We are grateful for the support from undergraduate assistants during the rearing for this work, in particular Regina Kurandina and Rhea Smykalski. Carolyn Kalinowski helped compile literature on metal toxicity in other Lepidoptera. This work was made possible by a University of Minnesota Department of Ecology, Evolution, and Behavior summer research grant.

This research was conducted under USDA APHIS permit P526P-13-02979.
1. Collection of experimental butterflies
<ol>
	<li>Catch adult female butterflies with an aerial insect net. Cabbage whites are generally found in open, disturbed habitats with nectar plants and host plants (in the family Brassicaceae) present.
	<ol>
		<li>Search when the sun is out and the temperature is warm. To target females, look for individuals fluttering slowly, close to the ground, and landing on plants to &#34;drum&#34; (taste) the leaves with their foretarsi.</li>
	</ol>
	</li>
	<li>Set up females in cages to harvest eggs. 
	NOTE: Field-collected females, on average, have mated with one or two males12, and should start laying fertile eggs shortly after capture. Wild-caught females need natural light to oviposit and mate, so place the cage in a greenhouse or windowsill.</li>
	<li>House females with a host plant to harvest eggs. 
	NOTE: Females will accept a variety of host plants, including green cabbage, radish, kale, collards, and Arabidopsis, but ensure that the plants have not been treated with any pesticides.
	<ol>
		<li>Present the host plants either in pots or in containers with water to maintain the leaf pressure, such as stems of kale in floral water tubes.</li>
		<li>If the researcher wishes to collect eggs and transfer them directly to diet, first use a rubber band to attach a host plant leaf to the top of a plastic cup of water, and then stretch a piece of parafilm around the edge-females touching the leaf will oviposit onto the parafilm (see5).</li>
	</ol>
	</li>
	<li>Ensure that the cage also contains something to keep the relative humidity high, for instance, through daily watering of a potted plant or wetting of a towel, especially in dry conditions. If potted plants are watered in the cage, ensure a towel is under the pot, as butterflies can get stuck in pooling water.</li>
	<li>Feed the butterflies with a 10% diluted honey water solution presented on a yellow sponge, which butterflies quickly learn to use, especially if housed with experienced individuals.
	<ol>
		<li>To encourage butterflies to feed from sponges, place them directly on the feeder, especially after lightly spraying with a water bottle, which often causes them to stick out their proboscis.</li>
		<li>To set up the feeder, first thoroughly rinse the yellow or orange sponges, and then cut them into small squares that fit into 60 mm plastic Petri dishes. Change the feeders daily and clean the sponges in a mild bleach solution, followed by thorough rinsing to prevent mold growth.</li>
	</ol>
	</li>
</ol>
2. Making artificial diets
<ol>
	<li>First, use the recipe in Table 1, or other relevant sources, to determine the relevant recipe for an experiment. Make necessary modifications specific to the focal species or experiment. Print out a recipe to follow while weighing ingredients.</li>
	<li>Weigh all the dry ingredients, except for the agar, into one container. Ensure the ingredients are put back into their respective storage location, noting that several ingredients are stored at 4&#176; C. Place the pre-weighed, dry ingredient mixture into a blender with 5 mL of flaxseed oil.</li>
	<li>For each diet batch, follow the steps detailed below.
	<ol>
		<li>Mix 15 g of fine-mesh agar with 400 mL of distilled water in a beaker at least 1 L in size. Microwave until the agar is close to boiling, with fine bubbles throughout the mixture, stirring the mixture every 30-60 s to prevent boiling over.</li>
		<li>To this hot agar mixture, add 400 mL of faucet-temperature distilled water to bring it to an appropriate temperature to mix with the dry ingredients, as the vitamin mixture is heat-sensitive.</li>
		<li>Add the agar mixture to the blender and thoroughly mix, scraping the edges of the blender if necessary.</li>
	</ol>
	</li>
	<li>As the agar is heating, place at least seventy four-ounce diet cups on the counter with the edges touching. After thoroughly mixing the diet, pour the mixture from the blender into diet cups, ensuring the diet covers the bottom of each cup.</li>
	<li>After the diet cools, place lids on the cups, label the diet cups with diet type, stack them on trays, and store for up to 1 month at 4 &#176;C until use.</li>
</ol>
3. Transfer and rearing on artificial diets
<ol>
	<li>House host plant leaves with butterfly eggs in 30 oz deli cups with a mesh cover in a 24 &#176;C climate chamber. After 1 week, check the cups-ensuring that the larvae are hatched and in the late first or early second instar stage, a good time for transfer to the artificial diet.</li>
	<li>Transfer the larvae to the artificial diet with a paintbrush, disinfecting it with bleach spray and a water rinse in between containers of larvae. Transfer three larvae into each 4 oz cup. While the artificial diet is energy dense and can support high densities of larvae, avoid packing larvae into cups, as diseases and mold can spread in cups with high larval density.</li>
	<li>Place the cups into a plastic bin on their sides so that frass falls to the bottom of the cups and away from the diet, reducing mold and disease risk.
	<ol>
		<li>House the diet cups in controlled temperature conditions with low to moderate light levels. Monitor the cups for mold and disease every 1-2 days by peeking through the clear cup lids.</li>
		<li>Cups with mold or disease can be quarantined or frozen to prevent spreading to other cups.</li>
	</ol>
	</li>
</ol>
4. Adult emergence and handling
<ol>
	<li>Allow the larvae to pupate and emerge in the diet cups. When adults emerge, give them a few hours for their wings to harden before removing them for marking. Remove adult butterflies from the cups with clean hands by gently grasping their wings, noting that grabbing all four wings closer to their body is a more stable hold.</li>
	<li>To mark the butterflies, hold dry individuals by the head and thorax and use a fine-tipped sharpie to lightly mark a number on their hindwing.
	<ol>
		<li>Sex individuals using a combination of wing markings and genitalia; females generally have two black spots on their dorsal forewing and darker, more yellowish hindwings, while males generally have one smaller black spot on the dorsal forewing on a brighter white background54.</li>
		<li>Given that this coloration shows individual and seasonal variation, confirm the sex using abdominal traits-males have two claspers at the distal end of their abdomen and a narrower abdomen in general, while females have a single genital opening.</li>
	</ol>
	</li>
	<li>Transfer the adults to wax glassine envelopes by opening the envelope with one hand, holding the butterfly by the head and thorax, sliding it into the envelope, and grabbing the wings through the envelope with the other hand.
	<ol>
		<li>Make sure all four wings are closed normally within the envelope.</li>
		<li>Maintain the butterflies in cold conditions (5-6 &#176;C) for up to 1 week prior to experimentation, but allow at least 1 day to acclimate when taken out of the fridge.</li>
	</ol>
	</li>
</ol>
5. Performance measures
<ol>
	<li>To measure wing traits on dead individuals, remove the wings of the butterfly by holding the thorax in one hand and using forceps to remove each wing at its base. Place the wings flat in a lightbox and take photographs for later measurements.</li>
	<li>To get estimates of fecundity, house the adults in mating cages, allowing at least 1 day for reproductive maturation of males and 1 day for mating. Sacrifice females at set time points for egg counts through dissection, or collect eggs each day on host plants.</li>
