Humana Na Eyyy Eyy Eyy
Humana Na Eyyy Eyy Eyy
Humana Na Eyyy Eyy Eyy
HANNAH GONZALES
JOENISON O. DAMULO
MIKYLLA DEPOSITARIO
APRIL 2024
CHAPTER 1
INTRODUCTION
in the Persian Gulf, finding that variations in otoliths were associated with ecological
populations in the western South Atlantic, revealing high levels of connectivity and
genetic diversity, as well as a historic population expansion coinciding with sea level
The researchers need to understand the two species of the Lutjanus family that is
accessible in Buenavista and Carmen Coastal waters better, which are the Lutjanus
campechanus and Ocysurus chrysurus accessible snappers in that area. This study's
intention is to look at their ecological roles and evolutionary relationships to help protect
The study of snappers In Buenavista and Carmen coastal waters offers important
knowledge into marine life and ecosystem health. By looking at how these fish live and
relate to their environment, researchers hope to learn more about the sea's equal and
variety to the ecosystem. Snappers, and their colored body and sizes, are important
participants in the coastal ecosystem. They have key roles in keeping the ocean
healthy. These studies can help us understand how we humans affect the coastal area.
From water pollution and over capturing fish, there are many dangers in the coastal
area today. The study of snappers in Buenavista and Carmen coastal waters is not just
about understanding the snappers. It's about their obstacles in the sea and how they
The findings of the study would contribute new information and a significant body of
This study will serve as a reference for further research on factors about ecological
investigating on how they relate and can adapt to their current and new environment.
The findings will contribute to the development of a more sophisticated and nuanced
the evolutionary relationships and ecological interaction. Finally, the study will
encourage future researchers to explore the factors of their ecological and phylogenetic
marine ecosystems. Snappers are a diverse group of fish species that play a crucial role
phylogenetic analysis of these sea creatures in specific coastal waters researchers can
gain valuable insights into their population dynamics distribution patterns evolutionary
preferred habitats is a crucial part of researching them in the Buenavista and Carmen
Coastal Waters. By identifying the specific environmental factors that influence the
understand the role of these fish species in the local ecosystem. Effective conservation
This study will be conducted through the accessibility of Snapper Fish in Buenavista
and Carmen Agusan del Norte Coastal Waters. Three fish of every type of Snapper
(Lutjanus campechanus and Ocysurus chrysurus) that is accessible will be our sample
to conduct analysis and. The sample size is dependent on what type is accessible in the
accessible in Selected Areas of Buenavista and Carmen Coastal Waters, we will define
ecological roles, etc. and gather information on the types of snappers found in
Buenavista and Carmen Coastal Waters and how they adapt to different kinds of water.
CHAPTER 2
This section contains the review of literature as well as relevant studies that support and
A series of studies have provided valuable insights into the ecological and phylogenetic
aspects of snappers. Silva (2023) used genetic and phylogenetic methods to validate
despite morphological similarities. Similarly, Sala (2023) identified nine red snapper
species in the Yapen Island Waters, Papua, using DNA barcode sequences and
highlighted the need for species-specific management. Guo (2008) contributed to the
snapper species from the South China Sea. These studies collectively highlight the
closely related, highlighting the importance of genetic analysis in taxonomy. Silva (2015)
and Gomes (2012) both identified high levels of genetic connectivity and a lack of
genetic differentiation among populations of the yellowtail snapper and red snapper,
respectively. These findings suggest a single genetic stock and a panmictic population,
no significant genetic differentiation between populations of the Pacific red snapper and
spotted rose snapper in the inshore Tropical Eastern Pacific. These studies collectively
provide valuable insights into the genetic and phylogenetic characteristics of snapper
species, which may have implications for their conservation and management.
during the growth of red snappers, identifying size and body depth as the main sources
of variance. These studies collectively highlight the diverse and significant role of
Authors, such as España (2003) and Erisman (2020) both highlight the importance of
snappers in ecosystem stability, with España emphasizing their role in resilience and
key drivers of snapper abundance. Schwartzkopf (2017) and Messias (2019) provide
more specific insights into the feeding ecology and ethnoecology of snappers,
feeding ecology, while Messias' study reveals the significant knowledge of artisanal
fishermen about snapper biology and ecology, particularly in relation to feeding and
habitat. These studies collectively underscore the ecological significance of snappers
and the need for further research to enhance our understanding of their role in marine
ecosystems.
