Description of Telamoptilia grewiae sp. n. and the consequences for the definition of the genera Telamoptilia and Spulerina (Lepidoptera, Gracillariidae, Gracillariinae)

Adult, host plant and mines of Telamoptilia grewiae sp. n. 1 Adult in habitus, paratype 2 Live adult 3 Host plant 4 Linear mines by early instar larvae 5 Blotch mine by later instar larva 6 Seriously damaged leaves found in September. Credit: Zookeys

The genus Telamoptilia Kumata & Kuroko, 1988 is globally represented by five species that may be found in the Oriental and African regions. The type species T. cathedraea (Meyrick, 1908) is geographically shared by the Oriental Region and Madagascar (De Prins and De Prins 2014). Three species are currently known from China, including T. cathedraea, T. hemistacta (Meyrick, 1924), and T. prosacta (Meyrick, 1918).

The larvae of Telamoptilia species are leaf miners. Three plant families are known as hosts for Telamoptilia: Malvaceae, Amaranthaceae and Convolvulaceae (De Prins and De Prins 2014). Vári (1961) briefly described the biology of T. geyeri (Vári, 1961). Kumata et al. (1988) described the biology and the larval body chaetotaxy of three species: T. cathedraea, T. prosacta and T. tiliae (Kumata & Ermolaev, 1988). However, no larval head chaetotaxy and pupal features of Telamoptilia have been described so far.

Telamoptilia grewiae sp. n. is associated with Malvaceae and is described in the present paper from adult external characters, male and female genitalia, wing venation and immature stages. The larval head and pupal features are described for the first time in Telamoptilia.

Methods

Field investigations were carried out in Mt. Baxian National Nature Reserves (40°11'N, 117°32'E), 300−600 m, Tianjin, China, from May to September in 2013 and June 2014. Leaves containing mines with larvae were placed in sealed plastic bags, or rearing containers with moist cotton. Larvae removed from mines were immersed in nearly boiling water for 30 seconds, and then were kept in 75% ethanol for morphological examination. Last instar larval skins, pupae, and exuviae were kept in 75% ethanol. Pupae in rearing containers were placed outdoors to overwinter, and were transferred into the laboratory at 20 °C on February 6, 2014. Emergence successively occurred from March 9 to early-April 2014. Adults were collected chiefly by rearing from immature stages, and occasionally by light trap.

Adult photographs were taken with a Leica M250A stereo microscope. Genitalia and wings were dissected and mounted according to the methods introduced by Li (2002), but stained with Eosin Y and/or Chlorazol Black, and the illustrations were prepared by using a Leica DM750 microscope, and refined in Photoshop® CS4 software. For scanning electron microscopy, larvae and pupae were dehydrated in gradient ethanol, dried in vacuum and coated with gold in a SCD 005 Sputter Coater (BAL-TEC), then operated with a voltage of 15 kV using Quanta 200 environmental scanning electron microscope (SEM) (FEI, Oregon). Line drawings were outlined from the photos taken by the Leica M250A stereo microscope, using path tool in Adobe Photoshop® CS4 software. Photographs of host plant, mines and a live adult were taken in the field using Canon PowerShot G10 digital camera.

Terminology of immature stages follows Davis and De Prins (2011) and De Prins et al. (2013), and that of adults follows Kumata et al. (1988). Thoracic segments I−III and abdominal segments 1−10 are abbreviated as TI−TIII and A1−A10, respectively.

All the specimens studied, including the types of the new species and the vouchered larvae and pupae, are deposited in the Insect Collection, Nankai University, Tianjin, China.

Taxonomy

Adults (Figs 1–2) with wing span 6.0−8.0 mm. Head silvery white, tinged with gray on face. Labial palpus grayish white, colored blackish gray on outer surface of distal half of second segment and before apex of third segment. Maxillary palpus white, with middle or distal half blackish fuscous. Antenna with scape white on posterior half, blackish gray on anterior half and distal portion, flap blackish gray tinged with white, as wide as scape in frontal view; flagellum silvery grayish fuscous, with each unit blackish distally. Thorax and tegula blackish gray mixed with white. Legs mostly white; foreleg with coxa blackish fuscous basally and distally, femur and tibia blackish fuscous, tarsus blackish gray distally on each except last segment; midleg with coxa blackish fuscous distally, femur blackish fuscous, except white medially and distally on dorsal surface, with ventral scale expansion blackish fuscous, tibia blackish fuscous basally and distally, white medially, tarsus white, each except last segment dotted blackish fuscous distally; hindleg with coxa blackish fuscous distally, femur blackish fuscous distally on outer surface, tibia blackish fuscous basally and distally, tarsus with basal three segments blackish fuscous distally, fourth segment dotted blackish fuscous dorso-distally. Forewing grayish fuscous to blackish fuscous; costal margin with a white spot basally at about 1/10 and one before apex, the former sometimes touching fold posteriorly, with white stria at distal 3/10 and 1/6 obliquely outward, reaching middle of wing and near termen respectively; transverse white fascia from costal 1/3 and 1/2 obliquely outward, reaching dorsal 1/2 and before end of fold respectively, edged with blackish fuscous to black scales, inner fascia wider than outer one, widened on posterior half; small white dot on distal end of M3, two or three small white dots along termen; apex blackish fuscous; cilia mostly blackish fuscous basally, gray distally, white adjacent to white markings, white on basal 1/4, black on median part, gray distally at apex, gray along dorsal margin. Hindwing and cilia uniformly gray.

Source: Read Full Artical at - ZOOKEYS

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Blue mussels not yet the bellwether of NE coastal environment

Marcy Cockrell installs cages to protect mussels from predators. In Maine, mussels inside cages faired as well as mussels in the wild. In Long Island Sound and Narragansett Bay it was a different story. Credit: Brown University

Ecologists sometimes look to mussel species, a well-studied and foundational genus in estuaries, as model organisms for assessing the condition of coastal habitats, which are crucial for people and well as the broader environment.

But a new study in the journal Ecosphere suggests that the seemingly simple blue mussel, when studied on regional scale from Maine to Connecticut, harbors at least three specific mysteries that must be solved if the mollusks are to serve as the "canaries in the coal mine" of the Northeast coast.

