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Team work in week two

The second week of the 2013 field season for Team Echinacea was excellent. We finished searching for seedlings and found a grand total of 102 seedlings in 13 remnant populations. We laid out the main common garden experiment with over a thousand orange, blue, and lime flags to guide our walking and to enable us to identify individual plants. We also began assessing survival in the recruitment experiment. On Wednesday Ilse presented results to the team on her aster analysis of 17-year fitness records for about 600 Echinacea plants in our main common garden experiment–details to follow. Pam took out her big new photosynthesis machine for its first trial run. Storms and wetness rained us out all day Thursday and we were without power for two hours on Thursday and about 18 hours on Friday. Team members are refining their ideas for independent projects and soon will be able to make their own posts. (IT folks at the UMN said they fixed the access problems-we’ll see.) Stay tuned to read about their awesome experimental plans!

You can read about some of our team-members on our their Echinacea Project webpages…
Pamela Kittelson
Ilse Renner
Dayvis Blasini
Kory Kolis
Sarah Baker
Marie Schaedel
Reina Nielsen
What a great team!

Next week we aim to finish assessing survival, flag another experimental plot, measure more plants, work on independent projects, and purchase/make/organize equipment and supplies for our experiments. We are also looking forward to Amy Dykstra’s visit. She will talk about her dissertation research.

We are making updates via twitter and facebook. These media have proved to be more reliable than this flog, but we hope that changes soon. See links on the Echinacea Project’s main web page. We hope to set up a venue for sharing more of our photos–stay tuned for that, but here are a few photos from this past week…

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Searching for seedlings at LF (the landfill site).

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An orchid (Cypripedium calceolus)
flowering at the KJ site.

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The team on the porch of the Hjelm house.

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First trial of the new phtosynthesis machine.

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Sorting flags to reuse & recycle.
We estimated 2600 flags here to reuse.

More defending your thesis

I defended my thesis on May 16th, presenting the results of my research on the hygroscopic motion of big bluestem and indian grass. I’ve attached the presentation to this post, though the presentation is a bit light on text. I’m putting together a section on my website with more text, which I’ll link when it’s ready.

drizin-seeds-presentation.pdf

Field trip to MN (22 – 26 May)

I drove from the Chicago Botanic Garden to our field site in western Minnesota hoping for a window of appropriate burning weather on Thursday afternoon or Friday afternoon. I also brought 297 Echinacea seedlings to plant as part of an experiment that investigates hybridization between native and non-native Echinacea. Several gallons of side-oats grama grass seed were waiting to be hand broadcast at two sites after the burn.

Why burn?
We want to burn our large Echinacea “common garden experiment.” In this abandoned field we have planted about 14000 individual Echinacea plants, starting in 1996, and measured their growth and flowering every year. We have burned this ~6 acre plot every other spring from 1998 to 2008. The weather didn’t cooperate in 2010, so we burned in 2011. We are trying to burn this year! Burning in the spring really increases the chance that an Echinacea plant will flower. We are planning a big crossing experiment this summer, so we want as many plants to flower as possible. Also, burning sets back the weeds–and that is a good thing.

Here’s the quick recap of major activities.
1. Packing
2. Driving to MN
3. Preparing to burn
4. The burn
5. Seeding after the burn
6. Preparing to plant
7. Planting
8. Seeding the phenology plot
9. Driving to IL

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Dwight makes sure the fire stays where it belongs

Read the gory details…

1. Packing
I loaded the truck with lots of field equipment to use during the summer. The seedlings in the hybridization experiment fit in three trays. I had two trays of “extra” seedlings that were still hanging on from Jill’s agar/blotter seed germination experiment. For the burn, I brought three backpack sprayers, the DNR burn permit, and batteries for radios. I forgot to bring a back-up drip torch.

2. Driving to MN
The drive to Minneapolis was generally uneventful, which is just what one wants when driving an 18-year old truck. Very early on Thursday I drove to the site. Shortly before arriving, I saw two Sandhill Cranes landing in a wet field near Holmes City. I think that’s the first time I’ve seen cranes on the ground in Douglas County–auspicious! I should mention that I also saw a Common Loon and Pelicans, which are common every summer in Douglas County. Seeing them makes for an auspicious day too.