	<li>To estimate egg loads, remove the abdomen of the female, place it in 1x PBS buffer, and cut a slit along the ventral side.
	<ol>
		<li>Use forceps to separate the innards from the cuticle, then pull the ovaries away from the gut, trachae, and other contents of the abdomen.</li>
		<li>Uncurl the four curled ovarioles within each of the two ovaries, noting where mature, yolked, and shelled eggs transition to immature follicles. Use a counter to help tally the total mature eggs, generally ranging from 0-200 eggs.</li>
	</ol>
	</li>
	<li>To determine the mating status of a dissected female, open the bursa copulatrix and separate the spermatophores within. As spermatophores are digested, they generally develop a &#34;tail&#34; and are nested within each other.</li>
</ol>
6. Case study
NOTE: Adult female cabbage white butterflies were collected from the wild in 2014 to found the experimental populations. Adult females originated from near Davis, California (N = 8 founding females).
<ol>
	<li>Housing the butterflies
	<ol>
		<li>House the females in &#34;BugDorm&#34; mesh cages (61 cm x 61 cm x 61 cm) under natural light in a greenhouse. Provide an organic leaf of the host plant cabbage (Brassica oleracea) for ovipositioning.</li>
		<li>To maintain humidity in the cages, include a small potted plant (Cosmos), watered daily, placed on top of a towel within each cage.</li>
		<li>Collect eggs daily by transferring leaves with new eggs to 473 mL plastic cups with holes in the lid and place in a climate chamber.</li>
		<li>Provide butterflies with ad libitum access to a 10% honey water solution (made by diluting organic honey with distilled water), accessible through a yellow sponge in a small Petri dish that is changed daily.</li>
	</ol>
	</li>
	<li>Preparing artificial diets
	<ol>
		<li>Prepare artificial diets for cabbage white larvae using modifications of previously developed Lepidoptera diets4. One batch of diet contained 50 g of wheat germ, 27 g of casein, 10 g of cellulose, 24 g of sucrose, 15 g of cabbage flour, 9 g of Wesson salt mix, 12 g of Torula yeast, 3.6 g of cholesterol, 10.5 g of Vanderzant vitamin mix, 1.1 g of methyl paraben, 1.5 g of sorbic acid, 3 g of ascorbic acid, and 0.175 g of streptomycin (see Table of Materials).</li>
		<li>Pre-weigh the dry ingredients for multiple diet batches (Table 1) and mix thoroughly to increase the homogeneity across diet types before being subdivided into separate batches for mixing with metal solutions.</li>
		<li>Place the dry ingredients in a blender with linseed oil and the corresponding metal mixture. 
		NOTE: Linseed oil was used in the present experiment as it was sold by a past provider of insect diets. Now, organic flaxseed oil is used exclusively, which is made from the same plant, but is less likely to contain any additives as commercial providers of linseed oil.</li>
		<li>Pour the prepared diet into 118 mL (4 oz) plastic deli cups. Use soluble metal salts to add focal metals to artificial diets. Aim for metal concentrations based on prior observations of the metal content of plants (e.g., nickel accumulation55,56,57 or roadside contamination of plants58,59,60) and tolerance of metals in other Lepidoptera49,50,51.</li>
		<li>Dissolve metal salts in 500-1,000 mL of distilled water prior to taking the corresponding amounts to add to artificial diets. For example, to make the 100 ppm nickel diet, add 317.6 mL of 1 M NiCl2 solution to the artificial diet before blending to give a final diet concentration of 100 mg/g Ni dry weight (approximately 53 mg/g wet weight). This amount translates into an average measured concentration of 109.6 ppm (Table 2) based on inductively-coupled plasma atomic emission spectroscopy. 
		NOTE: The levels of metals were estimated by the University of Minnesota&#39;s Research Analytical Labs with six samples.</li>
	</ol>
	</li>
	<li>Maintenance
	<ol>
		<li>Maintain the eggs harvested on host plants in climate chambers at 23 &#176;C on 14:10 photoperiods for 7 days. After this, transfer the early second instar larvae to the artificial diet.</li>
		<li>At transfer, evenly divide the larvae from a given plant across the four diet types to avoid confounding batches of larvae with diet type. Transfer the larvae (N = 346 total) as two individuals per 118 mL diet cup to reduce disease incidence from overcrowding and allow for ample space for adults to eventually eclose.</li>
		<li>Punch holes (three per lid) in the lids of the rearing cups. Place the cups in shoebox-sized plastic bins for rearing, with the different diets interspersed to avoid any systematic effects of location in the rearing chamber.</li>
		<li>House the cups of larvae in climate chambers at 23 &#176;C on 14:10 photoperiods (with bins of water at the bottom of the chamber to keep the humidity around 50%-60%, monitored with a home humidity sensor). In the event that the cups became moldy (about eight total cups in this case study), remove the cups from the chamber and remove those individuals from the experiment.</li>
		<li>Allow larvae&#160;to pupate and emerge in the rearing cups (N = 162 total). 
		NOTE: For the rearing conditions in this study, the development time from egg collection to adult emergence averaged around 25-30 days (ranging from 20-40 days, e.g.,25,28).</li>
		<li>As the pupae approach adult emergence, check the cups daily for newly-eclosed individuals and remove adults with dried wings. Label the adults on their hindwings with their corresponding individual number (assigned at larval transfer) using a fine-tipped black sharpie. Determine the sex of each individual and mark on a glassine envelope along with their number and emergence date. Place the adult butterflies in glassine envelopes and store at -20&#176; C until further processing. 
		NOTE: A small fraction of emerging adults show wing deformities that would interfere with flight and adult survival (5%-8%); these individuals are excluded from survival analyses for these experiments.</li>
	</ol>
	</li>
	<li>Measurement and data analysis
	<ol>
		<li>Measure the survival as survival from second instar (when the caterpillars were placed on diet) to adult emergence. 
		NOTE: The present study focused on survival and development time as measures of performance on the different diets.</li>
		<li>Measure the development time as the number of days between transfer to diets and adult emergence in the climate chamber.</li>
		<li>For data analysis, run two sets of models that included interactions between the metal and concentration. 
		NOTE: As both interactions were significant (F2,194 = 4.56, p = 0.01 for development time and X2 = 12.1, p = 0.002 for survival), the study proceeded with separate analysis of each metal.</li>
		<li>To analyze survival, run chi-square tests for each metal to test the effects of metal dose (treated as four categories) on survival to adulthood with wings fully intact.</li>
		<li>When a significant effect of dose is detected, perform a follow-up chi-square to compare each level to the control diet. To analyze the development time (from time of transfer to emergence as an adult), test for effects of sex on development time. 
		NOTE: As there was no effect of sex on development time, (p &#62; 0.10) for any metal in this experiment, we dropped it from consideration in the model.</li>
		<li>Run a separate ANOVA for each metal to test for the effect of the four concentrations on development time. Additionally, run t-tests for each concentration relative to the control to determine the minimum concentration where a performance effect is seen. 
		NOTE: In this study, JMP v16 was used for all analyses. All raw data are available on Mendeley61.</li>
	</ol>
	</li>
</ol>

