Funding was provided by the US National Science Foundation (NSF OCE&#160;2023420 and DEB 2231250, P. Sikkel PI). We thank the municipality of Dumaguete City, Negros Oriental, Philippines, for permission to conduct this study. We also thank the many volunteers for their field assistance and the staff and our colleagues at the Silliman University Institute for Environmental and Marine Sciences for their support.

Collection of samples was permitted by the Department of Agriculture-Bureau of Fisheries and Aquatic Resources (0154-18 DA-BFAR) in accordance with Philippine laws and regulations (RA 9147; FAO 233) and approved by the Silliman University (SU) animal ethics committee.
1. Light Traps
<ol>
	<li>Construction
	<ol>
		<li>Construct light traps from commercial polyvinyl chloride (PVC) tubes originally designed for plumbing. Use 10-15&#160;cm diameter PVC cut to 30-40 cm length (Figure 1).</li>
		<li>To both ends of the tubes, add PVC &#34;caps&#34; with a transparent acrylic funnel inserted in the center of the opening and glue in place with transparent epoxy glue (Figure 1). Let it dry.</li>
		<li>Ensure that one end of the tube has a screw-on or otherwise removable lid and that both ends are water-tight when the trap is &#34;closed&#34; (e.g., with the addition of an O-ring).</li>
	</ol>
	</li>
	<li>Light source
	<ol>
		<li>Before deployment, turn on an underwater light/torch (see Table of Materials) and place it in the tube, facing one of the transparent funnels, such that the light from the underwater torch illuminates the area in front of one side of the tube. If necessary, chemical glow sticks can be used in place of underwater torches, although their light intensity is lower. 
		NOTE: The light attracts a variety of small nocturnal organisms31, including gnathiids, and drives them to swim into the tube through the clear funnel. Once they have entered the tube, they are unable to escape due to the geometry of the light trap (small funnel opening) and the continued presence of a light source.</li>
	</ol>
	</li>
	<li>Placement
	<ol>
		<li>When in the water at the deployment site, fill light traps, with the light turned on, with seawater, and secure both ends. To ensure that the torch is not below or blocking the funnel tip, tilt the &#34;front&#34; of the tube upward to allow the torch to slide back away from the funnel.</li>
		<li>Place traps on the seafloor, in the sand or rubble, next to coral heads or other complex structures known to attract fish. Focus the light cone &#34;inwards&#34;, towards areas where fish aggregate. 
		NOTE: In shallow water, traps can be placed by breath-hold diving. Deeper deployment requires scuba.</li>
	</ol>
	</li>
	<li>Retrieval
	<ol>
		<li>Immediately prior to retrieving the trap, seal the openings of both the funnels (on either end of the tube) with a piece of modeling clay or rubber stopper sealing, keeping all the seawater and the contained organisms inside. 
		NOTE: The organisms will remain in the trap once the batteries of the lights have expired and the light is no longer illuminated. This provides flexibility when the traps are retrieved (&#34;soak time&#34;). Factors to consider when deciding on soak time are presented below (see Discussion).</li>
	</ol>
	</li>
	<li>Transport
	<ol>
		<li>Once the traps have been retrieved from the bottom, carry them to a boat, or swim ashore.</li>
		<li>Maintain traps close to ambient seawater temperature once removed from the ocean.</li>
		<li>Transport them to the laboratory for processing as soon as possible since no gas or water exchange will take place once removed from the ocean.</li>
	</ol>
	</li>
</ol>
2 Laboratory processing
<ol>
	<li>Storing and filtering of the samples
	<ol>
		<li>Once the light traps are removed from the ocean and brought back to the lab, empty their contents into buckets with fresh seawater.</li>
		<li>Add aeration to keep organisms alive until filtering.</li>
		<li>Filter the contents of the bucket by pouring through a funnel lined with 50-100 &#181;m plankton mesh, then empty the contents into a 100 mL container of fresh seawater.</li>
		<li>Use a pipette to draw from this smaller container to place aliquots of the sample into a Petri dish for microscopy. Repeat until the entire sample has been processed.</li>
	</ol>
	</li>
	<li>Gnathiid isopod identification and rearing
	<ol>
		<li>Because light trap samples attract multiple species of small invertebrates, carefully screen the samples to identify and remove gnathiid isopods. 10-20x magnification is the best for this task (Figure 2). 
		NOTE: Identifying gnathiids at the family level does not require living specimens. However, adult gnathiids, which are seldom caught in light traps, are needed for morphological species identification and breeding (see reference1,3,9 for a methodology for breeding and rearing gnathiids in captivity).</li>
		<li>In cases where gnathiids need to be kept alive for rearing, gently remove them with a pipette and place them in small plastic containers of fresh seawater.</li>
	</ol>
	</li>
</ol>

