Song Sparrow recordings

Inspired by Monday’s post about Margaret Morse Nice I looked up recordings of Song Sparrows in our collection. I found more than 1,600 recordings from 27 states in the USA and Canada. I was hoping to find recordings from Margaret Morse Nice’s former study area in her backyard, now Tuttle park, just north of the Lane Avenue bridge along the east side of the Olentangy river.

map of Recording locations on OSU main campus

Recording locations on OSU main campus

Instead I located a cluster of recordings in Franklin County: Don Borror, founder of our lab, recorded Song Sparrows on the OSU main campus in 1948 and 1953. [Note that these are among the earliest preserved sound recordings – the earliest existing recording in the USA is of a Song Sparrow recorded by Cornell Lab founder and pioneer in sound recording Arthur Allen in 1929.]

When we describe variation within and differences among songs, in addition to listening to recordings we often visualize sounds. We use sound analysis software to produce spectrograms that show the frequency of sound vibrations, which we perceive as pitch, over time. The darkness of the spectrogram indicates the loudness of the sound. See for yourself in this short video of one song of a Song Sparrow played in the software RAVEN, follow the moving bar while you listen – can you hear the difference among the notes?

 

Now listen to the variety of songs that Don Borror recorded on OSU campus and try to match them with the corresponding sonograms.   Tip: Hover your mouse over each of the spectrograms to reveal the number corresponding to the sound files below. This will help you to verify your match.

If you have enjoyed this sound matching game, I can recommend playing “Bird Song Hero“, a matching game set up by the Cornell Lab of Ornithology. You will not only perfect your skills in matching spectrograms to heard sound but will also learn the songs of some common garden birds. Enjoy!

 

About the Author: Angelika Nelson is the curator of the Borror Laboratory of Bioacoustics. Her recent research has focused on song and behavioral ecology of the White-crowned Sparrow in Oregon; each spring Angelika teaches the OSU course “Ohio Birds” where students learn about the life of birds and how to identify them in the field – by sight and sound.

 

Mites and moths

Following some earlier blogs about recently acquired collections I present to you here the Treat collection. This collection was assembled by Asher E. Treat a researcher at City University of New York and the American Museum of Natural History, also New York. This collection is one of the best in the world for mites associated with Lepidoptera (butterflies and moths). Mites have been found associated with most terrestrial and many aquatic organisms, but when it comes to insect hosts, mites on Coleoptera (beetles) and Hymenoptera (bees and wasps) are clearly the most numerous, diverse, and well-known. Still, Lepidoptera have a variety of associated mites.

The Acarology Collection acquired this collection 4 years ago, some years after Treat’s death. The collection consisted of about 37 slide boxes of exceptionally well labelled microscope slides and half a dozen insect drawers of pinned moths (all labelled as hosts of specific mite specimens). The Lepidoptera are being processed at the Triplehorn Insect collection, while we, the Acarology collection, have been working on processing (mostly databasing) the slides. This is proving to be a major job.

 

Image of a female of Dicrocheles phalaenodectes, the moth ear mite

Image of a female of Dicrocheles phalaenodectes, the moth ear mite

Treat got interested in mites associated with moths after finding mites in the ears of noctuid moths. In the process, he figured out the quite amazing life histories of some mites associated with these moths. The most famous is Dicrocheles phalaenodectes, the moth ear mite (family Laelapidae).

These mites break through the tympanic membrane of the ear of the moth and form small colonies inside the ear. By itself not too surprising, but the interesting part Treat discovered was that these mites are always found in one ear only, rarely if ever in both ears. In a way this makes sense. By breaking the tympanic membrane the mites make the moth deaf in that ear. Moths need their hearing to avoid predators (for example bats) so a deaf moth would be easy prey. However, a moth with one functional ear is still able to avoid bats, perhaps not as well as if it had two functional ears, but close enough. Which leaves the question: how do the mites manage to limit infestations to one ear?

Treat did many careful observations and follow-up experiments on this aspect and found that the mites have a very specific set of behaviors ensuring only one ear will be parasitized. The first female to get on a moth (nearly always a fertilized female, the immatures and males do not colonize) crawls to the dorsal part of the thorax, explores a little, after which she proceeds to one ear. Any future colonizers will first go to that same dorsal part of the thorax of the moth and follow the initial female to the same ear. It appears the mites lay a pheromone trail that guides newcomers to the already infested ear, and away from the uninfested one.

