Category: Data Nugget | Page 9

12.6.16

Sticky situations: big and small animals with sticky feet

Travis in the lab measuring the stickiness of a gecko’s toe.

The activities are as follows:

Species are able to do so many amazing things, from birds soaring in the air, lizards hanging upside-down from ceilings, and trees growing hundreds of feet tall. The study of biomechanics looks at living things from an engineering point of view to study these amazing abilities and discover why species come in such a huge variety of shapes and sizes. Biomechanics can improve our understanding of how plants and animals have adapted to their environments. We can also take what we learn from biology and apply it to our own inventions in a process called biomimicry. Using this approach, scientists have built robotic jellyfish to survey the oceans, walking robots to help transport goods, and fabrics that repel stains like water rolling off a lotus leaf.

Travis studies biomechanics and is interested in the ability of some species to climb and stick to walls. Sticky, or adhesive, toe pads have evolved in many different kinds of animals, including insects, arachnids, reptiles, amphibians, and mammals. Some animals, like frogs, bats, and bugs use suction cups to hold up their weight. Others, like geckos, beetles, and spiders have toe pads covered in tiny, branched hairs. These hairs actually adhere to the wall! Electrons in the molecules that make up the hairs interact with electrons in the molecules of the surface they’re climbing on, creating a weak and temporary attraction between the hairs and the surface. These weak attractions are called van der Waals forces.

Travis catching lizards in the Dominican Republic.

The heavier the animal, the more adhesion they will need to stick and support their mass. With a larger toe surface area, more hairs can come in contact with the climbing surface, or the bigger the suction cup can be. For tiny species like mites and flies, tiny toes can do the job. Each fly toe only has to be able to support a small amount of weight. But when looking at larger animals like geckos, their increased weight means they need much larger toe pads to support them.

When comparing large and small objects, the mass of large objects grows much faster then their surface area does. As a result, larger species have to support more mass per amount of toe area and likely need to have non-proportionally larger toes than those needed by lighter species. This results in geckos having some crazy looking feet! This relationship between mass and surface area led Travis to hypothesize that larger species have evolved non-proportionally larger toe pads, which would allow them to support their weight and stick to surfaces.

To investigate this idea, Travis looked at the data published in a paper by David Labonte and fellow scientists. In their paper they measured toe pad surface area and mass of individual animals from 17 orders (225 species) including insects, arachnids, reptiles, amphibians, and mammals. From their data, Travis calculated the average toe pad area and mass for each order.

Travis then plotted each order’s mass and toe pad area on logarithmic axes so it is easier to compare very small and very large values. Unlike a standard axis where the amount represented between tick marks is always the same, on logarithmic axes each tick mark increases by 10 times the previous value. For example, if the first tick represents 1.0, the second tick will be 10, and the next 100. As an example, look at the graphs below.

The left plot shows hypothetical gecko species of different sizes, but with proportional toes. Their mass per toe pad area ratio (g/mm²) varies, with larger species having larger g/mm² ratios. In this case, larger species have to support more mass per toe pad area. In the right plot, larger gecko species have disproportionally larger toes. These differences change each species’ mass per toe pad area ratios, so that all species, regardless of their size, have the same mass per toe pad area ratio.

Featured scientists: David Labonte, Christofer J. Clemente, Alex Dittrich, Chi-Yun Kuo, Alfred J. Crosby, Duncan J. Irschick, and Walter Federle. Written by: Travis Hagey

Data Nugget Flesch–Kincaid Reading Grade Level = 10.3

Scaling Up – Math Activity Flesch–Kincaid Reading Grade Level = 9.5

There is a scientific paper associated with the data in this Data Nugget. The data was used with permission from D. Labonte.

Labonte, D., Clemente, C.J., Dittrich, A., Kuo, C.Y., Crosby, A.J., Irschick, D.J. and Federle, W., 2016. Extreme positive allometry of animal adhesive pads and the size limits of adhesion-based climbing. Proceedings of the National Academy of Sciences, p.201519459.

To learn more about Travis and his research on geckos, read this blog post, “An evolving sticky situation” and check out the video below!

Sticky situations video

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For a video and article on using “gecko power” to scale a building, check out this article – Climbing a Glass Building? Try a Gecko’s Sticky Pads

About Travis: Ever since Travis was a kid, he was interested in animals and wanted to be a paleontologist. He even had many dinosaur names memorized to back it up! In college he discovered evolutionary biology, which drove him to apply for graduate school and become a scientist. There, he fell in love with comparative biomechanics, which combines evolutionary biology and mechanical engineering. Today Travis studies geckos and their sticky toes that allow them to scale surfaces like glass windows and tree branches.

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12.2.16

Are you my species?

Michael holding a male darter. The bright color patterns differ for each of the over 200 species. Photo by Tamra Mendelson.

The activities are as follows:

What is a species? The biological species concept says species are groups of organisms that can mate with each other but do not reproduce with members of other similar groups. How then do animals know who to choose as a mate and who is a member of their own species? Communication plays an important role. Animals collect information about each other and the rest of the world using multiple senses, including sight, sound, sonar, and smell. These signals may be used to figure out who would make a good mate and who is a member of the same species.

