<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJE</journal-id><journal-title-group><journal-title>Open Journal of Ecology</journal-title></journal-title-group><issn pub-type="epub">2162-1985</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oje.2015.510043</article-id><article-id pub-id-type="publisher-id">OJE-60733</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Earth&amp;Environmental Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Experimental Study in Out-Door Tanks of N and P Uptake by the Aquatic Communities of Lake Kinneret
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>oshe</surname><given-names>Gophen</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Andre</surname><given-names>Janurik</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Szarvas Research Station, Annaliget, Hungary</addr-line></aff><aff id="aff1"><addr-line>Migal-Scientific Research Institute, Kiryat Shmone, Israel</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>Gophen@Migal.org.il(OG)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>09</day><month>10</month><year>2015</year></pub-date><volume>05</volume><issue>10</issue><fpage>528</fpage><lpage>536</lpage><history><date date-type="received"><day>9</day>	<month>September</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>26</month>	<year>October</year>	</date><date date-type="accepted"><day>29</day>	<month>October</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Two trials (1
  <sup>st</sup> Trial-46 and 2
  <sup>nd</sup> Trial-64 hrs duration) experiment in 8 out-door tanks (5 m
  <sup>3</sup>) were carried out with similar design: 4 fish densities (0, 1, 5, and 10), 2 densities of zooplankton (high and low) and 4 increasing levels of P and N concentrations of nutrient enrichments. The consecutive changes of N and P concentrations were measured at 3 (Trial 1) and 4 (Trial 2) time intervals. It was found that nutrient uptake of the entire community, which is the differences between initial and final concentrations, was mostly affected by the initial enrichment. The ecological implications are discussed.
 
</p></abstract><kwd-group><kwd>Kinneret</kwd><kwd> N &amp; P</kwd><kwd> Community Uptake</kwd><kwd> Zooplankton</kwd><kwd> Common Carp</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The research of nutrient uptake by zooplankton is a worldwide investigated issue. The majority of these studies were experimentally carried out under laboratory conditions. Nevertheless a move from isolated artificial small volume systems (jars, bottles, test-tubes etc.) to larger volumes is becoming more common. The usage of large outdoor tanks, shallow ponds, mesocosms and others for the study of nutrient uptake, or interrelationships between food-web compartments is commonly used in Marine and Freshwater ecosystems [<xref ref-type="bibr" rid="scirp.60733-ref1">1</xref>] -[<xref ref-type="bibr" rid="scirp.60733-ref5">5</xref>] .</p><p>The epilimnetic biota of deep lakes is mostly comprised of three major components: phytoplankton (small and large size algae), zooplankton (micro and macro animals) and fish (large adults, small larvae and fingerlings). In Lake Kinneret the component of large body invertebrates is absent. The nutrient cycles, inputs and outputs as well as mass balances were intensively explored accompanied by long-term record of their availabilities. Moreover, indirect evaluation of nutrients utilization by plankton and geochemical transfer and losses were carried out and models were created. We studied the N and P uptake by the entire community in large volume facility (5 m<sup>3</sup> tanks) where three variables (zooplankton and fish densities and nutrient concentrations) were modified. Similar studies were also performed by monitoring of ecological variables in natural ecosystems. In this paper we present results of 46 and 64 hours experimental study of nitrogen and phosphorus uptake by the entire community (zooplankton, phytoplankton and fish). The experiments were carried out in out-door large tanks (5 m<sup>3</sup>) and three levels of the variables: fish and zooplankton densities and nutrient (P and N) availabilities.