Effects of open- and closed-system temperature changes on blood oxygen dissociation curves of skipjack tuna, Katsuwonus pelamis, and yellowfin tuna, Thunnus albacares

1991 ◽  
Vol 69 (7) ◽  
pp. 1814-1821 ◽  
Author(s):  
Richard W. Brill ◽  
Peter G. Bushnell

Tunas often experience rapid temperature changes of 10 °C or more during their daily vertical movements. Their blood is therefore subjected to open-system (i.e., constant O2 and CO2 partial pressure, variable O2 and CO2 content) temperature changes during passage through the gills. In addition, tunas possess vascular countercurrent heat exchangers and can have deep red muscle temperatures as much as 20 °C above ambient. Their blood also experiences closed-system (i.e., constant O2 and CO2 content, variable O2 and CO2 partial pressure) temperature changes during passage through the heat exchangers. Temperature-independent blood O2 binding could be expected. We found blood oxygen dissociation curves of skipjack tuna (Katsuwonus pelamis) and yellowfin tuna (Thunnus albacares) to be temperature independent during open-system temperature changes. Although blood from both species showed unsually large Bohr effects (−0.986 and −0.865 Δlog P50∙ΔpH−1 for skipjack and yellowfin tuna, respectively) when subjected to CO2 partial pressure alterations in the open system, the oxygen dissociation curves of skipjack tuna blood were nearly temperature independent during closed-system temperature changes. In other words, blood from skipjack tuna showed a reduced Bohr effect when subjected to the inevitable CO2 partial pressure changes that accompany closed-system temperature shifts. Since skipjack tuna blood shows temperture-independent O2 binding during closed-system temperature changes whereas yellowfin tuna blood does not, this unusual feature is not obligatory in thermoconserving fishes.

2017 ◽  
Vol 14 (3) ◽  
pp. 313 ◽  
Author(s):  
Budi Nugraha ◽  
Enjah Rahmat

Tulisan ini menyajikan tentang status perikanan huhate di Bitung meliputi deskripsi unit penangkapan, daerah penangkapan, komposisi hasil tangkapan, catch per unit of effort, dan ukuran ikan pertama kali tertangkap. Data dikumpulkan selama tahun 2004 sampai dengan 2005. Hasil penelitian menunjukkan bahwa huhate yang terdapat di Bitung dioperasikan dengan kapal penangkapan yang terbuat dari kayu berukuran 50 sampai dengan 80 GT. Daerah penangkapan di sekitar lokasi rumpon di Laut Sulawesi dan Laut Maluku. Hasil tangkapan yang diperoleh terdiri atas cakalang (Katsuwonus pelamis), madidihang (Thunnus albacares), baby tuna (Thunnus spp.), dan tongkol (Auxis spp.) serta hasil tangkapan sampingan yaitu lemadang (Coryphaena hippurus) dan sunglir (Elagatis bipinnulatus). Hasil analisis catch per unit of effort diperoleh bahwa nilai catch per unit of effort baby tuna (Thunnus spp.) mengalami kenaikan pada bulan Agustus 2004, dan cakalang (Katsuwonus pelamis) mengalami kenaikan pada bulan September 2004. Hasil analisis terhadap ukuran pertama kali cakalang (Katsuwonus pelamis) tertangkap oleh huhate 49,3 FLcm. Ukuran ini lebih panjang dibandingkan ukuran pertama kali cakalang (Katsuwonus pelamis) matang gonad. Sedangkan hasil analisis terhadap ukuran pertama kali madidihang (Thunnus albacares) tertangkap oleh huhate 51,6 FLcm. Ukuran ini lebih pendek dibandingkan ukuran pertama kali madidihang (Thunnus albacares) matang gonad. This paper presents the status of pole and line fishery in Bitung of North Sulawesi, consisting of description of fishing gear, fishing ground, catch composition, catch per unit of effort, and length at first capture. Data were collected during the period of 2004 until 2005. Results show that the pole and line in Bitung operated by wooden vessels of 50 until 80 GT. The fishing grounds were the waters around FADs location in Sulawesi Sea and Maluku Sea. Catch composition consists of skipjack tuna (Katsuwonus pelamis), yellow fin tuna (Thunnus albacares), baby tuna (Thunnus spp.), and frigate tuna (Auxis spp.), while the bycatch consisted of dolphinfish (Coryphaena hippurus) and rainbow runner (Elagatis bipinnulatus). Catch per unit of effort analysis shows that catch per unit of effort value of baby tuna (Thunnus spp.) increased on August 2004, whereas catch per unit of effort value of skipjack tuna (Katsuwonus pelamis) increased on September 2004. The length at first capture of skipjack tuna (Katsuwonus pelamis) was 49,3 FLcm. The catch size was bigger than the length at first maturity for skipjack tuna (Katsuwonus pelamis). The length at first capture of yellowfin tuna (Thunnus albacares) was 51,6 FLcm. This catch size was smaller than the length at first maturity for yellowfin tuna (Thunnus albacares).


