We Are Family

By Alexa Kownacki, Ph.D. Student, OSU Department of Fisheries and Wildlife, Geospatial Ecology of Marine Megafauna Lab

The GEMM Lab celebrating Leigh’s birthday with homemade baked goods and discussions about science.

A lab is a family. I know there is the common saying about how you cannot choose your family and you can only choose your friends. But, I’d beg to differ. In the case of graduate school, especially in departments similar to OSU’s Fisheries and Wildlife, your lab is your chosen family. These are the people who encourage you when you’ve hit a roadblock, who push you when you need extra motivation, who will laugh with you when you’ve reached the point of hysteria after hours of data analysis, who will feed you when you’re too busy to buy groceries, and who will always be there for you. That sure sounds a lot like a family to me.

GEMM Lab members at the Society for Marine Mammalogy 2017 Conference in Halifax, Nova Scotia at the masquerade ball. Photo source: Florence Sullivan

Many of us spend weeks—if not months—conducting field research for our various projects. None of us do this work from the main campus…seeing as the main campus for Oregon State University is located Corvallis, Oregon which is approximately 50 miles inland from the Pacific Ocean. The GEMM Lab isn’t actually based on the main campus; instead, you’ll find the lab at the Hatfield Marine Science Center in Newport, Oregon, within a two-minute stroll of the picturesque Yaquina Bay. However, many of the core classes we need are only offered on main campus. This results in the GEMM Lab members being spread across Corvallis, Newport, and the dominant fieldwork site for their project (which could be locally in Oregon, or in the waters off of New Zealand). So rather than your typical, weekly, hour-long lab meetings, the GEMM Lab meetings are monthly and last on the order of 3-5 hours. Others hear this and think that must be overwhelming to have such a long lab meeting. On the contrary, these are scheduled to fit into all of our chaotic schedules. One day a month, all of us gather together as a family unit, share what’s new about our lives, be sounding boards for each other, solve problems, and do so in a supportive environment. Hopefully you’re getting the picture that just because we’re all part of the same lab, it doesn’t mean we’re geographically close. This is exactly why we cultivate meaningful relationships while we are together. The Harvard Business Review published an article 2015 based on multiple peer-reviewed journals, summarizing the six dominant characteristics necessary to foster a positive workplace:

  1. Caring for colleagues as friends
  2. Supporting each other
  3. Avoiding blame and forgiving mistakes
  4. Inspiring each other at work
  5. Emphasizing the meaningfulness of the work
  6. Treating each other with respect

And I can attest that every member within the GEMM Lab embraces all of these characteristics and I have a feeling that none of them have read that article prior to today. Family naturally follows those basic guidelines. And, our lab, is a family.

My very first GEMM Family Dinner.

Case and Point: when I was applying for graduate programs, I made a point of traveling to meet the GEMM Lab members at the monthly lab meeting. Sure, I also wanted to make sure that both Newport and Corvallis would be good fits in terms of locations. But, mostly, I needed to see if this Lab would be a strong family unit for my graduate school career and beyond. The moment I arrived at Hatfield Marine Science Center in Newport, it was clear, this was a family that I could see myself being a part of. Not only had all the members brought some kind of food item to share at the lab meeting (this was important to me), but Florence had baked homemade bread, Dawn had offered to show me around Hatfield, and Leila had set up a time to take me around main campus with other grad students. During the lab meeting discussions, I was welcomed to contribute and I felt comfortable doing so. That was another big moment where something “clicked” and I knew I had found a great group of amazing scientists who were also amazing human beings.

GEMM Lab members at the Port Orford Field Station in August 2017.

Flash forward a few months, and now I am one of those lab members who is bringing food to lab meetings. More than that, we have GEMM Lab dinners and game nights. I may be based in Corvallis, but I commute out to Newport just for these fun activities because this is my family. I want to be with them—not only when we’re talking about our research—but when we’re laughing about the silly things that happen in our daily lives, comically screaming at each other in an effort to win whatever game is on the table, and enjoying home-cooked meals. This is my family.

GEMM Lab members helping some friends at South Coast Tours build a dirt-bag house in August 2017.

I guess I’d like to plug this message to any potential graduate student regardless of discipline(s): find a lab with people that you truly want to surround yourselves with—day and night—in good times and in bad times—because undoubtedly, you’ll need those kinds of people. And, to current lab constituents in any lab: it’s up to us to create a supportive family which will make everyone successful.

Sister Sledge knew just this when the group sang this verse of their hit, “We Are Family”:

Living life is fun and we’ve just begun
To get our share of this world’s delights
High, high hopes we have for the future
And our goal’s in sight
We, no we don’t get depressed
Here’s what we call our golden rule
Have faith in you and the things you do
You won’t go wrong, oh-no
This is our family Jewel

I’m grateful to have found a lab that embodies the lyrics of one of my favorite childhood karaoke songs. The GEMM Lab is not only a lab that produces cutting-edge science; it is a family that encourages one another in all facets of life—creating an environment where people can have high-quality lives and generate high-quality science.

GEMM Lab Family Dinner complete with the board game, Evolution, and homemade pizza. October 2017.

Hearing is believing

Dr. Leigh Torres, Geospatial Ecology of Marine Megafauna Lab, Marine Mammal Institute, Oregon State University

Dr. Holger Klinck, Bioacoustics Research Program, Cornell Lab of Ornithology, Cornell University

For too long the oil and gas industry has polluted the ocean with seismic airgun noise with little consequence. The industry uses seismic airguns in order to find their next lucrative reserve under the seafloor, and because their operations are out of sight and the noise is underwater many have not noticed this deafening (literally1) noise. As terrestrial and vision-dependent animals, we humans have a hard time appreciating the importance of sound in the marine environment. Most of the ocean is a dark place, where vision does not work well, so many animals are dependent on sound to survive. Especially marine mammals like whales and dolphins.

But, hearing is believing, so let’s have a listen to a recording of seismic airguns firing in the South Taranaki Bight (STB) of New Zealand, a known blue whale feeding area. This is a short audio clip of a seismic airgun firing every ~8 seconds (a typical pattern). Before you hit play, close your eyes and imagine you are a blue whale living in this environment.

Now, put that clip on loop and play it for three months straight. Yes, three months. This consistent, repetitive boom is what whales living in a region of oil and gas exploration hear, as seismic surveys often last 1-4 months.

So, how loud is that, really? Your computer or phone speaker is probably not good enough to convey the power of that sound (unless you have a good bass or sub-woofer hooked up). Industrial seismic airgun arrays are among the loudest man-made sources2 and the noise emitted by these arrays can travel thousands of kilometers3. Noise from a single seismic airgun survey can blanket an area of over 300,000 km2, raising local background noise levels 100-fold4.

Now, oil and gas representatives frequently defend their seismic airgun activities with two arguments, both of which are false. You can hear both these arguments made recently in this interview by a representative of the oil and gas industry in New Zealand defending a proposal to conduct a 3 month-long seismic survey in the STB while blue whales will be feeding there.