"Mussels could indeed be a good sentinel species for rocky shores, but what our work suggests is that we need to know a lot more about how they behave in these different estuarine settings to use them as an indicator of ecosystem health," said conservation scientist and study senior author Heather Leslie, the Peggy and Henry D. Sharpe Assistant Professor of Environmental Studies.

For the study, Leslie and former students Marcy Cockrell and Joanna Bernhardt monitored and experimented with mussels at 18 sites in the Casco Bay of Maine, the Narragansett Bay of Rhode Island, and the Long Island Sound of Connecticut and New York in 2010 and 2011 (a region spanning about 600 kilometers of coastline). They measured the abundance of mussels both at adult and larval stages, studied the populations of neighboring rocky shore animals and marine algae, and tracked data on ecosystem factors such as water salinity, temperature, nutrients, oxygen, and local human population density. In the experiments, the team protected some mussels with cages to expose the effect that birds, crabs and other predators have on their numbers.

In the end, the research uncovered three intriguing mysteries of mussel life across the region, particularly in Casco Bay:

Generation gaps: Adults were populous but "recruitment" of young mussels from surrounding waters was low in Long Island Sound and Narragansett Bay. The opposite was true in Casco Bay. There, juvenile recruitment was high but adult populations were low. Few Maine predators: The cage experiments showed a significant role for mussel predators in Long Island Sound and Narragansett Bay, but not in Casco Bay. There, unprotected mussels fared about as well as the protected ones. Inner vs. outer: In each estuary, Leslie's team made measurements at sites nestled well within the bay, as well as at sites closer to the open ocean. Prior research suggested that higher levels of food within the bay would promote growth and abundance for the filter-feeding mussels (due to higher levels of nutrients and phytoplankton at the inner estuary sites). The study results were notably mixed across the whole region, however, providing little support for that hypothesis.

Explanations await further research. Genetic studies could determine, for example, whether the young mussels that are so abundant in Casco Bay may be floating up from the more southerly shores. If so, that suggests that mussel population dynamics can only be understood on regional (or multi-estuary) geographic scale.

Meanwhile, understanding why predator activity seems low in Casco Bay might require learning more about the local predator populations there. The findings could shed light on whether the ecosystem is in balance or other factors are at play.

"We did this because we want to understand how these systems work," Leslie said. "Given their accessibility and how well-studied they have been in other locations, rocky shores are logical sentinel ecosystems. They provide an opportunity to investigate how climate change and other more local-scale human activities are affecting New England's coast."

It may take more work to crack open the mussels' mysteries, but the stakes are high enough to make it worthwhile, Leslie said.

Source: Brown University

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Bugs life: The nerve cells that make locusts ‘gang up’

Computer reconstruction of nerve cells in a desert locust that produce the neurochemical serotonin. The colors indicate each cell's response to the social stimuli that cause gregarious behavior. The green cells contain less serotonin after a life-time of crowding with other locusts. The blue cells contain more serotonin after a locust has seen and smelled other locusts for just one hour. The yellow cells increase their serotonin content within an hour of exposing a locust to any of the social stimuli that induce gregarious behavior. Credit: University of Leicester

A team of biologists has identified a set of nerve cells in desert locusts that bring about 'gang-like' gregarious behaviour when they are forced into a crowd.

Dr Swidbert Ott from the University of Leicester's Department of Biology, working with Dr Steve Rogers at the University of Sydney, Australia, has published a study that reveals how newly identified nerve cells in locusts produce the neurochemical serotonin to initiate changes in their behaviour and lifestyle.

The findings demonstrate the importance of individual history for understanding how brain chemicals control behaviour, which may apply more broadly to humans also.

Locusts are normally shy, solitary animals that actively avoid the company of other locusts. But when they are forced into contact with other locusts, they undergo a radical change in behaviour -- they enter a 'bolder' gregarious state where they are attracted to the company of other locusts. This is the critical first step towards the formation of the notorious locust swarms.

Dr Ott said: "Locusts only have a small number of nerve cells that can synthesise serotonin. Now we have found that of these, a very select few respond specifically when a locust is first forced to be with other locusts. Within an hour, they produce more serotonin.

"It is these few cells that we think are responsible for the transformation of a loner into a gang member. In the long run, however, many of the other serotonin-cells also change, albeit towards making less serotonin."

When a locust is first forced into contact with other locusts, a specific set of nerve cells that produce the neurochemical serotonin is responsible for reconfiguring its behaviour so that the previously solitary locust becomes a member of the gang, which is known as 'gregarious' behaviour.

An entirely different set of its serotonin-producing nerve cells is then affected by life in the group in the long run.

Dr Ott added: "The key to our success was to look in locusts that have just become gregarious and that had never met another locust until an hour earlier. If we had looked only in solitary locusts and in locusts that had a life-long history of living in crowds, we would have missed the nerve cells that are the key players in the transformation.

"There is an important lesson here for understanding the mechanisms that drive changes in social behaviour in general, both in locusts and in humans. We have shown how important it is to look at what happens when a new social behaviour is first set up, not just at the long-term outcome.

"Research in insects can give us deep insights into how brains work in general, including our own."

Studies have previously shown that the change from solitary to gregarious behaviour is caused by serotonin.

The new study, which was funded by the Leverhulme Trust, the Biotechnology and Biological Sciences Research Council (BBSRC) and the Royal Society, has identified the individual serotonin-producing nerve cells that are responsible for the switch from solitary to gregarious behaviour.

The scientists used a fluorescent stain that reveals the serotonin-producing nerve cells under the microscope. This allowed them to measure the amount of serotonin in individual nerve cells -- the brighter a nerve cell lights up, the more serotonin it contains. The newly identified cells were much brighter in locusts that had just been forcedly crowded with other locusts. Moreover, the same cells were also brighter in locusts that had their hind legs tickled by the researchers for an hour -- which is sufficient to make the locusts behave gregariously.

Serotonin has important roles in the brains of all animals that include the regulation of moods and social interactions.

In humans, there are strong links between changes in serotonin and mental disorders such as depression and anxiety.