Snappers play a crucial role in marine ecosystems, with their diet and habitat
preferences varying by species. Rigoberto (2021) found that snappers in the Caribbean
Sea primarily consume crustaceans, while Parsons (2014) highlighted the importance of
estuarine habitats for post-settlement snapper in New Zealand. Chỉ (2017) identified
rocky habitats in brackish water as key for juvenile mangrove red snapper in Vietnam,
and Simonsen (2014) observed differences in the feeding ecology of red snapper
between artificial and natural reefs in the Gulf of Mexico. These studies collectively
Snappers, any of about 103 species of fishes of the family Lutjanidae are marine
saltwater fish, Amy Tikkanen (2024). Salt water fish can't survive in freshwater because
their bodies are highly concentrated of salt solution. The water would flow into their
body until all their cells accumulate so much water that they bloat and die eventually,
this is because their bodies are more salty than fresh water, so they absorb water via
the process of Osmosis, Helen Scales (2022). Although some of the fishes of the family
Lutjanidae are mainly marine fishes, some are rarely inhabiting Estuaries, Skelton, P.H.,
intermediate depths (<100 m), but the majority of the species on the subfamily Etelinae
and some members of the Apsilinae are confined to deeper water (100 to 500 m). Most
lutjanids are solitary in habit and exhibit territorial behavior, Allen 1985. The Red
Snapper (Lutjanus campechanus) fish prefer deep reefs or rocky banks, these species
commonly inhabit waters from 9–60 m (30–200 ft). the Yellowtail Snapper (Ocysurus
chrysurus) fish prefers schooling in small groups in and around reefs, they occur at
depths of from near the surface to 180 meters (590 ft), though mostly between 10 and
Morphological characteristics
forms, many with special modifications. The shape, size, and structure of body parts
permit different fishes to live in different environments or in different parts of the same
environment. The external anatomy of a fish can reveals a great deal about where and
The eyes of these Snapper Fishes are eyes are similar to terrestrial vertebrates like
birds and mammals, but have a more spherical lens. Fish can detect color reported by
(Densmore, 2019) in fishes. Fish eyes are rounder than in mammals because of the
refractive index of water and focus is achieved by moving the lens in and out not
distorting it as in mammals. Fish eyes are usually placed just dorsal of and above the
mouth as it was observed by (Menke, 2011). It has a terminal mouth and generally feed
on other fish as it was reported by (Densmore,2019). Although most teeth in the upper
jaw are densely packed, fine, or hair like “villiform” teeth, there are several canine teeth
present as well – the latter constituting a definitive characteristic of all snappers. These
fishes have nostril, each nostril in a fish actually consists of two openings which is
located in the dorsal to the mouth, (Menke, 2011). Pair of small rounded nostrils on each
side of snout with very low flap on outer edge of anterior nostril. Paired nostrils or
snares in fish are used to detect odors in water and can be quite sensitive. Sense of
smell is well developed in fishes. Gills are the breathing apparatus of fish and are highly
vascularized, which gives them their bright red color, (Saha et al., 2018). The lateral line
is a sensory organ consisting of fluid filled sacs with hair like- sensory apparatus that
are open to the water through a series of pores, the lateral line system consists of a
long canal that runs along each side of the body, and contains a series of sensory
organs that can detect small pressure changes and vibrations from water currents. This
helps fish sense movements nearby, alerting them to prey or predator activity in fishes
tissues covered with calcium; also have a very important mucus layer covering the body
that helps prevent infection, (Robert, 2011). Fins are appendages used by the fish to
maintain position, move steer and stop. There are two kind of fins median and paired.
