Manseguiaopaper
Manseguiaopaper
Manseguiaopaper
net/publication/274017898
CITATION READS
1 243
6 authors, including:
Some of the authors of this publication are also working on these related projects:
All content following this page was uploaded by Mark Ronald Manseguiao on 25 May 2016.
Squares (GLS) Procrustes superimposition method was done Cluster Analysis was used to compare similarities among
to standardize the coordinates and to remove variation due to populations based on centroid size.
differences in translation, orientation and size [14], [15].
398
International Journal of Bioscience, Biochemistry and Bioinformatics, Vol. 4, No. 5, September 2014
Fig. 3. Summary of the geometric morphometric relative warp analysis of the Fig. 4. Summary of the geometric morphometric relative warp analysis of the
left wing showing the consensus morphology (uppermost panel) and the right wing showing the consensus morphology (uppermost panel) and the
variation in the shapes of the pronotum among the three populations of P. variation in the shapes of the pronotum among the three populations of P.
reichei. reichei.
399
International Journal of Bioscience, Biochemistry and Bioinformatics, Vol. 4, No. 5, September 2014
400
International Journal of Bioscience, Biochemistry and Bioinformatics, Vol. 4, No. 5, September 2014
Overall, the contraction and expansion of the landmark Cluster analysis of the centroid sizes of the wing
points suggest that the overall shape of the wings become morphology showed that the left and right wings were
shorter from proximal to distal landmark points and broader grouped according to geographic location. Each location is
between points in the upper margins to the lower margins. seen to be significantly different from each other (p<0.5; Fig.
Also, the proximal points become closer together suggesting 7). Left and right wings were also significantly different
a slender wing. except for BAL indicating functional asymmetry arises in the
According to Chapman [20], narrower and petiolate bases wings. Functional asymmetry is deviations in the bilateral
are characteristics of slow-flying insects while those with symmetry of an organism believed to be induced by stresses
broader bases are faster. Based on the data, the wings of in the environment. Furthermore, it shows that these
P.reicheifrom the three populations are observed to be more environmental factors might be similar in BAL and WAO
narrow proximally, shorter in length and broader between the despite a large geographic distance between the two
leading edge to the trailing edge of the wing. This suggests locations.
that wing shape contribute to a slower flight but more The variations observed in P.reichei may be attributed to
powerful since more force is produced to lift the body up. the effects of latitude and altitude as has been observed in
Drosophila melanogaster [21], [22]. Moreover these wing
TABLE XI: INTERLANDMARK (INTER-LM) DISTANCES WITH THE BOTTOM morphology changes including wing asymmetry may also be
10% PCA SCORES FOR THE SIGNIFICANT COMPONENTS OF THE PROCRUSTES attributed to the diet during development [23], relative
TRANSFORMED LANDMARK COORDINATES OF THE RIGHT WING OF P.
REICHEI FROM THREE LOCATIONS IN MINDANAO humidity and rainfall [24], [25].
PC1 PC2 PC3 PC4 PC5
%var=24.22% %var=15.75% %var=12.33 %var=6.39 %var=5.25
LM value LM value LM value LM value LM value IV. CONCLUSION
14-19 -0.0949 3-18 -0.0955 4-5 -0.0987 4-21 -0.0737 5-16 -0.0874
1-10 -0.0950 1-19 -0.0960 3-12 -0.1001 2-3 -0.0746 5-20 -0.0895 This study has clearly described the variations in the wings
9-21 -0.0957 2-18 -0.0960 17-21 -0.1005 8-19 -0.0841 10-18 -0.0903 of three geographically distant populations of P. reichei using
18-21 -0.0967 8-11 -0.101 3-20 -0.1019 3-21 -0.0845 3-20 -0.0936
19-21 -0.0971 2-8 -0.102 2-13 -0.1047 11-16 -0.0861 8-10 -0.0948 landmark-based geometric morphometric analysis. While
16-21 -0.0975 3-4 -0.1026 4-7 -0.108 4-14 -0.0900 16-18 -0.1005 differences were observed between geographical locations,
14-16 -0.0997 3-8 -0.1077 14-17 -0.109 8-14 -0.0911 3-17 -0.1006 distance was not a factor for the differences which may
10-21 -0.1006 2-5 -0.1083 11-17 -0.1116 2-18 -0.0934 4-10 -0.1007
11-13 -0.1006 7-11 -0.1084 15-17 -0.113 10-11 -0.0949 8-16/ -0.1048
indicate differences in the genetic structure of the populations.
