs like Brontosaurus carry so much weight...

Many <a href="https://www.earth.com/news/dinosaurs-self-regulated-their-body-temperature/">dinosaurs</a> replaced their teeth as they fell out - a trait that is shared with modern crocodilians and sharks. Tooth replacement is useful for predatory animals whose teeth are used to hold struggling prey animals and are often broken off.&nbsp;



Now, new research shows that spinosaurids (a group that includes spinosaurus) replaced their teeth even faster than many other dinosaurs. This helps explain why so many spinosaurid teeth have been found littering dinosaur digs.&nbsp;&nbsp;&nbsp;



A team of scientists led by the <a href="https://www.ehu.eus/en">University of the Basque Country</a> assessed a partial spinosaurid jaw from the Late Cretaceous found in La Rioja, Spain. The jaw contained eight alveoli or tooth sockets and tooth remains. Indeed, the researchers found up to three teeth in a single alveolus.&nbsp;



“We recognized up to three generations of teeth in the same alveolus: the functional tooth of the animal, another tooth being formed and which would replace the first, and the germ of the one that would end up replacing the second,” explained Pablo Navarro, co-author of the research published in the journal <a href="https://www.tandfonline.com/doi/full/10.1080/08912963.2022.2069019">Historical Biology</a>.



“This suggests very rapid tooth replacement and is probably one of the reasons why so many spinosaurid teeth can be&nbsp; found on the Iberian Peninsula during the Lower Cretaceous."



Previous research showed that some species of spinosaurids were able to quickly replace their conical teeth, with an estimated time of 60 to 68 days. This research not only verifies the trait for the entire group, but also explains the mechanism of how this regeneration is possible.&nbsp;&nbsp;&nbsp;



“Throughout their lives these animals grew new teeth that gradually replaced the original ones and caused them to fall out. This means that the same animal could generate multiple teeth,” said Navarro.



“These teeth, more or less conical in shape and a centimetre in size, were transported by rivers, accumulated in lake areas and, over time, became fossilised,” said the researcher. They are one of the most common vertebrate remains in Iberian sites of the Lower Cretaceous (between 145 and 113 million years ago)”.



Although scientists aren’t entirely sure why spinosaurid teeth were replaced so quickly, it’s likely this ability gave them an edge over other predators.&nbsp;



The study is published in the journal <a href="https://dx.doi.org/10.1080/08912963.2022.2069019">Historical Biology&nbsp;</a>



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By <a href="mailto:nire518@gmail.com">Erin Moody </a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Spinosaurids rapidly replaced their teeth

Many dinosaurs replaced their teeth as they fell out -...

A new study from <a href="https://www.ncsu.edu/">North Carolina State University</a> explores the connection between hearing loss and dementia in geriatric <a href="https://www.earth.com/news/playfulness-is-a-key-personality-trait-of-gifted-dogs/">dogs</a>. These findings could support treatment of aging dogs and advance our understanding of the relationship between sensory loss and cognitive function.



“In humans, we know that age-related hearing loss is estimated to affect one-third of people over age 65,” said study co-author Natasha Olby.&nbsp;



“We also know that the rate of cognitive decline is approximately 30-40% faster in people with age-related hearing loss and that hearing loss is a greater contributor to dementia risk than other factors such as hypertension or obesity. But we don’t understand whether the same holds true for dogs.”



The researchers evaluated 39 senior or geriatric dogs. Auditory and cognitive tests were performed and owners were asked to fill out questionnaires focused on cognitive ability and quality of life. Cognitive testing, questionnaire scores and age were compared between hearing groups.



The “average” dog can hear tones at 50 decibels (dBs) with no difficulty. Of the study cohort, 19 of the dogs could hear at 50 dBs, 12 at 70 dBs, and eight at 90 dBs (roughly equivalent to the noise made by a jet plane at takeoff).&nbsp;



When the hearing results were compared with quality of life questionnaire responses, scores related to vitality and companionship declined significantly as hearing deteriorated. The results from cognitive testing were similar - as hearing declined, so did the dog’s ability to perform tasks.



“Hearing loss is one of the biggest predictors of dementia in people,” said Olby. “Hearing loss also contributes to falls in elderly people, as sensory decline contributes to a loss in motor skills. So the connection between physical and neurological decline is clear for humans.”



These findings suggest that the same connection happens with aging dogs. Understanding these changes in elderly dogs enhances the ability to identify and treat these issues in pets, but also improves the understanding of the same issues among humans.



