The ecology of eelgrass meadows in the Pacific Northwest: A ...
The ecology of eelgrass meadows in the Pacific Northwest: A ...
The ecology of eelgrass meadows in the Pacific Northwest: A ...
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great annual range <strong>of</strong> water temperature<br />
(-6' C to 27' C <strong>in</strong> Izembek riagoon; Nova<br />
Scotia: -2O C to 2 4 O C; Rhode Island:<br />
-2' C to 27' C; North Carol<strong>in</strong>a: 0' C to<br />
27O C) m hilli ips unpubl. data). <strong>The</strong>re is<br />
evidence that <strong>eelgrass</strong> at <strong>the</strong> nor<strong>the</strong>rn and<br />
sou<strong>the</strong>rn limits <strong>of</strong> distribution on <strong>the</strong><br />
<strong>Pacific</strong> coast and on <strong>the</strong> Atlantic coast<br />
may have much greater <strong>the</strong>rmal tolerances<br />
than that <strong>in</strong> <strong>the</strong> midportion <strong>of</strong> <strong>the</strong> <strong>Pacific</strong><br />
coast range (Phillips et al. 1983b). In<br />
Puget Sound, <strong>the</strong> normal annual range <strong>of</strong><br />
water temperature is 6O C to 13O C.<br />
Occasionally, dur<strong>in</strong>g low tides on sunny<br />
days <strong>in</strong> summer, <strong>the</strong>re may be brief periods<br />
<strong>of</strong> elevated water temperatures over<br />
<strong>eelgrass</strong> (up to 18O C), but this is rare.<br />
In 1974, Phillips warned that heated water<br />
released <strong>in</strong>to <strong>eelgrass</strong> habitats could<br />
disrupt <strong>the</strong> reprductive cycle, presumably<br />
<strong>in</strong>terfer<strong>in</strong>g with <strong>the</strong> normal temperaturedependent<br />
periodicity <strong>of</strong> flower<strong>in</strong>g and<br />
germ<strong>in</strong>ation. Consider<strong>in</strong>g <strong>the</strong> present<br />
contributions <strong>of</strong> McMillan (1978) and<br />
McMillan and Phillips (1979), we now know<br />
that <strong>the</strong> developmental cycle <strong>of</strong> <strong>eelgrass</strong>,<br />
as well as its presence <strong>in</strong> an area, is<br />
temperature related. Populations <strong>of</strong> <strong>the</strong><br />
plant have specific <strong>the</strong>rmal adaptive<br />
limits. <strong>The</strong> <strong>Pacific</strong> <strong>Northwest</strong> does not<br />
have a significant problem with <strong>the</strong>rmal<br />
water release from power plants or<br />
<strong>in</strong>dustry. We know from work done <strong>in</strong><br />
Biscayne Bay on Thalassia (reviewed by<br />
Zieman 1982) that plants were killed when<br />
<strong>the</strong> water temperature was elevated C<br />
above ambient and were harmed by an<br />
elevation <strong>of</strong> 3O C. If <strong>the</strong> <strong>Northwest</strong><br />
should encounter such <strong>the</strong>rmal releases, we<br />
must consider <strong>the</strong> impacts on <strong>eelgrass</strong>.<br />
McRoy and Helfferich (1980) noted <strong>the</strong><br />
susceptibility <strong>of</strong> <strong>eelgrass</strong> <strong>in</strong> <strong>the</strong> North<br />
Atlantic to a- very slight <strong>in</strong>crease <strong>in</strong><br />
water temperature <strong>in</strong> 1931. Dur<strong>in</strong>g that<br />
period over 90% <strong>of</strong> all <strong>eelgrass</strong> died.<br />
Recent evidence shows that <strong>the</strong>se stra<strong>in</strong>s<br />
have a greater <strong>the</strong>rmal tolerance range<br />
than do <strong>Pacific</strong> coast stocks.<br />
Consider<strong>in</strong>g its worldwide distribution,<br />
<strong>eelgrass</strong> grows <strong>in</strong> a wide range <strong>of</strong><br />
sal<strong>in</strong>ity. It is euryhal<strong>in</strong>e. Biebl and<br />