</p><p>There are 24 fish species in Lake Kinneret of which 5 are exotics. The exotic Mugilids and Silver Carp are not reproduced in the lake and therefore annually introduced. Oreochromis aureus, and the Common Carp, Cyprinus carpio are reproduced in the lake and therefore not additionally introduced. The present existence of the latter two in the lake was resulted by old introductions which later totally stopped. The impact of the exotic fishes, excluding Common Carp, on the Lake Kinneret water quality was previously studied. The present study is aimed at both, N and P uptake indication accompanied by an attempt to evaluate potential effect of Common Carp on the Kinneret water quality. The Kinneret ecosystem structure has been modified and nutrient availabilities was shifted from P to N limitation [<xref ref-type="bibr" rid="scirp.60733-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.60733-ref7">7</xref>] . Consequently trophic relations between food-web compartment were modified [<xref ref-type="bibr" rid="scirp.60733-ref8">8</xref>] -[<xref ref-type="bibr" rid="scirp.60733-ref10">10</xref>] .</p></sec><sec id="s2"><title>2. Material and Methods</title><p>The experiments were carried out in eight 5 m<sup>3</sup> outdoor tanks directly supplied by Lake Kinneret waters (intake depth- 1.5 m 100 m from shoreline). The tanks are equipped with compressed air lift aeration system. The experiments design is given in <xref ref-type="table" rid="table1">Table 1</xref>. The fishes were 100 - 150 g/Ind. of Common Carp (Cyprinus carpio). Two densities level (high and low) of Zooplankton were maintained. The lake density of large body zooplankton was about 50 per 1 liter. For the experimental addition we collected zooplankton in the open water zone (&gt;20 m depth) of the lake, by down (15 m) and up 15 time hauls of 100 μ mesh plankton net with 25 cm diameter open mouth. The total quantity of filtered lake water was approximated as 2.5 m<sup>3</sup>. Collected animals were carefully flushed from the net collector (bucket) into 20 L (lake water) pail and continuously mixed. One liter and 0.5 liter were removed from the pail while mixing into each of the experimental tanks with “High” and “Low” additional zooplankton respectfully. The initial zooplankton densities were approximated as 70 and 60 organisms per liter in the “High” and “Low” tanks respectively. The zooplankton addition was done separately for Trial 1 and 2 (<xref ref-type="table" rid="table1">Table 1</xref>). In order to emphasize temporal changes, 2 trials were carried out: the time duration of the 1<sup>st</sup> trial was 46 hours and for the second-64 hours. The two trials were carried out with similar fish number (densities) and the same individuals. The zooplankton was collected separately for each trial by the same procedure and time interval between the two trials was 3 days. Evaporated water loss was compensated by pumped lake water during the 3 days interval between trials. Additional nutrients were given initially to the tanks in 2 (Trial 1) and 3 levels (Trial 2). The nutrients initial concentrations in the tanks are given in <xref ref-type="table" rid="table2">Table 2</xref>. In the first trial, three samples were collected: (initial, 24 and 46 hours); in the second Trial-4 samples (initial, 41, 48 and 64 hours). Added nutrients were NH<sub>4</sub>Cl and Na<sub>3</sub>PO<sub>4</sub>. Nutrients were added at three levels and their averages (SD) of all treatments for each sampling time (1<sup>st</sup> Trial-3, and 2<sup>nd</sup> Trial-4) are given in <xref ref-type="table" rid="table2">Table 2</xref> (Trial 1) and <xref ref-type="table" rid="table3">Table 3</xref> (Trial 2). Aeration was operated 2 hours during day time every 24 hours.</p><p>To determine concentrations of P-PO<sub>4</sub> and N-NH<sub>4</sub> we used analysis procedures given in [<xref ref-type="bibr" rid="scirp.60733-ref11">11</xref>] .</p></sec><sec id="s3"><title>3. Results</title><p>ANOVA comparative tests (p &lt; 0.05) were carried out aimed at indication if there is an impact of zooplankton and fish densities and enrichment levels on the community uptake of nutrients. The uptake measure was considered as the nutrient concentration differences between initial and final time. Results of Trial 1 indicates: zooplankton and fish densities did not have significant impact (all p values were higher than 0.05) on the total (include: initial, 24 hr and 46 hr) averages of P-PO<sub>4</sub> and N-NH<sub>4</sub> concentrations. The only significant effect on community uptake of nutrients was that of enrichment levels. Similarly, in the 2<sup>nd</sup> Trial, the only significant (p &lt; 0.05) impact on the total (including all samples) averaged concentrations of P-PO<sub>4</sub> and N-NH<sub>4</sub> was that of nutrient enrichments. Nevertheless, successive processes evaluation presented as a continuous figures plotting;</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Experimental design: zooplankton addition (H = High; L = Low) and fish number in the tanks</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Tank No.