1992 ◽  
Vol 70 (4) ◽  
pp. 654-662 ◽  
Author(s):  
Richard W. Brill ◽  
Peter G. Bushnell ◽  
David R. Jones ◽  
Manabu Shimizu

In most fishes, blood acid–base regulation following a temperature change involves active adjustments of gill ion-exchange rates which take hours or days to complete. Previous studies have shown that isolated blood from skipjack tuna, Katsuwonus pelamis, and albacore, Thunnus alalunga, had rates of pH change with temperature (in the open system) equivalent to those necessary to retain net protein charge in vivo (≈ −0.016 ΔpH∙ °C−1). It was postulated that this is due to protons leaving the hemoglobin combining with plasma bicarbonate [Formula: see text], which is removed as gaseous CO2, and that this ability evolved so that tunas need not adjust gill ion-exchange rates to regulate blood pH appropriately following ambient temperature changes. We reexamined this phenomenon using blood and separated plasma from yellowfin tuna, Thunnus albacares. Unlike previous studies, our CO2 levels (0.5 and 1.5% CO2) span those seen in yellowfin tuna arterial and venous blood. Various bicarbonate concentrations [Formula: see text] were obtained by collecting blood from fully rested as well as vigorously exercised fish. We use our in vitro data to calculate basic physiochemical parameters for yellowfin tuna blood: nonbicarbonate buffering (β), the apparent first dissociation constant of carbonic acid (pKapp), and CO2 solubility (αCO2). We also determined the effects of acute temperature change on arterial pH, [Formula: see text], and partial pressures of O2 and CO2in vivo. The pH shift of yellowfin tuna blood subjected to a closed-system temperature change did not differ from previous studies of other teleosts (≈ −0.016 ΔpH∙ °C−1). The pH shift in blood subjected to open-system temperature change was Pco2 dependent and lower than that in skipjack tuna or albacore blood in vitro, but identical with that seen in yellowfin tuna blood in vivo. However, pH adjustments in vivo were caused by changes in both [Formula: see text] and Pco2. The exact mechanisms responsible for these changes remain to be elucidated.


2021 ◽  
Vol 944 (1) ◽  
pp. 012009
Author(s):  
I Ayuningtias ◽  
I Jaya ◽  
M Iqbal

Abstract Yellowfin tuna (Thunnus albacares), mackerel tuna (Euthynnus affinis), and skipjack tuna (Katsuwonus pelamis) have important economic values for the capture fisheries in Indonesia. Activities of identifying these fish and other types of tuna have been done manually, which can lead to errors and ultimately affect statistics, stock estimates, or traceability. The aim of this research is to use deep learning methods in identifying three species of tuna, specifically yellowfin tuna, mackerel tuna, and skipjack tuna. YOLO’s newest model, YOLOv5, was used to identify the fish. The number of epochs that produces the optimum accuracy value for use in the YOLOv5 model is 400. The values for training loss, accuracy, precision, recall and F1-Score when the model is learning with a total of 400 epochs are 0.000253, 95%, 98.1%, 93.9%, and 96%. Based on these results, the three species of tuna can be identified with high accuracy.


1984 ◽  
Vol 30 (10) ◽  
pp. 1646-1651 ◽  
Author(s):  
O Siggaard-Andersen ◽  
P D Wimberley ◽  
I Göthgen ◽  
M Siggaard-Andersen