<ol>
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A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=First+record+and+molecular+characterisation+of+two+Gnathia+species+(Crustacea,+Isopoda,+Gnathiidae)+from+Philippine+coral+reefs,+including+a+summary+of+all+Central-Indo+Pacific+Gnathia+species.">First record and molecular characterisation of two Gnathia species (Crustacea, Isopoda, Gnathiidae) from Philippine coral reefs, including a summary of all Central-Indo Pacific Gnathia species.</a> International Journal for Parasitology: Parasites and Wildlife. 14, 355-367 (2021).</li><li>Losey, G. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cleaning+symbiosis+in+Puerto+Rico+with+comparison+to+the+tropical+Pacific.">Cleaning symbiosis in Puerto Rico with comparison to the tropical Pacific.</a> 4 (4), 960-970 (1974).</li><li>Grutter, A. 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J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+curious+life-style+of+the+parasitic+stages+of+gnathiid+isopods.">The curious life-style of the parasitic stages of gnathiid isopods.</a> Advances in Parasitology. 58. , 289-391 (2004).</li><li>Tanaka, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Life+history+of+gnathiid+isopods-current+knowledge+and+future+directions.">Life history of gnathiid isopods-current knowledge and future directions.</a> Plankton and Benthos Research. 2 (1), 1-11 (2007).</li><li>Sikkel, P. C., Schaumburg, C. S., Mathenia, J. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Diel+infestation+dynamics+of+gnathiid+isopod+larvae+parasitic+on+Caribbean+reef+fish.">Diel infestation dynamics of gnathiid isopod larvae parasitic on Caribbean reef fish.</a> Coral Reefs. 25, 683-689 (2006).</li><li>Santos, T. R. N., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Habitat+associations+of+fish-parasitic+gnathiid+isopods+in+a+shallow+reef+system+in+the+central+Philippines.">Habitat associations of fish-parasitic gnathiid isopods in a shallow reef system in the central Philippines.</a> Marine Biodiversity. 4, 83-96 (2019).</li><li>Nagel, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+role+of+vision+in+host-finding+behaviour+of+the+ectoparasite+Gnathia+falcipenis+(Crustacea).">The role of vision in host-finding behaviour of the ectoparasite Gnathia falcipenis (Crustacea).</a> Isopoda). Marine and Freshwater Behaviour and Physiology. 42 (1), 31-42 (2009).</li><li>Sikkel, P. C., Sears, W. T., Weldon, B., Tuttle, B. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+experimental+field+test+of+host-finding+mechanisms+in+a+Caribbean+gnathiid+isopod.">An experimental field test of host-finding mechanisms in a Caribbean gnathiid isopod.</a> Marine Biology. 158, 1075-1083 (2011).</li><li>Vondriska, C., Dixson, D. L., Packard, A. J., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differentially+susceptible+host+fishes+exhibit+similar+chemo-attractiveness+to+a+common+coral+reef+ectoparasite.">Differentially susceptible host fishes exhibit similar chemo-attractiveness to a common coral reef ectoparasite.</a> Symbiosis. 81 (3), 247-253 (2020).</li><li>Grutter, A. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Parasite+infection+rather+than+tactile+stimulation+is+the+proximate+cause+of+cleaning+behaviour+in+reef+fish.">Parasite infection rather than tactile stimulation is the proximate cause of cleaning behaviour in reef fish.</a> Proceedings of the Royal Society of London. Series B: Biological Sciences. 268 (1474), 1361-1365 (2001).</li><li>Sikkel, P. C., Cheney, K. L., C&#244;t&#233;, I. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+situ+evidence+for+ectoparasites+as+a+proximate+cause+of+cleaning+interactions+in+reef+fish.">In situ evidence for ectoparasites as a proximate cause of cleaning interactions in reef fish.</a> Animal Behaviour. 68 (2), 241-247 (2004).</li><li>Sikkel, P. C., Herzlieb, S. E., Kramer, D. 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J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Unexpected+response+of+a+captive+blackeye+thicklip,+Hemigymnus+melapterus+(Bloch),+from+Lizard+Island,+Australia,+exposed+to+juvenile+isopods+Gnathia+aureamaculosa+Ferreira+&amp;+Smit.">Unexpected response of a captive blackeye thicklip, Hemigymnus melapterus (Bloch), from Lizard Island, Australia, exposed to juvenile isopods Gnathia aureamaculosa Ferreira &amp; Smit.</a> Journal of Fish Diseases. 34 (7), 563-566 (2011).</li><li>Grutter, A. S., Pickering, J. L., McCallum, H., McCormick, M. I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Impact+of+micropredatory+gnathiid+isopods+on+young+coral+reef+fishes.">Impact of micropredatory gnathiid isopods on young coral reef fishes.</a> Coral Reefs. 27 (3), 655-661 (2008).</li><li>Artim, J. M., Sellers, J. C., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Micropredation+by+gnathiid+isopods+on+settlement-stage+reef+fish+in+the+eastern+Caribbean+Sea.">Micropredation by gnathiid isopods on settlement-stage reef fish in the eastern Caribbean Sea.</a> Bulletin of Marine Science. 91 (4), 479-487 (2015).