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Epibiosis occur frequently on the shells of some marine crustaceans, which often serve as substrate for various species of algae, there is few information on the associations between these. The objective of this study was to determine if the gastropod mollusk Aliger gigas (formerly Lobatus gigas) in larval had some sort of the association with algal. To the above was carried out collecting egg masses in the environment, the larvae were cultivated in seawater filtered 5 μm. The algal material found was observed in electron microscopy, for its identification and quantification. We analyzed 60 larvae aged 2–44 days for analyzing the structure of the shell and its epibionts. Of the larvae analyzed, 50 larvae presented epizoic. The algae community consisted of 28 taxa, and composed of 25 diatoms (Bacillariophyta) and three cyanophytes (Cyanobacteria). The H´ diversity values fluctuated between 0.2 a 1.2. The dominant and frequent species were formed by diatoms: Nitzschia panduriformis var. minor, Halamphora sp. and Cyclophora sp.
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Chapter
First Report on the Diversity of
Epizoic Algae in Larval of Shellfish
Gastropod Aliger gigas
Rocío ElizabethMuciño-Márquez,
DalilaAldana-Aranda, María GuadalupeFigueroa-Torres
and OscarHernández-Almeida
Abstract
Epibiosis occur frequently on the shells of some marine crustaceans, which
often serve as substrate for various species of algae, there is few information on
the associations between these. The objective of this study was to determine if
the gastropod mollusk Aliger gigas (formerly Lobatus gigas) in larval had some
sort of the association with algal. To the above was carried out collecting egg
masses in the environment, the larvae were cultivated in seawater filtered 5μm.
The algal material found was observed in electron microscopy, for its identifica-
tion and quantification. We analyzed 60 larvae aged 2–44days for analyzing the
structure of the shell and its epibionts. Of the larvae analyzed, 50 larvae presented
epizoic. The algae community consisted of 28 taxa, and composed of 25 diatoms
(Bacillariophyta) and three cyanophytes (Cyanobacteria). The H´ diversity values
fluctuated between 0.2 a 1.2. The dominant and frequent species were formed by
diatoms: Nitzschia panduriformis var. minor, Halamphora sp. and Cyclophora sp.
Keywords: cyanophyte, diatom, epibiont, Aliger gigas
. Introduction
Epibiotic is a type of association in which an organism lives on the surface layer
of another organism called basibiont, these nonparasitic organisms are known
as epibionts [1, 2]. The shells of gastropod and bivalve mollusks represent a suit-
able habitat for the settlement of various species of algae, viruses or fungi [3–6].
Different studies have focused on epiphytic diatoms of grasses and marine mac-
roalgae [7–9]; in copepods of the species Farranula gibbula, the epibiotic diatom
Pseudohimantidium pacificum has been observed [10]. Very little information exists
on symbiotic associations between algae and crustaceans or marine planktonic
mollusks, being able to cite what was observed in Peringia ulvae (formerly Hydrobia
ulvae) and diatoms Cocconeis placentula and Achnanthes lemmermannii, also cyano-
phytes and bacteria in its Shell [5]. Based on the above, the objective of this work
was to identify epizoic species present in the shells of the larval stages of the marine
gastropod mollusk, Aliger gigas.
Plankton Communities
. Material and methods
An egg mass of Aliger gigas was incubated in filtered seawater with a 5μm mesh,
until hatching. Later, the larvae were cultured with seawater filtered with a 50μm
mesh and fed with Nannochloropsis oculata (Ochrophyta, Eustigmatophyceae) at a con-
centration of 1 000 cells per larva, at a density of 100 larvae/L. The larvae were fixed
in glutaraldehyde, cacodylate and dehydrated in alcohols from 70 to 100% and dried
at a critical point. The shells of 60 larvae between 2 and 44days old were processed.
The specimens were observed in a JEOL field emission scanning electron microscope
(JSM-7600F), of the National Laboratory of Nano and Biomaterials of Cinvestav IPN
Mérida, the presence of epizoic algae was analyzed and to its quantification was car-
ried out. For the identification of phytoplankton, the works of [1116], among others.
The AlgaeBase system was consulted to verify accepted taxonomic names [17].
To obtain the relative abundance index, the proportion of abundance of each
species (organism number) was quantified in relation to the total abundance of organ-
isms counted in each larva of different ages [18]. The contribution of the abundance
of the epizoic algae species of each larva was determined by means of the SIMPER
analysis [19]. This analysis determines the species that most contribute to the similar-
ity between sample. A cumulative similarity discrimination value of 90% was applied.
