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Devorah A. N. Bennu, GrrlScientist - Science Kit

Devorah A. N. Bennu, GrrlScientist
Devorah A. N. Bennu, PhD. Chapman Postdoctoral Fellow. Independent Scholar. American Museum of Natural History, New York City
  • 30,000 Facets Give Dragonflies a Different Perspective
  • Why Are Bluebirds Blue?
  • Catching Dinner on the Fly
  • It's All in the Olfactory Pits
  • Take a Peek at Nature's Web Site
  • Back to Science Online Table of Contents


    30,000 Facets Give Dragonflies a Different Perspective: The Big Compound Eye in the Sky


    Color vision in humans depends upon three light-sensitive proteins, called opsins, that are present in our retinas. Each type of opsin absorbs one color of light in the spectrum. In humans, the colors absorbed by these opsins are red, green or blue. The many wavelengths of light reflected into our eyes from the surfaces of objects around us mix together to provide a rich palette of color. Yet, despite our visual color range, there is a creature with even greater scope; the dragonfly.

    Unlike humans, day-flying species of dragonflies have four or five opsins, allowing them to see colors that are beyond human visual capabilities, such as ultraviolet (UV) light. Their opsins are grouped in specific ways within small hexagonal packages, called facets. Together, these facets comprise the insect's compound eye. "They are segregated in the compound eye so that the upwards facing eye has only blue and UV receptors, and the downwards facing eye has receptors for longer wavelengths, [such as] green and orange," says Robert Olberg, dragonfly vision expert and professor of biology at Union College in Schenectady.

    This patterned concentration of opsin types, particularly those sensitive to blue and UV, gives special advantages to hunting dragonflies. For example, it is thought that the sky appears to be very bright to a dragonfly, thereby providing a clear background against which small moving prey can be easily detected, according to Dennis Paulson, dragonfly expert and director of the Slater Museum of Natural History at the University of Puget Sound, in Tacoma.

    Are there color-blind dragonflies? "We don't know," replies Paulson. "There are some [species] that tend to fly only at dusk; perhaps some of them have limited color vision."

    Dusk-active dragonflies have sacrificed most of their color vision in favor of increased light-collecting capacity by having fewer, larger facets in their eyes. They also lack all color sensitive opsins except green, which provides the broadest range of light sensitivity for any opsin. As a result, these dragonfly species probably also have a corresponding decrease in overall color perception.

    Dragonflies (and bees) have the largest compound eyes of any insect; each containing up to 30,000 facets, and the eyes cover most of the insect's head, resembling a motorcycle helmet. In contrast to a human eye, each facet within the compound eye points in a slightly different direction and perceives light emanating from only one particular direction in space, creating a mosaic of partially overlapping images.

    Does this mean that dragonflies have 30,000 eyes? "No," replies Olberg. "It's more like a human having 10,000 to 30,000 photoreceptors spread out across the retina -- but better than that because each facet has several spectral types of receptors."

    Dragonflies can also detect the plane of polarization of light, which humans cannot do without the aid of sunglasses. The advantages of this capability are unknown for dragonflies, but other insects are known to use polarized light as a sort of "sky compass" by which they navigate.

    Another visual advantage of the multifaceted eye is a dragonfly's acute sensitivity to movement, as anyone who has tried to catch one can tell you. "Dragonflies can see in all directions at the same time. That's one of many advantages of a compound eye; you can wrap it around your head," explains Olberg. "The spherical field of vision means that dragonflies are still watching you after they have flown by. However, the backward-looking part of the eye has rather low resolution. So, if you want to catch a dragonfly, let it go by you and then swing your net like a baseball bat from behind. If you swing at them while they are approaching they'll usually see the net coming and easily avoid it. They are awfully good at what they do." Olberg concludes.

    Many thanks to Robert Olberg, a PhD graduate of the UW's Zoology Department, Dennis Paulson and David O'Carroll for allowing me to interview them for this story.

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    Why are Bluebirds Blue? The Physics of Structural Colors in Bird Feathers [Schemochromes]


    Most avian colors are the result of different types of pigments that are deposited into the developing feather. However, pigments alone do not produce all avian feather colors. Blues and whites typically result from small changes in feather structure that alters their light reflective properties. These fundamental modifications cause blue light to be selectively reflected from the feather surface in the case of blue feathers, while white feathers reflect all visible light. In short, blues and whites are structural colors, or schemochromes.

