Lessonia spicata (Suhr) Santelices is the most ecologically and economically important kelp from Pacific South America. Here, we contribute to the bioinformatics and evolutionary systematics of the species by performing high throughput sequencing on L. spicata from Valparaiso, Chile. The L. spicata complete mitogenome is 37,097 base pairs (bp) in length and contains 66 genes (GenBank accession MK965907), the complete plastid genome is 130,305 bp and has 173 genes (accession MK965908), and the data assembled 7,630 bp of the nuclear ribosomal cistron (accession MK965909). The organellar genomes are similar in structure and content to others published from the Laminariales.

The Peruvian sea is one of the most productive ecosystems in the world. Phytoplankton production provides food for fish, mammals, mollusks and birds. This trophic network is affected by the presence of toxic phytoplankton species. In July 2017, samples of phytoplankton were obtained from Paracas Bay, an important zone for scallop (Argopecten purpuratus) aquaculture in Peru. Morphological analysis revealed the presence of the genus Pseudo-nitzschia, which was isolated and cultivated in laboratory conditions. Subsequently, the monoclonal cultures were observed by scanning electron microscopy (SEM), and identified as P. multistriata, based on both the morphological characteristics, and internal transcribed spacers region (ITS2) sequence phylogenetic analysis. Toxin analysis using liquid chromatography (LC) with high-resolution mass spectrometry (HRMS) revealed the presence of domoic acid (DA) with an estimated amount of 0.004 to 0.010 pg cell−1. This is the first report of DA from the coastal waters of Peru and its detection in P. multistriata indicates that it is a potential risk. Based on our results, routine monitoring of this genus should be considered in order to ensure public health.

During the austral winter of 2017, a bloom of Prorocentrum spp. occurred, reaching a cell density of 2.73 × 106 cells L−1, in Paracas Bay, Peru. In order to identify which, type of species generated this event and determine its toxicity, the values of the environmental parameters (temperature, winds and salinity) that induced the rapid growth of the dinoflagellate in this bloom were identified. A clonal culture was established for taxonomic (SEM), phylogenetic (ITS) and toxicological analysis via LC-MS/MS to determine the presence of tetrodotoxin (TTX) and whether the species represents a food safety hazard. This event coincided with the coastal upwelling process, which generated high concentrations of phytoplankton biomass (>10 mg m−3 chlorophyll-a) and allowed the rapid growth of P. cordatum (IMP-BG 450) in Paracas Bay. However, toxicological analyses of the IMP-BG 450 strain culture did not show the presence of TTX quantifiable through the technique used. Due to the antecedents of the presence of TTX in mollusks from other latitudes during blooms of this species, it is recommended that analyses of this toxin be carried out both in filter-feeding mollusks and in this species during a new bloom.

Siete especies de Rhodymenia han sido registradas para la costa de Perú, donde seis de ellas crecen en la costa central: R. corallina, R. howeana, R. multidigitata, R. flabellifolia, R. skottsbergii y R. californica. La más conflictiva taxonómicamente es R. corallina, de la cual se han segregado R. howeana y R. multidigitata, solo en base a caracteres morfológicos externos (forma del estipe y hábito de la fronda). Recolecciones recientes e intensivas de este complejo de especies en la costa central del Perú (9°S hasta 15°S) han permitido reunir varios morfotipos, evidenciando la alta variabilidad morfológica presente, que dificulta el poder diferenciar cada uno de los taxones involucrados. El objetivo del presente trabajo fue esclarecer la taxonomía de este complejo mediante la combinación de datos morfológicos, tanto vegetativos como reproductivos, y de secuencias genéticas utilizando los marcadores rbcL y COI-5P. Especímenes de Callao, localidad tipo de R. howeana y R. multidigitata, fueron analizados molecularmente junto con material de la costa central (Casma hasta Marcona, 9-15°S) y norte de Perú (Piura, 6°S), así como del norte chico de Chile (Coquimbo, 30°S), resolviendo dos grupos de Rhodymenia: un primer grupo filogenético asociado a R. corallina de Chile (Coquimbo, 30°S), distribuido a lo largo de toda la costa central peruana (Casma hasta Marcona, 9-15°S) y un segundo grupo restringido a la costa norte de Perú (Piura a Casma, 6-9°S). Estos grupos se diferencian en caracteres de la morfología externa y reproductiva. Basado en características del soro tetrasporangial, se reconoce a R. howeana para el norte del Perú.

Phyllophorella was recently described from two localities on the central coast of Peru (12°S), based on the endemic species Phyllophora (Ph.) peruviana. The genus currently accommodates three species, Phyllophorella (P.) peruviana, P. humboldtiana and P. limaensis. Recent field surveys for Phyllophorella on the central coast of Peru led to the discovery of collections outside the originally reported ranges. Morphological, anatomical, and genetic characterization of the specimens confirms range extensions for P. peruviana to 9° S and 15° S, and P. humboldtiana to 12° S and 15° S. A combined phylogenetic analysis of rbcL and COI-5P gene sequences supports the taxonomic status of these two species and reasserts the genus as monophyletic. Anatomically, the two species differ in nemathecial structure. Phyllophorella peruviana displays dome-shaped and well-defined circular nemathecia, whereas in P. humboldtiana they are irregular and diffuse in form. Mature cystocarps were observed for the first time in Phyllophorella, in P. humboldtiana from Lima and Ica, Peru. Phyllophorella, as well as the other genera classified to the family Phyllophoraceae, have a procarpic sexual system, with a carpogonial branch of three cells; the cystocarp develops a thickened cortex, is immersed in the medulla, and lacks a pericarp and an ostiole. This study demonstrates that field work, together with morphological, developmental, and genetic analyses, are useful methods for improving our understanding of seaweed distributions and systematics.