Michael snorkeling, looking for darters.

Michael is a scientist interested in studying how individuals communicate within and across the boundaries of species. He studies darters, a group of over 200 small fish species that live on the bottom of streams, rivers, and lakes. Michael first chose to study darters because he was fascinated by the bright color patterns the males have on their bellies during the breeding season. Female darters get to select which males to mate with and the males fight with each other for access to the females during the mating season. Species identification is very important during this time. Females want to make sure they choose a member of their own species to mate with. Males want to make sure they only spend energy fighting off males of their own species who are competing for the same females. What information do females and males use to guide their behavior and how do they know which individuals are from their own species?

Across all darter species, there is a huge diversity of color patterns. Because only males are brightly colored and there is such a diversity of colors and patterns, Michael wondered if males use the color patterns to communicate species identity during mating. Some darter species have color patterns that are very similar to those of other darter species. Perhaps, Michael thought, the boundaries of species are not as clear as described by the biological species concept. Some darter species may be able to hybridize, or mate with members of a different species if their color patterns are very close. Thus, before collecting any data, Michael predicted that the more similar the color patterns between two males, the more likely they would be to hybridize and act aggressively towards each other. If this is the case, it would serve as evidence that color pattern may indeed serve as a signal to communicate darter species identity.

Michael (right) in the field, collecting darters. Photo by Tamra Mendelson.

Michael collected eight pairs of darter species (16 species in all) from Alabama, Mississippi, Tennessee, Kentucky, South Carolina, and North Carolina and brought them all back to the lab. In some species pairs the color patterns were very similar, and in some they were very different. For each species pair, he put five males of both species and five females of both species in the same fish tank and observed their behavior for five hours. He did this eight times, once for each species pair (for a total of 1,280 fish!). During the five-hour observation period, he recorded (1) how many times females mated with males of their own species or of a different species and (2) how many times males were aggressive towards males of their own species or of a different species. He used these data to calculate an index of bias for each behavior, to show whether individuals had stronger reactions towards members of their own species.

Featured scientist: Michael Martin from the University of Maryland, Baltimore County

Flesch–Kincaid Reading Grade Level = 10.9

Videos showing darter behavior:

Darter species used in the experiment:

darters

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11.17.16

When a species can’t stand the heat

An adult male tuatara. Photo by Scott Jarvie.

The activities are as follows:

Tuatara are a unique species of reptile found only in New Zealand. Tuatara look like lizards but they are actually in their own reptile group. Tuatara are the only species remaining on the planet from this lineage, one that dates to the time of the dinosaurs! Tuatara are similar to tortoises in that they are extremely long-lived and can sometimes live over 100 years. Tuatara start reproducing when they are about 15–20 years old and they breed infrequently.

North Brother Island, one of the small New Zealand islands where tuatara are still found today. Photo by Jo Monks.

The sex of tuatara is not determined by sex chromosomes (X or Y) as in humans. Instead, the temperature of the nest during egg development is the only factor that determines the sex of tuatara embryos. If the egg develops with a low temperature in the nest it will be female, but if it develops with a high temperature it will be male. This process happens in many other species, too, including some turtles, crocodiles, lizards, and fish. However, most species are the opposite of tuatara and produce females at the warmest temperatures.

Today, tuatara face many challenges. Humans introduced new predators to the large North and South Islands of New Zealand. Tuatara used to live on these main islands, but predators drove the island populations to extinction. Today, the tuatara survive only on smaller offshore islands where they can escape predation. Because many of these islands are small, tuatara can have low population numbers that are very vulnerable to a variety of risk factors. One of the current challenges faced by these populations is climate change. Similar to the rest of the world, New Zealand is experiencing higher and higher temperatures as a result of climate change, and the warm temperatures may impact tuatara reproduction.

Kristine collecting data on a tuatara in the field. Photo by Sue Keall.

North Brother Island has a small population of tuatara (350–500 individuals) that has been studied for decades. Every single tuatara has been marked with a microchip (like the ones used on pet dogs and cats), which allows scientists to identify and measure the same individuals repeatedly across several years. In the 1990s, a group of scientists studying the tuatara on this island noticed that there were more males than females (60% males). The scientists started collecting data on the number of males and females so they could track whether the sex ratio, or the ratio of males and females in the population, became more balanced or became even more male-biased over time. The sex ratio is important because when there are fewer females in a population, there are fewer individuals that lay eggs and produce future offspring. Generally, a population that is highly male-biased will have lower reproduction rates than a population that is more balanced or is female-biased.

The fact that tuatara are long-lived and breed infrequently meant that the scientists needed to follow the sex ratio for many years to be sure they were capturing a true shift in the sexes over time, not just a short-term variation. In 2012, Kristine and her colleagues decided to use these long-term data to see if the increasing temperatures from climate change were associated with the changing sex ratio. They predicted that there would be a greater proportion of males in the population over time. This would be reflected in an unbalanced sex ratio that is moving further and further away from 50% males and 50% females and toward a male-biased population.