Based on the composition and abundance of the epizoic algae species, the community
was characterized by the following descriptors: to evaluate the diversity, the species
richness of Margalef (S), the Shannon-Wiener index (H) and Pielou’s equity (J’)
considering to according to in accordance with [20], through the ODI program of the
Interdisciplinary Center for Marine Sciences, Department of Plankton.
To obtain dominance of the species, an Olmstead & Tukey test was used [21].
The dominant, constant, occasional and rare species were determined from the
relationship between the densities of the organisms and their frequencies of
appearance. The statistical programs used were Primer-E and R.
. Results
Of the 60 specimens of A. gigas larvae analyzed, 83% presented epizoic algae.
The epizoic algae community consisted of 28 taxa, made up of 25 diatoms and
three cyanophytes. It should be noted that one of the recorded diatom species
Cylindrotheca closterium is considered a species that can be harmful and forms algal
blooms (Table).
. Specific diversity
The diversity values H´ fluctuated between 0.9 and 1.2. The 28-day-old pre-
metamorphic larval shells presented the highest value of H´ 1.2 with an equity of
J´ 0.4, and a species richness of S 14. These values of H´ 1.2 with a J 0.5 and an S 9,
were slightly higher in the 30-day-old larvae, which already had foot formation.
For the 20-day-old larvae, H ‘was 1.1, J’ was 0.4 and S was 11 and in the 18-day-old
larvae, H ‘was 0.9, J’ was 0.4 and S was 9 species (Figure , Table  ). Following the
same behavior, the youngest veliger larvae, 8days old, presented the lowest diver-
sity with values of H ‘of 0.2, J’ of 0.42 and S of 4 species (Figure , Table).
. Dominant species
Based on the Olmstead and Tukey test, the epizoic algae community consisted
of 17 rare species, followed by five common, three abundant and three dominant
First Report on the Diversity of Epizoic Algae in Larval of Shellfish Gastropod Aliger gigas
DOI: http://dx.doi.org/10.5772/intechopen.95113
Larva age in days          FR At.
Number of larvae analyzed     
Bacillariophyta
Amphora sp. 0 0 0 0 0 0 0 2.5 0 0 10 R
Cocconeis lineata 0 0 0 0 0.1 1.5 0 3 0 0 30 R
Cocconeis scutellum 0 0 0 0 0.1 20.1 0 0 0 30 O
Craspedostauros sp. 0 5 0 0 0 0 12 00.1 030 R
Cyclophora sp. 0 66 10 3 5 1.9 0.3 15 76 70 90 D
Cylindrotheca closterium 17.5 1.5 54.4 1.3 0.3 0 0 0 70 C
Entomoneis paludosa 0 0 19 3.6 717 16 11 8.5 480 C
Halamphora coffeaeformis 0 0 0 0 0 0 0 0 0.1 0.1 20 R
Halamphora sp. 0 1.7 47 30 10 70.2 0 0 0 70 D
Haslea tsukamotoi 0 0 0 0 0 1 0.1 7.5 0 1 40 R
Hippodonta pseudacceptata 0 0 0 0 54.3 0 0 0 0 0 10 R
Hyalosynedra sp. 0 0 0 0 0 0.4 0.1 0 0 1.2 30 R
Licmophora sp. 0 0 0 0.3 0 0 0 0 0 0 10 R
Navicula radiosa 0 0 0 2.6 019 1 9 0 0 40 O
Nitzschia dissipata 0 0 0 0 0.1 00.1 0 0 0 20 R
Nitzschia inconspicua 0 0 0 0 0 8 0 0 0 2.8 20 R
Nitzschia linearis 0 0 0 0 0 0 0 0 0 0.3 10 R
Nitzschia microcephala 0 0 0.4 0 0 0 0.1 0 0 0 20 R
Nitzschia panduriformis var. minor 64 18 851 94.5 1.1 20 7. 5 0.2 100 D
Nitzschia sp. 0 0 3.6 4 5 0 0 0 0 0 30 O
Pleurosigma sp. 5 0 0 0.5 0 0 0 0 0 0 20 R
Plankton Communities
Psammodictyon panduriforme 0 0 2.2 0 0 0 0 0 0 0 10 R
Pseudachnanthidium sp. 0 0 0 0 0 0.3 0 0 0 0 10 R
Scalariella sp. 0 0 8 0 0 0 0 0 0.2 0.1 30 R
Stephanodiscus minutulus 0 0 0.3 0 0 0 0 0 0 0 10 R
Cyanophyta
Haloleptolyngbya sp. 0 0 0 0 5 32 68 30 7.6 20 60 C
Richelia intracellularis 0 0 0 0 0 0 0 2 0 0 10 R
Arthrospira sp. 0 1.8 0 0 0 4.1 0 .6 0 0 0.3 40 R
S     
H. . . . . . . . . .
J. . . . . . . . . .
Table 1.