</li><li>Sellers, J. C., Holstein, D. M., Botha, T. L., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Lethal+and+sublethal+impacts+of+a+micropredator+on+post-settlement+Caribbean+reef+fishes.">Lethal and sublethal impacts of a micropredator on post-settlement Caribbean reef fishes.</a> Oecologia. 189, 293-305 (2019).</li><li>Allan, B. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Parasite+infection+directly+impacts+escape+response+and+stress+levels+in+fish.">Parasite infection directly impacts escape response and stress levels in fish.</a> Journal of Experimental Biology. 223 (16), (2020).</li><li>Spitzer, C. A., Anderson, T. W., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Habitat+associations+and+impacts+on+a+juvenile+fish+host+by+a+temperate+gnathiid+isopod.">Habitat associations and impacts on a juvenile fish host by a temperate gnathiid isopod.</a> International Journal for Parasitology: Parasites and Wildlife. 17, 65-73 (2022).</li><li>Sikkel, P. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nocturnal+migration+reduces+exposure+to+micropredation+in+a+coral+reef+fish.">Nocturnal migration reduces exposure to micropredation in a coral reef fish.</a> Bulletin of Marine Science. 93 (2), 475-489 (2017).</li><li>Artim, J. M., Hook, A., Grippo, R. S., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Predation+on+parasitic+gnathiid+isopods+on+coral+reefs:+a+comparison+of+Caribbean+cleaning+gobies+with+non-cleaning+microcarnivores.">Predation on parasitic gnathiid isopods on coral reefs: a comparison of Caribbean cleaning gobies with non-cleaning microcarnivores.</a> Coral Reefs. 36, 1213-1223 (2017).</li><li>Artim, J. M., Sikkel, P. 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C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Changes+in+abundance+of+fish-parasitic+gnathiid+isopods+associated+with+warm-water+bleaching+events+on+the+northern+Great+Barrier+Reef.">Changes in abundance of fish-parasitic gnathiid isopods associated with warm-water bleaching events on the northern Great Barrier Reef.</a> Coral Reefs. 38 (4), 721-730 (2019).</li><li>Shodipo, M. O., Duong, B., Graba-Landry, A., Grutter, A. S., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effect+of+acute+seawater+temperature+increase+on+the+survival+of+a+fish+ectoparasite.">Effect of acute seawater temperature increase on the survival of a fish ectoparasite.</a> In Oceans. 1 (4), (2020).</li><li>Artim, J. M., Nicholson, M. D., Hendrick, G. C., Brandt, M., Smith, T. B., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Abundance+of+a+cryptic+generalist+parasite+reflects+degradation+of+an+ecosystem.">Abundance of a cryptic generalist parasite reflects degradation of an ecosystem.</a> Ecosphere. 11 (10), (2020).</li><li>Richardson, A. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Using+continuous+plankton+recorder+data.">Using continuous plankton recorder data.</a> Progress in Oceanography. 68 (1), 27-74 (2006).</li><li>McLeod, L. E., Costello, M. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Light+traps+for+sampling+marine+biodiversity.">Light traps for sampling marine biodiversity.</a> Helgoland Marine Research. 71 (1), 1-8 (2017).</li><li>Artim, J. M., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Comparison+of+sampling+methodologies+and+estimation+of+population+parameters+for+a+temporary+fish+ectoparasite.">Comparison of sampling methodologies and estimation of population parameters for a temporary fish ectoparasite.</a> International Journal for Parasitology: Parasites and Wildlife. 5 (2), 145-157 (2016).</li><li>Pag&#225;n, J. A., Ver&#237;ssimo, A., Sikkel, P. C., Xavier, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hurricane-induced+disturbance+increases+genetic+diversity+and+population+admixture+of+the+direct-brooding+isopod,+Gnathia+marleyi.">Hurricane-induced disturbance increases genetic diversity and population admixture of the direct-brooding isopod, Gnathia marleyi.</a> Scientific reports. 10 (1), (2020).</li><li>Doherty, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Light-traps:+selective+but+useful+devices+for+quantifying+the+distributions+and+abundances+of+larval+fishes.">Light-traps: selective but useful devices for quantifying the distributions and abundances of larval fishes.</a> Bulletin of Marine Science. 41, 423-431 (1987).</li><li>Jones, C. M., Nagel, L., Hughes, G. L., Cribb, T. H., Grutter, A. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Host+specificity+of+two+species+of+Gnathia+(Isopoda)+determined+by+DNA+sequencing+blood+meals.">Host specificity of two species of Gnathia (Isopoda) determined by DNA sequencing blood meals.</a> International Journal for Parasitology. 37 (8-9), 927-935 (2007).</li><li>Hendrick, G. C., Dolan, M. C., McKay, T., Sikkel, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Host+DNA+integrity+within+blood+meals+of+hematophagous+larval+gnathiid+isopods+(Crustacea).">Host DNA integrity within blood meals of hematophagous larval gnathiid isopods (Crustacea).</a> Isopoda, Gnathiidae). Parasites &amp; Vectors. 12 (1), 1-9 (2019).</li></ol>