Artificial Rearing and Heavy Metal Tolerance in Cabbage White Butterflies

The authors have no conflicts of interest to declare.

In this research, cabbage white butterflies (Pieris rapae) were raised on an artificial diet to examine differences in heavy metal toxicity. In doing so, this study provides general methods for rearing and laboratory studies of this easy-to-manipulate butterfly system. This discussion first considers more general questions about the methods reviewed here, then reviews our scientific findings before concluding with reflections on the components of the artificial diet.
The protocol reviewed here gives steps of a general rearing method for cabbage white butterflies, but there are many points within this protocol that can be tweaked. For instance, while the case study presented here uses sponges for feeding, other researchers have had luck with dental wicks and silk flowers filled with honey water5. While the present study uses honey water as food, other researchers have used sugar solutions and even Gatorade. If pupae need to be weighed, or moved to other conditions for emergence (e.g., inducing diapause and needing to cold store for 1 month), the researcher can easily remove them from the cups by spritzing them with water to moisten their silk attachments and grab them with feather forceps, then re-hanging them using double-sided tape. If researchers need more flexibility in terms of when adult butterflies are moved into cages for adult behavior, they can be held in the refrigerator for several weeks, but they need to be fed. Every several days, the butterflies should be taken out to be fed a dilute honey water solution. Under indoor lighting, this can be done by using a pin to unroll their proboscis into the food. On the adult performance end, a wide range of fitness measures can be taken on cabbage white butterflies. Body size can be measured as the wet or dry mass of larvae at certain stages, pupae, or adults (sacrificed, or held in glassine envelopes), or through the measurement of wing length in the program ImageJ (see12,24,25,28). The lifetime fecundity of females can be measured through daily egg collections on host plants25,69,70, and the size of specific traits can be measured as a metric of performance; for instance, the mass or volume of the brain or individual brain regions62,71,72, or the mass or protein content of the thorax or flight muscle62,70. Finally, adults can be used in behavioral studies to test any number of questions examining the effect of diet manipulation on foraging or oviposition choice27,73.
If the rearing protocol is not working as expected, there are a few aspects to troubleshoot. First, one can ask whether the light levels are high enough to elicit normal adult behavior. While lab-adapted lines of Pieris will lay eggs under fluorescent light, the only artificial light that works for wild-type lines are powerful broad-spectrum greenhouse lights. Natural light in greenhouses, windowsills, or outdoors works best to elicit mating and egg-laying behavior. Second, if eggs are not hatching or if larvae are dying early in development, there are a few things to consider. The host plant material must be organic, noting that &#34;organic&#34; plants from stores are sometimes treated with chemicals that can kill larvae, so raising one&#39;s own host plants is often best. If the host acceptance rate is lower, younger leaves with higher nitrogen content can be attempted, presenting potted plants instead of individual leaves and ensuring females are mated. Females will accept seeding Brassica, even small sprouts that are 2 weeks of age. The paraffin method works well to transfer eggs to different conditions, but it should be noted that the acceptance rate tends to be lower than whole plants. Third, all the components of the diet must be of high quality and not expired. Flaxseed oil should be replaced annually and stored in the fridge24,25. Wheat germ, the vitamin mix, and antibiotics should also be kept cool. Fourth, one can consider tweaking the diet cup setup. Any number of disposable plastic cup types can be used for rearing, from 1 oz to 15 oz. We have found that 4 oz is a good size to allow for adult emergence and packs nicely into our climate chambers. Holes poked in the lids allow for airflow, but too many holes can dry the diet in low humidity conditions, so this number may need to be adjusted. Fifth, the conditions in the climate chamber may need to be adjusted in combination with the cup conditions. If the conditions are too dry, host plants with eggs may dry out before larvae can be transferred, and cups with diet may dry out before butterflies emerge. On the other hand, if the conditions are too wet, the cups can harbor mold and disease. Researchers may need to adjust the airflow in cups through the use of mesh lids, or more or less holes in the lids. Another common issue is chamber lights that are bright enough to cause temperature swings in the cups and a build-up of condensation; using dimmer lights is an easy option for larval rearing.
With respect to the research questions in this paper, this study found that cabbage whites were relatively more sensitive to copper than to nickel or zinc. Copper had significant negative impacts on development time at concentrations as low as 50 ppm (Figure 3 and Table 3) and on survival at 500 ppm (Figure 4, Table 4). In contrast, there were no negative effects of nickel on survival (up to 500 ppm; Figure 3) or negative effects on development time at 100 ppm (Figure 4). Cabbage whites were fairly tolerant of zinc, with survival effects seen only at 1,000 ppm (Figure 3) and negative effects on development time starting at 100 ppm (Figure 4). Based on the relatively greater concentrations of zinc in butterfly tissue and mustards (their host plant; Figure 1), it was expected that a relatively greater tolerance to zinc would be seen. However, the sensitivity to copper and the tolerance of nickel were somewhat unexpected given the very low levels of nickel in butterfly tissue (Figure 1) and the necessity of copper as a micronutrient. These unexpected findings are discussed below after considering the tolerance of these metals in other butterflies and moths.
To compare the present data with metal sensitivity measured in other Lepidoptera, data from existing studies were compiled on the minimum concentration, where heavy metals negatively impacted survival49,50,51,56,63,64,65,66,67,68; these studies focused on moths, especially pest species (Galleria mellonella, Lymantria dispar, Plutella xylostella, Spodoptera sp.). All of the measured sensitivity values in this study fall close to the range measured for these other species (Figure 5). However, the measure of nickel tolerance in this study does seem to be higher than expected-while there was not a significant effect of survival at 500 ppm, the previous study on Pieris rapae also found a very high tolerance for nickel (significant effects starting at 1,000 ppm56), despite low levels in their tissue naturally (Figure 1). The measure of copper sensitivity in this study also seems to be at the low end for studies of Lepidoptera. While the use of an artificial diet allows a convenient and controlled comparison of relative metal sensitivity, it is important to note that components of the diet could alter the measurement of absolute metal sensitivity. For instance, vitamin C in the diet could offset metal-induced oxidative stress74, or antibiotics in the diet could alter any effects of microbes on the processing of metals75. An interesting line of future research would be to systematically manipulate such diet components to test effects on metal toxicity, especially given questions about the functional role of lepidopteran gut microbes76,77&#160;and nectar components that may have antioxidant properties78. In addition, variation in dietary requirements across species can make interspecific comparisons challenging, and artificial diet-based methods should be complemented with manipulations of host plants.
These butterflies are particularly tolerant of nickel and sensitive to copper. Previous research has noted that many plants in the mustard family, which includes plants favored by Pieridae, hyper-accumulate nickel as a defensive mechanism against herbivores55,56,63,79,80,81. This hyper-accumulation is over 1,000 ppm in plant tissue, which is orders of magnitude greater than what is seen in most plants (Figure 1). It is possible that Pieris have a particularly high tolerance for nickel due to past selection by such nickel accumulators, as previously speculated26. While copper has been less frequently studied as a micronutrient in insect diets, there is some evidence that it plays a small role in reproduction and immunity, although primarily in blood-feeding insects (e.g.,82,83). It is possible that copper plays a less important physiological role in butterflies than in other animals84,85,86, consistent with recent work highlighting how copper may be as concerning of a pollutant for insects as lead, cadmium, and mercury (e.g.,87,88,89). While Pieris have been shown to avoid copper contamination at low levels90, the mobility of copper in plants (e.g., moving into leaves and flowers) has also flagged it as a metal contaminant of concern91.
While these results provide interesting data on the relative toxicity of these metals to cabbage white butterflies, this paper also aims to be of general use as a detailed visual illustration of methods for rearing this powerful system. Cabbage whites are easy to rear and manipulate in controlled lab experiments4,5 facilitating studies of host searching6,7,8, foraging9,10,11, and sexual selection12,13,14. The ability to rear these butterflies on an artificial diet is key in creating common garden conditions for comparisons and to manipulate nutrients, toxins, and even novel host plants. However, it is important to note that this artificial diet is not necessarily the optimal artificial diet for this species, and could likely be improved with future manipulations. For instance, the salt mix in this diet (and other lepidopteran diets) was originally developed for vertebrates and has higher calcium levels than what most insects need92,93. Thus, some of our rearing efforts have made custom salt mixes with lower calcium levels (e.g.,62), and others make use of &#34;Beck&#39;s salt mix&#34;, which may be more appropriate for many insect species94. In our own manipulations, we also found that butterflies performed better with relatively less wheat germ and relatively more cellulose compared to original concentrations4. One area in need of further attention is the lipid source and concentration in the diet. For instance, past work has shown that shifting from linseed oil (used in this study) to phospholipids increased the mating rates and growth rates of Pieris on artificial diets95. Supplementation of specific fatty acids in artificial diets may have additional positive effects96,97. Optimizing the artificial diet of Pieris98,99&#160;creates opportunities for addressing interesting questions about nutritional ecology100,101,102, evolutionary ecology, and ecotoxicology. These artificial diet approaches allow researchers to address questions about the role of specific lipids in cognitive evolution103, pre-adaptation to toxins28, dietary components that reduce the toxicity of pollutants104, or stoichiometric interactions between nutrients105.