    Visible light is composed of many colors of light, each with distinct wavelengths. Red light, for example, has a long wavelength (~700nm) while blue light has a much shorter wavelength (~400nm). When visible light encounters particles with the same diameter or larger than its component wavelengths, those specific light photons are reflected. Such reflected light photons are collected and seen by the observer's eye, thereby imparting color to the perceived image. Because blue light has a very short wavelength, it is selectively reflected more easily than other colors of light with longer wavelengths. This was first understood in 1869, when scientist John Tyndall noted that miniscule particles in earth's atmosphere preferentially scattered blue light resulting in the familiar "sky blue" of a clear summer day. Shortly afterward, Rayleigh demonstrated that Tyndall's "fine particles" are gases in our atmosphere, specifically, nitrogen and oxygen. Tyndall's contribution is widely recognized by describing this phenomenon as "Tyndall scattering" and referring to structural blue colors as "Tyndall Blues."

    Tyndall scattering can be demonstrated at home using a simple experiment to produce a pale Tyndall blue color. First, mix one or two drops of milk into a glass of water then place this glass in a dark room and focus a flashlight upon it, and the fluid will appear bluish. This bluish color results from blue light bouncing off milk particles suspended in the water while other, longer, light wavelengths pass through the fluid, unobstructed. Of course, milk has some larger diameter particles in it that reflect other wavelengths of light that slightly longer than blue, thereby contaminating the pure "Tyndall" blue color.

    Blue coloring in most bird species results from preferential scattering of blue light by the feather structure. When a blue feather is observed under a powerful microscope, the surface layer of keratin appears cloudy or milky due to the presence of small air cavities. A cross-section of the feather reveals an underlying layer of melanin granules and tiny air pockets in the middle of the feather barb. These small air cavities act like tiny particles because they selectively scatter blue light while the melanin granules absorb longer wavelengths of light, intensifying the blue. Structural differences are immediately obvious when a red feather, which derives its color from pigments, is viewed under the same microscope. The surface of the red feather is transparent and colorless while the underlying structures are filled with red pigment granules that reflect only red light.

    The differences between structural and pigment colors can be demonstrated using several simple experiments. Because blue color is entirely dependent upon the reflective structure of the feather, it turns dark when ground up into a powder. However, a red or yellow feather retain their original color when subjected to the same treatment because pigments are not damaged when the feather structure is ruined. Pigments can also be removed from the feather without damaging its structure. When a red or yellow feather is placed into an appropriate solvent, the pigment granules will dissolve into the solvent, leaving behind a colorless feather. Blue feathers can also lose their blue coloring when placed into a liquid with a particular optical density, such as balsam, that fills the air cavities in the feather structure, thereby preventing reflection of blue light. Thus, such a feather appears dark when it is wet, but its lovely blue color returns after it has dried.

    The physical phenomena that generate structural blue colors are similar, but not identical to, those that produce iridescent colors, such as those seen in purple martins and magpies. For example, iridescent feathers often appear to be very bright when compared to a structural blue feather viewed under the same light. Unlike iridescent feathers, blue feathers remain blue to the observer when the feather is rotated in relation to the light source whereas the coloring of iridescent feathers will vary and then become black as the angle of the light shifts. Similar to an iridescent feather, a structural blue feather will appear dark when it is placed directly between the light source and the observer because light cannot be reflected from the feather surface into the observer's eye.

    White also is also a structural feather color that relies upon the same principles described for blue feathers, except that white is produced when all wavelengths of light are reflected. A white feather also shows comparable structural characteristics. When a white feather is observed under a powerful microscope, the surface structure appears crystalline, resembling cut glass or snow, clearly capable of reflecting all visible light. White feathers also contain many air cavities in the feather barbs that increase the total reflection of all spectrums of visible light. As previously described, both melanin granules and air pockets are found in the middle of blue feathers; however, white feathers lack melanin but contain many more air cavities. This lack of underlying melanin granules can be easily demonstrated because a lustrous white feather becomes transparent when it is immersed in balsam.

    Touracos (Family: Musophagidae) are unique among birds because they alone produce their own green (and blue) pigments. However, all other birds make green feathers using a combination of both structural and pigment colors. Basically, the feather retains its blue-reflecting structures but embedded within its keratin structure are either yellow carotenoids (producing pure bright greens) or melanins (producing darker olive greens). Thus, it is possible to produce either blue or yellow birds from green parents, through the loss of either a yellow pigment or blue-reflecting feather structures -- a fact that has provided thousands of bird breeders with many decades of pleasure.

    Surprisingly, despite humanity's deep appreciation for colors, there remain many questions yet to be answered about colors in animals. For example, why do birds rarely produce blue pigments? Why do they instead rely upon structural changes within their plumage to provide the lovely blue color that so many humans associate with "the bluebird of happiness?"

