Download (20MB) - Repository@Napier
Download (20MB) - Repository@Napier Download (20MB) - Repository@Napier
1.2 -0.4 "a 0.8 > (i) % Water content (1) (iii) % Water content (3) 2 3 4 Distance class 1.2 (v) % Silt/clay (2) 0.4 -0.4 2 3 4 1.2 (vii) % Organic content (1) 1 0.8 . 4.0 4- °8 Distance class Distance class Distance class p
DISCUSSION This study specifically addressed 2 questions, these were: (1) what is the micro-scale spatial distribution of dense populations of tube-building spionids and what does it suggest about intraspecific interactions?; (2) what are the roles of larval recruitment, interspecific interactions and abiotic variables in determining spatial patterns? These questions were addressed using P. elegans as an example. The micro-scale spatial patterns of P. elegans within high density patches on Drum Sands. Linear transects of 32 contiguous cores were taken monthly from 3 small-scale P. elegans patches from March to August 1997, and then every other month until February 1998. Dispersion indices suggested that all through the sampling period (except October 1997) the distribution of adult P. elegans individuals showed a significant departure from random (in at least 2 of the 3 replicates), all of these were aggregated distributions, i.e., their variances were significantly greater than their means. There was generally a very good agreement between the 3 dispersion indices used (I, Id and Ii.,) which suggests that confident statements can be made about these results (Myers, 1978). The form of these patterns were investigated using mapping (nearest-neighbour gridding technique) and spatial autocorrelation analysis. Spatial autocorrelation analysis allowed the nature of patterns and estimates of patch sizes to be made. In general, these patches of increased adult P. elegans densities were smaller than the sampling units (i.e.,
- Page 160 and 161: of non-patch areas (Figure 6.3(vi))
- Page 162 and 163: the individuals colonising patch az
- Page 164 and 165: Multivariate analysis of community
- Page 166 and 167: Month Sample statistic (Global R) N
- Page 168 and 169: 2NP 3NP 4NP .•,, 6NP 5NP 6P 1NP i
- Page 170 and 171: Figure 6.8: Two-dimensional MDS ord
- Page 172 and 173: - - 5P ... 4P . 6P • .‘2NP 1NP
- Page 174 and 175: I 50. 1 60. 70. 80. 90. 100. BRAY-C
- Page 176 and 177: 'P2-AZ P3-AZ N2-AZ .- - - " .„ ..
- Page 178 and 179: o • o -o + 350 — 300 = 250 7 g
- Page 180 and 181: The importance of the ambient commu
- Page 182 and 183: In April, when P. elegans larval av
- Page 184 and 185: not only for errant polychaetes, bu
- Page 186 and 187: observed in this study. How crucial
- Page 188 and 189: Micro-scale spatial patterns of mac
- Page 190 and 191: METHODS Experimental design - A pre
- Page 192 and 193: study. These individuals would not
- Page 194 and 195: RESULTS Pilot survey - The pilot su
- Page 196 and 197: Transect survey - Micro-scale patte
- Page 198 and 199: Month v:m ratio pattern Id pattern
- Page 200 and 201: (i) March 1997, replicate 1 -iAlmiA
- Page 202 and 203: (xix) October 1997, replicate 1 (ra
- Page 204 and 205: The new recruits were only sufficie
- Page 206 and 207: The results of correlation analyses
- Page 208 and 209: cf.) . crt N ,—, Cr) C,1 ,—, Cr
- Page 212 and 213: examine the micro-scale spatial pat
- Page 214 and 215: Invertebrate larvae, those of polyc
- Page 216 and 217: laboratory observations are needed
- Page 218 and 219: CHAPTER 8 THE FAUNAL COMMUNITIES OF
- Page 220 and 221: Other theories have been postulated
- Page 222 and 223: RESULTS Univariate analysis of spec
- Page 224 and 225: -T. g 80 g 50 40 30 20 10 (i) Adult
- Page 226 and 227: in significant differences in size
- Page 228 and 229: 8.2). This was mainly because of th
- Page 230 and 231: 120 100 80 60 - 40 20 0. cn1 c.n (i
- Page 232 and 233: 3NP 6NP 4NP 1 NP 5NP 2NP : 3P 1P 6P
- Page 234 and 235: 4P 3P 5P 5NP 6P 2P 1P Figure 8.8: T
- Page 236 and 237: Figure 8.10 shows the dendrogram pr
- Page 238 and 239: NP1 NP2 NP2 NP2 NP1 NP1 NP2 NP2 NP2
- Page 240 and 241: Sediment water, organic and silt/cl
- Page 242 and 243: 5 350 — 300 250 200 — ISO — 1
- Page 244 and 245: abundances of P. ciliata had more d
- Page 246 and 247: levels of silt/clay and organics. S
- Page 248 and 249: 1973; Noji and Noji, 1991). Competi
- Page 250 and 251: shown to consume up to 68% of a 0-g
- Page 252 and 253: In Chapter 7 the micro-scale spatia
- Page 254 and 255: and positions of patches. Consequen
- Page 256 and 257: epresent those found establishing i
- Page 258 and 259: distribution at the micro-scale. Ad
DISCUSSION<br />
This study specifically addressed 2 questions, these were:<br />
(1) what is the micro-scale spatial distribution of dense populations of tube-building<br />
spionids and what does it suggest about intraspecific interactions?;<br />
(2) what are the roles of larval recruitment, interspecific interactions and abiotic<br />
variables in determining spatial patterns?<br />
These questions were addressed using P. elegans as an example.<br />
The micro-scale spatial patterns of P. elegans within high density patches on<br />
Drum Sands.<br />
Linear transects of 32 contiguous cores were taken monthly from 3 small-scale P.<br />
elegans patches from March to August 1997, and then every other month until<br />
February 1998. Dispersion indices suggested that all through the sampling period<br />
(except October 1997) the distribution of adult P. elegans individuals showed a<br />
significant departure from random (in at least 2 of the 3 replicates), all of these were<br />
aggregated distributions, i.e., their variances were significantly greater than their<br />
means. There was generally a very good agreement between the 3 dispersion indices<br />
used (I, Id and Ii.,) which suggests that confident statements can be made about these<br />
results (Myers, 1978).<br />
The form of these patterns were investigated using mapping (nearest-neighbour<br />
gridding technique) and spatial autocorrelation analysis. Spatial autocorrelation<br />
analysis allowed the nature of patterns and estimates of patch sizes to be made. In<br />
general, these patches of increased adult P. elegans densities were smaller than the<br />
sampling units (i.e.,