First, the oil and gas industry claim that whales and dolphins can just leave the area if they choose. But this is their home, where they live, where they feed and breed. These habitats are not just anywhere. Blue whales come to the STB to feed, to sustain their bodies and reproductive capacity. This habitat is special and is not available anywhere else nearby, so if a whale leaves the STB because of noise disturbance it may starve. Similarly, oil and gas representatives have falsely claimed that because whales stay in the area during seismic airgun activity this indicates they are not being disturbed. If you had the choice of starving or listening to seismic booming you might also choose the latter, but this does not mean you are not disturbed (or annoyed and stressed). Let’s think about this another way: imagine someone operating a nail gun for three months in your kitchen and you have nowhere else to eat. You would stay to feed yourself, but your stress level would elevate, health deteriorate, and potentially have hearing damage. During your next home renovation project you should be happy you have restaurants as alternative eateries. Whales don’t.

Second, the oil and gas industry have claimed that the frequency of seismic airguns is out of the hearing range of most whales and dolphins. This statement is just wrong. Let’s look at the spectrogram of the above played seismic airgun audio clip recorded in the STB. A spectrogram is a visual representation of sound (to help us vision-dependent animals interpret sound). Time is on the horizontal axis, frequency (pitch) is on the vertical axis, and the different colors on the image indicate the intensity of sound (loudness) with bright colors illustrating areas of higher noise. Easily seen is that as the seismic airgun blasts every ~8 seconds, there is elevated noise intensity across all frequencies (bright yellow, orange and green bands). This noise intensity is especially high in the 10 – 80 Hz frequency range, which is exactly where many large baleen whales – like the blue whale – hear and communicate.

A spectrogram of the above played seismic airgun audio clip recorded in the South Taranaki Bight, New Zealand. Airgun pulses every ~8 seconds are evident by elevated noise intensity across all frequencies (bright yellow, orange and green bands), which are especially intense in the 10 – 80 Hz frequency range.

In the big, dark ocean, whales use sound to communicate, find food, and navigate. So, let’s try to imagine what it’s like for a whale trying to communicate in an environment with seismic airgun activity. First, let’s listen to a New Zealand blue whale call (vocalization) recorded in the STB. [This audio clip is played at 10X the original speed so that it is more audible to the human hearing frequency range. You can see the real time scale in the top plot.]

Now, let’s look at a spectrogram of seismic airgun pulses and a blue whale call happening at the same time. The seismic airgun blasts are still evident every ~8 seconds, and the blue whale call is also evident at about the 25 Hz frequency (within the pink box). Because blue whales call at such a low frequency humans cannot hear their call when played at normal speed, so you will only hear the airgun pulses if you hit play. But you can see in the spectrogram that five airgun blasts overlapped with the blue whale call.

No doubt this blue whale heard the repetitive seismic airgun blasts, and vocalized in the same frequency range at the same time. Yet, the blue whale’s call was partially drowned out by the intense seismic airgun blasts. Did any other whale hear it? Could this whale hear other whales? Did it get the message across? Maybe, but probably not very well.

Some oil and gas representatives point toward their adherence to seismic survey guidelines and use of marine mammal observers to reduce their impacts on marine life. In New Zealand these guidelines only stop airgun blasting when animals are within 1000 m of the vessel (1.5 km if a calf is present), yet seismic airgun blasts are so intense that the noise travels much farther. So, while these guidelines may be a start, they only prevent hearing damage to whales and dolphins by stopping airguns from blasting right on top of animals.

So, what does this mean for whales and other marine animals living in habitat where seismic airguns are operating? It means their lives are disturbed and dramatically altered. Multiple scientific studies have shown that whales change behavior5, distribution6, and vocalization patterns7 when seismic airguns are active. Other marine life like squid8, spiny lobster9, scallops10, and plankton11 also suffer when exposed to airgun noise. The evidence has mounted. There is no longer a scientific debate: seismic airguns are harmful to marine animals and ecosystems.

What we are just starting to study and understand is the long-term and population level effects of seismic airguns on whales and other marine life. How do short term behavioral changes, movement to different areas, and different calling patterns impact an individual’s ability to survive or a population’s ability to persist? These are the important questions that need to be addressed now.

Seismic airgun surveys to find new oil and gas reserves are so pervasive in our global oceans, that airgun blasts are now heard year round in the equatorial Atlantic3, 12. As reserves shrink on land, the industry expands their search in our oceans, causing severe and persistent consequences to whales, dolphins and other marine life. The oil and gas industry must take ownership of the impacts of their seismic airgun activities. It’s imperative that political, management, scientific, and public pressure force a more complete assessment of each proposed seismic airgun survey, with an honest evaluation of the tradeoff between economic benefits and costs to marine life.

Here are a few ways we can reduce the impact of seismic airguns on marine life and ecosystems:

  • Restrict seismic airgun operation in and near sensitive environmental areas, such as marine mammal feeding and breeding areas.
  • Prohibit redundant seismic surveys in the same area. If one group has already surveyed an area, that data should be shared with other groups, perhaps after an embargo period.
  • Cap the number and duration of seismic surveys allowed each year by region.
  • Promote the use of renewable energy sources.
  • Develop new and quieter survey methods.

Even though we cannot hear the relentless booming, this does not mean it’s not happening and harming animals. Please listen one more time to 1 minute of what whales hear for months during seismic airgun operations.

 

More information on seismic airgun surveys and their impact on marine life:

Boom, Baby, Boom: The Environmental Impacts of Seismic Surveys

A Review of the Impacts of Seismic Airgun Surveys on Marine Life

Sonic Sea: Emmy award winning film about ocean noise pollution and its impact on marine mammals.

Atlantic seismic will impact marine mammals and fisheries

 

References:

  1. Gordon, J., et al., A review of the effects of seismic surveys on marine mammals. Marine Technology Society Journal, 2003. 37(4): p. 16-34.
  2. National Research Council (NRC), Ocean Noise and Marine Mammals. 2003, National Academy Press: Washington. p. 204.
  3. Nieukirk, S.L., et al., Sounds from airguns and fin whales recorded in the mid-Atlantic Ocean, 1999–2009. The Journal of the Acoustical Society of America, 2012. 131(2): p. 1102-1112.
  4. Weilgart, L., A review of the impacts of seismic airgun surveys on marine life. 2013, Submitted to the CBD Expert Workshop on Underwater Noise and its Impacts on Marine and Coastal Biodiversity 25-27 February 2014: London, UK. .
  5. Miller, P.J., et al., Using at-sea experiments to study the effects of airguns on the foraging behavior of sperm whales in the Gulf of Mexico. Deep Sea Research Part I: Oceanographic Research Papers, 2009. 56(7): p. 1168-1181.
  6. Castellote, M., C.W. Clark, and M.O. Lammers, Acoustic and behavioural changes by fin whales (Balaenoptera physalus) in response to shipping and airgun noise. Biological Conservation, 2012. 147(1): p. 115-122.
  7. Di lorio, L. and C.W. Clark, Exposure to seismic survey alters blue whale acoustic communication. Biology Letters, 2010. 6(1): p. 51-54.
  8. Fewtrell, J. and R. McCauley, Impact of air gun noise on the behaviour of marine fish and squid. Marine pollution bulletin, 2012. 64(5): p. 984-993.
  9. Fitzgibbon, Q.P., et al., The impact of seismic air gun exposure on the haemolymph physiology and nutritional condition of spiny lobster, Jasus edwardsii. Marine Pollution Bulletin, 2017.
  10. Day, R.D., et al., Exposure to seismic air gun signals causes physiological harm and alters behavior in the scallop Pecten fumatus. Proceedings of the National Academy of Sciences, 2017. 114(40): p. E8537-E8546.
  11. McCauley, R.D., et al., Widely used marine seismic survey air gun operations negatively impact zooplankton. Nature Ecology & Evolution, 2017. 1(7): p. s41559-017-0195.
  12. Haver, S.M., et al., The not-so-silent world: Measuring Arctic, Equatorial, and Antarctic soundscapes in the Atlantic Ocean. Deep Sea Research Part I: Oceanographic Research Papers, 2017. 122: p. 95-104.

