The authors acknowledge the Water Quality Analysis Laboratory at the University of New Hampshire for assistance with sample analysis. The authors also thank two anonymous reviewers whose comments have helped to improve the manuscript. This work is funded by the National Science Foundation (DEB-1556603). Partial funding was also provided by the EPSCoR Ecosystems and Society Project (NSF EPS-1101245), New Hampshire Agricultural Experiment Station (Scientific Contribution #2662, USDA National Institute of Food and Agriculture (McIntire-Stennis) Project (1006760), the University of New Hampshire Graduate School, and the New Hampshire Water Resources Research Center.

1. Identifying and Characterizing the Ideal Experimental Stream Reach
<ol>
	<li>Ensure that experimental stream reaches are long enough to promote complete mixing of solutes11 and long enough where biological uptake can occur. Reach lengths can vary among streams and experiments. In small first-order headwater streams, reach length may vary from 20-150 m (or longer if the system requires it) depending on discharge and other physical properties of the stream.
	<ol>
		<li>Exclude large pools from experimental reaches, as they retard the downstream movement of solutes, minimal flow sections, and tributaries that dilute the added solution. Times of low discharge may require shortening the reach length while higher discharge may require a longer reach.</li>
		<li>Identify a location at the top of the experimental stream reach above a riffle to facilitate mixing of the added solutes. This will be the addition site. At the bottom of the experimental stream reach, identify a location where flow is constricted and representative of about 90% of the total flow (Figure 1). This will be the sample collection site.</li>
	</ol>
	</li>
</ol>
<img alt="Figure 1" src="/files/ftp_upload/54704/54704fig1.jpg" /> 
Figure 1: Example of Downstream Sampling Site. An ideal sampling site is where the majority of flow is constricted and easily accessible without disturbance of the stream channel and benthos. Here a fallen piece of wood debris has created this sampling point in a small first-order headwater stream. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54704/54704fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<ol start="2">
	<li>Obtain discharge measurement and background nutrient concentrations of the solutes of interest prior to experiments in order to calculate the mass of solutes needed for the manipulations. Please see calculations in step 2.2.1.
	<ol>
		<li>Obtain background concentration data for the target solute of manipulation (e.g. NO3-) and chloride (Cl-) which is often used as the conservative tracer. Use the conservative tracer in the context of these experiments, to track changes in conductivity, which indicate the arrival of the nutrient pulse at the sampling station and the rate in which the pulse is passing through. Conductivity, or specific conductance, is a surrogate for in-situ changes in concentration of the conservative tracer.</li>
		<li>Characterize the physio-chemical properties of the experimental reach by collecting ancillary data such as reach width and depth, temperature, pH and dissolved oxygen.
		<ol>
			<li>Perform measurements that cannot be made with the use of an environmental probe (e.g. width and depth), the day before or immediately after the experiment in order to minimize any benthic or chemical disturbance within the stream channel. Divide the experimental reach in equidistant transects (e.g. every 10 m) where width and at least 3 depth measurements can be assessed (e.g. right bank, thalweg, and left bank). These data are valuable to connect the physical properties of a stream to biogeochemical measurements and if the researchers are also interested in calculating nutrient uptake kinetics and parameters6.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
2. Preparation for Experiment
<ol>
	<li>Determine the mass (kg) of solute required for manipulation using the outlined equations below. 
	Note: The example below applies to a nitrate-based experiment with NO3- in the form of sodium nitrate (NaNO3) and assumes a targeted increase of 3x above background (equations are based on those of Kilpatrick and Cobb12). In this example the following assumptions have been made with respect to background conditions: discharge = 10 L/sec; [Cl] = 10 mg/L; [NO3-] = 50 &#181;g N/L. Due to variation among experiments, adjust required input data.
	<ol>
		<li>Calculate the Targeted increase (Equation 1): 
		Targeted [NO3- &#956;g N/L] increase = expected background [NO3- &#956;g N/L] * targeted increase 
		150 &#956;g N/L = 50 &#956;g N/L * 3</li>
		<li>Calculate the total atomic mass flux (Equation 2): 
		Total atomic mass flux (NO3- &#956;g N) = 30 min * 60 sec * Q(L/sec) * targeted [NO3- &#956;g N/L] increase 
		Where 30 minutes is the assumed duration of solute peak12 and Q is discharge 
		2 700 000 &#956;g N = 30 min * 60 sec * 10 L/s * 150 &#956;g N/L</li>
		<li>Calculate the total molecular mass flux (Equation 3): 
		Total molecular mass flux (NO3- &#956;g N) = total atomic mass flux (NO3- &#956;g N)/atomic mass (14) * molecular weight (85) 
		Where atomic mass refers to N and molecular weight refers to NaNO3. 
		16,392,857.14 &#956;g N = 2,700,000 &#956;g N/(14 * 85)&#160;</li>
		<li>Calculate the mass to add (Equation 4): 
		Mass to add (g) = total molecular mass flux (NO3- &#956;g N)/1,000,000 g/&#956;g 
		16.39 g NaNO3 = 16,392,857.14 &#956;g N/1,000,000 g/&#956;g 
		Note: Follow the above calculations for any other solutes including the conservative tracer (e.g. sodium chloride). Make sure to adjust the atomic and molecular masses for the solute of interest.</li>
	</ol>
	</li>
	<li>Prepare all solutes one day prior to field experiments. Weigh out enough solutes to raise the ambient concentration of both the biological tracer and the conservative tracer three times (or desired amount) above background. It is important that the quantity of added solutes causes a measureable change above background concentration that is sufficient to create a wide dynamic range in added nutrient concentration.
	<ol>
		<li>Weigh solutes using analytical scales and subsequently store in clean acid-washed high-density polyethylene bottles with appropriate labels. Examples of biological tracers include: NO3-: sodium nitrate (NaNO3); NH4+: ammonium chloride (NH4Cl); PO4-3: potassium phosphate (K2HPO4). However, the choice of biological tracer will be a function of the biogeochemical question being asked. Options for conservative tracers include sodium chloride (NaCl) and sodium bromide (NaBr).</li>
	</ol>
	</li>
	<li>Collect remaining materials: field book, labeling tape and pen, field measuring tape, cooler, conductivity meter, ~ 20 L bucket and large stirring rod (e.g. beer paddle, rebar, large stick), approximately 50 clean and acid-washed 125 ml high-density polyethylene bottles. Label the 125 ml bottles #1-50. 
	Note: Less than 50 samples can be taken per experiment and background samples are included in the 50 total bottles.</li>
	<li>Optional: Depending on the numbers of field personnel, perform sample filtering on-site (see section #5). If this option is chosen, bring 50 clean, pre-labeled and acid-washed 60 ml high-density polyethylene bottles into the field. Label the 60 ml bottles #1-50 to match the 125 ml collection bottles.</li>
</ol>
3. Day of Set Up
<ol>
	<li>Deploy the field conductivity meter at the collection site. Place the instrument upstream (approximately 0.5-1.0 m) of where samples will be taken so sample collection does not interfere with instrument readings. The meter will remain in place throughout the experiment. A field conductivity meter is best as it provides real-time conductivity readings, which are required to determine the sampling rate (see step 5.2) and filtration and analysis order (steps 5.3 and 6.1).</li>
	<li>Collect 125 ml background samples in triplicate at the addition site and at the collection site of the experimental reach prior to the addition of the solution. These data will be used to verify day-of ambient concentration and to determine variation in solute concentration along the stream reach. These data are also valuable to connect ambient stream chemistry (e.g. DOC: NO3- ratios13) to the biogeochemical measurements of interest.</li>
	<li>Record the time and conductivity of background samples collected.</li>
	<li>Record the background conductivity of stream prior to addition of solutions.</li>
</ol>
4. Adding Solutes
<ol>