</th><th align="center" valign="middle" >Additional Zooplankton Level</th><th align="center" valign="middle" >Number of Fishes</th></tr></thead><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >H</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >L</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >H</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >L</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >5</td><td align="center" valign="middle" >H</td><td align="center" valign="middle" >5</td></tr><tr><td align="center" valign="middle" >6</td><td align="center" valign="middle" >L</td><td align="center" valign="middle" >5</td></tr><tr><td align="center" valign="middle" >7</td><td align="center" valign="middle" >H</td><td align="center" valign="middle" >10</td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >L</td><td align="center" valign="middle" >10</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Three sampled (0, 24, 46 hours) averages (SD) concentrations of N-NH<sub>4</sub> and P-PO<sub>4</sub> in 8 tanks, and 3 levels of enrichment</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Nutrient</th><th align="center" valign="middle" >Enrichment levels (ppm)</th><th align="center" valign="middle" >Averaged concentration (ppm) (SD) of all treatments in three samples: 0, 24, 46 hrs</th></tr></thead><tr><td align="center" valign="middle" >N-NH<sub>4</sub></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.599 (0.140)</td></tr><tr><td align="center" valign="middle" >N-NH<sub>4</sub></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.036 (0.169)</td></tr><tr><td align="center" valign="middle" >N-NH<sub>4</sub></td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >1.554 (0.117)</td></tr><tr><td align="center" valign="middle" >P-PO<sub>4</sub></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.275 (0.023)</td></tr><tr><td align="center" valign="middle" >P-PO<sub>4</sub></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.522 (0.033)</td></tr><tr><td align="center" valign="middle" >P-PO<sub>4</sub></td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >0.758 (0.103)</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Initial averaged (SD) concentration of N-NH<sub>4</sub> and P-PO<sub>4</sub> in 8 tanks of Trial 2 respective to enrichment level: 0, 1, 2 and 3. Original concentrations were: N-NH<sub>4</sub> = 0.1939 ppm and P-PO<sub>4</sub> = 0.0362 ppm</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Nutrient</th><th align="center" valign="middle" >Enrichment levels: 1, 2, 30.</th><th align="center" valign="middle" >Averaged concentration (ppm) (SD) of all treatments in four samples: 0, 41, 48, 64 hrs</th></tr></thead><tr><td align="center" valign="middle" >N-NH<sub>4</sub></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.8178 (0.3026)</td></tr><tr><td align="center" valign="middle" >N-NH<sub>4</sub></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.3985 (0.2481)</td></tr><tr><td align="center" valign="middle" >N-NH<sub>4</sub></td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >2.1352 (0.3636)</td></tr><tr><td align="center" valign="middle" >P-PO<sub>4</sub></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.2684 (0.0096)</td></tr><tr><td align="center" valign="middle" >P-PO<sub>4</sub></td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.5369 (0.0202)</td></tr><tr><td align="center" valign="middle" >P-PO<sub>4</sub></td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >0.8095 (0.0388)</td></tr></tbody></table></table-wrap><p>several impact factors were indicated as follows:</p><p>Trial 1 (Figures 1-4): <xref ref-type="fig" rid="fig1">Figure 1</xref> indicates that as the initial concentration is increasing, the difference between initial and final (46 hr) time concentration is elevated proportionally too. This difference is a measure of biotic community uptake. The pattern of the changes of the difference between initial time and final time N-NH<sub>4</sub> vs initial time concentration of N-NH<sub>4</sub> changes is similar to those of P-PO<sub>4</sub> (<xref ref-type="fig" rid="fig2">Figure 2</xref>) but not higher than 1.0 ppm of the initial concentration when it is declining. It is not impossible that other processes are involved, such as geochemical oxygenation of NH<sub>4</sub> to be converted to nitrate, also took place. Especially affected by the daily 2 hours aeration in the tanks continuously. Nevertheless the impact of this factor and probably others, was the same in all tanks and therefore differences could be attributed solely to enrichments levels. Results in <xref ref-type="fig" rid="fig2">Figure 2</xref> indicate that not like the uptake of P-PO<sub>4</sub> (<xref ref-type="fig" rid="fig1">Figure 1</xref>) there is a decline of N uptake if initial concentration of NH<sub>4</sub> is above 1.0 ppm. Compatible results are presented in <xref ref-type="fig" rid="fig3">Figure 3</xref>: uptake of P increase while N intake increase up to a level below 0.2 ppm whilst the elevation of P uptake continued slightly. <xref ref-type="fig" rid="fig4">Figure 4</xref> is indicating the trend of uptake elevation of P and N respectively whilst Figures 1-3 emphasize dynamical changes.