Until the 1930s Germany had been the international leader in biochemistry, chemistry, and areas of biology. After WWII, however, molecular biology as a new interdisciplinary scientific enterprise was scarcely represented in Germany for almost 20 years. Three major reasons for the low performance of molecular biology are discussed: first, the forced emigration of Jewish scientists after 1933, which not only led to the expulsion of future distinguished molecular biologists, but also to a strong decline of ''dynamic biochemistry'', a field which (...) contributed greatly to molecular biology. Second, German university structures that strongly impeded interdisciplinary research. Third, the international isolation and self-isolation of German scientists that was a major obstacle to the implementation of new fields of research developed elsewhere. Despite the fact that there was no official boycott against Germany as there had been after WWI and despite the Cold War policy of integrating Germans into the West, as a consequence of National Socialism and WWI for many years only very few German scientists gained access to the international community of molecular biologists. Max Delbruck played an important role in helping the Germans establish modern, mostly molecular, biology because he retained strong connections to Germany. Most importantly, it required a new generation of young scientists who had received part of their training in the US to establish modern molecular biology at German universities and Max Planck Institutes. (shrink)

Berichte zur Wissenschaftsgeschichte, Volume 45, Issue 3, Page 301-305, September 2022.

This paper aims to provide a fresh historical perspective on the debates on vitalism and holism in Germany by analyzing the work of the zoologist Hans Spemann (1869–1941) in the interwar period. Following up previous historical studies, it takes the controversial question about Spemann’s affinity to vitalistic approaches as a starting point. The focus is on Spemann’s holistic research style, and on the shifting meanings of Spemann’s concept of an organizer. It is argued that the organizer concept unfolded multiple layers (...) of meanings (biological, philosophical, and popular) during the 1920s and early 1930s. A detailed analysis of the metaphorical dynamics in Spemann’s writings sheds light on the subtle vitalistic connotations of his experimental work. How Spemann’s work was received by contemporary scientists and philosophers is analyzed briefly, and Spemann’s holism is explored in the broader historical context of the various issues about reductionism and holism and related methodological questions that were so prominently discussed not only in Germany in the 1920s. (shrink)

This article explores the collaborative research of the Nobel laureate Hans Spemann (1869–1941) and the Swiss zoologist Fritz Baltzer (1884–1974) on problems at the intersection of development and heredity and raises more general questions concerning science and politics in Germany in the interwar period. It argues that Spemann and Baltzer’s collaborative work made a significant contribution to the then ongoing debates about the relation between developmental physiology and hereditary studies, although Spemann distanced himself from _Drosophila_ genetics because of his anti-reductionist (...) position. The article analyzes how Spemann framed the issues of heredity in terms of an epigenetic principle in the context of his work on the “organizer,” and it explores the experimental dynamics of research on newt merogones carried out by Baltzer in a methodological development of Spemann’s constriction experiments. Finally, these research attempts are discussed as part of a broader “prehistory” of the mid-twentieth century cell nuclear transplantation experiments, which provided the basis for later animal cloning. (shrink)

Model organisms became an indispensable part of experimental systems in molecular developmental and cell biology, constructed to investigate physiological and pathological processes. They are thought to play a crucial role for the elucidation of gene function, complementing the sequencing of the genomes of humans and other organisms. Accordingly, historians and philosophers paid considerable attention to various issues concerning this aspect of experimental biology. With respect to the representational features of model organisms, that is, their status as models, the main focus (...) was on generalization of phenomena investigated in such experimental systems. Model organisms have been said to be models for other organisms or a higher taxon. This, however, presupposes a representation of the phenomenon in question. I will argue that prior to generalization, model organisms allow researchers to built generative material models of phenomena – structures, processes or the mechanisms that explain them – through their integration in experimental set-ups that carve out the phenomena from the whole organism and thus represent them. I will use the history of zebrafish biology to show how model organism systems, from around 1970 on, were developed to construct material models of molecular mechanisms explaining developmental or physiological processes. (shrink)