	<li>Pour all reagents (16.39 g NaNO3 and 1483 g NaCl) into a large container (e.g. 20 L bucket) and add enough stream water to completely dissolve the solutes. Rinse reagent vessels thrice with additional stream water and pour rinse into solution container. Keep track of amount of water added.
	<ol>
		<li>For example, use a 500 ml bottle to pour stream water into the container. Stir solution until all reagents have been completely dissolved.</li>
	</ol>
	</li>
	<li>Collect 60 ml aliquot of the addition solution. Keep this highly concentrated sample separate (e.g. zip-lock bag) from all other samples to minimize cross contamination. Such samples are important if calculating nutrient uptake kinetics6 is an additional goal of the research project as these samples can be used to determine the exact mass of solutes added.</li>
	<li>Pour solution into addition site. Do this by pouring the solution in a smooth and quick motion to minimize travel lag time and splashing that could reduce the amount of reagents added. Rinse the container and the stir stick three times in the stream immediately after the addition to guarantee all reagents have been added to the stream.
	<ol>
		<li>Record the time the solution was added: hr:min:sec.</li>
		<li>Record the masses of tracers added (e.g. NaNO3 and NaCl).</li>
		<li>After the solution has been added, do not disturb the stream. Make sure that all travel along the stream occurs on the banks to ensure that the stream benthos and the solution itself are not disturbed.</li>
	</ol>
	</li>
</ol>
5. Field Sampling
<ol>
	<li>Order sampling bottles in ascending order while waiting for solution to arrive to the sampling location. Travel time will be a function of discharge and reach length and can be determined ahead of time (one-day prior) either with a NaCl-only injection or rhodamine dye (which can be used to establish travel time14). 
	Note: If working on a DON-themed project, avoid using rhodamine dye as it is a type of DON and will therefore alter the ambient DON pool if any remains in the study reach.</li>
</ol>
<img alt="Figure 2" src="/files/ftp_upload/54704/54704fig2.jpg" /> 
Figure 2: Example Schematic of Solute Breakthrough Curve (BTC). A BTC represents changes in solute concentration over time and can be used to explain the transit and biogeochemical cycling of a tracer in a stream. Grab samples should be taken across the BTC with a frequency that gives equal representation to both the ascending and descending limbs of the BTC. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54704/54704fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<ol start="2">
	<li>Sample Collection 
	Note: The over-arching objective of sample collection, is to adequately represent changes in solute concentration along both the rising and falling limbs of the break through curve (BTC) (Figure 2).
	<ol>
		<li>Upon arrival of the solution (detected via an increase in conductivity), collect samples in 125 ml bottles throughout the BTC by holding a 125 ml bottle into the main flow of water at the sampling point. Quickly rinse the bottle with stream water and discard rinse downstream and then take sample. Cap sample and place into cooler.</li>
		<li>Record the time (hr:min:sec) and conductivity of each sample taken along the BTC into a field book (Table 1).</li>
		<li>Collect samples based on time (e.g. 1 min intervals) or based on the rate at which conductivity changes. For example, if conductivity is changing quickly, sample every 30-60 sec until changes in conductivity slow, at which time samples can be taken every 5-10 min. For intervals based on conductivity, take samples every 15-30 units depending on the rate at which conductivity is changing.</li>
		<li>Sample until conductivity returns to background or within 5 &#181;S/cm of background conditions. Intervals of sample collection can be adjusted during the experiment as long as the BTC is well represented in the grab samples.</li>
	</ol>
	</li>
</ol>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Bottle #</td>
			<td>Specific Conductance</td>
			<td>Time</td>
			<td>Notes</td>
		</tr>
		<tr>
			<td>1</td>
			<td></td>
			<td>hr:min:sec</td>
			<td>e.g. background (downstream)</td>
		</tr>
		<tr>
			<td>2</td>
			<td></td>
			<td></td>
			<td>e.g. background (downstream)</td>
		</tr>
		<tr>
			<td>3</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>4</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>5</td>
			<td></td>
			<td></td>
			<td>e.g. sample at peak conductance</td>
		</tr>
		<tr>
			<td>.</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>.</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>.</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Highest Bottle #</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
	</tbody>
</table>
Table 1PField book: Example Page from Lab Book and Required Information
<ol start="3">
	<li>Sample Filtering 
	Note: Filtering of samples can occur either in the field or upon returning to the laboratory.
	<ol>
		<li>Filter samples from the rising limb in order of ascending specific conductivity until the peak in specific conductivity. Wait for the experiment to be over and filter samples from the falling limb in ascending order of specific conductivity (i.e. start with the last sample and work backwards toward peak specific conductivity). 
		Note: This order of samples minimizes cross contamination between samples and allows for the same filter, syringe, and filter holder to be used as long as the filter, syringe and filter holder are appropriately rinsed in between each sample (see steps 5.3.2-5.3.4).</li>
		<li>Remove plunger from a 60 ml syringe and then close stop-cock. Pour ~10 ml of sample into syringe and return plunger to syringe. Shake syringe so that sample rinses internal walls of syringe. Attached syringe to filter-holder and open stop-cock. Push sample through filter-holder and discard rinse.</li>
		<li>Remove plunger and close stop-cock. Pour ~30 ml of sample into syringe and return plunger to syringe. Open stock-cock and expel ~10 ml through filter-holder and into 60 ml sampling bottle. Cap the bottle, swirl with filtrate and discard. Repeat this step for a total of 3 rinses. This will ensure any impurities have been removed from the 60 ml sample bottle and that the walls are coated with sample.</li>
		<li>Remove plunger and close stop-cock. Pour ~60 ml of sample into syringe and return plunger to syringe. Push the sample through the filter holder and into the 60 ml sample bottle. Fill bottles up to the shoulder to prevent cracking of bottles when frozen. Cap bottle and place into cooler.</li>
		<li>Repeat steps 5.3.2-5.3.4 for all remaining samples. Change filter between rising and falling limb samples to minimize contamination.</li>
		<li>Transport samples back to the laboratory on the same day and on ice.</li>
	</ol>
	</li>
</ol>
6. Preparation for Laboratory Analysis
<ol>
	<li>If filtering of samples is to occur in the laboratory, follow protocol as outlined in section 5.3.1. Filter samples from both the ascending and descending limbs of the BTC in order of increasing conductivity. Change the filter between rising limb and falling limb samples.</li>
	<li>Freeze filtered samples at -20 &#176;C until analysis.</li>
	<li>Ensure that analytical facilities are equipped to handle highly concentrated samples. 
	Note: Some laboratories are not equipped to run highly concentrated samples and thus care should be taken. Incorporate prepared standards that capture that higher end of expected solute concentrations. High concentration standards will help to ensure a standard curve that captures the expected range of manipulated solute concentrations.</li>
	<li>Analyze samples from low to high conductivity on all analytical instruments. Ordering samples from low to high specific conductance prevents contamination of low salt/nutrient samples by high salt/nutrient samples. This means samples from the rising and falling limbs will be mixed with respect to sequence.
	<ol>
		<li>Analyze samples for total dissolved organic carbon, total dissolved nitrogen, nitrate and ammonium, although the exact combination of solute analysis will be a function of the research question (see Wymore et al.10 for example).</li>
	</ol>
	</li>
</ol>
7. Data Analysis
<ol>
	<li>Analyze the data using simple linear regression. The independent variable is the concentrations of the added nutrient and the dependent variable is DOM concentration either as DOC or DON. Each point on the figure represents one grab sample from the breakthrough curve and that sample&#39;s nutrient and DOC/DON concentration.</li>
</ol>