The study appears in the <a href="https://onlinelibrary.wiley.com/doi/full/10.1111/jvim.16510">Journal of Veterinary Internal Medicine</a>.&nbsp;



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By <a href="mailto:katherinebucko@gmail.com">Katherine Bucko</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Hearing loss linked to dementia in aging dogs

A new study from North Carolina State University explores the...

Oak savannas are grassy and shrubby areas, featuring oaks as the dominant <a href="https://www.earth.com/news/heat-makes-pine-trees-more-susceptible-to-disease/">tree</a> species. Since oaks require a dry environment, in North America these savannas are frequently found in the rain shadow of the West Coast’s mountain range. Oaks host a vast diversity of insect species, such as oak gall wasps, which form striking growths known as galls. However, the expansion of this invasive wasp species has usually been kept in check by a wide range of parasitoid wasps, which lay their eggs inside the galls, and, after hatching, their larvae feed upon the oak gall wasp larvae.&nbsp;



According to a new study led by <a href="https://www.binghamton.edu/">Binghamton University</a> in New York, climate change has led to warming temperatures in the Pacific Northwest, leading some insect species – including the oak gall wasps - to expand their range into more northerly oak savannas, where they encounter less competition and they can proliferate. “In the native range, you might find a handful of galls on a single leaf. In the expanded range, sometimes you’re finding thousands on a single tree,” said study senior author Kirsten Prior, an assistant professor of Biological Sciences at Binghamton. “This is pretty prevalent throughout Vancouver Island.”



Biodiversity tends to work on a latitudinal gradient: while there is a vast multitude of species closer to the equator, their numbers gradually decrease at higher latitudes. Thus, when species expand their range northwards due to warming temperatures, they often move into areas without a diversity of predators and competitors, eventually overwhelming the ecosystems they encounter.



“When species undergo poleward range expansions in response to anthropogenic change, they likely encounter less diverse communities in new locations. If low diversity communities provide weak biotic interactions, such as reduced competition or predation, range-expanding species may experience high niche opportunities,” the study authors explained.



This seems to happen currently with oak gall wasps, which exhibit unusual population growths at higher latitudes, where they need to face less competition – a phenomenon highlighting the importance of biodiversity for keeping invasive species in check, as well as the potential long-term ramifications of climate change.



“Biodiversity can be really important in potentially protecting areas from invading species. If we have strong competitors and predators, this might make areas less susceptible to invading species,” concluded study lead author Dylan Jones, a doctoral student in Biology at Binghamton.



The study is published in the <a href="http://dx.doi.org/10.1111/1365-2656.13780">Journal of Animal Ecology</a>.&nbsp;



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By <a href="mailto:andrei.ionescu5891@gmail.com">Andrei Ionescu</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer&nbsp;&nbsp;

Invasive wasps are expanding northward on the West Coast

Oak savannas are grassy and shrubby areas, featuring oaks as...

A new study led by <a href="https://www.cornell.edu/">Cornell University</a> has examined how the geographical characteristics of the world’s islands influence the seasonal variation in the number of <a href="https://www.earth.com/news/new-report-confirms-that-bird-species-are-steadily-declining/">bird species</a>. The experts have shown that the seasonal species richness of birds is affected by the size of an island, how isolated it is from the mainland, and the latitude at which it is located.&nbsp;



“We used 21 years of bird observations on 690 islands from the Cornell Lab of Ornithology’s eBird program,” said study lead author Frank La Sorte, an expert in Avian Ecology and Behavior. “In addition to resident bird species that occur year-round on islands, islands can also host migratory bird species during the breeding or non-breeding seasons, or as transients during migration.”



The analysis revealed that species numbers peaked on islands located in the Northern Hemisphere at mid-latitudes during migration seasons. However, during non-breeding periods, the number of bird species increased on tropical islands, reflecting the fact that the majority of bird species breed in the Northern Hemisphere and migrate towards the tropics to spend their autumns and winters.



Moreover, the researchers found an unmistakable correlation between the size of an island and the number of species present there: the bigger the island, the more bird species. By contrast, islands that are more distant from the mainland usually host a smaller number of species.&nbsp;&nbsp;



“These findings emphasize the importance of evolutionary processes on the largest islands and the unique ecology of the world’s most remote islands,” Dr. La Sorte explained. “Overall, species richness was lowest across all four seasons on the smallest, most remote islands and species richness was highest across all four seasons on the largest islands located at intermediate distances from the mainland.”