3. Preparing to burn
Thursday morning the ground was wet and the wet grass duff (fuel) didn’t look very promising for burning. The erosion in the surrounding corn fields indicated it had rained a lot. Our rain gauge confirmed that showing 3.65 inches (93 mm) of precipitation in the previous week. Light winds and cool temps weren’t helping dry it out, but the sun and low humidity offered a glimmer of hope. It’s rather stressful trying to predict burn weather and decide whether to rally folks to make a long trip to help burn.

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The plot before the burn

Dwight and I began preparations for the burn. Just after noon, it looked like the fuel might dry out enough to burn and the weather forecast looked great, so I let folks know that we were going to attempt to burn in late afternoon. I should add that the fire forecast for Friday was getting worse, so that a burn was going to happen on Thursday or never (well, June or 2014).

Here’s our pre-burn to do list:
Prepare burn break (mower, weed whip, chain saw)
Fill water tank on truck (70 – 80 gallons)
Put six buckets in tractor trailer
Set up hoses [I forgot to set up hoses this year, thus this list]
Fill backpack sprayers
Fill drip torch(es)
Get matches
Activate burn permit
Call sheriff
Call neighbors
Walk burn break with crew & place buckets
Check radios

What to wear during a burn:
100% cotton long-sleeved shirt and long pants
Hat
Leather boots (over ankle, if you have them)
Leather work gloves

4. The burn
Amy, Brad, Dwight, Jean, and I conducted the burn and it went smoothly. Amy made a nice post with photos. The burn was slow and thorough. Ignition initiated at 5:20 and we were done at 8:20. Winds were light ESE ~ 8 mph. We had a great dinner afterward.

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Amy keeps the fire from jumping the road

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Brad and Amy through the smoke

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A slow and thorough burn

Post burn to do list:
Call sheriff
Put everything away–dry out tanks
Broadcast seed

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Some grass is still green right after the fire

5. Seeding after the burn
On Friday I hand broadcast about 2 gallons (8 liters) of native grass seed. More warm season grasses will provide fuel for future fires! The Soras chattering in the neighboring wetland kept me company. Here’s the seed sources–keeping it local!
grocery bag: Bouteloua curtipendula from cg1 10 Aug 2012
grocery bag: Bouteloua curtipendula from Krus 14 Aug 2012
#1 bag: Bouteloua curtipendula (& some Elymus canadensis) from Backhill 19 Aug 2012
#2 bag: Bouteloua curtipendula from Backhill 19 Aug 2012
#2 bag: Bouteloua curtipendula from cg1 22 Aug 2012

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Much of the grass that was green right after the fire is now brown

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I found this Sharpie while broadcasting side-oats grama


6. Preparing to plant

Next job was getting those seedlings in the ground! The forecast was for lots of rain during the upcoming week, which is great for seedlings, and for lots of rain in the afternoon, which is not so great for a person planting seedlings. I had to hurry.

I was quite efficient, except that I paused to watch a pair of Trumpeter Swans at Hegg Lake WMA–another first for me in Douglas County. I got a very nice look at the birds up close and saw the shape and color of their bills–straight and all black. I didn’t hear them, so I’m not 100% positive they were trumpeters. Tundra swans apparently look similar, but I haven’t seen them up close for years.

I chose a uniform location in an area that was planted with warm season grasses in 2000 for this experimental plot. I was considering mowing the area, or at least the rows to facilitate making straight rows and putting the plugs in, but I decided against it.
I laid out 300 planting locations (10 m x 30 m) with meter tapes and pin flags. A 9m x 29m grid would be sufficient for 300 locations, but I don’t like to plant at 0m on a tape and I planned to leave a few flags at locations with no plants.

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Setting up planting locations

7. Planting

These seedlings all originate from plants that flowered at Hegg Lake last summer. Shona conducted the summer experiment and prepared the seeds for germination. Read about Shona’s project. Jill germinated the seeds this spring and measured the seedlings multiple times. Read about Jill’s project.

I ended up planting one tray (~100 seedlings) on Friday before getting rained out. Planting in the light rain worked for a while, but it was slow. When it really started coming down, I bagged it.

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tools of the trade

On Saturday morning I saw the pair of Trumpeters at the flooded field SW of MN27 & CR1. The nearby Canada Geese were much smaller. A black tern flew overhead. When I arrived at Hegg, I saw fresh truck tracks and what looked like a can of beer and a pair of underwear right in the middle of the parking area. They were not there the day before! Upon closer inspection I realized that it was a can of Nos energy drink, not beer.