Drawing of relative positions of mites in a moth ear

Drawing of relative positions of mites in a moth ear

To complete the cycle, young females leaving the ear initially wander around the hosts body (mostly the thorax), congregating around the head at night. They leave the moth by running down its proboscis when it is feeding on flowers. On the flowers, the mites wait for their next host.
Another mite family that is specialized on Lepidoptera, the Otopheidomenidae, is also parasitic, and they will also show up near the ears, but they do not pierce the tympanic membrane, so they do not cause deafness. Unfortunately, we know much less about them, Treat was never able to study their behavior. A range of other mite families have representatives that are regularly found on Lepidoptera, but they are not specialists at the family level: Ameroseiidae, Melicharidae, Erythraeidae, Iolinidae, Cheyletidae, Acaridae, Carpoglyphidae, and Histiostomatidae. That list excludes the occasional “vagrants” that can be found on moths, but that are unlikely to be living on them for extended periods of time. All in all, quite a diverse community.
For those interested in knowing more, Treat wrote a book “Mites of Moths and Butterflies” (1975, Cornell University Press) that is a rare combination of good scholarship (especially natural history) and readability.

Title page of Treat's book on moth mites

Title page of Treat’s book on moth mites

Treat was very careful and noted things like host specimen numbers (if available), which allows current researchers to track down the exact moth from which a given mite came.

This is currently a common approach, but Treat started this in the 1950-ies. And there is more. Based on Treat’s label data we know not only the name of the hosts and the specific locality, but also gender of the host, whether the left or right ear was infested, and the exact part of the body the mites were found on. So we have excellent information, directly from the slides, showing that Proctolaelaps species (family Melicharidae) are nearly always found near the base of the palps [as an aside, Proctolaelaps is a bit of an unfortunate generic name, combining “procto-” = anus and “laelaps” = hurricane; presumably the name

Microscope slide from the Treat collection

Slide from the Treat collection

refers to a relatively large anal shield]. Such complete data are fantastic for future research, but they also mean a lot more work processing these slides, as every slide has lots of unique data. I want to thank George Keeney, part-time curator of the acarology collection and a series of volunteers, Ben Carey, Rachel Hitt, Mitchell Maynard, Ben Mooney, Jake Waltermyer, and Elijah Williams, for their hard work in accessioning this material.

 

About the Author: Dr. Hans Klompen is professor in the department of Evolution, Ecology and Organismal Biology and director of the Ohio State University Acarology Collection.

Images from Botany 2016

Now back from this week’s Botany 2016 meeting in Savannah, Georgia, I have some photos to share with you.  As I mentioned in the previous post, meetings like this provide us with a number of benefits — connecting with colleagues, seeing what others are doing in research, and just experiencing a new city.  I had not been to Savannah before and I enjoyed it.  The famous garden squares that the city is built around give it a unique feel.  The meeting was well-attended and had an especially large component of presentations about outreach from academic units to the broader public — something that we are trying to do with this blog.

 

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I could not resist stopping along the highway on the way down to photograph this rock face that had been dislodged by roots growing into a crevice and ultimately causing it to fall, illustrating the power of plants!

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Savannah is a port city, near the Atlantic Ocean and served by the Savannah River, meaning the the city sees a lot of large container ships; here is a view of part of the city from the convention center at which our meeting was held.

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These meetings are held at large convention centers these days, as opposed to college campuses, where we used to meet. It is convenient in that all of the presentations are closer together and there are large open spaces for meeting with colleagues, as shown here.

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Most of the formal exchange at a meeting like this consists of talks presented by the attendees; you can do a lot of sitting throughout the day.

 

 

 

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Posters are also a popular way of presenting your research results. Here, a former student in our program, Dr. Lisa Wallace, explains the status of the Mississippi herbarium databasing effort.

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Paul Blischak, one of our current EEOB students, explains some of his work during the poster session.

 

 

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Savannah is famous as the setting for John Berendt’s novel Midnight in the Garden of Good and Evil. Local cemeteries are not only historic and atmospheric, but also reveal plants growing wherever they can — here in a brick wall.

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The fact that the Palmetto (Sabal palmetto) is frequent and native in the area reminds us that we are approaching the subtropics and tropics, home to most palm diversity.

