Reference health

Establishing the thermal window for aerobic scope in New Zealand geoduck clams (Panopea zelandica)

https://doi.org/10.1007/s00360-016-1038-5
CiteStamped reference-health badge
51/51 checkable references clean · checked 2026-07-21

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

12 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 51 checked references that resolve
resolves10.1016/0044-8486(94)90048-5
Determination of optimal thermal conditions for growth of clam (Venerupis pullastra) seed
resolves10.1016/j.cbpa.2009.12.018
Response of Mytilus galloprovincialis (L.) to increasing seawater temperature and to marteliosis: Metabolic and physiological parameters
resolves10.2983/035.034.0107
Temperature and Food-Ration Optimization in the Hatchery Culture of Juveniles of the Pacific Geoduck<i>Panopea generosa</i>
resolves10.1080/00785236.2001.10409466
Reply to comment by H.U. RiisgÅrd
resolves10.1007/BF00349561
Comparison of the scope for growth with the growth performance of Ostrea edulis seed reared at different food concentrations in an open-flow system
resolves10.1007/s10811-013-0037-0
On the description of Tisochrysis lutea gen. nov. sp. nov. and Isochrysis nuda sp. nov. in the Isochrysidales, and the transfer of Dicrateria to the Prymnesiales (Haptophyta)
resolves10.1007/s10811-014-0284-8
Erratum to: On the description of Tisochrysis lutea gen. nov. sp. nov. and Isochrysis nuda sp. nov. in the Isochrysidales, and the transfer of Dicrateria to the Prymnesiales (Haptophyta)
resolves10.1080/00288330.1991.9516475
Preliminary estimates of age, mortality, growth, and reproduction in the hiatellid clam <i>Panopea zelandica</i> in New Zealand
resolves10.1016/S0022-0981(00)00215-X
Effect of reproduction on escape responses and muscle metabolic capacities in the scallop Chlamys islandica Müller 1776
resolves10.3354/meps006073
Response-Surface Analysis of the Combined Effects of Exposure and Acclimation Temperatures on Filtration, Oxygen Consumption and Scope for Growth in the Oyster Ostrea edulis
resolves10.1098/rstb.2007.2099
Linking environmental variability and fish performance: integration through the concept of scope for activity
resolves10.1007/BF00355716
The estimation of filtering rate from the clearance of suspensions
resolves10.4319/lom.2006.4.284
Flow‐through chamber method for clearance rate measurements in bivalves: design and validation of individual chambers and mesocosm
resolves10.2983/035.034.0103
Developing Fisheries and Aquaculture Industries for<i>Panopea zelandica</i>in New Zealand
resolves10.1007/s10499-012-9550-4
Feeding physiology and scope for growth of the oyster Crassostrea corteziensis (Hertlein, 1951) acclimated to different conditions of temperature and salinity
resolves10.1007/s10499-007-9133-y
The effect of temperature on the energy budget of the Manila clam, Ruditapes philippinarum
resolves10.1007/s00360-007-0243-7
Effects of body-size and season on digestive organ size and the energy balance of cockles fed with a constant diet of phytoplankton
resolves10.1111/j.1095-8649.1981.tb05847.x
Temperature tolerance and the final preferendum—rapid methods for the assessment of optimum growth temperatures
resolves10.1080/10417946609371849
A word from the editor
resolves10.3354/meps305147
Effect of temperature on filtration rate in the mussel Mytilus edulis: no evidence for temperature compensation
resolves10.1016/0022-0981(87)90080-3
Interactive effect of diet and temperature on the growth of juvenile clams
resolves10.1016/j.jembe.2009.09.021
Viscosity and not biological mechanisms often controls the effects of temperature on ciliary activity and swimming velocity of small aquatic organisms
resolves10.1080/00288330.2014.918548
Broodstock conditioning of New Zealand geoduck ( <i>Panopea zelandica</i> ) within different temperature and feeding ration regimes
resolves10.1016/j.aquaculture.2016.05.008
Aerobic scope and oxygen regulation of New Zealand geoduck (Panopea zelandica) in response to progressive hypoxia
resolves10.1086/BBLv224n2p79
Energetics of Byssus Attachment and Feeding in the Green-Lipped Mussel <i>Perna canaliculus</i>
resolves10.1242/jeb.093450
Seasonal changes in the behaviour and respiration physiology of the freshwater duck mussel<i>Anodonta anatina</i>.
resolves10.1016/j.jtherbio.2014.04.005
The effect of seasonal temperature variation on behaviour and metabolism in the freshwater mussel (Unio tumidus)
resolves10.1007/s00442-007-0720-4
Hypoxia tolerance associated with activity reduction is a key adaptation for Laternula elliptica seasonal energetics
resolves10.1080/17451000701635128
Metabolic adjustments in the oyster<i>Crassostrea gigas</i>according to oxygen level and temperature
resolves10.3354/meps298205
Effects of food availability and hypoxia on bivalves: the value of using multiple parameters to measure bivalve condition in environmental studies
resolves10.1139/f04-136
Precaution in the harvest of Methuselah's clams — the difficulty of getting timely feedback from slow-paced dynamics
resolves10.1111/j.0269-8463.2004.00903.x
Extreme sensitivity of biological function to temperature in Antarctic marine species
resolves10.1007/s00442-007-0858-0
Thermal limits of burrowing capacity are linked to oxygen availability and size in the Antarctic clam Laternula elliptica
resolves10.1126/science.1163156
Physiology and Climate Change
resolves10.1111/j.1095-8649.2010.02783.x
Climate change effects on fishes and fisheries: towards a cause‐and‐effect understanding
resolves10.1242/jeb.114181