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    Catching Dinner on the Fly ...The Night is Alive With the Sound of Echoes


    The evening was peaceful as the sun settled below the horizon. Suddenly, the orange and red sky was dotted with flying blue-grey silhouettes zigzagging above Lake Union. Bats! Some bats dipped low over the water's surface to drink in a manner similar to swallows, while others followed erratic courses above, consuming mosquitoes and other insects in flight.

    How do bats find and capture insects in darkness? All insect-eating bats produce sounds -- either with open mouths or through an elaborate nose-leaf that functions like a megaphone -- that are reflected as faint echoes from objects in the environment, providing bats an accurate picture of their environment and allowing them to maneuver in complete darkness.

    We didn't always know that bats rely on sound to move through dark surroundings. In the late 1800s, Swiss zoologist Charles Jurine's suggestion that bats could "see" using their ears was rejected as preposterous by most of his colleagues. However, in 1944, Donald Griffin, then an undergrad at Harvard University, used special microphones to show that bats generate ultrasonic sounds above the range of human hearing to create echoes that reveal the locations of objects. As a result, Griffin coined the term "echolocation" to describe this phenomenon.

    bats communicate using a variety of squeaks and squeals that human ears can hear, but bat species in the taxonomic suborder Microchiroptera emit high-frequency (high-pitched) sounds for echolocation. Even though low frequency sounds travel farther, only small ultrasonic sound waves used for echolocation can provide detailed information about tiny objects in the environment, such as flying mosquitoes.

    Echolocation sounds are not the same pitch for all bat species. High frequency echolocation calls produced by bats range from 20-200 kilohertz (kHz) or more (humans cannot hear sounds above 20kHz). There are differences in the pattern of echolocation calls, as well. Some species produce a constant frequency (CF) cry, while others use a frequency modulated (FM) call that descends in pitch. However, most bat species can choose to use either type of call.

    CF and FM sounds reveal different types of information to the bat. CF is used to detect objects while FM provides distance and other finely detailed data about the nature of the object. For example, by comparing the time elapsed between outgoing calls and returning echoes, bats accurately estimate distance to an object. Deviations in echo intensity and pitch reveal important details about the target, such as direction, size, shape and velocity. Most bat species produce a complicated sequence of CF and FM calls that they modify apparently depending upon differences in habitat, such as open areas versus dense vegetation.

    Because air absorbs energy contained in sound waves, the usefulness of high-pitched (short wave) sounds such as those produced by echolocating bats are limited to a range of 50 feet or less, making echolocationg bats nearsighted. To partially compensate for this energy loss and to increase their range, most bats produce high intensity sounds of up to 120 decibels, which is as loud as a smoke detector held four inches from your ear. These "shouting" bat species include the Little Brown Bat, Myotis lucifugus, and the Big Brown Bat, Eptesicus fuscus, which are common in Seattle neighborhoods.

    How do bats make such loud sounds without deafening themselves? Shortly before the bat's larynx muscles contract to produce an ultrasonic call, special muscles in the middle ear contract, separating the three inner ear bones (the malleus, incus and stapes or "hammer," "anvil" and "stirrup"), causing momentary deafness. After the call has been made, the middle ear muscles relax, restoring the bat's hearing in time to receive echoes from objects that are as close as one meter away.

    There still are many unanswered questions about the acoustic abilities of bats. However, research into echolocation is already yielding practical benefits for humans. For example, sonar is a primitive form of echolocation (from a bat's perspective!) that is widely used for navigation, tracking aircraft, ships, submarines and missiles, and for forecasting weather.

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    It's All in the Olfactory Pits: Going Home Makes Scents to a Salmon


    On a cool autumn afternoon, I stepped outside of my friend's house and witnessed a phenomenon of nature I have never seen before. In a stream flowing through the back yard, the bodies of spawning coho salmon, Oncorhynchus kisutch, shone blood-red in the bright sunlight. These fish battered themselves mercilessly against the stream bed, digging shallow nests in which to lay their eggs. Against all odds, they had survived the rigors of ocean life, returning to their birthplace to spawn.

    There are eight species of Salmonidae (salmon) that are native throughout many parts of the western United States, including the Seattle area. Salmon begin their lives in freshwater stream beds, where they stay from several months to as long as two years, depending upon the species. After they have reached about an inch in length, the young fish travel downstream to open ocean, where they remain for two to seven years, until they reach sexual maturity. Oceanic salmon live in large groups, or shoals, that wander throughout the northern Pacific Ocean and into the Bering Sea, as far as 1000 miles or more away from their birth streams. Yet, despite their wanderlust, reproductively mature salmon overcome enormous challenges to return to their natal streams to reproduce.

    How do salmon find their way back home to spawn? The cues used by salmon to find their way home from the ocean are not fully understood. But many scientists believe that a combination of geographic features, temperature, magnetic, celestial and chemical cues, hearing and other factors are involved.