The small cabbage white butterfly (Pieris rapae, hereafter &#34;cabbage white&#34;) is a cosmopolitan pest species of mustard crops, such as cabbage, broccoli, and canola1,2,3. At the same time, the cabbage white is a powerful system for research in biology and a commonly used butterfly model, as they can be easily reared and manipulated in controlled lab experiments4,5. Research on cabbage white butterflies has provided critical insights with respect to host searching6,7,8, nectar resource use9,10,11, mate choice and sexual selection12,13,14, wing pattern development and evolution15,16,17, and responses to novel and changing environments18,19. Many of these insights rely on the fact that cabbage whites can be reared on artificial diets4,20,21, which can be precisely manipulated to reflect poor nutritional conditions22,23, ecologically relevant pollutant levels24,25,26,27, or transitions to novel host plants28,29. The present study uses an experiment on exposure to heavy metals to illustrate basic methods for rearing cabbage white butterflies on an artificial diet in the laboratory and key performance measures of larvae and adults. Many aspects of these methods apply to other butterflies30,31 and moths32,33,34 that can be reared on an artificial diet.
In this paper, an experiment on metal tolerance is used to illustrate the general methods of rearing cabbage white butterflies. Heavy metals are a common anthropogenic pollutant stemming from the degradation of human products, industrial processes, and legacy contamination from historical use in pesticides, paints, and other products35,36,37,38. Many heavy metals, including lead, copper, zinc, and nickel, can move from soil and water into plant tissue39,40,41,42, and metals in dust can be deposited on plant leaves43,44,45, resulting in multiple routes of exposure to phytophagous insect larvae. Heavy metal exposure early in life can have negative effects on animal development, especially on neural tissue, and high levels can be lethal35,36,46,47,48. A number of studies have shown the negative effects of metal exposure on developing insects, including both pests and beneficial insects49,50,51. The large number of heavy metal pollutants, and the fact that they often co-occur in human environments52, means that precise lab methods are needed in which researchers can expose developing insects to different levels and combinations of diverse metals to understand and mitigate their environmental effects.
The present work contrasts the impacts of common metals on cabbage white survival and development, focusing on copper (Cu), zinc (Zn), and nickel (Ni), three common pollutants in human environments. For instance, forbs from rural Minnesota roadsides contain up to 71 ppm Zn, 28 ppm Cu, and 5 ppm Ni53. This experiment manipulates the levels of these metals in artificial diets of cabbage white butterflies at levels corresponding to, and exceeding, the levels seen in the environment. An artificial diet is used to contrast the relative toxicity of these metals, predicting that cabbage whites would be more sensitive to metal pollutants that are not an integral part of their physiology (nickel) relative to those that occur, albeit at small levels, in enzymes and tissue (copper and zinc; Figure 1). Throughout, this text provides methodological details and accompanying video visualizations to illustrate the rearing and research methods of this important butterfly model system.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1-L Pyrex beaker</td>
			<td>Fisher Scientific</td>
			<td>07-250-059</td>
			<td></td>
		</tr>
		<tr>
			<td>500 mL graduated cylinder</td>
			<td>Fisher Scientific</td>
			<td>03-007-43</td>
			<td></td>
		</tr>
		<tr>
			<td>60-mm plastic petri dish lid</td>
			<td>Fisher Scientific</td>
			<td>08-757-100B</td>
			<td></td>
		</tr>
		<tr>
			<td>Ascorbic Acid</td>
			<td>Frontier</td>
			<td>6015</td>
			<td></td>
		</tr>
		<tr>
			<td>Blender</td>
			<td>Amazon - Ninja Store</td>
			<td>BL610 Professional</td>
			<td></td>
		</tr>
		<tr>
			<td>Cabbage Flour</td>
			<td>Frontier</td>
			<td>1086</td>
			<td></td>
		</tr>
		<tr>
			<td>Casein</td>
			<td>Frontier</td>
			<td>1100</td>
			<td></td>
		</tr>
		<tr>
			<td>Celluose</td>
			<td>Frontier</td>
			<td>3425</td>
			<td></td>
		</tr>
		<tr>
			<td>Cholsterol</td>
			<td>Sigma</td>
			<td>C3045</td>
			<td></td>
		</tr>
		<tr>
			<td>Cups for rearing (4 oz)</td>
			<td>Wasserstrom</td>
			<td>6094583</td>
			<td>purchase with matching lids</td>
		</tr>
		<tr>
			<td>Fine Mesh Agar</td>
			<td>Sigma</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Flaxseed Oil</td>
			<td>amazon</td>
			<td>B004R63VI6</td>
			<td></td>
		</tr>
		<tr>
			<td>Floral water tubes, 2.8 x 0.8inch</td>
			<td>Amazon - Yimaa Direct</td>
			<td>B08BZ969DK</td>
			<td></td>
		</tr>
		<tr>
			<td>Glassine envelopes (1 3/4 x 2 7/8 INCHES)</td>
			<td>Amazon - Wizard Coin Supply</td>
			<td>B0045FG90G</td>
			<td></td>
		</tr>
		<tr>
			<td>Mesh Cages (15.7 x 15.7 x 23.6&#34;)</td>
			<td>Amazon</td>
			<td>B07SK6P94S</td>
			<td></td>
		</tr>
		<tr>
			<td>Methyl Paraben</td>
			<td>Frontier</td>
			<td>7685</td>
			<td></td>
		</tr>
		<tr>
			<td>Ohaus Portable Scale</td>
			<td>Fisher Scientific</td>
			<td>02-112-228</td>
			<td></td>
		</tr>
		<tr>
			<td>Organic Honey</td>
			<td>Amazon</td>
			<td>B07DHQQFGM</td>
			<td></td>
		</tr>
		<tr>
			<td>Photo studio portable lightbox</td>
			<td>Amazon</td>
			<td>B07T6TNYJ1</td>
			<td></td>
		</tr>
		<tr>
			<td>Plastic bin, shoebox size</td>
			<td>Amazon</td>
			<td>B09L3B3V1R</td>
			<td></td>
		</tr>
		<tr>
			<td>Plastic disposable transfer pipets</td>
			<td>Fisher Scientific</td>
			<td>13-680-50</td>
			<td></td>
		</tr>
		<tr>
			<td>Sorbic Acid</td>
			<td>Sigma</td>
			<td>S1626</td>
			<td></td>
		</tr>
		<tr>
			<td>Spatulas</td>
			<td>Fisher Scientific</td>
			<td>14-357Q</td>
			<td></td>
		</tr>
		<tr>
			<td>Streptomycin</td>
			<td>Sigma</td>
			<td>S9137</td>
			<td></td>
		</tr>
		<tr>
			<td>Sucrose</td>
			<td>Target</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Torula Yeast</td>
			<td>Frontier</td>
			<td>1720</td>
			<td></td>
		</tr>
		<tr>
			<td>Vanderzant vitamin mix</td>
			<td>Frontier</td>
			<td>F8045</td>
			<td></td>
		</tr>
		<tr>
			<td>Weigh boats</td>
			<td>Fisher Scientific</td>
			<td>01-549-750</td>
			<td></td>
		</tr>
		<tr>
			<td>Wesson Salt Mix</td>
			<td>Frontier</td>
			<td>F8680</td>
			<td></td>
		</tr>
		<tr>
			<td>Wheat Germ</td>
			<td>Frontier</td>
			<td>G1659</td>
			<td></td>
		</tr>
		<tr>
			<td>Wooden handled butterfly net, 12&#34; hoop</td>
			<td>Amazon - Educational Science</td>
			<td>B00O5JDLVC</td>
			<td></td>
		</tr>
		<tr>
			<td>Yellow sponges</td>
			<td>Amazon-Celox</td>
			<td>B0B8HTHY5B</td>
			<td></td>
		</tr>
	</tbody>
</table>

rearing the cabbage white butterfly (pieris rapae) in controlled conditions: a case study with heavy metal tolerance