10-14 -0.1023 9-11 -0.1137 1-19 -0.1161 7-11 -0.0996 17-21 -0.1085 Environmental differences may also have triggeredwing
14-17 -0.1025 6-11 -0.1142 2-21 -0.1181 9-17 -0.1006 17-19 -0.1089 development. Similar environmental cues may produce
1-4 -0.1026 2-17 -0.1181 12-17 -0.1247 3-14 -0.1011 4-15 -0.1121
17-21 -0.103 10-11 -0.1195 1-17 -0.1252 18-21 -0.1091 4-20 -0.1161
similarity in wing landmarksbut distinct geographically.
8-14 -0.1065 2-7 -0.125 3-21 -0.1262 18-20 -0.1099 4-16 -0.1219
8-21 -0.1092 11-19 -0.1318 13-17 -0.1273 8-17 -0.1102 2-17 -0.1375 ACKNOWLEDGEMENT
4-14 -0.1199 2-6 -0.141 2-14 -0.1282 18-19 -0.1214 19-20 -0.1545
4-21 -0.1263 2-19 -0.1429 3-13 -0.1287 17-18 -0.1263 16-17 -0.1577 Thanks are owed to Philippine Department of Science and
11-21 -0.1278 3-5 -0.1494 3-14 -0.1368 14-18 -0.1318 15-19 -0.1588 Technology under the Accelerated Science and Technology
1-11 -0.1323 3-7 -0.1507 4-6 -0.1379 9-11 -0.163 16-19 -0.1603 Human Resource Development Program for their prompt
2-4 -0.1361 11-17 -0.1558 1-2 -0.156 8-11 -0.1636 15-17 -0.1699
11-14 -0.1416 3-6 -0.1779 1-3 -0.166 11-18 -0.1752 17-20 -0.1753 responses to queries regarding the study.
REFERENCES
WAO RW
WAO LW
WAL RW
BAL RW
[1]
BAL LW
1600 [4] B. Cui and G. Liu, “Research significant of wing and vein among
Insecta,” International Journal of Biology, vol. 3, pp. 80-183, 2011.
[5] M. A. Sturtevant and E. Bier, “Analysis of the genetic hierarchy
2000 guiding wing vein development in Drosophila,” Development 121, no.
3, pp. 785-801, 1995.
64
[6] S. F. Gilbert, J. M. Opitz, and R. A. Raff, “Resynthesizing evolutionary
2400 and developmental biology,” Dev. Biol., vol. 173, pp 357–372, 1996.
[7] M. A. J. Torres, L. A. Adamat, M. M. E. Manting, S. R. M. Tabugo, R.
C. Joshi, L. Sebastian, A. T. Barrion, and C. G. Demayo,
2800 “Developmental modules defining the shapeof the forewing of
Scotinopharacoarctata,” Egypt. Acad. J. biolog. Sci., vol. 3, no. 1, pp.
105-112, 2010.
3200
100 [8] T. M. Francoy, R. A. O. Silva, P. Nunes-Silva, C. Menezes, and V. L.
Imperatriz-Fonseca, “Gender identification of five genera of stingless
Fig. 7. Dendrogram of centroid size comparison using ward’s method from bees (Apidae, Meliponini) based on wing morphology,” Genetics and
three populations of P. reichei. molecular research, vol. 8, no. 1, pp. 207-214, 2009.
401
International Journal of Bioscience, Biochemistry and Bioinformatics, Vol. 4, No. 5, September 2014
[9] F. J. Rohlf, Geometric morphometrics and phylogeny, Stony Brook, Jessie G. Gorospe is a faculty and the dean of the
NY: State University of New York, pp. 175-193, 2002. School of Graduate Studies at the Naawan Campus of
[10] P. Mitteroecker and P. Gunz, “Advances in geometric morphometrics,” the Mindanao State University system.