Median fin is single running down the midline of the body. Dorsal fin is a median fin
located on the dorsal side of the fish. The anal fin and caudal fin are median fin. Caudal
fin act like a propeller for the fish and caudal peduncle act like a motor. The paired fin
are arranged in pair, the pelvic and pectoral fin. Pectoral fins are vertical and are located
on the sides of fish. Pelvic fin is horizontally on the ventral side of the fish part the
pectoral fins in fish (Densmore., 2019). Pectoral fins are similar to animal arms which
are found near the pectoral muscles. Pelvic fins are similar to legs. Vent is a small
opening in the skin, has anal, genital, and urinary pores, the analpore is where feces
exits the fish body. The anus is the largest and most anterior of the pores, the genital
Research Design:
This study aims to determine the Ecological and Phylogenetic differences between
This can provide an understanding about this species behavior, habitat preference, DNA
The factors being considered, and the data that will be collected. In this study, a
Research Environment:
This study was conducted in two different places where we have taken snapper
fishes as samples, these locations are Carmen Fish Port (fig.1) and Brgy. 8 Buenavista
(fig.2).
Figure.1 Figure.2
Methods:
To perform this study, we need data’s that is collected and determined by these
methods.
Sample collection;
Four samples of Snapper fish to be collected in the coastal waters of Carmen and
Buenavista randomly. Two Red snapper ((Lutjanus campechanus) sample from Carmen
Observations;
aquatic waters (fresh and salt water), and comparing DNA sequences and
Upon utilizing the findings of Drummond et al., (2012) for BEAST v. 1.8.4 and Miller et
al. (2010) for the CIPRES Science Gateaway V. 3.3, the diversification analysis image
species of snappers. Note that this analysis tends to focus only on the
Biotechnology Information (NCBI) and were used to analyze genetic diversity and
and were used to analyze genetic diversity and compare evolutionary relationships
among snapper species. The image below shows the DNA sequence of the Red
Snapper:
Comparison of Morphological Characteristic
The eyes of these fishes, Red Snapper (Lutjanus campechanus) has a round lens and
very red coloration in the eyes (fig.1), while Yellowtail Snapper (Ocyurus chrysurus) has
also a round lens though the coloration in the eyes are mostly silver with hints of red
(fig.2).
Figure.1 Figure.2
The mouth position of these fishes, Red Snapper (Lutjanus campechanus) (fig.1), and
Figure.1 Figure.2
The gills of both Red Snapper (Lutjanus campechanus) (fig.1) and Yellowtail
filamentous structures called gill filaments. Overall, their gills serve the same essential
The noses, or snouts, of red snapper and yellowtail snapper exhibit subtle
snapper (Ocyurus chrysurus) (fig.2) tends to have a shorter, more rounded snout. Both
species have nostrils located on either side of the snout, allowing them to detect scent
molecules in the water. These differences in snout shape may be related to their feeding
behaviors and habitats, with red snapper often found in deeper waters and yellowtail
Figure.1 Figure.2
Red snapper (Lutjanus campechanus) (fig.1) has relatively large scales that
are firmly embedded in their skin, giving them a rough texture. Yellowtail snapper
(Ocyurus chrysurus) (fig.2) have smaller, more closely spaced scales compared
Figure.1 Figure.2
Lateral lines of the two species Red and Yellowtail snappers are visible, but the red
snapper’s lateral line is more noticeable due to the larger size of a red snapper.
The fins of red snapper and yellowtail snapper exhibit some similarities but also
notable differences. Both species have dorsal, anal, pelvic, and caudal fins. The
snapper has continuous, big and pointy dorsal and anal fin while the yellowtail
snapper’s dorsal and anal fin is not continuous nor big and it is round. Red snapper
typically has a slightly forked caudal fin, with the upper and lower lobes being roughly
equal in size. In contrast, yellowtail snapper possesses a deeply forked caudal fin, with
the upper lobe significantly longer and more pronounced than the lower lobe. These
differences in fin morphology may reflect adaptations to their respective habitats and
swimming behaviors, with red snapper often found in deeper waters and yellowtail
body with a moderately pointed snout. Red snapper has a deep reddish-pink coloration
on their upper body, fading to a lighter pink or silver on the lower body. They can grow
quite large, reaching lengths of up to 40 inches. While Yellowtail snapper have a more
slender, smooth body compared to red snapper, with a distinct yellow stripes running
laterally along their body. They are typically smaller, reaching lengths of around 20
inches.