Source: University of Leicester

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Small, fast, and crowded: Mammal traits amplify tick-borne illness

Chipmunks are small-bodied animals with fast lives and dense populations. When ticks feed on them, they are more likely to pick up multiple disease-causing pathogens. Credit: © dwags / Fotolia

In the U.S., some 300,000 people are diagnosed with Lyme disease annually. Thousands also suffer from babesiosis and anaplasmosis, tick-borne ailments that can occur alone or as co-infections with Lyme disease. According to a new paper published in PLOS ONE, when small, fast-living mammals abound, so too does our risk of getting sick.

In eastern and central North America, blacklegged ticks are the primary vectors for Lyme disease, babesiosis, and anaplasmosis. The pathogens that cause these illnesses are widespread in nature; ticks acquire them when they feed on infected animals.

Richard S. Ostfeld, the paper's lead author and a scientist at the Cary Institute of Ecosystem Studies, has researched the ecology of Lyme disease since 1992. "A pattern emerged in our long-term studies. Ticks that fed on certain rodents and shrews were much more likely to pick up multiple pathogens, making the environment riskier for people."

To investigate why mammals differ in their 'reservoir competence' or ability to transmit pathogens to ticks, Ostfeld and his co-authors from Bard College, Oregon State University, the University of South Florida, and EcoHealth Alliance took a two-pronged approach.

First, they looked at life history traits for nine mammals known to harbor Lyme disease, babesiosis, and anaplasmosis. Attributes like body size, litter size, and life span were taken into consideration.

Then they looked at the role of mammal population density. As 'sit and wait' parasites, ticks are much more likely to encounter animals with dense populations. This, in turn, could help pathogens evolve to exploit specific hosts, resulting in more effective transmission rates.

For Lyme disease and anaplasmosis, fast life history features were a strong predictor of an animal's ability to transmit infection to ticks. Body size was inversely related to reservoir competence. Raccoon, skunk, opossum, squirrel, and deer infected fewer ticks than their mouse, chipmunk, and shrew counterparts.

Ostfeld notes, "This is consistent with past research on Lyme disease, West Nile virus, and Eastern Equine encephalitis. There is evidence that animals that mature early and have frequent, large litters invest less in some immune defenses, making them better pathogen hosts."

Population density was the best predictor of species' abilities to transmit all three pathogen groups, with animals that ticks encountered most frequently being the most effective at transferring infection. Co-author Felicia Keesing of Bard College explains, "Fast life history and high population density often go hand-in-hand. In rodents and shrews, pathogen adaptation and poor immune defense may be working together to amplify disease spread."

With Ostfeld concluding, "In our struggle to manage the ever-growing list of tick-borne diseases, we need to understand which animals magnify human disease risk. Our results suggest when generalist pathogens emerge, small mammals with large populations and a fast pace of life warrant careful monitoring."

Source: Cary Institute of Ecosystem Studies

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Teeth, sex and testosterone reveal secrets of aging in wild mouse lemurs

A brown mouse lemur in the wild. Mouse lemurs, weighing a mere 30 to 80 grams, are the world's smallest primates. Credit: Jukka Jernvall

Mouse lemurs can live at least eight years in the wild -- twice as long as some previous estimates, a long-term longitudinal study finds.

PLOS ONE published the research on brown mouse lemurs (Microcebus rufus) led in Madagascar by biologist Sarah Zohdy, a post-doctoral fellow in Emory's Department of Environmental Sciences and the Rollins School of Public Health. Zohdy conducted the research while she was a doctoral student at the University of Helsinki.

"It's surprising that these tiny, mouse-sized primates, living in a jungle full of predators that probably consider them a bite-sized snack, can live so long," Zohdy says. "And we found individuals up to eight years of age in the wild with no physical symptoms of senescence like some captive mouse lemurs start getting by the age of four."

It is likely that starvation, predation, disease and other environmental stressors reduce the observed rate of senescence in the wild, Zohdy notes, but a growing body of evidence also suggests that captive conditions may affect mental and physical function.

"We focused on wild mouse lemurs because we want to know what happens naturally when a primitive primate is exposed to all of the extrinsic and intrinsic mortality factors that shaped them as a species," Zohdy says. "Comparing longevity data of captive and wild mouse lemurs may help us understand how the physiological and behavioral demands of different environments affect the aging process in other primates, including humans."

The study determined ages of wild mouse lemurs in Madagascar's Ranomafana National Park through a dental mold method that had not previously been used with small mammals. In addition to the high-resolution tooth-wear analysis for aging, fecal samples underwent hormone analysis.

The researchers found no difference between the longevity of male and female mouse lemurs, unlike most vertebrates where males tend to die first.

"And even more interestingly, we found no difference in testosterone levels between males and females," Zohdy says. Mouse lemurs are female dominant, which may explain why their testosterone levels are on a par with males.

"While elevated male testosterone levels have been implicated in shorter lifespans in several species, this is one of the first studies to show equivalent testosterone levels accompanying equivalent lifespans," Zohdy says.

A co-author of the study is primatologist Patricia Wright of the Centre ValBio Research Station in Madagascar and Stony Brook University. Other institutions involved in the study include Colorado State University, Duke University and the University of Arizona, Tucson.
Mouse lemurs, found only on the island of Madagascar, are the world's smallest primates. They are among nearly 100 species of lemurs that arrived in Madagascar some 65 million years ago, perhaps floating over from mainland Africa on mats of vegetation.

Mouse lemurs weigh a mere 30 to 80 grams but in captivity they live six times longer than mammals of similar body size, such as mice or shrews. Captive gray mouse lemurs (Microcebus murinus) can live beyond age 12. By age four, however, they can start exhibiting behavioral and neurologic degeneration. In addition to slowing of motor skills and activity levels, reduced memory capacity and sense of smell, the captive four-year-olds can start developing gray hair and cataracts, Zohdy says.

The wild brown mouse lemurs in the study were trapped, marked and released during the years 2003 to 2010. A total of 420 dental impressions were taken from the lower-right mandibular tooth rows of 189 unique individuals. Over the course of seven years, 270 age estimates were calculated. For 23 individuals captured three or more times during the duration of the study, the regression slopes of wear rates were calculated and the mean slope was used to calculate ages for all individuals.