The authors declare no disclosures to make.

Traditional light traps, such as those used for collecting larval fishes, are large and are suspended in water column34. In contrast, the light traps described here are small and deployed on the sea bottom. These traps can be easily transported and rapidly deployed. They can be placed by breath-hold (free)-diving in shallow sites (as in this study) or on scuba in deeper sites, and attract both fed and unfed 
juvenile stages.
Variations of the benthic light traps de...

Parasitic crustaceans are important in the ecology and life histories of reef fishes. The biomass and energy they remove from their hosts are considerable and influence behavior, physiology, and survivorship1. Gnathiid isopod crustaceans represent the most prominent group of fish parasites in tropical and subtropical reef systems, where they are both abundant and diverse2,3 and are the primary food item of cleaner fishes4,5. Gnathiids are generally 1-3 mm in size. They have unusual life histories in which only the three juvenile stages feed on the blood and body fluids of fishes6,7. They are most active at night8,9, and while vision appears to play some role, host-finding10 relies heavily on olfactory cues to find hosts11,12. Each of the three juvenile feeding stages feeds on a single host fish, with each feed separated by a molting phase. After the final feed, third-stage larvae metamorphose into non-feeding adults, which reproduce and then die. Given that feeding requires only brief association with the host, while each inter-feeding interval lasts days, gnathiids spend most of their life free-living in the benthos.
Gnathiids impact hosts in multiple ways1. Aside from their role as drivers of interactions between cleaner fish and clients13,14,15, gnathiids can increase cortisol levels and decrease hematocrit in adult fish hosts16 and in high numbers, can even cause death17. For juvenile fish, even a single gnathiid can be fatal18,19,20, and even if the fish survives, its ability to compete for space and escape predators is compromised20,21,22. Avoiding gnathiids may even constitute one of the benefits of nocturnal migration in some reef fishes23.
In addition to cleaner fishes, gnathiid populations can be impacted by other micro carnivorous fishes24, as well as corals25,26. Ocean warming and the associated loss of live corals appear to have opposing impacts on gnathiids27,28,29.
Given their clear ecological importance and the likely influence of anthropogenic environmental change on their populations, there are compelling reasons to include them in ecological studies of coral reefs. However, their unique life history and the small number of researchers who study them create a barrier to the development, implementation, and dissemination of reliable, reproducible sampling methods to collect them for research.
Light traps have long been used to collect small marine organisms at night30,31. They take advantage of and are based on the fact that many nocturnally active organisms, including arthropods, are attracted to light. Traditionally they have been used to collect planktonic organisms in the water column30. However, the basic principles can be applied to collecting free-swimming organisms that are active near the benthos. Here we present a light trapping method adapted for collecting free-living stages of gnathiid isopods near the ocean bottom in remote coral reef environments such as the Philippines. For collecting in remote areas, these light traps (Figure 1) offer some advantages over other methods developed for collecting these organisms32. They are highly portable and durable, requiring only three parts, which are easily obtainable and inexpensive. They are also negatively buoyant, as when deployed, they are completely filled with seawater. Because they depend on light for attraction, they are only effective at night for collecting nocturnally active species. They also attract more than the target species, requiring sorting of the samples under a dissecting scope to obtain the target organisms. Three methods have thus far been used by our team and collaborators to collect gnathiids in coral reef systems throughout the world32. These include emergence traps, live fish-baited traps, and light traps, each with advantages and limitations.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Buckets, small sample containers</td>
			<td></td>
			<td>hardware store</td>
			<td></td>
		</tr>
		<tr>
			<td>Funnels</td>
			<td>Supplier No. 2209-03</td>
			<td>Funnels: AMERICAN SCIENTIFIC LLC SE&#160;-&#160;75 mm (3&#8221;)&#160;</td>
			<td>https://us.vwr.com/store/product/8884369/plastic-funnels</td>
		</tr>
		<tr>
			<td>Main body of light traps (made from commercially available PVC sanitarty pipes)</td>
			<td>(SKU 145640)&#160;</td>
			<td>Alasco Sanitary uPVC Pipes Series 1000 107mm/4&#39;&#160;</td>
			<td>https://alascopvcpipes.com/product/alasco-standard-sanitary-upvc-pipe-series-1000/.&#160; This brand can be found in the Philippines. Other simular brands can also be used</td>
		</tr>
		<tr>
			<td>Modeling clay&#160;</td>
			<td></td>
			<td>Can be found in art suppliy and childreans toy stores</td>
			<td>To seal the funnel after retreival</td>
		</tr>
		<tr>
			<td>Plankton mesh (50-100 &#181;m)</td>
			<td></td>
			<td>any reputable brand and source</td>
			<td>https://www.adkinstruments.in/products/plankton-nets-in-various-mesh-size-1633936883</td>
		</tr>
		<tr>
			<td>Screw on lids for the light trap</td>
			<td></td>
			<td>Alasco&#160; Sanitary &#160;Clean-Out&#160; 4&#34;</td>
			<td>https://alascopvcpipes.com/product/alasco-standard-sanitary-upvc-clean-out/. This brand can be found in the Philippines. Other simular brands can also be used</td>
		</tr>
		<tr>
			<td>Scuba/snorkel equipment</td>
			<td></td>
			<td>any reputable brand and source</td>
			<td></td>
		</tr>
		<tr>
			<td>Stereo-microscopes</td>
			<td></td>
			<td>Scientific suppliers</td>
			<td></td>
		</tr>
		<tr>
			<td>Underwater touches</td>
			<td></td>
			<td>Princeton Tec Ecoflare or&#160;Fantasea Nanospotter 6023</td>
			<td></td>
		</tr>
	</tbody>
</table>