CONCLUSION
analysis of the two available species Lutjanus campechanus and Ocysurus chrysurus in
Carmen and Buenavista Agusan del Norte. A significant genetic diversity was found
among sites. However, they seem to have shown genetic connectivity among sites.
and Ocysurus chrysurus) are predators that regulate the populations of their prey,
habitats, and participate in nutrient cycling within marine ecosystems. They play crucial
Comparative analysis of the phylogenetic tree for the Red snapper and Yellowtail
evolutionary relationship between the two species. Both shares common ancestor in the
Snapper family, but may have diverged over time due to various factors. Red Snapper
to Yellowtail Snapper (Ocyurus chrysurus), this suggest that the Red Snapper is more
derived and Yellowtail Snapper retains more characteristics of the common ancestor
to have a more robust body, large eyes, and a distinct red coloration. It also has a
pointed anal fin and lacks a yellow stripe along its body. On the other hand, the
yellowtail snapper (Ocyurus chrysurus) typically has a more streamlined body shape
with a yellow stripe running along its side, and a yellow tail, hence its name.
REFERENCES
da Silva, R., Veneza, I., Sampaio, I., Araripe, J., Schneider, H., & Gomes, G. (2015).
High levels of genetic connectivity among populations of yellowtail snapper, Ocyurus
chrysurus (Lutjanidae–Perciformes), in the Western South Atlantic revealed through
multilocus analysis. PLoS One, 10(3), e0122173. Retrieved from
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0122173
Sadighzadeh, Z., Otero-Ferrer, J. L., Lombarte, A., Fatemi, M. R., & Tuset, V. M. (2014).
An approach to unraveling the coexistence of snappers (Lutjanidae) using otolith
morphology. Scientia Marina, 78(3), 353-362. Retrieved from
https://www.torrossa.com/gs/resourceProxy?an=2984549&publisher=FZ1670#page=43
da Silva, R., Veneza, I., Sampaio, I., Araripe, J., Schneider, H., & Gomes, G. (2015).
High levels of genetic connectivity among populations of yellowtail snapper, Ocyurus
chrysurus (Lutjanidae–Perciformes), in the Western South Atlantic revealed through
multilocus analysis. PLoS One, 10(3), e0122173.
https://doi.org/10.1371/journal.pone.0122173
Silva, D., Veneza, I., Silva, R. D., Sampaio, I., & Evangelista-Gomes, G. (2023).
Molecular delimitation methods validate morphologically similar species of red snappers
(Perciformes: Lutjanidae). Anais da Academia Brasileira de Ciências, 95, e20210997.
https://doi.org/10.1590/0001-3765202320210997
Sala, R., Kusuma, A. B., & Pranata, B. (2023). Phylogenetic of Red Snapper
(Lutjanidae) in Yapen Island Waters, Papua, Indonesia. Retrieved from
http://repository.unipa.ac.id:8080/xmlui/handle/123456789/1420
Guo, Y., Wang, Z., Liu, C., & Liu, Y. (2008). Sequencing and analysis of the complete
mitochondrial DNA of Russell’s snapper (L. russellii). Progress in Natural
Science, 18(10), 1233-1238. https://doi.org/10.1016/j.pnsc.2008.07.001
Gomes, G., Sampaio, I., & Schneider, H. (2012). Population Structure of Lutjanus
purpureus (Lutjanidae-Perciformes) on the Brazilian coast: further existence evidence of
a single species of red snapper in the western Atlantic. Anais da Academia Brasileira de
Ciências, 84, 979-999. https://doi.org/10.1590/S0001-37652012000400013
Chu, C., Idid, M., Chong V. (2013) Phylogenetic relationships of selected genera of
Lutjanidae inferred from mitochondrial regions, with a note on the taxonomic status of
Pinjalo pinjalo. http://dx.doi.org/10.7773/cm.v39i4.2287
Schwartzkopf, B. D., Langland, T. A., & Cowan Jr, J. H. (2017). Habitat selection
important for red snapper feeding ecology in the northwestern Gulf of Mexico. Marine
and Coastal Fisheries, 9(1), 373-387.