"We found that wild brown mouse lemurs can live at least eight years," Zohdy says. "In the population that we studied, 16 percent lived beyond four years of age. And we found no physical signs of senescence, such as graying hair or cataracts, in any wild individual."

Limitations of the study include the inability to document gradual physiological symptoms of senescence in the wild. "Our results do not provide information about wild brown mouse lemurs that can be directly compared to senescence in captive gray mouse lemurs," Zohdy says. "Further research, using identical measures of senescence, will help to reveal whether patterns of physiological senescence occur consistently across the genus and in both captive and wild conditions."

Another confounding factor Zohdy cites is "the Sleeping Beauty effect," the fact that wild mouse lemurs hibernate for half the year, possibly boosting their life span.
"We now know that mouse lemurs can live a relatively long time in the wild," she says, "but we don't know the exact mechanisms behind why they live so long."

Source: Emory Health Sciences

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The science behind swimming: From whales to larvae, common principles at work in swimming

Whale and diver (stock illustration). Using simple hydrodynamics, researchers were able to show that a handful of principles govern how virtually every animal -- from the tiniest fish to birds to gigantic whales propel themselves though the water. Credit: © James Thew / Fotolia

At nearly 100 feet long and weighing as much as 170 tons, the blue whale is the largest creature on the planet, and by far the heaviest living thing ever seen on Earth. So there's no way it could have anything in common with the tiniest fish larvae, which measure millimeters in length and tip the scales at a fraction of a gram, right?

Not so fast, says L. Mahadevan, the Lola England de Valpine Professor of Applied Mathematics, of Organismic and Evolutionary Biology, and of Physics.

Using simple hydrodynamics, a team of researchers led by Mahadevan was able to show that a handful of principles govern how virtually every animal -- from the tiniest fish to birds to gigantic whales propel themselves though the water. The study is described in a September 14 paper in Nature Physics.

"What we wanted to investigate was how the speed of an organism changes as a function of how large it is, how quickly it moves and how much it moves," Mahadevan said. "To resolve that in detail, however, is very complex, because there is a great deal of differences in morphology and what parts of the body different creatures use to swim. The question is: Is there anything in common across all these organisms? The answer, we found, is yes."

In an effort to uncover those common principles, Mahadevan working with a postdoctoral fellow in his group , Mattia Gazzola, and a colleague Mederic Argentina from the University of Nice, began by trying to unpack the physics of how different creatures swim.

"The traditional approach to swimming phenomena is to take a certain specimen and accurately characterize it via experiments and/or simulations, and try to generalize from there, but it is very hard to strip out specific biological effects from general principles," Gazzola said. "We instead thought that while swimmers exhibit a huge diversity in shapes and kinematics, at the end of the day they all live in the same media, water.

"Therefore we thought that if a unifying mechanistic principle existed, it had to lie in the constraints that the flow environment poses to all its inhabitants," he continued. "And this is a purely physical problem, much easier to solve since it is not affected by biological vagaries. What I like about this paper is that in one line of algebra we derived a compact formula that accounts for 50 years of experiments. This is an example of how powerful minimal modeling can be."

"The basic relationship we wanted to understand was how the input variables -- namely the size of the organism, the amount an organism moves and how quickly it moves -- control the output variable, which is effectively the speed at which it moves," Mahadevan explained. "What we found is that there is a specific relationship, which can be described by in terms of a simple scaling law with two limits."

The first, which corresponds to creatures moving at intermediate speeds, describes situations where the bulk of the resistance is caused by skin friction, because water "sticks" to the organism's body. At faster speeds, Mahadevan said, the resistance organisms face largely comes from pressure that builds up in front of and around them, which is described by the second limit.

"While it wasn't a surprise that the resistance changed at organisms moved faster, the fact that those challenges could be so simply described was interesting and provocative, because we are talking about organisms that range in size from a few millimeters to the size of a blue whale," Mahadevan said.

Armed with those observations, Mahadevan and colleagues turned to a host of empirical observations that had been made over the past 50-plus years. When those data were plotted on a graph, the researchers found that the swimming speed of virtually every organism, from fish larvae to frogs to birds, amphibians and even whales, could be described by one of the two equations.

The same also held true, Mahadevan said, when Gazzola created complex computer models to solve the governing equations of fluid dynamics to describe how different organisms swim.

"What is particularly interesting is that all the organisms essentially reach the hydrodynamic limits of performance," he said. "Our simple theory, which doesn't distinguish in any detailed way between something like a blue whale and fish larvae, except in the parameters of how large you are, much you move and how quickly you move, can describe all this diversity. That suggests there are general principles at work here."


Source: Harvard University

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For tiger populations, a new threat

This is an Amur tiger photographed by camera trap. Credit: WCS Russia Program

Along with the pressures of habitat loss, poaching and depletion of prey species, a new threat to tiger populations in the wild has surfaced in the form of disease, specifically, canine distemper virus (CDV). According to a new study from the Wildlife Conservation Society (WCS) and its partners, CDV has the potential to be a significant driver in pushing the animals toward extinction.

While CDV has recently been shown to lead to the deaths of individual tigers, its long-term impacts on tiger populations had never before been studied.

The authors evaluated these impacts on the Amur tiger population in Russia's Sikhote-Alin Biosphere Zapovednik (SABZ), where tiger numbers declined from 38 individuals to 9 in the years 2007 to 2012. In 2009 and 2010, six adult tigers died or disappeared from the reserve, and CDV was confirmed in two dead tigers -- leading scientists to believe that CDV likely played a role in the overall decline of the population. Joint investigations of CDV have been an ongoing focus of WCS and Russian scientists at Sikhote-Alin Zapovednik and veterinarians at the regional Primorye Agricultural College since its first appearance in tigers in 2003.

A key finding of this study: Modeling shows that smaller populations of tigers were found to be more vulnerable to extinction by CDV. Populations consisting of 25 individuals were 1.65 times more likely to decline in the next 50 years when CDV was present. The results are profoundly disturbing for global wild tigers given that in most sites where wild tigers persist they are limited to populations of less than 25 adult breeding individuals.