Evolutionary Biology, vol. 36, no. 2, pp. 235-247, 2009.
[11] R. Laffont, C. Firmat, P. Alibert, B. David, S. Montuire, and, T.
Saucède, “Biodiversity and evolution in the light of morphometrics:
From patterns to processes,” ComptesRendusPalevol, vol. 10, no. 2, pp.
133-142, 2011.
[12] C. L. Staines. (2012). Hispines of the World. USDA/APHIS/PPQ.
Center for Plant Health Science and Technology and National Natural
History Museum. [Online]. Available:
http://idtools.org/id/beetles/hispines
[13] F. J. Rohlf, TPSDig version 2.12, Stony Brook, NY: State University of
New York, 2008. Sharon Rose M. Tabugo is an associate professor in
[14] F. L. Bookstein, Morphometric tools for landmark data: geometry and the Department of Biological Sciences in Mindanao
biology, London, UK: Cambridge University Press, 1991. State University – Iligan Institute Technology.
[15] I. L. Dryden and K. V. Mardia, Statistical analysis of shape, Chichester,
U.K: Wiley, 1998.
[16] F. J. Rohlf, TPSRelw version 1.46, Stony Brook, NY: State University
of New York, 2008.
[17] Ø. Hammer, D. A. T. Harper, and P. D. Ryan. (2001). Past:
Paleontological Statistics Software Package for education and data
analysis. Paleontologí aElectrónica. [Online] 4. pp. 1-9. Available:
http://palaeo-electronica.org/2001_1/past/issue1_01.html
[18] S. Lele and J. T. Richtsmeier, “Euclidean distance matrix analysis:
confidence intervals for form and growth differences,” American
Journal of Physical Anthropology, vol. 98, no. 1, pp. 73-86, 1995. MuhminMichael E. Manting is an instructor in the
[19] I. T. Jolliffe, “Principal component analysis,” Springer series in Department of Biological Sciences in Mindanao State
statistics, vol. 29, 2002. University – Iligan Institute Technology.
[20] R. F. Chapman, The insects: structure and function, Cambridge, UK:
Cambridge University Press, pp. 193-225, 1998.
[21] W. Pitchers, J. E. Pool, and I. Dworkin, “Altitudinal clinal variation in
wing size and shape in African Drosophila melanogaster: one cline or
many?” Evolution, vol. 67, no. 2, pp. 438-452, 2013.
[22] H. Johnson, M. J. Solensky, D. A. Satterfield, and A. K. Davis, “Does
Skipping a Meal Matter to a Butterfly's Appearance? Effects of Larval
Food Stress on Wing Morphology and Color in Monarch Butterflies,”
PloS one, vol. 9, no. 4, p. e93492, 2014.
[23] E. J. Márquez and C. I. Saldamando-Benjumea, “Rhodniusprolixus and
Rhodniusrobustus–like (Hemiptera, Reduviidae) wing asymmetry
under controlled conditions of population density and feeding Mark Anthony J. Torres is an associate professor in
frequency,” Journal of biosciences, vol. 38, no. 3, pp. 549-560, 2013. the Department of Biological Sciences in Mindanao
[24] G. F. Gómez, E. J. Márquez, L. A. Gutiérrez, J. E. Conn, and M. M. State University – Iligan Institute Technology. He is
Correa, “Geometric morphometric analysis of Colombian Anopheles also a director at the Institute for Peace and
albimanus (Diptera: Culicidae) reveals significant effect of Development in Mindanao of the University.
environmental factors on wing traits and presence of a metapopulation,”
Actatropica, vol. 135, pp. 75–85, 2014.
[25] M. J. D. Juri, J. Liria, J. C. Navarro, R. Rodriguez, and G. N. Fritz,
“Morphometric Variability of Anopheles pseudopunctipennis (Diptera:
Culicidae) from Different Ecoregions of Argentina and Bolivia,”
Florida Entomologist, vol. 94, no. 3, pp. 428-438, 2011.
402