A mysterious parthenogenetic cambarid crayfish (the Marmorkrebs) has been spreading across the globe for the past decade. We compare this crayfish directly to two other cambarids, Procambarus fallax and P. alleni, that have been suggested to be related or even identical to the Marmorkrebs. Using external morphology and sequences of two mitochondrial genes we show clear correspondences between Marmorkrebs and P. fallax, a species found natively throughout peninsular Florida, USA. Based on these congruent results we suggest that the Marmorkrebs is the parthenogenetic form of P. fallax. This finding has potential evolutionary and ecological implications at several levels. The Marmorkrebs might be a type of geographical parthenogenesis, but a natural population in the wild is so far unknown. Furthermore, challenges arise in regard to the respective species status of the Marmorkrebs. Taxonomically we suggest that the Marmorkrebs is treated as ‘parthenogenetic form’ of P. fallax. Last but not least, the identity of this animal and its ecology has an impact for considering potential spread and effects of this species across the globe.
Genetically identical animals are very much in demand as laboratory objects because they allow conclusions about environmental and epigenetic effects on development, structures, and behavior. Furthermore, questions about the relative fitness of various genotypes can be addressed. However, genetically identical animals are relatively rare, in particular, organisms that combine a high reproduction rate and a complex organization. Based on its exclusively parthenogenetic reproduction mode, it has been suggested that the Marmorkrebs (Crustacea, Decapoda, Astacida), a recently discovered crayfish, is an excellent candidate for research addressing the aforementioned questions. However, until now, a study using molecular markers that clearly proves the genetic uniformity of the offspring has been lacking. Here, with this first molecular study, we show that this crayfish indeed produces genetically uniform clones. We tested this with 19 related individuals of various generations of a Marmorkrebs population by means of six different microsatellite markers. We found that all examined specimens were identical in their allelic composition. Furthermore, half of the analyzed loci were heterozygous. These results and the absence of meioses in previous histological studies of the ovaries lead us to conclude the Marmorkrebs propagates apomictically. Thus, a genetically uniform organism with complex morphology, development, and behavior is now available for various laboratory studies.
There is a close association between parthenogenesis and polyploidy. For this reason, we undertook a karyological analysis to test whether the parthenogenetic Marmorkrebs, Procambarus fallax forma virginalis, possesses an enlarged set of chromosomes. For this purpose, we karyotyped the Marmorkrebs, the sexual form of P. fallax (together called P. fallax complex), and the closely related species P. alleni. The latter shows 94 chromosomes in the haploid condition. In contrast to this, we found a haploid set of 92 chromosomes in individuals of the P. fallax complex. However, in mitotic metaphases the sexual form shows 184 chromosomes, whereas the Marmorkrebs possesses 276 chromosomes. Hence, the parthenogenetic Marmorkrebs reveals a triple amount of the haploid chromosome number. In addition, we detected a strikingly large subtelocentric chromosome which appears once in haploid and twice in diploid cells of sexual individuals of the P. fallax complex. In the parthenogenetic Marmorkrebs, this prominent chromosome occurs thrice. All this clearly reveals that the Marmorkrebs is a triploid organism. The applicability of the used methods, the significance of polyploidy in evolution of Decapoda, putative pathways to parthenogenetic triploidy, a possible hybrid origin and the scientific and ecological consequences of an increased chromosome set in Marmorkrebs are discussed.
Two specimens of an unknown jellyfish species were collected in Bat Gallim and Beit Yannai, on the Mediterranean coast of Israel, in June and July 2010. Morphological characters identified it as a cepheid (Cnidaria, Scyphozoa, Rhizostomeae). However, the specimens showed remarkable differences from other cepheid genera; unlike Cephea and Netrostoma it lacks warts or knobs centrally on the exumbrella and filaments on oral disk and between mouths, and it differs from Cotylorhiza in its proximally loose anastomosed radial canals and in lacking stalked suckers and filaments on the moutharms. We thus describe it herein as Marivagia stellata gen. et sp. nov. We also present the results of molecular analyses based on mitochondrial cytochrome oxidase I (COI) and 28S ribosomal DNA, which support its placement among the Cepheidae and also provide its barcode signature. This new find is the fourth introduced scyphozoan species recorded in the Mediterranean. The presence of a sexually mature specimen collected as far back as 2006, and the occurrence of the species this summer at sites nearly 90 kms apart, indicate the existence of an established population.
Three alien macrophytes, Ascophyllum nodosum, Colpomenia peregrina and Polysiphonia morrowii, are reported for the first time from the Mar Piccolo of Taranto (southern Italy, Mediterranean Sea). Two other species, Agardhiella subulata and Codium fragile subsp. fragile that were not, or were sporadically, detected in the basin since their first record in 1987 and 2002, respectively, were also recorded. In the Mar Piccolo, there appears to be a close link between establishment of alien species and the regular import of shellfish for direct sale. To limit the flow of accidental species introductions, a continuous and rigorous control of all the economic activities performed along the coast is recommended through the enforcement of effective laws and an early detection of new introductions.
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