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  1. Cats are not necessarily animals.Margarida Hermida - 2024 - Erkenntnis 89 (4):1387-1406.
    Some plausibly necessary a posteriori theoretical claims include ‘water is H 2 O’, ‘gold is the element with atomic number 79’, and ‘cats are animals’. In this paper I challenge the necessity of the third claim. I argue that there are possible worlds in which cats exist, but are not animals. Under any of the species concepts currently accepted in biology, organisms do not belong essentially to their species. This is equally true of their ancestors. In phylogenetic systematics, monophyletic clades (...)
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  • The Origins of Species Concepts.John Simpson Wilkins - 2003 - Dissertation, University of Melbourne
    The longstanding species problem in biology has a history that suggests a solution, and that history is not the received history found in many texts written by biologists or philosophers. The notion of species as the division into subordinate groups of any generic predicate was the staple of logic from Aristotle through the middle ages until quite recently. However, the biological species concept during the same period was at first subtly and then overtly different. Unlike the logic sense, which relied (...)
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  • Understanding scientific types: holotypes, stratotypes, and measurement prototypes.Alisa Bokulich - 2020 - Biology and Philosophy 35 (5):1-28.
    At the intersection of taxonomy and nomenclature lies the scientific practice of typification. This practice occurs in biology with the use of holotypes (type specimens), in geology with the use of stratotypes, and in metrology with the use of measurement prototypes. In this paper I develop the first general definition of a scientific type and outline a new philosophical theory of types inspired by Pierre Duhem. I use this general framework to resolve the necessity-contingency debate about type specimens in philosophy (...)
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  • Naming and contingency: the type method of biological taxonomy.Joeri Witteveen - 2015 - Biology and Philosophy 30 (4):569-586.
    Biological taxonomists rely on the so-called ‘type method’ to regulate taxonomic nomenclature. For each newfound taxon, they lay down a ‘type specimen’ that carries with it the name of the taxon it belongs to. Even if a taxon’s circumscription is unknown and/or subject to change, it remains a necessary truth that the taxon’s type specimen falls within its boundaries. Philosophers have noted some time ago that this naming practice is in line with the causal theory of reference and its central (...)
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  • How to misidentify a type specimen.Matthew H. Haber - 2012 - Biology and Philosophy 27 (6):767-784.
    Type specimens are used to designate species. What is the nature of the relation between a type specimen and the species it designates? If species names are rigid designators, and type specimens ostensively define species, then that relation is, at the very least, a close one. Levine :325–338, 2001) argues that the relationship of type specimen to a named species is one of necessity—and that this presents problems for the individuality thesis. Namely, it seems odd that a contingently selected specimen (...)
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  • Taxon names and varieties of reference.Joeri Witteveen - 2021 - History and Philosophy of the Life Sciences 43 (2):1-12.
    Linnaean-style, rank-based codes of taxonomic nomenclature provide stability to the relation between taxon names and their referents through the device of nomenclatural types. The practice of using types to tether names to taxa is uncontroversial and well-understood. But the nature of the relation between types, names, and taxa continues to be a topic of philosophical debate. A particularly contested issue is whether it is necessary for taxa that have a type specimen to contain their type specimen. Jerzy Brzozowski has recently (...)
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  • Type Specimens and Scientific Memory.Lorraine Daston - 2004 - Critical Inquiry 31 (1):153.
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  • A Logic of Temporal Contingency.Jie Fan - 2024 - Erkenntnis 89 (7):2611-2640.
    We propose a logic of temporal contingency, which has operators of past and future contingency as primitive modalities. This logic is less expressive than standard temporal logic over the class of bidirectional frames, and cannot define some basic frame properties such as bidirectionality and transitivity. We present a minimal system based on two key ‘bridge axioms’ and a bimodal version of a so-called ‘almost definability’ schema in the literature. The completeness proof is highly nontrivial due to the requirement that the (...)
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  • Individual essentialism in biology.Michael Devitt - 2018 - Biology and Philosophy 33 (5-6):39.
    A few philosophers of biology have recently explicitly rejected Essential Membership, the doctrine that if an individual organism belongs to a taxon, particularly a species, it does so essentially. But philosophers of biology have not addressed the broader issue, much discussed by metaphysicians on the basis of modal intuitions, of what is essential to the organism. In this paper, I address that issue from a biological basis, arguing for the Kripkean view that an organism has a partly intrinsic, partly historical, (...)
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  • Taxa, individuals, clusters and a few other things.Donald H. Colless - 2006 - Biology and Philosophy 21 (3):353-367.
    The recognition of species proceeds by two fairly distinct phases: (1) the sorting of individuals into groups or basic taxa (‘discovery’) (2) the checking of those taxa as candidates for species-hood (‘justification’). The target here is a rational reconstruction of phase 1, beginning with a discussion of key terms. The transmission of ‘meaning’ is regarded as bimodal: definition states the intension of the term, and diagnosis provides a disjunction of criteria for recognition of its extension. The two are connected by (...)
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  • Reflections on Naming and Necessity.Michael Devitt - 2021 - Theoria 88 (2):406-433.
    Theoria, Volume 88, Issue 2, Page 406-433, April 2022.
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  • How to Frege–Dummett a Putnam.Jerzy Brzozowski - 2013 - Principia: An International Journal of Epistemology 17 (2):301.
    The object of this paper is to suggest how the Frege–Dummettian notions of criterion of identity and criterion of application can be put to work within Putnam’s account of reference for natural kind terms in “Meaning of ‘Meaning’ ”. By doing so, some light can be shed on Putnam’s earlier views on “necessity relative to a body of knowledge” as well as his later views on sortal identity. If the Frege–Dummettian criteria are indeed at work within Putnam’s account, then we (...)
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  • Outlining Species: Drawing as a Research Technique in Contemporary Biology.Barbara Wittmann - 2013 - Science in Context 26 (2):363-391.
    ArgumentBiological drawings of newly described or revised species are expected to represent the type specimen with greatest possible accuracy. In taxonomic practice, illustrations assume the function of mobile representatives of relatively immobile specimens. In other words, such illustrations serve as “immutable mobiles” in the Latourian sense. However, the significance of drawing in the context of first descriptions goes far beyond that of illustration in the conventional sense. Not only does it synthesize the verbal catalogue of the type's morphological characteristics: it (...)
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  • Does a type specimen necessarily or contingently belong to its species?Joseph LaPorte - 2003 - Biology and Philosophy 18 (4):583-588.
    In a recent article, Alex Levine raises a paradox. It appears that, given some relatively uncontroversial premises about how a species term comes to refer to its species, a type specimen belongs necessarily and contingently to its species. According to Levine, this problem arises if species are individuals rather than natural kinds. I argue that the problem can be generalized: the problem also arises if species are kinds and type specimens are paradigmatic members used to baptize names for species. Indeed, (...)
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  • Biological taxon names are descriptive names.Jerzy A. Brzozowski - 2020 - History and Philosophy of the Life Sciences 42 (3):1-25.
    The so-called ‘type method’ widely employed in biological taxonomy is often seen as conforming to the causal-historical theory of reference. In this paper, I argue for an alternative account of reference for biological nomenclature in which taxon names are understood as descriptive names. A descriptive name, as the concept came to be known from the work of Gareth Evans, is a referring expression introduced by a definite description. There are three main differences between the DN and the causal account. First, (...)
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