The cabbage white butterfly (Pieris rapae) is an important system for applied pest control research and basic research in behavioral and nutritional ecology. Cabbage whites can be easily reared in controlled conditions on an artificial diet, making them a model organism of the butterfly world. In this paper, a manipulation of heavy metal exposure is used to illustrate basic methods for rearing this species. The general protocol illustrates how butterflies can be caught in the field, induced to lay eggs in greenhouse cages, and transferred as larvae to artificial diets. The methods show how butterflies can be marked, measured, and studied for a variety of research questions. The representative results give an idea of how artificial diets that vary in components can be used to assess butterfly performance relative to a control diet. More specifically, butterflies were most tolerant to nickel and least tolerant to copper, with a tolerance of zinc somewhere in the middle. Possible explanations for these results are discussed, including nickel hyper-accumulation in some mustard host plants and recent evidence in insects that copper may be more toxic than previously appreciated. Finally, the discussion first reviews variations to the protocol and directions for troubleshooting these methods, before considering how future research might further optimize the artificial diet used in this study. Overall, by providing a detailed video overview of the rearing and measurement of cabbage whites on artificial diets, this protocol provides a resource for using this system across a wide range of studies.

Overview 
Artificial diet can be used to raise cabbage white butterflies in standard conditions to test the effects of certain diet ingredients on butterfly performance. In the present work, artificial diets were used to study the toxicity of different metals found in host plants growing in polluted areas (Figure 1). Larvae were raised on diets containing increasing concentrations of three different metals (Figure 2; specific methodological details presented in section 6 of the protocol). Butterfly survival and development were more impacted by copper and zinc and least impacted by nickel (Figure 3 and Figure 4), with a sensitivity comparable to other studies with butterflies and moths raised on artificial diets (Figure 5).
Survival 
Butterfly larvae were transferred to artificial diets containing copper, nickel, zinc, or control, where each metal type varied in concentration at three levels (Table 3). A representative image of larvae at an increasing dosage of toxin is shown in Figure 2. There was no effect of metal concentration on survival for nickel, but there was a significant effect for both copper and zinc (Table 3 and Figure 3). Post-hoc chi-square comparisons demonstrated that zinc showed a decline in survival relative to the control diet at only the highest level of zinc (1,000 ppm, post-hoc comparison X12 = 8.41, p = 0.004; Figure 1). Copper also showed a significant decline in survival only at the highest levels used (500 ppm, X12 = 7.00, p = 0.008), although there was a non-significant beneficial increase in survival at the two lowest levels (50 ppm and 100 ppm; Figure 3).
Development time 
There was a significant effect of copper and zinc concentration on development time (Table 4 and Figure 4). As copper concentration increased, there was an increase in development time, with a significant deviation from the control starting at 50 ppm (p = 0.027; Figure 3). As zinc concentration increased, there was an increase in development time, with a significant deviation from the control starting at 100 ppm (p = 0.03; Figure 4). There was a trend for increasing nickel to result in longer developmental times (p = 0.08; Table 4), and comparisons of each diet with the control showed significant effects starting at 100 ppm (p = 0.022; Figure 4).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/65383/65383fig01.jpg" /> 
Figure 1: Observed levels of focal metals in butterfly tissue and host plants. (Data from62.)&#160;Levels of copper, nickel, and zinc are shown for Pieris butterfly tissue (reared on bok choy in the lab) and wild-collected mustards (Bertorea sp.). Cars indicate the levels seen in plant leaves along high-traffic roads53. The levels of metals in artificial diets used in this study are reported in Table 1; points represent means, and error bars represent standard error. <a href="https://www.jove.com/files/ftp_upload/65383/65383fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/65383/65383fig02.jpg" /> 
Figure 2:&#160;Image of cabbage white larvae transferred on the same day to artificial diets of increasing concentration of a toxin. This image shows larvae from a dose-response study (presented in 28 using dried plant material for the toxic plant Aristolochia). Photo by ESR. <a href="https://www.jove.com/files/ftp_upload/65383/65383fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/65383/65383fig03.jpg" /> 
Figure 3: Variation in survival across metal diets of increasing concentrations. Asterisks indicate significant deviation in survival relative to the control diet. The exact metal concentrations in the diets are listed in Table 2. <a href="https://www.jove.com/files/ftp_upload/65383/65383fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/65383/65383fig04.jpg" /> 
Figure 4: Effects of metal concentration on development time. The asterisks indicate the lowest metal concentration for which there is a significant difference relative to the control (using a t-test). The exact metal concentrations in the diets are listed in Table 2. Points represent means, and error bars represent standard error. <a href="https://www.jove.com/files/ftp_upload/65383/65383fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/65383/65383fig05.jpg" /> 
Figure 5: Summary of metal tolerance in other Lepidoptera. Shown are composite survival data plotted from 11 existing studies49,50,51,56,63,64,65,66,67,68. The response variable is the level (in ppm) of metal concentration where negative effects on survival are first seen. Butterflies indicate results from this study, noting that the tolerance values for nickel were higher than those measured in this study. Points represent means, and error bars represent standard error. <a href="https://www.jove.com/files/ftp_upload/65383/65383fig05large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Ingredient</td>
			<td>Weigh as</td>
			<td>g</td>
			<td>mL</td>
		</tr>
		<tr>
			<td>Wheat Germ</td>
			<td>dry ingredients</td>
			<td>50</td>
			<td></td>
		</tr>
		<tr>
			<td>Cellulose</td>
			<td>dry ingredients</td>
			<td>10</td>
			<td></td>
		</tr>
		<tr>
			<td>Cabbage flour</td>
			<td>dry ingredients</td>
			<td>15</td>
			<td></td>
		</tr>
		<tr>
			<td>Casein</td>
			<td>dry ingredients</td>
			<td>27</td>
			<td></td>
		</tr>
		<tr>
			<td>Sucrose</td>
			<td>dry ingredients</td>
			<td>24</td>
			<td></td>
		</tr>
		<tr>
			<td>Wesson Salt Mix</td>
			<td>dry ingredients</td>
			<td>9</td>
			<td></td>
		</tr>
		<tr>
			<td>Torula Yeast</td>
			<td>dry ingredients</td>
			<td>12</td>
			<td></td>
		</tr>
		<tr>
			<td>Cholesterol</td>
			<td>dry ingredients</td>
			<td>3.6</td>
			<td></td>
		</tr>
		<tr>
			<td>Vitamin Mix</td>
			<td>dry ingredients</td>
			<td>10.5</td>
			<td></td>
		</tr>
		<tr>
			<td>Methyl Paraben</td>
			<td>dry ingredients</td>
			<td>0.75</td>
			<td></td>
		</tr>
		<tr>
			<td>Sorbic Acid</td>
			<td>dry ingredients</td>
			<td>1.5</td>
			<td></td>
		</tr>
		<tr>
			<td>Ascorbic Acid</td>
			<td>dry ingredients</td>
			<td>3</td>
			<td></td>
		</tr>
		<tr>
			<td>Streptomycin</td>
			<td>dry ingredients</td>
			<td>0.175</td>
			<td></td>
		</tr>
		<tr>
			<td>Flaxseed oil</td>
			<td>wet ingredients</td>
			<td></td>
			<td>5</td>
		</tr>
		<tr>
			<td>Agar&#160;</td>
			<td>agar</td>
			<td>15</td>
			<td></td>
		</tr>
	</tbody>
</table>
Table 1: Recipe for artificial diet. Shown are the weights (and volumes) of ingredients in one batch of cabbage white butterfly diet. The dry ingredients (and flaxseed oil) are prepared separately from the agar mixture (dissolved in 400 mL of boiling water, then brought to a cooler temperature with 400 mL of room temperature water).
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Diet type</td>
			<td>Copper (ppm)</td>
			<td>Nickel (ppm)</td>
			<td>Zinc (ppm)</td>
		</tr>
		<tr>
			<td>Copper-&#8220;100 ppm&#8221;</td>
			<td>96.1</td>
			<td>1.75</td>
			<td>69.9</td>
		</tr>
		<tr>
			<td>Nickel-&#8220;100 ppm&#8221;</td>
			<td>7.29</td>
			<td>109.6</td>
			<td>68.9</td>
		</tr>
		<tr>
			<td>Zinc-&#8220;100 ppm&#8221;</td>
			<td>7.96</td>
			<td>1.06</td>
			<td>186.2</td>
		</tr>
		<tr>
			<td>Zinc-&#8220;500 ppm&#8221;</td>
			<td>6.51</td>
			<td>1.16</td>
			<td>708</td>
		</tr>
		<tr>
			<td>Control</td>
			<td>5.89</td>
			<td>0.59</td>
			<td>59.3</td>
		</tr>
	</tbody>
</table>
Table 2: Measures of metals in diets. Shown are the mean levels of copper, nickel, and zinc in a subset of the artificial diets used in the study. The diet name (&#34;type&#34; in the analysis) is shown on the left, with values in quotes being the calculated level. The target concentration is shown in quotation marks. A subset of diets used in the study was analyzed to ensure the calculated values were on target with realized values; it should be noted that there is often some small degree of variation in the composition of diet components, and each line reported represents only one replicate.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Metal</td>
			<td>Pearson X32</td>
			<td>P</td>
		</tr>
		<tr>
			<td>Copper (N = 118)</td>
			<td>17.82</td>
			<td>0.0005</td>
		</tr>
		<tr>
			<td>Nickel (N = 152)</td>
			<td>3.45</td>
			<td>0.33</td>
		</tr>
		<tr>
			<td>Zinc (N = 152)</td>
			<td>12.52</td>
			<td>0.006</td>
		</tr>
	</tbody>
</table>
Table 3: Effects of metal concentration on survival. Shown are the results of a chi-square test for each metal, contrasting three concentrations of metal relative to a control diet.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Metal</td>
			<td>F</td>
			<td>P</td>
		</tr>
		<tr>
			<td>Copper (N = 61)</td>
			<td>F3,57 = 9.84</td>
			<td>&#60;0.0001</td>
		</tr>
		<tr>
			<td>Nickel (N = 75)</td>
			<td>F3,71 = 2.35</td>
			<td>0.079</td>
		</tr>
		<tr>
			<td>Zinc (N = 64)</td>
			<td>F3,60 = 3.79</td>
			<td>0.015</td>
		</tr>
	</tbody>
</table>
Table 4: Effects of metal concentration on development time. Shown are the results of individual ANOVAs for each metal.
Data Availability:
All data are available on Mendeley61.

