ALBERT

Description: lm Zusammenhang mit den hydrographischen Untersuchungen in der Irminger See, welche im Juni 1955 auf dem Fischerei-Forschungsschiff "Anton Dohrn" ausgeführt wurden und deren Ergebnisse in der vorhergehenden Arbeit: Schichtung und Zirkulation in der Irminger See im Juni 1955 von G. Dietrich (1957) niedergelegt sind, wurden auch Untersuchungen über die Verteilung chemischer Faktoren in den verschiedenen Wassermassen angestellt. Das Gebiet der lrminger See ist gerade in dieser Beziehung von besonderem Interesse, weil, wie wir im einzelnen durch die Untersuchungen von G. Böhnecke, E. Hentschel und H. Wattenberg (1930) und G. Böhnecke, B. Føyn und H. Wattenberg (1931) wissen, hier die verschiedenen Wassermassen der Golfstrom-Ausläufer, des nordatlantischen Wassers und des Ostgrönlandstromes aufeinandertreffen und sich in einer großen Anzahl größerer und kleinerer Wirbel mitinander vermischen. Diese bewirken ihrerseits durch mit ihnen gekoppelten Hebungs- und Senkungsbewegungen eine recht verwickelte Verschiebung der Wassermassen in vertikaler Richtung. Die große Ausdehnung des befahrenen Gebietes im Verlauf der etwa 5 wöchigen Untersuchungsdauer gestattete nur, den chemischen Untersuchungen ein ganz weitmaschiges Stationsnetz zugrunde zu legen. Von den insgesamt durchgeführten 140 hydrographischen Stationen konnten daher nur 50 Stationen mit den vollen Tiefenserien chemisch bearbeitet werden. Bei der Wahl der Stationen wurde so verfahren, daß der Untersuchungsraum einigermaßen gleichmäßig durch Meßpunkte aufgeteilt wurde (Abb . 17). Auf Feinheiten im Chemismus der Wasserkörper mußte daher von vornherein verzichtet werden. Das Hauptgewicht liegt vielmehr auf der großräurnigen Verteilung und dem chemischen Aufbau der verschiedenen Wasserkörper im Untersuchungsgebiet. Untersucht wurden: der Phosphat-Gehalt, der Gehalt an gelöstem Sauerstoff sowie die Fluoreszenz und die optische Trübung in mit dem Wasserschöpfer in verschiedenen Tiefen dem Meere entnommenen Wasserproben. Der Phosphat-Gehalt wurde nach der in der Meereskunde seit langem üblichen kolorimetrischen Methode nach G. Denigès {1920) mittels Ammoniummolybdat-Schwefelsaure und Zinnchlorür (K. Kalle, 1934) an 25 ccm messenden Proben mittels des elektrischen Kolorimeters "Elko II" der Fa. C. Zeiß bestimmt. Zur Sauerstoff-Bestimmung diente die gleichfalls seit langem übliche Winkler'sche Methode an 50 ccm Meerwasserproben (K. Kalle, 1939). Die Fluoreszenzstärke wurde an 1 ccm Meerwasserproben nach der vom Verfasser entwickelten Methode (K. Kalle, 1951) mittels des Zeiß'schen Pulfrichphotometer gemessen, während für die optische Trübung der mit dem Farbfilter "S 72" (720 mμ) an 5 cm dicken Wasserschichten gewonnene Extinktionswert diente. Für diesen Zweck wurde wiederum das "Elko II"-Gerät benutzt, weil die Messung mit diesem Gerat nur 20 ccm Wasser benötigt und die Meßgenauigkeit trotz der verhältnismäßig geringen Schichtdicke extrem genau durchführbar ist (Fehlergröße = ± 0,000 2 E)1). Die Meßwerte für den Phosphat- und den Sauerstoff-Gehalt werden zusammen mit den zugehörigen Temperatur- und Salzgehaltswerten im Bulletin Hydrographique 1955 (Kopenhagen) erscheinen. Die entsprechenden Werte für die Fluoreszenzstärke und die optische Trübung sind in Zahlentafel 1 niedergelegt. An je drei Vertikalschnitten durch das Untersuchungsgebiet (A, B, C) (Abb. 1-12), deren Lage aus Abb. 17 hervorgeht, sowie an je 4 Horizontal-Schnitten in den Tiefen-Niveaus von O m, 200 m, 500 m und 1000 m (Abb. 13-16 und 18-28) soll versucht werden, die Verteilung der chemischen Faktoren im Untersuchungsgebiet in großen Zügen deutlich zu machen.

Description: Geologische Karte 1: 25 000 mit Erläuterungen. Digitalisat des FID GEO (Fachinformationsdienst Geowissenschaften der festen Erde), erstellt durch das GDZ (Göttinger Digitalisierungszentrum, SUB Göttingen), Karte aus dem Bestand der SUB Göttingen. GeoTIFF erstellt durch FID GEO, SUB Göttingen.