 

 

 

Finding the hot spot: incorporating thermal imagery into our whale research

By Leila Lemos and Leigh Torres

A couple weeks ago the GEMM Lab trialed something new in our gray whale research: the addition of a thermal imaging camera to our drone.

For those who do not know what a thermal imaging camera is, it is a device that uses infrared radiation to form an object, and operates in wavelengths as long as 14,000 nm (14 µm). A thermal camera uses a similar procedure as a normal camera, but responds to infrared radiation rather than visible light. It is also known as an infrared or thermographic camera.

All objects with a temperature above absolute zero emit infrared radiation, and thermography makes it possible to see with or without visible light. The amount of radiation emitted by an object intensifies with temperature, thus thermography allows for perception of temperature variations. Humans and other warm-blooded animals are easily detectable via infrared radiation, during the day or the night.

Infrared radiation was first discovered in 1800, by the astronomer Frederick William Herschel. He discovered infrared light by using a prism and a thermometer (Fig.1). He called it the infrared spectrum “dark heat”, which falls between the visible and microwave bands on the electromagnetic spectrum (Hitch 2016).

Figure 1: Astronomer Frederick William Herschel discovers infrared light by using a prism and a thermometer.
Source: NASA, 2012.

 

Around 30 years later it was possible to detect a person using infrared radiation within ten meters distance, and around 50 years later it was possible to detect radiation from a cow at 400 meters distance, as technology became gradually more sensitive (Langley, 1880).

Thermography nowadays is applied in research and development in a variety of different fields in industry (Vollmer and Möllmann 2017). Thermal imaging is currently applied in many applications, such as night vision, predictive maintenance, reducing energy costs of processes and buildings, building and roof inspection, moisture detection in walls and roofs, energy auditing, refrigerant leaks and detection of gas, law enforcement and anti-terrorism, medicinal and veterinary thermal imaging, astronomy, chemical imaging, pollution effluent detection, archaeology, paranormal investigation, and meteorology.

Some of the most interesting examples of its application are:

  • Detection of the presence of icebergs, increasing safety for navigators.
  • Detection of bombs
  • Non-invasive detection of breast cancer (Fig.2)
  • Detection of fire, and detection of fire victims in smoke-filled rooms or hidden under plywood, by the fire departments (Fig.3)
Figure 2: Thermography approved in 1982 to detect breast cancer. Method is able to detect 95% of early stages cancers.
Source: Hitch, 2016.

 

Figure 3: The use of thermal imaging cameras by the fire departments.
Source: MASC, 2017.

 

In environmental research, the thermal imaging camera is an interesting tool used to detect wildlife presence (especially for nocturnal species), to monitor wildlife and detect disease (Fig.4), and to better understand thermal patterns in animals (Fig.5), among others.

Figure 4: Wildlife monitoring: detection of mange infection in wolves of Yellowstone National Park. During winter, wolves infected with mange can suffer a substantial amount of heat loss compared to those without the disease, according to a study by the U.S. Geological Survey and its partners.
Source: Wildlife Research News 2012; USGS 2016.

 

Figure 5: Study on thermal patterns and thermoregulation abilities of emperor penguins in Antarctica.
Source: BBC 2013.

 

Now that thermal cameras are small enough for attachment to drones, we are eager to monitor whales with this device to potentially identify injuries and infections. This non-invasive method could contribute another aspect to our on-going blue and gray whale health assessment work. However, dealing with new technology is never easy and we are working to optimize settings to collect the data needed. Our test flights with the thermal camera were successful – we captured images and retrieved the expensive camera (always a good thing!) – but the whale images were less clear than desired. The camera was able to detect thermal variation between our research vessel and the ocean (Fig. 6: boat and people are displayed as hot coloration (yellow, orange and red tones), while the ocean exhibited a cold coloration (purple). Yet, the camera’s ability to differentiate thermal content of the whale while surfacing from the ocean was less evident (Fig. 7). We believe this problem is due to automatic gain control settings by the camera that essentially continually shifts the baseline temperature in the image so that thermal contrast between the whale and ocean was not very strong, except for those hot blow holes shinning like devil eyes (Fig. 7). We are working to adjust these gain settings so that our next trial will be more successful, and next time we will see our whales in all their colorful thermal glory.

Figure 6: Thermal image of the R/V Ruby captured by a thermal camera flown on a drone by the GEMM Lab on September 09th, 2017.
Source: GEMMLab 2017.
Figure 7. Thermal image of a gray whale captured by a thermal camera flown on a drone by the GEMM Lab on September 09th, 2017. Notice the ‘hot’ color (yellow-orange) of the blow holes indicating the heat within the whale’s body. (Image captured under NOAA/NMFS permit #16111).

 

References

BBC. 2013. In pictures: Emperor penguins’ ‘cold coat’ discovered. Available at: http://www.bbc.co.uk/nature/21669963

Hitch J. 2016. A Brief History of Thermal Cameras. Available at: http://www.newequipment.com/technology-innovations/brief-history-thermal-cameras /gallery?slide=1

Langley SP. 1880. The bolometer. Vallegheny Observatory, The Society Gregory, New York, NY, USA.

MASC. 2017. Thermal Imaging Camera. Available at: https://duckduckgo.com/ ?q=detection+of+victim+fire+department+thermal+camera&atb=v76-7_u&iax=1&ia= images&iai=http%3A%2F%2Fwww.masc.sc%2FSiteCollectionImages%2Fuptown%2F Super_Red_Hot.jpg

NASA. 2012. Beyond the Visible Light. Available at: https://www.nasa.gov/topics/ technology/features/webb-beyond-vis.html

USGS. 2016. Study Shows Cold and Windy Nights Physically Drain Mangy Wolves. Available at: https://www.usgs.gov/news/study-shows-cold-and-windy-nights-physically-drain-mangy-wolves

Vollmer M. and Möllmann KP. 2018. Infrared Thermal Imaging: Fundamentals, research and Applications. Second Edition. Wiley-VCH: Weinheim, Germany.

Wildlife Research News, 2012. Tool: Infrared Monitoring. Available at: https://wildliferesearchnews.wordpress.com/2012/04/24/tool-infrared-monitoring/

Diving Deeper

By Taylor Mock, GEMM Lab intern

Greetings, all!

My name is Taylor Mock. Since February I have been volunteering in the GEMM Lab and am ecstatic to make my online debut as part of the team!

For many years, I had a shallow relationship with Hatfield Marine Science Center. As a Newport native, I would spend mornings and evenings glancing over at the Hatfield buildings while driving over the bridge to and from school. I was always intrigued. Sure, I would hear snippets of research from my peers about what projects their parents were involved in, but the inner workings of the complex mystified me.