 

DSC00047blog1

Although not native to the US, the Crepe Myrtle (Lagerstroemia) is used widely in plantings in the south as a street tree and provides a lot of color.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 
 

 

 

 

 
 
 
 

About the Author: Dr. John Freudenstein is a Professor in the Department of Evolution, Ecology and Organismal Biology and Director of the OSU Herbarium.

Summer – time for fieldwork and meetings

For many university faculty who are associated with museum collections, summer is a very different time than the academic year.  Many of us do not have teaching and departmental responsibilities then and so we are able to get out to do fieldwork, focus more intensively on research projects, and attend meetings.

When I say meetings, what do I mean?  Most scientific societies hold meetings for their members periodically – many on an annual basis.  These meetings bring together researchers and educators to exchange ideas about their work.  We present talks and posters that summarize results of projects.  As a plant systematist, I usually attend the “Botany” meeting that is held this week in Savannah, GA.

Logo Botany Conference 2016The meeting is large enough (with over a thousand attendees) that there are many parallel sessions on different topics, so it is not possible for one person to attend all of the talks.  You just have to make a schedule and choose what you want to hear – and talk to your colleagues to find out about talks that you missed.

In addition to oral presentations with projected graphics, posters are a great way to communicate the results of your scientific work.  The nice thing about posters is that they are available for viewing for several days and you can take your time reading them (usually they are assembled in a large room or two).  In addition during “poster sessions” – dedicated times when there are no talks going on – individuals will be standing by their posters to speak with meeting attendees about their work.  Another nice thing about posters is that after the meeting they can be brought back to your institution and displayed there.

What about biological collections and their relevance to these meetings?  Biological collections come into play in several ways.  First, much of the work that is being presented at evolutionarily-ecologically focused meetings is based in some way on specimens, so they are important as the basis for the data.  Second, there are often sessions at these meetings that are focused on specimens and museum collections – including exchanging ideas about best practices in curation and organizing larger-scale initiatives for the community.  At this year’s Botany meeting, for example, I will attend a session for herbarium curators and for anyone who is involved with and interested in aspects of herbaria.  Perhaps not surprisingly, much of the discussion in recent years at those sessions has centered on specimen databasing initiatives and how we can better work together across the community.  Lastly, there are professional societies dedicated to the promotion, improvement and educational aspects of natural history collections, such as the Society for the Preservation of Natural History Collections and the Natural Science Collections Alliance.  These societies also have meetings for individuals who are curate and develop natural history collections.

Check this blog on Friday – I’ll post some photos from the Botany 2016 meeting in Savannah so that you can see some of what has gone on there.  If you can’t wait, you can follow the meeting on Twitter (#botany2016).

 

About the AuthorDr. John Freudenstein is a Professor in the Department of Evolution, Ecology and Organismal Biology and Director of the OSU Herbarium.

Vertebrates in Bits and Pieces: Space Conservation in Vertebrate Collections

Bird specimens that are part of the Tetrapod collection

Bird specimens that are part of the Tetrapod collection

When you picture a vertebrate collection, you probably think of a collection of taxidermied birds and mammals or jars of pickled fish. But when you actually visit the collection, you will find the typical research study skins, and pelts and – out of necessity- preserved parts of specimens such as jars with tongues, eyes, stomach contents, brains, boxes of horns, eggs, nests, wings etc. These are organized as sub-collections within a vertebrate collection and are known under varying names such as the osteological or oological collections. These “sub-collections” can be used as educational tools, in research projects, or in art classes. But when we salvage or collect a specimen, why don’t we keep the entire specimen? One may argue that a whole specimen would have higher value to a researcher than the bits and pieces found in these sub-collections.

 

Indeed it is useful to preserve the entire specimen but there are many constraints that vertebrate and other museum collections face that prevent us from keeping an intact specimen.

One big issue museums face is space. For vertebrate collections, though it would be lovely to

A walrus skin

A walrus as a whole specimen takes up a large space but when folded up it can fit in a cabinet. (S. Malinich, 2013)

have an entire whale or elephant in the collection, such a specimen would take up a large part of our collection area. If a museum has a whale in its collection it may only keep parts that researchers have requested in the past such as particular vertebrae, a manus, or a partial skull. A great example of this can be found in the AudioVision “Whale Warehouse”  video episode. Within the episode, Grant Slater and Mae Ryan, producers for Southern California public radio, explore the L. A. Natural History Museum’s over-sized specimen storage facility, a place where curators store parts of large aquatic mammal specimens. Not only are the specimen parts inside large but they take up an entire warehouse off grounds from the main facility!