collecting marine gnathiid isopod fish parasites with light traps

A method to collect marine gnathiid isopod fish parasites with the use of light traps is presented. Gnathiid isopods are a major group of marine fish parasites that feed on blood and fluid from host fishes, mostly at night. Like ticks and mosquitos on land, they associate only temporarily with their host and spend most of their life free-living in the benthos. Given their high mobility and transient and predominantly nocturnal association with hosts, they cannot easily be collected by capturing free-living hosts. However, they are readily attracted to underwater light sources, creating the opportunity to collect them in light traps. Here the design and individual steps involved in the deployment and processing of specially adapted light traps for collecting free-living stages of gnathiid isopods are outlined. Sample results and possible modifications of the basic protocol for a variety of different sampling needs are presented and discussed.

For sampling in the central Philippines, the outlined trap design (Figure 1) was used. When 36 traps were set overnight (in one site), 1 to 1343 gnathiids per trap (275 &#177; 54) were collected. These included both fed and unfed juvenile stages (Figure 2; Table 1, 2). These results demonstrate the effectiveness of light traps for collecting gnathiid isopods under the study conditions. Figure 3 shows the placement o...

Watch this Scientific Journal Video about Collecting Marine Gnathiid Isopod Fish Parasites with Light Traps at JoVE.com

Collecting Marine Gnathiid Isopod Fish Parasites with Light Traps

We present a method to collect marine gnathiid isopod fish parasites using light traps placed at field sites via breath-hold diving or scuba diving.

A method to collect marine gnathiid isopod fish parasites with the use of light traps is presented. Gnathiid isopods are a major group of marine fish ...

collecting-marine-gnathiid-isopod-fish-parasites-with-light-traps

Research

JoVE Journal

Biology

1.3K Views.  Silliman University. We present a method to collect marine gnathiid isopod fish parasites using light traps placed at field sites via breath-hold diving or scuba diving.

Video: Collecting Marine Gnathiid Isopod Fish Parasites with Light Traps

Collecting and Measuring Nociceptive and Inflammatory Mediators in Surgical Wounds 

We describe a methodology by which we are able to collect and measure inflammatory and nociceptive biochemical mediators at the surgical wound site. Collecting site-specific biochemical markers allows us to evaluate the relationship between surgical wound and serum levels; determine any associations between mediator release, pain and analgesic consumption; and evaluate the effect of systemic and peripheral drug administration on surgical wound biochemistry.
This methodology has been applied to healthy women undergoing elective cesarean delivery with spinal anesthesia. Wound exudate and serum mediators, in conjunction with pain scores and analgesics consumption were measured at 1, 6, 24, and 48 hours post-cesarean delivery. Biochemical mediators that were detected included IL-1&beta;, IL-2, IL-4, IL-6, IL-7, IL-8, IL-10, IL-12, IL-13, IL-17, TNF&alpha;, INF&gamma;, G-CSF, GM-CSF, MCP-1 and MIP-1&beta;, nerve growth factor (NGF), prostaglandin E2 (PG-E2) and substance P. We found no correlations between wound and serum cytokines concentrations or time-release profiles (J Pain. 2008 Jul 9(7):650-7). This article describes and demonstrates the feasibility of collecting and assaying nociceptive and inflammatory mediators in surgical wounds at specific time points. The lack of significant correlations between serum and wound levels shows the importance of determining site-specific release if surgical wounds and localized pathologies are to be studied.