Toward the end of my Freshman year in 2012 at Westmont College in Santa Barbara, California, my mom asked me what my summer plans were. I replied with the typical “I don’t know… Get a job?” She insisted that instead of a job I think about getting an internship; experience that will last more than a summer. I inquired through a family friend (because every person in this little community is woven together some way or another) if any internships or volunteer opportunities were available at Hatfield. She pointed me in the direction of the Environmental Protection Agency and thus began my Hatfield volunteering saga. I worked that summer, and the next, at the EPA under the direction of Ted DeWitt and Jody Stecher on denitrification studies in estuarine marshes. That summer provided me a glorious front row seat to field research and a greater understanding of my potential as a person and as a scientist. Now, this experience was marvelous, but I knew shortly after starting that my heart was elsewhere.

It was during my study abroad semester in Belize as part of my internship at the Toledo Institute for Development and Environment (TIDE) that I realized I wanted to work with marine macroorganisms. At TIDE, I engaged in radio telemetry conservation efforts tracking Hicatee (Dermatemys mawii) aquatic turtles. We would spend days on a small boat floating through canals and setting nets in hopes of capturing individuals of this small population to outfit them with radio tracking devices. These would be later used to track foraging, mating, and travel patterns in the region. It was an amazing time, to say the least. I remember waking up on my 21st birthday from my camping hammock and staring up at the lush rainforest above my head with a warm breeze across my face, followed by spending the day in the presence of these glorious creatures. It was heaven. I returned to Westmont the following term and took a Marine Mammal Eco-Physiology course and absolutely fell in love with Cetacea. Yes, I had always been captivated by this clade of beings (and truthfully when I was eight years old had a book on “How to Become a Marine Mammal Trainer”), but this was deeper. Of course, pinnipeds and otters and polar bears and manatees were enjoyable to learn about. There was something about the Cetacea though and how they migrated up and down the coast (just like me!) that I really connected with. My time learning about these animals created an intimate understanding of another group of species that developed into a rich, indescribable empathetic connection. I had to take a couple years away from scholastics and away from biology for health and wellness reasons. One day, though, a couple years after graduating and returning to Newport I rekindled with Jody from the EPA. He asked me if I would like to volunteer under Leigh Torres in the Marine Mammal Institute at HMSC. I do not think I could have possibly said no. I have been enjoying my time in the GEMM Lab ever since!

Though I am available to help anyone with any task they need, the work I do mostly centers around photogrammetry.

Using photogrammetry skills to measure gray whales in the GEMM Lab.

Photogrammetry, essentially, means geo-spatially measuring objects using photographs. What that looks like for me is taking an aerial photograph (extracted from overhead drone video footage) of a whale, running the image through a computer program called “Matlab”, taking a series of measurements from the whale (e.g., tip of the mandible to the notch of the fluke, distance between each tip of the fluke, and several measurements across the midsection of the whale). Several images of individuals are processed in order to find an average set of measurements for each whale.

Final result of the photogrammetry method on a gray whale

You might be wondering, “How can one measure the distance accurately from just a photograph?” I am glad you asked! The drones are outfitted with a barometer to measure the atmospheric pressure and, in turn, altitude. The changing altitudes are recorded in a separate program that is run simultaneously with the video footage. Thus, we have the altitudinal measurements for every millisecond of the drone’s flight. To monitor the accuracy and functionality of the barometer, calibrations are completed upon deployment and retrieval of each drone flight. To calibrate: the initial takeoff height is measured, a board of known length is thrown into the water, the drone will then rise or lower slowly above the board between 10 and 40 m, photographs of the board are then taken from varying altitudes, and are processed in Matlab.

During my time in the GEMM Lab, I have had the pleasure of completing photogrammetry assignments for both Leila on the Oregon Coast gray whale and for Dawn on the New Zealand blue whale projects. These ladies, and the other members of the GEMM Lab, have been so patient and gracious in educating me on the workings of Matlab and the video processing systems. It is a distinct honor working with them and to delight in the astounding nature of these creatures together. Each day I am struck in sheer awe of how beautiful and powerful these whales truly are. Their graceful presence and movement through the water rivals even the most skillful dancer.

Over the last 6 years, I am delighted to say that my relationship with Hatfield has become much deeper. The people and the experiences I have encountered during my time here, especially in the GEMM Lab, have been nothing short of incredible. I am sincerely grateful for this continued opportunity. It fills my soul with joy to engage in work that contributes to the well being of the ocean and its inhabitants.

Thank you, Leigh and all of the GEMM Lab members. I hope to continue volunteering with you for as long as you will have me.

Where are the eggs? Studying red-legged kittiwakes in a time of change

By Rachael Orben, Research Associate, Department of Fisheries and Wildlife, Oregon State University

In late May, I returned to St. George Island, Alaska to study the foraging ecology of red-legged kittiwakes using a mix of high-tech biologging tags, physiology measurements, and observations.  The study was designed to identify differences in behavior and physiology between birds that reproduce successfully and birds that don’t and then to see how this might carry over to the winter season (and vice versa).  Things didn’t go as planned.

A red-legged kittiwake on St. George Island. Photo C. Kroeger

This was my fourth spring on the island, and like prior seasons we arrived in late May, when birds should be building nests. However, unlike previous seasons, red-legged kittiwake’s didn’t look like they had done much nest building. I was accompanied by Abram Fleishman, a superstar MS student from San Jose State who is studying the winter spatial ecology of red-legged kittiwakes in relationship to mercury concentration in their feathers.

We immediately set about recapturing birds that had carried geolocation data loggers over the winter. We wanted to catch as many as possible before eggs were laid, so that their blood samples would represent the pre-lay period. The weather was wonderful, so it wasn’t until three weeks after we arrived that we had our first day-off. It was at about this time that I finally lost my optimism and realized the majority of red-legged kittiwakes were not going to lay eggs. By late June kittiwakes are usually incubating eggs. We only saw a handful of eggs and very few of these were being incubated. Most birds didn’t even build nests, or if they did, the nest was dismantled by other birds when the nest building pair didn’t stick around to guard their pile of mud and moss.

Nests in 2016. Laying success was also low in 2016, but even if birds didn’t lay many pairs built nests.
Same cliff (and birds) without nests in 2017.

When I designed the study, I thought collecting enough data to answer my questions about successful versus failed breeders would be hard, since failed breeders would be challenging to work with and red-legged kittiwakes typically have high breeding success, meaning that sample sizes of failed breeders would be small. Instead our three seasons occurred with progressively worse breeding success and we will now have to shift the focus of our analysis to see if we can find differences between birds that laid eggs and birds that didn’t, if we have the sample sizes! With ~80% laying success in the 9 years preceding the beginning of our study in 2015, this is something I would never have expected! The egg laying failure of 2017 is unprecedented in the productivity monitoring time series collected by the Alaska Maritime Wildlife Refuge.

Seabirds are often touted as indicator species of marine health (Cairns 1988, Piatt et al 2007), and while there are always caveats and additional questions to be answered, seabirds are reliant on the ocean for food and observing their behavior and condition tells us something about how easy (or hard) it is for them to find food.