In 1937, a group of researchers in Nazi Germany began investigating tobacco mosaic virus with the hope of using the virus as a model system for understanding gene behavior in higher organisms. They soon developed a creative and interdisciplinary work style and were able to continue their research in the postwar era, when they made significant contributions to the history of molecular biology. This group is significant for two major reasons. First, it provides an example of how researchers were able (...) to produce excellent scientific research in the midst of dictatorship and war. Coupled with the group's ongoing success in postwar Germany, the German TMV investigators provide a dramatic example of how scientific communities deal with adversity as well as rapid political and social change. Second, since the researchers focused heavily on TMV, their story allows us to analyze how an experimental system other than phage contributed to the emergence of molecular biology. (shrink)

This paper emphasizes the crucial role of variation, at several different levels, for a detailed historical understanding of the development of the biomedical sciences. Going beyond valuable recent studies that focus on model organisms, experimental systems and instruments, we argue that all of these categories can be accommodated within our approach, which pays special attention to organismal and cultural variation. Our empirical examples are drawn in particular from recent historical studies of nineteenth- and early twentieth-century genetics and physiology. Based on (...) the quasi-paradoxical conclusion that biological and cultural variation both constrains and enables innovation in the biomedical sciences, we argue that more attention should be paid to variation as an analytical category in the historiography of the life sciences. (shrink)

Berichte zur Wissenschaftsgeschichte, Volume 45, Issue 3, Page 306-316, September 2022.

Muriel Wheldale, a distinguished graduate of Newnham College, Cambridge, was a member of William Bateson's school of genetics at Cambridge University from 1903. Her investigation of flower color inheritance in snapdragons (Antirrhinum), a topic of particular interest to botanists, contributed to establishing Mendelism as a powerful new tool in studying heredity. Her understanding of the genetics of pigment formation led her to do cutting-edge work in biochemistry, culminating in the publication of her landmark work, The Anthocyanin Pigments of Plants (1916). (...) In 1915, she joined Frederick Gowland Hopkin's Department of Biochemistry as assistant and in 1926 became one of the first women to be appointed university lecturer. In 1919 she married the biochemist Huia Onslow, with whom she collaborated until his death in 1922. This paper examines Wheldale's work in genetics and especially focuses on the early linkage of Mendelian methdology with new techniques in biochemistry that eventually led to the founding of biochemical genetics. It highlights significant issues in the early history of women in genetics, including the critical role of mentors, funding opportunities, and career strategies. (shrink)

Der Artikel führt den Begriff der epistemischen Konkurrenz ein. Im Gegensatz zu „wissenschaftliche Kontroverse“ beschreibt er eine Situation, in der sich zwei Forschungsfelder gegenseitig als mit demselben Bereich von Phänomen befasst wahrnehmen, wobei ihre methodischen Ansätze und theoretischen Erklärungen jedoch so unterschiedlich sind, dass ein offener Konflikt über die Wahrheit oder Falschheit bestimmter Aussagen oder die Genauigkeit in der Anwendung einer Methode nicht stattfindet. Nichtsdestotrotz streben beide Parteien danach, die maßgebliche Erklärung der entsprechenden Phänomene anzubieten. Indem die erweiterte Gemeinschaft der (...) Forschenden oder die Öffentlichkeit einen Ansatz als maßgeblich anerkennt, handeln sie als eine dritte, gewissermaßen neutrale Partei, die einen Preis vergibt, um den die anderen Parteien konkurrieren. Der Artikel beschreibt das Verhältnis von Genetik und Entwicklungsbiologie um 1900 als epistemische Konkurrenz. Diese Forschungsfelder geben unterschiedliche Erklärungen für die Phänomene der organischen Reproduktion. Die Erklärungen unterscheiden sich bezüglich der Formbegriffe und entsprechend hinsichtlich der Begriffe der Vererbung von Aspekten der Form eines Organismus. Zudem basieren die Erklärungen der beiden Felder auf unterschiedlichen Arten kausalen Schließens, die in unterschiedliche experimentelle Ansätze eingebettet sind. Diese Unterschiede können als Instanzen eines allgemeineren Unterschieds zwischen der Tradition der Naturgeschichte, die sich mit Unterschieden zwischen Organismen auseinandersetzt, und der Tradition der Anatomie, die sich mit den Teilen der Organismen beschäftigt, angesehen werden. Dieses Bild der Genetik und Entwicklungsbiologie als Zweige unterschiedlicher fest verankerter Traditionen widerspricht dem Narrativ der Trennung des Begriffs der Vererbung von dem der Entwicklung im Zuge einer Trennung der Disziplinen der Genetik und der Embryologie, das in der Historiographie der Biologie nach wie vor weit verbreitet ist. (shrink)

