Hydro-ecological relations in the Delta Waters
Hydro-ecological relations in the Delta Waters Hydro-ecological relations in the Delta Waters
period 1980-19$3 in an increase of the anaerobic sed-t suzface area of 4 ta 258 of she entire bottom awfkce (Stronlrhorst. et al. 1985). Qbvioualy, the Veerse Meer is vulnerable to eutreghicatian, owing to the long resid&&e the of water msses, the low extinetian coefficient and the ;Umost permanent stratification. The Oastesschelde estuary has a very low N-lead re6nlting in low chlorophyl concentratisne (Table 2). Wing to the execwtina af the Deltaplan (Pig. 1) the Oostarnehelde estuary has mainly been depriVed recently from its Bhinewater loading (Table 1). Model calculations revealed that a reduction of 50% of the nitrosen bed of the river W e would only lead to a rsduetian of less than 6% for nitrogen eoneentratlons in the 0oster.jkbelde estuary (Smobs-swdel; X. Scholten, peraerial co~u~ication). The Uoster~ohelde estuary is rnainly ir;fluenced by tearhe foastalwffter, containing low conewtrations of total nrtrogen (less than 0.5 slg N 1-l; Srockolano, et al. 1988). Contkaq to the Veerse Meer lag~an. the Creveliagen lagoon has an -2 -1 e%treaely Low N-load (4 g N m y ; Table 2). The CaeWA~mdel (De Vries, et al. 19BEI) revealed that Khe prodtlrcim of phytop.lanktan La the Gzevelingen is liodted by nitrogerl availability and not by light availability. The hl : P ratio of tae dlsselved nufkiems in cke watercolm of the GrwsMngenmeer durins winter is 2-4, poirtcing into the direction of a large surplus af phosphate, notwithstanding Che dominance of nitrogen in the discharge utatet, loading the lagoon Eff : P = 22 : I f. Model calculations showed s Mgh tunrover of ni~rog.~u, in the watercolumn. The chain of processes: nutrient uptake by phpoplanktaa - forslation d organic matter in algal cells - mherallzation of dead algae - regeneratbn of nutrients etc.. occurs 8 tWs a year. &out 90X of the anme1 prisary pr&uction of phytoplanktoa occurs on the baeis of resewrated nutrients, especialLy NB4 CDe Vtim, et al. lS88).
In the GZ3WQ-model ~alculatians CDe VrieB, et al, 19881 it is hypotkerriaed that in the Grevelingen lagoon the process of eutra@ication is prevented by the rate of the denitiificatian process. Dnnit-rifioation is undoubtedly a significant process in marine and estuarine ecaqstems. Rates of gaseous losses af nitr-en in the range -2 -1 of 5-70 mg N m d were determined in Bebgi-an, Dutch and Danish caastsl sedimnts, representing 8-23% of tha amount of nirrwen dnerdtliration in the benthic subaystein Caillen and Lancelot, 1987). Notwithstanding the Eaet that no actual measurements exist on denirrification rates in the Grevelingemeer, it is assumed in the OReWQ-model that deeitrificatiw compensates the load of nitrogen, especially in the benthic bonndary layer in the sedismnr, where aerobic and anaerobic 'patches' o;f sediment join each other. In mahp sballw estuarine waters the nain Foed chain ia dpminated by phyto~laakron and bmthir Eilterf eeders (mussels. cockles) , Just as ie the case in the Greoelingenmeer, Oosterschalde and Wadden Sea. T3e rumover rate sf nutrients in these ecosystems is deteraELned bp the filtering capacity of bsnthic filterfeeders. Theoretieally, every 5 to 10 days the entire valme of water of the estuaries circulates through the filtering apparatus of suspension feeders. Filterfeedem act as natuzal cantrollers of the eutrophicatian psocess (Office, et al. 1982): they deposit organic material from the watercolmn Dntn the bottom mdiments. Mnreover, they accelerate the regeneration of nutrients from the deposited perticulate o~anicarbon, thereby enhancing the primary produetion of pbytopLimktun, as was assuxned for the @xevali~enmeer (De Vries, et al. l$&%) 'be chain of pzoeesses - parcly measered. partly cheureticel - from biode~osition to reaenesation of nutrients and the coupling between nitrification and denicr%£icatie$n is limited by the load of szgani~ nace~ial ro t&e sediment. men the increaeing load of ozgulic material runs faster t4w Ehe grocess of heaerotrophic lotneralization. anaerobic cQndFeions wlll prevail in the sediment leading to death of bottom Fauna and a disconnection BE nitrification and dea5trification. GREWAQ- .