So, what do I think the red-legged kittiwakes told us this year? I think they were squawking loud and clear, that they were not able to find myctophid fishes within their foraging range to the south and west of the Pribilofs. Myctophids are small fatty mesopelagic bioluminescent fish that come to the surface at night where red-legged kittiwakes catch them.

Besides just observing the laying failure, we were able to GPS track a few birds, collect a few diet samples, catch birds for blood and feather samples, and resight banded individuals. It is these pieces of information that I will be analyzing in the coming months to try to understand why some individuals were able to lay eggs during our study years, while most were not.  These years should also help us understand what capacity red-legged kittiwakes have to cope (or not) with changes in prey availability. However, after three years, I still don’t know what a ‘good’ year looks like for red-legged kittiwakes. Fingers crossed next season is finally a decent year for this sentinel seabird of the pelagic Bering Sea.

Pre-lay foraging trips of red-legged kittiwakes in 2015.
Pre-lay foraging trips of red-legged kittiwake in 2017. Two birds were heading north when their GPS loggers stopped recording.

You can read more about our red-legged kittiwake research in a series of blog posts written for the Seabird Youth Network, a partnership between the Pribilof School District, the Aleut Community of St. Paul Island, the City of St. Paul, Tanadgusix Corporation, the St. George Traditional Council, St. George Island Institute, the Alaska Maritime National Wildlife Refuge, and the wider scientific community. The network creates opportunities for youth to learn about seabirds with the aim of building local capacity for the collection of long-term seabird monitoring data on the Pribilof Islands.

New and old methods in our gray whale field season 2017

By Leila Lemos, Ph.D. Student, Department of Fisheries and Wildlife, OSU

On June 6th the GEMM Lab officially started the second year of fieldwork of our “Noise Physiology” Project with gray whales along the Oregon coast. To date, we have spent 14 days at sea (12 around the Newport area and 2 in Port Orford, our control area), with a total of 32:31 hrs of effort. In 29 whale sightings of approximately 40 whales we have been able to collect 6 fecal samples for hormonal analysis, to fly the drone 17 times over the whales, to deploy a GoPro 6 times for qualitative prey analysis, and to deploy a light trap 2 times for quantitative prey analysis. While this sounds good, we have only just begun, with our field season extending into October. The graph below displays the sightings and data collection by area.

Figure 1: Sightings and data collection by area and month.

We have added a couple new components to our project this year. First, we are now using a “the light trap”, as mentioned above, to capture zooplankton prey of gray whales. The light trap (Figure 2), designed by our collaborator of Kim Bernard (OSU, College of Earth, Ocean, and Atmospheric Sciences). The light trap is composed of a water jug with a cut-out cone entrance where prey might enter the jug after being attracted by the chem lights we put in the jug. The jug is weighted down to maintain position, but swivels off the drop line by its own floats; and it’s all connected to a surface float.

Figure 2: Components of the light trap.
Source: Leila Lemos

The light trap is left overnight and recovered in the next day. Trapped prey are sieved (Figure 4), stored in properly labeled jars or Ziploc bags, and kept frozen until analysis (Figure 5 and 6) including species identification, community analysis, and caloric content.

Figure 3: Todd Chandler, our research technician, preparing the light trap to be deployed in Port Orford.
Source: Leila Lemos
Figure 4: Collected preys with our light trap being sieved for storage on June 27th.
Source: Dawn Barlow
Figure 5: Kim Bernard proud of the zooplankton sample collected in Newport on June 26th.
Source: Dawn Barlow
Figure 6: Our GEMM Lab intern Alyssa holds the prey sample collected in July 1st.
Source: Leigh Torres

The second component we have added this year is the fixed-location hydrophone (Figure 7) to record acoustic noise data over the entire summer season. Last year we used a temporarily deployed “drifting hydrophone” that only recorded noise data punctually. Because of the fixed hydrophone, this year we will be able to compare our hormone data with a wider range of acoustic data, and improve our analyses.

Figure 7: Joe Haxel, our acoustician, checking the hydrophone in July 14th that was previously deployed in Newport at the beginning of the summer season.
Source: Leila Lemos

We also made our first trip down to Port Orford, our control area, to intensively collect data over only two days (July 5th and 6th). Since Port Orford is a smaller city with reduced vessel traffic, we want to evaluate if whales observed in this area show a reduced stress response when compared to the whales that inhabit the area around Newport and Depoe Bay, where vessel traffic is higher. However, we were not able to collect any fecal sample during this trip to Port Orford, so more trips south to come!

Figure 8: Sharon Nieukirk, our acoustician, Leigh Torres, and Todd Chandler checking on RV Ruby before being lifted into the water at the port of Port Orford on July 5th.
Source: Leila Lemos
Figure 9: Our mascots Pepper and Avery didn’t get to go out in the boat with us, but they enjoyed our trip to Port Orford so much that they couldn’t stay awake on the way back to Newport.
Source: Leila Lemos and Leigh Torres

The other components we used last year such as photo identification (Figure 10), fecal samples (Figures 11 and 12), drones, and GoPros are still being put to use this year. If you want to know more about our Noise Physiology project, check here.

Figure 10: Me in our boat platform waiting for whales to appear to photograph them in July 13th.
Source: Joe Haxel
Figure 11: Joe Haxel collecting a fecal sample in Newport in July 13th.
Source: Leila Lemos
Figure 12: Fecal sample collected in Newport on July 13th.
Source: Leila Lemos

We are progressively spotting more gray whales along the Oregon coast and we will continue our field efforts and data collection until October. So, for now enjoy some photos taken during the last couple of months. Until next time!

Figure 13: Gray whale’s fluke just south of the Yaquina Lighthouse, in Newport, on July 13th.
Source: Leila Lemos
Figure 14: Gray whale breaching just north of the Yaquina Lighthouse, in Newport, on July 9th.
Source: Leila Lemos
Figure 15: Gray whale breaching in Newport, on June 6th.
Source: Leigh Torres

Life in the lab: notes from a lab meeting

By Florence Sullivan, MSc, Oregon State University

One of my favorite parts about working as a member of the GEMM lab is our monthly lab meeting. It’s a chance for everyone to share exciting news or updates about their research, discuss recent advances in our field, and of course, make the schedule for who is in charge of writing the blog each week!  Our fearless leader, Leigh, usually also has an exercise for us to complete. These have varied from writing and editing abstracts for conferences, conducting mock interviews of each other, reading and discussing relevant papers, R coding exercises, and other useful skills. Our most recent meeting featured an exciting announcement, as well as a really interesting discussion of the latest International Whaling Commission (IWC) reports of the scientific committee (SC) that I felt might be interesting to share with our readers.

First, the good news – Six GEMM lab members submitted abstracts to the 2017 Society of Marine Mammalogy Conference, and all six were accepted for either a speed talk or an oral presentation! We are very proud and excited to present our research and support each other at the conference in October.

And now, a little science history:

The IWC was originally formed as a management body, to regulate the global catch of great whales. However, it never had much legal power to enforce its edicts, and was largely ineffective in its task.  By 1986 whale populations had been decimated to such low numbers by commercial whaling efforts that a worldwide moratorium on harvest was imposed. The SC of the IWC meets on an annual basis, and is made up of leading experts in the field who give advice and recommendations to the commission.  If you are interested in seeing reports from over the years, follow this link to the IWC Archive.  The reports presented by the various sub committees of the Scientific Committee are dense, packed full of interesting information, but also contain lots of procedural minutiae.  Therefore, for this lab meeting, each of us took one of the 2017 Annexes, and summarized it for the group.