Watch this Scientific Journal Video about Investigating the Tolerance of Cabbage Butterflies to Urban Pollutants at JoVE.com

Author Spotlight: Investigating the Tolerance of Cabbage Butterflies to Urban Pollutants 

This paper presents a detailed protocol for rearing the cabbage white butterfly in controlled lab conditions with an artificial diet, which allows precise manipulations of early-life nutrition and toxin exposure. The representative results show how heavy metal toxicity can be assayed with this protocol.

Rearing the Cabbage White Butterfly (Pieris rapae) in Controlled Conditions: A Case Study with Heavy Metal Tolerance

The cabbage white butterfly (Pieris rapae) is an important system for applied pest control research and basic research in behavioral and nutritional ...

rearing-cabbage-white-butterfly-pieris-rapae-controlled-conditions

Research

JoVE Journal

Biology

3.2K Views.  University of Minnesota. This paper presents a detailed protocol for rearing the cabbage white butterfly in controlled lab conditions with an artificial diet, which allows precise manipulations of early-life nutrition and toxin exposure. The representative results show how heavy metal toxicity can be assayed with this protocol.

Video: Author Spotlight: Investigating the Tolerance of Cabbage Butterflies to Urban Pollutants 

Testing Visual Sensitivity to the Speed and Direction of Motion in Lizards

Testing visual sensitivity in any species provides basic information regarding behaviour, evolution, and ecology. However, testing specific features of the visual system provide more empirical evidence for functional applications. Investigation into the sensory system provides information about the sensory capacity, learning and memory ability, and establishes known baseline behaviour in which to gauge deviations (Burghardt, 1977). However, unlike mammalian or avian systems, testing for learning and memory in a reptile species is difficult. Furthermore, using an operant paradigm as a psychophysical measure of sensory ability is likewise as difficult. Historically, reptilian species have responded poorly to conditioning trials because of issues related to motivation, physiology, metabolism, and basic biological characteristics. Here, I demonstrate an operant paradigm used a novel model lizard species, the Jacky dragon (Amphibolurus muricatus) and describe how to test peripheral sensitivity to salient speed and motion characteristics. This method uses an innovative approach to assessing learning and sensory capacity in lizards. I employ the use of random-dot kinematograms (RDKs) to measure sensitivity to speed, and manipulate the level of signal strength by changing the proportion of dots moving in a coherent direction. RDKs do not represent a biologically meaningful stimulus, engages the visual system, and is a classic psychophysical tool used to measure sensitivity in humans and other animals. Here, RDKs are displayed to lizards using three video playback systems. Lizards are to select the direction (left or right) in which they perceive dots to be moving. Selection of the appropriate direction is reinforced by biologically important prey stimuli, simulated by computer-animated invertebrates.

Testing visual sensitivity in lizards using an operant conditioning paradigm that employs video playback of random-dot kinematograms and computer-generated invertebrates.

Testing visual sensitivity in any species provides basic information regarding behaviour, evolution, and ecology. However, testing specific features of ...

Computer-Generated Animal Model Stimuli

Communication between animals is diverse and complex. Animals may communicate using auditory, seismic, chemosensory, electrical, or visual signals. In particular, understanding the constraints on visual signal design for communication has been of great interest. Traditional methods for investigating animal interactions have used basic observational techniques, staged encounters, or physical manipulation of morphology. Less intrusive methods have tried to simulate conspecifics using crude playback tools, such as mirrors, still images, or models. As technology has become more advanced, video playback has emerged as another tool in which to examine visual communication (Rosenthal, 2000). However, to move one step further, the application of computer-animation now allows researchers to specifically isolate critical components necessary to elicit social responses from conspecifics, and manipulate these features to control interactions. Here, I provide detail on how to create an animation using the Jacky dragon as a model, but this process may be adaptable for other species. In building the animation, I elected to use Lightwave  3D to alter object morphology, add texture, install bones, and provide comparable weight shading that prevents exaggerated movement. The animation is then matched to select motor patterns to replicate critical movement features. Finally, the sequence must rendered into an individual clip for presentation. Although there are other adaptable techniques, this particular method had been demonstrated to be effective in eliciting both conspicuous and social responses in staged interactions.