Saturday proved to be cold but not too cold. It was 54 degrees F and very windy. I wore nitrile gloves and that kept my hands warm. I planted almost twice as fast as I did when it was raining. The Bobolinks kept me entertained all morning with their bubbling songs.

8. Seeding the phenology plot Saturday 1:11 – 1:42 pm
Right after finishing planting I went to the phenology plot and broadcast some native seeds that we collected last fall. I broadcast the seed fast and it dispersed well in the strong and gusty wind. There is a new fox den with a big pile of dirt in the middle of the plot. The only plants I saw flowering were Sambucus, Dandelion, and Antennaria. I’m sure others have been flowering, but it was overcast and cold and I was moving fast. As I left Hegg Lake a wild Turkey walked out in the road in front of my truck. So nice to see.

I planted ~ 2.5 gallons of seed from three collections:
1. Bouteloua curtipendula from Hegg Lake WMA 13 Aug 2012 (#4 bag). 2. Bouteloua curtipendula from NE corner of Hegg Lake WMA 27 Aug 2012 (grocery bag). 3. Schizachyrium scoparium (& some Bouteloua curtipendula) from along CR 15 at Hegg Lake WMA 16 Sept 2012 (grocery bag).

9. Driving to IL
I left around 5:45 AM on Sunday. As I climbed in the truck I heard a Great-crested flycatcher–first of the season–so, I suspected it would be an auspicious trip. It was a boring drive, just the way I like it. I talked to myself about mating isolation and asynchrony to help prepare for writing a proposal to NSF on this topic.


Postscript.
I didn’t have time to plant a few of Maria’s left-over Dichanthelium plants. Jean said she would be glad to plant them in her prairie garden. photo(7)May2013.JPG

Maria’s Dichanthelium plants. Some have been exposed to cold temperatures for the past month or so.

until next year

There was one project we did not get to this year. In the summer of 2012, field intern Kelly Kapsar observed flowering times for Echinacea in burned and unburned areas of the Staffanson prairie preserve. At the end of the summer, she collected the flowering heads in order to assess the relationship between flowering time and seed set. Various students have worked on aspects of the project. In November, Mindy Runge and Ale Mendoza (Lakeforest College) extracted and weighed achenes (click here to see their poster). In December, Marie Schaedel (Carleton College) weighed additional achenes and assessed our methods of judging whether an achene is full or empty (click here to read her results ). Most recently, Jill Pastick (Lakeforest College) finished extracting achenes and helped organize the collection.

These steps (extracting and weighing achenes) allow us to draw a relationship between flowering time and seed set (i.e. the proportion of full vs. empty achenes). The next step of this study will be to germinate the achenes and plant them in the field. Unfortunately, that will have to wait until next year. In the meantime, the collection of weighed and organized achenes will be stored in the freezer.

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Maria’s Poster for MEEC 2013!

Hi everyone,

I presented a poster at MEEC 2013 (which Katherine wrote on in the previous entry) and just got back from another poster presentation at Chicago Area Undergraduate Research Symposium (CAURS) today!

Here’s my poster – enjoy looking at it to see what I found out from my summer fieldwork!
Wang_MEEC2013-Poster36x44-pdf.pdf

MEEC 2013

This past weekend, three students associated with the Echinacea Project presented their work at the Midwest Ecology and Evolution Conference at Notre Dame.

Kelly Kapsar (Carleton College, 2014) spent the winter analyzing her data on flowering phenology in prairie remants and presented her results in a poster.

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Maria Wang (Northwestern, 2013) presented the results of her undergraduate honors thesis on pollen limitation in the prairie grass Dicanthelium.

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Master’s student Katherine Muller gave an oral presentation on her research on the relationship between Echinacea and its specialist aphid.

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I should mention that Maria was recently accepted as a Master’s student in the Northwestern Program in Plant Biology and Conservation. She will graduate this summer and remain in Chicago another year to finish her M.S.. She will be working with Dr. Nyree Zerega investigating the genetic origins of tropical crops. Although we will miss her in the Echinacea Project, we wish her the best in her next endeavor.

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More work with E. angustifolia x E. pallida crosses

This January Stuart and Gretel kindly hosted me in Chicago and gave me the opportunity to spend a few weeks working in the Echinacea Project lab continuing my research from the summer. Here is my final paper with some interesting results.