Featured scientists: Kristine Grayson from University of Richmond, Nicola Mitchell from University of Western Australia, and Nicola Nelson from Victoria University of Wellington

Flesch–Kincaid Reading Grade Level = 11.9

Additional teacher resources related to this Data Nugget:

Video Recording from Headwaters Institute: Lunch with a scientist – Meet Dr. Kristine Grayson!
Want to learn more about tuatara or introduce students to this species before beginning the Data Nugget? Check out this video by “It’s ok to be smart”.
There are two publications associated with the research in this activity:
- Grayson, Kristine L., Nicola J. Mitchell, Joanne M. Monks, Susan N. Keall, Joanna N. Wilson, and Nicola J. Nelson (2014). Sex Ratio Bias and Extinction Risk in an Isolated Population of Tuatara (Sphenodon punctatus). PLoS ONE 9(4): e94214.
- Grayson, Kristine L., Nicola J. Mitchell, and Nicola J. Nelson (2014). A Threat to New Zealand’s Tuatara Heats Up. American Scientist 102: 350-357.
For a popular science article about tuatara research, written for students, check out Science News for Student’s article “When a species can’t stand the heat: Global warming could leave New Zealand’s tuatara dangerously short of females” (PDF for printing, Word Search!)
Students can access the National Institute of Water and Atmospheric Research (NIWA) New Zealand weather station data here.

About Kristine: Kristine L. Grayson is an Associate Professor in the Biology Department at University of Richmond, where she teaches Intro Ecology/Evolution, Field Ecology, Ecophysiology, and Data Visualization. She is an HHMI BioInteractive Ambassador and facilitator with the Quantitative Undergraduate Biology Education and Synthesis (QUBES) project, where you can find additional teaching resources she has authored. Kristine runs an undergraduate research lab studying invasive insects, salamanders, and aquatic macroinvertebrates. Her work on tuatara was conducted during a postdoc at Victoria University of Wellington funded by an NSF International Research Fellowship. One of her claims to fame is capturing the state record holding snapping turtle for North Carolina – 52 pounds! To read more about Kristine and her interest in science from a young age, check out this article.

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11.1.16

Finding Mr. Right

Mountain chickadee, photo by Vladimir Pravosudov

The activities are as follows:

Depending on where they live, animals can face a variety of challenges from the environment. For example, animal species that live in cold environments may have adaptive traits that help them survive and reproduce under those conditions, such as thick fur or a layer of blubber. Animals may also have adaptive behaviors that help them deal with the environment, such as storing food for periods when it is scarce or hibernating during times of the year when living conditions are most unfavorable. These adaptations are usually consistently seen in all individuals within a species. However, sometimes populations of the same species may be exposed to different conditions depending on where they live. The idea that populations of the same species have evolved as a result of certain aspects of their environment is called local adaptation.

Mountain chickadees are small birds that live in the mountains of western North America. These birds do not migrate to warmer locations like many other bird species; they remain in the same location all year long. To deal with living in a harsh environment during the winter, mountain chickadees store large amounts of food throughout the forest during the summer and fall. They eat this food in the winter when very little fresh food is available. There are some populations of the species that live near the tops of mountains, and some that live at lower elevations. Birds at higher elevations experience harsher winter conditions (lower temperature, more snow) compared to birds living at lower elevations. This means that birds higher in the mountains depend more on their stored food to survive winter.

Carrie conducting field research in winter, photo by Vladimir Pravosudov

Carrie studies mountain chickadees in California. Based on previous research that was done in the lab she works in, she learned these birds have excellent spatial memory, or the ability to recall locations or navigate back to a particular place. This type of memory makes it easier for the mountain chickadees to find the food they stored. Carrie’s lab colleagues previously found that populations of birds from high elevations have much better spatial memory compared to low-elevation birds. Mountain chickadees also display aggressive behaviors and fight to defend resources including territories, food, or mates. Previous work that Carrie and her lab mate conducted found that male birds from low elevations are socially dominant over male birds from high elevations, meaning they are more likely to win in a fight over resources. Taken together, these studies suggest that birds from high elevations would likely do poorly at low elevations due to their lower dominance status, but low-elevation birds would likely do poorly at high elevations with harsher winter conditions due to their inferior memory for finding stored food items. These populations of birds are likely locally adapted – individuals from either population would likely be more successful in their own environments compared to the other.

In this species, females choose which males they will mate with. Males from the same elevation as the females may be best adapted to the location where the female lives. This means that when the female lays her eggs, her offspring will likely inherit traits that are well suited for that environment. If she mates with males that match her environment, she is setting up her offspring to be more successful and have higher survival where they will live. Carrie wondered if female mountain chickadees prefer to mate with males that are from the same elevation and therefor contribute to local adaptation by passing the adaptive behaviors on to the offspring. This process could contribute to the populations becoming more and more distinct. Offspring born in the high mountains will continue to inherit genes for good spatial memory, and those born at low elevations will inherit genes that allow them to be socially dominant.