</p><p>Trial 2 (Figures 5-10): Similar to the 1<sup>st</sup> Trial results presented in <xref ref-type="fig" rid="fig5">Figure 5</xref> indicates increase of N uptake with elevation of P uptake up to 0.1 ppm of NH<sub>4</sub> and decline afterwards. The positive relation between N and P uptake and enrichment levels is presented in <xref ref-type="fig" rid="fig6">Figure 6</xref> and <xref ref-type="fig" rid="fig7">Figure 7</xref> but P uptake slightly declined in the highest (3) level of enrichment. The interpretation of the slight decline of P uptake when N uptake is increasing above</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Trial 1: Fractional polynomial regression between initial PO<sub>4</sub> concentration (ppm) and consumed PO<sub>4</sub> (concentrations difference between initial and 46 hr)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x5.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Trial 1: Fractional polynomial regression between initial NH<sub>4</sub> concentration (ppm) and consumed NH<sub>4</sub> (concentrations difference between initial and 46 hr)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x6.png"/></fig><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Trial 1: Fractional polynomial regression between consumed NH<sub>4</sub> and consumed PO<sub>4</sub> (concentrations (ppm) difference between initial and 46 hr)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x7.png"/></fig><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Trial 1: Polynomial regression (r<sup>2</sup> and p values are given) between total averages (Init., 24, 46 hrs) of NH<sub>4</sub> vs PO<sub>4</sub> concentrations (ppm)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x8.png"/></fig><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> Trial 2: Fractional polynomial regression between consumed (initial minus 64 hr) NH<sub>4</sub> concentration and consumed PO<sub>4</sub> (initial minus 64 hr concentrations, ppm)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x9.png"/></fig><fig id="fig6"  position="float"><label><xref ref-type="fig" rid="fig6">Figure 6</xref></label><caption><title> Trial 2: Fractional polynomial regression between four levels (1 - 4) of enrichments and consumed NH<sub>4</sub> (ppm)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x10.png"/></fig><fig id="fig7"  position="float"><label><xref ref-type="fig" rid="fig7">Figure 7</xref></label><caption><title> Trial 2: Fractional polynomial regression between four levels (1 - 4) of enrichments and consumed PO<sub>4</sub> (ppm)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x11.png"/></fig><fig id="fig8"  position="float"><label><xref ref-type="fig" rid="fig8">Figure 8</xref></label><caption><title> Trial 2: Fractional polynomial regression between 64 hr concentration (ppm) of NH<sub>4</sub> and PO<sub>4</sub></title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x12.png"/></fig><fig id="fig9"  position="float"><label><xref ref-type="fig" rid="fig9">Figure 9</xref></label><caption><title> Trial 2: Polynomial regression (r<sup>2</sup> and p values are given) between consumed (Init. minus 64 hr concentrations, ppm) of NH<sub>4</sub> and PO<sub>4</sub></title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x13.png"/></fig><fig id="fig10"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref>0</label><caption><title> Trial 2: Polynomial regression (r<sup>2</sup> and p values are given) between total averages (Init., 41, 48, 64 hrs) of NH<sub>4</sub> vs PO<sub>4</sub> concentrations (ppm)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1380420x14.png"/></fig><p>1.5 ppm (<xref ref-type="fig" rid="fig8">Figure 8</xref>) is probably an indirect confirmation of stoichiometric regulation (homeostasis) of nutrients uptake [<xref ref-type="bibr" rid="scirp.60733-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.60733-ref13">13</xref>] . The overall comprehensive simultaneous increase of P and N uptake is shown in the regressions presented in <xref ref-type="fig" rid="fig9">Figure 9</xref>, <xref ref-type="fig" rid="fig1">Figure 1</xref>0.