Golden Eagles

Larger birds, such as these Golden Eagles, take up space where hundreds of smaller song birds could fit. (S. Malinich, 2013)

Here at the Museum of Biological Diversity, we do not face the challenge of storing whales, but smaller specimens in large numbers can soon turn into a space problem, too. Over 20 swan specimens, can take up the same cabinet that could be holding over a thousand smaller song birds. This puts constraints on how many specimens of a species we can accession per year and the maximum size of specimens that we can accept.

 

 

 

Another problem museum collections face is the condition of a specimen. Upon receiving specimens we conduct quality checks on varying aspects of the specimen.

Smelling a specimen before preparing it can save a lot of decision making it it smells rotten.

Smelling a specimen before preparing it can help make decisions if it smells rotten.

 

First, we conduct a sniff check: if the specimen smells rotten, it is past the point of return and we do not attempt to make it into a study skin, because it would continue to decay at a rapid pace.

 

 

A student prepares a specimen skin. While she prepares she looks it over for any reasons why it could not be made into a full study skin.

A student prepares a specimen skin. While she prepares it she checks it for any reasons why it could not be made into a full study skin.

Second, we do a visual look over on the outside of the specimen: We look for maggots, large wounds, as well as gangrenous flesh which would prevent us from turning the specimen into a whole study skin.

 

Third, we consider acceptance of certain specimens over the yearThough

Examining a large Great Horned Owl before making it into a parts specimen.

Examining a large Great Horned Owl before salvaging parts of this specimen.

it would be nice to make every specimen we receive into a study skin, we simply cannot  fit them all into cabinets. So only the specimens that are clean (or cleanable) and not losing feathers or fur will be preserved as full skins.

 

 

Sub-collections may arise because of a researcher’s fascination with a particular feature of a specimen, but they have become important parts of modern collections. Some sub-collections of the Tetrapod Collection are: skeletons, wings, feet, tails or samples of feathers. This way important research material is preserved, but instead of taking up a large portion of a cabinet these specimens can be filed just like documents into filing cabinets. This also makes sure that valuable records of species are kept even though a full skin could not be made because of how they were found when salvaged. These parts collections can still be valuable for research, for example, when scientists need DNA samples of a particular species. New molecular techniques allow extracting DNA from small tissue samples. To make up for the loss of a full skin, we take multiple images and measurements during processing to accompany the specimen in the collection.

A typical set up for preparing study skins.

A typical set up for preparing study skins.

Though it would be ideal for museum’s to preserve an entire specimen it may not be possible in the future as museum collections continue to grow. However as science progresses we are finding that even the smallests amounts of tissue samples of specimens can reveal much about a species. Entire collections of just tissue samples are being formed all around the world focusing on specific taxons or groups of species. In the future, as collections continue to grow it will become more beneficial to create more sub-collections with tissue samples to further the research value of museum collections.

 

About the author: Stephanie Malinich manages the tetrapods collection at the MBD.

Happy 4th of July!

I am currently traveling along the coast of Maine after teaching Field Ornithology and Hands-on Bird Science at the Hog island Audubon summer camp.

Don Borror, founder of the Borror Laboratory of Bioacoustics, used to teach at the same camps in the 1950s and ’60s. Like me, he recorded singing birds while identifying birds for campers. Sixty years ago to this day, on July 4th 1956, Don Borror took campers on a short boat ride to Eastern Egg Rock, one of the islands in the Muscongus Bay.

Boat ride from Hog Island to Eastern Egg Rock

Boat ride from Hog Island to Eastern Egg Rock

This island is now famous for its Atlantic Puffins that were brought back to this area by Steve Kress through Audubon Project Puffin (more about this on Friday’s post!).

Among gulls that breed on the island Don Borror discovered a little songbird, a male Savannah Sparrow, that had established a territory and was singing his heart out to attract a female.

Savannah Sparrow

Savannah Sparrow

 

 

 

 

 

 

 

Enjoy the day with listening to the song of the Savannah Sparrow with the soundscape of coastal Maine.

 

About the author: Angelika Nelson is curator of the Borror Laboratory of Bioacoustics and instructor for Hog island Audubon camps.

Plants included in the Calinger et al. study

Here are just of few of the species that were included in the Calinger et al. study of flowering time.

Cercis canadensis (Redbud), a tree in the bean family (Fabaceae).