Collecting and Measuring Nociceptive and Inflammatory Mediators in Surgical Wounds

A technique to collect and measure surgical wound biochemical mediators at specific time points.

We describe a methodology by which we are able to collect and measure inflammatory and nociceptive biochemical mediators at the surgical wound site. ...

Presynaptically Silent Synapses Studied with Light Microscopy

Synaptic plasticity likely underlies the nervous system's ability to learn and remember and may also represent an adaptability that prevents otherwise damaging insults from becoming neurotoxic.  We have been studying a form of presynaptic plasticity that is interesting in part because it is expressed as a digital switching on and off of a presynaptic terminal s ability to release vesicles containing the neurotransmitter glutamate.  Here we demonstrate a protocol for visualizing the activity status of presynaptic terminals in dissociated cell cultures prepared from the rodent hippocampus.  The method relies on detecting active synapses using staining with a fixable form of the styryl dye FM1-43, commonly used to label synaptic vesicles.  This staining profile is compared with immunostaining of the same terminals with an antibody directed against the vesicular glutamate transporter 1 (vGluT-1), a stain designed to label all glutamate synapses regardless of activation status.   We find that depolarizing stimuli induce presynaptic silencing.  The population of synapses that is silent under baseline conditions can be activated by prolonged electrical silencing or by activation of cAMP signaling pathways.

Glutamatergic synapses can switch from an active mode to a silent mode. We demonstrate that presynaptic activity status in dissociated culture of rodent neurons is visualized using a fixable form of the FM1-43 dye to visualize active synapses and immunostaining with vGluT-1 antibody to visualize all glutamate synapses.

Synaptic plasticity likely underlies the nervous system's ability to learn and remember and may also represent an adaptability that prevents otherwise ...

Culturing Primary Rat Inner Medullary Collecting Duct Cells

Arginine-vasopressin (AVP) facilitates water reabsorption by renal collecting duct principal cells and thereby fine-tunes body water homeostasis. AVP binds to vasopressin V2 receptors (V2R) on the surface of the cells and thereby induces synthesis of cAMP. This stimulates cellular signaling processes leading to changes in the phosphorylation of the water channel aquaporin-2 (AQP2). Protein kinase A phoshorylates AQP2 and thereby triggers the translocation of AQP2 from intracellular vesicles into the plasma membrane facilitating water reabsorption from primary urine. Aberrations of AVP release from the pituitary or AVP-activated signaling in principal cells can cause central or nephrogenic diabetes insipidus, respectively; an elevated blood plasma AVP level is associated with cardiovascular diseases such as chronic heart failure and the syndrome of inappropriate antidiuretic hormone secretion.
Here, we present a protocol for cultivation of primary rat inner medullary collecting duct (IMCD) cells, which express V2R and AQP2 endogenously. The cells are suitable for elucidating molecular mechanisms underlying the control of AQP2 and thus to discover novel drug targets for the treatment of diseases associated with dysregulation of AVP-mediated water reabsorption. IMCD cells are obtained from rat renal inner medullae and are used for experiments six to eight days after seeding. IMCD cells can be cultured in regular cell culture dishes, flasks and micro-titer plates of different formats, the procedure only requires a few hours, and is appropriate for standard cell culture laboratories.

Arginine-vasopressin (AVP) controls fine-tuning of body water homeostasis through facilitating water reabsorption by renal principal cells. Here, we present a protocol for the cultivation of primary rat inner medullary collecting duct cells suitable for the elucidation of molecular mechanisms underlying AVP-mediated water reabsorption.

Arginine-vasopressin (AVP) facilitates water reabsorption by renal collecting duct principal cells and thereby fine-tunes body water homeostasis. AVP ...

Assessing Species-specific Contributions To Craniofacial Development Using Quail-duck Chimeras

The generation of chimeric embryos is a widespread and powerful approach to study cell fates, tissue interactions, and species-specific contributions to the histological and morphological development of vertebrate embryos. In particular, the use of chimeric embryos has established the importance of neural crest in directing the species-specific morphology of the craniofacial complex. The method described herein utilizes two avian species, duck and quail, with remarkably different craniofacial morphology. This method greatly facilitates the investigation of molecular and cellular regulation of species-specific pattern in the craniofacial complex.&#160;Experiments in quail and duck chimeric embryos have already revealed neural crest-mediated tissue interactions and cell-autonomous behaviors that regulate species-specific pattern in the craniofacial skeleton, musculature, and integument. The great diversity of neural crest derivatives suggests significant potential for future applications of the quail-duck chimeric system to understanding vertebrate development, disease, and evolution.