Computer-generated stimuli using the Jacky dragon as a model.

Communication between animals is diverse and complex. Animals may communicate using auditory, seismic, chemosensory, electrical, or visual signals. In ...

Surgical Induction of Endolymphatic Hydrops by Obliteration of the Endolymphatic Duct

Surgical induction of endolymphatic hydrops (ELH) in the guinea pig by obliteration and obstruction of the endolymphatic duct is a well-accepted animal model of the condition and an important correlate for human Meniere's disease. In 1965, Robert Kimura and Harold Schuknecht first described an intradural approach for obstruction of the endolymphatic duct (Kimura 1965). Although effective, this technique, which requires penetration of the brain's protective covering, incurred an undesirable level of morbidity and mortality in the animal subjects. Consequently, Andrews and Bohmer developed an extradural approach, which predictably produces fewer of the complications associated with central nervous system (CNS) penetration.(Andrews and Bohmer 1989) 
The extradural approach described here first requires a midline incision in the region of the occiput to expose the underlying muscular layer. We operate only on the right side. After appropriate retraction of the overlying tissue, a horizontal incision is made into the musculature of the right occiput to expose the right temporo-occipital suture line. The bone immediately inferio-lateral the suture line (Fig 1) is then drilled with an otologic drill until the sigmoid sinus becomes visible. Medial retraction of the sigmoid sinus reveals the operculum of the endolymphatic duct, which houses the endolymphatic sac. Drilling medial to the operculum into the area of the endolymphatic sac reveals the endolymphatic duct, which is then packed with bone wax to produce obstruction and ultimately ELH. 
In the following weeks, the animal will demonstrate the progressive, fluctuating hearing loss and histologic evidence of ELH.

This video shows how to surgically obstruct the guinea pig's endolymphatic duct to produce endolymphatic hydrops.

Surgical induction of endolymphatic hydrops (ELH) in the guinea pig by obliteration and obstruction of the endolymphatic duct is a well-accepted animal ...

Do-It-Yourself Device for Recovery of Cryopreserved Samples Accidentally Dropped into Cryogenic Storage Tanks

Liquid nitrogen is colorless, odorless, extremely cold (-196 &deg;C) liquid kept under pressure. It is commonly used as a cryogenic fluid for long term storage of biological materials such as blood, cells and tissues 1,2. The cryogenic nature of liquid nitrogen, while ideal for sample preservation, can cause rapid freezing of live tissues on contact - known as 'cryogenic burn'2, which may lead to severe frostbite in persons closely involved in storage and retrieval of samples from Dewars. Additionally, as liquid nitrogen evaporates it reduces the oxygen concentration in the air and might cause asphyxia, especially in confined spaces2.
In laboratories, biological samples are often stored in cryovials or cryoboxes stacked in stainless steel racks within the Dewar tanks1. These storage racks are provided with a long shaft to prevent boxes from slipping out from the racks and into the bottom of Dewars during routine handling. All too often, however, boxes or vials with precious samples slip out and sink to the bottom of liquid nitrogen filled tank. In such cases, samples could be tediously retrieved after transferring the liquid nitrogen into a spare container or discarding it. The boxes and vials can then be relatively safely recovered from emptied Dewar. However, the cryogenic nature of liquid nitrogen and its expansion rate makes sunken sample retrieval hazardous. It is commonly recommended by Safety Offices that sample retrieval be never carried out by a single person. Another alternative is to use commercially available cool grabbers or tongs to pull out the vials3. However, limited visibility within the dark liquid filled Dewars poses a major limitation in their use.
In this article, we describe the construction of a Cryotolerant DIY retrieval device, which makes sample retrieval from Dewar containing cryogenic fluids both safe and easy.

Here we present a low cost, durable cryotolerant device for sample retrieval from Dewar tanks filled with liquid nitrogen. The ease of construction and modular design of the device makes the process of sample retrieval from cryogenic tanks safe and easy.

Liquid nitrogen is colorless, odorless, extremely cold (-196 &deg;C) liquid kept under pressure. It is commonly used as a cryogenic fluid for long term ...

Flow Cytometry-based Purification of S. cerevisiae Zygotes

Zygotes are essential intermediates between haploid and diploid states in the life cycle of many organisms, including yeast (Figure 1) 1. S. cerevisiae zygotes result from the fusion of haploid cells of distinct mating type (MATa, MATalpha) and give rise to corresponding stable diploids that successively generate as many as 20 diploid progeny as a result of their strikingly asymmetric mitotic divisions 2. Zygote formation is orchestrated by a complex sequence of events: In this process, soluble mating factors bind to cognate receptors, triggering receptor-mediated signaling cascades that facilitate interruption of the cell cycle and culminate in cell-cell fusion. Zygotes may be considered a model for progenitor or stem cell function.
Although much has been learned about the formation of zygotes and although zygotes have been used to investigate cell-molecular questions of general significance, almost all studies have made use of mating mixtures in which zygotes are intermixed with a majority population of haploid cells 3-8. Many aspects of the biochemistry of zygote formation and the continuing life of the zygote therefore remain uninvestigated.
Reports of purification of yeast zygotes describe protocols based on their sedimentation properties 9; however, this sedimentation-based procedure did not yield nearly 90% purity in our hands. Moreover, it has the disadvantage that cells are exposed to hypertonic sorbitol. We therefore have developed a versatile purification procedure. For this purpose, pairs of haploid cells expressing red or green fluorescent proteins were co-incubated to allow zygote formation, harvested at various times, and the resulting zygotes were purified using a flow cytometry-based sorting protocol. This technique provides a convenient visual assessment of purity and maturation. The average purity of the fraction is approximately 90%. According to the timing of harvest, zygotes of varying degrees of maturity can be recovered. The purified samples provide a convenient point of departure for "-omic" studies, for recovery of initial progeny, and for systematic investigation of this progenitor cell.

Flow Cytometry-based Purification of S. cerevisiae Zygotes

To purify zygotes of S. cerevisiae, haploid cells of opposite mating type were engineered to express red or green fluorescent proteins, co-incubated to allow zygote formation, and fractionated using a flow cytometry-based protocol. The highly-enriched fraction enables subsequent "-omic" studies, recovery of initial progeny, and systematic investigation of zygote morphogenesis.

Zygotes are essential intermediates between haploid and diploid states in the life cycle of many organisms, including yeast (Figure 1) 1. S. cerevisiae ...

Using Caenorhabditis elegans as a Model System to Study Protein Homeostasis in a Multicellular Organism

The folding and assembly of proteins is essential for protein function, the long-term health of the cell, and longevity of the organism. Historically, the function and regulation of protein folding was studied in vitro, in isolated tissue culture cells and in unicellular organisms. Recent studies have uncovered links between protein homeostasis (proteostasis), metabolism, development, aging, and temperature-sensing. These findings have led to the development of new tools for monitoring protein folding in the model metazoan organism Caenorhabditis elegans. In our laboratory, we combine behavioral assays, imaging and biochemical approaches using temperature-sensitive or naturally occurring metastable proteins as sensors of the folding environment to monitor protein misfolding. Behavioral assays that are associated with the misfolding of a specific protein provide a simple and powerful readout for protein folding, allowing for the fast screening of genes and conditions that modulate folding. Likewise, such misfolding can be associated with protein mislocalization in the cell. Monitoring protein localization can, therefore, highlight changes in cellular folding capacity occurring in different tissues, at various stages of development and in the face of changing conditions. Finally, using biochemical tools ex vivo, we can directly monitor protein stability and conformation. Thus, by combining behavioral assays, imaging and biochemical techniques, we are able to monitor protein misfolding at the resolution of the organism, the cell, and the protein, respectively.

