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16 results for “Spiny lobster”

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edi52/100

SBC LTER: Reef: Abundance, size and fishing effort for California Spiny Lobster (Panulirus interruptus), ongoing since 2012

Data on abundance, size and fishing pressure of California spiny lobster (Panulirus interruptus) are collected along the mainland coast of the Santa Barbara Channel. Spiny lobsters are an important predator in giant kelp forests off southern California. Two SBC LTER study reefs are located in or near the California Fish and Game Network of Marine Protected Areas (MPA), Naples and Isla Vista, both established as MPAs on 2012-01-01. MPAs provide a unique opportunity to investigate the effects of fishing on kelp forest community dynamics. Sampling began in 2012 and is ongoing. This dataset contains two tables. 1) Abundance and size data collected annually by divers in late summer before the start of the fishing season at five SBC LTER long term kelp forest study sites: two within MPAs (Naples and Isla Vista) and three outside (Arroyo Quemado, Mohawk and Carpinteria). 2) Fishing pressure, as determined by counting the number of commercial trap floats. Data are collected every two to four weeks during the lobster fishing season (October to March) at nine sites along the mainland, eight of which are also SBC LTER long-term kelp forest study reefs. See Methods for more information.

openCC (other)May 2024View details →
zenodo48/100

DATASET: De novo assembly and functional annotation of the heart + hemolymph transcriptome in the Caribbean spiny lobster Panulirus argus

<p>The spiny lobster <em>Panulirus argus</em> is an ecologically relevant species in shallow water coral reefs and target of the most lucrative fishery in the greater Caribbean region. This study reports, for the first time, the heart + hemolymph transcriptome of the Caribbean spiny lobster<em> Panulirus argus</em> assembled from short Illumina 150&thinsp;bp PE raw reads. A total 80,152,094 raw reads were assembled using the Oyster River Protocol pipeline that aspires to become the standard protocol for <em>de novo</em> transcriptome assembly. The assembly resulted in a total of 254,773 transcripts. Functional gene annotation was conducted using the software package &#39;dammit&#39; that also aspires to become the standard protocol for <em>de novo</em> transcriptome annotation. Lastly, gene enrichment analyses were conducted using the Gene Ontology (GO), KEGG pathway analyses (Kaas), and KOG (WebMGA) databases. This resource will be of utmost importance in future research aiming at exploring the effect of local and regional anthropogenic disturbances as well as global climate change on the molecular physiology of this overexploited species.</p>

opencc-by-4.0Dec 2019View details →
dryad32/100

Data from: Temporal genetic patterns of diversity and structure evidence sweepstakes in reproductive success of a spiny lobster

Population structure of many marine organisms is spatially patchy and varies within and between years, a phenomenon defined as chaotic genetic patchiness. This results from the combination of planktonic larval dispersal and environmental stochasticity. Additionally, in species with bi-partite life, post-settlement selection can magnify these genetic differences. The high fecundity (up to 500,000 eggs annually) and protracted larval duration (12-24 months) and dispersal of the southern rock lobster, Jasus edwardsii, make it a good test species for chaotic genetic patchiness and selection during early benthic life. Here we used double digest restriction-site associated DNA sequencing (ddRADseq) to investigate chaotic genetic patchiness and post-settlement selection in this species. We assessed differences in genetic structure and diversity of recently settled pueruli across four settlement years and between two sites in southeast Australia separated by approximately 1,000 km. Post-settlement selection was investigated by identifying loci under putative positive selection between recently settled pueruli and post-pueruli and quantifying differences in the magnitude and strength of the selection at each year and site. Genetic differences within and among sites through time in neutral SNP markers indicated chaotic genetic patchiness. Recently settled pueruli at the southernmost site exhibited lower genetic diversity during years of low pueruli catches, further supporting this hypothesis. Finally, analyses of outlier SNPs detected fluctuations in the magnitude and strength of the markers putatively under positive selection over space and time. One locus under putative positive selection was consistent at both locations during the same years, suggesting the existence of weak post-settlement selection.

opencc-zeroDec 2016View details →
dryad32/100

Data from: Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster (Palinurus elephas)

Defining population structure and genetic diversity levels is of the utmost importance for developing efficient conservation strategies. Overfishing has caused mean annual catches of the European spiny lobster (Palinurus elephas) to decrease alarmingly along its distribution area. In this context, there is a need for comprehensive studies to evaluate the genetic health of the exploited populations. The present work is based on a set of 10 nuclear markers amplified in 331 individuals from 10 different localities covering most of P. elephas distribution area. Samples from Atlantic and Mediterranean basins showed small but significant differences, indicating that P. elephas populations do not behave as a single panmictic unit but form two partially-overlapping groups. Despite intense overfishing, our dataset did not recover a recent bottleneck signal, and showed a large and stable historical effective size instead. This result could be accounted for by specific life history traits (reproduction and longevity) and the limitations of molecular markers in covering very recent timescales for non temporal samples. Our study emphasizes the necessity of integrating information on effective population sizes and life history parameters when evaluating population connectivity levels from genetic data.

opencc-zeroDec 2010View details →
dryad32/100

Data from: Oceanographic currents and local ecological knowledge indicate, and genetics does not refute, a contemporary pattern of larval dispersal for the ornate spiny lobster, Panulirus ornatus in the South-East Asian archipelago