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The authors have nothing to disclose.

The objective of the nutrient pulse method, as presented here, is to characterize and quantify the response of the highly diverse pool of ambient stream water DOM across a dynamic range of an added inorganic nutrient. If the added solute sufficiently increases the concentration of the reactive solute, a large inferential space can be created to understand how the biogeochemical cycling of DOM is linked to nutrient concentrations. This nutrient pulse approach is ideal as it involves none of the machinery associated with plateau-style addition (e.g. peristaltic pump) and does not involve expensive isotopic techniques. These manipulations are easily reproducible and multiple experiments can be conducted during a single day. We do recommend however, that if replicating experiments on the same day within a single stream reach, that additions are separated by several hours to allow for sufficient flushing of residual solutes.
In these ecosystem manipulations we are able to measure changes in the concentration of the ambient pool of DOM in response to the addition of nutrients. However, with this approach it is not possible to comment on which component of the DOM pool actually decreased or increased beyond changes in the concentration of DON and DOC. We cannot discern if it is a certain form of DON for example, that is preferentially consumed with the addition of NO3-. Changes could be due to a highly abundant and available forms of DON (e.g. amino acids) that were altered enough to change the overall concentration. However, this field-based approach could be easily paired with high-resolution analytical chemistry methods (e.g. fluorescence spectroscopy, Fourier transform ion cyclotron resonance mass spectroscopy) to determine what components or classes of molecules are directly responding to the experimental manipulation.
In addition to DOM chemistry, other biological and environmental factors may influence the response of DOM to the added nutrient. To understand this multifactor interaction other field data can be collected to examine other important variables. Temporal changes in the direction of the DON response to nitrate (Figure 3A-3F) may reflect autotrophic vs. heterotrophic dominated processes. For example, the positive relationship in Figure 3A, may reflect the activity of autotrophic organisms. It is likely that in May there is still adequate photosynthetically active radiation reaching the stream (prior to riparian canopy closure) and the observed pattern reflects these organisms shifting from DON to NO3- as their source of nitrogen, which results in an increase in DON concentration. The negative relationship observed later in the season (e.g. Figure 3E), likely represents the activity of heterotrophic microorganisms who are mining DON for its energy content. To test this type of biologically-based hypothesis, future research could incorporate concurrent measurements of autotrophic standing stock, microbial activity levels or enzymes concentrations, for example. Examining DOM-nitrate interactions across other environmental gradients, including dissolved oxygen and temperature, could help to elucidate the role of other physio-chemical parameters in driving the coupled biogeochemistry of DOM and nitrate.
The selection of low NO3- streams is essential for the success of these experiments and to retain the ability to measure changes in the DON pool. Studies examining the interaction between NO3- and DON for example, should occur in streams where NO3- makes up less than 50% of the TDN pool. The precision of measuring DON via subtraction is greatly reduced when NO3- contributes too large a fraction of the TDN pool since there is a multiplicative error term surrounding DON measurements that results from the analysis of TDN, NO3- and NH4+. Such sub-optimal conditions can result in negative DON concentrations. Thus this technique may be limited in systems which are heavily impaired by NO3- such as estuaries.
Although larger streams and rivers present their own set of challenges, this method may be applicable to higher-order systems. For example, Tank et al.5 performed a nutrient pulse experiment in the 7th-order Upper Snake River in Wyoming to examine the uptake kinetics of dissolved inorganic N. There may be ways to perform similar experiments in either lakes, soils or groundwater. However, such experiments are difficult due to the challenges associated with exposing a system to a gradient of nutrient concentrations or containing experimental units in ways that minimize disruption and experimental artefacts. This is one of the advantages of using stream ecosystems for these types of manipulative experiments. Nonetheless, the development of similar methods for other ecosystems, especially systems impaired by excessive N loading (e.g. estuaries), could have important management implications as we begin to understand the ways in which different forms of N drive eutrophication and toxic algal blooms in coastal waters.