Cercis canadensis (Redbud), a tree in the bean family (Fabaceae), flowers in spring.

Aesculus glabra (Ohio Buckeye; Sapindaceae), flowering in spring.

Aesculus glabra (Ohio Buckeye; Sapindaceae), flowering in spring.

 

 

 

 

 

 

 

 

Podophyllum

Podophyllum peltatum (Mayapple), flowering in spring.

Sabatia

Sabatia angularis (Rose Pink) flowers in summer. It is a member of the gentian family.

 

 

 

 

 

 

 

 

Cyp parvi

Cypripedium parviflorum (Yellow Lady’s Slipper) is an orchid that flowers in spring.

Cyp acaule

Cypripedium acaule (Pink Lady’s Slipper) also flowers in spring.

 

 

 

 

 

 

 

 

Hypo

Hypopitys americana (Pinesap) is a leafless member of the blueberry family that flowers in summer.

Monotropa

Monotropa uniflora is also leafless and a member of the blueberry family.

 

 

 

 

 

 

 

 

Calopogon

Calopogon tuberosus (Grass Pink) flowers in summer and is limited to bogs and wet sand.

Chimaphila maculata (Spotted Pipsissewa) is a small, almost herbaceous member of the blueberry family (Ericaceae). It flowers in summer.

 

 

 

 

 

 

 

 

 

Tipularia2

Tipularia discolor (Cranefly Orchid) has leaves that are present during the winter and flowers in late summer.

Tipularia1

The flowers of the Cranefly Orchid are unusual in that they are asymmetric — the petal on the left side of the flower is shifted downward.

 

 

 

 

 

 

 

 

 

Corallorhiza

Corallorhiza maculata (Spotted Coralroot) is a leafless orchid that flowers in late summer.

Acer

Acer saccharum (Sugar Maple) flowers in spring, but is well-known for its autumn foliage colors.

 

 

 

 

 

 

 

 

About the AuthorDr. John Freudenstein is a Professor in the Department of Evolution, Ecology and Organismal Biology and Director of the OSU Herbarium.  All phots by the author except those of Corallorhiza and Tipularia, which were taken by Erich DeLin.

Science from specimens

We frequently talk about the nature of our collections, the techniques that we use to preserve specimens, and sometimes about the living organisms that they represent. This time I would like to comment on what we can DO with the specimens. We are preserving them for the information that they contain, so let’s look at an example of how we can use that information.

A key point about museum collections is that, if done correctly, they preserve the organism with data about where and when it was collected. That spatial and temporal information is valuable and is why individual specimens are truly irreplaceable – you cannot go back in time to recollect something.

Climate change is a big topic in the news these days and because it is about change – something different in one time from another – museum specimens can be relevant to studying it. If in fact the climate is warming in a particular area, one expectation is that the growing season may lengthen – it might start a little earlier in spring and end a little later in autumn. If we could compare when plants begin flowering in spring, for example, we might find that for various species they flower somewhat earlier on average in the climate has warmed.

Calinger titleA study performed by one of the graduate students in our department was designed to investigate this. Kellen Calinger used herbarium specimens from our collection from across Ohio. She targeted plants at the peak of bloom, which meant that she needed to be careful that she was comparing plants in the same state of flowering (not just opening and not getting past), which she was easily able to do by examining each sheet. She restricted her sampling to a fairly narrow area to prevent the confounding effects of north-south variation in seasons. She analyzed 141 species collected over 115 years, including those flowering in spring, early and late summer. She also considered whether the species were herbaceous or woody, annual or perennial, wind or insect pollinated, and whether they were native or introduced.

Calinger graph

A graph from the Calinger et al. paper showing the gradual upward trend in temperatures over the past century.

What did she find? First, she found that there was considerable variation among the species with respect to how they responded to warming temperature. Sixty-six species (46%) showed significant advancement of flowering time with increasing temperature, while only two species (1%) showed a delay in flowering time. The remainder did not show a statistically significant change. Overall, flowering advanced 3.4 days per every degree (F) of warming for those 46% of species that were most sensitive, it was 5.2 days per degree. Spring flowering species were more responsive than those that flower in early or mid-summer, suggesting that there is a “buffering effect” as you move into the growing season. Wind-pollinated species (such as oaks) were more strongly affected than insect pollinated species, and introduced species were markedly more affected than native species. Annuals were more affected than perennials.

Phacelia_purshii

Phacelia purshii with a visiting bee. Photo by John Andersland.