The scientists used computer modeling to simulate the effects of CDV infection on isolated tiger populations of various sizes and through a series of transmission scenarios. These included tiger-to-tiger transmission and transmission through predation on CDV-infected domestic dogs and/or infected wild carnivores (such as foxes, raccoon dogs and badgers). High and low-risk scenarios for the model were created based on variation in the prevalence of CDV and the tigers' contact with sources of exposure.

Results showed that CDV infection increased the 50-year extinction probability of tigers in SABZ as much as 55.8 percent compared to CDV-free populations of equivalent size.

"Although we knew that individual tigers had died from CDV in the wild, we wanted to understand the risk the virus presents to whole populations," said WCS veterinarian Martin Gilbert. "Tigers are elusive, however, and studying the long-term impact of risk factors is very challenging. Our model, based on tiger ecology data collected over 20 years in SABZ, explored the different ways that tigers might be exposed to the virus and how these impact the extinction risk to tiger populations over the long term."

WCS Russia Program Director Dale Miquelle said, "Tigers face an array of threats throughout their range, from poaching to competition with humans for space and for food. 

Consequently, many tiger populations have become smaller and more fragmented, making them much more susceptible to diseases such as CDV. While we must continue to focus on the primary threats of poaching and habitat destruction, we now must also be prepared to deal with the appearance of such diseases in the future."

Priorities for future research, according to the authors, include identifying the domestic and wild carnivore species that contribute to the CDV reservoir, and those that are the most likely sources of infection for tigers. Tigers are too rare to sustain the virus in the long term, so CDV must rely on more abundant carnivore species to persist in the environment. 

Understanding the structure of the CDV reservoir will be a critical first step in identifying measures that might prevent or control future outbreaks. In addition, since we now know that small tiger populations are at greater risk to diseases such as CDV than larger populations, conservation strategies focusing on connectedness between populations become all the more important. "Estimating the potential impact of canine distemper virus on the Amur tiger population (Panthera tigris altaica) in Russia," appears in the current online edition of PloSONE. Authors include: Martin Gilbert of WCS and Boyd Orr Centre for Population and Ecosystem Health at the University of Glasgow; Dale G. Miquelle of WCS; John M. Goodrich of Panthera; Richard Reeve, Sarah Cleaveland and Louise Matthews of Boyd Orr Centre for Population and Ecosystem Health at the University of Glasgow; and Damien Joly of WCS and Metabiota.

This study was made possible through generous support from Morris Animal Foundation, Zoo Boise Conservation Fund, AZA Tiger Species Survival Plan Tiger Conservation Campaign, and the Biotechnology and Biological Sciences Research Council.

"Morris Animal Foundation is thankful to Dr. Miquelle and his team for helping protect the Amur Tigers," said Diane Brown, DVM, PhD, DACVP and Chief Scientific Officer for Morris Animal Foundation. "Our Foundation values their hard work and dedication to this study and we look forward to many more partnerships with the Wildlife Conservation Society."

Source: Wildlife Conservation Society

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Lemurs: Gardeners of Madagascar rainforest at risk

Onja Razafindratsima, a graduate student at Rice University, observes a lemur in a Madagascar rainforest. Razafindratsima led a three-year study to explore the relationship between lemurs and trees. Lemurs eat the fruit and spread its seeds far from the parent tree to help ensure its survival. Credit: Photo courtesy of Onja Razafindratsima/Rice University

A majority of Madagascar's 101 species of lemurs are threatened with extinction, and that could have serious consequences for the rainforests they call home. A new study by Rice University researchers shows the positive impacts lemurs can have on rainforest tree populations, which raises concerns about the potential impact their disappearance could have on the region's rich biodiversity.

A large proportion of trees in Madagascar's rainforest have fruits eaten by lemurs. Lemurs in turn disperse the seeds of their fruit trees throughout the forest with their scat. Such dispersal can play a crucial role for a tree species' ability to regenerate, but effects are poorly understood, especially when there are multiple dispersers.

For the tree, the evolutionary advantage of having animal-dispersed seeds may be that the seeds land well away from their parent trees where survival is low or that seeds are directed into spots where they are the most likely to sprout and survive.

Amy Dunham, an assistant professor of biosciences, and graduate student Onja Razafindratsima set out to detail the symbiotic relationship between fruit-eating lemurs and the trees that feed them through a three-year study in a rainforest in southeastern Madagascar.

Their data from observations, experiments and mathematical models demonstrate that seeds of a common canopy tree have a 300 percent higher chance of sprouting and becoming a sapling when dispersed by lemurs versus simply falling to the ground. One of the three lemur species is particularly good at dropping seeds in spots that are most advantageous for sprouting and survival. Other lemurs are not so selective, but still benefit the tree by moving seeds away from the parent tree. By acting as forest gardeners, these animals give the tree's population a boost.

The study appeared online in the Ecological Society of America journal Ecology.

As part of the study, the researchers followed the seed-dispersal patterns of three of Madagascar's lemur species: the red-fronted brown lemur, the red-bellied lemur and the southern black-and-white ruffed lemur. That meant tracking and observing groups of lemurs as the animals leaped from tree to tree through the forest, dined in the 65-foot-high canopies and dropped their undigested seeds at ground level.

Razafindratsima led the study as part of a thesis project she expects to complete early next year. She built a team of local researchers near Ranomafana National Park, the home of Centre ValBio, a research station founded by Dunham's former Ph.D. adviser, primatologist Patricia Wright.

"We have a team of up to 10 local villagers who are trained to do research," said Razafindratsima, a native of Madagascar. "Their exceptional knowledge of the forest is very important to us when we're trying to track lemurs and identify seeds and seedlings in a forest with over 300 species of trees."

The research team tracked 24 groups of lemurs over a year without the benefit of radio collars, said Razafindratsima, who keeps in touch with her team via phone and Skype when she's at Rice. She said the study sites were as close as a short hike from Centre ValBio and as far as a two-day trek through steep terrain that entailed camping overnight.

In addition to tracking lemurs and their dispersed seeds, the research team spent three years carrying out experiments on seed sprouting and survival. They found that dispersal by lemurs dramatically increased the odds that seeds would take root and survive. In particular, the red-fronted brown lemurs tended to drop seeds away from their parent trees and in places where there were gaps in the canopy. This gave individual seeds the best shot at taking root.