</p></sec><sec id="s4"><title>4. Discussion</title><p>The use of nutrient concentration as a measure for community uptake was documented worldwide in aquatic research [<xref ref-type="bibr" rid="scirp.60733-ref14">14</xref>] -[<xref ref-type="bibr" rid="scirp.60733-ref19">19</xref>] . The uniqueness trait of the experimental design presented in this paper is an achievement of experimental structure simplicity by the usage of low number of variables. The outdoor tanks dimensions, the initially usage of lake water composition (chemical and biological) and the aeration procedure and regime were all the same in the tanks. The only independently dissimilar variables between tanks were: nutrient enrichments, zooplankton and fish densities. Several ecological factors were a priori accounted as similar in all tanks: light and temperature conditions, nitrification and de-nitrification processes, photosynthetic activity, and Diurnal Vertical Migration (DVM) of plankton. The focus is given in this paper to the community uptake of N and P nutrients. The ecological conditions (parameters) in the tanks were considered as similar except nutrient concentrations (enrichments), and fish and zooplankton densities. Therefore evaluations of temporal changes (days) were done on these parameters only. Results indicated temporal dissimilarities of community uptake rates of nutrients. The changes of nutrient uptake rates were prominently dissimilar at the final stages of the two trials. Due to the differences in zooplankton and fish densities, variability of N and P consumption were predicted. There are two methods for the analysis of the temporal changes of community consumptions of nutrients: 1) regressive relation between averages and time intervals or in-between nutrients; and 2) regressive relation between continual consequent changes of the parameters of the studied variables with time and in between nutrients. In our study, the 1<sup>st</sup> method resulted similarity between nutrients, on the other hand the 2<sup>nd</sup> method represented only partial similarity. This later dissimilarity was termed by scientists as homeostasis or stoichiometric regulation. It was indicated that during low level of N and P concentration, the uptake of both is maintained simultaneously whilst when N is increasing higher P uptake relatively decline [<xref ref-type="bibr" rid="scirp.60733-ref6">6</xref>] . Significant impact on this was only due to the variable changes of P and N concentration (“Enrichment” in our study) but not zooplankton and fish densities within the frame of the present study. The fish densities in this study were ranged between 20 - 200 g/m<sup>3</sup> whilst the averaged lake density is approximated as 2.5 - 3.5 g/m<sup>3</sup>. The experimental densities did not affect significantly, indirectly or directly, the nutrient uptake regime. The nutrient uptake by biota in the tanks was represented by the left-over of subtraction of the final from initial time concentration. This value represents an overall change where several processes are involved. Nevertheless, the impact of fish and zooplankton densities was found to be an insignificant differ, and it is probable that their effect in all tanks were similar. On the contrary, the impact of nutrient concentrations was significantly dissimilar between tanks. Stoichiometric regulation of N and P uptake in fish is not well known as in zooplankton. Therefore, it is conclusively suggested that zooplankton homeosthasis is involved in the present study conditions. Limiting nutrients are utilized for growth at high efficiency whilst non limiting elements must be therefore disposed off or recycled [<xref ref-type="bibr" rid="scirp.60733-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.60733-ref13">13</xref>] . Hessen [<xref ref-type="bibr" rid="scirp.60733-ref12">12</xref>] stated that there is a tradeoff between metabolic demands of P and the dietary deficiencies of P and/or N. Zooplankton consumption (uptake/excretion) of P and N in Lake Kinneret resulted nutrients turnover time of 8 and 2 days for N and P respectively during summer-fall season [<xref ref-type="bibr" rid="scirp.60733-ref20">20</xref>] . Time durations of the two trials presented here were 1.9 (1<sup>st</sup> Trial) and 2.6 (2<sup>nd</sup> Trial) days which are both shorter (equal for P in 2<sup>nd</sup> Trial) than those measured for N and P in the lake by Rachamim [<xref ref-type="bibr" rid="scirp.60733-ref20">20</xref>] . The