Mountain chickadee, photo by Vladimir Pravosudov

To test whether female mountain chickadees contribute to local adaptation by choosing and mating with males from their own elevation, Carrie brought high- and low-elevation males and females into the lab. Carrie made sure that the conditions in the lab were similar to the light conditions in the spring when the birds mate (14 hours of light, 10 hours of dark). Once a female was ready, she was given time to spend with both males in a cage that is called a two-choice testing chamber. On one side of the testing chamber was a male from a low-elevation population, and on the other side was a male from a high-elevation population. Each female could fly between the two sides of the testing chamber, allowing her to “choose” which male she preferred to spend time close to (measured in seconds [s]). There was a cardboard divider in the middle of the cage with a small hole cut into it. This allowed the female to sit on the middle of the cardboard, which was not counted as preference for either male. Females from both high- and low-elevation populations were tested in the same way. The female bird’s preference was determined by comparing the amount of time the female spent on either side of the cage. The more time a female spent on the side of the cage near one male, the stronger her preference for that male.

Watch a video of one of the experimental trials:

Featured scientist: Carrie Branch from University of Nevada Reno

Flesch–Kincaid Reading Grade Level = 11.5

Additional teacher resources related to this Data Nugget include:

Carrie’s lab’s website, for more information on chickadee cognition!
A YouTube video of one of Carrie’s experimental trials showing a female in the two-choice testing chamber. Students can observe the female chickadee as she decides between the males on her left or the one on her right.
The paper published using these data and testing alternative hypotheses:
- Branch, C.L., Kozlovsky, D.Y., and V.V. Pravosudoc. 2015. Elevation-related differences in female mate preferences in mountain chickadees: are smart chickadees choosier? Animal Behavior 99: 89-94.

About Carrie: I have been interested in animal behavior and behavioral ecology since my second year in college at the University of Tennessee. I am primarily interested in how variation in ecology and environment affect communication and signaling in birds. I have also studied various types of memory and am interested in how animals learn and use information depending on how their environment varies over space and time. I am currently working on my PhD in Ecology, Evolution, and Conservation Biology at the University of Nevada Reno and once I finish I hope to become a professor at a university so that I can continue to conduct research and teach students about animal behavior. In my spare time I love hiking with my friends and dogs, and watching comedies!

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11.1.16

Why so blue? The determinants of color pattern in killifish, Part II

In Part 1, you examined the effects of genetics and environment on anal fin color in male bluefin killifish. The data from Becky’s experiment showed that both genetics and environment work together to determine whether male offspring had blue, yellow, or red anal fins. You will now examine how the father’s genetics, specifically their fin color pattern, affects anal fin color in their sons. When we factor in the genetics of the father, and not just the population he came from, does this influence our interpretation of the data?

The color polymorphism in bluefin killifish – males display anal fins in blue, red, or yellow.

The activities are as follows:

For her experiment, Becky collected male and female fish from both a swamp (26 Mile Bend) and a spring (Wakulla) population. Most of the males in the swamp have blue anal fins, but some have red or yellow. Most of the males from the spring have red or yellow anal fins, but some have blue. Becky decided to add data about the father’s fin color pattern into her existing analysis from Part 1 to see how it affected her interpretation of the results.

In Part 1, Becky was looking at the genetics from the population level. Looking at the data this way, we saw parents from the 26 Mile Bend swamp population were more likely to have sons with blue anal fins than parents from the Wakulla spring. Parents from the 26 Mile Bend were also much more likely to have sons with higher levels of plasticity, meaning they responded more to the environment they were raised in. This means there was a big difference between the proportion sons with blue anal fins in the clear and brown water treatments.

Bringing in the color pattern of the fathers now allows Becky to look at the genetics from both the population and the individual level. From both the swamp and spring population, Becky collected males of all colors. Becky measured the color pattern of the fathers and recorded the color of their anal fins and the rear part of their dorsal fins. She used males that were red on the rear portion of the dorsal fin with a blue anal fin (rb), males that were red on both fins (rr), males that were yellow on both fins (yy), and males that were yellow on the rear portion of the dorsal fin with blue a blue anal fin (yb).

She randomly assigned each father’s sons into one of the water treatments, either clear or brown water. Once the sons developed their fin colors, she recorded the anal fin color. This experimental design allowed her to test whether sons responded differently to the treatment depending on the genetics of their father. She thought that the anal fin color of the sons would be inherited genetically from the father, but would also respond plastically to the environment they were raised in. She predicted fathers with blue anal fins would be more likely to have sons with blue anal fins, especially if they were raised in the brown water treatment. She also predicted that fathers with red and yellow anal fins could have sons with blue anal fins if they were raised in the brown water treatment, but not as many as the blue fathers.

Featured scientist: Becky Fuller from The University of Illinois

Flesch–Kincaid Reading Grade Level = 10.9

About Becky: I consider myself to be an evolutionary biologist who studies fishes. I grew up in a small town riding horses in 4-H and working in a veterinary clinic. As an undergraduate at the University of Nebraska at Lincoln, I was interested in biology and considering either medical or veterinary school. Two things led to me research in ecology and evolution. In the summer of 1991, I was taking courses at Cedar Point Biological Field Station which was run by the University of Nebraska. I met Dr. Anthony Joern (Tony) who was studying grasshopper community ecology. Tony hired me onto his field crew that summer after the courses were finished. I went on to do an undergraduate thesis under Tony’s mentorship where I studied predation on grasshoppers. I caught the “science bug” and never looked back. Following my undergraduate work, I went to Uppsala University in Sweden on a Fulbright Scholarship. Here, I developed my love for fish and aquatics. I worked with Dr. Anders Berglund on pipefish in a fjord on the west coast of Sweden. Since then, I have had many wonderful advisers, instructors, mentors, and collaborators who have helped me develop skills along the numerous fronts required for a successful career in science. I consider myself very fortunate to have a job where I can do science and teach young, enthusiastic undergraduates.