Abstract A mathematical model is described giving the oxygen saturation fraction (s) as a function of the oxygen partial pressure (p): y - y0 = x - x0 + h X tanh [k X (x - x0)], where y = kn[s/(1-s)] and x = ln(p/kPa). The parameters are: y0 = 1.875; x0 = 1.946 + a + b; h = 3.5 + a; k = 0.5343; b = 0.055 X [T/(K - 310.15)]; a = 1.04 X (7.4 - pH) + 0.005 X Cbase/(mmol/L) + 0.07 X [[CDPG/(mmol/L)] - 5], where Cbase is the base excess of the blood and CDPG is the concentration of 2,3-diphosphoglycerate in the erythrocytes. The Hill slope, n = dy/dx, is given by n = 1 + h X k X [1 - tanh2[k X (x - x0)]]. n attains a maximum of 2.87 for x = x0, and n----1 for x----+/- infinity. The model gives a very good fit to the Severinghaus standard oxygen dissociation curve and the parameters may easily be fitted to other oxygen dissociation curves as well. Applications of the model are described including the solution of the inverse function (p as a function of s) by a Newton-Raphson iteration method. The po2-temperature coefficient is given by dlnp/dT = [A X alpha X p + CHb X n X S X (1 - s) X B]/[alpha X p + CHB X n X s X (1 - s)], where A = -dln alpha/dT approximately equal to 0.012 K-1; B = (lnp/T)s = 0.073 K-1 for y = y0; alpha = the solubility coefficient of O2 in blood = 0.0105 mmol X L-1 X kPa-1 at 37 degrees C; CHb = concentration of hemoglobin iron in the blood. Approximate equations currently in use do not take the variations of the po2-temperature coefficient with p50 and CHb into account.


1995 ◽  
Vol 73 (9) ◽  
pp. 1681-1688 ◽  
Author(s):  
John E. Keen ◽  
Richard W. Brill ◽  
Sumi Aota ◽  
Anthony P. Farrell ◽  
David J. Randall

Tonic cholinergic and adrenergic control of heart rate and ventral aorta pressure was examined in two species of tropical tunas, the skipjack tuna (Katsuwonus pelamis) and the yellowfin tuna (Thunnus albacares). Unlike that of many other teleosts, the basal heart rate in spinally blocked tunas (at 25 °C) was dominated by a cholinergic rather than an adrenergic tonus. Infusion of atropine increased the heart rate by 143 and 58% in skipjack and yellowfin tunas, respectively. Ventral aortic pulse pressure was significantly decreased and mean ventral aortic pressure was slightly increased. Blockade of β-adrenergic receptors with propranolol produced small (<6%) decreases in both heart rate and mean ventral aortic pressure, indicating a low level of tonic β-adrenergic stimulation. The small magnitude of the drop, however, suggests that tonic adrenergic regulation of heart rate and pressure is of less importance in tunas than in other teleosts, despite comparable circulating levels of adrenaline and noradrenaline. The α-adrenergic blocker phentolamine did not affect either heart rate or pressure. The intrinsic heart rate (i.e., the heart rate in the absence of cholinergic or adrenergic stimulation) was 180 beats/min in skipjack tuna and 119 beats/min in yellowfin tuna; these are the highest reported values for any teleost to date.


DEPIK ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 167-173
Author(s):  
M.A. Chaliluddin ◽  
Rizka Alfita ◽  
Thaib Rizwan ◽  
Rahmat Rizqi ◽  
Rosi Rahayu ◽  
...  

Large pelagic fish live on the water surface in groups. Skipjack tuna (Katsuwonus pelamis), yellowfin tuna (Thunnus albacares), mackerel tuna (Euthynnus affinis), mackerel (Scomberomous guttatus) are species of fishes that mainly catches by fishermen using purse seines. This study aims to determine the length and weight of large pelagic fish in the water of Idi Rayeuk and best the fishing season. This research was conducted in one month. Fish samples were collected from fishermen that used purse seine and landed their catches at the Idi Rayeuk Fishing Port, East Aceh. Additionally, the data was derived from the fishing port time-series during 2015 to 2019. The result showed that the yellowfin tuna (Thunnus albacares) has a length between 37 - 58 cm with a weight of 1.0 - 3.2 kg, skipjack tuna (Katsuwonus pelamis) 32 - 58 cm in length and weight 0.5 - 3.0 kg, mackerel tuna has 33 - 54 cm of length with a weight of 0.6 - 2.5 kg, and mackerel has 44 - 66 cm of length and weighing 0.7 - 1.7 kg. Its also found that the peak season for catching yellowfin tuna (Thunnus albacares) and mackerel tuna is May and June, and the lowest season in December for the yellowfin tuna, and December and January for the mackerel tuna. The peak season for skipjack fishing occurs in May, August, and October, and the low season occurs in November and December. Meanwhile, the peak season for fishing mackerel occurs in May, September, and October, while the low season occurs in January, February, and March.Keywords:Fishing seasonLarge pelagicPurse seineIdi RayeukAceh


Sign in / Sign up

Export Citation Format

Share Document