Description: map

Description: DFG, SUB Göttingen

Description: Among some coccids from Indonesia, received from Dr. L. G. E. KALSHOVEN, four large specimens were found which by their well developed ovisac showed some resemblance to Icerya purchasi MASK. After comparing the specimens with the photographs in MORRISON\xe2\x80\x99S Classification of the Margarodidae (1928) it appeared, however, that the wax covering of the body was more alike that of Walkeriana floriger (WALKER).\nThe old pinned specimens were not labelled, but Dr. KALSHOVEN remembered that they had been collected by Prof. ROEPKE on \xe2\x80\x9etjemara\xe2\x80\x9d (Casuarina). Upon inquiry Prof. ROEPKE informed me that in 1910 he had collected a giant coccid on old stems of Casuarina Junghuhniana MIQ. in the Tengger Mts. (East-Java). The specimens were found on trees near the last bend of the road leading to Tosari, a well-known health-resort at an elevation of about 1750 m, where Europeans often used to spend their holidays. Some specimens had been sent to Mr. E. E. GREEN in Ceylon who replied that it was a species of Walkeriana, but that he wanted the larvae for a description of this new species.

Description: In May 1938 I had the opportunity to observe seven living Aplysia depilans in the Zoological Station Naples. Notes on the size and colour were made and different methods of preservation were tried.\nAs one often wonders how much of the original colour pattern has been preserved in museum specimens of Aplysia, it seems important to give the result of the comparison of the living specimens as studied in 1938 and the same specimens after 18 years of preservation, in 1956. The best way of preservation appears to be killing in diluted alcohol as specimen nr. V shows.

Description: In an adult female of the common eel Anguilla anguilla a large lipoma was found, situated on the left side, caudally of the left operculum. Microscopically, the tumour, which originated from the subcutaneous connective tissue, was composed of areas of adipose tissue and areas of fibrous connective tissue.\nThe tumour belongs to the fibrolipomatous type and shows a striking resemblance with the lipoma, described by Stolk (in press) in the lizard Lacerta muralis.

Description: Twenty-one species of Distichopora have been described after specimens from various localities in the Indo-Pacific region, viz., D. violacea (Pallas, 1766) from \xe2\x80\x9cMare Indicum\xe2\x80\x9d, D. cinnabarina Nardo, 1844, from the Red Sea (?), D. gracilis Dana, 1848, from the Tuamotu Islands, D. coccinea Gray, 1860, from New Caledonia, D. fulvacea Michelin, 1862, from R\xc3\xa9union, D. nitida Verrill, 1864, from the Marshall Islands, D. rosea Kent, 1871, from the East coast of Australia, D. purpurea Schmeltz, 1875 (nomen nudum), from the Marshall Islands (?), D. irregularis Moseley, 1879, from the Philippine Islands, D. livida Tenison-Woods, 1879, from the Solomon Islands, D. brasseyi Wright, 1882, from the Gilbert Islands, D. allnutti Wright, 1882, from the Gilbert Islands (?), D. breviserialis Quelch, 1884, from unknown locality, D. milesii Quelch, 1884, from the Pacific (probably from the region of the Society and Tuamotu Islands), D. granulosa Quelch, 1885, from Rarotonga (?), D. conferta Quelch, 1885, from Rarotonga, D. ochracea Quelch, 1885, from the Solomon Islands, D. profunda Hickson & England, 1909, from the Chagos Archipelago, D. borealis Fisher, 1938, from the Aleutian Islands, D. fisheri Broch, 1942, from the Fiji Islands, and D. serpens Broch, 1942, from the Philippine Islands. Most of the described species came from shallow water, only three species were collected from great depths, viz., D. profunda (187\xe2\x80\x94274 m), D. borealis (518\xe2\x80\x94881 m), and D. serpens (91\xe2\x80\x94183 m). The type specimen of D. irregularis came from a depth of 10 fathoms (18 m).\nTo the species enumerated above should be added D. providentiae (Hickson & England, 1909) from off Providence Island in the Western Indian Ocean, collected at a depth of 125 fathoms (228 m). This species was originally placed in the genus Sporadopora, but the manner of arrangement of the gastropores and the dactylopores indicate that it presents at least some affinity to the genus Distichopora, and accordingly it may provisionally find a place here.