Percentage of the relative abundance of the epizoic algae community in the shells of Aliger gigas larvae. % FR: Percentage of the relative frequency. At: Attribute, D: D: Dominant, C: Constant,
O: Occasional and R: Rare. S: Species richness, H: Diversity and J: Equity.
First Report on the Diversity of Epizoic Algae in Larval of Shellfish Gastropod Aliger gigas
DOI: http://dx.doi.org/10.5772/intechopen.95113
species (Table). The dominant species were made up by the diatom Nitzschia
panduriformis var. minor, whose highest relative abundance was 68% in 8-day-old
larvae; Hippodonta pseudacceptata with a relative abundance of 54% in 20-day-old
larvae; Halamphora sp. with a relative abundance of 47% in 16-day-old larvae and
Cyclophora sp. with 70 and 76% in larvae of 36 and 44days respectively (Figure ,
Table). In addition, of the cyanophyte Haloleptolyngbya sp. with a relative abun-
dance of 68% in 28-day-old larvae (Figure , Table ).
. Characteristics of Aliger gigas larvae, observed in the development of this
work
The two to five-day old larvae have a shell formed by two turns in a spiral pre-
senting small granule at the apex and a velum characterized by having two lobes and
the right tentacle, corresponding to a young veliger larva. The shell of eight-day-old
Figure 1.
(A) Species richness (S), (B) diversity (H) and (C) equity (J’) of the epizoic algae community in the shells of
Aliger gigas larvae.
Plankton Communities
larvae is characterized by having three coils, showing well-defined lines of ornamen-
tation on the body of the shell. As regards its development; the velum has four lobes;
with the right tentacle well differentiated and the formation of the left tentacle.
The 15–18-day old larvae have a carapace with three and a half turns in the
spiral, the body has four parallel lines ending at the end of the siphon channel and
is highly ornamented. The velum has six lobes, tentacles, and proboscis. In larvae
from 20 to 28day of development, their shell has three and a half turns, with a band
of uniform striations on the body of the shell, the radula is already observed and the
velum begins the process of reabsorption therefore the larva begins to have a creep-
ing shape beginning its benthic phase. It is a stage known as a precompetent larva.
Regarding larvae between 30 and 44days old, at this stage the larvae are ready to
metamorphosis (30days). Post-metamorphic larvae or post larvae of 44days, pres-
ent a foot with an active crawling behavior. The shell is characterized by presenting
four turns, with a well-developed band of striae, the proboscide and the radula are
present and active, as is the foot with its operculum.
. Discussion
Diatoms have been reported in the literature as the main group of epizoic micro-
algae species attached to different types of animals that can be copepods [10, 2224];
cladocerans [25], hydrozoans [2627], krill [28] even in whales [2930]. Diatoms are
also present in diving birds [3132] and reptiles such as crocodiles [33].
As mentioned by [34], the first phase of the colonization of a substrate occurs
mainly by bacteria with diatoms, fungi and protozoa; which generate a film on the
surface of the basibiont. The results of this study showed that the shells of larvae
of the marine gastropod mollusk, Aliger gigas, provide an adequate and frequent
substrate for the settlement of epizoic microalgae, in the case of diatoms and
cyanophytes. A dominance of diatom species was also observed. Nitzschia panduri-
formis var. minor was reported in 8-day-old larvae, Halamphora sp. was present in
16-day-old larvae, Hippodonta pseudacceptata, in larvae of 20days and Cyclophora
sp., in larvae of 36 and 44days. Obtaining low values of diversity H(0.2 to 0.9) and
J’ (0.2 to 0.5), in these phases of the larvae. [35] mentions that diversity is low when
there is a dominance of some species.
Likewise, it was found that the diatom and cyanophyte populations were not stable.
It is interesting to note that, although the larvae were under the same culture condi-
tions, in the larvae of different ages, the structure of their epizoic microalgae com-
munity changed. In larvae less than 20days old, the cells of the dominant microalgae
Figure 2.
SIMPER analysis, percentage contribution of epizoic algae species from the shells of the larvae of the marine
gastropod mollusk Aliger gigas.