11.1.16

Why so blue? The determinants of color pattern in killifish, Part I

The color polymorphism in bluefin killifish – males display anal fins in blue, red, or yellow.

The activities are as follows:

In nature, animals can be found in a dazzling display of different colors and patterns. Color patterns serve as signals to members of the animal’s own species, or to other species. They can be used to attract mates, camouflage with the environment, or warn predators to stay away. When looking at the diversity of colors found in nature, you may wonder, why do animals have the color patterns they do? One way to study this question is to look at a single species that has individuals of different colors. This variation can be used to uncover the mechanisms that determine color.

The bluefin killifish is a freshwater species that is found mostly in Florida. They are found in two main habitats, springs and swamps. An intriguing aspect of this species is that male bluefin killifish are brightly colored with many different color patterns. The brightest part of the fish is the anal fin, which is found on the bottom of the fish by the tail. Some males have red anal fins, some have yellow anal fins, and others have blue anal fins. This variation in color is called a polymorphism, meaning that in a species there are multiple forms of a single trait. In a single spring or swamp you may see all three colors!

Becky in the field, with her colleague Katy, collecting fish in 26 Mile Bend Swamp.

Becky is a biologist studying bluefin killifish. One day, while out snorkeling for her research, she noticed an interesting pattern. She observed that there were differences in the polymorphism depending on whether she was in a spring or swamp. Springs have crystal clear water that can appear blue-tinted. Becky noticed that most of the males in springs had either red or yellow anal fins. Swamps have brown water, the color of iced tea, due to the dissolved plant materials in the water. Becky noticed that most of the males in swamps had blue anal fins. After noticing this pattern she wanted to find out why this variation in color existed. Becky came up with two possible explanations. She thought males in swamps might be more likely to be blue (1) because of the genes they inherit from their parents, or (2) because individual color is responding to environmental conditions. This second case, where the expression of a trait is directly influenced by the environment that an individual experiences, is known as phenotypic plasticity.

Becky had to design an experiment that could tease apart whether genes, plasticity, or both were responsible for male anal fin color. She did this by collecting male and female fish from the two habitat types, breeding them, and raising their offspring in clear or brown water. If a father’s genes are responsible for anal fin color in their sons, then fathers from swamps would be more likely to leave behind blue sons. If environmental conditions determine the color of sons, then sons raised in brown water will be blue, regardless of the population origin of their father.

Becky’s family helping her out in the field!

Becky and her colleagues collected fish from two populations in the wild – Wakulla Spring, and 26 Mile Bend Swamp – and brought them into the lab. These two populations represent the genetic stocks for the experiment. Fish from Wakulla are more closely related to each other than they are to fish from 26 Mile Bend. In the lab, they mated female fish with male fish from the same population: females from Wakulla mated with males from Wakulla, and females from 26 MB mated with males from 26 MB. The female fish then laid eggs, and after the offspring hatched from their eggs, half were put into tanks with clear water (which mimics spring conditions) and half in tanks with brown water (which mimics swamp conditions). For the brown water treatment, Becky colored the water using ‘Instant, De-caffeinated, No-Sugar, No-Lemon’ tea. They raised the fish to adulthood (3-6 months) so they could determine their sex and the color of the son’s anal fins. Becky then counted the total number of male offspring, and the number of male offspring that had blue anal fins. She used these numbers to calculate the proportion of sons that had blue anal fins in each treatment.

Featured scientist: Becky Fuller from The University of Illinois

Flesch–Kincaid Reading Grade Level = 9.4

To introduce students to bluefin killifish, there is a video showing the blue and red color morphs. Video can be shown on mute (background music is a little corny)!

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10.21.16

Bon Appétit! Why do male crickets feed females during courtship?

Mating pair of Hawaiian swordtail cricket with macrospermatophore on the male (left). The male and female (right) are marked with paint pens for individual identification.

The activities are as follows:

In many species of insects and spiders, males provide females with gifts of food during courtship and mating. This is called nuptial feeding. These offerings are eaten by the female and can take many forms, including prey items the male captured, substances produced by the male, or parts from the male’s body. In extreme cases the female eats the male’s entire body after mating! Clearly these gifts can cost the male a lot, including time and energy, and sometimes even their lives.

So why do males give these gifts? There are two main hypotheses explaining why nuptial feeding has evolved in so many different species. First, giving a gift may attract a female and improve a male’s chance of getting to mate with her, or of fathering her young. This is known as the mating effort hypothesis. Second, giving a gift may provide the female with the energy and nutrients she needs to produce young. The gift helps the female have more, or healthier, offspring. This is known as the paternal investment hypothesis. These two hypotheses are not mutually exclusive – meaning, for any given species, both mechanisms could be operating, or just one, or neither.