溶存有機物（DOM）は、生態系を淡水する重要なエネルギー及び栄養源を提供し、0.7μmのフィルターを通過する有機物として定義されます。水界生態系の中では、DOMは、光の減衰と金属錯体形成に影響を与えることができます。 DOMは、種々の官能基を有する有機化合物、並びに窒素（N）とリン（P）などの必須栄養素の非常に多様かつ不均一な混合物です。用語「DOM」はそのC、NおよびP成分を含むプール全体を説明しているが、その濃度は、溶存有機炭素（DOC）として測定されます。 DOMプールの固有の分子の複雑さは、しかし、その研究への挑戦を作成します。例えば、このような溶存有機態窒素（DON）と溶存有機リン（DOP）などの有機栄養素からなる総DOMプールの割合を測定する直接的な方法はありません。代わりに、有機栄養素の濃度の差によって決定されなければなりません（ <em&gt;例えば[DON] = [総溶存窒素] - [溶存無機窒素]）。 ストリームに現実的なDOMの修正を追加することは、周囲のDOMプールの多様性のために困難です。以前の研究では、単一の炭素源（ 例えば、グルコース、尿素1）を追加しました または落葉浸出液2のような特定のソースは、フィールド中の濃度を操作することができます。しかし、これらのソースは、周囲のDOMプールの特に代表的なものではありません。その後の実験のために周囲のDOMを絞り込むか、集中しようとすると、処理中の特定の画分（ 例えば 、高度に不安定な部品）の損失を含む困難に細工されています。その結果、我々は、現在、直接周囲DOMプールを操作する任意の方法を持たないように、周囲のDOMプールのコントロールを理解することは困難です。しかし、DOMの生物地球化学は、 例えば 、NIT（一般的な環境で見つかった栄養素にリンクされているので、レート[NO 3 - ] 3）、私たちは生態系をストリーミングし、これらの操作にDOMプールの応答を測定する他の溶質を追加することができます。 DOMプールは、我々はDOMは環境条件の変動にどのように応答するかをより深い洞察を得るために願って実験的に課せられた栄養広範囲の濃度にどのように応答するかを調べることによって。 一般的にストリームの生物地球化学に使用される1つの方法は、栄養添加方法です。栄養添加実験は、伝統的に取り込み速度または添加溶質4,5,6,7-の運命を理解するために使用されてきました。栄養添加物は、複数年8にわたって日スケール4、または長期的な操作に時間6に短期的であることができます。生物地球化学反応を介して追加された栄養素をトレースする-栄養添加物はまた、同位体標識された栄養素（ 例えば、15 N-NO 3）を含むことができます。しかし、同位体ベースの研究は、多くの場合、EXPEですnsiveと同位体で標識された栄養素を保持することができる複数の底生区画の挑戦的な分析（ 例えば消化）が必要です。最近の実験はその場生物地球化学的反応でリアルタイムに検討することにより、新しい方法を明らかにし、そのようなDOM 9,10-などの非添加し、周囲の溶質上のコントロールを解明する短期的な栄養パルスの有用性を明らかにしました。ここでは説明し、非常に多様なDOMプールでCとNと特異的にコントロールの結合された生物地球化学を理解することを目的とした短期的な栄養パルスを実施するための鍵の方法論の手順を示しています。この簡単に再現性のある方法は、実験的なストリームリーチに栄養パルスを追加し、操作溶質と関心の応答変数（ 例えば DOC、DON、DOP）の両方の濃度の変化を測定することを含みます。直接その場で栄養濃度を操作することによって、我々は間接的にDOMを変更することができます栄養濃度10のダイナミックレンジ全体でどのようにDOMの濃度変化をプールし、検討します。

<table border="0" cellpadding="0" cellspacing="0" width="593">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Sodium Nitrate</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td style="width:167px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Sodium Chloride</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td>Store purchased table salt can be used as well, however, it does contain trace levels of impurities</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:216px;">Whatman GFF glass-fiber filters</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">BD Filtering Syringe</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:216px;">EMD Millipore Swinnex Filter Holders</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Syringe stop-cock</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="84">
			<td height="84" style="height:84px;width:216px;">YSI Multi-parameter probe</td>
			<td style="width:91px;">Yellow Springs International</td>
			<td>556-01</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:216px;">Wide mouth HDPE 125 ml bottles</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">60 ml HDPE bottles</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">20 L bucket</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Field measuring tape</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Lab labeling tape</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Stir stick</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Cooler</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Sharpie pen</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Field notebook</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Tweezers</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Zip-lock bags</td>
			<td style="width:91px;">Any</td>
			<td style="width:119px;">Any</td>
			<td></td>
		</tr>
	</tbody>
</table>

understanding dissolved organic matter biogeochemistry through in situ nutrient manipulations in stream ecosystems