This essay details a historical crossroad in biochemistry and microbiology in which penicillin was a co-agent. I narrate the trajectory of the bacterial cell wall as the precise target for antibiotic action. As a strategic object of research, the bacterial cell wall remained at the core of experimental practices, scientific narratives and research funding appeals throughout the antibiotic era. The research laboratory was dedicated to the search for new antibiotics while remaining the site at which the mode of action of (...) this new substance was investigated. This combination of circumstances made the bacterial wall an ontology in transit. As invisible as the bacterial wall was for clinical purposes, in the biological laboratory, cellular meaning in regard to the action of penicillin made the bacterial wall visible within both microbiology and biochemistry. As a border to be crossed, some components of the bacterial cell wall and the biochemical destruction produced by penicillin became known during the 1950s and 1960s. The cell wall was constructed piece by piece in a transatlantic circulation of methods, names, and images of the shape of the wall itself. From 1955 onwards, microbiologists and biochemists mobilized new names and associated conceptual meanings. The composition of this thin and rigid layer would account for its shape, growth and destruction. This paper presents a history of biochemical morphology: a chemistry of shape – the shape of bacteria, as provided by its wall – that accounted for biology, for life itself. While penicillin was being established as an industrially-manufactured object, it remained a scientific tool within the research laboratory, contributing to the circulation of further scientific objects. (shrink)

Berichte zur Wissenschaftsgeschichte, Volume 45, Issue 3, Page 301-305, September 2022.

ZusammenfassungDer Artikel führt den Begriff der epistemischen Konkurrenz ein. Im Gegensatz zu „wissenschaftliche Kontroverse“ beschreibt er eine Situation, in der sich zwei Forschungsfelder gegenseitig als mit demselben Bereich von Phänomen befasst wahrnehmen, wobei ihre methodischen Ansätze und theoretischen Erklärungen jedoch so unterschiedlich sind, dass ein offener Konflikt über die Wahrheit oder Falschheit bestimmter Aussagen oder die Genauigkeit in der Anwendung einer Methode nicht stattfindet. Nichtsdestotrotz streben beide Parteien danach, die maßgebliche Erklärung der entsprechenden Phänomene anzubieten. Indem die erweiterte Gemeinschaft der (...) Forschenden oder die Öffentlichkeit einen Ansatz als maßgeblich anerkennt, handeln sie als eine dritte, gewissermaßen neutrale Partei, die einen Preis vergibt, um den die anderen Parteien konkurrieren. Der Artikel beschreibt das Verhältnis von Genetik und Entwicklungsbiologie um 1900 als epistemische Konkurrenz. Diese Forschungsfelder geben unterschiedliche Erklärungen für die Phänomene der organischen Reproduktion. Die Erklärungen unterscheiden sich bezüglich der Formbegriffe und entsprechend hinsichtlich der Begriffe der Vererbung von Aspekten der Form eines Organismus. Zudem basieren die Erklärungen der beiden Felder auf unterschiedlichen Arten kausalen Schließens, die in unterschiedliche experimentelle Ansätze eingebettet sind. Diese Unterschiede können als Instanzen eines allgemeineren Unterschieds zwischen der Tradition der Naturgeschichte, die sich mit Unterschieden zwischen Organismen auseinandersetzt, und der Tradition der Anatomie, die sich mit den Teilen der Organismen beschäftigt, angesehen werden. Dieses Bild der Genetik und Entwicklungsbiologie als Zweige unterschiedlicher fest verankerter Traditionen widerspricht dem Narrativ der Trennung des Begriffs der Vererbung von dem der Entwicklung im Zuge einer Trennung der Disziplinen der Genetik und der Embryologie, das in der Historiographie der Biologie nach wie vor weit verbreitet ist. (shrink)