Alyssa and Dawn reviewed Annex J: Report of the working group on non-deliberate human induced mortality of cetaceans.  The report shared new data about scarring rates of bowhead whales in the Bering Sea, notably, that 2.4% of the population will acquire a new scar each year, and that by the time an individual is 25 years old, it has a 40% chance of being scarred from a human derived interaction. The study noted that advances in drone technology may be an effective tool to assess scarring rates in whale populations, but emphasized that it is important to examine stranded carcasses to ground truth the rates we are able to capture from aerial and boat based photography.  The discussion then turned to the section about ship strikes, where we learned that in a comparison of fresh scars on humpback whales, and rates of voluntarily reported ship strikes, collisions were vastly under reported. Here it was noted that injuries that did not cause visible trauma could still be lethal to cetaceans, and that even moderate speed collisions can cause non-immediate lethal injury.

Leila walked us through Annex K: Report of the standing working group on environmental concerns. This subcommittee was the first one formed by the SC, and their report touched on issues such as bioaccumulation of heavy metals in whales, global oil spill emergency response training, harmful algal blooms (HABs), marine debris, diseases of concern, strandings and related mortality, noise, climate change, loss of arctic sea ice, and models of cetacean reaction to these impacts.

A few notes of particular interest:

-PCBs and other toxins are known to accumulate in killer whales, but this report discussed high levels of lead and cadmium in gray whales, leading to the question of what might be the source – sediment deposits? Fish?

-Lots of research has been done on the outfall of HABs involving domoic acid; now there is a need for research on other types of HABs

-A website has been created to increase surveillance, diagnosis and risk management of cetacean diseases, and is currently being refined: https://cdoc.iwc.int

-Changing climate is prompting distribution shifts in a number of species, putting animals at risk of interactions with shipping lanes, and increasing contact with invasive species.

-Models of cetacean bioenergetics have found that being entangled has energy costs equivalent to migration or pregnancy. Another model found that naval noise increased the metabolic rate of individuals by 30%. Models are becoming more and more accurate and complex every year, and each new one helps provide a framework to begin to assess cumulative impacts of human-cetacean interactions.

To wrap things up, I gave a brief overview of Annex N: Report of the subcommittee on whalewatching. This report gave quick updates on a number of different whale watching research projects around the world:

-Humpback whales in Hawaii change their swim speed and dive time when they encounter vessels.

-Endangered humpbacks in the Arabian Sea may need management intervention because there have been minimal advances in standards and attitudes by whale watching outfits or recreational boaters in Oman.

-Increased interactions and close encounters may be eroding the protective social barriers between bottlenose dolphins and the public.  The committee emphasizes that cetacean habituation to humans is a serious conservation cause of concern.

After research updates, the document then details a review from the working group on swim-with-whale operations. They emphasize the need for a global database, and note that the Convention on Migratory Species and the World Cetacean Alliance are both conducting reviews of this section of the whale watching industry and that a collaboration could be beneficial. Finally, this committee often gives feedback to ongoing projects and local management efforts, but is not convinced that their recommendations are being put into practice.

As one reads this litany of issues that face cetaceans in the modern world, it can be quite disheartening. However, reports like these keep researchers up to date on the current state of knowledge, areas of concern, and questions that need answering.  They help us set our priorities and determine which piece of the puzzle we are capable of tackling.  For more on some of the projects that our lab has under taken to help tackle these issues, check out Leila’s work on stress in gray whales, Dawn’s work looking at blue whales in New Zealand, Solene’s work on humpback habitat selection, or my work on vessel interactions. Individually, it’s easy to feel small, but when you look through the archives of the IWC, and realize how far we’ve come from extractive management to active conservation, you realize that every little project adds to those before it, and together, we can make a difference.

 

 

 

Migrating to higher latitudes

By Leila Lemos, Ph.D. Student, Department of Fisheries and Wildlife, OSU

On September 10th of 2015 I was catching an airplane to start a whole new phase of my life in Oregon, United States. Many thoughts, many doubts, many fears, many expectations, and one big dream that was about to come true: I was finally going to United States to work with whales.

I am from Rio de Janeiro, Brazil, a big city known for pretty beaches, tropical weather and restless nights. Thus, to arrive in a really small city on the countryside that usually rains for about six months a year was the opposite of what I was always used to. Trying to understand another language and culture differences was also not an easy step.

In addition, taking my first classes was a big challenge. It was hard to understand everything that was being said, but recording and listening to the classes afterwards definitely was what helped me the most. Also, my first meetings and discussions where I needed to explain my thoughts in another language was difficult, but when I look back and I can now see how much I have improved and it is gratifying to know that all of my efforts were worth it.

Feeling welcome was essential to start overcoming all of the difficulties. My advisor Leigh and my lab mates (Florence, Amanda, Rachael, Erin, Dawn and Courtney) always created a friendly atmosphere and I started being more confident over time. I also had amazing and understanding teachers who were patient and helped me along the way. My first roommates Jane and Angie, from US, and the students and teachers from Crossroads (an English group that I attend) made me practice English every day and I started feeling more comfortable about speaking (and also thinking) in English, and they became my “Oregon family” together with new friends I made from different nationalities. Also important were my family and friends back in Brazil that never stopped encouraging and supporting me.

Figure 1: GEMM-Lab, from left to right, starting at the top: Leigh Torres, me, Erin, Amanda, Dawn, Rachael, our interns from 2016 season (Catherine, Cat and Kelli), and Florence.

 

Figure 2: Practicing English at Crossroads.

 

The weather and seasons here are also very different from Brazil. We don’t have cold weather or snow, and we don’t see all of the changes that happen here from season to season. The first season I saw was the fall. Seeing all of the fall colors in the trees for the first time was magical and I can already say that fall is my favorite season here. The winter was a bit cruel for me, not because of the cold or eventually the snow, but because of the rain. There is a saying in my city that “people from Rio de Janeiro do not like gray days” and it is true: my mood changes with weather. However, I did travel a bit around Oregon during winter and got to enjoy the snow, and how fun is to slide in the snow, make snow angels and throw snowballs. The spring starts bringing sunny days after cold months and endless rain. Also all of the flowers around the Corvallis campus are so pretty and colorful. Finally the summer is hot, and in some days it can almost be as hot as Rio de Janeiro. However, I spend summer days in the coast, where the temperature is mild. For me, summer days are synonymous with fieldwork, since gray whales are migrating northbound and becoming resident along the Oregon coast to feed, and this is right when the fun begins!

Figure 3: Different seasons in Oregon: (A) Trees during the fall in Corvallis, (B) Winter in Crater Lake, (C) Spring at OSU campus: my office at Hovland Building, and (D) fieldwork in Port Orford during the summer.

 

I finally saw my first gray whale in July of 2016 and got to dive into all of the methodologies we wanted to apply in this project. I learned how to photograph whales for photo-identification, how to take important notes, how to collect fecal samples for hormonal analysis, and how to fly with a drone for the photogrammetry method.