Dissolved organic matter (DOM) is a highly diverse mixture of molecules providing one of the largest sources of energy and nutrients to stream ecosystems. Yet the in situ study of DOM is difficult as the molecular complexity of the DOM pool cannot be easily reproduced for experimental purposes. Nutrient additions to streams however, have been shown to repeatedly alter the in situ and ambient DOM pool. Here we demonstrate an easily replicable field-based method for manipulating the ambient pool of DOM at the ecosystem scale. During nutrient pulse experiments changes in the concentration of both dissolved organic carbon and dissolved organic nitrogen can be examined across a wide-range of nutrient concentrations. This method allows researchers to examine the controls on the DOM pool and make inferences regarding the role and function that certain fractions of the DOM pool play within ecosystems. We advocate the use of this method as a technique to help develop a deeper understanding of DOM biogeochemistry and how it interacts with nutrients. With further development this method may help elucidate the dynamics of DOM in other ecosystems.

<img alt="Figure 3" src="/files/ftp_upload/54704/54704fig3.jpg" /> 
Figure 3: Example Results from Nitrate (NO3-) Additions with Dissolved Organic Nitrogen (DON) as the Response Variable. Analyses are linear regressions. Asterisks represent statistical significance at &#945; = 0.05. Note the dynamic range in NO3- concentration that was achieved with the nutrient pulse method. Different panels represent different experiments across months and sites. Site acronyms refer to the three experimental streams10. Positive correlations are interpreted to reflect DON&#39;s role as a nutrient source while negative correlations are interpreted to reflect DON&#39;s role as an energy source. Experiments that resulted in no significant relationship are interpreted as either to reflect a non-responsive DON pool (i.e. highly recalcitrant) or that nutrient-based processes and energy-based process are off-setting. Please see Wymore et al.10 for additional discussion of results. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54704/54704fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" src="/files/ftp_upload/54704/54704fig4.jpg" /> 
Figure 4: Example Results from Nitrate (NO3-) Additions with Dissolved Organic Carbon (DOC) as the Response Variable. Analyses are linear regressions. Asterisks represent statistical significance at &#945; = 0.05. Different panels represent different experiments across months and sites. Site acronyms refer to the three experimental streams10. Across the majority of experiments no significant changes in the ambient DOC pool were observed. Negative results can be revealing about coupled biogeochemical processes. Please see Wymore et al.10 for additional discussion of results. <a href="https://www-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54704/54704fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Through the direct in situ manipulation of NO3-, we were able to indirectly alter concentrations of the DOM pool providing insight into the biogeochemical controls on the ambient DOM pool. Figure 3 shows results from a study that examined the interaction between NO3- and DON10. Although the exact magnitude of solute increase varied across experiments (due to variation in background solute concentration) sufficiently large gradients of NO3- were created via the nutrient addition approach. From this set of experiments, across three watersheds in New Hampshire, USA, we are able to make inferences about the ecological role of DON in headwater streams. As an organic nutrient, DON may serve as either an energy source (carbon) or as a nitrogen source. In these low NO3- streams, we interpreted the increase in DON concentration to reflect its utilization as a nutrient source. By providing the microbial communities with a highly available form of N as NO3-, the community shifted from DON to this newly available form. This has previously been referred to as the DON release hypothesis15. In contrast, the negative correlations we observed during these nitrate manipulations are interpreted to reflect DON utilization as an energy source. This heterotrophic process has been termed the passive-carbon vehicle hypothesis1,15. The highly variable response of DON throughout the growing season suggests strong seasonality in how DON responds to added nutrients. These data provide some of the first field-based experimental results regarding the ecological role that DON serves within stream ecosystems.
Negative results from these ecosystem manipulations are also revealing with respect to controls on biogeochemical processes. For example, Figure 4 shows no measurable response in the ambient DOC pool to the addition of NO3-. This suggests that the ambient pool of DOC is highly recalcitrant (i.e. not bioreactive). When nutrient pulses are repeatedly performed over the growing season for example, we can make inferences and conclusions about how and when the different fractions of the DOM pool are used by aquatic microbial communities. Through these manipulative ecosystem-scale experiments we were able to discern interactions between certain fractions of the DOM pool across a dynamic range of the added nutrient. These results in particular suggest that the N-rich fraction and C-rich fraction of the DOM pool cycle independently and may have their own unique set of ecological and biogeochemical controls16,17. By using this nutrient addition method we have been able to provide manipulative field-based data which provides strong evidence and support to patterns of DON lability that had only previously been observed in laboratory incubations18,19.

Watch this Scientific Journal Video about Understanding Dissolved Organic Matter Biogeochemistry Through In Situ Nutrient Manipulations in Stream Ecosystems at JoVE.com

河川生態系におけるその場での栄養塩操作を通じた溶存有機物の生物地球化学の理解 |環境 |ビデオ

Understanding Dissolved Organic Matter Biogeochemistry Through In Situ Nutrient Manipulations in Stream Ecosystems

Dissolved organic matter provides an important source of energy and nutrients to stream ecosystems. Here we demonstrate a field-based method to manipulate the ambient pool of dissolved organic matter in situ through easily replicable nutrient pulses.

溶存有機物生物地球化学を理解します<em&gt;その場で</em&gt;ストリーム生態系における栄養操作を

Dissolved organic matter (DOM) is a highly diverse mixture of molecules providing one of the largest sources of energy and nutrients to stream ecosystems. ...

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Understanding Dissolved Organic Matter Biogeochemistry Through In Situ Nutrient Manipulations in Stream Ecosystems

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10.1K ビュー.  University of New Hampshire. Dissolved organic matter provides an important source of energy and nutrients to stream ecosystems. Here we demonstrate a field-based method to manipulate the ambient pool of dissolved organic matter in situ through easily replicable nutrient pulses.