McRoy (1971) reported that <strong>eelgrass</strong> <strong>in</strong><br />
Izembek Lagoon, Alaska, ma<strong>in</strong>ta<strong>in</strong>ed an<br />
osmotic resistence to sal<strong>in</strong>ity changes<br />
from freshwater to 93 ppt. At 124 ppt<br />
leaves were killed. Positive net<br />
production was maximum at 31 ppt, as was<br />
photosyn<strong>the</strong>tic rate, but was found <strong>in</strong> a<br />
range from freshwater to 56 ppt<br />
(photosyn<strong>the</strong>tic rate was zero <strong>in</strong><br />
freshwater and at 62 ppt). Respiration<br />
was depressed <strong>in</strong> freshwater but only<br />
slightly affected from 31 ppt to 93 ppt.<br />
Ostenfeld (1908) considered that a<br />
sal<strong>in</strong>ity range for <strong>eelgrass</strong> <strong>in</strong> Denmark<br />
from 10 ppt to 30 ppt was optimum for<br />
growth. In Japan, Arasaki (1950) reported<br />
that <strong>eelgrass</strong> growth was best from 23.5<br />
ppt to 31 ppt but poor at 18.0 ppt and<br />
stop@ below 9.1 ppt, although plants did<br />
not die. Tut<strong>in</strong> (1938) observed <strong>eelgrass</strong><br />
<strong>in</strong> a bay <strong>in</strong> England <strong>in</strong> 42 ppt with no<br />
damage. He grew plants for a considerable<br />
period <strong>in</strong> <strong>the</strong> laboratory <strong>in</strong> sal<strong>in</strong>ities<br />
rang<strong>in</strong>g from 10 ppt to 40 ppt without<br />
harm. It is known that <strong>eelgrass</strong> can<br />
acclimate to a chang<strong>in</strong>g sal<strong>in</strong>ity regime.<br />
Often extensive <strong>meadows</strong> grow <strong>of</strong>f <strong>the</strong><br />
mouths <strong>of</strong> streams where <strong>the</strong> sal<strong>in</strong>ity drops<br />
to freshwater level at low tide. <strong>The</strong><br />
plants appear to flourish. Low sal<strong>in</strong>ities<br />
appear to enhance seed germ<strong>in</strong>ation <strong>in</strong><br />
spr<strong>in</strong>g (Tut<strong>in</strong> 1938; Arasaki 1950; Phillips<br />
1972).<br />
6.6 MANAGENENI! NEEDS<br />
Wilson (1981) noted that <strong>in</strong> order to<br />
manage our coastal estuaries properly, we<br />
need a better understand<strong>in</strong>g <strong>of</strong> <strong>the</strong> <strong>ecology</strong><br />
<strong>of</strong> <strong>eelgrass</strong>, which requires knowledge <strong>of</strong><br />
<strong>the</strong> causes <strong>of</strong> its distributional patterns.<br />
<strong>The</strong>se patterns are affected <strong>in</strong> <strong>the</strong> short<br />
term by <strong>the</strong> <strong>in</strong>creas<strong>in</strong>g demands by modern<br />
man on <strong>the</strong> coastal and estuar<strong>in</strong>e<br />
environments. Sedimentation, dredg<strong>in</strong>g,<br />
storms, currents, sewage, power-plant<br />
effluents, and factors such as<br />
adaptational tolerances <strong>of</strong> <strong>the</strong> plants as<br />
regulated by <strong>the</strong>ir genetic patterns, all<br />
affect <strong>the</strong>se distributional patterns.<br />
Cont<strong>in</strong>ued monitor<strong>in</strong>g <strong>of</strong> our estuar<strong>in</strong>e<br />
areas is necessary if we desire to rema<strong>in</strong><br />
aware <strong>of</strong> biological and environmental<br />
changes. This awareness is needed for<br />
<strong>in</strong>tellisent manaqement <strong>of</strong> this resource.<br />
S arti-na alternif lora (saltmarsh<br />
9---T<br />
cordsrass was <strong>in</strong>troduced <strong>in</strong>to Willapa Bay<br />
dur&g <strong>the</strong> 1940's or early 1950's: <strong>The</strong><br />
species has rapidly spread <strong>in</strong>to upper<br />
<strong>in</strong>tertidal and mudflat communities and is<br />
displac<strong>in</strong>g <strong>the</strong> more productive native