Biz is a scientist who studies nuptial gifts, and they work with the Hawaiian swordtail cricket. They chose this species because it uses a particularly interesting example of nuptial feeding. In most other cricket species, the male provides the female with a single package of sperm, called a spermatophore. After sperm transfer, the female removes the spermatophore from her genitalia and eats it. However, in the Hawaiian swordtail cricket, males produce not just one but a whole bunch of spermatophores over the course of a single mating. Most of these are smaller, and contain no sperm – these are called “micros”. Only the last and largest spermatophore to be transferred, called the “macro” actually contains sperm. The number of micros that a male gives changes from mating to mating.

From some of their previous research, and from reading papers written by other scientists, Biz learned that micros increase the chance that a male’s sperm will fertilize some of the female’s eggs. Also, the more micros the male gives, the more of the female’s offspring he will father. This research supports the mating effort hypothesis for the Hawaiian swordtail cricket. Knowing this, Biz wanted to test the paternal investment hypothesis as well. They wanted to know whether the “micro” nuptial gifts help females lay more eggs, or help more of those eggs hatch into offspring.

Biz used two experiments to test the paternal investment hypothesis. In the first experiment, 20 females and 20 males were kept in a large cage outside in the Hawaiian rainforest. The crickets were allowed to mate as many times as they wanted for six weeks. In the second experiment, 4 females and 4 males were kept in cages inside in a lab. Females were allowed to mate with up to 3 different males, and were then moved to a new cage to prevent them from mating with the same male more than once. In both experiments Biz observed all matings. They recorded the number of microspermatophores transferred during each mating and the number of eggs laid. If females that received a greater number of total micros over the course of all matings produced more eggs, or if their eggs had a higher rate of hatching, then the paternal investment hypothesis would be supported.

Featured scientist: Biz Turnell from Cornell University and Technische Universität Dresden

Flesch–Kincaid Reading Grade Level = 8.9

Additional teacher resources related to this Data Nugget include:

The data in this activity has been published. The citation for the paper, and a link to the PDF, are below:
- Turnell, B.R. and K.L. Shaw (2015) High opportunity for postcopulatory sexual selection under field conditions. Evolution 69(8): 2094–2104
For a popular science article about nuptial feeding in a different system, check out these articles
- “Nuptial gifts and other romantic gestures of the bug world“
- “Ultimate sacrifice: Spider’s post-sex cannibalism aids offspring“

10.13.16

Winter is coming! Can you handle the freeze?

Doug, and two members of his team, setting up the reciprocal transplant experiment in Scandinavia.

Doug with the reciprocal transplant experiment in Scandinavia.

The activities are as follows:

Doug is a biologist who studies plants from around the world. He often jokes that he chose to work with plants because he likes to take it easy. While animals rarely stay in the same place and are hard to catch, plants stay put and are always growing exactly where you planted them! Using plants allows Doug to do some pretty cool and challenging experiments. Doug and his research team carry out experiments with the plant species Mouse-ear Cress, or Arabidopsis thaliana. They like this species because it is easy to grow in both the lab and field. Arabidopsis is very small and lives for just one year. It grows across most of the globe across a wide range of latitudes and climates. Arabidopsis is also able to pollinate itself and produce many seeds, making it possible for researchers to grow many individuals to use in their experiments.

Doug, and two members of his team, setting up the reciprocal transplant experiment in Scandinavia.

Part I: Doug wanted to study how Arabidopsis is able to survive in such a range of climates. Depending on where they live, each population faces its own challenges. For example, there are some populations of this species growing in very cold habitats, and some populations growing in very warm habitats. He thought that each of these populations would adapt to their local environments. An Arabidopsis population growing in cold temperatures for many generations may evolve traits that increase survival and reproduction in cold temperatures. However, a population that lives in warm temperatures would not normally be exposed to cold temperatures, so the plants from that population would not be able to adapt to cold temperatures. The idea that populations of the same species have evolved as a result of certain aspects of their environment is called local adaptation.

To test whether Arabidopsis is locally adapted to its environment, Doug established a reciprocal transplant experiment. In this type of experiment, scientists collect seeds from plants in two different locations and then plant them back into the same location (home) and the other location (away). For example, seeds from population A would be planted back into location A (home), but also planted into location B (away). Seeds from population B would be planted back into location B (home), but also planted at location A (away). If populations A and B are locally adapted, this means that A will survive better than B in location A, and B will survive better than A in location B. Because each population would be adapted to the conditions from their original location, they would outperform the plants from away when they are at home (“home team advantage”).

In this experiment, Doug collected many seeds from warm Mediterranean locations at low latitudes, and cold Scandinavian locations at high latitudes. He used these seeds to grow thousands of seedlings. Once these young plants were big enough, they were planted into a reciprocal transplant experiment. Seedlings from the Mediterranean location were planted alongside Scandinavian seedlings in a field plot in Scandinavia. Similarly, seedlings from the Scandinavian locations were planted alongside Mediterranean seedlings in a field plot in the Mediterranean. By planting both Mediterranean and Scandinavian seedlings in each field plot, Doug can compare the relative survival of each population in each location. Doug made two local adaptation predictions:

Scandinavian seedlings would survive better than Mediterranean seedlings at the Scandinavian field plot.
Mediterranean seedlings would survive better than Scandinavian seedlings planted at the Mediterranean field plot.