Dunham said trees benefit from the wide dispersal of their seeds, and for some species in Madagascar, lemurs are the primary or only animal that can distribute those seeds. As the largest fruit-eaters in the system, these lemurs swallow seeds that may be too large for other fruit-eating animals, such as birds or bats.

"Seeds away from the parent tree survive better because there's less competition among seedlings," Razafindratsima said. "If they're close by the parent, they may also share the same natural enemies, like soil pathogens and seed predators, so there's higher mortality."

Trees that lose their dispersers will simply drop their seeds to the ground beneath their canopies, where chances of survival are slim, Dunham said. "Lemurs fill an important role as the gardeners for these trees. By ensuring that some seeds land in spots suitable for germination and survival, they increase the ability of these trees to replace themselves"

Dunham hopes the study will contribute to growing efforts to protect lemurs, and therefore the rainforest, which has been impacted in recent years by economic and political instability.

She noted grassroots efforts within Madagascar led to the first World Lemur Festival in late October to celebrate and protect the animals and their habitats in Madagascar.

"What got us interested is that frugivorous lemur populations are declining across the island, and we know very little about how these seed dispersers actually affect tree populations," she said. "Once we understand that better, maybe we'll have a better idea of how the community might change if the lemurs disappear.

"If some species suddenly lose their dispersers, but others dispersed by birds or the wind are doing fine, it may change population trajectories and alter which tree species are dominant in a community. To understand what happens when these species are lost, we need to understand their role in the ecosystem," she said.

Source: Rice University

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Scientists find 240-million-year-old parasite that infected mammals' ancestor

Scott Gardner. Credit: Craig Chandler, University Communications.

An egg much smaller than a common grain of sand and found in a tiny piece of fossilized dung has helped scientists identify a pinworm that lived 240 million years ago.

It is believed to be the most ancient pinworm yet found in the fossil record.

The discovery confirms that herbivorous cynodonts -- the ancestors of mammals -- were infected with the parasitic nematodes. It also makes it even more likely that herbivorous dinosaurs carried pinworms.

Scott Gardner, a parasitologist and director of the Harold W. Manter Laboratory of Parasitology at the University of Nebraska-Lincoln, was among an international group of scientists who published the study in the journal Parasites & Vectors.

"This discovery represents a first for our team and I think it opens the door to finding additional parasites in other species of fossil organisms," he said.

The team found the pinworm egg in a coprolite -- fossilized feces -- collected in 2007 at an excavation site in Rio Grande do Sul state in southern Brazil.

The coprolite was collected at a site with abundant fossilized remains of cynodonts. Previously, an Ascarid-like egg -- resembling a species of nematode commonly found in modern-day mammals -- was found in the coprolite.

The pinworm egg, representing an undescribed or "new species," was named Paleoxyuriscockburni, in honor of Aidan Cockburn, founder of the Paleopathology Association.

The structure of the pinworm egg placed it in a biological group of parasites that occur in animals that ingest large amounts of plant material. Its presence helped scientists deduce which cynodont species, of several found at the collection site, most likely deposited the coprolite.

Since the field of paleoparasitology, or the study of ancient parasites, emerged in the early 20th century, scientists have identified parasites of both plants and animals that date back as far as 500 million years ago.

The study of parasites in ancient animals can help determine the age of fossilized organisms and help establish dates of origin and diversification for association between host species and parasites. Coprolites are a key part of the study, enabling a better understanding of the ecological relationships between hosts and parasites.

Other members of the team were Jean-Pierre Hugot of the National Museum of Natural History in Paris; Victor Borba, Juliana Dutra, Luiz Fernando Ferreira and Adauto Araujo of Oswaldo Cruz Foundation in Rio de Janeiro; Prisiclla Araujo and Daniela Leles of Fluminense Federal University in Rio de Janeiro; and Atila August Stock Da-Rosa of the Federal University of Santa Maria in Rio Grande do Sul.

Source: University of Nebraska-Lincoln

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Kudzu can release soil carbon, accelerate global warming

This layer of decomposing knotweed will eventually form soil organic matter in invaded ecosystems.
 Credit: Image courtesy of Clemson University

Clemson University scientists are shedding new light on how invasion by exotic plant species affects the ability of soil to store greenhouse gases. The research could have far-reaching implications for how we manage agricultural land and native ecosystems.

In a paper published in the scientific journal New Phytologist, plant ecologist Nishanth Tharayil and graduate student Mioko Tamura show that invasive plants can accelerate the greenhouse effect by releasing carbon stored in soil into the atmosphere.
Since soil stores more carbon than both the atmosphere and terrestrial vegetation combined, the repercussions for how we manage agricultural land and ecosystems to facilitate the storage of carbon could be dramatic.

In their study, Tamura and Tharayil examined the impact of encroachment of Japanese knotweed and kudzu, two of North America's most widespread invasive plants, on the soil carbon storage in native ecosystems.

They found that kudzu invasion released carbon that was stored in native soils, while the carbon amassed in soils invaded by knotweed is more prone to oxidation and is subsequently lost to the atmosphere.

The key seems to be how plant litter chemistry regulates the soil biological activity that facilitates the buildup, composition and stability of carbon-trapping organic matter in soil.

"Our findings highlight the capacity of invasive plants to effect climate change by destabilizing the carbon pool in soil and shows that invasive plants can have profound influence on our understanding to manage land in a way that mitigates carbon emissions," Tharayil said.

Tharayil estimates that kudzu invasion results in the release of 4.8 metric tons of carbon annually, equal to the amount of carbon stored in 11.8 million acres of U.S. forest.
This is the same amount of carbon emitted annually by consuming 540 million gallons of gasoline or burning 5.1 billion pounds of coal.

"Climate change is causing massive range expansion of many exotic and invasive plant species. As the climate warms, kudzu will continue to invade northern ecosystems, and its impact on carbon emissions will grow," Tharayil said.

The findings provide particular insight into agricultural land-management strategies and suggest that it is the chemistry of plant biomass added to soil rather than the total amount of biomass that has the greatest influence on the ability of soil to harbor stable carbon.

"Our study indicates that incorporating legumes such as beans, peas, soybeans, peanuts and lentils that have a higher proportion of nitrogen in its biomass can accelerate the storage of carbon in soils," Tharayil said.