Figure 4: Learning how to fly with a drone over gray whales.
Source: Florence Sullivan

 

I had to digest a lot of information while trying to equilibrate in the boat and to not get seasick. However, it was so pleasurable to see how my field skills were getting better over time and how close I was to the Pacific marine fauna.

During my master’s degree I worked on toxicology in dolphins, which means working with dead carcasses. I remember telling myself all of the time that I wanted to do something different for my PhD – that I would be involved in a project with live animals. I am very glad I could accomplish that goal. Gray whales, sea lions, seals and a variety of marine birds are just some examples of the great diversity the Pacific Ocean has to offer and I am totally amazed.

Figure 5: Great diversity of the Oregon coast. Source: GEMMLab (Leila Lemos, Leigh Torres and Florence Sullivan)

After months of fieldwork it was time to return to the land and start learning how to work with all of the data we collected. We have amazing collaborators working with us and I have had wonderful opportunities to learn from all of them about the different methods we are applying in our project.

Figure 6: Learning the hormonal analysis technique at the Seattle Aquarium.

 

Thus, after one year and a half in Oregon I can already say that I feel home. The experience as an international student is not easy, but that’s what makes it such a valuable and gratifying experience. It has been a great journey, and I hope to continue to see improvements over time and keep learning throughout this amazing project studying gray whales.

 

How Unmanned Aircraft Systems (UAS, aka “drones”) are being applied in conservation research

By Leila Lemos, Ph.D. Student, Department of Fisheries and Wildlife, OSU

 

Unmanned Aircraft Systems (UAS), also known as “drones”, have been increasingly used in many diverse areas. Concerning field research, the use of drones has brought about reduced errors, increased safety and survey efforts, among other benefits, as described in a previous blog post of mine.

Several study groups around the world have been applying this new technology to a great variety of research applications, aiding in the conservation of certain areas and their respective fauna and flora. Examples of these studies include forest monitoring and tree cover analyses, .

Using drones for forest monitoring and tree cover analyses allows for many applications, such as biodiversity and tree height monitoring, forest classification and inventory, and plant disease and detection. The Ugalla Primate Project, for example, performed an interesting study on tree coverage mapping in western Tanzania (Figure 1).

Figure 1: Tree coverage analyses in Tanzania.
Source: Conservation Drones, 2016.

 

The access to this data (not possible before from the ground) and the acquired knowledge on tree density and structure were important to better understand how wild primates exploit a mosaic landscape. Here is a video about this project:

 

Forest restoration activities can also be monitored by drones. Rainforests around the world have been depleted through deforestation, partly to open up space for agriculture. To meet conservation goals, large areas are being restored to rainforests today (Elsevier 2015). It is important to monitor the success of the forest regeneration and to ensure that the inspected area is being replenished with the right vegetation. Since inspection events can be costly, labor intensive and time consuming, drones can facilitate these procedures, making the monitoring process more feasible.

Zahawi et al. (2015) conducted an interesting study in Costa Rica, being able to keep up with the success of the forest regeneration. They were also able to spot many fruit-eating birds important for forest regeneration (eg. mountain thrush, black guan and sooty-capped bush tanager). Researchers concluded that the automation of the process lead to equally accurate results.

Drones can also be used to inspect areas for illegal logging and habitat destruction. Conservationists have struggled to identify illegal activities, and the use of drones can accelerate the identification process of these activities and help to monitor their spread and ensure that they do not intersect with protected areas.

The Amazon Basin Conservation Association Los Amigos conservancy concession (LACC) has been monitoring 145,000 hectars of the local conservation area. Illegal gold mining and logging activities were identified (Figure 2) and drones have aided in tracking the spread of these activities and the progress of reforestation efforts.

Figure 2: Identification of illegal activities in the Amazon Basin.
Source: NPR, 2015.

 

Another remarkable project was held in Mexico, in one of the most important sites for monarch butterflies in the country: the Monarch Butterfly Biosphere Reserve. Around 10 hectars of vital trees were cut down in the reserve during 2013-2015, and a great decrease of the monarch population was perceived. The reserve did not allow researchers to enter in the area for inspection due to safety concerns. Therefore, drones were used and were able to reveal the illegal logging activity (Figure 3).

Figure 3: Identification of illegal logging at the Monarch Butterfly Biosphere Reserve, Mexico.
Source: Take Part, 2016.

 

Regarding the use of drones for mapping vulnerable areas, this new technology can be used to map potential exposed areas to avoid catastrophes. Concerning responses to fires or other natural disasters, drones can fly immediately, while planes and helicopters require a certain time. The drone material also allows for operating successfully under challenging conditions such as rain, snow and high temperatures, as in the case of fires. Data can be assessed in real time, with no need to have firefighters or other personnel at a dangerous location anymore. Drones can now fulfill this role. Examples of drone applications in this regard are the detection, monitoring and support for catastrophes such as landslides, tsunamis, ship collisions, volcanic eruptions, nuclear accidents, fire scenes, flooding, storms and hurricanes, and rescue of people and wildlife at risk. In addition, the use of a thermal image camera can better assist in rescue operations.

Researchers from the Universidad Politécnica de Madrid (UPM) are developing a system to detect forest fires by using a color index (Cruz et al. 2016). This index is based on vegetation classification techniques that have been adapted to detect different tonalities for flames and smoke (Figure 4). This new technique would result in more cost-effective outcomes than conventional systems (eg. helicopters, satellites) and in reaching inaccessible locations.

Figure 4: Fire detection with Forest Fire Detection Index (FFDI) in different scenes.
Source: UPM, 2016.

 

Marine debris detection by drones is another great functionality. The right localization and the extent of the problem can be detected through drone footage, and action plans for clean-ups can be developed.

A research conducted by the Duke University Marine Lab has been detecting marine debris on beaches around the world. They indicate that marine debris impacts water quality, and harms wildlife (eg. whales, sea birds, seals and sea turtles) that might confuse floating plastic with food. You can read a bit more about their research and its importance for conservation ends here.

Drones are also being extensively used for wildlife monitoring. Through drone footage, researchers around the world have been able to detect and map wildlife and habitat use, estimate densities and evaluate population status, detect rare behaviors, combat poaching, among others. One of the main benefits of using a drone instead of using helicopters or airplanes, or having researchers in the area, is the lower disturbance it may cause on wildlife.

A research team from Monash University is using drones for seabird monitoring in remote islands in northwestern Australia (Figure 5). After some tests, researchers were able to detect which altitude (~75 meters) the drone would not cause any disturbances to the birds. Results achieved by projects like this should be used in the future for approaching the species safely.

Figure 5: Photograph taken by a drone of a crested tern colony on a remote island in Australia.
Source: Conservation Drones, 2014.

 

Drones are also being used to combat elephant and rhino poaching in Africa. They are being implemented to predict, trace, track and catch suspects of poaching. The aim is to reduce the number of animals being killed for the detusking and dehorning practices and the illegal trade. You can read more about this theme here. The drone application on combating one of these illegal practices is also shown here in this video.

As if the innovation of this device alone was not enough, drones are also being used to load other tools. A good example is the collection of whale breath samples by attaching Petri dishes or sterile sponges in the basal part of the drones.