Doug’s team in the Mediterranean prepped and ready to set up the experiment.

Part II: The data from Doug’s reciprocal transplant experiment show that the Arabidopsis populations are locally adapted to their home locations. Now that Doug confirmed that populations were locally adapted, he wanted to know how it happened. What is different about the two habitats? What traits of Arabidopsis are different between these two populations? Doug now wanted to figure out the mechanism causing the patterns he observed.

Doug originally chose Arabidopsis populations in Scandinavia and the Mediterranean for his research on local adaptation because those two locations have very different climates. The populations may have adapted to have the highest survival and reproduction based on the climate of their home location. To deal with sudden freezes and cold winters in Scandinavia, plants may have adaptations to help them cope. Some plants are able to protect themselves from freezing temperatures by producing chemicals that act like antifreeze. These chemicals accumulate in their tissues to keep the water from turning into ice and forming crystals. Doug thought that the Scandinavian population might have evolved traits that would allow the plants to survive the colder conditions. However, the plants from the Mediterranean aren’t normally exposed to cold temperatures, so they wouldn’t have necessarily evolved freeze tolerance traits.

To see whether freeze tolerance was driving local adaptation, he set up an experiment to identify which plants survived after freezing. Doug again collected seeds from several different populations across Scandinavia and across the Mediterranean. He chose locations that had different latitudes because latitude affects how cold an area gets over the year. High latitudes (closer to the poles) are generally colder and low latitudes (closer to the equator) are generally warmer. Doug grew more seedlings for this experiment, and then, when they were a few days old, he put them in a freezer. Doug counted how many seedlings froze to death, and how many survived, and he used these numbers to calculate the percent survival for each population. To gain confidence in his results, he did this experiment with three replicate genotypes per population.

Doug predicted that if freeze tolerance was a trait driving local adaptation, the seedlings originally from colder latitudes (Scandinavia) would have increased survival after the freeze. Seedlings originally from lower latitudes would have decreased survival after the freeze because the populations would not have evolved tolerance to such cold temperatures.

Featured scientist: Doug Schemske from Michigan State University (MSU). Written by Christopher Oakley from MSU and Purdue University, and Marty Buehler (RET) from Hastings High School.

Flesch–Kincaid Reading Grade Level = 12.0

There is one scientific paper associated with the data in this Data Nugget. The citation and PDF of the paper is below.

Agren, J. and D.W. Schemske (2012). Reciprocal transplants demonstrate strong adaptive differentiation of the model organism Arabidopsis thaliana in its native range. New Phytologist 194:1112–1122.

10.6.16

Gene expression in stem cells

Adam working in the lab at Colorado State University.

The activities are as follows:

Every cell in your body contains the same DNA. How is it that genetically identical skin, brain, and muscle cells can look very different and perform very different functions from each other? Cells differentiate, or become different from one another, by turning certain genes on and off. This process is called gene expression. For example, when you spend time in the sun your skin cells turn on the gene for pigment, which protects your cells from bright sunlight. In the winter when there is less sunlight, your cells turn off this gene. This process your body uses to turn genes on and off is the same one it uses to develop from one cell into the many different cell types that make up your body. Stem cells have the ability to turn into any other type of cell in the body, an ability known as pluripotency. Your body retains some stem cells for your entire life.

Some genes are only turned on in specific types of cells because they have specialized jobs for those cell types, like muscle or brain cells. Other genes are more like managers, controlling which genes are turned on and off. The activity of these manager genes may be more common in stem cells because they could control which type of cell the stem cell will become. In recent years, scientists discovered they could reprogram specialized cells back into non-specialized stem cells, simply by turning on several manager genes. They call these reprogrammed cells induced pluripotent, or iPS.

Adam working under the hood, reprogramming specialized cells into induced pluripotent stem cells for his experiments.

Adam was working as a biologist in Colorado when he learned that many cool medical advances in regenerative and personalized medicine will happen when we figure out which genes are turned on, and which are turned off, in pluripotent stem cells. In his research, Adam wanted to look at gene expression for two genetically identical cell lines, those that have specialized and those that have been reprogrammed to be iPS stem cells. He was interested to see which genes are expressed by both types of cells and which genes are only expressed in one type of cell.

He decided to work with fibroblast cells because they are easy to grow in the lab. Fibroblasts cells are mainly responsible for production and maintenance of the extracellular matrix (including joints, ligaments, tendons and connective tissues), which is critical in holding the body’s tissues together. From reading the work of other scientists, Adam learned how to transform fibroblast cells into iPS stem cells. This knowledge lead him to two genetically identical types of cells – (1) specialized fibroblast cells and (2) unspecialized iPS cells. When fibroblast cells are transformed into unspecialized iPS cells, their function changes and they become responsible for wound healing and generating new tissues, acting like a reserve set of cells. Because fibroblast and iPS cells perform very different functions, Adam thinks it is likely that each cell line will expresses genes that are specific to its individual function.

