2021
DOI: 10.3390/jmse9050495
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Hiding in Fouling Communities: A Native Spider Crab Decorating with a Cryptogenic Bryozoan in a Mediterranean Marina

Abstract: Camouflage is the method by which animals conceal by blending in with the environment, and may be achieved by fixed or changing color, shape, texture, chemical secretions, and/or behavior [...]

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Cited by 7 publications
(5 citation statements)
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“…Total genomic DNA was extracted using the DNeasy® Blood & Tissue kit (QIAGEN). Partial sequences of the 16S ribosomal ribonucleic acid (16S rRNA) were amplified, purified, Sanger sequenced and finally checked, assembled and edited as in Tanduo et al (2021aTanduo et al ( , 2021b. They were compared with reference sequences from the NCBI nucleotide database both by using BLASTn (Morgulis et al, 2008) and by calculating the genetic P-distances between our samples and the sequences of the two species already deposited.…”
Section: Methodsmentioning
confidence: 99%
“…Total genomic DNA was extracted using the DNeasy® Blood & Tissue kit (QIAGEN). Partial sequences of the 16S ribosomal ribonucleic acid (16S rRNA) were amplified, purified, Sanger sequenced and finally checked, assembled and edited as in Tanduo et al (2021aTanduo et al ( , 2021b. They were compared with reference sequences from the NCBI nucleotide database both by using BLASTn (Morgulis et al, 2008) and by calculating the genetic P-distances between our samples and the sequences of the two species already deposited.…”
Section: Methodsmentioning
confidence: 99%
“…The colonies of Arthropoma cecilii (the only species of this genus known from the Mediterranean) reported from the Tyrrhenian Sea by Chimenz Gusso et al (2014) possibly belong to a different species, as suggested by Min et al (2017). Another example is Bugula neritina consisting of three cryptogenic species only recognizable through molecular analyses (Fehlauer-Ale et al, 2014), two of which presumably occur in the Mediterranean (Tanduo et al, 2021).…”
Section: Future Challenges Relating To Improved Technologies Global C...mentioning
confidence: 99%
“…Amplification was performed with an initial denaturation at 95 • C (5 min), followed by 39 cycles of denaturation at 95 • C (1 min), annealing at 47 • C (1 min), extension at 72 • C (1 min), with a final extension at 72 • C (5 min). The PCR products were purified and Sanger sequenced as in Tanduo et al [22]. The chromatograms for each sequence obtained were checked, assembled, edited using BioEdit version 7.0.0, and compared with reference sequences from the NCBI nucleotide (NT) database using the Basic Local Alignment Search Tool (BLAST; www.ncbi.nih.gov/BLAST/, accessed on 1 December 2021) [23].…”
Section: Sampling and Molecular Identificationmentioning
confidence: 99%