Sanford-Long_EchinaceaHybridization.doc

the phenology of aphids on Echinacea

During the summers of 2011 and 2012, I conducted a survey of aphid infestation in a section of the main experimental plot to track, among other things, seasonal changes in the distribution and abundance of Aphis echinaceae on Echinacea. With help from members of team Echinacea, I conducted 6 bi-weekly surveys in 2011 and 3 monthly surveys in 2012. In both years there was a sharp rise and fall in the frequency of aphid infestation. The plot below shows the percentage of plants in the survey area observed to have 1 or more aphids on each dates. In 2011, the peak of aphid infestation (i.e. when the highest percentage of plants hosted aphids) was around August 12th. In 2012, the peak date of aphid infestation occurred some time between July 13th and August 9th. I was not able to observe the peak directly due to a sudden die-off of aphids before my third survey. I estimated the peak frequency of aphids as the percentage of plants with live or dead aphids on August 10th (indicated by the asterix and x-error bar).

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I was also able to get a sense of aphid phenology from my aphid addition/exclusion experiment. In 2011 and 2012, I added or excluded aphids from 100 plants that were not flowering in 2011. The graph below shows the mean abundance of aphids in each experimental group over the summer of 2012:

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Based on this graph, I estimate that the peak of aphid infestation for 2012 occurred around July 22nd (202 days after January 1st), about two weeks before last year’s peak.

Dichanthelium Flowering!

Hi everyone,

Maria here at CBG. On Tuesday, I came back from Thanksgiving break to find that one of the Dichanthelium plants in the growth chamber was flowering like crazy!

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So many flowers! It was also interesting that the plant that flowered looked more stressed (yellow leaves) than some of the other plants.

Today, I collected some pollen (shook the spikelets) on glass slides, stained them with 0.1% toluidine blue, and looked at them under the microscope. It was amazing to see the stained pollen, and how different the viable and inviable pollen looked! I wish I had pictures. I will be learning how to take digital microscopic images (hopefully tomorrow?). So hopefully I’ll be able to stain pollen from all flowers tomorrow, take pictures of the stains, and count pollen to get a sense of levels of viability in Dichanthelium pollen.

Sync-ing in the Rain (Aug 30)

Maria here.

Woke up this morning to some rumbling thunder in the distance.

The skies looked grey, but nothing too bad. We discussed how to do all the things we had to do at Staffanson: demo rechecks, harvesting Kelly’s Echinacea heads, removing twist-ties and flags from heads/plants that Kelly won’t harvest, figuring out 6 nearest neighboring Echinacea plants to each of Kelly’s plants that was going to be harvested, and pulling up ant traps. Whew!

We did some individual project stuff from 9 to 11am. Jill finished up sorting ants. Katherine and Kelly went to NWLF and NNWLF to pull ant traps and remove twist-ties from heads. I was in CG 99 South, measuring Dichanthelium from my maternal lines experiment, and got 4 rows done before 11am.

We set off for Staffanson, all 5 of us cozy in the truck. The corn and perennial weeds greeted us happily on the dirt road leading into Staffanson. Jill went to pull up her ant traps and then helped Kelly to remove twist-ties and flags. Stuart, Katherine and I brought out Sulu (the GPS), R2D2 (the netbook), and paper datasheets, and tried to figure out how to determine the 6 nearest neighbors to Kelly’s harvest heads. We concluded that the most efficient way was to use R to determine the 6 mapped nearest neighbors, obtain the distance to the 6th neighbor, then use a reel tape to measure out the distance and search to see if there are any other nearest neighbors closer than the mapped one. We would have to do it another day.

Here’s a fancy spider Stuart found on his knee today. Photo courtesy of Katherine.
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On the way back for lunch, Stuart and Kelly belabored the pros and cons of color coding the top and bottom GPS poles.

After lunch we set out for Staffanson again. Kelly worked solo to harvest heads, while the four of us split into 2 teams (1 GPS + 1 clipboard) to do demo rechecks. After a little while, it started sprinkling and we heard some distant portentous thunder, so we turned back and left Staffanson.

Back at Hjelm House, Jill and Katherine cleaned up the ant traps and went to pull ant traps at Nessman. Stuart demonstrated dissecting achenes from Echinacea heads for Kelly, so she can dissect the heads she harvested when she’s at Carleton.

Lastly, as requested by Stuart, the “Sync Your Visor” song I came up with as an alternative to “Sync, Sync, Visor Sync”:

(To the tune of “Oh My Darling Clementine”)

Sync your visor, sync your visor,
Sync your visor everytime;
Data lost and gone forever
Don’t be sorry – sync it now!

Any suggestions for improvement are much welcome.