Here we utilize a combination of genetic data, oceanographic data, and local ecological knowledge to assess connectivity patterns of the ornate spiny lobster Panulirus ornatus (Fabricius, 1798) in the South-East Asian archipelago from Vietnam to Australia. Partial mitochondrial DNA control region and 10 polymorphic microsatellites did not detect genetic structure of 216 wild P. ornatus samples from Australia, Indonesia and Vietnam. Analyses show no evidence for genetic differentiation among populations (mtDNA control region sequences ΦST = -0.008; microsatellite loci FST = 0.003). A lack of evidence for regional or localized mtDNA haplotype clusters, or geographic clusters of microsatellite genotypes, reveals a pattern of high gene flow in P. ornatus throughout the South-East Asian Archipelago. This lack of genetic structure may be due to the oceanography-driven connectivity of the pelagic lobster larvae between spawning grounds in Papua New Guinea, the Philippines and, possibly, Indonesia. The connectivity cycle necessitates three generations. The lack of genetic structure of P. ornatus population in the South-East Asian archipelago has important implications for the sustainable management of this lobster in that the species within the region needs to be managed as one genetic stock.

opencc-zeroDec 2014View details →
dryad32/100

Data from: Effect of oceanographic barriers and overfishing on the population genetic structure of the European spiny lobster (Palinurus elephas)

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publicMay 2011View details →
dryad32/100

Data from: Temporal genetic patterns of diversity and structure evidence sweepstakes in reproductive success of a spiny lobster

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publicNov 2017View details →
dryad32/100

Data from: Seascape genetics of the spiny lobster Panulirus homarus in the Western Indian Ocean: understanding how oceanographic features shape the genetic structure of species with high larval dispersal potential

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publicNov 2018View details →
dryad32/100

Data from: Oceanographic currents and local ecological knowledge indicate, and genetics does not refute, a contemporary pattern of larval dispersal for the ornate spiny lobster, Panulirus ornatus in the South-East Asian archipelago

Open the record for dataset details and reuse information.

publicAug 2015View details →
zenodo28/100

Figure 6 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 289-311. https://doi.org/10.3897/zookeys.457.6669

Figure 6 - Diet of Panulirus argus and Panulirus guttatus from Puerto Morelos, Mexico. For each food item the index of relative importance (IRI) is estimated as IRI = (% frequency × % weight)/100. (Data from Colinas-Sánchez and Briones-Fourzán 1990).

opencc-by-4.0Nov 2014View details →
zenodo28/100

Figure 3 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 289-311. https://doi.org/10.3897/zookeys.457.6669

Figure 3 - Diet of Panulirus gracilis and Panulirus inflatus from Zihuatanejo, Mexico. For each food item the index of relative importance (IRI) is estimated as IRI = (% frequency × % weight)/100. (Data from Lozano-Álvarez and Aramoni-Serrano 1996).

opencc-by-4.0Nov 2014View details →
zenodo28/100

Figure 2 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 289-311. https://doi.org/10.3897/zookeys.457.6669

Figure 2 - Differences in some life-history traits between Panulirus gracilis and Panulirus inflatus from Zihuatanejo, Mexico. A carapace length (CL) distribution (n Panulirus gracilis: 2162, n Panulirus inflatus: 1873) B mean size C growth rate of males (mm CL week–1, n Panulirus gracilis: 148, n Panulirus inflatus: 34) D brood size (number of eggs per clutch) versus CL relationship. Error bars denote 95% confidence intervals. (Data from A, B Briones-Fourzán and Lozano-Álvarez 1992, C Briones-Fourzán and Lozano-Álvarez 2003, D Gracia 1985, Fernández-Lomelín 1992).

opencc-by-4.0Nov 2014View details →
zenodo28/100

Figure 5 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 289-311. https://doi.org/10.3897/zookeys.457.6669

Figure 5 - Differences in some life-history traits between Panulirus argus and Panulirus guttatus from Puerto Morelos, Mexico. A carapace length (CL) distribution (n Panulirus argus: 717, n Panulirus guttatus: 450) B mean size C growth rate of males (mm CL week–1, n Panulirus argus: 148, n Panulirus guttatus: 57) D brood size (number of eggs per clutch) versus CL relationship. Error bars denote 95% confidence intervals. (Data from A, B Lozano-Álvarez et al. 2007, Briones-Fourzán and Lozano-Álvarez 2013, C Negrete-Soto et al. 2002, D Fonseca-Larios and Briones-Fourzán 1998, Briones-Fourzán and Contreras-Ortiz 1999).

opencc-by-4.0Nov 2014View details →
zenodo28/100

Figure 1 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 289-311. https://doi.org/10.3897/zookeys.457.6669

Figure 1 - Geographic distribution of the two pairs of sympatric Panulirus species addressed in the text.

opencc-by-4.0Nov 2014View details →
zenodo28/100

Figure 4 from: Briones-Fourzán P (2014) Differences in life-history and ecological traits between co-occurring Panulirus spiny lobsters (Decapoda, Palinuridae). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 289-311. https://doi.org/10.3897/zookeys.457.6669

Figure 4 - Potential ecological interactions between Panulirus gracilis and Panulirus inflatus in a rocky site ("Site A") in Zihuatanejo, Mexico. A lobster density (number of individuals ha–1) B relative abundance of molluscs (percentage of molluscs in benthic samples) C condition factor of lobsters. Error bars denote 95% CI. (Data from A Lozano et al. 1982, B Aramoni-Serrano 1982, C Lozano-Álvarez and Aramoni-Serrano 1996).

opencc-by-4.0Nov 2014View details →
dryad28/100

Data from: Efficiency of ddRAD target enriched sequencing across spiny rock lobster species (Palinuridae: Jasus)

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publicJul 2018View details →

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