https://doi.org/10.1080/19425120.2017.1347117
Messias, M. A., Alves, T. I., Melo, C. M., Lima, M., Rivera-Rebella, C., Rodrigues, D. F.,
& Madi, R. R. (2019). Ethnoecology of Lutjanidae (snappers) in communities of artisanal
fisheries in northeast Brazil. Ocean & coastal management, 181, 104866.
https://doi.org/10.1016/j.ocecoaman.2019.104866
Rigoberto, R. L., & Alexei, E. V. (2021). Trophic resource partitioning among four
sympatric lutjanid species in the southern Mexican Caribbean Sea. Marine Biology
Research, 17(7-8), 615-624.
https://doi.org/10.1080/17451000.2021.2009872
Parsons, D. M., Sim-Smith, C. J., Cryer, M., Francis, M. P., Hartill, B., Jones, E. G., ... &
Zeldis, J. (2014). Snapper (Chrysophrys auratus): a review of life history and key
vulnerabilities in New Zealand. New Zealand Journal of Marine and Freshwater
Research, 48(2), 256-283. https://doi.org/10.1080/00288330.2014.892013
Chi, V. V., & True, J. D. (2017). Recruitment and habitat ecology of juvenile mangrove
red snapper (Lutjanus argentimaculatus Forsskal, 1775) in central
Vietnam. International Journal of Fisheries and Aquatic Studies, 5(6), 103-107.
Retrieved from https://www.fisheriesjournal.com/archives/2017/vol5issue6/PartB/5-5-53-
406.pdf
Simonsen, K. A., Cowan, J. H., & Boswell, K. M. (2015). Habitat differences in the
feeding ecology of red snapper (Lutjanus campechanus, Poey 1860): a comparison
between artificial and natural reefs in the northern Gulf of Mexico. Environmental
Biology of Fishes, 98, 811-824. https://doi.org/10.1007/s10641-014-0317-9
Wang, Z., Guo, Y., Tan, W., Li, L., Tang, E., Liu, C., & Liu, Y. (2010). DNA barcoding,
phylogenetic relationships and speciation of snappers (genus Lutjanus). Science China
Life Sciences, 53, 1025-1030.
https://doi.org/10.1007/s11427-010-4034-0
Mendoza-Barrera, E. T., Vega-Cendejas, M. E., Améndola-Pimenta, M., & Rodríguez-
Canul, R. (2018). Morphometric Analysis on Shape Transition during Growth of the Red
Snapper (Lutjanus campechanus, Poey, 1860). Open Journal of Marine Science, 8(04),
407. http://www.scirp.org/journal/PaperInformation.aspx?PaperID=87830&#abstract
da Silva R, Veneza I, Sampaio I, Araripe J, Schneider H, Gomes G (2015) High Levels
of Genetic Connectivity among Populations of Yellowtail Snapper, Ocyurus
chrysurus (Lutjanidae – Perciformes), in the Western South Atlantic Revealed through
Multilocus Analysis. PLoS ONE 10(3): e0122173.
https://doi.org/10.1371/journal.pone.0122173
Morais P and Dias E (2021) Estuaries, A Happy Place For Fish. Front. Young Minds.
9:613862. doi: 10.3389/frym.2021.613862
Berg, L.S., 1958. System der rezenten und fossilen Fischartigen und Fische. VEB
Verlag der Wissenschaften, Berlin.
Nelson, J.S., 1984. Fishes of the world. 2nd edition. John Wiley & Sons, Inc., New York.
523 p.
Currie, S., & Evans, D.H. (Eds.). (2020). The Physiology of Fishes (5th ed.). CRC Press.
https://doi.org/10.1201/9781003036401