How and how not to investigate the oxygen and capacity limitation of thermal tolerance (OCLTT) and aerobic scope – remarks on the article by Gräns et al.
resolves10.3354/meps211275
On measurement of filtration rate in bivalves-the stony road to reliable data: review and interpretation
resolves10.1007/s00227-014-2548-x
Escape performance of temperate king scallop, Pecten maximus under ocean warming and acidification
resolves10.1242/jeb.118851
The effects of temperature on aerobic metabolism: towards a mechanistic understanding of the responses of ectotherms to a changing environment
resolves10.1080/11250000509356677
Functional responses and scope for growth of two non‐indigenous bivalve species in the Sacca di Goro (northern Adriatic Sea, Italy)
resolves10.1111/j.1365-2109.2006.01527.x
Frequent monitoring of temperature: an essential requirement for site selection in bivalve aquaculture in tropical-temperate transition zones
resolves10.1007/s002270050033
Influence of hypoxia and anoxia on the physiological responses of the clam Ruditapes decussatus from southern Portugal
resolves10.1242/jeb.00054
Metabolic plasticity and critical temperatures for aerobic scope in a eurythermal marine invertebrate (<i>Littorina saxatilis</i>, Gastropoda: Littorinidae) from different latitudes
resolves10.1098/rspb.2010.1295
Global analysis of thermal tolerance and latitude in ectotherms
resolves10.1038/nclimate1539
Thermal tolerance and the global redistribution of animals
resolves10.1007/s00360-013-0764-1
Thermal dependence of clearance and metabolic rates in slow- and fast-growing spats of manila clam Ruditapes philippinarum
resolves10.1016/0022-0981(72)90011-1
Active metabolism associated with feeding in the mussel Mytilus edulis L.
resolves10.1007/bf00350733
Calorimetric studies on the energy metabolism of an infaunal bivalve, Abra tenuis, under normoxia, hypoxia and anoxia
resolves10.1007/s00442-013-2767-8
Low global sensitivity of metabolic rate to temperature in calcified marine invertebrates
resolves10.1016/0077-7579(73)90060-4
The effects of temperature on the metabolism and activity of mytilus edulis
resolves10.1016/0044-8486(78)90124-2
A review on the knowledge of suspension-feeding in lamellibranchiate bivalves, with special reference to artificial aquaculture systems
The 12 references without a DOI — listed, not checked
no DOI — not checkedBayne BL, Newell RC (1983) Physiological energetics of marine molluscs. In: Saleuddin ASM, Wilbur KM (eds) The Mollusca, vol 4., Physiology (Part 1)Academic Press, New York, pp 407–515
no DOI — not checkedBayne BL, Thompson RJ, Widdows J (1976) Physiology: I. In: Bayne BL (ed) Marine mussels their ecology and physiology. Cambridge University Press, London, pp 121–206
no DOI — not checkedCampbell A, Harbo RM, Hand CM Harvesting and distribution of Pacific geoduck clams, Panopea abrupta, in British Columbia. In: Jamieson GS, Campbell A (eds) Proceedings of the North Pacific Symposium on Invertebrate Stock Assessment and Management, Ottawa, 1998. National Research Council of Canada Research Press, pp 349–358
no DOI — not checkedCrisp DJ (1971) Energy flow measurements. In: Holme NA, McIntyre AD (eds) Methods for the study of marine benthos. Blackwell, Oxford, pp 197–323
no DOI — not checkedFry FEJ (1947) Effects of the environment on animal activity. In: University of Toronto Studies, Biological Series, No. 55, pp 2–62
no DOI — not checkedGoodwin L (1976) Observations on spawning and growth of subtidal geoducks (Panopea generosa, Gould). Proc Natl Shellfish Assoc 65:49–58
no DOI — not checkedGoodwin CL, Pease B (1989) Species profiles: life histories and environmental requirements of coastal fishes and invertebrates (Pacific Northwest)—Pacific Geoduck Clam United States of Fish and Wildlife Service. Biol Rep 82:1–14
no DOI — not checkedGribben PE, Creese RG (2005) Age, growth, and mortality of the New Zealand geoduck clam, Panopea zelandica (Bivalvia: Hiatellidae) in two north island populations. Bull Mar Sci 77:119–135
no DOI — not checkedGribben PE, Helson J, Jeffs AG (2004) Reproductive cycle of the New Zealand geoduck, Panopea zelandica, in two north island populations. Veliger 47:53–65
no DOI — not checkedIPCC (2014) Climate change 2014: impacts, adaptation, and vulnerability. Part B: regional aspects. Contribution of working group ii to the fifth assessment report of the intergovernmental panel on climate change. Barros VR, Field CB, Dokken DJ, Mastrandrea MD, Mach KJ, Bilir TE, Chatterjee M, Ebi KL, Estrada YO, Genova RC, Girma B, Kissel ES, Levy AN, MacCracken S, Mastrandrea PR, White LL (eds) Cambridge University Press, Cambridge
no DOI — not checkedLe Gall J-L, Raillard O (1988) Influence de la température sur la physiologie de l’huître Crassostrea gigas. Oceanis 14:603–608
no DOI — not checkedVerberk WCEP, Bilton DT (2013) Respiratory control in aquatic insects dictates their vulnerability to global warming. Biol Lett 9(2013047):1–4
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

checked 2026-07-21 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record

Embed this badge

Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.

<a href="https://citestamp.com/citestamped/10.1007/s00360-016-1038-5"><img src="https://citestamp.com/citestamped/10.1007/s00360-016-1038-5/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[![CiteStamped reference-health badge](https://citestamp.com/citestamped/10.1007/s00360-016-1038-5/badge.svg)](https://citestamp.com/citestamped/10.1007/s00360-016-1038-5)