ビデオ: Understanding Dissolved Organic Matter Biogeochemistry Through In Situ Nutrient Manipulations in Stream Ecosystems

VacuSIP, an Improved InEx Method for In Situ Measurement of Particulate and Dissolved Compounds Processed by Active Suspension Feeders

Benthic suspension feeders play essential roles in the functioning of marine ecosystems. By filtering large volumes of water, removing plankton and detritus, and excreting particulate and dissolved compounds, they serve as important agents for benthic-pelagic coupling. Accurately measuring the compounds removed and excreted by suspension feeders (such as sponges, ascidians, polychaetes, bivalves) is crucial for the study of their physiology, metabolism, and feeding ecology, and is fundamental to determine the ecological relevance of the nutrient fluxes mediated by these organisms. However, the assessment of the rate by which suspension feeders process particulate and dissolved compounds in nature is restricted by the limitations of the currently available methodologies. Our goal was to develop a simple, reliable, and non-intrusive method that would allow clean and controlled water sampling from a specific point, such as the excurrent aperture of benthic suspension feeders, in situ. Our method allows simultaneous sampling of inhaled and exhaled water of the studied organism by using minute tubes installed on a custom-built manipulator device and carefully positioned inside the exhalant orifice of the sampled organism. Piercing a septum on the collecting vessel with a syringe needle attached to the distal end of each tube allows the external pressure to slowly force the sampled water into the vessel through the sampling tube. The slow and controlled sampling rate allows integrating the inherent patchiness in the water while ensuring contamination free sampling. We provide recommendations for the most suitable filtering devices, collection vessel, and storing procedures for the analyses of different particulate and dissolved compounds. The VacuSIP system offers a reliable method for the quantification of undisturbed suspension feeder metabolism in natural conditions that is cheap and easy to learn and apply to assess the physiology and functional role of filter feeders in different ecosystems.

VacuSIP, an Improved InEx Method for In Situ Measurement of Particulate and Dissolved Compounds Processed by Active Suspension Feeders

We introduce the VacuSIP, a simple, non-intrusive, and reliable method for clean and accurate point sampling of water. The system was developed and evaluated for the simultaneous collection of the water inhaled and exhaled by benthic suspension feeders in situ, to cleanly measure removal and excretion of particulate and dissolved compounds.

VacuSIP、のための改良INEX方法<em&gt;その場で</em&gt;微粒子と溶解した化合物の測定は、アクティブサスペンションフィーダによって処理します

Benthic suspension feeders play essential roles in the functioning of marine ecosystems. By filtering large volumes of water, removing plankton and ...

環境学

Production and Measurement of Organic Particulate Matter in a Flow Tube Reactor

Organic particulate matter (PM) is increasingly recognized as important to the Earth's climate system as well as public health in urban regions, and the production of synthetic PM for laboratory studies have become a widespread necessity. Herein, experimental protocols demonstrate approaches to produce aerosolized organic PM by &#945;-pinene ozonolysis in a flow tube reactor. Methods are described for measuring the size distributions and morphology of the aerosol particles. The video demonstrates basic operations of the flow tube reactor and related instrumentation. The first part of the video shows the procedure for preparing gas-phase reactants, ozonolysis, and production of organic PM. The second part of the video shows the procedures for determining the properties of the produced particle population. The particle number-diameter distributions show different stages of particle growth, namely condensation, coagulation, or a combination of both, depending on reaction conditions. The particle morphology is characterized by an aerosol particle mass analyzer (APM) and a scanning electron microscope (SEM). The results confirm the existence of non-spherical particles that have grown from coagulation for specific reaction conditions. The experimental results also indicate that the flow tube reactor can be used to study the physical and chemical properties of organic PM for relatively high concentrations and short time frames.

This paper describes the operation procedure for the flow tube reactor and related data collection. It shows the protocols for setting the experiments, recording data and generating the number-diameter distribution as well as the particle mass information, which gives useful information about chemical and physical properties of the organic aerosols.

生産と流管炉の粒子状有機物の測定

Organic particulate matter (PM) is increasingly recognized as important to the Earth's climate system as well as public health in urban regions, and the ...

Production and Measurement of Organic Particulate Matter in the Harvard Environmental Chamber

The production and the evolution of atmospheric organic particulate matter (PM) are insufficiently understood for accurate simulations of atmospheric chemistry and climate. The complex production mechanisms and reaction pathways make this a challenging research topic. To address these issues, an environmental chamber, providing enough residence time and close-to-ambient concentrations of precursors for secondary organic materials, is needed. The Harvard Environmental Chamber (HEC) was built to serve this need, simulating the production of gas and particle phase species from volatile organic compounds (VOCs). The HEC has a volume of 4.7 m3 and a mean residence time of 3.4 h under typical operating conditions. It is operated as a completely mixed flow reactor (CMFR), providing the possibility of indefinite steady-state operation across days for sample collection and data analysis. The operation procedures are described in detail in this article. Several types of instrumentation are used to characterize the produced gas and particles. A High-Resolution Time-of-Fight Aerosol Mass Spectrometer (HR-ToF-AMS) is used to characterize particles. A Proton-Transfer-Reaction Mass Spectrometer (PTR-MS) is used for gaseous analysis. Example results are presented to show the use of the environmental chamber in a wide variety of applications related to the physicochemical properties and reaction mechanisms of organic atmospheric particulate matter.

This paper describes operation procedures for the Harvard Environmental Chamber (HEC) and related instrumentation for measuring gaseous and particle species. The environmental chamber is used to produce and study secondary organic species produced from the organic precursors, especially related to atmospheric organic particulate matter.

生産およびハーバード大学環境チャンバーにおける有機粒子状物質の測定

The production and the evolution of atmospheric organic particulate matter (PM) are insufficiently understood for accurate simulations of atmospheric ...