This article describes a method to generate chimeric embryos that are&#160;designed to test the species-specific contributions of neural crest and/or other tissues to craniofacial development.

The generation of chimeric embryos is a widespread and powerful approach to study cell fates, tissue interactions, and species-specific contributions to ...

Characterization of Calcification Events Using Live Optical and Electron Microscopy Techniques in a Marine Tubeworm

Characterizing the first event of biological production of calcium carbonate requires a combination of microscopy approaches. First, intracellular pH distribution and calcium ions can be observed using live microscopy over time. This allows identification of the life stage and the tissue with the feature of interest for further electron microscopy studies. Life stage and tissues of interest are typically higher in pH and Ca signals. 
Here, using H. elegans, we present a protocol to characterize the presence of calcium carbonate structures in a biological specimen on the scanning electron microscope (SEM), using energy-dispersive X-ray spectroscopy (EDS) to visualize elemental composition, using electron backscatter diffraction (EBSD) to determine the presence of crystalline structures, and using transmission electron microscopy (TEM) to analyze the composition and structure of the material. In this protocol, a focused ion beam (FIB) is used to isolate samples with dimension suitable for TEM analysis. As FIB is a site specific technique, we demonstrate how information from the previous techniques can be used to identify the region of interest, where Ca signals are highest.

We demonstrate the use of various microscopy methods that are useful in observing the calcification of a tubeworm, Hydroides elegans, as well as locating and characterizing the first calcified material. Live microscopy and electron microscopy are used together to provide functional and material information that are important in studying biomineralization.

Characterizing the first event of biological production of calcium carbonate requires a combination of microscopy approaches. First, intracellular pH ...

Preparation and Observation of Thick Biological Samples by Scanning Transmission Electron Tomography

This report describes a protocol for preparing thick biological specimens for further observation using a scanning transmission electron microscope. It also describes an imaging method for studying the 3D structure of thick biological specimens by scanning transmission electron tomography. The sample preparation protocol is based on conventional methods in which the sample is fixed using chemical agents, treated with a heavy atom salt contrasting agent, dehydrated in a series of ethanol baths, and embedded in resin. The specific imaging conditions for observing thick samples by scanning transmission electron microscopy are then described. Sections of the sample are observed using a through-focus method involving the collection of several images at various focal planes. This enables the recovery of in-focus information at various heights throughout the sample. This particular collection pattern is performed at each tilt angle during tomography data collection. A single image is then generated, merging the in-focus information from all the different focal planes. A classic tilt-series dataset is then generated. The advantage of the method is that the tilt-series alignment and reconstruction can be performed using standard tools. The collection of through-focal images allows the reconstruction of a 3D volume that contains all of the structural details of the sample in focus.

This report describes a sample preparation protocol and specific imaging conditions for performing scanning transmission electron tomography of thick biological specimens.

This report describes a protocol for preparing thick biological specimens for further observation using a scanning transmission electron microscope. It ...

Analysis of the Gap Junction-dependent Transfer of miRNA with 3D-FRAP Microscopy

Small antisense RNAs, like miRNA and siRNA, play an important role in cellular physiology and pathology and, moreover, can be used as therapeutic agents in the treatment of several diseases. The development of new, innovative strategies for miRNA/siRNA therapy is based on an extensive knowledge of the underlying mechanisms. Recent data suggest that small RNAs are exchanged between cells in a gap junction-dependent manner, thereby inducing gene regulatory effects in the recipient cell. Molecular biological techniques and flow cytometric analysis are commonly used to study the intercellular exchange of miRNA. However, these methods do not provide high temporal resolution, which is necessary when studying the gap junctional flux of molecules. Therefore, to investigate the impact of miRNA/siRNA as intercellular signaling molecules, novel tools are needed that will allow for the analysis of these small RNAs at the cellular level. The present protocol describes the application of three-dimensional fluorescence recovery after photobleaching (3D-FRAP) microscopy to elucidating the gap junction-dependent exchange of miRNA molecules between cardiac cells. Importantly, this straightforward and non-invasive live-cell imaging approach allows for the visualization and quantification of the gap junctional shuttling of fluorescently labeled small RNAs in real time, with high spatio-temporal resolution. The data obtained by 3D-FRAP confirm a novel pathway of intercellular gene regulation, where small RNAs act as signaling molecules within the intercellular network.