potential impact of fish on the nutrients availabilities can be evaluated through their densities in the tanks in comparison with lake conditions. Fish densities in the tanks varied between 20 - 200 g/m<sup>3</sup> whilst fish stock in the lake is approximately ranged between 2.5 - 3.5 g/m<sup>3</sup> and Zooplankton concentration―3.5 - 4.5 g/m<sup>3</sup>. According to the procedure of zooplankton collection by net hauls it can be approximated that its densities in the tanks was slightly higher than in the lake and turnover time of both N and P was therefore shorter than measured by Rachamim [<xref ref-type="bibr" rid="scirp.60733-ref20">20</xref>] under natural conditions in the lake. Consequently it is suggested that recycled elements partly supported N and P for zooplankton requirements. The results documented in the present study does not confirm impact of the Common Carp densities ranged between 20 - 200 g/m<sup>3</sup> on the Kinneret water quality within the time exposure of 46 - 64 hours. Similar conclusion is also attributed to the ranged densities of zooplankton (high and low) and time duration that were examined in the present research.</p></sec><sec id="s5"><title>5. Summary</title><p>Experimental study of the impact of fish and zooplankton densities and nutrient concentrations on N and P community uptake was carried out in 5 m<sup>3</sup> out-door tanks. Two trial durations were tested: 46 and 64 hrs. It was found that increase of initial concentration of N &amp; P was accompanied by increase rate of community uptake of those nutrients. When community uptake of N increased, respective elevation of P consumption was documented but not above 0.2 ppm of N. Then P consumption was increasing irrespective (lower) to N uptake. Moreover, when initial concentration of N increased above 1 ppm, community uptake of N declined. Statistical results analysis indicates significant impacts of initial nutrient concentrations and insignificant effects of zooplankton density level (experimental “High” and “Low”) and fish densities ranged from 20 to 200 g/m<sup>3</sup>.</p></sec><sec id="s6"><title>Cite this paper</title><p>MosheGophen,AndreJanurik, (2015) Experimental Study in Out-Door Tanks of N and P Uptake by the Aquatic Communities of Lake Kinneret. Open Journal of Ecology,05,528-536. doi: 10.4236/oje.2015.510043</p></sec></body><back><ref-list><title>References</title><ref id="scirp.60733-ref1"><label>1</label><mixed-citation publication-type="book" xlink:type="simple">Grice, G.D. and Reeve, M.R., Eds. (1982) Marine Mesocosms: Biological and Chemical Research in Experimental Ecosystems. Heidelberg, New-York, Berlin, 430 p. http://dx.doi.org/10.1007/978-1-4612-5645-8</mixed-citation></ref><ref id="scirp.60733-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Stewart, R.I.A., Dossena, M., Bohan, D.A., Jepppessen, E., et al. (2013) Mesocosm Experiments as a Tool for Ecological Climate-Change Research. Advances in Ecological Research, 48, 71-181. http://dx.doi.org/10.1016/B978-0-12-417199-2.00002-1</mixed-citation></ref><ref id="scirp.60733-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Soto, D. (1989) The Relevance of Reproductive Characteristics of Zooplankton to Experimental Studies in Outdoor Enclosures. Hydrobiologia, 182, 35-47. http://dx.doi.org/10.1007/BF00006366</mixed-citation></ref><ref id="scirp.60733-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Threlkeld, T.S. (1988) Planktivory and Planktivore Biomas Effects on Zooplankton Phytoplankton and Trophic Cascade. Limnology and Oceanography, 33, 1362-1375. http://dx.doi.org/10.4319/lo.1988.33.6.1362</mixed-citation></ref><ref id="scirp.60733-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Drenner, R.W., Threlkeld, S.T. and McCracken, M.D. (1986) Experimental Analysis of the Direct and Indirect Effects of an Omnivorous Filter-Feeding Clupeid on Plankton Community Structure. Canadian Journal of Fisheries and Aquatic Sciences, 43, 1935-1945. http://dx.doi.org/10.1139/f86-239</mixed-citation></ref><ref id="scirp.60733-ref6"><label>6</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Gophen</surname><given-names> M. </given-names></name>,<etal>et al</etal>. (<year>2011</year>)<article-title>The Cladoceran Trophic Status in the Nitrogen Limited Ecosystem of Lake Kinneret (Israel)</article-title><source> Journal of Environmental Biology</source><volume> 32</volume>,<fpage> 455</fpage>-<lpage>462</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.60733-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Gophen, M. (2015) The Impact of Available Nitrogen