Bioindication Testing of Stream Environment Suitability for Young Freshwater Pearl Mussels Using In Situ Exposure Methods

Knowledge of habitat suitability for freshwater mussels is an important step in the conservation of this endangered species group. We describe a protocol for performing in situ juvenile exposure tests within oligotrophic river catchments over one-month and three-month periods. Two methods (in both modifications) are presented to evaluate the juvenile growth and survival rate. The methods and modifications differ in value for the locality bioindication and each has its benefits as well as limitations. The sandy cage method works with a large set of individuals, but only some of the individuals are measured and the results are evaluated in bulk. In the mesh cage method, the individuals are kept and measured separately, but a low individual number is evaluated. The open water exposure modification is relatively easy to apply; it shows the juvenile growth potential of sites and can also be effective for water toxicity testing. The within-bed exposure modification needs a high workload but is closer to the conditions of a natural juvenile environment and it is better for reporting the real suitability of localities. On the other hand, more replications are needed in this modification due to its high-hyporheic environment variability.

Bioindication Testing of Stream Environment Suitability for Young Freshwater Pearl Mussels Using In Situ Exposure Methods

In situ bioindications enable determination of the suitability of an environment for endangered mussel species. We describe two methods based on the juvenile exposure of freshwater pearl mussels in cages to oligotrophic river habitats. Both methods are implemented in variants for open water and hyporheic water environments.

若い淡水パール ムール貝原露出メソッドを使用して Bioindication ストリーム環境適合性のテスト

Knowledge of habitat suitability for freshwater mussels is an important step in the conservation of this endangered species group. We describe a protocol ...

Improving Infrared Spectroscopy Characterization of Soil Organic Matter with Spectral Subtractions

Soil organic matter (SOM) underlies numerous soil processes and functions. Fourier transform infrared (FTIR) spectroscopy detects infrared-active organic bonds that constitute the organic component of soils. However, the relatively low organic matter content of soils (commonly &#60; 5% by mass) and absorbance overlap of mineral and organic functional groups in the mid-infrared (MIR) region (4,000-400 cm-1) engenders substantial interference by dominant mineral absorbances, challenging or even preventing interpretation of spectra for SOM characterization. Spectral subtractions, a post-hoc mathematical treatment of spectra, can reduce mineral interference and enhance resolution of spectral regions corresponding to organic functional groups by mathematically removing mineral absorbances. This requires a mineral-enriched reference spectrum, which can be empirically obtained for a given soil sample by removing SOM. The mineral-enriched reference spectrum is subtracted from the original (untreated) spectrum of the soil sample to produce a spectrum representing SOM absorbances. Common SOM removal methods include high-temperature combustion (&#39;ashing&#39;) and chemical oxidation. Selection of the SOM removal method carries two considerations: (1) the amount of SOM removed, and (2) absorbance artifacts in the mineral reference spectrum and thus the resulting subtraction spectrum. These potential issues can, and should, be identified and quantified in order to avoid fallacious or biased interpretations of spectra for organic functional group composition of SOM. Following SOM removal, the resulting mineral-enriched sample is used to collect a mineral reference spectrum. Several strategies exist to perform subtractions depending on the experimental goals and sample characteristics, most notably the determination of the subtraction factor. The resulting subtraction spectrum requires careful interpretation based on the aforementioned methodology. For many soil and other environmental samples containing substantial mineral components, subtractions have strong potential to improve FTIR spectroscopic characterization of organic matter composition.

SOM underlies many soil functions and processes, but its characterization by FTIR spectroscopy is often challenged by mineral interferences. The described method can increase the utility of SOM analysis by FTIR spectroscopy by subtracting mineral interferences in soil spectra using empirically obtained mineral reference spectra.

スペクトル減算と土壌有機物の赤外分光特性の向上

Soil organic matter (SOM) underlies numerous soil processes and functions. Fourier transform infrared (FTIR) spectroscopy detects infrared-active organic ...

Single-throughput Complementary High-resolution Analytical Techniques for Characterizing Complex Natural Organic Matter Mixtures

Natural organic matter (NOM) is composed of a highly complex mixture of thousands of organic compounds which, historically, proved difficult to characterize. However, to understand the thermodynamic and kinetic controls on greenhouse gas (carbon dioxide [CO2] and methane [CH4]) production resulting from the decomposition of NOM, a molecular-level characterization coupled with microbial proteome analyses is necessary. Further, climate and environmental changes are expected to perturb natural ecosystems, potentially upsetting complex interactions that influence both the supply of organic matter substrates and the microorganisms performing the transformations. A detailed molecular characterization of the organic matter, microbial proteomics, and the pathways and transformations by which organic matter is decomposed will be necessary to predict the direction and magnitude of the effects of environmental changes. This article describes a methodological throughput for comprehensive metabolite characterization in a single sample by direct injection Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS), gas chromatography mass spectrometry (GC-MS), nuclear magnetic resonance (NMR) spectroscopy, liquid chromatography mass spectrometry (LC-MS), and proteomics analysis. This approach results in a fully-paired dataset which improves statistical confidence for inferring pathways of organic matter decomposition, the resulting CO2 and CH4 production rates, and their responses to environmental perturbation. Herein we present results of applying this method to NOM samples collected from peatlands; however, the protocol is applicable to any NOM sample (e.g., peat, forested soils, marine sediments, etc.).

This protocol describes a single throughput for complementary analytical and omics techniques culminating in a fully-paired characterization of natural organic matter and microbial proteomics in different ecosystems. This approach permits robust comparisons for identifying metabolic pathways and transformations important for describing greenhouse gas production and predicting responses to environmental change.

シングル スループット複雑な天然有機物の混合物の評価の補完的な高解像度分析の手法

Natural organic matter (NOM) is composed of a highly complex mixture of thousands of organic compounds which, historically, proved difficult to ...