Using Caenorhabditis elegans as a Model System to Study Protein Homeostasis in a Multicellular Organism

To study the relationship between protein homeostasis, stress and aging, we monitored changes in protein folding by following protein dysfunction, protein localization in the cell and protein stability at the organismal, cellular and protein levels, using the genetically tractable metazoan Caenorhabditis elegans as a model system.

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Floral-Dip Transformation of Flax (Linum usitatissimum) to Generate Transgenic Progenies with a High Transformation Rate

Agrobacterium-mediated plant transformation via floral-dip is a widely used technique in the field of plant transformation and has been reported to be successful for many plant species. However, flax (Linum usitatissimum) transformation by floral-dip has not been reported. The goal of this protocol is to establish that Agrobacterium and the floral-dip method can be used to generate transgenic flax. We show that this technique is simple, inexpensive, efficient, and more importantly, gives a higher transformation rate than the current available methods of flax transformation.
In summary, inflorescences of flax were dipped in a solution of Agrobacterium carrying a binary vector plasmid (T-DNA fragment plus the Linum Insertion Sequence, LIS-1) for 1 - 2 min. The plants were laid flat on their side for 24 hr. Then, plants were maintained under normal growth conditions until the next treatment. The process of dipping was repeated 2 - 3 times, with approximately 10 - 14 day intervals between dipping. The T1 seeds were collected and germinated on soil. After approximately two weeks, treated progenies were tested by direct PCR; 2 - 3 leaves were used per plant plus the appropriate T-DNA primers. Positive transformants were selected and grown to maturity. The transformation rate was unexpectedly high, with 50 - 60% of the seeds from treated plants being positive transformants. This is a higher transformation rate than those reported for Arabidopsis thaliana and other plant species, using floral-dip transformation. It is also the highest, which has been reported so far, for flax transformation using other methods for transformation.

Floral-Dip Transformation of Flax Linum usitatissimum to Generate Transgenic Progenies with a High Transformation Rate

Here, we present a protocol to transform flax using Agrobacterium-mediated plant transformation via floral-dip. This protocol is simple to perform and inexpensive, yet yields a higher transformation rate than the current available methods for flax transformation.

Agrobacterium-mediated plant transformation via floral-dip is a widely used technique in the field of plant transformation and has been reported to be ...

Determining Membrane Protein Topology Using Fluorescence Protease Protection (FPP)

The correct topology and orientation of integral membrane proteins are essential for their proper function, yet such information has not been established for many membrane proteins. A simple technique called fluorescence protease protection (FPP) is presented, which permits the determination of membrane protein topology in living cells. This technique has numerous advantages over other methods for determining protein topology, in that it does not require the availability of multiple antibodies against various domains of the membrane protein, does not require large amounts of protein, and can be performed on living cells. The FPP method employs the spatially confined actions of proteases on the degradation of green fluorescent protein (GFP) tagged membrane proteins to determine their membrane topology and orientation. This simple approach is applicable to a wide variety of cell types, and can be used to determine membrane protein orientation in various subcellular organelles such as the mitochondria, Golgi, endoplasmic reticulum and components of the endosomal/recycling system. Membrane proteins, tagged on either the N-termini or C-termini with a GFP fusion, are expressed in a cell of interest, which is subject to selective permeabilization using the detergent digitonin. Digitonin has the ability to permeabilize the plasma membrane, while leaving intracellular organelles intact. GFP moieties exposed to the cytosol can be selectively degraded through the application of protease, whereas GFP moieties present in the lumen of organelles are protected from the protease and remain intact. The FPP assay is straightforward, and results can be obtained rapidly.

Determining Membrane Protein Topology Using Fluorescence Protease Protection FPP

Here, we present a protocol to determine the orientation and topology of integral membrane proteins in living cells. This simple protocol relies on selective protease sensitivity of chimeras between the protein of interest and GFP.

The correct topology and orientation of integral membrane proteins are essential for their proper function, yet such information has not been established ...

Genetic and Biochemical Approaches for In Vivo and In Vitro Assessment of Protein Oligomerization: The Ryanodine Receptor Case Study

Oligomerization is often a structural requirement for proteins to accomplish their specific cellular function. For instance, tetramerization of the ryanodine receptor (RyR) is necessary for the formation of a functional Ca2+ release channel pore. Here, we describe detailed protocols for the assessment of protein self-association, including yeast two-hybrid (Y2H), co-immunoprecipitation (co-IP) and chemical cross-linking assays. In the Y2H system, protein self-interaction is detected by &#946;-galactosidase assay in yeast co-expressing GAL4 bait and target fusions of the test protein. Protein self-interaction is further assessed by co-IP using HA- and cMyc-tagged fusions of the test protein co-expressed in mammalian HEK293 cells. The precise stoichiometry of the protein homo-oligomer is examined by cross-linking and SDS-PAGE analysis following expression in HEK293 cells. Using these different but complementary techniques, we have consistently observed the self-association of the RyR N-terminal domain and demonstrated its intrinsic ability to form tetramers. These methods can be applied to protein-protein interaction and homo-oligomerization studies of other mammalian integral membrane proteins.

Genetic and Biochemical Approaches for In Vivo and In Vitro Assessment of Protein Oligomerization: The Ryanodine Receptor Case Study

Oligomerization of the ryanodine receptor, a homo-tetrameric ion channel mediating Ca2+ release from intracellular stores, is critical for skeletal and cardiac muscle contraction. Here, we present complementary in vivo and in vitro methods to detect protein self-association and determine homo-oligomer stoichiometry.

Oligomerization is often a structural requirement for proteins to accomplish their specific cellular function. For instance, tetramerization of the ...

The Assembly and Application of 'Shear Rings': A Novel Endothelial Model for Orbital, Unidirectional and Periodic Fluid Flow and Shear Stress

Deviations from normal levels and patterns of vascular fluid shear play important roles in vascular physiology and pathophysiology by inducing adaptive as well as pathological changes in endothelial phenotype and gene expression. In particular, maladaptive effects of periodic, unidirectional flow induced shear stress can trigger a variety of effects on several vascular cell types, particularly endothelial cells. While by now endothelial cells from diverse anatomic origins have been cultured, in-depth analyses of their responses to fluid shear have been hampered by the relative complexity of shear models (e.g., parallel plate flow chamber, cone and plate flow model). While these all represent excellent approaches, such models are technically complicated and suffer from drawbacks including relatively lengthy and complex setup time, low surface areas, requirements for pumps and pressurization often requiring sealants and gaskets, creating challenges to both maintenance of sterility and an inability to run multiple experiments. However, if higher throughput models of flow and shear were available, greater progress on vascular endothelial shear responses, particularly periodic shear research at the molecular level, might be more rapidly advanced. Here, we describe the construction and use of shear rings: a novel, simple-to-assemble, and inexpensive tissue culture model with a relatively large surface area that easily allows for a high number of experimental replicates in unidirectional, periodic shear stress studies on endothelial cells.

Different levels and patterns of fluid shear are known to modulate endothelial gene expression, phenotype and susceptibility to disease. We discuss the assembly and use of 'shear rings': a model that produces unidirectional, periodic shear stress patterns. Shear rings are simple to assemble, economical and can produce high cell yields.

Deviations from normal levels and patterns of vascular fluid shear play important roles in vascular physiology and pathophysiology by inducing adaptive as ...