Publications by authors named "M E Witt"

Understanding the spatial ecology of commercially exploited species is vital for their conservation. Atlantic bluefin tuna (Thunnus thynnus, ABT) are increasingly observed in northeast Atlantic waters, yet knowledge of these individuals' spatial ecology remains limited. We investigate the horizontal and vertical habitat use of ABT (158 to 241 cm curved fork length; CFL) tracked from waters off the United Kingdom (UK) using pop-up satellite archival tags (n = 63).

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Article Synopsis
  • Biologging technology has been employed to track the behaviors and migrations of various wild animals, including a notable event involving the predation of an Atlantic bluefin tuna by an orca.
  • The study details a 19-minute predation sequence where the tuna displayed high activity levels during its capture and subsequent handling by the orca.
  • Unique datasets collected from both the tuna and orca give valuable insights into their energetic behaviors and patterns of interaction in the ocean.
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Author's response to letter concerning article: Witt, M, A Ring: Handley's Thread Lymphangioplasty Vs. BioBridge Collagen Matrix for Lymphedema Therapy-Old Wine in New Bottles? Lymphology 56 (2023) 110-120.

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Introduction: The throwing motion in the javelin throw applies high loads to the musculoskeletal system of the shoulder, both in the acceleration and deceleration phases. While the loads occurring during the acceleration phase and their relationship to kinematics and energy flow have been relatively well investigated, there is a lack of studies focusing the deceleration phase. Therefore, the aim of this study is to investigate how the throwing arm is brought to rest, which resultant joint torques are placed on the shoulder and how they are influenced by the kinematics of the acceleration phase.

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Comprehensive characterization of AML-associated T cells during disease progression is essential to identify relevant immune escape mechanisms and new immunotherapeutic approaches. Investigating the processes that lead to an immunosuppressive environment under progression of AML is difficult in humans, because by the time of diagnosis the disease is often progressed far beyond the initial stages. Therefore, to investigate T-cell phenotypes during progression a C57BL/6 mouse model was used.

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