Adam looked at expression in 10 different genes that are thought to have important functions for fibroblast or iPS cells. Adam measured the expression for each gene by looking at RNA abundance of each gene in the different cell types. RNA is the intermediate between DNA (the genetic blueprint) and protein (the functional worker of the cell). Adam chose to look at RNA, because it is often representative of how much protein is present in a cell, which is very difficult to measure directly. Adam analyzed three replicates for each cell type. He replicated in order to get a more accurate representation for each cell type. This is important in case the samples were in slightly different conditions, like warmer or cooler temperatures, which could alter gene expression. This experiment allowed Adam to figure out which genes are turned on in iPS cells, allowing him to better understand how stem cells work.

iPS cells display different gene expression and physical appearance than HFF cells: Figures A and B are low magnification images of two different iPS cell colonies. iPS cells are usually small, round, and like to grow in circular-like colonies. Figures C is a low magnification image of HFF cells. HFF cells tend to appear long and slender almost like trees. Generally, HFF cells like to grow near each other, but not in colonies. Figure D is a higher magnification image of the black box in figure C, showing a group of HFF cells growing in close proximity with each other.

Featured scientist: Adam Heck from Colorado State University. Written with Sandra Weeks from the Poudre Valley School District.

Flesch–Kincaid Reading Grade Level = 10.6

The gene expression data found in this activity was gathered from the following paper – citation and link below:

Neff, A. T., Lee, J. Y., Wilusz, J., Tian, B., & Wilusz, C. J. (2012). Global analysis reveals multiple pathways for unique regulation of mRNA decay in induced pluripotent stem cells. Genome Research, 22(8), 1457–1467.

10.5.16

Raising Nemo: Parental care in the clown anemonefish

Clown anemonefish caring for their eggs.

The activities are as follows:

When animals are born, some offspring are able to survive on their own, while others rely on parental care. Parental care can take many forms. One or both parents might help raise the young, or in some species other members of the group help them out. The more time and energy the parents invest, the more likely it is that their offspring will survive. However, parental care is costly for the parents. When a parent invests time, energy, and resources in their young, they are unable to invest as much in other activities, like finding food for themselves. This results in a tradeoff, or a situation where there are costs and benefits to the decisions that must be made. Parents must balance their time between caring for their offspring and other activities.

The severity of the tradeoff between parental care and other activities may depend on environmental conditions. For example, if there is a lot of food available, parents may spend more time tending to their young because finding food for themselves takes less time and energy. Scientists wonder if parents are able to adjust their parental care strategies in response to environmental changes.

Photo of Tina (left) with other members of her lab. The glowing blue tanks around them all contain anemonefish!

Tina is a scientist studying the clown anemonefish. She is interested in how parental care in this species changes in response to the environment. She chose to study anemonefish because they use an interesting system to take care of their young, and because the environment is always changing in the coral reefs where they live.

Anemonefish form monogamous pairs and live in groups of up to six individuals. The largest female is in charge of the group. Only the largest male and female get to mate and take care of the young. Both parents care for eggs by tending them, mouthing the eggs to clean the nest and remove dead eggs, and fanning eggs with their fins to oxygenate them. A single pair may breed together tens or even hundreds of times over their lifetimes. But here is the cool part – anemonefish can change their sex! If the largest female dies, the largest male changes to female, and the next largest fish in line becomes the new breeding male. That means that a single parent may have the opportunity to be a mother and a father during its lifetime.

Parents will fan the eggs to increase oxygen by the nest, or mouth them to remove dead eggs and clean the nest.

On the reef, anemonefish groups also experience shifts in how much food is available. In years with lots of food, the breeding pair has lots of young, and in years with little food they do not breed as often. Tina presumed that food availability determines how much time and energy the parents invest in parental care behaviors. She collected data from 20 breeding pairs of fish, 10 of which she gave half rations of food, and 10 of which she gave full rations. The experiment ran for six lunar months. Every time a pair laid a clutch of eggs, Tina waited 7 days and then took a 15-minute video of the parents and their nest. She watched the videos and measured three parental care behaviors: mouthing, fanning, and total time spent tending for both males and females. Some pairs laid eggs more than once, so she averaged these behaviors across the six months of the experiment. Tina predicted that parents fed a full ration would perform more parental care behaviors, and for a longer amount of time, than parents fed a half ration.

Watch video of the experimental trials, demonstrating the mouthing and fanning behaviors:

Featured scientist: Tina Barbasch from Boston University

Flesch–Kincaid Reading Grade Level = 9.4

About Tina: I first became interested in science catching frogs and snakes in my backyard in Ithaca, NY. This inspired me to major in Biology at Cornell University, located in my hometown. As an undergraduate, I studied male competition and sperm allocation in the local spotted salamander, Ambystoma maculatum. After graduating, I joined the Peace Corps and spent 2 years in Morocco teaching environmental education and 6 months in Liberia teaching high school chemistry. As a PhD student in the Buston Lab, I study how parents negotiate over parental care in my study system the clownfish, Amphiprion percula, otherwise known as Nemo. More here!

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