Here, we describe the application of three-dimensional fluorescence recovery after photobleaching (3D-FRAP) for the analysis of the gap junction-dependent shuttling of miRNA. In contrast to commonly applied methods, 3D-FRAP allows for the quantification of the intercellular transfer of small RNAs in real time, with high spatio-temporal resolution.

Small antisense RNAs, like miRNA and siRNA, play an important role in cellular physiology and pathology and, moreover, can be used as therapeutic agents ...

Assessing Mineral Availability in Fish Feeds using Complementary Methods Demonstrated with the Example of Zinc in Atlantic Salmon

Assessing the availability of dietary micro-minerals is a major challenge in mineral nutrition of fish species. The present article aims to describe a systematic approach combining different methodologies to assess the availability of zinc (Zn) in Atlantic salmon (Salmo salar). Considering that several Zn chemical species can be present in an Atlantic salmon feed, it was hypothesised that Zn availability is influenced by the Zn chemical species present in the feed. Thus, in this study, the first protocol is about how to extract the different Zn chemical species from the feed and to analyze them by a size exclusion chromatography-inductively coupled plasma mass spectroscopy (SEC-ICP-MS) method. Subsequently, an in vitro method was developed to evaluate the solubility of dietary Zn in Atlantic salmon feeds. The third protocol describes the method to study the impact of changing Zn chemical species composition on the uptake of Zn in a fish intestinal epithelial model using a rainbow trout gut cell line (RTgutGC). Together, the findings from the in vitro methods were compared with an in vivo study examining the apparent availability of inorganic and organic sources of Zn supplemented to Atlantic salmon feeds. The results showed that several Zn chemical species can be found in feeds and the efficiency of an organic Zn source depends very much on the amino acid ligand used to chelate Zn. The findings of the in vitro methods had less correlation with that outcome of the in vivo study. Nevertheless, in vitro protocols described in this article provided crucial information regarding Zn availability and its assessment in fish feeds.

This article explains in detail a systematic approach to assess micro-mineral availability in Atlantic salmon. The methodology includes tools and models with increasing biological complexity: (1) chemical speciation analysis, (2) in vitro solubility, (3) uptake studies in cell lines, and (4) in vivo fish studies.&#160;

Assessing the availability of dietary micro-minerals is a major challenge in mineral nutrition of fish species. The present article aims to describe a ...

Nucleofection and In Vivo Propagation of Chicken Eimeria Parasites

Transfection is a technical process through which genetic material, such as DNA and double-stranded RNA, are delivered into cells to modify the gene of interest. Currently, transgenic technology is becoming an indispensable tool for the study of Eimeria, the causative agents of coccidiosis in poultry and livestock. This protocol provides a detailed description of stable transfection in eimerian parasites: purification and nucleofection of sporozoites or second-generation merozoites, and in vivo propagation of transfected parasites. Using this protocol, we achieved transfection in several species of Eimeria. Taken together, nucleofection is a useful tool to facilitate genetic manipulation in eimerian parasites.

Nucleofection and In Vivo Propagation of Chicken Eimeria Parasites

Here, we provided a method to achieve stable transfection of chicken Eimeria parasites by nucleofecting sporozoites or second-generation merozoites. Genetically modified eimerian parasites expressing heterologous antigenic genes could be used as vaccine delivery vehicles.

Transfection is a technical process through which genetic material, such as DNA and double-stranded RNA, are delivered into cells to modify the gene of ...

Apoptosis Induction and Detection in a Primary Culture of Sea Cucumber Intestinal Cells

Primary cultured cells are used in a variety of scientific disciplines as exceptionally important tools for the functional evaluation of biological substances or characterization of specific biological activities. However, due to the lack of universally applicable cell culture media and protocols, well described cell culture methods for marine organisms are still limited. Meanwhile, the commonly occurring microbial contamination and polytropic properties of marine invertebrate cells further impede the establishment of an effective cell culture strategy for marine invertebrates. Here, we describe an easy-to-handle method for culturing intestinal cells from sea cucumber Apostichopus japonicus; additionally, we provide an example of in vitro apoptosis induction and detection in primary cultured intestinal cells. Moreover, this experiment provides details about the appropriate culture medium and cell collection method. The described protocol is compatible with a variety of widely available tissue samples from marine organisms including Echinodermata, Mollusca, and Crustacea, and it can provide sufficient cells for multiple in vitro experimental applications. This technique would enable researchers to efficiently manipulate primary cell cultures from marine invertebrates and to facilitate the functional evaluation of targeted biological materials on cells.

This protocol provides an easy-to-handle method to culture the intestinal cells from sea cucumber Apostichopus japonicus and is compatible with a variety of widely available tissue samples from marine organisms including Echinodermata, Mollusca, and Crustacea.

Primary cultured cells are used in a variety of scientific disciplines as exceptionally important tools for the functional evaluation of biological ...