First Report on the Diversity of Epizoic Algae in Larval of Shellfish Gastropod Aliger gigas
DOI: http://dx.doi.org/10.5772/intechopen.95113
were shed from the larvae shells allowing the colonization of other microalgae; on the
other hand, in larvae of 20 to 30days a higher H diversity of 1.0 to 1.2 was reported. In
another study with gastropods, carried out by [6] reviewed the shells of seven gas-
tropods (Alvania lineata, Bittium reticulatum, Clanculus cruciatus, Columbella rustica,
Gibbula adansoni, Nassarius incrassatus and Jujubinus striatus), reporting a richness of 19
to 25 species and a high J’ equity of 0.70 to 0.80 and [36] in Lepidochelys olivacea (olive
ridley) shells, recorded a diversity of 1.1 to 2.1 and a high J’ equity of 0.56 to 0.86.
From what was observed in this study, the size and structure of the shell of
A. gigas larvae on the different days of development provide a substrate for the
epizoic microalgae.
The two to five-day old larvae did not have microalgae, the size of the shell is
small, thin, smooth, the shell is formed through a transient amorphous calcium
carbonate that acts as a precursor in the aragonite crystallization sequence [37–38].
In addition, the time for colonization is still short.
In the case of larvae from 26 to 44days, the highest species richness was
reported, the shell is larger about 1 200μm with greater ornamentation and with
greater adhesion surface. Especially the 44-day-old larvae present a periostracum,
outermost layer of the shell composed of an organic matrix [38–39], which offers a
better substrate, rich in proteins, which permit the growth of epizoic microalgae. In
28-day-old larvae, the number of spirals and shell ornamentation may be the factors
that support the presence of Haloleptolyngbya sp., in addition to the mucus secreted
by the microalgae themselves to adhere to the substrate. The 30 to 36-day old larvae
showed a lower species richness and a dominance of Cyclophora sp. This diatom
forms colonies in a zigzag shape, occupying the entire larva shell and preventing
other microalgae from adhering. In several studies they have agreed to point out
that gastropod shells are good microenvironments, due to their different structures
and sizes. [6] Size does influence the colonization of epizoic microalgae, observing
that the largest shells (Bittium reticulatum, Gibbula adansoni, Columbella rustica
and Clanculus cruciatus) presented greater abundance and the small shells (Alvania
lineata, Nassarius incrassatus and Jujubinus striatus) higher species richness, unlike
what was found in this work.
Some microalgae produce allelopathic substances that inhibit the growth of
others [40]. This could explain why some larvae had fewer epizoic microalgae than
others, or for the fact that some had successfully colonized earlier and no longer left
space for the colonization of more species. In addition to the changes in the abun-
dances of the epizoic microalgae community, it is important to study the physical
and chemical factors that influence their succession and to analyze whether A. gigas
larvae fed on the epizoic microalgae reported. Epizoic microalgae associated with
the velum of the larvae analyzed in this study were reported, Cylindrotheca closte-
rium, Hippodonta pseudacceptata and Cyclophora sp.
The ecology studies of epizoic microalgae on the larvae of A. gigas, allows to
know which species of phytoplankton or phytobenthos are present in the system
where these larvae inhabit of the Mexican Caribbean. There are few studies focused
on the study of diatoms and even less if they are found as epizoic microalgae. As
the knowledge of the factors that regulate the competitive ability of the different
epizoic microalgae species increases, the degree of interaction between them and
their basibiont will also be understood.
Acknowledgements
We thank the National Council for Science and Technology (Conacyt) for grant
N° 269167 and the project The pink snail as an indicator of climate change in the
Plankton Communities
Author details
Rocío ElizabethMuciño-Márquez1,3*, DalilaAldana-Aranda2,
María GuadalupeFigueroa-Torres3 and OscarHernández-Almeida4
1 Biological and Health Sciences, Autonomous Metropolitan University,
Xochimilco Unit, Mexico
2 Cinvestav IPN, Mérida Unit Marine Ressources Departement, Mexico
3 Phycology Laboratory, Autonomous Metropolitan University, Xochimilco Unit,
Mexico
4 Autonomous University of Nayarit, Mexico
*Address all correspondence to: mucinoelizabeth@gmail.com
Caribbean: Ocean Warming and Acidification” (CB-2011-2101/181329). To the
electron microscopy laboratory of the Mérida Unit of Cinvestav and to Ana Ruth
Cristóbal Ramos and Dora Huerta for their work on electron microscopy.
© 2020 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms
of the Creative Commons Attribution License (http://creativecommons.org/licenses/
by/3.0), which permits unrestricted use, distribution, and reproduction in any medium,
provided the original work is properly cited.
First Report on the Diversity of Epizoic Algae in Larval of Shellfish Gastropod Aliger gigas
DOI: http://dx.doi.org/10.5772/intechopen.95113
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