Evolution and disappearance of sympatric Coregonus albula in a changing environment—A case study of the only remaining population pair in Sweden

During the past 50 years, Fennoscandian populations of spring‐spawning Baltic cisco (Coregonus albula), sympatric to common autumn‐spawners, have declined or disappeared; for example, three out of four known spring‐spawning populations in Sweden are regarded as extinct. Over the same period, the climate has changed and populations have been subject to other anthropogenic stressors. We compared historic (1960s) and recent (1990–2000s) morphological data from the still‐existent sympatric cisco populations in Lake Fegen, Sweden. Phenotypic changes were found for spring‐spawners making them more similar to the sympatric autumn‐spawners that had remained virtually unchanged. Based on results for other salmoniform fishes, a phenotypically plastic response to increased temperature during early development appears unlikely. The recent material was also analyzed with microsatellite markers; long‐term effective population size in spring‐spawners was estimated to be about 20 times lower than autumn‐spawners, with signs of long‐term gene flow in both directions and a recent genetic bottleneck in spring‐spawners. We suggest the change toward a less distinct phenotype in spring‐spawners to reflect a recent increase in gene flow from autumn‐spawners. Time since divergence was estimated to only c. 1,900 years (95% CI: 400–5,900), but still the Fegen populations represent the most morphologically and genetically distinct sympatric populations studied. Consequently, we hypothesize that less distinct population pairs can be even younger and that spring‐spawning may have repeatedly evolved and disappeared in several lakes since the end of the last glaciation, concurrent with changed environmental conditions.     

An alternative classification of trypanorhynch cestodes considering the tentacular armature as being of limited importance

Based on a light- and scanning electron microscopical study of scolex morphology, tentacles and surface structures of 31 trypanorhynch species, an alternative classification of the trypanorhynch cestodes, adults, plerocerci and postlarvae, is presented. The arrangement of the tentacular armature is no longer used as a distinguishing feature for four different superfamilies. Instead, the presence or absence of ciliated pits and prebulbular organs is used to define three superfamilies: Tentacularioidea Poche, 1926; Otobothrioidea Dollfus, 1942; and Eutetrarhynchoidea Guiart, 1927. A total of 12 families are defined by the characters: the presence/absence of blastocysts, the number of bothridia and the reduction of the rhyncheal apparatus, together with a new character, complete rows of tentacular hooks (homeoacanth and heteroacanth typica) versus rows of hooks partly reduced (heteroacanth atypica and poeciloacanth). Of the 19 families previously accepted, 10 are retained (Eutetrarhynchidae, Gilquiniidae, Lacistorhynchidae, Mixodigmatidae, Otobothriidae, Paranybeliniidae, Pterobothriidae, Shirleyrhynchidae, Sphyriocephalidae and Tentaculariidae, all sensu nov.); one family is reinstated (i.e. Aporhynchidae Poche, 1926 sensu nov.) and a new one is added (i.e. Pseudotobothriidae n. fam.). Advantages of this alternative classification of trypanorhynch cestodes are: (i) the resolution of incongruities and questions caused by the use of the tentacular armature to distinguish superfamilies; (ii) the criteria for the establishment of higher taxa, superfamilies and families are clearly defined; (iii) with the findings of new species with different character combinations, this system can be enlarged up to 4 superfamilies and 48 families without loosing its stability; and (iv) all existing genera are easily re-assigned to the superfamilies and families.     

The molecular structure of a dimer composed of the variable portions of the Bence-Jones protein REI refined at 2.0-A resolution.

The structure of the variable portions of a K-type Bence-Jones protein REI forming a dimer has been determined by X-ray diffraction to a resolution of 2.0 A. The structure has been refined using a constrained crystallographic refinement procedure. The final R value is 0.24 for 15000 significantly measured reflections; the estimated standard deviation of atomic positions is 0.09 A. A more objective assessment of the error in the atomic positions is possible by comparing the two independently refined monomers. The mean deviation of main-chain atoms of the two chains in internal segments in 0.22 A, of main-chain dihedral angles 6.3 degrees for these segments. The unrefined molecular structure of the VREI dimer has been published (Epp, O., Colman, P., Fehlhammer, H., Bode, W., Schiffer, M., Huber, R., and Palm, W. (1974), Eur. J. Biochem. 45, 513). Now a detailed analysis is presented in terms of hydrogen bonds and conformational angles. Secondary structural elements (antiparallel beta structure, reverse turns) are defined. A more precise atomic arrangement of the amino acid residues forming the contact region and the hapten binding site is given as well as the localization of solvent molecules. Two cis-prolines (Pro-8 and Pro-95) were detected. The intrachain disulfide bridge (Cys-23-Cys-88) occurs statistically in two alternative conformations. The structure suggests reasons for strong conservation of several amino acid residues. The knowledge of the refined molecular structure enables crystal structure analyses of related molecules to be made by Patterson search techniques. The calculated phases based on the refined structure are much improved compared to isomorphous phases. Therefore the effects of hapten binding on the molecular structure can be analyzed by the difference Fourier technique with more reliability. Hapten binding studies have been started.     

The primary structure of crystallizable monoclonal immunoglobulin IgG1 Kol. II. Amino acid sequence of the L-chain, gamma-type, subgroup I

The immunoglobulin Kol was the first intact antibody molecule which was characterized by high-resolution X-ray crystallography. Furthermore the complete amino-acid sequence of the heavy (H)-chain is known. Here we report the complete amino-acid sequence of the light (L)-chain of the monoclonal immunoglobulin Kol (IgG1). The polypeptide has an Mr of 22,781, consists of 216 amino acids and due to its structure is of the lambda-type. With the characteristic amino acids threonine, asparagine, threonine, glycine and lysine in positions 101, 114, 116, 154, and 165, respectively the Kol L-chain is of the Mcg isotype. With the proteins Mcg, Mot, Bur, Loc and Mem six myeloma-derived amino-acid sequences of the same isotype are known. The amino-acid sequence of the N-terminal variable part is characteristic of subgroup 1. This contribution completes the primary structure of IgG1 Kol.     

Letter: Preliminary x-ray data from well-ordered crystals of a human immunoglobulin G molecule

Crystals of an intact immunoglobulin G molecule, which are suitable for high resolution X-ray analysis, have been grown. The space group is P3₁21 (or enantiomorph) and the crystallographic diad relates the two halves of one molecule.