Description: The results of a complete census of the breeding population of the White Stork (Ciconia ciconia) in the Netherlands, carried out in the year 1950 by the State Forestry Service, have been published by M\xc3\x96RZER BRUIJNS and BRAAKSMA in Beaufortia 5, Nr. 45, April 15, 1955, p. 23\xe2\x80\x9442.\nA new census was performed during the year 1955 ; it is the intention to repeat the census from now on every year.\nThe results of the last census are even more alarming than those from 1950 (see table, p. 113). The number of occupied nests decreased from 83 nests in 1950 to 58 nests in 1955. The number of fledged young decreased from 195 in 1950 to 96 in 1955. Many nests, still occupied in 1950, were either in a state that they could no longer be used or they had vanished altogether in 1955. On the other hand some new nests have been erected in recent time, some of them yielding good breeding results. The data have been arranged in tables according to the provinces. Every nest is numbered. The numbers of the 1950 census are given in parentheses. Nests marked + means that the nest was occupied by a pair of birds, but that no young were fledged. Nests marked \xe2\x80\x94 means that the nest was not inhabited, or that it was visited irregularly or else occupied by one solitary bird. The number of young fledged is marked by a figure. A gale in the spring of 1955 destroyed 4 nests ; 12 eggs got lost.\nFighting was reported frequently, the unfortunate result being that 3 young storks and at least 37 eggs got lost. These figures probably indicate that at present an insufficient number of nesting sites is avaible in the Netherlands. Therefore it seems worth while to try to erect new nests in localities where fighting has been frequently reported, and to repair those nests that have been visited, but remained unoccupied, owing to the poor state of the nest. In this connection Mr. W. DRIESSEN got most remarkable results with a newly erected nest, made according to a special method. This method should be used for the nests which we hope can be erected or repaired before the new breeding season. Surely the alarming decrease of the White Stork in the Netherlands is not primarily caused by housing problems, but a more appropriate condition and a greater number of nesting sites probably helps to prevent the yearly destruction of perhaps ten or twenty eggs or chicks.\nPhotomechanical reproduction

Description: The main purpose of this study is to search for an explanation of the curious differentiation within the genus Chamaeleo. Since the species of this genus are rather doubtful units, I have studied the geograpical distribution of characters, not of the species, a method first used in botany (BAUR, ROTHMALER a.o.). I found that the number of characters is largest in east Afrika, gradually decreasing from this area to the periphery of the total range of the genus. East Africa proved to be still more important, as practically all the characters occur in it. This means that the chameleons in the other areas practically never possess characters that are not found in east Africa.\nThis pattern of distribution fits in rather well with REINIG\xe2\x80\x99S elimination theory (1938): \xe2\x80\x9e.. bei Einzelwanderungen wird nur ein Teil des gesamten Allelbestandes einer Art mitgef\xc3\xbchrt... eine durch Einzelwanderung entstandene Population weist eine geringere Zahl von Allelen auf als die Ausgangspopulation.\xe2\x80\x9d The existence of many parallel series of variation (meaning that several characters originated several times independently in different groups) led me to the conclusion that the mechanism described in REINIG\xe2\x80\x99S theory as elimination, has consequences also for the genes predisposed to change into others.\nThis reasoning gave a key to the reconstruction of the ancestral chameleon. By two different ways I arrived at the same conclusion, viz. the ancestral chameleon was probably an animal resembling mostly Chamaeleo chamaeleon s.l. (\xc2\xa7 21).\nAs for this theoretical part of my study a survey of the species was needed, I first made an attempt at a natural system. I have divided the genus into groups of related species. For practical reasons the chameleons of Madagascar are treated separately. Their connections with the species of the African continent are examined in a special section (\xc2\xa7 11).\nAs a result of my investigations I had to propose the following taxonomic changes: Ch. rhinoceratus var. lineatus + Ch. labordi + Ch. voeltzkowi + Ch. barbouri = Ch. rhinoceratus (\xc2\xa7 3), Ch. lambertoni = Ch. lateralis (\xc2\xa7 4), Ch. semicristatus = \xe2\x99\x80 Ch. verrucosus (\xc2\xa7 5), Ch. guibei nov. spec. (\xc2\xa7 6), Ch. calcarifer = Ch. chamaeleon calcarifer, Ch. zeylanicus = Ch. chamaeleon zeylanicus, Ch. etiennei = Ch. gracilis etiennei (\xc2\xa7 12), Ch. anchietae vinkei + Ch. anchietae mertensi + Ch. marunguensis = Ch. anchietae (\xc2\xa7 13), Ch. unicornis = Ch. oweni unicornis (\xc2\xa7 14), Ch. pumilus = Ch. pumilus pumilus, Ch. melanocephalus = Ch. pumilus melanocephalus, Ch. gutturalis = Ch. pumilus gutturalis, Ch. ventralis = Ch. pumilus ventralis, Ch. ventralis occidentalis = Ch. pumilus occidentalis, Ch. ventralis karrooicus = Ch. pumilus karrooicus, Ch. damaranus = Ch. pumilus damaranus, Ch. caffer = Ch. pumilus caffer, Ch. taeniobronchus = Ch. pumilus taeniobronchus. (\xc2\xa7 16).