How much of an effect is this? For Phacelia purshii (common name: Miami Mist) in northeastern Ohio, where the temperature effect seems strongest, it is flowering now two weeks earlier than it did a century ago. Many species in the study showed this pattern. One of the most troubling findings was the fact that introduced species seem to be very responsive to warming, suggesting that invasives may become an increasing problem.

Enough of the bad news – my point here was to emphasize what we can learn from museum collections that we could not otherwise know. Without the documentation of the presence of species at particular places and times, we would have no way to perform this kind of analysis. It’s just one example of what we can learn from our collections.

 

About the AuthorDr. John Freudenstein is a Professor in the Department of Evolution, Ecology and Organismal Biology and Director of the OSU Herbarium. 

Different songs for different places

In my last post I talked about how Carolina Chickadee songs have changed (or not) in Columbus and the surrounding areas over the past ~60 years. This post takes a different perspective on how Carolina Chickadee songs can vary: over geographic space. If you were paying close attention in the last post, you may have gotten a sense of geographic variation in song even on a scale as small as Columbus – some songs only appeared in certain areas during certain time periods.

One major component of my dissertation here at OSU has been to quantify how Carolina chickadee songs vary over their entire range, the southeastern United States, and compare this variation to geographic variation in their sister species, the Black-capped Chickadee. Despite Carolina Chickadees being very common birds, not many recordings of their songs were archived in museum collections for me to use. The Borror Lab had the most recordings, but the vast majority of those were made in Ohio.

So in spring of 2014 I embarked on an expedition to record as many Carolina Chickadees in as many different places as possible. Over 5 and a half weeks (divided into three trips), I drove about 6,000 miles through 22 states and recorded over 120 chickadees.

Sample locations during recording trip in 2014

Sample locations during recording trip in 2014

Below are samples of some of the atypical songs that I recorded on my trip. The full Carolina chickadee range is shaded in orange. All the spectrograms shown are on the same scale, so you can directly compare them to one another (the upper limit of each spectrogram image is about 10 kHz). Not included are songs or spectrograms of the typical alternating high-low-high-low Carolina chickadee song, which was also present at most sample locations.

  1. Newark, Delaware

CACH-DE

 

 

 

 

2. Kensington, Maryland

CACH-MD

 

 

 

 

3. Asheboro, North Carolina

CACH-NC

 

 

 

 

 

4. Cartersville, Georgia

CACH-GA

 

 

 

 

5. Camden, Alabama

CACH-AL

 

 

 

 

6. Ajax, Louisiana

CACH-LA

 

 

 

 

7. Meridian, Texas

CACH-TX

 

 

 

 

8. Moyers, Oklahoma

CACH-OK

 

 

 

 

9. Crossville, Tennessee

CACH-TN

 

 

 

10. Salem, Missouri

CACH-MO

 

 

 

 

11. Makanda, Illinois

CACH-IL

 

 

 

 

12. Mammoth Cave, Kentucky

CACH-KY

 

 

 

 

 

About the author:  Stephanie Wright Nelson is a graduate student in the department of EEOBiology. She studies song learning in chickadees and is particularly interested in the consequences of hybridization between Carolina and Black-capped Chickadees.

Time travels with the Borror Lab of Bioacoustics

Carolina Chickadee by Dan Pancamo

Carolina Chickadee by Dan Pancamo

One thing that is unique about the sound archive of the Borror Laboratory of Bioacoustics is that it not only contains a wide diversity of animal sounds, but a great number of recordings for certain species. When I started my Ph.D. research here at OSU, I was pleasantly surprised to find that this depth of recordings also included one of my study species, the Carolina Chickadee (Poecile carolinensis).

The namesake of the Borror Laboratory of Bioacoustics (BLB), Dr. Donald J. Borror, was one of the first biologists to take recording equipment out into the field to record animal sounds. And he started in and around Columbus. Because Carolina Chickadees are rather common birds here in the central and southern portions of Ohio, Carolina Chickadees were some of the first animals Dr. Borror recorded. The oldest recording he archived in the collection dates back to 1948. Listen to a 30-second excerpt of Dr. Borror’s recording of a typical four-note whistled Carolina Chickadee song from April 1948 (note: You can listen to the entire recording (BLB21) on the BLB’s website):

You may not think that having all these chickadee recordings across a long time period is super duper exciting, but I do. See, I study chickadee song. And we know that chickadees, like other songbirds, learn their song: young chickadees must hear other individuals of their species singing and imitate those sounds in order to produce normal adult song. However, like learning in humans, song learning in birds is not always a perfect process. As young birds make imperfect copies of the songs of the adult birds they hear, variation is introduced into the songs of a population of birds. Think about how the English language has changed in the past 100 years – some words have stopped being used, new ones have come into fashion – this is analogous to what happens with song in bird populations.