    However, when migrating salmon make the transition from marine into fresh water, it appears that they rely primarily upon their sense of smell (olfaction) to locate their birth streams. This hypothesis was first tested in 1954, when Wisby and Halser, two Canadian scientists, captured migrating salmon and plugged their nostrils before releasing them downstream. Those salmon with plugged olfactory pits (a salmon's nose) took the wrong fork in the stream about half the time, which is to be expected if they were randomly choosing. Those fishes without plugged olfactory pits returned to the correct stream fork 100% of the time.

    Amazingly, salmon memorize and later recognize distinctive odors that characterize their particular spawning streams. But scientists still do not know exactly which molecules are used as olfactory cues by salmon. It is thought that these scents are probably a unique combination of rotting vegetation, insects, fish and dust released from local rocks and soils. However, there is some evidence that amino acids (basic building blocks of all proteins) dissolved in the water, may also play an important role in salmon olfaction.

    Salmon are very sensitive to odors, particularly their predators' smells. For example, author C. Herb Williams, in the November 1978 issue of Pacific Search , described a study in which a solution containing one part of human skin dissolved in 80 billion parts of water was dumped into a river. The scent from this solution was sufficient to stop migrating salmon for as long as half an hour. Further, experiments by Canadian scientists show that salmon will slow or stop their migrations when certain human smells are present in the water. Additionally, trout -- another salmonid -- show distinct flight responses when a fisherman washes his hands upstream.

    Even though it is poorly understood at present, olfaction plays a critical role in the life cycle of salmon. They travel thousands of miles during their lifetimes and yet they rely upon their sense of smell to locate their natal streams, passing by hundreds of suitable rivers occupied by other salmon populations on their way home. Their ability to make such fine distinctions is truly remarkable.

    Thanks to my colleague, Nat Scholz, a newly-minted Ph.D. from the Zoology Department at the UW and now a famous scientist at NOAA, for answering my questions at the last minute for this story.

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    Take a Peek at Nature's Website: Spiders Spin Steely Silken Splendor


    On foggy mornings, Charlotte's web was truly a thing of beauty. This morning each thin strand was decorated with dozens of tiny beads of water. The web glistened in the light and made a pattern of loveliness and mystery, like a delicate veil.-- E. B. White, Charlotte's Web

    Perhaps the highest achievement of spiders is the orb-web. Orb-weaving spiders (Family: Araneidae) are remarkable artists fabricating intricate webs from the finest silks. Late autumn and early spring is when most display their best work.

    Orb-weavers (and cob-web weavers) can produce up to six different types of silk from a different set of silk glands located in the spider's abdomen. Each variety of spider silk is somewhat different in protein composition and is used for distinct parts of the web or for different purposes. These special silks are drawn out of the appropriate silk gland as the weaver needs it. Spider silk has great tensile strength and elasticity; easily supporting the combined weight of spider and struggling prey, weighing thousands of times more than the web itself.

    The large geometric webs found at this season of the year in urban and suburban yards are creations of the introduced orb-weaver, Araneus diadematus. This species gained fame as the first spiders to leave our planet when Arabella and Anita demonstrated their weaving skills in the absence of a gravitational field aboard Skylab. Another common introduced species, the large brown Giant House Spider, Tegenaria gigantea, lives mainly in buildings. Mature males of this species, which have leg spans of 2-4 inches, are roaming through bathrooms and bedrooms in the early autumn seeking mates and inadvertently terrifying sleepy-eyed humans.

    Despite my fear of spiders, I think the small Jumping Spiders (Family: Salticidae) patrolling the library stacks are quite cute and interesting. According to Rod Crawford, Curator of Arachnids at the Burke Museum, they are unusual spiders because they are very visual and perceive the world in much the same way that humans do. They rely upon keen eyesight to find and stalk prey during daylight hours. Like many spiders, Jumping Spiders don't weave webs at all, although they do construct silken nighttime retreats and egg sacs. Jumping Spiders also use silk as a safety line by attaching it to the substrate prior to pouncing upon their prey.

    Spiders are highly beneficial to humans because they prey upon insects and small animals. Unlike most predacious insects such as Ladybirds, spiders are active year-round. Additionally, spiders are generalist predators. They don't require prey populations to reach peak numbers before controlling them, contrary to many predacious insects that often are picky eaters. Crawford says, "Spiders are THE dominant terrestrial predators; one year's worth of spider prey outweighs all land vertebrates on the planet. Without spiders, the world would be a vastly different place."

    Thanks to Rod Crawford from the University of Washington's Burke Museum for allowing me to interview him for this story.

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