Thrarayil's lab is following up this research to gain a deeper understanding of soil carbon storage and invasion.

Tharayil leads a laboratory and research team at Clemson that studies how the chemical and biological interactions that take place in the plant-soil interface shape plant communities. He is also the director of Clemson's Multi-User Analytical Laboratory, which provides researchers with access to highly specialized laboratory instruments.

Source: Clemson University

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Tree diseases can help forests

A healthy seedling of the tree Castilla elastica is on the left, while a dying seedling, attacked by a plant pathogen, is on the right. A study in the Journal of Ecology by University of Utah biologists shows that such tree diseases, while killing individual seedlings, can increase forest biodiversity. Credit: Erin Spear, University of Utah.

Plant diseases attack trees and crops and can hurt lumber and food production, but University of Utah biologists found that pathogens that kill tree seedlings actually can make forests more diverse.

While low rainfall has been blamed for a lack of drought-sensitive trees near the Pacific side of the Panama Canal, the new study answers a mystery about what keeps drought-tolerant trees from that area from living along the wetter Caribbean side of the canal. The answer: disease-causing plant pathogens, the researchers report in their study, published online Wednesday, Nov. 12 by the Journal of Ecology.

"Because seedlings of disease-sensitive tree species can't survive in the wetter forests and drought-sensitive tree species cannot survive in the drier forests, different tree species inhabit the wetter and drier forests even though they are only 30 miles apart" in Panama, says Phyllis Coley, a senior author of the study and a distinguished professor of biology.
In other words, tree pathogens contribute to the staggering diversity of trees in Panama's tropical forests, she adds.

The study's first author, biology doctoral student Erin Spear, says that is important because "conservation planning and predictions about how tree species distributions may shift with climate change require an understanding of the factors currently influencing where species can and cannot survive."

That is particularly important in tropical forests and other forests that are under elevated threat of deforestation.

Funding for the study came from Sigma Xi -- The Scientific Research Society, the Smithsonian Institution and the National Science Foundation.

Of Forests and Pathogens

Tropical forests are threatened, and dry tropical forests are even more threatened because sunnier, drier climates are better for growing crops and are favored by people. Some 90 percent of Panama's residents live on the nation's drier Pacific slope.

Forests are essential for feeding and sheltering animals, providing important medicines, storing carbon and water, and reducing erosion by holding soil in place. These functions are influenced by different species inhabiting a forest, so it is essential to understand why certain tree species can survive in certain areas but not others.

Panama's forests also are important economically because tree roots limit how much soil erodes into the Panama Canal, ensuring that huge container ships can pass. Researchers also believe the forests help maintain water levels in the canal because forest soil stores water, slowly releasing it into streams feeding the canal during the dry season.

Diversity is high in tropical forests. A 930-square-mile area bordering the Panama Canal has more than 800 tree species. By comparison, about half the state of Rhode Island -- or some 610 square miles -- is forested, and that area has only 51 tree species.

Part of the reason Panama's forests have more species is because the Pacific end of the canal receives less annual rainfall -- about 5.9 feet -- than the Caribbean end, where 9.8 feet of rain falls annually.

"While there is considerable evidence that less rain in the drier, Pacific forests means that drought-sensitive tree species can't survive there, it has been unclear what prevents the drought-tolerant species of the drier forests from living in the wetter forests," says University of Utah biology professor Tom Kursar, the study's other senior author. "Our study tackled that unanswered question."

So Spear braved mud, rain, insects and snakes to monitor seedlings of a variety of tree species in the wetter and drier forests of central Panama for pathogen-caused damage and death. Plant pathogens that make plants sick include bacteria, viruses and fungi.

Spear says the researchers' findings suggest that "all seedlings are at a greater risk of being injured and killed by pathogens in the wetter forests than in the drier forests." This could be because the damp environment of the wetter forests helps pathogens survive, and more rainfall helps pathogens move from one seedling to another.

But that's only half the story. Coley says that their study indicates "pathogens are implicated in the absence of the dry-forest tree species from the wetter forests, where they might otherwise be able to live. That is because dry-forest tree species are more likely to die from pathogen attack than wet-forest species."

Diagnosing Sick Seedlings

Spear collected the seeds for the study by hiking for miles, kayaking in the canal to collect fruit from overhanging branches, and even riding a crane-carried gondola more than 100 feet upward into the forest canopy.

She conducted the study at two forest sites in central Panama: one at the large Metropolitan Natural Park in Panama City on the drier Pacific side, and one on private property in the Santa Rita Ridge area on the wetter Caribbean side. She planted "gardens" of tree seeds -- including species typical of wetter and drier forests -- in 30 locations at each site. More than 1,000 seeds were planted; 725 of them sprouted.

Once the seeds were planted, the researchers covered them with wire mesh to protect the seeds and seedlings from being crushed by tree branches or eaten by animals.

Spear visited both sites weekly and took notes on the 725 seedlings. Weekly visits were essential because, diseased seedlings can be dead and decomposing within days.

"We monitored when the seeds germinated, the occurrence of and date when symptoms of pathogen attack were observed, if and when a seedling died, and we ascribed a cause of death," Spear says. Pathogen symptoms included patches of black, dead tissue in the leaves or stem. "In some cases, we could actually see the pathogen growing on the seedling," she says.

Of the 725 seedlings that germinated, 38 percent suffered pathogen-caused damage, including 11 percent of seedlings killed by pathogens.

Compared with seedlings in the drier forest, seedlings in the wetter forest were 74 percent more likely to suffer pathogen-caused damage and 65 percent more likely to be killed by pathogens.

"But what was really striking was that pathogen-caused damage was five times more likely to be lethal for seedlings of dry-forest species than for wet-forest species," suggesting dry- and wet-forest species differ in their ability to halt or slow infection, Spear says.

The researchers next plan to identify specific fungi, bacteria and other pathogens and whether they differ in wetter and drier forests.

During her study at the drier park site in Panama City, Spear discussed her research with tourists and other park visitors.

"I'd emerge from the tangles of vines sweaty, muddy and generally disheveled and people couldn't help but ask what I was doing," Spear recalls. "It was heartening to hear how the forest had touched these very different people."