- Page 15 and 16: 2 CHIWGES XN TEE DELTA The Delta ar
- Page 17 and 18: area decltned cnnside~ably, leadins
- Page 19 and 20: Plan, then it is apparent tbt the s
- Page 21 and 22: Tiddl flats df the Eastem Seheldt v
- Page 23 and 24: tracefore possible to convert the a
- Page 25 and 26: Figsrlre 7 Changes in the cadrnrum
- Page 27 and 28: prevention measures are desirable h
- Page 29 and 30: elationships between different spec
- Page 31 and 32: Bio-essay Weriments with polluted s
- Page 33 and 34: considerable thought to drawing up
- Page 35 and 36: ShLOUONS, W. and BYSINK, W.D., 1981
- Page 37 and 38: are taken. The first year after the
- Page 39 and 40: The Hollands DiepJnaringpllet is pa
- Page 41 and 42: In 1976 the determination of chlozo
- Page 43 and 44: , 0.66 m 0,s - 0.02 1989 I 0.86 - 0
- Page 45 and 46: Table 3 Eutrophication of the Volke
- Page 47 and 48: Laks Volkarek ---- Lake Zoom 0.40 0
- Page 49 and 50: 4 WAGBEET MEdSIIRaS TO PEEVBT OR LT
- Page 51 and 52: Table 5 gives estimtes of the phosp
- Page 53 and 54: In principle, two states of equilib
- Page 55 and 56: Zooplankton (Alma affinis) Pike (Es
- Page 58 and 59: EUTROPHICATION OF ESTUAAIES AND BRA
- Page 60 and 61: The average discharge of Xhine and
- Page 62 and 63: and only l-2% cows frm the aive Sch
- Page 64 and 65: highest trophic potential: nutrient
- Page 68 and 69: model calculations reveal that a ni
- Page 70 and 71: Table 3 PreUmInary carbon budget of
- Page 72 and 73: Water life of Lake Grevelingen
- Page 74 and 75: macrophytes livkg on or rooting in
- Page 76 and 77: less predictable for water managers
- Page 78 and 79: ILWNEWIJK, A.. KEIP, C., 1988. De v
- Page 80 and 81: XBE CHANGING TmAL LAMXiCAPE I N TEE
- Page 82 and 83: The storm surke of L&Z1 A.D., knorm
- Page 84 and 85: osi* rn@8IOIP m .SL 4 Has F~~ULB 3
- Page 86 and 87: During the 19th century man starts
- Page 88 and 89: mudflats have retreated some 100-20
- Page 90 and 91: aq811~33a.e~ pue 3pTatlJS uxaJsafi
- Page 92 and 93: Erosion by waves of sandy shoals (c
- Page 94 and 95: Lt has been estimated that the sedi
- Page 96 and 97: Implementafion of the Delta Project
- Page 98 and 99: ECOLOGICAL DEVELOWdENT OF SALT MAKS
- Page 100 and 101: fn tidal water systems sedimentatio
- Page 102 and 103: hierarchical position. Tn the egtua
- Page 104 and 105: Of course. tke environmental change
- Page 106 and 107: wind erasson, desaliuation, aeratio
- Page 108 and 109: Fonner tirtal flats with saltmarsh
- Page 110 and 111: Grevelingen. Lake Veere and Krammer
- Page 112 and 113: As mentioned above aa important que
- Page 114 and 115: A seaond important perspective for
period 1980-19$3 <strong>in</strong> an <strong>in</strong>crease of <strong>the</strong> anaerobic sed-t suzface area<br />
of 4 ta 258 of she entire bottom awfkce (Stronlrhorst. et al. 1985).<br />
Qbvioualy, <strong>the</strong> Veerse Meer is vulnerable to eutreghicatian, ow<strong>in</strong>g to<br />
<strong>the</strong> long resid&&e <strong>the</strong> of water msses, <strong>the</strong> low ext<strong>in</strong>etian coefficient<br />
and <strong>the</strong> ;Umost permanent stratification.<br />
The Oastesschelde estuary has a very low N-lead re6nlt<strong>in</strong>g <strong>in</strong> low<br />
chlorophyl concentratisne (Table 2).<br />
W<strong>in</strong>g to <strong>the</strong> execwt<strong>in</strong>a af <strong>the</strong><br />
<strong>Delta</strong>plan (Pig. 1) <strong>the</strong> Oostarnehelde estuary has ma<strong>in</strong>ly been depriVed<br />
recently from its Bh<strong>in</strong>ewater load<strong>in</strong>g (Table 1). Model calculations<br />
revealed that a reduction of 50% of <strong>the</strong> nitrosen bed of <strong>the</strong> river<br />
W e<br />
would only lead to a rsduetian of less than 6% for nitrogen<br />
eoneentratlons <strong>in</strong> <strong>the</strong> 0oster.jkbelde estuary (Smobs-swdel; X. Scholten,<br />
peraerial co~u~ication). The Uoster~ohelde estuary is rna<strong>in</strong>ly ir;fluenced<br />
by tearhe foastalwffter, conta<strong>in</strong><strong>in</strong>g low conewtrations of total<br />
nrtrogen (less than 0.5 slg N 1-l; Srockolano, et al. 1988).<br />
Contkaq to <strong>the</strong> Veerse Meer lag~an. <strong>the</strong> Creveliagen lagoon has an<br />
-2 -1<br />
e%treaely Low N-load (4 g N m y ; Table 2). The CaeWA~mdel (De<br />
Vries, et al. 19BEI) revealed that Khe prodtlrcim of phytop.lanktan La<br />
<strong>the</strong> Gzevel<strong>in</strong>gen is liodted by nitrogerl availability and not by light<br />
availability. The hl<br />
: P ratio of tae dlsselved nufkiems <strong>in</strong> cke<br />
watercolm of <strong>the</strong> GrwsMngenmeer dur<strong>in</strong>s w<strong>in</strong>ter is 2-4,<br />
poirtc<strong>in</strong>g <strong>in</strong>to<br />
<strong>the</strong> direction of a large surplus af phosphate, notwithstand<strong>in</strong>g Che<br />
dom<strong>in</strong>ance of nitrogen <strong>in</strong> <strong>the</strong> discharge utatet, load<strong>in</strong>g <strong>the</strong> lagoon<br />
Eff : P = 22 : I f. Model calculations showed s Mgh tunrover of ni~rog.~u,<br />
<strong>in</strong> <strong>the</strong> watercolumn. The cha<strong>in</strong> of processes: nutrient uptake by<br />
phpoplanktaa - forslation d organic matter <strong>in</strong> algal cells -<br />
mherallzation of dead algae - regeneratbn of nutrients etc.. occurs 8<br />
tWs a year. &out<br />
90X of <strong>the</strong> anme1 prisary pr&uction of<br />
phytoplanktoa occurs on <strong>the</strong> baeis of resewrated nutrients, especialLy<br />
NB4 CDe Vtim, et al. lS88).