However, the scientists stress that there are significant variations in these relationships. For instance, even though large islands usually contain more species of birds, if these islands are very remote, they host fewer species, much like the extremely remote small islands.



“Our findings show that islands play a pivotal role as stopover sites and as wintering grounds for the world’s migratory birds. A better understanding of the geographical relationships between migratory birds and islands across seasons will improve our ability to practice effective bird conservation in these unique places,” Dr. La Sorte concluded.



The study is published in the journal <a href="http://dx.doi.org/10.1098/rspb.2022.1105">Proceedings of the Royal Society B Biological Sciences</a>.



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By <a href="mailto:andrei.ionescu5891@gmail.com">Andrei Ionescu</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer&nbsp;&nbsp;

What types of islands attract migratory birds?

A new study led by Cornell University has examined how...

Bats are known to have relatively long lifespans, with some common species living an astonishing 30–40 years. Longevity in mammals is usually related to body size, with larger species living for longer, but <a href="https://www.earth.com/news/wild-bats-have-a-long-term-memory-of-sounds/">bats</a> as a group fall above the regression line for mammals as they live longer than other mammals of similar body size. House mice, which have a weight similar to that of some bats, live only two years in captivity.&nbsp;



Scientists have long wondered why there is this difference, and a new study led by <a href="https://www.umd.edu/">University of Maryland</a> researchers has identified one of the potential reasons; it has to do with genes involved in hibernation.&nbsp;



“Hibernation has allowed bats, and presumably other animals, to stay in northerly or very southerly regions where there’s no food in the winter,” said study senior author Professor Gerald Wilkinson. “Hibernators tend to live much longer than migrators. We knew that,&nbsp;but we didn’t&nbsp;know if we would detect changes in epigenetic age due to hibernation.”



The researchers worked on big brown bats (Eptesicus fuscus) kept in a research colony at McMaster University. These are the most common bats in the United States and they can live up to 19 years of age. The research colony contained individuals of between one and ten years old. Data was collected by taking a small sample of wing tissue from the 20 captive bats on two occasions. One sample was taken in summer when the bats were active, and the other in winter, when the bats were hibernating.&nbsp;



During the genetic analysis, the researchers investigated changes in DNA methylation between samples taken from the same animal during active and hibernating periods. Methylation is a process whereby methyl groups are added to a DNA molecule, thereby changing the activity of a gene. Their results, published in the Proceedings of the Royal Society B, Biological Sciences, showed that changes in DNA methylation occurred at certain sites in the bat’s genome, particularly sites involved in regulating metabolism during hibernation.&nbsp;



“It’s pretty clear that the sites that decrease methylation in the winter are the ones that appear to be having an active effect,” said Professor Wilkinson. “Many of the genes that are nearest to them are known to be involved in regulating metabolism, so they presumably keep metabolism down.”



Some of these genes are the same ones that Wilkinson and fellow researchers identified as “longevity genes” in a&nbsp;<a href="https://cmns.umd.edu/news-events/features/4745">previous study</a>. Wilkinson said that there is significant overlap between the hibernation genes and the longevity genes, further highlighting the link between hibernation and longer lifespans.&nbsp;



The earlier study also established the first epigenetic clock for bats, capable of accurately predicting the age of any bat in the wild. That clock was applied in this latest study, enabling the researchers to demonstrate that hibernation reduces a bat’s epigenetic age in comparison to a non-hibernating animal of the same age. In fact, the researchers found that by hibernating over just one winter, a big brown bat’s epigenetic clock – a biological marker of aging – extends by three-quarters of a year.&nbsp;



This, say the researchers, may be one of the secrets to the extraordinary longevity found in some species of bats.&nbsp;



“We still don’t have a very good understanding of why some bats can live a really long time and other ones don’t,” said Professor Wilkinson. “We’ve shown that the ones that live a really long time all share the ability to hibernate, or to go into torpor frequently. That seems to be a corollary, but it’s not sufficient because hibernating rodents don’t live 20 years.”



Wilkinson said he is planning a follow-up study to compare epigenetic aging in big brown bats in Canada, where they hibernate, with the same species in Florida, where they do not hibernate. In doing so, Wilkinson hopes to get an even clearer picture of the role that hibernation plays in prolonging lifespans.&nbsp;



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By <a href="mailto:bosman@truewan.co.za">Alison Bosman</a>, <a href="https://www.earth.com/staff/">Earth.com</a> Staff Writer

Hibernation may be key to extraordinary longevity in bats

Bats are known to have relatively long lifespans, with some...

Pseudamussium alicei

Taxonomic tree: