Tidepool # 10 at Race Rocks

In May 2004 the biology class measured features of several pools, including this one, pool 10.

This file has been started to present some of the information we have accumulated on the pool in order to stimulate students to raise further questions and devise problems that can be investigated at the pool. It is also intended to be part of a cumulative digital legacy that those examining the pool can pass on to future students.

This pool has a diameter of less than half a meter .This pool is characterized by having a base of white crystalline quartz. It is also shaded for much of the day, and is usually filled with harpacticoids.

white quartz with harpactacoids visible

SEE THIS REFERENCE in the Race Rocks Taxonomy on Harpacticoids

A large amphipod and the small red harpacticoids in pool 10

Tidepool Studies at Race Rocks Pool #4 Peg6

A general view of the pool.It is perched on a shelf which easily gets flooded when there is a slight swell in the ocean. Polymorphism in the Snails of Pool # 4, Extended essay in Environmental Systems,
A student examines the life of pool 4 Amphipods collected with a suction bottle from pool#4.
A microscopic picture of the diatoms that grow as a fuzz in the pool in the early spring. They remain a few months until they are grazed off.
Roberto and the Biology Class measure salinity in pool 4.. May 2004
Enteromorpha growing in the pool. May 2004. Bay mussels, Mytilus trossulus in the brackish water of Pool#4
In May 2004,it is clear where the grazers, Littorina snails and amphipods) have trimmed off the diatoms on the bottom. Arunas measures the depth of pool 4 while watching for swells
In February, 2007, the diatoms cover almost the entire bottom of the pool. This is the winter pattern. Grazing as shown above gradually removes the covering of diatoms.

 

January, 2007. The tide is at its peak today, showing pool 4 being entirely submerged.
On February 11, 2008 a beast is photographed in the tidepool. Close up of the Filamentous golden algae filling the tidepools in early spring.
Weird form shades a covering of diatom fuzz!

 

Some ideas to consider:

Invitations to Inquiry:

This pool is unique in a number of ways. The white substrate in the bottom of the pool is the result of a quartz intrusion that has flooded while molten, through the cracks of the basalt.
What is the effect of this white reflective surface on the temperature of the pool and the organisms that live in the pool?

In 1997 while doing a detailed analysis of the organisms in the pool, we noticed for the first time that there were white periwinkles. At that time 26 were counted by Nadia and Catherine. Speculate on the evolutionary implications here.

The mussels in pool #4 are Mytilus trossulus, the bay mussel. Mussels that you can see on the surrounding intertidal areas are the Mytilus californianis. Why the species difference?

The pattern of diatom distribution changes in the bottom of the pool. In the winter, it covers the pool with a thick felt-like appearance, as spring approaches, the cover of diatoms starts to disappear, starting along the cracks where the mussels are anchored.. could one measure the rate of grazing from the amphipods in the cracks?

Temperature and Salinity in the pool fluctuate widely and at times form stratified layers. How does this affect organism distribution.?

The biotic and abiotic features of this pool vary considerably from other pools in the near vicinity. Quantify and explain the differences or similarities.

The only other pool that resembles this one is found over on the north-east corner of the island, at location peg15-pool #14. Compare the biotic and abiotic factors of these two pools, and explain the differences.

The following lab on tidepool abiotic factor measurement was done by Chiara Ravetti in September,2005.
Biology Laboratory

Analysis of the Abiotic Factors in Race Rocks Tidepools

The measurements of salinity, ph, and temperatures of different tidepools at Race Rocks was done September19, after 11.30 a.m., with high tide. For this reason the pools selected were only five, two (pool 7 and 8) several meters away from the sea at that time of the day, the other three (pool 1, 2 and 4) closer to the water and larger.
Data analysis and further note

pool 1 pool 2 pool 4 pool 7 pool 8 Ocean water
Salinity 62.1 32.8 21.9 45.3 45 30
Temperature 14.4 C 14.4 14.2 15.4 15.2 10
ph 8 6.8 6.9 7 8


The measurement of salinity is expressed in parts per thousand; the instrument utilizes electricity, that passing through salt ions determines its quantity.
The pools were contaminated by sealions excrement, which reduced the visibility inside the pool and probably altered the pH of the water.
Other factors which might affect these values in a tidepool are: evaporation, precipitation, and in general pollution, scarce precipitation at that time of the year, the presence of the estuary, (The Strait of Juan de Fuca) with the influence of fresh water. The salinity in a tidepool is higher than the sea, for the evaporation and the little exchange of water, therefore the organisms living in it must tolerate high salinity, as well as variations in temperature. The smaller tidepools further from the sea present even more significant changes.

 

Carmen’s lab on Transects

Race Rocks Transect Lab

Kite Diagrams

BELT TRANSECT PROCEDURE

About 20 meters from the dock on the north side of Great Race Rocks, we plotted our transect. Starting at the shore and going 15 m inland, we laid a tape measure and at every half-meter we made a 50cm-by-50cm quadrant and counted the species in the plot.

ANALYSIS:  We counted the algae by percent cover and the invertebrates by number. Some species overlapped, such as anthopleura and halosaccion. This coexistence was possible because the two species were not vying for the same food source. Species such as thatched barnacles and acorn barnacles did not live in the same quadrants, however. This may be because they are competing for the same substrate and nutrients and each prevents the other from invading into their space. As well, the thatched barnacles stopped growing at quadrant 15 but that is just where its competition, acorn barnacles began to grow. Perhaps one species was better suited to surviving farther up the shore.

That was the case for many of the species along the transect. Invertebrates like chiton, limpets and snails needed to be covered by the tide for most of its cycle. If these species tried to grow where they were exposed for a longer period of time, they would dry out and die. Other species like lichen need to be out of the water and as expected, were only found at high elevations on the transect.

The topography also affected the species diversity. The California Mussel, for example, was found only in quadrants that had crevices and rough substrate on which to grow.

In general, the abiotic factor that had the greatest affect on species diversity on the transect was the elevation and amount of tide cover the area got during a tide cycle. Below are kite diagrams of each species we found on the transect.

Carmen and Jana Environmental Systems class April 2003

LINK to photographic transect strip of this area

This x-axis represents percentage cover for the macroalgaes. Note it may be a different scale in the graphs. The y-axis represents the .5meter quadrat location from the peg #15.

The “series” 1 and 2 just represent half of the value for each quadrat for the species, a way to get EXCEL to plot a symmetrical “kite” shape

Anthopleura elegantisima ( green intertidal anemone)

Hedophylum sp. ( Brown wrinkled algae)

Analepus sp. ( rare algae)

Praseola sp. (green mat algae)

Xanthorea sp. (yellow Lichen)

Porphyra.sp

Hildenbrandia sp. ( red thin cust algae)

Alaria marginata ( brown Algae)

Coralina sp. ( pink coraline algae)

Fucus sp.

Gigartina sp. (red algae)

Cryptosiphonia sp. (like wet dog hair)

Halosaccion sp.. (salt sac algae)

Golden Diatom

Ulva lactuca Sea lettuce

Mitylis californianus California mussel

Searlesia dira ( Spindle Whelk)

Amphysia sp. Snail

Neomolgis sp. Red Spider Mite

Purple Nucella Snail

Limpet

Acorn Barnacles

Thatched Barnacles

Littorina Periwinkle snail

Katharina sp. (leather chiton)

 

See Transect A0050101
See Transect A0050102
See Transect A0050103

Return to the Contents page for Environmental modelling with Transects..

Tidepool # 3 at Race Rocks

This file has been started to present some of the information we have acumulated on the pool in order to stimulate students to raise further questions and devise problems that can be investigated at the pool. It is also intended to be part of a cumulative digital legacy that those examining the pool can pass on to future students.

Some ideas to consider:

  • This pool is very shallow and has a very low biodiversity. Diatoms, amphipods and a few barnacles live here. Since it is only a few centimeters higher up the shore than pool 4, note how elevation makes a significant impact on the abiotic factors of Temperature and salinity.

Intertidal Zonation of Halosaccion glandiforme:

EXTENDED ESSAY IN BIOLOGY
INTERTIDAL ZONATION OF HALOSACCION GLANDIFORME:
A FOCUS ON HEIGHT AND SLOPE AS FACTORS OF ZONATION

LESTER B. PEARSON COLLEGE

ALEX C. FLETCHER

JANUARY 14, 2002

ABSTRACT:
An intertidal study of the organism Halosaccion glandiforme was performed at Race Rocks Marine Protected Area a unique and undisturbed island located seventeen kilometres southwest of Victoria in the Strait of Juan de Fuca . Belt transects from three similar locations on the island were taken from the zero tide level up past the high tide mark. These transect photos were combined with other measurements and calculations to look at the variables influencing growth in the intertidal zone. The intertidal zone is unique in its numerous abiotic and biotic factors that influence life in the region. For the purpose of this study two of these factors were chosen in an attempt to quantify the possible relation that exists between them and the ecological niche of Halosaccion glandiforme. Vertical elevation from the zero tide level and angle of inclination of the rocky shore were compared with population density of the species. While analysis of slope and population density relation proved fairly inconclusive, simple statistical testing showed that a trend does exist between intertidal height and population density of Halosaccion glandiforme.  

Table of Contents

List of Figures and Tables

Introduction………………………………………………………………………1

The Problem

            Purpose and Background of the Study

            Hypotheses

            Limitations  

Review of Literature and Related Research…………………………..……….3

Introduction, Information about the organism

            The Theory

            Research Results in Related Areas

Research Design and Procedures……………………………………………7

The Setting and Population of the Study

            The Experimental and Control Groups Used

            Instruments Used

Analysis of Data…………………………………………………………….…10

Introduction

            Findings that Relate to Hypotheses 1 and 2

            Statistical Analysis

            Findings that Relate Hypotheses 3 and 4

Conclusions and Recommendations for Further Study…………….…….20

Interpretations and Implications of the Findings

            Recommendations

References Cited…………………………………………………………..…..…22

Appendix………………………………………………………………………..23

Transect-peg 5

            Transect-peg 5b1

            Transect-peg 6

List of Figures and Tables

Figure 1.   A small cluster of Halosaccion glandiforme, among barnacles, is shown growing next to a tide pool. …………………………………………………………………………. 1

Figure 3.   Areal view of Race Rocks Marine protected Area. Yellow markers indicate locations of study pegs and belt transect line ……………………………………………… 6

Figure 4. Working with H.glandiforme at the race Rocks Marine Protected Area…………………………………………………………………………………………………………7 
Figure 5.
  This image represents an example of a meter segment from the belt transect (taken from peg 6 at meter 4). …………………………………………………………………….. 8

Figure 6.   This image is an example of a meter segment from a belt transect (peg6, meter segment 4).  ………………………………………………………………………………………. 9

Table 1. Population density (in percent coverage of each meter segment) is shown in relation to the mean
of vertical height of the corresponding meter segment from measurements at peg 5. ………………………………………………………………………………………………………….. 10

Table 2. Population density (in percent coverage of each meter segment) is listed in relation to the mean of vertical height of the corresponding meter segment from measurements at peg 5b1. …………………………………………………………………. 10

Table 3. Population density (in percent coverage from each meter segment) is shown in relation to the mean of vertical height of the corresponding meter segment from measurements at peg 6. ……………………………………………………………………… 10

Figure 7. Graph of data from table one, peg 5.………………………………………… 11

Figure 8. Graph of data from table 2, peg 5b1.………………………………………… 11

Figure 9. Graph of data from table 3, peg 6……………………………………………… 12

Figure 10. Graph of population density in relation to mean of intertidal vertical height with

the three belt transects combined. ………………………………………………………….. 12

Table 4. Table of combined data of the significant values for the analysis of normal distribution from three pegs. …………………………………………………………………… 13

Table 5. Data table of expected normal distribution values and obtained distribution values used in conjunction to perform chi-squared test.………………………………………… 13

Figure 11. Graph of percent coverage vs. vertical height, comparing obtained values to normal distribution values………………………………………………………………………… 14

Figure 12. Graph of peg 5, belt transect terrain profile. ………………………………. 15

Figure 13. Graph of peg 5b1, belt transect terrain profile…………………………….. 16

Figure 14. Graph of peg 6, belt transect terrain profile………………………………… 17

Table 6. This data shows percent coverage in relation to the slope of the intertidal zone. …………………………………………………………………………………………………………..  18

Figure 15. Graph of table 6, the relation between population density and intertidal slope……………………………………………………………………………………………………..18

Introduction

image001

Figure 1. A small cluster of Halosaccion glandiforme among barnacles, ius shown growing next to a tidepool

The Problem:The purpose of this study is to try and quantify certain factors that are a part of the ecological niche of the sea sac Halosaccion glandiforme (figure 1) from the Rhodophyta division. From observing this plant on numerous occasions it is clear that this organism grows in a limited vertical range on the intertidal zone, the threshold between marine aquatic and terrestrial environments. It is likely that a specific physical setting exists for this species, and similarly with other intertidal species, where growing conditions are optimal. The main focus will be to look at the extent to which slope and elevation, in the tidal zone, affect the ideal habitat conditions of the Halosaccion glandiforme.

Purpose and background of the Study

image004

Figure 2. Picture showing Halosaccion glandiforme growing up to but not on a vertical surface.

Similar to all rocky intertidal dwelling species Halosaccion glandiforme is well adapted to survive the dynamic conditions presented in this ecosystem. This zone is characterized by the rapid changes and variability of temperature, light, moisture, salinity, and water movement. The aqua dynamics of the sea sac’s streamlined shape decreases the friction between it and the constantly moving marine waters. H. glandiforme are well anchored to surfaces (usually rock) by strong attachment devices as well as by growing in clusters of its own kind it is more protected. Being a water-filled sac the plant is less susceptible to the changes in moisture and temperature as a result of the tidal waters that are more limiting to other algae such as sea lettuce (Ulva fenestrata) and Purple laver (Porphyra perforata). From observations a growth trend along certain elevations, where the appropriate conditions of moisture and sunlight are found, appears to exist for H. glandiforme and other intertidal species. Also based on observation (figure 2) it seems as though the inclination of rock

surface influences the location of intertidal species including the H. glandiforme. This may be caused by the force of water movement along flatter, less restrictive surfaces, compared to steeper surfaces where friction between rock and water results in turbulence and a rough growing site for organisms. The characteristics and adaptations of each intertidal organism determine its niche. In looking at some of the many determining variables that exist along the seashore we can attempt to quantify this area.

Hypotheses

Hypothetically there is a measurable height at which this alga prospers as well as a preferred degree of inclination for its growth. A higher density population trend along the intertidal zone at this level would represent this.

  1. Ho- There is no significant relation between Halosaccion glandiforme population density and the vertical elevation on the tidal zone.
  2. Ha- there is a significant relation between Halosaccion glandiforme population density and the vertical elevation on the tidal zone
  3. Ho- There is no significant relation between inter tidal angle of slope and population density of the Halosaccion glandiforme.
  4. Ha- There is a significant relation between inter tidal angle of slope and population density of the Halosaccion glandiforme.

Limitations

This study is limited by only taking data at one point in the growing season of the plant and by not having the time to repeat collections of data several times over an extended period of time. The site of study, performed at Race Rocks Marine Protected Area is a prime location for flourishing intertidal life. However, taking measurements and data from three locations in one confined area is limiting in respect to the broadness of the viability of the results. Due to restrictions of time it was not possible to explore further relations and effects of abiotic and biotic factors. In addition many of the highly influential factors (such as wave motion, temperature, etc.) are not easily quantified and are not easily controlled thereby limiting the accuracy and broadness of the study and it’s findings.

Review of Literature and Related Research

Introduction, Information about the Organism

Specific information on Halosaccion glandiforme is limited beyond short physical descriptions and categorization. In Pacific Coastal marine texts Halosaccion is often referred to for its intertidal qualities while actual studies on the plant were not found while researching the topic. Typical descriptions of Halosaccion glandiforme depict the plant as a thin-walled elongated sausage-shaped sac found in the mid-intertidal region of rock dominated shores. The plant is identifiable by its rounded head and short stipe anchored by a small circular holdfast. Also, resulting from the water it contains, applying pressure to the plant produces fine sprays of water emitted from the pores.     In Common Seaweeds of the Pacific Coast (by J. Robert Waaland) it is stated that “Halosaccion glandiforme may reach lengths up to 25 cm and 3 to 4 cm in diameter; typical sizes are about 15 cm long by 2 to 3 cm in diameter.” The maximum length (25cm) is far greater than those studied in this paper. Typical sizes, in the populations and the physical vicinity of the study for this paper, were closer to a range of 1 to 10 cm in length.

The Theory

While theory in the area of inter tidal zone life is limited there is literature that states observations relating to the structured zonation that occurs in the intertidal zone. The slope hypothesis is related to a general description of the influence of shoreline gradient on intertidal zonation provided in Pacific Seashores A Guide to Intertidal Ecology (Carefoot, 1977). “Generally, where the range of the tides is small, or where the slope of the beach is steep, the bands are narrow; where the range of the tides is great, or where the slope of the beach is flat, the zones are wide.” From this statement it is clear that physical factors such as slope are influential on the intertidal zonation and banding of species. In Seashore Life of the Northern Pacific (Kozloff, 1996) it is stated that “On flat-topped reefs and rocks that do not have steep slopes, there should be plenty of Halosaccion glandiforme.” This provides a basis for the concept that shoreline gradient is plausible as a factor influencing the growth of Halosaccion. Therefore such factors of the intertidal zone directly affect the band of ideal growing conditions for organisms.

A theoretical description for universal zonation is presented by Stephenson’s “universal” scheme of zonation (Stephenson, 1949). This scheme is representative of the diverse zonal patterns around the world. It divides tidal shores into five main categories. From highest to lowest is the Supralittoral zone above the tidemark being mainly terrestrial however influenced by spray from waves and ocean mist. Below is the supralittorial fringe that encompasses the upper intertidal zone including the highest living barnacle and lowest limits of lichens. The Midlittoral zone is the whole intertidal area from the most elevated barnacles to the most elevated brown algae. The lowest edge of the intertidal zone represents the beginning of the Infralittoral fringe that continues to the lowest mark visible between waves at low tide. Bellow is the final tidal zone called the Infralittoral zone being almost constantly submerged. In this scheme Halosaccion glandiforme is situated between the extreme high water mark and the extreme low water mark somewhat centrally in the midlittoral zone.

Research Results in related areas

The most significant research results that relate to this paper involve work done on the abiotic features that affect the growth of intertidal organisms. While the research is not specific to Halosaccion glandiforme it is relevant to the intertidal zone occupied by this species.

The primary factor in determining growing location for algae results from the production of their many spores and the conditions that affect where the spores choose to settle. The few spores that survive and continue to develop into their gametophyte forms will only survive if they are in appropriate niche for that species.

There is much research that has gone into the effect of tidal levels and variation on zonation. The theory of zonation is based on the relationship between intertidal zones and tide levels. However it is not “universal” as it has been found (even by the Stephensons) to be inaccurate in certain situations. This comes from the influence of other factors that cause variance between intertidal zones and that must be considered when studying this area. The cycles that tides go through, in accordance with the sun and predominantly the moon, will affect the intertidal zone configuration by controlling the submersion of the intertidal zone and its organisms.

The upper limits of the intertidal zone are subject to temperature fluctuations and other abiotic terrestrial environmental factors such as air movement and fresh water that effect growth. Water retention enables certain species to survive for longer periods of time out of the water and therefore higher in the intertidal zone. The effects of exposure on seaweeds has been studied by Kanwisher (Kanwisher, J, 1957). In his article “Freezing and drying in intertidal algae” he measures water loss in certain algal species of the intertidal area. A brown alga Fucus vesiculosus was recorded as having lost 91% of its moisture to evaporation from solar heat. In laboratory work performed he found that this level of evaporation would occur in a period of about an hour and half. Similarly Enteromorpha linza demonstrated an 84 percent loss of water and Ulva lactuca a 77 percent loss of water when subject to terrestrial conditions. It is likely that the structure of Halosaccion glandiforme, being a water retentive sac, permits for lengthier exposure time with a higher level of water retention.

Light is a very influential aspect on intertidal life and zonation. As the source for photosynthesis it is vital to plant life. However it is also harmful in that ultra violet light can damage plant tissue. The sun’s UV rays can bleach marine plants that spend extended periods of time out of the water.

There is also the factor of competition for growing space amongst the many species and individuals occupying the limited space of the intertidal zone. As well predation and grazing by herbivores will affect the growing conditions of intertidal species.   The abrasive action by waves is a determinate in zonation separating stronger better-adapted organisms from those that are not able to endure the conditions. Some organisms have greater survivability in such conditions through growing in clusters, having streamlined shapes, sturdy holdfasts, and other such features.

Research Design and Procedures

image008

Figure 3, Aerial view of Race Rocks Ecological Reserve. Yellow markers denote location of study pegs and belt transect lines.

The Setting and Population of the Study

The data collection for this study was carried out at Race Rocks Marine Protected Area located 17 kilometres southwest of Victoria in the eastern Juan de Fuca Straight. Of the nine islets in the area, the main rock (with the lighthouse) was the site of this study. Three locations on the West facing side of the island were selected for the belt transects. Two of the three locations were already marked with study pegs, pegs 5 and 6. The other site located in between peg 6 and peg 5 was not pre-marked and is therefore referred to as peg 5b1 for this and future studies. The peg locations are visible in the diagram of Race Rocks (figure 3). The transect photographs were taken consecutively from the waters edge (at low tide, approximately 0m tide) up perpendicularly to a point beyond the intertidal zone. This point varied with each transect as the intertidal zone varies with the height and slope.

image010

The author working with Halosaccion glandiforme at Race Rocks Ecological Reserve.

The Experimental and Control Groups Used  

In using three transect belts the correlation between variables is based on a wider average of results. By setting all three transects to begin at the zero meter tide level they can be accurately compared. In taking the transect belts in proximity to one another they are more likely to be of similar conditions. For example, all three transects were on the same side of Race Rocks facing the same swell and wind directions. Therefore more variables are eliminated that could make comparison amongst them more obscure.

Instruments used

In creating the belt transects, a measuring tape over 10 meters long with markers for every meter was placed along the tidal zone tight to the rocks. The photos were taken along the measuring tape with a Sony Digital Camera. The photos were taken from about 1 meter above the ground (approximately waist height). One photo would cover a section of about fifty centimeters. The photos were taken overlapping the previous so that they could be fit together appropriately at a later time.

With the measuring tape in place the next step was to measure the physical height of the rock slope along the transect line. Height was measured at every 50 cm interval. A meter stick would be held perpendicular to (for example) the 1 meter mark and the 1.5 meter mark. By placing a third meter stick with a liquid level attached perpendicular to the initial stick and butting up horizontally to the second stick the difference in height was obtained.

These values were recorded in a chart and then used in the making of a height and slope outline graph of the rock surface at the transect belts.  In collating the individual transect photos into one cohesive transect belt the computer imaging program Adobe Photo 4 was used. After splicing the pictures appropriately the meter marks were marked by a line and each cluster of Halosaccion glandiforme was outlined for further analysis (figure 5).

image013Figure 5. This image represents an example of a meter segment from the belt transect (taken from peg 6 at meter 4). The measuring tape is visible as yellow line at the top of the image. The meter segments can be seen marked by white vertical lines at the sides of the image.

Further computer analysis was carried out using Scion Image for Windows. This program provided the capability of measuring the population density of Halosaccion glandiforme along the transect belt. The area of each transect section was measured scaled to the according meter segment length. Each meter section on the belt transect varied slightly from the others, as did the area of each meter segment. This is because of discrepancies in the distance between the camera and the shore, a source of error that is hard to avoid completely with such rough rocky intertidal terrain. Finally the total area covered by Halosaccion glandiforme clusters, as seen outlined in orange (figure 6), was measured in each meter segment. When compared to the corresponding area measurements of their meter segment the population density of Halosaccion glandiforme could be determined as a percentage covering of that area.
image015Figure 6. This image is an example of a meter segment from a belt transect (peg6, meter segment 4). The orange outlines represent the area covered by Halosaccion glandiforme. With measurements scaled to the according meter as presented by the measuring tape the area of the meter segment and the Halosaccion coverage was calculated and compared.(For complete belt transect of peg 6 see appendix.)

Analysis of Data

Introduction

With the data obtained from the belt transects of the intertidal zone the results of height and population density were compiled into tables and subsequently graphs to represent the possible relation. Also the data for the effect of surface slope on population density was converted into a graph.

Findings that relate to Hypothesis 1 and 2

Transect meter segment Mean of height Percent coverage of area
1 0 0
2 35 0
3 60 0
4 85 3.4
5 115 60.9
6 145 89.6
7 170 1
8 165 14.1
9 200 0

Table 1.  Population density (in percent coverage of each meter segment) is shown in relation to the mean of vertical height of the corresponding meter segment from measurements at peg 5.

 

Transect meter segment Mean of Height Percent coverage of area
1 5 0
2 17 0
3 21 0
4 70 1.6
5 110 23.8
6 160 46.8
7 190 10.7
8 230 0

Table 2. Population density (in percent coverage of each meter segment) is listed in relation to the mean of vertical height of the corresponding meter segment from measurements at peg 5b1.

 

Transect meter segment Mean of height Percent coverage
1 2 0
2 50 0
3 132 26.6
4 170 49.5
5 190 0
6 203 7.1
7 210 1.4
8 230 0
9 258 0

Table 3. Population density (in percent coverage from each meter segment) is shown in relation to the mean of vertical height of the corresponding meter segment from measurements at peg 6.image019

Figure 7.  Graph of data from table one, peg 5. This figure represents the relation between population density (in percent coverage from each meter segment) and vertical height.image022

Figure 8. Graph of data from table 2, peg 5b1. This figure represents the relation between population density (in percent coverage from each meter segment) and vertical height.image025

Figure 9. Graph of data from table 3, peg 6. This figure represents the relation between population density (in percent coverage from each meter segment) and vertical height.image028

Figure 10. Graph of population density in relation to mean of intertidal vertical height with the three belt transects combined.

Statistical Analysis

Vertical height Percent coverage
70 1.6
85 3.4
110 23.8
115 60.9
132 26.6
145 89.6
160 46.8
165 14.1
170 49.5
170 1
190 25.4
190 10.7
200 0
203 7.1
210 1.4

From the compiled data the significant values, those values that fell within the extremes of the range of population occurrence (table 4), were used for further analysis by means of normal distribution calculations. To test the obtained values against the values expected of a normal distribution curve a graph (figure 11) was produced.   Of the fifteen obtained values for vertical height the mean is 154.33 meters. Therefore the standard deviation is 43.71 meters from the mean. In accordance with a normal distribution the first standard deviation (from the mean to 110.62 and 198.04 cm) is expected to hold 34% of the values. At the second standard deviation (at 110.62 cm and 241.75 cm) 13.6% of the values are expected to be present. Finally the third standard deviation (at 23.2 cm and 285.46 cm) is expected to contain 2% of the values. With 15 values in this data set (table 4) the expected number of values for each deviation can be calculated from the expected percent (table 5).

Expected percent 2% 13.6% 34% 34% 13.6% 2%
Expected 0.3 2.04 5.1 5.1 2.04 0.3
Observed 0 3 3 6 3 0

Table 5. Data table of expected normal distribution values and obtained distribution values used in conjunction to perform chi-squared test.

The chi-squared statistic was calculated from this table (table 5) as 2.864. When this number is checked with the chi-square distribution table at five degrees of freedom it falls bellow the critical 95 percent value of 11.1. Therefore, there is a 95 percent certainty that the results fit the expectations and that the obtained values represent a normal distribution.

Findings that relate to hypotheses 3 and 4

To obtain the angle of inclination for the terrain of the belt transects it was necessary to create three graphs (figures 12, 13, and 14) from the height measurements (see Instruments used) taken along the three transect lines. With the use of a protractor the angles were extrapolated from each graph (table 6). The angle measurements represent the mean of inclination for each meter segment from each transect. The calculated angles were compared to the percent coverage values that they represented. The angles are only calculated from the meter segments where a significant population density of Halosaccion glandiforme is present as slope will only be influential in the identified zone where H. glandiforme usually grows. Therefore it is mainly from the 100cm to 200cm vertical height sections of each transect belt that angle of inclination is measured.

Figure 11 (To be scanned and added later)

Figure 12 (To be scanned and added later)
Figure 13 (To be scanned and added later)
Figure 14 (To be scanned and added later)

Angle of inclination Percent coverage
10 25.4
10 49.5
15 46.8
15 89.6
15.5 60.9
20 23.8
20 10.7
21 26.6

Table 6. This data shows percent coverage in relation to the slope of the intertidal zone. Slope is measured to represent the mean slope of each meter transect segment. Slope is only taken from the segments of the three transects where there is significant population density of Halosaccion glandiforme. Therefore it is mainly from the 100cm to 200cm vertical height sections of each transect belt.image031

Figure 15. Graph of table 6, the relation between population density and intertidal slope.

Conclusions and Recommendations for Further Study

Interpretation and Implications of the Findings

The three individual transect graphs (Figures 7, 8, and 9) show a trend between the relationship of vertical intertidal height and the population density of Halosaccion glandiforme. The majority of Halosaccion glandiforme were found to grow between vertical heights of 100 cm and 200cm from the zero tide level. The highest recorded level of population density in each belt transect varied slightly, ranging from 145 cm vertically to 160 cm vertically. When the distribution of obtained values for height and percent coverage were compared to the normal distribution it was found that the observed results fit with 95% confidence of the expected. This suggests that the observed results are not distributed by chance occurrence but are due to a trend. The null hypothesis (Ho) is disproved and the hypothesis (Ha) is accepted, as a significant relation does exist between Halosaccion glandiforme population density and the vertical elevation on the tidal zone. It is important to place this in context however as the results are based on data from a close proximity as to decrease the variability of results. It is likely that H. glandiforme populations even on the opposite side of Race Rocks, subject to different lighting, swell action, and other possible conditions, could demonstrate a different set of results.   Therefore this part of the experiment could be repeated and produce similar distribution results in the same vicinity and perhaps exhibit similar trends in a wider range of locations.

The slope percent coverage relation graph needed more data taken at more specific intervals to produce significant results. Since this relation could only be studied at heights where predetermined growth was expected it limited the data to eight significant values.   The graph suggests that growth is optimum on gradients of 10 to 20 degrees with the higher population densities at 15 degrees. Yet this is not reliable as it is clear from the terrain profile graphs (figures 11, 12, and 13) that there is not a great level of variance in shoreline slope at the sites of the belt transects. There was no data collected from terrain that exhibited more extreme angles. Slope most likely affects the growing conditions of Halosaccion glandiforme however it is only one several variables that together create intertidal zonation and is therefore difficult to quantify. This study was not sufficient to come to any conclusions concerning the hypothesis and the hypothesis (Ha) is not accepted.

Recommendations

While trends were observed in this study there are many conditions that must be taken into account. The data was collected at Race Rocks in July and cannot be considered relevant for the whole year. While the H. glandiforme populations are anchored to the rock and are not likely to vary extensively in position over time, the data would be of greater accuracy if it were collected and compared over an extended time. The data collection, as previously stated, is from one limited range and has not been tested or compared with intertidal zones in any other area. For further study it would be interesting to compare growth trends in different locations. Also the percent coverage values, that were vital to findings, were calculated (using Scion Image pro.) are covered by the species. For a more in depth study, population density calculations would be more accurate if they took into account the size and number of the individual organisms. One of the most limiting factors encountered in the analysis resulted from the scale of the measurements taken. For both hypotheses the results were based on data collected from intervals of one meter along the belt transects. Any discrepancy or variation that occurred in vertical height, slope, or population density inside the transect meter segment could not be taken into account. If repeated the data analysis would be far more conclusive had measurements been taken at smaller intervals of, for example, 10cm instead of 100cm.   This study focused on the intertidal organism Halosaccion glandiforme and the effects of elevation and slope on its population density. There are, however, many other variables and species that affect and grow in the intertidal zone and could be considered and tested similarly to analyze and quantify the intertidal area.

References Cited

  1. Waaland, Robert J. 1977, “Common Seaweeds of the Pacific Coast”. J.J. Douglas Ltd. Vancouver.
  2. Stephenson, T. A. and Stephenson, A. 1949, “The Universal features of zonation between tide-marks on rocky coasts.” Journal of Ecology. 37, 289-305.
  3. Kanwisher, J. 1957, “Freezing and drying in intertidal algae.” Biological Bulletin 113: 275-285.
  4. Carefoot, Thomas. 1977, “Pacific Seashores A Guide to Intertidal Ecology”. J.J. Douglas Ltd. Vancouver.
  5. Kozloff, Eugene N. 1996, “Seashore Life of the Northern Pacific Coast”. University of Washington Press. Seattle.
  • Appendix
PHOTO STRIP OF BELT TRANSECT FROM PEG#5 PHOTO STRIP OF BELT TRANSECT FROM PEG#5b1 PHOTO STRIP OF BELT TRANSECT FROM PEG#6

 

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Webcast to Conference in New York from underwater Race Rocks

During a presentation to the ETC conference at the United Nations School in New York in the spring of 2001, we tried out the underwater audio link from DIVELINK . An audio signal is relayed by SONAR for Ryan to a receiver near the docks. This receiver was connected to the audio input on the G3 laptop computer and to the shore tender as well. Both voices could be carried by the Sorenson Broadcaster first by wireless AirPort and then onto the internet. In this way we were able to communicate from underwater in the Pacific Ocean live by internet to the Altlantic coast. In this video, Ryan Murphy, a student at Pearson College, operates the device and the camera was operated by Jean-Olivier Dalphond, also a student at the college.

Fouling on Sensor bar

Already by March, the growth of algae on the environmental sensors and the aluminum bar has been prolific. Regular dives have to be made to keep the sensors free of algae. The predominant Genus here is Laminaria.

Turbulence and Mixing Estimates Using a Towed Horizontal microstructure Profiler

Paul Macoun: Turbulence and Mixing Estimates Using a Towed Horizontal microstructure Profiler

Turbulence and mixing estimates using a towed horizontal microstructure profiler.
Paul Macoun

The Ocean Turbulence Laboratory

University of Victoria

The Purpose

Mixing is the key element in the redistribution of salt, heat and energy in the ocean. Understanding the mechanisms and magnitude of turbulence and other mixing processes is crucial to the improvement of models that predict oceanic and atmospheric change. Our elusive goal is the parameterization of the vertical fluxes of salt and heat based upon the physics of oceanic mixing processes.

The horizontal profiler TOMI (Towed Ocean Microstructure Instrument) is used to make simultaneous measurements of temperature, conductivity, vertical velocity, and their fluctuations. The measurement of vertical velocity provides a means of estimating the rate of dissipation of turbulent kinetic energy. The respective products of instantaneous velocity and temperature, and that of velocity and conductivity, provide a direct measure of the vertical fluxes of heat and salt.

Simultaneous vertical profiles of current and its shear from a ship mounted ADCP (Acoustic Doppler Current Profiler) provide a means to relate the measured fluxes to the Froude Number and the Buoyancy Reynolds Number over a wide range of these parameters. The efficiency of mixing, the ratio of buoyancy-to-kinetic energy production, reaches 0.5 in near coastal regions and is generally much larger than the value of 0.2 assumed to apply to the open ocean.

This analysis is to be the first task to undertake with respect to the data set collected at Race Rocks on August 17th, 2000. At present, the processing is at a preliminary stage.

The Instrument

TOMI is a towed oceanographic vehicle designed to measure turbulence in both shallow and deep water. TOMI can support a multitude of instruments, from sonar to underwater cameras. Its primary oceanographic and electronic sensors are as follows:

1) Four airfoil shear probes and two fast-response thermistors on the nose.

2) A seabird temperature and conductivity sensor adjacent to the nose probes.

3) A seabird temperature and conductivity sensor, and a flowmeter, on the upper mast.

4) A seabird temperature and conductivity sensor, and a flowmeter, on the lower mast.

5) A pressure sensor mounted mid-body, internally.

6) An inertial motion sensor package, internal.

The sample rates for these instruments vary from 64 samples per second up to 512 samples per second. The airfoil shear probe is a unique instrument that measures the cross-stream component of velocity. The force generated by cross-stream flow bends a tiny ceramic bi-morph beam, which generates a voltage that is amplified and recorded. The motion sensor contains accelerometers and gyros. Its presence is required because of low frequency body motion contamination that finds its way into the shear probe signals. By having a record of the vehicle’s behaviour, the probe signals can be decontaminated through processing.

(Photos to be added)

Return to P. Macoun- Oceanographic Research

 A dive with Dr. Scott Wallace for the Discovery Channel,

Scott Wallace did research in 1997 and 1998 at Race Rocks with Pearson College divers. He studied the population dynamics of the Northern Abalone,Haliotis kamtchatkana
His research was done as part of a PhD thesis in Resource Management from the University of British Columbia in Vancouver :

Wallace, S. S. 1999. Fisheries Impacts on Marine Ecosystems and Biological Diversity: The role for marine protected areas in British Columbia. Ph.D. Dissertation. The University of British Columbia. Pp. 198.

 In May of 2000, he returned to Race Rocks for a dive with Garry and Hana and an interview with Stephanie Paine and Director Julia Nunes for the Discovery Channel. In this video he demonstrates the measurement technique he used in his research.

Wallace, Scott, S. 1999, Evaluating the Effects of Three Forms of Marine Reserve on Northern Abalone Populations in British Columbia, Canada.

Conservation Biology, Vol 13 No 4, August, 1999, pages 882-887.

ABSTRACT: :Marine reserves have been suggested as tools for assisting the management of fisheries by protecting vulnerable marine species from overexploitation. Although there is a theoretical basis for believing that marine reserves may serve as management tools, there are few marine reserves in the world in which to test their effectiveness. My research evaluated three forms of marine reserve on the south coast of Vancouver Island, British Columbia, Canada. I used northern abalone (Haliotis kamtschatkana), a severely depleted shellfish in this region, as an indicator of the effectiveness of the reserves. Abalone populations in eight sites receiving different degrees of spatial protection were counted and measured in situ during the spring of 1996 and 1997. In all sites with enforced harvest closures, populations of abalone were greater, and one site with nearly 40 years of protection had on average much larger (older) abalone. Reproductive output, as a function of abundance and size, was also greater in the enforced reserve areas. Larval dispersal from reserves, and hence the benefit to exploited areas, was not formally surveyed. Nevertheless, the results of my study, combined with knowledge of present abalone populations, life history, and regional hydrodynamics, suggest that establishment of reserves is justified in the absence of perfect knowledge of larval dispersal.

This video was taken by Garry Fletcher of Scott as he was involved in measuring abalone at Race Rocks:

Articles published by Scott Wallace: 

Wallace, Scott, S. 1999, Evaluating the Effects of Three Forms of Marine Reserve on Northern Abalone Populations in British Columbia, Canada. Conservation Biology, Vol 13 No 4, August, 1999, pages 882-887.

 

Out of Sight, Out of Mind, and Almost out of Time:

Out of sight, almost out of time–mpa