The collection of lung samples allows many health-monitoring applications, such as the analysis of virus and bacteria loads, DNA, hormones, and the detection of environmental toxins in their organisms. This non-invasive physiological tool, known as “Snotbot”, allows sampling collection without approaching closely the individuals and with minimal or no disturbance of the animals. The following video better describes about this amazing project:

It is inspiring to look at all of these wonderful applications of drones in conservation research. Our GEMM Lab team is already applying this great tool in the field and is hoping to support the conservation of wildlife.

 

 

References

Conservation Drones. 2014. Conservation Drones for Seabird Monitoring. Available at: https://conservationdrones.org/2014/05/05/conservation-drones-for-seabird-monitoring/

Conservation Drones. 2016. Tree cover analyses in Tanzania in collaboration with Envirodrone. Available at: https://conservationdrones.org/2016/09/17/tree-cover-analyses-in-tanzania-in-collaboration-with-envirodrone/

Cruz H, Eckert M, Meneses J and Martínez JF. 2016. Efficient Forest Fire Detection Index for Application in Unmanned Aerial Systems (UASs). Sensors 16(893):1-16.

Elsevier. 2015. Drones Could Make Forest Conservation Monitoring Significantly Cheaper: new study published in the Biological Conservation wins Elsevier’s Atlas award for September 2015. Available at: https://www.elsevier.com/about/press-releases/research-and-journals/drones-could-make-forest-conservation-monitoring significantly-cheaper

NPR. 2015. Eyes In The Sky: Foam Drones Keep Watch On Rain Forest Trees. Available at: http://www.npr.org/sections/goatsandsoda/2015/05/19/398765759/eyes-in-the-sky-styrofoam-drones-keep-watch-on-rainforest-trees

Take Part. 2016. Drones Uncover Illegal Logging in Critical Monarch Butterfly Reserve. Available at: http://www.takepart.com/article/2016/06/22/drones-uncover-illegal-logging-monarch-butterfly-habitat

UPM. 2016. New automatic forest fire detection system by using surveillance drones. Available at: http://www.upm.es/internacional/UPM/UPM_Channel/News/dc52fff26abf7510VgnVCM10000009c7648aRCRD

Zahawi RA, Dandois JP, Holl KD, Nadwodny D, Reid JL and Ellis EC. 2015. Using lightweight unmanned aerial vehicles to monitor tropical forest recovery. Biological Conservation 186:287–295.

 

Beyond the Rock: Using Satellite Trackers to Study the Lives of Common Murres

By Stephanie Loredo, Seabird Oceanography Lab, OSU

Photo credit: Seabird Oceanography Lab

Common murres (Uria aalgee) are the most abundant seabird on the Oregon Coast. At least half of the population in the California Current Ecosystem breeds on the Oregon Coast (half a million seabirds). This makes them ecologically important consumers of forage fish, especially during the breeding season when they use state-waters.

While they spend most of their time at sea, murres must come to shore to breed. During this time, they are highly visible by humans as they breed in large masses on rocky islands. While they are not the most agile on land, due to their short and stubby legs, they are actually amazing divers. Their short flipper-like wings help them swim, and they typically reach depths of 30-60m to catch their prey.

Aside from their underwater aviation skills, they make great parents as well. Both parents will incubate and care for their chick – murres only lay one egg a year – until they fledge; once they leave the rock, male murres take full responsibility for their chicks while the moms go on vacation (they worked hard to lay the egg so they need some time to recuperate). After the breeding season, murres leave the rock in large quantities – this is often the last time humans will see them this year in large aggregations from shore.

Despite their omnipresence and importance as a marine predator in Oregon, there is still a lot we don’t know about murres. Where do murres go when they are not breeding? Do they migrate? Where do they feed during the breeding and non-breeding period? What habitat characteristics are associated with feeding areas? By answering these questions, we increase knowledge of murre ecology in Oregon. Moreover, a more comprehensive understanding of the year-round movements of murres aids marine spatial planners take more informed actions on the current decisions regarding offshore renewable energy development. This is what I hope to achieve through my Masters research project at OSU.

Most of what is known about the offshore distribution of murres in Oregon comes from vessel observations. However, vessel data only provide snapshots in time, and not a continuous picture of area-use. Within the Seabird Oceanography Lab (SOL), we are using individual satellite tracking devices to follow the movements of murres associated with the Yaquina Head colony, which is a prominent breeding colony in Oregon located near Newport.

A common murre displaying a satellite tag prior to release.

SOL was able to track 15 common murres associated with the Yaquina Head colony in 2015 and 2016.  These tags were deployed periodically throughout the breeding period and have been successful in tracking birds for up to three months. Thus far, we have tracking data ranging from May to December (only one bird tracked during December).

Tracking data from 2015 and 2016 of murres off the Yaquina Head colony provide an interesting comparison.  In both years, murres experienced warmer ocean conditions, high Bald eagle disturbance rates, and consequently high Western gull egg predation at the colony. Some data also indicate low prey availability.  The combination of all these factors is most likely the reason for the observed reproductive failure at the colony in both years. Tracking data showed that 13 of the 15 birds tagged dispersed from the colony earlier than expected. The maps below summarize the dispersal of birds by year and by time of deployment.

 

Each map (Left: 2015, Right: 2016) illustrates all birds that dispersed from the colony and did not engage in central-place foraging (feeding trips to and from the colony). Sample size: n2015=7, n2016_spring=1, n2016_summer=3.

Most birds made a northward movement and traveled as far north as British Columbia, Canada.  Along their movement north, they used inlets and bays, but one of the most prominent areas used was the Columbia River plume. Birds used the Columbia River mouth area during the summer and fall, with the most time spent there during the summer. Dispersal from the colony was not what we expected; we expected individuals to breed on colony and engage in central-place foraging  (feeding to and from the breeding site) nearshore until mid-August when they usually leave the rock. However, we are still interested in the habitat characteristics of feeding areas and the conditions that led to movement from one feeding area to the next.

Prior to examining habitat associations of murre feeding areas, we must first determine their behavior state at each point location derived from the satellite tags.  After data cleaning and filtering out erroneous locations, we applied a behavioral analysis (Residence in Space and Time method) to determine behaviors associated with each point location. This analysis has allowed us to distinguish between intensive foraging, transiting, and extensive foraging. Extensive foraging locations can be interpreted as a set of locations that are mostly spread out in space, where murres searched for prey. On the other hand, intensive foraging locations can be interpreted as a set of locations that are very close together in space where murres likely found prey, and thus spent more time.

We are finalizing the extraction of environmental data for each point location from satellite data. Once all data are extracted, we can begin analysis for determining what environmental conditions were sought during dispersal and what types of habitats are preferred. Some of the ocean conditions that will be examined are sea surface temperate, wind, upwelling index, and primary net productivity. Some other habitat descriptors we are interested in assessing are substrate, distance to river mouth, salinity, depth, distance to the 200-m isobath, and distance to shore. For now, exploration of data indicates differences in habitat associations by behavior and between seasons.

Sample size means everything in a study like this so I am happy to say that more data is yet to come: SOL plans to deploy 15 more tags during spring and summer of 2017. I am excited to see what the additional tagged murres will do, and whether they will follow a pattern similar to those tracked in 2015 and 2016. However this time around, we will deploy tags as late in the summer/early fall as we can, in hope of acquiring some novel winter data to fill this knowledge gap. If we are successful, we may finally have a better idea of what life is like for common murres during more of the year beyond the rock.