Deficiency on Long-Term Changes in the Lake Kinneret Ecosystem. Open Journal of Ecology, 5, 147-157. http://dx.doi.org/10.4236/oje.2015.54013</mixed-citation></ref><ref id="scirp.60733-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Gophen, M. (2014) Competitive Consumption of the Lake Kinneret (Israel) Plankton by Hypophthalmichthys molitrix and Sarotherodon galilaeus. Open Journal of Ecology, 4, 532-542. http://dx.doi.org/10.4236/oje.2014.49043</mixed-citation></ref><ref id="scirp.60733-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Gophen, M. (2015) Experimental Study of the Aphanizomenon ovalisporum Response to Nitrogen Fertilization in the Sub-Tropical Eu-Mesotrophic Lake Kinneret (Israel). Open Journal of Ecology, 5, 259-265. http://dx.doi.org/10.4236/oje.2015.56020</mixed-citation></ref><ref id="scirp.60733-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Gophen, M., Smith, V.H., Nishri, A. and Threlkeld, S.T. (1999) Nitrogen Deficiency, Phosphorus Sufficiency, and the Invasion of Lake Kinneret, Israel, by N2-Fixing Cyanobacterium Aphanizomenon ovalisporum. Aquatic Sciences, 1, 1-14. http://dx.doi.org/10.1007/pl00001326</mixed-citation></ref><ref id="scirp.60733-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Wetzel, R.G. and Likens, G.E. (2000) Limnological Analyses. 3rd Edition, Springer, New York, Chapter: Nitrogen, Phosphorus, and Other Nutrients, 85-113. http://dx.doi.org/10.1007/978-1-4757-3250-4</mixed-citation></ref><ref id="scirp.60733-ref12"><label>12</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Hessen</surname><given-names> D.O. </given-names></name>,<etal>et al</etal>. (<year>2005</year>)<article-title>Aquatic Food Webs: Stoiciometric Regulation of Flux and Fate of Carbon. Peter Kilham Memorial Lecture</article-title><source> Verhandlungen des Internationalen Verein Limnologie</source><volume> 29</volume>,<fpage> 39</fpage>-<lpage>49</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.60733-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Elser, J.J., Hayakawa, K. and Urabe, J. (2001) Nutrient Limitation Reduces Food Quality for Zooplankton: Daphnia Response to Seston Phosphorus Enrichment. Ecology, 82, 898-903. http://dx.doi.org/10.1890/0012-9658(2001)082[0898:NLRFQF]2.0.CO;2</mixed-citation></ref><ref id="scirp.60733-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Haggard, B.E., Stanley, E.H. and Storm, D.E. (2005) Nutrient Retention in a Point-Source-Enriched Stream. Journal of the North American Benthological Society, 24, 29-47. http://dx.doi.org/10.1899/0887-3593(2005)024&lt;0029:NRIAPS&gt;2.0.CO;2</mixed-citation></ref><ref id="scirp.60733-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Kemp, M.J. and Dodds, W.K. (2002) The Influence of Ammonium, Nitrate, and Dissolved Oxygen Concentrations on Uptake, Nitrification, and Denitrification Rates Associated with Prairie Stream Substrata. Limnology and Oceanography, 47, 1380-1393. http://dx.doi.org/10.4319/lo.2002.47.5.1380</mixed-citation></ref><ref id="scirp.60733-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Marti, E.J., Gode, A.J., et al. (2004) Nutrient Retention Efficiency in Stream Receiving Inputs from Waste Water Treatment Plants. Journal of Environmental Quality, 33, 285-293. http://dx.doi.org/10.2134/jeq2004.2850</mixed-citation></ref><ref id="scirp.60733-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Mulholland, P.J., Tank, J.L., Webster, R.J., et al. (2002) Can Uptake Length in Stream Be Determined by Nutrient Addition Experiments? Results from an Interbiome Comparison Study. Journal of the North American Benthological Society, 21, 544-560. http://dx.doi.org/10.2307/1468429</mixed-citation></ref><ref id="scirp.60733-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">O’Brien, J.M. and Dodds, W.K. (2009) Ammonium Uptake and Mineralizaqtion in Prairie Stream: Chamber Incubation and Short Term Nutrient Addition Experiments. Freshwater Biology, 53, 102-112.</mixed-citation></ref><ref id="scirp.60733-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Payn, R.A., Webster, J.R., Mulholland, P.J., et al. (2005) Estimation of Stream Nutrient Uptake from Nutrient Addition Experiments. Limnology and Oceanography: Methods, 3, 174-182. http://dx.doi.org/10.4319/lom.2005.3.174</mixed-citation></ref><ref id="scirp.60733-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Rachamim, T., Zohary, T., Berman-Frank, I. and Gal, G. (2009) Nutrient Recycling by Zooplankton in Lake Kinneret (Israel). Poster Presentation in ASLO Aquatic Sciences Meeting 2009, Nice, France, 2009, 25-30.</mixed-citation></ref></ref-list></back></article>