Leaf Area Index Estimation Using Three Distinct Methods in Pure Deciduous Stands

Accurate estimations of leaf area index (LAI), defined as half of the total leaf surface area per unit of horizontal ground surface area, are crucial for describing the vegetation structure in the fields of ecology, forestry, and agriculture. Therefore, procedures of three commercially used methods (litter traps, needle technique, and a plant canopy analyzer) for performing LAI estimation were presented step-by-step. Specific methodological approaches were compared, and their current advantages, controversies, challenges, and future perspectives were discussed in this protocol. Litter traps are usually deemed as the reference level. Both the needle technique and the plant canopy analyzer (e.g., LAI-2000) frequently underestimate LAI values in comparison with the reference. The needle technique is easy to use in deciduous stands where the litter completely decomposes each year (e.g., oak and beech stands). However, calibration based on litter traps or direct destructive methods is necessary. The plant canopy analyzer is a commonly used device for performing LAI estimation in ecology, forestry, and agriculture, but is subject to potential error due to foliage clumping and the contribution of woody elements in the field of view (FOV) of the sensor. Eliminating these potential error sources was discussed. The plant canopy analyzer is a very suitable device for performing LAI estimations at the high spatial level, observing a seasonal LAI dynamic, and for long-term monitoring of LAI.

An accurate estimation of leaf area index (LAI) is crucial for many models of material and energy fluxes within plant ecosystems and between an ecosystem and the atmospheric boundary layer. Therefore, three methods (litter traps, needle technique, and PCA) for taking precise LAI measurements were in the presented protocol.

純粋な落葉スタンドにおける3つの異なる方法を用いてリーフエリア指数推定

Accurate estimations of leaf area index (LAI), defined as half of the total leaf surface area per unit of horizontal ground surface area, are crucial for ...

Fluorescently Labeled Bacteria as a Tracer to Reveal Novel Pathways of Organic Carbon Flow in Aquatic Ecosystems

Elucidating trophic interactions, such as predation and its effects, is a frequent task for many researchers in ecology. The study of microbial communities has many limitations, and determining a predator, prey, and predatory rates is often difficult. Presented here is an optimized method based on the addition of fluorescently labelled prey as a tracer, which allows for reliable quantitation of the grazing rates in aquatic predatory eukaryotes and estimation of nutrient transfer to higher trophic levels.

Presented here is a protocol for a single-cell, epifluorescence microscopy-based technique to quantify grazing rates in aquatic predatory eukaryotes with high precision and taxonomic resolution.

水生生態系における有機炭素流の新しい経路を明らかにするトレーサーとしての蛍光標識細菌

Elucidating trophic interactions, such as predation and its effects, is a frequent task for many researchers in ecology. The study of microbial ...

Modeling the Size Spectrum for Macroinvertebrates and Fishes in Stream Ecosystems

The size spectrum is an inverse, allometric scaling relationship between average body mass (M) and the density (D) of individuals within an ecological community or food web. Importantly, the size spectrum assumes that individual size, rather than species&#8217; behavioral or life history characteristics, is the primary determinant of abundance within an ecosystem. Thus, unlike traditional allometric relationships that focus on species-level data (e.g., mean species&#8217; body size vs. population density), size spectra analyses are &#8216;ataxic&#8217; &#8211; individual specimens are identified only by their size, without consideration of taxonomic identity. Size spectra models are efficient representations of traditional, complex food webs and can be used in descriptive as well as predictive contexts (e.g., predicting responses of large consumers to changes in basal resources). Empirical studies from diverse aquatic ecosystems have also reported moderate to high levels of similarity in size spectra slopes, suggesting that common processes may regulate the abundances of small and large organisms in very different settings. This is a protocol to model the community-level size spectrum in wadable streams. The protocol consists of three main steps. First, collect quantitative benthic fish and invertebrate samples that can be used to estimate local densities. Second, standardize the fish and invertebrate data by converting all individuals to ataxic units (i.e., individuals identified by size, irrespective of taxonomic identity), and summing individuals within log2 size bins. Third, use linear regression to model the relationship between ataxic M and D estimates. Detailed instructions are provided herein to complete each of these steps, including custom software to facilitate D estimation and size spectra modeling.

This is a protocol to model the size spectrum (scaling relationship between individual mass and population density) for combined fish and invertebrate data from wadable streams and rivers. Methods include: field techniques to collect quantitative fish and invertebrate samples; lab methods to standardize the field data; and statistical data analysis.

河川生態系におけるマクロ無脊椎動物と魚類のサイズスペクトルのモデリング

The size spectrum is an inverse, allometric scaling relationship between average body mass (M) and the density (D) of individuals within an ecological ...

Combining Fluidic Devices with Microscopy and Flow Cytometry to Study Microbial Transport in Porous Media Across Spatial Scales

Understanding the transport, dispersion and deposition of microorganisms in porous media is a complex scientific task comprising topics as diverse as hydrodynamics, ecology and environmental engineering. Modeling bacterial transport in porous environments at different spatial scales is critical to better predict the consequences of bacterial transport, yet current models often fail to up-scale from laboratory to field conditions. Here, we introduce experimental tools to study bacterial transport in porous media at two spatial scales. The aim of these tools is to obtain macroscopic observables (such as breakthrough curves or deposition profiles) of bacteria injected into transparent porous matrices. At the small scale (10-1000 &#181;m), microfluidic devices are combined with optical video-microscopy and image processing to obtain breakthrough curves and, at the same time, to track individual bacterial cells at the pore scale. At larger scale, flow cytometry is combined with a self-made robotic dispenser to obtain breakthrough curves. We illustrate the utility of these tools to better understand how bacteria are transported in complex porous media such as the hyporheic zone of streams. As these tools provide simultaneous measurements across scales, they pave the way for mechanism-based models, critically important for upscaling. Application of these tools may not only contribute to the development of novel bioremediation applications but also shed new light on the ecological strategies of microorganisms colonizing porous substrates.

Breakthrough curves (BTCs) are efficient tools to study the transport of bacteria in porous media. Here we introduce tools based on fluidic devices in combination with microscopy and flow cytometric counting to obtain BTCs.

流体デバイスと顕微鏡とフローサイトメトリーを組み合わせて、空間スケールを越えた多孔質培地における微生物輸送を研究

Understanding the transport, dispersion and deposition of microorganisms in porous media is a complex scientific task comprising topics as diverse as ...