A brief time-lapse video of a seedling dying from pathogen attack during a period of several days can be seen at: http://vimeo.com/58026978 Video by Erin Spear, University of Utah.


Source: University of Utah

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Mountain pine beetles get bad rap for wildfires, study says

Following wildfires in 2011, a UW-Madison research team studied lodgepole pine trees in the Northern Rocky Mountains to examine whether earlier outbreaks of mountain pine beetles changed the ecological impact of the wildfires. Credit: Turner Lab

Mountain pine beetles get a bad rap, and understandably so. The grain-of-rice-sized insects are responsible for killing pine trees over tens of millions of acres in the Western U.S. and Canada over the last decade.

But contrary to popular belief, these pests may not be to blame for more severe wildfires like those that have recently swept through the region. Instead, weather and topography play a greater role in the ecological severity of fires than these bark-boring beetles.

New research led by the University of Wisconsin-Madison and the Washington State Department of Natural Resources provides some of the first rigorous field data to test whether fires that burn in areas impacted by mountain pine beetles are more ecologically severe than in those not attacked by the native bug.

In a study published this week in the Proceedings of the National Academy of Sciences, UW-Madison zoology professor Monica Turner and her graduate student, Brian Harvey, show pine beetle outbreaks contributed little to the severity of six wildfires that affected more than 75,000 acres in the Northern Rocky Mountains in 2011. They also show that the beetle outbreaks, which occurred from 2000 through 2010, have not directly impacted post-fire recovery of the forests. The study does not, however, address fire behavior, such as how quickly fires spread or how dangerous they are to fight.

While the findings may exonerate the insect scapegoats, they should also help ecosystem managers better respond to changes in the face of climate-driven disturbances, like drought and warmer temperatures.

Large, severe fires are typical in the lodgepole pine forests found throughout the region, even without mountain pine beetle outbreaks. However, as the climate has warmed, outbreaks and big fires have both become more common. The phenomenon of more beetles has meant more dead trees, and some have grown concerned about how beetle attacks and wildfires may interact.

"The conventional wisdom is that a forest of dead trees is a tinder box just waiting to burn up," says Turner, who has long studied the forest landscape of the Mountain West. "There were very little data out there but a lot of concern."

Forests attacked by bark beetles -- which burrow into the bark of lodgepole pines to mate and incubate their larvae -- can seem nothing more than ample kindling for a raging blaze, with their dead wood and dry, reddish-brown needles.

The burrows the beetles carve under the bark of pines, called galleries, choke off water and nutrient circulation in the trees. The trees die and, for the first couple of years, they hold on to their dry, lifeless needles. Scientists call this the "red stage," and some believe these trees could fuel more severe fires.

By year three, most beetle-attacked trees have entered the "gray stage," dropping their once green pine foliage, becoming needleless wood carcasses.

Earlier studies from Turner's group suggested that beetle outbreaks would not lead to more severe fires. But without actual fires, the interaction could not be tested.

However, in 2011, wildfires throughout eastern Idaho and western Montana -- in forests that had experienced varying mountain pine beetle outbreak impacts -- provided opportunity for the research team to begin to answer the question: Do the two disturbances, beetle attacks and wildfire, together change the ecological response of the forest to fire?

Fortunately for the team, among the burned areas studied were pine stands that had not been attacked by beetles. These areas served as controls. Others suffered a range of mortality from the beetles; in some stands, beetles killed nearly 90 percent of the trees prior to wildfire. The fires that raged also ran the spectrum of severity, allowing the researchers to compare a number of variables.

Some study plots comprised mostly live trees, while others contained mostly red-stage or gray-stage trees -- allowing the researchers to assess whether plots with red-stage trees (with dry needles) experienced greater levels of fire severity than plots with mostly gray-stage trees (no needles), as they and others had expected.

The study team examined ecosystem indicators of fire severity, such as how many trees were killed by fire and how much char covered the forests.

Engaging in what Harvey calls "post-fire detective work," in 2012, the scientific team evaluated fire severity in each study plot and stripped sections of bark from over 10,000 trees to determine what killed them, beetles or fire. Beetle galleries can remain visible under the bark even after fire.

As they sifted through the blackened trees and forest floor, the team became covered with ash and soot.

"We looked like coal miners when we were done," says Harvey.

They found that the severity of the outbreak and whether trees were in the red or gray stage had almost no effect on fire severity under moderate burning conditions.

Only under more extreme fire-burning conditions -- when it was hot, dry and windy -- did areas with more beetle-killed trees show signs of more ecologically severe fires, such as more deeply burned trunks and crowns (the part of the tree that includes its limbs and needles). The presence of more gray-stage trees actually had a stronger impact on fire severity than the amount of red-stage trees, to the surprise of the scientists.

Overall, however, Turner says the effects of beetle outbreaks on fire severity took a back seat to stronger drivers -- primarily weather and topography. Fire severity increased under more extreme weather, regardless of pre-fire outbreaks, and forest stands higher in the landscape burned more severely than those at lower elevation as fires moved uphill, building momentum.

"No one says beetle-killed forests won't burn," says Turner. "The data set looks at whether they burn with different severity compared to unattacked forests burning under similar conditions."

The team was also interested in whether beetle outbreaks slowed the recovery of the forests after fires. Lodgepole pines are adapted to fire, containing two types of seed-carrying cones: those that release seeds as soon as they mature and those that require fire to open, blanketing the forest floor with potential new life following a blaze.

By counting the number of post-fire tree seedlings in their plots, the researchers found very little beetle-related impact. Tree seedlings were most numerous where more of the fire-killed trees bore the fire-adapted, or serotinous, cones. Beetle-killed trees likely contributed to post-fire seedling establishment, too, as their seeds remain viable in cones if they are not consumed in fire. Only high-reaching char from tall flames reduced the number of seed-spreading cones.

The scientists emphasize the results may differ in other forest types or with different lengths of time between beetle outbreaks and fire.

"These are both natural disturbances, fire and beetle outbreaks," says Turner. "It's not surprising the ecosystem has these mechanisms to be resilient. What we as people see as catastrophes are not always catastrophes to the ecosystem."

Source: University of Wisconsin-Madison

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