The end result is that not every chickadee sings exactly the same song and the acoustic traits of chickadee songs can change slightly from generation to generation. Using the BLB collection I can actually look at how Carolina Chickadee song has changed in the Columbus area over the past 65+ years.

What you are going to see below are a series of maps with representative spectrograms of chickadee songs from all over Columbus for different decade ranges. If you have never seen a spectrogram before, it is essentially a visual representation of sound, with time on the x-axis, frequency (or pitch) on the y-axis, and the darker color representing more energy (or the loudness) of the sound. Here is the spectrogram of one song of a Carolina Chickadee from the 1948 recording by Don Borror above:

Spectrogram of one song of a Carolina Chickadee recorded by Don Borror in Columbus OH in 1948

For each map below I encourage you to visually compare the different chickadee songs using the spectrograms (I have left the axes off for simplicity’s sake) and then listen to the recording containing those songs using the links below each map. Any overlapping spectrograms are from the same individual bird: Carolina Chickadees can sing up to 4 different song types each, although most only sing one or two types. If you want to listen to the original recording archived in the BLB, please click on the link for each BLB cut number.

map11950s

As you can see, Carolina Chickadees usually have a four-note song of alternating high and low whistled notes, but check out the weird song at Blacklick Woods Metro Park (#3)! Dr. Borror’s 1948 recording is actually quite unique in that the notes in the chickadee’s song are not very different in pitch from one another; usually Carolina Chickadee songs sound and look more like the spectrograms seen in examples 1 and 4b.

 

#1 (BLB1354)

#2 (BLB2451)

#3 (BLB3909)

#4 (BLB3947)

 

1960s

map2The unique song type seen before persists at Blacklick Woods Metro Park through the 1960s. Also note that some Carolina Chickadee songs start with a note much lower in pitch than others (like song number 1 here, or song 4a in the 1950s map). Carolina Chickadees also sometimes add notes onto the end of their songs, resulting in five-, six-, and sometimes up to twelve-note songs, although they usually keep the alternating high-low pattern (see #4).

 

#1 (BLB6374)

#2 (BLB9942)

#3 (BLB5112)

#4 (BLB9026)

#5 (BLB7966)

 

map31970s

Many of the songs in this decade are very similar, but one individual at Blendon Woods Metro Park (#2b) showed an interesting song with an additional introductory note. This song type is not seen in any other bird in any other decade, so it is possible this song type was never sung by any bird but this one.

 

#1 (BLB11032)

#2 (BLB14217)

#3 (BLB13312)

#4 (BLB11030)

1980s

map4As you can see, not much song variation was recorded in the 1980s, except for that three-note song up in Delware. While most of the songs follow the typical high-low-high-low pattern, there are subtle differences between individuals, like in the downward sweep of the first note.

 

 

#1 (BLB17075)

#2 (BLB17078)

Note the Black-capped Chickadee singing in the background of recording #2:

#3 (BLB15737)

#4 (BLB17063)

 

map51990s

In Delaware a three-note song type persists in the population from the 1980s into the 1990s. Also, the song type that starts with a lower-pitched note continues to pop up in various areas of northern Columbus (e.g. 3b), but is not seen in the southern portions of the city. Interestingly, I had not heard that song type myself while living in Columbus until moving to Clintonville this past March; up near Dublin that song type is not common anymore.

 

#1 (BLB17435)

#2a (BLB17433)

#2b

#3 (BLB21124)

In the past 14 years none of the recordings in the BLB collection specifically target Carolina chickadee songs. It would be interesting to know if those strange songs from Blacklick Woods Metro Park are still sung in that area, or if any other unique song types have appeared in the Columbus area.

So, as you travel throughout the Columbus area, keep an ear out for some odd chickadee songs … you may even hear something that has not been recorded before.

About the author: Stephanie Wright Nelson is a graduate student in the department of EEOBiology. She studies song learning in chickadees and is particularly interested in the consequences of hybridization between Carolina and Black-capped Chickadees.